PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
11076105-7	2000	Multivariable linear regression analysis yielded three significant predictors of PTH: calcium, phosphorus, and vintage (5.8% (4.0-7.5%) expected increase in PTH per year of vintage).	Phosphorus	95-105	parathyroid hormone	Homo sapiens	81-84
12089954-3	2000	PTH synthesis is mainly controlled by changes in calcium-phosphorus balance and calcitriol production by the kidneys.	Phosphorus	57-67	parathyroid hormone	Homo sapiens	0-3
10801911-2	2000	Recent studies in mature (3-4 mo) rats demonstrated that insulin-like growth factor-I (IGF-I) restored stimulation of renal 1,25-dihydroxycholecalciferol [1,25(OH)(2)D(3)] production by low phosphorus diet (LPD), another major stimulus of 1-OHase.	Phosphorus	190-200	insulin-like growth factor 1	Rattus norvegicus	57-85
10945855-2	2000	We demonstrate that p-fluorofentanyl more potently activates GIRK1/GIRK2 channels through opioid receptors than fentanyl and that the p-fluoro substitution also changes the potency profile from mu > kappa > delta (fentanyl) to mu > delta > or = kappa (p-fluorofentanyl).	Phosphorus	20-21	potassium inwardly rectifying channel subfamily J member 3	Homo sapiens	61-66
10945855-2	2000	We demonstrate that p-fluorofentanyl more potently activates GIRK1/GIRK2 channels through opioid receptors than fentanyl and that the p-fluoro substitution also changes the potency profile from mu > kappa > delta (fentanyl) to mu > delta > or = kappa (p-fluorofentanyl).	Phosphorus	20-21	potassium inwardly rectifying channel subfamily J member 6	Homo sapiens	67-72
10990401-1	2000	An enantiomeric excess of up to 94% was obtained using 0.5% Cu(OTf)2 and 1% of chiral trivalent phosphorus ligand.	Phosphorus	96-106	POU class 2 homeobox 2	Homo sapiens	63-74
10861245-5	2000	Therefore we generated a model of the PH domain of GAP1(IP4BP) in complex with Ins(1,3,4,5)P(4) based on the Btk-Ins(1,3,4,5)P(4) complex crystal structure.	Phosphorus	38-39	RAS p21 protein activator 3	Homo sapiens	51-61
10861245-5	2000	Therefore we generated a model of the PH domain of GAP1(IP4BP) in complex with Ins(1,3,4,5)P(4) based on the Btk-Ins(1,3,4,5)P(4) complex crystal structure.	Phosphorus	38-39	Bruton tyrosine kinase	Homo sapiens	109-112
12089922-3	2000	PTH synthesis is mainly controlled by changes in calcium-phosphorus balance and calcitriol production by the kidneys.	Phosphorus	57-67	parathyroid hormone	Homo sapiens	0-3
11832092-4	2000	In the tissues, apoptotic cells were examined by TUNEL method, and the expression of PCNA was examined by S-P staining.	Phosphorus	106-109	proliferating cell nuclear antigen	Homo sapiens	85-89
10896239-8	2000	Upregulation of LPS-induced TF activity but not the antigen by platelets in the presence of granulocytes suggests that the increased TF activity could be the result of PS enrichment of monocytes by fusion or platelets with activated monocytes.	Phosphorus	17-19	coagulation factor III, tissue factor	Homo sapiens	28-30
10896239-8	2000	Upregulation of LPS-induced TF activity but not the antigen by platelets in the presence of granulocytes suggests that the increased TF activity could be the result of PS enrichment of monocytes by fusion or platelets with activated monocytes.	Phosphorus	17-19	coagulation factor III, tissue factor	Homo sapiens	133-135
10787443-3	2000	After exhaustive extraction of lipids, apoB of native LDL contained 4 +/- 3 moles of phosphorus/mole protein.	Phosphorus	85-95	apolipoprotein B	Homo sapiens	39-43
10787443-4	2000	In contrast, apoB of OxLDL contained approximately 75 moles of phosphorus/mole protein.	Phosphorus	63-73	apolipoprotein B	Homo sapiens	13-17
10787443-5	2000	Saponification of this apoB released phosphorus, choline, and saturated fatty acids in a molar ratio of 1.0:0.98:0.84.	Phosphorus	37-47	apolipoprotein B	Homo sapiens	23-27
10917452-6	2000	The beta-glycosidic carbohydrate template (Nbeta-Fmoc-3Ala)4-beta-D-Galp-(1-O)-MBA-OPfp thus obtained was coupled to a PAL-PEG-PS resin and simultaneously extended at the four arms to yield, after cleavage from the solid support, a carbopeptide with four identical peptide strands.	Phosphorus	127-129	galanin like peptide	Homo sapiens	68-72
10821578-0	2000	Milk production, reproductive performance, and fecal excretion of phosphorus by dairy cows fed three amounts of phosphorus.	Phosphorus	112-122	Weaning weight-maternal milk	Bos taurus	0-4
10821580-0	2000	Milk production and reproductive performance of dairy cows fed two concentrations of phosphorus for two years.	Phosphorus	85-95	Weaning weight-maternal milk	Bos taurus	0-4
10801911-2	2000	Recent studies in mature (3-4 mo) rats demonstrated that insulin-like growth factor-I (IGF-I) restored stimulation of renal 1,25-dihydroxycholecalciferol [1,25(OH)(2)D(3)] production by low phosphorus diet (LPD), another major stimulus of 1-OHase.	Phosphorus	190-200	insulin-like growth factor 1	Rattus norvegicus	87-92
10927882-6	2000	Calcium and phosphorus contents in the bone and serum levels of parathyroid hormone and osteocalcin were not significantly different between Cd-treated and control rats.	Phosphorus	12-22	bone gamma-carboxyglutamate protein	Rattus norvegicus	88-99
10917001-14	2000	Patients with PTH equal or lower than 60 have serum Ca levels significantly higher than the remaining patients, on the contrary, serum P, Ca-P product and Al levels were significantly lower.	Phosphorus	0-1	parathyroid hormone	Homo sapiens	14-17
10917001-18	2000	Patients on haemodialysis showed serum Ca, P, PTH and Al levels higher than patients on peritoneal dialysis.	Phosphorus	0-1	parathyroid hormone	Homo sapiens	46-49
10750035-10	2000	Therefore we conclude that (33)P-labelled probes are preferred for detection of mRNAs encoding PGHS-2 in ovine uterine tissues.	Phosphorus	31-32	prostaglandin G/H synthase 2	Ovis aries	95-101
10783050-1	2000	The effect of angiotensin converting enzyme (ACE) inhibitor, temocaprilat and/or angiotensin II type 1 (AT1) receptor antagonist, CV-11974 on myocardial metabolism and contraction during ischemia and reperfusion was examined by phosphorus 31-nuclear magnetic resonance (31P-NMR) in Langendorff rabbit hearts.	Phosphorus	228-238	type-1 angiotensin II receptor	Oryctolagus cuniculus	81-117
10782830-8	2000	The concentration of Ca and P and their ratio increased inside the ALP-rich MV in relation to the proximity to subchondral bone.	Phosphorus	28-29	alkaline phosphatase, placental	Homo sapiens	67-70
10656319-4	2000	NaF (1.3% by weight in the mixed cement) was added to the powder components of a glass ionomer based on LG30 glass (which contains Al, Si, Ca, P, and O only).	Phosphorus	143-144	C-X-C motif chemokine ligand 8	Homo sapiens	0-3
10702277-3	2000	However, most reported PTP inhibitors have been phosphorus-containing compounds, tight binding inhibitors, and/or inhibitors that covalently modify the enzymes.	Phosphorus	48-58	protein tyrosine phosphatase receptor type U	Homo sapiens	23-26
10853197-7	2000	Dietary phosphorus restriction resulted in a significant decrease in PTH levels and a significant increase in serum calcitriol concentrations.	Phosphorus	8-18	parathyroid hormone	Homo sapiens	69-72
10617616-9	2000	Our data suggest a previously unrecognized chaperone-dependent pathway involving the sequential actions of Hsp70 and Hsp90/Cdc37 in the stabilization/folding of Cdk9 as well as the assembly of an active Cdk9/cyclin T1 complex responsible for P-TEFb-mediated Tat transactivation.	Phosphorus	242-243	cell division cycle 37, HSP90 cochaperone	Homo sapiens	123-128
10639156-8	2000	Likewise, topical application of B[a]P (200 microg) at weekly intervals to the skin of female mice for 25 weeks produced skin tumors only in the AhR-positive mice.	Phosphorus	37-38	aryl-hydrocarbon receptor	Mus musculus	145-148
10672034-1	2000	Complexes of the HMG box protein SRY with two duplexes of 8 and 14 base pairs have been studied by 31P NMR and complete assignment of all phosphorus signals of the bound DNA duplexes are presented.	Phosphorus	138-148	sex determining region Y	Homo sapiens	33-36
10617616-9	2000	Our data suggest a previously unrecognized chaperone-dependent pathway involving the sequential actions of Hsp70 and Hsp90/Cdc37 in the stabilization/folding of Cdk9 as well as the assembly of an active Cdk9/cyclin T1 complex responsible for P-TEFb-mediated Tat transactivation.	Phosphorus	242-243	heat shock protein family A (Hsp70) member 4	Homo sapiens	107-112
10617616-9	2000	Our data suggest a previously unrecognized chaperone-dependent pathway involving the sequential actions of Hsp70 and Hsp90/Cdc37 in the stabilization/folding of Cdk9 as well as the assembly of an active Cdk9/cyclin T1 complex responsible for P-TEFb-mediated Tat transactivation.	Phosphorus	242-243	heat shock protein 90 alpha family class A member 1	Homo sapiens	117-122
10617616-9	2000	Our data suggest a previously unrecognized chaperone-dependent pathway involving the sequential actions of Hsp70 and Hsp90/Cdc37 in the stabilization/folding of Cdk9 as well as the assembly of an active Cdk9/cyclin T1 complex responsible for P-TEFb-mediated Tat transactivation.	Phosphorus	242-243	cyclin dependent kinase 9	Homo sapiens	161-165
10617616-9	2000	Our data suggest a previously unrecognized chaperone-dependent pathway involving the sequential actions of Hsp70 and Hsp90/Cdc37 in the stabilization/folding of Cdk9 as well as the assembly of an active Cdk9/cyclin T1 complex responsible for P-TEFb-mediated Tat transactivation.	Phosphorus	242-243	cyclin dependent kinase 9	Homo sapiens	203-207
10617616-9	2000	Our data suggest a previously unrecognized chaperone-dependent pathway involving the sequential actions of Hsp70 and Hsp90/Cdc37 in the stabilization/folding of Cdk9 as well as the assembly of an active Cdk9/cyclin T1 complex responsible for P-TEFb-mediated Tat transactivation.	Phosphorus	242-243	cyclin T1	Homo sapiens	208-217
11216506-0	2000	High phosphorus feeding decreases the expression of renal PTH/PTHRP-receptor mRNA in rats.	Phosphorus	5-15	parathyroid hormone	Rattus norvegicus	58-61
11216506-1	2000	Dietary intake of high phosphorus (P) is well-described to increase serum levels of PTH, however, how this increased serum PTH affects the PTH actions in major target tissues, particularly in kidney, remains uncovered.	Phosphorus	23-33	parathyroid hormone	Rattus norvegicus	84-87
11216506-1	2000	Dietary intake of high phosphorus (P) is well-described to increase serum levels of PTH, however, how this increased serum PTH affects the PTH actions in major target tissues, particularly in kidney, remains uncovered.	Phosphorus	23-33	parathyroid hormone	Rattus norvegicus	123-126
11216506-1	2000	Dietary intake of high phosphorus (P) is well-described to increase serum levels of PTH, however, how this increased serum PTH affects the PTH actions in major target tissues, particularly in kidney, remains uncovered.	Phosphorus	23-33	parathyroid hormone	Rattus norvegicus	123-126
11095097-5	2000	The double staining for actin and PS exposure, quantitatively analysed by flow cytometry in HL-60 cells after different treatment times, demonstrated that the decrease of Annexin V binding in the late stages of apoptosis is associated with the strong reduction of actin labelling probably also due to a proteolytic cleavage.	Phosphorus	34-36	annexin A5	Homo sapiens	171-180
10611385-0	1999	Psr1, a nuclear localized protein that regulates phosphorus metabolism in Chlamydomonas.	Phosphorus	49-59	uncharacterized protein	Chlamydomonas reinhardtii	0-4
11052464-6	2000	On the other hand, urinary excretion of phosphorus (u-P/GF) after CAC load decreased to 60.0% +/- 32.4% (P < 0.01) and that in the BEC group showed no significant change (92.5% +/- 49.5%).	Phosphorus	40-50	carbonic anhydrase 2	Homo sapiens	66-69
10674850-4	2000	The serum phosphorus and magnesium concentrations decreased to nadirs of 1.6 mg/dl and 1.6 mg/dl respectively 7 hours after insulin injection.	Phosphorus	10-20	insulin	Homo sapiens	124-131
10611385-2	1999	Here we describe a gene encoding a regulator of phosphorus metabolism, designated Psr1 (phosphorus starvation response), from a photosynthetic eukaryote.	Phosphorus	48-58	uncharacterized protein	Chlamydomonas reinhardtii	82-86
10611385-2	1999	Here we describe a gene encoding a regulator of phosphorus metabolism, designated Psr1 (phosphorus starvation response), from a photosynthetic eukaryote.	Phosphorus	88-98	uncharacterized protein	Chlamydomonas reinhardtii	82-86
10611385-3	1999	The Psr1 protein is critical for acclimation of the unicellular green alga Chlamydomonas reinhardtii to phosphorus starvation.	Phosphorus	104-114	uncharacterized protein	Chlamydomonas reinhardtii	4-8
10611385-5	1999	The level of Psr1 increases at least 10-fold upon phosphate starvation, and immunocytochemical studies demonstrate that this protein is nuclear-localized under both nutrient-replete and phosphorus-starvation conditions.	Phosphorus	186-196	uncharacterized protein	Chlamydomonas reinhardtii	13-17
10611385-6	1999	Finally, Psr1 and angiosperm proteins have domains that are similar, suggesting a possible role for Psr1 homologs in the control of phosphorus metabolism in vascular plants.	Phosphorus	132-142	uncharacterized protein	Chlamydomonas reinhardtii	9-13
10611385-6	1999	Finally, Psr1 and angiosperm proteins have domains that are similar, suggesting a possible role for Psr1 homologs in the control of phosphorus metabolism in vascular plants.	Phosphorus	132-142	uncharacterized protein	Chlamydomonas reinhardtii	100-104
10611385-7	1999	With the identification of regulators such as Psr1 it may become possible to engineer photosynthetic organisms for more efficient utilization of phosphorus and to establish better practices for the management of agricultural lands and natural ecosystems.	Phosphorus	145-155	uncharacterized protein	Chlamydomonas reinhardtii	46-50
10619932-8	1999	Midterm clinical effectiveness of PC P/P includes the requisite lowering of the erythropoietin dose and improvement in skin pigmentation.	Phosphorus	34-35	erythropoietin	Homo sapiens	80-94
10602225-0	1999	Experimental Evidence for the Existence of Neutral P(6): A New Allotrope of Phosphorus.	Phosphorus	76-86	S100 calcium binding protein A12	Homo sapiens	51-55
10602225-1	1999	High-energy collisions of Cp*P(6)(+) cations yield neutral P(6) molecules (see reaction), thus providing the first experimental evidence for the existence of this new allotrope of phosphorus.	Phosphorus	180-190	S100 calcium binding protein A12	Homo sapiens	29-33
10602225-1	1999	High-energy collisions of Cp*P(6)(+) cations yield neutral P(6) molecules (see reaction), thus providing the first experimental evidence for the existence of this new allotrope of phosphorus.	Phosphorus	180-190	S100 calcium binding protein A12	Homo sapiens	59-63
10599719-6	1999	Compared with no HRT, the breast epithelium of women who had received either E+P or E alone had significantly higher PCNA proliferation indices, and treatment with E+P had a significantly higher index (PCNA and Ki67) than treatment with E alone.	Phosphorus	79-80	proliferating cell nuclear antigen	Homo sapiens	117-121
33862859-0	1999	A Lycopersicon esculentum phosphate transporter (LePT1) involved in phosphorus uptake from a vesicular-arbuscular mycorrhizal fungus.	Phosphorus	68-78	phosphate transporter 1	Solanum lycopersicum	49-54
10633458-6	1999	Phosphorus induces hyperplasia of the parathyroid glands independent of calcium and calcitriol, and by a post-transcriptional mechanism increases PTH synthesis and secretion.	Phosphorus	0-10	parathyroid hormone	Homo sapiens	146-149
10633458-8	1999	If the diet is then reduced in phosphorus, the levels of PTH return to normal.	Phosphorus	31-41	parathyroid hormone	Homo sapiens	57-60
10542201-1	1999	The Na/K-ATPase has been shown to bind 1 and 0.5 mol of (32)P/mol of alpha-chain in the presence [gamma-(32)P]ATP and [alpha-(32)P]ATP, respectively, accompanied by a maximum accumulation of 0.5 mol of ADP-sensitive phosphoenzyme (NaE1P) and potassium-sensitive phosphoenzyme (E2P).	Phosphorus	59-61	Fc gamma receptor and transporter	Homo sapiens	69-80
10596962-0	1999	Impaired parathyroid hormone action on urinary phosphorus excretion in isolated perfused kidney of streptozotocin-induced diabetic rats.	Phosphorus	47-57	parathyroid hormone	Rattus norvegicus	9-28
10654293-8	1999	Phosphorus NMR spectroscopy shows that phosphatidylcholine, phosphatidylinositol, sphingomyelin, and phosphatidylserine increase steadily from F15 to P21.	Phosphorus	0-10	cyclin-dependent kinase inhibitor 1A (P21)	Mus musculus	150-153
10596962-5	1999	In the control rat kidney, the addition of PTH increased urinary cAMP excretion from 8 +/- 3 to 190 +/- 49 pmol/5 min and urinary phosphorus excretion from 11.3 +/- 4.4 to 33.6 +/- 10.8 microg/5 min.	Phosphorus	130-140	parathyroid hormone	Rattus norvegicus	43-46
10500204-6	1999	Using phosphorus magnetic resonance spectroscopy we demonstrated a maximum rate of muscle mitochondrial ATP production (V(max)) below the normal range in all 12 FRDA patients and a strong negative correlation between mitochondrial V(max) and the number of GAA repeats in the smaller allele.	Phosphorus	6-16	frataxin	Homo sapiens	161-165
10683811-5	1999	In rats fed Na5P3O10 or K5P3O10, urinary albumin excretion and N-acetyl-beta-D-glucosaminidase (NAG) activity in the urine were increased in rats fed the high phosphorus diet.	Phosphorus	159-169	O-GlcNAcase	Rattus norvegicus	63-94
10683811-5	1999	In rats fed Na5P3O10 or K5P3O10, urinary albumin excretion and N-acetyl-beta-D-glucosaminidase (NAG) activity in the urine were increased in rats fed the high phosphorus diet.	Phosphorus	159-169	O-GlcNAcase	Rattus norvegicus	96-99
15348109-5	1999	Immersion of HA/G1 and HA coatings in culture medium resulted in significant alterations to the levels of calcium and phosphorus in the medium, leading to surface modifications.	Phosphorus	118-128	thioredoxin domain containing 12	Homo sapiens	13-18
10495131-13	1999	IN CONCLUSION: (1) uremia and phosphorus each had separate and major effects on skeletal resistance to PTH; (2) skeletal resistance to PTH was an important cause of secondary hyperparathyroidism, even in moderate renal failure; (3) during PTH infusion, the dynamics of skeletal resistance to PTH changed because all groups received a low phosphorus diet, and the adaptation to a new steady state was delayed by the degree of renal failure and the previous dietary phosphorus burden; and (4) normal serum phosphorus may not be indicative of body phosphorus stores during states of disequilibrium.	Phosphorus	338-348	parathyroid hormone	Rattus norvegicus	135-138
10495131-13	1999	IN CONCLUSION: (1) uremia and phosphorus each had separate and major effects on skeletal resistance to PTH; (2) skeletal resistance to PTH was an important cause of secondary hyperparathyroidism, even in moderate renal failure; (3) during PTH infusion, the dynamics of skeletal resistance to PTH changed because all groups received a low phosphorus diet, and the adaptation to a new steady state was delayed by the degree of renal failure and the previous dietary phosphorus burden; and (4) normal serum phosphorus may not be indicative of body phosphorus stores during states of disequilibrium.	Phosphorus	338-348	parathyroid hormone	Rattus norvegicus	135-138
10495131-13	1999	IN CONCLUSION: (1) uremia and phosphorus each had separate and major effects on skeletal resistance to PTH; (2) skeletal resistance to PTH was an important cause of secondary hyperparathyroidism, even in moderate renal failure; (3) during PTH infusion, the dynamics of skeletal resistance to PTH changed because all groups received a low phosphorus diet, and the adaptation to a new steady state was delayed by the degree of renal failure and the previous dietary phosphorus burden; and (4) normal serum phosphorus may not be indicative of body phosphorus stores during states of disequilibrium.	Phosphorus	338-348	parathyroid hormone	Rattus norvegicus	135-138
10495131-13	1999	IN CONCLUSION: (1) uremia and phosphorus each had separate and major effects on skeletal resistance to PTH; (2) skeletal resistance to PTH was an important cause of secondary hyperparathyroidism, even in moderate renal failure; (3) during PTH infusion, the dynamics of skeletal resistance to PTH changed because all groups received a low phosphorus diet, and the adaptation to a new steady state was delayed by the degree of renal failure and the previous dietary phosphorus burden; and (4) normal serum phosphorus may not be indicative of body phosphorus stores during states of disequilibrium.	Phosphorus	338-348	parathyroid hormone	Rattus norvegicus	135-138
10495131-13	1999	IN CONCLUSION: (1) uremia and phosphorus each had separate and major effects on skeletal resistance to PTH; (2) skeletal resistance to PTH was an important cause of secondary hyperparathyroidism, even in moderate renal failure; (3) during PTH infusion, the dynamics of skeletal resistance to PTH changed because all groups received a low phosphorus diet, and the adaptation to a new steady state was delayed by the degree of renal failure and the previous dietary phosphorus burden; and (4) normal serum phosphorus may not be indicative of body phosphorus stores during states of disequilibrium.	Phosphorus	338-348	parathyroid hormone	Rattus norvegicus	135-138
10495131-13	1999	IN CONCLUSION: (1) uremia and phosphorus each had separate and major effects on skeletal resistance to PTH; (2) skeletal resistance to PTH was an important cause of secondary hyperparathyroidism, even in moderate renal failure; (3) during PTH infusion, the dynamics of skeletal resistance to PTH changed because all groups received a low phosphorus diet, and the adaptation to a new steady state was delayed by the degree of renal failure and the previous dietary phosphorus burden; and (4) normal serum phosphorus may not be indicative of body phosphorus stores during states of disequilibrium.	Phosphorus	338-348	parathyroid hormone	Rattus norvegicus	135-138
10495131-13	1999	IN CONCLUSION: (1) uremia and phosphorus each had separate and major effects on skeletal resistance to PTH; (2) skeletal resistance to PTH was an important cause of secondary hyperparathyroidism, even in moderate renal failure; (3) during PTH infusion, the dynamics of skeletal resistance to PTH changed because all groups received a low phosphorus diet, and the adaptation to a new steady state was delayed by the degree of renal failure and the previous dietary phosphorus burden; and (4) normal serum phosphorus may not be indicative of body phosphorus stores during states of disequilibrium.	Phosphorus	30-40	parathyroid hormone	Rattus norvegicus	103-106
10495131-13	1999	IN CONCLUSION: (1) uremia and phosphorus each had separate and major effects on skeletal resistance to PTH; (2) skeletal resistance to PTH was an important cause of secondary hyperparathyroidism, even in moderate renal failure; (3) during PTH infusion, the dynamics of skeletal resistance to PTH changed because all groups received a low phosphorus diet, and the adaptation to a new steady state was delayed by the degree of renal failure and the previous dietary phosphorus burden; and (4) normal serum phosphorus may not be indicative of body phosphorus stores during states of disequilibrium.	Phosphorus	338-348	parathyroid hormone	Rattus norvegicus	135-138
10495131-13	1999	IN CONCLUSION: (1) uremia and phosphorus each had separate and major effects on skeletal resistance to PTH; (2) skeletal resistance to PTH was an important cause of secondary hyperparathyroidism, even in moderate renal failure; (3) during PTH infusion, the dynamics of skeletal resistance to PTH changed because all groups received a low phosphorus diet, and the adaptation to a new steady state was delayed by the degree of renal failure and the previous dietary phosphorus burden; and (4) normal serum phosphorus may not be indicative of body phosphorus stores during states of disequilibrium.	Phosphorus	338-348	parathyroid hormone	Rattus norvegicus	135-138
10495131-13	1999	IN CONCLUSION: (1) uremia and phosphorus each had separate and major effects on skeletal resistance to PTH; (2) skeletal resistance to PTH was an important cause of secondary hyperparathyroidism, even in moderate renal failure; (3) during PTH infusion, the dynamics of skeletal resistance to PTH changed because all groups received a low phosphorus diet, and the adaptation to a new steady state was delayed by the degree of renal failure and the previous dietary phosphorus burden; and (4) normal serum phosphorus may not be indicative of body phosphorus stores during states of disequilibrium.	Phosphorus	338-348	parathyroid hormone	Rattus norvegicus	135-138
10495131-13	1999	IN CONCLUSION: (1) uremia and phosphorus each had separate and major effects on skeletal resistance to PTH; (2) skeletal resistance to PTH was an important cause of secondary hyperparathyroidism, even in moderate renal failure; (3) during PTH infusion, the dynamics of skeletal resistance to PTH changed because all groups received a low phosphorus diet, and the adaptation to a new steady state was delayed by the degree of renal failure and the previous dietary phosphorus burden; and (4) normal serum phosphorus may not be indicative of body phosphorus stores during states of disequilibrium.	Phosphorus	338-348	parathyroid hormone	Rattus norvegicus	135-138
10495131-13	1999	IN CONCLUSION: (1) uremia and phosphorus each had separate and major effects on skeletal resistance to PTH; (2) skeletal resistance to PTH was an important cause of secondary hyperparathyroidism, even in moderate renal failure; (3) during PTH infusion, the dynamics of skeletal resistance to PTH changed because all groups received a low phosphorus diet, and the adaptation to a new steady state was delayed by the degree of renal failure and the previous dietary phosphorus burden; and (4) normal serum phosphorus may not be indicative of body phosphorus stores during states of disequilibrium.	Phosphorus	338-348	parathyroid hormone	Rattus norvegicus	135-138
10495131-13	1999	IN CONCLUSION: (1) uremia and phosphorus each had separate and major effects on skeletal resistance to PTH; (2) skeletal resistance to PTH was an important cause of secondary hyperparathyroidism, even in moderate renal failure; (3) during PTH infusion, the dynamics of skeletal resistance to PTH changed because all groups received a low phosphorus diet, and the adaptation to a new steady state was delayed by the degree of renal failure and the previous dietary phosphorus burden; and (4) normal serum phosphorus may not be indicative of body phosphorus stores during states of disequilibrium.	Phosphorus	338-348	parathyroid hormone	Rattus norvegicus	135-138
10472841-0	1999	A bioassay to determine the effect of phytase on phytate phosphorus hydrolysis and total phosphorus retention of feed ingredients as determined with broilers and laying hens.	Phosphorus	57-67	phytase	Zea mays	38-45
11379859-16	1999	After controlling for the effect of other variables by partial correlation analysis, a significant positive association between P and PTH (r= 0.25, p < 0.05), and a negative relationship between Mg and PTH (r= -0.57, p < 0.001) were evident.	Phosphorus	128-129	parathyroid hormone	Homo sapiens	134-137
10454642-2	1999	This replacement confers chirality to the phosphorus atom (PSS or PSR) and alters the energetic, structural and biological properties of B-DNA.	Phosphorus	42-52	PSS	Homo sapiens	59-62
10472841-5	1999	The addition of phytase increased total phosphorus retention from 34.8, 27.0, 16.0, 31.9, 40.3, 15.5, and 39.4% to 40.9, 58.0, 33.8, 43.4, 55.5, 26.5, and 45.7%, respectively.	Phosphorus	40-50	phytase	Zea mays	16-23
10461992-2	1999	The efficacy of phytase in releasing phytate-bound Fe and P from soybean meal in vitro and in improving dietary Fe bioavailability for hemoglobin repletion in young, anemic pigs was examined.	Phosphorus	58-59	putative glycerophosphoryl diester phosphodiesterase	Glycine max	16-23
10472841-8	1999	Total phosphorus retention of soybean meal, corn, and rice bran increased from 36.8, 28.6, and 35.9% to 53.4, 44.7, and 43.0%, respectively, with the addition of phytase.	Phosphorus	6-16	phytase	Zea mays	162-169
10791913-4	1999	Thus, FAD-linked mutations in PS exacerbate the production of Abeta42, the readily aggregable Abeta species corresponding to one of the main constituents of the senile plaques that invade the cortical areas of affected brains.	Phosphorus	30-32	presenilin 1	Homo sapiens	6-9
10510732-3	1999	Relative to the limits of normalcy, fasting serum levels of gastrin were low, but normal for calcium, phosphorus, parathyroid hormone, calcitonin and vitamin D, while the level of total alkaline phosphatase was elevated; fasting urine pH and calcium were low, while phosphorus and net acid were high.	Phosphorus	102-112	gastrin	Homo sapiens	60-67
10510732-3	1999	Relative to the limits of normalcy, fasting serum levels of gastrin were low, but normal for calcium, phosphorus, parathyroid hormone, calcitonin and vitamin D, while the level of total alkaline phosphatase was elevated; fasting urine pH and calcium were low, while phosphorus and net acid were high.	Phosphorus	266-276	gastrin	Homo sapiens	60-67
10372708-5	1999	Serum PTH levels were significantly higher in the BB genotype at baseline and remained so under either a low or a high calcium-phosphorus diet.	Phosphorus	127-137	parathyroid hormone	Homo sapiens	6-9
10416917-9	1999	At a low cTNI concentration (0.32 microg/l), interference was observed with SS and HES at 40 and 80% dilution and with P and Alb at 80%.	Phosphorus	119-120	troponin I3, cardiac type	Homo sapiens	9-13
10416917-12	1999	CONCLUSIONS: SS, P, Alb, and HES interfere in this cTNI immunoassay.	Phosphorus	17-18	troponin I3, cardiac type	Homo sapiens	51-55
10879277-6	1999	We also have demonstrated that P/N ratio possesses added value in evaluation of cell reactivity in immunophenotyping, based upon the apparent nonspecific cytoplasmic staining of MPO in the lymphocyte population.	Phosphorus	31-32	myeloperoxidase	Homo sapiens	178-181
10513211-6	1999	In addition, its content was negatively associated with Ca and P in the elastin fraction and with the aortic Mg.	Phosphorus	63-64	elastin	Homo sapiens	72-79
10445851-5	1999	Expression of a dominant negative mutant of mitogen-activated protein kinase kinase 4 (MKK4), a direct activator of JNK/SAPK, prevented T/P-induced JNK/SAPK activation.	Phosphorus	122-123	mitogen-activated protein kinase kinase 4	Mus musculus	44-85
10445851-5	1999	Expression of a dominant negative mutant of mitogen-activated protein kinase kinase 4 (MKK4), a direct activator of JNK/SAPK, prevented T/P-induced JNK/SAPK activation.	Phosphorus	122-123	mitogen-activated protein kinase kinase 4	Mus musculus	87-91
10445851-5	1999	Expression of a dominant negative mutant of mitogen-activated protein kinase kinase 4 (MKK4), a direct activator of JNK/SAPK, prevented T/P-induced JNK/SAPK activation.	Phosphorus	122-123	mitogen-activated protein kinase 8	Mus musculus	116-119
10232696-0	1999	Effect of histamine H2-receptor antagonist on the phosphorus-binding abilities of calcium carbonate and calcium lactate in hemodialysis patients.	Phosphorus	50-60	histamine receptor H2	Homo sapiens	10-31
11593511-3	1999	P&Q is specific for 5" and 3" flanking regions of F8A1 respectively.	Phosphorus	0-2	coagulation factor VIII associated 1	Homo sapiens	54-58
10232696-1	1999	The effect of histamine H2-receptor antagonist (famotidine) on the phosphorus-binding abilities of calcium carbonate and calcium lactate were examined in 13 chronic hemodialysis patients.	Phosphorus	67-77	histamine receptor H2	Homo sapiens	14-35
10232696-8	1999	A careful observation of changes in the serum phosphorus level should be required in hemodialysis patients receiving calcium carbonate and histamine H2-receptor antagonists.	Phosphorus	46-56	histamine receptor H2	Homo sapiens	139-160
11674206-4	1999	Data obtained from spin trapping experiments of a wide variety of free radicals generated in situ showed the formation of two diastereoisomers spin adducts with different phosphorus and hydrogen coupling constants.	Phosphorus	171-181	spindlin 1	Homo sapiens	19-23
10077579-5	1999	We found that P-TEFb complexes containing human cyclin T1 complexed with either human or rodent Cdk9 supported Tat transactivation and interacted with the Tat activation domain and the HIV-1 TAR RNA element to form TAR loop-dependent ribonucleoprotein complexes.	Phosphorus	14-15	cyclin T1	Homo sapiens	48-57
10077579-5	1999	We found that P-TEFb complexes containing human cyclin T1 complexed with either human or rodent Cdk9 supported Tat transactivation and interacted with the Tat activation domain and the HIV-1 TAR RNA element to form TAR loop-dependent ribonucleoprotein complexes.	Phosphorus	14-15	cyclin dependent kinase 9	Homo sapiens	96-100
10077579-5	1999	We found that P-TEFb complexes containing human cyclin T1 complexed with either human or rodent Cdk9 supported Tat transactivation and interacted with the Tat activation domain and the HIV-1 TAR RNA element to form TAR loop-dependent ribonucleoprotein complexes.	Phosphorus	14-15	tyrosine aminotransferase	Homo sapiens	111-114
10077579-5	1999	We found that P-TEFb complexes containing human cyclin T1 complexed with either human or rodent Cdk9 supported Tat transactivation and interacted with the Tat activation domain and the HIV-1 TAR RNA element to form TAR loop-dependent ribonucleoprotein complexes.	Phosphorus	14-15	Tat	Human immunodeficiency virus 1	155-158
10090754-0	1999	Stereochemical retention of the configuration in the action of Fhit on phosphorus-chiral substrates.	Phosphorus	71-81	fragile histidine triad diadenosine triphosphatase	Homo sapiens	63-67
10090754-6	1999	In this work, the Fhit-catalyzed cleavage of (RP)- and (SP)-gamma-(m-nitrobenzyl) adenosine 5"-O-1-thiotriphosphate (mNBATPalphaS) in H218O to adenosine 5"-[18O]thiophosphate is shown to proceed with overall retention of configuration at phosphorus.	Phosphorus	238-248	fragile histidine triad diadenosine triphosphatase	Homo sapiens	18-22
10052949-8	1999	With the aid of computer simulations of the lateral motion of PC molecules, based on the 2-D crystalline networks formed by annexin V in contact with the lipid bilayer, these FRAP results may be accounted for by considering a rather simple model of a proteolipidic complex consisting of an extended 2-D crystalline protein network facing the lipid bilayer and stabilized by strong interactions between annexin V and PS molecules.	Phosphorus	416-418	mechanistic target of rapamycin kinase	Homo sapiens	175-179
11674206-4	1999	Data obtained from spin trapping experiments of a wide variety of free radicals generated in situ showed the formation of two diastereoisomers spin adducts with different phosphorus and hydrogen coupling constants.	Phosphorus	171-181	spindlin 1	Homo sapiens	143-147
11834176-4	1999	RESULTS: DPP contained high organic phosphorus, 23.8% of aspartic residue and 19.1% serine residue; their molecular weight were 141, 000, 124, 000, 108, 000 respectively.	Phosphorus	36-46	dentin sialophosphoprotein	Homo sapiens	9-12
10090614-7	1999	Thus, the present study indicates that HLA alleles, or closely linked loci, may be involved in the pathogenesis of CL/P.	Phosphorus	118-119	major histocompatibility complex, class II, DR beta 1	Homo sapiens	39-42
10093058-8	1999	In addition, PS-519 significantly reduced PMN accumulation in the ischemic myocardium from 25.1 +/- 2.1 PMNs/mm2 in untreated hearts to 7.3 PMNs/mm2, and attenuated P-selectin surface expression on coronary vascular endothelium from 7.1 +/- 0.3% to 1.4 +/- 0.2% (P < 0.01).	Phosphorus	13-15	selectin P	Rattus norvegicus	165-175
10090614-2	1999	Two HLA-B alleles, B*1501 and B*5101, showed a significant positive association with CL/P.	Phosphorus	88-89	major histocompatibility complex, class I, B	Homo sapiens	4-9
9888830-4	1999	Among the analogues studied are new non-phosphorus-containing pTyr mimetics 23a and 23b which, when incorporated into tripeptide structures 18f and 20f, are able to inhibit Grb2 SH2 domain binding with affinities among the best yet reported for non-phosphorus-containing SH2 domain inhibitors (IC50 values of 6.7 and 1.3 microM, respectively).	Phosphorus	40-50	growth factor receptor bound protein 2	Homo sapiens	173-177
9888835-2	1999	Compounds with an R configuration at phosphorus were found to be potent MMP inhibitors while molecules with the S configuration were almost inactive.	Phosphorus	37-47	matrix metallopeptidase 1	Homo sapiens	72-75
9888830-4	1999	Among the analogues studied are new non-phosphorus-containing pTyr mimetics 23a and 23b which, when incorporated into tripeptide structures 18f and 20f, are able to inhibit Grb2 SH2 domain binding with affinities among the best yet reported for non-phosphorus-containing SH2 domain inhibitors (IC50 values of 6.7 and 1.3 microM, respectively).	Phosphorus	249-259	growth factor receptor bound protein 2	Homo sapiens	173-177
9934857-7	1999	The intensity and speed of induction in Ahr-responsive animals was such that the genotoxic effect of a single injection of B[a]P could not be augmented by prior treatment with non-genotoxic inducers such as beta-napthoflavone and TCDD.	Phosphorus	127-128	aryl-hydrocarbon receptor	Mus musculus	40-43
9826125-6	1998	Electron probe microanalysis revealed that the localization of OP was associated with matrices of calcified cartilage and osteoid nodules that contained calcium and phosphorus.	Phosphorus	165-175	secreted phosphoprotein 1	Homo sapiens	63-65
11938755-3	1999	ET-1(10(-11)-10(-8) mol.L-1) enhanced PS synthesis of cultured AT II cells in a dose-dependent manner.	Phosphorus	38-40	endothelin 1	Homo sapiens	0-4
11938755-5	1999	The minimum effective concentration of ET-1 enhanced PS synthesis of cultured AT II cells was higher than that of lung explants.	Phosphorus	53-55	endothelin 1	Homo sapiens	39-43
11938755-11	1999	The effect of ET-1 on PS synthesis was not induced by changing the number of AT II cells.	Phosphorus	22-24	endothelin 1	Homo sapiens	14-18
10086886-3	1999	Heat-denatured type I collagen (gelatin) was incubated with p-aminophenylmercuric acetate-activated MMP-2 and siderophores.	Phosphorus	17-18	matrix metallopeptidase 2	Homo sapiens	100-105
11670819-20	1998	On the basis of the above findings, a mechanistic scheme for the TNP hydrolysis by 2 is proposed; a TNP molecule is bound to the Pb center, and the hydroxide on the adjacent Zn ion attacks the phosphorus nucleus of TNP, leading to the formation of the BNP complex 3.	Phosphorus	193-203	natriuretic peptide B	Homo sapiens	252-255
10188194-7	1999	Vinclozolin, P, and DDE, known AR ligands, produce similar profiles of toxicity.	Phosphorus	13-14	androgen receptor	Rattus norvegicus	31-33
11670831-9	1998	Heating the anti complexes results in the clean conversion to the syn complexes, with pyramidal inversion observed at phosphorus.	Phosphorus	118-128	synemin	Homo sapiens	66-69
9930400-2	1998	31P nuclear magnetic resonance analysis of such apolipoprotein showed an organic phosphorus peak at -0.55 ppm, which suggests the formation of adducts (most probably Schiff bases) of oxidized phospholipids with apolipoprotein B.	Phosphorus	81-91	apolipoprotein B	Homo sapiens	211-227
9770443-3	1998	The phosphorylated hexapeptide, DpSpSEEK (N6, where pS denotes phosphorylated serine), was derived from the N terminus of the salivary protein statherin.	Phosphorus	33-35	statherin	Homo sapiens	143-152
9793786-0	1998	Effects of variations in dietary calcium and phosphorus supply on plasma and bone osteocalcin concentrations and bone mineralization in growing pigs.	Phosphorus	45-55	osteocalcin	Sus scrofa	82-93
9776793-7	1998	LPD"s low acid load and phosphorus content, the reduced synthesis of uremic toxins derived from alimentary protein, or both may explain these effects, which are indirectly protective against atherosclerosis.	Phosphorus	24-34	acyl-CoA synthetase bubblegum family member 1	Homo sapiens	0-3
9794568-14	1998	The percentage increase in PTH concentrations after phosphorus supplementation were similar in patients with optimal and suboptimal allograft function (33 vs 36%).	Phosphorus	52-62	parathyroid hormone	Homo sapiens	27-30
9794568-16	1998	Changes in 1,25(OH)(2)D concentrations after phosphorus supplementation, expressed as a percentage of the initial concentrations, correlated positively with the percentage changes in PTH concentrations for the whole group, as well as for each subgroup.	Phosphorus	45-55	parathyroid hormone	Homo sapiens	183-186
9794568-17	1998	The best determinants for the percentage and the absolute increase in PTH concentration after phosphorus supplementation was the final serum phosphate concentration (F=4.84, r=0.37, P=0.035) and the increase in serum phosphate (F=7.69, r=0.45, P= 0.009) respectively.	Phosphorus	94-104	parathyroid hormone	Homo sapiens	70-73
9794568-18	1998	CONCLUSIONS: Oral phosphorus supplementation led to a significant increase in the PTH concentration of kidney transplant recipients.	Phosphorus	18-28	parathyroid hormone	Homo sapiens	82-85
9687513-6	1998	Binding of E1A to P/CAF is direct, independent of CBP and requires residues within E1A conserved region 1.	Phosphorus	18-19	lysine acetyltransferase 2B	Homo sapiens	20-23
9761513-13	1998	The rise in serum phosphorus and decline in serum calcium during washout resulted in an increase in median intact parathyroid hormone (iPTH) levels from 292 pg/ml to 395 pg/ml.	Phosphorus	18-28	parathyroid hormone	Homo sapiens	114-133
9689058-9	1998	These results suggest that the enzymes in the PLD superfamily use the conserved histidine for nucleophilic attack on the substrate phosphorus atom and most likely proceed via a common two-step catalytic mechanism.	Phosphorus	131-141	glycosylphosphatidylinositol specific phospholipase D1	Homo sapiens	46-49
9687513-6	1998	Binding of E1A to P/CAF is direct, independent of CBP and requires residues within E1A conserved region 1.	Phosphorus	18-19	CREB binding protein	Homo sapiens	50-53
9737949-1	1998	To elucidate the difference in the mechanisms for alkalization during ischemic acidosis between diabetic and non-diabetic hearts, intracellular pH (pHi) was measured by phosphorus-31 magnetic resonance spectroscopy.	Phosphorus	169-179	glucose-6-phosphate isomerase	Rattus norvegicus	148-151
9683588-5	1998	Previously reported LD for TGFA with both CL/P and CPO could not be confirmed, except in CL/P patients with a positive family history.	Phosphorus	0-1	transforming growth factor alpha	Homo sapiens	27-31
9649438-4	1998	Only wild-type P-TEFb complex with an active CDK9 kinase was able to hyperphosphorylate the C-terminal domain of RNA polymerase II and mediate Tat transactivation in P-TEFb-depleted HeLa nuclear extract.	Phosphorus	15-16	cyclin dependent kinase 9	Homo sapiens	45-49
10806740-5	1998	CONCLUSION: The increase of cholesterol content and C/P ratio in the erythrocyte membrane might be involved in the pathophysiology of PIH.	Phosphorus	54-55	pregnancy-induced hypertension (pre-eclampsia, eclampsia, toxemia of pregnancy included)	Homo sapiens	134-137
9649438-4	1998	Only wild-type P-TEFb complex with an active CDK9 kinase was able to hyperphosphorylate the C-terminal domain of RNA polymerase II and mediate Tat transactivation in P-TEFb-depleted HeLa nuclear extract.	Phosphorus	15-16	tyrosine aminotransferase	Homo sapiens	143-146
9873382-0	1998	Evaluation of phosphorus-containing inhibitors of gamma-glutamyl hydrolase.	Phosphorus	14-24	gamma-glutamyl hydrolase	Homo sapiens	50-74
9625870-0	1998	Differential inhibition of N and P/Q Ca2+ currents by 5-HT1A and 5-HT1D receptors in spinal neurons of Xenopus larvae.	Phosphorus	33-34	5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled L homeolog	Xenopus laevis	54-71
9873382-1	1998	Several putative, phosphorus-containing inhibitors of gamma-glutamyl hydrolase were synthesized and evaluated for inhibitory activity.	Phosphorus	18-28	gamma-glutamyl hydrolase	Homo sapiens	54-78
29711272-0	1998	Ylidic Four pi Electron Four-Membered lambda5 -Phosphorus Heterocycles: Electronical Isomers of Heterocyclobutadienes.	Phosphorus	47-57	immunoglobulin lambda like polypeptide 1	Homo sapiens	38-45
9650801-8	1998	These compounds were about 10 times more potent than the 5-HT1A receptor antagonists, p-MPPI and NDL-249 and 100 times more potent than (S)-UH-301.	Phosphorus	9-10	5-hydroxytryptamine (serotonin) receptor 1A	Mus musculus	57-72
9613109-3	1998	Antisense oligonucleotides to hTR synthesized with peptide nucleic acids and phosphorothioate deoxyribonucleic acids(PS) also inhibited telomerase activity in vitro.	Phosphorus	117-119	telomerase RNA component	Homo sapiens	30-33
9613109-4	1998	Furthermore, PS antisense hTR had significant effect to decrease tumor size and a number of metastatic nodules in a xenograft human cancer-nude mouse model.	Phosphorus	13-15	telomerase RNA component	Homo sapiens	26-29
9492012-4	1998	When the mice were fed a diet high in lactose, calcium, and phosphorus, intestinal calbindin-D9k mRNA levels in the homozygous mice were restored to those in their control littermates.	Phosphorus	60-70	S100 calcium binding protein G	Mus musculus	83-96
9492012-7	1998	These data also demonstrate that in the absence of a functional VDR, a high local concentration of calcium, phosphorus, and/or lactose in the intestinal lumen can normalize intestinal calbindin-D9k mRNA levels.	Phosphorus	108-118	S100 calcium binding protein G	Mus musculus	184-197
9566902-7	1998	Replacement of both P and Q residues with A"s in LMP1 reduced EGFR induction by >75%, while deletion of PXQXT blocked EGFR induction.	Phosphorus	20-21	PDZ and LIM domain 7	Homo sapiens	49-53
9566902-7	1998	Replacement of both P and Q residues with A"s in LMP1 reduced EGFR induction by >75%, while deletion of PXQXT blocked EGFR induction.	Phosphorus	20-21	epidermal growth factor receptor	Homo sapiens	62-66
9561967-2	1998	Previous studies in our laboratory have demonstrated, however, that dosages of the OPs chlorpyrifos (CPF) or parathion (PS), which cause similar degrees of brain AChE inhibition in adult male rats, can produce marked differences in toxicity.	Phosphorus	120-122	acetylcholinesterase	Rattus norvegicus	162-166
9481529-8	1998	RESULTS: Study 1, administration of 32.2 mmol/d phosphorus resulted in a mean increase of 13.2 mmol/d urinary phosphorus, a mean decrease of 1.1 mmol/d urinary calcium, and a mean increase of 7 ng/mL in serum intact PTH.	Phosphorus	48-58	parathyroid hormone	Homo sapiens	216-219
9477969-1	1998	The consequences of the binding of annexin V on the structure and dynamics of PC/PS bilayers were studied by means of fluorescence polarization, 31P NMR, 2H NMR, and fluorescence recovery after photobleaching (FRAP).	Phosphorus	81-83	annexin A5	Homo sapiens	35-44
9477969-8	1998	These combined experiments are consistent with a model in which annexin V enters a proteolipidic complex in the form of an extended 2D network, stabilized by specific interactions with PS.	Phosphorus	185-187	annexin A5	Homo sapiens	64-73
10322647-10	1998	CONCLUSIONS: The down-regulation of renal PTH/PTHrP receptor mRNA occurs much earlier than the changes of renal function, plasma PTH, serum phosphorus and calcium in the course of human renal disease.	Phosphorus	140-150	parathyroid hormone 1 receptor	Homo sapiens	42-60
9473433-1	1998	The PD2 radical was generated in a free-space absorption cell by a dc glow discharge of D2 over red phosphorus grains which were placed in the middle of the Pyrex glass cell.	Phosphorus	96-110	PAF1 homolog, Paf1/RNA polymerase II complex component	Homo sapiens	4-7
9473433-4	1998	The phosphorus nuclear spin-rotation coupling constants were found to have relatively large values: Caa(P) = 0.4815(89) MHz, Cbb(P) = 0.2501 (104) MHz, and Ccc(P) = 0.0564 (74) MHz, as suggested from those of PH2.	Phosphorus	4-14	polyhomeotic homolog 2	Homo sapiens	209-212
9481529-10	1998	Study 2, administration of 64.4 mmol/d phosphorus resulted in a mean increase of 27.2 mmol/d urinary phosphorus, a mean decrease of 2.4 mmol/d urinary calcium, with no change in serum phosphate, PTH or urinary deoxypyridinoline.	Phosphorus	39-49	parathyroid hormone	Homo sapiens	195-198
9401762-8	1997	By an in situ hybridization, the alpha 1a and alpha 1d mRNAs were recognized in the smooth muscle cells of the E-vas and the P-vas, and the distribution pattern the same in both tissue.	Phosphorus	125-126	calcium voltage-gated channel subunit alpha1 A	Homo sapiens	33-41
9568815-1	1998	High extracellular phosphorus directly increases parathyroid hormone (PTH) secretion and gene transcription.	Phosphorus	19-29	parathyroid hormone	Rattus norvegicus	49-68
9530615-6	1997	The beta 2-microglobulin concentration in the urine of rats fed the high-phosphorus diet was significantly increased at 14 d, and increased more toward 21 d. We concluded that nephrocalcinosis and injury to the proximal tubules are rapidly induced in rats fed a high-phosphorus diet.	Phosphorus	73-83	beta-2 microglobulin	Rattus norvegicus	4-24
9530615-6	1997	The beta 2-microglobulin concentration in the urine of rats fed the high-phosphorus diet was significantly increased at 14 d, and increased more toward 21 d. We concluded that nephrocalcinosis and injury to the proximal tubules are rapidly induced in rats fed a high-phosphorus diet.	Phosphorus	267-277	beta-2 microglobulin	Rattus norvegicus	4-24
10822605-3	1998	Binding constants of L22 for dioleoylphosphatidylserine [di(C18 : 1)PS] or dioleoylphosphatidic acid [di(C18 : 1)PA] relative to dieoleoylphosphatidylcholine [di(C18 : 1)PC] were close to 1.	Phosphorus	68-70	ribosomal protein L22	Homo sapiens	21-24
10822605-5	1998	Assuming just one high affinity binding site on L16 for anionic lipid, the affinity of the site for di(C18 : 1)PS was calculated to be ca.	Phosphorus	111-113	immunoglobulin kappa variable 3D-15	Homo sapiens	48-51
9705570-2	1998	BACKGROUND: Hypophosphatemia is common in acutely ill patients and possibly may occur in the acute-phase response syndrome (APR), secondary to hyperglycemia and shifts of extracellular phosphorus into cells.	Phosphorus	185-195	phorbol-12-myristate-13-acetate-induced protein 1	Homo sapiens	124-127
9647491-7	1998	These findings confirm that even in severe chronic uremic patients dietary phosphorus restriction and calcium carbonate supplementation lower i-PTH serum levels.	Phosphorus	75-85	parathyroid hormone	Homo sapiens	144-147
9428931-8	1997	Interestingly, neoplastic cells reacting to ED1 (rat macrophage/histiocyte-specific antibody) and alpha-smooth muscle actin (alpha-SMA) appeared in SS tumours and tumours induced by SS-P and SS-A3-1 and by SS-P and SS-A3-1 cultures.	Phosphorus	185-186	actin gamma 2, smooth muscle	Rattus norvegicus	98-123
9428931-8	1997	Interestingly, neoplastic cells reacting to ED1 (rat macrophage/histiocyte-specific antibody) and alpha-smooth muscle actin (alpha-SMA) appeared in SS tumours and tumours induced by SS-P and SS-A3-1 and by SS-P and SS-A3-1 cultures.	Phosphorus	185-186	actin gamma 2, smooth muscle	Rattus norvegicus	125-134
9386122-7	1997	ET-1 correlated significantly with Pp/Ps at 6 hours (r2=.43, P<.005).	Phosphorus	38-40	endothelin 1	Homo sapiens	0-4
9401762-11	1997	In a functional study, l-phenylephrine produced concentration-dependent contraction in the E-vas (Emax = 2.24 +/- 0.70 g; pD2 = 5.32 +/- 0.09) and the P-vas (Emax = 2.46 +/- 0.46 g; pD2 = 5.07 +/- 0.12).	Phosphorus	151-152	PAF1 homolog, Paf1/RNA polymerase II complex component	Homo sapiens	182-185
9330592-1	1997	Parathyroid hormone (PTH) acts on bone and kidneys by binding to PTH/PTH-related protein (PTHrP) receptors and regulating calcium (Ca) and phosphorus (P) homeostasis.	Phosphorus	139-149	parathyroid hormone	Rattus norvegicus	0-19
9360138-8	1997	The optical density at a wavelength of 450 nm for CD42b was 1.47 +/- 0.35 in polypropylene, 1.16 +/- 0.38 in silicone, and 1.85 +/- 0.19 in double polyolefin (p < 0.01 vs silicone) and for CD61 0.98 +/- 0.39 in polypropylene, 0.91 +/- 0.22 in silicone, and 1.69 +/- 0.25 in double polyolefin (p < 0.01 vs silicone and polypropylene).	Phosphorus	5-6	glycoprotein Ib platelet subunit alpha	Homo sapiens	50-55
9360138-8	1997	The optical density at a wavelength of 450 nm for CD42b was 1.47 +/- 0.35 in polypropylene, 1.16 +/- 0.38 in silicone, and 1.85 +/- 0.19 in double polyolefin (p < 0.01 vs silicone) and for CD61 0.98 +/- 0.39 in polypropylene, 0.91 +/- 0.22 in silicone, and 1.69 +/- 0.25 in double polyolefin (p < 0.01 vs silicone and polypropylene).	Phosphorus	5-6	integrin subunit beta 3	Homo sapiens	192-196
9330592-1	1997	Parathyroid hormone (PTH) acts on bone and kidneys by binding to PTH/PTH-related protein (PTHrP) receptors and regulating calcium (Ca) and phosphorus (P) homeostasis.	Phosphorus	139-149	parathyroid hormone	Rattus norvegicus	21-24
9330592-1	1997	Parathyroid hormone (PTH) acts on bone and kidneys by binding to PTH/PTH-related protein (PTHrP) receptors and regulating calcium (Ca) and phosphorus (P) homeostasis.	Phosphorus	139-149	parathyroid hormone-like hormone	Rattus norvegicus	90-95
11670072-0	1997	Rapid Inversion at Phosphorus in the [eta(4)-(C(6)H(11))(3)SnP(7)W(CO)(3)](2)(-) and [(en)(CO)(3)W(eta(1),eta(4)-P(7))M(CO)(3)](3)(-) Ions Where M = Cr, W. Ethylenediamine (en) solutions of [eta(4)-P(7)M(CO)(3)](3)(-) ions [M = Cr (1a), W (1b)] react with (mesitylene)W(CO)(3) to form the bimetallic complexes [(en)(CO)(3)W(eta(1),eta(4)-P(7))M(CO)(3)](3)(-) where M = Cr (3a), W (3b) in good yield.	Phosphorus	19-29	integrin subunit alpha M	Homo sapiens	369-375
9316879-3	1997	We found that chronic proteasome inhibition using MG-341 significantly attenuated the peptidoglycan/polysaccharide (PG/PS)-induced up-regulation of iNOS in the colon and spleen and the consequent increase in plasma levels of nitrate and nitrite.	Phosphorus	119-121	nitric oxide synthase 2	Homo sapiens	148-152
9316879-6	1997	Treatment with MG-341 also significantly reduced PG/PS-induced increases in macroscopic spleen inflammation, spleen weight and spleen MPO activity.	Phosphorus	52-54	myeloperoxidase	Homo sapiens	134-137
9316879-7	1997	We conclude that the 26S proteasome complex plays an important role in regulating the PG/PS-induced up-regulation of iNOS and VCAM-1 in vivo and appears to be important in regulating colonic and splenic inflammation.	Phosphorus	89-91	nitric oxide synthase 2	Homo sapiens	117-121
9316879-7	1997	We conclude that the 26S proteasome complex plays an important role in regulating the PG/PS-induced up-regulation of iNOS and VCAM-1 in vivo and appears to be important in regulating colonic and splenic inflammation.	Phosphorus	89-91	vascular cell adhesion molecule 1	Homo sapiens	126-132
9228870-9	1997	RESULTS: Patients with SCI had significant suppression in PTH (p < .000009) and 1,25-D (p < .02) levels with elevated phosphorus (p < 0.03) and prolactin (p < .03) levels compared to patients with TBI.	Phosphorus	124-134	prolactin	Homo sapiens	153-162
9313859-2	1997	The pH-dependence of inactivation of thrombin by (-)-PMN is sigmoidal and consistent with the participation of a catalytic residue with a pKa of 8.0 +/- 0.1 in 0.15 M NaCl and a pKa of 7.4 +/- 0.2 in 0.15 M choline chloride in the nucleophilic attack of the catalytic Ser at phosphorus.	Phosphorus	275-285	coagulation factor II, thrombin	Homo sapiens	37-45
9148928-5	1997	The presence of PS was found to be crucial for the incorporation into and ribosome binding activity of p180 in liposomes.	Phosphorus	16-18	ribosome binding protein 1	Canis lupus familiaris	103-107
9232886-1	1997	Phytase, an enzyme that degrades the phosphorus storage compound phytate, has the potential to enhance phosphorus availability in animal diets when engineered into soybean (Glycine max) seeds.	Phosphorus	37-47	putative glycerophosphoryl diester phosphodiesterase	Glycine max	0-7
9232886-1	1997	Phytase, an enzyme that degrades the phosphorus storage compound phytate, has the potential to enhance phosphorus availability in animal diets when engineered into soybean (Glycine max) seeds.	Phosphorus	103-113	putative glycerophosphoryl diester phosphodiesterase	Glycine max	0-7
9236437-9	1997	The T/P ratio for ACE, which is membrane bound, was fivefold the ratio for albumin.	Phosphorus	6-7	angiotensin I converting enzyme	Homo sapiens	18-21
9195116-2	1997	Fosinopril is a phosphorus-containing ester prodrug of an angiotensin-converting enzyme (ACE) inhibitor.	Phosphorus	16-26	angiotensin I converting enzyme	Homo sapiens	58-87
9195116-2	1997	Fosinopril is a phosphorus-containing ester prodrug of an angiotensin-converting enzyme (ACE) inhibitor.	Phosphorus	16-26	angiotensin I converting enzyme	Homo sapiens	89-92
9129485-1	1997	A low-protein, low-phosphorus diet (LPD) has been shown to improve insulin sensitivity in uremic patients; however, this improvement has not been studied at low physiologic concentrations of plasma insulin, and the metabolic pathways concerned with this improvement have not been located.	Phosphorus	19-29	insulin	Homo sapiens	67-74
11669832-7	1997	The observation of the coupling only between p-H and the hydride in [(eta(6)-toluene)Fe(H)(SiCl(3))(2)](-) and (eta(6)-toluene)Fe(H)(py)(SiCl(3)) indicates that the configuration with the hydride trans to p-H is dominant in solution and the rotation of the toluene is not fast at room temperature.	Phosphorus	26-27	endothelin receptor type A	Homo sapiens	70-73
11669832-7	1997	The observation of the coupling only between p-H and the hydride in [(eta(6)-toluene)Fe(H)(SiCl(3))(2)](-) and (eta(6)-toluene)Fe(H)(py)(SiCl(3)) indicates that the configuration with the hydride trans to p-H is dominant in solution and the rotation of the toluene is not fast at room temperature.	Phosphorus	26-27	endothelin receptor type A	Homo sapiens	112-115
9079918-8	1997	Human placental protein tyrosine phosphatase 1B, with absolute specificity for P-Tyr, liberated significant quantities of 32Pi from four of the polypeptides, confirming that a portion of the protein-bound phosphate was present as 32P-Tyr.	Phosphorus	79-80	protein tyrosine phosphatase non-receptor type 1	Homo sapiens	16-47
9169286-1	1997	Brain creatine kinase (CK) catalyzed phosphorus fluxes between phosphocreatine (PCr) and ATP and changes in reactant concentrations were measured using [31P] nuclear magnetic resonance spectroscopy ([31P]NMR) before and during pentylenetetrazole-induced seizures in 7 and 21 day old rats.	Phosphorus	37-47	creatine kinase B	Rattus norvegicus	0-21
9158070-3	1997	The levels of PS4 were highly correlated with the corresponding TRH (p-Glu-His-Pro-NH2) and TRH-Gly (p-Glu-His-Pro-Gly) levels in hippocampus, amygdala, and pyriform cortex, consistent with the prepro-TRH source of all of these peptides.	Phosphorus	56-57	thyrotropin releasing hormone	Rattus norvegicus	64-67
9128259-5	1997	Further studies using CHO-E and -P monolayers demonstrate that the first 19 amino acids of PSGL-1 are sufficient for attachment and rolling on both E- and P-selectin and suggest that a sialyl Lewis x-containing glycan at Threonine-16 is critical for this sequence of amino acids to mediate attachment to E- and P-selectin.	Phosphorus	33-34	selectin P ligand	Homo sapiens	91-97
9228465-2	1997	m-PTH correlated positively and more significantly with serum calcium (Ca), serum phosphorus (P), Ca-P solubility products (Ca x P) and LS-BMD than i-PTH did (P = 0.024 vs. 0.531, 0.001 vs. 0.061, 0.0001 vs. 0.125, and 0.017 vs. 0.284, respectively).	Phosphorus	82-92	parathyroid hormone	Homo sapiens	2-5
9090882-11	1997	Deprivation of nitrogen, phosphorus, potassium, and sulfur changed spatial expression as well as the expression level of StPT1.	Phosphorus	25-35	inorganic phosphate transporter	Solanum tuberosum	121-126
9062504-6	1997	PTHrP-(1-36) administered sc in three doses (0.82, 1.64, and 3.28 micrograms/kg) to 21 normal women produced increases in circulating PTHrP-(1-36), reductions in serum phosphorus and the renal phosphorus threshold, increments in fractional calcium excretion and nephrogenous cAMP excretion, and increases in plasma 1,25-dihydroxyvitamin D.	Phosphorus	168-178	parathyroid hormone like hormone	Homo sapiens	0-5
9062504-6	1997	PTHrP-(1-36) administered sc in three doses (0.82, 1.64, and 3.28 micrograms/kg) to 21 normal women produced increases in circulating PTHrP-(1-36), reductions in serum phosphorus and the renal phosphorus threshold, increments in fractional calcium excretion and nephrogenous cAMP excretion, and increases in plasma 1,25-dihydroxyvitamin D.	Phosphorus	193-203	parathyroid hormone like hormone	Homo sapiens	0-5
9077579-7	1997	These data suggest that JTP-4819 ameliorates age-related impairment of spatial memory and partly reverses central cholinergic dysfunction, possibly due to the enhancement of neuropeptide function by inhibition of PEP mediated degradation of substance P, arginine-vasopressin, and thyrotropin-releasing hormone.	Phosphorus	26-27	arginine vasopressin	Rattus norvegicus	263-274
9077579-7	1997	These data suggest that JTP-4819 ameliorates age-related impairment of spatial memory and partly reverses central cholinergic dysfunction, possibly due to the enhancement of neuropeptide function by inhibition of PEP mediated degradation of substance P, arginine-vasopressin, and thyrotropin-releasing hormone.	Phosphorus	26-27	thyrotropin releasing hormone	Rattus norvegicus	280-309
9076897-4	1997	Activated charcoal treatment and phopholipase C digestion reduced the procoagulant-inducing activity of Pro-Alb, and Pro-Alb contained 2.3-fold more phosphorus than inactive albumin.	Phosphorus	149-159	albumin	Homo sapiens	121-124
9073589-0	1997	The cigarette tar component p-benzoquinone blocks T-lymphocyte activation by inhibiting interleukin-2 production, but not CD25, ICAM-1, or LFA-1 expression.	Phosphorus	21-22	interleukin 2	Homo sapiens	88-101
9062674-3	1997	At nanomolar concentration, JTP-4819 inhibited the degradation of substance P, arginine-vasopressin, and thyrotropin-releasing hormone by PEP in supernatants of the rat cerebral cortex and hippocampus.	Phosphorus	30-31	arginine vasopressin	Rattus norvegicus	88-99
9020139-3	1997	The P-2-linked [3H]BZDC-IP6 showed efficient, IP6-displaceable labeling of the GST-Syt II-C2B.	Phosphorus	4-5	glutathione S-transferase kappa 1	Homo sapiens	79-82
9020139-3	1997	The P-2-linked [3H]BZDC-IP6 showed efficient, IP6-displaceable labeling of the GST-Syt II-C2B.	Phosphorus	4-5	synaptotagmin 1	Homo sapiens	83-86
8840951-7	1996	Treatment of phosphorus-restricted HPX rats with IGF-I resulted in a decrease in serum phosphorus by 2 hours that preceded a fourfold increase in enzyme activity between 6 and 10 hours.	Phosphorus	13-23	insulin-like growth factor 1	Rattus norvegicus	49-54
9065184-6	1997	RESULTS: Incubation of phosphorus 32-labeled membranes with a gonadotropin-releasing hormone analog in the presence of guanosine thiotriphosphate caused a remarkable loss of phosphoprotein from 35 kd protein.	Phosphorus	23-33	gonadotropin releasing hormone 1	Homo sapiens	62-92
9179627-8	1997	The temporal expression of TNF, IL-1, IL-6 and NO suggest a cascade of inflammatory mediators in which monocytes and macrophages respond to PG/PS with enhanced synthesis of TNF and IL-1, which may in turn promote the synthesis of IL-6 and NO.	Phosphorus	143-145	tumor necrosis factor	Homo sapiens	27-30
9179627-8	1997	The temporal expression of TNF, IL-1, IL-6 and NO suggest a cascade of inflammatory mediators in which monocytes and macrophages respond to PG/PS with enhanced synthesis of TNF and IL-1, which may in turn promote the synthesis of IL-6 and NO.	Phosphorus	143-145	interleukin 6	Homo sapiens	38-42
9179627-8	1997	The temporal expression of TNF, IL-1, IL-6 and NO suggest a cascade of inflammatory mediators in which monocytes and macrophages respond to PG/PS with enhanced synthesis of TNF and IL-1, which may in turn promote the synthesis of IL-6 and NO.	Phosphorus	143-145	tumor necrosis factor	Homo sapiens	173-176
9179627-8	1997	The temporal expression of TNF, IL-1, IL-6 and NO suggest a cascade of inflammatory mediators in which monocytes and macrophages respond to PG/PS with enhanced synthesis of TNF and IL-1, which may in turn promote the synthesis of IL-6 and NO.	Phosphorus	143-145	interleukin 1 alpha	Homo sapiens	181-185
9179627-8	1997	The temporal expression of TNF, IL-1, IL-6 and NO suggest a cascade of inflammatory mediators in which monocytes and macrophages respond to PG/PS with enhanced synthesis of TNF and IL-1, which may in turn promote the synthesis of IL-6 and NO.	Phosphorus	143-145	interleukin 6	Homo sapiens	230-234
9038860-4	1997	ATP, creatine phosphate, creatine, and P, were inversely related to GLUT-4 protein concentration.	Phosphorus	2-3	solute carrier family 2 member 4	Rattus norvegicus	68-74
9503598-4	1997	The ranges of SCP under the influence of temperature, light, nitrate, ammonia, phosphorus, iron, carbonate, and sodium chloride were in the following respective order (% dry wt): 18.4-43.3, 20.5-42.3, 12.4-35.8, 15.7-41.8, 15.8-49.4, 17.4-49.7, 13.8-35.6, and 0.0-37.7.	Phosphorus	79-89	solute carrier family 50 member 1	Homo sapiens	14-17
9037126-11	1997	The results of this study confirmed the actions of GH on renal tubules with increases in calcium excretion and phosphorus reabsorption, and indicate that the action of GH on modulating vitamin D metabolism may be IGF-I mediated, not PTH mediated.	Phosphorus	111-121	growth hormone 1	Homo sapiens	51-53
8943469-2	1996	However, a direct effect of high extracellular phosphorus on parathyroid (PTH) function, gene expression, and cell proliferation is still controversial.	Phosphorus	47-57	parathyroid hormone	Rattus norvegicus	74-77
8943469-11	1996	In conclusion, parathyroid gene expression per cell and parathyroid cell hyperplasia are stimulated by high dietary phosphorus independently of calcium and calcitriol.	Phosphorus	116-126	parathyroid hormone	Rattus norvegicus	15-26
9014481-0	1996	[Effect of histamine H2-receptor antagonists on the phosphorus-binding ability of phosphate binders in hemodialysis patients].	Phosphorus	52-62	histamine receptor H2	Homo sapiens	11-32
9014481-1	1996	We examined the effects of histamine H2-receptor antagonists on the phosphorus binding ability of phosphate binders.	Phosphorus	68-78	histamine receptor H2	Homo sapiens	27-48
9062674-3	1997	At nanomolar concentration, JTP-4819 inhibited the degradation of substance P, arginine-vasopressin, and thyrotropin-releasing hormone by PEP in supernatants of the rat cerebral cortex and hippocampus.	Phosphorus	30-31	thyrotropin releasing hormone	Rattus norvegicus	105-134
9025264-5	1997	Conalbumin (low iron content) separated into three major components with p/s of 7.2, 6.6 and 6.2.	Phosphorus	32-33	transferrin (ovotransferrin)	Gallus gallus	0-10
8967953-5	1996	Although E1A displaces P/CAF from CBP, it does not disrupt the CBP-associated HAT activity.	Phosphorus	23-24	CREB binding protein	Homo sapiens	34-37
8943469-2	1996	However, a direct effect of high extracellular phosphorus on parathyroid (PTH) function, gene expression, and cell proliferation is still controversial.	Phosphorus	47-57	parathyroid hormone	Rattus norvegicus	61-72
9014481-5	1996	Furthermore, serum phosphorus levels decreased significantly eight weeks after the discontinuation of treatment with histamine H2-receptor antagonists.	Phosphorus	19-29	histamine receptor H2	Homo sapiens	117-138
9014481-8	1996	With the 4-week administration of histamine H2-receptor antagonists accompanied by calcium carbonate, the serum phosphorus level increased, similarly to that of the first study (from 6.3 +/- 0.9 to 7.1 +/- 0.5 mg/dl).	Phosphorus	112-122	histamine receptor H2	Homo sapiens	34-55
9014481-10	1996	These results suggest that histamine H2-receptor antagonists significantly affect the phosphorus binding ability of calcium carbonate, but not of calcium lactate.	Phosphorus	86-96	histamine receptor H2	Homo sapiens	27-48
9014481-12	1996	Careful observation of changes in the serum phosphorus level is required in hemodialysis patients receiving calcium carbonate and histamine H2-receptor antagonists.	Phosphorus	44-54	histamine receptor H2	Homo sapiens	130-151
11667736-6	1996	In the low energy conformation, the phosphole and phenyl ring planes are approximately orthogonal, with the 2-tert-butyl group in the less crowded position that is syn to the lone pair on phosphorus.	Phosphorus	188-198	synemin	Homo sapiens	164-167
8911021-7	1996	Phosphorus restriction through a combination of diet and intestinal phosphate binders is important to allow calcitriol therapy to successfully lower PTH levels, but it likely has no direct effects that are independent of interactions involving calcitriol.	Phosphorus	0-10	parathyroid hormone	Canis lupus familiaris	149-152
8840951-7	1996	Treatment of phosphorus-restricted HPX rats with IGF-I resulted in a decrease in serum phosphorus by 2 hours that preceded a fourfold increase in enzyme activity between 6 and 10 hours.	Phosphorus	87-97	insulin-like growth factor 1	Rattus norvegicus	49-54
8840951-10	1996	Although these growth factors may have a direct effect on the 1alpha-hydroxylase, these data suggest that the influence of GH, IGF-I, and insulin on transcellular phosphorus flux may have an independent effect on enzyme activity.	Phosphorus	163-173	gonadotropin releasing hormone receptor	Rattus norvegicus	123-125
8840951-10	1996	Although these growth factors may have a direct effect on the 1alpha-hydroxylase, these data suggest that the influence of GH, IGF-I, and insulin on transcellular phosphorus flux may have an independent effect on enzyme activity.	Phosphorus	163-173	insulin-like growth factor 1	Rattus norvegicus	127-132
8961134-2	1996	It is hypothesized that the elevation of serum PTH level was induced either by the rise in phosphorus levels induced by GH or by a direct stimulatory effect of IGF-I on PTH production.	Phosphorus	91-101	parathyroid hormone	Homo sapiens	47-50
23282563-11	1996	SAZ significantly attenuated the PG/PS-induced increases in myeloperoxidase (MPO) activity as well as significantly reduced the PG/PS-induced increases in liver and spleen weights.	Phosphorus	36-38	myeloperoxidase	Rattus norvegicus	60-75
23282563-11	1996	SAZ significantly attenuated the PG/PS-induced increases in myeloperoxidase (MPO) activity as well as significantly reduced the PG/PS-induced increases in liver and spleen weights.	Phosphorus	36-38	myeloperoxidase	Rattus norvegicus	77-80
23282563-14	1996	The FOS and XOS diets significantly attenuated the PG/PS-induced increases in liver weights when compared with PG/PS + chow-fed animals.	Phosphorus	54-56	Fos proto-oncogene, AP-1 transcription factor subunit	Rattus norvegicus	4-7
8961134-2	1996	It is hypothesized that the elevation of serum PTH level was induced either by the rise in phosphorus levels induced by GH or by a direct stimulatory effect of IGF-I on PTH production.	Phosphorus	91-101	growth hormone 1	Homo sapiens	120-122
8768839-9	1996	These results suggest a selective modulation by vitamin D of the renal response to PTH; 1,25-(OH)2D3 facilitates PTH-induced calcium and sodium reabsorption, but does not influence PTH-induced cAMP excretion; phosphorus, potassium, and bicarbonate tubular transport, or 1 alpha-hydroxylation of 25-hydroxyvitamin D3.	Phosphorus	209-219	parathyroid hormone	Homo sapiens	83-86
8869046-8	1996	Analysis of correlation allowed to identify a relation between: 1) dT and Tb [dT = Tb/[-0.305 + (0.0388)(Tb)]; P < 10(-4)]; 2) the slope of CA 125 initial regression (P) and DFS [DFS = 201.9e (-16.64*P); P < 10(-8)]; 3) P and OS [OS = 285.0e(-17.00*P); P < 10(-7)].	Phosphorus	111-112	mucin 16, cell surface associated	Homo sapiens	143-149
8718893-7	1996	Docking of Sp and Rp cycloheptyl methylphosphonyl thiocholines and thioethylates in AChE as models of the reversible complex and transition state using molecular dynamics affords structural insight into the spatial arrangement of the substituents surrounding phosphorus prior to and during reaction.	Phosphorus	259-269	acetylcholinesterase (Cartwright blood group)	Homo sapiens	84-88
8818805-12	1996	Phosphorus equivalency of microbial phytase was calculated by using response equations for ADG and apparent P absorption.	Phosphorus	0-10	ADG	Sus scrofa	91-94
8797118-0	1996	Direct effect of phosphorus on PTH secretion from whole rat parathyroid glands in vitro.	Phosphorus	17-27	parathyroid hormone	Rattus norvegicus	31-34
8797118-2	1996	In vivo manipulation of phosphorus is associated with changes in serum calcium and calcitriol levels which in turn can modify parathyroid hormone synthesis and secretion.	Phosphorus	24-34	parathyroid hormone	Rattus norvegicus	126-145
8663221-4	1996	In the presence of PS and Ca2+, plasmin was shown to convert FXaalpha to a FXabeta-like species at least 3 orders of magnitude faster than the autoproteolytic mechanism.	Phosphorus	19-21	plasminogen	Homo sapiens	32-39
8797118-3	1996	The present in vitro study evaluates whether high extracellular phosphorus has a direct effect on parathyroid hormone secretion.	Phosphorus	64-74	parathyroid hormone	Rattus norvegicus	98-117
8797118-5	1996	In 1.25 mM calcium, the parathyroid hormone secretion rate was similar in 1 and 2 mM phosphorus; however, a phosphorus concentration of 3 and 4 mM produced a 3- and 4-fold increase in the parathyroid hormone secretion, respectively, as compared with 1 mM phosphorus.	Phosphorus	85-95	parathyroid hormone	Rattus norvegicus	24-43
8797118-5	1996	In 1.25 mM calcium, the parathyroid hormone secretion rate was similar in 1 and 2 mM phosphorus; however, a phosphorus concentration of 3 and 4 mM produced a 3- and 4-fold increase in the parathyroid hormone secretion, respectively, as compared with 1 mM phosphorus.	Phosphorus	108-118	parathyroid hormone	Rattus norvegicus	188-207
8797118-5	1996	In 1.25 mM calcium, the parathyroid hormone secretion rate was similar in 1 and 2 mM phosphorus; however, a phosphorus concentration of 3 and 4 mM produced a 3- and 4-fold increase in the parathyroid hormone secretion, respectively, as compared with 1 mM phosphorus.	Phosphorus	108-118	parathyroid hormone	Rattus norvegicus	188-207
8797118-7	1996	Furthermore, the addition of arachidonic acid 20 microM, a substrate for inhibitory intracellular signal pathway, to the 4 mM phosphorus-1.35 mM calcium incubation media reduced the parathyroid hormone secretion to 34.5% (p < 0.05).	Phosphorus	126-136	parathyroid hormone	Rattus norvegicus	182-201
8797118-8	1996	In conclusion, our results indicate that in vitro, high phosphorus directly increases parathyroid hormone secretion.	Phosphorus	56-66	parathyroid hormone	Rattus norvegicus	86-105
8729088-5	1996	Consumption of a high P/S diet decreased mRNA levels for fatty acid synthase, acetyl-CoA carboxylase, malic enzyme, and pyruvate kinase in obese and lean animals.	Phosphorus	22-23	fatty acid synthase	Mus musculus	57-76
11666582-3	1996	The spans of the phosphorus chemical shift tensors for DBP and its chalcogenides are comparable to those of the corresponding compounds of triphenylphosphine; however, the asymmetry of the tensors for the DBP series reflects the reduced local symmetry at phosphorus.	Phosphorus	17-27	D-box binding PAR bZIP transcription factor	Homo sapiens	55-58
11666582-4	1996	For the complexes (DBP)M(CO)(5) and cis-(DBP)(2)M(CO)(4), where M is a group 6 transition metal (Cr, Mo, W), the most shielded component of the phosphorus shift tensor is found to be relatively independent of the metal or complex, delta(33) = -41 +/- 8 ppm, and is thought to lie along or close to the P-M bond axis direction.	Phosphorus	144-154	D-box binding PAR bZIP transcription factor	Homo sapiens	19-22
11666582-4	1996	For the complexes (DBP)M(CO)(5) and cis-(DBP)(2)M(CO)(4), where M is a group 6 transition metal (Cr, Mo, W), the most shielded component of the phosphorus shift tensor is found to be relatively independent of the metal or complex, delta(33) = -41 +/- 8 ppm, and is thought to lie along or close to the P-M bond axis direction.	Phosphorus	144-154	D-box binding PAR bZIP transcription factor	Homo sapiens	41-44
11666582-7	1996	The phosphorus shift tensors of the two nonequivalent DBP ligands of (DBP)(2)PtX(2) (X = Cl, Br) exhibit quite different principal components.	Phosphorus	4-14	D-box binding PAR bZIP transcription factor	Homo sapiens	54-57
11666582-7	1996	The phosphorus shift tensors of the two nonequivalent DBP ligands of (DBP)(2)PtX(2) (X = Cl, Br) exhibit quite different principal components.	Phosphorus	4-14	D-box binding PAR bZIP transcription factor	Homo sapiens	70-73
8652526-7	1996	The results clearly suggest that PS binding regulates the rate of prothrombin activation.	Phosphorus	33-35	coagulation factor II, thrombin	Homo sapiens	66-77
8665042-12	1996	Significant reductions in MI, W/D, and T/P in the organs sampled were observed in the rh-TM pretreated groups (p < 0.05).	Phosphorus	41-42	thrombomodulin	Rattus norvegicus	89-91
8737837-10	1996	These results show that microbial phytase supplementation of a low-P diet increased growth and relative retention of total P, Ca, Cu, and Zn and improved bone mineralization in broiler chickens.	Phosphorus	67-68	putative glycerophosphoryl diester phosphodiesterase	Glycine max	34-41
8639532-9	1996	We find the ATPase activity of Rep is influenced dramatically by both dimerization and ss DNA ligation state, with the following kcat values for ATP hydrolysis increasing by over 4 orders of magnitude: 2.1 x 10(-3) s(-1) for P, 2.17 +/- 0.04 s(-1) for PS, 16.5 +/- 0.2 s(-1) for P2S, and 71 +/- 2.5 s(-1) for P2S2 (20 mM Tris-HCl, pH 7.5, 6mM NaCl, 5 mM MgCl2, 10% glycerol, 4 degrees C).	Phosphorus	252-254	ATPase	Escherichia coli	12-18
8722816-1	1996	Phosphorus magnetic resonance spectroscopy (31P MRS) at 1.5 T was performed on nine polysubstance abusing men.	Phosphorus	0-10	MROS	Homo sapiens	48-51
8657749-3	1996	When Ho-0, an elution with n-hexane, and Ho-1 were administrated to the rachitic rats fed with a vitamin D-free, low-phosphorus diet, they not only increased significantly the concentration of inorganic phosphorus in serum, but also significantly promoted bone calcification.	Phosphorus	117-127	heme oxygenase 1	Rattus norvegicus	41-45
8676336-4	1996	For phosphonate-based pTyr mimetics such as phosphonomethyl phenylalanine (Pmp,2) introduction of fluorines alpha to the phosphorus has provided higher affinity pTyr mimetics.	Phosphorus	121-131	peripheral myelin protein 2	Homo sapiens	75-80
8647946-1	1996	High phosphorus directly stimulates PTH secretion in vitro.	Phosphorus	5-15	parathyroid hormone	Rattus norvegicus	36-39
8639532-9	1996	We find the ATPase activity of Rep is influenced dramatically by both dimerization and ss DNA ligation state, with the following kcat values for ATP hydrolysis increasing by over 4 orders of magnitude: 2.1 x 10(-3) s(-1) for P, 2.17 +/- 0.04 s(-1) for PS, 16.5 +/- 0.2 s(-1) for P2S, and 71 +/- 2.5 s(-1) for P2S2 (20 mM Tris-HCl, pH 7.5, 6mM NaCl, 5 mM MgCl2, 10% glycerol, 4 degrees C).	Phosphorus	252-254	replication protein	Escherichia coli	31-34
8799692-2	1996	While SHBG decreased significantly (from 56.0 +/- 20.0 to 43.9 +/- 16.1 nM, P = 0.009) phosphorus and urea increased (from 2.8 +/- 0.4 to 4.0 +/- 0.5 mg/dl, P = 0.00006 and from 32.1 +/- 9.4 to 42.3 +/- 11.0 mg/dl, P = 0.03, respectively).	Phosphorus	87-97	sex hormone binding globulin	Homo sapiens	6-10
8799692-5	1996	Plasma levels of SHBG were negatively correlated with phosphorus.	Phosphorus	54-64	sex hormone binding globulin	Homo sapiens	17-21
8809687-2	1996	Feeding a high Ca/P diet for more than 10 days resulted in an increase in the serum phosphate level in Hyp mice to one similar to that of normal mice.	Phosphorus	18-19	phosphate regulating endopeptidase homolog, X-linked	Mus musculus	103-106
8820410-7	1996	Addition of PKC resulted in a significantly slower decay of the fluorescence anisotropy of both DPH-DG and DPH-PC even in the absence of calcium, indicating a calcium independent complexation of PKC with the PS containing micelles.	Phosphorus	208-210	proline rich transmembrane protein 2	Homo sapiens	12-15
8820410-7	1996	Addition of PKC resulted in a significantly slower decay of the fluorescence anisotropy of both DPH-DG and DPH-PC even in the absence of calcium, indicating a calcium independent complexation of PKC with the PS containing micelles.	Phosphorus	208-210	proline rich transmembrane protein 2	Homo sapiens	195-198
8820410-9	1996	Similar specific interactions with PKC resulted in a slower decay of dansylated PMA when calcium and PS were present.	Phosphorus	101-103	proline rich transmembrane protein 2	Homo sapiens	35-38
8789108-6	1996	We used this method to construct a modeled structure for the bacteriophage lambda cro operator for which the phosphorus coordinates were known from 3.5-angstrum resolution crystal data (4CRO).	Phosphorus	109-119	cro	Escherichia virus Lambda	82-85
8789108-6	1996	We used this method to construct a modeled structure for the bacteriophage lambda cro operator for which the phosphorus coordinates were known from 3.5-angstrum resolution crystal data (4CRO).	Phosphorus	109-119	cro	Escherichia virus Lambda	187-190
8821836-3	1996	Calcium absorption and gene expression of calbindin-D9k were decreased in uremia and were also improved by phosphorus restriction.	Phosphorus	107-117	S100 calcium binding protein G	Rattus norvegicus	42-55
8882734-4	1996	Similar immunogenicity was displayed by free Gfpt1 in muramyldipeptide-phosphoethanolamine-containing phosphatidyl-choline, -serine (PC,PS) liposomes.	Phosphorus	136-138	glutamine fructose-6-phosphate transaminase 1	Mus musculus	45-50
8620724-7	1996	SP-A (in microgram/mL) was enhanced in Asb but not affected by smoking: 5.4 +/- 1.5 in Asb vs 1.6 +/- 0.4 in N (p < 0.05), whereas SP-A to phosphorus ratio was increased in Asb but affected by smoking.	Phosphorus	142-152	surfactant protein A2	Homo sapiens	0-4
8821836-7	1996	Phosphorus restriction prevented increases in the expression of ODC, c-fos and c-jun observed in uremia.	Phosphorus	0-10	ornithine decarboxylase 1	Rattus norvegicus	64-67
8821836-7	1996	Phosphorus restriction prevented increases in the expression of ODC, c-fos and c-jun observed in uremia.	Phosphorus	0-10	Fos proto-oncogene, AP-1 transcription factor subunit	Rattus norvegicus	69-74
8946100-4	1996	This could be modified by supplementing with calcium and phosphorus to the levels present in bovine milk.	Phosphorus	57-67	Weaning weight-maternal milk	Bos taurus	100-104
8834546-5	1996	Since the forearm ischemic exercise test induced a sub-normal production of serum lactate, the patient underwent phosphorus magnetic resonance spectroscopy (31P-MRS), a non-invasive method that allows in vivo assessment of the functional status of the glycolytic pathway and mitochondrial oxidative metabolism by measuring the high-energy phosphates and cytosolic pH.	Phosphorus	113-123	MROS	Homo sapiens	161-164
8550752-6	1996	Both hPTH(1-34) and hPTHrP(1-36) caused an increase in serum ionized calcium, a decrease in serum phosphorus, an increase in the fractional excretion of phosphorus, a decrease in the tubular maximum for phosphorus, an increase in nephrogenous cAMP excretion, and suppression of endogenous PTH(1-84).	Phosphorus	98-108	parathyroid hormone like hormone	Homo sapiens	20-26
8599879-9	1996	Both IgG and IgM aPS were beta 2 GPI dependent and did not bind PS in the absence of the glycoprotein.	Phosphorus	18-20	apolipoprotein H	Mus musculus	26-36
8550752-6	1996	Both hPTH(1-34) and hPTHrP(1-36) caused an increase in serum ionized calcium, a decrease in serum phosphorus, an increase in the fractional excretion of phosphorus, a decrease in the tubular maximum for phosphorus, an increase in nephrogenous cAMP excretion, and suppression of endogenous PTH(1-84).	Phosphorus	153-163	parathyroid hormone like hormone	Homo sapiens	20-26
8550752-6	1996	Both hPTH(1-34) and hPTHrP(1-36) caused an increase in serum ionized calcium, a decrease in serum phosphorus, an increase in the fractional excretion of phosphorus, a decrease in the tubular maximum for phosphorus, an increase in nephrogenous cAMP excretion, and suppression of endogenous PTH(1-84).	Phosphorus	153-163	parathyroid hormone like hormone	Homo sapiens	20-26
9064563-2	1996	Amongst these factors, phosphorus retention plays a crucial role in moderate and advanced CRF, by inhibiting renal calcitriol synthesis, lowering serum calcium levels and stimulating PTH secretion.	Phosphorus	23-33	parathyroid hormone	Homo sapiens	183-186
8840328-6	1996	It is clear now that phosphorus per se independent of the levels of ionized calcium and 1,25D3 can increase the synthesis and secretion of PTH in vivo and in vitro.	Phosphorus	21-31	parathyroid hormone	Homo sapiens	139-142
8619364-14	1995	Serum phosphorus concentrations increased with GH (21.2 +/- 3.3%) and high-dose IGF-I (8.8 +/- 3.6%) by day 21 but actually decreased by day 28 (-9.7 +/- 2.7, p < 0.02) with low-dose IGF-I.	Phosphorus	6-16	growth hormone 1	Homo sapiens	47-49
21799547-7	1995	Thus, RNase A enhances the rate of UpA cleavage by 3 x 10(11)-fold by binding to the transition state for P-O(5") bond cleavage with a dissociation constant of <2 x 10(-15) M.	Phosphorus	106-107	ribonuclease pancreatic	Bos taurus	6-13
21799547-7	1995	Thus, RNase A enhances the rate of UpA cleavage by 3 x 10(11)-fold by binding to the transition state for P-O(5") bond cleavage with a dissociation constant of <2 x 10(-15) M.	Phosphorus	106-107	plasminogen activator, urokinase	Bos taurus	35-38
8929628-7	1996	Patients with oxytocin resistant labour had lower intracellular potassium (p < .0006) and phosphorus (p < .02), and higher chloride (p < .05) and sodium (p < .03) compared to levels found in patients who responded to oxytocin treatment.	Phosphorus	93-103	oxytocin/neurophysin I prepropeptide	Homo sapiens	14-22
8619364-14	1995	Serum phosphorus concentrations increased with GH (21.2 +/- 3.3%) and high-dose IGF-I (8.8 +/- 3.6%) by day 21 but actually decreased by day 28 (-9.7 +/- 2.7, p < 0.02) with low-dose IGF-I.	Phosphorus	6-16	insulin like growth factor 1	Homo sapiens	80-85
8619364-14	1995	Serum phosphorus concentrations increased with GH (21.2 +/- 3.3%) and high-dose IGF-I (8.8 +/- 3.6%) by day 21 but actually decreased by day 28 (-9.7 +/- 2.7, p < 0.02) with low-dose IGF-I.	Phosphorus	6-16	insulin like growth factor 1	Homo sapiens	186-191
8619364-15	1995	Urinary phosphorus excretion decreased with high-dose IGF-I only.	Phosphorus	8-18	insulin like growth factor 1	Homo sapiens	54-59
8808193-5	1995	Based on Factor Analysis as well as Regression Analysis there is evidence of a high correlation between Fe and P contents in beta-thalassemia.	Phosphorus	111-112	general transcription factor IIE subunit 1	Homo sapiens	104-106
8720036-4	1995	(2) ANP infusion significantly increased urine flow rate (UFR), creatinine clearance (CCr), fractional excretion rates of sodium (FENa) and chloride (FECl), and urinary phosphorus and magnesium (Mg) excretions in a dose-dependent manner without affecting renal plasma flow and fractional excretion rates of potassium and urea in cisplatin-treated rats.	Phosphorus	169-179	natriuretic peptide A	Rattus norvegicus	4-7
8808193-6	1995	The latter finding led us to propose tentatively an accumulation of Fe as a complex with P-containing molecules.	Phosphorus	89-90	general transcription factor IIE subunit 1	Homo sapiens	68-70
7556531-7	1995	This is diagnostic for the presence of eIF-2 alpha(P)-GDP in cell lysates and suggests that regulation of GEF activity may occur by one or more mechanisms other than eIF-2(alpha) phosphorylation.	Phosphorus	50-53	eukaryotic translation initiation factor 2, subunit 2 (beta)	Mus musculus	39-44
8544403-3	1995	Patients using PS/PA membranes disclosed a further decreased CD14 expression than patients with CU/HE membranes.	Phosphorus	15-17	CD14 molecule	Homo sapiens	61-65
7574708-7	1995	The long range (through 4-bond: P-2, O-2, C-2, C-3, and H-3) coupling between P-2 and H-3, 4JH-3, P-2, was found to be 1.06 Hz and provides strong evidence for the beta-anomer.	Phosphorus	32-33	complement C2	Rattus norvegicus	42-45
7574708-7	1995	The long range (through 4-bond: P-2, O-2, C-2, C-3, and H-3) coupling between P-2 and H-3, 4JH-3, P-2, was found to be 1.06 Hz and provides strong evidence for the beta-anomer.	Phosphorus	32-33	complement C3	Rattus norvegicus	47-50
7664677-11	1995	Furthermore, the up-regulation of intestinal VDR observed in older (5- to 8-week-old) mutants may reflect a compensatory mechanism to help establish and maintain normal serum calcium and phosphorus levels.	Phosphorus	187-197	vitamin D receptor	Rattus norvegicus	45-48
8837895-2	1995	It exhibits 92% nucleotide identity with the ORF 5 of an LDV isolate that lacks neuropathogenicity, LDV-P, and the amino acid identities of the predicted VP-3Ps of the two strains is 90%.	Phosphorus	104-105	CWC15 spliceosome associated protein homolog	Homo sapiens	45-50
8593248-4	1995	Here we investigate the effect of well-known PKC activator 12-O-tetradecanoyl-2 phorbol-13-acetate (TPA), on the levels of 32P incorporation into EGF induced phosphatidylinositols (PI, PI4P, PI4, 5P2) and different phospholipids (PC, PA, PS) as well as on induced tyrosine kinase activity.	Phosphorus	238-240	epidermal growth factor	Homo sapiens	146-149
7556531-7	1995	This is diagnostic for the presence of eIF-2 alpha(P)-GDP in cell lysates and suggests that regulation of GEF activity may occur by one or more mechanisms other than eIF-2(alpha) phosphorylation.	Phosphorus	50-53	rho/rac guanine nucleotide exchange factor (GEF) 2	Mus musculus	106-109
7582503-0	1995	Phosphorus-containing peptides as mixed inhibitors of endopeptidase 3.4.24.15 and 3.4.24.16: effect on neurotensin degradation in vitro and in vivo.	Phosphorus	0-10	neurotensin	Mus musculus	103-114
7496492-9	1995	Phosphorus analysis revealed that the Glut1 zone at pH 8 contained more phospholipids than did the other one.	Phosphorus	0-10	solute carrier family 2 member 1	Homo sapiens	38-43
8527730-1	1995	Phosphorus magnetic resonance spectroscopy was used to determine effects of acute and chronic alcohol exposure on brain intracellular free magnesium concentration (Mgf) and bioenergetic state in rats.	Phosphorus	0-10	KIT ligand	Rattus norvegicus	164-167
7668251-12	1995	These results suggest that BCL3, or a nearby gene, plays a role in the etiology of CL/P in some families.	Phosphorus	86-87	BCL3 transcription coactivator	Homo sapiens	27-31
7636265-4	1995	That the 120-kDa phosphoprotein coimmunoprecipitated by anti-lyn Abs is the beta subunit of GM-CSFR was confirmed in the immunoprecipitates (IP) of M-07e cells with the use of an agarose-conjugated anti-p-tyr mAb.	Phosphorus	17-18	LYN proto-oncogene, Src family tyrosine kinase	Homo sapiens	61-64
7636265-4	1995	That the 120-kDa phosphoprotein coimmunoprecipitated by anti-lyn Abs is the beta subunit of GM-CSFR was confirmed in the immunoprecipitates (IP) of M-07e cells with the use of an agarose-conjugated anti-p-tyr mAb.	Phosphorus	17-18	colony stimulating factor 1 receptor	Homo sapiens	95-99
7582503-2	1995	We have examined several phosphorus-containing peptides as potential mixed inhibitors of two neurotensin-degrading zinc metallopeptidases, endopeptidase 3.4.24.15 and endopeptidase 3.4.24.16.	Phosphorus	25-35	neurotensin	Mus musculus	93-104
7893699-5	1995	Mutation of Tyr79, the residue equivalent to a p-cresol target in D beta M, to Phe79 altered the kinetic parameters of PHM.	Phosphorus	47-48	peptidylglycine alpha-amidating monooxygenase	Homo sapiens	119-122
7628521-0	1995	PC:PS liposomes induce a recruitment of neutrophils and the release of TNF alpha in the lungs of mice sensitized with Saccharopolyspora rectivirgula.	Phosphorus	3-5	tumor necrosis factor	Mus musculus	71-80
7537224-3	1995	In addition HPLC amino acid analysis of acid-hydrolyzed t-PA, PG and u-PA, shows that: (i) P-Ser and P-Tyr residues are present in t-PA; (ii) P-Thr and P-Tyr are present in PG; (iii) P-Ser, P-Thr and P-Tyr are present in u-PA.	Phosphorus	13-14	plasminogen activator, tissue type	Homo sapiens	56-60
7537224-3	1995	In addition HPLC amino acid analysis of acid-hydrolyzed t-PA, PG and u-PA, shows that: (i) P-Ser and P-Tyr residues are present in t-PA; (ii) P-Thr and P-Tyr are present in PG; (iii) P-Ser, P-Thr and P-Tyr are present in u-PA.	Phosphorus	13-14	plasminogen activator, urokinase	Homo sapiens	69-73
7537224-3	1995	In addition HPLC amino acid analysis of acid-hydrolyzed t-PA, PG and u-PA, shows that: (i) P-Ser and P-Tyr residues are present in t-PA; (ii) P-Thr and P-Tyr are present in PG; (iii) P-Ser, P-Thr and P-Tyr are present in u-PA.	Phosphorus	13-14	plasminogen activator, tissue type	Homo sapiens	131-135
7537224-3	1995	In addition HPLC amino acid analysis of acid-hydrolyzed t-PA, PG and u-PA, shows that: (i) P-Ser and P-Tyr residues are present in t-PA; (ii) P-Thr and P-Tyr are present in PG; (iii) P-Ser, P-Thr and P-Tyr are present in u-PA.	Phosphorus	13-14	plasminogen activator, urokinase	Homo sapiens	221-225
7891095-6	1995	[octyl-3H]-Octyl-BDPO is an improved probe for NTE in terms of its potency, reactivity, selectivity, and the formation of 3H-labeled NTE with a stable phosphorus-carbon bond.	Phosphorus	151-161	patatin like phospholipase domain containing 6	Homo sapiens	47-50
7891095-6	1995	[octyl-3H]-Octyl-BDPO is an improved probe for NTE in terms of its potency, reactivity, selectivity, and the formation of 3H-labeled NTE with a stable phosphorus-carbon bond.	Phosphorus	151-161	patatin like phospholipase domain containing 6	Homo sapiens	133-136
7714086-9	1995	Serum Ca, phosphorus, alkaline phosphatase, osteocalcin, and 2-h fasting and 24-h urinary Ca excretion levels all increased significantly in subjects treated with the GnRH-a alone, whereas a decrement or no changes occurred for these measurement in the other two groups.	Phosphorus	10-20	gonadotropin releasing hormone 1	Homo sapiens	167-171
7752492-3	1995	The main factors inducing hyperparathyroidism which is a well known complication in patients with renal failure include (a) phosphorus retention: 1) hypocalcemia and 2) decreased levels of 1 alpha, 25(OH)2 Vitamin D3, (b) reduced number of 1 alpha, 25(OH)2 Vitamin D3 receptors in parathyroid tissue, (c) skeletal resistance to set-point for calcium-regulated parathyroid hormone secretion.	Phosphorus	124-134	parathyroid hormone	Homo sapiens	360-379
7773697-6	1995	CA1 orthodromic evoked PS was lost completely at an average 12.4 +/- 1.6 h after NMDA exposure.	Phosphorus	23-25	carbonic anhydrase 1	Homo sapiens	0-3
7754807-0	1995	Tissue specificity and mechanism of vitamin D receptor up-regulation during dietary phosphorus restriction in the rat.	Phosphorus	84-94	vitamin D receptor	Rattus norvegicus	36-54
7843719-3	1995	Phosphomonoester expressed as a fraction of total phosphorus (PME/P) showed a correlation with abnormal serum aspartate transaminase (AST), histological intralobular degeneration/focal necrosis, portal inflammation, and piecemeal necrosis.	Phosphorus	50-60	cystatin B	Homo sapiens	62-65
7843719-3	1995	Phosphomonoester expressed as a fraction of total phosphorus (PME/P) showed a correlation with abnormal serum aspartate transaminase (AST), histological intralobular degeneration/focal necrosis, portal inflammation, and piecemeal necrosis.	Phosphorus	50-60	solute carrier family 17 member 5	Homo sapiens	134-137
7754807-1	1995	Dietary phosphorus restriction up-regulates intestinal vitamin D receptor (VDR), but the tissue specificity of the up-regulation and the mechanism of receptor accumulation remain unknown.	Phosphorus	8-18	vitamin D receptor	Rattus norvegicus	55-73
7754807-1	1995	Dietary phosphorus restriction up-regulates intestinal vitamin D receptor (VDR), but the tissue specificity of the up-regulation and the mechanism of receptor accumulation remain unknown.	Phosphorus	8-18	vitamin D receptor	Rattus norvegicus	75-78
7754807-11	1995	The results of these studies indicate that VDR up-regulation during dietary phosphorus restriction is tissue-specific and that the mechanism of the up-regulation is time-dependent.	Phosphorus	76-86	vitamin D receptor	Rattus norvegicus	43-46
7754807-12	1995	Acutely (D1-D5), phosphorus restriction up-regulates intestinal VDR through increased VDR gene expression, whereas chronic (D5-D10) phosphorus restriction appears to alter VDR metabolism through nongenomic mechanisms that are consistent with prolongation of the half-life of the receptor.	Phosphorus	17-27	vitamin D receptor	Rattus norvegicus	64-67
7754807-12	1995	Acutely (D1-D5), phosphorus restriction up-regulates intestinal VDR through increased VDR gene expression, whereas chronic (D5-D10) phosphorus restriction appears to alter VDR metabolism through nongenomic mechanisms that are consistent with prolongation of the half-life of the receptor.	Phosphorus	17-27	vitamin D receptor	Rattus norvegicus	86-89
7754807-12	1995	Acutely (D1-D5), phosphorus restriction up-regulates intestinal VDR through increased VDR gene expression, whereas chronic (D5-D10) phosphorus restriction appears to alter VDR metabolism through nongenomic mechanisms that are consistent with prolongation of the half-life of the receptor.	Phosphorus	17-27	vitamin D receptor	Rattus norvegicus	86-89
7754807-13	1995	The nature of the tissue-specific regulation of VDR during phosphorus restriction remains to be determined.	Phosphorus	59-69	vitamin D receptor	Rattus norvegicus	48-51
7748436-0	1994	[Risk of anthropogenic nitrogen and phosphorus entry into the North Sea ecosystem].	Phosphorus	36-46	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	68-71
7547182-1	1995	Phosphorus-31 NMR spectra in rabbit liver were successively observed for more than 5 months in a chronic CCl4 intoxication model using implanted wireless surface coils.	Phosphorus	0-10	C-C motif chemokine 4	Oryctolagus cuniculus	105-109
7706613-8	1995	High dietary phosphorus decreased the activity of glutamine synthetase and increased the activity of glutaminase I in kidney.	Phosphorus	13-23	glutamate-ammonia ligase	Rattus norvegicus	50-70
7853797-1	1994	Phosphorus retention as a result of chronic renal failure (CRF) induces secondary hyperparathyroidism (HPT II) while supplemented low-phosphorus low-protein diets (LPD) prevent it.	Phosphorus	134-144	Ras association (RalGDS/AF-6) and pleckstrin homology domains 1	Homo sapiens	164-167
7977355-4	1994	These data provide evidence from within families that a gene for susceptibility to CL/P is in significant linkage disequilibrium with the C2 allele of the TGFA locus.	Phosphorus	86-87	transforming growth factor alpha	Homo sapiens	155-159
7963147-10	1994	The only differences between our two groups in terms of serum or urinary parameters were for mean osteocalcin level, which was lower in group A (2.16 +/- 1.09 ng/ml) than in group B (2.70 +/- 0.98 ng/ml) (p = 0.029), and in mean urinary phosphorous level, which was higher in group A (1.44 +/- 0.76 mmol/2 hr) than in group B (1.26 +/- 0.89 mmol/2 hr (p = 0.034).	Phosphorus	237-248	bone gamma-carboxyglutamate protein	Homo sapiens	98-109
7853797-2	1994	The aim of this study was to assess in seven patients with advanced CRF and biological HPT II the effects of a LPD providing daily 5 to 7 mg/kg phosphorus, 0.4 g/kg protein, 300 mg calcium (Ca) and supplemented with amino acids, ketoacids, CaCO3 and vitamin D2, on the relationship between ionized Ca (iCa) and PTH concentrations.	Phosphorus	144-154	Ras association (RalGDS/AF-6) and pleckstrin homology domains 1	Homo sapiens	111-114
7853797-4	1994	After three months of LPD, serum phosphorus decreased from 1.59 +/- 0.15 to 1.26 +/- 0.24 mmol/liter (mean +/- SEM, P < 0.02), basal PTH levels from 251 +/- 25 to 127 +/- 16 pg/ml (P < 0.03), while basal iCa and GFR did not vary.	Phosphorus	33-43	Ras association (RalGDS/AF-6) and pleckstrin homology domains 1	Homo sapiens	22-25
7918481-1	1994	The interaction of the actin-binding protein filamin with mixtures of zwitterionic and anionic phospholipids (DMPC, DMPG, PC, PS) was studied in reconstituted lipid monolayers and bilayers.	Phosphorus	126-128	filamin C	Homo sapiens	45-52
8086425-0	1994	Phosphorus-31 nuclear magnetic resonance studies of complexes of thymidylate synthase.	Phosphorus	0-10	thymidylate synthetase	Homo sapiens	65-85
7892964-0	1994	Effects of ACTH treatment on cerebral phosphorus metabolites in infants with the West syndrome.	Phosphorus	38-48	proopiomelanocortin	Homo sapiens	11-15
7841319-7	1994	On the other hand, in LA patients without a CL antibodies, the fPS deficiency is unrelated to an increase in C4b-BP levels and may be due to abnormal binding of PS to C4b-BP.	Phosphorus	64-66	complement C4B (Chido blood group)	Homo sapiens	167-170
8034070-3	1994	RESULTS: Linear correlations between P and 1/DTs of hCG were poor.	Phosphorus	37-38	hypertrichosis 2 (generalised, congenital)	Homo sapiens	52-55
7749371-12	1994	These data therefore suggest that physiological concentrations of P(i) and Zn(II) may be sufficient for a low-level turnover of the contact system in plasma which in turn may be responsible for the background levels of cleaved HK and BK found in normal plasma.	Phosphorus	66-68	kininogen 1	Homo sapiens	234-236
8145072-7	1994	Serum phosphorus varied consistently after each meal with a net efflux from circulation that preceded an efflux of zinc by 2 h. The postprandial response of serum glucose and insulin were related to the postprandial plasma zinc response measured 6 h earlier; the variables were not correlated at concurrent time points.	Phosphorus	6-16	insulin	Homo sapiens	175-182
8025106-3	1994	D21E enhances the paramagnetic effects of Co2+ on 1/T1 and 1/T2 of the phosphorus and on 1/T1 of four proton resonances of dTdA, and these effects are abolished by the binding of the competitive inhibitor 3",5"-pdTp.	Phosphorus	71-81	interleukin 1 receptor like 1	Homo sapiens	42-60
7942157-8	1994	PTH(1-84) increased to a peak at week 2 (p < 0.02), after both the 1,25(OH)2D peak and the serum phosphorus nadir.	Phosphorus	100-110	parathyroid hormone	Homo sapiens	0-3
8075308-4	1994	PS levels, as estimated by binding of 125I-annexin V, were high on two of the cell lines tested, equivalent to 24 x 10(6) sites per cell for HepG2 (Kd 128 nM) and 6.5 x 10(6) sites per cell for MKN-28 (Kd 50 nM).	Phosphorus	0-2	annexin A5	Homo sapiens	43-52
7517468-8	1994	While, the mean +/- SDs of P/S ratio were 12.447 +/- 44.353 in 91 patients with CaP and 2.052 +/- 0.751 in 39 Cap patients with serum PSA level of < or = 10 ng/ml.	Phosphorus	27-28	kallikrein related peptidase 3	Homo sapiens	134-137
8069231-1	1994	The inhibition mechanism of the dimeric human placenta glutathione transferase (GST P1-1) by the antibiotic p-carboxyphenylazoxycyanide (calvatic acid) has been investigated at pH 7.0 and 30.0 degrees C. Experiments performed at different calvatic acid/GST P1-1 molar ratios indicate that one mole of calvatic acid inactivates one mole of the homodimeric enzyme molecule, containing two catalytically equivalent active sites.	Phosphorus	46-47	glutathione S-transferase pi 1	Homo sapiens	80-88
8069231-1	1994	The inhibition mechanism of the dimeric human placenta glutathione transferase (GST P1-1) by the antibiotic p-carboxyphenylazoxycyanide (calvatic acid) has been investigated at pH 7.0 and 30.0 degrees C. Experiments performed at different calvatic acid/GST P1-1 molar ratios indicate that one mole of calvatic acid inactivates one mole of the homodimeric enzyme molecule, containing two catalytically equivalent active sites.	Phosphorus	46-47	glutathione S-transferase pi 1	Homo sapiens	253-261
8187073-7	1994	At incubation of tissues with [3H]Trp-P-1 (0.75 microM) there was also a selective binding of radioactive substance in endothelial cells of the lung and liver and in the vena cava from BNF-treated mice but not from vehicle-treated control mice.	Phosphorus	38-39	natriuretic peptide type B	Mus musculus	185-188
8105683-2	1993	Previous studies have confirmed an association of alleles for TGFA with nonsyndromic cleft lip with or without cleft palate (CL/P) in humans.	Phosphorus	0-1	transforming growth factor alpha	Homo sapiens	62-66
8117706-0	1994	Resolution of individual lipids in mixed phospholipid membranes and specific lipid-cytochrome c interactions by magic-angle spinning solid-state phosphorus-31 NMR.	Phosphorus	145-155	cytochrome c, somatic	Homo sapiens	83-95
8116546-0	1994	Effects of a low-protein, low-phosphorus diet on metabolic insulin clearance in patients with chronic renal failure.	Phosphorus	30-40	insulin	Homo sapiens	59-66
8107105-6	1994	Titration of accessible PS molecules showed that annexin V molecules bind equally well to liposomes of PC/PS ratio ranging from 1 to 400.	Phosphorus	24-26	annexin A5	Homo sapiens	49-58
8107105-6	1994	Titration of accessible PS molecules showed that annexin V molecules bind equally well to liposomes of PC/PS ratio ranging from 1 to 400.	Phosphorus	106-108	annexin A5	Homo sapiens	49-58
8126026-5	1994	Analyses of the evolution of crystalline phases indicates that Ca4(PO4)2O is consumed prior to complete reaction resulting in a phase assemblage of hydroxyapatite (CA/P > 1.5) and CaHPO4.	Phosphorus	67-68	carbonic anhydrase 4	Homo sapiens	63-66
7936038-0	1994	Does erythropoietin have a beneficial effect on calcium, phosphorus and parathyroid hormone levels in pediatric hemodialysis patients?	Phosphorus	57-67	erythropoietin	Homo sapiens	5-19
8152267-4	1994	Immunoblotting with anti-P-tyr Abs demonstrated a prominent 62 kDa phosphotyrosyl protein (pp62) constitutively present in 11/11 Ph+ chronic phase linblasts while being virtually undetectable in equivalent amounts of protein derived from 15/15 and 2/2 comparable normal and Ph-negative chronic phase blast populations, respectively.	Phosphorus	25-26	docking protein 1	Homo sapiens	91-95
8117705-1	1994	Phosphorus-31 NMR has been used to investigate the interaction of cytochrome c with bilayers of the anionic lipids dioleoylphosphatidylglycerol (DOPG), dioleoylphosphatidylserine (DOPS), and diacylphosphatidylinositol (diacylPI).	Phosphorus	0-10	cytochrome c, somatic	Homo sapiens	66-78
8107105-7	1994	The stoichiometry of the binding between annexin V and PS, determined at low PS content, is eight annexin V molecules per one PS molecule.	Phosphorus	55-57	annexin A5	Homo sapiens	41-50
8107105-7	1994	The stoichiometry of the binding between annexin V and PS, determined at low PS content, is eight annexin V molecules per one PS molecule.	Phosphorus	55-57	annexin A5	Homo sapiens	98-107
7857077-1	1994	Calcium and phosphorus metabolism is mainly regulated by PTH through its actions on kidney and bone.	Phosphorus	12-22	parathyroid hormone	Rattus norvegicus	57-60
8253768-6	1993	Insulin increased the glycogen synthase ratio (-Glc-6-P/+Glc-6-P) by 7.5- and 3.5-fold in the presence and absence of glucose, respectively.	Phosphorus	53-55	insulin	Homo sapiens	0-7
8210358-4	1993	ACP has a higher phosphomonoester-phosphocreatine ratio than normal glandular tissue at phosphorus spectroscopy.	Phosphorus	88-98	CPAT1	Homo sapiens	0-3
8222031-9	1993	The P/N2O group (255 +/- 80 micrograms.kg-1 x min-1) received less propofol than the P/O2 group (344 +/- 60 micrograms.kg-1 x min-1) (P < or = 0.0001) and had shorter extubation (P < 0.001) and recovery (P < 0.01) times.	Phosphorus	4-5	CD59 molecule (CD59 blood group)	Homo sapiens	46-51
8361956-6	1993	About 1 mole phosphorus per mole of kappa-casein was also detected.	Phosphorus	13-23	casein kappa	Homo sapiens	36-48
8292752-4	1993	The isomalathion stereoisomers with the R configuration at phosphorus were 4.3-8.8-fold stronger inhibitors of rat brain acetylcholinesterase, yet 3.4-5.8-fold weaker inhibitors of electric eel acetylcholinesterase, than the isomalathion stereoisomers with the S configuration at phosphorus.	Phosphorus	59-69	acetylcholinesterase	Rattus norvegicus	121-141
8292752-5	1993	The rat brain acetylcholinesterase spontaneous (k0 = approximately 13.0 x 10(-3) min-1) and oxime-mediated (koxime) = 51.0 x 10(-3) min-1) reactivation rate constants following inhibition by isomalathion stereoisomers with the R configuration at phosphorus were comparable to spontaneous (11.3 x 10(-3) min-1) and oxime-mediated (50.2 x 10(-3) min-1) reactivation rates obtained for (S)-isoparathion methyl.	Phosphorus	246-256	acetylcholinesterase	Rattus norvegicus	14-34
8292752-7	1993	Rat brain acetylcholinesterase inhibited by the isomalathion stereoisomers with the S configuration at phosphorus were refractory to reactivation, suggesting an alternate mechanism of inhibition, i.e., the loss of the methylthio ligand.	Phosphorus	103-113	acetylcholinesterase	Rattus norvegicus	10-30
8246314-3	1993	These results indicate that monkey CYP1A1 cDNA encoded a functional protein and that the expressed CYP1A1 enzyme is active for the activation of B[a]P as well as AFB1 to produce toxic metabolites.	Phosphorus	37-38	cytochrome P450, family 1, subfamily a, polypeptide 1	Mus musculus	99-105
8399288-11	1993	The present study extends this work to investigate the effects of PC and PS on platelet responses to a natural agonist, thrombin.	Phosphorus	73-75	coagulation factor II, thrombin	Homo sapiens	120-128
8399288-15	1993	Incorporation of PS inhibits thrombin-induced platelet shape change, granule secretion, and protein phosphorylation.	Phosphorus	17-19	coagulation factor II, thrombin	Homo sapiens	29-37
8117245-3	1993	The naturally occurring phosphorus nucleus (P-31) is visible by NMR and phosphorus-31 NMR spectra contain signals from the major components of energy metabolism.	Phosphorus	24-34	ATPase H+ transporting V1 subunit E1	Homo sapiens	44-48
8237476-4	1993	Particulates (titanium, Ti; polymethylmethacrylate, PMMA; and polystyrene, PS) only with phagocytosable size stimulated peritoneal macrophages to secrete IL-1 and PGE2 in a dose- and time-dependent manner.	Phosphorus	75-77	interleukin 1 alpha	Homo sapiens	154-158
8393626-3	1993	pHi was measured from the phosphorus-31 nuclear magnetic resonance chemical shift of 2-deoxy-D-glucose 6-phosphate.	Phosphorus	26-36	glucose-6-phosphate isomerase	Homo sapiens	0-3
8396450-1	1993	Deuterium and phosphorus nuclear magnetic resonance (NMR) has been used to investigate the dynamics of slow motional processes induced in bilayer cardiolipin upon binding with cytochrome c.	Phosphorus	14-24	cytochrome c, somatic	Homo sapiens	176-188
8218573-4	1993	Gold colloid of 5 nm diameter particle size prepared with white phosphorus minimized nonspecific background labeling of beta-casein in paraffin embedded sections of the mammary epithelium of pregnant mice.	Phosphorus	58-74	casein beta	Mus musculus	120-131
8374598-7	1993	Cultures with B(a)P and DMN-OAc showed significantly higher AHH levels as compared with untreated cultures.	Phosphorus	18-19	aryl hydrocarbon receptor repressor	Homo sapiens	60-63
8374037-6	1993	It is likely that the substrate specificity observed for cDNA-expressed adult human liver FMO-D may have consequences for the metabolism and distribution of tertiary amines and phosphorus- and sulfur-containing drugs in humans and may provide insight into the physiologic substrate(s) for adult human liver FMO.	Phosphorus	177-187	fibromodulin	Homo sapiens	90-95
8369987-6	1993	In acromegalic patients, positive correlations were found among serum bone Gla protein and serum growth hormone and serum insulin-like growth factor I levels, as well as among levels of insulin-like growth factor I and serum phosphorus, serum alkaline phosphatase, and urinary hydroxyproline.	Phosphorus	225-235	insulin like growth factor 1	Homo sapiens	186-214
8344001-8	1993	charge distribution) in the region of the phosphorus atom determines that disturbance in the molecular environment of NTE which initiates DN.	Phosphorus	42-52	patatin like phospholipase domain containing 6	Gallus gallus	118-121
8387920-1	1993	N-Isopropyl-p-iodoamphetamine (IMP) receptors in normal human lung tissue were characterized using a radioligand binding assay with iodine-125 IMP as the ligand.	Phosphorus	11-13	BRCA1 associated protein	Homo sapiens	31-34
8513570-3	1993	The concentration of PAF in 26 samples taken during symptomatic PDA (median 16 pg/micrograms lipid phosphorus, range 1.4-1,200 pg/micrograms lipid phosphorus) was significantly higher than that of 31 samples from the same three patients during the periods without symptomatic PDA (median 1.9 pg/micrograms lipid phosphorus, range 0-12 pg/micrograms lipid phosphorus; P < 0.001).	Phosphorus	99-109	PCNA clamp associated factor	Homo sapiens	21-24
8513570-3	1993	The concentration of PAF in 26 samples taken during symptomatic PDA (median 16 pg/micrograms lipid phosphorus, range 1.4-1,200 pg/micrograms lipid phosphorus) was significantly higher than that of 31 samples from the same three patients during the periods without symptomatic PDA (median 1.9 pg/micrograms lipid phosphorus, range 0-12 pg/micrograms lipid phosphorus; P < 0.001).	Phosphorus	147-157	PCNA clamp associated factor	Homo sapiens	21-24
8343991-3	1993	Studies with many organophosphates, phosphinates and chiral phosphonates are entirely consistent with a 2-step process of initiation referred to as "NTE (70-80%) aging": about 70-80% of available nervous system NTE is first covalently phosphylated causing inhibition of esterase activity, and then the molecules of inhibited NTE undergo a covalent bond-cleavage leaving a negative charge in the region of the still-bound phosphorus.	Phosphorus	421-431	patatin like phospholipase domain containing 6	Gallus gallus	149-152
7688442-11	1993	While, the mean +/- SD of P/S ratio was 16.295 +/- 58.584 in all prostate cancer patients, and 2.031 +/- 0.654 in 27 prostate cancer patients with serum PSA level of < or = 20 ng/ml.	Phosphorus	26-27	kallikrein related peptidase 3	Homo sapiens	153-156
8476011-10	1993	The increase in var(s)p was presumed to reflect La(3+)-induced release of Ca2+ from intracellular organelles.	Phosphorus	20-23	carbonic anhydrase 2	Homo sapiens	74-77
8096116-6	1993	[1989, Am J Hum Genet, 45:348-353] that TFGA itself or a closely linked gene contributes to the development of CL/P in humans.	Phosphorus	114-115	transforming growth factor alpha	Homo sapiens	40-44
8280375-1	1993	In this study we analyzed the mutations in c-Ha-ras from skin papillomas initiated with benzo[a]pyrene (B[a]P), 7-methylbenz[a]anthracene (7-MBA), and 10-fluoro-7-methylbenz[a]anthracene (10-F-7-MBA) and from papillomas induced by treatment with tumor promoter alone.	Phosphorus	108-109	Harvey rat sarcoma virus oncogene	Mus musculus	43-51
8094269-0	1993	Resolving an apparent paradox concerning the role of TGFA in CL/P.	Phosphorus	64-65	transforming growth factor alpha	Homo sapiens	53-57
8456422-3	1993	Between August 1991 and October 1991 a clinically important factor VIII inhibitor was detected in five out of the 109 patients receiving factor VIII-P while none of the 109 patients receiving factor VIII-SD developed such antibodies.	Phosphorus	149-150	cytochrome c oxidase subunit 8A	Homo sapiens	67-71
8456422-3	1993	Between August 1991 and October 1991 a clinically important factor VIII inhibitor was detected in five out of the 109 patients receiving factor VIII-P while none of the 109 patients receiving factor VIII-SD developed such antibodies.	Phosphorus	149-150	cytochrome c oxidase subunit 8A	Homo sapiens	144-148
8456422-3	1993	Between August 1991 and October 1991 a clinically important factor VIII inhibitor was detected in five out of the 109 patients receiving factor VIII-P while none of the 109 patients receiving factor VIII-SD developed such antibodies.	Phosphorus	149-150	cytochrome c oxidase subunit 8A	Homo sapiens	144-148
8419119-5	1993	Our studies indicate that IGF-I administration to normal mice results in a dose-dependent (0-10 micrograms/h) increase in 1(OH)ase with maximum effects evident after 24 h, independent of changes in serum calcium, phosphorus, and glucose levels.	Phosphorus	213-223	insulin-like growth factor 1	Mus musculus	26-31
8384200-0	1993	Complexes of myosin subfragment 1 with pyrophosphate and with adenosine diphosphate as studied by phosphorus-31 nuclear magnetic resonance.	Phosphorus	98-108	myosin heavy chain 14	Homo sapiens	13-19
8352890-3	1993	A Ki-ras gene mutation (G-->T at the second position in codon 12) was found in one Glu-P-1-induced colon adenocarcinoma.	Phosphorus	90-91	KRAS proto-oncogene, GTPase	Rattus norvegicus	2-8
1446632-9	1992	Only in the case of EB+P-treated rats did coadministration of 5 micrograms NPY along with LHRH significantly enhance LHRH-stimulated LH secretion (P < 0.001).	Phosphorus	23-24	neuropeptide Y	Rattus norvegicus	75-78
1342184-9	1992	The milk of this region is a good source of calcium, magnesium, phosphorus and zinc, with 35%, 7.4%, 19% and 9% respectively of the RDA being obtained from a 237 ml portion of milk.	Phosphorus	64-74	Weaning weight-maternal milk	Bos taurus	4-8
1416985-1	1992	Gd3+ was evaluated as a probe for Ca2+ sites on protein kinase C (PKC) by studying its ability to replace Ca2+ in activation of PKC isozymes II (beta) and III (alpha) in the lipid systems phosphatidylserine/1,2-dioleoyl-sn-glycerol (PS/DO) and diheptanoylphosphatidylcholine (PC7)/DO.	Phosphorus	233-235	GRDX	Homo sapiens	0-3
1338049-4	1992	PIP like PS, activated Ca(2+)-ATPase activity by modifying ATP activation curve with increasing Vmax of the high affinity site.	Phosphorus	9-11	prolactin induced protein	Homo sapiens	0-3
1338049-4	1992	PIP like PS, activated Ca(2+)-ATPase activity by modifying ATP activation curve with increasing Vmax of the high affinity site.	Phosphorus	9-11	dynein axonemal heavy chain 8	Homo sapiens	30-36
1466489-6	1992	The acute, but transient, effect of IL-1 beta treatment was to cause a decrease in plasma calcium and phosphorus concentrations.	Phosphorus	102-112	interleukin 1 beta	Bos taurus	36-45
1416985-1	1992	Gd3+ was evaluated as a probe for Ca2+ sites on protein kinase C (PKC) by studying its ability to replace Ca2+ in activation of PKC isozymes II (beta) and III (alpha) in the lipid systems phosphatidylserine/1,2-dioleoyl-sn-glycerol (PS/DO) and diheptanoylphosphatidylcholine (PC7)/DO.	Phosphorus	233-235	protein kinase C alpha	Homo sapiens	66-69
1416985-1	1992	Gd3+ was evaluated as a probe for Ca2+ sites on protein kinase C (PKC) by studying its ability to replace Ca2+ in activation of PKC isozymes II (beta) and III (alpha) in the lipid systems phosphatidylserine/1,2-dioleoyl-sn-glycerol (PS/DO) and diheptanoylphosphatidylcholine (PC7)/DO.	Phosphorus	233-235	protein kinase C alpha	Homo sapiens	128-131
1400474-7	1992	Differential substrate phosphorylation by PS/PMA also occurred for PKC isozymes resolved by hydroxylapatite chromatography and was most dramatic for PKC-alpha, which could no longer phosphorylate histone or GS1-12.	Phosphorus	42-44	protein kinase C alpha	Homo sapiens	67-70
1400474-7	1992	Differential substrate phosphorylation by PS/PMA also occurred for PKC isozymes resolved by hydroxylapatite chromatography and was most dramatic for PKC-alpha, which could no longer phosphorylate histone or GS1-12.	Phosphorus	42-44	protein kinase C alpha	Homo sapiens	149-158
1400474-7	1992	Differential substrate phosphorylation by PS/PMA also occurred for PKC isozymes resolved by hydroxylapatite chromatography and was most dramatic for PKC-alpha, which could no longer phosphorylate histone or GS1-12.	Phosphorus	42-44	pseudouridine 5'-phosphatase	Homo sapiens	207-213
1513251-0	1992	Direct measurement of spin-lattice relaxation times of phosphorus metabolites in human myocardium.	Phosphorus	55-65	spindlin 1	Homo sapiens	22-26
1417956-3	1992	With histone or GS1-12 as substrates, protein kinase C was maximally activated by Ca/PS, or to maxima of 62%, 89% or 82% with PS/PMA, Ca/AA or PKC530-558, respectively.	Phosphorus	85-87	pseudouridine 5'-phosphatase	Homo sapiens	16-22
1420963-5	1992	Stacking interactions in the phosphorus-linked morpholino analogues are at least as strong as those found in d(ApA).	Phosphorus	29-39	glutamyl aminopeptidase	Homo sapiens	111-114
1461114-1	1992	In order to examine the mechanisms underlying radiation-induced changes in phosphorus metabolite levels observed in RIF-1 tumors in vivo, RIF-1 cells in culture were perfused for up to 70 h following gamma-irradiation with 0-25 Gy and monitored continuously by 31P NMR spectroscopy at 8.5 T. Cells immobilized in the sample volume by incorporation into calcium alginate beads were bioenergetically stable, but did not replicate at the cell density used.	Phosphorus	75-85	replication timing regulatory factor 1	Homo sapiens	116-121
1441598-10	1992	NAT1 shows marked kinetic selectivity for "monomorphic" substrates (e.g. p-aminobenzoic acid) whose in vivo acetylation rates do not correlate with the acetylation polymorphism.	Phosphorus	50-51	N-acetyltransferase 1	Homo sapiens	0-4
1518087-7	1992	On the other hand, Ps in a class I pseudogene (HLA-H) was 57%, which was in good agreement with Ps in other pseudogenes.	Phosphorus	19-21	major histocompatibility complex, class I, H (pseudogene)	Homo sapiens	47-52
1518087-7	1992	On the other hand, Ps in a class I pseudogene (HLA-H) was 57%, which was in good agreement with Ps in other pseudogenes.	Phosphorus	96-98	major histocompatibility complex, class I, H (pseudogene)	Homo sapiens	47-52
1318746-7	1992	(Rp)- and (Sp)-[16O,17O]DPPI were then converted into trans- and cis-[16O,17O]IcP, respectively, by PI-PLC from Bacillus cereus, which had been shown to proceed with inversion of configuration at phosphorus [Lin, G., Bennett, F. C., & Tsai, M.-D. (1990) Biochemistry 29, 2747-2757].	Phosphorus	196-206	phospholipase C beta 1	Homo sapiens	100-106
1282334-5	1992	In addition, our data suggest that, after synapsin I has reached the nerve endings, the relative proportions of variously phosphorylated synapsin I molecules change, and that these changes lead to a decrease in the overall content of phosphorus.	Phosphorus	234-244	synapsin I	Mus musculus	42-52
1282334-5	1992	In addition, our data suggest that, after synapsin I has reached the nerve endings, the relative proportions of variously phosphorylated synapsin I molecules change, and that these changes lead to a decrease in the overall content of phosphorus.	Phosphorus	234-244	synapsin I	Mus musculus	137-147
1507727-5	1992	There was a significant correlation between the value of %TRP in pre-load of h-PTH and the rate of urinary phosphorus (P) increment between pre-load and post-load of h-PTH in the NO and NH groups.	Phosphorus	107-117	parathyroid hormone	Homo sapiens	79-82
1507727-5	1992	There was a significant correlation between the value of %TRP in pre-load of h-PTH and the rate of urinary phosphorus (P) increment between pre-load and post-load of h-PTH in the NO and NH groups.	Phosphorus	107-117	parathyroid hormone	Homo sapiens	168-171
1319327-0	1992	Inhibition by human interleukin-1 alpha of parathyroid hormone-related peptide effects on renal calcium and phosphorus metabolism in the rat.	Phosphorus	108-118	interleukin 1 alpha	Rattus norvegicus	20-39
1514221-3	1992	Hypercalcemia induced by malignancy or parathyroid hormone-related protein infusion was associated with low serum phosphorus concentration, a decrease in the number of secretory and prosecretory granules in the parathyroid chief cells, and an increase in the cytoplasmic area of chief cells.	Phosphorus	114-124	parathyroid hormone like hormone	Homo sapiens	39-74
1520567-15	1992	Ellthworth-Howard test was positive, in that the infusion of parathyroid hormone (100 u) elicited a marked increment of the urinary excretions of phosphorus and cAMP.	Phosphorus	146-156	parathyroid hormone	Homo sapiens	61-80
15159922-2	1992	),they were the constructed with hexosamine,fatty acids and phosphorus etc.On the other hand,they showed much distinct differences from the enterobacterial LPS structure as follow:(1) 2-keto-3-deoxy-D-mannooctonate(KDO) was not detected by routine procedure.	Phosphorus	60-70	interferon regulatory factor 6	Homo sapiens	156-159
1533622-6	1992	In the presence of Ca2+/calcyclin, CAP-50 formed a complex with calcyclin and bound to the PS-containing vesicles.	Phosphorus	91-93	protein S100-A6	Oryctolagus cuniculus	24-33
1533622-6	1992	In the presence of Ca2+/calcyclin, CAP-50 formed a complex with calcyclin and bound to the PS-containing vesicles.	Phosphorus	91-93	annexin A11	Oryctolagus cuniculus	35-41
1500034-1	1992	Solid-phase extraction with the weak cation-exchange resin Fractogel TSK CM650(S) (TSK CM) was used to optimize the sensitivity and chromatographic resolution by HPLC of the mutagenic heterocyclic aromatic amines MeIQx, 4,8-DiMeIQx, IQ, MeIQ, PhIP, Trp-P-1, Trp-P-2, amino-alpha-carboline and the co-mutagens norharman and harman.	Phosphorus	163-164	tsukushi, small leucine rich proteoglycan	Homo sapiens	69-72
1500034-1	1992	Solid-phase extraction with the weak cation-exchange resin Fractogel TSK CM650(S) (TSK CM) was used to optimize the sensitivity and chromatographic resolution by HPLC of the mutagenic heterocyclic aromatic amines MeIQx, 4,8-DiMeIQx, IQ, MeIQ, PhIP, Trp-P-1, Trp-P-2, amino-alpha-carboline and the co-mutagens norharman and harman.	Phosphorus	163-164	tsukushi, small leucine rich proteoglycan	Homo sapiens	83-86
1557403-0	1992	Synthesis of 5-methylaminomethyl-2-selenouridine in tRNAs: 31P NMR studies show the labile selenium donor synthesized by the selD gene product contains selenium bonded to phosphorus.	Phosphorus	171-181	selenophosphate synthetase 1	Homo sapiens	125-129
1533057-6	1992	Binding of ADP favored Rep dimers in which both protomers bound single-stranded DNA, whereas binding of AMPP(NH)P favored simultaneous binding of both single-stranded and duplex DNA to the Rep dimer.	Phosphorus	111-113	replication protein	Escherichia coli	189-192
1565618-6	1992	A striking feature of syndecan 3 is an extensive (182 amino acid) threonine, serine, and proline (T+S+P)-rich domain that closely resembles T+S+P-rich regions in several mucin-like proteins in which O-linked oligosaccharides are bound to the threonine and serine residues.	Phosphorus	102-103	syndecan 3	Gallus gallus	22-32
1313807-10	1992	We find that Rep monomers (P) can bind either ss-DNA (S) or ds-DNA (D) to form PS or PD, respectively, which can then dimerize to form P2S or P2D.	Phosphorus	79-81	replication protein	Escherichia coli	13-16
1376958-0	1992	Dietary restriction of calcium, phosphorus, and vitamin D elicits differential regulation of the mRNAs for avian intestinal calbindin-D28k and the 1,25-dihydroxyvitamin D3 receptor.	Phosphorus	32-42	vitamin D (1,25- dihydroxyvitamin D3) receptor	Gallus gallus	147-180
1376958-8	1992	However, a more complex regulation of VDR expression occurs in that low-phosphorus restriction enhances VDR mRNA levels, possibly via increased circulating 1,25-(OH)2D3.	Phosphorus	72-82	vitamin D (1,25- dihydroxyvitamin D3) receptor	Gallus gallus	38-41
1376958-8	1992	However, a more complex regulation of VDR expression occurs in that low-phosphorus restriction enhances VDR mRNA levels, possibly via increased circulating 1,25-(OH)2D3.	Phosphorus	72-82	vitamin D (1,25- dihydroxyvitamin D3) receptor	Gallus gallus	104-107
1575962-7	1992	In conclusion, the dietary P/S ratio is well reflected in the fatty acid composition of serum cholesteryl esters and phospholipids, the intake of saturated fats less well, and the intake of monounsaturated fats not at all.	Phosphorus	27-28	chromosome 10 open reading frame 90	Homo sapiens	206-210
1311313-4	1992	Acetylation of bovine fragment 1 in the absence of Ca(II) or Mg(II) ions results in the loss of the metal ion-promoted quenching of the intrinsic Trp fluorescence of the protein and the Ca(II)-mediated binding to phosphatidylserine/phosphatidylcholine (PS/PC) vesicles.	Phosphorus	253-255	carbonic anhydrase 2	Bos taurus	186-192
1573080-8	1992	The ten days" feeding of the high-Ca/-P diet significantly elevated the serum P level in Hyp mice, and it reached a level similar to that of the normal mice.	Phosphorus	38-39	phosphate regulating endopeptidase homolog, X-linked	Mus musculus	89-92
1812274-0	1991	Pharmacology of a phosphorus-containing novel angiotensin converting enzyme inhibitor, SQ 29 852 in anesthetized dogs.	Phosphorus	18-28	angiotensin I converting enzyme	Canis lupus familiaris	46-75
1356882-4	1992	Comparing the difference between basal and intervention (delta 1) and between switchback and intervention diets (delta 2), changes in dchol and P/S ratio correlated significantly with changes in serum total, high-density lipoprotein (HDL) and LDL cholesterol, and apo B levels.	Phosphorus	144-145	apolipoprotein B	Homo sapiens	264-269
1361822-8	1992	It is concluded that on LCD 1) the number of episodes of hypercalcemia was markedly reduced, 2) higher calcium carbonate doses could be used, and thus 3) the control of serum phosphorus improved.	Phosphorus	175-185	transforming growth factor beta induced	Homo sapiens	24-29
1338283-4	1992	Haemoglobin percent, packed cell volume, and serum calcium, phosphorus and vitamin C were also increased in response to dietary F-2.	Phosphorus	60-70	prothrombin	Oryctolagus cuniculus	128-131
1283426-9	1992	Fosinopril, a new phosphorus-containing ACE inhibitor, is administered as a prodrug and is hydrolyzed to the pharmacologically active diacid, fosinoprilat.	Phosphorus	18-28	angiotensin I converting enzyme	Homo sapiens	40-43
1584590-2	1992	PAF was quantitated by platelet-aggregating activity and was found to be 7.8 +/- 1.8 pg/micrograms phosphorus of polyp phospholipid (mean +/- SE; n = 23).	Phosphorus	99-109	PCNA clamp associated factor	Homo sapiens	0-3
1764451-4	1991	It was found that chronic ethanol-induced modifications to each of the major phospholipid classes was responsible to some extent for the resistance to phospholipase A2, however, PS was particularly potent considering it is a compositionally minor constituent.	Phosphorus	178-180	phospholipase A2 group IB	Homo sapiens	151-167
1777593-9	1991	Plasma insulin-like growth factor I levels rose significantly, and serum phosphorus and intact parathyroid hormone levels fell significantly during growth hormone administration.	Phosphorus	73-83	growth hormone 1	Homo sapiens	148-162
1791469-4	1991	At Fe/P ratios above 0.5, the Fe(III)-phosvitin complex becomes increasingly soluble.	Phosphorus	6-7	casein kinase 2 beta	Homo sapiens	38-47
1668076-4	1991	HAp-coated film had a slightly higher Ca/P ratio than the original material and was stoichiometrically Ca10(PO4)6(OH)2 by EPMA analysis.	Phosphorus	41-42	reticulon 3	Homo sapiens	0-3
1798061-2	1991	The blood clearances of 99mTc-P and ICG in dogs decreased with increase in doses of CCl4 and with elapsed time after CCl4 administration.	Phosphorus	30-31	C-C motif chemokine 4	Canis lupus familiaris	84-88
1798061-2	1991	The blood clearances of 99mTc-P and ICG in dogs decreased with increase in doses of CCl4 and with elapsed time after CCl4 administration.	Phosphorus	30-31	C-C motif chemokine 4	Canis lupus familiaris	117-121
1895299-0	1991	Phosphorus-containing inhibitors of HMG-CoA reductase.	Phosphorus	0-10	3-hydroxy-3-methylglutaryl-CoA reductase	Homo sapiens	36-53
1681489-3	1991	Somatostatin decreases the renal plasma flow, glomerular filtration rate, osmotic and free water clearances, sodium and potassium excretion and the tubular reabsorption of phosphorus while urinary osmolality increases.	Phosphorus	172-182	somatostatin	Homo sapiens	0-12
1715393-4	1991	In addition, our data suggest that, after synapsin I has reached the nerve endings, the relative proportion of differently phosphorylated molecules of synapsin I changes, and that these changes lead to a decrease of the overall content of phosphorus.	Phosphorus	239-249	synapsin I	Mus musculus	42-52
1715393-4	1991	In addition, our data suggest that, after synapsin I has reached the nerve endings, the relative proportion of differently phosphorylated molecules of synapsin I changes, and that these changes lead to a decrease of the overall content of phosphorus.	Phosphorus	239-249	synapsin I	Mus musculus	151-161
1757329-2	1991	Infusion of Ps induced significant elevations (greater than 4-fold increase in units/ml of TNF by 60 min, P less than 0.05) in plasma TNF activity (L929 cytolysis assay) and alterations (P less than 0.05) in all hemodynamic and pulmonary parameters within 30-60 min.	Phosphorus	12-14	tumor necrosis factor	Sus scrofa	91-94
1757329-2	1991	Infusion of Ps induced significant elevations (greater than 4-fold increase in units/ml of TNF by 60 min, P less than 0.05) in plasma TNF activity (L929 cytolysis assay) and alterations (P less than 0.05) in all hemodynamic and pulmonary parameters within 30-60 min.	Phosphorus	12-14	tumor necrosis factor	Sus scrofa	134-137
1858733-6	1991	Serum parathyroid hormone level on day 6 correlated with phosphorus intake among formula-fed neonates.	Phosphorus	57-67	parathyroid hormone	Bos taurus	6-25
1713578-6	1991	Within a minute following stimulation of these cells with IL-2, PI 3-kinase activity could be detected in antiphosphotyrosine (anti-P-Tyr) antibody immunoprecipitates.	Phosphorus	64-65	interleukin 2	Mus musculus	58-62
1905108-8	1991	The authors" findings demonstrate that cynomolgus monkey and perhaps other primates provide a close animal model for examining the early transcriptional and post-translational processing of beta APP that precedes A beta P deposition during aging and in Alzheimer"s disease.	Phosphorus	196-197	amyloid beta precursor protein	Homo sapiens	213-219
1768103-1	1991	An extracellular p-coumaroyl esterase produced by the anaerobic fungus Neocallimastix strain MC-2 released p-coumaroyl groups from 0-[5-0-((E)-p-coumaroyl)-alpha-L-arabinofuranosyl]-(1----3)-0-beta -D-xylopyranosyl-(1----4)-D-xylopyranose (PAXX).	Phosphorus	17-19	melanocortin 5 receptor	Homo sapiens	93-97
1854746-2	1991	The enzyme enhances the paramagnetic effects of Co2+ on 1/T1 and 1/T2 of the phosphorus and on 1/T1 of six proton resonances of dTdA, and these effects are abolished by binding of the competitive inhibitor 3",5"-pdTp.	Phosphorus	77-87	interleukin 1 receptor like 1	Homo sapiens	48-66
1710622-1	1991	Plasma concentrations of PTH are much lower for a given calcium or phosphorus level in patients with familial benign hypercalcemia (FBH, or familial hypocalciuric hypercalcemia) than in those with primary hyperparathyroidism; these and other data suggest that there might be tissue hypersensitivity to PTH in FBH.	Phosphorus	67-77	parathyroid hormone	Homo sapiens	25-28
2057347-1	1991	Phosphorus-31 NMR has been applied to the characterization of terminal phosphates on fragments of calf thymus DNA induced by three different nuclease systems: DNase I, DNase II and the artificial nuclease "Mn-TMPyP/KHSO5".	Phosphorus	0-10	deoxyribonuclease 1	Bos taurus	159-166
1902470-6	1991	This rate, adjusted per micromole of lipid phosphorus, is 1636 +/- 358 nM factor Xa/min on monocyte, and 1569 +/- 54 nM factor Xa/min on platelets.	Phosphorus	43-53	coagulation factor X	Homo sapiens	74-83
1802021-2	1991	However, tetraplatin was a much more potent inhibitor than cisplatin, with its I50 values being 1/25, 1/45, and 1/130 that of cisplatin in the presence of DA/Gpp(NH)p, NaF/AlCl3, and forskolin/Gpp(NH)p respectively.	Phosphorus	14-15	C-X-C motif chemokine ligand 8	Homo sapiens	168-171
2010536-10	1991	These data indicate that IGF-I increases SNGFR, SNPF, and SNBF primarily by increasing LpA and also by decreasing RE without affecting delta P. Short-term starvation lowers SNGFR, SNPF, and SNBF primarily by decreasing delta P and possibly by lowering LpA and increasing RA and RE.	Phosphorus	50-51	insulin-like growth factor 1	Rattus norvegicus	25-30
1848101-5	1991	At subsaturating concentrations, histone III-S and protamine sulfate each accelerated the ATPase activity of PKC in the presence of Ca2+ and PS by as much as 1.5-fold.	Phosphorus	141-143	protein kinase C, gamma	Rattus norvegicus	109-112
1999147-9	1991	However, in the absence of apparent P-mediated stimulation of enzyme activity, identical treatment of Hyp mice increased the serum phosphorus level comparably, but paradoxically enhanced 25OHD-1 alpha-hydroxylase (3.1 +/- 0.4 vs. 11.7 +/- 2.0 fmol/mg.min).	Phosphorus	131-141	phosphate regulating endopeptidase homolog, X-linked	Mus musculus	102-105
1997510-8	1991	There was a negative correlation between PTH and phosphorus (P) in 1 degree HPT (r = -0.39; P less than 0.01) and in FBH (r = -0.41; P less than 0.03), but, again, the slopes differed greatly: 1 degree HPT, -6.57; FBH, -1.95 (P less than 0.0001).	Phosphorus	49-59	parathyroid hormone	Homo sapiens	41-44
1997510-11	1991	Thus, PTH values are lower at given Ca and P levels in patients with FBH than in those with 1 degree HPT, suggesting that PTH is more effective in raising Ca and lowering P in FBH than in 1 degree HPT.	Phosphorus	6-7	parathyroid hormone	Homo sapiens	122-125
1704190-5	1991	Because many A beta P-containing plaques in neocortex, cerebellum, and striatum were found to be devoid of any APP labeling, as were vascular A beta P deposits, it is unlikely that the extracellular A beta P is principally derived from the APP found within dystrophic neurites.	Phosphorus	20-21	amyloid beta precursor protein	Homo sapiens	13-19
1782102-4	1991	The increased crystal perfection was confirmed by chemical analyses which showed an increased calcium to phosphorus ratio in the Hyp/Y bones.	Phosphorus	105-115	phosphate regulating endopeptidase homolog, X-linked	Mus musculus	129-132
1856053-0	1991	Decreased plasma esterase-1 activity in rats fed a high-phosphorus diet.	Phosphorus	56-66	kallikrein 1-related peptidase C2	Rattus norvegicus	17-27
1908695-1	1991	Proteose peptone (p.peptone) remarkably induced tissue plasminogen activator (t-PA) activity in the conditioned medium of confluently cultured human embryonic lung diploid fibroblast, IMR-90 cells, in a dose-dependent manner.	Phosphorus	9-10	plasminogen activator, tissue type	Homo sapiens	48-82
1960892-0	1991	Dose effects of cholecystokinin and acetylcholine on phosphorus compounds and secretory responses in isolated perfused pancreas of rat.	Phosphorus	53-63	cholecystokinin	Rattus norvegicus	16-31
1847732-4	1991	However, when hepatic fructose-1-P concentration is elevated in response to a fructose load, inhibition of glucose-6-phosphatase by fructose-1-P may play a regulatory role, along with fructose-1-P-associated deinhibition of glucokinase, by directing glucose-6-P away from glucose formation and towards glycogen synthesis and glycolysis.	Phosphorus	32-34	glucose-6-phosphatase catalytic subunit 1	Rattus norvegicus	107-128
2260979-0	1990	Phosphorus-31 nuclear magnetic resonance spectroscopy reveals two conformational forms of chloroacetol phosphate-bound triosephosphate isomerase.	Phosphorus	0-10	triosephosphate isomerase 1	Homo sapiens	119-144
2240002-4	1990	Neither drug produced any significant change in blood levels of total and ionized calcium, magnesium, or phosphorus, which affect the regulation of parathyroid hormone and vitamin D.	Phosphorus	105-115	parathyroid hormone	Homo sapiens	148-167
2099369-4	1990	Plasma concentrations of osteocalcin did not correlate significantly with those of 1,25-dihydroxyvitamin D, but it was significantly proportional to that of Ca and inorganic P.	Phosphorus	0-1	bone gamma-carboxyglutamate protein	Bos taurus	25-36
2101404-6	1990	Plasma osteocalcin levels increased steadily during the perinatal period; at most stages of perinatal life, and already from the fetal period was osteocalcin higher in the low Ca-P diet rats than in the high Ca-P diet rats (in 22-day-old pups: 1106 +/- 47 ng/ml versus 429 +/- 14 ng/ml).	Phosphorus	0-1	bone gamma-carboxyglutamate protein	Rattus norvegicus	7-18
2146493-0	1990	Molecular analysis of nuc-1+, a gene controlling phosphorus acquisition in Neurospora crassa.	Phosphorus	49-59	ribonuclease	Saccharomyces cerevisiae S288C	22-27
2146493-8	1990	Analysis of nuc-2 and nuc-1; nuc-2 strains transformed by the nuc-1+ gene suggests that phosphate directly affects the level or activity of the negative regulatory factor(s) controlling phosphorus acquisition.	Phosphorus	186-196	ribonuclease	Saccharomyces cerevisiae S288C	22-27
2146493-8	1990	Analysis of nuc-2 and nuc-1; nuc-2 strains transformed by the nuc-1+ gene suggests that phosphate directly affects the level or activity of the negative regulatory factor(s) controlling phosphorus acquisition.	Phosphorus	186-196	ribonuclease	Saccharomyces cerevisiae S288C	62-67
2177024-6	1990	The gene dose effect of HPDR, Hyp and Gy on serum phosphorus values is consistently deviant and heterozygotes resemble affected hemizygotes.	Phosphorus	50-60	phosphate regulating endopeptidase homolog, X-linked	Mus musculus	24-28
2177024-6	1990	The gene dose effect of HPDR, Hyp and Gy on serum phosphorus values is consistently deviant and heterozygotes resemble affected hemizygotes.	Phosphorus	50-60	phosphate regulating endopeptidase homolog, X-linked	Mus musculus	30-33
2402437-1	1990	The determination of configuration at phosphorus in diastereomeric dinucleoside-methylphosphonates having the -O-P(= O)(-CH3)-O- internucleotide linkage with the NOE derived ROESY NMR technique is described for ApT, TpT, ApA, TpA and CpG.	Phosphorus	38-48	limb development membrane protein 1	Homo sapiens	216-219
2092741-6	1990	This animal model for macroscopically heterogenous brain ischemia may be useful for the evaluation of therapeutic interventions in stroke, and as an aid in the interpretation of phosphorus spectra from mixed volumes of ischemic and non-ischemic brain.	Phosphorus	178-188	activation-induced cytidine deaminase	Rattus norvegicus	149-152
2136468-6	1990	The combination of calcium, small doses of vitamin D, NaF and exercise used in the treatment of diabetic osteoporoses leads in general to a significant rise of the calcium serum level, an insignificant rise of the phosphorus level and it reduces alkaline phosphatase activity.	Phosphorus	214-224	C-X-C motif chemokine ligand 8	Homo sapiens	54-57
2229600-6	1990	Milk whey (10 microliters) from quarters with clinical mastitis and from quarters with SCC greater than 900,000 inhibited 96 to 100%, 84 to 100%, and 69 to 100% of DNA synthesis in 3-d cultures of lymphocytes stimulated with Concanavalin A, phytohemagglutinin P, and pokeweed mitogen, respectively.	Phosphorus	260-261	Weaning weight-maternal milk	Bos taurus	0-4
2225770-0	1990	Phosphorus nuclear magnetic resonance of diverse phosvitin species.	Phosphorus	0-10	Casein kinase II subunit beta	Gallus gallus	49-58
2106127-4	1990	Parathyroid hormone concentrations were high in furosemide-treated patients (0.95 +/- 0.15 ng/mL) compared with patients not treated with furosemide and receiving either moderate (0.49 +/- 0.05 ng/mL) or low (0.42 +/- 0.07 ng/mL) phosphorus intakes.	Phosphorus	230-240	parathyroid hormone	Homo sapiens	0-19
2183563-5	1990	Thus the immunoenhancing soluble mediator, i.e., IL-1, is induced equally by PS or LPS and has immunorestorative activity for FLV infected animals.	Phosphorus	77-79	interleukin 1 complex	Mus musculus	49-53
2099214-4	1990	The hydrophobic PS beads were used after coated with different alkylamine monomers (i.e. EDA, ALAM, TEA) by plasma polymerization process.	Phosphorus	16-18	ectodysplasin-A	Mesocricetus auratus	89-92
2177015-0	1990	Modulation of chick intestinal and renal calbindin gene expression by dietary vitamin D3, 1,25-dihydroxyvitamin D3, calcium and phosphorus.	Phosphorus	128-138	calbindin 1	Gallus gallus	41-50
2177015-6	1990	In vitamin D3-fed chicks, dietary calcium (Ca) or phosphorus (P) restriction induced, and high dietary Ca inhibited, intestinal calbindin and its mRNA synthesis.	Phosphorus	50-60	calbindin 1	Gallus gallus	128-137
2177015-6	1990	In vitamin D3-fed chicks, dietary calcium (Ca) or phosphorus (P) restriction induced, and high dietary Ca inhibited, intestinal calbindin and its mRNA synthesis.	Phosphorus	62-63	calbindin 1	Gallus gallus	128-137
2116905-8	1990	The dimethyl ester of phosphatidic acid is degraded efficiently in a calcium-dependent and positional-specific way by native phospholipase A2 and by the mutants, indicating that a negative charge at phosphorus is not an absolute substrate requirement.	Phosphorus	199-209	phospholipase A2 group IB	Homo sapiens	125-141
2335575-0	1990	Persistently elevated parathyroid hormone secretion and action in young women after four weeks of ingesting high phosphorus, low calcium diets.	Phosphorus	113-123	parathyroid hormone	Homo sapiens	22-41
2335575-1	1990	In an earlier 8-day study, we showed increased immunoreactive PTH (iPTH) levels in young adults fed high phosphorus (P), low calcium (Ca) diets assembled from common grocery foods, a dietary pattern characteristic of teens and young adults.	Phosphorus	105-115	parathyroid hormone	Homo sapiens	62-65
2107967-2	1990	For this purpose, quinone reductase [NAD(P)H:quinone oxidoreductase, EC 1.6.99.2] (QR) activity in the forestomach of ICR/Ha mice was investigated at successive time points during benzo(a)pyrene (BP)-induced carcinogenesis.	Phosphorus	40-43	crystallin, zeta	Mus musculus	18-35
2379442-1	1990	Blood phosphorus was measured in consecutive 136 admitted patients in the department of general surgery between Oct.	Phosphorus	6-16	plexin A2	Homo sapiens	112-115
2158363-8	1990	Cis- and trans-tamoxifen inhibited the Ca2(+)- and phosphatidylserine- (PS-) dependent activity of purified rat brain PKC with indistinguishable potencies, but cis-tamoxifen was somewhat more potent than the trans isomer in the inhibition of the Ca2(+)- and PS-independent activity of PKC.	Phosphorus	72-74	protein kinase C, gamma	Rattus norvegicus	118-121
2094538-7	1990	Patients with end-stage CRF (CRp greater than 4 mg/dl) and those on hemodialysis had elevated mean serum phosphorus levels and decreased mean serum total calcium concentrations compared with those with mild and moderate CRF, and more pronounced increases in both mean plasma PTH-COOH and PTH-NH2.	Phosphorus	105-115	C-reactive protein	Homo sapiens	29-32
2094538-9	1990	The logarithm of plasma PTH-NH2, but not PTH-COOH, concentration correlated positively with FEP and serum phosphorus concentration and negatively with total serum calcium concentration, while the logarithms of both PTH-NH2 and PTH-COOH levels correlated positively with CRp.	Phosphorus	106-116	parathyroid hormone	Homo sapiens	24-27
2225770-6	1990	The resolution of numerous additional phosphorus resonances provides the basis for further investigation of the particular molecular environments of phosvitin-bound phosphoryl groups and their involvement in the diverse binding modes for metal complex formation by phosvitins.	Phosphorus	38-48	Casein kinase II subunit beta	Gallus gallus	149-158
2092043-2	1990	Treatment of Jurkat T cells with PS, results in a strong decrease of Interleukin-2 synthesis.	Phosphorus	33-35	interleukin 2	Homo sapiens	69-82
2318237-5	1990	In the high PTH-M patients, corrected calcium was low (7.8 +/- 0.4 mg/dl) as compared to normal PTH-M patients (9.2 +/- 0.5 mg/dl, p less than 0.001), and this was also the case for serum phosphorus (2.2 +/- 0.6 vs. 3.2 +/- 0.3 and 3.4 +/- 0.4 mg/dl, respectively p less than 0.001).	Phosphorus	188-198	parathyroid hormone	Homo sapiens	12-15
33773722-7	2021	Consequently, the proposed AptVEGF/CDs/p-COF fluorescence biosensor offered excellent analytical performances for the VEGF165 detection, displaying a detection limit of 20.9 fg mL-1 within a wide linear range of the VEGF165 concentration of 1.0 pg mL-1-100 ng mL-1.	Phosphorus	18-19	vascular endothelial growth factor A	Homo sapiens	27-34
15236013-5	1990	When the patients were divided into two groups according to the degree of Pp/Ps change by declamping, significant elevation of L/P ratio and C3a level were observed in the group with higher increase (Post-/Pre-declamp value >/=1.25) of Pp/Ps compared to the lower (>>1.25) group.	Phosphorus	77-79	complement C3	Homo sapiens	141-144
15236013-6	1990	After declamping, in the higher Pp/Ps group, a positive correlation existed not only between Pp/Ps change and aortic clamp time, but also between L/P ratio and C3a level.	Phosphorus	35-37	complement C3	Homo sapiens	160-163
33798474-5	2021	When TrpRS was immobilized on Streptavidin (SA) sensor chip, the substrate competitive inhibitor indolmycin exhibited the best binding affinity in HBS-P (10 mM HEPES, 150 mM NaCl, 0.05% surfactant P-20, pH 7.4), 1 mM ATP and MgCl2, with a KD (dissociation equilibrium constant) value of 0.6 +- 0.1 muM.	Phosphorus	151-152	tryptophanyl-tRNA synthetase 1	Homo sapiens	5-10
2149400-1	1990	The ATPase activity of RecA protein was examined by monitoring the changes of NMR phosphorus signals of ATP, ADP and inorganic phosphate.	Phosphorus	82-92	RAD51 recombinase	Homo sapiens	23-27
2348827-1	1990	Calculations using a molecular mechanics methods of the effect of configuration at the asymmetrical phosphorus atom in phosphonic and triester derivatives of d(TpCH3)6, d(TpOEt)6 on the structure and stability of their complexes with dA6].	Phosphorus	100-110	a6	Drosophila melanogaster	234-237
2348827-3	1990	Duplexes of dA6 and non-ionic oligonucleotide analogs with Rp enantiomeric configuration of modified phosphorous groups in d(TpCH3) and Sp in d(TpOEt) turned out to be more stable than those with second enantiomeric configurations Sp and Rp, respectively.	Phosphorus	101-112	a6	Drosophila melanogaster	12-15
33773722-7	2021	Consequently, the proposed AptVEGF/CDs/p-COF fluorescence biosensor offered excellent analytical performances for the VEGF165 detection, displaying a detection limit of 20.9 fg mL-1 within a wide linear range of the VEGF165 concentration of 1.0 pg mL-1-100 ng mL-1.	Phosphorus	18-19	L1 cell adhesion molecule	Mus musculus	177-181
33773722-7	2021	Consequently, the proposed AptVEGF/CDs/p-COF fluorescence biosensor offered excellent analytical performances for the VEGF165 detection, displaying a detection limit of 20.9 fg mL-1 within a wide linear range of the VEGF165 concentration of 1.0 pg mL-1-100 ng mL-1.	Phosphorus	18-19	L1 cell adhesion molecule	Mus musculus	248-252
33773722-7	2021	Consequently, the proposed AptVEGF/CDs/p-COF fluorescence biosensor offered excellent analytical performances for the VEGF165 detection, displaying a detection limit of 20.9 fg mL-1 within a wide linear range of the VEGF165 concentration of 1.0 pg mL-1-100 ng mL-1.	Phosphorus	18-19	L1 cell adhesion molecule	Mus musculus	248-252
33761853-6	2021	OBJECTIVE: The present study aimed to investigate neuroprotective properties of PS against Abeta-in- duced neurotoxicity and to evaluate its potential mechanism of action.	Phosphorus	80-82	amyloid beta precursor protein	Homo sapiens	91-96
33765129-9	2021	Further, consistent with reduced accumulation of free amino acids, ZmPHR1s directly down-regulate ZmAAP2 and ZmLHT1 expression as direct linkers of phosphorus and nitrogen nutrition independent of NIGT1 in the LP maize ear.	Phosphorus	148-158	LHT1	Zea mays	109-115
33055433-6	2021	Among the membranes tested, PCL10%HA favored positive cell attachments, upregulated expression of DSPP and ALP gene and higher Ca/P ratio compared to PCL and PCL15%HA.	Phosphorus	28-29	dentin sialophosphoprotein	Homo sapiens	98-102
33055433-6	2021	Among the membranes tested, PCL10%HA favored positive cell attachments, upregulated expression of DSPP and ALP gene and higher Ca/P ratio compared to PCL and PCL15%HA.	Phosphorus	28-29	ATHS	Homo sapiens	107-110
33761853-13	2021	Although ex- tracts of PS inhibited Abeta-induced ROS production, it was unlikely that neuroprotective effects were simply due to the anti-oxidant capacity of PS.	Phosphorus	23-25	amyloid beta precursor protein	Homo sapiens	36-41
33761853-14	2021	Further, mechanistic study suggested that the neuroprotective effects of PS might be due to its capability to regulate amyloidogenesis through the down regulation of BACE and APP.	Phosphorus	73-75	beta-secretase 1	Homo sapiens	166-170
33761853-15	2021	CONCLUSION: These findings suggest that hexane extracts of PS confer neuroprotection against Abeta- induced neurotoxicity in SH-SY5Y cells by attenuating amyloidogenesis and tau hyperphosphoryla- tion.	Phosphorus	59-61	amyloid beta precursor protein	Homo sapiens	93-98
33761853-15	2021	CONCLUSION: These findings suggest that hexane extracts of PS confer neuroprotection against Abeta- induced neurotoxicity in SH-SY5Y cells by attenuating amyloidogenesis and tau hyperphosphoryla- tion.	Phosphorus	59-61	microtubule associated protein tau	Homo sapiens	174-177
33773251-4	2021	In this paper, a new acidic phosphoric-based geopolymer (named APG binder) was synthesized with fly ash as a raw material and aluminum dihydrogen phosphate as the reactant, and the APG binder was used for Pb2+ S/S for the first time.	Phosphorus	28-38	Mothers against dpp	Drosophila melanogaster	63-66
33773251-4	2021	In this paper, a new acidic phosphoric-based geopolymer (named APG binder) was synthesized with fly ash as a raw material and aluminum dihydrogen phosphate as the reactant, and the APG binder was used for Pb2+ S/S for the first time.	Phosphorus	28-38	Mothers against dpp	Drosophila melanogaster	181-184
33587587-2	2021	Hereby, a bimetallic phosphide embedded in a N and P co-doped porous carbon (FeCoP2@NPPC) material was synthesized by using sustainable biomass-derived N- and P-containing carbohydrates and non-noble metal salts as precursors.	Phosphorus	51-52	natriuretic peptide C	Homo sapiens	77-88
33804795-4	2021	The results showed that the specific surface area and pore size of the phosphorus-modified alumina sample AP7 (prepared with a P/Al molar ratio of 0.07) reached 496.2 m2 g-1 and 21.9 nm, while the specific surface area and pore size of the carbon-covered phosphorus-modified alumina sample CAP7-27 (prepared by using AP7 as a carrier for glucose at a glucose/Al molar ratio of 0.27) reached 435.3 m2 g-1 and 21.2 nm.	Phosphorus	71-81	cathelicidin antimicrobial peptide	Homo sapiens	290-297
33816432-2	2021	The synthesized SA/p(AAc)/o-MWCNTs HNC was used to remove methylene blue (MB) from aqueous solution.	Phosphorus	19-20	glycine-N-acyltransferase	Homo sapiens	21-24
33816432-8	2021	The SA/p(AAc)/o-MWCNTs HNC exhibited a maximum adsorption capacity of 1596.0 mg/g at 25 C. This adsorbent showed excellent MB uptake and good regeneration ability.	Phosphorus	7-8	glycine-N-acyltransferase	Homo sapiens	9-12
32796530-5	2020	We found that embryonic exposure of B[a]P downregulates shh and isl1, causing morphological hypoplasia in the telencephalon, ventral thalamus, hypothalamus, epiphysis and posterior commissure.	Phosphorus	40-41	sonic hedgehog signaling molecule a	Danio rerio	56-59
33236627-0	2021	Electrocatalytic Water Oxidation by a Phosphorus-Nitrogen O PN3-Pincer Cobalt Complex.	Phosphorus	38-48	sodium voltage-gated channel alpha subunit 10	Homo sapiens	60-63
32796530-5	2020	We found that embryonic exposure of B[a]P downregulates shh and isl1, causing morphological hypoplasia in the telencephalon, ventral thalamus, hypothalamus, epiphysis and posterior commissure.	Phosphorus	40-41	ISL LIM homeobox 1a	Danio rerio	64-68
33034465-1	2020	We report on a novel dynamical phenomenon in electron spin resonance experiments of phosphorus donors.	Phosphorus	84-94	spindlin 1	Homo sapiens	54-58
24682550-1	2015	BACKGROUND/AIMS: Fibroblast growth factor 23 (FGF23) and soluble alpha-Klotho are emerging potential biomarkers of phosphorus and vitamin D metabolism which change in concentration in early chronic kidney disease (CKD) in order to maintain normal phosphorus levels.	Phosphorus	115-125	fibroblast growth factor 23	Homo sapiens	17-44
28657671-9	2018	Collectively, APS improves the damage caused by H/P by mediating PI3K/Akt/eNOS signaling pathway.	Phosphorus	15-16	AKT serine/threonine kinase 1	Rattus norvegicus	70-73
24520728-4	2013	The annual total phosphorus (TP) export in stream-flow was 2.61, 2.48 and 1.61 kg P/ha for the 17, 211 and 1524 ha catchments, respectively, compared with a maximum permissible (by regulation) annual export of ca.	Phosphorus	17-27	lamin B receptor	Homo sapiens	82-86
24955930-7	2010	After 12 h and 24 h of incubation, the ALP activity of P-COS was higher compared with the control group.	Phosphorus	55-57	alkaline phosphatase, placental	Homo sapiens	39-42
34923106-0	2022	LncRNA H19 sponges miR-103-3p to promote the high phosphorus-induced osteoblast phenotypic transition of vascular smooth muscle cells by upregulating Runx2.	Phosphorus	50-60	RUNX family transcription factor 2	Rattus norvegicus	150-155
25311553-13	2015	cS and pS increased from CT1 to ST8 (rs: +0.60 and +0.34, respectively).	Phosphorus	7-9	cardiotrophin 1	Homo sapiens	25-28
25311553-13	2015	cS and pS increased from CT1 to ST8 (rs: +0.60 and +0.34, respectively).	Phosphorus	7-9	Oncogene OVC (ovarian adenocarcinoma oncogene)	Homo sapiens	32-35
34678255-1	2022	Dam construction causes phosphorus (P) accumulation in reservoir sediments and significantly affects the generation of available P. However, the effect of dam construction on the activity of sediment alkaline phosphatase (ALP), which is encoded by the bacterial phoD gene and participates in P mineralization, in river sediments remains unclear.	Phosphorus	24-38	alkaline phosphatase, placental	Homo sapiens	200-220
34678255-1	2022	Dam construction causes phosphorus (P) accumulation in reservoir sediments and significantly affects the generation of available P. However, the effect of dam construction on the activity of sediment alkaline phosphatase (ALP), which is encoded by the bacterial phoD gene and participates in P mineralization, in river sediments remains unclear.	Phosphorus	24-38	alkaline phosphatase, placental	Homo sapiens	222-225
34923106-9	2022	Collectively, the lncRNA H19 promoted osteogenic differentiation by modulating the miR-103-3p/Runx2 axis in the process of VSMC calcification induced by a high phosphorus concentration.	Phosphorus	160-170	RUNX family transcription factor 2	Rattus norvegicus	94-99
34923106-4	2022	H19 was expressed at high levels in high phosphorus-induced primary rat VSMCs.	Phosphorus	41-51	H19, imprinted maternally expressed transcript (non-protein coding)	Rattus norvegicus	0-3
34838376-9	2022	The maximum environmental capacity of P in SG soils was 187 Mg ha-1, and the maximum number of years for safe planting was 38 yrs.	Phosphorus	38-39	Rho GTPase activating protein 45	Homo sapiens	63-67
34891056-0	2022	Combined effect of tetracycline and copper ion on catalase activity of microorganisms during the biological phosphorus removal.	Phosphorus	108-118	catalase	Homo sapiens	50-58
34891056-3	2022	To reveal the effect of the mixed pollutants on catalase activity of microorganisms, the present study investigated tetracycline and copper ion as pollutants during the biological phosphorus removal.	Phosphorus	180-190	catalase	Homo sapiens	48-56
34651249-1	2022	One of the physiologic mechanisms responsible to maintain asymmetric phospholipid distribution (in particular phosphatidylserine, PS) in human erythrocyte membranes is orchestrated by the balance between enzymes responsible for active transport of PS from the outer to the inner leaflet (ATP11C) and those whose counteracts these activities (PLSCR1).	Phosphorus	130-132	ATPase phospholipid transporting 11C	Homo sapiens	288-294
34651249-1	2022	One of the physiologic mechanisms responsible to maintain asymmetric phospholipid distribution (in particular phosphatidylserine, PS) in human erythrocyte membranes is orchestrated by the balance between enzymes responsible for active transport of PS from the outer to the inner leaflet (ATP11C) and those whose counteracts these activities (PLSCR1).	Phosphorus	130-132	phospholipid scramblase 1	Homo sapiens	342-348
34651249-1	2022	One of the physiologic mechanisms responsible to maintain asymmetric phospholipid distribution (in particular phosphatidylserine, PS) in human erythrocyte membranes is orchestrated by the balance between enzymes responsible for active transport of PS from the outer to the inner leaflet (ATP11C) and those whose counteracts these activities (PLSCR1).	Phosphorus	248-250	ATPase phospholipid transporting 11C	Homo sapiens	288-294
34651249-2	2022	Using quantitative real-time polymerase chain reaction and standard flow cytometry procedures, we hypothesized that the aberrant expression of either or both ATP11C and PLSCR1 transcripts may disrupt the PS internalization/externalization process and become clinically relevant for patients with sickle cell anemia (SCA).	Phosphorus	204-206	ATPase phospholipid transporting 11C	Homo sapiens	158-164
34651249-2	2022	Using quantitative real-time polymerase chain reaction and standard flow cytometry procedures, we hypothesized that the aberrant expression of either or both ATP11C and PLSCR1 transcripts may disrupt the PS internalization/externalization process and become clinically relevant for patients with sickle cell anemia (SCA).	Phosphorus	204-206	phospholipid scramblase 1	Homo sapiens	169-175
34651249-5	2022	Most importantly, there was a strong inverse correlation between PS exposure and ATP11C/PLSCR1 ratio in sickle erythrocytes (Pearson correlation coefficient, r: - 0.78).	Phosphorus	65-67	ATPase phospholipid transporting 11C	Homo sapiens	81-87
34651249-5	2022	Most importantly, there was a strong inverse correlation between PS exposure and ATP11C/PLSCR1 ratio in sickle erythrocytes (Pearson correlation coefficient, r: - 0.78).	Phosphorus	65-67	phospholipid scramblase 1	Homo sapiens	88-94
34740654-1	2022	Antibiotic resistance gene (ARG) pollution in estuarine environment has drawn great attention, and it is not clear if the physical and chemical parameters such as salinity, total organic carbon, total nitrogen, total phosphorus and antibiotics affects the distribution of ARGs.	Phosphorus	217-227	serpin family A member 2 (gene/pseudogene)	Homo sapiens	272-276
34798712-3	2022	Monoammonium phosphate (MAP) coating with biodegradable organic polymers and the addition of magnesium (Mg) - a nutrient with a synergistic effect on the uptake of P, zinc (Zn), and boron (B) - emerge as a smart strategy to applying these micronutrients uniformly in soils.	Phosphorus	164-165	MAX dimerization protein MGA	Homo sapiens	93-111
34523500-6	2022	The kinetic model was successfully used to predict the binary competitive adsorption of Ni(II)-Co(II) and Cr(VI)-P(V), and especially the overshooting of Cr(VI) induced by P(V).	Phosphorus	172-173	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	95-101
34890944-17	2022	Conversely, cholecystokinin (CCK) mRNA was downregulated (P < 0.01) in birds fed P-deficient diets.	Phosphorus	81-82	cholecystokinin	Gallus gallus	12-27
34890944-18	2022	Anorexia-related hypothalamic cholecystokinin receptor (CCKAR) and melanocortin receptors (MC3R and MC4R) were upregulated (P < 0.05) in birds fed P-deficient diets, in both experiments.	Phosphorus	147-148	cholecystokinin B receptor	Gallus gallus	30-54
34890944-18	2022	Anorexia-related hypothalamic cholecystokinin receptor (CCKAR) and melanocortin receptors (MC3R and MC4R) were upregulated (P < 0.05) in birds fed P-deficient diets, in both experiments.	Phosphorus	147-148	cholecystokinin A receptor	Gallus gallus	56-61
34890944-18	2022	Anorexia-related hypothalamic cholecystokinin receptor (CCKAR) and melanocortin receptors (MC3R and MC4R) were upregulated (P < 0.05) in birds fed P-deficient diets, in both experiments.	Phosphorus	147-148	melanocortin 3 receptor	Gallus gallus	91-95
34890944-18	2022	Anorexia-related hypothalamic cholecystokinin receptor (CCKAR) and melanocortin receptors (MC3R and MC4R) were upregulated (P < 0.05) in birds fed P-deficient diets, in both experiments.	Phosphorus	147-148	melanocortin 4 receptor	Gallus gallus	100-104
34700087-3	2022	A phosphorus saturation ratio (PSR = P/(Fe + Al)) can be used to classify high and low risk soils based on a commonly applied Mehlich-3 soil test.	Phosphorus	2-12	jumonji domain containing 6, arginine demethylase and lysine hydroxylase	Homo sapiens	31-34
34896856-6	2022	Langmuir adsorption isotherm, quasi-second-order kinetic equation and mass transfer kinetics was found to describe the phosphorus adsorption process of CAs-4 and CA-4 in better way.	Phosphorus	119-129	Cas scaffold protein family member 4	Homo sapiens	152-157
34896856-6	2022	Langmuir adsorption isotherm, quasi-second-order kinetic equation and mass transfer kinetics was found to describe the phosphorus adsorption process of CAs-4 and CA-4 in better way.	Phosphorus	119-129	carbonic anhydrase 4	Homo sapiens	162-166
34910460-5	2022	H33A also greatly slows P formation, while H5A modestly slows both formation of Q and its reactions with substrates.	Phosphorus	24-25	H3.3 histone A	Homo sapiens	0-4
34346349-0	2022	Trends of the response-relationship between net anthropogenic nitrogen and phosphorus inputs (NANI/NAPI) and TN/TP export fluxes in Raohe basin, China.	Phosphorus	75-85	C-type lectin domain family 3 member B	Homo sapiens	109-111
34928309-6	2022	Biol.https://doi.org/10.1083/jcb.202103141) demonstrate exchange of endosomal PI4P for PS by ORP10 at ER-endosome contact sites, with the consequent recruitment of endosomal fission factors.	Phosphorus	87-89	oxysterol binding protein like 10	Homo sapiens	93-98
34928309-6	2022	Biol.https://doi.org/10.1083/jcb.202103141) demonstrate exchange of endosomal PI4P for PS by ORP10 at ER-endosome contact sites, with the consequent recruitment of endosomal fission factors.	Phosphorus	87-89	epiregulin	Homo sapiens	102-104
34560496-0	2022	Riverine flux of dissolved phosphorus to the coastal sea may be overestimated, especially in estuaries of gated rivers: Implications of phosphorus adsorption/desorption on suspended sediments.	Phosphorus	27-37	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	53-56
34755431-0	2022	Configurational Lability at Tetrahedral Phosphorus: syn/anti-Isomerization of a P-Stereogenic Phosphiranium Cation by Intramolecular Epimerization at Phosphorus.	Phosphorus	40-50	synemin	Homo sapiens	52-55
34755431-0	2022	Configurational Lability at Tetrahedral Phosphorus: syn/anti-Isomerization of a P-Stereogenic Phosphiranium Cation by Intramolecular Epimerization at Phosphorus.	Phosphorus	150-160	synemin	Homo sapiens	52-55
34786856-0	2022	Recent Developments in the Chemistry of Pn(I) (Pn = N, P, As, Sb, Bi) Cations.	Phosphorus	55-56	serpin family E member 2	Homo sapiens	40-45
34786856-1	2022	The Group 15 Pn(I) cations (Pn = N, P, As, Sb and Bi), which are isoelectronic with the donor-stabilized carbones, have emerged recently.	Phosphorus	36-37	serpin family E member 2	Homo sapiens	13-18
34563780-11	2022	For P adsorption isotherm process the Langmuir"s isotherms showed a good fit, with a maximum adsorption capacity of 90.8, 134.0, and 67.9 mgg-1 for ES, ESF-1:1, and ESF-1:10, respectively.	Phosphorus	4-5	ESF1 nucleolar pre-rRNA processing protein homolog	Homo sapiens	165-170
34333009-11	2022	Combination use of P (25 kg ha-1) and Zn fertilizer on maize enhanced its nutritional supply ability regarding Zn and Cu, and simultaneously mitigated potential human health risks associated with Cd and Pb.	Phosphorus	19-20	1,4-alpha-glucan-branching enzyme 2, chloroplastic/amyloplastic	Zea mays	28-32
34346349-3	2022	Based on the variation of net anthropogenic N and P inputs (NANI/NAPI) in the Raohe basin from 1990 to 2018, we constructed the response relationship between NANI/NAPI and total nitrogen and phosphorus (TN/TP) export fluxes in the riverine, which successfully predicted N and P export at the basin scale management.	Phosphorus	191-201	C-type lectin domain family 3 member B	Homo sapiens	203-205
34358891-1	2022	This work discussed the feasibility and stability of utilizing C-S-H phosphorus recovered products, HAP/C-S-H, to remove Zn(II) from aqueous solution and in-situ immobilize Zn(II) in contaminated soil.	Phosphorus	69-79	reticulon 3	Homo sapiens	100-103
34341919-1	2022	A new multi-point inflow pre-anoxic/oxic/anaerobic/anoxic/oxic (A1/O2/A3/A4/O5) sludge-membrane coupling process and pilot plant were developed and designed to solve the problem of nitrogen and phosphorus removal of low carbon and nitrogen (C/N) ratio domestic sewage in southern China.	Phosphorus	194-204	immunoglobulin kappa variable 2D-36 (pseudogene)	Homo sapiens	70-78
34761518-5	2022	CoP-HS exhibits the best catalytic activity for HER among these CoPx -HS in both acidic and alkaline media, originating from the adjusted electronic density of phosphorus to affect absorption-desorption process on H. Moreover, the calculated DeltaGH* based on P-sites of CoP-HS follows a quite similar trend with the normalized overpotential and Tafel slope, indicating the important role of P-sites for the HER process.	Phosphorus	160-170	caspase recruitment domain family member 16	Homo sapiens	0-3
34529316-7	2022	The results showed that pretreatment of neurons with roscovitine partially rescued cells from B(a)P-induced apoptosis, and alleviated B(a)P-induced upregulation of phosphorylated p53 at Ser15.	Phosphorus	138-139	Wistar clone pR53P1 p53 pseudogene	Rattus norvegicus	179-182
34529316-8	2022	Our results suggest that Cdk5/p53 signaling pathway may be involved in B(a)P-induced neuronal apoptosis, which will provide information to further elucidate the molecular mechanisms of B(a)P-induced neurotoxicity.	Phosphorus	75-76	cyclin-dependent kinase 5	Rattus norvegicus	25-29
34529316-8	2022	Our results suggest that Cdk5/p53 signaling pathway may be involved in B(a)P-induced neuronal apoptosis, which will provide information to further elucidate the molecular mechanisms of B(a)P-induced neurotoxicity.	Phosphorus	75-76	Wistar clone pR53P1 p53 pseudogene	Rattus norvegicus	30-33
34529316-8	2022	Our results suggest that Cdk5/p53 signaling pathway may be involved in B(a)P-induced neuronal apoptosis, which will provide information to further elucidate the molecular mechanisms of B(a)P-induced neurotoxicity.	Phosphorus	189-190	cyclin-dependent kinase 5	Rattus norvegicus	25-29
34529316-8	2022	Our results suggest that Cdk5/p53 signaling pathway may be involved in B(a)P-induced neuronal apoptosis, which will provide information to further elucidate the molecular mechanisms of B(a)P-induced neurotoxicity.	Phosphorus	189-190	Wistar clone pR53P1 p53 pseudogene	Rattus norvegicus	30-33
34732508-1	2022	Background Some reports indicate that serum phosphorus levels in the range seen clinically among patients undergoing dialysis attenuate calcium receptor activation and modify parathyroid hormone (PTH) release from isolated parathyroid glands in vitro Some clinicians and providers of dialysis thus have suggested that calcimimetic agents are ineffective and should not be used to manage secondary hyperparathyroidism among those undergoing dialysis when serum phosphorus concentrations exceed certain threshold levels.	Phosphorus	44-54	parathyroid hormone	Homo sapiens	175-194
34732508-1	2022	Background Some reports indicate that serum phosphorus levels in the range seen clinically among patients undergoing dialysis attenuate calcium receptor activation and modify parathyroid hormone (PTH) release from isolated parathyroid glands in vitro Some clinicians and providers of dialysis thus have suggested that calcimimetic agents are ineffective and should not be used to manage secondary hyperparathyroidism among those undergoing dialysis when serum phosphorus concentrations exceed certain threshold levels.	Phosphorus	44-54	parathyroid hormone	Homo sapiens	196-199
34732508-4	2022	However, with each calcimimetic agent, the decreases in PTH from baseline were less at each interval of follow-up during the trials among participants with serum phosphorus levels above one of three prespecified threshold values compared with those with serum phosphorus levels below these thresholds.	Phosphorus	162-172	parathyroid hormone	Homo sapiens	56-59
34825490-1	2022	The catalytic hydrogen-evolving activities of transition-metal phosphides are greatly related to the phosphorus content, but the physical origin of performance enhancement remains ambiguous, and tuning the catalytic activity of nickel phosphides (NiP2 /Ni5 P4 ) remains challenging due to unfavorable H* adsorption.	Phosphorus	101-111	BCL2 interacting protein 2	Homo sapiens	247-251
34761518-5	2022	CoP-HS exhibits the best catalytic activity for HER among these CoPx -HS in both acidic and alkaline media, originating from the adjusted electronic density of phosphorus to affect absorption-desorption process on H. Moreover, the calculated DeltaGH* based on P-sites of CoP-HS follows a quite similar trend with the normalized overpotential and Tafel slope, indicating the important role of P-sites for the HER process.	Phosphorus	160-170	caspase recruitment domain family member 16	Homo sapiens	271-274
34438149-4	2021	In this study, a microcosm experiment with different initial DOM contents elucidated that the biomass, and biomass nitrogen and phosphorus contents were greatly influenced by humic-like substances (C2 and C3), while the growth of periphytic biofilms increased the contents of humic-like (C1 and C2) and tryptophan-like substances (C5) in soil.	Phosphorus	128-138	complement C2	Homo sapiens	198-207
34968051-0	2022	Red Phosphorus: An Up-and-Coming Photocatalyst on the Horizon for Sustainable Energy Development and Environmental Remediation.	Phosphorus	0-14	secreted LY6/PLAUR domain containing 1	Homo sapiens	16-21
34890370-8	2021	In obese women, the levels of CRP positively correlated with Zn, TNFalpha with Mg, IFNgamma with Cu and P.	Phosphorus	104-105	C-reactive protein	Homo sapiens	30-33
34677901-1	2021	By employing the highly reducing aluminyl complex (K{(NON)Al}) 2 (NON = 4,5- bis (2,6-diisopropylanilido)-2,7-di- tert -butyl-9,9-dimethylxanthene), we demonstrate the controlled formation of P 4 2- and P 4 4- complexes from white phosphorus, and chemically reversible inter-conversion between them.	Phosphorus	231-241	erythrocyte membrane protein band 4.2	Homo sapiens	192-208
34542128-1	2021	Long-chain n-alkyl-H-phosphinic acids (Alk = C4-C18) are chemoselectively synthesized in yields up to 90% via the direct one-pot alkylation/oxidation of red phosphorus (Pn) in the multi-phase alkyl bromide/KOH/H2O/toluene system with alkyl-PEG recyclable micellar catalysts, which demonstrate good recyclability.	Phosphorus	153-167	ALK receptor tyrosine kinase	Homo sapiens	39-42
34894207-3	2021	METHODS: We explored eryptosis using the annexin V-binding assay, taken as an indicator of PS exposure at the erythrocyte surface.	Phosphorus	91-93	annexin A5	Homo sapiens	41-50
34836491-6	2021	Nor was RA-induced upregulation of p-tyr phosphorylation of p47phox, a member of the NADPH complex that produces ROS, a putative phosphorylation dependent signaling regulator.	Phosphorus	35-36	neutrophil cytosolic factor 1	Homo sapiens	60-67
34947158-0	2021	Potential Application of Pin-to-Liquid Dielectric Barrier Discharge Structure in Decomposing Aqueous Phosphorus Compounds for Monitoring Water Quality.	Phosphorus	101-111	dynein light chain LC8-type 1	Homo sapiens	25-28
34947158-4	2021	Moreover, we proposed that the pin-to-liquid DBD reactor could be used to decompose phosphorus compounds in water in the form of phosphate as a promising pretreatment method for monitoring total phosphorus in water.	Phosphorus	84-94	dynein light chain LC8-type 1	Homo sapiens	31-34
34855407-4	2022	Fusion of single unilamellar vesicles equipped with syt-1 and synaptobrevin 2 with planar pore-spanning target membranes containing PS and PI(4,5)P2 shows an almost complete suppression of stalled intermediate fusion states and an accelerated fusion kinetics in the presence of Ca2+, which is further enhanced upon addition of ATP.	Phosphorus	132-134	synaptotagmin 1	Homo sapiens	52-57
34855407-4	2022	Fusion of single unilamellar vesicles equipped with syt-1 and synaptobrevin 2 with planar pore-spanning target membranes containing PS and PI(4,5)P2 shows an almost complete suppression of stalled intermediate fusion states and an accelerated fusion kinetics in the presence of Ca2+, which is further enhanced upon addition of ATP.	Phosphorus	132-134	vesicle associated membrane protein 2	Homo sapiens	62-77
34536830-12	2021	For measurements related to quartz, especially for natural radiation background dose measurement, the most suitable TLDs are Al2O3:C and LiF:Mg,Cu,P.	Phosphorus	147-148	LIF interleukin 6 family cytokine	Homo sapiens	137-140
34947158-4	2021	Moreover, we proposed that the pin-to-liquid DBD reactor could be used to decompose phosphorus compounds in water in the form of phosphate as a promising pretreatment method for monitoring total phosphorus in water.	Phosphorus	195-205	dynein light chain LC8-type 1	Homo sapiens	31-34
34947158-5	2021	The decomposition of phosphorus compounds using the pin-to-liquid DBD reactor demonstrated excellent performance-comparable to the thermochemical pretreatment method-which could be a standard pretreatment method for decomposing phosphorus compounds in water.	Phosphorus	21-31	dynein light chain LC8-type 1	Homo sapiens	52-55
34947158-5	2021	The decomposition of phosphorus compounds using the pin-to-liquid DBD reactor demonstrated excellent performance-comparable to the thermochemical pretreatment method-which could be a standard pretreatment method for decomposing phosphorus compounds in water.	Phosphorus	228-238	dynein light chain LC8-type 1	Homo sapiens	52-55
34878213-0	2022	Red Phosphorus Anchored on Nitrogen-Doped Carbon Bubble-Carbon Nanotube Network for Highly Stable and Fast-Charging Lithium-Ion Batteries.	Phosphorus	4-14	Fas activated serine/threonine kinase	Homo sapiens	102-106
34738873-5	2021	In contrast, repression of IDO attenuated p-CA functions regulating BMDMs through IL-4.	Phosphorus	42-43	indoleamine 2,3-dioxygenase 1	Mus musculus	27-30
34738873-5	2021	In contrast, repression of IDO attenuated p-CA functions regulating BMDMs through IL-4.	Phosphorus	42-43	interleukin 4	Mus musculus	82-86
34217932-8	2021	Concerning phosphorus, competition with hydroxide ions for sorption site or dissolution of phosphate minerals in alkaline pH caused release of dissolved P to solution and decrease of P content in recovered colloids.	Phosphorus	153-154	phenylalanine hydroxylase	Homo sapiens	122-124
34217932-8	2021	Concerning phosphorus, competition with hydroxide ions for sorption site or dissolution of phosphate minerals in alkaline pH caused release of dissolved P to solution and decrease of P content in recovered colloids.	Phosphorus	183-184	phenylalanine hydroxylase	Homo sapiens	122-124
34930854-1	2021	INTRODUCTION: Fibroblast growth factor-23 (FGF23) is responsible for regulating the metabolism of phosphorus and vitamin D by affecting the kidneys and parathyroid gland.	Phosphorus	98-108	fibroblast growth factor 23	Homo sapiens	14-41
34091747-12	2021	In the NF1 group, tubular phosphorus reabsorption was significantly lower and uric acid excretion significantly higher than in the control group.Conclusion: Hypertension, urinary tract anomalies, and impaired renal function were more common in NF1 patients than healthy controls.	Phosphorus	26-36	neurofibromin 1	Homo sapiens	7-10
34091747-12	2021	In the NF1 group, tubular phosphorus reabsorption was significantly lower and uric acid excretion significantly higher than in the control group.Conclusion: Hypertension, urinary tract anomalies, and impaired renal function were more common in NF1 patients than healthy controls.	Phosphorus	26-36	neurofibromin 1	Homo sapiens	244-247
34918979-10	2021	The present study further suggests that PAX3 may be associated with CL/P etiology.	Phosphorus	71-72	paired box 3	Mus musculus	40-44
34926505-4	2021	There was no association between serum phosphorus with all-cause and cardiovascular mortality, but significant interactions (p = 0.02) between phosphorus and albumin existed in overall population.	Phosphorus	143-153	albumin	Homo sapiens	158-165
34930854-1	2021	INTRODUCTION: Fibroblast growth factor-23 (FGF23) is responsible for regulating the metabolism of phosphorus and vitamin D by affecting the kidneys and parathyroid gland.	Phosphorus	98-108	fibroblast growth factor 23	Homo sapiens	43-48
34747490-8	2021	In phase 1, reducing Ca and P did not reduce gastric pH or fecal score, but pigs fed the 50% diets had reduced (P < 0.05) average daily gain (ADG) and average daily feed intake (ADFI) compared with pigs fed the 100% diets.	Phosphorus	28-29	ADG	Sus scrofa	142-145
34861810-5	2021	RESULTS: A high-phosphorus intervention increased systolic blood pressure (SBP) and parathyroid hormone (PTH) in CTL and CKD rats but did not change serum creatinine and 25(OH)D levels.	Phosphorus	16-26	parathyroid hormone	Rattus norvegicus	84-103
34987718-8	2021	The CD90 + cells exhibited higher amounts of P, S, Cl, K, and Ca, while the Cu and Zn exhibited more than CD146-.	Phosphorus	45-46	Thy-1 cell surface antigen	Homo sapiens	4-8
34861810-6	2021	After the high-phosphorus diet, serum phosphate and fibroblast growth factor 23 (FGF23) increased in the CKDP group compared with the CKD group.	Phosphorus	15-25	fibroblast growth factor 23	Rattus norvegicus	52-79
34541999-10	2021	Furthermore, serum phosphorus level was positively correlated with phosphate tubular maximum per volume of filtrate (TmP/GFR) (Pearson r = 0.66, p < .001) in subgroup analysis, indicating renal phosphate loss via proximal renal tubular dysfunction.	Phosphorus	19-29	epithelial membrane protein 1	Homo sapiens	117-120
34861810-5	2021	RESULTS: A high-phosphorus intervention increased systolic blood pressure (SBP) and parathyroid hormone (PTH) in CTL and CKD rats but did not change serum creatinine and 25(OH)D levels.	Phosphorus	16-26	parathyroid hormone	Rattus norvegicus	105-108
34861810-6	2021	After the high-phosphorus diet, serum phosphate and fibroblast growth factor 23 (FGF23) increased in the CKDP group compared with the CKD group.	Phosphorus	15-25	fibroblast growth factor 23	Rattus norvegicus	81-86
34837246-3	2022	The multi-elemental analysis highlighted that the concentrations of nutrients in white lupin plants were mainly affected by P availability.	Phosphorus	124-125	5'-nucleotidase, cytosolic IIIA	Homo sapiens	87-92
34861810-9	2021	The Chao1 and Ace indexes were decreased in the CTL group after high-phosphorus diet intervention.	Phosphorus	69-79	angiotensin I converting enzyme	Rattus norvegicus	14-17
34885804-2	2021	Reactions of EBr3 (E = P, As) with iPr2PAcenapLi (Acenap = acenaphthene-5,6-diyl) afforded the thermally stable peri-substitution supported donor-acceptor complexes, iPr2PAcenapEBr23 and 4.	Phosphorus	23-24	EBR3	Homo sapiens	13-17
34846946-9	2022	In summary, our researches suggested that SET8 overexpression ameliorated high phosphorus induced calcification of vascular smooth muscle cells via activating PI3K/Akt mediated anti-apoptotic effects.	Phosphorus	79-89	lysine methyltransferase 5A	Homo sapiens	42-46
34837246-2	2022	In this study, under N- and P-free nutrient solution (-N-P), nodulating white lupin plants developed some nodules and analogous cluster root structures characterized by different morphological, physiological, and molecular responses than those observed upon single nutrient deficiency (strong acidification of external media, a better nutritional status than -N+P and +N-P plants).	Phosphorus	28-29	5'-nucleotidase, cytosolic IIIA	Homo sapiens	78-83
34837246-7	2022	They contribute to the good development of nodulating white lupin plants when grown on N- and P-free media.	Phosphorus	94-95	5'-nucleotidase, cytosolic IIIA	Homo sapiens	60-65
34837246-2	2022	In this study, under N- and P-free nutrient solution (-N-P), nodulating white lupin plants developed some nodules and analogous cluster root structures characterized by different morphological, physiological, and molecular responses than those observed upon single nutrient deficiency (strong acidification of external media, a better nutritional status than -N+P and +N-P plants).	Phosphorus	371-372	5'-nucleotidase, cytosolic IIIA	Homo sapiens	78-83
34837246-8	2022	This study provides evidence that limited N and P availability in the nutrient solution can promote white lupin-Bradyrhizobium symbiosis, which is favorable for the sustainability of legume production.	Phosphorus	48-49	5'-nucleotidase, cytosolic IIIA	Homo sapiens	106-111
34392097-6	2021	It was proposed that these conjugates with PS as skeleton (PS-PN) dominate granular stability by affecting hydrophobicity interactions and hydrogen bonds system, which are two important parameters to gel properties, constituting a crucial finding of this work.	Phosphorus	43-45	persephin	Homo sapiens	59-64
34739538-3	2021	Herein, binder-free, phosphorus-doped NiCo2S4/CFP (Ni-Co-S-P) was synthesized under hydrothermal conditions, followed by surface phosphorization via solid reaction.	Phosphorus	21-31	complement factor properdin	Homo sapiens	38-49
34789346-7	2021	The diet containing the highest STPP inclusion level and lowest Ca:P induced the highest peaks in post-prandial plasma P and PTH levels (1.8mmol/l and 27.2pg/ml, respectively) and the longest duration of concentrations raised above baseline were observed at 3 hours for P and 6 hours for PTH.	Phosphorus	67-68	parathyroid hormone	Felis catus	125-128
34789346-8	2021	Data indicate that Ca:P modulates postprandial plasma P and PTH.	Phosphorus	22-23	parathyroid hormone	Felis catus	60-63
34831089-5	2021	Thus lipopolysaccharide (LPS) induced microglial exosomes to contain more inflammatory signals, whilst stimulation with the TREM2 ligand phosphatidylserine (PS+) increased metabolic signals within the microglial exosomes.	Phosphorus	157-160	triggering receptor expressed on myeloid cells 2	Homo sapiens	124-129
34773306-0	2021	Phosphorus equivalency of phytase with various evaluation indicators of duck in starter.	Phosphorus	0-10	putative glycerophosphoryl diester phosphodiesterase	Glycine max	26-33
34773306-1	2021	This study was conducted to evaluate phosphorus (P) equivalency of phytase with various evaluation indicators of ducks in starter (0-14 days).	Phosphorus	37-47	putative glycerophosphoryl diester phosphodiesterase	Glycine max	67-74
34773306-7	2021	With the increase of dietary phytase level (treatments V-VIII), the apparent utilization of Ca and P showed no significant difference (p > 0.05) but an increasing trend.	Phosphorus	99-100	putative glycerophosphoryl diester phosphodiesterase	Glycine max	29-36
34773306-10	2021	Based on corn-soybean-rapeseed meal diet, with the evaluation indexes of FI, BWG, tibia ash, tibia Ca, tibia P, and apparent utilization of Ca and P, the addition of 500 U/kg phytase could release aP of 0.03%, 0.04%, 0.02%, 0.01%, 0.02%, 0.08%, and 0.07%, respectively.	Phosphorus	147-148	putative glycerophosphoryl diester phosphodiesterase	Glycine max	175-182
34358989-5	2021	The results indicate sea salt is a better trigger for treating wastewater (nearly 100% total nitrogen and total phosphorus removal) and producing high-quality biodiesel (330 mg/L d).	Phosphorus	112-122	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	21-24
34678656-6	2021	Normalization of serum phosphorus levels by low phosphate diet (LPD) rescued Klotho deficiency-induced heart failure and extended lifespan in male mice.	Phosphorus	23-33	klotho	Mus musculus	77-83
34717015-2	2022	Creating p-n junctions by bulk chemical doping in a single organic material (like silicon doped by boron and phosphorus) may capitalize the vast scientific and technological groundwork established in the inorganic semiconducting field.	Phosphorus	109-119	U6 snRNA biogenesis phosphodiesterase 1	Homo sapiens	9-12
34714475-5	2022	Finally, PS and SMZ exposure also induced extensive endocrine toxicities in zebrafish as confirmed by increases in various biomarkers including vitellogenin, 17beta-estradiol, testosterone, and triiodothyronine.	Phosphorus	9-11	vitellogenin	Danio rerio	144-156
34637261-0	2021	End Group Modification for Black Phosphorus: Simultaneous Improvement of Chemical Stability and Gas Sensing Performance.	Phosphorus	33-43	gastrin	Homo sapiens	96-99
34637261-1	2021	Black phosphorus (BP) nanosheets have been receiving attention for gas sensing showing superior sensitivity and selectivity among various two-dimensional materials.	Phosphorus	0-16	gastrin	Homo sapiens	67-70
34637261-1	2021	Black phosphorus (BP) nanosheets have been receiving attention for gas sensing showing superior sensitivity and selectivity among various two-dimensional materials.	Phosphorus	18-20	gastrin	Homo sapiens	67-70
34637261-9	2021	This work offers an effective means for preventing degradation of BP in ambient environments and provides a promising solution to solve the issue regarding humidity dependence in gas sensors.	Phosphorus	66-68	gastrin	Homo sapiens	179-182
34481009-9	2021	Therefore, in an acidic tumor microenvironment containing MMP-9, PEG-MAF=P disintegrated and rapidly released the drug.	Phosphorus	73-74	matrix metallopeptidase 9	Homo sapiens	58-63
34689162-6	2021	sEH deletion also abolished high phosphorus (Pi)-induced phenotypic transition of vascular smooth muscle cells (VSMCs) independent of its epoxyeicosatrienoic acids (EETs) hydrolysis.	Phosphorus	33-43	epoxide hydrolase 2, cytoplasmic	Mus musculus	0-3
34676404-0	2021	The phospho-base N-methyltransferases PMT1 and PMT2 produce phosphocholine for leaf growth in phosphorus-starved Arabidopsis.	Phosphorus	94-104	polyol/monosaccharide transporter 2	Arabidopsis thaliana	47-51
34771191-2	2021	Herein, BP was chemically functionalized by aliphatic amine (DETA), aromatic amine (PPDA) and cyclamine (Pid) via a nucleophilic substitution reaction, aiming to develop an intensively reactive BP flame retardant for epoxy resin (EP).	Phosphorus	8-10	metastasis associated 1 family member 2	Homo sapiens	105-108
34771191-2	2021	Herein, BP was chemically functionalized by aliphatic amine (DETA), aromatic amine (PPDA) and cyclamine (Pid) via a nucleophilic substitution reaction, aiming to develop an intensively reactive BP flame retardant for epoxy resin (EP).	Phosphorus	8-10	epiregulin	Homo sapiens	230-232
34636529-5	2021	The chemical states of the K-In-Se phase, which have a beneficial effect on the solar-cell performance owing to the formation of durable and improved p-n junctions, are formed only at a KF PDT process time of 50 s. We derived band alignments from the XPS depth profiles by extracting the conduction- and valence-band offsets, and we used optical-pump-THz-probe spectroscopy to measure the ultrafast photocarrier lifetimes related to the defect states following KF PDT.	Phosphorus	150-151	arylformamidase	Homo sapiens	461-463
34771191-2	2021	Herein, BP was chemically functionalized by aliphatic amine (DETA), aromatic amine (PPDA) and cyclamine (Pid) via a nucleophilic substitution reaction, aiming to develop an intensively reactive BP flame retardant for epoxy resin (EP).	Phosphorus	194-196	metastasis associated 1 family member 2	Homo sapiens	105-108
34771191-2	2021	Herein, BP was chemically functionalized by aliphatic amine (DETA), aromatic amine (PPDA) and cyclamine (Pid) via a nucleophilic substitution reaction, aiming to develop an intensively reactive BP flame retardant for epoxy resin (EP).	Phosphorus	194-196	epiregulin	Homo sapiens	230-232
34771191-3	2021	The -NH2 group on BP-DETA, BP-PPDA and BP-Pid reacted with the epoxide group at different temperatures.	Phosphorus	39-41	metastasis associated 1 family member 2	Homo sapiens	42-45
34771191-5	2021	The impacts of three BP-NH2 were compared on the flame retardancy and thermal decomposition of EP.	Phosphorus	21-23	epiregulin	Homo sapiens	95-97
34677215-6	2021	Results: The results revealed that the relationship between intracellular-P and single-cell alkaline phosphatase (SC-ALP) activity was inverse; SC-ALP activity was the highest (around 50 U g-1) when intracellular-P was the lowest possible (around 1.7 mg-P g-1) and decreased gradually as P availability increased reaching around 0.5 U g-1 in the control cultures.	Phosphorus	288-289	alkaline phosphatase, placental	Homo sapiens	117-120
34677215-6	2021	Results: The results revealed that the relationship between intracellular-P and single-cell alkaline phosphatase (SC-ALP) activity was inverse; SC-ALP activity was the highest (around 50 U g-1) when intracellular-P was the lowest possible (around 1.7 mg-P g-1) and decreased gradually as P availability increased reaching around 0.5 U g-1 in the control cultures.	Phosphorus	288-289	alkaline phosphatase, placental	Homo sapiens	147-150
34091333-10	2021	More than 50% of LBP in the LBP/PVP-ZIF-67 can degrade to dissolvable phosphorus in oxygenated water after 17 days, indicating the nanomaterial will not be persistent in the environment.	Phosphorus	70-80	lipopolysaccharide binding protein	Homo sapiens	17-20
34426389-5	2021	A solubilization test manifested that PS and its major components (dipalmitoyl phosphatidylcholine, DPPC; bovine serum albumin, BSA) could in turn accelerate the dissolution of BaP, which followed the order: PS > DPPC > BSA, and mixed phospholipids were significantly responsible for the solubilization of BaP by PS.	Phosphorus	313-315	albumin	Homo sapiens	113-126
34647497-5	2021	The expression of miR-375 was positively associated with the consumption of selenium (beta = 1.52), vitamin C (beta = 0.17) and vitamin D (beta = 13.01), and inversely associated with the consumption of added sugar (beta = -0.49), phosphorus (beta= -0.27) and vitamin B12 (beta = -10.80).	Phosphorus	231-241	microRNA 375	Homo sapiens	18-25
34091333-10	2021	More than 50% of LBP in the LBP/PVP-ZIF-67 can degrade to dissolvable phosphorus in oxygenated water after 17 days, indicating the nanomaterial will not be persistent in the environment.	Phosphorus	70-80	lipopolysaccharide binding protein	Homo sapiens	28-42
34354264-2	2021	Here we show that black phosphorus (BP) nanomaterials directly affect the cell cycle"s centrosome machinery.	Phosphorus	18-34	growth differentiation factor 5	Mus musculus	36-38
34746458-6	2021	In the meat from the three snail species, a strong significant positive correlation between Ca and P levels was observed, and the Cu and Fe (p < 0.05).	Phosphorus	99-100	snail family transcriptional repressor 1	Homo sapiens	27-32
34659853-7	2021	In TIO, hypersecretion of FGF-23 leads to increased renal excretion of phosphorus, increased bone resorption of calcium and phosphorus, decreased osteoblastic bone mineralization, and decreased gastrointestinal absorption of calcium and phosphorus, leading to insufficiency fractures and delayed fracture unions.	Phosphorus	71-81	fibroblast growth factor 23	Homo sapiens	26-32
34659853-7	2021	In TIO, hypersecretion of FGF-23 leads to increased renal excretion of phosphorus, increased bone resorption of calcium and phosphorus, decreased osteoblastic bone mineralization, and decreased gastrointestinal absorption of calcium and phosphorus, leading to insufficiency fractures and delayed fracture unions.	Phosphorus	124-134	fibroblast growth factor 23	Homo sapiens	26-32
34659853-7	2021	In TIO, hypersecretion of FGF-23 leads to increased renal excretion of phosphorus, increased bone resorption of calcium and phosphorus, decreased osteoblastic bone mineralization, and decreased gastrointestinal absorption of calcium and phosphorus, leading to insufficiency fractures and delayed fracture unions.	Phosphorus	237-247	fibroblast growth factor 23	Homo sapiens	26-32
34147926-5	2021	Reusability of p(MAA-NIPAAM)-CB-Fe3+ sorbent was determined after by determining the appropriate desorption agent for desorption of adsorbed catalase in the developed sorbent.	Phosphorus	15-16	catalase	Homo sapiens	141-149
34599185-1	2021	The synthesis of phosphines is based on white phosphorus, which is usually converted to PCl3, to be afterwards substituted step by step in a non-atomic efficient manner.	Phosphorus	46-56	PHD finger protein 19	Homo sapiens	88-92
34500180-7	2021	Based on urban land use grouping, nutrient elements could predict dCH4 well in rivers draining higher urban areas (urban >= 2%), which also reflected the lateral input of pollutants (TN, ammonia nitrogen, and total phosphorus).	Phosphorus	215-225	COP9 signalosome subunit 4	Drosophila melanogaster	66-70
34509868-8	2021	Also, AHLs improved intracellular P entrapment potential by regulating genes involved in inorganic-P accumulation (ppk, ppx) and P uptake and transport (pit, pstSCAB).	Phosphorus	34-35	kallikrein B1	Homo sapiens	115-118
34509868-8	2021	Also, AHLs improved intracellular P entrapment potential by regulating genes involved in inorganic-P accumulation (ppk, ppx) and P uptake and transport (pit, pstSCAB).	Phosphorus	98-100	kallikrein B1	Homo sapiens	115-118
34550535-9	2022	The reduction of P in the plasma induced by supplementation with Cr in the form of Cr-Pic or Cr-NP may exacerbate the adverse effect of a high-fat diet on the level of this element.	Phosphorus	17-18	calbindin 2	Rattus norvegicus	65-67
34547962-10	2022	Bax activity was increased in the D, P and DP groups.	Phosphorus	37-38	BCL2 associated X, apoptosis regulator	Rattus norvegicus	0-3
34550535-9	2022	The reduction of P in the plasma induced by supplementation with Cr in the form of Cr-Pic or Cr-NP may exacerbate the adverse effect of a high-fat diet on the level of this element.	Phosphorus	17-18	calbindin 2	Rattus norvegicus	83-85
34550535-9	2022	The reduction of P in the plasma induced by supplementation with Cr in the form of Cr-Pic or Cr-NP may exacerbate the adverse effect of a high-fat diet on the level of this element.	Phosphorus	17-18	calbindin 2	Rattus norvegicus	93-95
34378575-0	2021	Enhanced photocatalytic activity of the direct Z-scheme black phosphorus/BiOX (X = Cl, Br, I) heterostructures.	Phosphorus	56-72	chromosome 12 open reading frame 73	Homo sapiens	87-89
34380211-2	2021	The effect of various phosphorus (P) precursors on adsorption-related properties, P speciation distribution pattern, and the passivation mechanism was investigated by BET, FTIR, XRD, XPS, and 31P NMR analysis.	Phosphorus	22-32	delta/notch like EGF repeat containing	Homo sapiens	167-170
34414725-4	2021	The contribution of dissolved inorganic phosphorus (DIP) to TP in the water (WTP) was the lowest, while the contribution of calcium-bound phosphorus (HCl-P) to TP in the surface sediments (STP) was the largest in the study area.	Phosphorus	138-148	thyroid hormone receptor interactor 10	Homo sapiens	189-192
34414725-6	2021	(2) The APCS-MLR receptor model indicated that the main pollution sources of phosphorus were industrial wastewater and domestic sewage (29.07%), and pesticides and fertilizers (29.00%).	Phosphorus	77-87	amyloid P component, serum	Homo sapiens	8-12
34378575-3	2021	In the present work, first-principles calculations have been performed to comprehensively explore the structural, electronic and optical properties of black phosphorus (BP)/BiOX (X = Cl, Br, I) heterostructures, revealing the inherent reasons for their enhanced photocatalytic performance.	Phosphorus	169-171	chromosome 12 open reading frame 73	Homo sapiens	187-189
34292627-7	2021	Moreover, for the first time, direct evidence is provided experimentally to present the electrochemical mechanism of BP anodes with three-step lithiation and delithiation using ex situ X-ray diffraction (XRD), ex situ X-ray absorption spectroscopy (XAS), ex situ X-ray emission spectroscopy, operando XRD, and operando XAS, which reveal the formation of Li3 P7 , LiP, and Li3 P. Furthermore, the study indicates an open-circuit relaxation effect of the electrode with ex situ and operando XAS analyses.	Phosphorus	117-119	cytochrome P450 family 4 subfamily F member 22	Homo sapiens	372-375
34296473-3	2021	Here, it is demonstrated that 2D black phosphorus (BP) acts as giant phosphorus (P) ligand to confine a high density of single atoms (e.g., Pd1 , Pt1 ) via atomic layer deposition.	Phosphorus	51-53	programmed cell death 1	Homo sapiens	140-143
34296473-3	2021	Here, it is demonstrated that 2D black phosphorus (BP) acts as giant phosphorus (P) ligand to confine a high density of single atoms (e.g., Pd1 , Pt1 ) via atomic layer deposition.	Phosphorus	51-53	zinc finger protein 77	Homo sapiens	146-149
34296473-3	2021	Here, it is demonstrated that 2D black phosphorus (BP) acts as giant phosphorus (P) ligand to confine a high density of single atoms (e.g., Pd1 , Pt1 ) via atomic layer deposition.	Phosphorus	69-79	programmed cell death 1	Homo sapiens	140-143
34296473-3	2021	Here, it is demonstrated that 2D black phosphorus (BP) acts as giant phosphorus (P) ligand to confine a high density of single atoms (e.g., Pd1 , Pt1 ) via atomic layer deposition.	Phosphorus	69-79	zinc finger protein 77	Homo sapiens	146-149
34474854-10	2021	Both M(LPS) and M(IL-4) cells on untreated hydrogels shifted to a more pro-inflammatory phenotype in the presence of aminated-PS particles.	Phosphorus	126-128	interleukin 4	Homo sapiens	18-22
34373722-0	2021	MicroRNA-103a regulates the calcification of vascular smooth muscle cells by targeting runt-related transcription factor 2 in high phosphorus conditions.	Phosphorus	131-141	RUNX family transcription factor 2	Rattus norvegicus	87-122
34155644-10	2021	A laboratory incubation of soils from the site confirmed that NO3 - inhibited P release.	Phosphorus	78-79	NBL1, DAN family BMP antagonist	Homo sapiens	62-65
34111672-7	2021	Furthermore, urinary phosphorus/creatinine and intact fibroblast growth factor 23 were significantly lowered by low phosphorus diet.	Phosphorus	116-126	fibroblast growth factor 23	Mus musculus	54-81
34385710-4	2021	Further sequencing of known CTNNB1-mutant APAs led to a total of 16 of 27 (59%) with a somatic p.Gln209His, p.Gln209Pro or p.Gln209Leu mutation of GNA11 or GNAQ.	Phosphorus	123-124	G protein subunit alpha 11	Homo sapiens	147-152
34431737-8	2021	In the multiple linear regression analysis, serum urea nitrogen concentration, serum phosphorus concentration and blood ionised calcium concentration were independent variables predicting serum FGF-23 concentration.	Phosphorus	85-95	fibroblast growth factor 23	Felis catus	194-200
34126199-10	2021	UAC stimulated cartilage degeneration and chondrocytes nucleic acid damage, increased PARP 1 and serum P content, and enhanced ossification and stiffening of the cartilage, all were suppressed by low phosphorus diet (all, p < 0.05).	Phosphorus	200-210	poly (ADP-ribose) polymerase 1	Rattus norvegicus	86-92
34502264-6	2021	We designed a complex with non-cytotoxic LMWP to prevent the degradation of Oct4 and revealed that the positively charged cell-permeable LMWP helped condense the size of the Oct4-LMWP complexes (1:5 N:P ratio).	Phosphorus	201-202	POU domain, class 5, transcription factor 1	Mus musculus	76-80
34502264-6	2021	We designed a complex with non-cytotoxic LMWP to prevent the degradation of Oct4 and revealed that the positively charged cell-permeable LMWP helped condense the size of the Oct4-LMWP complexes (1:5 N:P ratio).	Phosphorus	201-202	POU domain, class 5, transcription factor 1	Mus musculus	174-178
34513902-6	2021	The sensitivity analysis and curve-fitting analysis also showed that ALB before CRRT was correlated with the 28 and 90 days mortality of critically ill patients with AKI and treated with CRRT and the removal efficiency of serum phosphorus.	Phosphorus	228-238	albumin	Homo sapiens	69-72
34513902-7	2021	Conclusion: The higher the serum ALB before CRRT, the lower the mortality of critically ill patients with AKI and treated with CRRT, and the higher the clearance efficiency of serum phosphorus.	Phosphorus	182-192	albumin	Homo sapiens	33-36
34589329-3	2021	Vitamin D (Vit D) regulates the absorption of calcium and phosphorus and thus, is universally accepted as an essential vitamin for bone strength as well as a facilitator of immune system function.	Phosphorus	58-68	vitrin	Homo sapiens	11-14
34533015-1	2021	Hypoparathyroidism is a rare disorder characterized by the absent or inappropriately decreased serum parathyroid hormone in the parathyroid glands, which is accompanied by impaired calcium-phosphorus metabolism.The main etiology of hypoparathyroidism remains damage or removal of the parathyroid glands during neck surgery.	Phosphorus	189-199	parathyroid hormone	Homo sapiens	101-120
34302157-2	2021	A series of P-Co3O4@NiCo-LDH/NF materials was firstly successfully synthesized by a hydrothermal method, high temperature calcination and an electrochemical deposition approach when sodium hypophosphite was used as the source of P and Ni(NO3)2 6H2O as the source of nickel and introduced cobalt at the same time.	Phosphorus	229-230	neurofascin	Homo sapiens	29-31
34484268-2	2021	Although previous studies have shown that 6-phosphogluconate dehydrogenase (6PGDH) plays an important role in plant resistance to adversity, its response to low phosphorus (P) stress remains unknown.	Phosphorus	161-171	6-phosphogluconate dehydrogenase	Glycine max	42-74
34484268-2	2021	Although previous studies have shown that 6-phosphogluconate dehydrogenase (6PGDH) plays an important role in plant resistance to adversity, its response to low phosphorus (P) stress remains unknown.	Phosphorus	161-171	6-phosphogluconate dehydrogenase	Glycine max	76-81
34456863-12	2021	After controlling for age, sex, disease duration, serum 25(OH)D, phosphorus, and calcium concentration, the positive correlation between OCN and PTH was still statistically significant (r = 0.323, p = 0.000).	Phosphorus	65-75	bone gamma-carboxyglutamate protein	Homo sapiens	137-140
34236859-4	2021	The process begins with regioselective trapping of a 3-trifloxybenzyne intermediate by an O-silyl phosphite in an Abramov-like reaction to bond the strained Csp carbons with phosphorus and silicon.	Phosphorus	174-184	DnaJ heat shock protein family (Hsp40) member C5	Homo sapiens	157-160
34242508-0	2021	Insertion of CS2 into a Phosphorus-Arsenic Single Bond and Investigations on Phosphane Arsanyldithiocarboxylates.	Phosphorus	24-34	chorionic somatomammotropin hormone 2	Homo sapiens	13-16
34260214-3	2021	For 107 countries, we analyze the colocation of human-derived nutrients (in urine) and crop demands for nitrogen, phosphorus, and potassium.	Phosphorus	114-124	LUC7 like 3 pre-mRNA splicing factor	Homo sapiens	87-91
34421960-5	2021	Our results suggest that high N availability (>100 kg N ha-1) could disadvantage the growth of ECM plants because of increased C costs associated with maintaining higher root N concentrations, while the insensitivity in SRR by AM plants to N fertilisation may be because AM fungi are more important for phosphorus (P) uptake.	Phosphorus	303-313	solute carrier family 9 member B1	Homo sapiens	54-60
34105846-2	2021	The P-Al bond added to ethylene and relatively small terminal alkenes (propylene and hex-1-ene) at room temperature to give the corresponding alkene-adducts.	Phosphorus	4-5	exonuclease 1	Homo sapiens	85-90
34440062-0	2021	Bovine Serum Albumin-Immobilized Black Phosphorus-Based gamma-Fe2O3 Nanocomposites: A Promising Biocompatible Nanoplatform.	Phosphorus	39-49	albumin	Homo sapiens	7-20
34112437-1	2021	We designed a signal-on photoelectrochemical (PEC) immunoassay for the sensitive monitoring of prostate-specific antigen (PSA) based on the etching reaction of hydrogen peroxide (H2O2) toward oxygen/phosphorus co-doped graphitic C3N4/AgBr/MnO2 nanosheets (OP-g-C3N4/AgBr/MnO2).	Phosphorus	199-209	kallikrein related peptidase 3	Homo sapiens	95-120
34112437-1	2021	We designed a signal-on photoelectrochemical (PEC) immunoassay for the sensitive monitoring of prostate-specific antigen (PSA) based on the etching reaction of hydrogen peroxide (H2O2) toward oxygen/phosphorus co-doped graphitic C3N4/AgBr/MnO2 nanosheets (OP-g-C3N4/AgBr/MnO2).	Phosphorus	199-209	basic transcription factor 3 pseudogene 11	Homo sapiens	256-260
34225874-5	2021	Moreover, GSH-ApoE-PC-liposomes benefited the 4 medicines in simultaneously transporting to Abeta1-42-insulted neurons, in functioning against hyperphosphorylated mitogen-activated protein kinases, including p-c-Jun N-terminal protein kinase, p-extracellular signal-regulated protein kinase 1/2 and p-p38, in downregulating tau protein at S202, caspase-3 and interleukin-6, and in upregulating p-cyclic adenosine monophosphate response element-binding protein.	Phosphorus	394-395	apolipoprotein E	Homo sapiens	14-18
34439437-4	2021	The B(a)P-induced dissociation of AHR from AHR-interacting protein (AIP) was suppressed by maclurin.	Phosphorus	8-9	aryl hydrocarbon receptor	Homo sapiens	34-37
34439437-4	2021	The B(a)P-induced dissociation of AHR from AHR-interacting protein (AIP) was suppressed by maclurin.	Phosphorus	8-9	aryl hydrocarbon receptor interacting protein	Homo sapiens	43-66
34439437-4	2021	The B(a)P-induced dissociation of AHR from AHR-interacting protein (AIP) was suppressed by maclurin.	Phosphorus	8-9	aryl hydrocarbon receptor interacting protein	Homo sapiens	68-71
34089433-4	2021	Altogether, seven minerals-Cu, Fe, K, Mg, Mn, Na, and P-were above the detection limit with the analysis revealing increased iron content in the heart of Fmr1 KO mice.	Phosphorus	54-55	fragile X messenger ribonucleoprotein 1	Mus musculus	154-158
34287525-8	2021	Maximum pods plant-1, seed pod, early seed filling, heavier seed weight, biological yield, seed yield, and harvest index were observed in plots treated with 130 kg.ha-1 phosphorous.	Phosphorus	169-180	Rho GTPase activating protein 45	Homo sapiens	164-168
34436123-9	2021	Cloning and overexpression of PHT1-1 and PHT1-3 genes in transgenic Arabidopsis thaliana plants significantly enriched total phosphorus and chlorophyll content, confirming that PHT1-1 and PHT1-3 gene functions are associated with the transport and absorption of phosphorus.	Phosphorus	125-135	phosphate transporter 1;1	Arabidopsis thaliana	30-36
34436123-9	2021	Cloning and overexpression of PHT1-1 and PHT1-3 genes in transgenic Arabidopsis thaliana plants significantly enriched total phosphorus and chlorophyll content, confirming that PHT1-1 and PHT1-3 gene functions are associated with the transport and absorption of phosphorus.	Phosphorus	125-135	phosphate transporter 1;3	Arabidopsis thaliana	41-47
34436123-9	2021	Cloning and overexpression of PHT1-1 and PHT1-3 genes in transgenic Arabidopsis thaliana plants significantly enriched total phosphorus and chlorophyll content, confirming that PHT1-1 and PHT1-3 gene functions are associated with the transport and absorption of phosphorus.	Phosphorus	262-272	phosphate transporter 1;1	Arabidopsis thaliana	30-36
34436123-9	2021	Cloning and overexpression of PHT1-1 and PHT1-3 genes in transgenic Arabidopsis thaliana plants significantly enriched total phosphorus and chlorophyll content, confirming that PHT1-1 and PHT1-3 gene functions are associated with the transport and absorption of phosphorus.	Phosphorus	262-272	phosphate transporter 1;3	Arabidopsis thaliana	41-47
34436123-9	2021	Cloning and overexpression of PHT1-1 and PHT1-3 genes in transgenic Arabidopsis thaliana plants significantly enriched total phosphorus and chlorophyll content, confirming that PHT1-1 and PHT1-3 gene functions are associated with the transport and absorption of phosphorus.	Phosphorus	262-272	phosphate transporter 1;1	Arabidopsis thaliana	177-183
34436123-9	2021	Cloning and overexpression of PHT1-1 and PHT1-3 genes in transgenic Arabidopsis thaliana plants significantly enriched total phosphorus and chlorophyll content, confirming that PHT1-1 and PHT1-3 gene functions are associated with the transport and absorption of phosphorus.	Phosphorus	262-272	phosphate transporter 1;3	Arabidopsis thaliana	188-194
34198270-3	2021	We calculated reaction pathways for PH3, PCl3, and BCl3adsorption on a bare and Cl-terminated Si(100)-2x1 surface, as well as for PH3adsorption on H-terminated Si(100)-2x1, which is widely used in current technologies for atomically precise doping of Si(100) with phosphorus.	Phosphorus	264-274	PHD finger protein 19	Homo sapiens	41-45
34291462-10	2022	Serum phosphorus was inversely correlated (weak correlation) with PIM2 (p = .017) CONCLUSION: : HP is common in critically ill pediatric patients, even when they are not under parenteral nutrition (PN).	Phosphorus	6-16	Pim-2 proto-oncogene, serine/threonine kinase	Homo sapiens	66-70
34357360-8	2021	In addition, PS (18:3/20:4) was significantly decreased in MDD2 group compared to MDD1, with AUC value of 0.785.	Phosphorus	13-15	MDD2	Homo sapiens	59-63
34357360-8	2021	In addition, PS (18:3/20:4) was significantly decreased in MDD2 group compared to MDD1, with AUC value of 0.785.	Phosphorus	13-15	MDD1	Homo sapiens	82-86
34336694-5	2021	Whole-body phosphorus autoradiography showed clear imaging at 48 h after injection of 125I-anti-TLR5 mAb and 125I-VEGF also provided clear imaging at 24 h. Biodistribution study demonstrated a higher tumor uptake of 125I-anti-TLR5 mAb in TLR5+ group compared with that in TLR5- group (P < 0.05), whereas tumor uptake of 125I-VEGF in TLR5+ group was lower than that in the TLR5- group (P < 0.05).	Phosphorus	11-21	toll-like receptor 5	Mus musculus	96-100
34336694-5	2021	Whole-body phosphorus autoradiography showed clear imaging at 48 h after injection of 125I-anti-TLR5 mAb and 125I-VEGF also provided clear imaging at 24 h. Biodistribution study demonstrated a higher tumor uptake of 125I-anti-TLR5 mAb in TLR5+ group compared with that in TLR5- group (P < 0.05), whereas tumor uptake of 125I-VEGF in TLR5+ group was lower than that in the TLR5- group (P < 0.05).	Phosphorus	11-21	vascular endothelial growth factor A	Mus musculus	114-118
34336694-5	2021	Whole-body phosphorus autoradiography showed clear imaging at 48 h after injection of 125I-anti-TLR5 mAb and 125I-VEGF also provided clear imaging at 24 h. Biodistribution study demonstrated a higher tumor uptake of 125I-anti-TLR5 mAb in TLR5+ group compared with that in TLR5- group (P < 0.05), whereas tumor uptake of 125I-VEGF in TLR5+ group was lower than that in the TLR5- group (P < 0.05).	Phosphorus	11-21	toll-like receptor 5	Mus musculus	226-230
34336694-5	2021	Whole-body phosphorus autoradiography showed clear imaging at 48 h after injection of 125I-anti-TLR5 mAb and 125I-VEGF also provided clear imaging at 24 h. Biodistribution study demonstrated a higher tumor uptake of 125I-anti-TLR5 mAb in TLR5+ group compared with that in TLR5- group (P < 0.05), whereas tumor uptake of 125I-VEGF in TLR5+ group was lower than that in the TLR5- group (P < 0.05).	Phosphorus	11-21	toll-like receptor 5	Mus musculus	238-242
34336694-5	2021	Whole-body phosphorus autoradiography showed clear imaging at 48 h after injection of 125I-anti-TLR5 mAb and 125I-VEGF also provided clear imaging at 24 h. Biodistribution study demonstrated a higher tumor uptake of 125I-anti-TLR5 mAb in TLR5+ group compared with that in TLR5- group (P < 0.05), whereas tumor uptake of 125I-VEGF in TLR5+ group was lower than that in the TLR5- group (P < 0.05).	Phosphorus	11-21	toll-like receptor 5	Mus musculus	272-276
34336694-5	2021	Whole-body phosphorus autoradiography showed clear imaging at 48 h after injection of 125I-anti-TLR5 mAb and 125I-VEGF also provided clear imaging at 24 h. Biodistribution study demonstrated a higher tumor uptake of 125I-anti-TLR5 mAb in TLR5+ group compared with that in TLR5- group (P < 0.05), whereas tumor uptake of 125I-VEGF in TLR5+ group was lower than that in the TLR5- group (P < 0.05).	Phosphorus	11-21	vascular endothelial growth factor A	Mus musculus	325-329
34336694-5	2021	Whole-body phosphorus autoradiography showed clear imaging at 48 h after injection of 125I-anti-TLR5 mAb and 125I-VEGF also provided clear imaging at 24 h. Biodistribution study demonstrated a higher tumor uptake of 125I-anti-TLR5 mAb in TLR5+ group compared with that in TLR5- group (P < 0.05), whereas tumor uptake of 125I-VEGF in TLR5+ group was lower than that in the TLR5- group (P < 0.05).	Phosphorus	11-21	toll-like receptor 5	Mus musculus	333-337
34377950-11	2021	Pigs fed diets with adequate Ca and P had greater (P < 0.05) albumin in serum than pigs fed the Ca- and P-deficient diets.	Phosphorus	36-37	albumin	Sus scrofa	61-68
34212682-4	2021	The results show that:(1) the average annual application intensity of nitrogen and phosphorus fertilizer in the study area from 2010 to 2015 is generally in the low and medium risk intensity of 120-360 kg hm-2 and 60-180 kg hm-2.	Phosphorus	83-93	cholinergic receptor muscarinic 2	Homo sapiens	205-209
34212682-4	2021	The results show that:(1) the average annual application intensity of nitrogen and phosphorus fertilizer in the study area from 2010 to 2015 is generally in the low and medium risk intensity of 120-360 kg hm-2 and 60-180 kg hm-2.	Phosphorus	83-93	cholinergic receptor muscarinic 2	Homo sapiens	224-228
34196610-0	2021	Phosphorus and sulfur SAD phasing of the nucleic acid-bound DNA-binding domain of interferon regulatory factor 4.	Phosphorus	0-10	interferon regulatory factor 4	Homo sapiens	82-112
34152156-1	2021	Industrially important triaryl phosphites, traditionally prepared from PCl3, have been synthesized by a diphenyl diselenide-catalyzed one-step procedure involving white phosphorus and phenols, which provides a halogen- and transition metal-free way to these compounds.	Phosphorus	169-179	PHD finger protein 19	Homo sapiens	71-75
34196610-4	2021	This article reports the use of native intrinsic phosphorus and sulfur single-wavelength anomalous dispersion methods to solve the complex of the DNA-binding domain (DBD) of interferon regulatory factor 4 (IRF4) bound to its interferon-stimulated response element (ISRE).	Phosphorus	49-59	interferon regulatory factor 4	Homo sapiens	174-204
34196610-4	2021	This article reports the use of native intrinsic phosphorus and sulfur single-wavelength anomalous dispersion methods to solve the complex of the DNA-binding domain (DBD) of interferon regulatory factor 4 (IRF4) bound to its interferon-stimulated response element (ISRE).	Phosphorus	49-59	interferon regulatory factor 4	Homo sapiens	206-210
34223733-10	2021	Furthermore, NA (75, 150, and 300 nmol) significantly reduced food intake in a dose-dependent manner (p &amp;lt;0.05).	Phosphorus	102-103	ATPase H+ transporting V0 subunit a2	Gallus gallus	77-78
34076417-3	2021	The resultant metal-organic framework (MOF)-based uranium ion trap (PCN-222-PA) with a high density of accessible phosphate groups exhibits a remarkable U(VI) uptake capacity (401.6 mg g-1), surpassing most of the reported phosphorus-modified MOFs and various other MOF adsorbents.	Phosphorus	223-233	TRAP	Homo sapiens	62-66
34313065-12	2021	Under the straw returning condition, phosphorus application rate for wheat of 105-150 kg hm-2 and the phosphorus application rate for maize of 63-90 kg hm-2 in Hebei fluvo-aquic soil could ensure the high crop yield, keep the phosphorus utilization efficiency at a high level, and reduce soil phosphorus accumulation and environmental risks.	Phosphorus	37-47	Putative anthocyanidin reductase	Zea mays	89-93
34313065-12	2021	Under the straw returning condition, phosphorus application rate for wheat of 105-150 kg hm-2 and the phosphorus application rate for maize of 63-90 kg hm-2 in Hebei fluvo-aquic soil could ensure the high crop yield, keep the phosphorus utilization efficiency at a high level, and reduce soil phosphorus accumulation and environmental risks.	Phosphorus	102-112	Putative anthocyanidin reductase	Zea mays	152-156
34313065-12	2021	Under the straw returning condition, phosphorus application rate for wheat of 105-150 kg hm-2 and the phosphorus application rate for maize of 63-90 kg hm-2 in Hebei fluvo-aquic soil could ensure the high crop yield, keep the phosphorus utilization efficiency at a high level, and reduce soil phosphorus accumulation and environmental risks.	Phosphorus	226-236	Putative anthocyanidin reductase	Zea mays	89-93
34313065-12	2021	Under the straw returning condition, phosphorus application rate for wheat of 105-150 kg hm-2 and the phosphorus application rate for maize of 63-90 kg hm-2 in Hebei fluvo-aquic soil could ensure the high crop yield, keep the phosphorus utilization efficiency at a high level, and reduce soil phosphorus accumulation and environmental risks.	Phosphorus	226-236	Putative anthocyanidin reductase	Zea mays	152-156
34313065-12	2021	Under the straw returning condition, phosphorus application rate for wheat of 105-150 kg hm-2 and the phosphorus application rate for maize of 63-90 kg hm-2 in Hebei fluvo-aquic soil could ensure the high crop yield, keep the phosphorus utilization efficiency at a high level, and reduce soil phosphorus accumulation and environmental risks.	Phosphorus	293-303	Putative anthocyanidin reductase	Zea mays	152-156
34203154-7	2021	Hydroxyapatite powder (HAp), yielding Ca, P, and O, is widely used to form biocompatible coatings.	Phosphorus	42-43	reticulon 3	Homo sapiens	23-26
34170851-0	2021	Bone mesenchymal stem cell derived exosomes alleviate high phosphorus-induced calcification of vascular smooth muscle cells through the NONHSAT 084969.2/NF-kappaB axis.	Phosphorus	59-69	nuclear factor kappa B subunit 1	Homo sapiens	153-162
34311526-8	2021	Results revealed that the repeated instillation of LPS/PS leads to voiding dysfunction, bladder urothelium denudation, and detrusor muscle fibrosis through the upregulation of the NLRP3 inflammasome/IL-1beta-related TGF-beta/Smad pathway and the increased epithelial-mesenchymal transition process in bladder tissues.	Phosphorus	55-57	NLR family, pyrin domain containing 3	Mus musculus	180-185
34120612-0	2021	Biomimetic black phosphorus quantum dots-based photothermal therapy combined with anti-PD-L1 treatment inhibits recurrence and metastasis in triple-negative breast cancer.	Phosphorus	11-27	CD274 molecule	Homo sapiens	87-92
34277092-8	2021	Calcium (Ca) and phosphorus (P) levels were lower in DCIR lesions when compared to controls.	Phosphorus	17-27	C-type lectin domain family 4 member A	Homo sapiens	53-57
34277092-8	2021	Calcium (Ca) and phosphorus (P) levels were lower in DCIR lesions when compared to controls.	Phosphorus	29-30	C-type lectin domain family 4 member A	Homo sapiens	53-57
34268038-20	2021	Interestingly, FGF-23 is shown to have a potential cardiovascular (CV) morbidity and mortality through various mechanisms like activation of myocardial FGF-23 receptors, endothelial dysfunction, inflammation, and altered phosphorus and vitamin D metabolisms.	Phosphorus	221-231	fibroblast growth factor 23	Homo sapiens	15-21
34154114-6	2021	With this method, we present a novel multi-layer graphene-BP-based dual-band anisotropic terahertz absorption structure (GBP-DATAS) and analyze its optical characteristics.	Phosphorus	58-60	transmembrane protein 132A	Homo sapiens	121-124
34154114-7	2021	Combining the advantages of graphene and BP localized surface plasmons, the GBP-DATAS demonstrates strong anisotropic plasmonic resonance and high absorption rate in the terahertz band.	Phosphorus	41-43	transmembrane protein 132A	Homo sapiens	76-79
34074247-7	2021	Urinary excretion of EVs expressing PiT1 and PiT2 negatively (P < 0.05) correlated with urinary phosphorus excretion, whereas excretion of EVs expressing FGF23 negatively (P < 0.05) correlated with both urinary calcium and phosphorus excretion.	Phosphorus	96-106	POU class 1 homeobox 1	Homo sapiens	36-40
34311526-8	2021	Results revealed that the repeated instillation of LPS/PS leads to voiding dysfunction, bladder urothelium denudation, and detrusor muscle fibrosis through the upregulation of the NLRP3 inflammasome/IL-1beta-related TGF-beta/Smad pathway and the increased epithelial-mesenchymal transition process in bladder tissues.	Phosphorus	55-57	interleukin 1 alpha	Mus musculus	199-207
34074247-7	2021	Urinary excretion of EVs expressing PiT1 and PiT2 negatively (P < 0.05) correlated with urinary phosphorus excretion, whereas excretion of EVs expressing FGF23 negatively (P < 0.05) correlated with both urinary calcium and phosphorus excretion.	Phosphorus	96-106	solute carrier family 20 member 2	Homo sapiens	45-49
34311526-8	2021	Results revealed that the repeated instillation of LPS/PS leads to voiding dysfunction, bladder urothelium denudation, and detrusor muscle fibrosis through the upregulation of the NLRP3 inflammasome/IL-1beta-related TGF-beta/Smad pathway and the increased epithelial-mesenchymal transition process in bladder tissues.	Phosphorus	55-57	transforming growth factor alpha	Mus musculus	216-224
34311526-9	2021	The downregulation of the NLRP3 inflammasome/IL-1beta-related TGF-beta/Smad pathway in bladder tissues through curcumin effectively mitigated bladder injury in the LPS/PS model.	Phosphorus	168-170	NLR family, pyrin domain containing 3	Mus musculus	26-31
34311526-10	2021	In conclusion, the NLRP3 inflammasome/IL-1beta-related TGF-beta/Smad pathway plays a crucial role in bladder injury in the LPS/PS model, and modulation of this pathway, such as by using curcumin, can effectively mitigate the sequelae of chronic inflammation-induced IC/BPS.	Phosphorus	127-129	NLR family, pyrin domain containing 3	Mus musculus	19-24
34311526-10	2021	In conclusion, the NLRP3 inflammasome/IL-1beta-related TGF-beta/Smad pathway plays a crucial role in bladder injury in the LPS/PS model, and modulation of this pathway, such as by using curcumin, can effectively mitigate the sequelae of chronic inflammation-induced IC/BPS.	Phosphorus	127-129	interleukin 1 alpha	Mus musculus	38-46
34311526-10	2021	In conclusion, the NLRP3 inflammasome/IL-1beta-related TGF-beta/Smad pathway plays a crucial role in bladder injury in the LPS/PS model, and modulation of this pathway, such as by using curcumin, can effectively mitigate the sequelae of chronic inflammation-induced IC/BPS.	Phosphorus	127-129	transforming growth factor alpha	Mus musculus	55-63
34163643-4	2021	In the presence of a third fac-positioned open coordination site, the P-C bond formation was found to be reversible, as shown for a series of molybdenum complexes.	Phosphorus	70-71	FA complementation group C	Homo sapiens	27-30
34068220-4	2021	Parathyroid hormone (PTH), Vitamin D, Fibroblast Growth Factor (FGF23) and other receptors or ion-transporters, work synergistically and establish a highly regulated signalling circuit between the bone, kidneys, and intestine to ensure the maintenance of Ca and P homeostasis.	Phosphorus	262-263	parathyroid hormone	Homo sapiens	0-19
34068220-4	2021	Parathyroid hormone (PTH), Vitamin D, Fibroblast Growth Factor (FGF23) and other receptors or ion-transporters, work synergistically and establish a highly regulated signalling circuit between the bone, kidneys, and intestine to ensure the maintenance of Ca and P homeostasis.	Phosphorus	262-263	parathyroid hormone	Homo sapiens	21-24
34068220-4	2021	Parathyroid hormone (PTH), Vitamin D, Fibroblast Growth Factor (FGF23) and other receptors or ion-transporters, work synergistically and establish a highly regulated signalling circuit between the bone, kidneys, and intestine to ensure the maintenance of Ca and P homeostasis.	Phosphorus	262-263	fibroblast growth factor 23	Homo sapiens	64-69
34374249-1	2021	Objective: To investigate the effects of estrogen receptor alpha (ERalpha) gene overexpression on bone metabolism and calcium and phosphorus metabolism in ovariectomized osteoporosis mice, and to provide experimental basis for targeted gene therapy of osteoporosis.	Phosphorus	130-140	estrogen receptor 1 (alpha)	Mus musculus	41-64
34374249-1	2021	Objective: To investigate the effects of estrogen receptor alpha (ERalpha) gene overexpression on bone metabolism and calcium and phosphorus metabolism in ovariectomized osteoporosis mice, and to provide experimental basis for targeted gene therapy of osteoporosis.	Phosphorus	130-140	estrogen receptor 1 (alpha)	Mus musculus	66-73
34374249-17	2021	Conclusion: ERalpha gene overexpression can improve osteoporosis by regulating bone mineral density, bone parameters, bone metabolism, calcium and phosphorus metabolic indicators and the expression levels of TIMP-1 and MCP-1 in tissues.	Phosphorus	147-157	estrogen receptor 1 (alpha)	Mus musculus	12-19
34141152-6	2021	Moreover, taurine effectively mitigated increase in myeloperoxidase activity, levels of reactive oxygen and nitrogen species, nitric oxide and interleukin-1beta in kidney and liver of rats treated with B(a)P.	Phosphorus	206-207	myeloperoxidase	Rattus norvegicus	52-67
34141152-6	2021	Moreover, taurine effectively mitigated increase in myeloperoxidase activity, levels of reactive oxygen and nitrogen species, nitric oxide and interleukin-1beta in kidney and liver of rats treated with B(a)P.	Phosphorus	206-207	interleukin 1 beta	Rattus norvegicus	143-160
34476094-13	2021	Conclusions: Higher serum phosphorus rather than serum calcium was independently associated with kidney disease progression in IgA nephropathy.	Phosphorus	26-36	CD79a molecule	Homo sapiens	127-130
34071151-0	2021	Study on Preparation and Interfacial Transition Zone Microstructure of Red Mud-Yellow Phosphorus Slag-Cement Concrete.	Phosphorus	86-96	adaptor related protein complex 5 subunit mu 1	Homo sapiens	75-78
34632163-8	2021	An appropriate Ca/P ratio in CaP can effectively promote the RANKL-RANK binding and evoke more activated NF-kappaB signaling transduction, which results in vigorous osteoclast differentiation.	Phosphorus	18-19	TNF superfamily member 11	Homo sapiens	61-66
34927824-4	2021	Here, since black phosphorus quantum dots (BPQDs), among many other types of QDs, increase the global m6A level and decrease the demethylase ALKBH5 level in lung cells, the epitranscriptome is taken into consideration for the first time to evaluate nanosafety.	Phosphorus	18-28	methyl-CpG binding domain protein 2	Homo sapiens	129-140
34927824-4	2021	Here, since black phosphorus quantum dots (BPQDs), among many other types of QDs, increase the global m6A level and decrease the demethylase ALKBH5 level in lung cells, the epitranscriptome is taken into consideration for the first time to evaluate nanosafety.	Phosphorus	18-28	alkB homolog 5, RNA demethylase	Homo sapiens	141-147
35513145-11	2022	Exposure of cells to large PS particles (500-5000 nm) upregulated interleukin-8 and the effect was enhanced at 24 h. Overall, the study demonstrated that smaller aminated particles were most toxic to hepatocytes, but larger particles induced apoptotic cell death or an inflammatory response depending on the length of exposure.	Phosphorus	27-29	C-X-C motif chemokine ligand 8	Homo sapiens	66-79
34090218-7	2021	PS applied cells showed increased motility in A549 cells as well as lost cell to cell connection in MCF7 and HCT116 cells, and induced expression of VIM, ZEB1 and SNAIL2 mRNA levels.	Phosphorus	0-2	vimentin	Homo sapiens	149-152
34090218-7	2021	PS applied cells showed increased motility in A549 cells as well as lost cell to cell connection in MCF7 and HCT116 cells, and induced expression of VIM, ZEB1 and SNAIL2 mRNA levels.	Phosphorus	0-2	zinc finger E-box binding homeobox 1	Homo sapiens	154-158
34090218-7	2021	PS applied cells showed increased motility in A549 cells as well as lost cell to cell connection in MCF7 and HCT116 cells, and induced expression of VIM, ZEB1 and SNAIL2 mRNA levels.	Phosphorus	0-2	snail family transcriptional repressor 2	Homo sapiens	163-169
34475317-5	2021	Furthermore, RA in combination with progesterone (RA?P) led to increased expression of Oct4, Fragilis, Stella, Dazl, Sycp3, Gdf9 and decreased expression of Mvh, and Stra8 genes compared to the RA-treated scenario.	Phosphorus	53-54	POU domain, class 5, transcription factor 1	Mus musculus	87-91
34475317-5	2021	Furthermore, RA in combination with progesterone (RA?P) led to increased expression of Oct4, Fragilis, Stella, Dazl, Sycp3, Gdf9 and decreased expression of Mvh, and Stra8 genes compared to the RA-treated scenario.	Phosphorus	53-54	developmental pluripotency-associated 3	Mus musculus	103-109
34475317-5	2021	Furthermore, RA in combination with progesterone (RA?P) led to increased expression of Oct4, Fragilis, Stella, Dazl, Sycp3, Gdf9 and decreased expression of Mvh, and Stra8 genes compared to the RA-treated scenario.	Phosphorus	53-54	deleted in azoospermia-like	Mus musculus	111-115
34475317-5	2021	Furthermore, RA in combination with progesterone (RA?P) led to increased expression of Oct4, Fragilis, Stella, Dazl, Sycp3, Gdf9 and decreased expression of Mvh, and Stra8 genes compared to the RA-treated scenario.	Phosphorus	53-54	synaptonemal complex protein 3	Mus musculus	117-122
34475317-5	2021	Furthermore, RA in combination with progesterone (RA?P) led to increased expression of Oct4, Fragilis, Stella, Dazl, Sycp3, Gdf9 and decreased expression of Mvh, and Stra8 genes compared to the RA-treated scenario.	Phosphorus	53-54	growth differentiation factor 9	Mus musculus	124-128
34475317-5	2021	Furthermore, RA in combination with progesterone (RA?P) led to increased expression of Oct4, Fragilis, Stella, Dazl, Sycp3, Gdf9 and decreased expression of Mvh, and Stra8 genes compared to the RA-treated scenario.	Phosphorus	53-54	DEAD box helicase 4	Mus musculus	157-160
34475317-5	2021	Furthermore, RA in combination with progesterone (RA?P) led to increased expression of Oct4, Fragilis, Stella, Dazl, Sycp3, Gdf9 and decreased expression of Mvh, and Stra8 genes compared to the RA-treated scenario.	Phosphorus	53-54	stimulated by retinoic acid gene 8	Mus musculus	166-171
35635968-2	2022	This work developed black phosphorus nanosheet loaded with CdTe quantum dots (BP-CdTe QDs) as dual-emitting luminophor, and TiO2 nanosheets (NSs) as dual-function moderator to construct single-luminophor-based ECL ratio biosensor for amyloid-beta protein (Abeta) detection.	Phosphorus	26-36	amyloid beta precursor protein	Homo sapiens	256-261
35461117-2	2022	Here, a fluorescent switch with high efficiency and regeneration by the black phosphorus (BP) nanosheets-regulated was developed to overcome false-positive issue in the assay of beta-amyloid1-42 oligomers (Abeta) process.	Phosphorus	72-88	amyloid beta precursor protein	Homo sapiens	206-211
35461117-2	2022	Here, a fluorescent switch with high efficiency and regeneration by the black phosphorus (BP) nanosheets-regulated was developed to overcome false-positive issue in the assay of beta-amyloid1-42 oligomers (Abeta) process.	Phosphorus	90-92	amyloid beta precursor protein	Homo sapiens	206-211
35461117-3	2022	The Abeta was rapidly recognized using the fluorescent emitter-nitrogen-doped carbon nanodots (N-CDs) under the regulation of BP nanosheets, while the N-CDs alone cannot recognize Abeta without the introduction of BP.	Phosphorus	126-128	amyloid beta precursor protein	Homo sapiens	4-9
35461117-3	2022	The Abeta was rapidly recognized using the fluorescent emitter-nitrogen-doped carbon nanodots (N-CDs) under the regulation of BP nanosheets, while the N-CDs alone cannot recognize Abeta without the introduction of BP.	Phosphorus	214-216	amyloid beta precursor protein	Homo sapiens	4-9
35461117-3	2022	The Abeta was rapidly recognized using the fluorescent emitter-nitrogen-doped carbon nanodots (N-CDs) under the regulation of BP nanosheets, while the N-CDs alone cannot recognize Abeta without the introduction of BP.	Phosphorus	214-216	amyloid beta precursor protein	Homo sapiens	180-185
35358526-3	2022	Two phosphorus materials from tailings, Ca(H2PO4)2 and Ca5(PO4)3(OH), were selected as modifier to load into biomass prior to pyrolysis.	Phosphorus	4-14	carbonic anhydrase 5A	Homo sapiens	55-64
35430311-9	2022	Conversely, increased proportions of bacillariophytes and total dissolved phosphorus in more mesotrophic lakes corresponded to greater periphyton Se uptake.	Phosphorus	74-84	squalene epoxidase	Homo sapiens	146-148
35078385-6	2022	In these gefitinib-containing nano-carrier, cyanine5 (Cy5) biotin-labeled black phosphorus was incorporated with cancer membrane and then consist of a nanomaterial (BPGM), which enabled to deliver gefitinib to the tumors effectively.	Phosphorus	74-90	bisphosphoglycerate mutase	Homo sapiens	165-169
35447191-5	2022	We found that the concentration of total phosphorus, which is mainly affected by land-use intensity and influenced by water depth, was the primary (positive) driver of changes in both FDc and FRic, while RUE was mainly explained by phytoplankton FD (i.e., FRic).	Phosphorus	41-51	CMD1B	Homo sapiens	184-187
35395261-4	2022	The characterizations and adsorption of MAF-HTCLs were studied for the selective adsorption of P, Cr, F, and Br.	Phosphorus	95-96	MAF bZIP transcription factor	Homo sapiens	40-43
35395261-9	2022	Finally, we determined that the selective adsorption mechanisms of P on MAF-HTCLs included strong ion exchange and surface chemical precipitation by analyzing the results of X-ray photoelectron spectroscopy.	Phosphorus	67-68	MAF bZIP transcription factor	Homo sapiens	72-75
35341854-4	2022	The bulk deposition fluxes of total nitrogen (TN) and total phosphorus (TP) over the network were 27.5 kg N ha-1 yr-1 and 0.92 kg P ha-1 yr-1, respectively.	Phosphorus	60-70	solute carrier family 9 member B1	Homo sapiens	106-117
35341854-4	2022	The bulk deposition fluxes of total nitrogen (TN) and total phosphorus (TP) over the network were 27.5 kg N ha-1 yr-1 and 0.92 kg P ha-1 yr-1, respectively.	Phosphorus	60-70	sodium channel epithelial 1 subunit gamma	Homo sapiens	130-141
35064296-7	2022	PRL-adjusted ACTH IPS/P ratios were > 1.3 in all patients with proven CD; it was 0.7 in the patient with EAS.	Phosphorus	22-23	prolactin	Homo sapiens	0-3
35064296-9	2022	CONCLUSION: Although PRL-adjusted ACTH IPS/P ratios can be helpful to improve the accuracy of results during IPSS procedures, a prolactin intersinus gradient towards the ACTH-dominant side in patients with CD may invalidate PRL as an indicator of pituitary venous outflow.	Phosphorus	43-44	prolactin	Homo sapiens	21-24
35567845-10	2022	Macrophytes were capable to preserve P in biomass in the macrophyte-dominated ecosystem, which released 150% and 72% of more labile organic P (NaOH25-nrP) and BD-P in the sediment after the deterioration than before, respectively.	Phosphorus	37-38	neuropilin 1	Homo sapiens	150-153
35567845-10	2022	Macrophytes were capable to preserve P in biomass in the macrophyte-dominated ecosystem, which released 150% and 72% of more labile organic P (NaOH25-nrP) and BD-P in the sediment after the deterioration than before, respectively.	Phosphorus	140-141	neuropilin 1	Homo sapiens	150-153
35248639-2	2022	Based on the soil sampling and survey data set, this study established the path analysis model of SANs (soil available nutrients, including ammonium nitrogen (AN), available phosphorus (AP) and available potassium (AK)) with topography, climate and vegetation in order to explore how environmental factors interact to affect the content of SANs.	Phosphorus	174-184	USH1 protein network component sans	Homo sapiens	98-102
35134405-5	2022	When the initial phosphorus concentration was 2.0 mg/L, the phosphorus adsorption capacity of Ca-GAT increased to 0.891 mg/g from 0.074 mg/g for GAT at 298 K and pH of 7.	Phosphorus	17-27	glycine-N-acyltransferase	Homo sapiens	145-148
35537585-3	2022	In this study, a multifunctional photothermal scaffold was developed: bone morphogenetic protein-2 (BMP-2)/polylactic-glycolic acid copolymers (PLGA) microspheres were prepared by a double emulsion method and then coated on the scaffolds prepared using a mixture of black phosphorus nanosheets (BPs) and PLGA, to form BMP-2@BPs scaffolds.	Phosphorus	272-282	bone morphogenetic protein 2	Homo sapiens	70-98
35537585-3	2022	In this study, a multifunctional photothermal scaffold was developed: bone morphogenetic protein-2 (BMP-2)/polylactic-glycolic acid copolymers (PLGA) microspheres were prepared by a double emulsion method and then coated on the scaffolds prepared using a mixture of black phosphorus nanosheets (BPs) and PLGA, to form BMP-2@BPs scaffolds.	Phosphorus	272-282	bone morphogenetic protein 2	Homo sapiens	100-105
35621115-0	2022	Strain-induced spin-gapless semiconductors and pure thermal spin-current in magnetic black arsenic-phosphorus monolayers.	Phosphorus	99-109	spindlin 1	Homo sapiens	60-64
35134405-5	2022	When the initial phosphorus concentration was 2.0 mg/L, the phosphorus adsorption capacity of Ca-GAT increased to 0.891 mg/g from 0.074 mg/g for GAT at 298 K and pH of 7.	Phosphorus	60-70	glycine-N-acyltransferase	Homo sapiens	145-148
35613118-5	2022	In sex-stratified analyses, we examined the cross-sectional associations between log-transformed sex hormones (per 1 SD) and log-transformed FGF-23 using multiple linear regression adjusted for socio-demographics, CVD risk factors, estimated glomerular filtration rate and mineral metabolites (25-hydroxyvitamin D, calcium, phosphorus and parathyroid hormone).	Phosphorus	324-334	fibroblast growth factor 23	Homo sapiens	141-147
35606353-6	2022	The above phenotypes were based on decreasing p-Ser9 and increasing p-Tyr216 by GSK3beta palmitoylation, which further activated the enhancer of the zeste homolog 2 (EZH2)-STAT3 pathway.	Phosphorus	46-47	glycogen synthase kinase 3 alpha	Homo sapiens	80-88
35606353-6	2022	The above phenotypes were based on decreasing p-Ser9 and increasing p-Tyr216 by GSK3beta palmitoylation, which further activated the enhancer of the zeste homolog 2 (EZH2)-STAT3 pathway.	Phosphorus	46-47	enhancer of zeste 2 polycomb repressive complex 2 subunit	Homo sapiens	166-170
35606353-6	2022	The above phenotypes were based on decreasing p-Ser9 and increasing p-Tyr216 by GSK3beta palmitoylation, which further activated the enhancer of the zeste homolog 2 (EZH2)-STAT3 pathway.	Phosphorus	46-47	signal transducer and activator of transcription 3	Homo sapiens	172-177
35065929-1	2022	The aerobic granular sludge simultaneous partial nitrification, denitrification and phosphorus removal (AGS-SPNDPR) process was carried out via tapered aeration in sequencing batch reactor (SBR) for treating low strength and low COD/TN ratio municipal wastewater.	Phosphorus	84-94	C-type lectin domain family 3 member B	Homo sapiens	233-235
35607373-1	2022	In patients with diabetes, the Wnt/beta-catenin pathway in vascular smooth muscle cells (VSMCs) is continuously activated by low-intensity inflammation, which leads to the osteoblastic differentiation of these cells and the deposition of calcium and phosphorus in blood vessels.	Phosphorus	250-260	catenin beta 1	Homo sapiens	35-47
35587600-11	2022	Participants with CKD and the minor allele of rs4074995 (RGS14) had lower phosphorus, lower plasma FGF23 and lower prevalence of hyperparathyroidism.	Phosphorus	74-84	regulator of G protein signaling 14	Homo sapiens	57-62
35590460-1	2022	To acquire phosphorus, cyanobacteria use the typical bacterial ABC-type phosphate transporter, which is composed of a periplasmic high-affinity phosphate-binding protein PstS and a channel formed by two transmembrane proteins PstC and PstA.	Phosphorus	11-21	phosphate ABC transporter substrate-binding protein PstS	Prochlorococcus phage P-SSM2	170-174
35594171-3	2022	Phosphinidenes, mono-valent phosphorus species, can be stabilized by phosphines, giving so-called phosphanylidenephosphoranes of the type RP(PR" 3 ).	Phosphorus	28-38	proteinase 3	Homo sapiens	138-146
35502857-1	2022	In this work, a phosphorus-doped mesoporous Au alloy film is grown on Ni foam (mAuP/NF) via a replacement reaction using diblock copolymers and NaH2PO2 as pore-forming agents and a phosphorus dopant, respectively.	Phosphorus	16-26	neurofascin	Homo sapiens	84-86
35502857-2	2022	Due to the phosphorus doping and well-developed mesoporous structure, the obtained mAuP/NF possesses superior NH3 yield (36.52 microg h-1 mg-1cat.)	Phosphorus	11-21	neurofascin	Homo sapiens	88-90
35589876-1	2022	Stanniocalcin-1 (STC-1) is a glycoprotein hormone involved in calcium/phosphorus metabolism and direct inhibition of bone and muscle growth.	Phosphorus	70-80	stanniocalcin 1	Sus scrofa	0-15
35589876-1	2022	Stanniocalcin-1 (STC-1) is a glycoprotein hormone involved in calcium/phosphorus metabolism and direct inhibition of bone and muscle growth.	Phosphorus	70-80	stanniocalcin 1	Sus scrofa	17-22
34999029-9	2022	Furthermore, the results from the Standards, Measurements and Testing (SMT) and X-Ray Diffraction (XRD) showed that phosphorus in the AGS mainly existed in the form of inorganic phosphorus (IP) and the proportion of Ca5(PO4)3(OH) in IP was up to 92%.	Phosphorus	116-126	carbonic anhydrase 5A	Homo sapiens	216-225
35592618-2	2022	Until recently, treatment of PH1 was supportive, consisting of intensive hyperhydration, use of crystallization inhibitors (citrate and neutral phosphorus), in a subset of responsive PH1 patients" pharmacologic doses of vitamin B6 (pyridoxine), and kidney and liver transplantation when patients progressed to kidney failure.	Phosphorus	144-154	alanine--glyoxylate and serine--pyruvate aminotransferase	Homo sapiens	29-32
35588886-0	2022	Rust triggers rapid reduction of Cr6+ by red phosphorus: The importance of electronic transfer medium of Fe3.	Phosphorus	45-55	teratocarcinoma-derived growth factor 1 pseudogene 6	Homo sapiens	33-36
35588886-2	2022	However, the activity of red P to reduce Cr6+ is limited.	Phosphorus	25-30	teratocarcinoma-derived growth factor 1 pseudogene 6	Homo sapiens	41-44
35588886-4	2022	Interestingly, we found that Fe3+ derived from rust, waste iron or Fe3+ reagents can be used as the electron transport medium to solve the electron transport obstacles between red P and Cr6+.	Phosphorus	176-181	teratocarcinoma-derived growth factor 1 pseudogene 6	Homo sapiens	186-189
35588886-5	2022	As a result, the reduction of Cr6+ by red P/rust system takes only 20 min, which is far lower than the 140 min of red P. The reduction rate of Cr6+ in the red P/rust system is about 12.3 times that of red P. The reaction mechanism is that red P is not easy to access chromate anions but can easily adsorb Fe3+.	Phosphorus	243-244	teratocarcinoma-derived growth factor 1 pseudogene 6	Homo sapiens	30-33
35588886-5	2022	As a result, the reduction of Cr6+ by red P/rust system takes only 20 min, which is far lower than the 140 min of red P. The reduction rate of Cr6+ in the red P/rust system is about 12.3 times that of red P. The reaction mechanism is that red P is not easy to access chromate anions but can easily adsorb Fe3+.	Phosphorus	243-244	teratocarcinoma-derived growth factor 1 pseudogene 6	Homo sapiens	143-146
35568694-6	2022	Additionally, a nanobody was screened via the domain where eIF4E2 bound to GSK3beta, and this nanobody inhibited S/T-P phosphorylation to promote senescence.	Phosphorus	117-118	eukaryotic translation initiation factor 4E family member 2	Homo sapiens	59-65
35629567-7	2022	The maximum adsorption capacity of Absodan Plus in terms of phosphorus and chromium amounts to 9.46 mg P/g and 39.1 mg Cr/g, respectively.	Phosphorus	60-70	chromodomain helicase DNA binding protein 7	Homo sapiens	119-123
35568694-6	2022	Additionally, a nanobody was screened via the domain where eIF4E2 bound to GSK3beta, and this nanobody inhibited S/T-P phosphorylation to promote senescence.	Phosphorus	117-118	glycogen synthase kinase 3 alpha	Homo sapiens	75-83
35403658-5	2022	Thus, the prepared P(AAm-co-AA)/CS-Fe3+ hybrid network hydrogel shows excellent mechanical properties in many aspects: a strength of up to 550 kPa, a broad strain-range up to 800%, fast self-recovery ability (30 min), and low hysteresis strain (<100%).	Phosphorus	19-20	citrate synthase	Homo sapiens	32-34
35560207-0	2022	The phospho-base N-methyltransferases PMT1 and PMT2 produce phosphocholine for leaf growth in phosphorus-starved Arabidopsis.	Phosphorus	94-104	polyol/monosaccharide transporter 2	Arabidopsis thaliana	47-51
35573870-13	2022	Binary logistic regression of low SMI showed that the odds ratio for PTH levels was greater than the upper limit of the normal range, which was 11.769 (p=0.043, 95% confidence interval: 1.078-128.536), and the model predictive power was 0.986 after correction for age, sex, height, weight, hemoglobin, serum calcium, serum phosphorus, serum total cholesterol, serum triglyceride, and basal metabolic rate.	Phosphorus	323-333	parathyroid hormone	Homo sapiens	69-72
35508846-0	2022	Recycling phosphorus and calcium from aquaculture waste as a precursor for hydroxyapatite (HAp) production: a review.	Phosphorus	10-20	reticulon 3	Homo sapiens	91-94
35605059-0	2022	High phosphorus mediated the release of C-X-C motif chemokine ligand 8 in valvular interstitial cells-induced endothelial-to-mesenchymal transition via miR-214/phosphatase and tensin homolog to promote valvular calcification in chronic kidney disease.	Phosphorus	5-15	microRNA 214	Homo sapiens	152-159
35385269-7	2022	The high gas response was attributed to the catalytic effect promoted by the uniformly distributed Co-exsolved nanoparticles and the formation of p-n junctions on the sensing surface during reduction.	Phosphorus	146-147	gastrin	Homo sapiens	9-12
35381273-2	2022	Herein, active photosynthetic Chlorophyceae (Chlorella, Chl) functionalized with black phosphorus nanosheets (BPNSs) through polyaspartic acid (PASP) and Fe3+ mediating "Lego building method" are utilized for photocatalyzed oxygen-evolving to realize photosynthesis enhanced synergistic photodynamic/chemodynamic/immune therapy.	Phosphorus	87-97	chordin like 1	Homo sapiens	56-59
35558889-0	2022	Dentin Matrix Protein 1 Silencing Inhibits Phosphorus Utilization in Primary Cultured Tibial Osteoblasts of Broiler Chicks.	Phosphorus	43-53	dentin matrix acidic phosphoprotein 1	Homo sapiens	0-23
35558889-1	2022	Three experiments were carried out in the present study to investigate whether dentin matrix protein 1 (DMP1) was involved in regulating phosphorus (P) metabolic utilization in primary cultured tibial osteoblasts of broiler chicks.	Phosphorus	149-151	dentin matrix acidic phosphoprotein 1	Homo sapiens	104-108
35558889-1	2022	Three experiments were carried out in the present study to investigate whether dentin matrix protein 1 (DMP1) was involved in regulating phosphorus (P) metabolic utilization in primary cultured tibial osteoblasts of broiler chicks.	Phosphorus	137-149	dentin matrix acidic phosphoprotein 1	Homo sapiens	79-102
35558889-7	2022	It is concluded that DMP1 silencing inhibited P utilization, and thus DMP1 was involved in regulating P metabolic utilization in primary cultured tibial osteoblasts of broiler chicks, which provides a novel insight into the regulation of the P utilization in the bone of broilers, and will contribute to develop feasible strategies to improve the bone P utilization efficiency of broilers so as to decrease its excretion.	Phosphorus	242-243	dentin matrix acidic phosphoprotein 1	Homo sapiens	70-74
35558889-1	2022	Three experiments were carried out in the present study to investigate whether dentin matrix protein 1 (DMP1) was involved in regulating phosphorus (P) metabolic utilization in primary cultured tibial osteoblasts of broiler chicks.	Phosphorus	137-149	dentin matrix acidic phosphoprotein 1	Homo sapiens	104-108
35558889-1	2022	Three experiments were carried out in the present study to investigate whether dentin matrix protein 1 (DMP1) was involved in regulating phosphorus (P) metabolic utilization in primary cultured tibial osteoblasts of broiler chicks.	Phosphorus	149-151	dentin matrix acidic phosphoprotein 1	Homo sapiens	79-102
35435133-0	2022	A long non-coding RNA H19/microRNA-138/TLR3 network is involved in high phosphorus-mediated vascular calcification and chronic kidney disease.	Phosphorus	72-82	H19, imprinted maternally expressed transcript (non-protein coding)	Rattus norvegicus	22-25
35630141-0	2022	Electrochemical Detection of Alpha-Fetoprotein Based on Black Phosphorus Nanosheets Modification with Iron Ions.	Phosphorus	62-72	alpha fetoprotein	Homo sapiens	29-46
35462447-6	2022	SIGNIFICANCE AND IMPACT OF THE STUDY: With superior genetic stability and production stability in non-selective medium during fermentation, the high-level p-CA-producing strain constructed via POT1-mediated delta integration could serve as an efficient platform strain, eliminating the threat of unstable and insufficient supply for future production of p-CA derivatives, making downstream processing and biosynthesis much simpler.	Phosphorus	155-156	acetyl-CoA C-acyltransferase	Saccharomyces cerevisiae S288C	193-197
35411891-3	2022	With 3V-PPh3 as the carrier, stable adsorption configurations of Rh and 3V-PPh3 were investigated, and the results showed that Rh and P had the strongest effects, while the vinyl group enhanced the adsorption strength of Rh.	Phosphorus	134-135	caveolin 1	Homo sapiens	5-12
35411891-3	2022	With 3V-PPh3 as the carrier, stable adsorption configurations of Rh and 3V-PPh3 were investigated, and the results showed that Rh and P had the strongest effects, while the vinyl group enhanced the adsorption strength of Rh.	Phosphorus	134-135	caveolin 1	Homo sapiens	72-79
35411891-5	2022	With 3V-PPh3 as the ligand, the properties of the HRh(CO)(P-frame)3 complex were investigated, and the results of structure analysis indicated that there were strong interactions between Rh and P, which contributed more to the non-loss of Rh.	Phosphorus	194-195	caveolin 1	Homo sapiens	5-12
35575337-9	2022	In the in vitro EFGR silencing study, the statistical glycopolymer-peptide (P3-P) polyplexes had superior EGFR silencing efficiency in comparison with the other polymers that were studied.	Phosphorus	78-80	epidermal growth factor receptor	Homo sapiens	106-110
35435133-0	2022	A long non-coding RNA H19/microRNA-138/TLR3 network is involved in high phosphorus-mediated vascular calcification and chronic kidney disease.	Phosphorus	72-82	toll-like receptor 3	Rattus norvegicus	39-43
35435133-6	2022	High phosphorus also increased the expression of RUNX2 whereas reduced the expression of alpha-SM actin in the aortic tissues and VSMCs.	Phosphorus	5-15	RUNX family transcription factor 2	Rattus norvegicus	49-54
35435133-6	2022	High phosphorus also increased the expression of RUNX2 whereas reduced the expression of alpha-SM actin in the aortic tissues and VSMCs.	Phosphorus	5-15	H19, imprinted maternally expressed transcript (non-protein coding)	Rattus norvegicus	89-97
35435133-10	2022	In conclusion, this study demonstrates that the H19/miR-138/TLR3 axis is involved in high phosphorus-mediated vascular calcification in rats with CKD.	Phosphorus	90-100	H19, imprinted maternally expressed transcript (non-protein coding)	Rattus norvegicus	48-51
35435133-10	2022	In conclusion, this study demonstrates that the H19/miR-138/TLR3 axis is involved in high phosphorus-mediated vascular calcification in rats with CKD.	Phosphorus	90-100	toll-like receptor 3	Rattus norvegicus	60-64
35416447-14	2022	Exp2% and Exp5% showed a higher Ca:P ratio after aging (p < 0.05).	Phosphorus	35-36	exportin 5	Homo sapiens	10-14
35426585-5	2022	Genetic variants in MTR, PCYT1A, ASS1, SLC 25A13, GSTM1, GSTT1, SUMO1 BHMT1, and BHMT2 are being reported to be linked with CL/P risk.	Phosphorus	127-128	phosphate cytidylyltransferase 1A, choline	Homo sapiens	25-31
35426585-5	2022	Genetic variants in MTR, PCYT1A, ASS1, SLC 25A13, GSTM1, GSTT1, SUMO1 BHMT1, and BHMT2 are being reported to be linked with CL/P risk.	Phosphorus	127-128	argininosuccinate synthase 1	Homo sapiens	33-37
35426585-5	2022	Genetic variants in MTR, PCYT1A, ASS1, SLC 25A13, GSTM1, GSTT1, SUMO1 BHMT1, and BHMT2 are being reported to be linked with CL/P risk.	Phosphorus	127-128	solute carrier family 25 member 13	Homo sapiens	39-48
35426585-5	2022	Genetic variants in MTR, PCYT1A, ASS1, SLC 25A13, GSTM1, GSTT1, SUMO1 BHMT1, and BHMT2 are being reported to be linked with CL/P risk.	Phosphorus	127-128	glutathione S-transferase mu 1	Homo sapiens	50-55
35426585-5	2022	Genetic variants in MTR, PCYT1A, ASS1, SLC 25A13, GSTM1, GSTT1, SUMO1 BHMT1, and BHMT2 are being reported to be linked with CL/P risk.	Phosphorus	127-128	glutathione S-transferase theta 1	Homo sapiens	57-62
35426585-5	2022	Genetic variants in MTR, PCYT1A, ASS1, SLC 25A13, GSTM1, GSTT1, SUMO1 BHMT1, and BHMT2 are being reported to be linked with CL/P risk.	Phosphorus	127-128	small ubiquitin like modifier 1	Homo sapiens	64-69
35426585-5	2022	Genetic variants in MTR, PCYT1A, ASS1, SLC 25A13, GSTM1, GSTT1, SUMO1 BHMT1, and BHMT2 are being reported to be linked with CL/P risk.	Phosphorus	127-128	betaine--homocysteine S-methyltransferase	Homo sapiens	70-75
35426585-5	2022	Genetic variants in MTR, PCYT1A, ASS1, SLC 25A13, GSTM1, GSTT1, SUMO1 BHMT1, and BHMT2 are being reported to be linked with CL/P risk.	Phosphorus	127-128	betaine--homocysteine S-methyltransferase 2	Homo sapiens	81-86
35051798-7	2022	Furthermore, we studied the surface enhancement effect of black phosphorus with different thicknesses as SERS substrates.	Phosphorus	64-74	seryl-tRNA synthetase 1	Homo sapiens	105-109
35498801-6	2022	The area under the curve of GDF15 for the diagnosis of PMDs was 0.891, which was higher than that of the other biomarkers, including FGF21 (0.814), lactate (0.863) and L/P ratio (0.671).	Phosphorus	170-171	growth differentiation factor 15	Homo sapiens	28-33
35363437-3	2022	Here we utilize mu-X-ray fluorescence imaging in combination with rapid freezing to resolve the elemental distribution of phosphorus, sulfur, potassium, and zinc in huntingtin exon-1-mYFP expressing HeLa cells.	Phosphorus	122-132	huntingtin	Homo sapiens	165-175
35416762-5	2022	Based on this aspect, this paper proposes a novel type of SN P system, namely, layered SN P system (LSN P system), to solve classification problems by supervised learning.	Phosphorus	61-62	sialophorin	Homo sapiens	100-103
35384052-12	2022	AT1 R inhibition abolished the rise in serum calcium and phosphorus and normalized serum superoxide dismutase and catalase.	Phosphorus	57-67	angiotensin II receptor, type 1b	Rattus norvegicus	0-5
35037420-8	2022	Using integrative transcriptomic and cistromic analyses, they identify CRTC2-regulated cystogenesis-associated genes, whose activation depends on CRTC2 condensate-facilitated P-TEFb recruitment and the release of paused RNA polymerase II.	Phosphorus	175-176	CREB regulated transcription coactivator 2	Mus musculus	71-76
35037420-8	2022	Using integrative transcriptomic and cistromic analyses, they identify CRTC2-regulated cystogenesis-associated genes, whose activation depends on CRTC2 condensate-facilitated P-TEFb recruitment and the release of paused RNA polymerase II.	Phosphorus	175-176	CREB regulated transcription coactivator 2	Mus musculus	146-151
35255258-11	2022	In vivo, Irisin decreased serum creatinine, urea and phosphorous levels in chronic kidney disease (CKD) mice.	Phosphorus	53-64	fibronectin type III domain containing 5	Homo sapiens	9-15
35088867-1	2022	Inorganic phosphate (Pi) is the predominant form of phosphorus (P) readily accessible to plants, and Phosphate Transporter 1 (PHT1) genes are the major contributors to root Pi uptake.	Phosphorus	52-62	solute carrier family 15 member 4 L homeolog	Xenopus laevis	126-130
35379968-1	2022	The main feedstock for the value-added phosphorus chemicals used in industry and research is white phosphorus (P4), from which the key intermediate for forming P(III) compounds is PCl3.	Phosphorus	39-49	PHD finger protein 19	Homo sapiens	180-184
35379968-1	2022	The main feedstock for the value-added phosphorus chemicals used in industry and research is white phosphorus (P4), from which the key intermediate for forming P(III) compounds is PCl3.	Phosphorus	93-109	PHD finger protein 19	Homo sapiens	180-184
35379968-3	2022	Our concept of oxidative onioation, where white phosphorus is selectively converted into triflate salts of versatile P1 transfer reagents such as (P(LN)3)(OTf)3 (LN is a cationic, N-based substituent; that is, 4-dimethylaminopyridinio), provides a convenient alternative for the implementation of P-O, P-N and P-C bonds while circumventing the use of PCl3.	Phosphorus	48-58	PHD finger protein 19	Homo sapiens	351-355
35088867-1	2022	Inorganic phosphate (Pi) is the predominant form of phosphorus (P) readily accessible to plants, and Phosphate Transporter 1 (PHT1) genes are the major contributors to root Pi uptake.	Phosphorus	64-65	solute carrier family 15 member 4 L homeolog	Xenopus laevis	126-130
35088867-8	2022	Furthermore, OsPHT1;7 showed an overwhelmingly higher transcript abundance in anthers than other PHT1 members, and ospht1;7 mutants were impaired in P accumulation in anthers but not in pistils or husks.	Phosphorus	149-150	solute carrier family 15 member 4 L homeolog	Xenopus laevis	97-101
35318578-7	2022	Under PHR control, several classes of PHTs, microRNAs, and proteins modulate root architecture, and metabolic processes to enable plants to adapt to low P.	Phosphorus	153-154	LY6/PLAUR domain containing 1	Homo sapiens	38-42
35392115-2	2022	We aimed to investigate the effects of inorganic P levels on P utilization, local bone-derived regulators and bone morphogenetic protein/mitogen-activated protein kinase (BMP/MAPK) pathway in primary cultured osteoblasts of broiler chicks in order to address whether local bone-derived regulators or BMP/MAPK pathway was involved in regulating the bone P utilization of broilers using an in vitro model.	Phosphorus	49-50	bone morphogenetic protein 1	Homo sapiens	110-136
35392115-2	2022	We aimed to investigate the effects of inorganic P levels on P utilization, local bone-derived regulators and bone morphogenetic protein/mitogen-activated protein kinase (BMP/MAPK) pathway in primary cultured osteoblasts of broiler chicks in order to address whether local bone-derived regulators or BMP/MAPK pathway was involved in regulating the bone P utilization of broilers using an in vitro model.	Phosphorus	49-50	bone morphogenetic protein 1	Homo sapiens	171-174
35392115-2	2022	We aimed to investigate the effects of inorganic P levels on P utilization, local bone-derived regulators and bone morphogenetic protein/mitogen-activated protein kinase (BMP/MAPK) pathway in primary cultured osteoblasts of broiler chicks in order to address whether local bone-derived regulators or BMP/MAPK pathway was involved in regulating the bone P utilization of broilers using an in vitro model.	Phosphorus	49-50	bone morphogenetic protein 1	Homo sapiens	300-303
35392115-8	2022	These results suggested that P utilization in primary cultured tibial osteoblasts of broiler chicks might be partly regulated by PHEX, DMP1, MEPE, BMP2, ERK1, and JNK1.	Phosphorus	29-30	phosphate regulating endopeptidase homolog X-linked	Homo sapiens	129-133
35392115-8	2022	These results suggested that P utilization in primary cultured tibial osteoblasts of broiler chicks might be partly regulated by PHEX, DMP1, MEPE, BMP2, ERK1, and JNK1.	Phosphorus	29-30	dentin matrix acidic phosphoprotein 1	Homo sapiens	135-139
35392115-8	2022	These results suggested that P utilization in primary cultured tibial osteoblasts of broiler chicks might be partly regulated by PHEX, DMP1, MEPE, BMP2, ERK1, and JNK1.	Phosphorus	29-30	matrix extracellular phosphoglycoprotein	Homo sapiens	141-145
35392115-8	2022	These results suggested that P utilization in primary cultured tibial osteoblasts of broiler chicks might be partly regulated by PHEX, DMP1, MEPE, BMP2, ERK1, and JNK1.	Phosphorus	29-30	bone morphogenetic protein 2	Homo sapiens	147-151
35392115-8	2022	These results suggested that P utilization in primary cultured tibial osteoblasts of broiler chicks might be partly regulated by PHEX, DMP1, MEPE, BMP2, ERK1, and JNK1.	Phosphorus	29-30	mitogen-activated protein kinase 3	Homo sapiens	153-157
35392115-8	2022	These results suggested that P utilization in primary cultured tibial osteoblasts of broiler chicks might be partly regulated by PHEX, DMP1, MEPE, BMP2, ERK1, and JNK1.	Phosphorus	29-30	mitogen-activated protein kinase 8	Homo sapiens	163-167
35369318-1	2022	Parathyroid hormone is the main endocrine regulator of extracellular calcium and phosphorus levels.	Phosphorus	81-91	parathyroid hormone	Homo sapiens	0-19
35334767-6	2022	A rapid adaptation of black phosphorus (BP) field-effect transistors (FETs) and gallium nitride (GaN) transistors in the CS field is also apparent.	Phosphorus	40-42	citrate synthase	Homo sapiens	121-123
35369063-0	2022	Dietary Phosphorus Reduced Hepatic Lipid Deposition by Activating Ampk Pathway and Beclin1 Phosphorylation Levels to Activate Lipophagy in Tilapia Oreochromis niloticus.	Phosphorus	8-18	beclin-1	Oreochromis niloticus	83-90
35369063-5	2022	Mechanistically, phosphorus increased the AMPKalpha1 phosphorylation level at S496 and Beclin1 phosphorylation at S90, and Beclin1 phosphorylation by AMPKalpha1 was required for phosphorus-induced lipophagy and lipolysis.	Phosphorus	17-27	beclin-1	Oreochromis niloticus	87-94
35369063-5	2022	Mechanistically, phosphorus increased the AMPKalpha1 phosphorylation level at S496 and Beclin1 phosphorylation at S90, and Beclin1 phosphorylation by AMPKalpha1 was required for phosphorus-induced lipophagy and lipolysis.	Phosphorus	17-27	beclin-1	Oreochromis niloticus	123-130
35369063-5	2022	Mechanistically, phosphorus increased the AMPKalpha1 phosphorylation level at S496 and Beclin1 phosphorylation at S90, and Beclin1 phosphorylation by AMPKalpha1 was required for phosphorus-induced lipophagy and lipolysis.	Phosphorus	178-188	beclin-1	Oreochromis niloticus	123-130
35369063-6	2022	Our study revealed a mechanism for Beclin1 regulation and autophagy induction in response to high-phosphorus diet, and provided novel evidences for the link between dietary phosphorus addition and lipolytic metabolism via the AMPK/Beclin1 pathway.	Phosphorus	98-108	beclin-1	Oreochromis niloticus	35-42
35369063-6	2022	Our study revealed a mechanism for Beclin1 regulation and autophagy induction in response to high-phosphorus diet, and provided novel evidences for the link between dietary phosphorus addition and lipolytic metabolism via the AMPK/Beclin1 pathway.	Phosphorus	173-183	beclin-1	Oreochromis niloticus	35-42
35369063-6	2022	Our study revealed a mechanism for Beclin1 regulation and autophagy induction in response to high-phosphorus diet, and provided novel evidences for the link between dietary phosphorus addition and lipolytic metabolism via the AMPK/Beclin1 pathway.	Phosphorus	173-183	beclin-1	Oreochromis niloticus	231-238
35290524-8	2022	The highest Phosphorus dissolving and IAA production capacity (in tryptophan-added medium) of isolates were  186.52 microg mL-1, and 50.05 mug mL-1  respectively, and 31 of 69 isolates were able to produce siderophore.	Phosphorus	12-22	L1 cell adhesion molecule	Mus musculus	123-127
35310951-4	2022	Herein, we determined the molecular basis of presentation of two P4/P6 double pS-containing peptides by HLA-B27 and compared them with unmodified and single-phosphorylated peptide complexes.	Phosphorus	78-80	major histocompatibility complex, class I, B	Homo sapiens	104-111
35294702-7	2022	Among these variants, only three different OTULIN variants (p.Val82Ile, p.Gln115His and p.Leu131_Arg132insLeuCysThrGlu) were detected.	Phosphorus	88-89	OTU deubiquitinase with linear linkage specificity	Homo sapiens	43-49
35290533-0	2022	Visualized SERS Imaging of Single Molecule by Ag/Black Phosphorus Nanosheets.	Phosphorus	55-65	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	11-15
35309424-2	2022	The addition of silica to P(NIPAAm-co-AAc) copolymer hydrogel has the potential to open up new applications in the development of thermosensitive building materials by leveraging the favorable thermal characteristics of P(NIPAAm-co-AAc).	Phosphorus	26-27	glycine-N-acyltransferase	Homo sapiens	38-41
35309424-2	2022	The addition of silica to P(NIPAAm-co-AAc) copolymer hydrogel has the potential to open up new applications in the development of thermosensitive building materials by leveraging the favorable thermal characteristics of P(NIPAAm-co-AAc).	Phosphorus	220-222	glycine-N-acyltransferase	Homo sapiens	38-41
35309424-4	2022	The P(NIPAAm-co-AAc) copolymer hydrogel was mixed with the m-silica to form the P(NIPAAm-co-AAc)-grafted m-silica nanocomposites.	Phosphorus	80-82	glycine-N-acyltransferase	Homo sapiens	16-19
35309424-4	2022	The P(NIPAAm-co-AAc) copolymer hydrogel was mixed with the m-silica to form the P(NIPAAm-co-AAc)-grafted m-silica nanocomposites.	Phosphorus	80-82	glycine-N-acyltransferase	Homo sapiens	92-95
35144130-0	2022	GSDMD-miR-223-NLRP3 axis involved in B(a)P-induced inflammatory injury of alveolar epithelial cells.	Phosphorus	41-42	NLR family pyrin domain containing 3	Homo sapiens	14-19
35144130-8	2022	Our results indicated that after B(a)P exposure, TNF-alpha and IL-6 in the supernatant were increased.	Phosphorus	37-38	tumor necrosis factor	Homo sapiens	49-58
35144130-8	2022	Our results indicated that after B(a)P exposure, TNF-alpha and IL-6 in the supernatant were increased.	Phosphorus	37-38	interleukin 6	Homo sapiens	63-67
35260475-9	2022	When stratified according to the plasma level of PS+ REVs, the group of patients with SLE with a high level of PS+ REVs presented a higher number of past thrombosis events and higher ATX levels.	Phosphorus	49-52	ectonucleotide pyrophosphatase/phosphodiesterase 2	Homo sapiens	183-186
35073420-2	2022	We calculated and evaluated the sensitivity coefficients of predicted STP and changes in STP using 1- and 10-yr simulations with and without P application.	Phosphorus	141-142	sulfotransferase family 1A member 1	Homo sapiens	89-92
35260475-9	2022	When stratified according to the plasma level of PS+ REVs, the group of patients with SLE with a high level of PS+ REVs presented a higher number of past thrombosis events and higher ATX levels.	Phosphorus	111-114	ectonucleotide pyrophosphatase/phosphodiesterase 2	Homo sapiens	183-186
35265269-1	2022	As an important hormone that regulates the balance of calcium and phosphorus, parathyroid hormone (PTH) has also been found to have an important function in intervertebral disc degeneration (IVDD).	Phosphorus	66-76	parathyroid hormone	Mus musculus	78-97
35424690-1	2022	In order to develop a liquid oxygen-compatible (LOX-compatible) matrix resins for polymer-based fiber-reinforced composites, a novel phosphorus-containing imidazole derivative called VAD containing multifunctional groups was synthesized and used as a co-curing agent for epoxy resin (EP) with simultaneous LOX-compatibility and mechanical improvement.	Phosphorus	133-143	lysyl oxidase	Homo sapiens	48-51
35424690-2	2022	A phosphorus group was introduced into the EP to capture the free radicals generated during the pyrolysis of the polymer to improve LOX compatibility, and the trimethylene group was introduced as a flexible spacer to enhance the toughness of the cured material.	Phosphorus	2-12	lysyl oxidase	Homo sapiens	132-135
35265269-1	2022	As an important hormone that regulates the balance of calcium and phosphorus, parathyroid hormone (PTH) has also been found to have an important function in intervertebral disc degeneration (IVDD).	Phosphorus	66-76	parathyroid hormone	Mus musculus	99-102
35089691-0	2022	Reversing the Epithelial-Mesenchymal Transition in Metastatic Cancer Cells Using CD146-Targeted Black Phosphorus Nanosheets and a Mild Photothermal Treatment.	Phosphorus	102-112	melanoma cell adhesion molecule	Homo sapiens	81-86
35089691-2	2022	Here, we present a nanomaterial-based approach to reverse the EMT in cancer cells by targeting an EMT inducer, CD146, using engineered black phosphorus nanosheets (BPNSs) and a mild photothermal treatment.	Phosphorus	141-151	melanoma cell adhesion molecule	Homo sapiens	111-116
35104121-6	2022	X-ray absorption fine structure spectroscopy and density functional theory calculation demonstrate that electrons transferred from Co and Se to P sites through Co-P and Se-P bonds in o-CoSe2-x P. P sites obtained plentiful electrons to form active centers, which also had a strong orbital coupling with As(III).	Phosphorus	144-145	membrane metalloendopeptidase like 1	Homo sapiens	169-173
35176981-5	2022	Then, DNA/LL-37 complexes were prepared by co-incubation of pEGFP-nef-vpr with LL-37 for 45 minutes at different nitrogen to phosphate (N/P) ratios.	Phosphorus	138-139	cathelicidin antimicrobial peptide	Homo sapiens	10-15
35216479-0	2022	Maize Transcription Factor ZmARF4 Confers Phosphorus Tolerance by Promoting Root Morphological Development.	Phosphorus	42-52	Auxin response factor 11	Zea mays	27-33
35177090-11	2022	Meanwhile, LHR, steroidogenic enzymes and StAR were downregulated with concentration-dependent on PS-MPs.	Phosphorus	98-100	luteinizing hormone/choriogonadotropin receptor	Mus musculus	11-14
35137736-2	2022	Herein, the effects of the size of BP nanosheets embedded in epoxy resin (EP) on flame retardancy are studied.	Phosphorus	35-37	epiregulin	Homo sapiens	74-76
35177090-11	2022	Meanwhile, LHR, steroidogenic enzymes and StAR were downregulated with concentration-dependent on PS-MPs.	Phosphorus	98-100	steroidogenic acute regulatory protein	Mus musculus	42-46
35214919-9	2022	The pp-LFER models performed well for predicting the Ead and K values, with external explained variance ranging from 0.90 to 0.97, and can serve as effective tools to rank adsorption capacities of organics onto BP.	Phosphorus	211-213	collagen like tail subunit of asymmetric acetylcholinesterase	Homo sapiens	53-56
35140213-1	2022	Parathyroid hormone (PTH) plays crucial role in maintaining calcium and phosphorus homeostasis.	Phosphorus	72-82	parathyroid hormone	Homo sapiens	0-19
35130971-8	2022	Notably, five proteins involved in phosphorus (P) metabolism-related nucleotide synthesis functions, including dUTPase, MazG, PhoH, Thymidylate synthase complementing protein (Thy1), and Ribonucleoside reductase (RNR), were mainly identified in agricultural soils.	Phosphorus	35-45	Deoxyuridine triphosphatase	Drosophila melanogaster	111-118
35133180-9	2022	Serum FGF-23 concentrations significantly correlated with serum tCa (r = 0.511, P = 0.003) and blood iCa concentrations (r = 0.425, P = 0.015) but not serum creatinine (r = 0.279, P = 0.122) or phosphorus concentrations (r = 0.208, P = 0.253).Conclusions and relevance Increased serum FGF-23 concentrations were associated with hypercalcaemia independently of creatinine and phosphate status in cats with CKD and upper urolithiasis.	Phosphorus	194-204	fibroblast growth factor 23	Felis catus	6-12
35130971-8	2022	Notably, five proteins involved in phosphorus (P) metabolism-related nucleotide synthesis functions, including dUTPase, MazG, PhoH, Thymidylate synthase complementing protein (Thy1), and Ribonucleoside reductase (RNR), were mainly identified in agricultural soils.	Phosphorus	35-45	Thy-1 cell surface antigen	Homo sapiens	176-180
35007810-16	2022	CONCLUSIONS: Adding phosphorus to PN in the first hours of life reduced the frequency of hypophosphatemia and hypercalcemia without any surge in hypernatremia or morbidity.	Phosphorus	20-30	U6 snRNA biogenesis phosphodiesterase 1	Homo sapiens	34-36
35042327-12	2022	By a logical selection of singlet carbenes, stable 2-phosha-1,3-butadiene and 2-arsa-1,3-butadiene compounds, as well as related radical cations and dications, can be prepared as crystalline solids.The relevance of NHV ligands as potent pi-donors has been demonstrated for the stabilization of elusive electrophilic phosphinidene and arsinidene complexes {(NHV)E}Fe(CO)4 (E = P or As).	Phosphorus	376-377	guided entry of tail-anchored proteins factor 3, ATPase	Homo sapiens	80-86
34571181-2	2022	METHODS: Eighty patients were divided into 2 groups randomly, the HTO-alone group (n = 41) and the HTO+P-PRP group (n = 39).	Phosphorus	103-104	prion protein	Homo sapiens	105-108
34571181-10	2022	The increase of the MJSW in the HTO+P-PRP group was significantly greater than that in the HTO-alone group during the first year, especially at 6 months (HTO alone, 3.8 +- 1.2 mm; HTO+P-PRP, 4.6 +- 1.1 mm; P = .001, 95% CI -1.27 to -0.35).	Phosphorus	36-37	prion protein	Homo sapiens	38-41
34571181-10	2022	The increase of the MJSW in the HTO+P-PRP group was significantly greater than that in the HTO-alone group during the first year, especially at 6 months (HTO alone, 3.8 +- 1.2 mm; HTO+P-PRP, 4.6 +- 1.1 mm; P = .001, 95% CI -1.27 to -0.35).	Phosphorus	36-37	prion protein	Homo sapiens	186-189
34571181-12	2022	Clinically, a higher proportion of patients in the HTO+P-PRP group exceeded the minimal clinically important difference (MCID) in the first year, especially at 6 months in Lysholm score (HTO alone, 65.9%; HTO+P-PRP, 97.4%) and WOMAC (HTO alone, 82.9%; HTO+P-PRP, 100.0%).	Phosphorus	209-210	prion protein	Homo sapiens	57-60
34571181-12	2022	Clinically, a higher proportion of patients in the HTO+P-PRP group exceeded the minimal clinically important difference (MCID) in the first year, especially at 6 months in Lysholm score (HTO alone, 65.9%; HTO+P-PRP, 97.4%) and WOMAC (HTO alone, 82.9%; HTO+P-PRP, 100.0%).	Phosphorus	256-257	prion protein	Homo sapiens	57-60
35007810-2	2022	We opted to carry out a study with the introduction of phosphorus as sodium glycerophosphate in PN from the first day onward to reveal the impact on serum phosphorus and calcium levels following the surge in the incidence of hypercalcemia and hypophosphatemia.	Phosphorus	55-65	U6 snRNA biogenesis phosphodiesterase 1	Homo sapiens	96-98
35159618-3	2022	The composition of BSM was the most advantageous in terms of non-fat solids, protein-which was the most abundant solid component-casein, calcium and phosphorus contents.	Phosphorus	149-159	mucin-19	Bos taurus	19-22
35072848-10	2022	Decrease in SOCS-3 expression was significant in Ob + D + M and Ob + D + P groups than other groups (p < 0.05).	Phosphorus	73-74	suppressor of cytokine signaling 3	Rattus norvegicus	12-18
34998548-13	2022	Compared with the 1 muM ISO treatment group, 1 microM ISO + 10 mM 3-MA downregulated the abundance of ATGL, the ratio of p-HSL to HSL and LC3-II to LC3-I, and the glycerol content, whereas it upregulated the abundance of PLIN1 and p62.	Phosphorus	121-122	lipase E, hormone sensitive type	Bos taurus	123-126
35067311-0	2022	GmWRKY46, a WRKY transcription factor, negatively regulates phosphorus tolerance primarily through modifying root morphology in soybean.	Phosphorus	60-70	WRKY transcription factor 49	Glycine max	12-16
34985865-3	2022	We found that the enzyme cascade comprising ferulic acid decarboxylase (FDC1) from Saccharomyces cerevisiae, styrene monooxygenase (SMO), styrene oxide isomerase (SOI) from Pseudomonas putida, and phenylacetaldehyde reductase (PAR) from Solanum lycopersicum could efficiently synthesize tyrosol from p-CA with a conversion rate over 90%.	Phosphorus	300-301	putative phenylacrylic acid decarboxylase FDC1	Saccharomyces cerevisiae S288C	72-76
35202131-5	2022	The model was built on STELLA, a dynamic modelling software, and is based on constitutive cell quota that varies with nitrogen, phosphorus, and temperature.	Phosphorus	128-138	developmental pluripotency associated 3	Homo sapiens	23-29
34935961-2	2022	While inactive P-TEFbs are mainly sequestered in the 7SK snRNP complex in a chromatin-free state, most of its active forms are in complex with its recruitment factors, Brd4 and SEC, in a chromatin-associated state.	Phosphorus	15-16	LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated	Homo sapiens	57-62
34935961-2	2022	While inactive P-TEFbs are mainly sequestered in the 7SK snRNP complex in a chromatin-free state, most of its active forms are in complex with its recruitment factors, Brd4 and SEC, in a chromatin-associated state.	Phosphorus	15-16	bromodomain containing 4	Homo sapiens	168-172
34935961-3	2022	Thus, switching from inactive 7SK snRNP to active P-TEFb (Brd4/P-TEFb or SEC/P-TEFb) is essential for global gene expression.	Phosphorus	50-51	bromodomain containing 4	Homo sapiens	58-62
34904988-4	2022	In most of the catalytic cycles, the P-H bond is cleaved to yield a phosphorus-based radical, which adds onto the unsaturated substrate followed by reduction of the corresponding radical yielding the product.	Phosphorus	68-78	phenylalanine hydroxylase	Homo sapiens	37-40
34951432-1	2022	Two dimensional black phosphorus nanosheets (BP NSs) have attracted plenty of attention in the research field of cancer photonic therapy.	Phosphorus	22-32	growth differentiation factor 5	Mus musculus	45-47
34951432-3	2022	To address these drawbacks, herein we report a red/black phosphorus (RP/BP) composite nanosheet, M-RP/BP@ZnFe2O4, which was synthesized by (1) partially converting red phosphorus (RP) to black phosphorus (BP) followed by liquid-phase ultrasonic exfoliation to form RP/BP NSs, (2) in situ synthesis of ZnFe2O4 nanoparticles on the surface of RP/BP NSs, (3) and wrapping with the MCF-7 cell membrane.	Phosphorus	57-67	growth differentiation factor 5	Mus musculus	205-207
34951432-3	2022	To address these drawbacks, herein we report a red/black phosphorus (RP/BP) composite nanosheet, M-RP/BP@ZnFe2O4, which was synthesized by (1) partially converting red phosphorus (RP) to black phosphorus (BP) followed by liquid-phase ultrasonic exfoliation to form RP/BP NSs, (2) in situ synthesis of ZnFe2O4 nanoparticles on the surface of RP/BP NSs, (3) and wrapping with the MCF-7 cell membrane.	Phosphorus	168-178	growth differentiation factor 5	Mus musculus	205-207
34951432-3	2022	To address these drawbacks, herein we report a red/black phosphorus (RP/BP) composite nanosheet, M-RP/BP@ZnFe2O4, which was synthesized by (1) partially converting red phosphorus (RP) to black phosphorus (BP) followed by liquid-phase ultrasonic exfoliation to form RP/BP NSs, (2) in situ synthesis of ZnFe2O4 nanoparticles on the surface of RP/BP NSs, (3) and wrapping with the MCF-7 cell membrane.	Phosphorus	193-203	growth differentiation factor 5	Mus musculus	205-207
34990129-3	2022	ESR investigations show that DMTP(O-) S reacts with Cl2 - to form the sigma2sigma*1 adduct radical -P-S(Formula: see text)Cl, which subsequently reacts with DMTP(O-) S to produce (-P-S(Formula: see text)S-P-)-.	Phosphorus	179-184	endogenous retrovirus group W member 5	Homo sapiens	52-55
34990129-4	2022	-P-S(Formula: see text)Cl in G-P(O-) S undergoes hole transfer to Gua, forming the cation radical (G +) via thermally activated hopping.	Phosphorus	0-4	DExD-box helicase 21	Homo sapiens	66-69
34990129-6	2022	Gua in G-P(O-) S is oxidized unimolecularly by the -P-S  intermediate in the sub-picosecond range.	Phosphorus	51-55	DExD-box helicase 21	Homo sapiens	0-3
35159667-5	2022	The natures of the interactions are similarly elucidated between the components of helicene dimers 6:6 and 7:7 with QTAIM-DFA, which have a p-CS/vdW nature.	Phosphorus	140-141	citrate synthase	Homo sapiens	142-144
34448875-3	2022	OBJECTIVE: To investigate the acute effect of excessive dietary phosphorus administered as sodium-dihydrogen phosphate on the postprandial levels of Pi and FGF23 and the response to food.	Phosphorus	64-74	fibroblast growth factor 23	Homo sapiens	156-161
35024716-6	2022	Synchrotron macro-attenuated total reflection-Fourier transform infrared (ATR-FTIR) micro-spectroscopy is used to elucidate the chemical changes occurring outside and within the cell of interest after exposure to BP nanoflakes.	Phosphorus	213-215	ATR serine/threonine kinase	Homo sapiens	74-77
35209305-0	2022	Simultaneous and ultra-sensitive SERS detection of SLPI and IL-18 for the assessment of donor kidney quality using black phosphorus/gold nanohybrids.	Phosphorus	121-131	secretory leukocyte peptidase inhibitor	Homo sapiens	51-55
35209305-0	2022	Simultaneous and ultra-sensitive SERS detection of SLPI and IL-18 for the assessment of donor kidney quality using black phosphorus/gold nanohybrids.	Phosphorus	121-131	interleukin 18	Homo sapiens	60-65
2706253-9	1989	The most downfield shifted phosphorus resonance in the GCG 13-mer duplex has been assigned to the phosphate in the C2-G3 step, and this observation demonstrates that the perturbation in the phosphodiester backbone extends to regions removed from the (G3-CX-G4).	Phosphorus	27-37	glucagon	Homo sapiens	55-58
34719849-0	2022	Metal-Free Phosphorus-Directed Borylation of C(sp2 )-H Bonds.	Phosphorus	11-21	Sp2 transcription factor	Homo sapiens	45-50
34873890-8	2022	CONCLUSION: Cow"s milk protein in the diet was associated with increased intake of energy, proteins, carbohydrates, calcium, phosphorus, and vitamin D, in addition to an increase in the Z-scores for weight-for-age and height-for-age.	Phosphorus	125-135	casein beta	Bos taurus	18-30
2560171-2	1989	Calmodulin inhibitors block vitamin D-induced Ca2+ transport in the gut and phosphorus uptake in renal BBMV"s.	Phosphorus	76-86	calmodulin 1	Rattus norvegicus	0-10
2628016-1	1989	The study of cerebral blood flow was performed with the aid of hydrogen clearance technique and the cinema-television method in alteration of cholinergic transmission by means of phosphorus-organic inhibitors of cholinesterase and a cholinolytic agent in unanesthetized rats.	Phosphorus	179-189	butyrylcholinesterase	Rattus norvegicus	212-226
2752025-2	1989	A consistent picture emerges from the application of infrared and 31P-NMR spectroscopy to Mg2+-PS interactions.	Phosphorus	95-97	mucin 7, secreted	Homo sapiens	90-93
2671232-0	1989	The calcium-phosphorus metabolism expert system module: a program developed in the ALEX Smalltalk/V shell.	Phosphorus	12-22	cilia and flagella associated protein 418	Homo sapiens	88-97
2917983-7	1989	These studies reveal that chiral reactions with acetylcholinesterase are dependent more on the nature of the groups surrounding the tetrahedral phosphorus than on the absolute configuration about the phosphorus atom and indicate that the active center comprises partially overlapping subsites that can accommodate the -OR and -SR" groups.	Phosphorus	144-154	acetylcholinesterase (Cartwright blood group)	Homo sapiens	48-68
2917983-7	1989	These studies reveal that chiral reactions with acetylcholinesterase are dependent more on the nature of the groups surrounding the tetrahedral phosphorus than on the absolute configuration about the phosphorus atom and indicate that the active center comprises partially overlapping subsites that can accommodate the -OR and -SR" groups.	Phosphorus	200-210	acetylcholinesterase (Cartwright blood group)	Homo sapiens	48-68
2920044-2	1989	Addition of purified PK-M to resting neutrophil light density membranes activated the NADPH-oxidase in the presence of PS, ATP and Mg2+.	Phosphorus	119-121	pyruvate kinase M1/2	Homo sapiens	21-25
2537025-6	1989	LPD decreased serum phosphorus and increased Ca2+.	Phosphorus	20-30	acyl-CoA synthetase bubblegum family member 1	Rattus norvegicus	0-3
2537025-10	1989	Thus the mechanism whereby PTH and phosphorus restriction stimulate 1,25(OH)2D3 production differ; increased Ca2+ blocks the PTH-mediated rise in 1,25(OH)2D3 but does not alter the 1,25(OH)2D3 response to phosphorus restriction.	Phosphorus	35-45	parathyroid hormone	Rattus norvegicus	125-128
2619121-5	1989	Erythropoietin concentration in dogs of the TRD groups was lower than that of controls, however, erythroid regenerative capacity was comparable with that of control dogs when plasma parathyroid hormone (PTH) concentration was lowered by reduced dietary intake of phosphorus.	Phosphorus	263-273	parathyroid hormone	Canis lupus familiaris	182-201
2516221-7	1989	A decrease of P/N ratio was also observed in the early phase after administration of erythropoietin, an agent which induces differentiation and multiplication of erythroblasts.	Phosphorus	14-15	erythropoietin	Homo sapiens	85-99
2516221-9	1989	However, following the initial decrease, the P/N ratio increased gradually 48 h after administration of erythropoietin.	Phosphorus	45-46	erythropoietin	Homo sapiens	104-118
2574956-2	1989	The biotinpentylamine substrate was incorporated into N,N-dimethylcasein by transglutaminase, the biotinylated products were adsorbed onto the membrane disks and conjugated with streptavidin-beta-galactosidase, and the absorbance resulting from the formation of p-nitrophenol from hydrolysis of p-nitrophenyl-beta-D-galactopyranoside was measured at 405 nm.	Phosphorus	10-11	protein-glutamine gamma-glutamyltransferase 2	Cavia porcellus	76-92
2752025-6	1989	One main conclusion of this work is that Mg2+ binding to PS bilayers shows a gradation, the binding is in the order DMPS greater than POPS greater than ox brain PS greater than DOPS.	Phosphorus	57-59	mucin 7, secreted	Homo sapiens	41-44
2737148-8	1989	Calcitonin ip decreased both serum calcium and phosphorus with an up to 5-fold increase in PTH mRNA at 1 h, thus demonstrating that the effect of phosphorus on PTH mRNA was due to the low serum calcium and not the high serum phosphorus.	Phosphorus	47-57	calcitonin-related polypeptide alpha	Rattus norvegicus	0-10
2737148-8	1989	Calcitonin ip decreased both serum calcium and phosphorus with an up to 5-fold increase in PTH mRNA at 1 h, thus demonstrating that the effect of phosphorus on PTH mRNA was due to the low serum calcium and not the high serum phosphorus.	Phosphorus	146-156	calcitonin-related polypeptide alpha	Rattus norvegicus	0-10
2737148-8	1989	Calcitonin ip decreased both serum calcium and phosphorus with an up to 5-fold increase in PTH mRNA at 1 h, thus demonstrating that the effect of phosphorus on PTH mRNA was due to the low serum calcium and not the high serum phosphorus.	Phosphorus	146-156	parathyroid hormone	Rattus norvegicus	91-94
2737148-8	1989	Calcitonin ip decreased both serum calcium and phosphorus with an up to 5-fold increase in PTH mRNA at 1 h, thus demonstrating that the effect of phosphorus on PTH mRNA was due to the low serum calcium and not the high serum phosphorus.	Phosphorus	146-156	parathyroid hormone	Rattus norvegicus	160-163
2737148-8	1989	Calcitonin ip decreased both serum calcium and phosphorus with an up to 5-fold increase in PTH mRNA at 1 h, thus demonstrating that the effect of phosphorus on PTH mRNA was due to the low serum calcium and not the high serum phosphorus.	Phosphorus	146-156	calcitonin-related polypeptide alpha	Rattus norvegicus	0-10
2737148-8	1989	Calcitonin ip decreased both serum calcium and phosphorus with an up to 5-fold increase in PTH mRNA at 1 h, thus demonstrating that the effect of phosphorus on PTH mRNA was due to the low serum calcium and not the high serum phosphorus.	Phosphorus	146-156	parathyroid hormone	Rattus norvegicus	91-94
2737148-8	1989	Calcitonin ip decreased both serum calcium and phosphorus with an up to 5-fold increase in PTH mRNA at 1 h, thus demonstrating that the effect of phosphorus on PTH mRNA was due to the low serum calcium and not the high serum phosphorus.	Phosphorus	146-156	parathyroid hormone	Rattus norvegicus	160-163
2737148-9	1989	When phosphorus and 1,25(OH)2D3 (100 pmol/100 g) were injected together, despite the low serum calcium, there was a decrease in PTH mRNA levels.	Phosphorus	5-15	parathyroid hormone	Rattus norvegicus	128-131
2498340-4	1989	Assignment of the phosphorus resonances of this complex was made by labeling the phosphoryl group at either C-1 or C-5 with 17O.	Phosphorus	18-28	heterogeneous nuclear ribonucleoprotein C	Homo sapiens	108-111
2498340-4	1989	Assignment of the phosphorus resonances of this complex was made by labeling the phosphoryl group at either C-1 or C-5 with 17O.	Phosphorus	18-28	complement C5	Homo sapiens	115-118
2498340-5	1989	The phosphorus atom closer to the paramagnetic metal ion, Ni2+, to which the broader of the phosphorus resonances is attributed, has been identified as that attached to C-1.	Phosphorus	4-14	heterogeneous nuclear ribonucleoprotein C	Homo sapiens	169-172
2498340-5	1989	The phosphorus atom closer to the paramagnetic metal ion, Ni2+, to which the broader of the phosphorus resonances is attributed, has been identified as that attached to C-1.	Phosphorus	92-102	heterogeneous nuclear ribonucleoprotein C	Homo sapiens	169-172
2917018-6	1989	Surprisingly, HLo-7 is highly active in reactivating human erythrocyte and rat diaphragm AChE inhibited by C(+)P(+/-)-and C(-)P(+/-)-soman, i.e. at least as active as HI-6, which is the most potent reactivator for soman-inhibited AChE reported so far.	Phosphorus	108-112	acetylcholinesterase	Rattus norvegicus	89-93
2785325-3	1989	The relationship between OC and the calcium-phosphorus regulating hormones (parathyroid hormone, calcitonin) and the biochemical parameters of bone metabolism (serum calcium, serum phosphorus and serum alkaline phosphatase) was studied in 30 patients on chronic hemodialysis (mean age: 51 years; mean duration of dialysis treatment: 39 months).	Phosphorus	44-54	bone gamma-carboxyglutamate protein	Homo sapiens	25-27
2541802-4	1989	Levels of cAMP (both urinary and nephrogenous) were significantly correlated with age, length, weight, and urinary phosphorus concentrations of the infants.	Phosphorus	115-125	cathelicidin antimicrobial peptide	Homo sapiens	10-14
2533973-5	1989	In healthy volunteers, however, the same dose of ANF increased urinary excretion of sodium, potassium, calcium, chloride and phosphorus as well as water, and creatinine clearances, and decreased plasma aldosterone.	Phosphorus	125-135	natriuretic peptide A	Homo sapiens	49-52
2912937-1	1989	Phosphorus-31 magnetic resonance spectra were obtained from the RIF-1 tumor in C3H mice before and up to 2 days after various doses of X rays.	Phosphorus	0-10	replication timing regulatory factor 1	Mus musculus	64-69
2910739-3	1989	In the normal rat stomach, the level of PAF was high in the antrum (940 +/- 200 nmol PAF/mol phosphorus of original phospholipids), especially in the antral mucosa (1801 +/- 426 nmol/mol phosphorus of original phospholipids).	Phosphorus	93-103	PCNA clamp associated factor	Rattus norvegicus	40-43
2910739-3	1989	In the normal rat stomach, the level of PAF was high in the antrum (940 +/- 200 nmol PAF/mol phosphorus of original phospholipids), especially in the antral mucosa (1801 +/- 426 nmol/mol phosphorus of original phospholipids).	Phosphorus	187-197	PCNA clamp associated factor	Rattus norvegicus	40-43
2803520-7	1989	Mouse IA2 was five- to sevenfold more active than the human enzyme for activation of the procarcinogens 2-acetylaminofluorene and benzo[a]pyrene-trans-7,8-dihydrodiol and the promutagens Glu-P-2 and Trp-P-1.	Phosphorus	191-192	protein tyrosine phosphatase, receptor type, N	Mus musculus	6-9
3210953-5	1988	PS/PC liposomes interact predominantely with the plasma membrane of TB cells and release Cat1 continuously, whereas the majority of PS/DSPC/DPPC liposomes are taken into the cells intact via endocytosis.	Phosphorus	0-2	GIT ArfGAP 1	Mus musculus	89-93
3219729-0	1988	Brain pH in migraine: an in vivo phosphorus-31 magnetic resonance spectroscopy study.	Phosphorus	33-43	glucose-6-phosphate isomerase	Homo sapiens	6-8
3219729-1	1988	The intracellular pH (pHi) of cerebral cortex was measured in migraine patients by use of in vivo phosphorus-31 NMR spectroscopy.	Phosphorus	98-108	glucose-6-phosphate isomerase	Homo sapiens	18-20
3219729-1	1988	The intracellular pH (pHi) of cerebral cortex was measured in migraine patients by use of in vivo phosphorus-31 NMR spectroscopy.	Phosphorus	98-108	glucose-6-phosphate isomerase	Homo sapiens	22-25
2903743-10	1988	In immunoblot experiments with anti-P-450Coh antibody, the amount of P-450Coh was considerably higher in DBA/2N mice treated with phenobarbital, TCPOBOP, or pyrazole in comparison with the AKR/J mice, indicating a strain specificity in the inducibility of coumarin 7-hydroxylase by pyrazole.	Phosphorus	36-37	cytochrome P450, family 2, subfamily a, polypeptide 5	Mus musculus	256-278
2723491-5	1989	II) In rats treated with PTH (PTH rats) both serum Ca and P levels were increased at the early stage.	Phosphorus	25-26	parathyroid hormone	Rattus norvegicus	30-33
2755909-7	1989	The activity of ALDH was found to be induced by PB in the liver and the intestinal mucosa, when measured with NAD and propionaldehyde (P/NAD) or phenylacetaldehyde (Ph/NAD).	Phosphorus	48-49	aldehyde dehydrogenase 3 family, member A1	Rattus norvegicus	16-20
2855193-4	1988	Serum phosphorus was decreased (p less than 0.01) in all three groups of mice infused with PTHrP (4.6 mg/dl, 5.0 micrograms/day; 6.7 mg/dl, 3.0 micrograms/day; and 6.4 mg/dl, 1.0 micrograms/day) compared with controls (8.5 mg/dl).	Phosphorus	6-16	parathyroid hormone-like peptide	Mus musculus	91-96
2855193-6	1988	The urinary calcium-creatinine ratio (0.74 compared with 0.034 in controls) was increased (p less than 0.03) in mice infused with PTHrP (5.0 micrograms/day), but the urinary phosphorus-creatinine ratio was not different from that in controls.	Phosphorus	174-184	parathyroid hormone-like peptide	Mus musculus	130-135
2855193-10	1988	The results of this study indicated that PTHrP increased serum calcium and 1,25-dihydroxycholecalciferol, decreased serum phosphorus, increased urinary excretion of calcium, phosphorus, and cAMP, and increased both bone resorption and formation in nude mice.	Phosphorus	122-132	parathyroid hormone-like peptide	Mus musculus	41-46
2855193-10	1988	The results of this study indicated that PTHrP increased serum calcium and 1,25-dihydroxycholecalciferol, decreased serum phosphorus, increased urinary excretion of calcium, phosphorus, and cAMP, and increased both bone resorption and formation in nude mice.	Phosphorus	174-184	parathyroid hormone-like peptide	Mus musculus	41-46
3191282-11	1988	These findings suggest that the abnormal bone mineralization in Hyp mice was mainly due to their abnormally low serum phosphorus level.	Phosphorus	118-128	phosphate regulating endopeptidase homolog, X-linked	Mus musculus	64-67
3220659-2	1988	The amino acid sequence G(1)-P(2)-P(3)-P(4)-H(5)-P(6)-G(7)-K(8)-P(9) occurs twice in the proline-rich glycoprotein (PRG) found in human parotid saliva.	Phosphorus	27-30	proline rich protein BstNI subfamily 3	Homo sapiens	89-114
3220659-2	1988	The amino acid sequence G(1)-P(2)-P(3)-P(4)-H(5)-P(6)-G(7)-K(8)-P(9) occurs twice in the proline-rich glycoprotein (PRG) found in human parotid saliva.	Phosphorus	27-30	proline rich protein BstNI subfamily 3	Homo sapiens	116-119
3406790-3	1988	During CPR, clinically important hypocalcemia or hyperkalemia was not detected, but serum phosphorus was significantly increased.	Phosphorus	90-100	cytochrome p450 oxidoreductase	Homo sapiens	7-10
3401510-6	1988	Phosphorus spectra of cells 1, 2 and 3 days post feeding showed a 40% decrease in the relative concentration of phosphorylcholine concentration over the 3 day period.	Phosphorus	0-10	carboxyl ester lipase pseudogene	Homo sapiens	22-38
3384820-12	1988	In dietary alteration studies results of Northern blot analysis indicate that low dietary phosphorus results in increased calbindin-D-mRNA in kidney but not in brain.	Phosphorus	90-100	calbindin 1	Rattus norvegicus	122-131
3402383-6	1988	Restriction of dietary phosphorus in rats receiving IGF-I increased (P less than 0.001) serum 1,25-(OH)2D from 33 +/- 5 to 94 +/- 11 pg/ml, or 185%, an increase equivalent to that observed in animals receiving GH.	Phosphorus	23-33	insulin-like growth factor 1	Rattus norvegicus	52-57
3402383-8	1988	These data indicate that IGF-I can restore the increase in serum 1,25-(OH)2D induced by restriction of dietary phosphorus to the same degree as GH.	Phosphorus	111-121	insulin-like growth factor 1	Rattus norvegicus	25-30
3402383-9	1988	This strongly suggests that the GH-dependent increase in serum 1,25-(OH)2D induced by restriction of dietary phosphorus is mediated by IGF-I.	Phosphorus	109-119	insulin-like growth factor 1	Rattus norvegicus	135-140
2845325-3	1988	Serum phosphorus values were the same by disease type and gender in patients with HBD and XLH.	Phosphorus	6-16	phosphate regulating endopeptidase homolog X-linked	Homo sapiens	90-93
3133995-5	1988	Daily balance studies demonstrated that administration of GH resulted in significant retention of nitrogen (+3.4 g/24 h) and phosphorus (+218 mg/24 h), despite provision of only 60% of caloric requirements.	Phosphorus	125-135	growth hormone 1	Homo sapiens	58-60
3379139-7	1988	In our patients a negative correlation was found between the serum PTH concentrations and both serum phosphorus levels and TmP/GFR values, respectively.	Phosphorus	101-111	parathyroid hormone	Homo sapiens	67-70
3171110-5	1988	CT caused a statistically significant drop in urine calcium, phosphorus and hydroxyproline (OH-proline) excretion in FH patients and a concomitant increase in serum PTH levels.	Phosphorus	61-71	calcitonin related polypeptide alpha	Homo sapiens	0-2
3379139-8	1988	We postulate that although the basic defect in tumoral calcinosis most likely resides in the proximal renal tubular cell, the variation in serum phosphorus levels and possibly disease expression is modulated in part by PTH.	Phosphorus	145-155	parathyroid hormone	Homo sapiens	219-222
2831248-0	1988	Elevated secretion and action of serum parathyroid hormone in young adults consuming high phosphorus, low calcium diets assembled from common foods.	Phosphorus	90-100	parathyroid hormone	Homo sapiens	39-58
2836111-3	1988	Three chemical classes of angiotensin converting-enzyme inhibitors have been introduced into clinical use, the sulfhydryl-containing inhibitors such as captopril and its analogs and prodrugs, carboxyalkyldipeptides such as enalapril and its analogs, and phosphorus-containing inhibitors such as fosinopril and the phosphonate SQ 29,852.	Phosphorus	254-264	angiotensin I converting enzyme	Homo sapiens	26-55
24226619-9	1988	Determinations of protein-bound phosphorus in the plasma of estradiol-treated juvenile brown trout correlated well with the RIA determinations of VTG.	Phosphorus	32-42	vitellogenin	Oncorhynchus mykiss	146-149
2831248-8	1988	Thus, short term ingestion of a diet typifying current levels of calcium and phosphorus intake resulted in elevated serum iPTH levels and indexes of PTH action in young adults.	Phosphorus	77-87	parathyroid hormone	Homo sapiens	123-126
3254691-4	1988	The LCAT activity was independent of the P/S ratio of the diet, but positively correlated with the percentage of linoleic acid in serum phospholipids and cholesteryl esters, and negatively correlated with the percentage of oleic acid in the same fractions.	Phosphorus	41-42	lecithin-cholesterol acyltransferase	Homo sapiens	4-8
2967089-1	1988	1 Fosinopril sodium is the first phosphorus-containing angiotensin-converting enzyme (ACE) inhibitor to be studied clinically as an antihypertensive agent.	Phosphorus	33-43	angiotensin I converting enzyme	Homo sapiens	55-84
2967089-1	1988	1 Fosinopril sodium is the first phosphorus-containing angiotensin-converting enzyme (ACE) inhibitor to be studied clinically as an antihypertensive agent.	Phosphorus	33-43	angiotensin I converting enzyme	Homo sapiens	86-89
3446806-0	1987	A phosphorus nuclear magnetic resonance study of metabolites and intracellular pH in rabbit vascular smooth muscle.	Phosphorus	2-12	glucose-6-phosphate isomerase	Oryctolagus cuniculus	79-81
3173616-6	1988	Blood phosphorus (P) and parathormone (PTH) levels were respectively reduced by 29% (p = 0.001) and 27% (p = 0.008) with CA.RP; and by 15% (p = 0.03) and 18% (p = 0.006) with CA.RN.	Phosphorus	6-16	carbonic anhydrase 8	Homo sapiens	121-126
3259355-4	1988	We found significant correlations between IL-1 and C3a des Arg, IL-1 and IC and C3a des Arg, and IC in Ps.A.	Phosphorus	103-105	complement C3	Homo sapiens	80-83
3685995-5	1987	PTHrP(1-34) strongly promoted the excretion of cAMP and phosphorus and reduced the excretion of calcium in the isolated, perfused rat kidney consistent with the symptoms seen in malignant hypercalcemia.	Phosphorus	56-66	parathyroid hormone like hormone	Bos taurus	0-5
3502402-4	1987	In the first group, a significant increase in serum osteocalcin and parathyroid hormone, after administration of phosphorus and persisting after treatment with salmon calcitonin, was found.	Phosphorus	113-123	bone gamma-carboxyglutamate protein	Homo sapiens	52-63
3502402-4	1987	In the first group, a significant increase in serum osteocalcin and parathyroid hormone, after administration of phosphorus and persisting after treatment with salmon calcitonin, was found.	Phosphorus	113-123	parathyroid hormone	Homo sapiens	68-87
3502402-7	1987	In accordance with the authors" results, phosphorus could be considered a useful activator of bone formation and this stimulus by parathyroid hormone was mediated.	Phosphorus	41-51	parathyroid hormone	Homo sapiens	130-149
3257266-10	1988	), a time point in which a CGRP-induced decrease in 45Ca++ uptake was observed, slightly potentiated morphine in the tail-flick and hot-plate tests, but not in the p-phenylquinone test.	Phosphorus	10-11	calcitonin/calcitonin-related polypeptide, alpha	Mus musculus	27-31
3325989-5	1987	The determination of the binding capacity and of the association constant for a definite system GnRH/lipid and, additionally, comparison of these data with analogous results concerning substance P [Pharmazie 39, 765 (1984)] furnish some new information with respect to the interaction of oppositely charged peptides and lipids.	Phosphorus	195-196	gonadotropin releasing hormone 1	Homo sapiens	96-100
3312937-0	1987	Low protein and low phosphorus diet in patients with chronic renal failure: influence on glucose tolerance and tissue insulin sensitivity.	Phosphorus	20-30	insulin	Homo sapiens	118-125
3476549-5	1987	The concentrations of acid-soluble calcium and phosphorus in CE, LMW, MMW, and HMW were 1509 and 462, 991 and 310, 231 and 7, and 162 and 3 micrograms/mL, respectively.	Phosphorus	47-57	cilia and flagella associated protein 97	Homo sapiens	79-82
3680505-1	1987	P-31 nuclear magnetic resonance (NMR) spectroscopy of the rat kidney with ureteral ligation resulted in a rapid and major increase in a peak resonating at 7096.63 +/- 0.65 Hz from the reference frequency of phosphorus (32.60 MHz).	Phosphorus	207-217	ATPase H+ transporting V1 subunit E1	Rattus norvegicus	0-4
9942490-0	1987	Sine-wave-to-helimagnetic transition in phosphorus-rich Eu(As1-xPx	Phosphorus	40-50	prostaglandin D2 receptor	Homo sapiens	59-62
3822837-6	1987	The rate variations with phosphorus substituents of 1a-h are NEt2 greater than NPri2 greater than N(CH2CH2)O greater than NMePh, and OMe greater than OCH2CH2CN greater than OCHMeCH2CN greater than OCMe2CH2CN much greater than OC6H4Cl.	Phosphorus	25-35	tetraspanin 12	Homo sapiens	61-65
3676290-2	1987	The action of residual phospholipase A2 in melittin samples resulted in mixtures of DMPC and its hydrolytic products that underwent reversible transitions at temperatures between 30 and 35 degrees C from extended bilayers to micellar particles which gave narrow single-line deuterium and phosphorus-31 NMR spectra.	Phosphorus	288-298	phospholipase A2 group IB	Homo sapiens	23-39
3611549-9	1987	An 8-fl oz serving of whole milk is an excellent source of iodine, calcium, phosphorus, and potassium.	Phosphorus	76-86	Weaning weight-maternal milk	Bos taurus	28-32
3307705-2	1987	Urinary trehalase was correlated with tubular reabsorption of phosphorus (%TRP): the lower the trehalase activity, the worse was %TRP.	Phosphorus	62-72	trehalase	Homo sapiens	8-17
3307705-2	1987	Urinary trehalase was correlated with tubular reabsorption of phosphorus (%TRP): the lower the trehalase activity, the worse was %TRP.	Phosphorus	62-72	trehalase	Homo sapiens	95-104
3295473-0	1987	Role of insulin in the stimulation of renal 25-hydroxyvitamin D3-1 alpha-hydroxylase by phosphorus deprivation in rats.	Phosphorus	88-98	cytochrome P450, family 27, subfamily b, polypeptide 1	Rattus norvegicus	44-84
2821148-8	1987	Parathyroid hormone significantly decreased tubular reabsorption of phosphorus, increased concentrations of urinary cyclic AMP (cAMP) and increased serum concentrations of calcium in all age groups.	Phosphorus	68-78	parathyroid hormone	Rattus norvegicus	0-19
2890182-8	1987	CCl4 changed the lipid composition of the liver plasma membrane by increasing PI and PC and decreasing SM, PS and PEA.	Phosphorus	107-109	C-C motif chemokine ligand 4	Rattus norvegicus	0-4
3583759-3	1987	Thus, in the present study, a glucose derivative substituted at the C-2 position by a p-iodobenzyl group, a 2-O-(p-iodobenzyl)-D-glucose (IBG) was designed and its synthesis was carried out.	Phosphorus	13-14	complement C2	Homo sapiens	68-71
3033178-2	1986	This rise in delta P was prevented by therapy with the angiotensin I converting enzyme inhibitor enalapril (15 mg/l drinking water, group DM + E) even though glomerular hyperperfusion and hyperfiltration persisted.	Phosphorus	19-20	angiotensin I converting enzyme	Rattus norvegicus	55-86
3029572-1	1986	Purified receptor-immunoglobulin E (IgE) complexes incubated with [gamma-32P]-ATP incorporated phosphorus into tyrosines on the beta and gamma chains of the receptor.	Phosphorus	95-105	immunoglobulin heavy constant epsilon	Homo sapiens	9-34
3029572-1	1986	Purified receptor-immunoglobulin E (IgE) complexes incubated with [gamma-32P]-ATP incorporated phosphorus into tyrosines on the beta and gamma chains of the receptor.	Phosphorus	95-105	immunoglobulin heavy constant epsilon	Homo sapiens	36-39
3503551-1	1986	Daily subcutaneous injection of a synthetic human parathyroid hormone fragment, combined with daily ingestion of 1,25(OH)2 vitamin D, significantly increased trabecular bone density in the spine (p less than .01), and improved intestinal calcium and phosphorus absorption and total body retention of dietary calcium and phosphorus in middle-aged men with idiopathic osteoporosis.	Phosphorus	250-260	parathyroid hormone	Homo sapiens	50-69
3100303-3	1986	Mean endogenous beta-glucuronidase activities at pH 5.2 were 12.0, 15.5, 44.5 and 147.7 nmol min-1 ml-1 for C, CS, black PS, and Brown PS, respectively, which correlated well with the degree of deconjugation of bilirubin in gall-bladder and hepatic biles and with the rate of deconjugation of hepatic bile incubated at 37 degrees C. Only four biles in brown PS exhibited bacterial enzyme activity.	Phosphorus	121-123	glucuronidase beta	Homo sapiens	16-34
3100303-3	1986	Mean endogenous beta-glucuronidase activities at pH 5.2 were 12.0, 15.5, 44.5 and 147.7 nmol min-1 ml-1 for C, CS, black PS, and Brown PS, respectively, which correlated well with the degree of deconjugation of bilirubin in gall-bladder and hepatic biles and with the rate of deconjugation of hepatic bile incubated at 37 degrees C. Only four biles in brown PS exhibited bacterial enzyme activity.	Phosphorus	135-137	glucuronidase beta	Homo sapiens	16-34
3503551-1	1986	Daily subcutaneous injection of a synthetic human parathyroid hormone fragment, combined with daily ingestion of 1,25(OH)2 vitamin D, significantly increased trabecular bone density in the spine (p less than .01), and improved intestinal calcium and phosphorus absorption and total body retention of dietary calcium and phosphorus in middle-aged men with idiopathic osteoporosis.	Phosphorus	320-330	parathyroid hormone	Homo sapiens	50-69
2411531-10	1985	Similarly, both the concentration of renal CaBP and renal CaBP mRNA levels increased 4-fold in rats fed low phosphorus diets, increased 2-fold in rats fed low calcium diets, and decreased 67% in rats fed low sodium diets, providing evidence that the nutritional induction or decrease in renal CaBP is accompanied by a corresponding alteration in the concentration of its specific translatable mRNA.	Phosphorus	108-118	hippocalcin	Rattus norvegicus	43-47
3090723-5	1986	Administration of GH decreased weight loss, caused retention of nitrogen, potassium, and phosphorus in amounts closely matching their proportions in skeletal muscle, and stimulated insulin production.	Phosphorus	89-99	growth hormone 1	Homo sapiens	18-20
3697510-8	1986	Phosphorus in fibrinogen did not correlate with fibrinogen degradation products or fibrinogen levels and became normal on adequate anticoagulation.	Phosphorus	0-10	fibrinogen beta chain	Homo sapiens	14-24
9936847-0	1985	Spin delocalization in phosphorus donor pairs in silicon.	Phosphorus	23-33	spindlin 1	Homo sapiens	0-4
3841078-0	1985	[Calcium and phosphorus metabolism in insulin dependent and non-insulin dependent diabetics, well-controlled and poorly-controlled].	Phosphorus	13-23	insulin	Homo sapiens	38-45
3487454-5	1986	Among different phospholipid mixtures tested, P-glycerol/P-choline vesicles were found most effective for C4b binding.	Phosphorus	46-47	complement C4B (Chido blood group)	Homo sapiens	106-109
3271417-2	1986	31P-1H and 1H-1H chemical shift correlation spectroscopies were jointly used to provide the assignment of the phosphorus resonances.	Phosphorus	110-120	minichromosome maintenance complex component 3	Homo sapiens	2-16
3485974-1	1986	Phosphorus nuclear magnetic resonance spectra of the Ha-ras oncogene product p21 and its nucleotide complexes have been obtained.	Phosphorus	0-10	H3 histone pseudogene 16	Homo sapiens	77-80
3954784-6	1986	From results with O-ethyl methylphosphonylated AChE prepared from two pairs of enantiomers as well as from the racemic fluoridate it was concluded that phosphonylation of AChE may not always occur via a mechanism involving inversion of configuration at phosphorus but can also occur with retention of configuration.	Phosphorus	253-263	acetylcholinesterase (Cartwright blood group)	Homo sapiens	171-175
2411531-10	1985	Similarly, both the concentration of renal CaBP and renal CaBP mRNA levels increased 4-fold in rats fed low phosphorus diets, increased 2-fold in rats fed low calcium diets, and decreased 67% in rats fed low sodium diets, providing evidence that the nutritional induction or decrease in renal CaBP is accompanied by a corresponding alteration in the concentration of its specific translatable mRNA.	Phosphorus	108-118	hippocalcin	Rattus norvegicus	58-62
2411531-10	1985	Similarly, both the concentration of renal CaBP and renal CaBP mRNA levels increased 4-fold in rats fed low phosphorus diets, increased 2-fold in rats fed low calcium diets, and decreased 67% in rats fed low sodium diets, providing evidence that the nutritional induction or decrease in renal CaBP is accompanied by a corresponding alteration in the concentration of its specific translatable mRNA.	Phosphorus	108-118	hippocalcin	Rattus norvegicus	58-62
4070136-6	1985	As both thyroid size and plasma GH are regulated partly by pituitary function, dietary phosphorus may alter endocrine function through changes in pituitary metabolism.	Phosphorus	87-97	growth hormone	Gallus gallus	32-34
2993522-3	1985	Data are presented to indicate that the following molecular interactions are essential for activation of the phosphorylation of MAP2: (a) hydrogen bond formation toward the 2", 3", or 5" position, (b) interaction with phosphorus, and (c) no hydrogen bonds but hydrophobic interactions at the base moiety.	Phosphorus	218-228	microtubule associated protein 2	Homo sapiens	128-132
3877954-2	1985	After intravenous administration, human and rat calcitonin, but neither human nor rat CGRP significantly decreased plasma calcium and phosphorus concentrations in awake, freely moving rats.	Phosphorus	134-144	calcitonin-related polypeptide alpha	Rattus norvegicus	48-58
3877954-6	1985	These studies indicate that calcitonin, but not CGRP, affects calcium and phosphorus homeostasis while both peptides decrease gastric acid secretion similarly.	Phosphorus	74-84	calcitonin-related polypeptide alpha	Rattus norvegicus	28-38
3877954-7	1985	Furthermore, these studies support the hypothesis that the calcium and phosphorus lowering effects of calcitonin are peripheral while the gastric inhibiting actions of the calcitonin and CGRP are mediated by the central nervous system.	Phosphorus	71-81	calcitonin-related polypeptide alpha	Rattus norvegicus	102-112
3935162-0	1985	Phosphorus-31 nuclear magnetic resonance study of the active site phosphohistidine and regulatory phosphoserine residues of rat liver ATP-citrate lyase.	Phosphorus	0-10	ATP citrate lyase	Rattus norvegicus	134-151
3893009-10	1985	PTH was equally effective in raising serum calcium, depressing serum phosphorus and tubular reabsorption of phosphate in non-diabetic as well as in diabetic rats.	Phosphorus	69-79	parathyroid hormone	Rattus norvegicus	0-3
4046610-3	1985	The results show that the major metabolite of P is 20 beta-hydroxy-4-pregnen-3-one (20 beta-DHP), representing up to 40% of the recovered radioactivity.	Phosphorus	46-47	dihydropyrimidinase	Homo sapiens	92-95
3997848-9	1985	This histidine decarboxylase (Vmax = 72 mumol X min-1 X mg-1) is much more active than "homogeneous" preparations of mammalian pyridoxal-P-dependent histidine decarboxylase (Vmax congruent to 1.0) and is about equal in activity to the pyruvoyl-dependent histidine decarboxylases from Gram-positive bacteria.	Phosphorus	136-138	histidine decarboxylase	Homo sapiens	5-28
3997848-9	1985	This histidine decarboxylase (Vmax = 72 mumol X min-1 X mg-1) is much more active than "homogeneous" preparations of mammalian pyridoxal-P-dependent histidine decarboxylase (Vmax congruent to 1.0) and is about equal in activity to the pyruvoyl-dependent histidine decarboxylases from Gram-positive bacteria.	Phosphorus	136-138	histidine decarboxylase	Homo sapiens	149-172
4015398-6	1985	One subfraction containing the highest antiChE activity and 88% phosphorus of F-5 was isolated.	Phosphorus	64-74	coagulation factor V	Homo sapiens	78-81
2993264-0	1985	Phosphorus-31 nuclear magnetic resonance and electronic spectroscopic studies of adrenodoxin reductase and its binary complex with NADP+.	Phosphorus	0-10	ferredoxin reductase	Homo sapiens	81-102
2993264-2	1985	The spectrum of adrenodoxin reductase showed two doublets arising from the phosphorus nuclei in the pyrophosphate group of FAD.	Phosphorus	75-85	ferredoxin reductase	Homo sapiens	16-37
2993264-4	1985	Further, one of the doublets of phosphorus nuclei of the pyrophosphate group of bound NADP+ in the complex of adrenodoxin reductase and NADP+ was considerably shifted upfield in comparison with that of free NADP+.	Phosphorus	32-42	ferredoxin reductase	Homo sapiens	110-131
2984059-2	1985	The response to Gpp(NH)p, ACTH1-24 + Gpp(NH)p and NaF was significantly lower in membranes from fetuses than from neonate lambs, whereas the response to forskolin was similar.	Phosphorus	7-8	C-X-C motif chemokine ligand 8	Homo sapiens	50-53
3980170-5	1985	Thirty-four phosphorus-containing metabolites were detected and quantitated by P-31 NMR from each of the three zones studied.	Phosphorus	12-22	ATPase H+ transporting V1 subunit E1	Homo sapiens	79-83
17793769-0	1985	Bacterial 5-nucleotidase in aquatic ecosystems: a novel mechanism of phosphorus regeneration.	Phosphorus	69-79	5'-nucleotidase ecto	Homo sapiens	10-24
3925810-1	1985	The use of ethylenediamine-N,N,N",N"-tetraacetic acid (EDTA) to sequester Mg2+ from samples containing ATP at acidic or neutral pH prior to 31P NMR spectroscopic analysis leads to significant broadening of the gamma- and beta-phosphorus resonances of ATP as compared to ATP alone.	Phosphorus	226-236	mucin 7, secreted	Homo sapiens	74-77
3925810-3	1985	At pH 7.0, 30 mM EDTA in the presence of 5 mM ATP and 7 mM Mg2+ leads to a threefold increase in the peak width of the gamma phosphorus of ATP as compared to 5 mM ATP alone.	Phosphorus	125-135	mucin 7, secreted	Homo sapiens	59-62
2982838-3	1985	Distances between enzyme-bound Mn2+ and the phosphorus atoms at C-6 of fructose-6-P and alpha-methyl-D-fructofuranoside 1,6-bisphosphate were identical, and the enzyme-Mn to phosphorus distance determined for the C-6 phosphorus atom of Fru-2,6-P2 was very similar to these values.	Phosphorus	44-54	complement C6	Bos taurus	64-67
3918116-1	1985	An average of 50% of anti-p-azophenylarsonate (Ars) antibodies bear a cross-reactive idiotype, IdCR, and an average of 15% bear a relatively minor idiotype, Id, in A/J mice.	Phosphorus	26-27	secreted Ly6/Plaur domain containing 1	Mus musculus	47-50
6541227-11	1984	Multivariate analysis, however, showed that the change in the serum concentration of 1 alpha,25-(OH)2-Vit D, as well as iPTH and CT, contributed to their correlation with the change in the serum concentrations of calcium and phosphorus.	Phosphorus	225-235	vitrin	Homo sapiens	102-105
4042628-5	1985	Phosphorus determinations on delipidated vitellogenin yield a phosphorus content of 0.63% in rainbow trout and 0.58% in sea trout vitellogenin.	Phosphorus	0-10	LOC100136735	Oncorhynchus mykiss	41-53
4042628-5	1985	Phosphorus determinations on delipidated vitellogenin yield a phosphorus content of 0.63% in rainbow trout and 0.58% in sea trout vitellogenin.	Phosphorus	0-10	LOC100136735	Oncorhynchus mykiss	130-142
4042628-5	1985	Phosphorus determinations on delipidated vitellogenin yield a phosphorus content of 0.63% in rainbow trout and 0.58% in sea trout vitellogenin.	Phosphorus	62-72	LOC100136735	Oncorhynchus mykiss	41-53
4029094-7	1985	Significant reductions (P less than 0.005) in G6PD, GSH-R, and GSH-P activities occurred on days 1-5, and SOD activity was significantly decreased (P less than 0.005) on days 4 and 5 by cyclophosphamide.	Phosphorus	24-25	glucose-6-phosphate dehydrogenase	Rattus norvegicus	46-50
2995196-5	1985	While a significant fall in urinary Na, K and phosphorus has been shown to occur following glucose and insulin administration, their effect on renal H+ excretion in man has not been investigated previously.	Phosphorus	46-56	insulin	Homo sapiens	103-110
4019944-6	1985	However, in the group of patients (n = 7) who started on the diet with P/S ratio 1.3 the low density lipoprotein cholesterol increased significantly (p less than 0.05) by 7% and the apolipoprotein B concentration by 10% (p less than 0.001) when shifting to the diet with P/S ratio 0.7.	Phosphorus	71-72	apolipoprotein B	Homo sapiens	182-198
3992058-3	1985	The dissociation constant for the AP4 X Mg2+ complex was estimated to be 10(-4) M from the downfield shift of the resonances assigned to the gamma- and delta-phosphorus nuclei.	Phosphorus	158-168	transcription factor AP-4	Homo sapiens	34-37
16453580-3	1984	We can show that most if not all incorporation of P into sp-I occurs in parallel with the incorporation of [S]-methionine in the giant polysomes that form sp-I and contain BR-derived mRNA.	Phosphorus	50-51	chromogranin A	Homo sapiens	57-61
6086272-1	1984	The mechanisms involved in the renal resistance to the phosphaturic action of PTH during dietary phosphorus deprivation remain ill defined.	Phosphorus	97-107	parathyroid hormone	Canis lupus familiaris	78-81
6087742-1	1984	The biochemical properties of a chick pancreatic calcium binding protein (CaBP) and its response to vitamin D status and dietary calcium and phosphorus levels were studied and compared with the known vitamin D-dependent CaBPs present in the chick intestine and kidney.	Phosphorus	141-151	calcium-binding protein	Gallus gallus	49-72
6087742-1	1984	The biochemical properties of a chick pancreatic calcium binding protein (CaBP) and its response to vitamin D status and dietary calcium and phosphorus levels were studied and compared with the known vitamin D-dependent CaBPs present in the chick intestine and kidney.	Phosphorus	141-151	calcium-binding protein	Gallus gallus	74-78
6087742-3	1984	Pancreatic levels of CaBP respond to changes in vitamin D status and dietary Ca and P level in a fashion similar to the intestinal CaBP.	Phosphorus	0-1	calcium-binding protein	Gallus gallus	21-25
6086272-3	1984	The present studies examine the initial events in the actions of PTH, namely receptor binding and adenylate cyclase activation, in renal cortical membranes from normal and phosphorus-deprived animals.	Phosphorus	172-182	parathyroid hormone	Canis lupus familiaris	65-68
6086272-13	1984	These data indicate that during dietary phosphorus deprivation there is uncoupling of the PTH receptor-adenylate system of canine kidney.	Phosphorus	40-50	parathyroid hormone	Canis lupus familiaris	90-93
6086272-14	1984	This abnormality may play a role in the renal resistance to PTH during dietary phosphorus deprivation.	Phosphorus	79-89	parathyroid hormone	Canis lupus familiaris	60-63
6378716-6	1984	In LH-RH-injected fish, there was a transient increase in plasma 17 alpha 20 beta P levels which persisted for less than 24 hr.	Phosphorus	82-83	gonadotropin releasing hormone 1	Homo sapiens	3-8
6589391-2	1984	Recent observations have suggested that PGE2 and vasopressin may interact and influence reabsorption of calcium and phosphorus in the cortical collecting duct.	Phosphorus	116-126	arginine vasopressin	Rattus norvegicus	49-60
6324253-5	1984	Parathyroid hormone may stimulate 1,25(OH)2D3 synthesis directly or via alterations (a decrease) in serum phosphorus or both.	Phosphorus	106-116	parathyroid hormone	Homo sapiens	0-19
6205387-3	1984	There was an association between levels of phosphorus and those of transferrin but not with those of seven other acute-phase associated proteins.	Phosphorus	43-53	transferrin	Homo sapiens	67-78
6712539-5	1984	It is concluded that a low-fat, high-P/S ratio diet lowers LDL and HDL2 cholesterol in healthy volunteers, but does not influence the level of HDL3 subfraction.	Phosphorus	37-38	junctophilin 3	Homo sapiens	67-71
6325646-5	1984	Low dietary intake of phosphorus resulted in an increase in 47Ca and 203Pb absorption and in CaBP synthesis when the animals were treated with cholecalciferol.	Phosphorus	22-32	centrin 1	Homo sapiens	93-97
6326109-1	1984	A family of murine anti-p-azophenylarsonate (Ars) antibodies share a variable (V) region serologically defined marker, the 36-60 idiotype (Id36-60).	Phosphorus	24-25	secreted Ly6/Plaur domain containing 1	Mus musculus	45-48
6735152-14	1984	Plasma concentrations of GH were reduced by the peripheral administration of NE, which might be expected not to cross the blood-brain-barrier (BBB), alpha 1/alpha 2 agonists clonidine and p-amino clonidine (which does not cross BBB), NE/E precursors L-DOPA and DOPS, and the beta agonist, isoproterenol.	Phosphorus	48-49	growth hormone 1	Homo sapiens	25-27
6719396-1	1984	By quantitative phosphorus determination on the single chains of human fibrinogen it is demonstrated that the covalently bound phosphorus of adult and fetal fibrinogen is exclusively located in the A alpha chain.	Phosphorus	16-26	fibrinogen beta chain	Homo sapiens	71-81
6719396-1	1984	By quantitative phosphorus determination on the single chains of human fibrinogen it is demonstrated that the covalently bound phosphorus of adult and fetal fibrinogen is exclusively located in the A alpha chain.	Phosphorus	16-26	fibrinogen beta chain	Homo sapiens	157-167
6719396-1	1984	By quantitative phosphorus determination on the single chains of human fibrinogen it is demonstrated that the covalently bound phosphorus of adult and fetal fibrinogen is exclusively located in the A alpha chain.	Phosphorus	127-137	fibrinogen beta chain	Homo sapiens	71-81
6719396-1	1984	By quantitative phosphorus determination on the single chains of human fibrinogen it is demonstrated that the covalently bound phosphorus of adult and fetal fibrinogen is exclusively located in the A alpha chain.	Phosphorus	127-137	fibrinogen beta chain	Homo sapiens	157-167
6719396-2	1984	The A alpha-chain of fetal fibrinogen contains about twice as much phosphorus as the adult A alpha-chain in the well known position of Ser 3 of fibrino-peptide A as well as in a hitherto unknown second position on the A alpha-chain.	Phosphorus	67-77	fibrinogen beta chain	Homo sapiens	27-37
6476785-4	1984	Changing from a low to a high P/S diet resulted in a significant decrease of total cholesterol (23%) and LDL cholesterol (18%) levels, but also HDL cholesterol (23%) and apolipoprotein A1 (Apo A1; 13%) concentrations fell significantly.	Phosphorus	30-31	apolipoprotein A1	Macaca mulatta	170-187
6476785-4	1984	Changing from a low to a high P/S diet resulted in a significant decrease of total cholesterol (23%) and LDL cholesterol (18%) levels, but also HDL cholesterol (23%) and apolipoprotein A1 (Apo A1; 13%) concentrations fell significantly.	Phosphorus	30-31	apolipoprotein A1	Macaca mulatta	189-195
6484303-8	1984	However, although total apparent absorption of magnesium and phosphorus was higher in CV rats ingesting MRP, the urinary excretion of these minerals was also higher and their retention was not better.	Phosphorus	61-71	ATP binding cassette subfamily C member 2	Rattus norvegicus	104-107
6588261-9	1983	Plasma PTH levels varied with each diet, but those rats with elevated PTH levels before dietary therapy experienced a fall in plasma PTH after the low-phosphorus diets were administered, with or without protein restriction.	Phosphorus	151-161	parathyroid hormone	Rattus norvegicus	70-73
6588261-9	1983	Plasma PTH levels varied with each diet, but those rats with elevated PTH levels before dietary therapy experienced a fall in plasma PTH after the low-phosphorus diets were administered, with or without protein restriction.	Phosphorus	151-161	parathyroid hormone	Rattus norvegicus	70-73
6227193-0	1983	Synthetic [Asu1,7] eel calcitonin increases phosphorus content in the hepatic mitochondria of rats.	Phosphorus	44-54	calcitonin-related polypeptide alpha	Rattus norvegicus	23-33
6227193-1	1983	The change of subcellular phosphorus content in the liver was investigated after a single sc administration of synthetic [Asu1,7] eel calcitonin (CT) to fed rats.	Phosphorus	26-36	calcitonin-related polypeptide alpha	Rattus norvegicus	134-144
6227193-2	1983	Administration of CT (80 MRC mU/100 g body weight) produced a significant increase in phosphorus content in the mitochondrial fraction, while this increase was not observed in fractions containing plasma membrane, nuclei, microsomes and cytosol.	Phosphorus	86-96	calcitonin-related polypeptide alpha	Rattus norvegicus	18-20
6227193-3	1983	A significant increase in the mitochondrial phosphorus content was observed even at the lowest dose of CT (40 MRC mU/100 g body weight).	Phosphorus	44-54	calcitonin-related polypeptide alpha	Rattus norvegicus	103-105
6227193-6	1983	These results suggest that phosphorus taken up by the liver cells after CT administration is largely located in the mitochondria, and that this increase is not related to oxidative phosphorylation.	Phosphorus	27-37	calcitonin-related polypeptide alpha	Rattus norvegicus	72-74
6227193-7	1983	Presumably the hepatic mitochondria play a role in the storage of intracellular phosphorus increased by CT.	Phosphorus	80-90	calcitonin-related polypeptide alpha	Rattus norvegicus	104-106
6658718-4	1983	However, the phosphorus content of cord fibrinogen was 3-4 times higher than that of adult fibrinogen.	Phosphorus	13-23	fibrinogen beta chain	Homo sapiens	40-50
6634712-3	1983	A low-phosphorus diet for 4 and 8 days increased serum calcium and decreased the elevated PTH level to the level of sham-operated rats.	Phosphorus	6-16	parathyroid hormone	Rattus norvegicus	90-93
6634712-5	1983	The low-phosphorus diet for 4 days, but not 8 days, increased the CT levels in uremic rats.	Phosphorus	8-18	calcitonin-related polypeptide alpha	Rattus norvegicus	66-68
6658718-6	1983	This might be explained by the higher phosphorus content of the cord fibrinogen molecule.	Phosphorus	38-48	fibrinogen beta chain	Homo sapiens	69-79
6619208-10	1983	Concentrations of phosphorus increased in the nucleus during S, G2 and M, and also showed fluctuations in the nucleolus during the cycle; these were not seen in the cytoplasm.	Phosphorus	18-28	crystallin gamma E, pseudogene	Homo sapiens	64-72
6633158-3	1983	The specific activity of renal CaBP (as measured by the chelex resin assay; Ca2+ bound protein/Ca2+ bound resin per mg protein) in the 28,000 Mr region was found to increase four fold in rats fed the low phosphorus diet and two fold in rats fed the low calcium diet when compared to rats fed the control diet.	Phosphorus	204-214	hippocalcin	Rattus norvegicus	31-35
6633158-6	1983	The greater response to dietary phosphorus restriction suggests that renal CaBP may be regulated by a mechanism different from that of intestinal CaBP.	Phosphorus	32-42	hippocalcin	Rattus norvegicus	75-79
6671454-0	1983	Suppressive effect of calcitonin on intestinal absorption of calcium and phosphorus in sheep.	Phosphorus	73-83	calcitonin-like	Ovis aries	22-32
6671454-1	1983	This study was carried out to determine the effect of calcitonin on calcium and phosphorus absorption in sheep.	Phosphorus	80-90	calcitonin-like	Ovis aries	54-64
6671454-6	1983	Calcitonin injection also reduced the serum phosphorus concentrations.	Phosphorus	44-54	calcitonin-like	Ovis aries	0-10
6639987-8	1983	During the interaction of the enanthiomers with the asymmetric phosphorus the stereospecificity of acetylcholinesterase is much higher than that of carboxylesterase.	Phosphorus	63-73	acetylcholinesterase (Cartwright blood group)	Homo sapiens	99-119
28310335-5	1983	This increased phosphorus uptake is attributed to abiotic sorption to inorganic surfaces exposed as a result of efficient removal of aufwuchs at high snail densities.	Phosphorus	15-25	snail family transcriptional repressor 1	Homo sapiens	150-155
6133867-6	1983	The results from these experiments show that the reaction catalyzed by guanylate cyclase proceeds with inversion of configuration at phosphorus and this indicates that the reaction proceeds by way of a single direct displacement reaction.	Phosphorus	133-143	guanylate cyclase	Bos taurus	71-88
6687344-4	1983	At this point, but not earlier, DBP was correlated with 25OHD (r = 0.69; P less than 0.01) and phosphorus (r = 0.49; P less than 0.05), and 25OHD was correlated with phosphorus (r = 0.48; P less than 0.05) and calcium (r = 0.44; P less than 0.05).	Phosphorus	95-105	D-box binding PAR bZIP transcription factor	Homo sapiens	32-35
6600222-2	1983	24-Hydroxylase activity and plasma concentrations of 24,25-dihydroxyvitamin D3 were significantly higher in Hyp mice than in normal mice when both groups were fed a normal diet containing 1.22% calcium (Ca) and 0.8% phosphorus (Pi).	Phosphorus	216-226	phosphate regulating endopeptidase homolog, X-linked	Mus musculus	108-111
6606303-4	1983	Injection of PS into mice or addition to normal mouse spleen cell cultures results in enhanced responses similar to that observed with LPS as well as with lipoteichoic acid derived from gram positive bacteria.	Phosphorus	13-15	toll-like receptor 4	Mus musculus	135-138
6647072-9	1983	The treatment with oral load of phosphates and 1,25(OH)2D3 in every patient with HBD, and so in our patient, is accompanied by increase in serum phosphorus, with improved tubular reabsorption of phosphate anion and a fall of hydrossiprolinuria with bone healing; this combination of responses is not present in XLH.	Phosphorus	145-155	HBD	Homo sapiens	81-84
6404142-4	1983	A phosphorus restriction test in 12 hypophosphatemic patients demonstrated that the reduced renal phosphorus reabsorption probably was due to both persisting hyperparathyroidism and a PTH-independent phosphorus leak.	Phosphorus	2-12	parathyroid hormone	Homo sapiens	184-187
6404142-4	1983	A phosphorus restriction test in 12 hypophosphatemic patients demonstrated that the reduced renal phosphorus reabsorption probably was due to both persisting hyperparathyroidism and a PTH-independent phosphorus leak.	Phosphorus	98-108	parathyroid hormone	Homo sapiens	184-187
6184178-2	1982	Here, the distribution of bovine myelin basic protein in dispersions with bovine brain L-alpha-diacylphosphatidylserine (PS) has been examined electronmicroscopically.	Phosphorus	121-123	myelin basic protein	Bos taurus	33-53
6606687-3	1983	It was found that the CSF generating component of the highly heterogeneous PS mixture is sensitive to acidic hydrolyses, but it is less sensitive than the toxic site in the lipid moiety of the LPS.	Phosphorus	75-77	colony stimulating factor 2 (granulocyte-macrophage)	Mus musculus	22-25
6606687-6	1983	Optimal dose of LPS and PS for CSF induction in mice differed widely.	Phosphorus	17-19	colony stimulating factor 2 (granulocyte-macrophage)	Mus musculus	31-34
6606687-8	1983	Optimal dose for PS was 160 micrograms, and this generated a significantly higher CSF level than 25 micrograms LPS.	Phosphorus	17-19	colony stimulating factor 2 (granulocyte-macrophage)	Mus musculus	82-85
6657667-2	1983	A positive correlation was found between calcium and phosphorus excretions and APRox and APRbr; no correlation was found between oxalate, uric acid, citrate and magnesium excretion and APR or FPR.	Phosphorus	53-63	phorbol-12-myristate-13-acetate-induced protein 1	Homo sapiens	79-82
7174666-0	1982	The stereochemical course at phosphorus of the reaction catalyzed by phosphoenolpyruvate carboxylase.	Phosphorus	29-39	phosphoenolpyruvate carboxykinase 1	Homo sapiens	69-100
7165551-10	1982	PTH mediates bone buffering capacity by activating intracellular shifts of calcium, phosphorus, and carbonate or by stimulation of bone carbonic anhydrase.	Phosphorus	84-94	parathyroid hormone	Homo sapiens	0-3
6848738-7	1983	Calcium and phosphorus intakes from SMA were also higher (P less than 0.01) than from human milk.	Phosphorus	12-22	survival of motor neuron 1, telomeric	Homo sapiens	36-39
6299313-0	1982	[Changes in Na+, K+-adenosinetriphosphatase and 5"-nucleotidase activities in cell membrane isolated from rat liver after acute white phosphorus poisoning].	Phosphorus	128-144	5' nucleotidase, ecto	Rattus norvegicus	48-63
6299313-1	1982	Na+, K+-ATPase and 5"-Nucleotidase activities in rat liver plasmamembranes after "in vivo" intoxication with a single dose of white phosphorus (10 mg/kg b.w.	Phosphorus	126-142	5' nucleotidase, ecto	Rattus norvegicus	19-34
6285369-0	1982	Phosphorus-containing inhibitors of angiotensin-converting enzyme.	Phosphorus	0-10	angiotensin I converting enzyme	Homo sapiens	36-65
6758781-0	1982	A phosphorus-containing pyrimidine analog as a potent inhibitor of cytidine deaminase.	Phosphorus	2-12	cytidine deaminase	Homo sapiens	67-85
7044148-1	1982	Phosphorus nuclear magnetic resonance spectroscopy (P-31 NMR) has been used to assess dynamic aspects of the metabolism of phosphorus-containing compounds in intact cells, organs, and animals.	Phosphorus	0-10	ATPase H+ transporting V1 subunit E1	Homo sapiens	52-56
7044148-1	1982	Phosphorus nuclear magnetic resonance spectroscopy (P-31 NMR) has been used to assess dynamic aspects of the metabolism of phosphorus-containing compounds in intact cells, organs, and animals.	Phosphorus	123-133	ATPase H+ transporting V1 subunit E1	Homo sapiens	52-56
7044148-3	1982	The P-31 NMR spectrum not only identifies which phosphorus-containing compounds are present in high concentration, namely adenosine 5"-triphosphate (ATP) and creatine phosphate, but also provides information about their chemical environment (including pH) and intracellular distribution.	Phosphorus	48-58	ATPase H+ transporting V1 subunit E1	Homo sapiens	4-8
7068846-14	1982	On the diet with low P/S ratio, HDL2 rose, whereas this effect was absent on diets with high P/S ratios.	Phosphorus	21-22	junctophilin 3	Homo sapiens	32-36
6294123-8	1982	Docosapentaenoate (22:5 omega 3) was the major omega 3 [14C] PUFA of PI + PS and PE.	Phosphorus	74-76	pumilio RNA binding family member 3	Homo sapiens	61-65
6215942-3	1982	Furthermore, preincubation of F1 with unlabeled AdoPP[NH]P, ADP, or ATP prevented the covalent labeling of the enzyme by [3H]NAP4-AdoPP[NH]P upon photoirradiation.	Phosphorus	51-52	suppressor of cytokine signaling 7	Homo sapiens	125-129
7151741-0	1982	Synthetic [Asu1,7] eel calcitonin increases phosphorus content in the hepatic bile of intact and nephrectomized rats.	Phosphorus	44-54	calcitonin-related polypeptide alpha	Rattus norvegicus	23-33
7151741-1	1982	The effect of synthetic [Asu1,7] eel calcitonin (CT) on phosphorus content in the hepatic bile was investigated in intact and nephrectomized rats.	Phosphorus	56-66	calcitonin-related polypeptide alpha	Rattus norvegicus	37-47
7151741-1	1982	The effect of synthetic [Asu1,7] eel calcitonin (CT) on phosphorus content in the hepatic bile was investigated in intact and nephrectomized rats.	Phosphorus	56-66	calcitonin-related polypeptide alpha	Rattus norvegicus	49-51
7151741-2	1982	The subcutaneous administration of CT (80 MRC mU/100 g BW) produced a significant fall in the serum inorganic phosphorus concentration and a corresponding increase in the amount of phosphorus in the liver and kidney.	Phosphorus	110-120	calcitonin-related polypeptide alpha	Rattus norvegicus	35-37
7151741-5	1982	CT also provoked a marked elevation of phosphorus excretion into the bile.	Phosphorus	39-49	calcitonin-related polypeptide alpha	Rattus norvegicus	0-2
7151741-7	1982	CT markedly increased phosphorus excretion into the bile of nephrectomized rats.	Phosphorus	22-32	calcitonin-related polypeptide alpha	Rattus norvegicus	0-2
7151741-9	1982	This effect of CT on the liver may be the cause of increased excretion of phosphorus into the bile.	Phosphorus	74-84	calcitonin-related polypeptide alpha	Rattus norvegicus	15-17
7067893-2	1982	Incubation of human citrated plasma with a concentrate of lipoprotein lipase (separated from the same plasma pool), for 6 hr at 37 degree C and pH 7.0, caused a marked decrease in the concentrations of calcium, triglycerides, total phosphorus, lipid phosphorus and total fatty acids.	Phosphorus	232-242	lipoprotein lipase	Homo sapiens	58-76
6284126-1	1982	Rat liver microsomal glucose 6-phosphatase catalyses phosphoryl transfer between D-glucose 6-[(R)-16O,17O,18O]phosphate and D-glucose with retention of configuration at the phosphorus atom.	Phosphorus	173-183	glucose-6-phosphatase catalytic subunit 1	Rattus norvegicus	21-42
7134871-11	1982	Among the B I and B II groups there was a change in the blood constituents B-hemoglobin, P-vitamin B12, S-calcium, S-ALP, and S-TIBC.	Phosphorus	89-90	calcium voltage-gated channel subunit alpha1 E	Homo sapiens	18-22
7302575-2	1981	Similarly, in vitamin D-deficient rats fed a diet low in calcium or phosphorus prolactin stimulated an increase in serum calcium in both groups and an increase in serum phosphorus in the rats fed the diet low in phosphorus.	Phosphorus	68-78	prolactin	Rattus norvegicus	79-88
6274981-4	1982	Fractionation of LTA after mild ammonia hydrolysis yielded a polyglycerophosphate and polar lipid fraction, both of which retained the glucose from the glycolipid moiety of the LTA molecule, and a neutral lipid fraction that was devoid of phosphorus or glucose.	Phosphorus	239-249	lymphotoxin alpha	Homo sapiens	17-20
7302575-2	1981	Similarly, in vitamin D-deficient rats fed a diet low in calcium or phosphorus prolactin stimulated an increase in serum calcium in both groups and an increase in serum phosphorus in the rats fed the diet low in phosphorus.	Phosphorus	169-179	prolactin	Rattus norvegicus	79-88
6787936-0	1981	Effect of metabolic acidosis on renal response to parathyroid hormone in phosphorus-deprived rats.	Phosphorus	73-83	parathyroid hormone	Rattus norvegicus	50-69
6269785-1	1981	Calcitonin and 1.25(OH)2D3 have opposite effects on the serum concentrations of Ca and P, as well as on bone resorption, and can be observed in the process of healing of standardized fracture in adult rats.	Phosphorus	87-88	calcitonin-related polypeptide alpha	Rattus norvegicus	0-10
6787936-1	1981	Both metabolic acidosis and phosphorus (Pi) deprivation have been shown to alter not only renal Pi metabolism independent of parathyroid hormone (PTH), but also the phosphaturic response to PTH.	Phosphorus	28-38	parathyroid hormone	Rattus norvegicus	125-144
6787936-1	1981	Both metabolic acidosis and phosphorus (Pi) deprivation have been shown to alter not only renal Pi metabolism independent of parathyroid hormone (PTH), but also the phosphaturic response to PTH.	Phosphorus	28-38	parathyroid hormone	Rattus norvegicus	146-149
6787936-1	1981	Both metabolic acidosis and phosphorus (Pi) deprivation have been shown to alter not only renal Pi metabolism independent of parathyroid hormone (PTH), but also the phosphaturic response to PTH.	Phosphorus	28-38	parathyroid hormone	Rattus norvegicus	190-193
6266866-2	1981	Over 90% and 70% of the phosphorus from dentine phosphoprotein and phosvitin were hydrolyzed in 2 h. The optimum pH of the enzyme for the dephosphorylation of phosvitin and dentine phosphoprotein was nearly 6.	Phosphorus	24-34	casein kinase 2 beta	Bos taurus	67-76
6266866-2	1981	Over 90% and 70% of the phosphorus from dentine phosphoprotein and phosvitin were hydrolyzed in 2 h. The optimum pH of the enzyme for the dephosphorylation of phosvitin and dentine phosphoprotein was nearly 6.	Phosphorus	24-34	casein kinase 2 beta	Bos taurus	159-168
6452904-0	1981	Phosphorus-31 nuclear magnetic resonance evidence for two conformations of myosin subfragment-1.nucleotide complexes.	Phosphorus	0-10	myosin heavy chain 14	Homo sapiens	75-81
6785276-2	1981	Measurements of phosphatidylinositol (PI) and phosphatidic acid (PA) by phosphorus assays and by radioactivity ([14C]arachidonate) indicate that thrombin induces the degradation of a given fraction of the total PI to PA.	Phosphorus	72-82	coagulation factor II, thrombin	Homo sapiens	145-153
7336952-5	1981	Cytochrome P-450LM3 had less activity towards the investigated substrates while cytochrome P-450LM4 preferentially formed 2- and 3-hexanol, resorufin and B(a)P-9,10-dihydrodiol.	Phosphorus	11-12	cytochrome P450 1A2	Oryctolagus cuniculus	80-99
6260260-7	1980	Blood phosphorus decrease and urinary phosphate excretion increase were observed only after the administration of 160 MRC units of pCT.	Phosphorus	6-16	calcitonin related polypeptide alpha	Homo sapiens	131-134
6259306-4	1981	Severe dietary restriction of either calcium or phosphorus resulted in a lower growth rate as well as a duodenal CaBP as compared to a moderate mineral restriction.	Phosphorus	48-58	centrin 1	Homo sapiens	113-117
6257868-7	1981	Both phosphorus supplements caused an increase in urinary cyclic AMP, indicating an increase in parathyroid hormone (PTH) secretion, but bone resorption as measured by urinary hydroxyproline was not affected by either phosphate supplement.	Phosphorus	5-15	parathyroid hormone	Homo sapiens	96-115
7318490-2	1981	The P-31 NMR spectra of intact rat lenses and rat lens PCA extracts provided comparable qualitative and quantitative results concerning the tissue levels of the phosphorus-containing metabolites of intermediate metabolism.	Phosphorus	161-171	ATPase H+ transporting V1 subunit E1	Rattus norvegicus	4-8
7471482-2	1980	The reaction includes neuraminidase hydrolysis of glycoprotein, cleavage of sialic acid to pyruvate by N-acetyl neuraminic acid (NANA)-aldolase, oxidation of pyruvate by pyruvate oxidase which produces hydrogen peroxide, and colorimetry of hydrogen peroxide using the peroxidase-p-chlorophenol-4-amino-antipyrine method.	Phosphorus	55-56	neuraminidase 1	Homo sapiens	22-35
7264020-4	1981	From wk 5 to 12, cows fed adequate phosphorus (98% of requirement) yielded 1.8 kg/day more milk than high phosphorus groups.	Phosphorus	35-45	Weaning weight-maternal milk	Bos taurus	91-95
7236251-2	1980	The 32P content of the myosin P-light chain was determined by radioautography after electrophoresis in the presence of sodium dodecyl sulphate.	Phosphorus	6-7	myosin X	Sus scrofa	23-29
6255990-12	1980	Therefore the hydrolysis of AMPS catalyze by the venom 5"-nucleotidase must proceed with inversion of configuration at phosphorus, which suggests that the reaction is most likely an "in line" single displacement without involving a phosphoryl-enzyme intermediate and without pseudorotation.	Phosphorus	119-129	5'-nucleotidase ecto	Homo sapiens	55-70
7375433-7	1980	Data from elution profiles and phosphorus assays indicated that CaBP(1) and CaBP(2) were different from phosvitin and the Ca-binding proteins of the duodenum and uterus.	Phosphorus	31-41	calcium binding protein 1	Gallus gallus	64-71
6998484-0	1980	Pyridoxal-5"-deoxymethylenephosphonate reconstituted D-serine dehydratase: a phosphorus-31 nuclear magnetic resonance study.	Phosphorus	77-87	serine racemase	Homo sapiens	53-73
6244292-3	1980	The partial sequence of the 17-amino acid peptide was found to be Ser-Arg-Pro-Ser(P)-Leu-Pro-Leu-Pro-(Ser2, Glx2, Pro2, Leu, Arg2).	Phosphorus	82-84	arginase 2	Rattus norvegicus	125-129
6993549-9	1980	These findings show that arginine is responsible for a fall in plasma phosphorus that may well be partly related to the insulin response, and an increase in plasma potassium of clinical significance, whose mechanism(s), however, are still obscure.	Phosphorus	70-80	insulin	Homo sapiens	120-127
6153466-2	1980	The p-n-butyl derivative (BuAU) was found to inhibit DNA polymerase alpha with a Ki of approximately 60 microM.	Phosphorus	4-5	DNA polymerase alpha 1, catalytic subunit	Homo sapiens	53-73
109470-12	1979	The modulation of the hydroxylase activities by vitamin D3 metabolites and parathyroid hormone suggests that these factors regulate the renal hydroxylase by direct actions, whereas it would appear that ethane-1-hydroxy-1,1-diphosphate, Ca, P, and steroid may exert their influence indirectly.	Phosphorus	240-241	dopamine receptor D3	Gallus gallus	56-58
6989167-2	1980	Furthermore, calcium and phosphorus metabolism in relation to serum gastrin was investigated in all 20 patients 5 weeks after transplantation.	Phosphorus	25-35	gastrin	Homo sapiens	68-75
6894195-3	1980	The resistance phenomenon may be due in part to a direct effect of phosphorus on the skeletal resorbing action of parathyroid hormone and in part to an indirect effect of phosphorus on 1,25(OH)2D3 production.	Phosphorus	67-77	parathyroid hormone	Homo sapiens	114-133
7337395-8	1980	There were fairly high correlations (about 0.4) between SAP and serum phosphorus for the calves but not for the cows.	Phosphorus	70-80	amyloid P component, serum	Bos taurus	56-59
7378419-1	1980	By phosphorus analysis of the fluorescent derivative produced by ultraviolet irradiation of carboxymethylated glyceraldehyde-3-phosphate dehydrogenase in the presence of NAD at saturation levels, it has been shown that the photochemical reaction leading to the formation of the new fluorophore is also a "half-of-the-sites" reaction.	Phosphorus	3-13	glyceraldehyde-3-phosphate dehydrogenase	Homo sapiens	110-150
44874-2	1979	Plasma phosphorus displayed a highly significant (p less than 0.001) fall with a maximum depression below baseline of 1.11 +/- 0.15 mg/100 ml or 33 +/- 3% (mean +/- SEM); there was a significant correlation (p less than 0.01) between this fall and the insulin peaks induced by arginine.	Phosphorus	7-17	insulin	Homo sapiens	252-259
233578-1	1979	The interaction of CrADP, an exchange-inert paramagnetic analogue of Mg-ADP, with yeast hexokinase has been studied by measuring the effects of CrADP on the longitudinal nuclear relaxation rate (1/T1) of the protons of water and the protons and phosphorus atom of enzyme-bound glucose-6-P.	Phosphorus	245-255	hexokinase	Saccharomyces cerevisiae S288C	88-98
34429-0	1979	Phosphorus-31 nuclear magnetic resonance study of D-serine dehydratase: pryridoxal phosphate binding site.	Phosphorus	0-10	serine racemase	Homo sapiens	50-70
582302-7	1979	Protein, calcium, magnesium, and phosphorus were also recovered from the ileum in greater quantities in lactase deficients after whole milk.	Phosphorus	33-43	lactase	Homo sapiens	104-111
457771-1	1979	Fibronectin isolated from cultures of chicken embryo fibroblasts (CEF) contains phosphorus linked to serine and threonine by monoester bonds.	Phosphorus	80-90	fibronectin 1	Gallus gallus	0-11
34630-2	1979	Recent observations indicate that in thyroparathyroidectomized (TPTX) rats fed a low (0.2 g/100 g) phosphorus diet, the tubular phosphaturic response to parathyroid hormone (PTH) remains markedly blunted even when it is assessed at normal or high plasma concentration and filtered load of inorganic phosphate (Pi).	Phosphorus	99-109	parathyroid hormone	Rattus norvegicus	153-172
206866-1	1978	Changes in serum calcium, phosphorus and plasma cyclic adenosine monophosphate levels under the effect of calcitonin in healthy subjects and uremic patients under chronic hemodialysis].	Phosphorus	26-36	calcitonin related polypeptide alpha	Homo sapiens	106-116
420284-9	1979	PTH decreased within 24 h from 243 +/- 59 to 36 +/- 0 pg/ml in phosphorus-depleted rats.	Phosphorus	63-73	parathyroid hormone	Rattus norvegicus	0-3
382751-6	1979	A significant relationship was found between serum calcitonin and serum phosphorus, whereas no significant correlation was present between serum calcitonin and serum creatinine or between serum calcitonin and serum calcium.	Phosphorus	72-82	calcitonin related polypeptide alpha	Homo sapiens	51-61
474191-4	1979	Between serum concentrations of calcitonin and phosphorus a significant positive correlation was found.	Phosphorus	47-57	calcitonin related polypeptide alpha	Homo sapiens	32-42
474191-6	1979	It is concluded that the elevated serum calcitonin in patients with chronic renal disease might be explained by a reduced renal degradation of calcitonin and/or an increased production due to stimulation by serum phosphorus.	Phosphorus	213-223	calcitonin related polypeptide alpha	Homo sapiens	40-50
703643-6	1978	Distribution of the label in the products of 14CH3OH assimilation and the presence of active hydroxypyruvate reductase in the extract suggest that the serine cycle is involved in methylotrophy of Ps.	Phosphorus	196-198	glyoxylate and hydroxypyruvate reductase	Homo sapiens	93-118
28181-0	1978	Complexes of trivalent oxygenated phosphorus compounds with cytochrome P-450 and cytochrome P-420: the origin of double Soret spectra.	Phosphorus	34-44	cytochrome P450 family 4 subfamily F member 3	Homo sapiens	60-76
351621-4	1978	Nonendotoxic, lipid-free, and polysaccharide-rich hydrolytic breakdown product of LPS (called PS) was less potent but still active in CSF induction.	Phosphorus	83-85	colony stimulating factor 2 (granulocyte-macrophage)	Mus musculus	134-137
641045-1	1978	The time course of oxygen-18 exchange between [18O]Pi and normal water, catalyzed by myosin subfragment 1 in the presence of MgADP, was followed using the shift in 31P NMR caused by the presence of oxygen-18 bound to the phosphorus.	Phosphorus	221-231	myosin heavy chain 14	Homo sapiens	85-91
720696-10	1978	The results may indicate that the acceptor site of the progesterone receptor is nonhistone protein over DNA of chromatin and may contain phosphorus moiety.	Phosphorus	137-147	progesterone receptor	Oryctolagus cuniculus	55-76
272381-2	1977	Incisor teeth lased in the presence of NaF released significantly less calcium and phosphorus into sodium acetate (pH 4.0) compared with unlased controls, suggesting a possible role for the laser in caries prevention.	Phosphorus	83-93	C-X-C motif chemokine ligand 8	Homo sapiens	39-42
672681-2	1978	Nucleic acids added to the medium as a source of nitrogen or phosphorus stimulated synthesis of ribonuclease.	Phosphorus	61-71	AKO65_RS07180	Bacillus pumilus	96-108
673095-4	1978	Coincident with the lowering of serum phosphorus concentrations, serum parathyroid hormone concentrations decreased approximately 30% from levels obtained while patients were taking placebo.	Phosphorus	38-48	parathyroid hormone	Homo sapiens	71-90
207065-4	1977	The decrease of phosphorus and the FFA rise were not affected and thus appear to be primarily dependent on beta2-receptors.	Phosphorus	16-26	potassium calcium-activated channel subfamily M regulatory beta subunit 2	Homo sapiens	107-112
914972-5	1977	A highly significant positive correlation was found between maternal and cord serum concentration of DBP (r = 0.59), total 25OHD (r = 0.79), "free 25OHD" (r = 0.86) and phosphorus (r = 0.73).	Phosphorus	169-179	D-box binding PAR bZIP transcription factor	Homo sapiens	101-104
18351-0	1977	A phosphorus-magnetic-resonance study of the interaction of Mg2+ with adenyl-5"-yl imidodiphosphate.	Phosphorus	2-12	mucin 7, secreted	Homo sapiens	60-63
196631-2	1977	Vitellogenin has a molecular weight of 235 000--240 000 and contains approximately 3% phosphorus by weight.	Phosphorus	86-96	vitellogenin 2	Gallus gallus	0-12
196631-5	1977	The phosphorus content and amino acid composition of vitellogenin are consistent with a model which contains two phosvitins and one lipovitellin.	Phosphorus	4-14	vitellogenin 2	Gallus gallus	53-65
889785-0	1977	Phosphorus-31 nuclear magnetic resonance of dihydroxyacetone phosphate in the presence of triosephosphate isomerase.	Phosphorus	0-10	triosephosphate isomerase 1	Homo sapiens	90-115
18351-2	1977	The interaction of Mg2+ ions with adenyl-5"-yl imidodiphosphate, AMP-P(NH)P, has been studied at basic and acidic pH values by phosphorus magnetic resonance spectroscopy in aqueous solution.	Phosphorus	127-137	mucin 7, secreted	Homo sapiens	19-22
142366-3	1977	Preparations of myosin, obtained by the method described, possessed the following properties: the ratio of extinctions at 280 and 260 nm 1.5-1.6; the Ca2+-activated ATPase activity--0.15-0.26 mM of phosphorus/mg of protein/min.	Phosphorus	198-208	myosin heavy chain 14	Homo sapiens	16-22
199335-0	1977	Differences in duodenal calcium-binding protein (CaBP) in response to a low-calcium or a low-phosphorus intake.	Phosphorus	93-103	centrin 1	Homo sapiens	24-47
199335-0	1977	Differences in duodenal calcium-binding protein (CaBP) in response to a low-calcium or a low-phosphorus intake.	Phosphorus	93-103	centrin 1	Homo sapiens	49-53
902906-0	1977	Triose phosphate isomerase: interactions with ligands studied by [31P]phosphorus nuclear magnetic resonance [proceedings].	Phosphorus	70-80	triosephosphate isomerase 1	Homo sapiens	0-26
191066-1	1977	Glycophorin A, the major human erythrocyte sialoglycoprotein, contains a significant amount of phosphorus when isolated by the lithium diiodosalicylate-phenol procedure.	Phosphorus	95-105	glycophorin A (MNS blood group)	Homo sapiens	0-13
14328-1	1977	The interaction of Mg2+ with nucleoside disphosphates : ADP, GDP, CDP and UDP has been studied by phosphorus magnetic resonance spectroscopy in aqueous solution.	Phosphorus	98-108	mucin 7, secreted	Homo sapiens	19-22
982945-1	1976	The effect of the proteins and vitamin "D" deficiency in the diet on the formation of the calcium-binding protein (CaBP), absorption of calcium in the small intestine and on the Ca and P content in blood serum of rats was studied.	Phosphorus	118-119	hippocalcin	Rattus norvegicus	90-113
885584-1	1977	Fab fragments of rabbit anti-p-azobenzoate antibody have been crystallized.	Phosphorus	29-30	FA complementation group B	Homo sapiens	0-3
191438-1	1977	Peptidyldipeptide hydrolase [angiotensin I-converting enzyme, EC 3.4.15.1] was inhibited by inorganic and organic phosphorus compounds tested, except for beta-glycerophosphate, 5"-AMP, and 5"-ADP, at the reagent concentrations used.	Phosphorus	114-124	angiotensin I converting enzyme	Homo sapiens	29-60
1000043-3	1976	In animals on low-phosphorous diet, the mucosal concentration of CaBP measured by a quantitative competitive binding assay has increased in parallel with the mucosal calcium concentration, the fractional absorption and the calcium transport capacity.	Phosphorus	18-29	S100 calcium binding protein G	Rattus norvegicus	65-69
828536-5	1976	The results indicated that phosphorus deprivation resulted in the increase in the vitamin D-dependent rCaBP as well as in the intestinal CaBP.	Phosphorus	27-37	S100 calcium binding protein G	Rattus norvegicus	102-107
828536-5	1976	The results indicated that phosphorus deprivation resulted in the increase in the vitamin D-dependent rCaBP as well as in the intestinal CaBP.	Phosphorus	27-37	S100 calcium binding protein G	Rattus norvegicus	103-107
1011167-0	1976	[Need of thyroxine in chronic effects of growth hormone (GH) on phosphorus and calcium metabolism of female adult rat (author"s transl)].	Phosphorus	64-74	gonadotropin releasing hormone receptor	Rattus norvegicus	41-55
1011167-0	1976	[Need of thyroxine in chronic effects of growth hormone (GH) on phosphorus and calcium metabolism of female adult rat (author"s transl)].	Phosphorus	64-74	gonadotropin releasing hormone receptor	Rattus norvegicus	57-59
127621-1	1975	Phosphate transport system II, previously shown to be responsible for high-affinity phosphate uptake under conditions of phosphorus starvation, is regulated by at least three genes: pcon-nuc-2, preg, and nuc-1.	Phosphorus	121-131	cell division cycle 27	Homo sapiens	187-192
942294-6	1976	In patients with SGV+P, the release of an insulinotropic intestinal factor and the preserved vagal innervation of the pancreas may be responsible for the accelerated insulin response of the undisturbed glucose tolerance.	Phosphorus	21-22	insulin	Homo sapiens	42-49
180750-2	1976	Our data confirm earlier observation that in evaluating the renal responsiveness to parathyroid hormone, urinary cyclic AMP is a better parameter than urinary phosphorus.	Phosphorus	159-169	parathyroid hormone	Homo sapiens	84-103
132455-4	1976	In 7 GH-deficient children and 3 adults with myotonic dystrophy, we measured the capacity of human GH (hGH), pGH, and pGH plasmin digests to cause: a) the retention of N, P, K, Na, and Cl; b) a rise in plasma free fatty acids; c) a fall in plasma alpha-amino NL d) impaired glucose tolerance; and e) hyperinsulinemia.	Phosphorus	171-172	gamma-glutamyl hydrolase	Homo sapiens	103-106
132455-4	1976	In 7 GH-deficient children and 3 adults with myotonic dystrophy, we measured the capacity of human GH (hGH), pGH, and pGH plasmin digests to cause: a) the retention of N, P, K, Na, and Cl; b) a rise in plasma free fatty acids; c) a fall in plasma alpha-amino NL d) impaired glucose tolerance; and e) hyperinsulinemia.	Phosphorus	171-172	plasminogen	Homo sapiens	122-129
127621-1	1975	Phosphate transport system II, previously shown to be responsible for high-affinity phosphate uptake under conditions of phosphorus starvation, is regulated by at least three genes: pcon-nuc-2, preg, and nuc-1.	Phosphorus	121-131	peroxisome proliferator activated receptor delta	Homo sapiens	204-209
171964-8	1975	This observation suggests that the mechanism underlying the enhanced tubular reabsorption of phosphorus is inhibition of the PTH-induced activation of adenylate cyclase in the kidney.	Phosphorus	93-103	parathyroid hormone	Rattus norvegicus	125-128
239391-0	1975	Interaction of Mg2+ ions with nucleoside triphosphates by phosphorus magnetic resonance spectroscopy.	Phosphorus	58-68	mucin 7, secreted	Homo sapiens	15-18
239391-1	1975	The interaction of Mg2+ with nucleoside triphosphates: ATP, GTP, CTP and UTP has been studied by phosphorus magnetic resonance spectroscopy in aqueous solution.	Phosphorus	97-107	mucin 7, secreted	Homo sapiens	19-22
167553-6	1975	The concentrations of PP1 in the plasma and urine remained unchanged when the patient"s intake of phosphorus was increased to 1.98 g/day.	Phosphorus	98-108	inorganic pyrophosphatase 1	Homo sapiens	22-25
1153373-3	1975	Supplemental methionine increased the phosphorus content of liver fat in strain A, but other parameters in the two strains were mot affected by the increase in dietary methionine.	Phosphorus	38-48	FAT atypical cadherin 1	Homo sapiens	66-69
124133-5	1975	The physiological response of the kidney to the elevated plasma parathyroid hormone appeared to be well preserved, as evidenced by the decreased fractional excretion of calcium and the increased fractional excretion of phosphorus in the urine; however, the fall in the clearance of calcium could be the result of the decreased filtered load.	Phosphorus	219-229	parathyroid hormone	Homo sapiens	64-83
239545-0	1975	Role of cytochrome b5 in NADPH-and NADH-dependent hydroxylation by the reconstituted cytochrome P-450- or P-448-containing system.	Phosphorus	28-29	cytochrome b5 type A	Homo sapiens	8-21
1229805-1	1975	The effect of propranolol on adrenaline- and insulin-induced changes in blood glucose pyruvate, lactate, phosphorus and potassium were examined in 29 apparently healthy volunteers.	Phosphorus	105-115	insulin	Homo sapiens	45-52
1229805-3	1975	There was no significant change in the blood glucose curve after insulin whereas insulin-induced increases in pyruvate and lactate were reduced by 44% +/- 17.7 (mean +/- SEM) and 78% +/- 5.4 respectively, and the fall in phosphorus by 48% +/- 3.1; the decrease in potassium, however, was not significantly modified.	Phosphorus	221-231	insulin	Homo sapiens	81-88
4655234-0	1972	[Changes in the phosphorus compound and electrolyte content of the blood during pregnancy and labor under the effect of drugs with tonomotoric action: vetrasine and ATP].	Phosphorus	16-26	ATPase phospholipid transporting 8A2	Homo sapiens	165-169
4812447-16	1974	These results indicate that 25HCC enhances tubular reabsorption of phosphorus in rats, only in the presence of either endogenous or exogenous circulating PTH, but not in its absence and thus imply a PTH-dependent mechanism of 25HCC action on the kidney.	Phosphorus	67-77	parathyroid hormone	Rattus norvegicus	199-202
4724585-12	1973	The incorporation of [(32)P]P(i) into vitellogenin followed a pattern identical with that found for [(3)H]leucine in the pulse-labelling experiments and this indicates that synthesis of the polypeptide chain and incorporation of P(i) are closely linked processes.	Phosphorus	26-27	a1-a	Xenopus laevis	38-50
1140742-0	1975	[Behavior of macroenergetic phosphorus compounds in the tissues in alloxan diabetes under the effect of insulin].	Phosphorus	28-38	insulin	Homo sapiens	104-111
1183901-0	1975	[Effect of oxytocin on the levels of macroenergetic phosphorus compounds in tissues].	Phosphorus	52-62	oxytocin/neurophysin I prepropeptide	Homo sapiens	11-19
32189809-4	1974	When treated as an adjustable constant, the Ca/P ratio in these beta-Ca3(PO4)2 solutions was found to have the value 1.514(0.010), confirming that the stoichiometry of the high temperature form of this salt is correctly indicated by the above formula.	Phosphorus	47-48	small nucleolar RNA, H/ACA box 3A	Homo sapiens	64-76
5173743-0	1971	[Determination of cholinesterase activity as an index of occupational exposure to phosphorus insecticides as inhibitors of this enzyme].	Phosphorus	82-92	butyrylcholinesterase	Homo sapiens	18-32
5065312-0	1972	Influence of organically bound phosphorus in foetal and adult fibrinogen on the kinetics of the interaction between thrombin and fibrinogen.	Phosphorus	31-41	fibrinogen beta chain	Homo sapiens	62-72
5065312-0	1972	Influence of organically bound phosphorus in foetal and adult fibrinogen on the kinetics of the interaction between thrombin and fibrinogen.	Phosphorus	31-41	coagulation factor II, thrombin	Homo sapiens	116-124
5065312-0	1972	Influence of organically bound phosphorus in foetal and adult fibrinogen on the kinetics of the interaction between thrombin and fibrinogen.	Phosphorus	31-41	fibrinogen beta chain	Homo sapiens	129-139
5077291-0	1972	[Nitrogen and phosphorus metabolism of helminthosporium sativum P K et B].	Phosphorus	14-24	endothelin receptor type B	Homo sapiens	68-72
5788793-0	1969	Effect of a cholinesterase inhibitor treatment on the phosphorus and nucleic acid metabolism in the stomach wall.	Phosphorus	54-64	butyrylcholinesterase	Homo sapiens	12-26
5124778-13	1971	The calcium and phosphorus contents were 0.85 and 1.65g/100g of vitellogenin respectively.	Phosphorus	16-26	a1-a	Xenopus laevis	64-76
5475987-1	1970	In man, oral administration of 1 g of phosphorus resulted in a 60-125% increase in serum immunoassayable parathyroid hormone (PTH) concentration.	Phosphorus	38-48	parathyroid hormone	Homo sapiens	105-124
5777010-0	1969	Changes in phytic acid and acid-soluble phosphorus in maturing Pinto beans.	Phosphorus	40-50	forkhead box L2	Homo sapiens	63-68
4178040-0	1968	The effect of age on the variation of the phosphorus content in the muscle, liver adn brain of rats.	Phosphorus	42-52	complement factor D	Rattus norvegicus	82-85
5726687-0	1968	[Effect of calcitonin and thyroxine on calcium and phosphorus metabolism.	Phosphorus	51-61	calcitonin related polypeptide alpha	Homo sapiens	11-21
6046883-0	1967	[The transphenoidal insertion of phosphorus (P 32) grains into the hypophysis of women with breast cancer].	Phosphorus	33-43	inhibitor of growth family member 2	Homo sapiens	45-49
5862426-0	1965	Molecular weight of human fibrinogen derived from phosphorus determinations.	Phosphorus	50-60	fibrinogen beta chain	Homo sapiens	26-36
5862426-4	1965	The ;cold insoluble residue" obtained during fibrinogen preparation has a higher phosphorus content than the purified fibrinogen.	Phosphorus	81-91	fibrinogen beta chain	Homo sapiens	45-55
5862426-6	1965	Evidence showed that adsorption of phospholipids or phosphorus-containing fibrinopeptides on purified fibrinogen or fibrin was unlikely.	Phosphorus	52-62	fibrinogen beta chain	Homo sapiens	102-112
5862426-10	1965	On the basis of phosphorus determinations the average molecular weight of human fibrinogen cannot be less than 342000 (304000-383000) for a group of ten donors, and 265000 for two other persons, assuming 1 phosphorus atom/molecule and incomplete splitting of the phosphorus-containing fibrinopeptide.	Phosphorus	16-26	fibrinogen beta chain	Homo sapiens	80-90
5862426-10	1965	On the basis of phosphorus determinations the average molecular weight of human fibrinogen cannot be less than 342000 (304000-383000) for a group of ten donors, and 265000 for two other persons, assuming 1 phosphorus atom/molecule and incomplete splitting of the phosphorus-containing fibrinopeptide.	Phosphorus	206-216	fibrinogen beta chain	Homo sapiens	80-90
5862426-10	1965	On the basis of phosphorus determinations the average molecular weight of human fibrinogen cannot be less than 342000 (304000-383000) for a group of ten donors, and 265000 for two other persons, assuming 1 phosphorus atom/molecule and incomplete splitting of the phosphorus-containing fibrinopeptide.	Phosphorus	206-216	fibrinogen beta chain	Homo sapiens	80-90
5862426-13	1965	Fibrinolysis was a possible cause of lower phosphorus contents found in isolated fibrinogen and fibrin from a donor who showed apprehension during blood collection and in a fibrinogen preparation that had been submitted to prolonged dialysis.	Phosphorus	43-53	fibrinogen beta chain	Homo sapiens	81-91
5862426-13	1965	Fibrinolysis was a possible cause of lower phosphorus contents found in isolated fibrinogen and fibrin from a donor who showed apprehension during blood collection and in a fibrinogen preparation that had been submitted to prolonged dialysis.	Phosphorus	43-53	fibrinogen beta chain	Homo sapiens	173-183
14212903-0	1964	[CONSIDERATIONS ON THE BLOOD CHOLINESTERASE LEVELS IN SUBJECTS HANDLING ORGANIC PHOSPHORUS INSECTICIDES.	Phosphorus	80-90	butyrylcholinesterase	Homo sapiens	29-43
14238892-0	1964	REACTIONS OF NAF AND SNF2 WITH DENTAL ENAMEL HAVING VARYING CA:P RATIOS.	Phosphorus	63-64	C-X-C motif chemokine ligand 8	Homo sapiens	13-16
14334161-0	1965	EFFECT OF INSULIN &amp; ASCORBIC ACID ON KIDNEY PHOSPHORUS &amp;  PHOSPHATASES OF SCORBUTIC GUINEA-PIGS.	Phosphorus	48-58	insulin	Cavia porcellus	10-17
14096425-0	1963	RELATIONSHIP BETWEEN DEPRESSION OF BRAIN OR PLASMA CHOLINESTERASE AND PARALYSIS IN CHICKENS CAUSED BY CERTAIN ORGANIC PHOSPHORUS COMPOUNDS.	Phosphorus	118-128	butyrylcholinesterase	Gallus gallus	51-65
5892305-0	1964	[Experimental studies on phosphorus metabolism in the retina and optic nerve using radioisotope P32.	Phosphorus	25-35	inhibitor of growth family member 2	Homo sapiens	96-99
14238892-0	1964	REACTIONS OF NAF AND SNF2 WITH DENTAL ENAMEL HAVING VARYING CA:P RATIOS.	Phosphorus	63-64	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	Homo sapiens	21-25
14159683-0	1964	[SIMPLE METHOD FOR HIGHLY SENSITIVE DETECTION OF ORGANIC PHOSPHORUS INHIBITORS OF CHOLINESTERASE AND FOR RAPID DETERMINATION OF PSEUDOCHOLINESTERASE].	Phosphorus	57-67	butyrylcholinesterase	Homo sapiens	82-96
14159683-0	1964	[SIMPLE METHOD FOR HIGHLY SENSITIVE DETECTION OF ORGANIC PHOSPHORUS INHIBITORS OF CHOLINESTERASE AND FOR RAPID DETERMINATION OF PSEUDOCHOLINESTERASE].	Phosphorus	57-67	butyrylcholinesterase	Homo sapiens	128-148
13941714-0	1963	[Action of human STH on blood phosphorus, pyruvic acid, lactic acid, alpha-ketoglutaric acid and ATP in man].	Phosphorus	30-40	saitohin	Homo sapiens	17-20
13971745-0	1963	On the occurrence of phosphorus in fibrinogen.	Phosphorus	21-31	fibrinogen beta chain	Homo sapiens	35-45
17793875-2	1962	The chief protein of the milk is casein, which has a lower phosphorus content than bovine casein.	Phosphorus	59-69	Weaning weight-maternal milk	Bos taurus	25-29
13864808-0	1962	[Phosphorus exchange of the phosphorylated fractions of the myocardium, studied with the use of P32.	Phosphorus	1-11	inhibitor of growth family member 2	Homo sapiens	96-99
13919398-0	1962	[Phosphorus metabolism of phosphorated fractions of the myocardium, studied by means of P32.	Phosphorus	1-11	inhibitor of growth family member 2	Homo sapiens	88-91
16655134-0	1958	Circulation Patterns for Phosphorus, Sulfur and Calcium in the Bean Plant.	Phosphorus	25-35	brain expressed associated with NEDD4 1	Homo sapiens	63-67
13776024-0	1961	[Variations of blood phosphorus by action of insulin].	Phosphorus	21-31	insulin	Homo sapiens	45-52
13911501-0	1961	[Effect of preliminary ACTH injections on muscle phosphorus fractions in anoxia].	Phosphorus	49-59	proopiomelanocortin	Homo sapiens	23-27
13480667-0	1957	[Effect of parathyroid hormone on renal clearance of phosphorus in hypoparathyroidism].	Phosphorus	53-63	parathyroid hormone	Homo sapiens	11-30
13512751-0	1957	Relations of organic phosphorus distributions in testes to P32 administration, testis growth, and hormonal effects.	Phosphorus	21-31	inhibitor of growth family member 2	Homo sapiens	59-62
13595588-0	1958	[Effect of estrogens, androgens, glucocorticoids, thyroid hormone &amp; growth hormone on phosphorus &amp; calcium metabolism].	Phosphorus	90-100	growth hormone 1	Homo sapiens	72-86
13579354-0	1957	[Effect of ACTH on blood &amp; urinary phosphorus in man under normal &amp; pathological conditions].	Phosphorus	39-49	proopiomelanocortin	Homo sapiens	11-15
13471110-0	1957	[Pituitary somatotropin extract &amp; phosphorus metabolism].	Phosphorus	38-48	growth hormone 1	Homo sapiens	11-23
13458807-0	1957	[Cholinesterase antagonists; pharmacological study of various phosphorus derivatives of military &amp; insecticidal importance].	Phosphorus	62-72	butyrylcholinesterase	Homo sapiens	1-15
13460971-0	1957	In vitro incorporation of P32 into phosphorus compounds of benign and malignant human ovarian tumors.	Phosphorus	35-45	inhibitor of growth family member 2	Homo sapiens	26-29
16654818-0	1955	Phosphorus and Sulfur Compounds in Plant Xylem Sap.	Phosphorus	0-10	SH2 domain containing 1A	Homo sapiens	47-50
13353998-0	1956	Cholinesterase activity levels among agricultural workers; a survey with respect to the degree of absorption by agricultural workers exposed to organic phosphorus insecticides.	Phosphorus	152-162	butyrylcholinesterase	Homo sapiens	0-14
13445027-0	1956	[Changes in acid-soluble phosphorus of the myometrium induced by insulin; experimental study with radiophosphorus].	Phosphorus	25-35	insulin	Homo sapiens	65-72
14365695-0	1955	Phosphorus metabolism of the adrenal gland: effect of hypophysectomy and administration of ACTH on the incorporation of radioactive phosphate into the RNA nucleotides.	Phosphorus	0-10	proopiomelanocortin	Homo sapiens	91-95
13244813-0	1955	Therapeutic factors in survival after lethal cholinesterase inhibition by phosphorus insecticides.	Phosphorus	74-84	butyrylcholinesterase	Homo sapiens	45-59
13276387-0	1955	Effect of insulin on the metabolism of phosphorus in human erythrocytes.	Phosphorus	39-49	insulin	Homo sapiens	10-17
14367417-0	1955	The use of radio-active phosphorus (P32) to determine the viability of the head of the femur.	Phosphorus	24-34	inhibitor of growth family member 2	Homo sapiens	36-39
13113216-0	1953	Comparative studies on the uptake of phosphorus by tissues under different doses of injected radioactive phosphorus P32.	Phosphorus	37-47	inhibitor of growth family member 2	Homo sapiens	116-119
16654677-2	1954	Comparative Effects of 2,4-Dichlorophenoxyacetic Acid and Other Plant Growth Regulators on Phosphorus Metabolism in Bean Plants.	Phosphorus	91-101	brain expressed associated with NEDD4 1	Homo sapiens	116-120
13186780-0	1954	Extrinsic (p32)/intrinsic (P31) phosphorus clearance ratio in man.	Phosphorus	32-42	ATPase H+ transporting V1 subunit E1	Homo sapiens	27-30
13259550-0	1955	[Studies with P32 on the phosphorus uptake of the human placenta].	Phosphorus	25-35	inhibitor of growth family member 2	Homo sapiens	14-17
16654717-2	1954	Comparative Effects of 2,4-Dichlorophenoxyacetic Acid and Other Plant Growth Regulators on Phosphorus Metabolism in Bean Plants (Continued).	Phosphorus	91-101	brain expressed associated with NEDD4 1	Homo sapiens	116-120
13155215-0	1954	[Effect of ACTH and cortisone on proteins, cholesterol, phosphorus, and phosphatase in the blood serum in chronic articular rheumatism].	Phosphorus	56-66	proopiomelanocortin	Homo sapiens	11-15
12979788-0	1952	[The phosphorus metabolism of plasma lipids of healthy persons without and after application of choline chloride, traced by radioactive phosphate (P 32); effects of lipotropic substances].	Phosphorus	5-15	inhibitor of growth family member 2	Homo sapiens	147-151
13039594-0	1953	Cholinesterase response and symptomatology from exposure to organic phosphorus insecticides.	Phosphorus	68-78	butyrylcholinesterase	Homo sapiens	0-14
13076905-0	1953	The effect of adrenocorticotrophic hormone (ACTH) on phosphorus metabolism in selected areas of monkey brain; preliminary report.	Phosphorus	53-63	proopiomelanocortin	Homo sapiens	14-42
13076905-0	1953	The effect of adrenocorticotrophic hormone (ACTH) on phosphorus metabolism in selected areas of monkey brain; preliminary report.	Phosphorus	53-63	proopiomelanocortin	Homo sapiens	44-48
16654469-0	1952	THE UPTAKE OF PHOSPHORUS BY BEAN PLANTS WITH PARTICULAR REFERENCE TO THE EFFECTS OF IRON.	Phosphorus	14-24	brain expressed associated with NEDD4 1	Homo sapiens	28-32
13105971-2	1953	Blood acid-soluble phosphorus fractions after the administration of insulin in muscle diseases and tetanus].	Phosphorus	19-29	insulin	Homo sapiens	68-75
13018676-0	1952	[Variations of acid-soluble serum phosphorus in diabetics treated with insulin].	Phosphorus	34-44	insulin	Homo sapiens	71-78
14844299-0	1951	Effect of prolactin on phosphorus metabolism of pigeon crop-sac; P31 and P32 analyses.	Phosphorus	23-33	ATPase H+ transporting V1 subunit E1	Homo sapiens	65-68
14948299-0	1952	[Blood phosphorus and phosphatases in children in Heine-Medin disease].	Phosphorus	7-17	milk fat globule EGF and factor V/VIII domain containing	Homo sapiens	56-61
18894879-0	1948	The relationship of cholinesterase inhibiting activity to the toxicity of some organic phosphorus compounds.	Phosphorus	87-97	butyrylcholinesterase	Homo sapiens	20-34
18112095-0	1949	Studies on the preparation of soy bean protein free from phosphorus.	Phosphorus	57-67	brain expressed associated with NEDD4 1	Homo sapiens	34-38
15436567-0	1950	The effect of hypophysectomy and growth hormone on phosphorus metabolism.	Phosphorus	51-61	growth hormone 1	Homo sapiens	33-47
17791179-0	1948	Determination of the Fate of Phosphorus in the Laying Hen by Means of Radiophosphorus (P32).	Phosphorus	29-39	inhibitor of growth family member 2	Homo sapiens	87-90
20786268-0	1945	First Aid for Phosphorus Burns.	Phosphorus	14-24	activation induced cytidine deaminase	Homo sapiens	6-9
18903402-0	1948	Inhibition of the cholinesterase activity of human blood plasma and erythrocyte stromata by alkylated phosphorus compounds.	Phosphorus	102-112	butyrylcholinesterase	Homo sapiens	18-32
16743345-2	1924	The Effect of Insulin Administration on the Distribution of Phosphorus Compounds in Blood and Muscle.	Phosphorus	60-70	insulin	Homo sapiens	14-21
19872627-7	1931	(21) have shown that potassium and phosphorus of the blood are decreased and Luck, Morrison, and Wilbur (22) indicate a reduction in the amino acids of the blood in insulin treatment.	Phosphorus	35-45	insulin	Bos taurus	165-172
33960368-8	2021	Mapping these pS/pT sites on the hTDO surface revealed their propinquity to acidic Asp/Glu (D/E) residues engendering negatively charged DEpSpT clusters vicinal to the ubiquitination K sites over the entire protein surface.	Phosphorus	14-16	tryptophan 2,3-dioxygenase	Homo sapiens	33-37
16693966-0	1931	STUDIES OF CALCIUM AND PHOSPHORUS METABOLISM: VIII.	Phosphorus	23-33	cytochrome c oxidase subunit 8A	Homo sapiens	46-50
33524753-5	2021	Compared with BTF1, the filler in BTF2 effectively delayed the increase in  P for 70 days or more and ensured stable operation for as long as 174 days.	Phosphorus	76-77	butyrophilin subfamily 2 member A2	Homo sapiens	34-38
33611046-9	2021	The excellent catalytic performance of Ru9.8/r-CoP is attributed to the abundant phosphorus vacancies along with a large specific surface area of r-CoP, which makes the Ru particles smaller and more uniformly dispersed on the surface, thereby exposing more active sites to show improved performance.	Phosphorus	81-91	caspase recruitment domain family member 16	Homo sapiens	47-50
33387018-9	2021	In a multivariate analysis, TNF-alpha positively associated with phosphorus, PTH, and alkaline phosphatase and inversely associated with height z-score, independent of kidney function, age, sex, and active vitamin D analogue use.	Phosphorus	65-75	tumor necrosis factor	Homo sapiens	28-37
20313181-0	1921	Cod-Liver Oil Without Phosphorus as Effective as Cod-Liver Oil with Phosphorus in Rickets and Tetany.	Phosphorus	68-78	small nuclear ribonucleoprotein polypeptides B and B1	Homo sapiens	49-52
16743045-0	1921	The Origin of Milk Fat and its Relation to the Metabolism of Phosphorus.	Phosphorus	61-71	FAT atypical cadherin 1	Homo sapiens	19-22
33440277-8	2021	Therefore, our data suggested that the CBP-1-mediated histone acetylation regulation in certain tissues is associated with the induction of protective response to PS-NPs in C. elegans.	Phosphorus	163-165	Protein cbp-1	Caenorhabditis elegans	39-44
33522635-6	2021	In simulations, we show we can preserve phosphorus-containing metabolite peaks that had an SNR < 1 before denoising.	Phosphorus	40-50	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1	Homo sapiens	91-98
34024107-8	2021	Therefore, the full cell of SnS2/GPE1/Na3V2(PO4)3 is evaluated and delivers good cycling stability of 500 cycles, holding a great prospect for the design and production of phosphorus-containing electrolytes for safer sodium-ion batteries.	Phosphorus	172-182	sodium voltage-gated channel alpha subunit 11	Homo sapiens	28-32
34042584-10	2021	After multiple Cox regression analysis adjusting for age, eGFR, cold ischemia time, HbA1c, phosphorus, calcium, and albumin, plasma levels of OPG remained an independent predictor of all-cause mortality (HR, 1.181; 95%CI 1.035 - 1.347; p = 0.014).	Phosphorus	91-101	TNF receptor superfamily member 11b	Homo sapiens	142-145
34042533-6	2021	The correlation analysis showed that serum adropin levels were correlated negatively with Age, CVD history, DM history, C-reactive protein, type B natriuretic peptide, phosphorus, intact parathyroid hormone, carotid artery plaque amount and carotid intima-media thickness (CIMT), left ventricular septal thickness (LVSTd), and left ventricular posterior wall thickness, whereas it was correlated positively with albumin, hemoglobin, serum creatinine and Kt/V, and ejection fraction value.	Phosphorus	168-178	energy homeostasis associated	Homo sapiens	43-50
34036706-8	2021	The FL community was enriched in predicted pathways for the metabolism of inositol phosphate, a potential phosphorus source, and of polycyclic aromatic hydrocarbons.	Phosphorus	106-116	fms related receptor tyrosine kinase 3 ligand	Homo sapiens	4-6
34015920-4	2021	Our results suggested that the phosphorus was substituted into carbon sites form P-N/P N bonds with four coordination, which contribute P 2p level donor states in the band gap to enhance light absorption and reduce charge separation.	Phosphorus	31-41	peripheral myelin protein 2	Homo sapiens	136-140
33744339-1	2021	Using neurokinin 1 receptor (NK1R) internalization to measure of substance P release in rat spinal cord slices, we found that it was induced by the adenylyl cyclase (AC) activator forskolin, by the protein kinase A (PKA) activators 6-Bnz-cAMP and 8-Br-cAMP, and by the activator of exchange protein activated by cAMP (Epac) 8-pCPT-2-O-Me-cAMP (CPTOMe-cAMP).	Phosphorus	75-76	tachykinin receptor 1	Rattus norvegicus	6-27
34011663-5	2021	Treatment with burosumab (an anti-FGF23 monoclonal antibody) normalised phosphorus and alkaline phosphatase levels and improved her bowing.	Phosphorus	72-82	fibroblast growth factor 23	Homo sapiens	34-39
33978034-5	2021	Decreased nitric oxide (NO) production resulting from endothelial NO synthase (eNOS) dysregulation is involved in the BP-induced endothelial dysfunction.	Phosphorus	118-120	nitric oxide synthase 3, endothelial cell	Mus musculus	54-77
33978034-5	2021	Decreased nitric oxide (NO) production resulting from endothelial NO synthase (eNOS) dysregulation is involved in the BP-induced endothelial dysfunction.	Phosphorus	118-120	nitric oxide synthase 3, endothelial cell	Mus musculus	79-83
33744339-1	2021	Using neurokinin 1 receptor (NK1R) internalization to measure of substance P release in rat spinal cord slices, we found that it was induced by the adenylyl cyclase (AC) activator forskolin, by the protein kinase A (PKA) activators 6-Bnz-cAMP and 8-Br-cAMP, and by the activator of exchange protein activated by cAMP (Epac) 8-pCPT-2-O-Me-cAMP (CPTOMe-cAMP).	Phosphorus	75-76	tachykinin receptor 1	Rattus norvegicus	29-33
34040623-6	2021	Such studies on the nutrient interaction pathways suggest that an MYB-like transcription factor, phosphate starvation response 1 (PHR1), acts as a master regulator of N, P, S, Fe, and Zn homeostasis.	Phosphorus	130-131	phosphate starvation response 1	Arabidopsis thaliana	97-128
33712426-3	2021	As the central biocatalyst, the cytochrome P450 monooxygenase CreJ oxidizes diverse p- and m-alkylphenyl phosphates with perfect stereoselectivity at different efficiencies.	Phosphorus	84-86	cytochrome P450 family 20 subfamily A member 1	Homo sapiens	32-61
33982720-2	2021	The Ni(I) species and chlorine atom radical Cl  were generated via the ligand to metal charge transfer (LMCT) process of the NiCl2(PPh3)2, which allows nickel(IV)-phosphorus species in situ formation, giving various tertiary phosphine oxides under photocatalyst-free conditions.	Phosphorus	163-173	protein phosphatase 4 catalytic subunit	Homo sapiens	125-137
33656230-7	2021	These results explain why excess phosphorus is needed for the preparation of Ni 2 P, and also demonstrate that the TPR-IR technique is an efficient method to understand the complex processes of catalyst preparation.	Phosphorus	33-43	translocated promoter region, nuclear basket protein	Homo sapiens	115-118
33618073-9	2021	However, males and females had similar blood phosphate, calcium, and creatinine levels irrespective of age, suggesting that female mice upregulated FGF23 to maintain blood phosphorus, and compromised renal function could not explain the increased serum iFGF23.	Phosphorus	172-182	fibroblast growth factor 23	Mus musculus	148-153
33963990-9	2021	Overall, biochar amendment at a dosage up to 10 t ha-1 could be a tool to enhance soil availability and plant uptake of phosphorus, particularly in acid, heavy textured P-poor soils.	Phosphorus	120-130	Rho GTPase activating protein 45	Homo sapiens	50-54
33471363-2	2021	Phosphorus homeostasis can be affected by diet and certain medications; some intravenous iron formulations can induce renal phosphate excretion and hypophosphatemia, likely through increasing serum concentrations of intact fibroblast growth factor 23.	Phosphorus	0-10	fibroblast growth factor 23	Homo sapiens	223-250
33579566-4	2021	Batch tests demonstrated that efficient PD with nitrate-to-nitrite transformation ratio of 97.67% supplying stable nitrite for anammox, and phosphorus was mainly removed using nitrate as electron acceptor via DPR with the ideal phosphorus release/uptake rate (7.73/22.17 mgP/gVSS/h).	Phosphorus	140-150	matrix Gla protein	Homo sapiens	271-274
33579566-4	2021	Batch tests demonstrated that efficient PD with nitrate-to-nitrite transformation ratio of 97.67% supplying stable nitrite for anammox, and phosphorus was mainly removed using nitrate as electron acceptor via DPR with the ideal phosphorus release/uptake rate (7.73/22.17 mgP/gVSS/h).	Phosphorus	228-238	matrix Gla protein	Homo sapiens	271-274
33949504-3	2021	The shortest cationanion distance between the phosphorus ion of the (PPh4)+ cation and the ferric ion of the [FeIII(HATD)2]- anion is 13.190 A in complex 1, whereas that between the ferrous ion of the [FeII(Phen)3]2+ cation and the ferric ion of the [FeIII(HATD)2]- anion is 7.821 A in complex 2.	Phosphorus	46-56	potassium two pore domain channel subfamily K member 3	Homo sapiens	69-73
33618073-14	2021	CONCLUSIONS: Our study demonstrates that aging female mice upregulate FGF23 to a greater degree during a mild phosphate challenge to maintain blood phosphorus versus young female and young/old male mice, potentially due to direct estradiol effects on osteocytes.	Phosphorus	148-158	fibroblast growth factor 23	Mus musculus	70-75
33465815-2	2021	ARHR2 patients are frequently treated with phosphate supplementation to ameliorate the rachitic phenotype, but elevating plasma phosphorus concentrations in ARHR2 patients may increase the risk of ectopic calcification without increasing bone mass.	Phosphorus	128-138	ectonucleotide pyrophosphatase/phosphodiesterase 1	Homo sapiens	157-162
33447973-3	2021	This study integrates empirical models into Geographic Information Systems to quantify total nitrogen and phosphorus (TN and TP) load and concentration in watercourses of Brazil"s Lobo Stream Hydrographic Basin (LSHB).	Phosphorus	106-116	C-type lectin domain family 3 member B	Homo sapiens	118-120
33742467-4	2021	Field-scale P balances were largely controlled by P application rate and exhibited a positive relationship with STP and runoff DRP flow-weighted mean concentration (FWMC).	Phosphorus	12-13	sulfotransferase family 1A member 1	Homo sapiens	112-115
33221241-1	2021	OBJECTIVES: This study aimed to explore echocardiographic characteristics of phospholamban (PLN) p.Arg14del mutation carriers to investigate whether structural and/or functional abnormalities could be identified before onset of symptoms.	Phosphorus	34-35	phospholamban	Homo sapiens	92-95
33259845-14	2021	The decrease of phosphorus metabolites in T1DM may be rather due to the pharmacological insulin supply.	Phosphorus	16-26	insulin	Homo sapiens	88-95
33893820-4	2021	CASE PRESENTATION: The patient was a 59-year-old asymptomatic woman who consistently showed elevated PTH levels (385-482 pg/ml) using the Roche Elecsys (Cobas e-411) and ADVIA Centaur assays, with normal calcium, phosphorus, vitamin D, and renal function parameters.	Phosphorus	213-223	parathyroid hormone	Homo sapiens	101-104
33947128-3	2021	The results of 2D-COS analysis indicated that the phase transition mechanism of P(NiPAAm-co-AAc) hydrogel at pH4 is different from that at pH2 due to the effect of COOH group of AAc.	Phosphorus	80-81	glycine-N-acyltransferase	Homo sapiens	92-95
33947128-3	2021	The results of 2D-COS analysis indicated that the phase transition mechanism of P(NiPAAm-co-AAc) hydrogel at pH4 is different from that at pH2 due to the effect of COOH group of AAc.	Phosphorus	80-81	glycine-N-acyltransferase	Homo sapiens	178-181
33910228-0	2021	Phosphorus-mediated sp2-sp3 couplings for C-H fluoroalkylation of azines.	Phosphorus	0-10	Sp2 transcription factor	Homo sapiens	20-23
33910228-0	2021	Phosphorus-mediated sp2-sp3 couplings for C-H fluoroalkylation of azines.	Phosphorus	0-10	Sp3 transcription factor	Homo sapiens	24-27
33370698-6	2021	100% of AO7 was removed within 30 min with conditions of 2 mM PS, 50 mg/L AO7 and 0.5 g/L RM-BC(HP), and the Fe leaching was negligible.	Phosphorus	62-64	ring finger protein 25	Homo sapiens	8-11
33891343-0	2021	One-Step Template/Solvent-Free Pyrolysis for in-situ  Immobilization of CoP Nanoparticles onto N and P co-Doped Carbon Porous Nanosheets towards High-efficiency Electrocatalytic Hydrogen Evolution.	Phosphorus	31-32	caspase recruitment domain family member 16	Homo sapiens	72-75
33880707-5	2021	Explicitly, the two probes (H and P) were able to collectively discriminate heavy metal cations such as Cd2+, Co2+, Zn2+, Cu2+, Ni2+, and Ag+, both in DMF, among all other heavy metal cations tested.	Phosphorus	34-35	CD2 molecule	Homo sapiens	104-107
33922173-2	2021	The study aims to reveal effector molecules driving the maintenance of phosphorus (P) homeostasis and parathyroid hormone (PTH) responsiveness to variable P supply throughout fetal and postnatal life.	Phosphorus	123-124	parathyroid hormone	Sus scrofa	102-121
33370698-9	2021	The mechanism studies demonstrated that PS was mainly activated by Fe0 and Fe2+ in RM-BC(HP) to produce different radicals, then 1O2 was generated by the reactions among these radicals to degrade AO7.	Phosphorus	40-42	ring finger protein 25	Homo sapiens	196-199
33789980-10	2021	Peritoneal macrophages from C57BL/6 mice produced TNF-alpha, IL-6, and IDO-1 via interaction with anti-P Abs through activating FcgammaRs, which were required for disease development.	Phosphorus	0-1	tumor necrosis factor	Mus musculus	50-59
33789980-10	2021	Peritoneal macrophages from C57BL/6 mice produced TNF-alpha, IL-6, and IDO-1 via interaction with anti-P Abs through activating FcgammaRs, which were required for disease development.	Phosphorus	0-1	interleukin 6	Mus musculus	61-65
33789980-10	2021	Peritoneal macrophages from C57BL/6 mice produced TNF-alpha, IL-6, and IDO-1 via interaction with anti-P Abs through activating FcgammaRs, which were required for disease development.	Phosphorus	0-1	indoleamine 2,3-dioxygenase 1	Mus musculus	71-76
33853500-0	2021	MYB30 and ETHYLENE INSENEITIVE3 antagonistically regulate root hair growth and phosphorus uptake under phosphate deficiency in Arabidopsis.	Phosphorus	79-89	myb domain protein 30	Arabidopsis thaliana	0-5
33832448-3	2021	In addition, fibroblast growth factor 23 (FGF23), which has been recognized as a phosphorus-regulating hormone, appears to be involved in haematopoietic regulation.	Phosphorus	81-91	fibroblast growth factor 23	Homo sapiens	13-40
33927739-0	2021	Spatiotemporal Pattern of Acid Phosphatase Activity in Soils Cultivated With Maize Sensing to Phosphorus-Rich Patches.	Phosphorus	94-104	acid phosphatase	Zea mays	26-42
33927739-1	2021	Aims: Acid phosphatase (APase) secretion by roots allows plants to mobilize organic phosphorus (P) in low P soils.	Phosphorus	25-26	acid phosphatase	Zea mays	6-22
33927739-1	2021	Aims: Acid phosphatase (APase) secretion by roots allows plants to mobilize organic phosphorus (P) in low P soils.	Phosphorus	96-97	acid phosphatase	Zea mays	6-22
33927739-1	2021	Aims: Acid phosphatase (APase) secretion by roots allows plants to mobilize organic phosphorus (P) in low P soils.	Phosphorus	96-97	acid phosphatase	Zea mays	24-29
33832448-3	2021	In addition, fibroblast growth factor 23 (FGF23), which has been recognized as a phosphorus-regulating hormone, appears to be involved in haematopoietic regulation.	Phosphorus	81-91	fibroblast growth factor 23	Homo sapiens	42-47
33835704-8	2021	The phosphate transporter PiT-1 knockdown prevented HP-mediated suppression of eNOS activity by impeding phosphorus influx in HUVECs.	Phosphorus	105-115	POU domain, class 1, transcription factor 1	Mus musculus	26-31
33897349-6	2021	RYR2 mutations were identified in five cases with BECTS, including one heterozygous frameshift mutation (c.14361dup/p.Arg4790Pro fs*6), two heterozygous missense mutations (c.2353G > A/p.Asp785Asn and c.8574G > A/p.Met2858Ile), and two pairs of compound heterozygous mutations (c.4652A > G/p.Asn1551Ser and c.11693T > C/p.Ile3898Thr, c.7469T > C/p.Val2490Ala and c.12770G > A/p.Arg4257Gln, respectively).	Phosphorus	114-115	ryanodine receptor 2	Homo sapiens	0-4
33835704-8	2021	The phosphate transporter PiT-1 knockdown prevented HP-mediated suppression of eNOS activity by impeding phosphorus influx in HUVECs.	Phosphorus	105-115	nitric oxide synthase 3, endothelial cell	Mus musculus	79-83
33578130-0	2021	A kinetic model for the thermoluminescent high dose response of LiF:Mg,Cu,P (MCP-N).	Phosphorus	74-75	LIF interleukin 6 family cytokine	Homo sapiens	64-67
33578130-0	2021	A kinetic model for the thermoluminescent high dose response of LiF:Mg,Cu,P (MCP-N).	Phosphorus	74-75	CD46 molecule	Homo sapiens	77-80
33578130-1	2021	This contribution describes a kinetic model attempting to reproduce the response of the thermoluminescent material LiF:Mg,Cu,P when it is irradiated to absorbed dose values in the kGy range.	Phosphorus	125-126	LIF interleukin 6 family cytokine	Homo sapiens	115-118
33394414-3	2021	A general formula for P adsorption was proposed that considers mineral composition through the component additivity method, also incorporating the effects of environmental factors, including the aqueous P concentration (Ce), pH, sediment concentration (S), and ionic strength (IS).	Phosphorus	22-23	phenylalanine hydroxylase	Homo sapiens	225-227
32803677-5	2021	RESULTS: In family 1, two DUOX2 missense mutations, namely, c.1060C>T/p.R354W in exon 10 and c.3200C>T/p.S1067L in exon 25, were found.	Phosphorus	70-71	dual oxidase 2	Homo sapiens	26-31
33388852-7	2021	In a recent publication, we demonstrated that the Golgi-localized P4 ATPase Dnf3p has a preference for PS as a substrate, can reach the plasma membrane in a cell cycle-dependent manner, and is regulated by the same kinases that activate Dnf1p and Dnf2p.	Phosphorus	103-105	aminophospholipid-translocating P4-type ATPase DNF3	Saccharomyces cerevisiae S288C	76-81
33388852-7	2021	In a recent publication, we demonstrated that the Golgi-localized P4 ATPase Dnf3p has a preference for PS as a substrate, can reach the plasma membrane in a cell cycle-dependent manner, and is regulated by the same kinases that activate Dnf1p and Dnf2p.	Phosphorus	103-105	aminophospholipid-translocating P4-type ATPase DNF1	Saccharomyces cerevisiae S288C	237-242
33388852-7	2021	In a recent publication, we demonstrated that the Golgi-localized P4 ATPase Dnf3p has a preference for PS as a substrate, can reach the plasma membrane in a cell cycle-dependent manner, and is regulated by the same kinases that activate Dnf1p and Dnf2p.	Phosphorus	103-105	aminophospholipid-translocating P4-type ATPase DNF2	Saccharomyces cerevisiae S288C	247-252
33394414-7	2021	Multivariable regression analysis was used to show that the amount of P adsorption was strongly correlated with Ce, followed by S, IS, and pH.	Phosphorus	70-71	phenylalanine hydroxylase	Homo sapiens	139-141
33869850-6	2021	Results revealed that interacted application of P and S at 22 and 15 kg ha-1 respectively increased grain yield of wheat by 40.1 % over control.	Phosphorus	48-49	plasma membrane ATPase	Triticum aestivum	72-76
33001224-5	2021	Concentrations of extractable calcium, iron, and phosphorus also varied significantly across the pH gradients.	Phosphorus	49-59	phenylalanine hydroxylase	Homo sapiens	97-99
33617039-0	2021	SPX4 interacts with both PHR1 and PAP1 to regulate critical steps in phosphorus-status-dependent anthocyanin biosynthesis.	Phosphorus	69-79	SPX domain-containing protein 4	Arabidopsis thaliana	0-4
33617039-0	2021	SPX4 interacts with both PHR1 and PAP1 to regulate critical steps in phosphorus-status-dependent anthocyanin biosynthesis.	Phosphorus	69-79	photolyase 1	Arabidopsis thaliana	25-29
33617039-0	2021	SPX4 interacts with both PHR1 and PAP1 to regulate critical steps in phosphorus-status-dependent anthocyanin biosynthesis.	Phosphorus	69-79	phosphatidic acid phosphatase 1	Arabidopsis thaliana	34-38
33596072-6	2021	When using CCl4 as a halogenating agent, the reaction of chlorinated spirophosphorane proceeds via SN2(P-V) mechanism, and the backside attack of P-Cl bond is the main pathway.	Phosphorus	103-104	C-C motif chemokine ligand 4	Homo sapiens	11-15
33372353-3	2021	Herein, we report a function-oriented strategy of deliberately constructing black phosphorus quantum dots-ZnIn 2 S 4 (BP/ZIS) heterostructures for solar-driven CO 2 reduction to syngas paired with selectively oxidative C-N bond formation in one redox cycle.	Phosphorus	82-92	zinc finger RANBP2-type containing 2	Homo sapiens	121-124
33367746-1	2021	BACKGROUND: In chronic kidney disease, serum phosphorus (P) elevations stimulate parathyroid hormone (PTH) production, causing severe alterations in the bone-vasculature axis.	Phosphorus	45-55	parathyroid hormone	Rattus norvegicus	81-100
33790413-8	2022	RESULTS: In this study, a novel homozygous BRAT1 variant c.233G > C with amino acid change of R with P at residue 78 (R78P) was identified.	Phosphorus	101-102	BRCA1 associated ATM activator 1	Homo sapiens	43-48
33720684-3	2021	This theranostic nanoplatform is constructed by using polyethyleneimine-modified black phosphorus nanosheets as a "fishnet" to attach l-Arginine (l-Arg) and glucose oxidase (GOx) and then depositing mini-sized MnO2 nanosheets (MNs) on the surface by a facile situ biomineralization method.	Phosphorus	87-97	hydroxyacid oxidase 1	Homo sapiens	157-172
33720684-3	2021	This theranostic nanoplatform is constructed by using polyethyleneimine-modified black phosphorus nanosheets as a "fishnet" to attach l-Arginine (l-Arg) and glucose oxidase (GOx) and then depositing mini-sized MnO2 nanosheets (MNs) on the surface by a facile situ biomineralization method.	Phosphorus	87-97	hydroxyacid oxidase 1	Homo sapiens	174-177
33109409-5	2021	The mucin corona would 1) stably adsorbed on PS@Bap at the early stages of endocytosis until degraded during the lysosomal transport and maturation process, 2) delay intracellular trafficking of PS@Bap and the progress of Bap detached from PS, 3) enhance uptake of PS@Bap but reduce the cytotoxicity elicited by PS@Bap, as indicated by cell viability, generation of reactive oxygen species, impairment on mitochondrial function, and further cell apoptosis.	Phosphorus	45-47	LOC100508689	Homo sapiens	4-9
33109409-5	2021	The mucin corona would 1) stably adsorbed on PS@Bap at the early stages of endocytosis until degraded during the lysosomal transport and maturation process, 2) delay intracellular trafficking of PS@Bap and the progress of Bap detached from PS, 3) enhance uptake of PS@Bap but reduce the cytotoxicity elicited by PS@Bap, as indicated by cell viability, generation of reactive oxygen species, impairment on mitochondrial function, and further cell apoptosis.	Phosphorus	195-197	LOC100508689	Homo sapiens	4-9
33109409-5	2021	The mucin corona would 1) stably adsorbed on PS@Bap at the early stages of endocytosis until degraded during the lysosomal transport and maturation process, 2) delay intracellular trafficking of PS@Bap and the progress of Bap detached from PS, 3) enhance uptake of PS@Bap but reduce the cytotoxicity elicited by PS@Bap, as indicated by cell viability, generation of reactive oxygen species, impairment on mitochondrial function, and further cell apoptosis.	Phosphorus	195-197	LOC100508689	Homo sapiens	4-9
33109409-5	2021	The mucin corona would 1) stably adsorbed on PS@Bap at the early stages of endocytosis until degraded during the lysosomal transport and maturation process, 2) delay intracellular trafficking of PS@Bap and the progress of Bap detached from PS, 3) enhance uptake of PS@Bap but reduce the cytotoxicity elicited by PS@Bap, as indicated by cell viability, generation of reactive oxygen species, impairment on mitochondrial function, and further cell apoptosis.	Phosphorus	195-197	LOC100508689	Homo sapiens	4-9
33109409-5	2021	The mucin corona would 1) stably adsorbed on PS@Bap at the early stages of endocytosis until degraded during the lysosomal transport and maturation process, 2) delay intracellular trafficking of PS@Bap and the progress of Bap detached from PS, 3) enhance uptake of PS@Bap but reduce the cytotoxicity elicited by PS@Bap, as indicated by cell viability, generation of reactive oxygen species, impairment on mitochondrial function, and further cell apoptosis.	Phosphorus	195-197	LOC100508689	Homo sapiens	4-9
33714972-10	2021	Serum phosphorus levels, alkaline phosphatase, hemoglobin, and triglycerides were found to be closely associated with CBS and CSE scores in femur tissues.	Phosphorus	6-16	cystathionine beta-synthase	Homo sapiens	118-121
33360171-4	2021	Results showed that dissolution of Ag2S-NPs fitted the pseudo-first-order kinetics and the kobs increased from 0.017 h-1 to 0.249 h-1 with increasing PS concentration from 2 mM to 10 mM (36 h, 40  C).	Phosphorus	150-152	angiotensin II receptor type 1	Homo sapiens	35-39
33714972-10	2021	Serum phosphorus levels, alkaline phosphatase, hemoglobin, and triglycerides were found to be closely associated with CBS and CSE scores in femur tissues.	Phosphorus	6-16	choreoathetosis/spasticity, episodic (paroxysmal choreoathetosis/spasticity)	Homo sapiens	126-129
33715866-11	2021	RESULTS: The groups with a diet high in phosphorus (CRF + H A and CRF + PTx + rPTH + HP) had a significant reduction in creatinine clearance and also in body weight with an increase in serum phosphorus regardless of parathyroidectomy, but not serum levels of calcium, FGF23 and calcitriol that were 2-3 times higher in the group with secondary hyperparathyroidism (CRF + HP).	Phosphorus	40-50	fibroblast growth factor 23	Rattus norvegicus	268-273
33439649-5	2021	Here, we disclose a Smiles-type rearrangement, triggered by a phosphorus-containing unit (arylphosphoramidate), therefore called "phospho-Smiles" rearrangement, allowing a Csp2-Csp2 bond formation thanks to a 1,4-aryl migration reaction.	Phosphorus	62-72	regulator of calcineurin 2	Homo sapiens	172-176
33912412-1	2021	Objective: Homeostasis of serum phosphorus and calcitriol level is regulated mainly by fibroblast growth factor 23 (FGF23).	Phosphorus	32-42	fibroblast growth factor 23	Homo sapiens	87-114
33912412-1	2021	Objective: Homeostasis of serum phosphorus and calcitriol level is regulated mainly by fibroblast growth factor 23 (FGF23).	Phosphorus	32-42	fibroblast growth factor 23	Homo sapiens	116-121
33439649-5	2021	Here, we disclose a Smiles-type rearrangement, triggered by a phosphorus-containing unit (arylphosphoramidate), therefore called "phospho-Smiles" rearrangement, allowing a Csp2-Csp2 bond formation thanks to a 1,4-aryl migration reaction.	Phosphorus	62-72	regulator of calcineurin 2	Homo sapiens	177-181
33660361-5	2021	We for the first time showed that CENP-R does not directly interact with CENP-O/P in vitro, but indeed interact with CENP-U and CENP-Q.	Phosphorus	37-38	centromere protein U	Homo sapiens	117-123
33660361-5	2021	We for the first time showed that CENP-R does not directly interact with CENP-O/P in vitro, but indeed interact with CENP-U and CENP-Q.	Phosphorus	37-38	centromere protein Q	Homo sapiens	128-134
33660361-4	2021	Here, we identified the fragment (residues 241-360) of CENP-U and the C-terminal half of CENP-Q are essential to form a hetero-complex and interact with CENP-O/P sub-complex in vitro.	Phosphorus	58-59	centromere protein O	Homo sapiens	153-159
33564801-5	2021	When the Cu-Ni-S and Cu-Ni-P materials were assembled into a two-electrode system, the Cu-Ni-S/NF//Cu-Ni-P/NF electrode pairs display superior water splitting activity (1.50 V@20 mA cm-2), which is one of the best electrocatalytic activities reported so far.	Phosphorus	27-28	solute carrier family 5 member 5	Homo sapiens	90-94
33248835-6	2021	Cd-only and B[a]P-only single toxicant exposures caused a significant downregulation of cytochrome p4501a (CYP1A1) and metallothionein-2 (MT2) mRNA in the gills, respectively, however binary co-exposures using both toxicants resulted in strong up-regulation of CYP1A1 and MT2.	Phosphorus	16-17	cytochrome P450, family 1, subfamily A	Danio rerio	107-113
33248835-6	2021	Cd-only and B[a]P-only single toxicant exposures caused a significant downregulation of cytochrome p4501a (CYP1A1) and metallothionein-2 (MT2) mRNA in the gills, respectively, however binary co-exposures using both toxicants resulted in strong up-regulation of CYP1A1 and MT2.	Phosphorus	16-17	metallothionein 2	Danio rerio	119-136
33248835-6	2021	Cd-only and B[a]P-only single toxicant exposures caused a significant downregulation of cytochrome p4501a (CYP1A1) and metallothionein-2 (MT2) mRNA in the gills, respectively, however binary co-exposures using both toxicants resulted in strong up-regulation of CYP1A1 and MT2.	Phosphorus	16-17	metallothionein 2	Danio rerio	138-141
33248835-6	2021	Cd-only and B[a]P-only single toxicant exposures caused a significant downregulation of cytochrome p4501a (CYP1A1) and metallothionein-2 (MT2) mRNA in the gills, respectively, however binary co-exposures using both toxicants resulted in strong up-regulation of CYP1A1 and MT2.	Phosphorus	16-17	cytochrome P450, family 1, subfamily A	Danio rerio	261-267
33248835-6	2021	Cd-only and B[a]P-only single toxicant exposures caused a significant downregulation of cytochrome p4501a (CYP1A1) and metallothionein-2 (MT2) mRNA in the gills, respectively, however binary co-exposures using both toxicants resulted in strong up-regulation of CYP1A1 and MT2.	Phosphorus	16-17	metallothionein 2	Danio rerio	272-275
33243515-4	2021	The activities of polyphosphate kinase (PPK) and exopolyphosphatase (PPX) tightly associated with phosphorus biological removal ranged from 0.356 to 11.844 mumol hydroxamic acid min-1 mg-1 protein, and 0.008 to 0.446 mumol p-nitrophenol min-1 mg-1 protein, respectively.	Phosphorus	98-108	CD59 molecule (CD59 blood group)	Homo sapiens	178-188
33221014-12	2021	The KF exhibited relatively high P and K use efficiency because of their low availability in karst soils.	Phosphorus	33-34	arylformamidase	Homo sapiens	4-6
33334509-2	2021	To search for the new commercial sorbent and treatment strategy, an organic acrylic amine fiber (AAF) and phosphorus loading inorganic-organic AAF (P-AAF) were prepared and used for lead (Pb) removal from water.	Phosphorus	106-116	proteasomal ATPase associated factor 1	Homo sapiens	148-153
33243515-4	2021	The activities of polyphosphate kinase (PPK) and exopolyphosphatase (PPX) tightly associated with phosphorus biological removal ranged from 0.356 to 11.844 mumol hydroxamic acid min-1 mg-1 protein, and 0.008 to 0.446 mumol p-nitrophenol min-1 mg-1 protein, respectively.	Phosphorus	98-108	CD59 molecule (CD59 blood group)	Homo sapiens	237-247
33555173-4	2021	The combination of the CrBr3 monolayer with N-terminated GaN nanosheets leads to enhanced FM coupling via superexchange interactions between the Cr-t2g and Cr-eg orbitals, consequently resulting in a Curie temperature of CrBr3 of up to 67 K. Moreover, self-doped p-n junctions can be naturally formed in the heterostructures without additional modulation of external fields.	Phosphorus	96-97	gigaxonin	Homo sapiens	57-60
33279197-4	2021	The results of characterization techniques indicate that the introduced B and P atoms most probably to substitute for sp2-hybridized C atoms in triazine rings.	Phosphorus	78-79	Sp2 transcription factor	Homo sapiens	118-121
33754556-9	2021	Phosphorus fertilizer application caused phosphorus surplus in soils, which was low when the application rate was less than 60 kg hm-2.	Phosphorus	0-10	cholinergic receptor muscarinic 2	Homo sapiens	130-134
33690044-2	2021	In this study, a novel phosphorus-modified bamboo biochar (PBC) cross-linked Mg-Al layered double-hydroxide (LDH) composite ("PBC@LDH") was successfully prepared by phosphate pre-impregnation and a hydrothermal method with Mg-Al LDH.	Phosphorus	23-33	dihydrolipoamide S-acetyltransferase	Homo sapiens	126-133
33367328-6	2021	P-adsorbed Ce3+ ions (P-Ce3+) in Vo-CNPLs were efficiently destabilized in H2O2 solution (pH 5-6) rather than in HCl and HNO3 solutions (pH 3), and the presence of H2O2 readily released P from Ce3+ sites.	Phosphorus	0-1	carboxylesterase 1 pseudogene 1	Homo sapiens	22-27
33606750-6	2021	RESULTS: Pi (KH2PO4, NaH2PO4) but not organic P caused an increased apparent P digestibility and significantly influenced kinetics of serum FGF23, parathyroid hormone, P, CrossLaps and bonespecific alkaline phosphatase, demonstrating a disrupted calcium (Ca) and P homeostasis with potential harm for renal, cardiovascular and skeletal health.	Phosphorus	9-10	fibroblast growth factor 23	Canis lupus familiaris	140-145
33622322-3	2021	Variations of tumor protein 63 (TP63) was reported to be related to the phenotype of CL/P.	Phosphorus	33-34	tumor protein p63	Homo sapiens	14-30
33603371-8	2021	Results: The developed HApN exhibited a favorable crystalline structure, Ca:P elemental ratio (1.67), mesoporous nature, and large surface area.	Phosphorus	76-77	alanyl aminopeptidase, membrane	Homo sapiens	23-27
33128336-2	2021	Here, via a controllable NH 3 treatment, we construct sandwiched p-n homojunctions in three-unit-cells n-type SnS 2 (n-SnS 2 ) nanosheet arrays using nitrogen (N) as acceptor dopants.	Phosphorus	65-66	sodium voltage-gated channel alpha subunit 11	Homo sapiens	110-115
33357879-0	2021	Ultrastretchable, self-adhesive, strain-sensitive and self-healing GO@DA/Alginate/P(AAc-co-AAm) multifunctional hydrogels via mussel-inspired chemistry.	Phosphorus	82-83	glycine-N-acyltransferase	Homo sapiens	84-87
33357879-2	2021	Herein, inspired by nanocomposite, double-network (DN) and mussel chemistry, a new Graphene oxide@Dopamine/Alginate/Poly(acrylic acid-co-acrylamide) [GO@DA/Alginate/P(AAc-co-AAm)] hydrogel was fabricated through one-pot in-situ radical copolymerization.	Phosphorus	116-117	glycine-N-acyltransferase	Homo sapiens	167-170
33357879-4	2021	Alginate/P(AAc-co-AAm) DN matrix, physically and chemically crosslinked by Fe3+ and N,N"-Methylenebisacrylamide, made hydrogels ultrastretchable, self-healing and biocompatible.	Phosphorus	9-10	glycine-N-acyltransferase	Homo sapiens	11-14
33347265-5	2021	We found that a single intravenous administration of siRNA (3 mg/kg BW) conjugated to GPR8 (GPR8:PCK-1siRNA(3 mg/kg BW) conjugate) in an optimized N/P ratio exploited as a therapeutic nanoformulation maintained glucose homeostasis for nearly 4 weeks in the T2DM mice.	Phosphorus	87-88	phosphoenolpyruvate carboxykinase 1, cytosolic	Mus musculus	97-102
33250417-7	2021	Whereas, the addition of inhibitor U0126 down-regulated sharply the expression level of p-ERK, which indicated that cellular osteogenic differentiation of MC3T3-E1 cells was governed through alpha2beta1 integrin-mediated MEK/ERK signaling pathways during CoFe2O4/P(VDF-TrFE) nanocomposite coatings were combined with SMF.	Phosphorus	263-264	mitogen-activated protein kinase 1	Mus musculus	90-93
33017791-0	2021	Laser-induced twisting of phosphorus functionalized thiazolotriazole as a way of cholinesterase activity change.	Phosphorus	26-36	butyrylcholinesterase	Homo sapiens	81-95
33614704-8	2020	The straightening of TM5 modifies the structure of the P-N linker that sits above it, and which comprises the 351DKTG354 conserved motif, resulting in an increase of the distance between ATP and the phosphorylation site.	Phosphorus	55-56	tropomyosin 3	Homo sapiens	21-24
33159888-0	2021	Lack of endothelial nitric oxide synthase accelerates ectopic calcification in uremic mice fed an adenine and high phosphorus diet.	Phosphorus	115-125	nitric oxide synthase 3, endothelial cell	Mus musculus	8-41
33078876-3	2021	Reaction of the P=C-O-P compound with (tht)AuCl (tht = tetrahydrothiophene) showed dominant coordination on the sp 3 phosphorus, and complete coordination on the sp 2 phosphorus required removal of tetrahydrothiophene.	Phosphorus	167-177	Sp2 transcription factor	Homo sapiens	162-166
33643037-6	2020	The LC3B1 to LC-3B2 conversion was decreased, with increased P62 accumulation and decreased p-P62 expression.	Phosphorus	92-93	nucleoporin 62	Mus musculus	94-97
33557562-0	2021	In search of phosphorus in astronomical environments: The reaction between the CP radical (X2Sigma+) and methanimine.	Phosphorus	13-23	ceruloplasmin	Homo sapiens	79-81
33533005-1	2021	The pyrolyzation of sewage sludge (SS) could efficiently transform inherent phosphorus (P) into bioavailable phosphate forms, which endows SS-derived biochar (SSB) the potential as a soil fertilizer.	Phosphorus	76-86	small RNA binding exonuclease protection factor La	Homo sapiens	159-162
33533005-1	2021	The pyrolyzation of sewage sludge (SS) could efficiently transform inherent phosphorus (P) into bioavailable phosphate forms, which endows SS-derived biochar (SSB) the potential as a soil fertilizer.	Phosphorus	88-89	small RNA binding exonuclease protection factor La	Homo sapiens	159-162
33533005-2	2021	However, the details about the release behavior of P in SSB have not been systematically investigated.	Phosphorus	51-52	small RNA binding exonuclease protection factor La	Homo sapiens	56-59
33533005-5	2021	Acidic and alkaline conditions were favorable for the fast release of P from SSB.	Phosphorus	70-71	small RNA binding exonuclease protection factor La	Homo sapiens	77-80
33536578-5	2021	Our study shows the utility of NGS in unravelling the genetic origin of some disorders of the calcium and phosphorus metabolism, and confirms the GCM2 gene as an important element for the maintenance of calcium homeostasis.	Phosphorus	106-116	glial cells missing transcription factor 2	Homo sapiens	146-150
33308018-8	2021	We demonstrated that the incorporation of FGF23 and the soft tissue compartment is essential for accurate modeling of the changes in calcium, phosphorus, iPTH and calcitriol in CKD-MBD.	Phosphorus	142-152	fibroblast growth factor 23	Homo sapiens	42-47
33040555-1	2021	BACKGROUND: This study aims to evaluate the association between serum alkaline phosphatase (ALP), calcium (Ca) and phosphorus (P), C-reactive protein (CRP) and D-dimer (D-D), and hemoglobin (Hb) in postoperative and preoperative osteoporotic hip fracture elderly patients.	Phosphorus	115-125	alkaline phosphatase, placental	Homo sapiens	70-90
33040555-1	2021	BACKGROUND: This study aims to evaluate the association between serum alkaline phosphatase (ALP), calcium (Ca) and phosphorus (P), C-reactive protein (CRP) and D-dimer (D-D), and hemoglobin (Hb) in postoperative and preoperative osteoporotic hip fracture elderly patients.	Phosphorus	115-125	alkaline phosphatase, placental	Homo sapiens	92-95
33040555-1	2021	BACKGROUND: This study aims to evaluate the association between serum alkaline phosphatase (ALP), calcium (Ca) and phosphorus (P), C-reactive protein (CRP) and D-dimer (D-D), and hemoglobin (Hb) in postoperative and preoperative osteoporotic hip fracture elderly patients.	Phosphorus	94-95	alkaline phosphatase, placental	Homo sapiens	70-90
33040555-10	2021	The serum levels of ALP, which were adjusted by Ca and P, were associated with Hb and CRP, but not with D-D.	Phosphorus	22-23	C-reactive protein	Homo sapiens	86-89
33257046-3	2021	The results showed that NO3--N and total phosphorus (TP) could be effectively removed with maximum NO3--N reduction and TP removal efficiencies of 94.2% and 75.8% at current intensities of 200 and 400 mA, respectively.	Phosphorus	41-51	NBL1, DAN family BMP antagonist	Homo sapiens	99-102
33250417-7	2021	Whereas, the addition of inhibitor U0126 down-regulated sharply the expression level of p-ERK, which indicated that cellular osteogenic differentiation of MC3T3-E1 cells was governed through alpha2beta1 integrin-mediated MEK/ERK signaling pathways during CoFe2O4/P(VDF-TrFE) nanocomposite coatings were combined with SMF.	Phosphorus	263-264	midkine	Mus musculus	221-224
33502255-3	2021	Materials & methods: Molecular dynamics tools were utilized to simulate the influence of CNTs doped with phosphorus, nitrogen and bromine and nitrogen on the formation of alpha-synuclein amyloid.	Phosphorus	105-115	synuclein alpha	Homo sapiens	171-186
33393160-12	2021	MEG3 silencing and miR-214 overexpression elevated Ca and P and reduced ALP in OP rat serum, elevated osteoblast viability, differentiation ability, COL-I and COL-Chi expression and ALP activity, and reduced COL-II expression of osteoblasts.	Phosphorus	58-59	microRNA 214	Rattus norvegicus	19-26
33579456-8	2021	The MSC spheroids incorporated with collagen and BP implanted into OPF porous hydrogel (Col+BP/OPF) elicited a higher expression of Runx2, osteopontin, and alkaline phosphatase than blank spheroids implanted into OPF porous hydrogel (Control/OPF).	Phosphorus	49-51	RUNX family transcription factor 2	Homo sapiens	132-137
33579456-8	2021	The MSC spheroids incorporated with collagen and BP implanted into OPF porous hydrogel (Col+BP/OPF) elicited a higher expression of Runx2, osteopontin, and alkaline phosphatase than blank spheroids implanted into OPF porous hydrogel (Control/OPF).	Phosphorus	49-51	secreted phosphoprotein 1	Homo sapiens	139-150
33502255-5	2021	Conclusion: Doped-CNTs, especially phosphorus-doped carbon nanotube could effectively prevent alpha-synuclein amyloid formation, thus, it could be considered as a potential treatment for Parkinson"s disease.	Phosphorus	35-45	synuclein alpha	Homo sapiens	94-109
33153966-7	2021	The patients not achieving remission showed longer diabetes durations; higher circulating glucose levels; more intensive antidiabetic drug treatment, including insulin; and significantly lower p-Mg concentrations (.73 [+-.08] mmol/L compared with .80-.82 [+-.07] mmol/L, respectively; P < .01) than the groups showing remission or without diabetes before surgery.	Phosphorus	4-5	insulin	Homo sapiens	160-167
33184936-8	2021	We also found differential phosphorylation in response to phosphate and phosphite in 69 proteins, including splicing factors, translation factors, the PHT1;4 phosphate transporter and the HAT1 histone acetyltransferase-potential phospho-switches signalling changes in phosphorus nutrition.	Phosphorus	268-278	Homeobox-leucine zipper protein 4 (HB-4) / HD-ZIP protein	Arabidopsis thaliana	188-192
33385780-8	2021	Klotho and phosphorus CSF levels were lower in both HCRT- and HCRT+ than controls.	Phosphorus	11-21	hypocretin neuropeptide precursor	Homo sapiens	52-56
33385780-8	2021	Klotho and phosphorus CSF levels were lower in both HCRT- and HCRT+ than controls.	Phosphorus	11-21	hypocretin neuropeptide precursor	Homo sapiens	62-66
33556674-6	2021	PLEs were common in this sample, with 67.5% of individuals experiencing at least one CAPE-P item "often" or "almost always".	Phosphorus	0-1	structural maintenance of chromosomes 2	Homo sapiens	85-89
33708111-15	2020	More importantly, we firstly found that beneficial effects in vivo and in vitro of FPS on phosphorus reabsorption are closely associated with regulation of FGF23-Klotho signaling axis and ERK1/2-SGK1-NHERF-1-NaPi-2a pathway in the kidney.	Phosphorus	90-100	farnesyl diphosphate synthase	Rattus norvegicus	83-86
33554120-4	2021	Methods: Using in vivo phosphorus magnetization transfer spectroscopy, we measured CK first-order forward rate constant (k f ) in the frontal lobe, in patients with first-episode psychosis (FEP; n = 16) and healthy controls (n = 34), at rest.	Phosphorus	23-33	cytidine/uridine monophosphate kinase 1	Homo sapiens	83-85
33280914-6	2021	The high efficiency in P removal under anoxia and resuspension, the low risk of toxicity and the high maximum adsorption capacity makes CFH-12  a promising adsorbent for lake restoration.	Phosphorus	23-24	complement factor H	Homo sapiens	136-139
33486840-9	2022	The FAM83H enamel had higher roughness and lower lightness, density, nanohardness, and calcium and phosphorus levels than controls.	Phosphorus	99-109	family with sequence similarity 83 member H	Homo sapiens	4-10
33486840-13	2022	CONCLUSIONS: FAM83H enamel demonstrated decreased lightness, density, hardness, calcium, phosphorus, and defective ultrastructure.	Phosphorus	89-99	family with sequence similarity 83 member H	Homo sapiens	13-19
33483870-8	2021	Girls in the CL/P group had a significant lower probability of having a CVM score of at least CS3 in the subsample with age 11 to 12 (p = 0.001) and a borderline non-significant lower probability of having a CVM score of at least CS5 in the subsample with age 12 to 13 (p = 0.055).	Phosphorus	16-17	myozenin 3	Homo sapiens	94-97
33483870-8	2021	Girls in the CL/P group had a significant lower probability of having a CVM score of at least CS3 in the subsample with age 11 to 12 (p = 0.001) and a borderline non-significant lower probability of having a CVM score of at least CS5 in the subsample with age 12 to 13 (p = 0.055).	Phosphorus	16-17	chorionic somatomammotropin hormone like 1	Homo sapiens	230-233
33038288-2	2021	Reduction yielded the corresponding 2-aza-1,3-diphospha-indane-1,3-diyls ( 1 ), which can be described as phosphorus-centered singlet biradical(oid)s. Their stability depends on the size of the substituent R: While derivatives with R = Dmp (2,6-dimethylphenyl) or Ter (2,6-dimesitylphenyl) underwent oligomerisation, the derivative with very bulky R = t Bu Bhp (2,6-bis(benzhydryl)-4-tertbutylphenyl) was stable with respect to oligomerisation in its monomeric form.	Phosphorus	106-116	trans-2,3-enoyl-CoA reductase	Homo sapiens	264-267
32927176-1	2021	Phosphorus-doped g-C3N4/ZnIn2S4 (PCN/ZIS) heterojunction photocatalysts were constructed by solvothermal method.	Phosphorus	0-10	zinc finger RANBP2-type containing 2	Homo sapiens	37-40
33254792-0	2021	Development of a fast and ultrasensitive black phosphorus-based colorimetric/photothermal dual-readout immunochromatography for determination of norfloxacin in tap water and river water.	Phosphorus	47-57	nuclear RNA export factor 1	Homo sapiens	160-163
33519420-8	2020	The MPTP/p-treated mice also showed the high levels of alpha-synuclein and low levels of TH and DJ-1 in striatum, substantia nigra, olfactory bulb, hippocampus, amygdala, prefrontal cortex, locus coeruleus, or colon.	Phosphorus	9-10	synuclein, alpha	Mus musculus	55-70
33254834-9	2021	However, the P to Fe removal ratio was 0.32 mgP/mgFe, similar to the ratio observed previously without primary sedimentation (0.36 mgP/mgFe).	Phosphorus	13-14	matrix Gla protein	Homo sapiens	44-47
33519420-8	2020	The MPTP/p-treated mice also showed the high levels of alpha-synuclein and low levels of TH and DJ-1 in striatum, substantia nigra, olfactory bulb, hippocampus, amygdala, prefrontal cortex, locus coeruleus, or colon.	Phosphorus	9-10	tyrosine hydroxylase	Mus musculus	89-91
33519420-8	2020	The MPTP/p-treated mice also showed the high levels of alpha-synuclein and low levels of TH and DJ-1 in striatum, substantia nigra, olfactory bulb, hippocampus, amygdala, prefrontal cortex, locus coeruleus, or colon.	Phosphorus	9-10	Parkinson disease (autosomal recessive, early onset) 7	Mus musculus	96-100
33519420-9	2020	In addition, the expression levels of phosphorylated-alpha-synuclein and GFAP were elevated in the striatum and substantia nigra in the MPTP/p-treated mice.	Phosphorus	19-20	synuclein, alpha	Mus musculus	53-68
33519420-9	2020	In addition, the expression levels of phosphorylated-alpha-synuclein and GFAP were elevated in the striatum and substantia nigra in the MPTP/p-treated mice.	Phosphorus	19-20	glial fibrillary acidic protein	Mus musculus	73-77
33519420-10	2020	Taken together, our study clarifies that the chronic MPTP/p-treated mice have a variety of non-motor dysfunctions as well as motor abnormalities by alpha-synuclein overexpression and dopaminergic depletion.	Phosphorus	58-59	synuclein, alpha	Mus musculus	148-163
33436713-8	2021	The main independent risk factors associated with 72-h mortality among patients with AST levels >= 3000 U/L included higher serum values of alkaline phosphatase, creatine kinase, serum sodium, potassium, and phosphorus.	Phosphorus	208-218	solute carrier family 17 member 5	Homo sapiens	85-88
33007762-1	2021	We report on a systematic analysis of phosphorus diffusion in silicon on insulator thin film via spin-on-dopant process (SOD).	Phosphorus	38-48	superoxide dismutase 1	Homo sapiens	121-124
33372500-7	2021	Among four biochar, the fixation rate of phosphorus was the highest under the B1 treatment.With the ratios of B1, B2, and B3 fertilizers, the order of the fixation rate of the four biochars to phosphorus was:M-YM > YM > JG > JZ.	Phosphorus	41-51	immunoglobulin kappa variable 7-3 (pseudogene)	Homo sapiens	110-124
33561925-6	2021	The birds fed diets with exogenous multi-enzyme containing phytase had a significantly greater digestibility of dry matter, gross energy, crude protein, calcium, and phosphorus compared with birds fed non-supplemented diets (p<0.05).	Phosphorus	166-176	putative glycerophosphoryl diester phosphodiesterase	Glycine max	59-66
33413534-10	2021	CONCLUSIONS: In conclusion, we believe that low VDR levels can affect DDH regardless of the serum levels of Ca, P, ALP, and vitamin D.	Phosphorus	112-113	vitamin D receptor	Homo sapiens	48-51
33057486-0	2021	Light-accelerating oxidase-mimicking activity of black phosphorus quantum dots for colorimetric detection of acetylcholinesterase activity and inhibitor screening.	Phosphorus	55-65	acetylcholinesterase (Cartwright blood group)	Homo sapiens	109-129
33057486-1	2021	A feasible and sensitive colorimetric platform was established for the assay of acetylcholinesterase (AChE) activity and evaluation of its inhibitor screening, based upon the light-accelerating oxidase-mimicking activity of black phosphorus quantum dots (BP QDs).	Phosphorus	230-240	acetylcholinesterase (Cartwright blood group)	Homo sapiens	80-100
33057486-1	2021	A feasible and sensitive colorimetric platform was established for the assay of acetylcholinesterase (AChE) activity and evaluation of its inhibitor screening, based upon the light-accelerating oxidase-mimicking activity of black phosphorus quantum dots (BP QDs).	Phosphorus	230-240	acetylcholinesterase (Cartwright blood group)	Homo sapiens	102-106
33561925-7	2021	The chickens fed diets with exogenous multi-enzyme containing phytase showed a higher concentration of Ca and P in the serum (p<0.05).	Phosphorus	110-111	putative glycerophosphoryl diester phosphodiesterase	Glycine max	62-69
33492304-0	2021	Effect of Parathyroid Hormone on Intestinal Mucosal Sodium Dependent Phosphorus Transporter.	Phosphorus	69-79	parathyroid hormone	Mus musculus	10-29
33150413-10	2021	High phosphate intake in Fgf23  +/- mice also increased maternal serum phosphorus and FGF23 but there was no change in PTH.	Phosphorus	71-81	fibroblast growth factor 23	Mus musculus	25-30
33492304-4	2021	Based on these clinical phenomena, we hypothesized that high levels of parathyroid hormone (PTH) might inhibit intestinal phosphorus absorption which mediated by sodium-dependent phosphorus transporters.	Phosphorus	122-132	parathyroid hormone	Mus musculus	71-90
33001513-5	2021	In addition, the RNA expression of fibroblast growth factor 23, a bone-derived factor involved in the regulation of vitamin D metabolism, was significantly reduced with dietary P restriction.	Phosphorus	177-178	fibroblast growth factor 23	Ovis aries	35-62
33536709-0	2021	SLC37A2, a phosphorus-related molecule, increases in smooth muscle cells in the calcified aorta.	Phosphorus	11-21	solute carrier family 37 member 2	Rattus norvegicus	0-7
32386937-1	2021	Bone and mineral metabolism becomes dysregulated with progression of chronic kidney disease (CKD), and increasing levels of parathyroid hormone serve as an adaptive response to maintain normal phosphorus and calcium levels.	Phosphorus	193-203	parathyroid hormone	Homo sapiens	124-143
33188848-10	2021	Post pH-cycling, Ca/P ratio with 1%/2% Arg-NaF was closest to hydroxyapatite (1.67).	Phosphorus	0-1	C-X-C motif chemokine ligand 8	Homo sapiens	43-46
33000126-7	2021	The protein levels of CCK, Dyn A, and BDNF were reduced in the colon of MPTP- or MPTP/p-treated mice compared to those of the vehicle-treated group.	Phosphorus	4-5	cholecystokinin	Mus musculus	22-25
33000126-7	2021	The protein levels of CCK, Dyn A, and BDNF were reduced in the colon of MPTP- or MPTP/p-treated mice compared to those of the vehicle-treated group.	Phosphorus	4-5	brain derived neurotrophic factor	Mus musculus	38-42
33360573-9	2021	In conclusion, the low phosphorus diet can induce layer fatigue syndrome and affect the content of OPG and E2 in serum and the expression of OCN, OPG, RANK and RANKL in femur protein, which leads to the imbalance of bone homeostasis, the thinning of femur cortex bone and the decrease of bone density.	Phosphorus	23-33	TNF receptor superfamily member 11b	Gallus gallus	99-102
32743932-8	2021	RESULTS: Patients with higher levels of FGF23 were younger and had higher levels of serum albumin, creatinine, albumin-corrected calcium, phosphorus, PTH, 25(OH)-vitamin D, and had higher percentages of intravenous (IV) iron, IV vitamin D and cinacalcet use.	Phosphorus	138-148	fibroblast growth factor 23	Homo sapiens	40-45
33360573-9	2021	In conclusion, the low phosphorus diet can induce layer fatigue syndrome and affect the content of OPG and E2 in serum and the expression of OCN, OPG, RANK and RANKL in femur protein, which leads to the imbalance of bone homeostasis, the thinning of femur cortex bone and the decrease of bone density.	Phosphorus	23-33	TNF receptor superfamily member 11b	Gallus gallus	146-149
33360573-9	2021	In conclusion, the low phosphorus diet can induce layer fatigue syndrome and affect the content of OPG and E2 in serum and the expression of OCN, OPG, RANK and RANKL in femur protein, which leads to the imbalance of bone homeostasis, the thinning of femur cortex bone and the decrease of bone density.	Phosphorus	23-33	tumor necrosis factor superfamily member 11	Gallus gallus	160-165
33360573-9	2021	In conclusion, the low phosphorus diet can induce layer fatigue syndrome and affect the content of OPG and E2 in serum and the expression of OCN, OPG, RANK and RANKL in femur protein, which leads to the imbalance of bone homeostasis, the thinning of femur cortex bone and the decrease of bone density.	Phosphorus	23-33	bone gamma-carboxyglutamate protein	Gallus gallus	141-144
33370441-1	2020	The thermoluminescence relative efficiency, etaTST, of LiF:Mg,Ti and LiF:Mg,Cu,P following heavy charged particle irradiation is calculated using track structure theory and compared with experimental measurements.	Phosphorus	79-80	LIF interleukin 6 family cytokine	Homo sapiens	55-58
33396842-12	2020	Therefore, the p-CA extracted from BC in Taeniam might be a good alternative medicine to growth hormone (GH) therapy.	Phosphorus	15-16	growth hormone 1	Homo sapiens	89-103
33396842-12	2020	Therefore, the p-CA extracted from BC in Taeniam might be a good alternative medicine to growth hormone (GH) therapy.	Phosphorus	15-16	growth hormone 1	Homo sapiens	105-107
33370441-1	2020	The thermoluminescence relative efficiency, etaTST, of LiF:Mg,Ti and LiF:Mg,Cu,P following heavy charged particle irradiation is calculated using track structure theory and compared with experimental measurements.	Phosphorus	79-80	LIF interleukin 6 family cytokine	Homo sapiens	69-72
33300892-6	2020	The interface of the BP/GaN heterostructure is atomically sharp, which is very critical for high-performance device fabrication using a direct step in the future.	Phosphorus	21-23	gigaxonin	Homo sapiens	24-27
33210699-4	2020	The goal of this work is to develop a self-degradable nanoplatform based on polylysine (PLL)-functionalized black phosphorus (PBP) for the delivery of Cas13a/crRNA complexes to specifically inhibit Mcl-1 at transcriptional level for breast cancer therapy.	Phosphorus	108-124	polycystin 1, transient receptor potential channel interacting	Homo sapiens	126-129
33300892-11	2020	Combining the results of the experiment and simulation, it can be revealed that the P adatom on undulatory GaN is sufficiently mobile and the undulating surface of GaN plays a major role in forming high-quality thin-films of BP.	Phosphorus	225-227	gigaxonin	Homo sapiens	107-110
33300892-3	2020	Here, a facile, direct synthesis of highly crystalline thin-film BP on GaN(001) substrates is achieved by conversion of red phosphorus to BP under atmospheric pressure.	Phosphorus	65-67	gigaxonin	Homo sapiens	71-74
33300892-3	2020	Here, a facile, direct synthesis of highly crystalline thin-film BP on GaN(001) substrates is achieved by conversion of red phosphorus to BP under atmospheric pressure.	Phosphorus	120-134	gigaxonin	Homo sapiens	71-74
33300892-11	2020	Combining the results of the experiment and simulation, it can be revealed that the P adatom on undulatory GaN is sufficiently mobile and the undulating surface of GaN plays a major role in forming high-quality thin-films of BP.	Phosphorus	225-227	gigaxonin	Homo sapiens	164-167
33300892-3	2020	Here, a facile, direct synthesis of highly crystalline thin-film BP on GaN(001) substrates is achieved by conversion of red phosphorus to BP under atmospheric pressure.	Phosphorus	138-140	gigaxonin	Homo sapiens	71-74
33300892-12	2020	The preferentially covered nearby step growth mechanism discovered here may enable the mass production of high-quality thin-film BP, and could also be instrumental in achieving the epitaxial growth of thin-film BP on GaN and other 2D materials.	Phosphorus	129-131	gigaxonin	Homo sapiens	217-220
33300892-12	2020	The preferentially covered nearby step growth mechanism discovered here may enable the mass production of high-quality thin-film BP, and could also be instrumental in achieving the epitaxial growth of thin-film BP on GaN and other 2D materials.	Phosphorus	211-213	gigaxonin	Homo sapiens	217-220
33296208-1	2020	The influence of adding nanoparticles on the ascast morphology of spin coated immiscible polystyrene/poly(methyl methacrylate) (PS/PMMA) thin films of different thickness (hE) and composition (RB, volume ratio of PS to PMMA) has been explored in this article.	Phosphorus	128-130	spindlin 1	Homo sapiens	66-70
33296208-2	2020	To understand the precise effect of nanoparticle addition, the morphology of PS/PMMA thin blend films spin cast from toluene on a native oxide covered silicon wafer substrate was first investigated.	Phosphorus	77-79	spindlin 1	Homo sapiens	102-106
33089319-8	2020	We also found three rare variants in the KISS1R gene in three patients with PA: p.C95W (rs141767649), p.A189T (rs73507527) and p.R229R (rs115335009).	Phosphorus	62-63	KISS1 receptor	Homo sapiens	41-47
32949090-2	2020	Herein, we developed a simplified pressurized gas-assisted process, and first reported a non-metal single-atom phosphorus with atomic-level dispersion on unique single-crystal Mo 2 C hexagonal nanosheet arrays with (001) plane exposure supported by carbon sheet (SAP-Mo 2 C-CS).	Phosphorus	111-121	SH2 domain containing 1A	Homo sapiens	263-266
33348538-9	2020	The method showed optimal precision and accuracy, whereas stability was adequate up to 4 h at 20  C, 24 h at 4  C and 6 months at -20  C. PTH was positively associated with creatinine, phosphorus and IRIS stage.	Phosphorus	185-195	parathyroid hormone	Homo sapiens	138-141
33066959-3	2020	CD34 expression was detected in nFib cultures following the addition of a culture supernatant of blood mononuclear cells stimulated with phytohemagglutinin (PHA)-P.	Phosphorus	161-163	CD34 molecule	Homo sapiens	0-4
33119209-3	2020	The heterojunction of p-CuInS2 and n-type polymer (both PNDI3OT-Se1 and Se2) successfully made p-n junctions and showed improved charge transfer.	Phosphorus	22-23	fucosyltransferase 2	Homo sapiens	72-75
33166399-3	2020	B[a]P-induced gene repression is caused by abrogated E2F1 signalling.	Phosphorus	4-5	E2F transcription factor 1 L homeolog	Xenopus laevis	53-57
33306729-1	2020	BACKGROUND: Concentrations of fibroblast growth factor 23 (FGF-23), a hormone that regulates phosphorus and vitamin D metabolism, increase as kidney function declines.	Phosphorus	93-103	fibroblast growth factor 23	Homo sapiens	30-57
33306729-1	2020	BACKGROUND: Concentrations of fibroblast growth factor 23 (FGF-23), a hormone that regulates phosphorus and vitamin D metabolism, increase as kidney function declines.	Phosphorus	93-103	fibroblast growth factor 23	Homo sapiens	59-65
33098910-4	2020	AF4 allows separation of the micelles from plasma proteins, which showed that small non-crosslinked pCL9-PEG (17 nm) and pCL15-PEG (22 nm) micelles had lower stability in plasma than pCL23-PEG micelles with larger size (43 nm) and higher degree of crystallinity of pCL, and had also lower stability than covalently crosslinked p(CL9-DTC3.9)-PEG and p(CL18-DTC7.5)-PEG micelles with similar small sizes (~20 nm).	Phosphorus	13-14	AF4/FMR2 family member 1	Homo sapiens	0-3
33098910-4	2020	AF4 allows separation of the micelles from plasma proteins, which showed that small non-crosslinked pCL9-PEG (17 nm) and pCL15-PEG (22 nm) micelles had lower stability in plasma than pCL23-PEG micelles with larger size (43 nm) and higher degree of crystallinity of pCL, and had also lower stability than covalently crosslinked p(CL9-DTC3.9)-PEG and p(CL18-DTC7.5)-PEG micelles with similar small sizes (~20 nm).	Phosphorus	43-44	AF4/FMR2 family member 1	Homo sapiens	0-3
33297383-3	2020	Identifying the crystalline orientation of black phosphorus through Ag1 and Ag2 modes under the parallel polarization has high requirements on the Raman system, while in the nonanalyzer configuration, the crystalline orientation of the thick black phosphorus may not be identified through Ag1 and Ag2 modes.	Phosphorus	49-59	thioredoxin domain containing 12	Homo sapiens	68-71
33297383-3	2020	Identifying the crystalline orientation of black phosphorus through Ag1 and Ag2 modes under the parallel polarization has high requirements on the Raman system, while in the nonanalyzer configuration, the crystalline orientation of the thick black phosphorus may not be identified through Ag1 and Ag2 modes.	Phosphorus	49-59	anterior gradient 2, protein disulphide isomerase family member	Homo sapiens	76-79
33297383-3	2020	Identifying the crystalline orientation of black phosphorus through Ag1 and Ag2 modes under the parallel polarization has high requirements on the Raman system, while in the nonanalyzer configuration, the crystalline orientation of the thick black phosphorus may not be identified through Ag1 and Ag2 modes.	Phosphorus	49-59	thioredoxin domain containing 12	Homo sapiens	289-292
33297383-3	2020	Identifying the crystalline orientation of black phosphorus through Ag1 and Ag2 modes under the parallel polarization has high requirements on the Raman system, while in the nonanalyzer configuration, the crystalline orientation of the thick black phosphorus may not be identified through Ag1 and Ag2 modes.	Phosphorus	49-59	anterior gradient 2, protein disulphide isomerase family member	Homo sapiens	297-300
33403267-2	2020	The advantage of oligo-ester-ether-diol obtained from waste PET glycolysis is its application in r-PUF, generating a durable foam with excellent fire resistance at rather low loadings of phosphorus-nitrogen FRs (P-N FRs), especially in high moisture environments.	Phosphorus	187-197	NME/NM23 nucleoside diphosphate kinase 2	Homo sapiens	99-102
32814290-7	2020	The declining soil pH and increasing Olsen-phosphorus in soils with chemical fertilization dramatically reduced the cbbL gene diversity and accA gene abundances and altered both the autotrophic bacterial and archaeal community compositions.	Phosphorus	43-53	G protein-coupled receptor 3	Homo sapiens	140-144
33551536-1	2020	The use of the bis(1-piperidinyl)-substituted carbodiphosphorane (Ph2(Pip)P)2C (1) as an NCN ligand for the stabilization of phosphorus cations was studied.	Phosphorus	125-135	prolactin induced protein	Homo sapiens	70-73
33273568-0	2020	Increased expression of fibroblast growth factor 23 is the signature of a deteriorated Ca/P balance in ageing laying hens.	Phosphorus	90-91	fibroblast growth factor 23	Gallus gallus	24-51
32820865-3	2020	Specimens were cycled for 30 days between a demineralization solution (pH = 4) composed of 0.1 M lactic acid and 3 mM Ca3 (PO4 )2 for 4 hours and a remineralization solution (pH = 7.0) composed of 1.5 mM Ca, 0.9 mM P, and 20 mM Tris(hydroxymethyl)-aminomethane for 20 hours.	Phosphorus	123-124	carbonic anhydrase 3	Homo sapiens	118-121
33123371-3	2020	The gene for the enzyme 5,10-methylentetrahydrofolate reductase (MTHFR) contributes to folic acid metabolism, and polymorphisms of this gene at C677T (rs1801133) and A1298C (rs1801131) are reported to alter its enzyme activity and are suggested to be involved in CL/P development.	Phosphorus	266-267	methylenetetrahydrofolate reductase	Homo sapiens	24-63
33123371-3	2020	The gene for the enzyme 5,10-methylentetrahydrofolate reductase (MTHFR) contributes to folic acid metabolism, and polymorphisms of this gene at C677T (rs1801133) and A1298C (rs1801131) are reported to alter its enzyme activity and are suggested to be involved in CL/P development.	Phosphorus	266-267	methylenetetrahydrofolate reductase	Homo sapiens	65-70
32847703-15	2020	In a study using infigratinib, a drug that targets mutations in a gene called fibroblast growth factor receptor 3 (FGFR3), we found that elevated levels of phosphorous were associated with greater clinical benefit.	Phosphorus	156-167	fibroblast growth factor receptor 3	Homo sapiens	78-113
32847703-15	2020	In a study using infigratinib, a drug that targets mutations in a gene called fibroblast growth factor receptor 3 (FGFR3), we found that elevated levels of phosphorous were associated with greater clinical benefit.	Phosphorus	156-167	fibroblast growth factor receptor 3	Homo sapiens	115-120
33256381-4	2020	PAI-1 is found to co-localize in the cap of PS-exposing platelets with its cofactor, vitronectin, and fibrinogen.	Phosphorus	44-46	serpin family E member 1	Homo sapiens	0-5
33256381-4	2020	PAI-1 is found to co-localize in the cap of PS-exposing platelets with its cofactor, vitronectin, and fibrinogen.	Phosphorus	44-46	vitronectin	Homo sapiens	85-96
32151295-9	2020	Nut consumption was associated with significantly greater intakes of fibre, vitamin E, Fe, Mg and P.	Phosphorus	98-99	NUT midline carcinoma family member 1	Homo sapiens	0-3
33037651-9	2020	Log creatinine, log intact parathyroid hormone and log product of total calcium and phosphorus were independent predictors of log fibroblast growth factor-23.	Phosphorus	84-94	fibroblast growth factor 23	Canis lupus familiaris	130-157
33230902-2	2020	Herein, a facile, fast, and versatile laser direct write micro/nanoprocessing to fabricate diode, NPN (PNP) bipolar junction transistor (BJT) simultaneously based on a pre-fabricated black phosphorus/molybdenum disulfide heterostructure is demonstrated.	Phosphorus	189-199	purine nucleoside phosphorylase	Homo sapiens	103-106
33230977-2	2020	Here, a bioinspired staged bone regeneration strategy which loads bone morphogenetic protein2 (BMP2 )-modified black phosphorus (BP@BMP2 ) nanosheets to a polylactic acid (PLLA) electrospun fibrous scaffold, with a combination of recruiting osteoblast precursor cells and biomineralization properties for bone regeneration, is constructed successfully by micro-sol electrospinning technique.	Phosphorus	111-127	bone morphogenetic protein 2	Homo sapiens	66-93
33230977-2	2020	Here, a bioinspired staged bone regeneration strategy which loads bone morphogenetic protein2 (BMP2 )-modified black phosphorus (BP@BMP2 ) nanosheets to a polylactic acid (PLLA) electrospun fibrous scaffold, with a combination of recruiting osteoblast precursor cells and biomineralization properties for bone regeneration, is constructed successfully by micro-sol electrospinning technique.	Phosphorus	111-127	bone morphogenetic protein 2	Homo sapiens	95-99
33230977-2	2020	Here, a bioinspired staged bone regeneration strategy which loads bone morphogenetic protein2 (BMP2 )-modified black phosphorus (BP@BMP2 ) nanosheets to a polylactic acid (PLLA) electrospun fibrous scaffold, with a combination of recruiting osteoblast precursor cells and biomineralization properties for bone regeneration, is constructed successfully by micro-sol electrospinning technique.	Phosphorus	111-127	bone morphogenetic protein 2	Homo sapiens	132-136
33241671-5	2020	Density functional theory calculations confirm that the higher substitution of S atoms by P in MoS2 can form strong Mo 3d-S 2p-P 2p hybridizations at Fermi level, resulting in the narrower bandgap and smaller  GH * of hydrogen (H*) adsorption, thereby leading to the promoted HER activity.	Phosphorus	90-91	gamma-glutamyl hydrolase	Homo sapiens	210-212
33247205-0	2020	High-phosphorus diets reduce aortic lesions and cardiomyocyte size and modify lipid metabolism in Ldl receptor knockout mice.	Phosphorus	5-15	low density lipoprotein receptor	Mus musculus	98-110
33218179-5	2020	In addition, P supply provided the highest levels of total phenols and flavonoids at leaf level, together with the maximum in vitro antioxidant activities (FRAP and ORAC).	Phosphorus	13-14	mechanistic target of rapamycin kinase	Homo sapiens	156-160
32567741-4	2020	Synthetic applications of K[(R 2 N) 2 P(BH 3 )] were studied in reactions with a 1,2-dichlorodisilane and CS 2 , which afforded either mono- or difunctional phosphine boranes with a rare combination of electronegative amino and electropositive functional disilanyl groups on phosphorus, or a phosphinodithioformate.	Phosphorus	275-285	chorionic somatomammotropin hormone 2	Homo sapiens	106-110
33125007-0	2020	Enhancing photoelectrochemical performance of ZnIn2S4 by phosphorus doping for sensitive detection of miRNA-155.	Phosphorus	57-67	microRNA 155	Homo sapiens	102-111
33185198-1	2020	The soil pH plays a substantial role in controlling phosphorus (P) adsorption and mobilization.	Phosphorus	52-62	phenylalanine hydroxylase	Homo sapiens	9-11
33185198-1	2020	The soil pH plays a substantial role in controlling phosphorus (P) adsorption and mobilization.	Phosphorus	64-66	phenylalanine hydroxylase	Homo sapiens	9-11
33185198-4	2020	Periodic density functional theory (DFT) calculations were carried out to provide a molecular level understanding of the pH dependence of P adsorption.	Phosphorus	0-1	phenylalanine hydroxylase	Homo sapiens	121-123
32297512-8	2020	The coordination of an electron-rich NHC (IMe4) to the phosphorus atom in 5 precludes the pi-electron density transfer from the NHV to the phosphorus atom.	Phosphorus	55-65	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	Homo sapiens	42-46
32297512-8	2020	The coordination of an electron-rich NHC (IMe4) to the phosphorus atom in 5 precludes the pi-electron density transfer from the NHV to the phosphorus atom.	Phosphorus	139-149	methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit	Homo sapiens	42-46
33164509-8	2020	Moreover, the lattice spacing (d) of PCs varied with the expansion and contraction of the hydrogels, which can cause the color of P(NIPAM-AAc) hydrogel-functionalized textiles to change.	Phosphorus	37-38	glycine-N-acyltransferase	Homo sapiens	138-141
33244257-10	2020	Conclusion: This study demonstrated that in Chinese children and adolescents with short stature, circulating calcium and phosphorus concentrations may be associated with the regulation of IGF-1 levels, and this relationship merits further investigation.	Phosphorus	121-131	insulin like growth factor 1	Homo sapiens	188-193
33244257-0	2020	Association Between Serum Calcium and Phosphorus Levels and Insulin-Like Growth Factor-1 in Chinese Children and Adolescents with Short Stature.	Phosphorus	38-48	insulin like growth factor 1	Homo sapiens	60-88
32937706-2	2020	Herein, the multifunctional BP-RGO nanohybrids was fabricated by solvothermal strategy to improve the dispersion state of BP in epoxy resin (EP) and enhance its fire safety performance, where the reduced graphene oxide (RGO) was attached on the surface of BP via PC and POC bonds.	Phosphorus	28-30	epiregulin	Homo sapiens	141-143
33244257-1	2020	Objective: The aim of this study was to investigate the effect of serum calcium and phosphorus levels on the insulin-like growth factor 1 (IGF-1) in Chinese children and adolescents with short stature.	Phosphorus	84-94	insulin like growth factor 1	Homo sapiens	109-137
33244257-1	2020	Objective: The aim of this study was to investigate the effect of serum calcium and phosphorus levels on the insulin-like growth factor 1 (IGF-1) in Chinese children and adolescents with short stature.	Phosphorus	84-94	insulin like growth factor 1	Homo sapiens	139-144
33244257-4	2020	The relationship between the serum calcium and phosphorus levels and IGF-1 was analysed.	Phosphorus	47-57	insulin like growth factor 1	Homo sapiens	69-74
33244257-5	2020	Results: The univariate analysis results showed that serum calcium or phosphorus was significantly associated with IGF-1 SDS.	Phosphorus	70-80	insulin like growth factor 1	Homo sapiens	115-120
33244257-6	2020	In addition, after adjusting for possible confounding factors, a linear relationship between serum calcium and IGF-1 SDS and a non-linear relationship between serum phosphorus and IGF-1 SDS were observed by smooth curve fitting.	Phosphorus	165-175	insulin like growth factor 1	Homo sapiens	180-185
33244257-8	2020	In the multivariate piecewise linear regression, when the serum phosphorus level was greater than 1.26 mmol/L, the IGF-1 SDS increased with the increase in serum phosphorus (beta 1.92, 95% CI 1.36, 2.48; p < 0.001).	Phosphorus	64-74	insulin like growth factor 1	Homo sapiens	115-120
33244257-8	2020	In the multivariate piecewise linear regression, when the serum phosphorus level was greater than 1.26 mmol/L, the IGF-1 SDS increased with the increase in serum phosphorus (beta 1.92, 95% CI 1.36, 2.48; p < 0.001).	Phosphorus	162-172	insulin like growth factor 1	Homo sapiens	115-120
32861771-4	2020	Next, the polyplexes of star poly[N,N"-dimethylaminoethyl methacrylate-ran-di(ethylene glycol) methacrylate] (S-P(DMAEMA-DEGMA)) with pDNA, exhibiting a phase transition temperature (TCP) in culture medium DMEM, were deposited on S-POEGMA layers when the temperature increased above the TCP of polyplex.	Phosphorus	110-113	steroidogenic acute regulatory protein	Homo sapiens	24-28
32937706-2	2020	Herein, the multifunctional BP-RGO nanohybrids was fabricated by solvothermal strategy to improve the dispersion state of BP in epoxy resin (EP) and enhance its fire safety performance, where the reduced graphene oxide (RGO) was attached on the surface of BP via PC and POC bonds.	Phosphorus	122-124	epiregulin	Homo sapiens	141-143
33030162-4	2020	Reaction of (6-Dipp)CuPPh2 with isocyanates, isothiocyanates and carbon disulfide results in the insertion of the heterocumulene into the Cu-P bond.	Phosphorus	22-23	nudix hydrolase 3	Homo sapiens	15-19
33118809-4	2020	The specific amino acid sequence DpSpSEEKC has been previously suggested to be responsible for the strong binding abilities of the protein statherin to hydroxyapatite, where pS denotes phosphorylated serine.	Phosphorus	34-36	statherin	Homo sapiens	139-148
33207858-7	2020	In conclusion, mGluR5 pharmacological blockade reduced fat accumulation in HepG2 cells incubated with O/P, probably by modulating the expression of SREBP-1 and PPAR-alpha.	Phosphorus	104-105	glutamate receptor, ionotropic, kainate 1	Mus musculus	15-21
33207858-7	2020	In conclusion, mGluR5 pharmacological blockade reduced fat accumulation in HepG2 cells incubated with O/P, probably by modulating the expression of SREBP-1 and PPAR-alpha.	Phosphorus	104-105	sterol regulatory element binding transcription factor 1	Homo sapiens	148-155
33158444-15	2020	The NSPA/PTPMEG pathway emerges as a new regulator of glutamatergic transmission and plasticity and may provide mechanistic clues and therapeutic opportunities for anti-P-mediated pathogenicity in SLE, a still unmet need.	Phosphorus	6-7	protein tyrosine phosphatase, non-receptor type 4	Mus musculus	9-15
33164007-1	2020	A copper-chitosan-black phosphorus nanocomposite (CuNPs-Chit-BP) was fabricated by electrochemically depositing copper nanoparticles onto a black phosphorus-modified glassy carbon electrode in chitosan solution.	Phosphorus	24-34	chitinase 1	Homo sapiens	56-60
33078928-0	2020	Chemoselectivity for B-O and B-H Bond Cleavage by Pincer-Type Phosphorus Compounds: Theoretical and Experimental Studies.	Phosphorus	62-72	bleomycin hydrolase	Homo sapiens	29-32
32311684-5	2020	Coating of P(NIPAM-MAm) layer and embedding Fe3O4 NPs on the surface of HmSiO2 NPs was revealed by HRTEM analysis.	Phosphorus	11-12	sarcoglycan gamma	Homo sapiens	19-22
33078928-2	2020	Theoretical calculations reveal that a pincer-type phosphorus compound with an [ONO]3- ligand reacts with HBpin, leading to cleavage of the stronger B-O bonds (DeltaG   = 23.2 kcal mol-1) rather than the weaker B-H bond (DeltaG   = 26.4 kcal mol-1).	Phosphorus	51-61	bleomycin hydrolase	Homo sapiens	211-214
33078928-3	2020	A pincer-type phosphorus compound with a [NNN]3- ligand reacts with HBpin, leading to the weaker B-H bond cleavage (DeltaG   = 16.2 kcal mol-1) rather than cleavage of the stronger B-O bond (DeltaG   = 33.0 kcal mol-1).	Phosphorus	14-24	bleomycin hydrolase	Homo sapiens	97-100
32623200-1	2020	In this work, iron (oxyhydr)oxide nanoparticle-doped expanded graphite (IO/EG-1 and IO/EG-2) was prepared via a hydrothermal reaction and applied for the phosphorus adsorption in the aqueous solutions.	Phosphorus	154-164	mediator complex subunit 28	Homo sapiens	75-79
32673974-0	2020	Phosphorus-rich biochar produced through bean-worm skin waste pyrolysis enhances the adsorption of aqueous lead.	Phosphorus	0-10	brain expressed associated with NEDD4 1	Homo sapiens	41-45
32901861-0	2020	Fortified phosphorus-lowering treatment through administration of lanthanum protects against vascular calcification via regulation of FGF23 in chronic kidney disease.	Phosphorus	10-20	fibroblast growth factor 23	Homo sapiens	134-139
32822094-5	2020	Phosphoenzyme and pathway prediction analyses imply that inorganic pyrophosphatase is the most likely catalytic agent to cycle P in these environments, and this process will rapidly overtake other P utilization strategies.	Phosphorus	0-1	inorganic pyrophosphatase 1	Homo sapiens	57-82
32822094-5	2020	Phosphoenzyme and pathway prediction analyses imply that inorganic pyrophosphatase is the most likely catalytic agent to cycle P in these environments, and this process will rapidly overtake other P utilization strategies.	Phosphorus	127-128	inorganic pyrophosphatase 1	Homo sapiens	57-82
32401115-6	2020	In addition, Gene Ontology enrichment, Kyoto Gene-Encyclopedia and genomic analyses were conducted for the mRNAs differentially expressed under high phosphorus.Result: RT-qPCR results confirmed that the expression of RUNX2, BMP2 and osteocalcin in HP group exhibited significant increases than in control group (p < .05).	Phosphorus	149-159	RUNX family transcription factor 2	Homo sapiens	217-222
33142484-7	2020	Dietary Ca and P deficiencies significantly decreased serum Ca and P concentrations and increased serum parathyroid hormone (PTH) concentration, and serum Ca and 25-OH-D3 concentrations were significantly increased by 25-OH-D3 supplementation.	Phosphorus	15-16	parathyroid hormone	Homo sapiens	104-123
33142484-7	2020	Dietary Ca and P deficiencies significantly decreased serum Ca and P concentrations and increased serum parathyroid hormone (PTH) concentration, and serum Ca and 25-OH-D3 concentrations were significantly increased by 25-OH-D3 supplementation.	Phosphorus	15-16	parathyroid hormone	Homo sapiens	125-128
32401115-6	2020	In addition, Gene Ontology enrichment, Kyoto Gene-Encyclopedia and genomic analyses were conducted for the mRNAs differentially expressed under high phosphorus.Result: RT-qPCR results confirmed that the expression of RUNX2, BMP2 and osteocalcin in HP group exhibited significant increases than in control group (p < .05).	Phosphorus	149-159	bone morphogenetic protein 2	Homo sapiens	224-228
32401115-6	2020	In addition, Gene Ontology enrichment, Kyoto Gene-Encyclopedia and genomic analyses were conducted for the mRNAs differentially expressed under high phosphorus.Result: RT-qPCR results confirmed that the expression of RUNX2, BMP2 and osteocalcin in HP group exhibited significant increases than in control group (p < .05).	Phosphorus	149-159	bone gamma-carboxyglutamate protein	Homo sapiens	233-244
32401115-11	2020	The mRNA expression of NT5E and ICAM1 were higher in group HP, while MAP3K7CL was lower than CON group (p < .05).Conclusion: This study provided a working list of lncRNAs that may be relevant to osteogenic differentiation, which presents a new insights into the mechanism of vascular calcification induced by high phosphorus in VSMCs.	Phosphorus	314-324	5'-nucleotidase ecto	Homo sapiens	23-27
32768871-8	2020	Our results showed that low dietary phosphorus decreased the production performance, phosphorus content, and E2 and OPG levels, while increased calcium and PTH levels, and ALP and TRACP activities in laying hens.	Phosphorus	36-46	TNF receptor superfamily member 11b	Gallus gallus	116-119
32835668-11	2020	The expression of TNF-alpha was decreased in P-317-treated mice as compared to the vehicle-treated group.	Phosphorus	45-46	tumor necrosis factor	Mus musculus	18-27
32768871-8	2020	Our results showed that low dietary phosphorus decreased the production performance, phosphorus content, and E2 and OPG levels, while increased calcium and PTH levels, and ALP and TRACP activities in laying hens.	Phosphorus	36-46	parathyroid hormone	Gallus gallus	156-159
33050443-7	2020	The content of inorganic P fractions, including solution phosphate (Sol-P), aluminum phosphate (Al-P), iron phosphate (Fe-P), reduction phosphate (Red-P), and calcium phosphate (Ca-P), significantly increased by 0.25, 16.22, 22.08, 2.04, and 5.08 mg kg-1, respectively, in surface soil per 100 kg ha-1 P accumulated in the soil.	Phosphorus	25-26	Rho GTPase activating protein 45	Homo sapiens	297-301
32966495-7	2020	We use these films as active layers to demonstrate mm-sized BP heterojunction photodetectors with mA W-1 scale responsivities from the visible to the near-infrared.	Phosphorus	60-62	alcohol withdrawal 4	Mus musculus	98-104
32991664-4	2020	Here, we developed a tumor vaccine (hEX@BP) by encapsulating black phosphorus quantum dots (BPQDs) with exosomes (hEX) against a murine subcutaneous lung cancer model.	Phosphorus	67-77	hematopoietically expressed homeobox	Homo sapiens	36-39
32935698-3	2020	Herein, phosphorus-doping modulation is utilized to fabricate monoclinic P-CoMoO4 with optimized electron structure supported on nickel foam (P-CoMoO4/NF) for alkaline HER via a facile hydrothermal method, followed by low-temperature phosphidation.	Phosphorus	8-18	neurofascin	Homo sapiens	142-153
33090502-1	2020	PURPOSE: Phosphorous MR spectroscopy (31P-MRS) forms a powerful, non-invasive research tool to quantify the energetics of the heart in diverse patient populations.	Phosphorus	9-20	MROS	Homo sapiens	42-45
32852547-11	2020	In conclusion, AXT914 increased PTH secretion in rat models of post-surgical hypoparathyroidism, thereby correcting abnormal calcium and phosphorus homeostasis.	Phosphorus	137-147	parathyroid hormone	Rattus norvegicus	32-35
32485516-1	2020	The effect of acetate (HAc) and propionate (HPr) on denitrifying phosphorus removal (DPR) was evaluated in a novel two-sludge A2/O - MBBR (anaerobic/anoxic/oxic - moving bed biofilm reactor) system.	Phosphorus	65-75	haptoglobin-related protein	Homo sapiens	44-47
32270379-4	2020	The main purpose of the present study was the design and synthesis of phosphorus-based peptidyl antagonists of IAPs that mimic the endogenous Smac protein, which blocks the interaction between IAPs and caspases.	Phosphorus	70-80	diablo IAP-binding mitochondrial protein	Homo sapiens	142-146
32583114-12	2020	These findings demonstrated the efficiency of HFe in removing of phosphorus from wastewater.	Phosphorus	65-75	homeostatic iron regulator	Homo sapiens	46-49
32511868-1	2020	Parathyroid glands (PTGs) are important endocrine organs being mainly responsible for the secretion of parathyroid hormone (PTH) to regulate the balance of calcium (Ca) /phosphorus (P) ions in the body.	Phosphorus	170-180	parathyroid hormone	Homo sapiens	103-122
32464336-5	2020	Moreover, the DFT calculation coupled with experiment (Mott-Schottky curves) illustrates the electron transfer behavior of CdS QDs/P-CNT, showing that the Cd-1 site should be the main active center and P doping is beneficial to increase H2 production.	Phosphorus	131-132	CD1c molecule	Homo sapiens	155-159
32511868-1	2020	Parathyroid glands (PTGs) are important endocrine organs being mainly responsible for the secretion of parathyroid hormone (PTH) to regulate the balance of calcium (Ca) /phosphorus (P) ions in the body.	Phosphorus	170-180	parathyroid hormone	Homo sapiens	124-127
32511868-1	2020	Parathyroid glands (PTGs) are important endocrine organs being mainly responsible for the secretion of parathyroid hormone (PTH) to regulate the balance of calcium (Ca) /phosphorus (P) ions in the body.	Phosphorus	0-1	parathyroid hormone	Homo sapiens	103-122
32511868-1	2020	Parathyroid glands (PTGs) are important endocrine organs being mainly responsible for the secretion of parathyroid hormone (PTH) to regulate the balance of calcium (Ca) /phosphorus (P) ions in the body.	Phosphorus	0-1	parathyroid hormone	Homo sapiens	124-127
32511868-2	2020	Once PTGs get injured or removed, their resulting defect or loss of PTH secretion should disturb the level of Ca/P in blood, thus damaging other related organs (bone, kidney, etc.)	Phosphorus	5-6	parathyroid hormone	Homo sapiens	68-71
33071826-11	2020	The first PC (PC-1; 63.12%) was positively related to P, Cl, and Na, and negatively related to C. The second principal component (23.01%) was mainly positively related to C. In the space defined by the two extracted PC (PC-1 and PC-2), the elementome of tick samples was clearly associated with tick species, but not with developmental stages, hosts or geographic locations.	Phosphorus	10-11	proprotein convertase subtilisin/kexin type 1	Homo sapiens	14-18
32988521-5	2020	Moreover, the addition of phytase linearly increased (P < 0.05) dietary protein, Ca, and phosphorus (P) utilization as well as nitrogen output, and excreta iron, copper, manganese, and zinc concentration quadratically increased (P < 0.05) as well as P output.	Phosphorus	89-99	putative glycerophosphoryl diester phosphodiesterase	Glycine max	26-33
32988521-5	2020	Moreover, the addition of phytase linearly increased (P < 0.05) dietary protein, Ca, and phosphorus (P) utilization as well as nitrogen output, and excreta iron, copper, manganese, and zinc concentration quadratically increased (P < 0.05) as well as P output.	Phosphorus	54-55	putative glycerophosphoryl diester phosphodiesterase	Glycine max	26-33
32812591-5	2020	The review is devoted to recent advances of using isolable silylenes and corresponding silylene-metal complexes for the activation of fundamental but inert molecules such as H2, COx, N2O, O2, H2O, NH3, C2H4 and E4 (E = P, As).	Phosphorus	219-220	cytochrome c oxidase subunit 8A	Homo sapiens	178-181
32833441-1	2020	Studies with acetylcholinesterase (AChE) inhibited by organophosphorus (OP) compounds with two chiral centers can serve as models or surrogates for understanding the rate, orientation and post-inhibitory mechanisms by the nerve agent, soman that possesses dual phosphorus and carbon chiral centers.	Phosphorus	60-70	acetylcholinesterase	Mus musculus	13-33
32833441-1	2020	Studies with acetylcholinesterase (AChE) inhibited by organophosphorus (OP) compounds with two chiral centers can serve as models or surrogates for understanding the rate, orientation and post-inhibitory mechanisms by the nerve agent, soman that possesses dual phosphorus and carbon chiral centers.	Phosphorus	60-70	acetylcholinesterase	Mus musculus	35-39
32909555-2	2020	In this work, the role of phosphorus as an acceptor from the pi electron cloud (Ppi pnicogen or phosphorus bonding) in PCl3-C2H2 and PCl3-C2H4 heterodimers is explored, by combining matrix isolation infrared spectroscopy with ab initio and DFT computational methodologies.	Phosphorus	26-36	PHD finger protein 19	Homo sapiens	119-123
32909555-2	2020	In this work, the role of phosphorus as an acceptor from the pi electron cloud (Ppi pnicogen or phosphorus bonding) in PCl3-C2H2 and PCl3-C2H4 heterodimers is explored, by combining matrix isolation infrared spectroscopy with ab initio and DFT computational methodologies.	Phosphorus	26-36	PHD finger protein 19	Homo sapiens	133-137
32909555-2	2020	In this work, the role of phosphorus as an acceptor from the pi electron cloud (Ppi pnicogen or phosphorus bonding) in PCl3-C2H2 and PCl3-C2H4 heterodimers is explored, by combining matrix isolation infrared spectroscopy with ab initio and DFT computational methodologies.	Phosphorus	96-106	PHD finger protein 19	Homo sapiens	119-123
32909555-2	2020	In this work, the role of phosphorus as an acceptor from the pi electron cloud (Ppi pnicogen or phosphorus bonding) in PCl3-C2H2 and PCl3-C2H4 heterodimers is explored, by combining matrix isolation infrared spectroscopy with ab initio and DFT computational methodologies.	Phosphorus	96-106	PHD finger protein 19	Homo sapiens	133-137
32909555-3	2020	The respective potential energy surfaces of the PCl3-C2H2 and PCl3-C2H4 heterodimers reveal unique minima stabilized by a concert of reasonably strong to weak interactions, of which Ppi phosphorus bonding was energetically dominant.	Phosphorus	186-196	PHD finger protein 19	Homo sapiens	48-52
32909555-3	2020	The respective potential energy surfaces of the PCl3-C2H2 and PCl3-C2H4 heterodimers reveal unique minima stabilized by a concert of reasonably strong to weak interactions, of which Ppi phosphorus bonding was energetically dominant.	Phosphorus	186-196	PHD finger protein 19	Homo sapiens	62-66
32909555-5	2020	The dominance of phosphorus bonding in the PCl3-C2H2 and PCl3-C2H4 heterodimers over other interactions (such as Hpi, HCl, HP, Clpi and lone pair-pi interactions) was confirmed and substantiated using extended quantum theory of atoms in molecules, natural bond orbital, electrostatic potential mapping and energy decomposition analyses.	Phosphorus	17-27	PHD finger protein 19	Homo sapiens	43-47
32909555-5	2020	The dominance of phosphorus bonding in the PCl3-C2H2 and PCl3-C2H4 heterodimers over other interactions (such as Hpi, HCl, HP, Clpi and lone pair-pi interactions) was confirmed and substantiated using extended quantum theory of atoms in molecules, natural bond orbital, electrostatic potential mapping and energy decomposition analyses.	Phosphorus	17-27	PHD finger protein 19	Homo sapiens	57-61
33455288-3	2020	Here we report a new inorganic nanosystem, which uses ultrathin black phosphorus (BP) nanosheets (minimum: 13 nm) as carriers and equips with up-conversion luminescence (UCL) nanoparticles as imaging probes, so that the system can generate photothermal and photodynamic effects to treat tumors together with immunotherapy.	Phosphorus	82-84	sulfite oxidase	Mus musculus	208-210
32812766-0	2020	Spin-polarized Molecular Triplet States as Qubits: Phosphorus Hyperfine Coupling in the Triplet State of Benzoisophosphinoline.	Phosphorus	51-61	spindlin 1	Homo sapiens	0-4
33047021-3	2020	Results show that compared with the base oil of liquid paraffin (LP), the coefficient of friction and wear rate of the BP nanosheets as the additives in liquid paraffin (BP-LP) are lower for the same loads.	Phosphorus	119-121	opiorphin prepropeptide	Homo sapiens	170-175
32897714-3	2020	Remarkably, the phosphorus center of the PS3 ligand undergoes protonation with hydrochloric acid.	Phosphorus	16-26	taste 2 receptor member 6 pseudogene	Homo sapiens	41-44
32789342-1	2020	Efficient synthesis of o-borylphenols is achieved through the Ru-catalyzed regio- and site-selective sp2 C-H borylation of aryl diphenylphosphinites followed by removal of the phosphorus directing group.	Phosphorus	176-186	Sp2 transcription factor	Homo sapiens	101-104
30888252-7	2020	In addition, the growth of internal pores in AACP promoted the removal of phosphorus and nitrogen.	Phosphorus	74-84	N-acetyltransferase pseudogene	Homo sapiens	45-49
33146328-0	2020	Calcium and Phosphorus Levels in Saliva are Influenced by Genetic Polymorphisms in Estrogen Receptor Alpha and Microrna17.	Phosphorus	12-22	estrogen receptor 1	Homo sapiens	83-106
33146328-0	2020	Calcium and Phosphorus Levels in Saliva are Influenced by Genetic Polymorphisms in Estrogen Receptor Alpha and Microrna17.	Phosphorus	12-22	microRNA 17	Homo sapiens	111-121
33146328-2	2020	The aim of this study was to evaluate if polymorphisms in ESR1 (Estrogen Receptor Alpha), ESR2 (Estrogen Receptor Beta) and miRNA17 (microRNA17) are associated with calcium and phosphorus levels in saliva.	Phosphorus	177-187	estrogen receptor 1	Homo sapiens	58-62
33146328-2	2020	The aim of this study was to evaluate if polymorphisms in ESR1 (Estrogen Receptor Alpha), ESR2 (Estrogen Receptor Beta) and miRNA17 (microRNA17) are associated with calcium and phosphorus levels in saliva.	Phosphorus	177-187	estrogen receptor 2	Homo sapiens	90-94
33146328-2	2020	The aim of this study was to evaluate if polymorphisms in ESR1 (Estrogen Receptor Alpha), ESR2 (Estrogen Receptor Beta) and miRNA17 (microRNA17) are associated with calcium and phosphorus levels in saliva.	Phosphorus	177-187	microRNA 17	Homo sapiens	124-131
33146328-2	2020	The aim of this study was to evaluate if polymorphisms in ESR1 (Estrogen Receptor Alpha), ESR2 (Estrogen Receptor Beta) and miRNA17 (microRNA17) are associated with calcium and phosphorus levels in saliva.	Phosphorus	177-187	microRNA 17	Homo sapiens	133-143
33146328-8	2020	The less common allele of ESR1 rs1884051 was associated with lower phosphorus levels (p=0.005) and there was an excess of heterozygotes for miRNA17 rs4284505 among individuals with lower calcium levels (p=0.002), both adjusted by sex.	Phosphorus	67-77	estrogen receptor 1	Homo sapiens	26-30
33146328-9	2020	This study provides evidence that genetic polymorphisms in ESR1 and miRNA17 are involved in determining salivary calcium and phosphorus levels.	Phosphorus	125-135	estrogen receptor 1	Homo sapiens	59-63
33146328-9	2020	This study provides evidence that genetic polymorphisms in ESR1 and miRNA17 are involved in determining salivary calcium and phosphorus levels.	Phosphorus	125-135	microRNA 17	Homo sapiens	68-75
32417213-3	2020	Parathyroid hormone (PTH) is a crucial hormone for the metabolism of calcium and phosphorus whose result can lead to erroneous diagnoses and medical actions if adequate reference intervals are not readily available.	Phosphorus	81-91	parathyroid hormone	Homo sapiens	0-19
32417213-3	2020	Parathyroid hormone (PTH) is a crucial hormone for the metabolism of calcium and phosphorus whose result can lead to erroneous diagnoses and medical actions if adequate reference intervals are not readily available.	Phosphorus	81-91	parathyroid hormone	Homo sapiens	21-24
33015068-2	2020	Physiologically, the maintenance of calcium and phosphorus homeostasis is achieved via a variety of concerted actions of hormones such as parathyroid hormone (PTH), vitamin D, and fibroblast growth factor (FGF23), which could be regulated mainly at three organs, the intestine, kidney, and bone.	Phosphorus	48-58	parathyroid hormone	Homo sapiens	138-157
33015068-2	2020	Physiologically, the maintenance of calcium and phosphorus homeostasis is achieved via a variety of concerted actions of hormones such as parathyroid hormone (PTH), vitamin D, and fibroblast growth factor (FGF23), which could be regulated mainly at three organs, the intestine, kidney, and bone.	Phosphorus	48-58	fibroblast growth factor 23	Homo sapiens	206-211
33015068-7	2020	Therefore, in this review, we will give a systematic introduction on PTH-1,25(OH)2D-FGF23 axis in the disorders of calcium and phosphorus metabolism, diagnostic biomarkers identified, and potential altered metabolic pathways involved.	Phosphorus	127-137	parathyroid hormone	Homo sapiens	69-74
33015068-7	2020	Therefore, in this review, we will give a systematic introduction on PTH-1,25(OH)2D-FGF23 axis in the disorders of calcium and phosphorus metabolism, diagnostic biomarkers identified, and potential altered metabolic pathways involved.	Phosphorus	127-137	fibroblast growth factor 23	Homo sapiens	84-89
32907583-9	2020	Interestingly, the protein corona formed by human albumin significantly induced the transfer of PS-particles across the tissue compared to the formed IgG-corona.	Phosphorus	96-98	albumin	Homo sapiens	50-57
33124283-8	2020	The TN/TP of lakes and reservoirs had a significant correlation with the lake depth in both spring and summer, indicating that lake depth is a key factor affecting the ratio of nitrogen and phosphorus.	Phosphorus	190-200	C-type lectin domain family 3 member B	Homo sapiens	4-9
33124283-9	2020	In addition, in eutrophic lakes with higher absolute nutrient concentrations, TN/TP has less effect on phytoplankton, while in deep-water lakes with lower absolute nutrient concentrations, TN/TP can determine the growth of phytoplankton limited by phosphorus.	Phosphorus	248-258	C-type lectin domain family 3 member B	Homo sapiens	78-80
32255272-6	2020	More importantly, the inactivation of CaMK II/PKC/PKA-ERK-CREB signaling pathways in hippocampus was detected at both the 2.5 and 6.25 mg/kg B[a]P-treated groups, indicating that multiple targets in NMDAR and downstream signaling pathways are involved in the B[a]P-induced neurotoxicity.	Phosphorus	46-47	Eph receptor B1	Rattus norvegicus	54-57
32255272-6	2020	More importantly, the inactivation of CaMK II/PKC/PKA-ERK-CREB signaling pathways in hippocampus was detected at both the 2.5 and 6.25 mg/kg B[a]P-treated groups, indicating that multiple targets in NMDAR and downstream signaling pathways are involved in the B[a]P-induced neurotoxicity.	Phosphorus	46-47	cAMP responsive element binding protein 1	Rattus norvegicus	58-62
32255272-6	2020	More importantly, the inactivation of CaMK II/PKC/PKA-ERK-CREB signaling pathways in hippocampus was detected at both the 2.5 and 6.25 mg/kg B[a]P-treated groups, indicating that multiple targets in NMDAR and downstream signaling pathways are involved in the B[a]P-induced neurotoxicity.	Phosphorus	50-51	protein kinase C, gamma	Rattus norvegicus	46-49
32255272-6	2020	More importantly, the inactivation of CaMK II/PKC/PKA-ERK-CREB signaling pathways in hippocampus was detected at both the 2.5 and 6.25 mg/kg B[a]P-treated groups, indicating that multiple targets in NMDAR and downstream signaling pathways are involved in the B[a]P-induced neurotoxicity.	Phosphorus	50-51	Eph receptor B1	Rattus norvegicus	54-57
32255272-6	2020	More importantly, the inactivation of CaMK II/PKC/PKA-ERK-CREB signaling pathways in hippocampus was detected at both the 2.5 and 6.25 mg/kg B[a]P-treated groups, indicating that multiple targets in NMDAR and downstream signaling pathways are involved in the B[a]P-induced neurotoxicity.	Phosphorus	50-51	cAMP responsive element binding protein 1	Rattus norvegicus	58-62
33419493-5	2020	The heat generated by black phosphorus (BP) under 808 nm near-infrared laser irradiation accelerates the F127 gel ablation and the release of GM-CSF, which recruit APC cells and prime the native T cells.	Phosphorus	22-38	colony stimulating factor 2 (granulocyte-macrophage)	Mus musculus	142-148
32552012-2	2020	In addition to vitamin D receptor activator, cinacalcet has recently been widely used for SHPT management, and the significant suppression of parathyroid hormone (PTH) with better control of serum calcium and phosphorus has been reported.	Phosphorus	209-219	parathyroid hormone	Homo sapiens	142-161
32552012-2	2020	In addition to vitamin D receptor activator, cinacalcet has recently been widely used for SHPT management, and the significant suppression of parathyroid hormone (PTH) with better control of serum calcium and phosphorus has been reported.	Phosphorus	209-219	parathyroid hormone	Homo sapiens	163-166
32913635-2	2020	The retention of phosphorus and the reductions in calcium and vitamin D levels stimulate the synthesis and secretion of parathyroid hormone as well as the proliferation rate of parathyroid cells.	Phosphorus	17-27	parathyroid hormone	None	120-139
33419493-5	2020	The heat generated by black phosphorus (BP) under 808 nm near-infrared laser irradiation accelerates the F127 gel ablation and the release of GM-CSF, which recruit APC cells and prime the native T cells.	Phosphorus	40-42	colony stimulating factor 2 (granulocyte-macrophage)	Mus musculus	142-148
32934772-6	2020	To target the interaction of 14-3-3epsilon with CDC25A for cancer therapy, we developed two novel phospho-peptides, pS and pT, corresponding to each of the 14-3-3 binding sites of CDC25A, to specifically interfere with 14-3-3epsilon binding to CDC25A.	Phosphorus	116-118	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon	Homo sapiens	29-42
32652893-7	2020	CONCLUSION: Our results reveal that affected children with the novel pathogenetic mutations p.C242R and p.S445* in the MCM8 gene are characterized by POI, short stature, cancer susceptibility, and genomic instability.	Phosphorus	69-70	minichromosome maintenance 8 homologous recombination repair factor	Homo sapiens	119-123
32934772-6	2020	To target the interaction of 14-3-3epsilon with CDC25A for cancer therapy, we developed two novel phospho-peptides, pS and pT, corresponding to each of the 14-3-3 binding sites of CDC25A, to specifically interfere with 14-3-3epsilon binding to CDC25A.	Phosphorus	116-118	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta	Homo sapiens	29-35
32934772-6	2020	To target the interaction of 14-3-3epsilon with CDC25A for cancer therapy, we developed two novel phospho-peptides, pS and pT, corresponding to each of the 14-3-3 binding sites of CDC25A, to specifically interfere with 14-3-3epsilon binding to CDC25A.	Phosphorus	116-118	cell division cycle 25A	Homo sapiens	180-186
32934772-6	2020	To target the interaction of 14-3-3epsilon with CDC25A for cancer therapy, we developed two novel phospho-peptides, pS and pT, corresponding to each of the 14-3-3 binding sites of CDC25A, to specifically interfere with 14-3-3epsilon binding to CDC25A.	Phosphorus	116-118	cell division cycle 25A	Homo sapiens	180-186
32934772-7	2020	Peptides pT (IC50 = 22.1 muM), and pS (IC50 = 29 muM) induced SCC cell death and blocked 14-3-3epsilon binding to CDC25A.	Phosphorus	35-37	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon	Homo sapiens	89-102
32934772-7	2020	Peptides pT (IC50 = 22.1 muM), and pS (IC50 = 29 muM) induced SCC cell death and blocked 14-3-3epsilon binding to CDC25A.	Phosphorus	35-37	cell division cycle 25A	Homo sapiens	114-120
32934772-8	2020	pS or pT treatment of SCC xenografts increased apoptotic cell death and decreased pro-survival P-Akt (S473) and Survivin, demonstrating the effectiveness of the peptides in vivo.	Phosphorus	0-2	AKT serine/threonine kinase 1	Homo sapiens	97-100
32680974-0	2020	Spatial divergence of PHR-PHT1 modules maintains phosphorus homeostasis in soybean nodules.	Phosphorus	49-59	CPD photolyase	Glycine max	22-25
32680974-0	2020	Spatial divergence of PHR-PHT1 modules maintains phosphorus homeostasis in soybean nodules.	Phosphorus	49-59	inorganic phosphate transporter 1-3	Glycine max	26-30
32871939-2	2020	The calcium-sensitive receptor (CaSR) plays an important role in calcium and phosphorus metabolism.	Phosphorus	77-87	calcium sensing receptor	Homo sapiens	4-30
32497684-5	2020	Passive dosing was applied in a novel format to expose the MCL-5 human lymphoblastoid cell line to the pro-carcinogen, benzo[a]pyrene (B[a]P) and was compared to solvent (dimethyl sulphoxide) spiked B[a]P exposures over 48 h. Passive dosing induced greater changes, at lower concentrations, to micronucleus frequency, p21 mRNA expression, cell cycle abnormalities, and cell and nuclear morphology.	Phosphorus	0-1	H3 histone pseudogene 16	Homo sapiens	318-321
32871939-2	2020	The calcium-sensitive receptor (CaSR) plays an important role in calcium and phosphorus metabolism.	Phosphorus	77-87	calcium sensing receptor	Homo sapiens	32-36
32824729-1	2020	Aprepitant, a lipophilic and small molecular representative of neurokinin 1 receptor antagonists, is known for its anti-proliferative activity on numerous cancer cell lines that are sensitive to Substance P mitogen action.	Phosphorus	205-206	tachykinin receptor 1	Rattus norvegicus	63-84
32417473-4	2020	A BC addition of 30 t ha-1 increased soil test phosphorus and decreased bulk density in the surface soil but did not significantly change pH or water retention properties, and most importantly, did not increase the yield.	Phosphorus	47-57	Rho GTPase activating protein 45	Homo sapiens	22-26
32417482-0	2020	Temporal and spatial variations of alkaline phosphatase activity related to phosphorus status of phytoplankton in the East China Sea.	Phosphorus	76-86	Alkaline phosphatase 4	Drosophila melanogaster	35-55
32784565-1	2020	Missense, nonsense, splice site and regulatory region variants in interferon regulatory factor 6 (IRF6) have been shown to contribute to both syndromic and non-syndromic forms of cleft lip and/or palate (CL/P).	Phosphorus	207-208	interferon regulatory factor 6	Homo sapiens	66-96
32824421-6	2020	The dietary supplementation of the MCPC increased (p < 0.05) the AID of phosphorus (P) and calcium (Ca) by 34.2% and 31.1% for BD1 and 26.7% and 41.3% for BD2, respectively, and increased (p < 0.05) ATTD of crude fat, P, and Ca by 1.4%, 45.6%, and 9.6% for BD1 and 3.1%, 66.0%, and 52.7% for BD2, respectively.	Phosphorus	37-38	beta-defensin 1	Sus scrofa	127-130
32824421-6	2020	The dietary supplementation of the MCPC increased (p < 0.05) the AID of phosphorus (P) and calcium (Ca) by 34.2% and 31.1% for BD1 and 26.7% and 41.3% for BD2, respectively, and increased (p < 0.05) ATTD of crude fat, P, and Ca by 1.4%, 45.6%, and 9.6% for BD1 and 3.1%, 66.0%, and 52.7% for BD2, respectively.	Phosphorus	37-38	beta-defensin 1	Sus scrofa	257-260
32784565-1	2020	Missense, nonsense, splice site and regulatory region variants in interferon regulatory factor 6 (IRF6) have been shown to contribute to both syndromic and non-syndromic forms of cleft lip and/or palate (CL/P).	Phosphorus	207-208	interferon regulatory factor 6	Homo sapiens	98-102
32802956-5	2020	Results: Using ES, we discovered individuals with known pathogenic SNVs in GBA (p.Glu365Lys, p.Thr408Met, p.Asn409Ser, and p.Leu483Pro) and LRRK2 (p.Arg1441Gly and p.Gly2019Ser).	Phosphorus	56-57	glucosylceramidase beta	Homo sapiens	75-78
32526547-5	2020	The effects of low dietary phosphorus on the endocrine and tibial osteoprotegerin (OPG)/nuclear factor kappa B receptor activating factor ligand (RANKL) signaling pathways of osteoporosis in caged laying hens were analyzed by serology, bone biomechanics, molecular biology and histopathology.	Phosphorus	27-37	TNF receptor superfamily member 11b	Gallus gallus	66-81
32526547-6	2020	The results showed that low dietary phosphorus decreased the production performance, and egg quality of laying hens and increased the contents of serum calcium (Ca), osteocalcin (OCN), alkaline phosphatase (ALP) and tartrate-resistant acid phosphatase (TRACP).	Phosphorus	36-46	bone gamma-carboxyglutamate protein	Gallus gallus	166-177
32526547-6	2020	The results showed that low dietary phosphorus decreased the production performance, and egg quality of laying hens and increased the contents of serum calcium (Ca), osteocalcin (OCN), alkaline phosphatase (ALP) and tartrate-resistant acid phosphatase (TRACP).	Phosphorus	36-46	bone gamma-carboxyglutamate protein	Gallus gallus	179-182
32526547-11	2020	Our results suggest that phosphorus may affect bone metabolism by regulating the OPG/RANKL signaling pathway.	Phosphorus	25-35	TNF receptor superfamily member 11b	Gallus gallus	81-84
32526547-11	2020	Our results suggest that phosphorus may affect bone metabolism by regulating the OPG/RANKL signaling pathway.	Phosphorus	25-35	tumor necrosis factor superfamily member 11	Gallus gallus	85-90
32731205-1	2020	Strain effects have been widely addressed in monolayer black phosphorus~(MBP) due to their significant influence on the orbital hybridization of atoms.	Phosphorus	61-71	myelin basic protein	Homo sapiens	73-76
32322911-1	2020	Substance P a neuro-immune mediator acts on Neurokinin-1 and -2 receptors (NK1R and NK2R).	Phosphorus	10-11	tachykinin receptor 1	Mus musculus	75-79
32322911-1	2020	Substance P a neuro-immune mediator acts on Neurokinin-1 and -2 receptors (NK1R and NK2R).	Phosphorus	10-11	tachykinin receptor 2	Mus musculus	84-88
32802956-5	2020	Results: Using ES, we discovered individuals with known pathogenic SNVs in GBA (p.Glu365Lys, p.Thr408Met, p.Asn409Ser, and p.Leu483Pro) and LRRK2 (p.Arg1441Gly and p.Gly2019Ser).	Phosphorus	56-57	leucine rich repeat kinase 2	Homo sapiens	140-145
32347320-4	2020	Functionally, we found that overexpression of GAS5 significantly attenuated the osteogenic differentiation and calcification of HASMCs induced by high levels of phosphorus.	Phosphorus	161-171	growth arrest specific 5	Homo sapiens	46-50
32347320-9	2020	In ex vivo models, GAS5 was significantly downregulated and its expression inversely related to the expression of miR-26b-5 and positively associated with the expression of PTEN in calcified aortic rings induced by high levels of phosphorus.	Phosphorus	230-240	growth arrest specific 5	Homo sapiens	19-23
32347320-9	2020	In ex vivo models, GAS5 was significantly downregulated and its expression inversely related to the expression of miR-26b-5 and positively associated with the expression of PTEN in calcified aortic rings induced by high levels of phosphorus.	Phosphorus	230-240	phosphatase and tensin homolog	Homo sapiens	173-177
32729680-3	2020	A stepwise mechanistic investigation into the doping process revealed that the decomposition of PPh3 triggered the release of both the elemental sulfur and phosphorus because of the reducing reaction environment.	Phosphorus	156-166	protein phosphatase 4 catalytic subunit	Homo sapiens	96-100
32468698-1	2020	The glycoprotein stanniocalcin-1 functions as a regulatory endocrine hormone that maintains the balance of calcium and phosphorus in bony fish and as a paracrine/autocrine factor involved in many physiological/pathological processes in humans, including carcinogenesis.	Phosphorus	119-129	stanniocalcin 1	Homo sapiens	17-32
32182536-11	2020	Phosphorus application at a rate of 50 kg ha-1 decreased total non-cancer and cancer risks by 15% and 21%, respectively, for both children and adults, compared to the highest value.	Phosphorus	0-10	Rho GTPase activating protein 45	Homo sapiens	42-46
32242612-7	2020	Ice-water swimming-induced increase in PTH correlated negatively with systemic calcium and positively with phosphorus.	Phosphorus	107-117	parathyroid hormone	Homo sapiens	39-42
32418499-1	2020	FGF-23 (fibroblast growth factor 23) regulates phosphorus and vitamin D.	Phosphorus	47-57	fibroblast growth factor 23	Homo sapiens	0-6
32418499-1	2020	FGF-23 (fibroblast growth factor 23) regulates phosphorus and vitamin D.	Phosphorus	47-57	fibroblast growth factor 23	Homo sapiens	8-35
32514747-4	2020	Subsequent analysis suggested that SAPK2 considerably influences the nitrogen, phosphorus, and potassium contents of rice grains.	Phosphorus	79-89	serine/threonine-protein kinase SAPK2	Oryza sativa Japonica Group	35-40
32545597-3	2020	The in vivo metabolic regulation of AOX activity by phosphorus (P) and nitrogen (N) and during plant symbioses with Arbuscular mycorrhizal fungi (AMF) and Rhizobium bacteria is still not fully understood.	Phosphorus	52-62	acyl-CoA oxidase 1	Homo sapiens	36-39
32818222-10	2020	Urine hepcidin/Cr was negatively correlated with tubular phosphorus reabsorption and was positively correlated with urine NGAL/Cr (r = -0.418, p = 0.019; r = 0.682, p = 0.000; respectively).	Phosphorus	57-67	hepcidin antimicrobial peptide	Homo sapiens	6-14
32484216-2	2020	14-3-3 proteins are gold-standard scaffold modules that recognize phosphoSer/Thr (pS/pT) containing conserved motifs, and confer conformational changes leading to modulation of functional parameters of their target proteins.	Phosphorus	82-84	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta	Homo sapiens	0-6
32517664-2	2020	We previously reported that calcium-sensing receptor (CaSR) mRNA and protein expression in parathyroid glands (PTGs) significantly decreased in a CKD rat model induced by a 5/6 nephrectomy that were fed a high phosphorus diet.	Phosphorus	210-220	calcium-sensing receptor	Rattus norvegicus	28-52
32517664-2	2020	We previously reported that calcium-sensing receptor (CaSR) mRNA and protein expression in parathyroid glands (PTGs) significantly decreased in a CKD rat model induced by a 5/6 nephrectomy that were fed a high phosphorus diet.	Phosphorus	210-220	calcium-sensing receptor	Rattus norvegicus	54-58
32347859-0	2020	Design of a LiF-rich solid electrolyte interface layer through salt-additive chemistry for boosting fast-charging phosphorus-based lithium ion battery performance.	Phosphorus	114-124	LIF interleukin 6 family cytokine	Homo sapiens	12-15
32347859-1	2020	A robust and conductive LiF-rich solid electrolyte interface layer was generated at the phosphorus surface through salt-additive chemistry, and it then served as a high-performance fast-charging lithium ion battery anode, delivering a high reversible capacity of 450 mA h g-1 after 450 cycles with a high charging current density of 8 A g-1 (about 3 min).	Phosphorus	88-98	LIF interleukin 6 family cytokine	Homo sapiens	24-27
32468656-2	2020	31-phosphorus magnetic resonance spectroscopy (31 P-MRS) is a powerful tool used to evaluate phosphorus metabolite levels in muscle.	Phosphorus	3-13	MROS	Homo sapiens	52-55
32581567-4	2020	Results: The SNP rs1790834 on CYB5A showed significant association with PSA response in CRPC patients treated with AA/P (P < 0.05), but rs743572, rs10883783 and rs1790858 did not.	Phosphorus	15-16	cytochrome b5 type A	Homo sapiens	30-35
31808570-3	2020	The first part of this review concentrated primarily on the computation of 31 P NMR chemical shifts, whereas the second part concerns the calculation of spin-spin coupling constants involving phosphorus nucleus, focusing primarily on their stereochemical dependencies and stereodynamic behavior in particular classes of organophosphorus compounds.	Phosphorus	192-202	spindlin 1	Homo sapiens	153-157
31707582-5	2020	Phosphorus burial is high in archipelagos with substantial sedimentation, but the stability of different burial forms varies across the Baltic Sea.	Phosphorus	0-10	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	143-146
32278118-8	2020	In conclusion, the study identifies weight, leptin and insulin as responsive to dietary phosphorus and that certain aspects of the systemic phosphorus response are attenuated by a corresponding high calcium intake.	Phosphorus	88-98	leptin	Homo sapiens	44-50
32278118-8	2020	In conclusion, the study identifies weight, leptin and insulin as responsive to dietary phosphorus and that certain aspects of the systemic phosphorus response are attenuated by a corresponding high calcium intake.	Phosphorus	88-98	insulin	Homo sapiens	55-62
32621455-7	2020	The results showed an increase in the formation of the perineurium and epineurium dose in the oat-treated groups (100, 200, and 400 mg/kg), compared to the control group after 2 weeks (P&amp;lt;0.05).	Phosphorus	185-186	ornithine aminotransferase	Rattus norvegicus	94-97
32621455-8	2020	Furthermore, the presence of inflammatory cells in the oat extract-treated groups (100, 200, and 400 mg/kg) decreased, compared to that in the control group after 2 weeks (P&amp;lt;0.05).	Phosphorus	172-173	ornithine aminotransferase	Rattus norvegicus	55-58
32621455-9	2020	In addition, the swelling of the axon significantly decreased in the oat extract-treated groups (200 and 400 mg/kg), compared to the control group (P&amp;lt;0.05).	Phosphorus	148-149	ornithine aminotransferase	Rattus norvegicus	69-72
32621455-10	2020	However, the axon dose-dependently increased in oat-treated groups (100, 200, and 400 mg/kg), compared to that in the control group after 4 weeks (P&amp;lt;0.05).	Phosphorus	147-148	ornithine aminotransferase	Rattus norvegicus	48-51
32028158-6	2020	Phosphorus transformed from water-soluble phosphorus (Ca(H2PO4)2, Ca(HPO4)) into insoluble Ca3(PO4)2.20 reducing-oxidizing cycles were investigated, and a less and less fluorine content in oxygen carrier was found because its phase transformation from solid NaF to gaseous HF, and the phosphorus content in oxygen carrier changed slightly under the current conditions.	Phosphorus	0-10	C-X-C motif chemokine ligand 8	Homo sapiens	258-261
31808570-3	2020	The first part of this review concentrated primarily on the computation of 31 P NMR chemical shifts, whereas the second part concerns the calculation of spin-spin coupling constants involving phosphorus nucleus, focusing primarily on their stereochemical dependencies and stereodynamic behavior in particular classes of organophosphorus compounds.	Phosphorus	192-202	spindlin 1	Homo sapiens	158-162
32475457-7	2020	Dietary P deficiency impaired the bone development by increasing serum Ca content and tibia ALP activity but decreasing serum P, 25-OHD3 contents, and tibia ash Ca and P contents of broilers.	Phosphorus	8-9	alkaline phosphatase, placental	Homo sapiens	92-95
32471062-5	2020	The results indicated that the proposed model sufficiently fitted the data (chi2&nbsp;(24) = 32.23,&nbsp;p&nbsp;< .12; CFI = .977; SRMR = .051; RMSEA = .034 (90% CI = .000 to .061)).	Phosphorus	31-32	complement factor I	Homo sapiens	119-122
32670863-6	2020	Experiments using AhR or GPR30 antagonists, siRNA strategies, and RNAseq analysis led us to propose a model in which AhR signaling plays a "driver role" in the AhR/GPR30 cross-talk in mediating long-term and low-dose exposure of B[a]P and/or BPA.	Phosphorus	26-27	aryl hydrocarbon receptor	Homo sapiens	117-120
32670863-6	2020	Experiments using AhR or GPR30 antagonists, siRNA strategies, and RNAseq analysis led us to propose a model in which AhR signaling plays a "driver role" in the AhR/GPR30 cross-talk in mediating long-term and low-dose exposure of B[a]P and/or BPA.	Phosphorus	26-27	aryl hydrocarbon receptor	Homo sapiens	117-120
32670863-6	2020	Experiments using AhR or GPR30 antagonists, siRNA strategies, and RNAseq analysis led us to propose a model in which AhR signaling plays a "driver role" in the AhR/GPR30 cross-talk in mediating long-term and low-dose exposure of B[a]P and/or BPA.	Phosphorus	26-27	G protein-coupled estrogen receptor 1	Homo sapiens	164-169
32483226-7	2020	Good separation of multiple CYP substrates was achieved without using organic solvents and any gradient methods by temperature-responsive chromatography utilizing a P(NIPAAm-co-n-butyl methacrylate (BMA))- and P(NIPAAm-co-N-acryloyl L-tryptophan methyl ester (L-Trp-OMe))-grafted silica column.	Phosphorus	165-167	cytochrome P450 family 4 subfamily F member 3	Homo sapiens	28-31
32364701-4	2020	The biochemical basis for ABHD12-dependent PS remodeling and its pathophysiological significance remain unknown.	Phosphorus	43-45	abhydrolase domain containing 12	Mus musculus	26-32
32364701-7	2020	Taken together, our findings reveal that ABHD12 and LPCAT3 coordinately regulate lyso-PS and C20:4 PS content in the CNS and point to lyso-PS lipids as the likely bioactive metabolites contributing to PHARC-related neuropathologies.	Phosphorus	86-88	abhydrolase domain containing 12	Mus musculus	41-47
32364701-7	2020	Taken together, our findings reveal that ABHD12 and LPCAT3 coordinately regulate lyso-PS and C20:4 PS content in the CNS and point to lyso-PS lipids as the likely bioactive metabolites contributing to PHARC-related neuropathologies.	Phosphorus	86-88	lysophosphatidylcholine acyltransferase 3	Mus musculus	52-58
32140723-8	2020	RESULTS: Two novel SRY gene mutations, p.Arg76Leu and p.Glu89flx15, were identified.	Phosphorus	39-40	sex determining region Y	Homo sapiens	19-22
32438707-0	2020	Inverse Correlation Between Grip Strength and Serum Phosphorus: A Retrospective Observational Study in Japanese Elderly with Poorly Controlled Type 2 Diabetes.	Phosphorus	52-62	glutamate receptor interacting protein 1	Homo sapiens	28-32
32438707-4	2020	Patients with a weakened hand grip (n = 21) scored worse on a mini-mental state examination (24.3 vs. 26.5, p = 0.04), showed a higher prevalence of diabetic peripheral neuropathy (76% vs. 40%, p = 0.03), and had a higher serum phosphorus concentration (3.8 vs. 3.3 mg/dL, p < 0.01) compared to those without a weakened hand grip (n = 20).	Phosphorus	228-238	glutamate receptor interacting protein 1	Homo sapiens	30-34
32438707-5	2020	The serum phosphorus concentration was inversely correlated to hand grip strength (r = -0.501, p < 0.001) among the total of 41 patients.	Phosphorus	10-20	glutamate receptor interacting protein 1	Homo sapiens	68-72
32243175-5	2020	We revealed that the decreased superoxide dismutase (SOD) activity by lipid peroxides could be an essential mechanism of the selectively higher ROS generation induced by BP-based nanosheets in cancer cells.	Phosphorus	170-172	superoxide dismutase 1	Homo sapiens	31-51
32243175-5	2020	We revealed that the decreased superoxide dismutase (SOD) activity by lipid peroxides could be an essential mechanism of the selectively higher ROS generation induced by BP-based nanosheets in cancer cells.	Phosphorus	170-172	superoxide dismutase 1	Homo sapiens	53-56
32524026-6	2020	Parathyroid hormone was mildly elevated at 90 pg/mL (reference range is 15 to 65 pg/mL), but she had persistently normal levels of total serum calcium at 9.9 mg/dL (reference range is 8.7 to 10.3 mg/dL), phosphorus at 3.5 mg/dL (reference range is 2.1 to 4.5 mg/dL), and albumin at 4.4 g/dL (reference range is 3.6 to 4.8 g/dL).	Phosphorus	204-214	parathyroid hormone	Homo sapiens	0-19
32608846-1	2020	Understanding the effect of calcite and chlorapatite mixture (CA/ClAP) addition on the mobilization of phosphorus (P) in sediments is crucial to the application of CA/ClAP as an amendment material to control the release of P from sediments.	Phosphorus	103-113	BCL10 immune signaling adaptor	Homo sapiens	65-69
32608846-1	2020	Understanding the effect of calcite and chlorapatite mixture (CA/ClAP) addition on the mobilization of phosphorus (P) in sediments is crucial to the application of CA/ClAP as an amendment material to control the release of P from sediments.	Phosphorus	115-116	BCL10 immune signaling adaptor	Homo sapiens	65-69
32608846-6	2020	The addition of CA/ClAP in sediments caused an increase in the content of P in the sediments, but the increased P mainly existed in the form of calcium-bound P (HCl-P), which was difficult to be re-released into the water column under anoxic and common pH (5-9) conditions.	Phosphorus	74-75	BCL10 immune signaling adaptor	Homo sapiens	19-23
32608846-6	2020	The addition of CA/ClAP in sediments caused an increase in the content of P in the sediments, but the increased P mainly existed in the form of calcium-bound P (HCl-P), which was difficult to be re-released into the water column under anoxic and common pH (5-9) conditions.	Phosphorus	74-75	BCL10 immune signaling adaptor	Homo sapiens	19-23
32608846-7	2020	The reduction of SRP in the pore water after the addition of CA/ClAP played an important role in the prevention of sedimentary P liberation into the overlying water by the CA/ClAP amendment.	Phosphorus	19-20	BCL10 immune signaling adaptor	Homo sapiens	64-68
32302111-4	2020	In the acidic media, the Co-SA/P-in situ catalyst with Co-P1N3 interfacial structure exhibits excellent activity and durability for hydrogen evolution reaction (HER) with a low overpotential of 98 mV at 10 mA cm-2 and a small Tafel slope of 47 mV dec-1, which are greatly superior to those of catalyst with Co-N4 interfacial structure.	Phosphorus	31-32	deleted in esophageal cancer 1	Homo sapiens	247-252
32372006-7	2020	In compost deficient in soluble P, supplemented with an insoluble inorganic form of P (Ca3(PO4)2), application of a phosphate solubilising Pseudomonas strain to plant roots provides a significant growth boost when compared with a Pseudomonas strain incapable of solubilising Ca3(PO4)2.	Phosphorus	84-85	ERC2 intronic transcript 1	Homo sapiens	87-97
32253237-4	2020	We previously demonstrated that mice lacking epithelial-specific splicing factor Esrp1 have fully penetrant bilateral CL/P.	Phosphorus	121-122	epithelial splicing regulatory protein 1	Mus musculus	81-86
32211705-1	2020	For the first time, electrochemiluminescence (ECL) emission was observed from black phosphorus quantum dots (BPQDs) in the presence of K2S2O8 as the co-reactant.	Phosphorus	84-94	C-C motif chemokine ligand 21	Homo sapiens	46-49
32253302-5	2020	The formation of covalent bonding P-O-C between BP and graphene oxide (GO) nanosheets not only reduces the voids of GO film but also improves the alignment degree of GO nanosheets, resulting in high compactness of the GO film.	Phosphorus	48-50	proopiomelanocortin	Homo sapiens	34-39
32266902-3	2020	Owing to the favorable degradability of BP, the nanosystem exhibited accelerated the release of the HSP90 inhibitor tanespimycin (17-AAG) and an apparent promotion in the reactive oxygen species (ROS) yield of PCN as well as expedited the degradation of the PCN-laden BP nanoplatforms.	Phosphorus	40-42	heat shock protein 90 alpha family class A member 1	Homo sapiens	100-105
32550215-2	2020	We aimed to assess the impact of PS supplementation on FBS, HbA1c and insulin levels by conducting a systematic review and meta-analysis of the available randomized controlled trials (RCTs).	Phosphorus	33-35	insulin	Homo sapiens	70-77
32337443-0	2020	Preparation of Fe3O4@SiO2@ P(AANa-co-AM) Composites and Their Adsorption for Pb(II).	Phosphorus	0-1	submaxillary gland androgen regulated protein 3B	Homo sapiens	77-83
32212616-2	2020	Herein, we address this challenge by developing a rapid electrochemical expansion strategy for scale preparation of fine crystal quality BPNSs from bulk black phosphorus, which was demonstrated to be an active cocatalyst for photocatalytic nitrogen fixation in the presence of CdS as a photocatalyst.	Phosphorus	159-169	CDP-diacylglycerol synthase 1	Homo sapiens	277-280
31991212-5	2020	At physiological pH, the degree of elastin mineralization is influenced by hydrolysis and complexity of medium composition, since ionic species, as sodium, potassium, magnesium, in addition to calcium and phosphorus, interfere with the calcification process.	Phosphorus	205-215	elastin	Homo sapiens	35-42
32045827-1	2020	Osteocytes play an important role in the regulation of serum phosphorus by producing fibroblast growth factor 23 (FGF23).	Phosphorus	61-71	fibroblast growth factor 23	Mus musculus	85-112
32045827-1	2020	Osteocytes play an important role in the regulation of serum phosphorus by producing fibroblast growth factor 23 (FGF23).	Phosphorus	61-71	fibroblast growth factor 23	Mus musculus	114-119
31951836-0	2020	Product and cost perspectives of phosphorus recovery from human urine using solid waste ash and sea salt addition - A case of Thailand.	Phosphorus	33-43	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	96-99
31951836-1	2020	Phosphorus (P) recovery from human urine was evaluated using the addition of MgCl2, sea salt and solid-waste (SW) incinerated ashes.	Phosphorus	0-1	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	84-87
32255892-13	2020	In Ethiopia, NE and soil-test based respectively recommended lower amounts of P by 8 and 19 kg ha-1 than the blanket recommendations, but maize yield (6 t ha-1) was similar among the three methods.	Phosphorus	78-79	1,4-alpha-glucan-branching enzyme 2, chloroplastic/amyloplastic	Zea mays	95-99
32431793-3	2020	Methods: We designed anti-VEGFR2 peptidomimetics with anti-angiogenic activity, including compound P (lactam derivative) and compound T (indole derivative) by using in silico methods.	Phosphorus	99-100	kinase insert domain receptor	Homo sapiens	26-32
32255892-7	2020	Although maize yield response to fertilizer differed with geographic location; on average, maize yield response to nitrogen (N), phosphorus (P) and potassium (K) were respectively 2.4, 1.6 and 0.2 t ha-1 in Nigeria, 2.3, 0.9 and 0.2 t ha-1 in Ethiopia, and 1.5, 0.8 and 0.2 t ha-1 in Tanzania.	Phosphorus	129-139	1,4-alpha-glucan-branching enzyme 2, chloroplastic/amyloplastic	Zea mays	199-203
32255892-10	2020	In Nigeria, NE recommended lower amounts of P by 9 and 11 kg ha-1 and K by 24 and 38 kg ha-1 than soil-test based and regional fertilizer recommendations, respectively.	Phosphorus	44-45	1,4-alpha-glucan-branching enzyme 2, chloroplastic/amyloplastic	Zea mays	61-65
32043188-7	2020	Using a single-pulse feeding-based fed-batch system, alkaline alpha-amylase activity of B. subtilis 168M P -27T was increased by 250.6-fold, compared with B. subtilis 168M A1.	Phosphorus	105-106	alpha-amylase	Bacillus subtilis subsp. subtilis str. 168	62-75
31919781-6	2020	In addition, some molecules involved in calcium/phosphorus metabolism, such as klotho and FGF23, have an involvement in the pathogenesis of diabetic vasculopathy, which appears to be dependent on the degree of vascular impairment.	Phosphorus	48-58	klotho	Homo sapiens	79-85
31919781-6	2020	In addition, some molecules involved in calcium/phosphorus metabolism, such as klotho and FGF23, have an involvement in the pathogenesis of diabetic vasculopathy, which appears to be dependent on the degree of vascular impairment.	Phosphorus	48-58	fibroblast growth factor 23	Homo sapiens	90-95
31841590-17	2020	Also, a significant negative correlation was found between PTHrP and phosphorus, again only in patients without calcitriol elevation.	Phosphorus	69-79	parathyroid hormone like hormone	Homo sapiens	59-64
31883475-11	2020	In addition, P.oil decreased the expressions of caspase-8, caspase-3, and Bax, and increased the expression of Bcl-2, thereby reducing the apoptosis of the intestinal mucosa.	Phosphorus	13-14	caspase 8	Rattus norvegicus	48-57
31987191-4	2020	Then, the LCN2 solution was incubated with the aptamer modified GSPE/P(ATT)-GO/AuNPs.	Phosphorus	66-67	lipocalin 2	Homo sapiens	10-14
31818557-3	2020	Our results showed that chloropicrin (CP) fumigation significantly increased the available-P, Leached-P and active-P fractionation (inorganic P extracted from H2O, NaHCO3 and NaOH) in Shangdong and Miyun soils in the early stages of culture, while soil alkaline phosphatase (ALP) activity and phoD gene abundance decreased significantly.	Phosphorus	39-40	alkaline phosphatase, placental	Homo sapiens	253-273
31818557-3	2020	Our results showed that chloropicrin (CP) fumigation significantly increased the available-P, Leached-P and active-P fractionation (inorganic P extracted from H2O, NaHCO3 and NaOH) in Shangdong and Miyun soils in the early stages of culture, while soil alkaline phosphatase (ALP) activity and phoD gene abundance decreased significantly.	Phosphorus	39-40	alkaline phosphatase, placental	Homo sapiens	275-278
31883475-11	2020	In addition, P.oil decreased the expressions of caspase-8, caspase-3, and Bax, and increased the expression of Bcl-2, thereby reducing the apoptosis of the intestinal mucosa.	Phosphorus	13-14	caspase 3	Rattus norvegicus	59-68
31883475-11	2020	In addition, P.oil decreased the expressions of caspase-8, caspase-3, and Bax, and increased the expression of Bcl-2, thereby reducing the apoptosis of the intestinal mucosa.	Phosphorus	13-14	BCL2 associated X, apoptosis regulator	Rattus norvegicus	74-77
31883475-11	2020	In addition, P.oil decreased the expressions of caspase-8, caspase-3, and Bax, and increased the expression of Bcl-2, thereby reducing the apoptosis of the intestinal mucosa.	Phosphorus	13-14	BCL2, apoptosis regulator	Rattus norvegicus	111-116
32210322-3	2020	This report examined the feasibility of degrading ciprofloxacin and sulfamethoxazole through photoelectrocatalytic oxidation using FTO-BiVO4/Ag2S with p-n heterojunction as anode.	Phosphorus	7-8	FTO alpha-ketoglutarate dependent dioxygenase	Homo sapiens	131-134
32210322-3	2020	This report examined the feasibility of degrading ciprofloxacin and sulfamethoxazole through photoelectrocatalytic oxidation using FTO-BiVO4/Ag2S with p-n heterojunction as anode.	Phosphorus	7-8	angiotensin II receptor type 1	Homo sapiens	141-145
31896473-6	2020	We found that micro-PS exposure caused oxidative stress and activated JNK and p38 MAPK.	Phosphorus	20-22	mitogen-activated protein kinase 8	Mus musculus	70-73
32184468-0	2020	Involvement of estrogen in phosphorus-induced nephrocalcinosis through fibroblast growth factor 23.	Phosphorus	27-37	fibroblast growth factor 23	Rattus norvegicus	71-98
32184468-2	2020	Estrogen is one of the factors affecting fibroblast growth factor 23 (FGF23), a phosphorus-regulating hormone.	Phosphorus	80-90	fibroblast growth factor 23	Rattus norvegicus	41-68
32184468-2	2020	Estrogen is one of the factors affecting fibroblast growth factor 23 (FGF23), a phosphorus-regulating hormone.	Phosphorus	80-90	fibroblast growth factor 23	Rattus norvegicus	70-75
32184468-8	2020	In addition, fibroblast growth factor receptor 1 (FGFR1: a predominant receptor of FGF23) inhibitor treatment partially decreased renal calcium concentrations in rats with high phosphorus intake.	Phosphorus	177-187	Fibroblast growth factor receptor 1	Rattus norvegicus	13-48
32184468-8	2020	In addition, fibroblast growth factor receptor 1 (FGFR1: a predominant receptor of FGF23) inhibitor treatment partially decreased renal calcium concentrations in rats with high phosphorus intake.	Phosphorus	177-187	Fibroblast growth factor receptor 1	Rattus norvegicus	50-55
32184468-8	2020	In addition, fibroblast growth factor receptor 1 (FGFR1: a predominant receptor of FGF23) inhibitor treatment partially decreased renal calcium concentrations in rats with high phosphorus intake.	Phosphorus	177-187	fibroblast growth factor 23	Rattus norvegicus	83-88
32184468-10	2020	Furthermore, FGF23 was involved in the nephrocalcinosis induced by high phosphorus intake partially through FGFR1 signaling.	Phosphorus	72-82	fibroblast growth factor 23	Rattus norvegicus	13-18
32184468-10	2020	Furthermore, FGF23 was involved in the nephrocalcinosis induced by high phosphorus intake partially through FGFR1 signaling.	Phosphorus	72-82	Fibroblast growth factor receptor 1	Rattus norvegicus	108-113
32608629-6	2020	The total phosphorus output was 0.534 kg hm-2, and the soluble total phosphorus (0.422kg hm-2) accounted for 79.00% of the total phosphorus flux.	Phosphorus	10-20	cholinergic receptor muscarinic 2	Homo sapiens	41-45
32608629-6	2020	The total phosphorus output was 0.534 kg hm-2, and the soluble total phosphorus (0.422kg hm-2) accounted for 79.00% of the total phosphorus flux.	Phosphorus	69-79	cholinergic receptor muscarinic 2	Homo sapiens	89-93
32608629-6	2020	The total phosphorus output was 0.534 kg hm-2, and the soluble total phosphorus (0.422kg hm-2) accounted for 79.00% of the total phosphorus flux.	Phosphorus	69-79	cholinergic receptor muscarinic 2	Homo sapiens	89-93
31896473-6	2020	We found that micro-PS exposure caused oxidative stress and activated JNK and p38 MAPK.	Phosphorus	20-22	mitogen-activated protein kinase 14	Mus musculus	78-86
31735793-2	2020	Although her disease was considered to be refractory to medical treatment, the serum intact parathyroid hormone (PTH) level remarkably improved without manifestation of hypercalcemia through only strict serum phosphorus control, mainly via intensification of dialysis.	Phosphorus	209-219	parathyroid hormone	Homo sapiens	92-111
31904454-0	2020	Conformational structure variation of human serum albumin after binding interaction with black phosphorus quantum dots.	Phosphorus	95-105	albumin	Homo sapiens	44-57
31904454-1	2020	Herein, binding interaction between black phosphorus quantum dots (BPQDs) and human serum albumin (HSA) was systematically characterized for deep illustration of conformational structure variation of HSA affected by BPQDs.	Phosphorus	42-52	albumin	Homo sapiens	84-103
31904454-1	2020	Herein, binding interaction between black phosphorus quantum dots (BPQDs) and human serum albumin (HSA) was systematically characterized for deep illustration of conformational structure variation of HSA affected by BPQDs.	Phosphorus	42-52	albumin	Homo sapiens	99-102
31735793-2	2020	Although her disease was considered to be refractory to medical treatment, the serum intact parathyroid hormone (PTH) level remarkably improved without manifestation of hypercalcemia through only strict serum phosphorus control, mainly via intensification of dialysis.	Phosphorus	209-219	parathyroid hormone	Homo sapiens	113-116
31735793-3	2020	The very strong correlation between the serum phosphorus level and serum intact PTH level suggested the possibility of secondary HPT.	Phosphorus	46-56	parathyroid hormone	Homo sapiens	80-83
32020436-1	2020	Excessive secretion of PTH leads to disturbance of calcium and phosphorus metabolism in the body, which promotes bone, kidney, digestive system and nervous system diseases.	Phosphorus	63-73	parathyroid hormone	Homo sapiens	23-26
32003386-4	2020	The first-principles calculations illustrate that the di-phosphorus bond of MoP2 is prone to break and the distal P atoms preferentially bind with Li atoms to form Li3P during lithiation, but MoP prefers to form ternary LixMoP.	Phosphorus	54-67	endothelial PAS domain protein 1	Homo sapiens	76-80
31924695-8	2020	A gel shift assay with a radiolabeled OARE module and nuclear extracts prepared from PB-treated mouse liver confirmed that HNF4alpha formed a complex with Ser 100-phosphorylated RORalpha, as shown by supershifted complexes with anti-p-Ser100 RORalpha and anti-HNF4alpha antibodies.	Phosphorus	71-72	hepatic nuclear factor 4, alpha	Mus musculus	123-132
32479276-5	2020	159 tons of nitrogen and 26.4 tons of phosphorus were estimated to be discharged to the Baltic Sea annually.	Phosphorus	38-48	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	95-98
32479276-7	2020	Nitrogen and phosphorus input from grey water contributes to 0.25% of the exceedance of, for the Baltic Sea set, eutrophication target.	Phosphorus	13-23	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	104-107
32003386-4	2020	The first-principles calculations illustrate that the di-phosphorus bond of MoP2 is prone to break and the distal P atoms preferentially bind with Li atoms to form Li3P during lithiation, but MoP prefers to form ternary LixMoP.	Phosphorus	54-67	opioid receptor mu 1	Homo sapiens	76-79
31919818-4	2020	Recovering phosphorus from these wastewaters is considered a big challenge due to the high phosphorus concentration (between 478 and 1756 mg L-1) and solids content (> 2-6% of total solids).	Phosphorus	11-21	immunoglobulin kappa variable 1-16	Homo sapiens	141-144
32608731-0	2020	[Phosphorus Storage Capacity and Loss Risk in Coastal Reed Wetland Surrounding Bohai Sea].	Phosphorus	1-11	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	85-88
32608731-6	2020	The P adsorption capacity was related to the contents of Ca, Mg, and TOC.	Phosphorus	4-5	rhomboid 5 homolog 2	Homo sapiens	69-72
31922740-3	2020	Benefitted from the uniform atomic blending of Co2+ ions in the Co-glycerate precursors, CoP NPs in situ formed in the confined space with NaH2PO2 as phosphorus source during the annealing process; meanwhile, glycerate suffered carbonization and transformed into P-doped dual carbon shells during the annealing process, including interior thin carbon coating, closely encircled CoP NP, and peripheral hollow carbon sphere loading a lot of CoP NPs.	Phosphorus	150-160	caspase recruitment domain family member 16	Homo sapiens	89-92
31840180-2	2020	Here, we examined the role of Golgi-endosome transport, specifically M6PR shuttling mediated by GCC2, in PS-ASO trafficking and activity.	Phosphorus	105-107	mannose-6-phosphate receptor, cation dependent	Mus musculus	69-73
31840180-3	2020	We found that reduction in cellular levels of GCC2 or M6PR impaired PS-ASO release from endosomes and decreased PS-ASO activity in human cells.	Phosphorus	68-70	GRIP and coiled-coil domain containing 2	Homo sapiens	46-50
31840180-3	2020	We found that reduction in cellular levels of GCC2 or M6PR impaired PS-ASO release from endosomes and decreased PS-ASO activity in human cells.	Phosphorus	68-70	mannose-6-phosphate receptor, cation dependent	Homo sapiens	54-58
31840180-3	2020	We found that reduction in cellular levels of GCC2 or M6PR impaired PS-ASO release from endosomes and decreased PS-ASO activity in human cells.	Phosphorus	112-114	GRIP and coiled-coil domain containing 2	Homo sapiens	46-50
31840180-3	2020	We found that reduction in cellular levels of GCC2 or M6PR impaired PS-ASO release from endosomes and decreased PS-ASO activity in human cells.	Phosphorus	112-114	mannose-6-phosphate receptor, cation dependent	Homo sapiens	54-58
31840180-4	2020	GCC2 relocated to LEs upon PS-ASO treatment, and M6PR also co-localized with PS-ASOs in LEs or on LE membranes.	Phosphorus	27-29	GRIP and coiled-coil domain containing 2	Homo sapiens	0-4
31699482-7	2020	TPR measurements revealed that phosphorus-promoted nanocatalysts had higher reduction potentials than nanocatalyst without promoter.	Phosphorus	31-41	translocated promoter region, nuclear basket protein	Homo sapiens	0-3
32116791-0	2020	Phosphorus Restriction Changes the Expression of Fibroblast Growth Factor 23 and Its Receptors in Laying Hens.	Phosphorus	0-10	fibroblast growth factor 23	Gallus gallus	49-76
32116791-11	2020	The laying hens adjusted to low-phosphorus diets by increasing intestinal NPt2b protein production, which was associated with decreased serum FGF23 concentration.	Phosphorus	32-42	fibroblast growth factor 23	Gallus gallus	142-147
31618470-7	2020	Gene expression of the major intestinal phosphorus transporter, NaPi-2b, was not different between CKD and NL rats in the jejunum but was lower in CKD rats versus NL rats in the duodenum.	Phosphorus	40-50	solute carrier family 34 member 2	Rattus norvegicus	64-71
31435005-8	2020	Increased urinary phosphorus excretion was associated with a significant increase in DBP [0.14 mmHg/100 mg (0.01, 0.28), adjusted].	Phosphorus	18-28	D-box binding PAR bZIP transcription factor	Homo sapiens	85-88
31435005-10	2020	For example, added phosphorus (but not plant or animal) was associated with increases in SBP and DBP, 1.24 mmHg/100 mg (0.36, 2.12) and 0.83 mmHg/100 mg (0.22, 1.44), respectively, crude.	Phosphorus	19-29	selenium binding protein 1	Homo sapiens	89-92
31435005-10	2020	For example, added phosphorus (but not plant or animal) was associated with increases in SBP and DBP, 1.24 mmHg/100 mg (0.36, 2.12) and 0.83 mmHg/100 mg (0.22, 1.44), respectively, crude.	Phosphorus	19-29	D-box binding PAR bZIP transcription factor	Homo sapiens	97-100
31654875-11	2020	New MARPOL regulations for passenger ships on the Baltic Sea require advanced treatment of pollutant nutrients, nitrogen and phosphorus, before sewage discharge in order to combat eutrophication of this sensitive area.	Phosphorus	125-135	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	57-60
31786156-8	2020	After birth, serum calcium falls and phosphorus rises, which trigger an increase in PTH and a subsequent rise in calcitriol.	Phosphorus	37-47	parathyroid hormone	Homo sapiens	84-87
31901221-4	2020	We identified 363 differentially p-Tyr residues, corresponding to the majority of proteins previously known to participate in CLEC-2 signaling and also novel ones, including adaptors (e.g., DAPP1, Dok1/3, CASS4, Nck1/2), kinases/phosphatases (e.g., FAK1, FES, FGR, JAK2, SHIP2), and membrane proteins (e.g., G6F, JAM-A, PECAM-1, TLT-1).	Phosphorus	33-34	C-type lectin domain family 1 member B	Homo sapiens	126-132
31913377-1	2020	We report the influence of N-heterocyclic carbenes (NHCs) on the hydrolysis of a diphosphene TerP[double bond, length as m-dash]PTer (1; Ter = 2,6-Mes2C6H3; Mes = 2,4,6-Me3C6H2), a phosphorus-analogue of an alkene.	Phosphorus	181-191	peroxisomal trans-2-enoyl-CoA reductase	Homo sapiens	93-97
31935810-2	2020	Herein, the synthesis of a macromolecular spirocyclic phosphorus/nitrogen-containing IFR poly sulfonamide spirocyclic pentaerythritol bisphosphonate (SAPC) is reported via a two-step method that uses pentaerythritol, phosphorus oxychloride and sulfonamide (SAA) as raw materials.	Phosphorus	42-64	serum amyloid A1 cluster	Homo sapiens	257-260
31860056-9	2020	Thus, higher FGF23 levels were needed to maintain phosphaturia and normal serum phosphorus values.	Phosphorus	80-90	fibroblast growth factor 23	Rattus norvegicus	13-18
31860056-10	2020	Renal Klotho expression was preserved in Nx rats on a 0.2% phosphorus diet, reduced on a 0.4% phosphorus diet, and markedly reduced in Nx rats receiving LPS.	Phosphorus	59-69	Klotho	Rattus norvegicus	6-12
31860056-10	2020	Renal Klotho expression was preserved in Nx rats on a 0.2% phosphorus diet, reduced on a 0.4% phosphorus diet, and markedly reduced in Nx rats receiving LPS.	Phosphorus	94-104	Klotho	Rattus norvegicus	6-12
31860056-11	2020	In ex vivo experiments, high phosphorus and LPS increased nuclear beta-catenin and p65-NFkappaB and decreased Klotho.	Phosphorus	29-39	catenin beta 1	Rattus norvegicus	66-78
31860056-11	2020	In ex vivo experiments, high phosphorus and LPS increased nuclear beta-catenin and p65-NFkappaB and decreased Klotho.	Phosphorus	29-39	synaptotagmin 1	Rattus norvegicus	83-86
31860056-11	2020	In ex vivo experiments, high phosphorus and LPS increased nuclear beta-catenin and p65-NFkappaB and decreased Klotho.	Phosphorus	29-39	Klotho	Rattus norvegicus	110-116
31860056-13	2020	In conclusion, strict control of phosphorus intake prevented the increase in FGF23 in renal failure, whereas inflammation independently increased FGF23 values.	Phosphorus	33-43	fibroblast growth factor 23	Rattus norvegicus	77-82
31938583-0	2020	Risk of phosphorus losses in surface runoff from agricultural land in the Baltic Commune of Puck in the light of assessment performed on the basis of DPS indicator.	Phosphorus	8-18	decaprenyl diphosphate synthase subunit 1	Homo sapiens	150-153
32038672-8	2019	These results suggested that tobacco NtMYB12 acts as a phosphorus starvation response enhancement factor and regulates NtCHS and NtPT2 expression, which results in increased flavonol and P accumulation and enhances tolerance to low Pi stress.	Phosphorus	55-65	inorganic phosphate transporter 1-4-like	Nicotiana tabacum	129-134
32065759-7	2020	Hyperoxia was also found to diminish DNA damage and generation of free radicals initiated in B[a]P-treated cells which was attributed to an significant rise of Nrf2, leading to elevated antioxidant activities or detoxification proteins including heme oxygenase 1 (HO-1), superoxide dismutase (SOD), glutathione peroxidase-1/2 (GPX-1/2), CAT, GST and glutathione (GSH).	Phosphorus	97-98	NFE2 like bZIP transcription factor 2	Homo sapiens	160-164
32065759-7	2020	Hyperoxia was also found to diminish DNA damage and generation of free radicals initiated in B[a]P-treated cells which was attributed to an significant rise of Nrf2, leading to elevated antioxidant activities or detoxification proteins including heme oxygenase 1 (HO-1), superoxide dismutase (SOD), glutathione peroxidase-1/2 (GPX-1/2), CAT, GST and glutathione (GSH).	Phosphorus	97-98	heme oxygenase 1	Homo sapiens	246-262
32065759-7	2020	Hyperoxia was also found to diminish DNA damage and generation of free radicals initiated in B[a]P-treated cells which was attributed to an significant rise of Nrf2, leading to elevated antioxidant activities or detoxification proteins including heme oxygenase 1 (HO-1), superoxide dismutase (SOD), glutathione peroxidase-1/2 (GPX-1/2), CAT, GST and glutathione (GSH).	Phosphorus	97-98	heme oxygenase 1	Homo sapiens	264-268
32065759-7	2020	Hyperoxia was also found to diminish DNA damage and generation of free radicals initiated in B[a]P-treated cells which was attributed to an significant rise of Nrf2, leading to elevated antioxidant activities or detoxification proteins including heme oxygenase 1 (HO-1), superoxide dismutase (SOD), glutathione peroxidase-1/2 (GPX-1/2), CAT, GST and glutathione (GSH).	Phosphorus	97-98	superoxide dismutase 1	Homo sapiens	271-291
32065759-7	2020	Hyperoxia was also found to diminish DNA damage and generation of free radicals initiated in B[a]P-treated cells which was attributed to an significant rise of Nrf2, leading to elevated antioxidant activities or detoxification proteins including heme oxygenase 1 (HO-1), superoxide dismutase (SOD), glutathione peroxidase-1/2 (GPX-1/2), CAT, GST and glutathione (GSH).	Phosphorus	97-98	superoxide dismutase 1	Homo sapiens	293-296
32065759-7	2020	Hyperoxia was also found to diminish DNA damage and generation of free radicals initiated in B[a]P-treated cells which was attributed to an significant rise of Nrf2, leading to elevated antioxidant activities or detoxification proteins including heme oxygenase 1 (HO-1), superoxide dismutase (SOD), glutathione peroxidase-1/2 (GPX-1/2), CAT, GST and glutathione (GSH).	Phosphorus	97-98	glutathione peroxidase 1	Homo sapiens	299-325
32065759-7	2020	Hyperoxia was also found to diminish DNA damage and generation of free radicals initiated in B[a]P-treated cells which was attributed to an significant rise of Nrf2, leading to elevated antioxidant activities or detoxification proteins including heme oxygenase 1 (HO-1), superoxide dismutase (SOD), glutathione peroxidase-1/2 (GPX-1/2), CAT, GST and glutathione (GSH).	Phosphorus	97-98	glutathione peroxidase 1	Homo sapiens	327-334
32065759-7	2020	Hyperoxia was also found to diminish DNA damage and generation of free radicals initiated in B[a]P-treated cells which was attributed to an significant rise of Nrf2, leading to elevated antioxidant activities or detoxification proteins including heme oxygenase 1 (HO-1), superoxide dismutase (SOD), glutathione peroxidase-1/2 (GPX-1/2), CAT, GST and glutathione (GSH).	Phosphorus	97-98	catalase	Homo sapiens	337-340
31606465-1	2020	Stanniocalcin (STC-1), a kind of glycoprotein hormone, was first found in fish and mainly regulates calcium/phosphorus metabolism in the body.	Phosphorus	108-118	stanniocalcin 1	Sus scrofa	15-20
31948015-2	2020	Herein, a novel MOF composite was designed through the generated cooperative role of MOF (NH2-MIL-101(Al)) and a phosphorus-nitrogen-containing ionic liquid ([DPP-NC3bim][PMO]).	Phosphorus	113-132	lysine acetyltransferase 8	Homo sapiens	16-19
31499302-0	2020	Phosphorus sorption and availability in an andosol after a decade of organic or mineral fertilizer applications: Importance of pH and organic carbon modifications in soil as compared to phosphorus accumulation.	Phosphorus	0-10	phenylalanine hydroxylase	Homo sapiens	127-129
32966995-1	2020	BACKGROUND: Calcimimetics are used to treat mineral and bone disorder by reducing parathyroid hormone (PTH), calcium (Ca), and phosphorus (Phos).	Phosphorus	139-143	parathyroid hormone	Homo sapiens	82-101
32674240-1	2020	BACKGROUND AND OBJECTIVES: Previous study has reported phosphorus intake is associated prostate cancer (PCa), but the association between phosphorus intake and serum prostate specific antigen (PSA) levels hasn"t been reported in non-history of PCa population.	Phosphorus	138-148	kallikrein related peptidase 3	Homo sapiens	166-191
32674240-1	2020	BACKGROUND AND OBJECTIVES: Previous study has reported phosphorus intake is associated prostate cancer (PCa), but the association between phosphorus intake and serum prostate specific antigen (PSA) levels hasn"t been reported in non-history of PCa population.	Phosphorus	138-148	kallikrein related peptidase 3	Homo sapiens	193-196
32674240-6	2020	Weighted linear regression and generalized additive models were used to addressing the linear and non-linear link of phosphorus intake to PSA level.	Phosphorus	117-127	kallikrein related peptidase 3	Homo sapiens	138-141
32674240-10	2020	CONCLUSIONS: There is a non-linear correlation between dietary phosphorus intake and PSA.	Phosphorus	63-73	kallikrein related peptidase 3	Homo sapiens	85-88
32674240-11	2020	Dietary phosphorus intake was positively associated with increased PSA when dietary phosphorus intake is beyond 1151 mg after adjusting other covariates.	Phosphorus	8-18	kallikrein related peptidase 3	Homo sapiens	67-70
32674240-11	2020	Dietary phosphorus intake was positively associated with increased PSA when dietary phosphorus intake is beyond 1151 mg after adjusting other covariates.	Phosphorus	84-94	kallikrein related peptidase 3	Homo sapiens	67-70
32674240-12	2020	Over 1151 mg per day dietary phosphorus intake may be the risk factor for PSA increasing.	Phosphorus	29-39	kallikrein related peptidase 3	Homo sapiens	74-77
31499302-2	2020	We aimed to highlight the impact of pH and organic C modifications in soil on the inorganic P (Pi) sorption capacity and availability as compared to the effect of P accumulation after mineral or organic fertilizers.	Phosphorus	92-93	phenylalanine hydroxylase	Homo sapiens	36-38
31499302-2	2020	We aimed to highlight the impact of pH and organic C modifications in soil on the inorganic P (Pi) sorption capacity and availability as compared to the effect of P accumulation after mineral or organic fertilizers.	Phosphorus	95-96	phenylalanine hydroxylase	Homo sapiens	36-38
33602093-6	2020	RESULTS: We demonstrated that a combination of L and P significantly enhances the anti-Abeta effect of L or P in the hippocampus of APP/PS1 mice.	Phosphorus	53-54	amyloid beta (A4) precursor protein	Mus musculus	87-92
31746731-8	2020	In the correlation analysis, the serum E-selectin level was significantly correlated to glucose, alanine transaminase, creatinine, calcium, phosphorus, total protein, albumin, and end diastolic volume (p = 0.0001, p = 0.001, p = 0.03, p = 0.021, p = 0.023, p = 0.002, p = 0.003, and p = 0.047, respectively).	Phosphorus	140-150	selectin E	Homo sapiens	39-49
33602093-6	2020	RESULTS: We demonstrated that a combination of L and P significantly enhances the anti-Abeta effect of L or P in the hippocampus of APP/PS1 mice.	Phosphorus	53-54	presenilin 1	Mus musculus	136-139
33602093-6	2020	RESULTS: We demonstrated that a combination of L and P significantly enhances the anti-Abeta effect of L or P in the hippocampus of APP/PS1 mice.	Phosphorus	108-109	amyloid beta (A4) precursor protein	Mus musculus	87-92
33602093-6	2020	RESULTS: We demonstrated that a combination of L and P significantly enhances the anti-Abeta effect of L or P in the hippocampus of APP/PS1 mice.	Phosphorus	108-109	presenilin 1	Mus musculus	136-139
33602093-7	2020	CONCLUSION: Our findings suggest that combining L and P significantly enhances the anti-Abeta effect of L or P in the hippocampus of APP/PS1 mice and maybe a potential new effective strategy for AD ther- apy.	Phosphorus	54-55	amyloid beta (A4) precursor protein	Mus musculus	88-93
33602093-7	2020	CONCLUSION: Our findings suggest that combining L and P significantly enhances the anti-Abeta effect of L or P in the hippocampus of APP/PS1 mice and maybe a potential new effective strategy for AD ther- apy.	Phosphorus	54-55	presenilin 1	Mus musculus	137-140
32071505-6	2020	PTH elevation is significant when Phosphorus is in the highest tertile.	Phosphorus	34-44	parathyroid hormone	Homo sapiens	0-3
32071505-10	2020	To conclude, ANFIS and machine learning algorithm are in agreement with each other in stating that 25-OHD deficiency triggers lower calcium levels, lower calcium and higher phosphorus trigger PTH production.	Phosphorus	173-183	parathyroid hormone	Homo sapiens	192-195
31498925-5	2020	What roles does XPR1 (the only known phosphate exporter) play in maintaining placental-fetal phosphorus homeostasis?	Phosphorus	93-103	xenotropic and polytropic retrovirus receptor 1	Mus musculus	16-20
32925065-10	2020	CONCLUSION: These findings demonstrated that chronic systemic exposure to P gLPS simultaneously induces inflammation-dependent bone loss and AD-like pathologies by elevating IL-6 and IL-17 from middle age, suggesting that periodontal bacteria induce exacerbation of bone loss and memory decline, resulting in AD progression.	Phosphorus	74-75	interleukin 6	Mus musculus	174-178
32925065-10	2020	CONCLUSION: These findings demonstrated that chronic systemic exposure to P gLPS simultaneously induces inflammation-dependent bone loss and AD-like pathologies by elevating IL-6 and IL-17 from middle age, suggesting that periodontal bacteria induce exacerbation of bone loss and memory decline, resulting in AD progression.	Phosphorus	74-75	interleukin 17A	Mus musculus	183-188
32455510-10	2020	The H&P score was positively correlated with GPA 1 (r = 0.512, P<0.001), with GPA 2 (r = 0.425, P<0.001) and with PANCE score (r = 0.448, P<0.001).	Phosphorus	6-7	glycoprotein hormone subunit alpha 2	Homo sapiens	78-83
31633765-0	2020	Circulating IGF-I independently predicts blood pressure in children with higher calcium-phosphorus product levels.	Phosphorus	80-98	insulin like growth factor 1	Homo sapiens	12-17
31491633-8	2019	Therefore, in anaerobic ecosystems, the effects of macro metals on APA under conditions of sulfide accumulation may have innovative implications for phosphorus management.	Phosphorus	149-159	glutamyl aminopeptidase	Homo sapiens	67-70
31309898-8	2020	RESULTS: The results of the docking studies showed that the newly designed phosphorus and thiophosphorus tacrine analogs, theoretically possess AChE and BChE-binding ability.	Phosphorus	75-85	acetylcholinesterase (Cartwright blood group)	Homo sapiens	144-148
31309898-8	2020	RESULTS: The results of the docking studies showed that the newly designed phosphorus and thiophosphorus tacrine analogs, theoretically possess AChE and BChE-binding ability.	Phosphorus	75-85	butyrylcholinesterase	Homo sapiens	153-157
31712405-0	2020	Phosphorus Availability Regulates TORC1 Signaling via LST8 in Chlamydomonas.	Phosphorus	0-10	uncharacterized protein	Chlamydomonas reinhardtii	54-58
31712405-4	2020	Here, we show that phosphorus (P) regulates TORC1 signaling in the model green alga Chlamydomonas reinhardtii via LST8, a conserved TORC1 subunit that interacts with the kinase domain of TOR.	Phosphorus	19-29	uncharacterized protein	Chlamydomonas reinhardtii	114-118
31732702-0	2020	Phosphorus Sensing by LST8 Acts as a TOR Guide for Cell Growth in Chlamydomonas.	Phosphorus	0-10	MTOR associated protein, LST8 homolog	Homo sapiens	22-26
30053139-5	2020	Per each 10% increase in transferrin saturation (TSAT), there was a 0.013 mmol/L decrease in phosphorus [95% confidence interval (CI) -0.021 to -0.004; P = 0.003] and a 0.022 nmol/L increase in logarithmic 25-hydroxyvitamin D (Ln-25OHD) levels (95% CI 0.005-0.040; P = 0.019).	Phosphorus	93-103	transferrin	Homo sapiens	25-36
30053139-7	2020	Meanwhile, beta (95% CI) per 1 unit increase in phosphorus, Ln-25OHD and Ln-iPTH for the square root of the serum hepcidin were 0.594 (0.257-0.932; P = 0.001), -0.270 (-0.431 to -0.108; P = 0.001) and 0.115 (0.004-0.226; P = 0.042), respectively.	Phosphorus	48-58	hepcidin antimicrobial peptide	Homo sapiens	114-122
30053139-8	2020	In subgroup analysis, the relationship between phosphorus, 25OHD and hepcidin was strongest in the positive-inflammation group.	Phosphorus	47-57	hepcidin antimicrobial peptide	Homo sapiens	69-77
31854604-4	2019	The average concentration of total nitrogen (TN) and total phosphorus (TP) reached 10.05 mg L-1 and 1.10 mg L-1, far exceeding the occurrence standard of eutrophication, which should be cause for concern.	Phosphorus	59-69	L1 cell adhesion molecule	Homo sapiens	92-101
32884998-11	2020	In conclusion, the results suggest c.1A > GAtg/Gtg in the FZD6 (NM_001164616) might be the genetic etiology for non-syndromic CL/P in this pedigree.	Phosphorus	129-130	gamma-glutamyltransferase 1	Homo sapiens	47-50
32884998-11	2020	In conclusion, the results suggest c.1A > GAtg/Gtg in the FZD6 (NM_001164616) might be the genetic etiology for non-syndromic CL/P in this pedigree.	Phosphorus	129-130	frizzled class receptor 6	Homo sapiens	58-62
32884998-12	2020	Furthermore, this finding provided new etiologic information, supplementing the evidence that FZD6 is a strong potential gene for CL/P.	Phosphorus	133-134	frizzled class receptor 6	Homo sapiens	94-98
31835304-2	2019	Treatment of isosorbide with diphenylchlorophosphate generates a mixture of phosphorus esters from which exo-5-(diphenylphosphato)isosorbide-2-endo-ol may be isolated using column chromatography.	Phosphorus	76-93	exonuclease 5	Homo sapiens	105-110
31861622-6	2019	i-Ca was negatively correlated with urea and serum phosphorus was positively correlated with FGF-23.	Phosphorus	51-61	fibroblast growth factor 23	Canis lupus familiaris	93-99
31563738-2	2019	Then the experimental results showed that the IA1 mode (4 h aeration and 1 h non-aeration) could improve the simultaneous nitrogen and phosphorus removal and the settleability of granules in continuous flow system.	Phosphorus	135-145	INSM transcriptional repressor 1	Homo sapiens	46-49
31689101-3	2019	Here we report the direct observation of symmetry-dependent electron-phonon coupling in black phosphorus (BP) by performing the polarization-selective resonance Raman measurement in the visible and ultraviolet regimes, focusing on the out-of-plane Ag1 and in-plane Ag2 phonon modes.	Phosphorus	94-104	NBPF member 10	Homo sapiens	248-251
31689101-3	2019	Here we report the direct observation of symmetry-dependent electron-phonon coupling in black phosphorus (BP) by performing the polarization-selective resonance Raman measurement in the visible and ultraviolet regimes, focusing on the out-of-plane Ag1 and in-plane Ag2 phonon modes.	Phosphorus	94-104	anterior gradient 2, protein disulphide isomerase family member	Homo sapiens	265-268
33015612-12	2020	The magnitude of the FGF-23 level reductions was strongly associated with concomitant changes in serum phosphorus levels but not with the changes in intact parathyroid hormone levels.	Phosphorus	103-113	fibroblast growth factor 23	Homo sapiens	21-27
33015612-16	2020	These results suggest that phosphorus is a strong inducer of FGF-23 production and that regulation of FGF-23 production is a rapid process.	Phosphorus	27-37	fibroblast growth factor 23	Homo sapiens	61-67
31831119-3	2019	Mineral bone abnormalities are common in chronic kidney disease; reduction in glomerular filtration rate and changes in vitamin D, parathyroid hormone, and fibroblast growth factor 23 result in the dysregulation of phosphorus and calcium metabolism.	Phosphorus	215-225	fibroblast growth factor 23	Homo sapiens	156-183
31854558-7	2019	The concentrations of total phosphorus averaged 0.228+-0.068, 0.258+-0.121, 0.219+-0.083, and 0.225+-0.121 mg L-1, respectively.	Phosphorus	28-38	immunoglobulin kappa variable 1-16	Homo sapiens	110-113
31597416-1	2019	A wide-spectrum-responsive paper-based photoelectrochemical (PEC) sensor based on black phosphorus quantum dots sensitized titanium dioxide (TiO2-BP QDs) for prostate-specific antigen (PSA) detection was presented herein.	Phosphorus	88-98	kallikrein related peptidase 3	Homo sapiens	158-189
31628909-1	2019	Human Vgamma9Vdelta2 T cells respond to small phosphorus-containing compounds, often called phosphoantigens, which are now known to be intracellular ligands of the immune receptor butyrophilin 3A1 (BTN3A1).	Phosphorus	46-56	butyrophilin subfamily 3 member A1	Homo sapiens	180-196
31628909-1	2019	Human Vgamma9Vdelta2 T cells respond to small phosphorus-containing compounds, often called phosphoantigens, which are now known to be intracellular ligands of the immune receptor butyrophilin 3A1 (BTN3A1).	Phosphorus	46-56	butyrophilin subfamily 3 member A1	Homo sapiens	198-204
31209480-8	2019	Egret-Burke TaMATE1B also had higher concentrations of water-extractable P, Fe and Al in the rhizosphere, indicating the release of mineral-protected C. In addition, citrate ligand facilitated Fe and Al release from soil, with their concentrations rising with increasing ligand concentration and incubation time.	Phosphorus	73-74	LOC101664696	Triticum aestivum	12-20
31831119-3	2019	Mineral bone abnormalities are common in chronic kidney disease; reduction in glomerular filtration rate and changes in vitamin D, parathyroid hormone, and fibroblast growth factor 23 result in the dysregulation of phosphorus and calcium metabolism.	Phosphorus	215-225	parathyroid hormone	Homo sapiens	131-150
31408100-14	2019	CONCLUSION: The majority of P/LP variants in patients with CACNA1C-mediated LQT8 cluster in an SH3-binding domain of the cytosolic II-III loop.	Phosphorus	28-29	calcium voltage-gated channel subunit alpha1 C	Homo sapiens	59-66
31598923-5	2019	The results showed that application of PM-PA at the highest rate, which caused maximum change in Pr (DeltaPr = 59%) in laboratory condition, also produced maximum P uptake by grain (190.3 mg pot-1) and grain yield (44.1 g pot-1) of wheat in greenhouse experiment.	Phosphorus	39-40	protection of telomeres 1	Homo sapiens	191-196
31598923-5	2019	The results showed that application of PM-PA at the highest rate, which caused maximum change in Pr (DeltaPr = 59%) in laboratory condition, also produced maximum P uptake by grain (190.3 mg pot-1) and grain yield (44.1 g pot-1) of wheat in greenhouse experiment.	Phosphorus	39-40	protection of telomeres 1	Homo sapiens	222-227
31408100-14	2019	CONCLUSION: The majority of P/LP variants in patients with CACNA1C-mediated LQT8 cluster in an SH3-binding domain of the cytosolic II-III loop.	Phosphorus	28-29	calcium voltage-gated channel subunit alpha1 C	Homo sapiens	76-80
31350858-0	2019	Lipid remodeling regulator 1 (LRL1) is differently involved in the phosphorus-depletion response from PSR1 in Chlamydomonas reinhardtii.	Phosphorus	67-77	uncharacterized protein	Chlamydomonas reinhardtii	102-106
31989808-0	2019	Influence of the Klotho/FGF23/Egr1 signaling pathway on calcium-phosphorus metabolism in diabetic nephropathy and the intervention of Shenyuan granules.	Phosphorus	56-74	klotho	Mus musculus	17-23
31989808-0	2019	Influence of the Klotho/FGF23/Egr1 signaling pathway on calcium-phosphorus metabolism in diabetic nephropathy and the intervention of Shenyuan granules.	Phosphorus	56-74	fibroblast growth factor 23	Mus musculus	24-29
31989808-0	2019	Influence of the Klotho/FGF23/Egr1 signaling pathway on calcium-phosphorus metabolism in diabetic nephropathy and the intervention of Shenyuan granules.	Phosphorus	56-74	early growth response 1	Mus musculus	30-34
31989808-10	2019	Shenyuan granules may partly intervene in the expressions of CYP24 and CYP27 through the Klotho/FGF23/Egr1 signaling pathway, thereby improving calcium and phosphorus metabolism and alleviating renal injury in diabetic nephropathy.	Phosphorus	156-166	cytochrome P450, family 24, subfamily a, polypeptide 1	Mus musculus	61-66
31989808-10	2019	Shenyuan granules may partly intervene in the expressions of CYP24 and CYP27 through the Klotho/FGF23/Egr1 signaling pathway, thereby improving calcium and phosphorus metabolism and alleviating renal injury in diabetic nephropathy.	Phosphorus	156-166	cytochrome P450, family 27, subfamily a, polypeptide 1	Mus musculus	71-76
31384956-3	2019	Serum FGF23 was negatively correlated with serum phosphorus.	Phosphorus	49-59	fibroblast growth factor 23	Homo sapiens	6-11
31384956-5	2019	INTRODUCTION: FGF23 is involved in the mineral homeostasis, especially the regulation of serum phosphorus.	Phosphorus	95-105	fibroblast growth factor 23	Homo sapiens	14-19
31384956-12	2019	Serum FGF23 was significantly and negatively correlated with phosphorus level after adjusted for age, gender, calcium, iPTH, and 25(OH)D in the euthyroid GD group.	Phosphorus	61-71	fibroblast growth factor 23	Homo sapiens	6-11
31384956-14	2019	Serum FGF23 was negatively correlated with serum phosphorus in euthyroid GD patients.	Phosphorus	49-59	fibroblast growth factor 23	Homo sapiens	6-11
32055385-1	2019	Condensed phase access to the unprecedented tetrahedral cations [EP3]+ (E = S, Se, Te) was achieved through the reaction of ECl3[WCA] with white phosphorus ([WCA]- = [Al(ORF)4]- and [F(Al(ORF)3)2]-; -RF = -C(CF3)3).	Phosphorus	145-155	prostaglandin E receptor 3	Homo sapiens	65-73
31300631-1	2019	We investigate the spin relaxation under conditions of optical excitation between the Rydberg orbital states of phosphorus donor impurities in silicon.	Phosphorus	112-122	spindlin 1	Homo sapiens	19-23
31320601-3	2019	Compared to pure TiO2 and TiO2/SnO with a microplate structure (TiO2/P-SnO), TiO2/F-SnO heterojunctions exhibited significantly enhanced photocatalytic performances for organics removal such as toluidine blue O (TBO) and methylene blue (MB) under daylight fluorescent lamp irradiation (350-800 nm).	Phosphorus	69-70	strawberry notch homolog 2	Homo sapiens	71-74
31320601-3	2019	Compared to pure TiO2 and TiO2/SnO with a microplate structure (TiO2/P-SnO), TiO2/F-SnO heterojunctions exhibited significantly enhanced photocatalytic performances for organics removal such as toluidine blue O (TBO) and methylene blue (MB) under daylight fluorescent lamp irradiation (350-800 nm).	Phosphorus	69-70	strawberry notch homolog 2	Homo sapiens	71-74
31726554-7	2019	Annual total soluble phosphorus yield (soluble phosphorus loading to stream) from subsurface drains and surface runoff could vary from 0.041 to 0.058 kg/ha under RCP 4.5 and 0.035 to 0.064 kg/ha under RCP 8.5 by the end of the 21st century while the values from the baseline model were 0.051 kg/ha.	Phosphorus	21-31	CGRP receptor component	Homo sapiens	162-165
31328421-3	2019	The activated Al@PS core-shell beads were involved to make a homogenous MOF-based layer in the presence of the organic linker.	Phosphorus	17-19	lysine acetyltransferase 8	Homo sapiens	72-75
31279186-1	2019	Calcium nitrate (Ca(NO3)2) addition can be used to control the release of phosphorus from sediments, however it can also cause an increase in the concentration of nitrate-nitrogen (NO3--N) in the water column.	Phosphorus	74-84	NBL1, DAN family BMP antagonist	Homo sapiens	20-23
31279186-6	2019	The combined treatment using Ca(NO3)2 and AER had a relatively small effect on the contents of mobile phosphorus in the sediments, but it could greatly increase the amount of residual phosphorus in the top 30mm sediments (increased by 27.7-42.9%).	Phosphorus	184-194	NBL1, DAN family BMP antagonist	Homo sapiens	32-35
31279186-8	2019	In conclusion, the combined use of Ca(NO3)2 addition and AER capping is a more promising strategy for the control of sedimentary phosphorus release than the single use of Ca(NO3)2 addition from the point of view of both the control efficiency of P release from sediments and the releasing risk of the added nitrate.	Phosphorus	129-139	NBL1, DAN family BMP antagonist	Homo sapiens	38-41
31653006-8	2019	Moreover, chromatography data showed that PS and PTS possessed 17 identical anthocyanins as a negative regulator of ERK.	Phosphorus	42-44	mitogen-activated protein kinase 1	Mus musculus	116-119
31653006-9	2019	These findings suggested that anthocyanins from PS and PTS inhibited melanogenesis in vitro and in vivo by activating the ERK signaling pathway.	Phosphorus	48-50	mitogen-activated protein kinase 1	Mus musculus	122-125
31560355-2	2019	The dense packing of POMe2/PSMe2 functional groups within UHM-60/UHM-61 (UHM: University of Hamburg Materials) with an underlying net of ucp topology was overcome by increasing the sterical demand of phosphorus substituents.	Phosphorus	200-210	proteasome activator subunit 2	Homo sapiens	27-32
31614948-6	2019	The nutrient-to-energy ratio for vitamins A, B1, B2, B6, C, folate and minerals Calcium, copper, iron, magnesium, phosphorus, potassium and zinc increased significantly.	Phosphorus	114-124	immunoglobulin kappa variable 5-2	Homo sapiens	33-55
31591515-1	2019	Phytase is one of the most effective feed additives to increase the availability of phosphorus and minerals by catalyzing the hydrolysis of phytic acid.	Phosphorus	84-94	putative glycerophosphoryl diester phosphodiesterase	Glycine max	0-7
31903094-11	2019	The study demonstrated reduced plasma levels of parathyroid hormone (PTH), reduced fluctuations in plasma phosphate and plasma PTH, and reduced renal phosphate excretion when ingesting phosphorus supplementation as milk compared to phosphate tablets.	Phosphorus	185-195	parathyroid hormone	Homo sapiens	48-67
31903094-11	2019	The study demonstrated reduced plasma levels of parathyroid hormone (PTH), reduced fluctuations in plasma phosphate and plasma PTH, and reduced renal phosphate excretion when ingesting phosphorus supplementation as milk compared to phosphate tablets.	Phosphorus	185-195	parathyroid hormone	Homo sapiens	69-72
31903094-11	2019	The study demonstrated reduced plasma levels of parathyroid hormone (PTH), reduced fluctuations in plasma phosphate and plasma PTH, and reduced renal phosphate excretion when ingesting phosphorus supplementation as milk compared to phosphate tablets.	Phosphorus	185-195	parathyroid hormone	Homo sapiens	127-130
31064011-8	2019	Anti-FGF-23 antibody tended to increase (0.05 < P <= 0.1) plasma phosphorus level of hens before adenine gavage, interestingly, and decreased (P <= 0.01) plasma FGF-23 level and kidney index (% of body weight) of hens after adenine gavage.	Phosphorus	65-75	fibroblast growth factor 23	Gallus gallus	5-11
31215115-5	2019	A variant in GDF11 (encoding growth differentiation factor 11), predicting a p.(Arg298Gln) substitution at the Furin protease cleavage site, was identified in one family that segregated with CL/P and both rib and vertebral hypersegmentation, mirroring that seen in Gdf11 knockout mice.	Phosphorus	194-195	growth differentiation factor 11	Mus musculus	13-18
31215115-5	2019	A variant in GDF11 (encoding growth differentiation factor 11), predicting a p.(Arg298Gln) substitution at the Furin protease cleavage site, was identified in one family that segregated with CL/P and both rib and vertebral hypersegmentation, mirroring that seen in Gdf11 knockout mice.	Phosphorus	194-195	growth differentiation factor 11	Homo sapiens	29-61
31215115-5	2019	A variant in GDF11 (encoding growth differentiation factor 11), predicting a p.(Arg298Gln) substitution at the Furin protease cleavage site, was identified in one family that segregated with CL/P and both rib and vertebral hypersegmentation, mirroring that seen in Gdf11 knockout mice.	Phosphorus	194-195	furin (paired basic amino acid cleaving enzyme)	Mus musculus	111-116
31215115-6	2019	In the second family in which CL/P was the only phenotype, a mutation in FST (encoding the GDF11 antagonist, Follistatin) was identified that is predicted to result in a p.(Cys56Tyr) substitution in the region that binds GDF11.	Phosphorus	33-34	growth differentiation factor 11	Mus musculus	91-96
31215115-6	2019	In the second family in which CL/P was the only phenotype, a mutation in FST (encoding the GDF11 antagonist, Follistatin) was identified that is predicted to result in a p.(Cys56Tyr) substitution in the region that binds GDF11.	Phosphorus	33-34	follistatin	Mus musculus	109-120
31226716-3	2019	The episodes were linked to biallelic variants in exon 2 of the TBC1D24 gene that lead to amino acid changes (c.304C >T/p.Pro102Ser and c.410T > C/p.Val137Ala), each variant being inherited from a parent.	Phosphorus	5-6	TBC1 domain family member 24	Homo sapiens	64-71
31660068-0	2019	Tailored Black Phosphorus for Erythrocyte Membrane Nanocloaking with Interleukin-1alpha siRNA and Paclitaxel for Targeted, Durable, and Mild Combination Cancer Therapy.	Phosphorus	15-25	interleukin 1 alpha	Homo sapiens	69-87
31453997-0	2019	Controlled nanofabrication of metal-free SERS substrate on few layered black phosphorus by low power focused laser irradiation.	Phosphorus	77-87	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	41-45
31453997-1	2019	Black Phosphorous (BP) has intrinsic in-plane ferroelectric properties that may have the inherent capability of SERS response and can be considered as a replacement of metal nanoparticle-based SERS substrates.	Phosphorus	6-17	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	112-116
31453997-1	2019	Black Phosphorous (BP) has intrinsic in-plane ferroelectric properties that may have the inherent capability of SERS response and can be considered as a replacement of metal nanoparticle-based SERS substrates.	Phosphorus	6-17	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	193-197
31150757-3	2019	To date, two independent GWAS have identified GADD45G as influencing risk for CL/P.	Phosphorus	81-82	growth arrest and DNA damage inducible gamma	Homo sapiens	46-53
31566311-8	2019	A description is given of a patient suffering from MD1 with a number of endocrine disorders, including hypergonadotropic hypogonadism, autoimmune thyroid disease, hyperinsulinism, and also impaired calcium-phosphorus metabolism.	Phosphorus	198-216	MAFD1	Homo sapiens	51-54
31854882-3	2019	When a phosphorus source was and was not added, the optimum conditions for recovering phosphorus were pH=9.5, N:P=0.8, and Mg:P=1.8 and pH=9.5, Mg:P=1.6, and speed=200 r min-1, respectively.	Phosphorus	86-96	CD59 molecule (CD59 blood group)	Homo sapiens	170-175
31008565-3	2019	In this work, phosphorus and polyamidoamine dendrimer (generation 3 and 4 of each type) are explored to address delivery challenges of PLK1 siRNA (siPLK1).	Phosphorus	14-24	polo like kinase 1	Homo sapiens	135-139
31201908-7	2019	Experimentally, P(DADMAC-AAm)CMC/Fe2O3 and P(DADMAC-SA)CMC/Fe2O3 show high sorption capacity of Co(II), i.e. 69.67 mg g-1 and 75.17 mg g-1, respectively, which makes them potential sorbents for Co(II) removal from water/wastewater.	Phosphorus	16-17	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	96-102
31201908-7	2019	Experimentally, P(DADMAC-AAm)CMC/Fe2O3 and P(DADMAC-SA)CMC/Fe2O3 show high sorption capacity of Co(II), i.e. 69.67 mg g-1 and 75.17 mg g-1, respectively, which makes them potential sorbents for Co(II) removal from water/wastewater.	Phosphorus	16-17	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	194-200
31157583-1	2019	PURPOSE: The KRISTINE study compared neoadjuvant trastuzumab emtansine plus pertuzumab (T-DM1+P) with docetaxel, carboplatin, trastuzumab plus P (TCH+P) for the treatment human epidermal growth factor receptor 2-positive stage II to III breast cancer.	Phosphorus	0-1	erb-b2 receptor tyrosine kinase 2	Homo sapiens	177-211
30712064-6	2019	The increased aortic phosphorus content as an index of vascular calcification was inhibited by both FYB-931 and etidronate in a dose-dependent manner; however, FYB-931 was 10 times more potent than etidronate.	Phosphorus	21-31	FYN binding protein 1	Rattus norvegicus	100-103
30712064-6	2019	The increased aortic phosphorus content as an index of vascular calcification was inhibited by both FYB-931 and etidronate in a dose-dependent manner; however, FYB-931 was 10 times more potent than etidronate.	Phosphorus	21-31	FYN binding protein 1	Rattus norvegicus	160-163
31262954-0	2019	SPX4 Acts on PHR1-Dependent and -Independent Regulation of Shoot Phosphorus Status in Arabidopsis.	Phosphorus	65-75	SPX domain-containing protein 4	Arabidopsis thaliana	0-4
31599133-1	2019	Fibroblast growth factor 23 (FGF23), one of the endocrine fibroblast growth factors, is a principal regulator in the maintenance of serum phosphorus concentration.	Phosphorus	138-148	fibroblast growth factor 23	Homo sapiens	0-27
31599133-1	2019	Fibroblast growth factor 23 (FGF23), one of the endocrine fibroblast growth factors, is a principal regulator in the maintenance of serum phosphorus concentration.	Phosphorus	138-148	fibroblast growth factor 23	Homo sapiens	29-34
31599133-4	2019	FGF23 reduces serum phosphorus concentration through decreased reabsorption of phosphorus in the kidney and by decreasing 1,25 dihydroxyvitamin D (1,25(OH)2D) concentrations.	Phosphorus	20-30	fibroblast growth factor 23	Homo sapiens	0-5
31599133-4	2019	FGF23 reduces serum phosphorus concentration through decreased reabsorption of phosphorus in the kidney and by decreasing 1,25 dihydroxyvitamin D (1,25(OH)2D) concentrations.	Phosphorus	79-89	fibroblast growth factor 23	Homo sapiens	0-5
30796757-6	2019	Parameters which were measured were serum Ca, P, parathyroid hormone (PTH), 25-OH vitamin D, albumin and creatinine).	Phosphorus	0-1	parathyroid hormone	Homo sapiens	49-68
30393914-11	2019	Parameters affecting PCPE-1 elevation in the patient group were identified as systolic blood pressure, blood urea nitrogen, phosphorus, haemoglobin, intact parathormone levels, glomerular filtration rate and body mass index.	Phosphorus	124-134	procollagen C-endopeptidase enhancer	Homo sapiens	21-27
31348670-1	2019	A straightforward method for the preparation of non-K region fused phosphorus- and nitrogen-containing (PN)-heterocyclic pyrenes has been accomplished.	Phosphorus	67-77	U6 snRNA biogenesis phosphodiesterase 1	Homo sapiens	104-106
31152194-2	2019	KEY MESSAGE: Piriformospora indica confers salt tolerance in tomato seedlings by increasing the uptake of nutrients such as N, P and Ca, improving K+/Na+ homoeostasis by regulating the expression of NHXs, SOS1 and CNGC15 genes, maintaining water status by regulating the expression of aquaporins.	Phosphorus	13-14	plasmalemma Na+/H+ antiporter	Solanum lycopersicum	205-209
31152194-2	2019	KEY MESSAGE: Piriformospora indica confers salt tolerance in tomato seedlings by increasing the uptake of nutrients such as N, P and Ca, improving K+/Na+ homoeostasis by regulating the expression of NHXs, SOS1 and CNGC15 genes, maintaining water status by regulating the expression of aquaporins.	Phosphorus	13-14	cyclic nucleotide gated channel 15	Solanum lycopersicum	214-220
31154128-4	2019	Results showed that chloramination could reduce formation of C-DBPs and total organic halogen (TOX) while increase N-DBP formation, and the introduction of TA/PS pretreatment process slightly increased the formation of C-DBPs and TOX but sharply reduced the formation of N-DBPs with higher toxicity as well as brominated CX3R-type DBPs that are more toxic than their chlorinated analogues.	Phosphorus	159-161	thymocyte selection associated high mobility group box	Homo sapiens	230-233
31122463-10	2019	The total phosphorus of a certified reference material (GSBZ50033-95) was 1.50 +- 0.04 mgP L-1 (n = 3), consistent with the certified value (1.51 +- 0.02 mgP L-1).	Phosphorus	10-20	immunoglobulin kappa variable 1-16	Homo sapiens	91-94
31416263-5	2019	Concentrations of macrominerals, including Ca, Mg, P, K, and Na, in the raw milk were greater in Alberta dairy farms than the WA (p &lt; 00.5; except Ca).	Phosphorus	51-52	Weaning weight-maternal milk	Bos taurus	76-80
31401975-2	2019	Here, neural-network analysis is used to test whether noninvasive phosphorus (31P) cardiovascular magnetic resonance spectroscopy (CMRS) measurements of cardiac adenosine triphosphate (ATP) energy, phosphocreatine (PCr), the first-order CK reaction rate kf, and the rate of ATP synthesis through CK (CK flux), can predict specific human heart disease and clinical severity.	Phosphorus	66-76	cytidine/uridine monophosphate kinase 1	Homo sapiens	237-239
31401975-2	2019	Here, neural-network analysis is used to test whether noninvasive phosphorus (31P) cardiovascular magnetic resonance spectroscopy (CMRS) measurements of cardiac adenosine triphosphate (ATP) energy, phosphocreatine (PCr), the first-order CK reaction rate kf, and the rate of ATP synthesis through CK (CK flux), can predict specific human heart disease and clinical severity.	Phosphorus	66-76	cytidine/uridine monophosphate kinase 1	Homo sapiens	296-298
31401975-2	2019	Here, neural-network analysis is used to test whether noninvasive phosphorus (31P) cardiovascular magnetic resonance spectroscopy (CMRS) measurements of cardiac adenosine triphosphate (ATP) energy, phosphocreatine (PCr), the first-order CK reaction rate kf, and the rate of ATP synthesis through CK (CK flux), can predict specific human heart disease and clinical severity.	Phosphorus	66-76	cytidine/uridine monophosphate kinase 1	Homo sapiens	296-298
31161541-5	2019	Short-chain n-alkanes (C15, C17, and C19) in the sediments varied in abundance from 10.0 to 76.2 mug/g TOC across the study and showed a moderate correlation with total phosphorus (TP) concentrations in the overlying water.	Phosphorus	169-179	placenta associated 8	Homo sapiens	23-26
31343838-5	2019	Also, 3 p exhibited weak inhibition of the enzymatic activity of human topoisomerase I. Molecular docking studies indicated preferential binding of the compounds to the ATP-binding pocket of the human checkpoint 2 kinase (Chk2) catalytic domain, thus, identifying a novel diaryl 2-propenone chemotype for the development of potent inhibitors of Chk2.	Phosphorus	8-9	checkpoint kinase 2	Homo sapiens	201-220
31343838-5	2019	Also, 3 p exhibited weak inhibition of the enzymatic activity of human topoisomerase I. Molecular docking studies indicated preferential binding of the compounds to the ATP-binding pocket of the human checkpoint 2 kinase (Chk2) catalytic domain, thus, identifying a novel diaryl 2-propenone chemotype for the development of potent inhibitors of Chk2.	Phosphorus	8-9	checkpoint kinase 2	Homo sapiens	222-226
31343838-5	2019	Also, 3 p exhibited weak inhibition of the enzymatic activity of human topoisomerase I. Molecular docking studies indicated preferential binding of the compounds to the ATP-binding pocket of the human checkpoint 2 kinase (Chk2) catalytic domain, thus, identifying a novel diaryl 2-propenone chemotype for the development of potent inhibitors of Chk2.	Phosphorus	8-9	checkpoint kinase 2	Homo sapiens	345-349
30728466-12	2019	Furthermore, the olfactory bulbs in MPTP/P-treated mice showed significantly increased levels of interleukin-1beta (IL-1beta), caspase-1, glial fibrillary acidic protein (GFAP), Toll receptor 4 (TLR4), phosphorylation of p65, as well as activated molecules of NOD-like receptor protein 3 (NLRP3) that were associated with neuroinflammation.	Phosphorus	37-38	interleukin 1 beta	Mus musculus	97-114
30728466-12	2019	Furthermore, the olfactory bulbs in MPTP/P-treated mice showed significantly increased levels of interleukin-1beta (IL-1beta), caspase-1, glial fibrillary acidic protein (GFAP), Toll receptor 4 (TLR4), phosphorylation of p65, as well as activated molecules of NOD-like receptor protein 3 (NLRP3) that were associated with neuroinflammation.	Phosphorus	37-38	interleukin 1 alpha	Mus musculus	116-124
30728466-12	2019	Furthermore, the olfactory bulbs in MPTP/P-treated mice showed significantly increased levels of interleukin-1beta (IL-1beta), caspase-1, glial fibrillary acidic protein (GFAP), Toll receptor 4 (TLR4), phosphorylation of p65, as well as activated molecules of NOD-like receptor protein 3 (NLRP3) that were associated with neuroinflammation.	Phosphorus	37-38	caspase 1	Mus musculus	127-136
30728466-12	2019	Furthermore, the olfactory bulbs in MPTP/P-treated mice showed significantly increased levels of interleukin-1beta (IL-1beta), caspase-1, glial fibrillary acidic protein (GFAP), Toll receptor 4 (TLR4), phosphorylation of p65, as well as activated molecules of NOD-like receptor protein 3 (NLRP3) that were associated with neuroinflammation.	Phosphorus	37-38	glial fibrillary acidic protein	Mus musculus	138-169
30728466-12	2019	Furthermore, the olfactory bulbs in MPTP/P-treated mice showed significantly increased levels of interleukin-1beta (IL-1beta), caspase-1, glial fibrillary acidic protein (GFAP), Toll receptor 4 (TLR4), phosphorylation of p65, as well as activated molecules of NOD-like receptor protein 3 (NLRP3) that were associated with neuroinflammation.	Phosphorus	37-38	glial fibrillary acidic protein	Mus musculus	171-175
30728466-12	2019	Furthermore, the olfactory bulbs in MPTP/P-treated mice showed significantly increased levels of interleukin-1beta (IL-1beta), caspase-1, glial fibrillary acidic protein (GFAP), Toll receptor 4 (TLR4), phosphorylation of p65, as well as activated molecules of NOD-like receptor protein 3 (NLRP3) that were associated with neuroinflammation.	Phosphorus	37-38	toll-like receptor 4	Mus musculus	178-193
30728466-12	2019	Furthermore, the olfactory bulbs in MPTP/P-treated mice showed significantly increased levels of interleukin-1beta (IL-1beta), caspase-1, glial fibrillary acidic protein (GFAP), Toll receptor 4 (TLR4), phosphorylation of p65, as well as activated molecules of NOD-like receptor protein 3 (NLRP3) that were associated with neuroinflammation.	Phosphorus	37-38	toll-like receptor 4	Mus musculus	195-199
30728466-12	2019	Furthermore, the olfactory bulbs in MPTP/P-treated mice showed significantly increased levels of interleukin-1beta (IL-1beta), caspase-1, glial fibrillary acidic protein (GFAP), Toll receptor 4 (TLR4), phosphorylation of p65, as well as activated molecules of NOD-like receptor protein 3 (NLRP3) that were associated with neuroinflammation.	Phosphorus	37-38	v-rel reticuloendotheliosis viral oncogene homolog A (avian)	Mus musculus	221-224
30728466-12	2019	Furthermore, the olfactory bulbs in MPTP/P-treated mice showed significantly increased levels of interleukin-1beta (IL-1beta), caspase-1, glial fibrillary acidic protein (GFAP), Toll receptor 4 (TLR4), phosphorylation of p65, as well as activated molecules of NOD-like receptor protein 3 (NLRP3) that were associated with neuroinflammation.	Phosphorus	37-38	NLR family, pyrin domain containing 3	Mus musculus	260-287
30728466-12	2019	Furthermore, the olfactory bulbs in MPTP/P-treated mice showed significantly increased levels of interleukin-1beta (IL-1beta), caspase-1, glial fibrillary acidic protein (GFAP), Toll receptor 4 (TLR4), phosphorylation of p65, as well as activated molecules of NOD-like receptor protein 3 (NLRP3) that were associated with neuroinflammation.	Phosphorus	37-38	NLR family, pyrin domain containing 3	Mus musculus	289-294
30728466-13	2019	Our results demonstrate that MPTP/P-caused olfactory bulb damage might be related to NLRP3-mediated inflammation.	Phosphorus	30-31	NLR family, pyrin domain containing 3	Mus musculus	85-90
31221281-8	2019	The non-adherence group showed a substantial increase of 0.74 mg/dL in serum phosphorus levels and 6.16 mg2/dL2 in the calcium-phosphorus product after the intervention.	Phosphorus	127-137	l(1)L2	Drosophila melanogaster	108-111
31221281-9	2019	Meanwhile, the calcium-phosphorus product improved from 56.42 +- 11.49 mg2/dL2 to 51.05 +- 10.67 mg2/dL2 in the adherence group.	Phosphorus	23-33	l(1)L2	Drosophila melanogaster	75-78
31221281-9	2019	Meanwhile, the calcium-phosphorus product improved from 56.42 +- 11.49 mg2/dL2 to 51.05 +- 10.67 mg2/dL2 in the adherence group.	Phosphorus	23-33	l(1)L2	Drosophila melanogaster	101-104
31161541-5	2019	Short-chain n-alkanes (C15, C17, and C19) in the sediments varied in abundance from 10.0 to 76.2 mug/g TOC across the study and showed a moderate correlation with total phosphorus (TP) concentrations in the overlying water.	Phosphorus	169-179	cytokine like 1	Homo sapiens	28-31
31085209-12	2019	In summary, the results of the present study demonstrate that B[a]P and BPDE induce mitochondrial damage through ROS production that suppresses SIRT1/TERT/PGC-1a signaling and mediate B[a]P- and BPDE-mediated reproductive toxicity.	Phosphorus	66-67	sirtuin 1	Rattus norvegicus	144-149
31085209-12	2019	In summary, the results of the present study demonstrate that B[a]P and BPDE induce mitochondrial damage through ROS production that suppresses SIRT1/TERT/PGC-1a signaling and mediate B[a]P- and BPDE-mediated reproductive toxicity.	Phosphorus	66-67	telomerase reverse transcriptase	Rattus norvegicus	150-154
31085209-12	2019	In summary, the results of the present study demonstrate that B[a]P and BPDE induce mitochondrial damage through ROS production that suppresses SIRT1/TERT/PGC-1a signaling and mediate B[a]P- and BPDE-mediated reproductive toxicity.	Phosphorus	66-67	PPARG coactivator 1 alpha	Sus scrofa	155-161
30991335-6	2019	The chemical elements As, B, Bi, Cd, Cu, P, Pb, Sb, Sn and Zn (PC2) are strongly spatially associated with soils sampled above high-density urban residential, commercial and industrial sites, and are interpreted to reflect heavy metal contamination from human activities.	Phosphorus	41-42	chromobox 4	Homo sapiens	63-66
31260305-1	2019	Phosphorus-carbon spin-spin coupling constants in a series of salient heterocyclic phosphines were calculated at the SOPPA(MP2) level including evaluation of relativistic and solvent effects.	Phosphorus	0-10	tryptase pseudogene 1	Homo sapiens	117-126
31319542-1	2019	A coinage-metal bond has been predicted and characterized in the complexes of [1.1.1]propellane (P) and M2/MCl/MCH3 (M = Cu, Ag, and Au).	Phosphorus	97-98	C-type lectin domain family 4 member D	Homo sapiens	107-110
31319542-1	2019	A coinage-metal bond has been predicted and characterized in the complexes of [1.1.1]propellane (P) and M2/MCl/MCH3 (M = Cu, Ag, and Au).	Phosphorus	97-98	caspase 7	Homo sapiens	111-115
31085402-0	2019	Porous graphene-black phosphorus nanocomposite modified electrode for detection of leptin.	Phosphorus	22-32	leptin	Homo sapiens	83-89
31085402-3	2019	This paper describes an environmentally friendly and label-free immunosensor based on porous graphene functionalized black phosphorus (PG-BP) composite to detect of leptin.	Phosphorus	117-133	leptin	Homo sapiens	165-171
31096080-1	2019	We propose the first black phosphorus (BP) - fiber optic biosensor for ultrasensitive diagnosis of human neuron-specific enolase (NSE) cancer biomarkers.	Phosphorus	21-37	enolase 2	Homo sapiens	105-128
31096080-1	2019	We propose the first black phosphorus (BP) - fiber optic biosensor for ultrasensitive diagnosis of human neuron-specific enolase (NSE) cancer biomarkers.	Phosphorus	21-37	enolase 2	Homo sapiens	130-133
31096080-1	2019	We propose the first black phosphorus (BP) - fiber optic biosensor for ultrasensitive diagnosis of human neuron-specific enolase (NSE) cancer biomarkers.	Phosphorus	39-41	enolase 2	Homo sapiens	105-128
31096080-1	2019	We propose the first black phosphorus (BP) - fiber optic biosensor for ultrasensitive diagnosis of human neuron-specific enolase (NSE) cancer biomarkers.	Phosphorus	39-41	enolase 2	Homo sapiens	130-133
31096080-5	2019	The anti-NSE immobilized BP-TFG biosensor has been implemented to detect NSE biomarkers demonstrating ultrahigh sensitivity with limit of detection down to 1.0 pg/mL, which is 4 orders magnitude lower than NSE cut-off value of small cell lung cancer.	Phosphorus	25-27	enolase 2	Homo sapiens	9-12
31096080-5	2019	The anti-NSE immobilized BP-TFG biosensor has been implemented to detect NSE biomarkers demonstrating ultrahigh sensitivity with limit of detection down to 1.0 pg/mL, which is 4 orders magnitude lower than NSE cut-off value of small cell lung cancer.	Phosphorus	25-27	enolase 2	Homo sapiens	73-76
31096080-5	2019	The anti-NSE immobilized BP-TFG biosensor has been implemented to detect NSE biomarkers demonstrating ultrahigh sensitivity with limit of detection down to 1.0 pg/mL, which is 4 orders magnitude lower than NSE cut-off value of small cell lung cancer.	Phosphorus	25-27	enolase 2	Homo sapiens	73-76
31336943-9	2019	The outcome of correlation and LASSO regression indicated that total phosphorus (TP) was the single most important factor for Fe(II), S(-II), and SSC in black bloom with explanation ratios (ERs) of 76.1%, 37.0%, and 12.9%, respectively.	Phosphorus	69-79	transcription elongation factor A1	Homo sapiens	134-139
31340920-7	2019	Acute exposure to isoflurane resulted in obviously increased cellular ROS, cytochrome C release and caspase-3 activity in the hippocampal neurons (P &amp;lt; 0.05), and these changes were significantly inhibited by ulinastatin pretreatment (P &amp;lt; 0.05).	Phosphorus	147-148	caspase 3	Rattus norvegicus	100-109
31247804-4	2019	Predicated on an efficient metal-free dehalogenation of aryl halides under mild organo-photoredox conditions, sulfur, phosphorus, and silicon heteroatoms capture the C(sp2)-centered radical in an intramolecular fashion.	Phosphorus	118-128	Sp2 transcription factor	Homo sapiens	166-171
31284582-8	2019	This assay allowed the isolation of the lpa1-5525 mutant characterized by a new mutation in the lpa1 locus associated with a lower amount of phytic phosphorus in the seeds in comparison with the wild type.	Phosphorus	148-158	inositol-3-phosphate synthase	Zea mays	40-44
31284582-8	2019	This assay allowed the isolation of the lpa1-5525 mutant characterized by a new mutation in the lpa1 locus associated with a lower amount of phytic phosphorus in the seeds in comparison with the wild type.	Phosphorus	148-158	inositol-3-phosphate synthase	Zea mays	96-100
29392983-7	2019	N-NO2 and N-NO3 removal efficiency was very low for both analysed systems where for total phosphorus and phosphates it oscillated around 83-84%.	Phosphorus	90-100	membrane frizzled-related protein	Homo sapiens	0-5
30939369-6	2019	Increasing the magnesite dosage from 0.83 to 3.33 g L-1 promoted the phosphorus recovery efficiency from 2.2% to 78.3% at 3 d, which was attributed to sufficient Mg2+ supply.	Phosphorus	69-79	immunoglobulin kappa variable 1-16	Homo sapiens	52-55
30939369-6	2019	Increasing the magnesite dosage from 0.83 to 3.33 g L-1 promoted the phosphorus recovery efficiency from 2.2% to 78.3% at 3 d, which was attributed to sufficient Mg2+ supply.	Phosphorus	69-79	serpin family C member 1	Homo sapiens	119-125
31270632-12	2019	Graphical abstract Schematic presentation of the quenching of the fluorescence of phosphorus and nitrogen dually-doped carbon quantum dots (PN-CQDs) by vitamin B12 (VB12) and Co(II).	Phosphorus	82-92	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	175-181
31001886-0	2019	Temperature and phosphorus interacts in controlling the picoplankton carbon flux in the Adriatic Sea: an experimental versus field study.	Phosphorus	16-26	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	97-100
31001886-3	2019	Therefore, in the global warming scenario, an increase of the picoplankton carbon flux towards higher trophic levels can be expected in the Adriatic Sea, particularly under unlimited phosphorus conditions.	Phosphorus	183-193	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	149-152
31037817-1	2019	FGF-23 is a 32 kDa protein that is a key regulator of phosphorus and vitamin D metabolism.	Phosphorus	54-64	fibroblast growth factor 23	Homo sapiens	0-6
31589667-0	2019	Long-term Variation in Agricultural Edge-of-Field Phosphorus Transport during Snowmelt, Rain, and Mixed Runoff Events.	Phosphorus	50-60	Ras interacting protein 1	Homo sapiens	88-92
31062421-0	2019	Effects of dietary calcium to available phosphorus ratios on bone metabolism and osteoclast activity of the OPG /RANK/RANKL signalling pathway in piglets.	Phosphorus	40-50	TNF receptor superfamily member 11b	Homo sapiens	108-111
31062421-3	2019	The aim of this study was to explore the effects of dietary calcium to available phosphorus ratios (Ca/AP) on bone metabolism and osteoclast activity of the osteoprotegerin (OPG)/receptor activator of nuclear factor kappa B ligand (RANKL) signalling pathway in piglets.	Phosphorus	81-91	TNF receptor superfamily member 11b	Homo sapiens	157-172
31062421-3	2019	The aim of this study was to explore the effects of dietary calcium to available phosphorus ratios (Ca/AP) on bone metabolism and osteoclast activity of the osteoprotegerin (OPG)/receptor activator of nuclear factor kappa B ligand (RANKL) signalling pathway in piglets.	Phosphorus	81-91	TNF receptor superfamily member 11b	Homo sapiens	174-177
31079202-4	2019	The whole-exome sequencing analysis revealed that both patients harbored compound heterozygous mutations (p.Lys14Arg and p.Trp74Cys) of COX20 gene.	Phosphorus	55-56	cytochrome c oxidase assembly factor COX20	Homo sapiens	136-141
30878613-5	2019	The results indicate that hexokinase has the capability to catalyze the phosphorylation of COS, resulting in an increase in the quantity of phosphorus in the SF-g-COS.	Phosphorus	140-150	hexokinase 1	Homo sapiens	26-36
30952291-0	2019	Electrogenerated chemiluminescence aptasensor for lysozyme based on copolymer nanospheres encapsulated black phosphorus quantum dots.	Phosphorus	109-119	lysozyme	Homo sapiens	50-58
30928749-8	2019	Ship-borne phosphorus input results in a decrease of phosphate content in the water and increase of phosphorus binding to sediments.	Phosphorus	11-21	inositol polyphosphate-5-phosphatase D	Homo sapiens	0-4
30928749-8	2019	Ship-borne phosphorus input results in a decrease of phosphate content in the water and increase of phosphorus binding to sediments.	Phosphorus	100-110	inositol polyphosphate-5-phosphatase D	Homo sapiens	0-4
31115502-3	2019	Western blotting results showed that phosphorylated (p)-AKT at Ser473 and at Thr308 and p-beta-catenin at Ser552 were downregulated.	Phosphorus	37-38	thymoma viral proto-oncogene 1	Mus musculus	56-59
31115502-3	2019	Western blotting results showed that phosphorylated (p)-AKT at Ser473 and at Thr308 and p-beta-catenin at Ser552 were downregulated.	Phosphorus	37-38	catenin (cadherin associated protein), beta 1	Mus musculus	90-102
31059083-8	2019	Expression of cleaved caspase-3, cleaved poly(ADP-ribose) polymerase and p-H2AX was enhanced by tranilast in combination with cisplatin.	Phosphorus	2-3	caspase 3	Homo sapiens	22-31
31059083-8	2019	Expression of cleaved caspase-3, cleaved poly(ADP-ribose) polymerase and p-H2AX was enhanced by tranilast in combination with cisplatin.	Phosphorus	2-3	H2A.X variant histone	Homo sapiens	75-79
31173609-5	2019	Patients with CRS were older (p<0.001), with more diabetes mellitus (p<0.001), coronary heart history (p<0.001), higher estimated glomerular filtration rate (eGFR) (p<0.001), lower serum creatinine (p<0.001) and phosphorus levels (p = 0.003) compared to non-CRS patients.	Phosphorus	212-222	twist family bHLH transcription factor 1	Homo sapiens	14-17
31174565-10	2019	Moreover, H. cordata and 2-undecanone effectively decreased B[a]P-induced intracellular reactive oxygen species (ROS) overproduction and further notably protected BEAS.2B cells from B[a]P-induced DNA damage and inflammation by significantly inhibiting phosphorylated H2A.X overexpression and interleukin-1beta secretion.	Phosphorus	64-65	H2A.X variant histone	Homo sapiens	267-272
31174565-10	2019	Moreover, H. cordata and 2-undecanone effectively decreased B[a]P-induced intracellular reactive oxygen species (ROS) overproduction and further notably protected BEAS.2B cells from B[a]P-induced DNA damage and inflammation by significantly inhibiting phosphorylated H2A.X overexpression and interleukin-1beta secretion.	Phosphorus	64-65	interleukin 1 beta	Homo sapiens	292-309
31249587-10	2019	In addition, nitrogen deposition and phosphorus inputs may also alter the status of some alien species.	Phosphorus	37-47	COP9 signalosome subunit 2	Homo sapiens	89-94
30740639-8	2019	However, patients with type 1 or type 2 diabetes and decreased concentrations of both elastase-1 and chymotrypsin had lower albumin, phosphorus, and vitamin A than patients with normal pancreatic exocrine function.	Phosphorus	133-143	chymotrypsin like elastase 1	Homo sapiens	86-96
31181709-4	2019	Incorporation of TSP-POSS further enhances the AO resistance of the FPI/TSP composite films via a Si-P synergic effect.	Phosphorus	19-20	thrombospondin 1	Homo sapiens	72-75
31002261-4	2019	This study aimed to investigate the effects of FcRn on nab-P elimination and distribution to targeted tissues.	Phosphorus	59-60	Fc fragment of IgG receptor and transporter	Mus musculus	47-51
31163520-1	2019	Objective:To investigate relationship between the level of estrogen, calcium and phosphorus concentration in serum with benign paroxysmal positional vertigo(BPPV).	Phosphorus	81-91	benign paroxysmal positional vertigo	Homo sapiens	157-161
30972678-6	2019	The effluent concentration of total phosphorus (TP) was lower than 0.3 mg L-1, and the maximum removal rate could reach 98%.	Phosphorus	36-46	immunoglobulin kappa variable 1-16	Homo sapiens	74-77
30927227-4	2019	The proteins of FGF19 subfamily influence the enterohepatic circulation of bile, participate in glucose and lipid metabolism regulation, and maintenance of phosphorus and vitamin D3 homeostasis.	Phosphorus	156-166	fibroblast growth factor 19	Homo sapiens	16-21
30907059-4	2019	Supplementation of 1alpha(OH)ase-/- mice with dietary calcium and phosphate, which normalized serum calcium and phosphorus, prolonged their average lifespan to more than 8 months with reduced oxidative stress and cellular senescence and SASP.	Phosphorus	112-122	cytochrome P450, family 27, subfamily b, polypeptide 1	Mus musculus	19-32
31019249-0	2019	Author Correction: Nitrate-NRT1.1B-SPX4 cascade integrates nitrogen and phosphorus signalling networks in plants.	Phosphorus	72-82	immunoglobulin superfamily member 9	Homo sapiens	27-31
30763810-6	2019	Significant correlation between total EDC abundance and COD contents was detected, and the concentrations of endogenous estrogens (E1, E2, and E3) were positively correlated with total nitrogen (TN) and total phosphorus (TP).	Phosphorus	209-219	small nucleolar RNA, H/ACA box 73A	Homo sapiens	131-145
31163776-3	2019	The asymmetric spin splitting can be flexibly tuned by the angles between the incident plane and the armchair crystalline directions of the top and bottom BP layers, i.e., phi1 and phi2.	Phosphorus	155-157	protein phosphatase 1 regulatory inhibitor subunit 14B	Homo sapiens	172-176
31136618-7	2019	Finally, we found that universal reactions are also associated with ancestral domains, such as those related to phosphorus-containing groups with a phosphate group as acceptor or those related to the ribulose-phosphate binding barrel, triosephosphate isomerase, and D-ribose-5-phosphate isomerase (RpiA) lid domain, among others.	Phosphorus	112-122	triosephosphate isomerase 1	Homo sapiens	235-260
31136618-7	2019	Finally, we found that universal reactions are also associated with ancestral domains, such as those related to phosphorus-containing groups with a phosphate group as acceptor or those related to the ribulose-phosphate binding barrel, triosephosphate isomerase, and D-ribose-5-phosphate isomerase (RpiA) lid domain, among others.	Phosphorus	112-122	ribose 5-phosphate isomerase A	Homo sapiens	266-296
31136618-7	2019	Finally, we found that universal reactions are also associated with ancestral domains, such as those related to phosphorus-containing groups with a phosphate group as acceptor or those related to the ribulose-phosphate binding barrel, triosephosphate isomerase, and D-ribose-5-phosphate isomerase (RpiA) lid domain, among others.	Phosphorus	112-122	ribose 5-phosphate isomerase A	Homo sapiens	298-302
31211210-1	2019	This DIB article provides details about transcriptional and physiological response of Fe- and P-deficient white lupin roots, an extensive and complete description of plant response is shown in the research article "Physiological and transcriptomic data highlight common features between iron and phosphorus acquisition mechanisms in white lupin roots" Venuti et al.	Phosphorus	296-306	5'-nucleotidase, cytosolic IIIA	Homo sapiens	112-117
31163776-5	2019	For the special case of phi1 = phi2 = 0 or 90 , the transmitted beam undergoes Goos-Hanchen shift, which varies with the carrier density of BP.	Phosphorus	140-142	protein phosphatase 1 regulatory inhibitor subunit 14B	Homo sapiens	24-28
31083335-4	2019	HDAC inhibitors such as scriptaid enhanced caspase-3/7, -8 and -9 activity induced by P/V-CPI- and overall cell toxicity.	Phosphorus	86-87	histone deacetylase 9	Homo sapiens	0-4
31126258-17	2019	DISCUSSION: Depending on the results of the INNOVATION trial, the addition of HER2 targeted treatment with either T or T and P to CT may inform future study designs or become a standard in the perioperative management HER2+ GC.	Phosphorus	125-126	erb-b2 receptor tyrosine kinase 2	Homo sapiens	78-82
30860308-2	2019	DFT calculations revealed that the preferred reaction mechanism involves the unsaturated 16-e mangana-substituted phosphonium ylide complex fac-[Mn(CO)3 (kappa2 P,C-Ph2 P=CHNHC)] (6 b) as key intermediate able to activate H2 via a non-classical mode of metal-ligand cooperation implying a formal lambda5 -P-lambda3 -P phosphorus valence change.	Phosphorus	318-328	immunoglobulin lambda like polypeptide 1	Homo sapiens	296-303
31075143-3	2019	The results showed that chemical fertilizers combined with manure (NPKM) significantly (P <= 0.05) increased the soil total phosphorus, Olsen P and soil organic matter (SOM) by 2, 3 and 1 times, respectively, compared with the NPK treatment, and by 4, 17 and 2 times, respectively, compared with the CK treatment.	Phosphorus	68-69	cytidine/uridine monophosphate kinase 1	Homo sapiens	300-302
31083335-4	2019	HDAC inhibitors such as scriptaid enhanced caspase-3/7, -8 and -9 activity induced by P/V-CPI- and overall cell toxicity.	Phosphorus	86-87	caspase 3	Homo sapiens	43-65
30858199-2	2019	The affinity of the TCR interaction with p:MHCII plays a role in Th differentiation by mechanisms that are not completely understood.	Phosphorus	41-42	T cell receptor alpha variable 6-3	Mus musculus	20-23
31080905-8	2019	The effect of extraction process and natural waste source on the critical properties of the HAp such as Ca/P ratio, crystallinity and phase assemblage, particle sizes, and morphology are discussed herein.	Phosphorus	107-108	reticulon 3	Homo sapiens	92-95
30289382-16	2019	There were no differences in intramuscular fat (IMF) content of LL muscle, however, IMF of ECO pigs had lower (P&amp;lt;0.05) proportion of saturated and higher (P&amp;lt;0.01) proportion of monounsaturated fatty acids accompanied by higher (P&amp;lt;0.001) values of thiobarbituric reactive substances (TBARS).	Phosphorus	111-112	IMF	Sus scrofa	84-87
30556299-10	2019	The mean salivary LL-37 concentration of PS-exposed children was significantly lower (100.71 +- 72.14 pg/mL) than that of PS-unexposed children (151.84 +- 107.89 pg/mL).	Phosphorus	41-43	cathelicidin antimicrobial peptide	Homo sapiens	18-23
30858199-2	2019	The affinity of the TCR interaction with p:MHCII plays a role in Th differentiation by mechanisms that are not completely understood.	Phosphorus	41-42	histocompatibility-2, MHC	Mus musculus	43-48
30901203-3	2019	This paper describes the direct and tin flux-assisted synthesis of phosphorus-rich metal phosphides with MP2 or MP3 compositions.	Phosphorus	67-77	tryptase pseudogene 1	Homo sapiens	105-108
31281748-0	2019	Association of ORAI1 Genetic Polymorphism with Serum Calcium and Phosphorus Levels in Non-dialysis Chronic Kidney Disease Patients: A Case-control Study.	Phosphorus	65-75	ORAI calcium release-activated calcium modulator 1	Homo sapiens	15-20
30944224-4	2019	Here we describe the crystal structure the C-terminal tail of FGF19 (FGF19CT) bound to sKLB and demonstrate that FGF19CT and FGF21CT bind to the same binding site on sKLB, via a multiturn D-P motif to site 1 and via a S-P-S motif to the pseudoglycoside hydrolase region (site 2).	Phosphorus	218-223	fibroblast growth factor 19	Homo sapiens	62-67
30944224-4	2019	Here we describe the crystal structure the C-terminal tail of FGF19 (FGF19CT) bound to sKLB and demonstrate that FGF19CT and FGF21CT bind to the same binding site on sKLB, via a multiturn D-P motif to site 1 and via a S-P-S motif to the pseudoglycoside hydrolase region (site 2).	Phosphorus	218-223	fibroblast growth factor 19	Homo sapiens	113-120
30896801-6	2019	SPL dose-dependently alleviated VC by suppressing the phenotypic transition of vascular smooth muscle cell (VSMCs) through downregulation of Pit-1 in a high phosphorus medium and even in a high phosphorus combined with high glucose medium.	Phosphorus	157-167	POU class 1 homeobox 1	Homo sapiens	141-146
31049400-6	2019	We show that enhancers established by p63 are highly enriched for single-nucleotide polymorphisms associated with nonsyndromic cleft lip +- cleft palate (CL/P).	Phosphorus	157-158	tumor protein p63	Homo sapiens	38-41
31049400-7	2019	These orthogonal approaches indicate a strong molecular link between p63 enhancer function and CL/P, illuminating molecular mechanisms underlying this developmental defect and revealing vital regulatory elements and new candidate causative genes.	Phosphorus	98-99	tumor protein p63	Homo sapiens	69-72
30690363-4	2019	The PAD was effective across a wide temperature range of 11-34  C, initial NO3--N range of 13-52 mg L-1 and PO43--P below 60 mg L-1.	Phosphorus	4-5	NBL1, DAN family BMP antagonist	Homo sapiens	75-78
30991634-5	2019	Our studies have established that a low protein to carbohydrate (P:C) ratio can increase lifespan, motor ability and mitochondrial function in a parkin mutant Drosophila model of PD.	Phosphorus	65-66	parkin	Drosophila melanogaster	145-151
30808201-4	2019	Results: Galectin-3 was significantly associated with dialysis vintage, calcium, phosphorus and low-density lipoprotein.	Phosphorus	81-91	galectin 3	Homo sapiens	9-19
31011377-2	2019	The pathogenesis relates to mutation in the gene SLC34A2 (solute carrier family 34 member 2) located on chromosome 4p15.2, which produces a defective sodium-phosphate cotransporter in alveolar epithelial type-2 cells, making these cells unable to clear phosphorus released during recycling of surfactant [1].	Phosphorus	253-263	solute carrier family 34 member 2	Homo sapiens	49-56
31011377-2	2019	The pathogenesis relates to mutation in the gene SLC34A2 (solute carrier family 34 member 2) located on chromosome 4p15.2, which produces a defective sodium-phosphate cotransporter in alveolar epithelial type-2 cells, making these cells unable to clear phosphorus released during recycling of surfactant [1].	Phosphorus	253-263	solute carrier family 34 member 2	Homo sapiens	58-91
30593010-0	2019	Spin-dependent carrier mobility and its gate-voltage modifying effects for functionalized single walled black phosphorus tubes.	Phosphorus	110-120	spindlin 1	Homo sapiens	0-4
30790353-7	2019	A predominant EBNA-1 variant (P-thr) was identified across the study groups.	Phosphorus	30-31	EBNA-1	Human gammaherpesvirus 4	14-20
30888091-2	2019	Furthermore, SIMesPK was used in reactions with potassium amides and alkoxides to form the molecular phosphorus-potassium clusters [K4 (SIMesP)2 (hmds)2 ] [5, hmds=N(SiMe3 )2 ] and [K6 (SIMesP)2 (OtBu)4 ] (6).	Phosphorus	101-111	keratin 4	Homo sapiens	132-144
30232627-8	2019	Implants showed no statistically significant differences (p &gt; 0.05) between or within groups at baseline or 12 months for any parameter, except MMP-8 decreased significantly for PS (14.50 +- 17.58 to 4.63 +- 7.56 ng; p = 0.044), and after 12 months, PCR showed a significant difference between TC and PS (p = 0.018).	Phosphorus	181-183	matrix metallopeptidase 8	Homo sapiens	147-152
30256395-9	2019	The current study revealed that P-nucleolin (Thr-76 and 84) increased in I/R injury myocardium, P-nucleolin was indispensable to upregulate miR-21 and inhibited apoptosis induced by H 2 O 2 in H9C2 cardiomyocytes.	Phosphorus	32-33	nucleolin	Rattus norvegicus	34-43
30256395-9	2019	The current study revealed that P-nucleolin (Thr-76 and 84) increased in I/R injury myocardium, P-nucleolin was indispensable to upregulate miR-21 and inhibited apoptosis induced by H 2 O 2 in H9C2 cardiomyocytes.	Phosphorus	32-33	nucleolin	Rattus norvegicus	98-107
30738820-7	2019	In a subset (n = 744) investigation of nutrient consumption related to salivary biomarkers, we found that elevated calorie-adjusted phosphorus intake was directly associated with salivary IL-1beta concentration (OR1.40, 95% CI 1.04-1.89), and inversely associated with salivary IL-4 concentration (OR0.62, 95% CI 0.46-0.84).	Phosphorus	132-142	interleukin 1 beta	Homo sapiens	188-196
30465136-4	2019	RESULTS: High levels of FGF-23 correlated with longer duration of dialysis (p = 0.002), elevated levels of calcium (p &lt; 0.001), phosphorus (p = 0.037) and low density lipoprotein cholesterol (p = 0.027).	Phosphorus	131-141	fibroblast growth factor 23	Homo sapiens	24-30
30738820-7	2019	In a subset (n = 744) investigation of nutrient consumption related to salivary biomarkers, we found that elevated calorie-adjusted phosphorus intake was directly associated with salivary IL-1beta concentration (OR1.40, 95% CI 1.04-1.89), and inversely associated with salivary IL-4 concentration (OR0.62, 95% CI 0.46-0.84).	Phosphorus	132-142	interleukin 4	Homo sapiens	278-282
30659931-7	2019	Taken together, B[a]P-induced aberrant EB development and apoptosis were related to EMT process and the Akt/GSK-3beta signaling pathway modulation.	Phosphorus	20-21	AKT serine/threonine kinase 1	Homo sapiens	104-107
30659931-7	2019	Taken together, B[a]P-induced aberrant EB development and apoptosis were related to EMT process and the Akt/GSK-3beta signaling pathway modulation.	Phosphorus	20-21	glycogen synthase kinase 3 alpha	Homo sapiens	108-117
31094460-11	2019	The increased amount of insulin decreased (p&amp;lt;0.01) in the main group, whereas in the control group these indicators almost did not change.	Phosphorus	43-44	insulin	Homo sapiens	24-31
31087985-4	2019	The results showed that when the influent ammonia concentration was below 45 mg L-1, the biological phosphorus removal granule system showed good performance.	Phosphorus	100-110	immunoglobulin kappa variable 1-16	Homo sapiens	80-83
30681211-5	2019	The eta1 -coordination via a P-W bond was observed for tungsten, while the side-on coordination via the P=C bond resulted with platinum.	Phosphorus	29-30	secreted phosphoprotein 1	Homo sapiens	4-8
31087986-6	2019	The final concentration of phosphorus was kept below 0.5 mg L-1, and the removal rate of COD and TP was stable at 80% and 95%, respectively, the accumulation rate of nitrite remained above 90%, and the SVI value decreased from the initial 63 mL g-1 to 35 mL g-1.	Phosphorus	27-37	immunoglobulin kappa variable 1-16	Homo sapiens	60-63
31087987-9	2019	The batch tests of phosphorus uptake by the sludge under different temperature conditions revealed that O2, NO3-, and NO2- could all be used as electron acceptors for phosphorus uptake.	Phosphorus	167-177	NBL1, DAN family BMP antagonist	Homo sapiens	108-111
31087987-11	2019	The phosphorus uptake rates of O2 and NO3- as electron acceptors were also found to be negatively correlated with temperature.	Phosphorus	4-14	NBL1, DAN family BMP antagonist	Homo sapiens	38-41
31087987-9	2019	The batch tests of phosphorus uptake by the sludge under different temperature conditions revealed that O2, NO3-, and NO2- could all be used as electron acceptors for phosphorus uptake.	Phosphorus	19-29	NBL1, DAN family BMP antagonist	Homo sapiens	108-111
30777436-1	2019	The central phosphorus atom of a novel hydroxyl-functionalized triarylphosphane was shown to reversibly insert into one of the molecule"s O-H bonds, which forms the basis for a tautomeric lambda3/lambda5-phosphane equilibrium.	Phosphorus	12-22	immunoglobulin lambda like polypeptide 1	Homo sapiens	196-203
29976269-3	2019	The milk concentration of calcium (Ca), potassium (K), magnesium (Mg), sodium (Na) and phosphorus (P) in the present study was quantified from mid-IR spectroscopy on 12 223 test-day records from 1717 Holstein-Friesian cows.	Phosphorus	87-97	Weaning weight-maternal milk	Bos taurus	4-8
30777436-5	2019	However, upon generation of an alkoxide via proton abstraction, the electrophilic character of the lambda5-phosphane in the equilibrium became evident since the alkoxide was found to attack the molecule"s phosphorus atom.	Phosphorus	205-215	immunoglobulin lambda like polypeptide 1	Homo sapiens	99-106
30716177-3	2019	A phosphorus analogue of p-quinodimethane (pQDM), (IPrC)2 P4 [5, IPr=C{N(Ar)CH2 }2 ; Ar=2,6-iPr2 C6 H3 ] featuring a planar P4 ring, was readily accessible by KC8 -reduction of (IPrC)(PCl2 )2 (2).	Phosphorus	2-12	metal response element binding transcription factor 2	Homo sapiens	184-188
29976269-3	2019	The milk concentration of calcium (Ca), potassium (K), magnesium (Mg), sodium (Na) and phosphorus (P) in the present study was quantified from mid-IR spectroscopy on 12 223 test-day records from 1717 Holstein-Friesian cows.	Phosphorus	99-100	Weaning weight-maternal milk	Bos taurus	4-8
29603070-6	2019	High Ca/P/VitD treatment induced vascular calcification only in CKD rats, suppressed serum parathyroid hormone levels and led to higher sclerostin, DKK1 and FGF23 serum levels.	Phosphorus	8-9	dickkopf WNT signaling pathway inhibitor 1	Rattus norvegicus	148-152
30659707-6	2019	The EGF supplementation significantly elevated (p &lt; 0.05) the coefficients of total tract apparent digestibility of crude protein, calcium and phosphorus, but tended to decrease sucrase activity (p &lt; 0.10) than the control group.	Phosphorus	146-156	epidermal growth factor	Homo sapiens	4-7
31218207-2	2019	Elevated serum phosphorus and 1,25dihydroxyvitaminD stimulates FGF23 production to promote renal phosphate excretion and decrease 1,25dihydroxyvitaminD synthesis.	Phosphorus	15-25	fibroblast growth factor 23	Homo sapiens	63-68
30445242-6	2019	Additionally, significant upregulation of PC, PE and PS with the same fatty acid chains of 18:0/18:2 was found after exposure to 0.05 mug mL-1 and 20 mug mL-1 PCB153 at 120 h. This study revealed that PCB153 exposure modulated 22 endogenous glycerophospholipids in PC12 cells and provided the basis for the further study of PCB153 on the effects of glycerophospholipids on PC12 cells.	Phosphorus	53-55	L1 cell adhesion molecule	Mus musculus	138-149
30584645-6	2019	Plasma sclerostin concentration positively correlated with serum 25-OH-D (tau = 0.204), phosphorus (tau = 0.1482), and TNF-alpha (tau = 0.183) and inversely with iPTH (tau = - 0.255), alkaline phosphatase (tau = - 0.203), IL-6 (tau =- 0.201), and beta-CTx (tau = - 0.099) levels.	Phosphorus	88-98	sclerostin	Homo sapiens	7-17
30584645-7	2019	In multivariate regression analysis, variability of sclerostin levels was explained by sex and 25-OH-D and phosphorus levels.	Phosphorus	107-117	sclerostin	Homo sapiens	52-62
29603070-6	2019	High Ca/P/VitD treatment induced vascular calcification only in CKD rats, suppressed serum parathyroid hormone levels and led to higher sclerostin, DKK1 and FGF23 serum levels.	Phosphorus	8-9	fibroblast growth factor 23	Rattus norvegicus	157-162
30792397-7	2019	This information can be used to aid in the understanding the impact that nitrogen and phosphorus have on the early summer CyanoHAB and the functional activities of Nostoc- and Anabaena-dominated or Microcystis-dominated communities, and aid in making management decisions related to harmful algal blooms.	Phosphorus	86-96	activation induced cytidine deaminase	Homo sapiens	32-35
30628347-2	2019	The results showed that the denitrifying phosphorus bacteria (DPBs) were successfully enriched within 46 d by controlling the nitrate recycling ratio (increasing from 150% to 300%), with a temperature of 30C+-2C, volume loading rate of 0.8 kg (m3 d)-1 and sludge reflux ratio of 80% in the ABR, sludge retention time (SRT) in the denitrifying phosphorus removal functional area of 25 d, and the dissolved oxygen (DO) of 1-2 mg L-1 in the MBR.	Phosphorus	41-51	immunoglobulin kappa variable 1-16	Homo sapiens	427-430
30628326-6	2019	Reducible phosphorus (BD-P) and iron-aluminum-bound phosphorus (NaOH-rP) were reversibly redistributed into weakly adsorbed phosphorus (NH4Cl-P), polyphosphorus/organophosphorous (NaOH-nrP), residual phosphorus (Rest-P), and interstitial water-soluble active phosphorus (SRP).	Phosphorus	10-20	neuropilin 1	Homo sapiens	185-188
30439425-4	2019	We showed that PS upregulated the expression of TLR1/3/4 and promoted the phosphorylation of Akt, Erk, JNK, following the activation of NF-kappaB, which led to the polarization towards M1.	Phosphorus	15-17	toll-like receptor 13	Mus musculus	48-54
30439425-4	2019	We showed that PS upregulated the expression of TLR1/3/4 and promoted the phosphorylation of Akt, Erk, JNK, following the activation of NF-kappaB, which led to the polarization towards M1.	Phosphorus	15-17	thymoma viral proto-oncogene 1	Mus musculus	93-96
30439425-4	2019	We showed that PS upregulated the expression of TLR1/3/4 and promoted the phosphorylation of Akt, Erk, JNK, following the activation of NF-kappaB, which led to the polarization towards M1.	Phosphorus	15-17	mitogen-activated protein kinase 1	Mus musculus	98-101
30439425-4	2019	We showed that PS upregulated the expression of TLR1/3/4 and promoted the phosphorylation of Akt, Erk, JNK, following the activation of NF-kappaB, which led to the polarization towards M1.	Phosphorus	15-17	mitogen-activated protein kinase 8	Mus musculus	103-106
30439425-4	2019	We showed that PS upregulated the expression of TLR1/3/4 and promoted the phosphorylation of Akt, Erk, JNK, following the activation of NF-kappaB, which led to the polarization towards M1.	Phosphorus	15-17	nuclear factor of kappa light polypeptide gene enhancer in B cells 1, p105	Mus musculus	136-145
30439425-5	2019	In a murine breast cancer model of tumor cell 4T1 inoculation, subcutaneous injection of PS induced effective antitumor effect through reprogramming M2 macrophages in the tumor microenvironment to M1, increased CD4+ and CD8+ T cells, and decreased the expression of CD31 in the tumor mass, which together inhibited the tumor progression and the metastasis in lung and liver, leading to the prolong of the mice survival.	Phosphorus	89-91	platelet/endothelial cell adhesion molecule 1	Mus musculus	266-270
30628326-6	2019	Reducible phosphorus (BD-P) and iron-aluminum-bound phosphorus (NaOH-rP) were reversibly redistributed into weakly adsorbed phosphorus (NH4Cl-P), polyphosphorus/organophosphorous (NaOH-nrP), residual phosphorus (Rest-P), and interstitial water-soluble active phosphorus (SRP).	Phosphorus	52-62	neuropilin 1	Homo sapiens	185-188
30628326-6	2019	Reducible phosphorus (BD-P) and iron-aluminum-bound phosphorus (NaOH-rP) were reversibly redistributed into weakly adsorbed phosphorus (NH4Cl-P), polyphosphorus/organophosphorous (NaOH-nrP), residual phosphorus (Rest-P), and interstitial water-soluble active phosphorus (SRP).	Phosphorus	52-62	neuropilin 1	Homo sapiens	185-188
30628347-3	2019	The net phosphorus release and phosphorus uptake of DPBs reached 20.56 mg L-1and 27.74 mg L-1, respectively.	Phosphorus	8-18	immunoglobulin kappa variable 1-16	Homo sapiens	74-77
30628326-6	2019	Reducible phosphorus (BD-P) and iron-aluminum-bound phosphorus (NaOH-rP) were reversibly redistributed into weakly adsorbed phosphorus (NH4Cl-P), polyphosphorus/organophosphorous (NaOH-nrP), residual phosphorus (Rest-P), and interstitial water-soluble active phosphorus (SRP).	Phosphorus	52-62	neuropilin 1	Homo sapiens	185-188
30628347-6	2019	The results also suggested that 0.83 mg L-1NO3--N was consumed per 1 mg L-1 PO43--P removed during the denitrifying phosphorus removal, indicating that the simultaneous nitrogen and phosphorus removal was achieved in the ABR-MBR system.	Phosphorus	116-126	immunoglobulin kappa variable 1-16	Homo sapiens	40-43
30628326-6	2019	Reducible phosphorus (BD-P) and iron-aluminum-bound phosphorus (NaOH-rP) were reversibly redistributed into weakly adsorbed phosphorus (NH4Cl-P), polyphosphorus/organophosphorous (NaOH-nrP), residual phosphorus (Rest-P), and interstitial water-soluble active phosphorus (SRP).	Phosphorus	52-62	neuropilin 1	Homo sapiens	185-188
30628347-6	2019	The results also suggested that 0.83 mg L-1NO3--N was consumed per 1 mg L-1 PO43--P removed during the denitrifying phosphorus removal, indicating that the simultaneous nitrogen and phosphorus removal was achieved in the ABR-MBR system.	Phosphorus	182-192	immunoglobulin kappa variable 1-16	Homo sapiens	40-43
30453214-3	2019	The hybridized nanoplatform (R-MnO2-FBP) was prepared by assembly of Rhodamine B (RhB)-encapsulated manganese dioxide (R-MnO2) as O2 supplier and indicator, and fluorescein isothiocyanate (FITC)-labelled peptide-functionalized black phosphorus as the theranostic agent.	Phosphorus	233-243	ECB2	Homo sapiens	36-39
30528454-7	2019	Higher circulating PTH levels were associated with lower body weight (beta = -0.048, P = .0003) independent of renal function, serum calcium, phosphorus,and albumin levels in PHPT patients.	Phosphorus	142-152	parathyroid hormone	Homo sapiens	19-22
30309249-2	2019	Gelatin prepared from calf bones (GCB) is a novel source of high-quality protein and phosphorus.	Phosphorus	85-95	natriuretic peptide receptor 2	Bos taurus	34-37
30309249-15	2019	Tibia calcium and phosphorus content were increased by GCB inclusion at 14 d of age (P &lt;= 0.001).	Phosphorus	18-28	natriuretic peptide receptor 2	Bos taurus	55-58
30309249-18	2019	Supplementation of diets with GCB increased phosphorus digestibility (P &lt;= 0.01) and suppressed ileum growth during the experimental period.	Phosphorus	44-54	natriuretic peptide receptor 2	Bos taurus	30-33
30870065-8	2019	The most significant CL/P-associated differentially methylated region encompassed the VTRNA2-1 gene, which was also hypomethylated in cases (FWER p = 0.014).	Phosphorus	24-25	vault RNA 2-1	Homo sapiens	86-94
30604360-4	2019	We found that the application of Ca2+ could regulate the activity of plasma membrane H+-ATPase, for mitigating the increase of ammonium and the decrease of nitrate and phosphorus in soybean roots, which mitigated the inhibition on growth and improved the yield and grain quality of soybean under simulated acid rain stress.	Phosphorus	168-178	plasma membrane ATPase 4	Glycine max	85-94
30870065-10	2019	Gene Set Enrichment Analysis of CL/P-associated DMRs showed an over-representation of genes involved in palate development such as WNT9B, MIR140 and LHX8.	Phosphorus	35-36	Wnt family member 9B	Homo sapiens	131-136
30870065-10	2019	Gene Set Enrichment Analysis of CL/P-associated DMRs showed an over-representation of genes involved in palate development such as WNT9B, MIR140 and LHX8.	Phosphorus	35-36	microRNA 140	Homo sapiens	138-144
30870065-10	2019	Gene Set Enrichment Analysis of CL/P-associated DMRs showed an over-representation of genes involved in palate development such as WNT9B, MIR140 and LHX8.	Phosphorus	35-36	LIM homeobox 8	Homo sapiens	149-153
30047165-8	2019	Downregulation of the osmosis regulatory gene, osr-1, might contribute to p-coumaric acids" effect on increased resistance to high osmolarity.	Phosphorus	74-76	Uncharacterized protein	Caenorhabditis elegans	47-52
30580950-7	2019	We showed 2 QTL regions on BTA1, one affecting alphaS2-CN production and the other harboring the SLC37A1 gene, which encodes a phosphorus antiporter and affects alphaS1- and alphaS2-CN PD.	Phosphorus	127-137	solute carrier family 37 member 1	Bos taurus	97-104
30712523-7	2019	Compared with native bone, the inorganic phase of Bact+ (i.e., CHAp) exhibits higher mineral crystallinity, lower carbonate content, and lower Ca/P, C/Ca, Mg/Ca, and Mg/P ratios.	Phosphorus	146-147	transcription factor like 5	Homo sapiens	63-67
30628292-4	2019	The highest phosphorus removal efficiency was achieved at a C/P ratio of 30, with the anaerobic phosphorus release rate (PRR) and aerobic phosphorus uptake rate (PUR, used as P/MLSS) reaching 3.5 mg (g h)-1 and 4.2 mg (g h)-1 respectively, and an average effluent PO43--P concentration below 0.3 mg L-1.	Phosphorus	12-22	immunoglobulin kappa variable 1-16	Homo sapiens	299-302
30272230-1	2019	The aim of the present study was to test whether different dietary corn sources and phytase supplementation affect the prececal phosphorus digestibility (pcdP) and appearance of inositol phosphates in the lower ileum of growing broiler chickens and turkeys.	Phosphorus	128-138	phytase	Zea mays	84-91
30172137-4	2019	As soil P fertility plays a central role in ES delivery, we argue that soil test phosphorus (STP) concentration provides a suitable common unit of measure by which delivering multiple ES can be economically valued relative to maximum potential yield, in $ ha-1 yr-1 units.	Phosphorus	81-91	Rho GTPase activating protein 45	Homo sapiens	256-265
30230960-3	2019	Variability between organophosphorus insecticides-in lipophilicity, speed of activation, speed and potency of acetylcholinesterase inhibition, and in the chemical groups attached to the phosphorus-results in variable speed of poisoning onset, severity, clinical toxidrome, and case fatality.	Phosphorus	26-36	acetylcholinesterase (Cartwright blood group)	Homo sapiens	110-130
30277286-1	2019	Insertion of PCl3 or PhBCl2 into 5,10,15,20-tetraaryl-p-benziporphyrin prompted an intramolecular fusion affording anti-aromatic phosphorus(V) and non-aromatic boron(III) complexes of two N-fused dihydro-p-benziporphyrin isomers.	Phosphorus	129-139	PHD finger protein 19	Homo sapiens	13-17
30176540-8	2019	FINDINGS: Bip-P-113 and Dip-P-113 had the longest and widest non-nature amino acids, respectively.	Phosphorus	14-15	heat shock protein 5	Mus musculus	10-13
30679396-2	2019	In the blood, phosphorus exists in the form of phosphate ions and colloidal particles composed of solid-phase calcium-phosphate and serum protein fetuin-A, which are termed calciprotein particles(CPP).	Phosphorus	14-24	alpha-2-HS-glycoprotein	Mus musculus	146-154
30551297-6	2019	Polymerase chain reaction analysis indicated that the SiO2/Si-p-rhOPN substrates with high level of immobilized p-rhOPN promoted MC-3T3-E1 cell differentiation, as demonstrated by the higher transcript expression levels of the osteogenic differentiation regulatory gene, Runt-related transcription factor 2, compared to cells cultured on SiO2/Si-OH or SiO2/Si-gelatin.	Phosphorus	62-63	runt related transcription factor 2	Mus musculus	271-306
30388580-5	2019	The optimal hydraulic retention time and interval time for biomass harvesting of FPCO-PBR were both 2 d. Nitrogen and phosphorus recovery rate were 30 mg L-1 d-1 and 7 mg L-1 d-1 respectively under optimal operating parameters.	Phosphorus	118-128	translocator protein	Homo sapiens	86-89
30641515-2	2019	Through the secretion of parathyroid hormone (PTH), the parathyroid glands are primarily responsible for maintaining extracellular calcium and phosphorus concentrations.	Phosphorus	143-153	parathyroid hormone	Homo sapiens	25-44
30641526-5	2019	PTHrP, although encoded by a distinct gene, shares amino acid sequence homology with PTH in the amino-terminal domain, which allows it to cross-react at a common G protein receptor, the type 1 PTH/PTHrP receptor (PTHR1), resulting in similar skeletal effects and effects on calcium and phosphorus metabolism.	Phosphorus	286-296	parathyroid hormone like hormone	Homo sapiens	0-5
30009339-7	2019	The expression of NaPi IIa and the corresponding renal Na+-dependent Pi capacity were modulated by high dietary phosphorus (P) intake in a parathyroid-dependent manner.	Phosphorus	112-122	solute carrier family 34 member 1	Homo sapiens	18-26
30031146-7	2019	The F1 to F4 generations of Cyp27b1 KO mice fed 25(OH)D3 showed normal growth, normal plasma levels of Ca, P, and parathyroid hormone, and normal bone mineral density.	Phosphorus	107-108	cytochrome P450, family 27, subfamily b, polypeptide 1	Mus musculus	28-35
29701806-2	2019	Recently it was shown that adiponectin modulates renal handling of calcium and phosphorus.	Phosphorus	79-89	adiponectin, C1Q and collagen domain containing	Homo sapiens	27-38
30009339-7	2019	The expression of NaPi IIa and the corresponding renal Na+-dependent Pi capacity were modulated by high dietary phosphorus (P) intake in a parathyroid-dependent manner.	Phosphorus	124-126	solute carrier family 34 member 1	Homo sapiens	18-26
30488924-5	2018	These distinct differences result from a significantly decreased interface trap density (Dit ~ 1011 cm-2 eV-1) and subthreshold gate swing (SS ~ 270 mV dec-1) in the BP device caused by the formation of stable energy states at the AlOx/oxidized BP interface, even with BP oxidized by air exposure.	Phosphorus	166-168	deleted in esophageal cancer 1	Homo sapiens	152-157
30693111-5	2018	The mean D-LDL-C (2.47+-0.71 mmol/L) was significantly lower compared to F-LDL-C (2.76+-1.05 mmol/L), N-LDL-C (2.74+-1.04 mmol/L), A-LDL-C (2.99+-1.02 mmol/L), and M-LDL-C (2.97+-1.08 mmol/L) p &lt; 0.001.	Phosphorus	64-65	component of oligomeric golgi complex 2	Homo sapiens	9-16
30693111-5	2018	The mean D-LDL-C (2.47+-0.71 mmol/L) was significantly lower compared to F-LDL-C (2.76+-1.05 mmol/L), N-LDL-C (2.74+-1.04 mmol/L), A-LDL-C (2.99+-1.02 mmol/L), and M-LDL-C (2.97+-1.08 mmol/L) p &lt; 0.001.	Phosphorus	64-65	component of oligomeric golgi complex 2	Homo sapiens	11-16
30521326-4	2018	The PA can not only slowly etch ZIF-67 and gain a hollow structure but also act as a source of phosphorus to prepare CoP/C nanoboxes.	Phosphorus	95-105	caspase recruitment domain family member 16	Homo sapiens	117-120
30427781-13	2018	There were significant relationships between AChE activity with P and PTH.	Phosphorus	64-65	acetylcholinesterase (Cartwright blood group)	Homo sapiens	45-49
30556287-1	2019	The sizeable direct bandgap, high mobility, and long spin lifetimes at room temperature offer black phosphorus (BP) potential applications in spin-based semiconductor devices.	Phosphorus	94-110	spindlin 1	Homo sapiens	53-57
30556287-1	2019	The sizeable direct bandgap, high mobility, and long spin lifetimes at room temperature offer black phosphorus (BP) potential applications in spin-based semiconductor devices.	Phosphorus	94-110	spindlin 1	Homo sapiens	142-146
30556287-1	2019	The sizeable direct bandgap, high mobility, and long spin lifetimes at room temperature offer black phosphorus (BP) potential applications in spin-based semiconductor devices.	Phosphorus	112-114	spindlin 1	Homo sapiens	142-146
30347158-7	2018	Reactions of 1 with phosphorus electrophiles proceed stereoconvergently at C-1 of 1a/b to give predominantly menthyl-configured substitution products: PCl3 and 2 equiv of 1 give Men2PCl (6), which hydrolyzes to dimenthylphosphine P-oxide (7), whereas Ph2PCl with 1 equiv of 1 gave P-menthyldiphenylphosphine oxide (27) after workup in air.	Phosphorus	20-30	PHD finger protein 19	Homo sapiens	151-155
30239752-9	2018	We conclude that compound heterozygous p.Asp148Tyr and p.Arg201GlyfsTer6 mutations in NHLRC2 lead to severe tissue fibrosis in humans by enhancing the differentiation of fibroblasts to myofibroblasts.	Phosphorus	20-21	NHL repeat containing 2	Homo sapiens	86-92
30372837-3	2018	Exploring the relationship between miR-14 2-3 p and gene SH2B1 expression is beneficial for the treatment of cardiac hypertrophy.	Phosphorus	2-3	SH2B adaptor protein 1	Rattus norvegicus	57-62
29730794-0	2018	Effects of an invasive polychaete on benthic phosphorus cycling at sea basin scale: An ecosystem disservice.	Phosphorus	45-55	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	67-70
29730794-12	2018	in the Baltic Sea enhance the phosphorus fluxes from sediment to water on a sea basin scale.	Phosphorus	30-40	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	14-17
29730794-12	2018	in the Baltic Sea enhance the phosphorus fluxes from sediment to water on a sea basin scale.	Phosphorus	30-40	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	76-79
30387610-3	2018	On the other hand, in situ generated phosphate anions via the Ag-catalyzed aerobic oxidation of phosphonyl reactants underwent SN2 reaction to provide branched phosphorus-containing amine products.	Phosphorus	160-170	solute carrier family 38 member 5	Homo sapiens	127-130
29936156-5	2018	The results showed that NO3--N removal efficiency of autotrophic and mixotrophic denitrification process increased by 40 and 35%, respectively, after phosphorus addition.	Phosphorus	150-160	NBL1, DAN family BMP antagonist	Homo sapiens	24-27
30266011-5	2018	The HAp was revealed to be a carbonated HAp exhibiting A- and B- type CO32- substitutions with CO32- content of 2.14 +- 1.36 wt.%, trace amounts of some important elements (Mg, Na, and K), and Ca/P atomic ratio of 1.54, thereby confirming that the HAp resembled the biological apatite in terms of morphology, structure, and composition.	Phosphorus	196-197	scaffold attachment factor B	Homo sapiens	4-7
30223019-7	2018	Through phosphorus colorimetric assay, we demonstrated that VAOS notably inhibited phosphatase and tensin homologue deleted on chromosome 10 (PTEN) dephosphorylation activity, another member of the protein tyrosine phosphatases (PTPases)-upstream factor of AKT.	Phosphorus	8-18	phosphatase and tensin homolog	Homo sapiens	142-146
30223019-7	2018	Through phosphorus colorimetric assay, we demonstrated that VAOS notably inhibited phosphatase and tensin homologue deleted on chromosome 10 (PTEN) dephosphorylation activity, another member of the protein tyrosine phosphatases (PTPases)-upstream factor of AKT.	Phosphorus	8-18	AKT serine/threonine kinase 1	Homo sapiens	257-260
30144171-10	2018	The PTH concentrations were reduced and ALP activity increased at certain time points during the low phosphorus feeding compared to the puppies being fed the control diet.	Phosphorus	101-111	alkaline phosphatase, biomineralization associated	Canis lupus familiaris	40-43
30268890-6	2018	This would then lead to an elevation of B[a]P levels, thus possibly suggesting a long-lasting stimulation of the transcription factor AhR.	Phosphorus	44-45	aryl hydrocarbon receptor	Homo sapiens	134-137
31089567-3	2018	The presence of vitamin D receptor in a number of tissues implies that vitamin D has various physiological roles apart from calcium and phosphorus metabolism.	Phosphorus	136-146	vitamin D receptor	Homo sapiens	16-34
30590821-9	2018	In summary, impact of Ca concentration on AID Ca and P was dependent on limestone particle size and phytase inclusion.	Phosphorus	53-54	phytase	Zea mays	100-107
30511626-8	2018	Adding a PLD inhibitor significantly reduced the elevation of cell viability and migration of the colon cancer cells exposed to fibroblasts conditioned medium (p&amp;lt;0.005).	Phosphorus	160-162	glycosylphosphatidylinositol specific phospholipase D1	Homo sapiens	9-12
30109784-10	2018	In addition, Ca-PS reduced serum phosphorus levels with no effects on serum levels of calcium and sodium, fluid volume, blood pressure, or interdialytic weight gain.	Phosphorus	33-43	calcyphosine	Homo sapiens	13-18
30109784-11	2018	Ca-PS treatment decreases serum levels of potassium and phosphorus in MHD patients with interdialytic hyperkalemia.	Phosphorus	56-66	calcyphosine	Homo sapiens	0-5
30098555-2	2018	The CMCS simultaneously removes ammonia nitrogen (NH4+) and phosphate (PO43-) by chemical precipitation and it can achieve recovery of nitrogen and phosphorus.	Phosphorus	148-158	G protein signaling modulator 2	Homo sapiens	4-8
30445969-6	2018	Across the three tertiles of serum Angpt-2, a significant trend effect was observed for body mass index, normalized protein catabolic rate, calcium x phosphorus product, hs-CRP, brain natriuretic peptide, lower-density lipoprotein cholesterol, left ventricular ejection fraction, total weekly urea clearance and residual renal function (all p &lt; 0.05).	Phosphorus	150-160	angiopoietin 2	Homo sapiens	35-42
30511620-8	2018	The lower constitutive phosphorylation of VEGF-A in the group 2 was also increased in coronary vessels after melatonin treatment (p&amp;lt;0.05).	Phosphorus	23-24	vascular endothelial growth factor A	Rattus norvegicus	42-48
30514687-8	2018	Knockdown of ADAM17 with siRNA 1 significantly increased the sensitivity of SW480 cells to tocetuximad (P &amp;lt; 0.05), obviously inhibited the cell proliferation, migration and invasion, and significantly reduced the expressions of p-EGFR and p-AKT in the cells (P &amp;lt; 0.001).	Phosphorus	104-105	ADAM metallopeptidase domain 17	Homo sapiens	13-19
31065446-4	2018	We found the standard OCT-based metric and PS-OCT-based metrics were complementary for the differentiation of healthy fibro-adipose tissue, healthy stroma, and IDC.	Phosphorus	43-45	plexin A2	Homo sapiens	46-49
30452474-9	2018	Our results show that phosphorus absorption was higher in 10-week-old rats compared with 20- and 30-week-olds and this corresponded to higher gene expression of the major phosphate transporter, NaPi-2b, as well as higher whole-body phosphorus balance and net phosphorus absorption.	Phosphorus	22-32	solute carrier family 34 member 2	Rattus norvegicus	194-201
29660161-1	2018	BACKGROUND: Fibroblast growth factor-23 (FGF-23) and klotho are key regulators of vitamin D and parathyroid hormone (PTH) synthesis as well as phosphorus and calcium homeostasis; however, information on the FGF-23/klotho axis in healthy and hospitalised foals is lacking.	Phosphorus	143-153	fibroblast growth factor 23	Homo sapiens	12-39
30413888-7	2018	The substantial amino acid substitutions in PstS most likely contribute to the successful adaptation of bacteria in different ecological condition dealing with different phosphorus availability.	Phosphorus	170-180	kallikrein related peptidase 4	Homo sapiens	44-48
30628225-9	2018	The sequential extraction analysis of phosphate-adsorbed MZ showed that 49.4% of phosphorus in MZ existed in the mobile form (NH4Cl-P, BD-P, and NaOH-nrP), which could be easily released from MZ.	Phosphorus	81-91	neuropilin 1	Homo sapiens	150-153
30354051-0	2018	Tip-Sonicated Red Phosphorus-Graphene Nanoribbon Composite for Full Lithium-Ion Batteries.	Phosphorus	14-28	TOR signaling pathway regulator	Homo sapiens	0-3
30187446-3	2018	The developed PEGylated SA lipoplexes (pegSA lipoplexes) showed a lower N/P ratio (1.5) for BMP-9 gene complexation while maintaining the SUV character with a unique shape (square and triangular lipoplexes).	Phosphorus	14-15	growth differentiation factor 2	Mus musculus	92-97
30239896-8	2018	STX5 can re-locate to LEs upon PS-ASO incubation, can bind PS-ASOs, and the binding appears to be required for this pathway.	Phosphorus	31-33	syntaxin 5	Homo sapiens	0-4
30239896-9	2018	Our study reveals a novel release pathway in which PS-ASO incubation causes LE re-localization of STX5, which mediates the recruitment of COPII vesicles to LEs to facilitate endosomal PS-ASO release, and identifies another key PS-ASO binding protein.	Phosphorus	51-54	syntaxin 5	Homo sapiens	98-102
29660161-8	2018	In hospitalised and septic foals, increased FGF-23 and aldosterone concentrations were associated with high phosphorus and PTH but not with TCa and vitamin D metabolite concentrations.	Phosphorus	108-118	fibroblast growth factor 23	Homo sapiens	44-50
29660161-12	2018	Elevated FGF-23 and reduced klotho, together with high phosphorus and PTH concentrations suggests FGF-23 resistance.	Phosphorus	55-65	fibroblast growth factor 23	Homo sapiens	98-104
29660161-1	2018	BACKGROUND: Fibroblast growth factor-23 (FGF-23) and klotho are key regulators of vitamin D and parathyroid hormone (PTH) synthesis as well as phosphorus and calcium homeostasis; however, information on the FGF-23/klotho axis in healthy and hospitalised foals is lacking.	Phosphorus	143-153	fibroblast growth factor 23	Homo sapiens	41-47
29660161-1	2018	BACKGROUND: Fibroblast growth factor-23 (FGF-23) and klotho are key regulators of vitamin D and parathyroid hormone (PTH) synthesis as well as phosphorus and calcium homeostasis; however, information on the FGF-23/klotho axis in healthy and hospitalised foals is lacking.	Phosphorus	143-153	klotho	Homo sapiens	53-59
30320513-1	2018	Compost is organic material that has been degraded into a nutrient-stabilized humus-like substance through intense microbial activity, which can provide essential plant nutrients (nitrogen, phosphorus) to aid in the growth of fruits and vegetables.	Phosphorus	190-200	activation induced cytidine deaminase	Homo sapiens	205-208
30766810-9	2018	A significant positive correlation found between PTH and phosphorous (P = 0.003; r = 0.378) and potassium (P &lt;= 0.001; r = 0.421).	Phosphorus	57-68	parathyroid hormone	Homo sapiens	49-52
30403605-7	2018	Bax and C-fos were positively expressed and significantly higher in the hippocampus of chronic cerebral ischemic vascular dementia rats (model group) than in the medicated thread moxibustion group after treatment (p &amp;lt;0.01).	Phosphorus	19-20	BCL2 associated X, apoptosis regulator	Rattus norvegicus	0-3
30338975-3	2018	Here, a novel and stable sodium titanate/carbon-black phosphorus (NTO/C-BP) hybrids are first fabricated as a promising anode material for advanced sodium-ion batteries.	Phosphorus	48-64	CREB binding protein	Homo sapiens	70-74
30413250-4	2018	However, assessment and treatment of MBD is rife with challenges owing to biological tensions between its many components, such as calcium and phosphorus with their regulatory hormones fibroblast growth factor 23 and parathyroid hormone; fibroblast growth factor 23 with its co-receptor klotho; and vitamin D with control of calcium and phosphorus.	Phosphorus	143-153	fibroblast growth factor 23	Homo sapiens	185-236
30403605-7	2018	Bax and C-fos were positively expressed and significantly higher in the hippocampus of chronic cerebral ischemic vascular dementia rats (model group) than in the medicated thread moxibustion group after treatment (p &amp;lt;0.01).	Phosphorus	19-20	Fos proto-oncogene, AP-1 transcription factor subunit	Rattus norvegicus	8-13
30240227-4	2018	After dripping onto a water surface, a drop of ethanol solution of poly(stearyl acrylate- co-acrylic acid) [P(SA- co-AAc)] spread quickly to form a thin film.	Phosphorus	108-109	glycine-N-acyltransferase	Homo sapiens	117-120
30374844-8	2018	TERF1 also regulates plant utilization of phosphorus (Pi) and nitrogen (N).	Phosphorus	42-52	ethylene-responsive transcription factor 1	Solanum lycopersicum	0-5
30365537-10	2018	The results suggest that applying 50 muM of GA3 to the development of Tifton 85 bermudagrass provides higher dry matter yield and removal of nitrogen, phosphorus, and sodium for the first crop cycle in CWs.	Phosphorus	151-161	succinyl-CoA:glutarate-CoA transferase	Homo sapiens	44-47
30322116-0	2018	Hypocaloric Diet Prevents the Decrease in FGF21 Elicited by High Phosphorus Intake.	Phosphorus	65-75	fibroblast growth factor 21	Rattus norvegicus	42-47
30323203-1	2018	The use of the dietary phosphorus-to-protein ratio (PPR) to reduce dietary phosphorus while maintaining protein intake is valuable for nutritional management in the dialysis population, but the actual PPR values in hospital meals have not been determined.	Phosphorus	23-33	PPR1	Homo sapiens	52-55
30323203-1	2018	The use of the dietary phosphorus-to-protein ratio (PPR) to reduce dietary phosphorus while maintaining protein intake is valuable for nutritional management in the dialysis population, but the actual PPR values in hospital meals have not been determined.	Phosphorus	75-85	PPR1	Homo sapiens	52-55
30221923-6	2018	Biochemical assays confirmed that DDHD1 hydrolyzes PI/PS to LPI/LPS with sn-1 selectivity and accounts for a substantial fraction of the PI/PS lipase activity in mouse brain tissue.	Phosphorus	54-56	DDHD domain containing 1	Mus musculus	34-39
30229610-0	2018	[Characteristics of Denitrifying Phosphorus Removal by A2/O-BAF at Low Temperatures].	Phosphorus	33-43	BAF nuclear assembly factor 1	Homo sapiens	60-63
30168321-3	2018	It was also found that racemic and enantiopure ( O-methyl)6-2,6-helic[6]arenes could be easily brominated by Br2 to give the corresponding hexabromo-substituted helic[6]arene derivatives rac-4, (+)- P-4, and (-)- M-4 in high yields.	Phosphorus	199-200	Rac family small GTPase 1 pseudogene 4	Homo sapiens	187-192
30214507-6	2018	Blood sample analysis revealed that B-type natriuretic peptide (BNP), troponin T, C-reactive protein (CRP), creatinine and phosphorus concentrations were increased in the PTH-untreated CM group compared with that in the control group, whereas PTH and calcium concentrations were decreased.	Phosphorus	123-133	parathyroid hormone	Rattus norvegicus	171-174
30217807-1	2018	BACKGROUND: Fibroblast growth factor 23 (FGF23), a bone-derived hormone that regulates phosphorus and vitamin D metabolism, contributes to the pathogenesis of mineral and bone disorders in CKD and is an emerging cardiovascular risk factor.	Phosphorus	87-97	fibroblast growth factor 23	Homo sapiens	12-39
30214507-7	2018	Administration of PTH dose-dependently decreased BNP, CRP, creatinine and phosphorus levels, and increased PTH and calcium levels.	Phosphorus	74-84	parathyroid hormone	Rattus norvegicus	18-21
30217807-1	2018	BACKGROUND: Fibroblast growth factor 23 (FGF23), a bone-derived hormone that regulates phosphorus and vitamin D metabolism, contributes to the pathogenesis of mineral and bone disorders in CKD and is an emerging cardiovascular risk factor.	Phosphorus	87-97	fibroblast growth factor 23	Homo sapiens	41-46
29891277-2	2018	In our previous study, we isolated a water-soluble polysaccharide (BCPS) from Bupleurum chinense and showed that it exhibits anti-inflammatory effect by antagonizing P-selectin-mediated adhesion of HL-60 cells to CHO-P cells.	Phosphorus	69-70	selectin P	Homo sapiens	166-176
30313075-6	2018	Meta-analysis showed that levels of serum phosphorus (SMD -1.06; 95% CI, -1.27 to -0.85, P &lt; .001), parathyroid hormone (SMD -1.09; 95% CI, -1.49 to -0.70, P &lt; .001), and calcium-phosphorus (SMD -0.65; 95% CI, -0.97 to -0.34, P &lt; .001) in the nicotinamide group were significantly lower than those of the control group.	Phosphorus	42-52	small nuclear ribonucleoprotein D1 polypeptide	Homo sapiens	54-60
30301506-8	2018	Following the infection of CD8+T cells with SMAR1-downregulated lentiviral system, cell apoptosis level was decreased significantly (control vs. sh-SMAR1: 32.23 +- 12.4 % vs. 18.28 +- 8.93 %, p &amp;lt; 0.05).	Phosphorus	89-90	BTG3 associated nuclear protein	Mus musculus	44-49
30301506-8	2018	Following the infection of CD8+T cells with SMAR1-downregulated lentiviral system, cell apoptosis level was decreased significantly (control vs. sh-SMAR1: 32.23 +- 12.4 % vs. 18.28 +- 8.93 %, p &amp;lt; 0.05).	Phosphorus	89-90	BTG3 associated nuclear protein	Mus musculus	148-153
29751303-5	2018	It also decreased the phosphorus export to downstream water bodies by 5.33 kg/hm2/yr because of widespread ditches and ponds, a lower hydraulic gradient, and increased retention times of surface water in ponds.	Phosphorus	22-32	cholinergic receptor muscarinic 2	Homo sapiens	78-81
30249044-3	2018	Phosphorus is regulated by multiple hormones (parathyroid hormone (PTH), 1,25-dihyxdroxyvitamin D (1,25D), and fibroblast growth factor 23 (FGF23)) and tissues (kidney, intestine, parathyroid glands, and bone) to maintain homeostasis.	Phosphorus	0-10	parathyroid hormone	Homo sapiens	46-65
30249044-3	2018	Phosphorus is regulated by multiple hormones (parathyroid hormone (PTH), 1,25-dihyxdroxyvitamin D (1,25D), and fibroblast growth factor 23 (FGF23)) and tissues (kidney, intestine, parathyroid glands, and bone) to maintain homeostasis.	Phosphorus	0-10	parathyroid hormone	Homo sapiens	67-70
30249044-3	2018	Phosphorus is regulated by multiple hormones (parathyroid hormone (PTH), 1,25-dihyxdroxyvitamin D (1,25D), and fibroblast growth factor 23 (FGF23)) and tissues (kidney, intestine, parathyroid glands, and bone) to maintain homeostasis.	Phosphorus	0-10	fibroblast growth factor 23	Homo sapiens	111-138
30249044-3	2018	Phosphorus is regulated by multiple hormones (parathyroid hormone (PTH), 1,25-dihyxdroxyvitamin D (1,25D), and fibroblast growth factor 23 (FGF23)) and tissues (kidney, intestine, parathyroid glands, and bone) to maintain homeostasis.	Phosphorus	0-10	fibroblast growth factor 23	Homo sapiens	140-145
30231858-7	2018	At baseline the plasma renin concentration (PRC) was similar in sham and BDL animals, but increased urinary excretion of ANGII and an increase P-Aldosterone was observed in the placebo treated BDL animals.	Phosphorus	44-45	renin	Rattus norvegicus	23-28
29633705-2	2018	Fibroblast growth factor 23 (FGF23) is a bone-derived hormone with a pivotal role in phosphorus and vitamin D metabolism.	Phosphorus	85-95	fibroblast growth factor 23	Homo sapiens	0-27
30213628-3	2018	In this study, we characterized four monoclonal antibodies (MAbs), designated as Pc7, Pc8, Pc11 and Pc25 MAbs against the P protein of CDV-PS strain.	Phosphorus	139-141	proprotein convertase subtilisin/kexin type 7	Homo sapiens	81-84
30213628-3	2018	In this study, we characterized four monoclonal antibodies (MAbs), designated as Pc7, Pc8, Pc11 and Pc25 MAbs against the P protein of CDV-PS strain.	Phosphorus	139-141	proprotein convertase subtilisin/kexin type 7	Homo sapiens	86-89
29633705-2	2018	Fibroblast growth factor 23 (FGF23) is a bone-derived hormone with a pivotal role in phosphorus and vitamin D metabolism.	Phosphorus	85-95	fibroblast growth factor 23	Homo sapiens	29-34
30159399-2	2018	The enzymes phospholipase C and D (PLC and PLD) both cleave the phosphorus-oxygen bonds of phosphate esters in phosphatidylcholine (PC) lipids.	Phosphorus	64-74	heparan sulfate proteoglycan 2	Homo sapiens	35-38
29853024-4	2018	Electrochemical polymerization and over-oxidation conditions were deeply optimized to increase the sensitivity of PG/p(Thp)-Ox.	Phosphorus	16-17	uromodulin	Homo sapiens	119-122
29853024-9	2018	Satisfactory recovery values (98.07-104.4%) were observed with PG/p(Thp)-Ox electrode during the analysis of PRO in PRO-spiked potato, urine and river water samples.	Phosphorus	66-67	uromodulin	Homo sapiens	68-71
29860070-11	2018	Moreover, normal phosphorus significantly up-regulated lipoprotein lipase (LPL) mRNA expression and down-regulated fatty acid synthase (FAS) mRNA in Nile tilapia"s liver while low phosphorus with or without phytase supplementation reduced LPL expression and relatively up-regulated FAS.	Phosphorus	17-27	lipoprotein lipase	Oreochromis niloticus	55-73
29860070-11	2018	Moreover, normal phosphorus significantly up-regulated lipoprotein lipase (LPL) mRNA expression and down-regulated fatty acid synthase (FAS) mRNA in Nile tilapia"s liver while low phosphorus with or without phytase supplementation reduced LPL expression and relatively up-regulated FAS.	Phosphorus	17-27	lipoprotein lipase	Oreochromis niloticus	75-78
29860070-11	2018	Moreover, normal phosphorus significantly up-regulated lipoprotein lipase (LPL) mRNA expression and down-regulated fatty acid synthase (FAS) mRNA in Nile tilapia"s liver while low phosphorus with or without phytase supplementation reduced LPL expression and relatively up-regulated FAS.	Phosphorus	17-27	fatty acid synthase	Oreochromis niloticus	115-134
29860070-11	2018	Moreover, normal phosphorus significantly up-regulated lipoprotein lipase (LPL) mRNA expression and down-regulated fatty acid synthase (FAS) mRNA in Nile tilapia"s liver while low phosphorus with or without phytase supplementation reduced LPL expression and relatively up-regulated FAS.	Phosphorus	17-27	fatty acid synthase	Oreochromis niloticus	136-139
29860070-11	2018	Moreover, normal phosphorus significantly up-regulated lipoprotein lipase (LPL) mRNA expression and down-regulated fatty acid synthase (FAS) mRNA in Nile tilapia"s liver while low phosphorus with or without phytase supplementation reduced LPL expression and relatively up-regulated FAS.	Phosphorus	17-27	lipoprotein lipase	Oreochromis niloticus	239-242
29860070-11	2018	Moreover, normal phosphorus significantly up-regulated lipoprotein lipase (LPL) mRNA expression and down-regulated fatty acid synthase (FAS) mRNA in Nile tilapia"s liver while low phosphorus with or without phytase supplementation reduced LPL expression and relatively up-regulated FAS.	Phosphorus	17-27	fatty acid synthase	Oreochromis niloticus	282-285
30159399-2	2018	The enzymes phospholipase C and D (PLC and PLD) both cleave the phosphorus-oxygen bonds of phosphate esters in phosphatidylcholine (PC) lipids.	Phosphorus	64-74	glycosylphosphatidylinositol specific phospholipase D1	Homo sapiens	43-46
29685880-5	2018	Strong p-S6 staining in patients with OCCC suggests high mTORC1/2 activity.	Phosphorus	7-8	CREB regulated transcription coactivator 1	Mus musculus	57-63
30134544-5	2018	We note that sepsis shock syndrome represents loss of regulation of inflammatory response to infection and that vitamin D, parathyroid hormone, fibroblast growth factor, and klotho interact with sepsis defense mechanisms in which movement of calcium and phosphorus are part of the process.	Phosphorus	254-264	parathyroid hormone	Homo sapiens	123-142
29999323-4	2018	The cooperative competition of the hydrophilic quaternary vinylimidazole moieties and hydrophobic long alkyl side chains determines the thermal sensitive behavior of the P(NIPAm/VIM nBr) microgels.	Phosphorus	170-171	vimentin	Homo sapiens	178-181
30123501-12	2018	LPS up-regulated expression of IL-1beta, IL-6 and IL-10 in cecum, and serum concentration of MDA, IL-1beta and IL-6 (P &lt; 0.05), whereas 0.40% dietary non-phytate phosphorus supplementation significantly increased (P &lt; 0.05) villi height/crypt depth ratio, decreased (P &lt; 0.05) serum MDA and IFN-gamma concentration compared with the 0.12% non-phytate phosphorus group.	Phosphorus	165-175	interleukin 1, beta	Gallus gallus	31-39
30123501-12	2018	LPS up-regulated expression of IL-1beta, IL-6 and IL-10 in cecum, and serum concentration of MDA, IL-1beta and IL-6 (P &lt; 0.05), whereas 0.40% dietary non-phytate phosphorus supplementation significantly increased (P &lt; 0.05) villi height/crypt depth ratio, decreased (P &lt; 0.05) serum MDA and IFN-gamma concentration compared with the 0.12% non-phytate phosphorus group.	Phosphorus	360-370	interleukin 1, beta	Gallus gallus	31-39
30123501-13	2018	Conclusion: In summary, this study demonstrates that 0.40% dietary non-phytate phosphorus supplementation significantly increased calcium and phosphorus levels of eggshell, increased villi height/crypt depth ratio, decreased serum MDA and IFN-gamma concentration compared with the 0.12% non-phytate phosphorus groups.	Phosphorus	79-89	interferon gamma	Gallus gallus	239-248
29998686-4	2018	However, when phenol was higher than 100 mg L-1, phosphorus removal performance of the reactor decreased drastically.	Phosphorus	49-59	immunoglobulin kappa variable 1-16	Homo sapiens	44-47
29998686-5	2018	When phenol concentration was 200 mg L-1, the system lost phosphorus removal performance after only 22 cycles.	Phosphorus	58-68	immunoglobulin kappa variable 1-16	Homo sapiens	37-40
29866645-5	2018	Changes in urinary Klotho, urinary TNF-alpha, and phosphorus were associated with changes in serum Klotho; changes in estimated glomerular filtration rate, urinary TNF-alpha, and albuminuria were related to urinary Klotho variation.	Phosphorus	50-60	klotho	Homo sapiens	99-105
30028452-2	2018	Herein, we demonstrate a facile strategy for the preparation of CoP quantum dots (QDs) embedded in S,N-codoped graphite carbon (CoP@SNC) by using organophosphoric acid as both phosphorus and carbon sources.	Phosphorus	176-186	caspase recruitment domain family member 16	Homo sapiens	64-67
30028452-2	2018	Herein, we demonstrate a facile strategy for the preparation of CoP quantum dots (QDs) embedded in S,N-codoped graphite carbon (CoP@SNC) by using organophosphoric acid as both phosphorus and carbon sources.	Phosphorus	176-186	caspase recruitment domain family member 16	Homo sapiens	128-131
29920895-1	2018	A mild phosphorization process in low-temperature molten salt (NaCl-KCl-AlCl3 ) has been developed to synthesize peapod-like CoP@C nanostructures by using low-toxicity industrial PCl3 as the phosphorus source and Mg as the reductant at 250  C. Importantly, high efficiency of the phosphorous source is achieved since only stoichiometric PCl3 is required to complete the reaction.	Phosphorus	191-201	caspase recruitment domain family member 16	Homo sapiens	125-128
29920895-1	2018	A mild phosphorization process in low-temperature molten salt (NaCl-KCl-AlCl3 ) has been developed to synthesize peapod-like CoP@C nanostructures by using low-toxicity industrial PCl3 as the phosphorus source and Mg as the reductant at 250  C. Importantly, high efficiency of the phosphorous source is achieved since only stoichiometric PCl3 is required to complete the reaction.	Phosphorus	280-291	caspase recruitment domain family member 16	Homo sapiens	125-128
29866645-5	2018	Changes in urinary Klotho, urinary TNF-alpha, and phosphorus were associated with changes in serum Klotho; changes in estimated glomerular filtration rate, urinary TNF-alpha, and albuminuria were related to urinary Klotho variation.	Phosphorus	50-60	klotho	Homo sapiens	99-105
29962149-3	2018	The results show that when the concentration of TP was 10 mg L-1 in the influent, the lowest concentration of COD for good performance of the biological phosphorus removal system was 175 mg L-1.	Phosphorus	153-163	immunoglobulin kappa variable 1-16	Homo sapiens	61-64
29958595-11	2018	The target gene transforming growth factor alpha (TGFA) of miR-199a-5p involved in CL/P is screened and verified.	Phosphorus	86-87	tumor necrosis factor	Homo sapiens	16-48
29958595-11	2018	The target gene transforming growth factor alpha (TGFA) of miR-199a-5p involved in CL/P is screened and verified.	Phosphorus	86-87	transforming growth factor alpha	Homo sapiens	50-54
29797482-5	2018	We also reported that Pbx1 loss from cephalic epithelial domains, on a Pbx2- or Pbx3-deficient background, results in CL/P via disruption of a regulatory network that controls apoptosis at the seam of frontonasal and maxillary process fusion.	Phosphorus	22-23	pre B cell leukemia homeobox 2	Mus musculus	71-75
29797482-5	2018	We also reported that Pbx1 loss from cephalic epithelial domains, on a Pbx2- or Pbx3-deficient background, results in CL/P via disruption of a regulatory network that controls apoptosis at the seam of frontonasal and maxillary process fusion.	Phosphorus	22-23	pre B cell leukemia homeobox 3	Mus musculus	80-84
29931419-6	2018	Analyzed SNPs in FGF23 (rs710498025) and TRAFD1 (rs345195312) were significantly (p &lt;= 0.05) associated with the serum calcium/phosphorus ratio and serum phosphorus levels, respectively.	Phosphorus	130-140	fibroblast growth factor 23	Sus scrofa	17-22
29931419-6	2018	Analyzed SNPs in FGF23 (rs710498025) and TRAFD1 (rs345195312) were significantly (p &lt;= 0.05) associated with the serum calcium/phosphorus ratio and serum phosphorus levels, respectively.	Phosphorus	130-140	TRAF-type zinc finger domain containing 1	Sus scrofa	41-47
29931419-6	2018	Analyzed SNPs in FGF23 (rs710498025) and TRAFD1 (rs345195312) were significantly (p &lt;= 0.05) associated with the serum calcium/phosphorus ratio and serum phosphorus levels, respectively.	Phosphorus	157-167	fibroblast growth factor 23	Sus scrofa	17-22
29931419-6	2018	Analyzed SNPs in FGF23 (rs710498025) and TRAFD1 (rs345195312) were significantly (p &lt;= 0.05) associated with the serum calcium/phosphorus ratio and serum phosphorus levels, respectively.	Phosphorus	157-167	TRAF-type zinc finger domain containing 1	Sus scrofa	41-47
29931419-8	2018	Furthermore, TRAFD1 is known to be involved in skeletal disorders which emphasize its link to phosphorus utilization and immune system.	Phosphorus	94-104	TRAF-type zinc finger domain containing 1	Sus scrofa	13-19
29637561-8	2018	CONCLUSION: 1,25(OH)2 D deficiency in the 1alpha(OH)ase-/- mice accelerated alveolar bone loss by inhibiting osteoblastic bone formation and enhancing periodontal tissue degeneration in a calcium- and phosphorus- as well as an age-independent manner.	Phosphorus	201-211	cytochrome P450, family 27, subfamily b, polypeptide 1	Mus musculus	42-55
29754326-0	2018	Acid phosphatase gene GmHAD1 linked to low phosphorus tolerance in soybean, through fine mapping.	Phosphorus	43-53	LOC547457	Glycine max	0-16
29754326-1	2018	KEY MESSAGE: Map-based cloning identified GmHAD1, a gene which encodes a HAD-like acid phosphatase, associated with soybean tolerance to low phosphorus stress.	Phosphorus	141-151	LOC547457	Glycine max	82-98
29790272-4	2018	The muon hyperfine coupling constant (Amu ) indicated that the phosphorus atom bearing the t-butyl group trapped muonium to provide a metastable P-heterocyclic radical involving the ylidic MuP(&lt;)=C moiety.	Phosphorus	63-73	major urinary protein, pseudogene	Homo sapiens	189-192
29962164-7	2018	The order of importance was phosphatase activity &gt; pH &gt; sucrase activity &gt; catalase activity &gt; total N &gt; available P &gt; available K &gt; soil moisture content &gt; urease activity &gt; electrical conductivity (EC); phosphatase activity, pH value, invertase activity, catalase activity, total nitrogen, available phosphorus, and available potassium showed significant correlation with SOC and SIC (P&lt;0.01).	Phosphorus	329-339	catalase isozyme 1-like	Gossypium hirsutum	84-92
29962149-3	2018	The results show that when the concentration of TP was 10 mg L-1 in the influent, the lowest concentration of COD for good performance of the biological phosphorus removal system was 175 mg L-1.	Phosphorus	153-163	immunoglobulin kappa variable 1-16	Homo sapiens	190-193
29962149-6	2018	When the concentration of TP was 6 mg L-1 in the influent, the lowest concentration of COD for good performance of the biological phosphorus removal system was 150 mg L-1.	Phosphorus	130-140	immunoglobulin kappa variable 1-16	Homo sapiens	167-170
29774606-4	2018	Nitrogen doping lowers the d-band of CoP and weakens the H adsorption on the surface of CoP because of the strong electronegativity of nitrogen as compared to phosphorus.	Phosphorus	159-169	caspase recruitment domain family member 16	Homo sapiens	88-91
29812941-6	2018	Using PARP-1 as a model protein, we report that treatment of ADP-ribosylated peptides with hydrofluoric acid generates a specific +132 Da mass signature that corresponds to the decomposition of mono- and poly(ADP-ribosylated) peptides into ribose adducts as a consequence of the cleavage of the phosphorus-oxygen bonds.	Phosphorus	295-305	poly(ADP-ribose) polymerase 1	Homo sapiens	6-12
29893020-5	2018	Here, a rare chemical form of arsenic, called black-arsenic (b-As), is reported as a cousin of black phosphorus, as an extremely anisotropic layered semiconductor.	Phosphorus	101-111	BAS	Homo sapiens	46-65
29882656-0	2018	Biodegradable Black Phosphorus Nanosheets Mediate Specific Delivery of hTERT siRNA for Synergistic Cancer Therapy.	Phosphorus	14-30	telomerase reverse transcriptase	Homo sapiens	71-82
29688456-0	2018	Fibroblast growth factor 23 mRNA expression profile in chickens and its response to dietary phosphorus.	Phosphorus	92-102	fibroblast growth factor 23	Gallus gallus	0-27
29688456-2	2018	FGF23 mRNA is highly expressed in bone and slightly expressed in liver, and is regulated by dietary phosphorus.	Phosphorus	100-110	fibroblast growth factor 23	Gallus gallus	0-5
29688456-5	2018	The effect of dietary phosphorus on FGF23 expression was measured.	Phosphorus	22-32	fibroblast growth factor 23	Gallus gallus	36-41
29688456-13	2018	In conclusion, FGF23 mRNA expression pattern in chicken was clearly different from that in mammals and dietary phosphorus regulated the expression of FGF23 in a tissue-specific way.	Phosphorus	111-121	fibroblast growth factor 23	Gallus gallus	15-20
29688456-13	2018	In conclusion, FGF23 mRNA expression pattern in chicken was clearly different from that in mammals and dietary phosphorus regulated the expression of FGF23 in a tissue-specific way.	Phosphorus	111-121	fibroblast growth factor 23	Gallus gallus	150-155
30045587-0	2018	Evaluation of dried amorphous ferric hydroxide CFH-12  as agent for binding bioavailable phosphorus in lake sediments.	Phosphorus	89-99	complement factor H	Homo sapiens	47-50
29882656-4	2018	In this work, we present small and thin black phosphorus (BP) nanosheets as a biodegradable delivery system for hTERT siRNA.	Phosphorus	46-56	telomerase reverse transcriptase	Homo sapiens	112-123
29882656-4	2018	In this work, we present small and thin black phosphorus (BP) nanosheets as a biodegradable delivery system for hTERT siRNA.	Phosphorus	58-60	telomerase reverse transcriptase	Homo sapiens	112-123
29882656-5	2018	The BP nanosheets prepared with poly(ethylene glycol) (PEG) and polyethylenimine (PEI) modification (PPBP), exhibited high siRNA loading capacity and robust cell uptake.	Phosphorus	4-6	pro-platelet basic protein	Homo sapiens	101-105
29747513-4	2018	The copolymer interacts with miR-34a at low N/P ratios (~2/1) to form nanoplexes of size ~108 nm and a zeta potential ~ +39 mV.	Phosphorus	46-47	microRNA 34a	Homo sapiens	29-36
30065132-7	2018	On the basis of the results obtained in this study, it can be concluded that efficient removal of BOD, T-N, and total phosphorus can be achieved by the B-MBR as long as appropriate recirculation intensity is selected.	Phosphorus	118-128	translocator protein	Homo sapiens	154-157
28648547-4	2018	Indeed, for an aqueous pH of 5.2 and a phosphorus concentration of 75 mg L-1, the recovered amounts increased from 19.2 mg g-1 to 33.8 mg g-1 when the used pyrolysis temperature was raised from 400  C to 600  C. For all the tested biochars, the phosphorus recovery kinetics data were well fitted by the pseudo-second-order model, and the equilibrium state was obtained after 180 min of contact time.	Phosphorus	39-49	L1 cell adhesion molecule	Homo sapiens	73-76
28648547-4	2018	Indeed, for an aqueous pH of 5.2 and a phosphorus concentration of 75 mg L-1, the recovered amounts increased from 19.2 mg g-1 to 33.8 mg g-1 when the used pyrolysis temperature was raised from 400  C to 600  C. For all the tested biochars, the phosphorus recovery kinetics data were well fitted by the pseudo-second-order model, and the equilibrium state was obtained after 180 min of contact time.	Phosphorus	245-255	L1 cell adhesion molecule	Homo sapiens	73-76
30857093-4	2018	The lower N/P ratio facilitated the production of leucine aminopeptidase, which was unexpectedly induced by high P but not by low N.	Phosphorus	12-13	carboxypeptidase Q	Homo sapiens	58-72
29965638-5	2018	The membrane was hung in the biological carrier when the reactor was operated for 10 d. After the hanging of the film succeeded, the effluent COD was below 50 mg L-1, the effluent phosphorus was close to zero, and the removal efficiency of phosphorus reached to above 95%.	Phosphorus	240-250	immunoglobulin kappa variable 1-16	Homo sapiens	162-165
29965638-10	2018	During the recovery period, the concentration of the phosphorus solution increased from 40mg L-1 to 82 mg L-1 by increasing the influent phosphate concentration and the COD concentration in the anaerobic phase, meeting the requirement of phosphorus recovery with the struvite method.	Phosphorus	53-63	immunoglobulin kappa variable 1-16	Homo sapiens	93-96
29965638-10	2018	During the recovery period, the concentration of the phosphorus solution increased from 40mg L-1 to 82 mg L-1 by increasing the influent phosphate concentration and the COD concentration in the anaerobic phase, meeting the requirement of phosphorus recovery with the struvite method.	Phosphorus	53-63	immunoglobulin kappa variable 1-16	Homo sapiens	106-109
29965638-10	2018	During the recovery period, the concentration of the phosphorus solution increased from 40mg L-1 to 82 mg L-1 by increasing the influent phosphate concentration and the COD concentration in the anaerobic phase, meeting the requirement of phosphorus recovery with the struvite method.	Phosphorus	238-248	immunoglobulin kappa variable 1-16	Homo sapiens	106-109
29893387-1	2018	Hydroalumination of R-P(H)-C[triple bond, length as m-dash]C-tBu with bulky H-Al[CH(SiMe3)2]2 afforded the new P-H functionalized Al/P-based frustrated Lewis pair R-P(H)-C[[double bond, length as m-dash]C(H)-tBu]-AlR2 [R = CH(SiMe3)2; FLP 7].	Phosphorus	21-23	aldo-keto reductase family 1 member B	Homo sapiens	213-217
29807433-1	2018	Phosphate is an essential component of cell functions, and the specific transport of phosphorus into a cell is mediated by phosphate-binding protein (PBP).	Phosphorus	85-95	phosphatidylethanolamine binding protein 1	Homo sapiens	123-148
29807433-1	2018	Phosphate is an essential component of cell functions, and the specific transport of phosphorus into a cell is mediated by phosphate-binding protein (PBP).	Phosphorus	85-95	phosphatidylethanolamine binding protein 1	Homo sapiens	150-153
30701904-10	2018	A direct correlation (r=0.445; p&amp;lt;0.05) was established between FGF-23 serum levels and serum phosphorus, which was more pronounced in HD patients (r=0.545; p&amp;lt;0.01).	Phosphorus	100-110	fibroblast growth factor 23	Homo sapiens	70-76
29377525-6	2018	A hydroxyl-carbonate apatite (HCAp) layer was formed on all samples after SBF immersion for 72 h. Pure MBG showed the highest chemical reactivity after 72 h, with the resulting apatite layer exhibiting a Ca/P ratio of ~1.6 in accordance to stoichiometric biological apatite.	Phosphorus	98-99	HCA1	Homo sapiens	30-34
29606600-4	2018	We hypothesize that these NanS-p proteins are involved in competitive growth of EHEC in the gastrointestinal tract of humans and animals.	Phosphorus	5-6	N-acetylneuraminate synthase	Homo sapiens	26-30
29442783-3	2018	There is a 0.18 eV interface dipole pointing from BP to C8-BTBT, which means a relative weak interaction of substrate BP and the C8-BTBT molecules.	Phosphorus	118-120	homeobox C8	Homo sapiens	129-136
29442783-1	2018	The interfacial electronic structure and morphology of nanofilm of 2,7-dioctyl[1]benzothieno[3,2-b]benzothiophene (C8-BTBT) on black phosphorus (BP) was investigated with photoemission spectroscopy (PES) and atomic force microscopy (AFM).	Phosphorus	133-143	homeobox C8	Homo sapiens	115-122
29442783-1	2018	The interfacial electronic structure and morphology of nanofilm of 2,7-dioctyl[1]benzothieno[3,2-b]benzothiophene (C8-BTBT) on black phosphorus (BP) was investigated with photoemission spectroscopy (PES) and atomic force microscopy (AFM).	Phosphorus	145-147	homeobox C8	Homo sapiens	115-122
29442783-2	2018	The heterojunction of C8-BTBT/BP is a straddling one with a hole injection barrier of 1.41 eV and electron injection barrier of 2.43 eV from BP to C8-BTBT.	Phosphorus	30-32	homeobox C8	Homo sapiens	22-29
29442783-2	2018	The heterojunction of C8-BTBT/BP is a straddling one with a hole injection barrier of 1.41 eV and electron injection barrier of 2.43 eV from BP to C8-BTBT.	Phosphorus	30-32	homeobox C8	Homo sapiens	147-154
29442783-2	2018	The heterojunction of C8-BTBT/BP is a straddling one with a hole injection barrier of 1.41 eV and electron injection barrier of 2.43 eV from BP to C8-BTBT.	Phosphorus	141-143	homeobox C8	Homo sapiens	22-29
29442783-3	2018	There is a 0.18 eV interface dipole pointing from BP to C8-BTBT, which means a relative weak interaction of substrate BP and the C8-BTBT molecules.	Phosphorus	50-52	homeobox C8	Homo sapiens	56-63
29442783-4	2018	Volmer-Weber growth mode of C8-BTBT nanofilm on BP was confirmed and the C8-BTBT molecules adopt standing up configuration.	Phosphorus	48-50	homeobox C8	Homo sapiens	28-35
29442783-3	2018	There is a 0.18 eV interface dipole pointing from BP to C8-BTBT, which means a relative weak interaction of substrate BP and the C8-BTBT molecules.	Phosphorus	50-52	homeobox C8	Homo sapiens	129-136
29781271-0	2018	Bronsted Acid/Organic Photoredox Cooperative Catalysis: Easy Access to Tri- and Tetrasubstituted Alkenylphosphorus Compounds from Alcohols and P-H Species.	Phosphorus	22-23	tRNA-Ile (anticodon AAT) 9-1	Homo sapiens	71-74
29442783-3	2018	There is a 0.18 eV interface dipole pointing from BP to C8-BTBT, which means a relative weak interaction of substrate BP and the C8-BTBT molecules.	Phosphorus	118-120	homeobox C8	Homo sapiens	56-63
29741082-4	2018	The thermoelectric properties are found to be greatly enhanced after the BP addition, with the power factor of the film, with 2 wt % BP (36.2 muW m-1 K-2) representing a 109% improvement over the pure PEDOT:PSS film (17.3 muW m-1 K-2).	Phosphorus	73-75	RBPJ pseudogene 3	Homo sapiens	150-153
29741082-4	2018	The thermoelectric properties are found to be greatly enhanced after the BP addition, with the power factor of the film, with 2 wt % BP (36.2 muW m-1 K-2) representing a 109% improvement over the pure PEDOT:PSS film (17.3 muW m-1 K-2).	Phosphorus	73-75	RBPJ pseudogene 3	Homo sapiens	230-233
29741082-4	2018	The thermoelectric properties are found to be greatly enhanced after the BP addition, with the power factor of the film, with 2 wt % BP (36.2 muW m-1 K-2) representing a 109% improvement over the pure PEDOT:PSS film (17.3 muW m-1 K-2).	Phosphorus	133-135	RBPJ pseudogene 3	Homo sapiens	150-153
29799517-1	2018	The ABP dendrimer, which is built on a phosphorus-based scaffold and bears twelve azabisphosphonate groups at its surface, is one of the dendrimers that has been shown to display immuno-modulatory and anti-inflammatory effects towards the human immune system.	Phosphorus	39-49	amine oxidase copper containing 1	Homo sapiens	4-7
29886473-5	2018	Presently, there are several ways to reduce FGF23 levels, including decrease of intake and block of phosphorus absorption, supplement of FGF23 antibody and pseudo calcium or renal transplantation.	Phosphorus	100-110	fibroblast growth factor 23	Homo sapiens	44-49
29717319-1	2018	A Cu2O/BiVO4 p-n heterojunction based photoanode in photoelectrochemical (PEC) water splitting is fabricated by a two-step electrodeposition method on an FTO substrate followed by annealing treatment.	Phosphorus	13-14	FTO alpha-ketoglutarate dependent dioxygenase	Homo sapiens	154-157
29806022-4	2018	We also show that phosphorus addition greatly accelerates the rate of succession for plants and for microbial phototrophs, even at the most extreme deglaciating site at over 5000 meters above sea level in the Andes of arid southern Peru.	Phosphorus	18-28	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	192-195
29804411-1	2018	Objective: To observe the expression of protein kinase B (Akt) / mammalian target of rapamycin (mTOR) induced by high phosphorus in rat vascular smooth muscle cells (VSMC) calcification model, and its modulation on the expression of core binding factor alpha 1 (Cbfalpha1).	Phosphorus	118-128	protein tyrosine kinase 2 beta	Homo sapiens	40-56
29804411-16	2018	Akt and mTOR are involved in VSMC calcification induced by high phosphorus through the activation of Cbfalpha1.	Phosphorus	64-74	AKT serine/threonine kinase 1	Rattus norvegicus	0-3
29804411-1	2018	Objective: To observe the expression of protein kinase B (Akt) / mammalian target of rapamycin (mTOR) induced by high phosphorus in rat vascular smooth muscle cells (VSMC) calcification model, and its modulation on the expression of core binding factor alpha 1 (Cbfalpha1).	Phosphorus	118-128	AKT serine/threonine kinase 1	Homo sapiens	58-61
29804411-16	2018	Akt and mTOR are involved in VSMC calcification induced by high phosphorus through the activation of Cbfalpha1.	Phosphorus	64-74	mechanistic target of rapamycin kinase	Rattus norvegicus	8-12
29804411-1	2018	Objective: To observe the expression of protein kinase B (Akt) / mammalian target of rapamycin (mTOR) induced by high phosphorus in rat vascular smooth muscle cells (VSMC) calcification model, and its modulation on the expression of core binding factor alpha 1 (Cbfalpha1).	Phosphorus	118-128	mechanistic target of rapamycin kinase	Homo sapiens	65-94
29804411-16	2018	Akt and mTOR are involved in VSMC calcification induced by high phosphorus through the activation of Cbfalpha1.	Phosphorus	64-74	RUNX family transcription factor 2	Rattus norvegicus	101-110
29804411-1	2018	Objective: To observe the expression of protein kinase B (Akt) / mammalian target of rapamycin (mTOR) induced by high phosphorus in rat vascular smooth muscle cells (VSMC) calcification model, and its modulation on the expression of core binding factor alpha 1 (Cbfalpha1).	Phosphorus	118-128	mechanistic target of rapamycin kinase	Homo sapiens	96-100
29804411-1	2018	Objective: To observe the expression of protein kinase B (Akt) / mammalian target of rapamycin (mTOR) induced by high phosphorus in rat vascular smooth muscle cells (VSMC) calcification model, and its modulation on the expression of core binding factor alpha 1 (Cbfalpha1).	Phosphorus	118-128	RUNX family transcription factor 2	Rattus norvegicus	233-260
29804411-1	2018	Objective: To observe the expression of protein kinase B (Akt) / mammalian target of rapamycin (mTOR) induced by high phosphorus in rat vascular smooth muscle cells (VSMC) calcification model, and its modulation on the expression of core binding factor alpha 1 (Cbfalpha1).	Phosphorus	118-128	RUNX family transcription factor 2	Rattus norvegicus	262-271
29804411-10	2018	The mRNA expressions of Cbfalpha1 and OPN increased significantly and the protein expressions of p-Akt, p-mTOR, Cbfalpha1 and OPN up-regulated significantly in high phosphorus group (all P&lt;0.05).	Phosphorus	165-175	RUNX family transcription factor 2	Rattus norvegicus	24-33
29804411-10	2018	The mRNA expressions of Cbfalpha1 and OPN increased significantly and the protein expressions of p-Akt, p-mTOR, Cbfalpha1 and OPN up-regulated significantly in high phosphorus group (all P&lt;0.05).	Phosphorus	165-175	AKT serine/threonine kinase 1	Rattus norvegicus	99-102
29804411-10	2018	The mRNA expressions of Cbfalpha1 and OPN increased significantly and the protein expressions of p-Akt, p-mTOR, Cbfalpha1 and OPN up-regulated significantly in high phosphorus group (all P&lt;0.05).	Phosphorus	165-175	mechanistic target of rapamycin kinase	Rattus norvegicus	106-110
29804411-10	2018	The mRNA expressions of Cbfalpha1 and OPN increased significantly and the protein expressions of p-Akt, p-mTOR, Cbfalpha1 and OPN up-regulated significantly in high phosphorus group (all P&lt;0.05).	Phosphorus	165-175	RUNX family transcription factor 2	Rattus norvegicus	112-121
29804411-11	2018	After treated with Wortmannin or Rapamycin for 24 h, compared with high phosphorus group, the mRNA expressions of Cbfalpha1 and OPN decreased significantly in high phosphorus + Wortmannin (30, 50 and 100 nmol/L) groups (all P&lt;0.05) and high phosphorus + Rapamycin (1, 10 and 100 ng/ml) groups (all P&lt;0.05).	Phosphorus	72-82	RUNX family transcription factor 2	Rattus norvegicus	114-123
29804411-11	2018	After treated with Wortmannin or Rapamycin for 24 h, compared with high phosphorus group, the mRNA expressions of Cbfalpha1 and OPN decreased significantly in high phosphorus + Wortmannin (30, 50 and 100 nmol/L) groups (all P&lt;0.05) and high phosphorus + Rapamycin (1, 10 and 100 ng/ml) groups (all P&lt;0.05).	Phosphorus	164-174	RUNX family transcription factor 2	Rattus norvegicus	114-123
29804411-11	2018	After treated with Wortmannin or Rapamycin for 24 h, compared with high phosphorus group, the mRNA expressions of Cbfalpha1 and OPN decreased significantly in high phosphorus + Wortmannin (30, 50 and 100 nmol/L) groups (all P&lt;0.05) and high phosphorus + Rapamycin (1, 10 and 100 ng/ml) groups (all P&lt;0.05).	Phosphorus	164-174	RUNX family transcription factor 2	Rattus norvegicus	114-123
29804411-12	2018	After treated with Wortmannin or Rapamycin for 48 h, compared with high phosphorus group, the protein expressions of p-Akt, Cbfalpha1 and OPN down-regulated significantly in high phosphorus + Wortmannin (30, 50 and 100 nmol/L) groups (all P&lt;0.05).	Phosphorus	72-82	AKT serine/threonine kinase 1	Rattus norvegicus	119-122
29462698-6	2018	In view of this, the present study aimed to investigate the anti-inflammatory actions of PS and its potential neuroprotective effects against beta-amyloid (Abeta)-induced microglia-mediated neurotoxicity.	Phosphorus	89-91	amyloid beta (A4) precursor protein	Mus musculus	156-161
29804411-12	2018	After treated with Wortmannin or Rapamycin for 48 h, compared with high phosphorus group, the protein expressions of p-Akt, Cbfalpha1 and OPN down-regulated significantly in high phosphorus + Wortmannin (30, 50 and 100 nmol/L) groups (all P&lt;0.05).	Phosphorus	72-82	RUNX family transcription factor 2	Rattus norvegicus	124-141
29462698-8	2018	Subsequently, MTT reduction assay was used to evaluate the neuroprotective effects of PS leaf extracts against Abeta-induced microglia-mediated neurotoxicity in SH-SY5Y neuroblastoma cells.	Phosphorus	86-88	amyloid beta (A4) precursor protein	Mus musculus	111-116
29804411-12	2018	After treated with Wortmannin or Rapamycin for 48 h, compared with high phosphorus group, the protein expressions of p-Akt, Cbfalpha1 and OPN down-regulated significantly in high phosphorus + Wortmannin (30, 50 and 100 nmol/L) groups (all P&lt;0.05).	Phosphorus	179-189	AKT serine/threonine kinase 1	Rattus norvegicus	119-122
29804411-12	2018	After treated with Wortmannin or Rapamycin for 48 h, compared with high phosphorus group, the protein expressions of p-Akt, Cbfalpha1 and OPN down-regulated significantly in high phosphorus + Wortmannin (30, 50 and 100 nmol/L) groups (all P&lt;0.05).	Phosphorus	179-189	RUNX family transcription factor 2	Rattus norvegicus	124-141
29965519-4	2018	When the PS concentration increased from 0.25 to 2 mmol  L-1 and the VUV intensity increased from 113.2 to 618.5 muW  cm-2, the removal rate of 2-MIB was increased by 42% and 39%, respectively, and the removal rate of GSM was increased by 34% and 16%, respectively.	Phosphorus	9-11	MIB E3 ubiquitin protein ligase 1	Homo sapiens	146-149
29584948-3	2018	In this work, we demonstrate that black arsenic phosphorus alloy (b-As xP1- x) formed by introducing arsenic into BP can significantly extend the operational wavelength range of photonic devices.	Phosphorus	114-116	XPA, DNA damage recognition and repair factor	Homo sapiens	71-74
29533492-4	2018	These compounds represent a new type of useful reagent, and their access paves the way for the concept of "RP synthons" (i.e., RP2- phosphandiides), likely to be the most flexible precursors of a variety of phosphorus targets.	Phosphorus	207-217	RP2 activator of ARL3 GTPase	Homo sapiens	127-130
29489415-9	2018	CONCLUSION: Our study demonstrated that there is low number of etiologic coding variants in GREM1, confirming earlier suggestions that variants in regulatory elements may largely account for the association between this locus and CL/P.	Phosphorus	233-234	gremlin 1, DAN family BMP antagonist	Homo sapiens	92-97
29458003-12	2018	The presence of VDR variants affect the protein expression of VD, phosphorus, FGF23 and PTH.	Phosphorus	66-76	vitamin D receptor	Homo sapiens	16-19
29655203-8	2018	Recurrent P/LP variants were observed in 14 distinct genes, most commonly in MECP2, KCNQ2, SCN1A, SCN2A, STXBP1, and PRRT2.	Phosphorus	10-11	methyl-CpG binding protein 2	Homo sapiens	77-82
29655203-8	2018	Recurrent P/LP variants were observed in 14 distinct genes, most commonly in MECP2, KCNQ2, SCN1A, SCN2A, STXBP1, and PRRT2.	Phosphorus	10-11	potassium voltage-gated channel subfamily Q member 2	Homo sapiens	84-89
29655203-8	2018	Recurrent P/LP variants were observed in 14 distinct genes, most commonly in MECP2, KCNQ2, SCN1A, SCN2A, STXBP1, and PRRT2.	Phosphorus	10-11	sodium voltage-gated channel alpha subunit 1	Homo sapiens	91-96
29655203-8	2018	Recurrent P/LP variants were observed in 14 distinct genes, most commonly in MECP2, KCNQ2, SCN1A, SCN2A, STXBP1, and PRRT2.	Phosphorus	10-11	sodium voltage-gated channel alpha subunit 2	Homo sapiens	98-103
29655203-8	2018	Recurrent P/LP variants were observed in 14 distinct genes, most commonly in MECP2, KCNQ2, SCN1A, SCN2A, STXBP1, and PRRT2.	Phosphorus	10-11	syntaxin binding protein 1	Homo sapiens	105-111
29655203-8	2018	Recurrent P/LP variants were observed in 14 distinct genes, most commonly in MECP2, KCNQ2, SCN1A, SCN2A, STXBP1, and PRRT2.	Phosphorus	10-11	proline rich transmembrane protein 2	Homo sapiens	117-122
29636481-7	2018	Furthermore, the PHR1 master regulator of the phosphorus-starvation response also directly promotes expression of NIGT1 family genes, leading to reductions in nitrate uptake.	Phosphorus	46-56	photolyase 1	Arabidopsis thaliana	17-21
29443694-0	2018	Exploration of two-dimensional bio-functionalized phosphorene nanosheets (black phosphorous) for label free haptoglobin electro-immunosensing applications.	Phosphorus	80-91	haptoglobin	Homo sapiens	108-119
29443694-1	2018	We report on the development of an antibody-functionalized interface based on electrochemically active liquid-exfoliated two-dimensional phosphorene (Ph) nanosheets-also known as black phosphorous nanosheets-for the label-free electrochemical immunosensing of a haptoglobin (Hp) biomarker, a clinical marker of severe inflammation.	Phosphorus	185-196	haptoglobin	Homo sapiens	262-273
29669938-9	2018	The increase in plasma FGF23 was correlated with the increase in serum phosphorus, and the decrease in plasma 1,25-dihydroxyvitamin D was correlated with the increase in plasma FGF23.	Phosphorus	71-81	fibroblast growth factor 23	Homo sapiens	23-28
29669938-10	2018	CONCLUSIONS: Canagliflozin induced a prompt increase in serum phosphorus, which triggers downstream changes in FGF23, 1,25-dihydroxyvitamin D, and PTH, with potential to exert adverse effects on bone health.	Phosphorus	62-72	fibroblast growth factor 23	Homo sapiens	111-116
29669938-10	2018	CONCLUSIONS: Canagliflozin induced a prompt increase in serum phosphorus, which triggers downstream changes in FGF23, 1,25-dihydroxyvitamin D, and PTH, with potential to exert adverse effects on bone health.	Phosphorus	62-72	parathyroid hormone	Homo sapiens	147-150
29662131-3	2018	The complex refractive index, normal-incidence reflectivity and birefringence are presented and a difference in the refractive index in the visible regime between GaN and GaNP alloys of ~0.3 can be engineered by adding minute amounts of phosphorus, indicating strong potential for refractive index tunability.	Phosphorus	237-247	minichromosome maintenance complex component 3 associated protein	Homo sapiens	171-175
29670389-1	2018	Background: FGF23 plays an important role in calcium-phosphorus metabolism.	Phosphorus	53-63	fibroblast growth factor 23	Mus musculus	12-17
29304459-3	2018	The aim of this study was to quantify the effect of temperature and cadmium (Cd) toxicity on alkaline phosphatase (ALP) produced by microbes to acquire phosphorus.	Phosphorus	152-162	alkaline phosphatase, placental	Homo sapiens	93-113
29304459-3	2018	The aim of this study was to quantify the effect of temperature and cadmium (Cd) toxicity on alkaline phosphatase (ALP) produced by microbes to acquire phosphorus.	Phosphorus	152-162	alkaline phosphatase, placental	Homo sapiens	115-118
29304459-12	2018	Our results suggest that global warming might accelerate the deficiency of available phosphorus in Cd contaminated soils due to higher inhibition of Cd on ALP activity, particularly in alkaline soils.	Phosphorus	85-95	alkaline phosphatase, placental	Homo sapiens	155-158
29290646-3	2018	On the supply side, we operate an auction with small-scale livestock owners who bid for contracts to implement site-specific manure management practices that reduce phosphorus loadings to a major reservoir.	Phosphorus	165-175	BH3 interacting domain death agonist	Homo sapiens	80-83
29679282-3	2018	Inhibition of FGF23 by burosumab results in increased renal phosphate reabsorption and increased serum levels of phosphorus and active vitamin D.	Phosphorus	113-123	fibroblast growth factor 23	Homo sapiens	14-19
29413630-4	2018	The green microalga was grown in a culture medium with a phosphorus (P) content of 4.55 mg L-1 simulating an industrial effluent; it was also exposed to a bimetal solution of copper (Cu) and nickel (Ni) for 2 days.	Phosphorus	57-71	immunoglobulin kappa variable 1-16	Homo sapiens	91-94
29623690-1	2018	There is evidence that nutritional phosphorus (P) excess may be a risk factor for chronic kidney disease (CKD) in humans and pets (Advances in Nutrition: An International Review Journal (2014), 5, 104; The American Journal of Clinical Nutrition, (2013), 98, 6; Journal of Feline Medicine and Surgery, (2017); The source of phosphorus influences serum PTH, apparent digestibility and blood levels of calcium and phosphorus in dogs fed high phosphorus diets with balanced Ca/P ratio.	Phosphorus	35-45	parathyroid hormone	Homo sapiens	351-354
29675099-11	2018	However, p-CtIP of HepG2.2.15 was significantly lower than that of HepG2 after DSB.	Phosphorus	9-10	RB binding protein 8, endonuclease	Homo sapiens	11-15
29325125-0	2018	Age, phosphorus, and 25-hydroxycholecalciferol regulate mRNA expression of vitamin D receptor and sodium-phosphate cotransporter in the small intestine of broiler chickens.	Phosphorus	5-15	vitamin D (1,25- dihydroxyvitamin D3) receptor	Gallus gallus	75-93
29559581-3	2018	The interaction between Tat and P-TEFb, which is a cellular protein complex composed of cyclin T1 and CDK9, delivers P-TEFb to the newly transcribed viral mRNAs where phosphorylation of RNA polymerase II by CDK9 leads to highly efficient mRNA transcription.	Phosphorus	32-33	cyclin T1	Homo sapiens	88-97
29559581-3	2018	The interaction between Tat and P-TEFb, which is a cellular protein complex composed of cyclin T1 and CDK9, delivers P-TEFb to the newly transcribed viral mRNAs where phosphorylation of RNA polymerase II by CDK9 leads to highly efficient mRNA transcription.	Phosphorus	32-33	cyclin dependent kinase 9	Homo sapiens	102-106
29559581-3	2018	The interaction between Tat and P-TEFb, which is a cellular protein complex composed of cyclin T1 and CDK9, delivers P-TEFb to the newly transcribed viral mRNAs where phosphorylation of RNA polymerase II by CDK9 leads to highly efficient mRNA transcription.	Phosphorus	32-33	cyclin dependent kinase 9	Homo sapiens	207-211
29287254-1	2018	A phosphorus-bearing product S-PAL obtained from nutrient-rich wastewater was reused as ameliorant for Cu, Pb and Cd immobilization in contaminated soil with three different rates (1%, 5% and 10% w/w).	Phosphorus	2-12	SHC binding and spindle associated 1	Homo sapiens	31-34
29518087-1	2018	The hormone fibroblast growth factor 23 (FGF23) is secreted from bone and is involved in phosphorus (P) metabolism.	Phosphorus	89-99	fibroblast growth factor 23	Rattus norvegicus	12-39
29518087-1	2018	The hormone fibroblast growth factor 23 (FGF23) is secreted from bone and is involved in phosphorus (P) metabolism.	Phosphorus	89-99	fibroblast growth factor 23	Rattus norvegicus	41-46
33418784-7	2018	In contrast to class C CpG ODNs, which also simultaneously induce IFN-alpha and IL-6, the ratio of IFN-alpha and IL-6 induced by PEI-CpG ODN NPs could be regulated by changing the N/P ratio.	Phosphorus	129-130	interferon alpha 1	Homo sapiens	99-108
33418784-7	2018	In contrast to class C CpG ODNs, which also simultaneously induce IFN-alpha and IL-6, the ratio of IFN-alpha and IL-6 induced by PEI-CpG ODN NPs could be regulated by changing the N/P ratio.	Phosphorus	129-130	interleukin 6	Homo sapiens	113-117
29911042-14	2018	Both HCY and CathK were found positively associated with serum phosphorus (r = 0.584, P &lt; 2.01 and r = 0.249, P &lt; 0.05, respectively).	Phosphorus	63-73	cathepsin K	Homo sapiens	13-18
28332409-7	2018	During monitoring of the adsorption tower (33 days), the influent total phosphorus (T-P) concentration was in the range of 0.020-0.046 mgP/L, whereas the effluent T-P concentration was in the range of 0.010-0.028 mgP/L.	Phosphorus	72-82	matrix Gla protein	Homo sapiens	135-138
29146137-6	2018	RESULTS: Phosphorus, potassium, and sodium additives were present on the ingredient list in 37%, 9%, and 72% of MPF, respectively.	Phosphorus	9-19	mesothelin	Homo sapiens	112-115
29146137-7	2018	Among MPF categories that contained a phosphorus additive, phosphorus content was significantly (P &lt; .05) higher in MPF with phosphorus additives versus MPF without phosphorus additives and MPF reference foods (median [min, max]): (270 [140, 500] mg/100 g) versus (200 [130, 510] mg/100 g) versus (210 [100, 260] mg/100 g), respectively.	Phosphorus	38-48	mesothelin	Homo sapiens	6-9
29146137-7	2018	Among MPF categories that contained a phosphorus additive, phosphorus content was significantly (P &lt; .05) higher in MPF with phosphorus additives versus MPF without phosphorus additives and MPF reference foods (median [min, max]): (270 [140, 500] mg/100 g) versus (200 [130, 510] mg/100 g) versus (210 [100, 260] mg/100 g), respectively.	Phosphorus	59-69	mesothelin	Homo sapiens	6-9
29146137-7	2018	Among MPF categories that contained a phosphorus additive, phosphorus content was significantly (P &lt; .05) higher in MPF with phosphorus additives versus MPF without phosphorus additives and MPF reference foods (median [min, max]): (270 [140, 500] mg/100 g) versus (200 [130, 510] mg/100 g) versus (210 [100, 260] mg/100 g), respectively.	Phosphorus	59-69	mesothelin	Homo sapiens	119-122
29146137-7	2018	Among MPF categories that contained a phosphorus additive, phosphorus content was significantly (P &lt; .05) higher in MPF with phosphorus additives versus MPF without phosphorus additives and MPF reference foods (median [min, max]): (270 [140, 500] mg/100 g) versus (200 [130, 510] mg/100 g) versus (210 [100, 260] mg/100 g), respectively.	Phosphorus	59-69	mesothelin	Homo sapiens	119-122
29413111-8	2018	Furthermore, cytokine concentrations were independently associated with several mineral concentrations: IL-1beta with higher phosphorus and iron, IL-6 with higher calcium, magnesium, copper and manganese, IL-8 with higher calcium and zinc, and TNF-alpha with lower iron and manganese.	Phosphorus	125-135	interleukin 1 beta	Homo sapiens	104-112
29146137-7	2018	Among MPF categories that contained a phosphorus additive, phosphorus content was significantly (P &lt; .05) higher in MPF with phosphorus additives versus MPF without phosphorus additives and MPF reference foods (median [min, max]): (270 [140, 500] mg/100 g) versus (200 [130, 510] mg/100 g) versus (210 [100, 260] mg/100 g), respectively.	Phosphorus	59-69	mesothelin	Homo sapiens	119-122
29488933-7	2018	Density functional theory calculations performed on PPh3 and PPh4+ revealed large differences in the molecular orbital energies that were ascribed to differences in the phosphorus oxidation state (III versus V) and molecular charge (neutral versus +1).	Phosphorus	169-179	protein phosphatase 4 catalytic subunit	Homo sapiens	52-56
29146137-7	2018	Among MPF categories that contained a phosphorus additive, phosphorus content was significantly (P &lt; .05) higher in MPF with phosphorus additives versus MPF without phosphorus additives and MPF reference foods (median [min, max]): (270 [140, 500] mg/100 g) versus (200 [130, 510] mg/100 g) versus (210 [100, 260] mg/100 g), respectively.	Phosphorus	59-69	mesothelin	Homo sapiens	6-9
29488933-7	2018	Density functional theory calculations performed on PPh3 and PPh4+ revealed large differences in the molecular orbital energies that were ascribed to differences in the phosphorus oxidation state (III versus V) and molecular charge (neutral versus +1).	Phosphorus	169-179	potassium two pore domain channel subfamily K member 3	Homo sapiens	61-65
29146137-7	2018	Among MPF categories that contained a phosphorus additive, phosphorus content was significantly (P &lt; .05) higher in MPF with phosphorus additives versus MPF without phosphorus additives and MPF reference foods (median [min, max]): (270 [140, 500] mg/100 g) versus (200 [130, 510] mg/100 g) versus (210 [100, 260] mg/100 g), respectively.	Phosphorus	59-69	mesothelin	Homo sapiens	119-122
29146137-7	2018	Among MPF categories that contained a phosphorus additive, phosphorus content was significantly (P &lt; .05) higher in MPF with phosphorus additives versus MPF without phosphorus additives and MPF reference foods (median [min, max]): (270 [140, 500] mg/100 g) versus (200 [130, 510] mg/100 g) versus (210 [100, 260] mg/100 g), respectively.	Phosphorus	59-69	mesothelin	Homo sapiens	119-122
29146137-7	2018	Among MPF categories that contained a phosphorus additive, phosphorus content was significantly (P &lt; .05) higher in MPF with phosphorus additives versus MPF without phosphorus additives and MPF reference foods (median [min, max]): (270 [140, 500] mg/100 g) versus (200 [130, 510] mg/100 g) versus (210 [100, 260] mg/100 g), respectively.	Phosphorus	59-69	mesothelin	Homo sapiens	119-122
29146137-7	2018	Among MPF categories that contained a phosphorus additive, phosphorus content was significantly (P &lt; .05) higher in MPF with phosphorus additives versus MPF without phosphorus additives and MPF reference foods (median [min, max]): (270 [140, 500] mg/100 g) versus (200 [130, 510] mg/100 g) versus (210 [100, 260] mg/100 g), respectively.	Phosphorus	59-69	mesothelin	Homo sapiens	6-9
29146137-7	2018	Among MPF categories that contained a phosphorus additive, phosphorus content was significantly (P &lt; .05) higher in MPF with phosphorus additives versus MPF without phosphorus additives and MPF reference foods (median [min, max]): (270 [140, 500] mg/100 g) versus (200 [130, 510] mg/100 g) versus (210 [100, 260] mg/100 g), respectively.	Phosphorus	59-69	mesothelin	Homo sapiens	119-122
29146137-7	2018	Among MPF categories that contained a phosphorus additive, phosphorus content was significantly (P &lt; .05) higher in MPF with phosphorus additives versus MPF without phosphorus additives and MPF reference foods (median [min, max]): (270 [140, 500] mg/100 g) versus (200 [130, 510] mg/100 g) versus (210 [100, 260] mg/100 g), respectively.	Phosphorus	59-69	mesothelin	Homo sapiens	119-122
29146137-7	2018	Among MPF categories that contained a phosphorus additive, phosphorus content was significantly (P &lt; .05) higher in MPF with phosphorus additives versus MPF without phosphorus additives and MPF reference foods (median [min, max]): (270 [140, 500] mg/100 g) versus (200 [130, 510] mg/100 g) versus (210 [100, 260] mg/100 g), respectively.	Phosphorus	59-69	mesothelin	Homo sapiens	119-122
29146137-9	2018	CONCLUSIONS: The use of additives in packaged MPF products as indicated by the ingredient list can significantly contribute to the dietary phosphorus and potassium loads in patients with CKD.	Phosphorus	139-149	mesothelin	Homo sapiens	46-49
29146137-10	2018	Patients with CKD should be educated to avoid MPF foods listing phosphorus and/or potassium additives on the ingredient list, which may lead to improved dietary adherence.	Phosphorus	64-74	mesothelin	Homo sapiens	46-49
29276822-5	2018	The optimum H2 and O2 production rates on BP/BiVO4 were approximately 160 and 102 mumol g-1  h-1 under irradiation of light with a wavelength longer than 420 nm, without using any sacrificial agents or external bias.	Phosphorus	42-44	relaxin 2	Homo sapiens	12-21
29344653-0	2018	A novel variant of osteogenesis imperfecta type IV and low serum phosphorus level caused by a Val94Asp mutation in COL1A1.	Phosphorus	65-75	collagen type I alpha 1 chain	Homo sapiens	115-121
29576814-10	2018	Conclusion: The majority of patients with low PS levels also had mutations in the fifteen exon of PROS 1 gene.	Phosphorus	46-48	protein S	Homo sapiens	98-104
29355264-1	2018	A phosphorus(v) complex of porphycene [P(OEPc)(OMe)2]PF6 (OEPc = 2,3,6,7,12,13,16,17-octaethylporphycenato dianion) has been synthesized and structurally characterized as the first porphycene derivative incorporating nonmetal elements in the macrocyclic cavity.	Phosphorus	2-12	sperm associated antigen 17	Homo sapiens	53-56
29571392-2	2018	Correlation analyses (DIP vs Chl a; R2 = 0.407, df = 31, p &lt; 0.001) suggested phosphorus limiting conditions in lakes, which was corroborated with the highest alkaline phosphatase activity (APA) that fluctuated from 0.38 to 41.14 nmol L-1 min-1.	Phosphorus	81-91	immunoglobulin kappa variable 1-16	Homo sapiens	238-247
29471799-6	2018	Sixteen participants (aged 13-16 years) with p-DCD (&lt;=16th percentile on the MABC-2 test) were recruited.	Phosphorus	8-9	dermcidin	Homo sapiens	47-50
29337188-2	2018	Putatively, the mineralization disorder is attributed to the elevated fibroblast growth factor 23 (FGF23), which reduced the serum phosphorus by suppressing the reabsorption of phosphorus in kidney.	Phosphorus	131-141	fibroblast growth factor 23	Mus musculus	70-97
29412679-1	2018	Organophosphorus compounds with a phosphorus atom attached to a phenyl group and two organothio/organoseleno groups were synthesized using the rhodium-catalyzed insertion reaction of the PhP group of pentaphenylcyclopentaphosphine (PhP)5 with acyclic disulfides and diselenides.	Phosphorus	6-16	N-acylsphingosine amidohydrolase 1	Homo sapiens	187-190
29412679-1	2018	Organophosphorus compounds with a phosphorus atom attached to a phenyl group and two organothio/organoseleno groups were synthesized using the rhodium-catalyzed insertion reaction of the PhP group of pentaphenylcyclopentaphosphine (PhP)5 with acyclic disulfides and diselenides.	Phosphorus	6-16	N-acylsphingosine amidohydrolase 1	Homo sapiens	232-235
29412679-2	2018	The method was applied to the synthesis of heterocyclic compounds containing the S-P-S group by the reaction of (PhP)5 and cyclic disulfides such as 1,2-dithietes, 1,2-dithiocane, 1,4,5-dithiopane, and 1,2-dithiolanes.	Phosphorus	81-84	N-acylsphingosine amidohydrolase 1	Homo sapiens	113-116
29337188-2	2018	Putatively, the mineralization disorder is attributed to the elevated fibroblast growth factor 23 (FGF23), which reduced the serum phosphorus by suppressing the reabsorption of phosphorus in kidney.	Phosphorus	131-141	fibroblast growth factor 23	Mus musculus	99-104
29337188-2	2018	Putatively, the mineralization disorder is attributed to the elevated fibroblast growth factor 23 (FGF23), which reduced the serum phosphorus by suppressing the reabsorption of phosphorus in kidney.	Phosphorus	177-187	fibroblast growth factor 23	Mus musculus	70-97
29337188-2	2018	Putatively, the mineralization disorder is attributed to the elevated fibroblast growth factor 23 (FGF23), which reduced the serum phosphorus by suppressing the reabsorption of phosphorus in kidney.	Phosphorus	177-187	fibroblast growth factor 23	Mus musculus	99-104
29354815-2	2018	CoP nanoparticles anchored on N,P-dual-doped mesoporous graphene-like carbon (CoP@NPMG) acts as an outstanding bifunctional electrocatalyst for both the hydrogen evolution reaction and the oxygen evolution reaction over a wide pH range.	Phosphorus	2-3	caspase recruitment domain family member 16	Homo sapiens	78-81
29394885-11	2018	High phosphorus diet-induced changes in bone microstructure were accompanied by increased serum parathyroid hormone and fibroblast growth factor 23 levels.	Phosphorus	5-15	parathyroid hormone	Rattus norvegicus	96-115
29394885-11	2018	High phosphorus diet-induced changes in bone microstructure were accompanied by increased serum parathyroid hormone and fibroblast growth factor 23 levels.	Phosphorus	5-15	fibroblast growth factor 23	Rattus norvegicus	120-147
28757361-9	2018	The treatment with Phosphorus caused a significant increase of INF-gamma and TNF-alpha on the 5th day of infection compared with the Control (p&lt;0.05), with reestablishment on the 24th day, as well as in the Control group.	Phosphorus	19-29	tumor necrosis factor	Rattus norvegicus	77-86
28726128-1	2018	Using a time-dependent phosphorus (P) budget model for the Baltic proper, describing sources and sinks at the external borders of the water column, one may compute the e-folding time T of the adjustment of the winter surface water P concentration c 1 to abruptly changed total P supply.	Phosphorus	23-33	heterogeneous nuclear ribonucleoprotein C	Homo sapiens	247-250
29370119-0	2018	Inadequate Dietary Phosphorus Levels Cause Skeletal Anomalies and Alter Osteocalcin Gene Expression in Zebrafish.	Phosphorus	19-29	bone gamma-carboxyglutamate (gla) protein	Danio rerio	72-83
29350657-1	2018	Hypoparathyroidism (HPT) is a rare disease with leading symptoms of hypocalcemia, associated with high serum phosphorus levels and absent or inappropriately low levels of parathyroid hormone (PTH).	Phosphorus	109-119	HPT	Homo sapiens	0-18
29350657-1	2018	Hypoparathyroidism (HPT) is a rare disease with leading symptoms of hypocalcemia, associated with high serum phosphorus levels and absent or inappropriately low levels of parathyroid hormone (PTH).	Phosphorus	109-119	HPT	Homo sapiens	20-23
30106322-2	2018	The protein kinase PINK1 and E3 ubiquitin ligase PRKN are the most well studied regulators of mitophagy, via a feedforward mechanism involving ubiquitin phosphorylation (p-Ser65-Ub) and accumulation at the damaged mitochondria.	Phosphorus	170-172	PTEN induced kinase 1	Homo sapiens	19-24
29219161-1	2018	A detailed mechanism of the I2-induced transformation of white phosphorus into PI3 emerges from a DFT analysis.	Phosphorus	57-73	peptidase inhibitor 3	Homo sapiens	79-82
29621752-1	2018	BACKGROUND: Fibroblast growth factor 23 (FGF-23) is a hormone that regulates phosphorus levels and vitamin D metabolism.	Phosphorus	77-87	fibroblast growth factor 23	Homo sapiens	12-39
29621752-1	2018	BACKGROUND: Fibroblast growth factor 23 (FGF-23) is a hormone that regulates phosphorus levels and vitamin D metabolism.	Phosphorus	77-87	fibroblast growth factor 23	Homo sapiens	41-47
29134946-1	2018	We study the conventional electron-phonon mediated superconducting properties of hole-doped black phosphorus by density functional calculations and get quite a large electron-phonon coupling (EPC) constant lambda ~ 1.0 with transition temperature T C ~ 10 K, which is comparable to MgB2 when holes are doped into the degenerate and nearly flat energy bands around the Fermi level.	Phosphorus	98-108	secretoglobin family 2A member 1	Homo sapiens	282-286
29152826-4	2018	Ultimately, on treatment of the (mu2 :eta2 ,eta2 -Pn2 ){Ni(IMes)(CO)}2 compounds with carbon monoxide, the Pn2 units can be released, affording P4 in the case of the phosphorus-containing species, and elemental arsenic in the case of (mu2 :eta2 ,eta2 -As2 ){Ni(IMes)(CO)}2 .	Phosphorus	166-176	adaptor related protein complex 1 subunit mu 2	Homo sapiens	33-36
29152826-4	2018	Ultimately, on treatment of the (mu2 :eta2 ,eta2 -Pn2 ){Ni(IMes)(CO)}2 compounds with carbon monoxide, the Pn2 units can be released, affording P4 in the case of the phosphorus-containing species, and elemental arsenic in the case of (mu2 :eta2 ,eta2 -As2 ){Ni(IMes)(CO)}2 .	Phosphorus	166-176	DNA polymerase iota	Homo sapiens	44-48
29152826-4	2018	Ultimately, on treatment of the (mu2 :eta2 ,eta2 -Pn2 ){Ni(IMes)(CO)}2 compounds with carbon monoxide, the Pn2 units can be released, affording P4 in the case of the phosphorus-containing species, and elemental arsenic in the case of (mu2 :eta2 ,eta2 -As2 ){Ni(IMes)(CO)}2 .	Phosphorus	166-176	amyloid beta precursor protein	Homo sapiens	50-53
29152826-4	2018	Ultimately, on treatment of the (mu2 :eta2 ,eta2 -Pn2 ){Ni(IMes)(CO)}2 compounds with carbon monoxide, the Pn2 units can be released, affording P4 in the case of the phosphorus-containing species, and elemental arsenic in the case of (mu2 :eta2 ,eta2 -As2 ){Ni(IMes)(CO)}2 .	Phosphorus	166-176	amyloid beta precursor protein	Homo sapiens	107-110
29152826-4	2018	Ultimately, on treatment of the (mu2 :eta2 ,eta2 -Pn2 ){Ni(IMes)(CO)}2 compounds with carbon monoxide, the Pn2 units can be released, affording P4 in the case of the phosphorus-containing species, and elemental arsenic in the case of (mu2 :eta2 ,eta2 -As2 ){Ni(IMes)(CO)}2 .	Phosphorus	166-176	DNA polymerase iota	Homo sapiens	44-48
29152826-4	2018	Ultimately, on treatment of the (mu2 :eta2 ,eta2 -Pn2 ){Ni(IMes)(CO)}2 compounds with carbon monoxide, the Pn2 units can be released, affording P4 in the case of the phosphorus-containing species, and elemental arsenic in the case of (mu2 :eta2 ,eta2 -As2 ){Ni(IMes)(CO)}2 .	Phosphorus	166-176	DNA polymerase iota	Homo sapiens	44-48
30106322-2	2018	The protein kinase PINK1 and E3 ubiquitin ligase PRKN are the most well studied regulators of mitophagy, via a feedforward mechanism involving ubiquitin phosphorylation (p-Ser65-Ub) and accumulation at the damaged mitochondria.	Phosphorus	170-172	parkin RBR E3 ubiquitin protein ligase	Homo sapiens	49-53
29597231-8	2018	Prolonged hypocalcemia and exposure to elevated PTH may also result in 1,25(OH)2D-mediated calcium and phosphorus release from bone.	Phosphorus	103-113	parathyroid hormone	Homo sapiens	48-51
29375690-0	2018	Effect of SLC34A2 gene mutation on extracellular phosphorus transport in PAM alveolar epithelial cells.	Phosphorus	49-59	solute carrier family 34 member 2	Homo sapiens	10-17
29597237-1	2018	The interplay between vitamin D and parathyroid hormone (PTH) represents one of the most important metabolic mechanisms of regulation of the calcium/phosphorus homeostasis.	Phosphorus	149-159	parathyroid hormone	Homo sapiens	36-55
29421132-0	2018	Bioavailability and geochemical speciation of phosphorus in surface sediments of the Southern Caspian Sea.	Phosphorus	46-56	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	102-105
29577851-6	2018	METHODS: Recombinant human alpha-synuclein was expressed and isolated and incubated in the presence of phosphatidylcholine and phosphatidylserine (PC/PS) containing liposomes.	Phosphorus	150-152	synuclein alpha	Homo sapiens	27-42
29207398-6	2018	Ginsenoside Rb3 significantly delayed the appearance of transient recovery of PS during OGD, and improved the recovery amplitudes of NMDA-PS and AMPA-PS after reoxygenation.	Phosphorus	78-80	stathmin 4	Rattus norvegicus	12-15
29210694-3	2017	In addition, the results of three inflow total phosphorus (TP) concentrations (5 mg L-1, 15 mg L-1, and 30 mg L-1) indicated that high-levels of phosphorus were more advantageous in regards to improving the activity of denitrifying bacteria in soil and strengthening the effect of nitrogen removal, suggesting that the effluent total nitrogen (TN) concentration could meet the primary grade A standard (TN &lt;= 15 mg L-1).	Phosphorus	145-155	immunoglobulin kappa variable 1-16	Homo sapiens	84-87
28926796-1	2017	LiF:Mg,Cu,P,Si (MCPS), a new tissue equivalent phosphor, was synthesized by solid state method.	Phosphorus	10-11	LIF interleukin 6 family cytokine	Homo sapiens	0-3
28923731-4	2017	Our results showed that the freshly adsorbed phosphorus dominantly exists in Occluded-P and Fe/AlP and their percentages increased with increasing phosphorus adsorbed.	Phosphorus	45-55	ATHS	Homo sapiens	95-98
28513870-6	2017	We discovered an increased calcium ion concentration and upregulated Runx2, BMP2, Nrf2, HO-1, gamma-GCS, NQO-1, and LC3II/LC3I expressions in the high phosphorous, si-NC and Nrf2-siRNA, and NC groups, compared with the normal control group.	Phosphorus	151-162	RUNX family transcription factor 2	Homo sapiens	69-74
28513870-6	2017	We discovered an increased calcium ion concentration and upregulated Runx2, BMP2, Nrf2, HO-1, gamma-GCS, NQO-1, and LC3II/LC3I expressions in the high phosphorous, si-NC and Nrf2-siRNA, and NC groups, compared with the normal control group.	Phosphorus	151-162	bone morphogenetic protein 2	Homo sapiens	76-80
28513870-6	2017	We discovered an increased calcium ion concentration and upregulated Runx2, BMP2, Nrf2, HO-1, gamma-GCS, NQO-1, and LC3II/LC3I expressions in the high phosphorous, si-NC and Nrf2-siRNA, and NC groups, compared with the normal control group.	Phosphorus	151-162	NFE2 like bZIP transcription factor 2	Homo sapiens	82-86
28513870-6	2017	We discovered an increased calcium ion concentration and upregulated Runx2, BMP2, Nrf2, HO-1, gamma-GCS, NQO-1, and LC3II/LC3I expressions in the high phosphorous, si-NC and Nrf2-siRNA, and NC groups, compared with the normal control group.	Phosphorus	151-162	heme oxygenase 1	Homo sapiens	88-103
28513870-6	2017	We discovered an increased calcium ion concentration and upregulated Runx2, BMP2, Nrf2, HO-1, gamma-GCS, NQO-1, and LC3II/LC3I expressions in the high phosphorous, si-NC and Nrf2-siRNA, and NC groups, compared with the normal control group.	Phosphorus	151-162	NAD(P)H quinone dehydrogenase 1	Homo sapiens	105-110
28513870-7	2017	Compared to the high phosphorus and si-NC groups, higher levels of Runx2 and BMP2 but decreased Nrf2, HO-1, gamma-GCS, NQO-1, and LC3II/LC3I expressions were detected in the Nrf2-siRNA group.	Phosphorus	21-31	RUNX family transcription factor 2	Homo sapiens	67-72
28513870-8	2017	The high phosphorus, si-NC and over-expressed Nrf2 experimental groups all had increased Nrf2, NQO-1, HO-1, gamma-GCS, and LC3II/LC3I expressions as well as high numbers of autophagosomes compared with the normal control group.	Phosphorus	9-19	NFE2 like bZIP transcription factor 2	Homo sapiens	89-93
28513870-8	2017	The high phosphorus, si-NC and over-expressed Nrf2 experimental groups all had increased Nrf2, NQO-1, HO-1, gamma-GCS, and LC3II/LC3I expressions as well as high numbers of autophagosomes compared with the normal control group.	Phosphorus	9-19	NAD(P)H quinone dehydrogenase 1	Homo sapiens	95-100
28513870-8	2017	The high phosphorus, si-NC and over-expressed Nrf2 experimental groups all had increased Nrf2, NQO-1, HO-1, gamma-GCS, and LC3II/LC3I expressions as well as high numbers of autophagosomes compared with the normal control group.	Phosphorus	9-19	heme oxygenase 1	Homo sapiens	102-117
29206257-2	2017	In this work, the interactions of H2O and/or O2 with BP are investigated using first-principles calculations.	Phosphorus	53-55	heme oxygenase 2	Homo sapiens	34-47
29206257-6	2017	The effects of H2O and/or O2 on the quasiparticle band gap and exciton binding energy of BP are also investigated.	Phosphorus	89-91	heme oxygenase 2	Homo sapiens	15-28
29336756-6	2017	The elevated ALP group had significantly higher levels of preoperative parathyroid hormone (PTH), lower preoperative serum calcium, higher preoperative phosphorus, lower postoperative hypocalcemia, and a longer hospital stay.	Phosphorus	152-162	alkaline phosphatase, placental	Homo sapiens	13-16
28783443-4	2017	The thermo-sensitivity of the Fe3O4/P(MMA-b-NIPAAm-b-AAc) magnetic composite nanosphere was confirmed via DLS at 40  C. DOX encapsulation efficiency was calculated to be 98.2%.	Phosphorus	36-37	glycine-N-acyltransferase	Homo sapiens	53-56
28513870-9	2017	Finally, we detected a lower amount of autophagosomes presence and Nrf2, NQO-1, HO-1 gamma-GCS, and LC3II/LC3 protein expression of Nrf2-siRNA group than that of the high phosphorus and si-NC groups.	Phosphorus	171-181	NFE2 like bZIP transcription factor 2	Homo sapiens	132-136
28531916-4	2017	In the solution, increased CO2 in air enhanced the dissolution of FAp, i.e., from 0.04 to 1.18ppm for P and from 2.48 to 13.61ppm for Ca.	Phosphorus	102-103	fibroblast activation protein alpha	Homo sapiens	66-69
29210694-3	2017	In addition, the results of three inflow total phosphorus (TP) concentrations (5 mg L-1, 15 mg L-1, and 30 mg L-1) indicated that high-levels of phosphorus were more advantageous in regards to improving the activity of denitrifying bacteria in soil and strengthening the effect of nitrogen removal, suggesting that the effluent total nitrogen (TN) concentration could meet the primary grade A standard (TN &lt;= 15 mg L-1).	Phosphorus	145-155	immunoglobulin kappa variable 1-16	Homo sapiens	95-98
29210694-3	2017	In addition, the results of three inflow total phosphorus (TP) concentrations (5 mg L-1, 15 mg L-1, and 30 mg L-1) indicated that high-levels of phosphorus were more advantageous in regards to improving the activity of denitrifying bacteria in soil and strengthening the effect of nitrogen removal, suggesting that the effluent total nitrogen (TN) concentration could meet the primary grade A standard (TN &lt;= 15 mg L-1).	Phosphorus	145-155	immunoglobulin kappa variable 1-16	Homo sapiens	95-98
29210694-3	2017	In addition, the results of three inflow total phosphorus (TP) concentrations (5 mg L-1, 15 mg L-1, and 30 mg L-1) indicated that high-levels of phosphorus were more advantageous in regards to improving the activity of denitrifying bacteria in soil and strengthening the effect of nitrogen removal, suggesting that the effluent total nitrogen (TN) concentration could meet the primary grade A standard (TN &lt;= 15 mg L-1).	Phosphorus	145-155	immunoglobulin kappa variable 1-16	Homo sapiens	95-98
29165378-4	2017	The main driving factors which influenced sediment phosphorus flux velocity in the sediment-water interface were sediment B-SO42-, B-MBN and A-MBP content.	Phosphorus	51-61	myelin basic protein	Homo sapiens	143-146
29185452-7	2017	We also revealed that while physiological agonist S1P-induced endocytosed S1P1R readily recycled back to PM, pharmacological FTY720-P-induced endocytosed S1P1R-positive vesicles became associated with DHHC5 in the later phase, persistently transmitting Gi signals there.	Phosphorus	131-133	zinc finger DHHC-type palmitoyltransferase 5	Homo sapiens	201-206
29077389-9	2017	The "luminescence-on" behavior of l-Y(OH)3:Ce,Tb by phosphate adsorption was employed to detect and recover phosphorus at low concentrations in deionized water, mineral water, tap water, and river water.	Phosphorus	108-118	nuclear RNA export factor 1	Homo sapiens	176-179
29165378-6	2017	Sediment B-SO42-, B-MBN and A-MBP content and the interaction between them were the main factors affecting sediment phosphorus release rates in the sediment-water interface.	Phosphorus	116-126	alpha-1-microglobulin/bikunin precursor	Homo sapiens	9-33
29035031-3	2017	Here, we report our first-principles calculations of spin-polarized electronic structure of monolayer black phosphorus (phosphorene) adsorbed on a magnetic europium oxide (EuO) substrate.	Phosphorus	102-118	spindlin 1	Homo sapiens	53-57
29167516-3	2017	Here we demonstrate that amino-functionalized polystyrene nanoparticles (PS-NH2), but not amino- or hydroxyl-functionalized silica particles, trigger cell death in hepatocellular carcinoma Huh7 cells.	Phosphorus	73-75	MIR7-3 host gene	Homo sapiens	189-193
29163142-9	2017	Furthermore, multiple regression analyses showed that a low level of serum phosphorus correlated with cerebral Abeta deposition, even when age, sex, apolipoprotein E epsilon4 genotype, and MMSE z-score were controlled for.	Phosphorus	75-85	apolipoprotein E	Homo sapiens	149-165
28843778-5	2017	Moreover, our study indicated that the B[a]P-induced autophagy was initiated through the activation of cytochrome P450 1B1 (CYP1B1) and the aryl hydrocarbon receptor (AhR) in HaCaT cells.	Phosphorus	43-44	cytochrome P450 family 1 subfamily B member 1	Homo sapiens	103-122
29148130-6	2017	Assuming those kinetic parameters remained constant for each patient, serum phosphorus concentrations during the second treatment were used to estimate the driving force concentration (Cdf ) for phosphorus mobilization from tissues during the second treatment.	Phosphorus	76-86	LIF interleukin 6 family cytokine	Homo sapiens	185-188
29148130-6	2017	Assuming those kinetic parameters remained constant for each patient, serum phosphorus concentrations during the second treatment were used to estimate the driving force concentration (Cdf ) for phosphorus mobilization from tissues during the second treatment.	Phosphorus	195-205	LIF interleukin 6 family cytokine	Homo sapiens	185-188
28985998-9	2017	In contrast, the configuration of the phosphorus atom is critical for GGT inhibitory activity.	Phosphorus	38-48	inactive glutathione hydrolase 2	Homo sapiens	70-73
28843778-5	2017	Moreover, our study indicated that the B[a]P-induced autophagy was initiated through the activation of cytochrome P450 1B1 (CYP1B1) and the aryl hydrocarbon receptor (AhR) in HaCaT cells.	Phosphorus	43-44	cytochrome P450 family 1 subfamily B member 1	Homo sapiens	124-130
28843778-5	2017	Moreover, our study indicated that the B[a]P-induced autophagy was initiated through the activation of cytochrome P450 1B1 (CYP1B1) and the aryl hydrocarbon receptor (AhR) in HaCaT cells.	Phosphorus	43-44	aryl hydrocarbon receptor	Homo sapiens	140-165
28843778-5	2017	Moreover, our study indicated that the B[a]P-induced autophagy was initiated through the activation of cytochrome P450 1B1 (CYP1B1) and the aryl hydrocarbon receptor (AhR) in HaCaT cells.	Phosphorus	43-44	aryl hydrocarbon receptor	Homo sapiens	167-170
29118269-8	2017	For example, the expression levels of miR-34a were correlated with serum phosphorus and cholesterin levels; miR-204, miR-15a and miR-16b were correlated with triglyceride.	Phosphorus	73-83	microRNA 34a	Sus scrofa	38-45
29293859-4	2017	Scanning fluorescence X-ray microscopy images of a 50-mum x 45-mum area of an organic soil sample showed heterogeneous distributions of P, Al, and Si.	Phosphorus	136-137	latexin	Homo sapiens	63-66
28885837-1	2017	The reaction of LGa (L = Dipp(4-(Dipp-imino)pent-2-en-2-yl)amide; Dipp: 2,6-diisopropylphenyl) and white phosphorus was revisited.	Phosphorus	105-115	glutaminase 2	Homo sapiens	16-19
29383117-7	2017	The agreement between P-TRG and MR-TRG was excellent (0.923).	Phosphorus	22-23	T cell receptor gamma locus	Homo sapiens	24-27
27882824-3	2017	A phosphorus level of at least 3 mM and K:P molar ratio over 3 were necessary to form MPP, which showed higher content rate of phosphorus and potassium in precipitate.	Phosphorus	2-12	M-phase phosphoprotein 6	Homo sapiens	86-89
28985224-4	2017	For two CASP8 variants, p.K148R and p.I298V, the association remained significant in a combined sample of 10,820 cases and 8,881 controls.	Phosphorus	24-25	caspase 8	Homo sapiens	8-13
27882824-3	2017	A phosphorus level of at least 3 mM and K:P molar ratio over 3 were necessary to form MPP, which showed higher content rate of phosphorus and potassium in precipitate.	Phosphorus	127-137	M-phase phosphoprotein 6	Homo sapiens	86-89
28677090-5	2017	In the simple linear regression model, Klotho levels were correlated with age, phosphorus, PTH, ACR, HOMA, IL-6, FGF-23, OxLDL, eGFR and vitamin D levels.	Phosphorus	79-89	klotho	Homo sapiens	39-45
28748724-4	2017	Areas covered: Sodium-glucose cotransporter 2 (SGLT2) inhibitors have been linked with the scarce, but serious, complication of euglycemic diabetic ketoacidosis, as well as with an increase in serum potassium, magnesium and phosphorus levels.	Phosphorus	224-234	solute carrier family 5 member 2	Homo sapiens	15-45
28748724-4	2017	Areas covered: Sodium-glucose cotransporter 2 (SGLT2) inhibitors have been linked with the scarce, but serious, complication of euglycemic diabetic ketoacidosis, as well as with an increase in serum potassium, magnesium and phosphorus levels.	Phosphorus	224-234	solute carrier family 5 member 2	Homo sapiens	47-52
28748724-7	2017	Insulin administration is associated with a reduction in serum potassium, magnesium and phosphorus concentration, along with reduced renal magnesium excretion.	Phosphorus	88-98	insulin	Homo sapiens	0-7
28656548-0	2017	Treadmill Exercise Attenuates alpha-Synuclein Levels by Promoting Mitochondrial Function and Autophagy Possibly via SIRT1 in the Chronic MPTP/P-Induced Mouse Model of Parkinson"s Disease.	Phosphorus	56-57	synuclein, alpha	Mus musculus	30-45
28882992-6	2017	Mouse glutathione S-transferase p1 (mGstp1) further enhanced P-GSH adduct formation in vitro.	Phosphorus	61-62	glutathione S-transferase, pi 1	Mus musculus	6-34
28882992-6	2017	Mouse glutathione S-transferase p1 (mGstp1) further enhanced P-GSH adduct formation in vitro.	Phosphorus	61-62	glutathione S-transferase, pi 1	Mus musculus	36-42
28921494-2	2017	Like a natural phosphodiester RNA backbone linkage, a PS2-modified backbone linkage is achiral at phosphorus.	Phosphorus	98-108	taste 2 receptor member 64 pseudogene	Homo sapiens	54-57
28731143-2	2017	In the present study, the contribution of TNX to liver dysfunction was investigated by administration of high-fat and high-cholesterol diet with high levels of phosphorus and calcium (HFCD) to wild-type (WT) and TNX-knockout (KO) mice.	Phosphorus	160-170	tenascin XB	Mus musculus	42-45
28741160-0	2017	Erratum to: Treadmill Exercise Attenuates alpha-Synuclein Levels by Promoting Mitochondrial Function and Autophagy Possibly via SIRT1 in the Chronic MPTP/P-Induced Mouse Model of Parkinson"s Disease.	Phosphorus	68-69	synuclein, alpha	Mus musculus	42-57
28667925-6	2017	Log serum FGF23 and age were significantly associated with IRIS stage (P=0.027 and P=0.032 respectively), while log serum phosphorus concentration (P&lt;0.001) was significantly associated with log serum FGF23 concentration.	Phosphorus	122-132	fibroblast growth factor 23	Canis lupus familiaris	204-209
28667925-7	2017	In summary, serum FGF23 concentration is increased in dogs with CKD, and is associated with serum phosphorus concentration.	Phosphorus	98-108	fibroblast growth factor 23	Canis lupus familiaris	18-23
28655510-7	2017	CIV and CXIV further blocked Ca/P-induced osteochondrocytic transdifferentiation of VSMC displayed e.g. by reduced gene expressions of Runx2, Sox9, osterix and increased expressions of alphaSMA and SM22alpha.	Phosphorus	32-33	RUNX family transcription factor 2	Homo sapiens	135-140
28655510-7	2017	CIV and CXIV further blocked Ca/P-induced osteochondrocytic transdifferentiation of VSMC displayed e.g. by reduced gene expressions of Runx2, Sox9, osterix and increased expressions of alphaSMA and SM22alpha.	Phosphorus	32-33	SRY-box transcription factor 9	Homo sapiens	142-146
28655510-7	2017	CIV and CXIV further blocked Ca/P-induced osteochondrocytic transdifferentiation of VSMC displayed e.g. by reduced gene expressions of Runx2, Sox9, osterix and increased expressions of alphaSMA and SM22alpha.	Phosphorus	32-33	Sp7 transcription factor	Homo sapiens	148-155
28655510-7	2017	CIV and CXIV further blocked Ca/P-induced osteochondrocytic transdifferentiation of VSMC displayed e.g. by reduced gene expressions of Runx2, Sox9, osterix and increased expressions of alphaSMA and SM22alpha.	Phosphorus	32-33	transgelin	Homo sapiens	198-207
32260683-2	2017	In this work, we prepared a highly active electrocatalyst containing phosphorus-doped NiCo2S4 nanocrystals grown on carbon nanotube embedded carbon nanofibers (P-NiCo2S4@CNT/CNF).	Phosphorus	69-79	NPHS1 adhesion molecule, nephrin	Homo sapiens	174-177
28828864-8	2017	Once arrived at the tumor site, the P-S-H nanoparticles were stimulated by overexpressed MMP2 and acidic pH, and subsequently the shedding of the PEG shell and protonation of the HLAH peptide induced the reassembly of nanoparticles, resulting in the formation of nanoparticles with activated cytotoxic peptides on the surface.	Phosphorus	36-37	major histocompatibility complex, class I, H (pseudogene)	Homo sapiens	179-183
29965245-5	2017	The concentration of total phosphorus (TP) in water ranged from 0.05 to 2.31 mg L-1 in May and from 0.03 to 0.1 mg L-1 in September.	Phosphorus	27-37	immunoglobulin kappa variable 1-16	Homo sapiens	80-83
28447218-11	2017	The highest pCR was reached by the BluePrint HER2-type patients treated with T/P (76%).	Phosphorus	39-40	erb-b2 receptor tyrosine kinase 2	Homo sapiens	45-49
27225727-1	2017	Pin1 is an enzyme that specifically recognizes the peptide bond between phosphorylated serine or threonine (pS/pT-P) and proline.	Phosphorus	108-110	peptidyl-prolyl cis/trans isomerase, NIMA-interacting 1	Mus musculus	0-4
28828864-8	2017	Once arrived at the tumor site, the P-S-H nanoparticles were stimulated by overexpressed MMP2 and acidic pH, and subsequently the shedding of the PEG shell and protonation of the HLAH peptide induced the reassembly of nanoparticles, resulting in the formation of nanoparticles with activated cytotoxic peptides on the surface.	Phosphorus	36-37	matrix metallopeptidase 2	Homo sapiens	89-93
29965259-3	2017	The results showed that the average effluent concentration of soluble phosphorus under different influent C/N conditions were 0.22, 0.34, 0.39, 0.42, and 2.45 mg L-1 and the low influent C/N ratio was beneficial to phosphate removal.	Phosphorus	70-80	L1 cell adhesion molecule	Homo sapiens	162-165
28838338-6	2017	Immunoreactivity of octanoylated ghrelin significantly increased in GI compared to GIII, GV, and GVI (p&amp;lt;0.05).	Phosphorus	102-104	ghrelin and obestatin prepropeptide	Rattus norvegicus	33-40
28648599-4	2017	Furthermore, the effect of BDM on the S1-bound adenosine 5"-(beta,gamma-imido) triphosphate (AMPPNP) 31P NMR spectrum suggests that BDM changes the microenvironment around the phosphorus atoms of myosin-bound nucleotide.	Phosphorus	176-186	myosin heavy chain 14	Homo sapiens	196-202
31457722-5	2017	Electrochemical impedance spectroscopic measurements clarified that the good electron transport proceeded throughout the developed conduction pathway to promote the phase transition to trisodium phosphide (Na3P), leading to a high reversible capacity for phosphorus; the as-prepared black phosphorus showed only a reversible capacity of 140 mA h g-1 at the 60th cycle, whereas the 30 wt % Ni-coated composite delivered a relatively high capacity of 780 mA h g(P)-1.	Phosphorus	255-265	GTP binding protein 1	Homo sapiens	458-464
28474853-1	2017	At 80 GPa, phases with the PH2 stoichiometry, which are composed of simple cubic like phosphorus layers capped with hydrogen atoms and layers of H2 molecules, are predicted to be important species contributing to the recently observed superconductivity in compressed phosphine.	Phosphorus	86-96	polyhomeotic homolog 2	Homo sapiens	27-30
28811481-3	2017	Earlier, we had demonstrated an LIF neuron by a novel 4-terminal impact ionization based n+/p/n+ with an extended gate (gated-INPN) device by physics simulation.	Phosphorus	67-68	LIF interleukin 6 family cytokine	Homo sapiens	32-35
28631314-2	2017	Several approaches are demonstrated here for covalent chemical modifications of layered black phosphorus in order to form P-C and P-O-C bonds.	Phosphorus	88-104	proopiomelanocortin	Homo sapiens	122-135
28425622-7	2017	In addition, calcium-phosphorus metabolism was significantly altered (calcium reduced; phosphorus reduced; parathyroid hormone [PTH] increased; 1,25(OH)2 D decreased).	Phosphorus	21-31	parathyroid hormone	Mus musculus	107-126
28715025-2	2017	Here, we identified a pressure-induced reversible phase transition on few-layer BP nanosheets by performing in situ ADXRD and Raman spectroscopy with the assistance of DAC apparatus.	Phosphorus	80-82	arylacetamide deacetylase	Homo sapiens	168-171
29137322-7	2017	In support of this, the administration of the JNK inhibitor, D-JNKI1, was able to counteract the Abeta and p-Tau accumulation in the retina of TgCRND8 mice, and consequently reduce RGCs loss.	Phosphorus	5-6	mitogen-activated protein kinase 8	Mus musculus	46-49
30034212-0	2017	IMPROVING PREDICTIVE MODELS OF IN-STREAM PHOSPHORUS CONCENTRATION BASED ON NATIONALLY-AVAILABLE SPATIAL DATA COVERAGES.	Phosphorus	41-51	thymus, brain and testes associated	Homo sapiens	96-103
27339879-5	2017	We further found that caspase-1 knockout decreased MPTP/p-induced caspase-7 cleavage, subsequently inhibited nuclear translocation of poly (ADP-ribose) polymerase 1 (PARP1), and reduced the release of apoptosis-inducing factor (AIF).	Phosphorus	25-26	caspase 7	Mus musculus	66-75
27339879-5	2017	We further found that caspase-1 knockout decreased MPTP/p-induced caspase-7 cleavage, subsequently inhibited nuclear translocation of poly (ADP-ribose) polymerase 1 (PARP1), and reduced the release of apoptosis-inducing factor (AIF).	Phosphorus	25-26	poly (ADP-ribose) polymerase family, member 1	Mus musculus	134-164
27339879-5	2017	We further found that caspase-1 knockout decreased MPTP/p-induced caspase-7 cleavage, subsequently inhibited nuclear translocation of poly (ADP-ribose) polymerase 1 (PARP1), and reduced the release of apoptosis-inducing factor (AIF).	Phosphorus	25-26	poly (ADP-ribose) polymerase family, member 1	Mus musculus	166-171
27339879-5	2017	We further found that caspase-1 knockout decreased MPTP/p-induced caspase-7 cleavage, subsequently inhibited nuclear translocation of poly (ADP-ribose) polymerase 1 (PARP1), and reduced the release of apoptosis-inducing factor (AIF).	Phosphorus	25-26	apoptosis-inducing factor, mitochondrion-associated 1	Mus musculus	201-226
27339879-5	2017	We further found that caspase-1 knockout decreased MPTP/p-induced caspase-7 cleavage, subsequently inhibited nuclear translocation of poly (ADP-ribose) polymerase 1 (PARP1), and reduced the release of apoptosis-inducing factor (AIF).	Phosphorus	25-26	apoptosis-inducing factor, mitochondrion-associated 1	Mus musculus	228-231
28425622-17	2017	Taken together, these results indicate that Nf1 deficiency in osteocytes dramatically increases FGF23 production and causes a mineralization defect (ie, hyperosteoidosis) via the alteration of calcium-phosphorus metabolism.	Phosphorus	201-211	neurofibromin 1	Homo sapiens	44-47
28588114-6	2017	C. reinhardtii knockdown mutants for GPD2 and GPD3 showed no difference in growth but displayed significant reduction in TAG concentration compared with the wild type in response to phosphorus or nitrogen starvation.	Phosphorus	182-192	glycerol-3-phosphate dehydrogenase (NAD(+)) GPD2	Saccharomyces cerevisiae S288C	37-41
28588114-6	2017	C. reinhardtii knockdown mutants for GPD2 and GPD3 showed no difference in growth but displayed significant reduction in TAG concentration compared with the wild type in response to phosphorus or nitrogen starvation.	Phosphorus	182-192	glycerol-3-phosphate dehydrogenase (NAD(+)) GPD2	Saccharomyces cerevisiae S288C	46-50
28477543-11	2017	To prevent phytoplankton blooms with 20 mug L-1 chlorophyll-a throughout Lake Taihu, both phosphorus and nitrogen loads need a nearly 90% reduction.	Phosphorus	90-100	immunoglobulin kappa variable 1-16	Homo sapiens	44-47
28755169-5	2017	The yield of Ps-bioemulsifier (pure bioemulsifier) was 0.68 +- 0.05 mg mL-1.	Phosphorus	13-15	L1 cell adhesion molecule	Mus musculus	71-75
28433878-7	2017	In the ambient sediments, smaller particle size and higher levels of organic matter and nutrients (nitrogen and phosphorus) were associated with increased persistence of the GB3 marker and culturable Escherichia coli (cEC) and enterococci (cENT).	Phosphorus	112-122	alpha 1,4-galactosyltransferase (P blood group)	Homo sapiens	174-177
28473187-5	2017	RESULTS: In univariable analysis, RBP4 was inversely related to renal function, age and HDL, and positively related to other lipids, insulinemia, HOMA, glycemia, albumin, phosphorus and right hepatic lobe diameter.	Phosphorus	171-181	retinol binding protein 4	Homo sapiens	34-38
28388470-0	2017	Binding of poly(amidoamine), carbosilane, phosphorus and hybrid dendrimers to thrombin-Constants and mechanisms.	Phosphorus	42-52	coagulation factor II, thrombin	Homo sapiens	78-86
28686649-5	2017	The average values of parathyroid hormone (PTH), calcium (Ca) and phosphorus (P) were 47.62 pg/mL, 2.26 mmol/L and 1.18 mmol/L, respectively.	Phosphorus	43-44	parathyroid hormone	Homo sapiens	22-41
28648030-18	2017	(3) Compared with control group, the mRNA and protein expressions of Runx2 and ALP were higher in high phosphorus+ pH7.4 group (0.60+-0.04 vs. 0.34+-0.03, 0.42+-0.04 vs. 0.21+-0.02, 67.2+-4.3 vs. 23.2+-2.3 respectively, all P&lt;0.05).	Phosphorus	103-113	RUNX family transcription factor 2	Rattus norvegicus	69-74
28482576-7	2017	The PEGylated triblock copolymer could chemically conjugate DOX onto PAH blocks via pH-responsive hydrazone bonds and simultaneously complex negatively charged Bcl-2 siRNA with cationic PDMAPMA blocks through electrostatic interactions at N/P ratios&gt;=32:1 to form multifunctional nanomicelleplexes.	Phosphorus	4-5	BCL2 apoptosis regulator	Homo sapiens	160-165
28486700-19	2017	Stimulation with ADAM17, H2O2 and Ps supernatant culture significantly increased Notch and fibrosis in both Ps and Cs.	Phosphorus	108-110	ADAM metallopeptidase domain 17	Homo sapiens	17-23
28648030-21	2017	Compared with high phosphorus+ pH7.6 group, the mRNA(1.11+-0.05) and protein(1.08+-0.06) expressions of Runx2 and ALP(197.0+-6.7) were higher in high phosphorus+ pH7.7 group (all P&lt;0.05).	Phosphorus	19-29	RUNX family transcription factor 2	Rattus norvegicus	104-109
28648030-18	2017	(3) Compared with control group, the mRNA and protein expressions of Runx2 and ALP were higher in high phosphorus+ pH7.4 group (0.60+-0.04 vs. 0.34+-0.03, 0.42+-0.04 vs. 0.21+-0.02, 67.2+-4.3 vs. 23.2+-2.3 respectively, all P&lt;0.05).	Phosphorus	103-113	PDZ and LIM domain 3	Rattus norvegicus	79-82
28648030-21	2017	Compared with high phosphorus+ pH7.6 group, the mRNA(1.11+-0.05) and protein(1.08+-0.06) expressions of Runx2 and ALP(197.0+-6.7) were higher in high phosphorus+ pH7.7 group (all P&lt;0.05).	Phosphorus	19-29	PDZ and LIM domain 3	Rattus norvegicus	114-117
28648030-21	2017	Compared with high phosphorus+ pH7.6 group, the mRNA(1.11+-0.05) and protein(1.08+-0.06) expressions of Runx2 and ALP(197.0+-6.7) were higher in high phosphorus+ pH7.7 group (all P&lt;0.05).	Phosphorus	150-160	RUNX family transcription factor 2	Rattus norvegicus	104-109
28648030-19	2017	Compared with high phosphorus+ pH7.4 group, the mRNA(0.76+-0.05) and protein(0.68+-0.03) expressions of Runx2 and ALP(102.1+-5.4) were higher in high phosphorus+ pH7.5 group (all P&lt;0.05).	Phosphorus	19-29	RUNX family transcription factor 2	Rattus norvegicus	104-109
28648030-21	2017	Compared with high phosphorus+ pH7.6 group, the mRNA(1.11+-0.05) and protein(1.08+-0.06) expressions of Runx2 and ALP(197.0+-6.7) were higher in high phosphorus+ pH7.7 group (all P&lt;0.05).	Phosphorus	150-160	PDZ and LIM domain 3	Rattus norvegicus	114-117
28648030-19	2017	Compared with high phosphorus+ pH7.4 group, the mRNA(0.76+-0.05) and protein(0.68+-0.03) expressions of Runx2 and ALP(102.1+-5.4) were higher in high phosphorus+ pH7.5 group (all P&lt;0.05).	Phosphorus	19-29	PDZ and LIM domain 3	Rattus norvegicus	114-117
28648030-19	2017	Compared with high phosphorus+ pH7.4 group, the mRNA(0.76+-0.05) and protein(0.68+-0.03) expressions of Runx2 and ALP(102.1+-5.4) were higher in high phosphorus+ pH7.5 group (all P&lt;0.05).	Phosphorus	150-160	RUNX family transcription factor 2	Rattus norvegicus	104-109
28648030-19	2017	Compared with high phosphorus+ pH7.4 group, the mRNA(0.76+-0.05) and protein(0.68+-0.03) expressions of Runx2 and ALP(102.1+-5.4) were higher in high phosphorus+ pH7.5 group (all P&lt;0.05).	Phosphorus	150-160	PDZ and LIM domain 3	Rattus norvegicus	114-117
28648030-20	2017	Compared with high phosphorus+ pH7.5 group, the mRNA(0.90+-0.05) and protein(0.90+-0.05) expressions of Runx2 and ALP(139.3+-4.9) were higher in high phosphorus+ pH7.6 group (all P&lt;0.05).	Phosphorus	19-29	RUNX family transcription factor 2	Rattus norvegicus	104-109
28648030-20	2017	Compared with high phosphorus+ pH7.5 group, the mRNA(0.90+-0.05) and protein(0.90+-0.05) expressions of Runx2 and ALP(139.3+-4.9) were higher in high phosphorus+ pH7.6 group (all P&lt;0.05).	Phosphorus	19-29	PDZ and LIM domain 3	Rattus norvegicus	114-117
28648030-20	2017	Compared with high phosphorus+ pH7.5 group, the mRNA(0.90+-0.05) and protein(0.90+-0.05) expressions of Runx2 and ALP(139.3+-4.9) were higher in high phosphorus+ pH7.6 group (all P&lt;0.05).	Phosphorus	150-160	RUNX family transcription factor 2	Rattus norvegicus	104-109
28648030-20	2017	Compared with high phosphorus+ pH7.5 group, the mRNA(0.90+-0.05) and protein(0.90+-0.05) expressions of Runx2 and ALP(139.3+-4.9) were higher in high phosphorus+ pH7.6 group (all P&lt;0.05).	Phosphorus	150-160	PDZ and LIM domain 3	Rattus norvegicus	114-117
28619026-10	2017	Furthermore, this relationship remained significant after additional adjustment for gender and factors potentially affecting serum FGF23 levels (serum calcium, serum phosphorus, and glomerular filtration rate), respectively (both P &lt; 0.01).	Phosphorus	166-176	fibroblast growth factor 23	Homo sapiens	131-136
28383662-0	2017	Phosphorus Taste Involves T1R2 and T1R3.	Phosphorus	0-10	taste receptor, type 1, member 2	Mus musculus	26-30
28430857-7	2017	We identified two compounds, trazodone hydrochloride and dibenzoylmethane, which reversed eIF2&alpha;-P-mediated translational attenuation in&nbsp;vitro and in&nbsp;vivo.	Phosphorus	102-103	eukaryotic translation initiation factor 2A	Homo sapiens	90-100
28383662-0	2017	Phosphorus Taste Involves T1R2 and T1R3.	Phosphorus	0-10	taste receptor, type 1, member 3	Mus musculus	35-39
28459587-3	2017	In situ low-temperature scanning tunneling microscopy (LT-STM) measurements were used to monitor the growth of the single-layer blue phosphorus, which forms triangular structures arranged hexagonally on the tellurium layer.	Phosphorus	133-143	sulfotransferase family 1A member 3	Homo sapiens	58-61
28526382-6	2017	RESULTS: MAR and NAR scores for phosphorus; vitamins A, B1, and B6; and niacin were negatively associated with IL-6 (beta = -0.006, -0.004, -0.004, -0.007, -0.004, and -0.005, respectively; P &lt; 0.05).	Phosphorus	32-42	interleukin 6	Homo sapiens	111-115
28546586-6	2017	The wide and tuneable band gap of monolayer penta-BP5 makes it more advantageous for high-frequency-response optoelectronic materials than the currently popular 2D systems, such as transition metal dichalcogenides and black phosphorus.	Phosphorus	224-234	BP5	Homo sapiens	50-53
29622969-9	2017	Serum osteoprotegerin correlated positively with serum phosphorus, calcium phosphorus product, alkaline phosphatase, iPTH, C-reactive protein, serum uric acid, low-density lipoprotein (LDL) and left ventricular mass index (LVMI) (p &lt; 0.005), and negatively with hemoglobin, ejection fraction (p &lt; 0.005) and HDL (p &lt; 0.05).	Phosphorus	55-65	TNF receptor superfamily member 11b	Homo sapiens	6-21
28611678-11	2017	EDX showed that KLK4 inner enamel contained less calcium and phosphorus and more nitrogen than control inner enamel and KLK4 outer enamel.	Phosphorus	61-71	kallikrein related-peptidase 4 (prostase, enamel matrix, prostate)	Mus musculus	16-20
28459587-4	2017	As revealed by in situ X-ray photoelectron spectroscopy, LT-STM measurements, and density functional theory calculation, the blue phosphorus layer weakly interacts with the underlying tellurium layer.	Phosphorus	130-140	sulfotransferase family 1A member 3	Homo sapiens	60-63
28242278-1	2017	Nitrogen and phosphorus loads are considered a major reason for the eutrophication of the Baltic Sea.	Phosphorus	13-23	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	97-100
28323996-1	2017	Fibroblast growth factor 23 (FGF23), a hormone required for phosphorus metabolism, was recently proposed to act on Ca2+ uptake; however, the available evidence of how FGF23 controls the body fluid Ca2+ homeostasis needs to be further clarified.	Phosphorus	60-70	fibroblast growth factor 23	Danio rerio	0-27
28469078-7	2017	Plasma miR-21 in children with PI+PS followed a similar pattern.	Phosphorus	34-36	microRNA 21	Homo sapiens	7-13
28498313-8	2017	These results provide important information concerning the AtWRKY6 regulation network and reveal potential vital target genes of AtWRKY6 under low phosphorus stress.	Phosphorus	147-157	WRKY family transcription factor	Arabidopsis thaliana	59-66
28498313-8	2017	These results provide important information concerning the AtWRKY6 regulation network and reveal potential vital target genes of AtWRKY6 under low phosphorus stress.	Phosphorus	147-157	WRKY family transcription factor	Arabidopsis thaliana	129-136
28323996-1	2017	Fibroblast growth factor 23 (FGF23), a hormone required for phosphorus metabolism, was recently proposed to act on Ca2+ uptake; however, the available evidence of how FGF23 controls the body fluid Ca2+ homeostasis needs to be further clarified.	Phosphorus	60-70	fibroblast growth factor 23	Danio rerio	29-34
27665015-2	2017	Hence, neutralization of FGF-23 should be additive with phytase in reducing dietary non-phytate phosphorus (nPP) needs in chickens fed plant-based diets rich in phytic acid.	Phosphorus	96-106	fibroblast growth factor 23	Gallus gallus	25-31
28246678-6	2017	Among the rejection groups, statistically significant differences for CXCL10 levels were found between ACR vs. NAD (p &lt; 0.001), ACR vs. BLR (p = 0.019) and AVR vs. NAD (p = 0.009).	Phosphorus	24-25	C-X-C motif chemokine ligand 10	Homo sapiens	70-76
28246678-6	2017	Among the rejection groups, statistically significant differences for CXCL10 levels were found between ACR vs. NAD (p &lt; 0.001), ACR vs. BLR (p = 0.019) and AVR vs. NAD (p = 0.009).	Phosphorus	24-25	acrosin	Homo sapiens	103-106
28419560-6	2017	OBJECTIVES: To measure FGF-23 concentration in dogs with different stages of CKD and determine its association with factors involved in CKD-MBD, including serum phosphorus and parathyroid hormone (PTH) concentrations.	Phosphorus	161-171	fibroblast growth factor 23	Canis lupus familiaris	23-29
28419560-13	2017	Serum creatinine and phosphorus concentrations were the strongest independent predictors of FGF-23 concentration.	Phosphorus	21-31	fibroblast growth factor 23	Canis lupus familiaris	92-98
28181071-5	2017	We further, revealed that AA treatment significantly inhibited the MPTP/p-induced phosphorylation of MAPK/P38 related proteins such as JNK and ERK.	Phosphorus	72-73	mitogen-activated protein kinase 8	Mus musculus	135-138
28181071-5	2017	We further, revealed that AA treatment significantly inhibited the MPTP/p-induced phosphorylation of MAPK/P38 related proteins such as JNK and ERK.	Phosphorus	72-73	mitogen-activated protein kinase 1	Mus musculus	143-146
28458511-12	2017	CONCLUSION: PGA/P-containing medications, including bim/tim, significantly reduced IOP in previously treated patients with open-angle glaucoma or OHT; most reached their target IOP or an IOP even lower than their target and reported good/very good tolerability.	Phosphorus	12-13	Rho guanine nucleotide exchange factor 5	Homo sapiens	56-59
28448530-0	2017	Response of Npt2a knockout mice to dietary calcium and phosphorus.	Phosphorus	55-65	solute carrier family 34 (sodium phosphate), member 1	Mus musculus	12-17
28458511-13	2017	PGA/P-containing medications such as bim/tim should be considered as a safe, effective therapeutic option for Turkish patients who exhibit poor response, tolerance, or adherence to their previous therapy.	Phosphorus	0-1	Rho guanine nucleotide exchange factor 5	Homo sapiens	41-44
29965146-6	2017	With Phoslock  added at the rate of 630 g m-2, sediment phosphorus release was successfully controlled, which reduced the phosphorus concentration in the lake water to less than 0.010 mg L-1.	Phosphorus	56-66	L1 cell adhesion molecule	Homo sapiens	187-190
27487524-7	2017	The presence of biomass improves the simultaneous removal efficiency of nitrogen and phosphorus in the IPC BAF.	Phosphorus	85-95	BAF nuclear assembly factor 1	Homo sapiens	107-110
28112857-0	2017	Sensitive Detection of Carcinoembryonic Antigen Using Stability-Limited Few-Layer Black Phosphorus as an Electron Donor and a Reservoir.	Phosphorus	88-98	CEA cell adhesion molecule 3	Homo sapiens	23-47
27647928-0	2017	Maternally derived anti-fibroblast growth factor 23 antibody as new tool to reduce phosphorus requirement of chicks.	Phosphorus	83-93	fibroblast growth factor 23	Gallus gallus	24-51
27647928-2	2017	Here we show that a maternally derived antibody to a fibroblast growth factor-23 (FGF-23) peptide (GMNPPPYS) alleviated phosphorus deficiency in chicks fed low non-phytate phosphorus (nPP) diets.	Phosphorus	120-130	fibroblast growth factor 23	Gallus gallus	53-80
27647928-2	2017	Here we show that a maternally derived antibody to a fibroblast growth factor-23 (FGF-23) peptide (GMNPPPYS) alleviated phosphorus deficiency in chicks fed low non-phytate phosphorus (nPP) diets.	Phosphorus	120-130	fibroblast growth factor 23	Gallus gallus	82-88
28086102-2	2017	In this paper a phosphorus recovery technology from Polish industrial Sewage Sludge Ashes was investigated (PolFerAsh - Polish Fertilizers form Ash).	Phosphorus	16-26	arylsulfatase family member H	Homo sapiens	84-87
28098948-0	2017	Phosphorus acquisition efficiency in arbuscular mycorrhizal maize is correlated with the abundance of root-external hyphae and the accumulation of transcripts encoding PHT1 phosphate transporters.	Phosphorus	0-10	phosphate transporter protein 1	Zea mays	168-172
27647928-8	2017	In conclusion, maternally-derived anti-FGF-23 antibody increased phosphorus retention in chicks fed diets containing either 0.13 or 0.20% nPP and thereby, reduced signs of phosphorus deficiency.	Phosphorus	65-75	fibroblast growth factor 23	Gallus gallus	39-45
28408819-4	2017	Both Sim and Sim/P pretreatment reduced intestinal oxidative damnification, restricted inflammatory harm, and downregulated the BMP4 and COX-2 expressions as compared to II/RI groups, while Sim/P remarkably improved this effect.	Phosphorus	17-18	bone morphogenetic protein 4	Rattus norvegicus	128-132
28271892-3	2017	The results show that C-O-P linkages of phosphorus-containing groups can progressively evolve into C-P-O, C3-P O, C3-P, and eventually elemental phosphorus as a result of heat treatment.	Phosphorus	40-50	translin	Homo sapiens	106-112
28218845-1	2017	Butyrophilin 3A1 (BTN3A1) binds small phosphorus-containing molecules, which initiates transmembrane signaling and activates butyrophilin-responsive cells.	Phosphorus	38-48	butyrophilin subfamily 3 member A1	Homo sapiens	0-16
28296648-3	2017	The initial six-peptide sequence DpSpSEEK (where pS denotes phosphorylated serine) of the N-terminus of statherin can be immobilized on a hydroxyapatite (HAP) surface and the negatively charged domains of the DpSpSEEK side chain can catch free Ca2+ in saliva due to the charge adsorption effect.	Phosphorus	34-36	statherin	Homo sapiens	104-113
28218845-1	2017	Butyrophilin 3A1 (BTN3A1) binds small phosphorus-containing molecules, which initiates transmembrane signaling and activates butyrophilin-responsive cells.	Phosphorus	38-48	butyrophilin subfamily 3 member A1	Homo sapiens	18-24
28060458-0	2017	TiL4 -Coordinated Black Phosphorus Quantum Dots as an Efficient Contrast Agent for In Vivo Photoacoustic Imaging of Cancer.	Phosphorus	24-34	toll like receptor 2	Homo sapiens	0-4
27927649-12	2017	Cilostazol with Axl knockdown have additive changes in downstream gene expression and cell functions in P-cresol culture.	Phosphorus	104-106	Axl receptor tyrosine kinase	Rattus norvegicus	16-19
27826644-2	2017	Great deal of data has accumulated to demonstrate increased FGF23 secretion from the bone to compensate for even subtle increases in serum phosphorus long before intact PTH.	Phosphorus	139-149	fibroblast growth factor 23	Homo sapiens	60-65
28265411-17	2017	CONCLUSIONS: Implementation of the CHOP inpatient nutritional rehabilitation protocol aimed at rapid, efficient, and safe weight gain and integration of caregivers in treatment of patients with diverse ED diagnoses led to excellent QI outcomes in percentage MBMI at discharge and 4-weeks follow-up, while maintaining a short LOS and low rates of RH phosphorus supplementation.	Phosphorus	349-359	DNA damage inducible transcript 3	Homo sapiens	35-39
28386345-5	2017	RESULTS: Compared with normal, negative control, BMSCs, and sp600125 groups, rats in the PS group exhibited decreased discharge volume, maximal micturition volume, contraction interval, and bladder capacity but increased residual urine volume, bladder pressure, bladder peak pressure, expression of TGF-beta/MAPK signaling pathway-related proteins, levels of inflammatory cytokines, and growth inhibition rate.	Phosphorus	89-91	transforming growth factor, beta 1	Rattus norvegicus	299-307
28009462-1	2017	Highly phosphorescent (Ph4 P)2 [MnBr4 ] as a low-cost and environmentally benign emitting material achieves peak current efficiency of 25.4 cd A-1 and external quantum efficiency (EQE) of 7.2% for nondoped organic light-emitting diodes, and peak current efficiency of 32.0 cd A-1 and EQE of 9.6% for doped devices with 20% (Ph4 P)2 [MnBr4 ]:27% TCTA:53% 6DCZPPY as a doping emitting layer.	Phosphorus	23-24	BCL2 related protein A1	Homo sapiens	143-146
28009462-1	2017	Highly phosphorescent (Ph4 P)2 [MnBr4 ] as a low-cost and environmentally benign emitting material achieves peak current efficiency of 25.4 cd A-1 and external quantum efficiency (EQE) of 7.2% for nondoped organic light-emitting diodes, and peak current efficiency of 32.0 cd A-1 and EQE of 9.6% for doped devices with 20% (Ph4 P)2 [MnBr4 ]:27% TCTA:53% 6DCZPPY as a doping emitting layer.	Phosphorus	23-24	BCL2 related protein A1	Homo sapiens	276-279
28009462-1	2017	Highly phosphorescent (Ph4 P)2 [MnBr4 ] as a low-cost and environmentally benign emitting material achieves peak current efficiency of 25.4 cd A-1 and external quantum efficiency (EQE) of 7.2% for nondoped organic light-emitting diodes, and peak current efficiency of 32.0 cd A-1 and EQE of 9.6% for doped devices with 20% (Ph4 P)2 [MnBr4 ]:27% TCTA:53% 6DCZPPY as a doping emitting layer.	Phosphorus	23-24	T cell leukemia translocation altered	Homo sapiens	345-349
28005411-4	2017	Previously, we demonstrated that a Phex mutation in mice creates a lower set point for extracellular phosphate, where an increment in phosphorus further stimulates Fgf23 production to maintain low serum phosphorus levels.	Phosphorus	134-144	phosphate regulating endopeptidase homolog, X-linked	Mus musculus	35-39
28005411-4	2017	Previously, we demonstrated that a Phex mutation in mice creates a lower set point for extracellular phosphate, where an increment in phosphorus further stimulates Fgf23 production to maintain low serum phosphorus levels.	Phosphorus	134-144	fibroblast growth factor 23	Mus musculus	164-169
28005411-4	2017	Previously, we demonstrated that a Phex mutation in mice creates a lower set point for extracellular phosphate, where an increment in phosphorus further stimulates Fgf23 production to maintain low serum phosphorus levels.	Phosphorus	203-213	phosphate regulating endopeptidase homolog, X-linked	Mus musculus	35-39
28005411-4	2017	Previously, we demonstrated that a Phex mutation in mice creates a lower set point for extracellular phosphate, where an increment in phosphorus further stimulates Fgf23 production to maintain low serum phosphorus levels.	Phosphorus	203-213	fibroblast growth factor 23	Mus musculus	164-169
28005411-8	2017	However, introduction of the Galnt3 null allele to Dmp1 knockout mice resulted in a significant increase in serum phosphorus and normalization of BMD.	Phosphorus	114-124	polypeptide N-acetylgalactosaminyltransferase 3	Mus musculus	29-35
28005411-8	2017	However, introduction of the Galnt3 null allele to Dmp1 knockout mice resulted in a significant increase in serum phosphorus and normalization of BMD.	Phosphorus	114-124	dentin matrix protein 1	Mus musculus	51-55
28005411-9	2017	This increased serum phosphorus was accompanied by markedly elevated Fgf23 expression and circulating Fgf23 levels, an attempt to reduce serum phosphorus in the face of improving phosphorus levels.	Phosphorus	21-31	fibroblast growth factor 23	Mus musculus	69-74
28005411-9	2017	This increased serum phosphorus was accompanied by markedly elevated Fgf23 expression and circulating Fgf23 levels, an attempt to reduce serum phosphorus in the face of improving phosphorus levels.	Phosphorus	21-31	fibroblast growth factor 23	Mus musculus	102-107
28005411-9	2017	This increased serum phosphorus was accompanied by markedly elevated Fgf23 expression and circulating Fgf23 levels, an attempt to reduce serum phosphorus in the face of improving phosphorus levels.	Phosphorus	143-153	fibroblast growth factor 23	Mus musculus	69-74
28005411-9	2017	This increased serum phosphorus was accompanied by markedly elevated Fgf23 expression and circulating Fgf23 levels, an attempt to reduce serum phosphorus in the face of improving phosphorus levels.	Phosphorus	143-153	fibroblast growth factor 23	Mus musculus	102-107
28005411-9	2017	This increased serum phosphorus was accompanied by markedly elevated Fgf23 expression and circulating Fgf23 levels, an attempt to reduce serum phosphorus in the face of improving phosphorus levels.	Phosphorus	143-153	fibroblast growth factor 23	Mus musculus	69-74
28005411-9	2017	This increased serum phosphorus was accompanied by markedly elevated Fgf23 expression and circulating Fgf23 levels, an attempt to reduce serum phosphorus in the face of improving phosphorus levels.	Phosphorus	143-153	fibroblast growth factor 23	Mus musculus	102-107
28369625-0	2017	Arabidopsis plasma membrane H+-ATPase genes AHA2 and AHA7 have distinct and overlapping roles in the modulation of root tip H+ efflux in response to low-phosphorus stress.	Phosphorus	153-163	plasma membrane H+-ATPase	Arabidopsis thaliana	12-37
28369625-0	2017	Arabidopsis plasma membrane H+-ATPase genes AHA2 and AHA7 have distinct and overlapping roles in the modulation of root tip H+ efflux in response to low-phosphorus stress.	Phosphorus	153-163	H[+]-ATPase 2	Arabidopsis thaliana	44-48
28369625-0	2017	Arabidopsis plasma membrane H+-ATPase genes AHA2 and AHA7 have distinct and overlapping roles in the modulation of root tip H+ efflux in response to low-phosphorus stress.	Phosphorus	153-163	H[+]-ATPase 7	Arabidopsis thaliana	53-57
28369625-2	2017	Plasma membrane H+-ATPase (PM H+-ATPase) plays an important role in the plant response to low-phosphorus stress (LP).	Phosphorus	94-104	plasma membrane H+-ATPase	Arabidopsis thaliana	0-25
28112865-1	2017	2D black phosphorus (BP) and rhenium dichalcogenides (ReX2 , X = S, Se) possess intrinsic in-plane anisotropic physical properties arising from their low crystal lattice symmetry, which has inspired their novel applications in electronics, photonics, and optoelectronics.	Phosphorus	21-23	RNA exonuclease 2	Homo sapiens	54-58
28049756-6	2017	Additionally, these S/T-P sites seem to be important for PRRXL1 conformation, and their point mutation to alanine or aspartate down-regulates PRRXL1 transcriptional activity.	Phosphorus	24-25	paired related homeobox protein-like 1	Mus musculus	57-63
28049756-6	2017	Additionally, these S/T-P sites seem to be important for PRRXL1 conformation, and their point mutation to alanine or aspartate down-regulates PRRXL1 transcriptional activity.	Phosphorus	24-25	paired related homeobox protein-like 1	Mus musculus	142-148
28110703-5	2017	High dietary intakes of bioavailable phosphorus and of calcium have been found to boost FGF23 levels, and this accords well with prospective epidemiology pointing to high intakes of both phosphate and calcium as risk factors for aggressive prostate cancer.	Phosphorus	37-47	fibroblast growth factor 23	Homo sapiens	88-93
26467655-9	2017	The reductions in both nitrogen and phosphorus loads have led to large-scale alleviation of eutrophication and to a healthier Baltic Sea.	Phosphorus	36-46	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	133-136
27929669-6	2017	Pth/Fgf23 double mutants had the same elevation in serum phosphorus as Pth null fetuses, as compared with normal serum phosphorus in Fgf23 nulls.	Phosphorus	57-67	parathyroid hormone	Mus musculus	0-3
27929669-6	2017	Pth/Fgf23 double mutants had the same elevation in serum phosphorus as Pth null fetuses, as compared with normal serum phosphorus in Fgf23 nulls.	Phosphorus	57-67	fibroblast growth factor 23	Mus musculus	4-9
27776874-0	2017	Innovative combination of Fe2+-BAF and ozonation for enhancing phosphorus and organic micropollutants removal treating petrochemical secondary effluent.	Phosphorus	63-73	BAF nuclear assembly factor 1	Homo sapiens	31-34
27671846-3	2017	The sorbed phosphorus mainly consisted of Ex-P and Fe-P, with Ex-P being the dominant.	Phosphorus	11-21	muscleblind like splicing regulator 1	Homo sapiens	42-46
28149680-4	2017	A loss-of-functionmutant of the candidate transcription factor gene WRKY6, which is involved in the acclimation of plants to low phosphorus, had increased root hair density.	Phosphorus	129-139	WRKY family transcription factor	Arabidopsis thaliana	68-73
28157376-1	2017	We report on electron spin resonance measurements of phosphorus donors localized in a 200  mum^{2} area below the inductive wire of a lumped element superconducting resonator.	Phosphorus	53-63	spindlin 1	Homo sapiens	22-26
28138323-1	2016	Hypoparathyroidism is a rare endocrine disorder in which parathyroid hormone (PTH) production is abnormally low or absent, resulting in low serum calcium and increased serum phosphorus.	Phosphorus	174-184	parathyroid hormone	Homo sapiens	57-76
27705923-8	2017	Finally, the decision tree model based marker panel (CA19-9/MUC17/MUC5AC) predicted HP, SSA/P and TA with SN/SP of 58%/95%, 79%/90% and 97%/83%, respectively.	Phosphorus	85-86	mucin 17, cell surface associated	Homo sapiens	60-65
27705923-8	2017	Finally, the decision tree model based marker panel (CA19-9/MUC17/MUC5AC) predicted HP, SSA/P and TA with SN/SP of 58%/95%, 79%/90% and 97%/83%, respectively.	Phosphorus	85-86	mucin 5AC, oligomeric mucus/gel-forming	Homo sapiens	66-72
29179169-3	2017	Vitamin D stimulates intestinal phosphorus absorption, and phosphorus promotes FGF23 secretion from osteocytes.	Phosphorus	59-69	fibroblast growth factor 23	Homo sapiens	79-84
28114997-4	2017	RESULTS: In the present study, we synthesized a kind of graphene-P-gp loaded with miR-122-InP@ZnS quantum dots nanocomposites (GPMQNs) that, in the presence of glutathione, provides controlled release of miR-122.	Phosphorus	65-66	microRNA 122	Homo sapiens	82-89
27900815-4	2017	These unprecedented pathways grant access to both P1 - and P3 -containing organophosphorus compounds in two simple steps from white phosphorus.	Phosphorus	126-142	crystallin gamma F, pseudogene	Homo sapiens	50-61
27733274-1	2017	HYPOTHESIS: Phosphorus and vitamin D (calcitriol) supplementation in the Phex mouse, a murine model for endolymphatic hydrops (ELH), will improve otic capsule mineralization and secondarily ameliorate the postnatal development of ELH and sensorineural hearing loss (SNHL).	Phosphorus	12-22	phosphate regulating endopeptidase homolog, X-linked	Mus musculus	73-77
27733274-8	2017	The Phex rescue group was also supplemented with phosphorus and calcium but only from P20 to P40.	Phosphorus	49-59	phosphate regulating endopeptidase homolog, X-linked	Mus musculus	4-8
27733274-14	2017	CONCLUSION: Supplementation with phosphorus and calcitriol improves otic capsule bone morphology in the Phex male mouse but does not alter development of ELH or SNHL.	Phosphorus	33-43	phosphate regulating endopeptidase homolog, X-linked	Mus musculus	104-108
27291250-3	2017	OBJECTIVE: In this study we have rationally modified the structure of existing p-coumaric acid and ferulic acid, which would selectively activate PPARgamma and exert their anti-proliferative effect at lower dose as compared to natural phytoconstituents.	Phosphorus	79-81	peroxisome proliferator activated receptor gamma	Homo sapiens	146-155
28578340-0	2017	MicroRNA-30b Regulates High Phosphorus Level-Induced Autophagy in Vascular Smooth Muscle Cells by Targeting BECN1.	Phosphorus	28-38	beclin 1	Rattus norvegicus	108-113
27565852-6	2016	The increase of available phosphorus in both SDS-nClAP and ClAP treated sediment samples verified dissolution-precipitation mechanism involved in Pb immobilization.	Phosphorus	26-36	BCL10 immune signaling adaptor	Homo sapiens	50-54
28182071-5	2017	FGF-23 levels were significantly associated with serum phosphorus and parathyroid hormone (PTH) levels in univariate and multivariate analysis.	Phosphorus	55-65	fibroblast growth factor 23	Homo sapiens	0-6
28182071-8	2017	There is a strong association between FGF-23 and phosphorus and PTH levels.	Phosphorus	49-59	fibroblast growth factor 23	Homo sapiens	38-44
27820122-4	2017	The patient was treated with oral phosphorus and calcitriol, surgical debulking, and intralesional corticosteroids, which resulted in tumor regression and normalization of serum fibroblast growth factor 23 and phosphorus.	Phosphorus	34-44	fibroblast growth factor 23	Homo sapiens	178-205
28606572-10	2017	Intake of phosphorus, calcium, zinc, magnesium, iron, and vitamin B12 during the luteal phase was positively correlated with serum DAO activity (P &lt; 0.05).	Phosphorus	10-20	amine oxidase copper containing 1	Homo sapiens	131-134
27241268-5	2017	Besides, a tobermorite-enriched material was added in the HF2 unit in order to improve phosphorus removal.	Phosphorus	87-97	complement factor H	Homo sapiens	58-61
27241268-9	2017	The tobermorite-enriched HF2 unit showed a distinct higher phosphate (60-67%) and total phosphorus (54%) removal.	Phosphorus	88-98	complement factor H	Homo sapiens	25-28
28145858-7	2016	On the other hand, magnesium level showed a significant decline at 24 hours (P = 0.005) while PTH increased significantly (p&amp;lt;0.000) and (p=0.005) for term and preterm groups respectively.	Phosphorus	123-125	parathyroid hormone	Homo sapiens	94-97
27959360-3	2016	An arrested alpha-hydride migration mechanism suggests increased nucleophilicity of the phosphorus atom facilitates [PPh] group transfer reactivity.	Phosphorus	88-98	enolase 1	Homo sapiens	117-120
27853782-1	2016	The trivalent phosphorus-bridged [2]ferrocenophane complex 2 having NEt2 groups on the respective phosphorus centers was prepared, and its reactions as a diphosphine ligand were examined for iron and chromium carbonyl complexes.	Phosphorus	14-24	tetraspanin 12	Homo sapiens	68-72
27853782-1	2016	The trivalent phosphorus-bridged [2]ferrocenophane complex 2 having NEt2 groups on the respective phosphorus centers was prepared, and its reactions as a diphosphine ligand were examined for iron and chromium carbonyl complexes.	Phosphorus	98-108	tetraspanin 12	Homo sapiens	68-72
27997532-7	2016	Further PS treatment resulted in recovery of axonal outgrowth and enhanced retrograde axonal transport by decreasing histone deacetylase 6 (HDAC6) levels and thus increasing acetylation of alpha-tubulin levels.	Phosphorus	8-10	histone deacetylase 6	Mus musculus	117-138
27997532-7	2016	Further PS treatment resulted in recovery of axonal outgrowth and enhanced retrograde axonal transport by decreasing histone deacetylase 6 (HDAC6) levels and thus increasing acetylation of alpha-tubulin levels.	Phosphorus	8-10	histone deacetylase 6	Mus musculus	140-145
27709557-15	2016	In the logistic regression models, SOD1 activity higher than 3.32 U/mg Hb was associated with protection of AKI development when adjusted by hemoglobin, phosphorus and APACHE II score (OR 0.309; CI 95 % 0.137-0.695; p = 0.005) and when adjusted by age, gender, chronic kidney disease, admission category (medical or surgery) and APACHE II score (OR 0.129; CI 95 % 0.033-0.508; p = 0.003).	Phosphorus	153-163	superoxide dismutase 1	Homo sapiens	35-39
27960475-2	2016	We report on the anisotropy of electron-phonon interactions through a polarization-resolved Raman study of the four vibrational modes of atomically thin black phosphorus (2D phosphane): the three bulk-like modes Ag1, B2g, and Ag2 and the Davydov-induced mode labeled Ag(B2u).	Phosphorus	153-169	NBPF member 10	Homo sapiens	212-215
27882369-0	2016	Regio- and stereo-selective polymerization of 1,3-butadiene catalyzed by phosphorus-nitrogen PN3-pincer cobalt(ii) complexes.	Phosphorus	73-83	sodium voltage-gated channel alpha subunit 10	Homo sapiens	93-96
27882369-3	2016	The cobalt center is chelated by the PN3 ligand through the pyridinyl nitrogen, the pyrazol nitrogen and the phosphorus donor, with a long Co-P bond distance indicating a labile character.	Phosphorus	109-119	sodium voltage-gated channel alpha subunit 10	Homo sapiens	37-40
27591802-2	2016	The objective of this study was to investigate the association between the BMP2 (bone morphogenetic protein 2) and BMP4 (bone morphogenetic protein 4) polymorphisms with non-syndromic CL/P to clarify the potential role of these genes in the etiology of CL/P in Iranian population.	Phosphorus	77-78	bone morphogenetic protein 2	Homo sapiens	81-109
27591802-2	2016	The objective of this study was to investigate the association between the BMP2 (bone morphogenetic protein 2) and BMP4 (bone morphogenetic protein 4) polymorphisms with non-syndromic CL/P to clarify the potential role of these genes in the etiology of CL/P in Iranian population.	Phosphorus	77-78	bone morphogenetic protein 4	Homo sapiens	115-119
27995584-4	2016	Although the samples" morphology was found to be affected by neither the amount of CA nor the soaking time in SBF, the soaking results revealed that the maximum changes in the Ca/P ratio were found for the HAp samples prepared in the presence of the highest amounts of CA, which pointed out to the highest bioactivity of these samples.	Phosphorus	179-180	reticulon 3	Homo sapiens	206-209
27654224-5	2016	Furthermore, the new process showed a broad spectrum of handling ability for different concentrations of phosphorus-containing solution in the range of 5-350 mg L-1, and the obtained results of phosphorus conversion ratio and recovery efficiency were more than 92% and 80%, respectively.	Phosphorus	105-115	immunoglobulin kappa variable 1-16	Homo sapiens	161-164
27654224-5	2016	Furthermore, the new process showed a broad spectrum of handling ability for different concentrations of phosphorus-containing solution in the range of 5-350 mg L-1, and the obtained results of phosphorus conversion ratio and recovery efficiency were more than 92% and 80%, respectively.	Phosphorus	194-204	immunoglobulin kappa variable 1-16	Homo sapiens	161-164
26410393-10	2016	CONCLUSION: Under the present experimental conditions, GOS/FOS  mixture induced colonic positive effects, which increased Ca, P and Mg absorption.	Phosphorus	126-127	Fos proto-oncogene, AP-1 transcription factor subunit	Rattus norvegicus	59-62
27916815-8	2016	Phosphorus intake increased sP, uP and uP/creat ratio and ALP (p &lt;= 0.02) and caused decrease in TrP (p = 0.00).	Phosphorus	0-10	ATHS	Homo sapiens	39-61
27775327-0	2016	lambda5-Phosphorus-Containing alpha-Diazo Compounds: A Valuable Tool for Accessing Phosphorus-Functionalized Molecules.	Phosphorus	8-18	immunoglobulin lambda like polypeptide 1	Homo sapiens	0-7
27062893-2	2016	2PAM reactivates nerve agent-inhibited AChE via direct nucleophilic attack by the oxime moiety on the phosphorus center of the bound nerve agent.	Phosphorus	102-112	acetylcholinesterase (Cartwright blood group)	Homo sapiens	39-43
27775327-0	2016	lambda5-Phosphorus-Containing alpha-Diazo Compounds: A Valuable Tool for Accessing Phosphorus-Functionalized Molecules.	Phosphorus	83-93	immunoglobulin lambda like polypeptide 1	Homo sapiens	0-7
27775327-1	2016	The compounds characterized by the presence of a lambda5-phosphorus functionality at the alpha-position with respect to the diazo moiety, here referred to as lambda5-phosphorus-containing alpha-diazo compounds (PCDCs), represent a vast class of extremely versatile reagents in organic chemistry and are particularly useful in the preparation of phosphonate- and phosphinoxide-functionalized molecules.	Phosphorus	57-67	immunoglobulin lambda like polypeptide 1	Homo sapiens	49-56
27775327-1	2016	The compounds characterized by the presence of a lambda5-phosphorus functionality at the alpha-position with respect to the diazo moiety, here referred to as lambda5-phosphorus-containing alpha-diazo compounds (PCDCs), represent a vast class of extremely versatile reagents in organic chemistry and are particularly useful in the preparation of phosphonate- and phosphinoxide-functionalized molecules.	Phosphorus	57-67	immunoglobulin lambda like polypeptide 1	Homo sapiens	158-165
27775327-1	2016	The compounds characterized by the presence of a lambda5-phosphorus functionality at the alpha-position with respect to the diazo moiety, here referred to as lambda5-phosphorus-containing alpha-diazo compounds (PCDCs), represent a vast class of extremely versatile reagents in organic chemistry and are particularly useful in the preparation of phosphonate- and phosphinoxide-functionalized molecules.	Phosphorus	166-176	immunoglobulin lambda like polypeptide 1	Homo sapiens	158-165
27714043-6	2016	Quantitative analyses of calcium, phosphorus and uranium performed using inductively coupled plasma/mass spectrometry (ICP/MS) demonstrated the inhibition of the precipitation of calcium phosphate by fetuin A and osteopontin for 2 h.	Phosphorus	34-44	alpha 2-HS glycoprotein	Homo sapiens	200-232
27895933-0	2016	Influence of proton pump inhibitors and histamine H2 receptor antagonists on serum phosphorus level control by calcium carbonate in patients undergoing hemodialysis: a retrospective medical chart review.	Phosphorus	83-93	histamine receptor H2	Homo sapiens	40-61
27854278-2	2016	Recent interventional trials using NAM to treat high levels of phosphorus in end-stage renal disease have highlighted new potential uremic toxicities of 2PY.	Phosphorus	63-73	SH3 and cysteine rich domain 3	Homo sapiens	35-38
28087877-1	2016	The article incorrectly stated: "Elevations of both fibroblast growth factor 23 (FGF23) and parathyroid hormone (PTH) lead to hyperphosphatemia and hypocalcemia because of decreased urinary excretion of phosphorus."	Phosphorus	203-213	fibroblast growth factor 23	Homo sapiens	52-79
27809761-12	2016	This confirmed a strong eQTL for SLC37A1, with peak association at the same imputed sequence variants that were most significant for phosphorus concentration.	Phosphorus	133-143	solute carrier family 37 member 1	Bos taurus	33-40
27867811-0	2016	Dramatic mitigation of bone pain after phosphorus replacement therapy in a subject with FGF23-related hypophosphatemic osteomalacia.	Phosphorus	39-49	fibroblast growth factor 23	Homo sapiens	88-93
27867811-1	2016	INTRODUCTION: Fibroblast growth factor 23 (FGF23) is secreted from bone and suppresses the absorption of phosphorus in renal proximal tubule and in intestinal tract.	Phosphorus	105-115	fibroblast growth factor 23	Homo sapiens	14-41
27867811-1	2016	INTRODUCTION: Fibroblast growth factor 23 (FGF23) is secreted from bone and suppresses the absorption of phosphorus in renal proximal tubule and in intestinal tract.	Phosphorus	105-115	fibroblast growth factor 23	Homo sapiens	43-48
27867811-7	2016	CONCLUSIONS: We should be aware of the possibility that phosphorus replacement therapy exert marked beneficial effects for the reduction of bone pain in subjects with FGF23-related hypophosphatemic osteomalacia even when we fail to identify tumor localization.	Phosphorus	56-66	fibroblast growth factor 23	Homo sapiens	167-172
27729116-3	2016	The purpose of this study was to investigate the contribution of MSX1 gene polymorphisms to the risk of developing CL/P in a sample of Mexican patients.	Phosphorus	118-119	msh homeobox 1	Homo sapiens	65-69
27729116-10	2016	RESULTS: In the cases and pseudo-controls, an association was found between CL/P and the SNP1-G allele (P = 0.031) and the SNP1-G/G genotype (P = 0.032), a polymorphism located near MSX1.	Phosphorus	79-80	small nuclear ribonucleoprotein U1 subunit 70	Homo sapiens	89-93
27729116-11	2016	Triad analysis showed a tendency toward CL/P susceptibility for the genotype SNP1-G/G (P = 0.075) and an association between CL/P and the haplotype GCTC (P = 0.037).	Phosphorus	43-44	small nuclear ribonucleoprotein U1 subunit 70	Homo sapiens	77-81
27729116-15	2016	CONCLUSIONS: The results of this study suggest an association between CL/P susceptibility and SNP1, located near the MSX1 gene, in the Mexican population.	Phosphorus	73-74	small nuclear ribonucleoprotein U1 subunit 70	Homo sapiens	94-98
27729116-15	2016	CONCLUSIONS: The results of this study suggest an association between CL/P susceptibility and SNP1, located near the MSX1 gene, in the Mexican population.	Phosphorus	73-74	msh homeobox 1	Homo sapiens	117-121
28087877-1	2016	The article incorrectly stated: "Elevations of both fibroblast growth factor 23 (FGF23) and parathyroid hormone (PTH) lead to hyperphosphatemia and hypocalcemia because of decreased urinary excretion of phosphorus."	Phosphorus	203-213	fibroblast growth factor 23	Homo sapiens	81-86
28087877-1	2016	The article incorrectly stated: "Elevations of both fibroblast growth factor 23 (FGF23) and parathyroid hormone (PTH) lead to hyperphosphatemia and hypocalcemia because of decreased urinary excretion of phosphorus."	Phosphorus	203-213	parathyroid hormone	Homo sapiens	92-111
28087877-1	2016	The article incorrectly stated: "Elevations of both fibroblast growth factor 23 (FGF23) and parathyroid hormone (PTH) lead to hyperphosphatemia and hypocalcemia because of decreased urinary excretion of phosphorus."	Phosphorus	203-213	parathyroid hormone	Homo sapiens	113-116
27801303-18	2016	In addition, blood lactate and cTnI levels were significanly lower in SG (P &amp;lt; .044).	Phosphorus	74-75	troponin I3, cardiac type	Homo sapiens	31-35
26690785-3	2016	When weanling Vdr-/- mice are fed a diet containing high levels of calcium, phosphorus and lactose, termed the rescue diet, normalisation of serum calcium, phosphate and parathyroid hormone levels results in prevention of rickets at 10 weeks of age.	Phosphorus	76-86	vitamin D (1,25-dihydroxyvitamin D3) receptor	Mus musculus	14-17
27043860-8	2016	We also found significant decreases in hepatic mRNA expression of interleukin (IL)-1beta, IL-12beta, toll-like receptor (TLR)-4 and cyclooxygenase (COX)-2 in the PV-, PI- and PS-treated groups compared with those of the EC group.	Phosphorus	175-177	interleukin 1 beta	Rattus norvegicus	66-88
27043860-8	2016	We also found significant decreases in hepatic mRNA expression of interleukin (IL)-1beta, IL-12beta, toll-like receptor (TLR)-4 and cyclooxygenase (COX)-2 in the PV-, PI- and PS-treated groups compared with those of the EC group.	Phosphorus	175-177	cytochrome c oxidase II, mitochondrial	Rattus norvegicus	132-154
27475981-7	2016	Stratified analyses revealed that elevated serum phosphorus significantly increased all-cause mortality risk among men (RR 1.33; 95% CI 1.11-1.60), but not in women (RR 1.09; 95% CI 0.89-1.33).	Phosphorus	49-59	ribonucleotide reductase catalytic subunit M1	Homo sapiens	120-124
27690395-2	2016	DFT, ONIOM(CCSD(T):MP2), and CCSD(T) computational results demonstrated that the reaction occurs through phosphorus-ligand cooperative catalysis, which provides an unprecedented protocol for metal-free CO2 conversion.	Phosphorus	105-115	tryptase pseudogene 1	Homo sapiens	19-22
29964426-1	2016	Based on test results and mass balance, PHA, TP metabolic regularity was revealed under different nitrate nitrogen concentrations in main anoxic stage [c(NO3)] for nitrogen and phosphorus removal in single sludge system with continuous flow, then the effectiveness of using c(NO3) as control parameter was proved from the perspective of the reaction mechanism.	Phosphorus	177-187	NBL1, DAN family BMP antagonist	Homo sapiens	154-157
29964426-6	2016	The phosphorus released in anaerobic stage changed along with increasing c(NO3), and the amount of phosphorus released obtained the maximum value 6.16 g d-1 when c(NO3) value was 2.5 mg L-1.	Phosphorus	4-14	NBL1, DAN family BMP antagonist	Homo sapiens	75-78
29964426-6	2016	The phosphorus released in anaerobic stage changed along with increasing c(NO3), and the amount of phosphorus released obtained the maximum value 6.16 g d-1 when c(NO3) value was 2.5 mg L-1.	Phosphorus	4-14	NBL1, DAN family BMP antagonist	Homo sapiens	164-167
29964426-6	2016	The phosphorus released in anaerobic stage changed along with increasing c(NO3), and the amount of phosphorus released obtained the maximum value 6.16 g d-1 when c(NO3) value was 2.5 mg L-1.	Phosphorus	4-14	immunoglobulin kappa variable 1-16	Homo sapiens	186-189
29964426-6	2016	The phosphorus released in anaerobic stage changed along with increasing c(NO3), and the amount of phosphorus released obtained the maximum value 6.16 g d-1 when c(NO3) value was 2.5 mg L-1.	Phosphorus	99-109	NBL1, DAN family BMP antagonist	Homo sapiens	75-78
29964426-6	2016	The phosphorus released in anaerobic stage changed along with increasing c(NO3), and the amount of phosphorus released obtained the maximum value 6.16 g d-1 when c(NO3) value was 2.5 mg L-1.	Phosphorus	99-109	NBL1, DAN family BMP antagonist	Homo sapiens	164-167
29964426-6	2016	The phosphorus released in anaerobic stage changed along with increasing c(NO3), and the amount of phosphorus released obtained the maximum value 6.16 g d-1 when c(NO3) value was 2.5 mg L-1.	Phosphorus	99-109	immunoglobulin kappa variable 1-16	Homo sapiens	186-189
29964426-7	2016	In addition, under c(NO3) value of 2.5 mg L-1, the amount of total phosphorus uptake and anoxic phosphorus uptake obtained the maximum values of 8.04 g d-1 and 3.67 g d-1, respectively.	Phosphorus	67-77	NBL1, DAN family BMP antagonist	Homo sapiens	21-24
29964426-7	2016	In addition, under c(NO3) value of 2.5 mg L-1, the amount of total phosphorus uptake and anoxic phosphorus uptake obtained the maximum values of 8.04 g d-1 and 3.67 g d-1, respectively.	Phosphorus	67-77	immunoglobulin kappa variable 1-16	Homo sapiens	42-45
29964426-7	2016	In addition, under c(NO3) value of 2.5 mg L-1, the amount of total phosphorus uptake and anoxic phosphorus uptake obtained the maximum values of 8.04 g d-1 and 3.67 g d-1, respectively.	Phosphorus	96-106	NBL1, DAN family BMP antagonist	Homo sapiens	21-24
29964426-7	2016	In addition, under c(NO3) value of 2.5 mg L-1, the amount of total phosphorus uptake and anoxic phosphorus uptake obtained the maximum values of 8.04 g d-1 and 3.67 g d-1, respectively.	Phosphorus	96-106	immunoglobulin kappa variable 1-16	Homo sapiens	42-45
27608178-3	2016	Phosphorus and halogen are introduced through the treatment of graphene oxide with PX3 gas (PCl3 , PBr3 , and PI3 ).	Phosphorus	0-10	pannexin 3	Homo sapiens	83-86
27608178-3	2016	Phosphorus and halogen are introduced through the treatment of graphene oxide with PX3 gas (PCl3 , PBr3 , and PI3 ).	Phosphorus	0-10	PHD finger protein 19	Homo sapiens	92-96
27608178-3	2016	Phosphorus and halogen are introduced through the treatment of graphene oxide with PX3 gas (PCl3 , PBr3 , and PI3 ).	Phosphorus	0-10	E2F transcription factor 1	Homo sapiens	99-103
27608178-3	2016	Phosphorus and halogen are introduced through the treatment of graphene oxide with PX3 gas (PCl3 , PBr3 , and PI3 ).	Phosphorus	0-10	peptidase inhibitor 3	Homo sapiens	110-113
27589858-9	2016	CaSR and VDR mRNA were reduced only in CKD rats fed the high-phosphorus diets (CKD HP), then CaSR and VDR immunohistochemical expressions were compatible with gene expression assay.	Phosphorus	61-71	calcium-sensing receptor	Rattus norvegicus	0-4
27164190-2	2016	The result is functional deficiency of, or resistance to, intact FGF23 (iFGF23), causing hyperphosphatemia, increased renal tubular reabsorption of phosphorus (TRP), elevated or inappropriately normal 1,25-dihydroxyvitamin D3 (1,25D), ectopic calcifications, and/or diaphyseal hyperostosis.	Phosphorus	148-158	fibroblast growth factor 23	Homo sapiens	65-70
27521658-7	2016	Exposed to high phosphate media and blocking core fucosylation in VSMCs by knocking down Fut8 using a siRNA markedly reduced calcium and phosphorus deposition and Cbfalpha1 expression (osteoblast-specific transcription factor), and increased alpha-Sma expression (smooth muscle cell marker).	Phosphorus	137-147	fucosyltransferase 8	Homo sapiens	89-93
27589858-9	2016	CaSR and VDR mRNA were reduced only in CKD rats fed the high-phosphorus diets (CKD HP), then CaSR and VDR immunohistochemical expressions were compatible with gene expression assay.	Phosphorus	61-71	vitamin D receptor	Rattus norvegicus	9-12
28298956-1	2016	Serum phosphorus levels stay relatively constant through the influence of multiple factors-such as parathyroid hormone, fibroblast growth factor 23, and vitamin D-on the kidney, bone, and digestive system.	Phosphorus	6-16	parathyroid hormone	Homo sapiens	99-118
27994294-3	2016	RESULTS: In 40 patients in high-flux membrane hemodialysis, we found negative correlation of beta2M with high density lipoprotein (r=-0.73, p&lt;0.001) and albumin (r= -0.53, p&lt;0.001) and positive correlation with triglycerides (r=0.69, p&lt;0.001), parathyroid hormone (r=0.58, p &lt; 0.05) and phosphorus (r= 0.53, p&lt;0.001).	Phosphorus	299-309	beta-2-microglobulin	Homo sapiens	93-99
28298956-1	2016	Serum phosphorus levels stay relatively constant through the influence of multiple factors-such as parathyroid hormone, fibroblast growth factor 23, and vitamin D-on the kidney, bone, and digestive system.	Phosphorus	6-16	fibroblast growth factor 23	Homo sapiens	120-147
27508925-0	2016	Nanostructured Aptamer-Functionalized Black Phosphorus Sensing Platform for Label-Free Detection of Myoglobin, a Cardiovascular Disease Biomarker.	Phosphorus	38-54	myoglobin	Homo sapiens	100-109
26790456-6	2016	Fibroblast growth factor 23 is produced by osteocytes to regulate phosphorus and 1,25(OH)2D3, but it also plays a major role in the adverse consequences of declining renal function, in particular with respect to the myocardium.	Phosphorus	66-76	fibroblast growth factor 23	Homo sapiens	0-27
29726164-6	2016	Catalase activity increased with the soil layer deepening, which was directly related to soil total potassium, and indirectly related to pH, organic matter, total nitrogen and total phosphorus through total potassium.	Phosphorus	182-192	catalase	Homo sapiens	0-8
27514745-8	2016	In addition, structural analysis coupled with the results of phosphorus NMR and time-resolved tryptophan fluorescence measurements suggest that 14-3-3zeta interacts with the kinase domain of ASK1 in close proximity to its active site, thus indicating this interaction might block its accessibility and/or affect its conformation.	Phosphorus	61-71	tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta	Homo sapiens	144-154
27514745-8	2016	In addition, structural analysis coupled with the results of phosphorus NMR and time-resolved tryptophan fluorescence measurements suggest that 14-3-3zeta interacts with the kinase domain of ASK1 in close proximity to its active site, thus indicating this interaction might block its accessibility and/or affect its conformation.	Phosphorus	61-71	mitogen-activated protein kinase kinase kinase 5	Homo sapiens	191-195
27648940-3	2016	In Arabidopsis (Arabidopsis thaliana), the AtPHO1 protein regulates and facilitates the distribution of phosphorus.	Phosphorus	104-114	phosphate 1	Arabidopsis thaliana	43-49
27766035-12	2016	Instead, the regulation of phosphate homeostasis by DMP1 via the axis of "FGF23-renal phosphorus reabsorption" is vital for maintaining a healthy joint.	Phosphorus	86-96	dentin matrix protein 1	Mus musculus	52-56
27766035-12	2016	Instead, the regulation of phosphate homeostasis by DMP1 via the axis of "FGF23-renal phosphorus reabsorption" is vital for maintaining a healthy joint.	Phosphorus	86-96	fibroblast growth factor 23	Mus musculus	74-79
27508925-1	2016	We report the electrochemical detection of the redox active cardiac biomarker myoglobin (Mb) using aptamer-functionalized black phosphorus nanostructured electrodes by measuring direct electron transfer.	Phosphorus	122-138	myoglobin	Homo sapiens	78-87
28497083-0	2017	Impact of FGF23 level on calcium and phosphorus levels in post-renal transplantation.	Phosphorus	37-47	fibroblast growth factor 23	Homo sapiens	10-15
28497083-9	2017	Conclusion: The level of postoperative FGF23 is an important marker for secretion of phosphorus from kidneys emphasizing the central role of FGF23 marker to regulate calcium and phosphorus metabolism after a successful renal transplantation.	Phosphorus	85-95	fibroblast growth factor 23	Homo sapiens	39-44
27721584-1	2016	BACKGROUND: The klotho (Klt)-fibroblast growth factor-23 (FGF-23)-vitamin D axis is the main component of calcium (Ca) and phosphorus (P) metabolisms; on the contrary, it is also secreted from the choroid plexus (CP).	Phosphorus	123-133	klotho	Homo sapiens	16-22
27382971-3	2016	Black phosphorus-assisted laser desorption/ionization mass spectrometry (BP/ALDI-MS) showed clear background and exhibited superior detection sensitivity toward quaternary ammonium compounds compared to carbon-based materials.	Phosphorus	0-16	methyltransferase like 7B	Homo sapiens	76-80
27721584-1	2016	BACKGROUND: The klotho (Klt)-fibroblast growth factor-23 (FGF-23)-vitamin D axis is the main component of calcium (Ca) and phosphorus (P) metabolisms; on the contrary, it is also secreted from the choroid plexus (CP).	Phosphorus	123-133	fibroblast growth factor 23	Homo sapiens	29-56
27721584-1	2016	BACKGROUND: The klotho (Klt)-fibroblast growth factor-23 (FGF-23)-vitamin D axis is the main component of calcium (Ca) and phosphorus (P) metabolisms; on the contrary, it is also secreted from the choroid plexus (CP).	Phosphorus	123-133	fibroblast growth factor 23	Homo sapiens	58-64
27349833-7	2016	Our results show that the food-sourced CNP had various metabolic fluxes through urban systems, with carbon mostly emitted into the air and nitrogen and phosphorus mostly discharged into landfills and water.	Phosphorus	152-162	2',3'-cyclic nucleotide 3' phosphodiesterase	Homo sapiens	39-42
28725361-1	2016	Soil total nitrogen (STN) and total phosphorus (STP) are important indicators of soil nutrients and the important indexes of soil fertility and soil quality evaluation.	Phosphorus	36-46	sulfotransferase family 1A member 1	Homo sapiens	48-51
26438400-8	2016	Consequently, significantly higher concentrations of B[a]P metabolites and DNA adducts were found in beta-glucuronidase-treated cells at 24 h. DNA adduct levels peaked at 48 h in cells that were exposed to B[a]P and treated with beta-glucuronidase.	Phosphorus	57-58	glucuronidase beta	Homo sapiens	101-119
27381982-3	2016	Increased phosphorylation promoted 14-3-3 binding to BLNK (37-fold) and SYK (2.5-fold) in a pS/pT-concentration dependent manner.	Phosphorus	92-94	B cell linker	Homo sapiens	53-57
26303194-10	2016	In contrast, PC4, characterized by protein, vitamin B2, phosphorus, and calcium, was associated with a weight gain of +41 g/year (95 % CI +2 to +80) and +88 g/year (95 % CI +36 to +140) in men and women, respectively.	Phosphorus	56-66	proprotein convertase subtilisin/kexin type 4	Homo sapiens	13-16
27381982-3	2016	Increased phosphorylation promoted 14-3-3 binding to BLNK (37-fold) and SYK (2.5-fold) in a pS/pT-concentration dependent manner.	Phosphorus	92-94	spleen associated tyrosine kinase	Homo sapiens	72-75
27668158-8	2016	Elevated serum phosphorus and C-reactive protein were independent determinants for plasma endocan, and elevated C-reactive protein was also an independent determinant for urine endocan levels in multivariate analysis.	Phosphorus	15-25	endothelial cell specific molecule 1	Homo sapiens	90-97
28494083-4	2016	We describe both the role of phosphorus in the regulation of G1 progression by means of the Cyclin Dependent Kinase (CDK) Pho85 and the stabilization of the cyclin Cln3, as well as the role of other molecule composed of phosphorus-the polyphosphate-in cell cycle progression, dNTP synthesis, and genome stability.	Phosphorus	29-39	cyclin-dependent serine/threonine-protein kinase PHO85	Saccharomyces cerevisiae S288C	122-127
27281157-9	2016	The percentage of individuals with unrepaired CL/P who were older than the respective target ages ranged from 37.0% (95% CI, 30.6%-43.8%) in Goa to 65.8% (95% CI, 60.3%-70.9%) in Bihar (median, 57.9%; interquartile range, 52.6%-63.4%).	Phosphorus	49-50	tripartite motif containing 47	Homo sapiens	141-144
24923416-2	2016	Some mesenchymal tumours (often resembling haemangiopericytomas) express molecules that normally regulate phosphorus metabolism; most frequently, fibroblast growth factor 23.	Phosphorus	106-116	fibroblast growth factor 23	Canis lupus familiaris	146-173
27484986-12	2016	Furthermore, the BDNF level was significantly elevated in the paeonol treatment group compared with mice treated with MPTP/p only.	Phosphorus	62-63	brain derived neurotrophic factor	Mus musculus	17-21
26976902-7	2016	In Exp.2, there was a linear relationship between phosphorus (P) intake and ileal P output for diets with increased levels of SFM and RB.	Phosphorus	50-60	expansin	Glycine max	3-8
27151498-1	2016	We tested the hypothesis that in shallow, eutrophic Lake Kasumigaura, the concentration of particulate phosphorus (PP) is controlled by biogenic P (P in living or dead phytoplankton and bacterial cells), rather than by resuspension of inorganic P in sediment.	Phosphorus	103-113	prion protein	Homo sapiens	115-117
27551266-4	2016	Our present study in isolated testicular germ cell population from adult male Wistar rats, highlighted the synergistic protective effect of curcumin and resveratrol against B(a)P induced p53 mediated germ cell apoptosis.	Phosphorus	177-178	Wistar clone pR53P1 p53 pseudogene	Rattus norvegicus	187-190
27435510-3	2016	In this chamber, nitrites specifically trigger a pH and laser irradiance-dependent diazotization starting from p-aminothiophenol (PATP) absorbed onto the surface of Au NPs to form p,p"-dimercaptoazobenzene (DMAB) molecules, in which the presence of NO2(-) ions above 30.7 muM (1.38 ppm) in the siphoned liquid sample can be identified relying on SERS peak (1141 cm(-1)) intensity of the emerging azo moiety.	Phosphorus	27-28	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	346-350
27545201-4	2016	We precisely controlled the MOS interface for diamond by wet annealing and fabricated p-channel and planar-type MOSFETs with phosphorus-doped n-type body on diamond (111) substrate.	Phosphorus	125-135	MOS proto-oncogene, serine/threonine kinase	Homo sapiens	28-31
29964742-6	2016	For the test reactor (R2) in which DO was controlled at the levels of 2, 1, 0.5, 0.2, 0.1 mg L-1 during the aerobic stage, respectively, the phosphorus removal performance showed a slight fluctuation at the beginning of each stage but rapidly increased to a stable state.	Phosphorus	141-151	L1 cell adhesion molecule	Homo sapiens	93-96
27315223-1	2016	Methylenetetrahydrofolate dehydrogenase (NAD(P)+ dependent) 2, methenyltetrahydrofolate cyclohydrolase (MTHFD2) is a mitochondrial enzyme involved in folate metabolism.	Phosphorus	45-47	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase	Homo sapiens	104-110
27371941-2	2016	Catalytically inactive OP-AChE conjugates formed between the active-center serine and phosphorus of OPs can, in principle, be reactivated by nucleophilic oxime antidotes.	Phosphorus	86-96	acetylcholinesterase (Cartwright blood group)	Homo sapiens	26-30
27371941-5	2016	We outline here the potential limitations of available AChE X-ray structures that preclude an accurate prediction of oxime structures, which are necessary for association in the OP-AChE gorge and nucleophilic attack of the OP-conjugated phosphorus.	Phosphorus	237-247	acetylcholinesterase (Cartwright blood group)	Homo sapiens	181-185
27187567-4	2016	In addition, the feeding rates of nitrogen and phosphorus were optimized in the AEM-PBR to maximize biomass production.	Phosphorus	47-57	translocator protein	Homo sapiens	84-87
27187567-5	2016	The maximum biomass concentration of 4.38g/L was obtained under synergistic regulation of nitrogen and phosphorus feeding rates at 19.0mgN/L/d and 4.2mgP/L/d.	Phosphorus	103-113	matrix Gla protein	Homo sapiens	150-153
26243062-6	2016	RESULTS: Klotho levels on admission were lower than expected for age, and correlated with lumbar spine BMD Z-score (r = -0.81, p &lt; 0.001) and alkaline phosphatase levels (r = 0.66, p = 0.003) but not with age, height-SDS, weight-SDS, BMI-SDS, or serum calcium, phosphorus and IGF-1 levels.	Phosphorus	264-274	klotho	Homo sapiens	9-15
27563628-12	2016	E-selectin was positively correlated only with phosphorus in ESRD children (r = 0.398, P = 0.018).	Phosphorus	47-57	selectin E	Homo sapiens	0-10
27446345-9	2016	Multivariate analysis showed that the serum expression levels of creatinine [micromol/l; odds radio (OR), 1.003; 95% confidence interval (CI), 1.002-1.004; P=0.001] and phosphorus (mmol/l; OR, 2.19; 95% CI, 1.254-3.826; P=0.006) in patients with CKD significantly influenced serum PTH expression levels.	Phosphorus	169-179	parathyroid hormone	Homo sapiens	281-284
27291294-7	2016	TRM, but not DEX, partially (47%) protected against PS, at 21 days.	Phosphorus	52-54	tremor	Mus musculus	0-3
27493655-0	2016	Molecular Evolution and Association of Natural Variation in ZmARF31 with Low Phosphorus Tolerance in Maize.	Phosphorus	77-87	Auxin response factor 13	Zea mays	60-67
27374927-0	2016	PCl3-C6H6 heterodimers: evidence for Ppi phosphorus bonding at low temperatures.	Phosphorus	41-51	PHD finger protein 19	Homo sapiens	0-4
27269194-6	2016	The [Cu(glygly)(PS)] complex exhibited a significant free radical-scavenging activity (60.1+-1.2%) and lipoxygenase (LOX-5) inhibitory activity (36.6+-1.3%) in comparison to PS which resulted in activity of 4.4+-1.4% and inhibition of 6.1+-2.6% respectively.	Phosphorus	16-19	arachidonate 5-lipoxygenase	Homo sapiens	117-122
27269194-6	2016	The [Cu(glygly)(PS)] complex exhibited a significant free radical-scavenging activity (60.1+-1.2%) and lipoxygenase (LOX-5) inhibitory activity (36.6+-1.3%) in comparison to PS which resulted in activity of 4.4+-1.4% and inhibition of 6.1+-2.6% respectively.	Phosphorus	16-18	arachidonate 5-lipoxygenase	Homo sapiens	117-122
27466293-8	2016	Furthermore, the cell viability was reduced by 500 muM O/P mixture at 6, 24, and 48 h in a time-dependent manner.	Phosphorus	57-58	latexin	Homo sapiens	51-54
27466293-10	2016	Furthermore, treatment with O/P mixture significantly enhanced the expression of NOX4 and caspase3 activation in a dose- and time- dependent manner.	Phosphorus	30-31	NADPH oxidase 4	Homo sapiens	81-85
27466293-10	2016	Furthermore, treatment with O/P mixture significantly enhanced the expression of NOX4 and caspase3 activation in a dose- and time- dependent manner.	Phosphorus	30-31	caspase 3	Homo sapiens	90-98
27191351-1	2016	PURPOSE OF REVIEW: Fibroblast growth factor 23 (FGF23) is a hormone secreted by osteocytes and osteoblasts that regulates phosphorus and vitamin D homeostasis.	Phosphorus	122-132	fibroblast growth factor 23	Homo sapiens	19-46
27129885-14	2016	C+P-IR or C/P-RIR were four to eight times more likely to exhibit low femoral neck CSMI or CSA when compared with C+P-R. Lumbar spine aBMD and Z-score were lower in C+P-IR when compared with C+P-R (p&lt;=0.003).	Phosphorus	2-3	ERCC excision repair 8, CSA ubiquitin ligase complex subunit	Homo sapiens	91-94
27191351-1	2016	PURPOSE OF REVIEW: Fibroblast growth factor 23 (FGF23) is a hormone secreted by osteocytes and osteoblasts that regulates phosphorus and vitamin D homeostasis.	Phosphorus	122-132	fibroblast growth factor 23	Homo sapiens	48-53
27347203-5	2016	The expression levels of STAT3 [total, tyrosine phosphorylated (p-Tyr) and serine phosphorylated (p-Ser)], JNK, c-Jun and cyclin D1 were assessed in the OSCC cell lines SCC25 and SCC9.	Phosphorus	6-7	signal transducer and activator of transcription 3	Homo sapiens	25-30
27347203-5	2016	The expression levels of STAT3 [total, tyrosine phosphorylated (p-Tyr) and serine phosphorylated (p-Ser)], JNK, c-Jun and cyclin D1 were assessed in the OSCC cell lines SCC25 and SCC9.	Phosphorus	6-7	cyclin D1	Homo sapiens	122-131
26928188-1	2016	UNLABELLED: There is growing need for a reliable assay for measuring fibroblast growth factor 23 (FGF23), a regulator of phosphorus and vitamin D.	Phosphorus	121-131	fibroblast growth factor 23	Homo sapiens	69-96
26928188-1	2016	UNLABELLED: There is growing need for a reliable assay for measuring fibroblast growth factor 23 (FGF23), a regulator of phosphorus and vitamin D.	Phosphorus	121-131	fibroblast growth factor 23	Homo sapiens	98-103
27106165-2	2016	Through direct surface modification with ammonium hexafluorophosphate (NH4 PF6 ), phosphorus can be successfully incorporated onto the surface of the carbon felt by forming phosphate functional groups with -OH chemical moieties that exhibit good hydrophilicity.	Phosphorus	82-92	sperm associated antigen 17	Homo sapiens	75-78
27346269-7	2016	(3) Both mRNA and protein expressions of Runx2 in high phosphorus groups were higher than in control group (0.630+-0.033 vs.0.340+-0.058 and 0.865+-0.031 vs.0.414+-0.011, both P&lt;0.05) and lower in TRAM-34 group (0.399+-0.023 and 0.575+-0.014, both P&lt;0.05 vs. high phosphorus group) in VSMCs simulated for 4 days.Besides, compared with high phosphorus group, the expression of Runx2 was decreased in control group(0.113+-0.010 vs.0.067+-0.008, P&lt;0.05) and TRAM-34 group (0.069+-0.006, P&lt;0.05) after aortic rings were cultured for 4 days.	Phosphorus	55-65	RUNX family transcription factor 2	Rattus norvegicus	41-46
27346269-7	2016	(3) Both mRNA and protein expressions of Runx2 in high phosphorus groups were higher than in control group (0.630+-0.033 vs.0.340+-0.058 and 0.865+-0.031 vs.0.414+-0.011, both P&lt;0.05) and lower in TRAM-34 group (0.399+-0.023 and 0.575+-0.014, both P&lt;0.05 vs. high phosphorus group) in VSMCs simulated for 4 days.Besides, compared with high phosphorus group, the expression of Runx2 was decreased in control group(0.113+-0.010 vs.0.067+-0.008, P&lt;0.05) and TRAM-34 group (0.069+-0.006, P&lt;0.05) after aortic rings were cultured for 4 days.	Phosphorus	55-65	RUNX family transcription factor 2	Rattus norvegicus	382-387
27346269-8	2016	(4) Compared with control group, the activity of ALP was significantly increased in high phosphorus group (96.56+-9.84 vs.46.92+-4.60, P&lt;0.05) and decreased in TRAM-34 group(70.20+-8.41, P&lt;0.05 vs. high phosphorus group) in VSMCs simulated for 12 days.	Phosphorus	89-99	PDZ and LIM domain 3	Rattus norvegicus	49-52
27346269-8	2016	(4) Compared with control group, the activity of ALP was significantly increased in high phosphorus group (96.56+-9.84 vs.46.92+-4.60, P&lt;0.05) and decreased in TRAM-34 group(70.20+-8.41, P&lt;0.05 vs. high phosphorus group) in VSMCs simulated for 12 days.	Phosphorus	209-219	PDZ and LIM domain 3	Rattus norvegicus	49-52
27513491-8	2016	There was a significant association between adiponectin concentrations with the healthy eating index, calories, lipids, proteins, fibers, riboflavin, and phosphorus, among others; and a tendency with carbohydrates and niacin.	Phosphorus	154-164	adiponectin, C1Q and collagen domain containing	Homo sapiens	44-55
27513491-9	2016	In multiple linear regression analysis, fiber and riboflavin (r2 = 0.0928; p = 0.0013) and carbohydrates and phosphorus were associated with the concentrations of adiponectin.	Phosphorus	109-119	adiponectin, C1Q and collagen domain containing	Homo sapiens	163-174
27172989-4	2016	The phosphidation degree, P/S ratio and work function (WF) of HF-MoSP can be tuned easily over broad range by changing the phosphidation temperature.	Phosphorus	26-27	dual specificity phosphatase 23	Homo sapiens	65-69
29964886-6	2016	The research will provide basic data for application of MRB in deep removal of low concentration phosphorus from sewage treatment plant and water body.	Phosphorus	97-107	roundabout guidance receptor 4	Homo sapiens	56-59
27180610-5	2016	Such a monovalent phosphorous(i) compound can undergo reactions with Cu(OAc)2, S, Se, (TMS)CHN2 and HCl to give various phosphorus(iii) species.	Phosphorus	18-29	chimerin 2	Homo sapiens	91-95
27180610-5	2016	Such a monovalent phosphorous(i) compound can undergo reactions with Cu(OAc)2, S, Se, (TMS)CHN2 and HCl to give various phosphorus(iii) species.	Phosphorus	120-130	chimerin 2	Homo sapiens	91-95
27060822-13	2016	Minerals (Mg, P, Na, K, Ca, Zn) in milk were not affected by the added iron in milk.	Phosphorus	14-15	Weaning weight-maternal milk	Bos taurus	35-39
26926422-7	2016	Molecular dynamics simulations of NTS1 in bilayers are in agreement with the ESR data, and point to sites in the receptor where PS could interact with higher affinity.	Phosphorus	128-130	neurotensin receptor 1	Rattus norvegicus	34-38
27070188-10	2016	CaSR expression was positively associated with serum phosphorus level (r = 0.274, P = .029) and GAD65/67 was negatively correlated with serum PTH level (r = -0.342, P = .005).	Phosphorus	53-63	calcium sensing receptor	Homo sapiens	0-4
27624533-1	2016	Fibroblast growth factor 23 (FGF23) is a potent regulator of phosphorus (P) and vitamin D metabolism.	Phosphorus	61-71	fibroblast growth factor 23	Rattus norvegicus	0-27
27624533-1	2016	Fibroblast growth factor 23 (FGF23) is a potent regulator of phosphorus (P) and vitamin D metabolism.	Phosphorus	61-71	fibroblast growth factor 23	Rattus norvegicus	29-34
26607678-5	2016	In serum-starved and re-feeding models of U251 and U373MG, we observed the rising expression of nucleostemin and p-beta-Catenin (p-Tyr645) were accompanied with cell proliferation markers (cyclin D1 and proliferating cell nuclear antigen (PCNA)).	Phosphorus	84-85	G protein nucleolar 3	Homo sapiens	96-108
26607678-5	2016	In serum-starved and re-feeding models of U251 and U373MG, we observed the rising expression of nucleostemin and p-beta-Catenin (p-Tyr645) were accompanied with cell proliferation markers (cyclin D1 and proliferating cell nuclear antigen (PCNA)).	Phosphorus	84-85	cyclin D1	Homo sapiens	189-198
26607678-5	2016	In serum-starved and re-feeding models of U251 and U373MG, we observed the rising expression of nucleostemin and p-beta-Catenin (p-Tyr645) were accompanied with cell proliferation markers (cyclin D1 and proliferating cell nuclear antigen (PCNA)).	Phosphorus	84-85	proliferating cell nuclear antigen	Homo sapiens	203-244
26895334-9	2016	Notably, the crown root had the strongest ZmCCD7 expression in the meristematic zone under phosphorus limitation.	Phosphorus	91-101	carotenoid cleavage dioxygenase	Zea mays	42-48
26970198-1	2016	The loss of diffuse phosphorus (P) presented different characteristics in the freeze-thaw area due to the combined impacts of precipitation and temperature, which caused spatiotemporal variations of the critical source area of diffuse P (CSAP).	Phosphorus	20-30	centriole, cilia and spindle associated protein	Homo sapiens	238-242
27025361-3	2016	It is the first time for the MOF which contains phosphorus for selective separation of methane from natural gas and pyrolysis gas.	Phosphorus	48-58	lysine acetyltransferase 8	Homo sapiens	29-32
27001892-7	2016	Accordingly, the VEGFR-1-targeted copolymer (P-(F56)-DOX) was more toxic towards bEnd.3 cells than to cancer cells, and exhibited significantly higher cytotoxicity than did the non-targeted control copolymer.	Phosphorus	45-46	FMS-like tyrosine kinase 1	Mus musculus	17-24
27001892-7	2016	Accordingly, the VEGFR-1-targeted copolymer (P-(F56)-DOX) was more toxic towards bEnd.3 cells than to cancer cells, and exhibited significantly higher cytotoxicity than did the non-targeted control copolymer.	Phosphorus	45-46	BEN domain containing 3	Mus musculus	81-87
26965530-10	2016	Phosphorus correlated with intact FGF23 (white women, r=0.120, p&lt;0.0001; black women r=0.163, p&lt;0.01).	Phosphorus	0-10	fibroblast growth factor 23	Homo sapiens	34-39
26965530-11	2016	However, phosphorus correlated with C-terminal FGF23 only in black women (r=0.157, p&lt;0.01).	Phosphorus	9-19	fibroblast growth factor 23	Homo sapiens	47-52
26965530-19	2016	Intact FGF23 correlated with serum phosphorus.	Phosphorus	35-45	fibroblast growth factor 23	Homo sapiens	7-12
27176000-8	2016	Among HIV-positive persons, factors independently associated with higher baseline FGF23 levels included female (adjusted ratio of geometric means [95% CI],1.46 [1.21,1.76]), serum phosphorus (1.20 [1.03,1.40]), HCV (1.31 [1.10,1.56]) and non-suppressed HIV RNA (1.27 [1.01,1.76]).	Phosphorus	180-190	fibroblast growth factor 23	Homo sapiens	82-87
26898284-7	2016	For mineral content, significant and consistent effects of the DGAT1 polymorphism on calcium, phosphorus, and zinc were detected.	Phosphorus	94-104	diacylglycerol O-acyltransferase 1	Bos taurus	63-68
26773479-9	2016	The importance of FGF-23 (phosphatonin) and parathyroid hormone in normalizing the dramatic changes in plasma calcium and phosphorus during the 24h egg-laying cycle is discussed.	Phosphorus	122-132	fibroblast growth factor 23	Homo sapiens	18-24
26593514-6	2016	In conclusion, the presence of FAME delayed PS degradation and postponed oxysterols formation.	Phosphorus	44-46	benign adult familial myoclonic epilepsy 1	Homo sapiens	31-35
26992746-2	2016	The theoretical scenario calculated in this study shows that the annually generated food waste onboard ships in traffic in the Baltic Sea contains about 182tonnes of nitrogen and 34tonnes of phosphorus.	Phosphorus	191-201	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	134-137
26992746-5	2016	Future regulations for sewage discharge in the Baltic Sea will require significant reduction of total nitrogen and phosphorus released.	Phosphorus	115-125	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	54-57
26898284-8	2016	In the Dutch HF population, the contribution of the DGAT1 K232A polymorphism to phenotypic variance was 12.0% for calcium, 8.3% for phosphorus, and 6.1% for zinc.	Phosphorus	132-142	diacylglycerol O-acyltransferase 1	Bos taurus	52-57
25743373-1	2016	The hydroxyl oxygen of the catalytic triad serine in the active center of serine hydrolase acetylcholinesterase (AChE) attacks organophosphorus compounds (OPs) at the phosphorus atom to displace the primary leaving group and to form a covalent bond.	Phosphorus	133-143	acetylcholinesterase (Cartwright blood group)	Homo sapiens	91-111
25770169-4	2016	The main hormones and factors that contribute to the kidney regulation of phosphorus and calcium include parathyroid hormone, FGF-23, klotho and 1,25-dihydroxyvitamin D (1,25(OH)2D).	Phosphorus	74-84	parathyroid hormone	Homo sapiens	105-124
25770169-6	2016	Despite FGF-23 and PTH having synergic effects regarding phosphorus removal, they have opposite effects on 1,25(OH)2D3.	Phosphorus	57-67	fibroblast growth factor 23	Homo sapiens	8-14
25770169-6	2016	Despite FGF-23 and PTH having synergic effects regarding phosphorus removal, they have opposite effects on 1,25(OH)2D3.	Phosphorus	57-67	parathyroid hormone	Homo sapiens	19-22
26846171-9	2016	The data revealed that the F-actin/G-actin ratio and cofilin were reduced, and p-cofilin increased conversely in cells with SEPT7 overexpression, indicating that SEPT7 reduced glioma cell migration by promoting cofilin phosphorylation and depolymerizing actin.	Phosphorus	79-80	cofilin 1	Homo sapiens	81-88
26846171-9	2016	The data revealed that the F-actin/G-actin ratio and cofilin were reduced, and p-cofilin increased conversely in cells with SEPT7 overexpression, indicating that SEPT7 reduced glioma cell migration by promoting cofilin phosphorylation and depolymerizing actin.	Phosphorus	79-80	septin 7	Homo sapiens	162-167
26846171-9	2016	The data revealed that the F-actin/G-actin ratio and cofilin were reduced, and p-cofilin increased conversely in cells with SEPT7 overexpression, indicating that SEPT7 reduced glioma cell migration by promoting cofilin phosphorylation and depolymerizing actin.	Phosphorus	79-80	cofilin 1	Homo sapiens	81-88
25743373-1	2016	The hydroxyl oxygen of the catalytic triad serine in the active center of serine hydrolase acetylcholinesterase (AChE) attacks organophosphorus compounds (OPs) at the phosphorus atom to displace the primary leaving group and to form a covalent bond.	Phosphorus	133-143	acetylcholinesterase (Cartwright blood group)	Homo sapiens	113-117
25743373-2	2016	Inhibited AChE can be reactivated by cleavage of the Ser-phosphorus bond either spontaneously or through a reaction with nucleophilic agents, such as oximes.	Phosphorus	57-67	acetylcholinesterase (Cartwright blood group)	Homo sapiens	10-14
27262192-2	2016	Interaction of NER protein XPC-RAD23B providing primary damage recognition with DNA duplexes containing a B[a]P-derived residue linked to the exocyclic amino group of a guanine (BPDE-N(2)-dG) in the central position of one strand and AP site in different positions of the other strand was analyzed.	Phosphorus	28-29	RAD23 homolog B, nucleotide excision repair protein	Homo sapiens	31-37
26769003-0	2016	Lamin A is involved in the development of vascular calcification induced by chronic kidney failure and phosphorus load.	Phosphorus	103-113	lamin A/C	Rattus norvegicus	0-7
26769003-3	2016	The main aim of this study was to analyse the effect of phosphorus load in the differential expression pattern of genes and proteins, particularly of lamin A/C, which are involved in phenotypic change of the vascular smooth muscle cells to osteoblast-like cells.	Phosphorus	56-66	lamin A/C	Rattus norvegicus	150-159
26769003-4	2016	The in vivo study of the calcified abdominal aortas from nephrectomized rats receiving a high phosphorus diet showed among others, a repression of muscle related proteins and overexpression of lamin A/C.	Phosphorus	94-104	lamin A/C	Rattus norvegicus	193-202
29997776-1	2016	Sodium phosphaethynolate reacts with [MCl(PDI)] (M = Co, Ir; PDI = pyridinediimine) to give metallaphosphaketenes, which in the case of iridium rearranges into a dimetalladiphosphene, via CO migration from phosphorus to the metal.	Phosphorus	206-216	peptidyl arginine deiminase 1	Homo sapiens	42-45
29997776-2	2016	Two different bonding modes of the PCO anion to CAAC-coinage metal complexes [CAAC: cyclic (alkyl)(amino)(carbene)] are reported, one featuring a strong Au-P bond and the other an eta2 coordination to copper.	Phosphorus	35-36	DNA polymerase iota	Homo sapiens	180-184
26187577-5	2016	Compared with controls and uremic rats fed a normal diet, uremic rats fed a high-phosphorous diet had lower levels of miR-133b and miR-211 and higher levels of miR-29b that correlated respectively with greater expression of osteogenic RUNX2 and with lower expression of several inhibitors of osteoblastic differentiation.	Phosphorus	81-92	microRNA 133b	Rattus norvegicus	118-126
26603871-5	2016	RESULTS: In the cross-sectional study, the main cTnT predictors were dialysis vintage, age, eQB, phosphorus, and C-reactive protein.	Phosphorus	97-107	troponin T2, cardiac type	Homo sapiens	48-52
26187577-5	2016	Compared with controls and uremic rats fed a normal diet, uremic rats fed a high-phosphorous diet had lower levels of miR-133b and miR-211 and higher levels of miR-29b that correlated respectively with greater expression of osteogenic RUNX2 and with lower expression of several inhibitors of osteoblastic differentiation.	Phosphorus	81-92	microRNA 211	Rattus norvegicus	131-138
26187577-8	2016	We conclude that miR-29b, miR-133b, and miR-211 have direct roles in the vascular smooth muscle calcification induced by high phosphorus and may be new therapeutic targets in the management of vascular calcification.	Phosphorus	126-136	microRNA 211	Rattus norvegicus	40-47
26997382-10	2016	Diabetes status, P, PTH, and low density lipoprotein-cholesterol had significant impact on the prescription pattern of phosphorous binders.	Phosphorus	119-130	parathyroid hormone	Homo sapiens	20-23
26821943-1	2016	We report ab initio time-domain simulations of nonradiative electron-hole recombination and electronic dephasing in ideal and defect-containing monolayer black phosphorus (MBP).	Phosphorus	154-170	myelin basic protein	Homo sapiens	172-175
26902190-4	2016	S-P staining of immunohistochemistry was used to detect the expression of Caspase 3 and Caspase 4 in temporal lobe neurocytes of TLE group and contrast group.	Phosphorus	0-3	caspase 3	Homo sapiens	74-83
26902190-4	2016	S-P staining of immunohistochemistry was used to detect the expression of Caspase 3 and Caspase 4 in temporal lobe neurocytes of TLE group and contrast group.	Phosphorus	0-3	caspase 4	Homo sapiens	88-97
26821943-2	2016	Our calculations predict that the presence of phosphorus divacancy in MBP (MBP-DV) substantially reduces the nonradiative recombination rate, with time scales on the order of 1.57 ns.	Phosphorus	46-56	myelin basic protein	Homo sapiens	70-73
26821943-2	2016	Our calculations predict that the presence of phosphorus divacancy in MBP (MBP-DV) substantially reduces the nonradiative recombination rate, with time scales on the order of 1.57 ns.	Phosphorus	46-56	myelin basic protein	Homo sapiens	75-81
26407302-2	2016	This intramolecular rearrangement was shown to occur in three steps: first, the hydride proton migrates to phosphorus, then the P-Aryl moiety rotates around the P-Ni bond, and finally the back migration of one proton to Ni completes the process.	Phosphorus	107-117	5'-nucleotidase, cytosolic IIIA	Homo sapiens	161-165
26777416-1	2016	Evolutionary algorithms (EAs) coupled with density functional theory (DFT) calculations have been used to predict the most stable hydrides of phosphorus (PHn, n = 1-6) at 100, 150, and 200 GPa.	Phosphorus	142-152	carbamoyl-phosphate synthase 1	Homo sapiens	154-157
26692521-3	2016	Mutations in IRF6 (Interferon Regulatory Factor 6) and GRHL3 (Grainyhead-like 3) cause Van der Woude syndrome, which includes CL/P.	Phosphorus	129-130	interferon regulatory factor 6	Homo sapiens	13-17
26692521-3	2016	Mutations in IRF6 (Interferon Regulatory Factor 6) and GRHL3 (Grainyhead-like 3) cause Van der Woude syndrome, which includes CL/P.	Phosphorus	129-130	interferon regulatory factor 6	Homo sapiens	19-49
26692521-3	2016	Mutations in IRF6 (Interferon Regulatory Factor 6) and GRHL3 (Grainyhead-like 3) cause Van der Woude syndrome, which includes CL/P.	Phosphorus	129-130	grainyhead like transcription factor 3	Homo sapiens	55-60
26692521-3	2016	Mutations in IRF6 (Interferon Regulatory Factor 6) and GRHL3 (Grainyhead-like 3) cause Van der Woude syndrome, which includes CL/P.	Phosphorus	129-130	grainyhead like transcription factor 3	Homo sapiens	62-79
26661117-4	2016	Herein, we report on the synthesis of Cs[E3 C2 (trip)2 ] (1 a: E=P; 1 b: E=As; trip=2,4,6-triisopropylphenyl) and Cs[E4 C(trip)] (2 a: E=P; 2 b: E=As).	Phosphorus	65-66	mediator complex subunit 1	Homo sapiens	44-54
26831224-9	2016	The P/S ratio showed the highest specificity in the case of CEA (97.14%).	Phosphorus	4-5	CEA cell adhesion molecule 3	Homo sapiens	60-63
26311115-5	2016	A more prolonged uremia due to an adenine high-phosphorus diet for 14 days resulted in high levels of FGF23 mRNA and serum FGF23 and PTH.	Phosphorus	47-57	fibroblast growth factor 23	Rattus norvegicus	102-107
26311115-5	2016	A more prolonged uremia due to an adenine high-phosphorus diet for 14 days resulted in high levels of FGF23 mRNA and serum FGF23 and PTH.	Phosphorus	47-57	fibroblast growth factor 23	Rattus norvegicus	123-128
26655748-9	2016	There was a significant positive correlation between serum PTH and salivary phosphorus (r=0.342, p=0.009), and between serum PTH and salivary potassium (r=0.306, p=0.020).	Phosphorus	76-86	parathyroid hormone	Homo sapiens	59-62
26510093-0	2016	Phosphorus cycling in deciduous forest soil differs between stands dominated by ecto- and arbuscular mycorrhizal trees.	Phosphorus	0-10	tripartite motif containing 33	Homo sapiens	80-84
26813507-1	2016	FGF23-related hypophosphatemic rickets is basically treated with active vitamin D and phosphorus.	Phosphorus	86-96	fibroblast growth factor 23	Homo sapiens	0-5
27134553-6	2016	Reactions between PCS- and W(CO)5(MeCN) similarly afford [W(CO)5(PCS)]-; however, due to the ambidentate nature of the anion, a mixture of both the phosphorus- and sulfur-bonded complexes (4a and 4b, respectively) is obtained.	Phosphorus	148-158	PCS	Homo sapiens	18-21
27440690-4	2016	The objective of this cross-sectional study was to examine the relationship between serum FGF-23 concentrations and phosphorus related factors in 182 young Japanese women (mean age, 19.5+-0.4 years).	Phosphorus	116-126	fibroblast growth factor 23	Homo sapiens	90-96
26673146-1	2016	The divalent europium complexes, and (L(Me/Et) = p-HC6F4N(CH2)2NMe2/Et2), have been prepared from redox-transmetallation/protolysis (RTP) reactions between Eu metal, Hg(C6F5)2 and L(Me/Et)H in thf.	Phosphorus	17-18	endothelin 2	Homo sapiens	68-71
26970791-2	2016	MPP was hydroxyalkylated with ethylene and propylene carbonates to get oligoetherols with 1,3,5-triazine ring and phosphorus.	Phosphorus	114-124	M-phase phosphoprotein 6	Homo sapiens	0-3
26723869-4	2016	The purpose of the present study was to evaluate these activities of Rg1 in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)/probenecid (MPTP/p)-induced PD mouse model for the first time and to elucidate the underlying mechanisms.	Phosphorus	4-5	protein phosphatase 1, regulatory subunit 3A	Mus musculus	69-72
26786148-13	2016	Plasma FGF23 concentrations increased four weeks after high phosphorus intake and normalized after eight weeks.	Phosphorus	60-70	fibroblast growth factor 23	Homo sapiens	7-12
26782594-1	2016	We investigated the effect of high phosphorus content on the sodium-phosphate cotransporter (NaPi-IIa and NaPi-IIl).	Phosphorus	35-45	solute carrier family 34 member 1	Rattus norvegicus	93-101
27440690-5	2016	We found that higher serum concentrations of inorganic phosphorus and lower serum concentrations of 1,25-dihydroxy vitamin D as well as lower fat but higher phosphorus and calcium intake were weakly but significantly associated with high serum concentrations of FGF-23, adjusted for postmenarcheal age and body weight.	Phosphorus	55-65	fibroblast growth factor 23	Homo sapiens	262-268
27440690-6	2016	These results suggested that in young Japanese women, serum FGF-23 might be indicative of phosphorus nutrition status.	Phosphorus	90-100	fibroblast growth factor 23	Homo sapiens	60-66
26395031-10	2016	Finally, p-S6 staining showed activation of mTOR pathway in human adenoid cystic carcinoma samples.	Phosphorus	9-10	mechanistic target of rapamycin kinase	Homo sapiens	44-48
27362907-4	2016	Our study demonstrated that a high concentration of phosphorus induced apoptosis and calcification of VSMCs, decreased expression of Axl, and reduced phosphorylation of Akt.	Phosphorus	52-62	Axl receptor tyrosine kinase	Rattus norvegicus	133-136
27362907-4	2016	Our study demonstrated that a high concentration of phosphorus induced apoptosis and calcification of VSMCs, decreased expression of Axl, and reduced phosphorylation of Akt.	Phosphorus	52-62	AKT serine/threonine kinase 1	Rattus norvegicus	169-172
27040054-0	2016	Effects of gender and body weight on fibroblast growth factor 23 responsiveness to estimated dietary phosphorus.	Phosphorus	101-111	fibroblast growth factor 23	Homo sapiens	37-64
27040054-3	2016	The purpose of this study was to evaluate whether sex could influence FGF23 responsiveness to dietary phosphorus intake in healthy individuals.	Phosphorus	102-112	fibroblast growth factor 23	Homo sapiens	70-75
28002816-6	2016	RESULTS: Osteocalcin was positively correlated with serum phosphorus (p = 0.001), alkaline phosphatase (ALP; p &lt; 0.001), PTH (p = 0.002) and beta-CTX (p &lt; 0.001), and negatively correlated with BMD at the lumbar spine (p &lt; 0.001) and total hip (p = 0.002).	Phosphorus	58-68	bone gamma-carboxyglutamate protein	Homo sapiens	9-20
28002816-8	2016	CONCLUSION: Our results suggest that osteocalcin was positively correlated with serum phosphorus, ALP, PTH, and beta-CTX, but negatively correlated with BMD at the lumbar spine and total hip.	Phosphorus	86-96	bone gamma-carboxyglutamate protein	Homo sapiens	37-48
26594136-9	2016	These results demonstrate that the PSR1 gene is an important determinant of lipid and starch accumulation in response to phosphorus starvation but not nitrogen starvation.	Phosphorus	121-131	uncharacterized protein	Chlamydomonas reinhardtii	35-39
30854527-4	2016	In a recent study we showed that uncontrolled PS production by these mutant PSS1 enzymes lead to the accumulation of PS in the ER where it is not detected in normal cells.	Phosphorus	46-48	phosphatidylserine synthase 1	Homo sapiens	76-80
30854527-5	2016	This increased PS in the ER in turn, activated the Sac1 phosphatase, which is responsible for the dephosphorylation of the minor lipid, phosphatidylinositol 4-phosphate (PI4P) in the ER.	Phosphorus	15-17	SAC1 like phosphatidylinositide phosphatase	Homo sapiens	51-55
25634900-1	2016	In this research, the effect of magnesium (Mg), copper (Cu) and phosphorus (P) impurities on dosimetry response of LiF:Mg,Cu,P phosphors is studied experimentally and by the simulation procedure.	Phosphorus	64-74	LIF interleukin 6 family cytokine	Homo sapiens	115-118
27885332-1	2016	The longevity gene klotho has numerous physiological functions, such as regulating calcium and phosphorus levels, delaying senescence, improving cognition, reducing oxidative stress, and protecting vascular endothelial cells.	Phosphorus	95-105	Klotho	Rattus norvegicus	19-25
26523947-2	2016	They are rich in phosphorus compounds in the form of orthophosphate (Pi), pyrophosphate (PPi), and polyphosphate (polyP) and their acidity is maintained by proton pumps such as the vacuolar proton pyrophosphatase (V-H+-PPase, or VP1), the vacuolar proton ATPase (V-H+-ATPase), or both.	Phosphorus	17-27	dynein axonemal heavy chain 8	Homo sapiens	255-261
26523947-2	2016	They are rich in phosphorus compounds in the form of orthophosphate (Pi), pyrophosphate (PPi), and polyphosphate (polyP) and their acidity is maintained by proton pumps such as the vacuolar proton pyrophosphatase (V-H+-PPase, or VP1), the vacuolar proton ATPase (V-H+-ATPase), or both.	Phosphorus	17-27	dynein axonemal heavy chain 8	Homo sapiens	263-274
26498828-4	2015	The P-O-C bonds formed in this process help maintain contact between phosphorus and CNTs, leading to a durable hybrid.	Phosphorus	69-79	proopiomelanocortin	Homo sapiens	4-9
27508374-1	2016	The degree of phosphorus saturation (DPS) of agricultural soils is studied worldwide for risk assessment of phosphorus (P) losses.	Phosphorus	14-24	decaprenyl diphosphate synthase subunit 1	Homo sapiens	37-40
27508374-1	2016	The degree of phosphorus saturation (DPS) of agricultural soils is studied worldwide for risk assessment of phosphorus (P) losses.	Phosphorus	108-118	decaprenyl diphosphate synthase subunit 1	Homo sapiens	37-40
27508376-7	2016	Phosphorus removal was significantly enhanced, exceeding 90% in E-BF by chemical precipitation, physical adsorption, and flocculation of phosphorus because of the in situ formation of ferric ions by the anodizing of sacrificial iron anodes.	Phosphorus	0-10	EBF transcription factor 1	Homo sapiens	64-68
27508376-7	2016	Phosphorus removal was significantly enhanced, exceeding 90% in E-BF by chemical precipitation, physical adsorption, and flocculation of phosphorus because of the in situ formation of ferric ions by the anodizing of sacrificial iron anodes.	Phosphorus	137-147	EBF transcription factor 1	Homo sapiens	64-68
27070162-7	2016	Along with this, a strong direct correlation (r=0.522; p&lt;0.001) was found between the concentration of FGF-23 in the serum and inorganic phosphorus; at the same time hyperphosphatemia was less significantly associated with higher serum intact parathyroid hormone (PTH) levels (r=0.398; p&lt;0.05).	Phosphorus	140-150	fibroblast growth factor 23	Homo sapiens	106-112
29297646-4	2016	Results: Ehen comparing the s-Klotho levels in patients with different CKD stages, it was found that the level change associated with the reduction of glomerular filtration rate (GFR) ahead of phosphorus and PTH increase in serum, stared at 3A CKD, whereas hyperphosphatemia and PTH increase started at 4-5 CKD stages.	Phosphorus	193-203	klotho	Homo sapiens	30-36
26675484-10	2015	PS alone induced differentiation and expression of p21WAF1/CIP1 and p53 and decreased CHK1 in all three cell lines, with almost no further effect when combined with erlotinib.	Phosphorus	0-2	cyclin dependent kinase inhibitor 1A	Homo sapiens	59-63
27081473-4	2015	There are several factors that regulate FGF23: phosphorus, vitamin D, and parathyroid hormone (PTH).	Phosphorus	47-57	fibroblast growth factor 23	Homo sapiens	40-45
26675484-10	2015	PS alone induced differentiation and expression of p21WAF1/CIP1 and p53 and decreased CHK1 in all three cell lines, with almost no further effect when combined with erlotinib.	Phosphorus	0-2	tumor protein p53	Homo sapiens	68-71
26675484-10	2015	PS alone induced differentiation and expression of p21WAF1/CIP1 and p53 and decreased CHK1 in all three cell lines, with almost no further effect when combined with erlotinib.	Phosphorus	0-2	checkpoint kinase 1	Homo sapiens	86-90
26565933-2	2015	The crystalline sample (NaK-D-1) of the water-soluble, mixed sodium/potassium salt of D-1 was obtained in the 14.7% yield, which has been characterized by complete elemental analysis, TG/DTA, FTIR, single-crystal X-ray structure analysis, and solution ((183)W, (31)P, (1)H and (13)C{(1)H}) NMR spectroscopy.	Phosphorus	265-266	TANK binding kinase 1	Homo sapiens	24-27
26494532-5	2015	The SMD simulations showed that the active pyridinium ring of K048 is directed towards the phosphorus atom conjugated to the active serine (SUN203) of tabun-mAChE(wild-type).	Phosphorus	91-101	acetylcholinesterase	Mus musculus	157-162
26494532-9	2015	Such displacement is causing the inaccessibility of the drug towards the phosphorus atom conjugated to the active serine (SUN203) of tabun-mutant mAChE(Y337A).	Phosphorus	73-83	acetylcholinesterase	Mus musculus	146-151
26494532-10	2015	Furthermore, the unbinding of the K048 with SMD studies showed that the active pyridinium ring of the drug undergoes a complete turn along the gorge axis and is directed away from the phosphorus atom conjugated to the active serine of the tabun-mutant mAChE(Y337A).	Phosphorus	184-194	acetylcholinesterase	Mus musculus	252-257
26423393-7	2015	Nematode Hsp70 were useful biosensors to monitor and assess the levels of nitrogen and phosphorus pollutions in wetlands.	Phosphorus	87-97	Heat Shock Protein	Caenorhabditis elegans	9-14
27194998-1	2015	BACKGROUND: The osteocyte-derived hormone, fibroblast growth factor 23 (FGF23), regulates the phosphorus metabolism and suppresses 1,25-dihydroxyvitamin D production, thereby mitigating hyperphosphatemia in patients with renal disorders.	Phosphorus	94-104	fibroblast growth factor 23	Homo sapiens	43-70
27194998-1	2015	BACKGROUND: The osteocyte-derived hormone, fibroblast growth factor 23 (FGF23), regulates the phosphorus metabolism and suppresses 1,25-dihydroxyvitamin D production, thereby mitigating hyperphosphatemia in patients with renal disorders.	Phosphorus	94-104	fibroblast growth factor 23	Homo sapiens	72-77
27194998-2	2015	An elevated FGF23 level is suggested to be an early biomarker of altered phosphorus metabolism in the initial stages of chronic kidney disease (CKD) and acts as a strong predictor of mortality in dialysis patients.	Phosphorus	73-83	fibroblast growth factor 23	Homo sapiens	12-17
26548556-1	2015	Spin states of the electrons and nuclei of phosphorus donors in silicon are strong candidates for quantum information processing applications given their excellent coherence times.	Phosphorus	43-53	spindlin 1	Homo sapiens	0-4
26888134-13	2015	Administration of rPTH(1-84) in the dose of 80 or 160 microg/kg made serum calcium and phosphorus back to normal levels, with no significant difference between the doses (P&gt;0.05).	Phosphorus	87-97	parathyroid hormone	Rattus norvegicus	18-27
26888134-18	2015	CONCLUSION: Calcium and phosphorus return to normal level by administration of rPTH(1-84) in the dose of 80 microg/kg or 160 microg/kg, with increase in BMD.	Phosphorus	24-34	parathyroid hormone	Rattus norvegicus	79-88
27011991-4	2015	1 mg   L-1 while the release of phosphorus was 10.43 mg   L-1 showing that 5.38 mg of VFA was required to release 1 mg PO43--P.	Phosphorus	32-42	immunoglobulin kappa variable 1-16	Homo sapiens	58-61
27011991-6	2015	35 mg   L-1, while the uptake of phosphorus of MBR tank was 1.33 mg   L-1.	Phosphorus	33-43	immunoglobulin kappa variable 1-16	Homo sapiens	70-73
26397709-0	2015	Phosphorus-Based Dendrimer ABP Treats Neuroinflammation by Promoting IL-10-Producing CD4(+) T Cells.	Phosphorus	0-10	interleukin 10	Mus musculus	69-74
26323022-9	2015	Similarly, high-phosphorus diets in mice significantly increased blood FGF23, osteopontin and osteocalcin, lowered sclerostin, and decreased bone mineral density (P &lt; .05 for all).	Phosphorus	16-26	fibroblast growth factor 23	Mus musculus	71-76
26392310-7	2015	The urinary phosphorus/creatinine ratio was increased in Pmca1(EKO) mice (P &lt; 0.004).	Phosphorus	12-22	ATPase, Ca++ transporting, plasma membrane 1	Mus musculus	57-62
26544186-15	2015	Diminished eGFR, age, diabetes, serum phosphorus and microalbuminurea demonstrate significant relationship with elevated IL-33 levels, supporting the possible pathognomonic role of IL-33 in the cardiovascular burden in RTR.	Phosphorus	38-48	interleukin 33	Homo sapiens	121-126
26323022-9	2015	Similarly, high-phosphorus diets in mice significantly increased blood FGF23, osteopontin and osteocalcin, lowered sclerostin, and decreased bone mineral density (P &lt; .05 for all).	Phosphorus	16-26	secreted phosphoprotein 1	Mus musculus	78-89
26323022-9	2015	Similarly, high-phosphorus diets in mice significantly increased blood FGF23, osteopontin and osteocalcin, lowered sclerostin, and decreased bone mineral density (P &lt; .05 for all).	Phosphorus	16-26	bone gamma-carboxyglutamate protein 2	Mus musculus	94-105
26296303-3	2015	By comparison with PA6/PS and PA6/PEG systems, it is denominated that the PEG blocks in PEG-b-PPG-b-PEG can effectively reduce the surface tension of PA6 droplets and further decrease the diameter of the PA6 microspheres.	Phosphorus	23-25	serglycin	Homo sapiens	94-97
26406962-3	2015	The WW domain of human Pin1 can recognize the phosphoserine/phosphothreonine-proline (pS/pT-P) motifs, while its PPIase domain catalyzes the cis/trans isomerization of prolyl bonds to regulate the cell cycle.	Phosphorus	86-88	peptidylprolyl cis/trans isomerase, NIMA-interacting 1	Homo sapiens	23-27
30090274-5	2015	However, taking advantage of the ligand optimization opportunities presented by the PNP system via the changes in the substitution at phosphorus led to the discovery of a catalyst whose activity, longevity, and scope far exceeded that of the original SiNN archetype.	Phosphorus	134-144	purine nucleoside phosphorylase	Homo sapiens	84-87
26514124-1	2015	BACKGROUND: Fasting serum phosphorus (P) was reported to be inversely related to serum glucose and insulin, while the impact of P ingestion is not well documented.	Phosphorus	26-36	insulin	Homo sapiens	99-106
26249563-8	2015	More importantly, the PGS polymer in the beta-TCP/PGS scaffolds could direct the biomineralization of Ca/P from particulate shape into a nanofiber-interweaved structure.	Phosphorus	22-23	adaptor related protein complex 1 subunit sigma 2	Homo sapiens	41-53
26451949-4	2015	The fabricated n-CdS/p-Si heterojunction exhibits promising power conversion efficiency close to 3%, up from a mere efficient 0.15% for a similar cell fabricated on a planar Si.	Phosphorus	21-22	CDP-diacylglycerol synthase 1	Homo sapiens	17-20
26605011-3	2015	In this study, the association of two important TGFA gene polymorphisms, BamHI (rs11466297) and RsaI (rs3732248), with CL/P was evaluated in an Iranian population.	Phosphorus	122-123	transforming growth factor alpha	Homo sapiens	48-52
26605011-8	2015	CONCLUSION: Our study showed that there was an association between the TGFA BamHI variation and nonsyndromic CL/P in Iranian population.	Phosphorus	112-113	transforming growth factor alpha	Homo sapiens	71-75
26483638-7	2015	Using Ser293-P antibody, which recognizes a phosphorylated form of connexin36, we found that phosphorylation of connexin36 in both slow and fast RD models was significantly greater than in wildtype controls.	Phosphorus	13-14	gap junction protein, delta 2	Mus musculus	67-77
26483638-7	2015	Using Ser293-P antibody, which recognizes a phosphorylated form of connexin36, we found that phosphorylation of connexin36 in both slow and fast RD models was significantly greater than in wildtype controls.	Phosphorus	13-14	gap junction protein, delta 2	Mus musculus	112-122
25896061-2	2015	Numerous studies in the past decade have implicated IRF6 in CL/P, but this has not often been replicated in other populations.	Phosphorus	63-64	interferon regulatory factor 6	Homo sapiens	52-56
26011613-2	2015	We estimated the effects of climate change and possible future scenarios of agricultural changes on the phosphorus and nitrogen loading to the Baltic Sea from Finnish catchments.	Phosphorus	104-114	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	150-153
26277886-3	2015	The as-fabricated 20 nm top-gated BP transistors exhibit respectable on-state current (174 muA/mum) and transconductance (70 muS/mum) at a VDS of 0.1 V. Due to the use of two-dimensional BP as the channel material, the transistors exhibit relatively small short channel effects, preserving a decent on-off current ratio of 10(2) even at an extremely small channel length of 20 nm.	Phosphorus	34-36	latexin	Homo sapiens	95-98
26277886-3	2015	The as-fabricated 20 nm top-gated BP transistors exhibit respectable on-state current (174 muA/mum) and transconductance (70 muS/mum) at a VDS of 0.1 V. Due to the use of two-dimensional BP as the channel material, the transistors exhibit relatively small short channel effects, preserving a decent on-off current ratio of 10(2) even at an extremely small channel length of 20 nm.	Phosphorus	34-36	latexin	Homo sapiens	129-132
26287312-6	2015	Iodine reacted with the starting complex as an electrophile under splitting of the P-P bond in the t-Bu2P P unit to yield [(1,2-eta-t-Bu2P-P-P-t-Bu2)W(2,6-i-Pr2C6H3N)2Cl], t-Bu2PI, and phosphorus polymers.	Phosphorus	185-195	endothelin receptor type A	Homo sapiens	128-131
25241022-11	2015	CONCLUSIONS: Supplementing diets with the GOS/FOS( ) mixture increased bone mineralization, density and structure due to an increase in Ca, P and Mg absorptions.	Phosphorus	140-141	Fos proto-oncogene, AP-1 transcription factor subunit	Rattus norvegicus	46-49
25896061-3	2015	In specific, the only etiologic single-nucleotide polymorphism (SNP) identified in the IRF6 locus (rs642961) has recently been shown not to be associated with CL/P in diverse populations.	Phosphorus	66-67	interferon regulatory factor 6	Homo sapiens	87-91
26018436-2	2015	However, over the past decade, substantial advances have been made in understanding the control of phosphorus by the so-called phosphatonin system, the lynchpin of which is fibroblast growth factor 23 (FGF23).	Phosphorus	99-109	fibroblast growth factor 23	Homo sapiens	202-207
26354558-2	2015	Elevated serum parathyroid hormone (PTH) and abnormal calcium (Ca) and phosphorus (P) balance have been implicated in vascular damage in chronic kidney disease (CKD) patients, but there is lack of histo-pathological studies.	Phosphorus	36-37	parathyroid hormone	Homo sapiens	15-34
26018436-2	2015	However, over the past decade, substantial advances have been made in understanding the control of phosphorus by the so-called phosphatonin system, the lynchpin of which is fibroblast growth factor 23 (FGF23).	Phosphorus	99-109	fibroblast growth factor 23	Homo sapiens	173-200
26018436-3	2015	FGF23 binds to the klotho/FGFR1c receptor complex in renal tubular epithelial cells, leading to upregulation of Na/Pi cotransporters and subsequent excretion of phosphorus from the body.	Phosphorus	161-171	fibroblast growth factor 23	Homo sapiens	0-5
26379630-8	2015	Gene expression study of CrPGP1 and CrPGP2 in nutrient-starved C. reinhardtii showed differential response to phosphorus and nitrogen deficiency.	Phosphorus	110-120	uncharacterized protein	Chlamydomonas reinhardtii	25-31
26379630-8	2015	Gene expression study of CrPGP1 and CrPGP2 in nutrient-starved C. reinhardtii showed differential response to phosphorus and nitrogen deficiency.	Phosphorus	110-120	uncharacterized protein	Chlamydomonas reinhardtii	36-42
25189433-8	2015	Multivariate linear regression analysis indicated normalized phosphorus intake, renal CPh and dietary protein intake were independently associated with serum phosphorus level.	Phosphorus	158-168	carboxypeptidase E	Homo sapiens	86-89
26264209-0	2015	Experimental Comparison of Efficiency of First Aid Dressings in Burning White Phosphorus on Bacon Model.	Phosphorus	72-88	activation induced cytidine deaminase	Homo sapiens	47-50
26176378-1	2015	A commercial phosphorus-based reagent (P(NMe2)3) mediates umpolung alkylation of methyl aroylformates with benzylic and allylic bromides, leading to either Barbier-type addition or ylide-free olefination products upon workup.	Phosphorus	13-23	NME/NM23 nucleoside diphosphate kinase 2	Homo sapiens	41-45
25962562-9	2015	Following treatment with bisperoxopicolinatooxovanadate (BPV) or metformin in the insulin-resistant skeletal muscle cells, there was an increase in the rate of glucose uptake, an increase in GLUT4 expression and its translocation, a reduction in the expression of PTEN and p-PTEN, and a decrease in cell apoptosis compared with untreated insulin-resistant cells.	Phosphorus	28-29	phosphatase and tensin homolog	Homo sapiens	264-268
25692973-6	2015	RESULTS: After adjustment for age, body mass index, lifestyle factors and serum levels of calcium, phosphorus, testosterone, 25-OH-vitamin D3 and cortisol, higher serum DHEA-S concentrations were associated with higher BMD values at all skeletal sites.	Phosphorus	99-109	sulfotransferase family 2A member 1	Homo sapiens	169-175
26321027-6	2015	In hypertensive patients, urine FGF23/creatinine positively correlated with serum calcium and negatively with serum 25(OH)D, urinary calcium, phosphorus, and magnesium.	Phosphorus	142-152	fibroblast growth factor 23	Homo sapiens	32-37
25954033-11	2015	This first finding of a DLX4 mutation in a family with CL/P establishes DLX4 as a potential cause of human clefts.	Phosphorus	58-59	distal-less homeobox 4	Homo sapiens	24-28
25954033-11	2015	This first finding of a DLX4 mutation in a family with CL/P establishes DLX4 as a potential cause of human clefts.	Phosphorus	58-59	distal-less homeobox 4	Homo sapiens	72-76
25962562-9	2015	Following treatment with bisperoxopicolinatooxovanadate (BPV) or metformin in the insulin-resistant skeletal muscle cells, there was an increase in the rate of glucose uptake, an increase in GLUT4 expression and its translocation, a reduction in the expression of PTEN and p-PTEN, and a decrease in cell apoptosis compared with untreated insulin-resistant cells.	Phosphorus	28-29	phosphatase and tensin homolog	Homo sapiens	275-279
25962562-9	2015	Following treatment with bisperoxopicolinatooxovanadate (BPV) or metformin in the insulin-resistant skeletal muscle cells, there was an increase in the rate of glucose uptake, an increase in GLUT4 expression and its translocation, a reduction in the expression of PTEN and p-PTEN, and a decrease in cell apoptosis compared with untreated insulin-resistant cells.	Phosphorus	28-29	insulin	Homo sapiens	82-89
25962562-9	2015	Following treatment with bisperoxopicolinatooxovanadate (BPV) or metformin in the insulin-resistant skeletal muscle cells, there was an increase in the rate of glucose uptake, an increase in GLUT4 expression and its translocation, a reduction in the expression of PTEN and p-PTEN, and a decrease in cell apoptosis compared with untreated insulin-resistant cells.	Phosphorus	28-29	solute carrier family 2 member 4	Homo sapiens	191-196
25962562-9	2015	Following treatment with bisperoxopicolinatooxovanadate (BPV) or metformin in the insulin-resistant skeletal muscle cells, there was an increase in the rate of glucose uptake, an increase in GLUT4 expression and its translocation, a reduction in the expression of PTEN and p-PTEN, and a decrease in cell apoptosis compared with untreated insulin-resistant cells.	Phosphorus	28-29	insulin	Homo sapiens	338-345
26123121-0	2015	Fabrication of SnO2-SnO nanocomposites with p-n heterojunctions for the low-temperature sensing of NO2 gas.	Phosphorus	31-32	strawberry notch homolog 2	Homo sapiens	15-18
26020100-7	2015	Our results show that anti-RhoC particles used at a low N/P ratio of 2.5/1 suppressed RhoC protein levels by 100% and 90% in SUM149 and MDA-MB-231 cells, respectively.	Phosphorus	58-59	ras homolog family member C	Homo sapiens	27-31
26183217-6	2015	In the low dosage group, down-regulated apoptosis cytokine p53 is associated with EAE-P effect, but it is inflammatory cytokine TNF-alpha that is related to the effect of EAE-P in the high dosage group.	Phosphorus	86-87	Wistar clone pR53P1 p53 pseudogene	Rattus norvegicus	59-62
26020100-7	2015	Our results show that anti-RhoC particles used at a low N/P ratio of 2.5/1 suppressed RhoC protein levels by 100% and 90% in SUM149 and MDA-MB-231 cells, respectively.	Phosphorus	58-59	ras homolog family member C	Homo sapiens	86-90
25939510-6	2015	Taken together, our data suggest that CD5 defines a functionally distinct population of B cells in humans in the anti-caps-PS immune response.	Phosphorus	123-125	CD5 molecule	Homo sapiens	38-41
25701423-9	2015	When applied to full lipid extracts from rat primary cardiomyocytes treated with peroxynitrite donor SIN-1, ten PL-bound oxoLPP were unambiguously identified by LC-MS, including two PC-, two PE-, one PG-, two PS-, and three PA-derived species.	Phosphorus	209-211	MAPK associated protein 1	Homo sapiens	101-106
26394465-3	2015	In the Archean hydrothermal conditions under the action of the phosphorus chemical potential the C-H-O system was transformed into a four-component system C-H-O-P setting up a gluconeogenic system, which became the basis of power supply for a protometabolism, and formation of a new cycle of CO2 fixation (reductive pentose phosphate pathway).	Phosphorus	63-73	DNA damage inducible transcript 3	Homo sapiens	155-162
25663376-3	2015	Animal models have shown the WNT signaling pathway plays an important role in mid-facial development, and various genes in this pathway have been associated with nonsyndromic CL/P in previous studies.	Phosphorus	178-179	Wnt family member 5A	Homo sapiens	29-32
24980682-10	2015	SP and NKA levels were higher in the ceramic, composite and amalgam groups than those in the enamel group (p&amp;lt;0.05).	Phosphorus	107-109	tachykinin precursor 1	Homo sapiens	7-10
26119308-6	2015	An adverse effect on parathyroid hormone (PTH) secretion from high phosphorus intake was seen only when calcium intake was inadequate.	Phosphorus	67-77	parathyroid hormone	Homo sapiens	21-40
25813681-3	2015	RESULTS: In grafts collected after G+P mobilization, we observed a significantly higher proportion of c-kit(+)Sca-1(+) hematopoietic stem cells compared with G-CSF.	Phosphorus	37-38	KIT proto-oncogene receptor tyrosine kinase	Mus musculus	102-107
25560538-7	2015	PNC resulted in a significant decrease in the prevalence of hyperkalemia, hypophosphatemia and also showed amelioration in Ca/P ratio, nPCR and an increase in P of hyphosphatemic patients.	Phosphorus	0-1	nasopharyngeal carcinoma-related protein	Homo sapiens	135-139
26123194-7	2015	Various PIPs directly enhance TRPM3 activity in cell-free inside-out patches, with a potency order PI(3,4,5)P3 &gt; PI(3,5)P2 &gt; PI(4,5)P2   PI(3,4)P2 &gt;&gt; PI(4)P.	Phosphorus	8-9	transient receptor potential cation channel subfamily M member 3	Homo sapiens	30-35
25922494-5	2015	The altered root growth in response to P and Mg supply was correlated with AUX1, PIN2, and PIN3 mRNA abundance and expression and the accumulation of the protein.	Phosphorus	39-40	Transmembrane amino acid transporter family protein	Arabidopsis thaliana	75-79
25922494-5	2015	The altered root growth in response to P and Mg supply was correlated with AUX1, PIN2, and PIN3 mRNA abundance and expression and the accumulation of the protein.	Phosphorus	39-40	Auxin efflux carrier family protein	Arabidopsis thaliana	81-85
25922494-5	2015	The altered root growth in response to P and Mg supply was correlated with AUX1, PIN2, and PIN3 mRNA abundance and expression and the accumulation of the protein.	Phosphorus	39-40	Auxin efflux carrier family protein	Arabidopsis thaliana	91-95
26007739-0	2015	A Highly Sensitive Porous Silicon (P-Si)-Based Human Kallikrein 2 (hK2) Immunoassay Platform toward Accurate Diagnosis of Prostate Cancer.	Phosphorus	19-20	kallikrein related peptidase 2	Homo sapiens	53-65
25846005-2	2015	While Plk1 is a promising target for antitumor therapy, Plk2 is regarded as a tumor suppressor even though the two Plks commonly recognize the S-pS/T-P motif through their PBD.	Phosphorus	145-147	polo like kinase 2	Homo sapiens	56-60
26191512-4	2015	Parathyroid hormone (PTH) insufficiency was defined as a serum PTH level of &lt;60 pg/mL or a serum phosphorus level higher than the serum calcium level in the presence of hypocalcemia.	Phosphorus	100-110	parathyroid hormone	Homo sapiens	0-19
26191512-4	2015	Parathyroid hormone (PTH) insufficiency was defined as a serum PTH level of &lt;60 pg/mL or a serum phosphorus level higher than the serum calcium level in the presence of hypocalcemia.	Phosphorus	100-110	parathyroid hormone	Homo sapiens	21-24
26191512-10	2015	Intact PTH was negatively correlated with serum phosphorus levels.	Phosphorus	48-58	parathyroid hormone	Homo sapiens	7-10
25346528-11	2015	cS and pS increased from CT1 to ST8 showing construct validity (rs : +0.348 and +0.354, respectively; P &lt; .001).	Phosphorus	7-9	cardiotrophin 1	Homo sapiens	25-28
25346528-11	2015	cS and pS increased from CT1 to ST8 showing construct validity (rs : +0.348 and +0.354, respectively; P &lt; .001).	Phosphorus	7-9	Oncogene OVC (ovarian adenocarcinoma oncogene)	Homo sapiens	32-35
25924954-0	2015	Cleavage of a P-N Bond in a Urea-Containing (Ph2 P(R)PPh2 )-Bridged Dinuclear Gold(I) Thiolate Complex by Fluoride and a Mechanistic Insight.	Phosphorus	14-15	relaxin 2	Homo sapiens	45-57
26028746-3	2015	The application of phospholipase A (PLA) - assisted degumming process could further reduce the residual phosphorus content of camellia oil (6.84 mg/kg) to make the oil suitable for physical refining while maintaining the maximal oil yield (98.2 %).	Phosphorus	104-114	phospholipase A and acyltransferase 1	Homo sapiens	19-34
26028746-3	2015	The application of phospholipase A (PLA) - assisted degumming process could further reduce the residual phosphorus content of camellia oil (6.84 mg/kg) to make the oil suitable for physical refining while maintaining the maximal oil yield (98.2 %).	Phosphorus	104-114	phospholipase A and acyltransferase 1	Homo sapiens	36-39
26093727-9	2015	Serum Fetuin-A levels were positively correlated with blood urea nitrogen level (r = .241, P = .025) and serum creatinine level (r = .262, P = .014), whereas it was negatively correlated with serum phosphorus level (r = -.409, P &lt; .001).	Phosphorus	198-208	alpha 2-HS glycoprotein	Homo sapiens	6-14
26007739-0	2015	A Highly Sensitive Porous Silicon (P-Si)-Based Human Kallikrein 2 (hK2) Immunoassay Platform toward Accurate Diagnosis of Prostate Cancer.	Phosphorus	19-20	RBPJ pseudogene 3	Homo sapiens	67-70
25901899-1	2015	Phytase is a phosphohydrolase considered highly specific for the degradation of phytate to release bound phosphorus for animal consumption and aid in the reduction of environmental nutrient loading.	Phosphorus	105-115	phytase	Zea mays	0-7
25843793-8	2015	The further study indicated that NAD(P)H oxidase inhibitor DPI and NF-kappaB inhibitor PDTC reduced NE-induced mRNA and protein expression of IL-6 in U937 macrophages.	Phosphorus	36-38	interleukin 6	Homo sapiens	142-146
25710805-8	2015	Serum phosphorus levels were inversely associated with eGFR, and levels above the recommended targets were associated with a higher risk of graft failure independently of eGFR.	Phosphorus	6-16	epidermal growth factor receptor	Homo sapiens	55-59
25871630-1	2015	C-F bond cleavage by transient phosphorus(III)-based dications [RP(C(PPh3)2)](2+) (4a(2+), R = Ph; 4b(2+), R = 4-F-Ph) is reported.	Phosphorus	31-41	protein phosphatase 4 catalytic subunit	Homo sapiens	69-73
25364865-9	2015	The S:PS ratio showed a strong correlation with SD1 (R2=.95) and SS (r=.87, R2=.88).	Phosphorus	6-8	CUP2Q35	Homo sapiens	48-51
25404658-0	2015	Gastrointestinal Inhibition of Sodium-Hydrogen Exchanger 3 Reduces Phosphorus Absorption and Protects against Vascular Calcification in CKD.	Phosphorus	67-77	solute carrier family 9 member A3	Rattus norvegicus	31-58
25155265-8	2015	For the haplotype CGT, a statistically difference was identified between the CL/P group and controls (P = 0.04).	Phosphorus	80-81	UDP glycosyltransferase 8	Homo sapiens	18-21
25051330-2	2015	Previously, we showed that a phosphorous-based dendrimer capped with anionic AzaBisPhosphonate groups (so-called ABP dendrimer) has immunomodulatory and anti-inflammatory properties toward the human immune system.	Phosphorus	29-40	amine oxidase copper containing 1	Homo sapiens	113-116
25600998-12	2015	Taken together, these results indicate that root uptake of arsenate is probably not via sulfate transporters, but the poor growth of the double mutant of sultr1;1 and sultr1;2 was due to its poor sulfate status and decreased levels of thiols, which had pleiotropic effects on the root uptake and translocation of potassium and phosphorus and arsenic tolerance.	Phosphorus	327-337	sulfate transporter 1;1	Arabidopsis thaliana	154-175
25048220-1	2015	Transgenic soybean plants overexpressing the Arabidopsis purple acid phosphatase gene AtPAP15 (OXp) or the soybean expansin gene GmEXPB2 (OXe) can improve phosphorous (P) efficiency in pure culture by increasing Apase secretion or changing root morphology.	Phosphorus	155-166	purple acid phosphatase 15	Arabidopsis thaliana	86-93
25048220-1	2015	Transgenic soybean plants overexpressing the Arabidopsis purple acid phosphatase gene AtPAP15 (OXp) or the soybean expansin gene GmEXPB2 (OXe) can improve phosphorous (P) efficiency in pure culture by increasing Apase secretion or changing root morphology.	Phosphorus	155-166	expansin 1	Glycine max	115-123
25404658-4	2015	Oral administration of tenapanor or other intestinal sodium-hydrogen exchanger 3 inhibitors increased fecal phosphorus, decreased urine phosphorus excretion, and reduced [(33)P]orthophosphate uptake in rats.	Phosphorus	108-118	solute carrier family 9 member A3	Rattus norvegicus	53-80
25797523-2	2015	By an in-tandem technique using an ultra-sharp tungsten probe as the nanomanipulator and an optical fiber as the optical waveguide the nanoscale CdS/p-Si axial nanowire junctions were fabricated, and in situ photocurrents from them were successfully measured.	Phosphorus	45-46	CDP-diacylglycerol synthase 1	Homo sapiens	145-148
25585525-9	2015	The serum alanine transaminase (ALT) and aspartate aminotransferase (AST) levels on postoperative days 1 and 3 were significantly higher in the PS group than in the AL group.	Phosphorus	144-146	solute carrier family 17 member 5	Homo sapiens	41-67
25585525-9	2015	The serum alanine transaminase (ALT) and aspartate aminotransferase (AST) levels on postoperative days 1 and 3 were significantly higher in the PS group than in the AL group.	Phosphorus	144-146	solute carrier family 17 member 5	Homo sapiens	69-72
25797523-3	2015	Compared to a single constituting nanowire, the CdS/p-Si axial nanowire junctions possess a photocurrent saturation effect, which protects them from damage under high voltages.	Phosphorus	3-4	CDP-diacylglycerol synthase 1	Homo sapiens	48-51
25897359-10	2015	However, the o-Tyr/p-Tyr ratio was an independent determinant of EPO-resistance indices in our human study.	Phosphorus	19-20	erythropoietin	Homo sapiens	65-68
26131269-9	2015	Compared with IR group, mRNA expression of MAP2K3 and Bax were significantly decreased with Bcl-2 was significantly increased in IR+P+S group (P&lt;0.05).	Phosphorus	132-134	BCL2 associated X, apoptosis regulator	Rattus norvegicus	54-57
26131269-9	2015	Compared with IR group, mRNA expression of MAP2K3 and Bax were significantly decreased with Bcl-2 was significantly increased in IR+P+S group (P&lt;0.05).	Phosphorus	132-134	BCL2, apoptosis regulator	Rattus norvegicus	92-97
25680792-0	2015	The transcription factor PHR1 regulates lipid remodeling and triacylglycerol accumulation in Arabidopsis thaliana during phosphorus starvation.	Phosphorus	121-131	photolyase 1	Arabidopsis thaliana	25-29
25880550-14	2015	In the majority of participants, increased CSF p-tau levels were associated with current neurocognitive impairment.	Phosphorus	19-20	microtubule associated protein tau	Homo sapiens	49-52
25318838-7	2015	After adjusting for age, gender, waist circumference, body mass index, smoking status, exercise, diabetes, hypertension, lipid profiles, and renal function, serum Cac , phosphorus, and Cac -phosphorus products were independent risk factors for fatty liver (odds ratio [OR]: 1.71, 95% confidence interval [CI]: 1.49-1.95, P &lt; 0.001; OR: 1.34, 95% CI: 1.22-1.48, P &lt; 0.001; and OR: 1.20, 95% CI: 1.14-1.26, P &lt; 0.001, respectively), and the risk of fatty liver increased in a graded manner over the quartiles.	Phosphorus	190-200	carbonic anhydrase 2	Homo sapiens	185-188
25772403-6	2015	Experimentally, 1:1 P-bonded PCl3-CH3OH adduct in nitrogen matrix was identified, where shifts in the P-Cl modes of PCl3, O-C, and O-H modes of CH3OH submolecules were observed.	Phosphorus	20-21	PHD finger protein 19	Homo sapiens	29-33
25772403-6	2015	Experimentally, 1:1 P-bonded PCl3-CH3OH adduct in nitrogen matrix was identified, where shifts in the P-Cl modes of PCl3, O-C, and O-H modes of CH3OH submolecules were observed.	Phosphorus	20-21	PHD finger protein 19	Homo sapiens	116-120
25677339-6	2015	Furthermore, the siRNA-PLGA/CSO micelles showed that the efficiencies of cellular uptake and STAT3 gene silencing gradually increased with increasing N/P ratios.	Phosphorus	23-24	signal transducer and activator of transcription 3	Homo sapiens	93-98
25446885-4	2015	The increases in calcium and phosphorus retention required for enhanced bone mineral accretion are brought about by changes in the vitamin D endocrine system, parathyroid hormone (PTH) and fibroblast growth factor-23 (FGF-23).	Phosphorus	29-39	fibroblast growth factor 23	Mus musculus	218-224
25446885-5	2015	Thus, in Sost knockout mice, concentrations of serum 1,25-dihydroxyvitamin D (1,25(OH)2D) are increased and concentrations of FGF-23 are decreased thereby allowing a positive calcium and phosphorus balance.	Phosphorus	187-197	sclerostin	Mus musculus	9-13
25446885-7	2015	Adaptations in vitamin D, PTH and FGF-23 physiology occur in the absence of sclerostin expression and mediate increased calcium and phosphorus retention required for the increase in bone mineralization.	Phosphorus	132-142	parathyroid hormone	Mus musculus	26-29
25446885-7	2015	Adaptations in vitamin D, PTH and FGF-23 physiology occur in the absence of sclerostin expression and mediate increased calcium and phosphorus retention required for the increase in bone mineralization.	Phosphorus	132-142	fibroblast growth factor 23	Mus musculus	34-40
26338395-3	2015	New factors and hormones have been identified, such as Klotho and fibroblast growth factor-23 (FGF-23) that interact with vitamin D and the parathyroid hormone in the renal management of calcium and phosphorus.	Phosphorus	199-209	klotho	Homo sapiens	55-61
26338395-3	2015	New factors and hormones have been identified, such as Klotho and fibroblast growth factor-23 (FGF-23) that interact with vitamin D and the parathyroid hormone in the renal management of calcium and phosphorus.	Phosphorus	199-209	fibroblast growth factor 23	Homo sapiens	66-93
26338395-3	2015	New factors and hormones have been identified, such as Klotho and fibroblast growth factor-23 (FGF-23) that interact with vitamin D and the parathyroid hormone in the renal management of calcium and phosphorus.	Phosphorus	199-209	fibroblast growth factor 23	Homo sapiens	95-101
25770497-3	2015	The kinetics of the FBN adsorption varies from a single-component Langmuir model on homogeneous hydrophilic PHEMA to a two-stage spreading relaxation model on homogeneous hydrophobic PS surface.	Phosphorus	183-185	fibrinogen beta chain	Homo sapiens	20-23
25770497-4	2015	On a heterogeneous PS-b-PHEMA surface with majority PS part, the initial FBN adsorption rate remains the same as that on the homogeneous PS surface.	Phosphorus	19-21	fibrinogen beta chain	Homo sapiens	73-76
25446885-2	2015	We review the mechanisms by which Sost knockout mice are able to accrete increased amounts of calcium and phosphorus required for the maintenance of a high bone mass.	Phosphorus	106-116	sclerostin	Mus musculus	34-38
25446885-4	2015	The increases in calcium and phosphorus retention required for enhanced bone mineral accretion are brought about by changes in the vitamin D endocrine system, parathyroid hormone (PTH) and fibroblast growth factor-23 (FGF-23).	Phosphorus	29-39	parathyroid hormone	Mus musculus	159-178
25446885-4	2015	The increases in calcium and phosphorus retention required for enhanced bone mineral accretion are brought about by changes in the vitamin D endocrine system, parathyroid hormone (PTH) and fibroblast growth factor-23 (FGF-23).	Phosphorus	29-39	parathyroid hormone	Mus musculus	180-183
25446885-4	2015	The increases in calcium and phosphorus retention required for enhanced bone mineral accretion are brought about by changes in the vitamin D endocrine system, parathyroid hormone (PTH) and fibroblast growth factor-23 (FGF-23).	Phosphorus	29-39	fibroblast growth factor 23	Mus musculus	189-216
25948212-10	2015	CONCLUSION: The reaction between PS on the MP and the PSR of HUVECs plays an important role in the internalization of MSC-MPs.	Phosphorus	33-35	jumonji domain containing 6, arginine demethylase and lysine hydroxylase	Homo sapiens	54-57
25730146-3	2015	The temperature dependent Raman spectroscopy experiments were carried out on a few-layer black phosphorus sample, which depicts softening of Ag(1), B2g, and Ag(2) modes as temperature increases from 77 to 673 K. The calculated temperature coefficients for Ag(1), B2g, and Ag(2) modes of the few-layer black phosphorus nanosheet sample were observed to be -0.01, -0.013, and -0.014 cm(-1) K(-1), respectively.	Phosphorus	95-105	NBPF member 10	Homo sapiens	141-146
25730146-3	2015	The temperature dependent Raman spectroscopy experiments were carried out on a few-layer black phosphorus sample, which depicts softening of Ag(1), B2g, and Ag(2) modes as temperature increases from 77 to 673 K. The calculated temperature coefficients for Ag(1), B2g, and Ag(2) modes of the few-layer black phosphorus nanosheet sample were observed to be -0.01, -0.013, and -0.014 cm(-1) K(-1), respectively.	Phosphorus	95-105	anterior gradient 2, protein disulphide isomerase family member	Homo sapiens	157-162
25730146-3	2015	The temperature dependent Raman spectroscopy experiments were carried out on a few-layer black phosphorus sample, which depicts softening of Ag(1), B2g, and Ag(2) modes as temperature increases from 77 to 673 K. The calculated temperature coefficients for Ag(1), B2g, and Ag(2) modes of the few-layer black phosphorus nanosheet sample were observed to be -0.01, -0.013, and -0.014 cm(-1) K(-1), respectively.	Phosphorus	95-105	NBPF member 10	Homo sapiens	256-261
25730146-3	2015	The temperature dependent Raman spectroscopy experiments were carried out on a few-layer black phosphorus sample, which depicts softening of Ag(1), B2g, and Ag(2) modes as temperature increases from 77 to 673 K. The calculated temperature coefficients for Ag(1), B2g, and Ag(2) modes of the few-layer black phosphorus nanosheet sample were observed to be -0.01, -0.013, and -0.014 cm(-1) K(-1), respectively.	Phosphorus	95-105	anterior gradient 2, protein disulphide isomerase family member	Homo sapiens	272-277
25853057-3	2015	Mutations in the gene for the interferon regulatory factor 6 (IRF6) cause a hereditary dominant malformation syndrome including CL/P, and polymorphisms are associated with non-syndromic CL/P (MIM 119530).	Phosphorus	131-132	interferon regulatory factor 6	Homo sapiens	30-60
25853057-3	2015	Mutations in the gene for the interferon regulatory factor 6 (IRF6) cause a hereditary dominant malformation syndrome including CL/P, and polymorphisms are associated with non-syndromic CL/P (MIM 119530).	Phosphorus	131-132	interferon regulatory factor 6	Homo sapiens	62-66
31245436-7	2015	Immunochemical analysis demonstrated that the amount of interleukin-6 (IL-6), a cytokine known to trigger osteoclast formation, was significantly reduced in the maternal milk of mice fed the low-phosphorus diet.	Phosphorus	195-205	interleukin 6	Mus musculus	56-69
24832558-6	2015	An increase in vtg production in whole body homogenate was observed in fish exposed to 0.2 and 2.0 microg l(-1) p,p"-DDE.	Phosphorus	19-20	vitellogenin	Danio rerio	15-18
25561469-2	2015	CDK9, as part of P-TEFb and the super elongation complex (SEC), is by far the best characterized of CDK9, CDK12, and CDK13.	Phosphorus	17-18	cyclin dependent kinase 9	Homo sapiens	0-4
25604963-5	2015	IR nu(CO) data support modest attenuation of PhBP3 donor ability at phosphorus upon eta(6)-phenyl substituent binding, representing a new inductive strategy for tuning tris(phosphino)phenylborate donation at the kappa(3)-phosphine-bound metal fragment.	Phosphorus	68-78	PHB1 pseudogene 3	Homo sapiens	45-50
25611334-2	2015	We found that Raman intensities of Ag(1), B2g, and Ag(2) modes of BP not only depend on the polarization angle alpha, but also relate to the sample rotation angle theta.	Phosphorus	66-68	NBPF member 10	Homo sapiens	35-40
25611334-2	2015	We found that Raman intensities of Ag(1), B2g, and Ag(2) modes of BP not only depend on the polarization angle alpha, but also relate to the sample rotation angle theta.	Phosphorus	66-68	anterior gradient 2, protein disulphide isomerase family member	Homo sapiens	51-56
31245436-7	2015	Immunochemical analysis demonstrated that the amount of interleukin-6 (IL-6), a cytokine known to trigger osteoclast formation, was significantly reduced in the maternal milk of mice fed the low-phosphorus diet.	Phosphorus	195-205	interleukin 6	Mus musculus	71-75
25674023-5	2015	PTH positively correlated with the duration of dialysis, serum phosphorus level, presence of calcific deposit, and increased thickness of the Achilles tendon.	Phosphorus	63-73	parathyroid hormone	Homo sapiens	0-3
25604868-3	2015	The best sensor for the assay of CEA was the one based on P/graphite (the limit of determination was 16 fg/ml and sensitivity was 2.32 x 10(7)  s mg(-1)  ml), while for the assay of NSE the, best sensor was the one based on P/graphene (the limit of determination was 7.45 pg/ml and sensitivity was 2.49 x 10(8)  s mg(-1)  ml).	Phosphorus	58-59	CEA cell adhesion molecule 3	Homo sapiens	33-36
26031087-4	2015	Anoxic phosphorus uptake rate decreased with added COD.	Phosphorus	7-17	small nuclear ribonucleoprotein polypeptides B and B1	Homo sapiens	51-54
24939836-5	2015	Furthermore, blood calcium and phosphorus homeostasis is maintained by an interplay between feedback loops of the 1,25(OH)2D/VDR system with parathyroid hormone and with fibroblast-growth factor (FGF) 23 respectively.	Phosphorus	31-41	vitamin D receptor	Homo sapiens	125-128
24939836-5	2015	Furthermore, blood calcium and phosphorus homeostasis is maintained by an interplay between feedback loops of the 1,25(OH)2D/VDR system with parathyroid hormone and with fibroblast-growth factor (FGF) 23 respectively.	Phosphorus	31-41	fibroblast growth factor 23	Homo sapiens	170-203
25604868-3	2015	The best sensor for the assay of CEA was the one based on P/graphite (the limit of determination was 16 fg/ml and sensitivity was 2.32 x 10(7)  s mg(-1)  ml), while for the assay of NSE the, best sensor was the one based on P/graphene (the limit of determination was 7.45 pg/ml and sensitivity was 2.49 x 10(8)  s mg(-1)  ml).	Phosphorus	58-59	enolase 2	Homo sapiens	182-185
25604868-4	2015	The sensor of choice for simultaneous detection of NSE and CEA is the one based on P/graphene because we need high sensitivity and low limit of determination for NSE.	Phosphorus	83-84	enolase 2	Homo sapiens	51-54
25604868-4	2015	The sensor of choice for simultaneous detection of NSE and CEA is the one based on P/graphene because we need high sensitivity and low limit of determination for NSE.	Phosphorus	83-84	CEA cell adhesion molecule 3	Homo sapiens	59-62
25604868-4	2015	The sensor of choice for simultaneous detection of NSE and CEA is the one based on P/graphene because we need high sensitivity and low limit of determination for NSE.	Phosphorus	83-84	enolase 2	Homo sapiens	162-165
25563643-1	2015	BACKGROUND AND PURPOSE: Fibroblast growth factor 23 (FGF23) is a hormone that regulates phosphorus and vitamin D metabolism.	Phosphorus	88-98	fibroblast growth factor 23	Homo sapiens	24-51
25563643-1	2015	BACKGROUND AND PURPOSE: Fibroblast growth factor 23 (FGF23) is a hormone that regulates phosphorus and vitamin D metabolism.	Phosphorus	88-98	fibroblast growth factor 23	Homo sapiens	53-58
25563643-6	2015	RESULTS: In multivariable-adjusted models, higher calcium and phosphorus concentrations, lower estimated glomerular filtration rate and higher urine albumin excretion were independently associated with higher FGF23.	Phosphorus	62-72	fibroblast growth factor 23	Homo sapiens	209-214
25277363-3	2015	The silver nanoparticles (nAg) were then decorated with covalently bound PS-SH macromolecules to improve the phase miscibility in the PS-Br-PVME blends.	Phosphorus	73-75	NBAS subunit of NRZ tethering complex	Homo sapiens	26-29
25277363-7	2015	Although the matrix and the grafted molecular weights were similar, PS-g-nAg particles were expelled from the PS phase and were localized in the PVME phase of the blends.	Phosphorus	68-70	NBAS subunit of NRZ tethering complex	Homo sapiens	73-76
26714388-10	2015	The nPCR correlated directly with albumin (r = 0.34, p = 0.012), magnesium (r = 0.48, p &lt; 0.0001), phosphorus (r = 0.42, p = 0.02), and the phase angle body composition parameter (r = 0.26, p = 0.049).	Phosphorus	102-112	nasopharyngeal carcinoma-related protein	Homo sapiens	4-8
25376759-5	2015	In contrast, with the N-phenylated ligands PNP(Ph)-Et and PNP(Ph)-nPr, despite small Et and nPr substituents at the phosphorus sites, complexes [Fe(kappa(3)-P,N,P-PNP(Ph)-Et)Cl2] and [Fe(kappa(3)-P,N,P-PNP(Ph)-nPr)Cl2] were formed, revealing that sterics can be also controlled by substituent variations at the amino N-sites.	Phosphorus	116-126	neuronal pentraxin receptor	Homo sapiens	66-69
25634106-0	2015	High phosphorus level leads to aortic calcification via beta-catenin in chronic kidney disease.	Phosphorus	5-15	catenin beta 1	Rattus norvegicus	56-68
26287973-11	2015	CONCLUSIONS: Aberrant phosphorus homeostasis, reflected by higher phosphorus and FGF23, may be a risk factor for mortality in patients initiating hemodialysis, particularly among African Americans.	Phosphorus	22-32	fibroblast growth factor 23	Homo sapiens	81-86
26288017-0	2015	Why Is the Association of Phosphorus and FGF23 with Mortality Stronger in African-American Hemodialysis Patients.	Phosphorus	26-36	fibroblast growth factor 23	Homo sapiens	41-46
26693712-1	2015	BACKGROUND: Fibroblast growth factor 23 (FGF23) is a phosphaturic hormone implicated in disorders of serum phosphorus concentration and vitamin D.	Phosphorus	107-117	fibroblast growth factor 23	Homo sapiens	12-39
26693712-1	2015	BACKGROUND: Fibroblast growth factor 23 (FGF23) is a phosphaturic hormone implicated in disorders of serum phosphorus concentration and vitamin D.	Phosphorus	107-117	fibroblast growth factor 23	Homo sapiens	41-46
25634106-14	2015	CONCLUSION: These results suggest that beta-catenin is an important player in high phosphorus level-induced aortic calcification in CKD.	Phosphorus	83-93	catenin beta 1	Rattus norvegicus	39-51
25864030-0	2015	A modified BAF system configuring synergistic denitrification and chemical phosphorus precipitation: Examination on pollutants removal and clogging development.	Phosphorus	75-85	BAF nuclear assembly factor 1	Homo sapiens	11-14
24437584-3	2015	The aim of this study was to evaluate the association between polymorphisms in WNT3 and WNT9B genes and CL/P in Brazilian families.	Phosphorus	107-108	Wnt family member 3	Homo sapiens	79-83
26649223-12	2015	Serum cTnI level significantly correlated with oxygen saturation (SpO2), ejection fraction (EF), Qp/Qs, and Pp/Ps ratios.	Phosphorus	111-113	troponin I3, cardiac type	Homo sapiens	6-10
24437584-3	2015	The aim of this study was to evaluate the association between polymorphisms in WNT3 and WNT9B genes and CL/P in Brazilian families.	Phosphorus	107-108	Wnt family member 9B	Homo sapiens	88-93
25676620-8	2015	Reduced association of A-PS particles in RAW264.7 cells following pre-incubation of SP-A was also observed with coherent anti-Stokes Raman spectroscopy.	Phosphorus	25-27	surfactant associated protein A1	Mus musculus	84-88
27149811-8	2015	All of them were followed up during 1 year Standard clinical and laboratory examination was supplemented by the measurement of the parathyroid hormone (PTH), Ca and P levels.	Phosphorus	152-153	parathyroid hormone	Homo sapiens	131-150
32262008-4	2014	FBP can control the morphology of calcium carbonate and provide the phosphorus source for the formation of CHA.	Phosphorus	68-78	fructose-bisphosphatase 1	Homo sapiens	0-3
26281189-10	2015	As CKD progressed, the serum concentrations of Klotho and sclerostin were inversely correlated with the levels of phosphorus and parathyroid hormone.	Phosphorus	114-124	klotho	Homo sapiens	47-53
24894834-0	2015	Identification of primary and secondary metabolites with phosphorus status-dependent abundance in Arabidopsis, and of the transcription factor PHR1 as a major regulator of metabolic changes during phosphorus limitation.	Phosphorus	197-207	photolyase 1	Arabidopsis thaliana	143-147
25182220-7	2014	Consistent with the in vitro results, we observed the formation of a homogeneous dentin bridge and the expression of odontogenic (dentin sialoprotein, dentin matrix protein 1) and focal adhesion molecules (Vinculin, p-Paxillin) at the injury site of pulp repair model by iRoot BP Plus.	Phosphorus	105-106	dentin sialophosphoprotein	Homo sapiens	130-149
25182220-7	2014	Consistent with the in vitro results, we observed the formation of a homogeneous dentin bridge and the expression of odontogenic (dentin sialoprotein, dentin matrix protein 1) and focal adhesion molecules (Vinculin, p-Paxillin) at the injury site of pulp repair model by iRoot BP Plus.	Phosphorus	105-106	dentin matrix acidic phosphoprotein 1	Homo sapiens	151-174
25433991-4	2014	Mechanism studies revealed that Cd(II) affected the transformations of intracellular PHAs and glycogen, and the activities of oxidoreductase and polyphosphate kinase, resulted in the decrease of nitrite oxidizing bacteria and polyphosphate accumulating organisms abundance, which might be the major reason for the negative effects of long-term exposure to 10 mg L(-1) Cd(II) on biological nitrogen and phosphorus removal.	Phosphorus	402-412	thioredoxin reductase 1	Homo sapiens	126-140
25428623-5	2014	Upon inactivation of AtPHT1;9, changes in the transcript profiles of several genes that respond to plant phosphorus (P) status indicated a possible role in the regulation of systemic signaling of P status within the plant.	Phosphorus	105-115	phosphate transporter 1;9	Arabidopsis thaliana	21-29
24578219-0	2014	Dietary phosphorus restriction by a standard low-protein diet decreased serum fibroblast growth factor 23 levels in patients with early and advanced stage chronic kidney disease.	Phosphorus	8-18	fibroblast growth factor 23	Homo sapiens	78-105
24578219-2	2014	Although recent studies demonstrated that FGF23 levels decreased in response to dietary restriction of phosphorus and/or use of phosphate binders, research on the effects of a standard low-protein diet is lacking.	Phosphorus	103-113	fibroblast growth factor 23	Homo sapiens	42-47
24578219-5	2014	Changes in FGF23 levels correlated with changes in 24 h urinary phosphorus excretion in the advanced CKD group.	Phosphorus	64-74	fibroblast growth factor 23	Homo sapiens	11-16
25132581-9	2014	Univariate analysis showed significant correlations of serum phosphorus with TMP/GFR, alkaline phosphatase, age, lactate dehydrogenase (LDH), and log intact FGF23.	Phosphorus	61-71	fibroblast growth factor 23	Homo sapiens	157-162
25132581-12	2014	CONCLUSION: The elevated serum phosphorus concentrations with simultaneously increased TMP/GFR and elevated FGF23 levels collectively suggest that patients with SCD display proximal tubular resistance to the action of FGF23 before any decline in GFR.	Phosphorus	31-41	fibroblast growth factor 23	Homo sapiens	218-223
25262405-1	2014	The aim of the paper was to evaluate 23 catchment factors that determine total phosphorus and total nitrogen load to the Baltic Sea.	Phosphorus	79-89	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	128-131
25147979-9	2014	Unexpectedly, the low-Ca-P diet attenuated the 5% casein diet-related reduction of serum IGF-1 and Ghr hepatic gene expression, as well as the low-protein diet-induced decrease in bone mass and strength.	Phosphorus	25-26	insulin-like growth factor 1	Rattus norvegicus	89-94
25174878-0	2014	Dietary phosphorus overload aggravates the phenotype of the dystrophin-deficient mdx mouse.	Phosphorus	8-18	dystrophin, muscular dystrophy	Mus musculus	60-70
25147979-9	2014	Unexpectedly, the low-Ca-P diet attenuated the 5% casein diet-related reduction of serum IGF-1 and Ghr hepatic gene expression, as well as the low-protein diet-induced decrease in bone mass and strength.	Phosphorus	25-26	growth hormone receptor	Rattus norvegicus	99-102
25147979-13	2014	These results suggest that hormonal modulation in response to a low-Ca-P diet may modify the low-protein diet-induced effect on Ghr hepatic mRNA levels and consequently the impact of low protein intakes on IGF-1 circulating levels and skeletal growth.	Phosphorus	71-72	growth hormone receptor	Rattus norvegicus	128-131
25878777-10	2014	The log-FGF23 strongly correlated with calcium levels at Months 1, 6 and 12, however, this relationship was blunted if serum phosphorus was &gt;6 mg/dL.	Phosphorus	125-135	fibroblast growth factor 23	Homo sapiens	8-13
25147979-13	2014	These results suggest that hormonal modulation in response to a low-Ca-P diet may modify the low-protein diet-induced effect on Ghr hepatic mRNA levels and consequently the impact of low protein intakes on IGF-1 circulating levels and skeletal growth.	Phosphorus	71-72	insulin-like growth factor 1	Rattus norvegicus	206-211
25443545-2	2014	Lisa Gutekunst, MSEd, RD, CSR, CDN, Chair of the National Kidney Foundation Council on Renal Nutrition, lobbied the FDA to add phosphorus to the Nutrition Facts Label.	Phosphorus	127-137	5', 3'-nucleotidase, cytosolic	Homo sapiens	31-34
25453654-1	2014	The Klotho protein, whose gene has predominant renal expression, acts in the control of serum phosphorus and 1,25-dihydroxyvitamin D3 and regulates the function of ion channels.	Phosphorus	94-104	klotho	Homo sapiens	4-10
25379382-0	2014	Contribution of protein phosphorylation to binding-induced folding of the SLBP-histone mRNA complex probed by phosphorus-31 NMR.	Phosphorus	110-120	stem-loop binding protein	Homo sapiens	74-78
25065802-0	2014	Fate of phosphorus in diluted urine with tap water.	Phosphorus	8-18	nuclear RNA export factor 1	Homo sapiens	41-44
25344353-7	2014	3) Serum phosphorus level positively correlated with cTnT, MYO, and BNP in CKD patients (p&lt;0.001).	Phosphorus	9-19	troponin T2, cardiac type	Homo sapiens	53-57
25344353-7	2014	3) Serum phosphorus level positively correlated with cTnT, MYO, and BNP in CKD patients (p&lt;0.001).	Phosphorus	9-19	myoglobin	Homo sapiens	59-62
25344353-7	2014	3) Serum phosphorus level positively correlated with cTnT, MYO, and BNP in CKD patients (p&lt;0.001).	Phosphorus	9-19	natriuretic peptide B	Homo sapiens	68-71
24935232-9	2014	In multivariable-adjusted Cox regression models, the highest quartile of serum phosphorus was associated with increased mortality in participants fasting 12 or more hours (adjusted HR, 1.74; 95% CI, 1.38-2.20; reference, lowest quartile) but not in participants fasting less than 12 hours (adjusted HR, 1.08; 95% CI, 0.89-1.32; P for interaction = 0.002).	Phosphorus	79-89	cytochrome c oxidase subunit 8A	Homo sapiens	26-29
25319440-6	2014	In the stratified analysis, patients with combined higher ALP (&gt;150 U/L) and hyperphosphatemia (&gt;7.0 mg/dL) had the greatest mortality risk (aHR: 2.25 [95% CI: 1.69-2.98] compared to the lowest HR group (ALP &lt;= 60 U/L and 4 mg/dL &lt;= phosphorus&lt;5 mg/dL).	Phosphorus	245-255	alkaline phosphatase, placental	Homo sapiens	58-61
25051439-10	2014	The stabilized Fgf23 ADHR allele reversed the Galnt3-null phenotype and normalized total Fgf23, serum phosphorus, and bone Fgf23 mRNA.	Phosphorus	102-112	fibroblast growth factor 23	Mus musculus	15-20
25051439-13	2014	Furthermore, the more stable Fgf23 ADHR mutant protein could normalize serum phosphorus in Galnt3 knockout mice.	Phosphorus	77-87	fibroblast growth factor 23	Mus musculus	29-34
25490830-3	2014	Afterward, CS, which exhibited five different molecular weights and deacetylation degrees, was complexed with pIRES2-EGFP-hBMP2-His to form CS/pIRES2-EGFP-hBMP2-His nanoparticles; in this procedure, a desolvent method was used at different N/P ratios (amino in CS to phospho in plasmid DNA).	Phosphorus	120-121	bone morphogenetic protein 2	Homo sapiens	122-127
25490830-3	2014	Afterward, CS, which exhibited five different molecular weights and deacetylation degrees, was complexed with pIRES2-EGFP-hBMP2-His to form CS/pIRES2-EGFP-hBMP2-His nanoparticles; in this procedure, a desolvent method was used at different N/P ratios (amino in CS to phospho in plasmid DNA).	Phosphorus	120-121	bone morphogenetic protein 2	Homo sapiens	155-160
25308005-4	2014	Preoperative laboratory testing [serum Ca and P, creatinine and parathormone levels (PTH)] which led to the diagnosis of P-HPT had been performed, the size and weight of the parathyroid glands measured, and postoperative serum PTH levels determined.	Phosphorus	0-1	parathyroid hormone	Homo sapiens	85-88
25705415-9	2014	Treatment of rats with lung injury with rhsTM (HV/TM) significantly attenuated the decrease in PaO2 and the increase in both mPAP and Pp/Ps, which was associated with a decrease in the lung protein permeability.	Phosphorus	137-139	thrombomodulin	Rattus norvegicus	43-45
25319440-7	2014	Although the effect of hyperphosphatemia on mortality seemed stronger in higher ALP levels, the interaction was not statistically significant (P=0.22).The association between serum phosphorus levels and mortality was not limited to higher ALP levels.	Phosphorus	181-191	alkaline phosphatase, placental	Homo sapiens	80-83
25319440-7	2014	Although the effect of hyperphosphatemia on mortality seemed stronger in higher ALP levels, the interaction was not statistically significant (P=0.22).The association between serum phosphorus levels and mortality was not limited to higher ALP levels.	Phosphorus	181-191	alkaline phosphatase, placental	Homo sapiens	239-242
25319440-9	2014	While considering the joint effect of ALP and hyperphosphatemia on mortality, the optimal phosphorus range should be stricter.	Phosphorus	90-100	alkaline phosphatase, placental	Homo sapiens	38-41
25147051-3	2014	Whereas Mes*N PCl (Mes*=2,4,6-tri-tert-butylphenyl) is stable in the solid state and in solution, the formal phosphorus congener Mes*P PCl is highly reactive and could not be observed.	Phosphorus	109-119	PHD finger protein 1	Homo sapiens	135-138
24674095-1	2014	Fibroblast growth factor 23 (FGF23) levels in dialysis patients are influenced by various factors, including phosphorus load.	Phosphorus	109-119	fibroblast growth factor 23	Homo sapiens	0-27
24674095-1	2014	Fibroblast growth factor 23 (FGF23) levels in dialysis patients are influenced by various factors, including phosphorus load.	Phosphorus	109-119	fibroblast growth factor 23	Homo sapiens	29-34
23647316-10	2014	FGF23 increased 50% with a positive correlation with the indexes of metabolic effort and, consequently, phosphorous decreased, although only in the first half.	Phosphorus	104-115	fibroblast growth factor 23	Homo sapiens	0-5
25205440-3	2014	Here, taking a phosphorus donor electron spin in a (29)Si nuclear spin bath as our model system, we discover both theoretically and experimentally that many-body correlations in nanoscale nuclear spin baths produce identifiable signatures in decoherence of the central spin under multiple-pulse dynamical decoupling control.	Phosphorus	15-25	spindlin 1	Homo sapiens	41-45
25205440-3	2014	Here, taking a phosphorus donor electron spin in a (29)Si nuclear spin bath as our model system, we discover both theoretically and experimentally that many-body correlations in nanoscale nuclear spin baths produce identifiable signatures in decoherence of the central spin under multiple-pulse dynamical decoupling control.	Phosphorus	15-25	spindlin 1	Homo sapiens	66-70
25205440-3	2014	Here, taking a phosphorus donor electron spin in a (29)Si nuclear spin bath as our model system, we discover both theoretically and experimentally that many-body correlations in nanoscale nuclear spin baths produce identifiable signatures in decoherence of the central spin under multiple-pulse dynamical decoupling control.	Phosphorus	15-25	spindlin 1	Homo sapiens	66-70
25205440-3	2014	Here, taking a phosphorus donor electron spin in a (29)Si nuclear spin bath as our model system, we discover both theoretically and experimentally that many-body correlations in nanoscale nuclear spin baths produce identifiable signatures in decoherence of the central spin under multiple-pulse dynamical decoupling control.	Phosphorus	15-25	spindlin 1	Homo sapiens	66-70
24692172-7	2014	However, regardless of the dietary phosphate contents, serum phosphorus levels were consistently elevated in Galnt3 knockout mice.	Phosphorus	61-71	polypeptide N-acetylgalactosaminyltransferase 3	Mus musculus	109-115
25054229-11	2014	CONCLUSIONS: B[alpha]P demonstrates inhibitory action on LSR and LDL-R, as well as ABCA1, which we propose leads to modified lipid status in B[alpha]P-treated mice, thus providing new insight into mechanisms underlying the involvement of pollutants in the disruption of lipid homeostasis, potentially contributing to dyslipidemia associated with obesity.	Phosphorus	20-22	lipolysis stimulated lipoprotein receptor	Mus musculus	57-60
25242761-7	2014	Multivariate analysis showed that Sclerostin levels were significantly positively correlated with serum phosphorus levels (P=.008) and inversely correlated with renal function (P=.026).	Phosphorus	104-114	sclerostin	Homo sapiens	34-44
24852682-8	2014	RESULTS: We found a significant biomarker interaction between CSF Abeta and CSF p-tau levels affecting brain structure.	Phosphorus	80-81	amyloid beta precursor protein	Homo sapiens	66-71
24373102-4	2014	Expression of an inorganic phosphate transporter (PTA3) was enriched ~10-fold under phosphorus-deficient conditions relative to a phosphorus-replete control, and this signal was rapidly lost upon phosphate resupply.	Phosphorus	84-94	PTA3	Aureococcus anophagefferens	50-54
25518667-11	2014	Thus, the contributions of the ABR and the MBR were intensified, guaranteeing the efficiency of nitrogen and phosphorus removal in the system.	Phosphorus	109-119	translocator protein	Homo sapiens	43-46
25036995-6	2014	FTIR (Fourier transform infrared spectroscopy) scans provided evidences of the existence of chemical reactions involving phosphorus, as revealed by a new absorption band from 1060 to 1180cm(-1), related to COP vibrations.	Phosphorus	121-131	caspase recruitment domain family member 16	Homo sapiens	206-209
24983310-6	2014	RESULTS: CD47mAb perfusion of donor kidneys resulted in marked improvement in posttransplant survival, lower levels of serum creatinine, blood urea nitrogen, phosphorus and magnesium, and less histological evidence of injury.	Phosphorus	158-168	CD47 molecule	Homo sapiens	9-13
24861054-6	2014	Blockade of ActRIIB signaling downregulates porin, a crucial ADP/ATP shuttle between cytosol and mitochondrial matrix leading to a consecutive deficiency of oxidative phosphorylation as measured by in vivo Phosphorus Magnetic Resonance Spectroscopy ((31)P-MRS).	Phosphorus	206-216	activin receptor IIB	Mus musculus	12-19
25054229-11	2014	CONCLUSIONS: B[alpha]P demonstrates inhibitory action on LSR and LDL-R, as well as ABCA1, which we propose leads to modified lipid status in B[alpha]P-treated mice, thus providing new insight into mechanisms underlying the involvement of pollutants in the disruption of lipid homeostasis, potentially contributing to dyslipidemia associated with obesity.	Phosphorus	20-22	low density lipoprotein receptor	Mus musculus	65-70
25015300-2	2014	Transforming growth factor alpha (TGFA) is a well characterized mammalian growth factor which might contribute to the development of CL/P.	Phosphorus	136-137	tumor necrosis factor	Homo sapiens	0-32
25015300-2	2014	Transforming growth factor alpha (TGFA) is a well characterized mammalian growth factor which might contribute to the development of CL/P.	Phosphorus	136-137	transforming growth factor alpha	Homo sapiens	34-38
25015300-11	2014	Stratified analyses suggested that the TGFA Taq I polymorphism was significantly associated with CL/P in Caucasians (C1C2 vs C1C1: OR = 1.95, 95% CI = 1.34-2.86; C2C2 + C1C2 vs C1C1: OR = 1.68, 95% CI = 1.18-2.38; C2 vs V1: OR = 1.52, 95% CI = 1.14 -2.02).	Phosphorus	100-101	transforming growth factor alpha	Homo sapiens	39-43
24927615-8	2014	CONCLUSION: PS-induced hepatic fibrosis results in up-regulation of the miR-27a and miR-146b in liver tissues, suggestingmiR-27a and miR-146b would be associated with the development of PS-induced liver fibrosis and be potential therapeutic targets during hepatic fibrosis.	Phosphorus	12-14	microRNA 27a	Rattus norvegicus	72-79
25002136-3	2014	Phosphorus (P) is reported to improve insulin sensitivity, which is involved in lipid metabolism, and thus we were interested in determining the impact of phosphorus ingestion on postprandial lipemia, a recognized CVD risk factor.	Phosphorus	0-10	insulin	Homo sapiens	38-45
25002136-7	2014	In the phosphorus (P) supplemented group, postprandial serum P increased (p=0.00), while changes in insulin, non-esterified fatty acids (NEFA) and triglyceride (TG) were not significantly different than that of placebo.	Phosphorus	7-17	insulin	Homo sapiens	100-107
25002136-8	2014	Concurrently, phosphorus supplementation increased postprandial concentrations of apolipoprotein B48 (ApoB48) (p&lt;0.05) and decreased that of apolipoprotein B100 (ApoB100) (p&lt;0.05).	Phosphorus	14-24	apolipoprotein B	Homo sapiens	82-100
25002136-8	2014	Concurrently, phosphorus supplementation increased postprandial concentrations of apolipoprotein B48 (ApoB48) (p&lt;0.05) and decreased that of apolipoprotein B100 (ApoB100) (p&lt;0.05).	Phosphorus	14-24	apolipoprotein B	Homo sapiens	102-108
25002136-8	2014	Concurrently, phosphorus supplementation increased postprandial concentrations of apolipoprotein B48 (ApoB48) (p&lt;0.05) and decreased that of apolipoprotein B100 (ApoB100) (p&lt;0.05).	Phosphorus	14-24	apolipoprotein B	Homo sapiens	144-163
25002136-8	2014	Concurrently, phosphorus supplementation increased postprandial concentrations of apolipoprotein B48 (ApoB48) (p&lt;0.05) and decreased that of apolipoprotein B100 (ApoB100) (p&lt;0.05).	Phosphorus	14-24	apolipoprotein B	Homo sapiens	165-172
24927615-8	2014	CONCLUSION: PS-induced hepatic fibrosis results in up-regulation of the miR-27a and miR-146b in liver tissues, suggestingmiR-27a and miR-146b would be associated with the development of PS-induced liver fibrosis and be potential therapeutic targets during hepatic fibrosis.	Phosphorus	12-14	microRNA 146b	Rattus norvegicus	84-92
24927615-8	2014	CONCLUSION: PS-induced hepatic fibrosis results in up-regulation of the miR-27a and miR-146b in liver tissues, suggestingmiR-27a and miR-146b would be associated with the development of PS-induced liver fibrosis and be potential therapeutic targets during hepatic fibrosis.	Phosphorus	12-14	microRNA 146b	Rattus norvegicus	133-141
24927615-8	2014	CONCLUSION: PS-induced hepatic fibrosis results in up-regulation of the miR-27a and miR-146b in liver tissues, suggestingmiR-27a and miR-146b would be associated with the development of PS-induced liver fibrosis and be potential therapeutic targets during hepatic fibrosis.	Phosphorus	186-188	microRNA 27a	Rattus norvegicus	72-79
24927615-8	2014	CONCLUSION: PS-induced hepatic fibrosis results in up-regulation of the miR-27a and miR-146b in liver tissues, suggestingmiR-27a and miR-146b would be associated with the development of PS-induced liver fibrosis and be potential therapeutic targets during hepatic fibrosis.	Phosphorus	186-188	microRNA 146b	Rattus norvegicus	84-92
24927615-8	2014	CONCLUSION: PS-induced hepatic fibrosis results in up-regulation of the miR-27a and miR-146b in liver tissues, suggestingmiR-27a and miR-146b would be associated with the development of PS-induced liver fibrosis and be potential therapeutic targets during hepatic fibrosis.	Phosphorus	186-188	microRNA 146b	Rattus norvegicus	133-141
24723407-0	2014	Over-expression of the Arabidopsis proton-pyrophosphatase AVP1 enhances transplant survival, root mass, and fruit development under limiting phosphorus conditions.	Phosphorus	141-151	Inorganic H pyrophosphatase family protein	Arabidopsis thaliana	58-62
25163127-6	2014	Additionally, N2O uptake was most responsive to dissolved inorganic nitrogen with phosphorus (DIN + DIP) addition, suggesting that the N2O consumption process may be P limited.	Phosphorus	82-92	DIP	Homo sapiens	100-103
24904159-5	2014	This quantum-mechanical process is present in all nuclear spin systems, such as phosphorus or bismuth atoms in silicon, and offers a general route toward the electrical control of nuclear-spin-based devices.	Phosphorus	80-90	spindlin 1	Homo sapiens	58-62
24824185-8	2014	RESULTS: The results demonstrated that high phosphorus induced the calcification of differentiated adipocytes with increased expression of osteopontin, the osteoblast transcription factor Runx2 and decreased expression of adipocyte transcription factors peroxisome proliferator-activated receptor gamma (PPARgamma) and CCAAT-enhancer-binding protein alpha (CEBPalpha), indicating that high phosphorus led to a phenotypic switch of adipocytes to an osteoblast like phenotype.	Phosphorus	44-54	secreted phosphoprotein 1	Homo sapiens	139-150
24824185-8	2014	RESULTS: The results demonstrated that high phosphorus induced the calcification of differentiated adipocytes with increased expression of osteopontin, the osteoblast transcription factor Runx2 and decreased expression of adipocyte transcription factors peroxisome proliferator-activated receptor gamma (PPARgamma) and CCAAT-enhancer-binding protein alpha (CEBPalpha), indicating that high phosphorus led to a phenotypic switch of adipocytes to an osteoblast like phenotype.	Phosphorus	44-54	RUNX family transcription factor 2	Homo sapiens	188-193
24824185-8	2014	RESULTS: The results demonstrated that high phosphorus induced the calcification of differentiated adipocytes with increased expression of osteopontin, the osteoblast transcription factor Runx2 and decreased expression of adipocyte transcription factors peroxisome proliferator-activated receptor gamma (PPARgamma) and CCAAT-enhancer-binding protein alpha (CEBPalpha), indicating that high phosphorus led to a phenotypic switch of adipocytes to an osteoblast like phenotype.	Phosphorus	44-54	peroxisome proliferator activated receptor gamma	Homo sapiens	254-302
24824185-8	2014	RESULTS: The results demonstrated that high phosphorus induced the calcification of differentiated adipocytes with increased expression of osteopontin, the osteoblast transcription factor Runx2 and decreased expression of adipocyte transcription factors peroxisome proliferator-activated receptor gamma (PPARgamma) and CCAAT-enhancer-binding protein alpha (CEBPalpha), indicating that high phosphorus led to a phenotypic switch of adipocytes to an osteoblast like phenotype.	Phosphorus	44-54	peroxisome proliferator activated receptor gamma	Homo sapiens	304-313
24824185-8	2014	RESULTS: The results demonstrated that high phosphorus induced the calcification of differentiated adipocytes with increased expression of osteopontin, the osteoblast transcription factor Runx2 and decreased expression of adipocyte transcription factors peroxisome proliferator-activated receptor gamma (PPARgamma) and CCAAT-enhancer-binding protein alpha (CEBPalpha), indicating that high phosphorus led to a phenotypic switch of adipocytes to an osteoblast like phenotype.	Phosphorus	44-54	CCAAT enhancer binding protein alpha	Homo sapiens	319-355
24824185-8	2014	RESULTS: The results demonstrated that high phosphorus induced the calcification of differentiated adipocytes with increased expression of osteopontin, the osteoblast transcription factor Runx2 and decreased expression of adipocyte transcription factors peroxisome proliferator-activated receptor gamma (PPARgamma) and CCAAT-enhancer-binding protein alpha (CEBPalpha), indicating that high phosphorus led to a phenotypic switch of adipocytes to an osteoblast like phenotype.	Phosphorus	44-54	CCAAT enhancer binding protein alpha	Homo sapiens	357-366
24904159-5	2014	This quantum-mechanical process is present in all nuclear spin systems, such as phosphorus or bismuth atoms in silicon, and offers a general route toward the electrical control of nuclear-spin-based devices.	Phosphorus	80-90	spindlin 1	Homo sapiens	188-192
24801272-11	2014	Pairwise comparison showed that both Cs and Ps increased from CT1 to ST3 (P = 0.005) but not from ST4 onwards (P = 0.198).	Phosphorus	44-46	cardiotrophin 1	Homo sapiens	62-65
24619246-11	2014	Pearson"s correlation analysis showed that AOA diversity had a positive significant correlation with available phosphorus.	Phosphorus	111-121	aprataxin	Homo sapiens	43-46
24801272-11	2014	Pairwise comparison showed that both Cs and Ps increased from CT1 to ST3 (P = 0.005) but not from ST4 onwards (P = 0.198).	Phosphorus	44-46	tumor-suppressor, HELA cell type	Homo sapiens	69-72
24699913-2	2014	This Article describes the emerging area of catalytic SN2 reactions with specific emphasis on the design and development of phosphorus(V) and cyclopropenone-based catalytic SN2 reactions of alcohols.	Phosphorus	124-134	solute carrier family 38 member 5	Homo sapiens	54-57
25158503-3	2014	The RSM analysis results demonstrated that the effect of individual operation parameter on phosphorus removal was followed as the order of Al/P &gt; pH &gt; MS, and the optimal process parameters with phosphorus removal efficiency of 97.8% were Al/P = 2.49, pH = 8.3 and MS 398 r x min(-1), respectively.	Phosphorus	91-101	CD59 molecule (CD59 blood group)	Homo sapiens	282-288
24742150-0	2014	Synthesis and evaluation of phosphorus containing, specific CDK9/CycT1 inhibitors.	Phosphorus	28-38	cyclin dependent kinase 9	Homo sapiens	60-64
24742150-0	2014	Synthesis and evaluation of phosphorus containing, specific CDK9/CycT1 inhibitors.	Phosphorus	28-38	cyclin T1	Homo sapiens	65-70
24742150-2	2014	The aim of this research was to develop novel and selective phosphorus containing CDK9/CycT1 inhibitors.	Phosphorus	60-70	cyclin dependent kinase 9	Homo sapiens	82-86
24742150-2	2014	The aim of this research was to develop novel and selective phosphorus containing CDK9/CycT1 inhibitors.	Phosphorus	60-70	cyclin T1	Homo sapiens	87-92
24814575-6	2014	All P, SS, and SP supplementation increased the superoxide dismutase activity (40.1, 53.0, and 64.5%), glutathione content (84.6, 104, and 165%), TCR-induced T lymphocyte proliferation (20.8, 26.4, and 50.0%), and IL-2 concentration (24.9, 27.2, and 46.2%) and decreased malondialdehyde content (25.1, 26.3, and 49.3%), respectively.	Phosphorus	4-5	interleukin 2	Homo sapiens	214-218
24699913-2	2014	This Article describes the emerging area of catalytic SN2 reactions with specific emphasis on the design and development of phosphorus(V) and cyclopropenone-based catalytic SN2 reactions of alcohols.	Phosphorus	124-134	solute carrier family 38 member 5	Homo sapiens	173-176
26425597-7	2014	In the patient presented in this study, in patients with surgically created hypoparathyroidism, and those receiving Cinacalcet or Velcalcetide, a fall in PTH was associated with hypophosphatemia or a fall in serum phosphorus.	Phosphorus	214-224	parathyroid hormone	Homo sapiens	154-157
24601885-1	2014	Fibroblast growth factor-23 (FGF23) controls serum phosphorus largely through actions on the kidneys to excrete phosphorus and reduce calcitriol.	Phosphorus	51-61	fibroblast growth factor 23	Mus musculus	0-27
23660507-8	2014	Compared to healthy controls, serum IL-10 levels of both the PSFA group and PS group were significantly lower (p&lt;=0.01), but TGF beta levels were significantly higher in the PSFA group (35.3+-5.6ng/ml vs. 31.2+-6.6ng/ml, respectively; p=0.037).	Phosphorus	61-63	interleukin 10	Homo sapiens	36-41
24749646-2	2014	Reductive quenching of the (3)MLCT excited state of the photosensitizer by NEt3 or N(CH2CH2OH)3 (TEOA) generates PS( -), and subsequent intermolecular electron transfer to 1 produces the reduced anionic form of 1.	Phosphorus	113-115	tetraspanin 2	Homo sapiens	75-79
24886973-7	2014	In particular, the ratio of P-S349 to total p62 levels was significantly increased in the brains with Alzheimer"s disease (AD) compared with controls.	Phosphorus	28-29	nucleoporin 62	Homo sapiens	44-47
24940459-5	2014	RESULTS: The rates of patients with initial PSA higher than 50 ng/mL, with a Gleason score of 8 or higher, and with clinical stage D were significantly lower in the PS group than those in the non-PS group.	Phosphorus	165-167	kallikrein related peptidase 3	Homo sapiens	44-47
24601885-1	2014	Fibroblast growth factor-23 (FGF23) controls serum phosphorus largely through actions on the kidneys to excrete phosphorus and reduce calcitriol.	Phosphorus	51-61	fibroblast growth factor 23	Mus musculus	29-34
24601885-2	2014	Although these actions are well established in adults and children, the role that FGF23 plays in regulating fetal phosphorus metabolism has not been previously studied.	Phosphorus	114-124	fibroblast growth factor 23	Homo sapiens	82-87
24601885-3	2014	We used several mouse models to study the effect of endogenous deficiency or excess of FGF23 on fetal phosphorus metabolism.	Phosphorus	102-112	fibroblast growth factor 23	Mus musculus	87-92
24601885-12	2014	The active delivery of phosphorus across the placenta does not require FGF23, and that process overrides any effects that absence or excess of FGF23 might otherwise have on phosphate handling by the fetal kidneys.	Phosphorus	23-33	fibroblast growth factor 23	Mus musculus	143-148
24559458-1	2014	New cyclic and acylic phosphorus-nitrogen compounds have been synthesized in reactions of Hyp-N(SiMe3)PCl2 (hypersilyl = Hyp = (Me3Si)3Si) with silver salts of the perfluorinated anions [CF3CO2](-), [CF3SO3](-), and [C6F5](-).	Phosphorus	22-32	metal response element binding transcription factor 2	Homo sapiens	102-106
24669256-2	2014	In addition, the correlation between serum FGF-23 and phosphorus (Pi) levels and the clinical implications were identified.	Phosphorus	54-64	fibroblast growth factor 23	Homo sapiens	43-49
24650647-10	2014	The use of the two models SWAP and ANIMO shows the magnitudes of nitrogen and phosphorus fluxes transported by natural and simulated intense rainfall in an agricultural area with different soil management procedures, as required by decision makers.	Phosphorus	78-88	splicing factor SWAP	Homo sapiens	26-30
24216259-2	2014	From a physiological perspective and supported by some data, phosphorus is the main driver for FGF-23 secretion.	Phosphorus	61-71	fibroblast growth factor 23	Homo sapiens	95-101
24216259-3	2014	Therefore, it is conceivable that interventions aiming at restriction of phosphorus uptake from the gastrointestinal tract may lower serum FGF-23 levels and improve cardiovascular risk and subsequently survival.	Phosphorus	73-83	fibroblast growth factor 23	Homo sapiens	139-145
24045674-1	2014	OBJECTIVE: GALNT3 gene encodes the glycosyltransferase polypeptide N-acetylgalactosaminyltransferase-3 (ppGalNacT3), which initiates the O-glycosylation of fibroblast growth factor 23 (FGF23) that is important in phosphorous regulation.	Phosphorus	213-224	polypeptide N-acetylgalactosaminyltransferase 3	Homo sapiens	11-17
24045674-1	2014	OBJECTIVE: GALNT3 gene encodes the glycosyltransferase polypeptide N-acetylgalactosaminyltransferase-3 (ppGalNacT3), which initiates the O-glycosylation of fibroblast growth factor 23 (FGF23) that is important in phosphorous regulation.	Phosphorus	213-224	fibroblast growth factor 23	Homo sapiens	156-183
24045674-1	2014	OBJECTIVE: GALNT3 gene encodes the glycosyltransferase polypeptide N-acetylgalactosaminyltransferase-3 (ppGalNacT3), which initiates the O-glycosylation of fibroblast growth factor 23 (FGF23) that is important in phosphorous regulation.	Phosphorus	213-224	fibroblast growth factor 23	Homo sapiens	185-190
24636907-6	2014	Meanwhile, the expression level of TaEXPB23 was up-regulated at excess-P condition, suggesting the involvement of TaEXPB23 in phosphorus adaptability.	Phosphorus	126-136	EXPB23	Triticum aestivum	35-43
24636907-6	2014	Meanwhile, the expression level of TaEXPB23 was up-regulated at excess-P condition, suggesting the involvement of TaEXPB23 in phosphorus adaptability.	Phosphorus	126-136	EXPB23	Triticum aestivum	114-122
24872881-0	2014	Effect of dietary phosphorus content on milk production and phosphorus excretion in dairy cows.	Phosphorus	18-28	Weaning weight-maternal milk	Bos taurus	40-44
24713147-6	2014	The expression of membrane-bound acid phosphatase (MBAcP) was strictly regulated with optimal expression at a concentration of phosphorus 5 mM.	Phosphorus	127-137	acid phosphatase	Burkholderia gladioli	33-49
24513883-1	2014	The synthesis of a novel PS conjugated with bovine and human serum albumin (BSA and HSA) and a monoclonal antibody anti-CD104 is reported, as well as their biological potential against the human bladder cancer cell line UM-UC-3.	Phosphorus	25-27	albumin	Bos taurus	61-74
24513883-1	2014	The synthesis of a novel PS conjugated with bovine and human serum albumin (BSA and HSA) and a monoclonal antibody anti-CD104 is reported, as well as their biological potential against the human bladder cancer cell line UM-UC-3.	Phosphorus	25-27	integrin subunit beta 4	Homo sapiens	120-125
24568660-4	2014	The molar yields of CNCl and NCl3 were observed to be as high as 44% (pH = 6.0, chlorine/precursor molar ratio [Cl/P] = 6.4) and 108% (pH = 7.0, Cl/P = 30), respectively, both being strong functions of Cl/P, pH, and temperature.	Phosphorus	115-116	calpain 5	Homo sapiens	29-33
24568660-4	2014	The molar yields of CNCl and NCl3 were observed to be as high as 44% (pH = 6.0, chlorine/precursor molar ratio [Cl/P] = 6.4) and 108% (pH = 7.0, Cl/P = 30), respectively, both being strong functions of Cl/P, pH, and temperature.	Phosphorus	148-149	calpain 5	Homo sapiens	29-33
24568676-7	2014	In contrast, phosphorus-rich phosphide NiP2 is formed on Ni/CNTs and NiO/CNTs.	Phosphorus	13-23	BCL2 interacting protein 2	Homo sapiens	39-43
24550322-4	2014	Therapy aims at counteracting consequences of FGF23 excess, i.e. oral phosphorus supplementation with multiple daily intakes to compensate for renal phosphate wasting and active vitamin D analogs (alfacalcidol or calcitriol) to counter the 1,25-diOH-vitamin D deficiency.	Phosphorus	70-80	fibroblast growth factor 23	Homo sapiens	46-51
32261282-6	2014	The complexes of Mag-VPCmns and nucleoside molecules with various N/P ratios were evaluated using gel electrophoresis, surface charge (zeta-potential) measurement, and particle size measurement.	Phosphorus	22-23	myelin associated glycoprotein	Homo sapiens	17-20
24423294-5	2014	PATIENTS AND METHODS: We quantified GNAS methylation alterations by both PCR-pyrosequencing and methylation specific-multiplex ligation-dependent probe amplification assay in genomic DNA from 63 patients with PHP-I and correlated these findings with clinical parameters (age at diagnosis; calcium, phosphorus, PTH, TSH levels; presence or absence of each AHO sign).	Phosphorus	298-308	GNAS complex locus	Homo sapiens	36-40
32261283-2	2014	Then, nanofibers composed of P(NIPAAm-co-AAc) and polyurethane (PU) were fabricated by the single-spinneret electrospinning technique and used as drug carriers by co-spinning with the water insoluble drug nifedipine (NIF).	Phosphorus	29-30	glycine-N-acyltransferase	Homo sapiens	41-44
24334408-1	2014	Calcium and phosphorus homeostasis is achieved by interplay among hormones, including 1,25(OH)2D3 (1,25D), parathyroid hormone, and fibroblast growth factor 23 (FGF23), and their interactions with other proteins.	Phosphorus	12-22	fibroblast growth factor 23	Mus musculus	132-159
24259513-8	2014	Despite the elevated FGF23 levels, Fgfr1-/-/Fgfr4-/- mice have elevated serum phosphorus levels, increased brush-border membrane vesicle (BBMV) phosphate transport, and increased Na-P(i) cotransporter 2c (NaPi-2c) protein expression compared with wild-type mice.	Phosphorus	78-88	fibroblast growth factor receptor 1	Mus musculus	35-40
24259513-8	2014	Despite the elevated FGF23 levels, Fgfr1-/-/Fgfr4-/- mice have elevated serum phosphorus levels, increased brush-border membrane vesicle (BBMV) phosphate transport, and increased Na-P(i) cotransporter 2c (NaPi-2c) protein expression compared with wild-type mice.	Phosphorus	78-88	fibroblast growth factor receptor 4	Mus musculus	44-49
24311704-9	2014	Serum phosphorus levels, adjusted for age, were significantly lower at GFR of 60-69 ml/min per 1.73 m(2) than higher GFR, but thereafter they became higher in parallel with fibroblast growth factor 23 as GFR declined.	Phosphorus	6-16	fibroblast growth factor 23	Homo sapiens	173-200
24334408-1	2014	Calcium and phosphorus homeostasis is achieved by interplay among hormones, including 1,25(OH)2D3 (1,25D), parathyroid hormone, and fibroblast growth factor 23 (FGF23), and their interactions with other proteins.	Phosphorus	12-22	fibroblast growth factor 23	Mus musculus	161-166
24009282-7	2014	While serum phosphorus levels correlated with FGF23 concentrations in each group separately [r=0.522 (P&lt;0.01) and r=0.42 (P&lt;0.01) in short daily and conventional in-center hemodialysis, respectively], FGF23 levels were lower [823 RU/mL (263, 2169)] in the patients receiving short daily hemodialysis than in patients treated with conventional hemodialysis [2521 RU/mL (909, 5556)] (P&lt;0.01 between groups).	Phosphorus	12-22	fibroblast growth factor 23	Homo sapiens	46-51
24009282-7	2014	While serum phosphorus levels correlated with FGF23 concentrations in each group separately [r=0.522 (P&lt;0.01) and r=0.42 (P&lt;0.01) in short daily and conventional in-center hemodialysis, respectively], FGF23 levels were lower [823 RU/mL (263, 2169)] in the patients receiving short daily hemodialysis than in patients treated with conventional hemodialysis [2521 RU/mL (909, 5556)] (P&lt;0.01 between groups).	Phosphorus	12-22	fibroblast growth factor 23	Homo sapiens	207-212
24593641-3	2014	At vacuum heating temperatures ranging from 325  C, red phosphorus evaporates solely as P4 molecules (P4/P2 ~ 2 x 10(5), P4/P ~ 10(21)).	Phosphorus	52-66	solute carrier family 10 member 4	Homo sapiens	121-130
24854458-7	2014	A significant decline from baseline (10.9%, p &lt; 0.01) in the serum FGF23 concentration was observed in the ERN group compared to placebo, but not in the ERN-L group compared to placebo (p = 0.36 and 0.97 for ERN-L and placebo, respectively), despite equivalent declines in serum phosphorus.	Phosphorus	282-292	fibroblast growth factor 23	Homo sapiens	70-75
24246761-2	2014	We previously showed that the PAH prototype, benzo[a]pyrene (B[a]P), triggers apoptosis via DNA damage-induced p53 activation (genotoxic pathway) and via remodeling of the membrane cholesterol-rich microdomains called lipid rafts, leading to changes in pH homeostasis (non-genotoxic pathway).	Phosphorus	30-31	tumor protein p53	Homo sapiens	111-114
23909275-3	2014	The vast majority of compounds that contain a phosphorus-carbon bond are manufactured using phosphorus trichloride (PCl3) as an intermediate.	Phosphorus	46-56	PHD finger protein 19	Homo sapiens	116-120
24425727-2	2014	A higher total habitual dietary phosphorus intake has been associated with higher serum parathyroid hormone (PTH) and lower serum calcium concentrations in healthy individuals.	Phosphorus	32-42	parathyroid hormone	Homo sapiens	88-107
24425727-2	2014	A higher total habitual dietary phosphorus intake has been associated with higher serum parathyroid hormone (PTH) and lower serum calcium concentrations in healthy individuals.	Phosphorus	32-42	parathyroid hormone	Homo sapiens	109-112
24425727-3	2014	Higher serum PTH concentrations have been shown in those who consume foods with phosphorus additives.	Phosphorus	80-90	parathyroid hormone	Homo sapiens	13-16
24425727-8	2014	In our loading test with a low-calcium, high-phosphorus lunch provided to healthy young men, serum PTH concentrations showed peaks at 1 and 6 h, and serum fibroblast growth factor 23 (FGF23) concentrations increased significantly at 8 h after the meal.	Phosphorus	45-55	parathyroid hormone	Homo sapiens	99-102
24425727-8	2014	In our loading test with a low-calcium, high-phosphorus lunch provided to healthy young men, serum PTH concentrations showed peaks at 1 and 6 h, and serum fibroblast growth factor 23 (FGF23) concentrations increased significantly at 8 h after the meal.	Phosphorus	45-55	fibroblast growth factor 23	Homo sapiens	184-189
24425727-9	2014	In contrast, the high-calcium, high-phosphorus meal suppressed the second PTH and FGF23 elevations until 8 h after the meal.	Phosphorus	36-46	parathyroid hormone	Homo sapiens	74-77
24425727-9	2014	In contrast, the high-calcium, high-phosphorus meal suppressed the second PTH and FGF23 elevations until 8 h after the meal.	Phosphorus	36-46	fibroblast growth factor 23	Homo sapiens	82-87
24425727-10	2014	This implies that adequate dietary calcium intake is needed to overcome the interfering effects of high phosphorus intake on PTH and FGF23 secretion.	Phosphorus	104-114	parathyroid hormone	Homo sapiens	125-128
24425727-10	2014	This implies that adequate dietary calcium intake is needed to overcome the interfering effects of high phosphorus intake on PTH and FGF23 secretion.	Phosphorus	104-114	fibroblast growth factor 23	Homo sapiens	133-138
24425727-13	2014	These findings suggest that long-term high-phosphorus diets may impair bone health mediated by FGF23 resistance both in chronic kidney disease patients and in the healthy population.	Phosphorus	43-53	fibroblast growth factor 23	Homo sapiens	95-100
25057492-4	2014	Mannosylated chitosan ODN nanoparticles (MCHODN NPs) were formulated by self-assembled method using various N/P ratio (moles of amine groups of MCH to phosphate moieties of ODNs) and characterized for gel retardation assay, physicochemical characteristics, cytotoxicity and transfection efficiency, and antisense assay.	Phosphorus	49-50	pro-melanin concentrating hormone	Homo sapiens	41-44
25057492-6	2014	On increasing the N/P ratio of MCH/ODN, particle size of the NPs decreased whereas zeta potential (ZV) increased.	Phosphorus	20-21	pro-melanin concentrating hormone	Homo sapiens	31-34
25088267-4	2014	Calciotropic hormones such as vitamin D and parathyroid hormone, as well as hormones controlling phosphorus homeostasis, such as fibroblast growth factor-23 (FGF-23), are essential in controlling these interactions.	Phosphorus	97-107	fibroblast growth factor 23	Homo sapiens	129-156
24246481-3	2014	Results obtained demonstrated a sound performance of synergistic denitrification and chemical precipitation in pre-denitrification of the modified BAF process when dosing Fe salts, which showed enhanced by using Fe(2+) as the dosed precipitant in increasing the denitrification loading rate, exhibiting a better controlling of the residual phosphorus in pre-denitrification effluent, and improving sludge settleability.	Phosphorus	340-350	BAF nuclear assembly factor 1	Homo sapiens	147-150
25088267-4	2014	Calciotropic hormones such as vitamin D and parathyroid hormone, as well as hormones controlling phosphorus homeostasis, such as fibroblast growth factor-23 (FGF-23), are essential in controlling these interactions.	Phosphorus	97-107	fibroblast growth factor 23	Homo sapiens	158-164
24270576-6	2014	Semi-quantitative western blot analysis further confirmed that the levels of ubiquitin and NF-kappaB p65 were decreased, while those of IkappaB-alpha (an inhibitor of NF-kappaB) were significantly increased in the PS-341 group compared with the shunt group (P&lt;0.05).	Phosphorus	214-216	synaptotagmin 1	Rattus norvegicus	101-104
24164913-10	2014	Younger age, lower prevalence of diabetes, longer dialysis vintage, and higher calcium and phosphorus were independently associated with higher FGF-23 levels.	Phosphorus	91-101	fibroblast growth factor 23	Homo sapiens	144-150
25132170-9	2014	Serum phosphorus levels were related to SOX6 rs7117858.	Phosphorus	6-16	SRY-box transcription factor 6	Homo sapiens	40-44
24720199-0	2014	[Study on distribution of phosphorus in surface sediments of the Yellow Sea and the East China Sea].	Phosphorus	26-36	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	72-75
24720199-0	2014	[Study on distribution of phosphorus in surface sediments of the Yellow Sea and the East China Sea].	Phosphorus	26-36	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	95-98
24270576-6	2014	Semi-quantitative western blot analysis further confirmed that the levels of ubiquitin and NF-kappaB p65 were decreased, while those of IkappaB-alpha (an inhibitor of NF-kappaB) were significantly increased in the PS-341 group compared with the shunt group (P&lt;0.05).	Phosphorus	214-216	NFKB inhibitor alpha	Rattus norvegicus	136-149
23296792-1	2014	Fibroblast growth factor-23 (FGF-23) has emerged as an important hormone involved in phosphorus and vitamin D homeostasis.	Phosphorus	85-95	fibroblast growth factor 23	Homo sapiens	0-27
23296792-1	2014	Fibroblast growth factor-23 (FGF-23) has emerged as an important hormone involved in phosphorus and vitamin D homeostasis.	Phosphorus	85-95	fibroblast growth factor 23	Homo sapiens	29-35
25593987-10	2014	T56-LIMKi reduced tumor size and p-cofilin levels in the Panc-1 tumors, leading us to propose T56-LIMKi as a candidate drug for cancer therapy.	Phosphorus	33-34	pancreas protein 1	Mus musculus	57-63
24975224-8	2014	Furthermore, rats treated with cinacalcet+human PTH (1-34) showed transiently but significantly higher plasma FGF23 levels at 3 h after oral phosphorus administration compared with cinacalcet-treated rats.	Phosphorus	141-151	fibroblast growth factor 23	Homo sapiens	110-115
24975224-9	2014	These results suggest that oral phosphorus supplementation secondarily increases circulating FGF23 levels at least partially by stimulation of PTH secretion.	Phosphorus	32-42	fibroblast growth factor 23	Rattus norvegicus	93-98
24975224-0	2014	Oral phosphorus supplementation secondarily increases circulating fibroblast growth factor 23 levels at least partially via stimulation of parathyroid hormone secretion.	Phosphorus	5-15	fibroblast growth factor 23	Rattus norvegicus	66-93
24975224-0	2014	Oral phosphorus supplementation secondarily increases circulating fibroblast growth factor 23 levels at least partially via stimulation of parathyroid hormone secretion.	Phosphorus	5-15	parathyroid hormone	Rattus norvegicus	139-158
24975224-1	2014	Oral phosphorus supplementation stimulates fibroblast growth factor 23 (FGF23) secretion; however, the underlying mechanism remains unclear.	Phosphorus	5-15	fibroblast growth factor 23	Rattus norvegicus	43-70
24975224-1	2014	Oral phosphorus supplementation stimulates fibroblast growth factor 23 (FGF23) secretion; however, the underlying mechanism remains unclear.	Phosphorus	5-15	fibroblast growth factor 23	Rattus norvegicus	72-77
24975224-2	2014	The aim of this study was to investigate the involvement of parathyroid hormone (PTH) in increased plasma FGF23 levels after oral phosphorus supplementation in rats.	Phosphorus	130-140	parathyroid hormone	Rattus norvegicus	60-79
24975224-2	2014	The aim of this study was to investigate the involvement of parathyroid hormone (PTH) in increased plasma FGF23 levels after oral phosphorus supplementation in rats.	Phosphorus	130-140	fibroblast growth factor 23	Rattus norvegicus	106-111
24173213-8	2014	Cellular PPIase Pin1 binds specifically to phosphoserine- or phosphothreonine-proline (pS/T-P) motifs in target proteins.	Phosphorus	87-89	peptidylprolyl cis/trans isomerase, NIMA-interacting 1	Homo sapiens	9-20
24864466-6	2014	In patients with different stages of CKD, the increase in FGF-23 levels, as glomerular filtration rate reduced, outstripped that in the serum levels of phosphorus and intact parathyroid hormone.	Phosphorus	152-162	fibroblast growth factor 23	Homo sapiens	58-64
23906857-1	2014	Rivers export increasing amounts of dissolved inorganic (DIN, DIP) and organic (DON, DOP) nitrogen and phosphorus to the Black Sea causing coastal eutrophication.	Phosphorus	103-113	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	127-130
23906857-6	2014	In these baselines, total N and P inputs to the Black Sea decrease between 2000 and 2050, but not for all rivers and nutrient forms.	Phosphorus	32-33	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	54-57
21576477-1	2013	Crop-livestock production systems are the largest cause of human alteration of the global nitrogen (N) and phosphorus (P) cycles.	Phosphorus	107-117	LUC7 like 3 pre-mRNA splicing factor	Homo sapiens	0-4
24228848-6	2013	ADP binding to the ATPase was triggered by photolytic release of ADP from P(3)-1-(2-nitro)phenylethyl ADP (caged ADP).	Phosphorus	2-3	dynein axonemal heavy chain 8	Homo sapiens	19-25
24121369-0	2013	Simultaneous removal of phosphorus and nitrogen from sewage using a novel combo system of fluidized bed reactor-membrane bioreactor (FBR-MBR).	Phosphorus	24-34	translocator protein	Homo sapiens	137-140
24121369-1	2013	A FBR-MBR combo system was designed as a novel approach for simultaneous phosphorus and nitrogen removal from sewage.	Phosphorus	73-83	translocator protein	Homo sapiens	6-9
24121369-3	2013	Prior recovery of phosphorus as struvite in the FBR enhanced nitrogen and COD removal efficiency in MBR.	Phosphorus	18-28	translocator protein	Homo sapiens	100-103
25019031-2	2013	Previous studies have suggested that both higher serum parathyroid hormone (PTH) level and higher dietary protein intake may contribute to higher serum phosphorus levels.	Phosphorus	152-162	parathyroid hormone	Homo sapiens	55-74
24039010-4	2013	As evidenced by cyclic voltammetry, galvanostatic charge/discharge, and wide potential window tests, a supercapacitor constructed from PC-2 (impregnation ratio of 2), with the highest phosphorus content, can operate very stably in 1 M H2 SO4 at 1.5 V with only 18 % degradation after 10 000 cycles at a current density of 5 A g(-1) .	Phosphorus	184-194	polycystin 2, transient receptor potential cation channel	Homo sapiens	135-139
24131677-10	2013	CRP was significantly positively associated with serum phosphorus, calcium, alkaline phosphatase, and PTH, and significantly inversely associated with HDL and albumin.	Phosphorus	55-65	C-reactive protein	Homo sapiens	0-3
25019031-2	2013	Previous studies have suggested that both higher serum parathyroid hormone (PTH) level and higher dietary protein intake may contribute to higher serum phosphorus levels.	Phosphorus	152-162	parathyroid hormone	Homo sapiens	76-79
25019031-6	2013	Logistic regression models were examined to assess the association between likelihood of hyperphosphatemia (serum phosphorus &gt;5.5 mg/dl) and serum PTH and nPCR increments.	Phosphorus	114-124	parathyroid hormone	Homo sapiens	150-153
25019032-1	2013	The combination of serum 25-hydroxyvitamin D (25D) and fibroblast growth factor 23 (FGF23) levels predict hard renal outcomes in patients with chronic kidney disease (CKD), independent of classical markers of mineral and bone disorders, including serum phosphorus, parathyroid hormone, 1,25-dihydroxyvitamin D levels, and active vitamin D therapy.	Phosphorus	253-263	fibroblast growth factor 23	Homo sapiens	84-89
23982515-5	2013	Phosphorus-31 NMR spectroscopy ((31)P-NMR) analysis confirms the site of attack and shows the capability of dUTPase to cleave the dUTP analogue alpha,beta-imido-dUTP, containing the imido linkage usually regarded to be non-hydrolyzable.	Phosphorus	0-10	Deoxyuridine triphosphatase	Drosophila melanogaster	108-115
24205842-1	2013	Hydrolysis of G- and V-series organophosphorus nerve agents (OPNAs) containing a phosphorus-methyl bond yields a methylphosphonic acid (MeP) product when adducted to human butyrylcholinesterase (BChE).	Phosphorus	36-46	butyrylcholinesterase	Homo sapiens	172-193
24205842-1	2013	Hydrolysis of G- and V-series organophosphorus nerve agents (OPNAs) containing a phosphorus-methyl bond yields a methylphosphonic acid (MeP) product when adducted to human butyrylcholinesterase (BChE).	Phosphorus	36-46	butyrylcholinesterase	Homo sapiens	195-199
23877588-6	2013	A prolonged oral phosphorus load increases FGF-23 expression by a mechanism that includes local changes in the ratio of inorganic phosphate to pyrophosphate in bone.	Phosphorus	17-27	fibroblast growth factor 23	Homo sapiens	43-49
24228204-4	2013	Fibroblast growth factor 23 and Klotho are novel mediators of phosphorus metabolism that are tightly linked to dietary phosphorus intake and show promise as integrated biomarkers of phosphorus excess and its long-term health consequences.	Phosphorus	62-72	fibroblast growth factor 23	Homo sapiens	0-27
24228204-4	2013	Fibroblast growth factor 23 and Klotho are novel mediators of phosphorus metabolism that are tightly linked to dietary phosphorus intake and show promise as integrated biomarkers of phosphorus excess and its long-term health consequences.	Phosphorus	62-72	klotho	Homo sapiens	32-38
24228204-4	2013	Fibroblast growth factor 23 and Klotho are novel mediators of phosphorus metabolism that are tightly linked to dietary phosphorus intake and show promise as integrated biomarkers of phosphorus excess and its long-term health consequences.	Phosphorus	119-129	fibroblast growth factor 23	Homo sapiens	0-27
24228204-4	2013	Fibroblast growth factor 23 and Klotho are novel mediators of phosphorus metabolism that are tightly linked to dietary phosphorus intake and show promise as integrated biomarkers of phosphorus excess and its long-term health consequences.	Phosphorus	119-129	klotho	Homo sapiens	32-38
24348506-8	2013	RESULTS: FGF-23 was elevated (mean: 4,681 pg/ml, SD: 3,906) and correlated with hsCRP, esRAGE, AOPP, dialysis vintage and phosphorus in univariate analysis.	Phosphorus	122-132	fibroblast growth factor 23	Homo sapiens	9-15
24348506-9	2013	In multiple regression analysis, hsCRP, AOPP and phosphorus but not esRAGE were all significantly correlated to FGF-23 (R2 = 0.7, p &lt; 0.001).	Phosphorus	49-59	fibroblast growth factor 23	Homo sapiens	112-118
23852336-4	2013	RESULTS: Circulating phosphate concentrations declined more rapidly and the fractional excretion of phosphorus was higher in the first week post-transplantation in subjects with higher FGF23 values.	Phosphorus	100-110	fibroblast growth factor 23	Homo sapiens	185-190
23892345-5	2013	The further magnetic study shows the two coordination polymers exhibit antiferromagnetic behavior for 1 between the mononuclear units, while ferromagnetic behavior for 2 derived from double O-P-O bridges in syn-anti mode between the metal centers.	Phosphorus	192-193	synemin	Homo sapiens	207-210
23933531-1	2013	Parathion (PS) and chlorpyrifos (CPF) are organophosphorus insecticides (OPs) that elicit acute toxicity by inhibiting acetylcholinesterase (AChE).	Phosphorus	11-13	acetylcholinesterase	Rattus norvegicus	119-139
23933531-1	2013	Parathion (PS) and chlorpyrifos (CPF) are organophosphorus insecticides (OPs) that elicit acute toxicity by inhibiting acetylcholinesterase (AChE).	Phosphorus	11-13	acetylcholinesterase	Rattus norvegicus	141-145
23933531-3	2013	We proposed that differential inhibition of eCB-degrading enzymes (fatty acid amide hydrolase, FAAH, and monoacylglycerol lipase, MAGL) by PS and CPF leads to differences in extracellular eCB levels and toxicity.	Phosphorus	139-141	fatty-acid amide hydrolase-like	Rattus norvegicus	95-99
23933531-3	2013	We proposed that differential inhibition of eCB-degrading enzymes (fatty acid amide hydrolase, FAAH, and monoacylglycerol lipase, MAGL) by PS and CPF leads to differences in extracellular eCB levels and toxicity.	Phosphorus	139-141	monoglyceride lipase	Rattus norvegicus	105-128
23933531-3	2013	We proposed that differential inhibition of eCB-degrading enzymes (fatty acid amide hydrolase, FAAH, and monoacylglycerol lipase, MAGL) by PS and CPF leads to differences in extracellular eCB levels and toxicity.	Phosphorus	139-141	monoglyceride lipase	Rattus norvegicus	130-134
23933531-7	2013	Cholinesterase inhibition was extensive in hippocampus with PS (89-90%) and CPF (78-83%) exposure.	Phosphorus	60-62	butyrylcholinesterase	Rattus norvegicus	0-14
23933531-11	2013	The cannabinoid CB1 receptor antagonist/inverse agonist AM251 (3mg/kg, ip) had no influence on functional signs after CPF but markedly decreased toxicity in PS-treated rats.	Phosphorus	157-159	cannabinoid receptor 1	Rattus norvegicus	16-19
23933531-13	2013	CB1-mediated signaling appears to play a role in the acute toxicity of PS but the role of eCBs in CPF toxicity remains unclear.	Phosphorus	71-73	cannabinoid receptor 1	Rattus norvegicus	0-3
24028402-5	2013	mRNA and protein expression of intestinal calbindin and vitamin D receptor correlated quadratically with dietary nonphytate phosphorus, and the highest expression was found when dietary available phosphorus was at 0.25% to 0.3%.	Phosphorus	124-134	calbindin 1	Gallus gallus	42-51
24083833-4	2013	This effect requires the C-terminal domain of complexin-1, which binds to the membrane, the presence of PS in the membrane, and the core region of complexin-1, which binds to the SNARE complex.	Phosphorus	104-106	complexin 1	Homo sapiens	46-57
24124568-7	2013	In addition, the abundances of the chiA and nosZ genes were sensitive to plant functional group removal, the AOB-amoA gene abundance to phosphorus enrichment when nitrogen was added simultaneously, and the nirS and nirK gene abundances responded to watering.	Phosphorus	136-146	chitinase acidic	Homo sapiens	35-39
23998855-4	2013	In situ labeling of all labile H groups (aliphatic and phenolic hydroxyls and carboxylic acids) with a phosphorus-containing reagent (Cl-TMDP) followed by quantitative 31P NMR acquisition constitutes a novel fast and reliable analytical tool for the analysis of tannins and proanthocyanidins with significant implications for the fields of food and feed analyses, tannery, and the development of natural polyphenolics containing products.	Phosphorus	103-113	dual specificity phosphatase 13	Homo sapiens	137-141
23868911-5	2013	In the NP fraction, GPs are enriched with a mixture of saturated, monounsaturated, and polyunsaturated fatty acid species, while PE and PS in the SF fractions are enriched with PUFA-containing molecular species.	Phosphorus	136-138	pumilio RNA binding family member 3	Homo sapiens	177-181
24028402-5	2013	mRNA and protein expression of intestinal calbindin and vitamin D receptor correlated quadratically with dietary nonphytate phosphorus, and the highest expression was found when dietary available phosphorus was at 0.25% to 0.3%.	Phosphorus	124-134	vitamin D (1,25- dihydroxyvitamin D3) receptor	Gallus gallus	56-74
24028402-5	2013	mRNA and protein expression of intestinal calbindin and vitamin D receptor correlated quadratically with dietary nonphytate phosphorus, and the highest expression was found when dietary available phosphorus was at 0.25% to 0.3%.	Phosphorus	196-206	calbindin 1	Gallus gallus	42-51
24028402-5	2013	mRNA and protein expression of intestinal calbindin and vitamin D receptor correlated quadratically with dietary nonphytate phosphorus, and the highest expression was found when dietary available phosphorus was at 0.25% to 0.3%.	Phosphorus	196-206	vitamin D (1,25- dihydroxyvitamin D3) receptor	Gallus gallus	56-74
24028402-7	2013	With this level of phosphorus supplementation, calbindin and vitamin D receptor reached their highest expression.	Phosphorus	19-29	calbindin 1	Gallus gallus	47-56
24028402-7	2013	With this level of phosphorus supplementation, calbindin and vitamin D receptor reached their highest expression.	Phosphorus	19-29	vitamin D (1,25- dihydroxyvitamin D3) receptor	Gallus gallus	61-79
24038251-5	2013	One of the hormonal factors acutely affected by dietary phosphorus loading is fibroblast growth factor-23, which may be a key factor responsible for many of the cardiovascular disease (CVD) complications of high phosphorus intake.	Phosphorus	56-66	fibroblast growth factor 23	Homo sapiens	78-105
24026993-9	2013	But based on some patients clinical features such as their history of preterm delivery, previous history of recurrent abortions and history of preterm delivery in their family, significant association was found with Hp2-2 compared with healthy control (P&amp;lt;0.003).	Phosphorus	253-254	ADP ribosylation factor like GTPase 6 interacting protein 5	Homo sapiens	216-221
23915305-4	2013	A series of oligo-2"-deoxyribonucleotides with parallel (ps) and antiparallel (aps) strand orientation were constructed containing isoguanine-cytosine, isoguanine-isocytosine, and adenine-thymine base pairs.	Phosphorus	57-59	oligodendrocyte transcription factor 2	Homo sapiens	12-19
24039837-0	2013	Surface display of recombinant Drosophila melanogaster acetylcholinesterase for detection of organic phosphorus and carbamate pesticides.	Phosphorus	101-111	Acetylcholine esterase	Drosophila melanogaster	55-75
24038251-5	2013	One of the hormonal factors acutely affected by dietary phosphorus loading is fibroblast growth factor-23, which may be a key factor responsible for many of the cardiovascular disease (CVD) complications of high phosphorus intake.	Phosphorus	212-222	fibroblast growth factor 23	Homo sapiens	78-105
23607609-5	2013	The results showed that, compared to mice consuming the HFE diet alone, those also consuming phytosterols (the HFE + PS diet) significantly decreased mean serum low-density lipoprotein cholesterol levels and altered brain NMDAR1 mRNA and protein expression and liver Cyp27a1 mRNA expression.	Phosphorus	117-119	glutamate receptor, ionotropic, NMDA1 (zeta 1)	Mus musculus	222-228
23702567-8	2013	CPAP reduced daytime sleepiness (ESS, -2.2; 95% CI, -3.0 to -1.5; P &amp;lt; .0001) compared with standard care.	Phosphorus	66-69	centromere protein J	Homo sapiens	0-4
23893290-2	2013	It has also recently been revealed that novel dendrimers with both viologen units and phosphorus groups in their structure show different antimicrobial, cytotoxic and hemotoxic properties, and have the ability to influence the activity of cholinesterases and to inhibit alpha-synuclein fibrillation.	Phosphorus	86-96	synuclein, alpha	Mus musculus	270-285
23607609-5	2013	The results showed that, compared to mice consuming the HFE diet alone, those also consuming phytosterols (the HFE + PS diet) significantly decreased mean serum low-density lipoprotein cholesterol levels and altered brain NMDAR1 mRNA and protein expression and liver Cyp27a1 mRNA expression.	Phosphorus	117-119	cytochrome P450, family 27, subfamily a, polypeptide 1	Mus musculus	267-274
23719553-5	2013	Although phosphorus is an essential nutrient, in excess it could be linked to tissue damage by a variety of mechanisms involved in the endocrine regulation of extracellular phosphate, specifically the secretion and action of fibroblast growth factor 23 and parathyroid hormone.	Phosphorus	9-19	fibroblast growth factor 23	Homo sapiens	225-252
23885974-3	2013	Electrophilic addition of Cl2( -) to phosphorothioate with elimination of Cl(-) leads to the formation of a two-center three-electron sigma(2)sigma*(1)-bonded adduct radical (-P-S-Cl).	Phosphorus	175-179	endogenous retrovirus group W member 5	Homo sapiens	26-29
23494951-5	2013	SEM/EDAX showed the presence of calcium-and phosphorus-containing particles on untreated and treated disks that were more numerous on fibronectin-coated disks.	Phosphorus	44-54	fibronectin 1	Mus musculus	134-145
23787444-2	2013	Maternal polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) gene have been associated with CL/P.	Phosphorus	108-109	methylenetetrahydrofolate reductase	Homo sapiens	30-65
23787444-2	2013	Maternal polymorphisms in the methylenetetrahydrofolate reductase (MTHFR) gene have been associated with CL/P.	Phosphorus	108-109	methylenetetrahydrofolate reductase	Homo sapiens	67-72
24032853-3	2013	The value of the o-Ps lifetime in the Sm-E liquid crystalline phase of 4TCB, i.e., 2.21 ns at room temperature, was explained by the formation of bubbles induced by Ps atoms, which are created due to a liquidlike state of the butyl chains of 4TCB molecules in the Sm-E phase.	Phosphorus	19-21	small nuclear ribonucleoprotein polypeptide E	Homo sapiens	38-42
24032853-3	2013	The value of the o-Ps lifetime in the Sm-E liquid crystalline phase of 4TCB, i.e., 2.21 ns at room temperature, was explained by the formation of bubbles induced by Ps atoms, which are created due to a liquidlike state of the butyl chains of 4TCB molecules in the Sm-E phase.	Phosphorus	19-21	small nuclear ribonucleoprotein polypeptide E	Homo sapiens	264-268
23789648-10	2013	A monotonic increase in barriers is observed for pseudorotation with the successive replacement of phosphorus with arsenic in methyl-DHP.	Phosphorus	99-109	dihydropyrimidinase	Homo sapiens	133-136
23841641-5	2013	The P-E bond dissociation enthalpies in EP2(C6H10)2 were measured via calorimetric studies to be 134.7 +- 2.1 kcal/mol for P-O, and 93 +- 3 kcal/mol for P-S, respectively, in good agreement with the computed values.	Phosphorus	4-5	prostaglandin E receptor 2	Homo sapiens	40-43
23486250-1	2013	The heterotrophic bacterial community of the Eastern Mediterranean Sea is believed to be limited by phosphorus (P) availability.	Phosphorus	100-114	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	67-70
23709217-7	2013	A screen for additional Dnf1 mutants capable of replacing Drs2 function identified substitutions of TM1 and 2 residues, within a region called the exit gate, that permit recognition of dually acylated PS.	Phosphorus	201-203	dishevelled segment polarity protein 1	Homo sapiens	58-62
23719553-5	2013	Although phosphorus is an essential nutrient, in excess it could be linked to tissue damage by a variety of mechanisms involved in the endocrine regulation of extracellular phosphate, specifically the secretion and action of fibroblast growth factor 23 and parathyroid hormone.	Phosphorus	9-19	parathyroid hormone	Homo sapiens	257-276
24409197-5	2013	In this review, we discuss the role of P-TEFb and the necessity for its mobilization in stimulating viral reactivation from latency upon treatment with HDAC and BET inhibitors.	Phosphorus	39-40	histone deacetylase 9	Homo sapiens	152-156
23919123-1	2013	BACKGROUND: Parathyroid hormone (PTH) secreted by parathyroid glands regulates the metabolism of calcium and phosphorus in bone and kidney.	Phosphorus	109-119	parathyroid hormone	Homo sapiens	33-36
23466546-4	2013	Insulin was complexed with MAH, and insulin-imprinted p(HEMA-MAH) [insulin-(MIP)] cryogel was prepared by free radical polymerization with 2-hydroxyethyl methacrylate (HEMA), N,N,N",N"-tetramethylethylenediamine (TEMED) and ammonium persulfate (APS) in an ice bath.	Phosphorus	15-16	insulin	Homo sapiens	0-7
23919123-1	2013	BACKGROUND: Parathyroid hormone (PTH) secreted by parathyroid glands regulates the metabolism of calcium and phosphorus in bone and kidney.	Phosphorus	109-119	parathyroid hormone	Homo sapiens	12-31
24350484-4	2013	Sludge, sludge sintered at 400 and 600 degrees C, and sea sand suppressed phosphorus release from sediments into the overlying water, whereas sludge and sludge sintered at 200 degrees C increased nitrogen release relative to that without capping.	Phosphorus	74-84	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	54-57
24409197-5	2013	In this review, we discuss the role of P-TEFb and the necessity for its mobilization in stimulating viral reactivation from latency upon treatment with HDAC and BET inhibitors.	Phosphorus	39-40	delta/notch like EGF repeat containing	Homo sapiens	161-164
23532406-3	2013	FGF23 regulates serum phosphorus and active vitamin D levels by action on proximal renal tubule cells.	Phosphorus	22-32	fibroblast growth factor 23	Homo sapiens	0-5
23961477-5	2013	The parathyroid hormone, vitamin D, Fibrogenic growth factor 23 (FGF23) and klotho coreceptor are the key regulators of phosphorus balance in body.	Phosphorus	120-130	fibroblast growth factor 23	Homo sapiens	36-63
23961477-5	2013	The parathyroid hormone, vitamin D, Fibrogenic growth factor 23 (FGF23) and klotho coreceptor are the key regulators of phosphorus balance in body.	Phosphorus	120-130	fibroblast growth factor 23	Homo sapiens	65-70
22025197-2	2013	Previous findings showed that the anticancer drugs p-N,N-bis(2-chloroethyl) amino-l-phenylalanine (melphalan, MEL) and p-N,N-bis(2-chloroethyl)aminophenylbutyric acid (chlorambucil, CAB) belonging to the nitrogen mustard group, in addition to their clastogenic activity, also exert aneugenic potential, nondisjunction and chromosome delay.	Phosphorus	51-52	neural proliferation, differentiation and control 1	Homo sapiens	182-185
23616621-8	2013	Externalization of phosphatidylserine after Ca/P stimulation and interaction of S100A9 and annexin V indicated that a phosphatidylserine-annexin V-S100A9 membrane complex facilitates hydroxyapatite nucleation within the macrophage-derived MV membrane.	Phosphorus	47-48	annexin A5	Homo sapiens	137-146
23616621-8	2013	Externalization of phosphatidylserine after Ca/P stimulation and interaction of S100A9 and annexin V indicated that a phosphatidylserine-annexin V-S100A9 membrane complex facilitates hydroxyapatite nucleation within the macrophage-derived MV membrane.	Phosphorus	47-48	S100 calcium binding protein A9 (calgranulin B)	Mus musculus	147-153
23536116-1	2013	Thermodynamic data for the reversible formation of cis-RuCl2(P-N)(PPh3)(eta(2)-H2) () from trans-RuCl2(P-N)(PPh3) in C6D6 are determined by variable temperature (31)P{(1)H} and (1)H NMR spectroscopy; P-N = o-diphenylphosphino-N,N"-dimethylaniline.	Phosphorus	61-62	protein phosphatase 4 catalytic subunit	Homo sapiens	66-70
23536116-1	2013	Thermodynamic data for the reversible formation of cis-RuCl2(P-N)(PPh3)(eta(2)-H2) () from trans-RuCl2(P-N)(PPh3) in C6D6 are determined by variable temperature (31)P{(1)H} and (1)H NMR spectroscopy; P-N = o-diphenylphosphino-N,N"-dimethylaniline.	Phosphorus	61-62	protein phosphatase 4 catalytic subunit	Homo sapiens	108-112
23717787-0	2013	Serum phosphorus reduction in dialysis patients treated with cinacalcet for secondary hyperparathyroidism results mainly from parathyroid hormone reduction.	Phosphorus	6-16	parathyroid hormone	Homo sapiens	126-145
23589634-8	2013	Over-expressing Ta-PHR1-A1 in wheat upregulated a subset of phosphate starvation response genes, stimulated lateral branching and improved phosphorus uptake when the plants were grown in soil and in nutrient solution.	Phosphorus	139-149	deoxyribodipyrimidine photo-lyase PHR1	Saccharomyces cerevisiae S288C	19-23
23210522-6	2013	In contrast, electron partitioning declined with increasing nitrogen/phosphorus (r(2)  = 0.23) and AOX activity correlated with phosphorus (r(2)  = 0.64).	Phosphorus	128-138	acyl-CoA oxidase 1	Homo sapiens	99-102
23624806-7	2013	This change may lead to an excess of phosphorus within the storage regions of grain, and in turn to the demonstrated increased association of phosphorus with zinc in ferritin-expressing grains.	Phosphorus	37-47	Fer2	Triticum aestivum	166-174
23624806-7	2013	This change may lead to an excess of phosphorus within the storage regions of grain, and in turn to the demonstrated increased association of phosphorus with zinc in ferritin-expressing grains.	Phosphorus	142-152	Fer2	Triticum aestivum	166-174
23434726-5	2013	Applying the (129)I exchange model, an estimate of total phosphorus and nitrogen inflow from the Baltic Proper to the Bothnian Sea indicates values of 20 +- 7 x 10(3) tons/y and 300 +- 50 x 10(3) tons/y respectively.	Phosphorus	57-67	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	127-130
23434726-6	2013	The values for the outflow from the Bothnian Sea to the Baltic Proper hold 12 +- 3 x 10(3) tons/y for total phosphorus and 283 +- 55 x 10(3) tons/y for total nitrogen.	Phosphorus	108-118	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	45-48
23521343-3	2013	EXPERT OPINION: The initial event in the pathogenesis of secondary hyperparathyroidism is the phosphorus overload per nephron that lead to the secretion of a new phosphaturic hormone, fibroblast growth factor 23 from the bone.	Phosphorus	94-104	fibroblast growth factor 23	Homo sapiens	184-211
23328887-0	2013	When phosphorus and NHC (N-heterocyclic carbene) meet each other.	Phosphorus	5-15	high mobility group nucleosomal binding domain 4	Homo sapiens	25-47
23328887-4	2013	This perspective will highlight the new synthetic routes for NHC bearing a phosphorus moiety such as NHC-phosphenium salt, N-phosphorylated-imidazolium salt, 4-phosphino or 4,5-diphosphino-imidazolium salt and tethered phosphino-imidazolium salt.	Phosphorus	75-85	high mobility group nucleosomal binding domain 4	Homo sapiens	61-64
23328887-4	2013	This perspective will highlight the new synthetic routes for NHC bearing a phosphorus moiety such as NHC-phosphenium salt, N-phosphorylated-imidazolium salt, 4-phosphino or 4,5-diphosphino-imidazolium salt and tethered phosphino-imidazolium salt.	Phosphorus	75-85	high mobility group nucleosomal binding domain 4	Homo sapiens	101-104
23376121-6	2013	Our findings show that HI-6 binds to tabun inhibited Homo sapiens AChE (hAChE) with an IC50 value of 300muM and suggest that the reactive nucleophilic moiety of HI-6 is excluded from the phosphorus atom of tabun.	Phosphorus	187-197	acetylcholinesterase (Cartwright blood group)	Homo sapiens	66-70
23376121-6	2013	Our findings show that HI-6 binds to tabun inhibited Homo sapiens AChE (hAChE) with an IC50 value of 300muM and suggest that the reactive nucleophilic moiety of HI-6 is excluded from the phosphorus atom of tabun.	Phosphorus	187-197	acetylcholinesterase (Cartwright blood group)	Homo sapiens	72-77
23430206-13	2013	Correcting the serum phosphorus level may be associated with lower sclerostin levels.	Phosphorus	21-31	sclerostin	Homo sapiens	67-77
23026737-6	2013	Phosphorus-31 magnetic resonance spectroscopy was used to track the changes of brain high-energy phosphates [i.e. adenosine triphosphate and phosphocreatine (PCr)] and intracellular pH (pHi).	Phosphorus	0-10	vasoactive intestinal peptide	Sus scrofa	186-189
24191467-6	2013	In the UK, food additives are estimated to contribute 29% of the domestic load; automatic dishwashing detergents contribute 9% and potentially increasing; domestic laundry 14%, including contributions from phosphonates, but decreasing; phosphorus dosing to reduce lead levels in tap water 6%; food waste disposed of down the drain 1%; and personal care products 1%.	Phosphorus	236-246	nuclear RNA export factor 1	Homo sapiens	279-282
23589853-8	2013	The results show that actin binding to the myosin.ADP.P complex straightens the relay helix before phosphate dissociation.	Phosphorus	52-53	myosin heavy chain 14	Homo sapiens	43-49
23611556-2	2013	Through independent and combined effects on renal phosphorus and vitamin D metabolism, alterations in FGF23 and Klotho expression are essential for maintaining mineral homeostasis in kidney disease.	Phosphorus	50-60	fibroblast growth factor 23	Homo sapiens	102-107
23511365-11	2013	CONCLUSION: On the same FiO2 and PEEP setting, breathing via T-piece improved oxygenation and resulted in increased ScvO2 as compared to breathing on CPAP with PS.	Phosphorus	160-162	centromere protein J	Homo sapiens	150-154
23592003-5	2013	The frequency of the C/C genotype of IL-1alpha was 55% in CP patients, while in the control group it was 20% (p&amp;lt;0.0001).	Phosphorus	31-32	interleukin 1 alpha	Homo sapiens	37-46
23534463-3	2013	Effect of FLRX on helicase ATPase activity was analyzed by phosphorus-free assay based on a colorimetric estimation of ATP hydrolysis-produced inorganic phosphate.	Phosphorus	59-69	helicase for meiosis 1	Homo sapiens	18-26
23534463-3	2013	Effect of FLRX on helicase ATPase activity was analyzed by phosphorus-free assay based on a colorimetric estimation of ATP hydrolysis-produced inorganic phosphate.	Phosphorus	59-69	dynein axonemal heavy chain 8	Homo sapiens	27-33
23514329-4	2013	Single-crystal X-ray diffraction studies revealed that the ligand in [(4a)W(CO)5] and [(4a)CpCo(CO)] binds through its phosphorus lone-pair; [(4a)SbCl3] and [(4a)(AsCl3)2] contain a T-shaped ECl3 unit which binds to the chelating diimine moiety, and associate further via chloride bridges to give centrosymmetric dimers.	Phosphorus	119-129	achaete-scute family bHLH transcription factor 3	Homo sapiens	163-168
23313279-12	2013	3) Micro-XRF imaging: Abnormal calcium and phosphorus inclusions were found within the inner longitudinal sections of tibiotarsi for the PGM-mixture treatment.	Phosphorus	43-53	versican	Gallus gallus	137-140
23298590-11	2013	Overall, the in vitro biocompatibilities of the nanoparticles depend on the chemical composition and size of the Fe(3)O(4)/P(NIPAAm-co-AAc) particles.	Phosphorus	123-124	glycine-N-acyltransferase	Mus musculus	135-138
23506394-12	2013	While MQSGA score, serum phosphorus and calcium x phosphorus product showed positive relationships with calcification score and the expressions of BMP2 and MGP.	Phosphorus	25-35	bone morphogenetic protein 2	Homo sapiens	147-151
23229416-4	2013	The percentage of 5-mC and the protein expression of IGF-2 in the fetal whole brain were both lower in the PD group than in the PS group.	Phosphorus	128-130	insulin-like growth factor 2	Rattus norvegicus	53-58
23506394-12	2013	While MQSGA score, serum phosphorus and calcium x phosphorus product showed positive relationships with calcification score and the expressions of BMP2 and MGP.	Phosphorus	50-60	bone morphogenetic protein 2	Homo sapiens	147-151
23506394-12	2013	While MQSGA score, serum phosphorus and calcium x phosphorus product showed positive relationships with calcification score and the expressions of BMP2 and MGP.	Phosphorus	50-60	matrix Gla protein	Homo sapiens	156-159
23520205-0	2013	Fractional excretion of phosphorus modifies the association between fibroblast growth factor-23 and outcomes.	Phosphorus	24-34	fibroblast growth factor 23	Homo sapiens	68-95
23464730-4	2013	Fibroblast growth factor-23 is now considered to be a key regulator of plasma phosphorus concentration in people but has only recently been investigated in companion animal species.	Phosphorus	78-88	fibroblast growth factor 23	Homo sapiens	0-27
23233539-1	2013	Calcium and phosphorus homeostasis are highly interrelated and share common regulatory hormones, including FGF23.	Phosphorus	12-22	fibroblast growth factor 23	Mus musculus	107-112
23281937-5	2013	The changes observed in the chemical shifts of (31)P MAS NMR spectra with x are found to be too large to be caused solely by changing sodium modification of the phosphate SRO structural groups, and this indicates that internetwork bonding between phosphorus and boron through bridging oxygens (BOs), P-O-B, must be a major contributor to the IRO structure of these glasses.	Phosphorus	247-257	ER membrane protein complex subunit 3	Homo sapiens	300-305
22959760-1	2013	Vitamin D-resistant rickets is the common clinical outcome of multiple genetic mutations that alter the regulation of phosphorus and vitamin D metabolism, mainly through their effects on fibroblast growth factor 23 (FGF-23).	Phosphorus	118-128	fibroblast growth factor 23	Homo sapiens	187-214
22959760-1	2013	Vitamin D-resistant rickets is the common clinical outcome of multiple genetic mutations that alter the regulation of phosphorus and vitamin D metabolism, mainly through their effects on fibroblast growth factor 23 (FGF-23).	Phosphorus	118-128	fibroblast growth factor 23	Homo sapiens	216-222
23413976-12	2013	The relationship between FGF-23 and Ca*P for the older group could be expressed by the exponential model FGF-23= 38.15 e0.4625Ca*P. CONCLUSION: Abnormal values of FGF-23 in adolescents and young adults with CKD correlate with Ca* P in the absence of vascular calcifications, and may serve as a biomarker for the risk of cardiovascular calcifications.	Phosphorus	39-40	fibroblast growth factor 23	Homo sapiens	25-31
23413976-12	2013	The relationship between FGF-23 and Ca*P for the older group could be expressed by the exponential model FGF-23= 38.15 e0.4625Ca*P. CONCLUSION: Abnormal values of FGF-23 in adolescents and young adults with CKD correlate with Ca* P in the absence of vascular calcifications, and may serve as a biomarker for the risk of cardiovascular calcifications.	Phosphorus	39-40	fibroblast growth factor 23	Homo sapiens	105-111
23413976-12	2013	The relationship between FGF-23 and Ca*P for the older group could be expressed by the exponential model FGF-23= 38.15 e0.4625Ca*P. CONCLUSION: Abnormal values of FGF-23 in adolescents and young adults with CKD correlate with Ca* P in the absence of vascular calcifications, and may serve as a biomarker for the risk of cardiovascular calcifications.	Phosphorus	39-40	fibroblast growth factor 23	Homo sapiens	105-111
23233539-4	2013	In wild-type, PTH KO, and PTH-CaSR DKO mice, elevation of either serum calcium or phosphorus by intraperitoneal injection increased serum FGF23 levels.	Phosphorus	82-92	calcium-sensing receptor	Mus musculus	30-34
23233539-4	2013	In wild-type, PTH KO, and PTH-CaSR DKO mice, elevation of either serum calcium or phosphorus by intraperitoneal injection increased serum FGF23 levels.	Phosphorus	82-92	fibroblast growth factor 23	Mus musculus	138-143
23233539-5	2013	In PTH KO and PTH-CaSR DKO mice, however, increases in serum phosphorus by dietary manipulation were accompanied by severe hypocalcemia, which appeared to blunt stimulation of FGF23 release.	Phosphorus	61-71	calcium-sensing receptor	Mus musculus	18-22
23075500-6	2013	We have successfully identified a 25-mer peptide, MARCKS-ED, based on the effector domain sequence of the intracellular membrane protein myristoylated alanine-rich C-kinase substrate that can recognize PS with preferences for highly curved vesicles in a sequence-specific manner.	Phosphorus	202-204	myristoylated alanine rich protein kinase C substrate	Homo sapiens	50-56
23233539-6	2013	Increases in dietary phosphorus in PTH-CaSR DKO mice markedly decreased serum 1,25-dihydroxyvitamin D(3) [1,25(OH)(2)D(3)] despite no change in FGF23, suggesting direct regulation of 1,25(OH)(2)D(3) synthesis by serum phosphorus.	Phosphorus	21-31	calcium-sensing receptor	Mus musculus	39-43
23233539-6	2013	Increases in dietary phosphorus in PTH-CaSR DKO mice markedly decreased serum 1,25-dihydroxyvitamin D(3) [1,25(OH)(2)D(3)] despite no change in FGF23, suggesting direct regulation of 1,25(OH)(2)D(3) synthesis by serum phosphorus.	Phosphorus	21-31	fibroblast growth factor 23	Mus musculus	144-149
23233539-7	2013	Calcium-mediated increases in serum FGF23 required a threshold level of serum phosphorus of about 5 mg/dl.	Phosphorus	78-88	fibroblast growth factor 23	Mus musculus	36-41
23233539-8	2013	Analogously, phosphorus-elicited increases in FGF23 were markedly blunted if serum calcium was less than 8 mg/dl.	Phosphorus	13-23	fibroblast growth factor 23	Mus musculus	46-51
23233539-9	2013	The best correlation between calcium and phosphorus and serum FGF23 was found between FGF23 and the calcium x phosphorus product.	Phosphorus	41-51	fibroblast growth factor 23	Mus musculus	62-67
23233539-9	2013	The best correlation between calcium and phosphorus and serum FGF23 was found between FGF23 and the calcium x phosphorus product.	Phosphorus	41-51	fibroblast growth factor 23	Mus musculus	86-91
23233539-9	2013	The best correlation between calcium and phosphorus and serum FGF23 was found between FGF23 and the calcium x phosphorus product.	Phosphorus	110-120	fibroblast growth factor 23	Mus musculus	62-67
23233539-9	2013	The best correlation between calcium and phosphorus and serum FGF23 was found between FGF23 and the calcium x phosphorus product.	Phosphorus	110-120	fibroblast growth factor 23	Mus musculus	86-91
23233539-11	2013	Thus the regulation of FGF23 by both calcium and phosphorus appears to be fundamentally important in coordinating the serum levels of both mineral ions and ensuring that the calcium x phosphorus product remains within a physiological range.	Phosphorus	49-59	fibroblast growth factor 23	Mus musculus	23-28
23233539-11	2013	Thus the regulation of FGF23 by both calcium and phosphorus appears to be fundamentally important in coordinating the serum levels of both mineral ions and ensuring that the calcium x phosphorus product remains within a physiological range.	Phosphorus	184-194	fibroblast growth factor 23	Mus musculus	23-28
23307792-5	2013	In addition, we observed that T(3) administration significantly decreased plasma 1,25(OH)(2)D and renal CYP27B1 mRNA levels that were increased by low-calcium or low-phosphorus diets and induced hypocalcemia in mice fed a low-calcium diet.	Phosphorus	166-176	cytochrome P450, family 27, subfamily b, polypeptide 1	Mus musculus	104-111
23163230-6	2013	Of the two conjugates, SOD1-(cc)-P(MeOx-b-BuOx) and SOD1-(cc)-P(EtOx-b-BuOx), compared, the latter was entering cells 4 to 7 times faster and at 6 h colocalized predominantly with endoplasmic reticulum (41 +- 3%) and mitochondria (21 +- 2%).	Phosphorus	32-34	superoxide dismutase 1, soluble	Mus musculus	23-27
23094926-4	2013	Through VDR, 1alpha,25(OH)2D3 regulates more than 200 genes in mammals, including those involved in the calcium and phosphorus homeostasis, immune function, reproduction, cardiovascular, central nerve system, inflammation, angiogenesis, and cellular proliferation, differentiation and apoptosis.	Phosphorus	116-126	vitamin D receptor	Homo sapiens	8-11
23353624-3	2013	In the present study, we investigated the effects of the TNSALP genotype on associations among serum bonespecific alkaline phosphatase (BAP), serum calcium, and phosphorus in healthy young Japanese subjects.	Phosphorus	161-171	alkaline phosphatase, biomineralization associated	Homo sapiens	57-63
23353624-6	2013	RESULTS: Grouped by the TNSALP genotype, a significant negative correlation between serum BAP and phosphorus was observed in 787T&gt;C homozygotes (CC-type), but not in heterozygotes (TCtype), nor in 787T homozygotes (TT-type).	Phosphorus	98-108	alkaline phosphatase, biomineralization associated	Homo sapiens	24-30
23353624-7	2013	CONCLUSIONS: In the present study, we revealed that the single nucleotide polymorphism 787T&gt;C in the TNSALP gene had effects on the correlation between serum BAP and phosphorus in young adult subjects.	Phosphorus	169-179	alkaline phosphatase, biomineralization associated	Homo sapiens	104-110
23186954-13	2013	Treatment with subcutaneous recombinant human parathyroid hormone teriparatide (rhPTH [1-34]) 20 mcg twice daily for three days normalized her calcium and phosphorus concentrations.	Phosphorus	155-165	parathyroid hormone	Homo sapiens	46-65
23748218-4	2013	FGF-23, the humoral factor involved in phosphate metabolism, is strongly associated with serum phosphorus level.	Phosphorus	95-105	fibroblast growth factor 23	Homo sapiens	0-6
23595379-8	2013	TXL pretreatment increased the PKA activity and the expression of Ser(133) p-CREB in the reflow and no-reflow myocardium (P &lt; 0.05).	Phosphorus	4-5	protein kinase cAMP-activated catalytic subunit alpha	Sus scrofa	31-34
23595379-8	2013	TXL pretreatment increased the PKA activity and the expression of Ser(133) p-CREB in the reflow and no-reflow myocardium (P &lt; 0.05).	Phosphorus	4-5	cAMP response element binding protein	Sus scrofa	77-81
25151822-15	2013	Our results showed an increase of both activities (LOX and POX) in wheat infected by Bgt for both (M) and (NM) plants by the inoculum SZE (Ri+Gm) at P/5 phosphorus concentration.	Phosphorus	153-163	LOC543232	Triticum aestivum	51-54
25151822-15	2013	Our results showed an increase of both activities (LOX and POX) in wheat infected by Bgt for both (M) and (NM) plants by the inoculum SZE (Ri+Gm) at P/5 phosphorus concentration.	Phosphorus	153-163	peroxidase-like	Triticum aestivum	59-62
23548855-9	2013	CONCLUSION: Our results indicate that Mg might not improve endothelial function (CRP level and FMD) and that a decreased cIMT as a marker of atherosclerosis may be due to the inhibition of calcification through the regulation parathormone, calcium, and phosphorus.	Phosphorus	253-263	CIMT	Homo sapiens	121-125
23781580-8	2013	CONCLUSION: UGT1A1 genotype-based RDs of irinotecan in CPT-P therapy were determined.	Phosphorus	56-57	UDP glucuronosyltransferase family 1 member A1	Homo sapiens	12-18
23705812-5	2013	Formulation PL6 was considered as desirable with highest EE% (72.3 +- 6.1%), PS (279.4 +- 1.8 nm), zeta potential (-29.4 +- 2.6 mV), and cumulative drug diffusion of 96.43 +- 3.1% in 24 h. The ANOVA results for the dependent variables demonstrated that the model was significant (p value &lt; 0.05) for response variables.	Phosphorus	77-79	transmembrane protein 115	Homo sapiens	12-15
23681536-2	2013	For instance, the involvement of plant PLD members has been shown or suggested in a wide variety of the cellular and physiological processes such as regulating stomatal opening and closure; signaling plant responses to drought, salt, and other abiotic and biotic stresses; organizing microtubule and actin cytoskeletal structures; promoting pollen tube growth; cycling phosphorus; signaling nitrogen availability; regulating N-acylethanolamine stress signaling; and remodeling membrane phospholipids in plant responses to phosphate deprivation and during and after freezing.	Phosphorus	369-379	phospholipase D alpha 1	Arabidopsis thaliana	39-42
23878759-8	2013	Serum DKK-1 levels correlated negatively with both lumbar T score (r = -0.69, P &lt; 0.001) and femur T score (r = -0.64, P &lt; 0.001) and correlated positively with duration of menopause (r = 0.61, P &lt; 0.001), while there was no significant correlation between serum levels of either calcium, phosphorus or alkaline phosphatase, and both serum Dickkopf-1 levels and the level of bone mineral density (P &gt; 0.05).	Phosphorus	298-308	dickkopf WNT signaling pathway inhibitor 1	Homo sapiens	6-11
23879172-3	2013	Phosphorus-containing sirolimus (FIM-A), which targets mTOR signaling, inhibits cancer cell growth in vitro.	Phosphorus	0-10	mechanistic target of rapamycin kinase	Homo sapiens	55-59
23774081-1	2013	The spin states of an electron bound to a single phosphorus donor in silicon show remarkably long coherence and relaxation times, which makes them promising building blocks for the realization of a solid-state quantum computer.	Phosphorus	49-59	spindlin 1	Homo sapiens	4-8
23774081-2	2013	Here we demonstrate, by high-fidelity (93%) electrical spin readout, that a long relaxation time T1 of about 2 s, at B=1.2 T and T 100 mK, is also characteristic of electronic spin states associated with a cluster of few phosphorus donors, suggesting their suitability as hosts for spin qubits.	Phosphorus	221-231	spindlin 1	Homo sapiens	55-59
23774081-2	2013	Here we demonstrate, by high-fidelity (93%) electrical spin readout, that a long relaxation time T1 of about 2 s, at B=1.2 T and T 100 mK, is also characteristic of electronic spin states associated with a cluster of few phosphorus donors, suggesting their suitability as hosts for spin qubits.	Phosphorus	221-231	spindlin 1	Homo sapiens	176-180
23774081-2	2013	Here we demonstrate, by high-fidelity (93%) electrical spin readout, that a long relaxation time T1 of about 2 s, at B=1.2 T and T 100 mK, is also characteristic of electronic spin states associated with a cluster of few phosphorus donors, suggesting their suitability as hosts for spin qubits.	Phosphorus	221-231	spindlin 1	Homo sapiens	176-180
23774081-3	2013	Owing to the difference in the hyperfine coupling, electronic spin transitions of such clusters can be sufficiently distinct from those of a single phosphorus donor.	Phosphorus	148-158	spindlin 1	Homo sapiens	62-66
23774081-4	2013	Our atomistic tight-binding calculations reveal that when neighbouring qubits are hosted by a single phosphorus atom and a cluster of two phosphorus donors, the difference in their electron spin resonance frequencies allows qubit rotations with error rates  10(-4).	Phosphorus	101-111	spindlin 1	Homo sapiens	190-194
23774081-4	2013	Our atomistic tight-binding calculations reveal that when neighbouring qubits are hosted by a single phosphorus atom and a cluster of two phosphorus donors, the difference in their electron spin resonance frequencies allows qubit rotations with error rates  10(-4).	Phosphorus	138-148	spindlin 1	Homo sapiens	190-194
23774446-2	2013	Studies in individuals without CKD suggest that FGF23 levels are regulated by dietary phosphorus; however, the effect of pharmacologic phosphorus restriction on FGF23 in CKD patients is uncertain.	Phosphorus	86-96	fibroblast growth factor 23	Homo sapiens	48-53
23443538-6	2013	Under phosphorus-depleted conditions, the Arabidopsis sqd2 mutant, which does not accumulate either sulfoquinovosyldiacylglycerol or glucuronosyldiacylglycerol, was the most severely damaged of three sulfoquinovosyldiacylglycerol-deficient mutants.	Phosphorus	6-16	sulfoquinovosyldiacylglycerol 2	Arabidopsis thaliana	54-58
23199690-0	2013	Nitrogen and phosphorus interaction and cytokinin: responses of the primary root of Arabidopsis thaliana and the pdr1 mutant.	Phosphorus	13-23	pleiotropic drug resistance 1	Arabidopsis thaliana	113-117
24068957-5	2013	Embryos that were compound mutant for miR-17-92 and the related miR-106b-25 cluster had completely penetrant CL/P.	Phosphorus	112-113	miR-17-92a-1 cluster host gene	Homo sapiens	38-47
24068957-5	2013	Embryos that were compound mutant for miR-17-92 and the related miR-106b-25 cluster had completely penetrant CL/P.	Phosphorus	112-113	membrane associated ring-CH-type finger 8	Homo sapiens	38-41
23866594-1	2013	AIM: To study the clinical significance of determining the serum concentration of phosphorus and calcium metabolism regulators--the morphogenetic proteins FGF-23 and Klotho in patients with different stages of chronic kidney disease (CKD).	Phosphorus	82-92	fibroblast growth factor 23	Homo sapiens	155-161
23866594-1	2013	AIM: To study the clinical significance of determining the serum concentration of phosphorus and calcium metabolism regulators--the morphogenetic proteins FGF-23 and Klotho in patients with different stages of chronic kidney disease (CKD).	Phosphorus	82-92	klotho	Homo sapiens	166-172
23092211-9	2012	Instead, it skews the oxyanion hole and makes the phosphorus more open to the nucleophilic water molecule, resulting in a remarkable change in the rate-determining step and significantly improved catalytic activity of human BChE.	Phosphorus	50-60	butyrylcholinesterase	Homo sapiens	224-228
23369255-3	2012	Using the Langmuir model equation, the monolayer removal capacity of PHEMA surface was found to be 0.7388, 0.8396 and 3.0367 mg/g for Co(II), Cu(IotaIota) and Pb(II) ions and removal capacity of P(MMA-HEMA) was found to be 28.8442, 31.1526 and 31.4465 mg/g for Co(II), Cu(IotaIota) and Pb(II) ions, respectively.	Phosphorus	69-70	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	134-140
23369255-3	2012	Using the Langmuir model equation, the monolayer removal capacity of PHEMA surface was found to be 0.7388, 0.8396 and 3.0367 mg/g for Co(II), Cu(IotaIota) and Pb(II) ions and removal capacity of P(MMA-HEMA) was found to be 28.8442, 31.1526 and 31.4465 mg/g for Co(II), Cu(IotaIota) and Pb(II) ions, respectively.	Phosphorus	69-70	submaxillary gland androgen regulated protein 3B	Homo sapiens	142-165
23369255-3	2012	Using the Langmuir model equation, the monolayer removal capacity of PHEMA surface was found to be 0.7388, 0.8396 and 3.0367 mg/g for Co(II), Cu(IotaIota) and Pb(II) ions and removal capacity of P(MMA-HEMA) was found to be 28.8442, 31.1526 and 31.4465 mg/g for Co(II), Cu(IotaIota) and Pb(II) ions, respectively.	Phosphorus	69-70	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	261-267
23369255-3	2012	Using the Langmuir model equation, the monolayer removal capacity of PHEMA surface was found to be 0.7388, 0.8396 and 3.0367 mg/g for Co(II), Cu(IotaIota) and Pb(II) ions and removal capacity of P(MMA-HEMA) was found to be 28.8442, 31.1526 and 31.4465 mg/g for Co(II), Cu(IotaIota) and Pb(II) ions, respectively.	Phosphorus	69-70	submaxillary gland androgen regulated protein 3B	Homo sapiens	269-292
23380985-8	2012	In Rtx patients, CIMT was positively correlated with age, BMI, serum phosphorus, low-density lipoprotein, and hs-CRP.	Phosphorus	69-79	CIMT	Homo sapiens	17-21
23072540-0	2012	Eliminating the purple acid phosphatase AtPAP26 in Arabidopsis thaliana delays leaf senescence and impairs phosphorus remobilization.	Phosphorus	107-117	purple acid phosphatase 26	Arabidopsis thaliana	40-47
23033062-3	2012	Notably, it is found that the devices based on phosphorus(V) porphyrins with a configuration structure of [ITO/PEDOT : PSS/organic active film/LiF/Al] give an incident-photon-to-current conversion efficiency (IPCE) response.	Phosphorus	47-57	LIF interleukin 6 family cytokine	Homo sapiens	143-146
22997345-1	2012	BACKGROUND AND OBJECTIVE: Fibroblast growth factor 23 (FGF-23), a regulator of phosphorus metabolism, is a risk marker in CKD.	Phosphorus	79-89	fibroblast growth factor 23	Homo sapiens	26-53
22997345-1	2012	BACKGROUND AND OBJECTIVE: Fibroblast growth factor 23 (FGF-23), a regulator of phosphorus metabolism, is a risk marker in CKD.	Phosphorus	79-89	fibroblast growth factor 23	Homo sapiens	55-61
23134409-6	2012	The heteroleptic 1:1 LP complexes 2-4 were also obtained by the one-pot reaction of Mes2Te, Ph3E (E = P, As, Sb) and HO3SCF3.	Phosphorus	22-23	H3 histone pseudogene 26	Homo sapiens	92-96
22962014-0	2012	Annexin V decreases PS-mediated macrophage efferocytosis and deteriorates elastase-induced pulmonary emphysema in mice.	Phosphorus	20-22	annexin A5	Mus musculus	0-9
21812703-6	2012	Most of the 11- to 14-year-old boys without CL/P were in CS3 and CS4, though it was not so obvious in boys with CL/P.	Phosphorus	47-48	myozenin 3	Homo sapiens	57-60
21812703-11	2012	By the age of 14, children with CL/P had a 4.679 times higher risk of delayed CS3, and the 95% confidence interval for the odds ratio was 2.129 to 10.286.	Phosphorus	35-36	myozenin 3	Homo sapiens	78-81
23026887-4	2012	Outflow median dissolved reactive phosphorus (DRP) and total phosphorus (TP) stream concentrations were significantly less in Period 2 compared to Period 1.	Phosphorus	34-44	period circadian regulator 2	Homo sapiens	126-134
22723123-5	2012	RESULTS: SLN-PS was &gt;4-fold more potent than PS in inhibiting the growth of A549 and H510 cells in vitro.	Phosphorus	13-15	sarcolipin	Mus musculus	9-12
22837529-8	2012	Preincubation of monocytes with molecules that bind PS protected these cells from hBD-3-induced membrane damage, suggesting that outer-membrane PS expression can at least partially explain monocyte susceptibility to hBD-3.	Phosphorus	52-54	defensin beta 103B	Homo sapiens	82-87
22837529-8	2012	Preincubation of monocytes with molecules that bind PS protected these cells from hBD-3-induced membrane damage, suggesting that outer-membrane PS expression can at least partially explain monocyte susceptibility to hBD-3.	Phosphorus	52-54	defensin beta 103B	Homo sapiens	216-221
22837529-8	2012	Preincubation of monocytes with molecules that bind PS protected these cells from hBD-3-induced membrane damage, suggesting that outer-membrane PS expression can at least partially explain monocyte susceptibility to hBD-3.	Phosphorus	144-146	defensin beta 103B	Homo sapiens	82-87
22837529-8	2012	Preincubation of monocytes with molecules that bind PS protected these cells from hBD-3-induced membrane damage, suggesting that outer-membrane PS expression can at least partially explain monocyte susceptibility to hBD-3.	Phosphorus	144-146	defensin beta 103B	Homo sapiens	216-221
22723123-6	2012	SLN-PS enhanced cellular uptake and facilitated PS accumulation in mitochondria, leading to oxidative stress and apoptosis via the mitochondrial-apoptosis pathway.	Phosphorus	4-6	sarcolipin	Mus musculus	0-3
22723123-7	2012	SLN-PS was highly effective in suppressing the growth of A549 xenografts (78% inhibition compared to control, p &lt; 0.01); while PS had no significant effect.	Phosphorus	4-6	sarcolipin	Mus musculus	0-3
23146451-0	2012	Role of fibroblast growth factor 23 (FGF23) in the metabolism of phosphorus and calcium immediately after kidney transplantation.	Phosphorus	65-75	fibroblast growth factor 23	Homo sapiens	8-35
22947512-11	2012	Interestingly, 1,2-DG6 (2.5 muM) and PS (1 muM) with calcium activated the enzyme activity to ~7 fold.	Phosphorus	37-39	latexin	Homo sapiens	43-46
23146451-0	2012	Role of fibroblast growth factor 23 (FGF23) in the metabolism of phosphorus and calcium immediately after kidney transplantation.	Phosphorus	65-75	fibroblast growth factor 23	Homo sapiens	37-42
23146451-9	2012	CONCLUSIONS: Elevated serum levels of FGF23 could explain the deficiency of calcitriol and elevated renal phosphorus wasting in the early posttransplant period.	Phosphorus	106-116	fibroblast growth factor 23	Homo sapiens	38-43
23599704-8	2012	Stepwise multiple regression analysis revealed that the percent change of the calcium-phosphorus product in the nondiabetic group and that of phosphorus in the diabetic group were predictive variables for the percent change of MDA-LDL/LDL, whereas the percent change of log high-sensitive C-reactive protein and that of systolic blood pressure in the nondiabetic group and that of diastolic blood pressure in the diabetic group were predictive variables for the percent change of plasma pentosidine.	Phosphorus	142-152	C-reactive protein	Homo sapiens	289-307
23071309-7	2012	Introducing Vam7(1-125)p as a separate recombinant protein suppresses the defect caused by N-domain deletion from Vam7tm, demonstrating that the function of this N-domain is not constrained to covalent attachment to Vam7p.	Phosphorus	23-24	Vam7p	Saccharomyces cerevisiae S288C	12-16
23233960-0	2012	[Forms and distributions of particulate phosphorus in the surface sediments of North Yellow Sea].	Phosphorus	40-50	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	92-95
22888742-4	2012	The relative MMP-2 stimulation of PS, PE, BS and BE loaded in elastic niosomes were 1.26 +/- 0.14, 1.34 +/- 0.15, 1.09 +/- 0.09 and 1.20 +/- 0.04 for the pro MMP-2 and 1.26 +/- 0.12, 1.41 +/- 0.23, 1.01 +/- 0.08 and 1.03 +/- 0.12 for the active MMP-2, respectively in comparing to the control which were similar activity to their free enzymes.	Phosphorus	34-36	matrix metallopeptidase 2	Homo sapiens	13-18
22865705-1	2012	More than LiP service: The adsorption of red phosphorus into porous carbon provides a composite anode material for lithium-ion batteries.	Phosphorus	41-55	SMG1 nonsense mediated mRNA decay associated PI3K related kinase	Homo sapiens	10-13
22673528-0	2012	Spin crossover in phosphorus- and arsenic-bridged cyclopentadienyl-manganese(II) dimers.	Phosphorus	18-28	spindlin 1	Homo sapiens	0-4
22622660-7	2012	Moreover, PUFA are incorporated in breast cancer lipid rafts with different specificity for the phospholipid moiety, in particular PUFA are incorporated in PI, PS, and PC phospholipids that may be relevant to the formation of PUFA metabolites (prostaglandins, prostacyclins, leukotrienes, resolvines, and protectines) of phospholipids deriving second messengers and signal transduction activation.	Phosphorus	160-162	pumilio RNA binding family member 3	Homo sapiens	10-14
22622660-7	2012	Moreover, PUFA are incorporated in breast cancer lipid rafts with different specificity for the phospholipid moiety, in particular PUFA are incorporated in PI, PS, and PC phospholipids that may be relevant to the formation of PUFA metabolites (prostaglandins, prostacyclins, leukotrienes, resolvines, and protectines) of phospholipids deriving second messengers and signal transduction activation.	Phosphorus	160-162	pumilio RNA binding family member 3	Homo sapiens	131-135
22622660-7	2012	Moreover, PUFA are incorporated in breast cancer lipid rafts with different specificity for the phospholipid moiety, in particular PUFA are incorporated in PI, PS, and PC phospholipids that may be relevant to the formation of PUFA metabolites (prostaglandins, prostacyclins, leukotrienes, resolvines, and protectines) of phospholipids deriving second messengers and signal transduction activation.	Phosphorus	160-162	pumilio RNA binding family member 3	Homo sapiens	131-135
22257707-8	2012	In addition, PS treatment inhibited the influx of inflammatory CD8(pos) and CD11b(pos) cells to kidney tissue.	Phosphorus	13-15	integrin subunit alpha M	Homo sapiens	76-81
22801440-9	2012	CONCLUSION: The lower VDR expression in osteoporotic could indicate a lower ability to respond to vitamin D, and could be the explanation of the increase in the PTH and decrease in the phosphorus levels in patients with respect to controls.	Phosphorus	185-195	vitamin D receptor	Homo sapiens	22-25
22581996-4	2012	Addition of high dietary phosphorus to this diet increased FGF23 except in rats with hypocalcemia despite high PTH levels.	Phosphorus	25-35	fibroblast growth factor 23	Rattus norvegicus	59-64
22703926-13	2012	CONCLUSIONS: FGF-23, a hormone involved in phosphorous and vitamin D homeostasis, is independently associated with all-cause death and incident HF in community-living older persons.	Phosphorus	43-54	fibroblast growth factor 23	Homo sapiens	13-19
22722629-2	2012	OBJECTIVE: To elucidate possible mechanisms leading to neurodegeneration in patients with glucocerebrosidase (GBA)-associated Parkinson disease (PD) using combined proton ((1)H) and phosphorus ((31)P) magnetic resonance spectroscopic imaging (MRSI) in vivo.	Phosphorus	182-192	glucosylceramidase beta	Homo sapiens	90-108
22722629-2	2012	OBJECTIVE: To elucidate possible mechanisms leading to neurodegeneration in patients with glucocerebrosidase (GBA)-associated Parkinson disease (PD) using combined proton ((1)H) and phosphorus ((31)P) magnetic resonance spectroscopic imaging (MRSI) in vivo.	Phosphorus	182-192	glucosylceramidase beta	Homo sapiens	110-113
22020549-15	2012	The relationship between CL/P and CDH1 needs further study to inform future parents from hereditary diffuse gastric cancer (HDGC) families adequately.	Phosphorus	28-29	cadherin 1	Homo sapiens	34-38
22406438-2	2012	Past roles have been to alter calcium and phosphorus metabolism to prevent or lessen bone disease and reduce PTH levels in dialysis patients and more recently, pre-dialysis patients.	Phosphorus	42-52	parathyroid hormone	Homo sapiens	109-112
22839363-12	2012	Adsorbed As(III) could be removed prior to fertilizer application, however coprecipitated As(V) will release upon mineral decomposition, linking its cycling to that of phosphorus.	Phosphorus	168-178	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	90-95
22863242-0	2012	Is serum phosphorus control related to parathyroid hormone control in dialysis patients with secondary hyperparathyroidism?	Phosphorus	9-19	parathyroid hormone	Homo sapiens	39-58
22863242-1	2012	BACKGROUND: Elevated serum phosphorus (P) levels have been linked to increased morbidity and mortality in dialysis patients with secondary hyperparathyroidism (SHPT) but may be difficult to control if parathyroid hormone (PTH) is persistently elevated.	Phosphorus	27-37	parathyroid hormone	Homo sapiens	201-220
22311343-4	2012	RESULTS: In bivariate analyses, C-terminal FGF23 levels were positively related to phosphorus and uric acid levels.	Phosphorus	83-93	fibroblast growth factor 23	Homo sapiens	43-48
22563127-6	2012	This mutant, named lpa1-7, is able to accumulate less phytic phosphorus and a higher level of free inorganic phosphate in the seeds compared with wild type.	Phosphorus	61-71	inositol-3-phosphate synthase	Zea mays	19-25
23214203-5	2012	High phosphorus intake, 1,25-dihydroxyvitamin D3 and PTH are the main stimuli for FGF-23 secretion.	Phosphorus	5-15	fibroblast growth factor 23	Homo sapiens	82-88
22578268-0	2012	The Pht1;9 and Pht1;8 transporters mediate inorganic phosphate acquisition by the Arabidopsis thaliana root during phosphorus starvation.	Phosphorus	115-125	phosphate transporter 1;9	Arabidopsis thaliana	4-10
22578268-0	2012	The Pht1;9 and Pht1;8 transporters mediate inorganic phosphate acquisition by the Arabidopsis thaliana root during phosphorus starvation.	Phosphorus	115-125	phosphate transporter 1;8	Arabidopsis thaliana	15-21
22595391-9	2012	Clinical examples show reduced FTRx despite increased TRx/GFR for phosphorus and urate, and analyses suggest that such discrepancies are often inevitable.	Phosphorus	66-76	Rap guanine nucleotide exchange factor 5	Homo sapiens	58-61
21932115-3	2012	Associations between serum phosphorus and PTH may vary by race.	Phosphorus	27-37	parathyroid hormone	Homo sapiens	42-45
21932115-11	2012	In whites only, lower serum phosphorus and lower serum retinol were associated with higher PTH.	Phosphorus	28-38	parathyroid hormone	Homo sapiens	91-94
21932115-12	2012	CONCLUSIONS: Numerous factors not classically associated with calcium-phosphorus homeostasis are independently associated with PTH and should be considered in future studies of PTH and chronic disease.	Phosphorus	70-80	parathyroid hormone	Homo sapiens	127-130
22492434-8	2012	Deletion of endA abolished both extracellular degradation of DNA by S. oneidensis MR-1 and the ability to use eDNA as a sole source of phosphorus.	Phosphorus	135-145	deoxyribonuclease	Shewanella oneidensis MR-1	12-16
22150777-12	2012	Expression of NKD-2 and DVL3 remained unchanged and the expression of active Tyr-p-GSK3beta increased significantly.	Phosphorus	2-3	NKD inhibitor of WNT signaling pathway 2	Homo sapiens	14-19
22150777-12	2012	Expression of NKD-2 and DVL3 remained unchanged and the expression of active Tyr-p-GSK3beta increased significantly.	Phosphorus	2-3	dishevelled segment polarity protein 3	Homo sapiens	24-28
22265240-7	2012	The prevalence of anemia, elevated PTH and high phosphorus showed an inverse relationship with eGFR.	Phosphorus	48-58	epidermal growth factor receptor	Homo sapiens	95-99
22265240-10	2012	Using an eGFR of 60 ml/min/1.73 m(2) modification of diet in renal disease equation (MDRD) as screening threshold for metabolic complications would result in a high incidence of missed complications: 29%, 28% and 40% for anemia, elevated PTH and high phosphorus, respectively.	Phosphorus	251-261	epidermal growth factor receptor	Homo sapiens	9-13
22265240-11	2012	CONCLUSION: The presence of anemia, an elevated PTH or an elevated serum phosphorus level increased with lower eGFR but even among patients with an eGFR &gt;60 ml/min/1.73 m(2), these complications are common.	Phosphorus	73-83	epidermal growth factor receptor	Homo sapiens	111-115
22265240-11	2012	CONCLUSION: The presence of anemia, an elevated PTH or an elevated serum phosphorus level increased with lower eGFR but even among patients with an eGFR &gt;60 ml/min/1.73 m(2), these complications are common.	Phosphorus	73-83	epidermal growth factor receptor	Homo sapiens	148-152
22353396-0	2012	Phosphorus-containing dendrimers against alpha-synuclein fibril formation.	Phosphorus	0-10	synuclein alpha	Homo sapiens	41-56
22365809-2	2012	The optimized PEI-PE/pDNA complexes at an N/P ratio of 16 had a particle size of 225 nm, a surface charge of +31 mV, and protected the pDNA from the action of DNase I.	Phosphorus	14-15	deoxyribonuclease I	Mus musculus	159-166
22353396-1	2012	The aim of this work was to study the effect of phosphorus-containing dendrimers (generations G3 and G4) on the fibrillation of alpha-synuclein (ASN).	Phosphorus	48-58	synuclein alpha	Homo sapiens	128-143
22025115-8	2012	RRF, serum phosphorus and calcium levels and active vitamin D therapy explain 69% of the variation in FGF-23.	Phosphorus	11-21	fibroblast growth factor 23	Homo sapiens	102-108
22343749-7	2012	Recombinant phosphatidylserine-specific phospholipase A(1) (PS-PLA(1)) that deacylates fatty acid at the sn-1 position of PS and produces 2-acyl-LysoPS, but not catalytically inactive mutant PS-PLA(1), stimulated the release of AP-TGFalpha from GPR34-expressing cells.	Phosphorus	60-62	phospholipase A1 member A	Homo sapiens	191-200
22343749-7	2012	Recombinant phosphatidylserine-specific phospholipase A(1) (PS-PLA(1)) that deacylates fatty acid at the sn-1 position of PS and produces 2-acyl-LysoPS, but not catalytically inactive mutant PS-PLA(1), stimulated the release of AP-TGFalpha from GPR34-expressing cells.	Phosphorus	60-62	transforming growth factor alpha	Homo sapiens	231-239
22343749-7	2012	Recombinant phosphatidylserine-specific phospholipase A(1) (PS-PLA(1)) that deacylates fatty acid at the sn-1 position of PS and produces 2-acyl-LysoPS, but not catalytically inactive mutant PS-PLA(1), stimulated the release of AP-TGFalpha from GPR34-expressing cells.	Phosphorus	60-62	G protein-coupled receptor 34	Homo sapiens	245-250
22087764-6	2012	Combining immunogold-silver EM and electron probe microanalysis further demonstrated that the OPN protein was localized at the periphery of cell debris or degenerating neurites, corresponding with locally higher concentrations of calcium and phosphorus, and that the relative magnitude of OPN accumulation was comparable to that of calcium and phosphorus.	Phosphorus	242-252	secreted phosphoprotein 1	Rattus norvegicus	94-97
22087764-6	2012	Combining immunogold-silver EM and electron probe microanalysis further demonstrated that the OPN protein was localized at the periphery of cell debris or degenerating neurites, corresponding with locally higher concentrations of calcium and phosphorus, and that the relative magnitude of OPN accumulation was comparable to that of calcium and phosphorus.	Phosphorus	344-354	secreted phosphoprotein 1	Rattus norvegicus	94-97
22852425-5	2012	Using the aforementioned gas-water ratio of 10 and a hydraulic residence time (HRT) of 2 days, the mean removal efficiencies of the multi-medium CFI for NH3-N and total phosphorus were 71.7% and 63.6%, respectively-approximately twice as great as those in the non-aerated system.	Phosphorus	169-179	complement factor I	Homo sapiens	145-148
22532149-10	2012	In OA cartilage, Akt decreased (p &amp;lt; 0.05) and PKCalpha increased (p &amp;lt; 0.05).	Phosphorus	32-33	AKT serine/threonine kinase 1	Homo sapiens	17-20
22589859-2	2012	deviation for Pd, P and Cl atoms = 0.024 A) with the PPh(3) and Cl ligands mutually trans.	Phosphorus	14-15	caveolin 1	Homo sapiens	53-59
21874319-1	2012	Parathyroid hormone (PTH) plays a critical role in calcium and phosphorus metabolism.	Phosphorus	63-73	parathyroid hormone	Homo sapiens	0-19
25049596-0	2012	The Influence of Dietary Calcium and Phosphorus Imbalance on Intestinal NaPi-IIb and Calbindin mRNA Expression and Tibia Parameters of Broilers.	Phosphorus	37-47	solute carrier family 34 member 2	Homo sapiens	72-80
25049596-1	2012	A 2x2 factorial experiment was conducted to study the effect of dietary calcium and non-phytate phosphorus (nPP) imbalance on calbindin and NaPi-IIb mRNA levels in the small intestine and tibia parameters of broiler chicks.	Phosphorus	96-106	calbindin 1	Homo sapiens	126-135
25049596-1	2012	A 2x2 factorial experiment was conducted to study the effect of dietary calcium and non-phytate phosphorus (nPP) imbalance on calbindin and NaPi-IIb mRNA levels in the small intestine and tibia parameters of broiler chicks.	Phosphorus	96-106	solute carrier family 34 member 2	Homo sapiens	140-148
19793331-14	2012	Regarding the mineral composition, in ML-GH group increments in concentrations of phosphorus (10.70 vs 10.34; p = .013) were observed at 2 weeks and of magnesium (0.29 vs 0.25; p = .019) 5 weeks after implantation.	Phosphorus	82-92	somatotropin	Canis lupus familiaris	41-43
21431856-7	2012	A sample study composed of 39 multiplex Italian pedigrees was enrolled to test linkage between two microsatellite flanking HAND2 locus and CL/P.	Phosphorus	142-143	heart and neural crest derivatives expressed 2	Mus musculus	123-128
22450905-8	2012	CONCLUSIONS This meta-analysis suggests that maternal MTHFR 677TT genotype might increase the risk of having a CL/P offspring in the white population.	Phosphorus	114-115	methylenetetrahydrofolate reductase	Homo sapiens	54-59
22330754-5	2012	The selective introduction of a phosphorus moiety in O-3 using chlorodiphenylphosphine has led to 3-O-diphenylphosphinito-N-phthaloyl-6-O-pivaloylchitosan with a ds of 0.97 from energy dispersive X-ray spectroscopy, which demonstrates the potential applications of O-6 pivaloyl protection.	Phosphorus	32-42	immunoglobulin kappa variable 2D-38 (pseudogene)	Homo sapiens	53-56
22330754-5	2012	The selective introduction of a phosphorus moiety in O-3 using chlorodiphenylphosphine has led to 3-O-diphenylphosphinito-N-phthaloyl-6-O-pivaloylchitosan with a ds of 0.97 from energy dispersive X-ray spectroscopy, which demonstrates the potential applications of O-6 pivaloyl protection.	Phosphorus	32-42	immunoglobulin kappa variable 1D-35 (pseudogene)	Homo sapiens	265-268
22362063-2	2012	The aim of this pilot study is to assess whether a very-low-protein diet (0.3 g/kg per day) with a consequent low intake of phosphorus would reduce fibroblast growth factor 23 compared with a low-protein diet (0.6 g/kg per day) in CKD patients not yet on dialysis.	Phosphorus	124-134	fibroblast growth factor 23	Homo sapiens	148-175
22334717-6	2012	Uremic rats fed with a high-phosphorus diet showed more severe sHPT, higher serum FGF23 levels and mortality, and decreased parathyroid Klotho gene expression.	Phosphorus	28-38	fibroblast growth factor 23	Rattus norvegicus	82-87
22334717-6	2012	Uremic rats fed with a high-phosphorus diet showed more severe sHPT, higher serum FGF23 levels and mortality, and decreased parathyroid Klotho gene expression.	Phosphorus	28-38	Klotho	Rattus norvegicus	136-142
21874319-1	2012	Parathyroid hormone (PTH) plays a critical role in calcium and phosphorus metabolism.	Phosphorus	63-73	parathyroid hormone	Homo sapiens	21-24
21874319-5	2012	In this model, an increase in PTH was induced by its autonomous production in PHP, while PTH in CKD was elevated by a decrease in feedback inhibition of 1,25(OH)2D in the serum, as well as an increase in stimulation by phosphorus in the serum.	Phosphorus	219-229	parathyroid hormone	Homo sapiens	30-33
21874319-5	2012	In this model, an increase in PTH was induced by its autonomous production in PHP, while PTH in CKD was elevated by a decrease in feedback inhibition of 1,25(OH)2D in the serum, as well as an increase in stimulation by phosphorus in the serum.	Phosphorus	219-229	parathyroid hormone	Homo sapiens	89-92
22357741-0	2012	Oat beta-glucan and dietary calcium and phosphorus differentially modify intestinal expression of proinflammatory cytokines and monocarboxylate transporter 1 and cecal morphology in weaned pigs.	Phosphorus	40-50	MCT1	Sus scrofa	128-157
21825304-11	2012	Phosphorus overload was associated with higher serum FGF-23 levels and Runx-2, as well as myocardial hypertrophy.	Phosphorus	0-10	fibroblast growth factor 23	Homo sapiens	53-59
22781422-3	2012	Our results showed that mothers who were carrying two copies of MTHFR C677T variant alleles appeared to have reduced the risk of CL/P in offspring, comparing to those with homozygous of wild-type allele.	Phosphorus	132-133	methylenetetrahydrofolate reductase	Homo sapiens	64-69
21825304-11	2012	Phosphorus overload was associated with higher serum FGF-23 levels and Runx-2, as well as myocardial hypertrophy.	Phosphorus	0-10	RUNX family transcription factor 2	Homo sapiens	71-77
22334667-3	2012	Here, we show that treatment of macrophages with low pH medium resulted in increased expression of stabilin-1 out of several receptors, which are known to be involved in PS-dependent removal of apoptotic cells.	Phosphorus	170-172	stabilin 1	Mus musculus	99-109
22300300-5	2012	Namely, that the formation of the so-called trans-resveratrol and tyrosinase (S)P complex with its O-O bridge plays a crucial role in the first steps of this enzymatic reaction and that the hydroxylation of the ortho C-H bond of the trans-resveratrol OH group occurs after O-O bond cleavage in the tyrosinase active site.	Phosphorus	77-81	tyrosinase	Homo sapiens	66-76
22324784-5	2012	X-ray crystallography of the syn isomer of complex 2 demonstrated that it has a distorted trigonal bipyramidal geometry with the nitrido group and the two sulfur atoms defining the equatorial plane, the phosphorus atom of the monophosphine and the protonated amine nitrogen of the tridentate ligand spanning the two reciprocal trans positions along the axis perpendicular to the trigonal plane.	Phosphorus	203-213	synemin	Homo sapiens	29-32
21541779-6	2012	Total phosphorus concentration in pore waters ranged from 0.5 to 8.1 mgP l(-1) (mean 3.2 mgP l(-1)).	Phosphorus	6-16	matrix Gla protein	Homo sapiens	69-72
21541779-6	2012	Total phosphorus concentration in pore waters ranged from 0.5 to 8.1 mgP l(-1) (mean 3.2 mgP l(-1)).	Phosphorus	6-16	matrix Gla protein	Homo sapiens	89-92
22186160-3	2012	Zn-doped HAp has the Ca(10)Zn(x)(PO(4))(6)(OH)(2-2)(x)O(2)(x) (0&lt;x&lt;=0.25) chemical composition with a constant Ca/P ratio of 1.67 due to the insertion mechanism into the hexagonal channel (partial occupancy of the 2b Wyckoff site with the formation of linear O-Zn-O entities).	Phosphorus	33-34	reticulon 3	Homo sapiens	9-12
22456089-4	2012	The TGF-beta1 level in on-ice serum was significantly lower than that in room-temperature serum (P&amp;#60;0.001), and both were significantly higher than that found in on-ice plasma (P&amp;#60;0.001).	Phosphorus	97-98	transforming growth factor beta 1	Homo sapiens	4-13
22300300-5	2012	Namely, that the formation of the so-called trans-resveratrol and tyrosinase (S)P complex with its O-O bridge plays a crucial role in the first steps of this enzymatic reaction and that the hydroxylation of the ortho C-H bond of the trans-resveratrol OH group occurs after O-O bond cleavage in the tyrosinase active site.	Phosphorus	77-81	tyrosinase	Homo sapiens	298-308
22125260-6	2012	Further analyses of specific classes showed an increased risk of CL/P associated with 2nd month use of doxycycline/tetracycline (2 exposed cases; POR, 7.30; 95%CI, 1.81-29.46) and sulfamethizole (18 exposed cases; POR, 1.76; 95%CI, 1.10-2.81).	Phosphorus	68-69	cytochrome p450 oxidoreductase	Homo sapiens	146-149
22125260-6	2012	Further analyses of specific classes showed an increased risk of CL/P associated with 2nd month use of doxycycline/tetracycline (2 exposed cases; POR, 7.30; 95%CI, 1.81-29.46) and sulfamethizole (18 exposed cases; POR, 1.76; 95%CI, 1.10-2.81).	Phosphorus	68-69	cytochrome p450 oxidoreductase	Homo sapiens	214-217
24323759-11	2012	The improved functional status of PS-519 treated animals correlated positively (p &lt; 0.01) with reduced expression of astroglial iNOS in areas adjacent to the hemorrhage 7 days post-ICH.	Phosphorus	34-36	nitric oxide synthase 2	Rattus norvegicus	131-135
22334743-0	2012	In vitro evaluation of limestone, dicalcium phosphate, and phytase on calcium and phosphorus solubility of corn and soybean meal.	Phosphorus	82-92	phytase	Zea mays	59-66
22360923-0	2012	FGF23/Klotho axis: phosphorus, mineral metabolism and beyond.	Phosphorus	19-29	fibroblast growth factor 23	Homo sapiens	0-5
22340148-3	2012	RESULTS: Significant correlations were found between GAF scores and energy (kilocalories), carbohydrates, fibre, total fat, linoleic acid, riboflavin, niacin, folate, vitamin B6, vitamin B12, pantothenic acid, calcium, phosphorus, potassium, and iron (all P values &lt; 0.05), as well as magnesium (r = 0.41, P &lt; 0.001) and zinc (r = 0.35, P &lt; 0.001).	Phosphorus	219-229	fibroblast growth factor 9	Homo sapiens	53-56
22237483-1	2012	The activation of phosphorus remains a popular and competitive area of research driven by the dual goals of finding ways to avoid the environmentally questionable P-Cl compounds applied in many industrial processes and the target of catalytic functionalization of P(4).	Phosphorus	18-28	solute carrier family 10 member 4	Homo sapiens	264-268
22237483-7	2012	Apart from these, a new entry point into phosphorus chemistry is the gentle activation of P(4) by an alkyne analogue of tin.	Phosphorus	41-51	solute carrier family 10 member 4	Homo sapiens	90-94
22272818-4	2012	Of particular interest is isolation of an intermediate [Ir(tpitH)(PPh(3))(2)Cl(2)] (1a) with monocyclometalated phosphite, together with the formation of [Ir(tpit)(tpitH)(PPh(3))] (3a) with all tripodal, bidentate, and monodentate phosphorus donors coexisting on the coordination sphere, upon treatment of 2a with a second equiv of triphenylphosphite.	Phosphorus	231-241	caveolin 1	Homo sapiens	66-71
22360923-0	2012	FGF23/Klotho axis: phosphorus, mineral metabolism and beyond.	Phosphorus	19-29	klotho	Homo sapiens	6-12
22396166-3	2012	Fibroblast growth factor 23 (FGF23) regulates phosphorus and vitamin D metabolism.	Phosphorus	46-56	fibroblast growth factor 23	Homo sapiens	0-27
21730210-7	2012	In multivariate regression analyses, changes from baseline in serum FGF23 were associated with changes in serum calcium and phosphorus but not with intact PTH at each time point of measurements (Week-12, Week-24 and Week-52).	Phosphorus	124-134	fibroblast growth factor 23	Homo sapiens	68-73
21380638-12	2012	Adjustment for plasma alpha(1)-antichymotrypsin or plasma creatinine reduced the significance of plasma phosphorus in men.	Phosphorus	104-114	serpin family A member 3	Homo sapiens	22-47
22126969-1	2012	The configuration at phosphorus in cyclic (S)-HPMPC (1, cidofovir) and (S)-HPMPA (2) phenyl ester (5 and 6, respectively) diastereomers ((R(p))-5, (R(p))-6, (S(p))-6) was determined by X-ray crystallography and correlated to their (1)H and (31)P NMR spectra in solution.	Phosphorus	21-31	RP6	Homo sapiens	147-155
22396166-3	2012	Fibroblast growth factor 23 (FGF23) regulates phosphorus and vitamin D metabolism.	Phosphorus	46-56	fibroblast growth factor 23	Homo sapiens	29-34
22213316-2	2012	The physiological actions of the VDR and its ligand are not only the well-known regulation of calcium and phosphorus uptake and transport controlling bone formation, but also their significant involvement in the control of immune functions and of cellular growth and differentiation.	Phosphorus	106-116	vitamin D receptor	Homo sapiens	33-36
22304717-4	2012	Over the past 15 years, tremendous efforts have been made in the discovery of potent GCPII inhibitors, particularly those with phosphorus-, urea- and thiol-based zinc binding groups.	Phosphorus	127-137	folate hydrolase 1	Homo sapiens	85-90
22246283-1	2012	BACKGROUND AND OBJECTIVES: Fibroblast growth factor 23 (FGF23) regulates phosphorus and vitamin D metabolism.	Phosphorus	73-83	fibroblast growth factor 23	Homo sapiens	27-54
22246283-1	2012	BACKGROUND AND OBJECTIVES: Fibroblast growth factor 23 (FGF23) regulates phosphorus and vitamin D metabolism.	Phosphorus	73-83	fibroblast growth factor 23	Homo sapiens	56-61
22754369-7	2012	We further show that miR P-27-5p targets the 3"-untranslated mRNA region (3"-UTR) of cyclin-dependent kinase 4 (CDK4) and reduces both the mRNA and protein level of CDK4, which in turn, interferes with phosphorylation of the retinoblastoma protein (RB1).	Phosphorus	25-26	RB transcriptional corepressor 1	Homo sapiens	249-252
22099949-5	2012	Independent predictors (estimate standard error) of log-transformed FGF-23 concentrations included phosphorus (0.75 [0.237], P = 0.002) and cardiac troponin T (1.04 [0.41], P = 0.01).	Phosphorus	99-109	fibroblast growth factor 23	Homo sapiens	68-74
22754369-7	2012	We further show that miR P-27-5p targets the 3"-untranslated mRNA region (3"-UTR) of cyclin-dependent kinase 4 (CDK4) and reduces both the mRNA and protein level of CDK4, which in turn, interferes with phosphorylation of the retinoblastoma protein (RB1).	Phosphorus	25-26	MLX interacting protein	Homo sapiens	21-24
22106404-3	2012	After 4 weeks of Nx, wild-type mice with renal mass reduction exhibited increased blood urea nitrogen, plasma creatinine and phosphorus concentrations, and defective urine concentrating capability, all of which were significantly attenuated by mPGES-1 deletion.	Phosphorus	125-135	prostaglandin E synthase	Mus musculus	244-251
22701173-2	2012	Decreased glomerular filtration of phosphorus is initially compensated by decreased tubular reabsorption, regulated by PTH and FGF23, maintaining normal serum phosphorus concentrations.	Phosphorus	35-45	fibroblast growth factor 23	Homo sapiens	127-132
22754369-7	2012	We further show that miR P-27-5p targets the 3"-untranslated mRNA region (3"-UTR) of cyclin-dependent kinase 4 (CDK4) and reduces both the mRNA and protein level of CDK4, which in turn, interferes with phosphorylation of the retinoblastoma protein (RB1).	Phosphorus	25-26	cyclin dependent kinase 4	Homo sapiens	85-110
22754369-7	2012	We further show that miR P-27-5p targets the 3"-untranslated mRNA region (3"-UTR) of cyclin-dependent kinase 4 (CDK4) and reduces both the mRNA and protein level of CDK4, which in turn, interferes with phosphorylation of the retinoblastoma protein (RB1).	Phosphorus	25-26	cyclin dependent kinase 4	Homo sapiens	112-116
22754369-7	2012	We further show that miR P-27-5p targets the 3"-untranslated mRNA region (3"-UTR) of cyclin-dependent kinase 4 (CDK4) and reduces both the mRNA and protein level of CDK4, which in turn, interferes with phosphorylation of the retinoblastoma protein (RB1).	Phosphorus	25-26	cyclin dependent kinase 4	Homo sapiens	165-169
22701173-8	2012	Phosphorus binders lower serum phosphorus and also FGF23 levels, without decreasing diet protein content.	Phosphorus	0-10	fibroblast growth factor 23	Homo sapiens	51-56
23208191-0	2012	Relationship between reductions in parathyroid hormone and serum phosphorus during the management of secondary hyperparathyroidism with calcimimetics in hemodialysis patients.	Phosphorus	65-75	parathyroid hormone	Homo sapiens	35-54
21412773-1	2012	The IGF-II/mannose 6-phosphate receptor (IGF-IIR/Man-6-P) up-regulation correlates with heart disease progression and its signaling cascades directly trigger pathological cardiac hypertrophy, fibrosis, and cardiomyocytes apoptosis.	Phosphorus	54-56	insulin-like growth factor 2 receptor	Rattus norvegicus	41-48
22031097-8	2012	Changes in FGF23 mirrored the rise in serum PTH and the decline in circulating 1,25(OH)(2)D. The rise in PTH and FGF23 in Col4a3 null mice coincided with an increase in the urinary fractional excretion of phosphorus and a progressive decline in sodium-phosphate cotransporter gene expression in the kidney.	Phosphorus	205-215	fibroblast growth factor 23	Mus musculus	11-16
22031097-8	2012	Changes in FGF23 mirrored the rise in serum PTH and the decline in circulating 1,25(OH)(2)D. The rise in PTH and FGF23 in Col4a3 null mice coincided with an increase in the urinary fractional excretion of phosphorus and a progressive decline in sodium-phosphate cotransporter gene expression in the kidney.	Phosphorus	205-215	collagen, type IV, alpha 3	Mus musculus	122-128
23419404-0	2012	A study of the association between serum bone-specific alkaline phosphatase and serum phosphorus concentration or dietary phosphorus intake.	Phosphorus	86-96	alkaline phosphatase, placental	Homo sapiens	55-75
23419404-0	2012	A study of the association between serum bone-specific alkaline phosphatase and serum phosphorus concentration or dietary phosphorus intake.	Phosphorus	122-132	alkaline phosphatase, placental	Homo sapiens	55-75
23075669-4	2012	Period 2 recruited patients taking &gt;=12 pills/day of binder with phosphorus of &gt;=3.5 mg/dl.	Phosphorus	68-78	period circadian regulator 2	Homo sapiens	0-8
26451072-12	2012	The direct association of the DDC haplotype with CL/P suggests that this haplotype may either have direct effects on clefts or it may influence clefting risks through other yet unexplored risk behavior(s).	Phosphorus	52-53	dopa decarboxylase	Homo sapiens	30-33
22777315-1	2012	BACKGROUND/AIMS: The link between CKD and CAC has been mostly established by studies of patients who have abnormally high phosphorus levels and advanced CKD or end-stage renal disease.	Phosphorus	122-132	carbonic anhydrase 2	Homo sapiens	42-45
22777315-2	2012	The aim of this study was to examine if there are distinct trajectory classes of serum phosphorus (controlling for eGFR) that are associated CAC in a relatively healthy, community sample.	Phosphorus	87-97	carbonic anhydrase 2	Homo sapiens	141-144
22777315-5	2012	RESULTS: Membership in one class of phosphorus trajectory versus the next lowest level was associated with a 97.9 Agatston unit increase in CAC (p &lt;.001).	Phosphorus	36-46	carbonic anhydrase 2	Homo sapiens	140-143
22777315-7	2012	CONCLUSIONS: Classification of phosphorus trajectories provides further definition for prediction of CAC within the conventional "normal" range.	Phosphorus	31-41	carbonic anhydrase 2	Homo sapiens	101-104
22679498-10	2012	Analysis of the water"s chemistry shows evidence of microbial activity along the path and suggests that the springs supply nitrogen, phosphorus and organic matter to the microbial communities in the Dead Sea.	Phosphorus	133-143	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	204-207
23029012-7	2012	Markers in and near IRF6 and TGFA were associated with CL/P in the Brazilian cohort (p&lt;10(-6)).	Phosphorus	58-59	interferon regulatory factor 6	Mus musculus	20-24
23029012-7	2012	Markers in and near IRF6 and TGFA were associated with CL/P in the Brazilian cohort (p&lt;10(-6)).	Phosphorus	58-59	transforming growth factor alpha	Mus musculus	29-33
23029012-11	2012	IRF6 and TGFA contribute to subsets of CL/P with specific dental anomalies.	Phosphorus	42-43	interferon regulatory factor 6	Mus musculus	0-4
23029012-11	2012	IRF6 and TGFA contribute to subsets of CL/P with specific dental anomalies.	Phosphorus	42-43	transforming growth factor alpha	Mus musculus	9-13
22970174-2	2012	Efforts to identify gene products whose transcription is directly regulated by FGF23 stimulation of fibroblast growth factor receptors (FGFR)/alpha-Klotho complexes in the kidney is confounded by both systemic alterations in calcium, phosphorus and vitamin D metabolism and intrinsic alterations caused by the underlying renal pathology in CKD.	Phosphorus	234-244	fibroblast growth factor 23	Mus musculus	79-84
22034506-1	2011	BACKGROUND AND OBJECTIVES: Fibroblast growth factor 23 (FGF23) regulates phosphorus and vitamin D metabolism.	Phosphorus	73-83	fibroblast growth factor 23	Homo sapiens	27-54
22235299-0	2012	High phosphorus diet-induced changes in NaPi-IIb phosphate transporter expression in the rat kidney: DNA microarray analysis.	Phosphorus	5-15	solute carrier family 34 member 2	Rattus norvegicus	40-48
22034506-1	2011	BACKGROUND AND OBJECTIVES: Fibroblast growth factor 23 (FGF23) regulates phosphorus and vitamin D metabolism.	Phosphorus	73-83	fibroblast growth factor 23	Homo sapiens	56-61
22034506-4	2011	RESULTS: In multivariable-adjusted analyses, each 5-year increase in age was associated with 2.1 RU/ml higher FGF23, each 500-mg increase in phosphorus intake was associated with 3.4 RU/ml higher FGF23, and each 0.1-mg/dl increase in creatinine was associated with 3.4 RU/ml higher FGF23.	Phosphorus	141-151	fibroblast growth factor 23	Homo sapiens	196-201
22034506-4	2011	RESULTS: In multivariable-adjusted analyses, each 5-year increase in age was associated with 2.1 RU/ml higher FGF23, each 500-mg increase in phosphorus intake was associated with 3.4 RU/ml higher FGF23, and each 0.1-mg/dl increase in creatinine was associated with 3.4 RU/ml higher FGF23.	Phosphorus	141-151	fibroblast growth factor 23	Homo sapiens	196-201
22034506-8	2011	CONCLUSIONS: In community-dwelling adults with largely preserved kidney function, established cardiovascular risk factors and higher phosphorus intake were associated with higher FGF23.	Phosphorus	133-143	fibroblast growth factor 23	Homo sapiens	179-184
21855188-2	2011	Fibroblast growth factor 23 (FGF-23) is a hormone originating from bone that regulates urine phosphorus excretion.	Phosphorus	93-103	fibroblast growth factor 23	Homo sapiens	0-27
22009723-8	2011	On all four phosphate diets, Galnt3 knockout mice had consistently higher phosphorus levels and lower alkaline phosphatase and intact Fgf23 concentrations than littermate controls.	Phosphorus	74-84	polypeptide N-acetylgalactosaminyltransferase 3	Mus musculus	29-35
21996606-2	2011	This molecule was designed on the basis of X-ray structure of the complex of d-myo-inositol 1,3,4,5-tetrakisphosphates, Ins(1,3,4,5)P(4), and Grp1 PH (general receptor of phosphoinositides pleckstrin homology) domain for the application to the widely employed biotin-avidin techniques.	Phosphorus	132-133	cytohesin 3	Homo sapiens	142-146
21855188-2	2011	Fibroblast growth factor 23 (FGF-23) is a hormone originating from bone that regulates urine phosphorus excretion.	Phosphorus	93-103	fibroblast growth factor 23	Homo sapiens	29-35
21855188-14	2011	In the context of prior literature, these data suggest that postmenopausal phosphorus retention may stimulate higher FGF-23 concentrations after menopause.	Phosphorus	75-85	fibroblast growth factor 23	Homo sapiens	117-123
21855107-3	2011	This study presents the first investigation on the sorption of phosphorus (P) in the presence of two model phosphonate compounds, 2-aminothylphosphonoic acid (2-AEP) and phosphonoformic acid (PFA), on marine carbonate sediments.	Phosphorus	63-73	legumain	Homo sapiens	161-164
21737371-6	2011	Compared with control cells, Leydig cells primed with B[a]P in vivo produced less testosterone in response to human chorionic gonadotropin (hCG) or dibutyl cyclic adenosine monophosphate in vitro.	Phosphorus	58-59	chorionic gonadotropin subunit beta 5	Homo sapiens	116-144
21855107-3	2011	This study presents the first investigation on the sorption of phosphorus (P) in the presence of two model phosphonate compounds, 2-aminothylphosphonoic acid (2-AEP) and phosphonoformic acid (PFA), on marine carbonate sediments.	Phosphorus	75-76	legumain	Homo sapiens	161-164
21839658-2	2011	On the first reaction route, one water molecule performs nucleophilic attack at the phosphorus center P(gamma) from ATP while the second water molecule in the closed protein cleft serves as a catalytic base assisted by the Glu residue from the myosin salt bridge.	Phosphorus	84-94	myosin heavy chain 14	Homo sapiens	244-250
21826734-5	2011	There was a significant positive correlation of blood FGF23 and phosphorus levels and blood FGF23 and urine phosphorus levels.	Phosphorus	64-74	fibroblast growth factor 23	Rattus norvegicus	54-59
21803396-4	2011	The effectiveness of the strategy was demonstrated using abattoir wastewater, containing nitrogen and phosphorus at approximately 250 mgN/L and 30 mgP/L, respectively.	Phosphorus	102-112	matrix Gla protein	Homo sapiens	147-150
21939286-6	2011	The calculated activation and reaction energy and free energy values obtained suggested the nucleophilic attack of the Ser92 alkoxide on the phosphorus atom of the substrate would be the rate-limiting step of the catalytic hydrolysis of alkyl phosphate monoesters by PLAP.	Phosphorus	141-151	alkaline phosphatase, placental	Homo sapiens	267-271
21913670-2	2011	The Co(II) complexes generally adopt a tetrahedral configuration of general formula [(NP2)Co(I)(2)], wherein the two phosphorus donors are bound to the metal center but the central N-donor remains unbound.	Phosphorus	117-127	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	4-10
21913670-2	2011	The Co(II) complexes generally adopt a tetrahedral configuration of general formula [(NP2)Co(I)(2)], wherein the two phosphorus donors are bound to the metal center but the central N-donor remains unbound.	Phosphorus	117-127	neuronal pentraxin 2	Homo sapiens	86-89
21519925-8	2011	Genome-wide gene expression profiling and molecular network analysis indicated activation of transcriptional regulation by sterol regulatory element-binding protein (SREBP) in FTY720-non-P-treated HMO6 cells.	Phosphorus	170-171	CCHC-type zinc finger nucleic acid binding protein	Homo sapiens	123-164
21960229-1	2011	Primary hyperparathyroidism (PHPT) is a disease to cause calcium, phosphorus, bone metabolism abnormality by the over secretion of parathyroid hormone (PTH) .	Phosphorus	66-76	parathyroid hormone	Homo sapiens	131-150
21780761-5	2011	Glucuronidation assays with HEK293 cell lines overexpressing individual human UGT enzymes demonstrated that UGTs 1A1, 1A4, 1A7, 1A8, 1A9, 1A10, and 2B7 glucuronidated one or both DB[a,l]P-trans-11,12-diol enantiomers.	Phosphorus	186-187	UDP glucuronosyltransferase family 1 member A complex locus	Homo sapiens	78-81
22345991-9	2011	Three of the four markers viz MIB,C1_4_1 and C1_2_5 showed a significant association of microsatellite alleles with CL/P.	Phosphorus	119-120	MIB E3 ubiquitin protein ligase 1	Homo sapiens	30-33
21788361-9	2011	Furthermore, an AtG3Pp4 knockdown mutant exhibited accentuated total lateral root lengths under +phosphorus and -phosphorus conditions compared with the wild type.	Phosphorus	97-107	Major facilitator superfamily protein	Arabidopsis thaliana	16-23
21788361-9	2011	Furthermore, an AtG3Pp4 knockdown mutant exhibited accentuated total lateral root lengths under +phosphorus and -phosphorus conditions compared with the wild type.	Phosphorus	113-123	Major facilitator superfamily protein	Arabidopsis thaliana	16-23
21739963-3	2011	After dissolving the PDP, the P4VP collapses onto the PS struts and a free-standing bicontinuous gyroid template of 50-100 mum thickness and interconnected, uniformly sized pores is formed.	Phosphorus	54-56	pyruvate dehydrogenase phosphatase catalytic subunit 1	Homo sapiens	21-24
21966280-0	2011	The abnormal phenotypes of cartilage and bone in calcium-sensing receptor deficient mice are dependent on the actions of calcium, phosphorus, and PTH.	Phosphorus	130-140	calcium-sensing receptor	Mus musculus	49-73
21966280-6	2011	Deletion of 1alpha(OH)ase in CaR(-/-) mice resulted in a longer lifespan, normocalcemia, lower serum phosphorus, greater elevation in PTH, slight improvement in skeletal growth with increased chondrocyte proliferation and PTHrP expression, and further increases in indices of osteoblastic bone formation.	Phosphorus	101-111	cytochrome P450, family 27, subfamily b, polypeptide 1	Mus musculus	12-25
21966280-7	2011	Deletion of PTH in CaR(-/-) mice resulted in rescue of early lethality, normocalcemia, increased serum phosphorus, undetectable serum PTH, normalization in skeletal growth with normal chondrocyte proliferation and enhanced PTHrP expression, and dramatic decreases in indices of osteoblastic bone formation.	Phosphorus	103-113	parathyroid hormone	Mus musculus	12-15
21966280-7	2011	Deletion of PTH in CaR(-/-) mice resulted in rescue of early lethality, normocalcemia, increased serum phosphorus, undetectable serum PTH, normalization in skeletal growth with normal chondrocyte proliferation and enhanced PTHrP expression, and dramatic decreases in indices of osteoblastic bone formation.	Phosphorus	103-113	calcium-sensing receptor	Mus musculus	19-22
21999742-3	2011	This program is known as phosphorus kinetic modeling or PKM.	Phosphorus	25-35	pyruvate kinase M1/2	Homo sapiens	56-59
21697018-1	2011	OBJECTIVES: Biochemical tests related to calcium and phosphorus metabolism have traditionally been considered as a reliable tool to differentiate familial hypocalciuric hypercalcemia (FHH) from primary hyperparathyroidism (PHPT).	Phosphorus	53-63	calcium sensing receptor	Homo sapiens	184-187
21561999-7	2011	Administration of FGF23 to FGFR3(-/-)FGFR4(-/-) mice resulted in a decrease in serum parathyroid hormone (PTH) levels and an increase in serum phosphorus levels mediated by increased renal phosphate reabsorption.	Phosphorus	143-153	fibroblast growth factor 23	Mus musculus	18-23
21600932-5	2011	The metabolism to the active 5"-triphosphate involves hydrolysis of the carboxyl ester by cathepsin A (Cat A) and carboxylesterase 1 (CES1) followed by a putative nucleophilic attack on the phosphorus by the carboxyl group resulting in the elimination of phenol and the alaninyl phosphate metabolite, PSI-353131.	Phosphorus	190-200	cathepsin A	Homo sapiens	90-101
21600932-5	2011	The metabolism to the active 5"-triphosphate involves hydrolysis of the carboxyl ester by cathepsin A (Cat A) and carboxylesterase 1 (CES1) followed by a putative nucleophilic attack on the phosphorus by the carboxyl group resulting in the elimination of phenol and the alaninyl phosphate metabolite, PSI-353131.	Phosphorus	190-200	carboxylesterase 1	Homo sapiens	114-132
21600932-5	2011	The metabolism to the active 5"-triphosphate involves hydrolysis of the carboxyl ester by cathepsin A (Cat A) and carboxylesterase 1 (CES1) followed by a putative nucleophilic attack on the phosphorus by the carboxyl group resulting in the elimination of phenol and the alaninyl phosphate metabolite, PSI-353131.	Phosphorus	190-200	carboxylesterase 1	Homo sapiens	134-138
21519253-4	2011	RECENT FINDINGS: Higher levels of serum phosphorus (including those within the normal range) and its regulatory hormone, fibroblast growth factor 23 (FGF-23), are associated with increased mortality in patients with all stages of CKD.	Phosphorus	40-50	fibroblast growth factor 23	Homo sapiens	121-148
21273999-8	2011	Present results suggest that (i) several adiposity-related factors may play a role in promoting the development of early arterial diseases in young subjects with a benign phenotype of obesity, (ii) a PTH rise resulting from a subclinical imbalance in calcium-phosphorus homeostasis may affect the biological process of vascular calcifications.	Phosphorus	259-269	parathyroid hormone	Homo sapiens	200-203
21792966-2	2011	Linkage studies have shown interferon regulatory factor 6 (IRF6) to be associated with CL/P in multiple populations, including one in Honduras.	Phosphorus	90-91	interferon regulatory factor 6	Homo sapiens	27-57
21792966-2	2011	Linkage studies have shown interferon regulatory factor 6 (IRF6) to be associated with CL/P in multiple populations, including one in Honduras.	Phosphorus	90-91	interferon regulatory factor 6	Homo sapiens	59-63
21519253-4	2011	RECENT FINDINGS: Higher levels of serum phosphorus (including those within the normal range) and its regulatory hormone, fibroblast growth factor 23 (FGF-23), are associated with increased mortality in patients with all stages of CKD.	Phosphorus	40-50	fibroblast growth factor 23	Homo sapiens	150-156
20146335-2	2011	Fibroblast growth factor 23 (FGF-23) mRNA is overexpressed in the tumor tissue, leading to impaired reabsorption of phosphorus in the renal tubules and hypophosphatemia.	Phosphorus	116-126	fibroblast growth factor 23	Homo sapiens	0-27
20146335-2	2011	Fibroblast growth factor 23 (FGF-23) mRNA is overexpressed in the tumor tissue, leading to impaired reabsorption of phosphorus in the renal tubules and hypophosphatemia.	Phosphorus	116-126	fibroblast growth factor 23	Homo sapiens	29-35
21453744-5	2011	Like benzo-[a]-pyrene (B[a]P), a well known AHR ligand, T-2 led to cytochrome P450 1A1 (CYP1A1) mRNA expression in Caco-2 cells, which could be inhibited by the AHR antagonist resveratrol.	Phosphorus	27-28	aryl hydrocarbon receptor	Homo sapiens	44-47
21453744-5	2011	Like benzo-[a]-pyrene (B[a]P), a well known AHR ligand, T-2 led to cytochrome P450 1A1 (CYP1A1) mRNA expression in Caco-2 cells, which could be inhibited by the AHR antagonist resveratrol.	Phosphorus	27-28	solute carrier family 25 member 5	Homo sapiens	56-59
21453744-5	2011	Like benzo-[a]-pyrene (B[a]P), a well known AHR ligand, T-2 led to cytochrome P450 1A1 (CYP1A1) mRNA expression in Caco-2 cells, which could be inhibited by the AHR antagonist resveratrol.	Phosphorus	27-28	cytochrome P450 family 1 subfamily A member 1	Homo sapiens	67-86
21453744-5	2011	Like benzo-[a]-pyrene (B[a]P), a well known AHR ligand, T-2 led to cytochrome P450 1A1 (CYP1A1) mRNA expression in Caco-2 cells, which could be inhibited by the AHR antagonist resveratrol.	Phosphorus	27-28	cytochrome P450 family 1 subfamily A member 1	Homo sapiens	88-94
21660675-10	2011	Further, the improvements in the ratio of T/P of SBP &amp; DBP and in the level of NO and ET-1 in the treatment group were more significant than those in the control group (P&lt;0.05).	Phosphorus	44-45	selenium binding protein 1	Homo sapiens	49-52
21660675-10	2011	Further, the improvements in the ratio of T/P of SBP &amp; DBP and in the level of NO and ET-1 in the treatment group were more significant than those in the control group (P&lt;0.05).	Phosphorus	44-45	D-box binding PAR bZIP transcription factor	Homo sapiens	59-62
22097096-8	2011	The CRP levels greater than 6.2, had a direct statistically significant correlation with duration of hemodialysis and phosphorus level (p = 0.01).	Phosphorus	118-128	C-reactive protein	Homo sapiens	4-7
21392948-1	2011	The polycarbonate copolymer poly(trimethylene carbonate-co-5,5-dimethyl trimethylene carbonate) (P(TMC-co-DTC)) was synthesized by the polymerization of trimethylene carbonate (TMC) and 5,5-dimethyl trimethylene carbonate (DTC) using tin (II) 2-ethylhexanoate [Sn(Oct)(2)] as a catalyst.	Phosphorus	97-98	plexin A2	Homo sapiens	264-267
21486785-7	2011	We found that both the PPi-induced locked-open time and the ATP/P-ATP ligand exchange time of DeltaF508-CFTR channels are dramatically shortened, suggesting that the DeltaF508 mutation destabilizes the full and partial NBD dimer states.	Phosphorus	23-24	CF transmembrane conductance regulator	Homo sapiens	104-108
21389978-1	2011	Fibroblast growth factor 23 (FGF23) regulates phosphorus metabolism and is a strong predictor of mortality in dialysis patients.	Phosphorus	46-56	fibroblast growth factor 23	Homo sapiens	0-27
21389978-1	2011	Fibroblast growth factor 23 (FGF23) regulates phosphorus metabolism and is a strong predictor of mortality in dialysis patients.	Phosphorus	46-56	fibroblast growth factor 23	Homo sapiens	29-34
21429060-16	2011	"Stepwise backward regression" revealed a significant inverse correlation between the serum level of PTH and the GFR of the transplanted kidney; this correlation was independent from the influence of other variables such as Ca, P, and Alk-P (p = 0.011, beta = -1.556).	Phosphorus	101-102	ALK receptor tyrosine kinase	Homo sapiens	235-238
21429060-18	2011	The BMD Z-scores showed statistically meaningful correlations with the serum level of Alk-P, which were independent from the influence of other variables such as Ca, P, and PTH (p &lt;= 0.002).	Phosphorus	90-91	ALK receptor tyrosine kinase	Homo sapiens	86-89
21699335-0	2011	Spin-polarized transient electron trapping in phosphorus-doped silicon.	Phosphorus	46-56	spindlin 1	Homo sapiens	0-4
21699335-1	2011	Experimental evidence of electron spin precession during travel through the phosphorus-doped Si channel of an all-electrical device simultaneously indicates two distinct processes: (i) short time scales ( 50 ps) due to purely conduction-band transport from injector to detector and (ii) long time scales ( 1 ns) originating from delays associated with capture or reemission in shallow impurity traps.	Phosphorus	76-86	spindlin 1	Homo sapiens	34-38
22097096-9	2011	Also, CRP levels above 10 mg L(-1) had a direct statistically significant correlation with age and phosphorus levels (p = 0.02).	Phosphorus	99-109	C-reactive protein	Homo sapiens	6-9
22097096-10	2011	According to the prevalence of high CRP level and it"s correlation with age, duration ofhemodialysis and phosphorus level in hemodialysis patients, CRP level should be screened in this group of patients routinely because of its prognostic importance.	Phosphorus	105-115	C-reactive protein	Homo sapiens	36-39
22097096-10	2011	According to the prevalence of high CRP level and it"s correlation with age, duration ofhemodialysis and phosphorus level in hemodialysis patients, CRP level should be screened in this group of patients routinely because of its prognostic importance.	Phosphorus	105-115	C-reactive protein	Homo sapiens	148-151
21754349-1	2011	Facile ligand substitution is observed when the ruthenium chloride complex [Ru(eta(5)-C(9)H(7))Cl(PPh(3))(2)] is treated with 1,4-bis-(diphenyl-phosphan-yl)butane in refluxing toluene yielding the title compound, [Ru(C(9)H(7))Cl(C(28)H(28)P(2))].	Phosphorus	238-240	endothelin receptor type A	Homo sapiens	79-82
21514417-6	2011	In line, kidneys of db/db mice on the phosphorus-rich diet displayed significantly increased mRNA expression of the T(H)1 cytokines interferon gamma, IL-6, and tumor necrosis factor alpha.	Phosphorus	38-48	interleukin 6	Mus musculus	150-187
21754296-1	2011	In the title complex, [Co(CN)(2)(C(18)H(18)N(4))]PF(6), the Co(III) atom together with one of the pyridyl rings and two cyanide anions are located on a mirror plane, while the P atom is located on an inversion centre.	Phosphorus	49-50	mitochondrially encoded cytochrome c oxidase III	Homo sapiens	60-67
21377185-6	2011	Phosphorus sorption kinetics were rapid for all size fractions of both Al-WTRs (&gt;98% P sorption effectiveness at shaking times &gt;=2 h).	Phosphorus	0-10	WTRS	Homo sapiens	74-78
21437516-9	2011	Using a backward conditional logistic regression model, age (p&lt;0.001), diabetes (p= 0.001), and C-reactive protein levels &gt;6 mg/L (p= 0.006) were associated with the presence of low AAI, whereas male gender (p&lt;0.001), diabetes (p= 0.001) and elevated calcium x phosphorus product (p= 0.026) were associated with high AAI.	Phosphorus	270-280	C-reactive protein	Homo sapiens	99-117
21113143-8	2011	The autophagic process is independent of the proapoptotic arms of ER stress, but Beclin-1 contributes to PS exposure and subsequent phagocytosis of oxLDLs exposed cells.	Phosphorus	105-107	beclin 1	Homo sapiens	81-89
21333302-2	2011	The appearance of induction concentration in the plots of k(obs) versus [MX] (where k(obs) is pseudo-first-order rate constants for the reaction of piperidine (Pip) with PS(-)) is attributed to the occurrence of two or more than two independent ion exchange processes between different counterions at the cationic micellar surface.	Phosphorus	170-172	prolactin induced protein	Homo sapiens	160-163
21493770-2	2011	Because insulin and IGF1 increase renal tubular calcium and phosphorus reabsorption, we examined GSK3 regulation of phosphate transporter activity and determined whether PKB/SGK inactivates GSK3 to enhance renal phosphate and calcium transport.	Phosphorus	60-70	insulin-like growth factor 1	Mus musculus	20-24
21310821-5	2011	By multivariable analysis, higher donor phosphorus correlated with higher recipient serum creatinine (slope=0.087, 95% confidence interval [CI]: 0.004 to 0.169, P=0.041) and lower recipient estimated GFR (slope=-4.321, 95% CI: -8.165 to -0.476, P=0.028) at 12 months.	Phosphorus	40-50	Rap guanine nucleotide exchange factor 5	Homo sapiens	200-203
21888062-0	2011	[Investigation of metabolism of high-molecular phosphorus-containing compounds of the nervous system at the Palladin Institute of Biochemistry of National Academy of Sciences of Ukraine (1951-1965)].	Phosphorus	47-57	palladin, cytoskeletal associated protein	Homo sapiens	108-116
21246268-4	2011	Under the optimal condition, fluorescence intensity at 460 nm of m-NQB and p-NQB provided two sets of linear ranges, 0.5-15 muM and 20-40 muM and the limit of cyanide detection of 1.4 muM.	Phosphorus	11-12	latexin	Homo sapiens	124-127
21246268-4	2011	Under the optimal condition, fluorescence intensity at 460 nm of m-NQB and p-NQB provided two sets of linear ranges, 0.5-15 muM and 20-40 muM and the limit of cyanide detection of 1.4 muM.	Phosphorus	11-12	latexin	Homo sapiens	138-141
21246268-4	2011	Under the optimal condition, fluorescence intensity at 460 nm of m-NQB and p-NQB provided two sets of linear ranges, 0.5-15 muM and 20-40 muM and the limit of cyanide detection of 1.4 muM.	Phosphorus	11-12	latexin	Homo sapiens	138-141
21449769-4	2011	Preoperative tests revealed hypercalcemia associated with elevation of parathyroid hormone (PTH) (calcium = 11.2 mg/dL, calcium ion = 1.48 mmol/L, phosphorus = 4.0 mg/dL, alkaline phosphatase = 625 U/L, parathyroid hormone (PTH) PTH = 998 pg/mL).	Phosphorus	147-157	parathyroid hormone	Homo sapiens	71-90
21449769-4	2011	Preoperative tests revealed hypercalcemia associated with elevation of parathyroid hormone (PTH) (calcium = 11.2 mg/dL, calcium ion = 1.48 mmol/L, phosphorus = 4.0 mg/dL, alkaline phosphatase = 625 U/L, parathyroid hormone (PTH) PTH = 998 pg/mL).	Phosphorus	147-157	parathyroid hormone	Homo sapiens	92-95
20733586-6	2011	In addition, male Tspan8 knockout mice showed significantly lower bone mineral density and phosphorus levels (6.2 and 16.6%, respectively).	Phosphorus	91-101	tetraspanin 8	Mus musculus	18-24
21371424-4	2011	In this study, OPG was found in an in vitro assay to significantly inhibit calcification of vascular smooth muscle cells (VSMC) induced by high calcium/phosphate (Ca/P) treatment (p=0.0063), although this effect was blunted at high OPG concentrations.	Phosphorus	16-17	TNF receptor superfamily member 11b	Homo sapiens	232-235
21731867-12	2011	Both PTH and FGF23 were positively correlated with phosphorus and negatively with hemoglobin levels.	Phosphorus	51-61	fibroblast growth factor 23	Homo sapiens	13-18
21295312-2	2011	After irradiation with UV-light and heat treatment, the films formed hemi-spherical pores due to the preferable deposition of CdS and Cd onto the PS spheres during the photochemical and interfacial reactions.	Phosphorus	146-148	CDP-diacylglycerol synthase 1	Homo sapiens	126-129
21462296-7	2011	CONCLUSIONS: Our results provide for the first time evidence implicating FGF1 in the occurrence of CL/P, and support TIMP2 and WNT9B as novel loci predisposing to CL/P.	Phosphorus	102-103	fibroblast growth factor 1	Homo sapiens	73-77
21239463-2	2011	Heteromeric Kir4.1-Kir5.1 channels are highly pH sensitive within the physiological range of pH changes and are strongly expressed by the peripheral chemosensors as well as in the brainstem pH-sensitive areas which mediate respiratory responses to changes in blood and brain levels of P(CO(2))/[H(+)].	Phosphorus	285-286	potassium inwardly-rectifying channel, subfamily J, member 16	Mus musculus	19-25
20813767-1	2011	BACKGROUND: Fibroblast growth factor-23 (FGF-23) is a phosphorus-regulating substance.	Phosphorus	54-64	fibroblast growth factor 23	Homo sapiens	12-39
20578976-0	2011	Unusual activity pattern of leucine aminopeptidase inhibitors based on phosphorus containing derivatives of methionine and norleucine.	Phosphorus	71-81	carboxypeptidase Q	Homo sapiens	36-50
20813767-1	2011	BACKGROUND: Fibroblast growth factor-23 (FGF-23) is a phosphorus-regulating substance.	Phosphorus	54-64	fibroblast growth factor 23	Homo sapiens	41-47
21406294-7	2011	Phosphorus stimulates FGF-23 secretion by osteocytes and expression of the osteoblastic transcriptome, thereby increasing extracellular matrix mineralization in atherosclerotic plaques, hypertrophic cartilage, and skeletal osteoblast surfaces.	Phosphorus	0-10	fibroblast growth factor 23	Homo sapiens	22-28
21941786-3	2011	Then serum K+ levels were measured; the activities of HK-ATPase (HKA) in kidneys were detected by the method of determinated phosphorus content; Western Blot assay and real-time PCR were used to exam the protein and mRNA expression levels of HKA in kidneys, respectively.	Phosphorus	125-135	ATPase H+/K+ transporting subunit alpha	Rattus norvegicus	54-63
21941786-3	2011	Then serum K+ levels were measured; the activities of HK-ATPase (HKA) in kidneys were detected by the method of determinated phosphorus content; Western Blot assay and real-time PCR were used to exam the protein and mRNA expression levels of HKA in kidneys, respectively.	Phosphorus	125-135	ATPase H+/K+ transporting subunit alpha	Rattus norvegicus	65-68
21522293-1	2011	In the title diaqua-cobalt complex, [Co(C(8)H(11)NO(5)PS)(2)(H(2)O)(2)], the Co(II) atom is surrounded by six O atoms belonging to the phosphoryl and sulfonyl groups of two deprotonated chelate ligands and two additional O atoms from water mol-ecules which are in cis positions with respect to one another.	Phosphorus	54-56	mitochondrially encoded cytochrome c oxidase II	Homo sapiens	77-83
21093110-2	2011	We evaluated in 867 AD subjects the association of AD + P with genes which may modify the pathological process via effects on the accumulation of amyloid beta (Abeta) protein and/or hyperphosphorylated microtubule-associated protein tau (MAPT): amyloid precursor protein (APP), beta-site amyloid precursor protein cleaving enzyme (BACE1), sortilin-related receptor (SORL1), and MAPT.	Phosphorus	56-57	amyloid beta precursor protein	Homo sapiens	146-158
21093110-2	2011	We evaluated in 867 AD subjects the association of AD + P with genes which may modify the pathological process via effects on the accumulation of amyloid beta (Abeta) protein and/or hyperphosphorylated microtubule-associated protein tau (MAPT): amyloid precursor protein (APP), beta-site amyloid precursor protein cleaving enzyme (BACE1), sortilin-related receptor (SORL1), and MAPT.	Phosphorus	56-57	microtubule associated protein tau	Homo sapiens	238-242
21093110-2	2011	We evaluated in 867 AD subjects the association of AD + P with genes which may modify the pathological process via effects on the accumulation of amyloid beta (Abeta) protein and/or hyperphosphorylated microtubule-associated protein tau (MAPT): amyloid precursor protein (APP), beta-site amyloid precursor protein cleaving enzyme (BACE1), sortilin-related receptor (SORL1), and MAPT.	Phosphorus	56-57	amyloid beta precursor protein	Homo sapiens	245-270
21093110-2	2011	We evaluated in 867 AD subjects the association of AD + P with genes which may modify the pathological process via effects on the accumulation of amyloid beta (Abeta) protein and/or hyperphosphorylated microtubule-associated protein tau (MAPT): amyloid precursor protein (APP), beta-site amyloid precursor protein cleaving enzyme (BACE1), sortilin-related receptor (SORL1), and MAPT.	Phosphorus	56-57	beta-secretase 1	Homo sapiens	331-336
21093110-2	2011	We evaluated in 867 AD subjects the association of AD + P with genes which may modify the pathological process via effects on the accumulation of amyloid beta (Abeta) protein and/or hyperphosphorylated microtubule-associated protein tau (MAPT): amyloid precursor protein (APP), beta-site amyloid precursor protein cleaving enzyme (BACE1), sortilin-related receptor (SORL1), and MAPT.	Phosphorus	56-57	sortilin related receptor 1	Homo sapiens	339-364
21093110-2	2011	We evaluated in 867 AD subjects the association of AD + P with genes which may modify the pathological process via effects on the accumulation of amyloid beta (Abeta) protein and/or hyperphosphorylated microtubule-associated protein tau (MAPT): amyloid precursor protein (APP), beta-site amyloid precursor protein cleaving enzyme (BACE1), sortilin-related receptor (SORL1), and MAPT.	Phosphorus	56-57	sortilin related receptor 1	Homo sapiens	366-371
21093110-2	2011	We evaluated in 867 AD subjects the association of AD + P with genes which may modify the pathological process via effects on the accumulation of amyloid beta (Abeta) protein and/or hyperphosphorylated microtubule-associated protein tau (MAPT): amyloid precursor protein (APP), beta-site amyloid precursor protein cleaving enzyme (BACE1), sortilin-related receptor (SORL1), and MAPT.	Phosphorus	56-57	microtubule associated protein tau	Homo sapiens	378-382
21440761-7	2011	RESULTS: Serum OPN correlated with first month phosphorus (r=0.33, P=.00), Caxproduct (r=0.41, P=.02), and proteinuria (r=0.34, P=.00) with negative relations to serum insulin (r=0.28, P=.04).	Phosphorus	47-57	secreted phosphoprotein 1	Homo sapiens	15-18
21087998-3	2011	Here, we identify a more general, P-TEFb-independent role of 7SK RNA in directly affecting the function of the architectural transcription factor and chromatin regulator HMGA1.	Phosphorus	34-35	high mobility group AT-hook 1	Homo sapiens	170-175
20093322-1	2011	The effects of RU486 and S-P, a more selective glucocorticoid receptor antagonist from Schering-Plough, were investigated on glucocorticoid receptor nuclear translocation and DNA binding.	Phosphorus	25-28	nuclear receptor subfamily 3, group C, member 1	Rattus norvegicus	125-148
21440839-5	2011	METHODS: The effects of Hg(2+) on biological activity and structure of BLM642-1290 recombinant helicase were determined by fluorescence polarized, ultraviolet spectroscopic, and free-phosphorus assay technologies, respectively.	Phosphorus	183-193	helicase for meiosis 1	Homo sapiens	95-103
21292848-9	2011	Directly treating phosphorus may be the most beneficial approach because this can reduce serum phosphorus, PTH, and FGF-23.	Phosphorus	18-28	fibroblast growth factor 23	Homo sapiens	116-122
21266088-8	2011	Indeed, a 2-APB analogue where the boron-oxygen core is replaced by a carbon-phosphorus core is devoid of potentiating capacity (while retaining inhibition capacity), highlighting the key role of the boron-oxygen core present in borinate esters for the potentiation function.	Phosphorus	77-87	arginyl aminopeptidase	Homo sapiens	12-15
20631407-0	2011	Pilot study of dietary phosphorus restriction and phosphorus binders to target fibroblast growth factor 23 in patients with chronic kidney disease.	Phosphorus	23-33	fibroblast growth factor 23	Homo sapiens	79-106
20631407-0	2011	Pilot study of dietary phosphorus restriction and phosphorus binders to target fibroblast growth factor 23 in patients with chronic kidney disease.	Phosphorus	50-60	fibroblast growth factor 23	Homo sapiens	79-106
20631407-2	2011	Reducing dietary phosphorus intake lowers FGF23 secretion in healthly individuals, but there is little data on its effects in patients with pre-dialysis CKD.	Phosphorus	17-27	fibroblast growth factor 23	Homo sapiens	42-47
20946192-2	2011	Although previously considered to be caused by tertiary hyperparathyroidism, recent evidence suggests a primary role for persistently elevated circulating levels of the phosphorus-regulating hormone, FGF23.	Phosphorus	169-179	fibroblast growth factor 23	Homo sapiens	200-205
20490785-7	2011	Serum 1,25 (OH)(2) vitamin D3 was associated with higher urinary excretion of calcium and phosphorus in ASF patients.	Phosphorus	90-100	arylsulfatase F	Homo sapiens	104-107
20837821-8	2011	RESULTS: Phosphorus 31 magnetic resonance spectroscopy showed reduced phosphorylation potential in the calf muscle at rest in patients with an OPA1 mutation (-24% from normal mean; P = .003) as well as a reduced maximum rate of mitochondrial adenosine triphosphate synthesis (-36%; P < .001; ranging from -28% to -49% in association with different mutations).	Phosphorus	9-19	OPA1 mitochondrial dynamin like GTPase	Homo sapiens	143-147
21791917-9	2011	High phosphorus increased MMP-2 and MMP-9 expressions in VSMC from normal rats but not from CKD rats.	Phosphorus	5-15	matrix metallopeptidase 2	Rattus norvegicus	26-31
21791917-9	2011	High phosphorus increased MMP-2 and MMP-9 expressions in VSMC from normal rats but not from CKD rats.	Phosphorus	5-15	matrix metallopeptidase 9	Rattus norvegicus	36-41
21135546-10	2011	CONCLUSION: We confirmed the high prevalence of LVH in nondialyzed CKD patients and showed that FGF23, an early marker of phosphorus load, was an important factor associated with LVH in these patients.	Phosphorus	122-132	fibroblast growth factor 23	Homo sapiens	96-101
21997255-7	2011	RESULTS: Significant correlations were found between HAp erosion and the concentration of phosphorus in unstimulated saliva (r = 0.40, p = 0.03) and between HAp erosion and the concentration of sodium (r = -0.40, p = 0.03), chloride (r = -0.47, p = 0.01), phosphorus (r = 0.45, p = 0.01) and flow (r = -0.39, p = 0.04) of stimulated saliva.	Phosphorus	90-100	reticulon 3	Homo sapiens	53-56
21865755-4	2011	This review summarizes the role of the FGF-23 axis on phosphorus metabolism, and presents the clinical entities that arise from activation or inactivation of the FGF-23 axis.	Phosphorus	54-64	fibroblast growth factor 23	Homo sapiens	39-45
21725161-6	2011	The active state of c-Src, p-Tyr416-c-Src, was positively correlated with tumour grade (P=0.062) but inversely correlated with vascular invasion (P=0.071).	Phosphorus	27-28	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	20-25
21725161-6	2011	The active state of c-Src, p-Tyr416-c-Src, was positively correlated with tumour grade (P=0.062) but inversely correlated with vascular invasion (P=0.071).	Phosphorus	27-28	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	36-41
21757825-8	2011	Furthermore, serum cTnI levels significantly correlated with Pp/Ps (r=0.745, P&lt;0.001) in VSD children.	Phosphorus	64-66	troponin I3, cardiac type	Homo sapiens	19-23
21335993-4	2011	Milk is an important source of minerals supporting growth (type II nutrients), such as potassium, magnesium, phosphorus and zinc, and the high lactose content also seems to support growth due to a prebiotic effect and improved absorption of minerals.	Phosphorus	109-119	Weaning weight-maternal milk	Bos taurus	0-4
20735471-10	2011	CONCLUSION: After 1-year follow-up, de novo arterial stiffness in dialysis patients as determined by CAVI was significantly associated with age and initial serum phosphorus.	Phosphorus	162-172	carbonic anhydrase 6	Homo sapiens	101-105
22145450-1	2011	BACKGROUND: Children with growth hormone deficiency (GHD) have increased renal phosphorus reabsorption during rhGH therapy, Fibroblast growth factor 23 (FGF23) is a known regulator of serum phosphorus and may be responsible for this effect.	Phosphorus	79-89	fibroblast growth factor 23	Homo sapiens	124-151
22145450-1	2011	BACKGROUND: Children with growth hormone deficiency (GHD) have increased renal phosphorus reabsorption during rhGH therapy, Fibroblast growth factor 23 (FGF23) is a known regulator of serum phosphorus and may be responsible for this effect.	Phosphorus	79-89	fibroblast growth factor 23	Homo sapiens	153-158
22145450-1	2011	BACKGROUND: Children with growth hormone deficiency (GHD) have increased renal phosphorus reabsorption during rhGH therapy, Fibroblast growth factor 23 (FGF23) is a known regulator of serum phosphorus and may be responsible for this effect.	Phosphorus	190-200	fibroblast growth factor 23	Homo sapiens	124-151
22145450-1	2011	BACKGROUND: Children with growth hormone deficiency (GHD) have increased renal phosphorus reabsorption during rhGH therapy, Fibroblast growth factor 23 (FGF23) is a known regulator of serum phosphorus and may be responsible for this effect.	Phosphorus	190-200	fibroblast growth factor 23	Homo sapiens	153-158
22145450-7	2011	The C-FGF23 rise persisted after adjusting for age, gender, sex, total calcium, and phosphorus (p &lt; 0.01) but attenuated after adjusting for TmP/GFR or IGF-1.	Phosphorus	84-94	fibroblast growth factor 23	Homo sapiens	6-11
21959717-2	2011	Recently, new factors such as FGF-23 have been added to the classic list of regulators of bone metabolism, which include calcium, phosphorus, PTH and calcitriol.	Phosphorus	130-140	fibroblast growth factor 23	Homo sapiens	30-36
21069224-3	2011	In 2008, the total simulated phosphorus contribution was 9634, 6524 and 3908 kg (P) y(-1) from sod farms, citrus farms and row crop farmlands, respectively.	Phosphorus	29-39	superoxide dismutase 1	Homo sapiens	95-98
21164011-3	2010	We demonstrated an ensemble nuclear spin memory in phosphorous-doped silicon, which can be read out electrically and has a lifetime exceeding 100 seconds.	Phosphorus	51-62	spindlin 1	Homo sapiens	36-40
22166756-3	2011	Upon stimulation by cAMP, HSL is phosphorylated at several serine residues (P-Ser(552), P-Ser(649) and P-Ser(650)) leading to enzymatic activation.	Phosphorus	23-24	lipase E, hormone sensitive type	Homo sapiens	26-29
22166756-3	2011	Upon stimulation by cAMP, HSL is phosphorylated at several serine residues (P-Ser(552), P-Ser(649) and P-Ser(650)) leading to enzymatic activation.	Phosphorus	76-77	lipase E, hormone sensitive type	Homo sapiens	26-29
22166756-3	2011	Upon stimulation by cAMP, HSL is phosphorylated at several serine residues (P-Ser(552), P-Ser(649) and P-Ser(650)) leading to enzymatic activation.	Phosphorus	76-77	lipase E, hormone sensitive type	Homo sapiens	26-29
20122814-10	2011	CONCLUSION: The consumption of a rich-MRP diet in male adolescents had a negative influence on dietary phosphorus absorption, tending to decrease the phosphorus balance.	Phosphorus	103-113	ATP binding cassette subfamily C member 1	Homo sapiens	38-41
20122814-10	2011	CONCLUSION: The consumption of a rich-MRP diet in male adolescents had a negative influence on dietary phosphorus absorption, tending to decrease the phosphorus balance.	Phosphorus	150-160	ATP binding cassette subfamily C member 1	Homo sapiens	38-41
20959465-10	2010	PKA inhibition (H89 or R(P)-adenosine-3",5"-cyclic monophosphorothioate (R(P)-cAMPS)) decreased butaprost-induced cAMP-response element-binding protein and ERK activation but did not affect EGFR activation, whereas beta-arrestin1 deficiency decreased EGFR activation but did not affect butaprost-induced PKA activation, thus indicating that they were independent EP2-mediated pathways.	Phosphorus	25-28	mitogen-activated protein kinase 1	Mus musculus	156-159
20959465-10	2010	PKA inhibition (H89 or R(P)-adenosine-3",5"-cyclic monophosphorothioate (R(P)-cAMPS)) decreased butaprost-induced cAMP-response element-binding protein and ERK activation but did not affect EGFR activation, whereas beta-arrestin1 deficiency decreased EGFR activation but did not affect butaprost-induced PKA activation, thus indicating that they were independent EP2-mediated pathways.	Phosphorus	25-28	epidermal growth factor receptor	Mus musculus	190-194
20959465-10	2010	PKA inhibition (H89 or R(P)-adenosine-3",5"-cyclic monophosphorothioate (R(P)-cAMPS)) decreased butaprost-induced cAMP-response element-binding protein and ERK activation but did not affect EGFR activation, whereas beta-arrestin1 deficiency decreased EGFR activation but did not affect butaprost-induced PKA activation, thus indicating that they were independent EP2-mediated pathways.	Phosphorus	25-28	epidermal growth factor receptor	Mus musculus	251-255
20959465-10	2010	PKA inhibition (H89 or R(P)-adenosine-3",5"-cyclic monophosphorothioate (R(P)-cAMPS)) decreased butaprost-induced cAMP-response element-binding protein and ERK activation but did not affect EGFR activation, whereas beta-arrestin1 deficiency decreased EGFR activation but did not affect butaprost-induced PKA activation, thus indicating that they were independent EP2-mediated pathways.	Phosphorus	25-28	prostaglandin E receptor 2 (subtype EP2)	Mus musculus	363-366
21164011-4	2010	The electronic spin information can be mapped onto and stored in the nuclear spin of the phosphorus donors, and the nuclear spins can then be repetitively read out electrically for time periods that exceed the electron spin lifetime.	Phosphorus	89-99	spindlin 1	Homo sapiens	15-19
21164011-4	2010	The electronic spin information can be mapped onto and stored in the nuclear spin of the phosphorus donors, and the nuclear spins can then be repetitively read out electrically for time periods that exceed the electron spin lifetime.	Phosphorus	89-99	spindlin 1	Homo sapiens	77-81
21164011-4	2010	The electronic spin information can be mapped onto and stored in the nuclear spin of the phosphorus donors, and the nuclear spins can then be repetitively read out electrically for time periods that exceed the electron spin lifetime.	Phosphorus	89-99	spindlin 1	Homo sapiens	77-81
20880712-1	2010	Following previous studies we herein report the synthesis and the pharmacological evaluation of a new class of human carbonic anhydrase (hCA) inhibitors, 1,5-diarylpyrrole-3-carboxamides prepared by a solid-phase strategy involving a PS(HOBt) resin.	Phosphorus	234-236	HCA1	Homo sapiens	137-140
20811335-5	2010	Serum parathyroid hormone (PTH) was outside the guideline targets in the majority of patients and associated with low calcium, high phosphorus, acidosis, dialysis vintage and female gender.	Phosphorus	132-142	parathyroid hormone	Homo sapiens	6-25
20811335-5	2010	Serum parathyroid hormone (PTH) was outside the guideline targets in the majority of patients and associated with low calcium, high phosphorus, acidosis, dialysis vintage and female gender.	Phosphorus	132-142	parathyroid hormone	Homo sapiens	27-30
20970329-3	2010	In the present study, the inhibitory effects of a series of styrylheterocycles having either a p-SO(2)NH(2) or p-SO(2)Me group on the production of cyclooxygenase-2-mediated PGE(2) were evaluated in lipopolysaccharide-stimulated RAW264.7 murine macrophages.	Phosphorus	7-8	prostaglandin-endoperoxide synthase 2	Mus musculus	148-164
20050948-12	2010	Addition of 1 g/kg MOS significantly increased the digestibility of Ca and P by 8.4% and 7.7% units, respectively; however, further increment did not enhance the absorption.	Phosphorus	75-76	MOS proto-oncogene, serine/threonine kinase	Homo sapiens	19-22
20707671-1	2010	UNLABELLED: Abstract Background: Fibroblast growth factor 23 (FGF-23), a phosphaturic peptide hormone secreted by the osteoblasts, is an important regulator of phosphorus and vitamin D metabolism.	Phosphorus	160-170	fibroblast growth factor 23	Homo sapiens	33-60
20707671-1	2010	UNLABELLED: Abstract Background: Fibroblast growth factor 23 (FGF-23), a phosphaturic peptide hormone secreted by the osteoblasts, is an important regulator of phosphorus and vitamin D metabolism.	Phosphorus	160-170	fibroblast growth factor 23	Homo sapiens	62-68
21113195-1	2010	Vitamin D is a seco-steroid involved in calcium and phosphorus metabolism, and bone formation and mineralization, through binding to a specific nuclear receptor, vitamin D receptor (VDR).	Phosphorus	52-62	vitamin D receptor	Homo sapiens	162-180
21113195-1	2010	Vitamin D is a seco-steroid involved in calcium and phosphorus metabolism, and bone formation and mineralization, through binding to a specific nuclear receptor, vitamin D receptor (VDR).	Phosphorus	52-62	vitamin D receptor	Homo sapiens	182-185
20876236-6	2010	Inhibition of B[a]P-mediated MAPK and neovasculogenesis was significantly rescued by pretreatment with alpha-naphthoflavone, an aryl hydrocarbon receptor (AhR) antagonist.	Phosphorus	18-19	aryl hydrocarbon receptor	Homo sapiens	128-153
20876236-6	2010	Inhibition of B[a]P-mediated MAPK and neovasculogenesis was significantly rescued by pretreatment with alpha-naphthoflavone, an aryl hydrocarbon receptor (AhR) antagonist.	Phosphorus	18-19	aryl hydrocarbon receptor	Homo sapiens	155-158
21034990-4	2010	Under the influence of parathyroid hormone, the kidney then converts 25-hydroxyvitamin D to 1,25-dihydroxyvitamin D, the biologically active, hormonal form of the nutrient that is important in the metabolism of calcium and phosphorus and is critical in building and maintaining healthy bones.	Phosphorus	223-233	parathyroid hormone	Homo sapiens	23-42
20852376-10	2010	Intact PTH level correlated negatively with serum ionized calcium and positively with serum phosphorus levels only in the predialysis samples with the use of low-flux but not high-flux filters.	Phosphorus	92-102	parathyroid hormone	Homo sapiens	7-10
21170873-7	2010	Other studies suggest that the opposite influences on TmP/GFR of growth hormone (stimulation) and estrogen (inhibition) are the determinants of the age-associated changes in TmP/GFR and serum phosphorus.	Phosphorus	192-202	growth hormone 1	Homo sapiens	65-79
20730242-0	2010	Zwitterionic and cationic P(5)-clusters from four-membered phosphorus-nitrogen-metal heterocycles.	Phosphorus	59-69	solute carrier family 10 member 5	Homo sapiens	26-30
20730242-1	2010	A general route for the functionalization of P(4) mediated by four-membered phosphorus-nitrogen-metal heterocycles is introduced yielding novel phosphorus-rich clusters.	Phosphorus	76-86	solute carrier family 10 member 4	Homo sapiens	45-49
20730242-1	2010	A general route for the functionalization of P(4) mediated by four-membered phosphorus-nitrogen-metal heterocycles is introduced yielding novel phosphorus-rich clusters.	Phosphorus	144-154	solute carrier family 10 member 4	Homo sapiens	45-49
20685823-4	2010	Remarkably, we show that PTH is necessary for the high-FGF23 levels of early kidney failure due to an adenine high-phosphorus diet.	Phosphorus	115-125	parathyroid hormone	Rattus norvegicus	25-28
20685823-4	2010	Remarkably, we show that PTH is necessary for the high-FGF23 levels of early kidney failure due to an adenine high-phosphorus diet.	Phosphorus	115-125	fibroblast growth factor 23	Rattus norvegicus	55-60
20708045-6	2010	(+)-Cholesten-3-one significantly increases the expression of BMPR IB, but not BMPR IA or BMPR II; p-Smad1/5/8 positive nuclei and expression of p-Smad1/5/8 were detected in NSCs treated with (+)-Cholesten-3-one, indicating that (+)-Cholesten-3-one may activate the BMP signaling.	Phosphorus	50-51	bone morphogenetic protein 1	Homo sapiens	62-65
20669901-6	2010	Photolysis of the Ni(p)(+)-CO state generates a novel Ni(p)(+) species (A(red)*) with a rhombic electron paramagnetic resonance spectrum (g values of 2.56, 2.10, and 2.01) and an extremely low (1 kJ/mol) barrier for recombination with CO. We suggest that the photolytically generated A(red)* species is (or is similar to) the Ni(p)(+) species that binds CO (to form the Ni(p)(+)-CO species) and the methyl group (to form Ni(p)-CH(3)) in the ACS catalytic mechanism.	Phosphorus	21-23	acyl-CoA synthetase short chain family member 2	Homo sapiens	441-444
20368306-9	2010	Suppression of MGP increased matrix calcium and phosphorus deposition by 90 +- 6% and 100 +- 4% at 1 mM ambient Ca(2+) and phosphorus concentration.	Phosphorus	48-58	matrix Gla protein	Homo sapiens	15-18
20368306-9	2010	Suppression of MGP increased matrix calcium and phosphorus deposition by 90 +- 6% and 100 +- 4% at 1 mM ambient Ca(2+) and phosphorus concentration.	Phosphorus	123-133	matrix Gla protein	Homo sapiens	15-18
20623795-0	2010	Measuring the acute effect of insulin infusion on ATP turnover rate in human skeletal muscle using phosphorus-31 magnetic resonance saturation transfer spectroscopy.	Phosphorus	99-109	insulin	Homo sapiens	30-37
21709748-2	2010	The crystal structure of a Tat:P-TEFb complex (Tahirov, T.H.	Phosphorus	31-32	tyrosine aminotransferase	Homo sapiens	27-30
20507957-3	2010	The primary systemic stimuli of FGF23 secretion are increased 1,25(OH)(2)D levels and increased dietary phosphorus intake.	Phosphorus	104-114	fibroblast growth factor 23	Homo sapiens	32-37
20395135-3	2010	The results show that BNP-TiO(2) possesses single anatase phase with mesopore structures, and nitrogen and phosphorus contained in original crop seeds are self-doped into the lattice as anions and cations, respectively.	Phosphorus	107-117	natriuretic peptide B	Homo sapiens	22-25
20507957-4	2010	In kidney failure, FGF23 levels increase early and steadily rise with progression of kidney disease, likely as an appropriate physiologic adaptation to maintain normal phosphorus balance by helping to augment urinary phosphate excretion in conjunction with increased parathyroid hormone levels and by decreasing gut phosphorus absorption through decreased 1,25(OH)(2)D. In the long term, this compensation may become maladaptive by causing a progressive decline in 1,25(OH)(2)D levels with attendant consequences such as secondary hyperparathyroidism.	Phosphorus	168-178	fibroblast growth factor 23	Homo sapiens	19-24
20507957-4	2010	In kidney failure, FGF23 levels increase early and steadily rise with progression of kidney disease, likely as an appropriate physiologic adaptation to maintain normal phosphorus balance by helping to augment urinary phosphate excretion in conjunction with increased parathyroid hormone levels and by decreasing gut phosphorus absorption through decreased 1,25(OH)(2)D. In the long term, this compensation may become maladaptive by causing a progressive decline in 1,25(OH)(2)D levels with attendant consequences such as secondary hyperparathyroidism.	Phosphorus	316-326	fibroblast growth factor 23	Homo sapiens	19-24
20580720-9	2010	Biochemical analyses indicated that PI3K-Akt signaling increased nuclear total beta-catenin and P-beta-catenin(552) levels and reduced N-terminal beta-catenin phosphorylation, which is associated with degradation.	Phosphorus	36-37	thymoma viral proto-oncogene 1	Mus musculus	41-44
20580720-9	2010	Biochemical analyses indicated that PI3K-Akt signaling increased nuclear total beta-catenin and P-beta-catenin(552) levels and reduced N-terminal beta-catenin phosphorylation, which is associated with degradation.	Phosphorus	36-37	catenin beta 1	Homo sapiens	98-110
20547979-3	2010	RESEARCH DESIGN AND METHODS: Five potential inhibitory Ser sites located proximally to the P-Tyr binding domain of IRS-2 were mutated to Ala.	Phosphorus	91-92	insulin receptor substrate 2	Mus musculus	115-120
20580720-9	2010	Biochemical analyses indicated that PI3K-Akt signaling increased nuclear total beta-catenin and P-beta-catenin(552) levels and reduced N-terminal beta-catenin phosphorylation, which is associated with degradation.	Phosphorus	36-37	catenin (cadherin associated protein), beta 1	Mus musculus	79-91
20580720-9	2010	Biochemical analyses indicated that PI3K-Akt signaling increased nuclear total beta-catenin and P-beta-catenin(552) levels and reduced N-terminal beta-catenin phosphorylation, which is associated with degradation.	Phosphorus	36-37	catenin (cadherin associated protein), beta 1	Mus musculus	98-110
20507943-2	2010	Excessive production of FGF23 by osteocytes is an appropriate compensation to help maintain normal phosphorus metabolism in these patients.	Phosphorus	99-109	fibroblast growth factor 23	Homo sapiens	24-29
20507943-3	2010	Beginning in early CKD, progressive increases in levels of FGF23 enhance phosphaturia on a per-nephron basis and inhibit calcitriol production, thereby contributing centrally to the predominant phosphorus phenotype of predialysis kidney disease: normal serum phosphate, increased fractional excretion of phosphate, and calcitriol deficiency.	Phosphorus	194-204	fibroblast growth factor 23	Homo sapiens	59-64
20691317-8	2010	There was a strong, positive association between the highest quartile of serum phosphorus (3.7 to 5.0 mg/dl) and high ABPI compared to the reference group (3.1 to 3.4 mg/dl) after adjustment for demographics, traditional CVD risk factors, kidney function, C-reactive protein, serum calcium, and 25-hydroxyvitamin D levels (adjusted odds ratio 4.78, 95% confidence interval 1.73 to 13.2, p = 0.003).	Phosphorus	79-89	C-reactive protein	Homo sapiens	256-274
20823673-4	2010	Organothiophosphorus pesticides (P=S type) are easily oxidized to their phosphorus compounds (P=O type) in chlorinated water containing HOCl as little as 0.5 mg/l, resulting in an increase in cholinesterase-inhibitory activity.	Phosphorus	10-20	butyrylcholinesterase	Homo sapiens	192-206
20672837-7	2010	In conclusion, annexin VI may have advantages over annexin V in certain situations for both in vitro and in vivo detection of apoptosis and therapeutic targeting of PS due to its lower calcium requirement for membrane binding and its higher molecular weight.	Phosphorus	165-167	annexin A5	Homo sapiens	15-24
20602355-9	2010	We have performed a new crystallographic refinement of the original diffraction map of the pentacoordinated phosphorus structure with the MgF(3)(-) TSA.	Phosphorus	108-118	signal transducer and activator of transcription 5A	Homo sapiens	138-141
20957167-3	2010	In the case of both N/P ratios (5, 25), nanoparticles started releasing EGFR antisense as soon as they were exposed to the medium and the release lasted for approximately 50 hours.	Phosphorus	22-23	epidermal growth factor receptor	Homo sapiens	72-76
20957167-6	2010	Agarose gel electrophoresis of the nanoparticles with the two different N/P ratios showed that these nanoparticles could protect EGFR antisense molecules for six hours.	Phosphorus	74-75	epidermal growth factor receptor	Homo sapiens	129-133
20551061-4	2010	Treatment of human PTEN null PC3 prostate and PIK3CA mutant HCT116 colon carcinoma cells with PI-103 resulted in a concentration- and time-dependent decrease in phosphocholine (PC) and total choline (tCho) levels (P &lt; 0.05) detected by phosphorus ((31)P)- and proton ((1)H)-MRS.	Phosphorus	239-249	phosphatase and tensin homolog	Homo sapiens	19-23
20472109-3	2010	Serum phosphorus level and urinary phosphorus excretion were slightly lower and higher, respectively, in SAP-sFRP4 compared to wild-type (WT) littermate, but the difference did not reach statistical significance.	Phosphorus	6-16	secreted frizzled-related protein 4	Mus musculus	109-114
21090295-4	2010	Moreover, at 0, 1, 6, 24 h after disturbance, the BAP gradually declined with the number of sediment disturbance increase, but the BAP at Oh after each disturbance was higher than that at 1 h, 6 h, 24 h. This may be attributed to the immediate release of bioavailable particulate phosphorus ( BAPP), as a result of sediment disturbance.	Phosphorus	280-290	prohibitin 2	Homo sapiens	131-134
21090303-0	2010	[Effect of the influent COD and C/N ratio on phosphorus removal of UCT system].	Phosphorus	45-55	small nuclear ribonucleoprotein polypeptides B and B1	Homo sapiens	24-27
21090303-5	2010	When the influent concentration of COD is lower than 350 mg/L, the phenomenon of denitrifying phosphorus-uptake is very remarkable.	Phosphorus	94-104	small nuclear ribonucleoprotein polypeptides B and B1	Homo sapiens	35-38
21090303-8	2010	The removal efficiency of total phosphorus achieve higher than 80% steadily when the influent concentration of COD in the range of 250-450 mg/L even in different influent C/N ratio.	Phosphorus	32-42	small nuclear ribonucleoprotein polypeptides B and B1	Homo sapiens	111-114
20077437-7	2010	Enzyme kinetics analysis indicated that p-CA is a mixed type (for tyrosine) or competitive inhibitor (for DOPA) of human TYR.	Phosphorus	40-41	tyrosinase	Homo sapiens	121-124
21090295-1	2010	The course of intermittent sediment disturbance-sedimentation, that sediment disturbance was for 10 min and succeeding sedimentation was for 1430 min each day over a 17-day period, was simulated to investigate the variation of bioavailable phosphorus (BAP) in overlying water.	Phosphorus	240-250	prohibitin 2	Homo sapiens	252-255
20649764-8	2010	Early intervention with intravenous or pulse oral vitamin D therapy at serum iPTH &lt;300 pg/mL can control serum phosphorus, calcium-phosphorus product, and PTH levels to the target ranges and slow the progression of secondary hyperparathyroidism.	Phosphorus	114-124	parathyroid hormone	Homo sapiens	78-81
20583336-6	2010	Emerging data highlight the potential of FGF23 as a novel diagnostic to identify CKD patients at the highest risk for disease progression, cardiovascular disease, and death, and those who might benefit from early phosphorus-related therapies before the onset of overt hyperphosphatemia.	Phosphorus	213-223	fibroblast growth factor 23	Homo sapiens	41-46
20558539-9	2010	Three loci were near genes encoding the kidney-specific type IIa sodium phosphate co-transporter (SLC34A1), the calcium-sensing receptor (CASR), and fibroblast growth factor 23 (FGF23), proteins that contribute to phosphorus metabolism.	Phosphorus	214-224	solute carrier family 34 member 1	Homo sapiens	98-105
20571400-5	2010	In-vivo and in-vitro experiments demonstrated that FGF23 positively correlated, also in a dose-dependent manner, with the dose of estrogens and with the observed changes in calcitriol and phosphorus.	Phosphorus	188-198	fibroblast growth factor 23	Homo sapiens	51-56
20408761-5	2010	The polymorphism of TGFbeta3 C641A participates in interaction effect for CL/P with environmental exposures, although the polymorphism was not associated with CL/P in single-locus analysis, and synergistic effect of TGFbeta3 C641A and maternal passive smoking could provide a new tool for identifying high-risk individuals of CL/P and also an additional evidence that CL/P is determined by both genetic and environmental factors.	Phosphorus	77-78	transforming growth factor beta 3	Homo sapiens	20-28
20408761-5	2010	The polymorphism of TGFbeta3 C641A participates in interaction effect for CL/P with environmental exposures, although the polymorphism was not associated with CL/P in single-locus analysis, and synergistic effect of TGFbeta3 C641A and maternal passive smoking could provide a new tool for identifying high-risk individuals of CL/P and also an additional evidence that CL/P is determined by both genetic and environmental factors.	Phosphorus	77-78	transforming growth factor beta 3	Homo sapiens	216-224
20408761-5	2010	The polymorphism of TGFbeta3 C641A participates in interaction effect for CL/P with environmental exposures, although the polymorphism was not associated with CL/P in single-locus analysis, and synergistic effect of TGFbeta3 C641A and maternal passive smoking could provide a new tool for identifying high-risk individuals of CL/P and also an additional evidence that CL/P is determined by both genetic and environmental factors.	Phosphorus	162-163	transforming growth factor beta 3	Homo sapiens	20-28
20408761-5	2010	The polymorphism of TGFbeta3 C641A participates in interaction effect for CL/P with environmental exposures, although the polymorphism was not associated with CL/P in single-locus analysis, and synergistic effect of TGFbeta3 C641A and maternal passive smoking could provide a new tool for identifying high-risk individuals of CL/P and also an additional evidence that CL/P is determined by both genetic and environmental factors.	Phosphorus	162-163	transforming growth factor beta 3	Homo sapiens	20-28
20558539-9	2010	Three loci were near genes encoding the kidney-specific type IIa sodium phosphate co-transporter (SLC34A1), the calcium-sensing receptor (CASR), and fibroblast growth factor 23 (FGF23), proteins that contribute to phosphorus metabolism.	Phosphorus	214-224	fibroblast growth factor 23	Homo sapiens	149-176
20558539-9	2010	Three loci were near genes encoding the kidney-specific type IIa sodium phosphate co-transporter (SLC34A1), the calcium-sensing receptor (CASR), and fibroblast growth factor 23 (FGF23), proteins that contribute to phosphorus metabolism.	Phosphorus	214-224	fibroblast growth factor 23	Homo sapiens	178-183
20585891-5	2010	Based on these results, SPS and PS may improve scratching behavioral reactions in skin by regulating the action of histamine and the activation of the transcription factors NF-kappaB and c-jun.	Phosphorus	25-27	jun proto-oncogene	Mus musculus	187-192
20399138-1	2010	The FT-Raman spectra of 10 generations of phosphorus-containing dendrimers containing P=S and P=O bonds with terminal benzaldehyde and P-Cl groups have been recorded and analyzed.	Phosphorus	42-52	polycystin 2 like 1, transient receptor potential cation channel	Homo sapiens	135-139
21393712-0	2010	Spin dynamics of isolated donor electrons in phosphorus-doped silicon from high-frequency electron spin resonance.	Phosphorus	45-55	spindlin 1	Homo sapiens	0-4
20572854-8	2010	This study provides further evidence implicating MSX1 and MTHFR in the etiology of nonsyndromic CL/P across different populations.	Phosphorus	99-100	msh homeobox 1	Homo sapiens	49-53
20572854-8	2010	This study provides further evidence implicating MSX1 and MTHFR in the etiology of nonsyndromic CL/P across different populations.	Phosphorus	99-100	methylenetetrahydrofolate reductase	Homo sapiens	58-63
19733931-7	2010	A significant interaction was found for CHRNA3 and PS (P=0.02).	Phosphorus	51-53	cholinergic receptor nicotinic alpha 3 subunit	Homo sapiens	40-46
20628536-1	2010	The mechanism of FGF23 action in calcium/phosphorus metabolism of patients with chronic kidney disease (CKD) was studied using a mathematical model and clinical data in a public domain.	Phosphorus	41-51	fibroblast growth factor 23	Homo sapiens	17-22
20628536-4	2010	Using the parameters identified from available clinical data, we observed that a transient decrease in the FGF23 level elevated the serum concentrations of PTH, calcitriol, and phosphorus.	Phosphorus	177-187	fibroblast growth factor 23	Homo sapiens	107-112
20628536-6	2010	This model-based prediction indicated that the therapeutic reduction of FGF23 by the neutralizing antibody did not reduce phosphorus burden of CKD patients and decreased the urinary phosphorous excretion.	Phosphorus	182-193	fibroblast growth factor 23	Homo sapiens	72-77
20628536-7	2010	Thus, the high FGF23 level in CKD patients was predicted to be a failure of FGF23-mediated phosphorous excretion.	Phosphorus	91-102	fibroblast growth factor 23	Homo sapiens	15-20
20628536-7	2010	Thus, the high FGF23 level in CKD patients was predicted to be a failure of FGF23-mediated phosphorous excretion.	Phosphorus	91-102	fibroblast growth factor 23	Homo sapiens	76-81
20550822-2	2010	Because phosphorus is an essential mineral for all living organisms, growing of phytase transgenic maize may affect the performance of the arthropod community in maize fields.	Phosphorus	8-18	phytase	Zea mays	80-87
20471598-4	2010	Based on adsorption yield and residual activity of glutathione S-transferase (GST) after fusion with the PS19-6 peptide or its variants, it was found that the basic amino acid in the PS-tags, i.e., Arg was essential for the strong binding affinity of PS-tags in both the peptide and peptide-fused protein forms The aliphatic amino acids in PS19-6 and PS19-6L, such as Ile or Leu, were also effective.	Phosphorus	105-107	glutathione S-transferase kappa 1	Homo sapiens	78-81
19452288-0	2010	New targets of PS-341: BAFF and APRIL.	Phosphorus	15-18	TNF superfamily member 13b	Homo sapiens	23-27
19452288-0	2010	New targets of PS-341: BAFF and APRIL.	Phosphorus	15-18	TNF superfamily member 13	Homo sapiens	32-37
21393712-0	2010	Spin dynamics of isolated donor electrons in phosphorus-doped silicon from high-frequency electron spin resonance.	Phosphorus	45-55	spindlin 1	Homo sapiens	99-103
21393712-1	2010	We present the spin dynamics of isolated donor electrons in phosphorus-doped silicon at low temperature and in a high magnetic field.	Phosphorus	60-70	spindlin 1	Homo sapiens	15-19
19955208-3	2010	Our results indicate that the combination of PIP(2), PIP(3), and PS generates a high negative charge (-8) at the plasma membrane of actin-rich pseudopods, where active Rac1 preferentially localizes during phagosome formation.	Phosphorus	65-67	Rac family small GTPase 1	Mus musculus	168-172
20366723-0	2010	Spin-dependent recombination between phosphorus donors in silicon and Si/SiO{2} interface states investigated with pulsed electrically detected electron double resonance.	Phosphorus	37-47	spindlin 1	Homo sapiens	0-4
20012997-1	2010	Recent studies have demonstrated that levels of fibroblast growth factor 23 (FGF-23), a key regulator of phosphorus and vitamin D metabolism, rise dramatically as renal function declines and may play a key initiating role in disordered mineral and bone metabolism in patients with chronic kidney disease (CKD).	Phosphorus	105-115	fibroblast growth factor 23	Homo sapiens	48-75
20012997-1	2010	Recent studies have demonstrated that levels of fibroblast growth factor 23 (FGF-23), a key regulator of phosphorus and vitamin D metabolism, rise dramatically as renal function declines and may play a key initiating role in disordered mineral and bone metabolism in patients with chronic kidney disease (CKD).	Phosphorus	105-115	fibroblast growth factor 23	Homo sapiens	77-83
20627041-2	2010	METHODS: Immunohistochemical method of S-P was used to examine Dkk-3 expression in 69 cases of esophageal squamous cell carcinoma and 5 cases of normal esophageal tissue with non-tumor tissue microarray and the results were analyzed and correlated with their clinical and pathological features.	Phosphorus	39-42	dickkopf WNT signaling pathway inhibitor 3	Homo sapiens	63-68
20641975-10	2004	PS is also accessible for annexin V binding in apoptosis and necrosis because of disruption of the plasma membrane.	Phosphorus	0-2	annexin A5	Homo sapiens	26-35
20641975-11	2004	Annexin V binds to PS with high affinity (dissociation constant = 7 nM).	Phosphorus	19-21	annexin A5	Homo sapiens	0-9
20217174-3	2010	The derivative technique also revealed for the first time a substantial increase in glassy-state expansivity with increasing nBMA content in S/nBMA random copolymers, from 1.4x10(-4) K-1 in PS to 3.5x10(-4) K-1 in PnBMA.	Phosphorus	190-192	keratin 1	Homo sapiens	183-186
20163832-6	2010	Interestingly, PDI reductase activity could maintain TF in the reduced monomeric form, while also maintaining low exposure of PS, both states correlated with low procoagulant function.	Phosphorus	126-128	protein disulfide isomerase family A member 2	Homo sapiens	15-18
20092876-1	2010	White phosphorus (P(4)) is a highly toxic compound used in various pyrotechnic products.	Phosphorus	0-16	solute carrier family 10 member 4	Homo sapiens	18-22
19230880-10	2010	In women with PCOS, phosphorus was correlated negatively with insulin and insulin resistance and positively with 1,25(OH)(2) D. In addition, in normal-weight patients, PTH correlated positively with insulin and insulin resistance.	Phosphorus	20-30	parathyroid hormone	Homo sapiens	168-171
19230880-11	2010	CONCLUSION(S): It is possible that elevated levels of phosphorus and PTH in women with PCOS, at least in part, through their effects on insulin levels and insulin resistance, are involved in pathogenesis of the syndrome.	Phosphorus	54-64	insulin	Homo sapiens	136-143
19230880-11	2010	CONCLUSION(S): It is possible that elevated levels of phosphorus and PTH in women with PCOS, at least in part, through their effects on insulin levels and insulin resistance, are involved in pathogenesis of the syndrome.	Phosphorus	54-64	insulin	Homo sapiens	155-162
19781123-0	2010	Low calcium:phosphorus ratio in habitual diets affects serum parathyroid hormone concentration and calcium metabolism in healthy women with adequate calcium intake.	Phosphorus	12-22	parathyroid hormone	Homo sapiens	61-80
19889793-7	2010	In addition to 4MUG, the PS(serosal) of the glucuronide conjugates of 7-ethyl-10-hydroxycamptothecin (SN-38) and acetaminophen in the jejunal everted sacs were also significantly reduced in Mrp3(-/-) mice compared with wild-type mice.	Phosphorus	25-27	ATP-binding cassette, sub-family C (CFTR/MRP), member 3	Mus musculus	190-194
20366723-1	2010	We investigate the spin species relevant for the spin-dependent recombination used for the electrical readout of coherent spin manipulation in phosphorus-doped silicon.	Phosphorus	143-153	spindlin 1	Homo sapiens	19-23
20366723-1	2010	We investigate the spin species relevant for the spin-dependent recombination used for the electrical readout of coherent spin manipulation in phosphorus-doped silicon.	Phosphorus	143-153	spindlin 1	Homo sapiens	49-53
20366723-1	2010	We investigate the spin species relevant for the spin-dependent recombination used for the electrical readout of coherent spin manipulation in phosphorus-doped silicon.	Phosphorus	143-153	spindlin 1	Homo sapiens	49-53
20366723-2	2010	Via a multifrequency pump-probe experiment in pulsed electrically detected magnetic resonance, we demonstrate that the dominant spin-dependent recombination transition occurs between phosphorus donors and Si/SiO_{2} interface states.	Phosphorus	183-193	spindlin 1	Homo sapiens	128-132
19957936-1	2010	Density functional theory (DFT) predicts a detailed mechanism for the reported potential photocatalytic system for solar hydrogen production from water, (P-da-PNN)RuH(CO) (1, P-da = dearomatized at the phosphorus side arm, PNN = (2-(di-tert-butylphosphinomethyl)-6-diethylaminomethyl)pyridine) (Science 2009, 324, 74).	Phosphorus	202-212	pinin, desmosome associated protein	Homo sapiens	159-162
20157217-13	2010	CONCLUSIONS: Primary hyperparathyroidism patients with lithiasis presented higher values of parathormone, alkaline phosphatase, osteocalcin, and Cl/P and calciuria indexes than lithiasis-free PHPT patients.	Phosphorus	13-14	bone gamma-carboxyglutamate protein	Homo sapiens	128-139
20059333-2	2010	Fibroblast growth factor 23 (FGF23) is part of a previously unrecognized hormonal bone-parathyroid-kidney axis, which is modulated by PTH, 1,25(OH)(2)-vitamin D (1,25(OH)(2)D), dietary and serum phosphorus levels.	Phosphorus	195-205	fibroblast growth factor 23	Homo sapiens	0-27
20059333-2	2010	Fibroblast growth factor 23 (FGF23) is part of a previously unrecognized hormonal bone-parathyroid-kidney axis, which is modulated by PTH, 1,25(OH)(2)-vitamin D (1,25(OH)(2)D), dietary and serum phosphorus levels.	Phosphorus	195-205	fibroblast growth factor 23	Homo sapiens	29-34
20059333-2	2010	Fibroblast growth factor 23 (FGF23) is part of a previously unrecognized hormonal bone-parathyroid-kidney axis, which is modulated by PTH, 1,25(OH)(2)-vitamin D (1,25(OH)(2)D), dietary and serum phosphorus levels.	Phosphorus	195-205	parathyroid hormone	Homo sapiens	134-137
20059333-3	2010	Synthesis and secretion of FGF23 by osteocytes are positively regulated by 1,25(OH)(2)D and serum phosphorus and negatively regulated, through yet unknown mechanisms, by the phosphate-regulating gene with homologies to endopeptidases on the X chromosome (PHEX) and by dentin matrix protein 1 (DMP1).	Phosphorus	98-108	fibroblast growth factor 23	Homo sapiens	27-32
19889624-7	2010	However, PKR gene silencing or treatment with a specific PKR inhibitor significantly prevented the increase in pT(451)-PKR and pS(194)-FADD levels in SH-SY5Y nuclei and completely inhibited activities of caspase-3 and -8.	Phosphorus	127-129	eukaryotic translation initiation factor 2-alpha kinase 2	Mus musculus	9-12
19889624-7	2010	However, PKR gene silencing or treatment with a specific PKR inhibitor significantly prevented the increase in pT(451)-PKR and pS(194)-FADD levels in SH-SY5Y nuclei and completely inhibited activities of caspase-3 and -8.	Phosphorus	127-129	eukaryotic translation initiation factor 2-alpha kinase 2	Mus musculus	57-60
19889624-7	2010	However, PKR gene silencing or treatment with a specific PKR inhibitor significantly prevented the increase in pT(451)-PKR and pS(194)-FADD levels in SH-SY5Y nuclei and completely inhibited activities of caspase-3 and -8.	Phosphorus	127-129	eukaryotic translation initiation factor 2-alpha kinase 2	Mus musculus	57-60
19889624-7	2010	However, PKR gene silencing or treatment with a specific PKR inhibitor significantly prevented the increase in pT(451)-PKR and pS(194)-FADD levels in SH-SY5Y nuclei and completely inhibited activities of caspase-3 and -8.	Phosphorus	127-129	Fas associated via death domain	Homo sapiens	135-139
20731105-4	2010	ACC, LV hypertrophy, and arterial hypertension (AH) were more significant in patients with higher serum levels PTH and P. CONCLUSION: In patients with early-stage CRD, phosphorus and calcium metabolic disturbances promote the development of AH, vascular and cardiac valvular calcification, myocardial hypertrophy, and HF.	Phosphorus	168-178	parathyroid hormone	Homo sapiens	111-114
19772957-7	2010	After 20 weeks, the rats fed with a high phosphorus diet showed a significant increase in serum phosphorus, PTH, and creatinine, together with aortic calcification and a decrease in bone mass.	Phosphorus	41-51	parathyroid hormone	Rattus norvegicus	108-111
20091488-8	2010	Multiple regression analysis showed that fetuin-A was independently associated with estimated glomerular filtration rate (beta=0.386; p&lt;0.001), IL-6 (beta=-0.393; p=0.001) and ET-1 (beta=-0.219; p=0.02), in a multivariate model including also sex, parathyroid hormone and the calcium x phosphorus product.	Phosphorus	289-299	alpha 2-HS glycoprotein	Homo sapiens	41-49
20936886-1	2010	BACKGROUND: Imbalanced levels of parathyroid hormone (PTH), serum calcium (Ca) and phosphorous (P) are associated with an increased risk of cardiovascular (CV) death and fracture in dialysis patients with secondary hyperparathyroidism (SHPT).	Phosphorus	54-55	parathyroid hormone	Homo sapiens	33-52
19949066-5	2010	IFN-alpha, generated by plasmacytoid dendritic cells, induced the expression of CD69 and suppressed the sphingosine-1-phosphate-induced chemotactic response, promoting FO-oriented Ag transport by MZ-P B cells.	Phosphorus	199-200	interferon alpha	Mus musculus	0-9
19642642-7	2009	Furthermore, the crystal structure of the ternary complex of the aged conjugate with 2-PAM revealed that the orientation of the oxime function does not permit nucleophilic attack on the phosphorus atom, thus providing a plausible explanation for its failure to reactivate the aged soman/AChE conjugate.	Phosphorus	186-196	peptidylglycine alpha-amidating monooxygenase	Homo sapiens	87-90
19782638-10	2009	An inverse correlation was found between CD4 and LPS levels (p=0.044) in PS group only.	Phosphorus	50-52	CD4 molecule	Homo sapiens	41-44
19452557-11	2009	Furthermore, similarity of the structure to the structure of RNase A, which is known to hydrolyze the O--P bond in RNA, grants it further credibility and suggests a mechanism for the OP hydrolysis.	Phosphorus	105-106	ribonuclease A family member 1, pancreatic	Homo sapiens	61-68
19696400-4	2009	The induction of KLF2 by PS led to the increase in eNOS and the suppression of ET-1, which could be reversed by KLF2 siRNA.	Phosphorus	25-27	DNA segment, Chr 9, MRC UK Mouse Genome Centre 40 expressed	Mus musculus	79-83
19696400-4	2009	The induction of KLF2 by PS led to the increase in eNOS and the suppression of ET-1, which could be reversed by KLF2 siRNA.	Phosphorus	25-27	Kruppel-like factor 2 (lung)	Mus musculus	112-116
19696400-5	2009	In addition, PS induced the phosphorylation of ERK5 and MEF2 which are necessary for the KLF2 expression.	Phosphorus	13-15	mitogen-activated protein kinase 7	Mus musculus	47-51
19696400-5	2009	In addition, PS induced the phosphorylation of ERK5 and MEF2 which are necessary for the KLF2 expression.	Phosphorus	13-15	myocyte enhancer factor 2C	Mus musculus	56-60
19696400-5	2009	In addition, PS induced the phosphorylation of ERK5 and MEF2 which are necessary for the KLF2 expression.	Phosphorus	13-15	Kruppel-like factor 2 (lung)	Mus musculus	89-93
19770756-2	2009	RECENT FINDINGS: FGF23 regulates phosphorus and vitamin D metabolism.	Phosphorus	33-43	fibroblast growth factor 23	Homo sapiens	17-22
19696400-4	2009	The induction of KLF2 by PS led to the increase in eNOS and the suppression of ET-1, which could be reversed by KLF2 siRNA.	Phosphorus	25-27	Kruppel-like factor 2 (lung)	Mus musculus	17-21
19809748-2	2009	Tertiary phosphorus donor ligands react with the mixture of [Rh(CO)2Tt] and [(RhTt)2(mu-CO)3] to give [Rh(CO)(PR3)Tt] (R = Cy, NMe(2), Ph or OPh) and [Rh{P(OPh)3}2Tt] in which rhodium is bound to two sulfur atoms of the scorpionate ligand; the B-H bond is directed towards the metal to give an agostic-like B-H...Rh interaction.	Phosphorus	9-19	proteinase 3	Homo sapiens	110-113
19656958-6	2009	Milk for males had a lower content in Ca and P, a greater content of K, and Mg, whereas no sex effects were found in Na, Fe, or Zn percentages.	Phosphorus	45-46	Weaning weight-maternal milk	Bos taurus	0-4
19775108-1	2009	The controlled activation of white phosphorus, P(4), provides a key entry point into many aspects of phosphorus chemistry.	Phosphorus	29-45	solute carrier family 10 member 4	Homo sapiens	47-51
19746466-1	2009	Insertion of PCl(3) into 5,10,15,20-tetraaryl-21-telluraporphyrin leads to a phosphorus complex of N-fused dihydrotelluraporphyrin with an inverted tellurophene ring.	Phosphorus	77-87	PHD finger protein 19	Homo sapiens	13-18
19968117-2	2009	The results showed that, when the concentration of COD in influential of anaerobic stage, the concentration of NO3 -N in influent of anoxic stage and pH value were 300 mg/L, 50 mg/L and 7.0 respectively, DPB could become dominant populations quickly in the system in two-time feeding mode, and the reactor performed well for denitrifying phosphorus removal.	Phosphorus	338-348	NBL1, DAN family BMP antagonist	Homo sapiens	111-114
19775108-1	2009	The controlled activation of white phosphorus, P(4), provides a key entry point into many aspects of phosphorus chemistry.	Phosphorus	35-45	solute carrier family 10 member 4	Homo sapiens	47-51
19775108-4	2009	This has enabled the targeted preparation of novel mono- and dicationic phosphorus-rich clusters [(DippNP)(2)(P(4))Cl](+) and [(DippNP)(2)(P(4))(2)](+).	Phosphorus	72-82	solute carrier family 10 member 4	Homo sapiens	110-114
19775108-4	2009	This has enabled the targeted preparation of novel mono- and dicationic phosphorus-rich clusters [(DippNP)(2)(P(4))Cl](+) and [(DippNP)(2)(P(4))(2)](+).	Phosphorus	72-82	solute carrier family 10 member 4	Homo sapiens	139-143
19680637-5	2009	These results indicate that strong and specific attachment of PS-tags onto the phi-PS surface prevented scFv conformational changes and consequently, the high antigen-binding activities of scFvs were preserved.	Phosphorus	62-64	immunglobulin heavy chain variable region	Homo sapiens	104-108
19760622-4	2009	Therefore, the aim of this study is to investigate the association between the maternal and child"s functional ABCB1 3435C > T polymorphism, periconceptional medication exposure, and the risk of a child with CL/P.	Phosphorus	211-212	ATP binding cassette subfamily B member 1	Homo sapiens	111-116
19216809-0	2009	Habitual high phosphorus intakes and foods with phosphate additives negatively affect serum parathyroid hormone concentration: a cross-sectional study on healthy premenopausal women.	Phosphorus	14-24	parathyroid hormone	Homo sapiens	92-111
19760622-10	2009	These data suggest that mothers who carry the ABCB1 3435C > T polymorphism are at significantly increased risk for having offspring with CL/P, especially mothers using medication in the periconceptional period.	Phosphorus	140-141	ATP binding cassette subfamily B member 1	Homo sapiens	46-51
19713292-5	2009	Patients with no RRF showed higher calcium-phosphorus product (Ca x P) and C-reactive protein (CRP).	Phosphorus	0-1	C-reactive protein	Homo sapiens	75-93
19713292-5	2009	Patients with no RRF showed higher calcium-phosphorus product (Ca x P) and C-reactive protein (CRP).	Phosphorus	0-1	C-reactive protein	Homo sapiens	95-98
19710229-0	2009	Abnormal physiological and molecular mutant phenotypes link chloroplast polynucleotide phosphorylase to the phosphorus deprivation response in Arabidopsis.	Phosphorus	108-118	polyribonucleotide nucleotidyltransferase	Arabidopsis thaliana	72-100
19710229-2	2009	In Chlamydomonas reinhardtii, PNPase regulates chloroplast transcript accumulation in response to phosphorus (P) starvation, and PNPase expression is repressed by the response regulator PSR1 (for PHOSPHORUS STARVATION RESPONSE1) under these conditions.	Phosphorus	98-108	polyribonucleotide nucleotidyltransferase	Arabidopsis thaliana	30-36
19710229-2	2009	In Chlamydomonas reinhardtii, PNPase regulates chloroplast transcript accumulation in response to phosphorus (P) starvation, and PNPase expression is repressed by the response regulator PSR1 (for PHOSPHORUS STARVATION RESPONSE1) under these conditions.	Phosphorus	98-108	uncharacterized protein	Chlamydomonas reinhardtii	186-190
19710229-2	2009	In Chlamydomonas reinhardtii, PNPase regulates chloroplast transcript accumulation in response to phosphorus (P) starvation, and PNPase expression is repressed by the response regulator PSR1 (for PHOSPHORUS STARVATION RESPONSE1) under these conditions.	Phosphorus	98-108	uncharacterized protein	Chlamydomonas reinhardtii	196-227
19714708-7	2009	It was also found that red phosphorus is a suitable MALDI matrix for peptides and proteins, illustrated by the examples of a Calmix mixture of bradykinin, angiotensin, renin, adrenocorticotropic hormone ACTH fragment 18-359 and insulin, and of insulin alone.	Phosphorus	23-37	kininogen 1	Homo sapiens	143-153
19714708-7	2009	It was also found that red phosphorus is a suitable MALDI matrix for peptides and proteins, illustrated by the examples of a Calmix mixture of bradykinin, angiotensin, renin, adrenocorticotropic hormone ACTH fragment 18-359 and insulin, and of insulin alone.	Phosphorus	23-37	renin	Homo sapiens	168-173
19714708-7	2009	It was also found that red phosphorus is a suitable MALDI matrix for peptides and proteins, illustrated by the examples of a Calmix mixture of bradykinin, angiotensin, renin, adrenocorticotropic hormone ACTH fragment 18-359 and insulin, and of insulin alone.	Phosphorus	23-37	proopiomelanocortin	Homo sapiens	203-207
19714708-7	2009	It was also found that red phosphorus is a suitable MALDI matrix for peptides and proteins, illustrated by the examples of a Calmix mixture of bradykinin, angiotensin, renin, adrenocorticotropic hormone ACTH fragment 18-359 and insulin, and of insulin alone.	Phosphorus	23-37	insulin	Homo sapiens	228-235
19714708-7	2009	It was also found that red phosphorus is a suitable MALDI matrix for peptides and proteins, illustrated by the examples of a Calmix mixture of bradykinin, angiotensin, renin, adrenocorticotropic hormone ACTH fragment 18-359 and insulin, and of insulin alone.	Phosphorus	23-37	insulin	Homo sapiens	244-251
19633233-7	2009	Therefore, AtPAP15 likely mobilizes phosphorus reserves in plants, particularly during seed and pollen germination.	Phosphorus	36-46	purple acid phosphatase 15	Arabidopsis thaliana	11-18
19809253-4	2009	The seed was coupled to PEGylated-PS beads to remove the monomeric beta2m from solution.	Phosphorus	34-36	beta-2-microglobulin	Homo sapiens	67-73
19830970-14	2009	The results of the current study indicated that the bond strength of P&amp;B NT might be compromised by the higher acidity of this adhesive compared to OS during each curing mode, especially PDI.	Phosphorus	69-71	peptidyl arginine deiminase 1	Homo sapiens	191-194
20069911-3	2009	The triterpenoid saponins are mainly oleanolic type and hederagenin type, most of which are bidesmosidic saponins, substituted with oligosaccharide chains at both C-3 and C-28, and some are substituted with acetyl, caffeoyl, isoferuloyl, p-methoxy cinnamyl and 3,4-dimethoxy cinnamyl groups in the oligosaccharide chains.	Phosphorus	10-11	complement C3	Homo sapiens	163-166
19444471-9	2009	Thus, TGFA appears to influence risk of CL/P through unconventional means with an apparent parent-of-origin effect (excess maternal transmission) and possible interaction with maternal exposures.	Phosphorus	43-44	transforming growth factor alpha	Homo sapiens	6-10
19295502-4	2009	In the absence of stage 3 or 4 CKD, patients with elevated serum cystatin C had a higher prevalence of low hemoglobin and elevated uric acid, homocysteine, phosphorus, fibrinogen, and C-reactive protein than patients with a normal serum cystatin C.	Phosphorus	156-166	cystatin C	Homo sapiens	65-75
19563773-1	2009	Phosphorus-containing pseudopeptides, racemic at the C-terminal alpha-carbon, are potent mechanism-based inhibitors of folylpolyglutamate synthetase (FPGS).	Phosphorus	0-10	folylpolyglutamate synthase	Homo sapiens	119-148
19563773-1	2009	Phosphorus-containing pseudopeptides, racemic at the C-terminal alpha-carbon, are potent mechanism-based inhibitors of folylpolyglutamate synthetase (FPGS).	Phosphorus	0-10	folylpolyglutamate synthase	Homo sapiens	150-154
19722630-11	2009	The increase of the thickness of the intermediate PDEA layer arises from the protonation and hydration, but the swelling is constrained by the PS layers.	Phosphorus	143-145	phosphodiesterase 6A	Homo sapiens	50-54
19722630-12	2009	The increase of the thickness of the two PS layers is a result of an increasing incompatibility and an accompanying sharpening of the interface between the PS layers and the PDEA layer.	Phosphorus	41-43	phosphodiesterase 6A	Homo sapiens	174-178
19722630-12	2009	The increase of the thickness of the two PS layers is a result of an increasing incompatibility and an accompanying sharpening of the interface between the PS layers and the PDEA layer.	Phosphorus	156-158	phosphodiesterase 6A	Homo sapiens	174-178
19722630-13	2009	Starting at a pH slightly below 6, progressive swelling of the PDEA layer with decreasing pH induces a cracking of the two PS layers and also a sharp increase of the vesicle size and the wall thickness.	Phosphorus	123-125	phosphodiesterase 6A	Homo sapiens	63-67
19515808-7	2009	Similarly, in FGFR4(-/-) mice, administration of FGF23 caused a small but significant decrease in serum phosphorus levels (8.7 +/- 0.3 vs. 7.6 +/- 0.4 mg/dl; p &lt; or = 0.001) and in renal BBM NaPi-2a and NaPi-2c protein abundance.	Phosphorus	104-114	fibroblast growth factor 23	Mus musculus	49-54
19775014-5	2009	PCB31 was the dominate PCB congener in all the p-DCB samples with the maximum 98.5% of the total PCBs.	Phosphorus	47-48	pyruvate carboxylase	Homo sapiens	0-3
19442720-1	2009	The present study was aimed to investigate the effects of polyoxyethylene (40) stearate (PS), a non-ionic surfactant, on the activity of P-glycoprotein (P-gp) and six major cytochrome P450 (CYP) isoforms.	Phosphorus	89-91	ATP binding cassette subfamily B member 1	Homo sapiens	137-151
19442720-1	2009	The present study was aimed to investigate the effects of polyoxyethylene (40) stearate (PS), a non-ionic surfactant, on the activity of P-glycoprotein (P-gp) and six major cytochrome P450 (CYP) isoforms.	Phosphorus	89-91	ATP binding cassette subfamily B member 1	Homo sapiens	153-157
19442720-4	2009	The obtained results showed that PS inhibited P-gp mediated efflux in a concentration-dependent manner mainly by modulating substrate-stimulated P-gp ATPase activity.	Phosphorus	33-35	ATP binding cassette subfamily B member 1	Homo sapiens	46-50
19442720-4	2009	The obtained results showed that PS inhibited P-gp mediated efflux in a concentration-dependent manner mainly by modulating substrate-stimulated P-gp ATPase activity.	Phosphorus	33-35	ATP binding cassette subfamily B member 1	Homo sapiens	145-149
19442720-7	2009	In conclusion, PS is potentially useful as a pharmaceutical ingredient to improve the oral bioavailability of coadministered P-gp substrates and substrates for certain CYP isoforms.	Phosphorus	15-17	ATP binding cassette subfamily B member 1	Homo sapiens	125-129
19282155-6	2009	The DNA arrays" hybridization efficiency was assessed by the molar ratio of chlorine to phosphorus in a DNA strand, which was determined from the relevant XPS Cl2p and P2p core-level peak areas after hybridization.	Phosphorus	88-98	endogenous retrovirus group W member 5	Homo sapiens	159-163
19282155-6	2009	The DNA arrays" hybridization efficiency was assessed by the molar ratio of chlorine to phosphorus in a DNA strand, which was determined from the relevant XPS Cl2p and P2p core-level peak areas after hybridization.	Phosphorus	88-98	pyrimidinergic receptor P2Y4	Homo sapiens	168-171
19586048-10	2009	Interestingly, phosphorylation of cTnT (cTnT-P) differentially regulates tension cost (an index of cross-bridge cycling rate): increased by cTn-del-P and decreased by intact cTn-wt-P. Like the isometric fiber data, sliding speed of thin filaments regulated by cTn-del is more sensitive to Ca(2+) compared with cTn-wt.	Phosphorus	45-46	troponin T2, cardiac type	Homo sapiens	34-38
19586048-10	2009	Interestingly, phosphorylation of cTnT (cTnT-P) differentially regulates tension cost (an index of cross-bridge cycling rate): increased by cTn-del-P and decreased by intact cTn-wt-P. Like the isometric fiber data, sliding speed of thin filaments regulated by cTn-del is more sensitive to Ca(2+) compared with cTn-wt.	Phosphorus	45-46	troponin T2, cardiac type	Homo sapiens	40-44
19542373-3	2009	Herein, we show that the positively charged residues of the BRS enable this region of CD3 epsilon to complex a subset of acidic phospholipids, including PI(3)P, PI(4)P, PI(5)P, PI(3,4,5)P(3), and PI(4,5)P(2).	Phosphorus	153-154	CD3 antigen, epsilon polypeptide	Mus musculus	86-89
19406976-3	2009	Exposing bovine aortic endothelial cells to a phosphorus load increased production of reactive oxygen species, which depended on phosphorus influx via sodium-dependent phosphate transporters, and decreased nitric oxide production via inhibitory phosphorylation of endothelial nitric oxide synthase.	Phosphorus	46-56	nitric oxide synthase 3	Bos taurus	264-297
19615558-1	2009	The calcium sensing receptor (CaSR) and fibroblast growth factor 23 (FGF-23) play central roles in the regulation of calcium and phosphorus metabolism, respectively.	Phosphorus	129-139	calcium sensing receptor	Homo sapiens	4-28
19615558-1	2009	The calcium sensing receptor (CaSR) and fibroblast growth factor 23 (FGF-23) play central roles in the regulation of calcium and phosphorus metabolism, respectively.	Phosphorus	129-139	calcium sensing receptor	Homo sapiens	30-34
19615558-1	2009	The calcium sensing receptor (CaSR) and fibroblast growth factor 23 (FGF-23) play central roles in the regulation of calcium and phosphorus metabolism, respectively.	Phosphorus	129-139	fibroblast growth factor 23	Homo sapiens	40-67
19615558-1	2009	The calcium sensing receptor (CaSR) and fibroblast growth factor 23 (FGF-23) play central roles in the regulation of calcium and phosphorus metabolism, respectively.	Phosphorus	129-139	fibroblast growth factor 23	Homo sapiens	69-75
19566760-6	2009	RESULTS: The results included the following findings: (i) the level of plasma SP in the PSD group (58.47 +/- 14.39) was higher than that of the PS group (36.98 +/- 9.49; P = 0.000), while the level of CSF SP in the PSD group (72.13 +/- 13.06) was higher than that of the post-stroke group (37.30 +/- 12.57; P = 0.03); (ii) the level of plasma SP was positively correlated with the HAMD and NIHSS score; (iii) the level of plasma SP (38.45 +/- 12.23), the HAMD score (9.08 +/- 8.72), and the NIHSS score (3.25 +/- 1.90) of the anterior stroke group (51.21 +/- 16.27, 17.46 +/- 15.96, and 6.91 +/- 3.30, respectively) were higher than those of the posterior stroke group (38.45 +/- 12.23, 9.08 +/- 8.7, and 3.25 +/- 1.90, respectively; P = 0.017, P = 0.001, and P = 0.000, respectively).	Phosphorus	88-90	tachykinin precursor 1	Homo sapiens	78-80
18990452-10	2009	The APOE genotypes epsilon4/4, epsilon4/3; epsilon3/3; epsilon4/2, and epsilon3/2 or epsilon2/2 were associated with decreasing levels of serum total and LDL cholesterol (Ps&lt;0.001), but not with increasing depressive symptoms (P=0.67).	Phosphorus	171-173	apolipoprotein E	Homo sapiens	4-8
19746344-5	2009	Dietary phosphorus restriction, intestinal phosphate binders, and calcitriol supplementation may slow the progression of renal disease and decrease PTH concentrations in animals with secondary hyperparathyroidism; however, the prognosis for these animals is guarded to poor.	Phosphorus	8-18	parathyroid hormone	Canis lupus familiaris	148-151
19490502-0	2009	Transgenic barley (Hordeum vulgare L.) expressing the wheat aluminium resistance gene (TaALMT1) shows enhanced phosphorus nutrition and grain production when grown on an acid soil.	Phosphorus	111-121	aluminum-activated malate transporter 1	Triticum aestivum	87-94
19490502-2	2009	In short-term pot trials (26 days), transgenic barley expressing TaALMT1 (GP-ALMT1) was more efficient than a non-transformed sibling line (GP) at taking up phosphorus on acid soil, but the genotypes did not differ when the soil was limed.	Phosphorus	157-167	aluminum-activated malate transporter 1	Triticum aestivum	65-72
19490502-2	2009	In short-term pot trials (26 days), transgenic barley expressing TaALMT1 (GP-ALMT1) was more efficient than a non-transformed sibling line (GP) at taking up phosphorus on acid soil, but the genotypes did not differ when the soil was limed.	Phosphorus	157-167	aluminum-activated malate transporter 1	Triticum aestivum	67-72
19558098-7	2009	Distribution characteristics of phosphorus forms were different between the sediment and soils of water-level-fluctuating zone: (1) The ratio of IP/TP in the surface sediments (average value 55.7%) was higher than that in soils of water-level-fluctuating zone (average value 49.4%); (2) The domination phosphorus forms of IP in surface sediments was Ca-P (average ratio 83.5%), and the ratio of (Fe/Al-P)/IP was only 15%.	Phosphorus	32-42	asparaginase and isoaspartyl peptidase 1	Homo sapiens	399-407
19291734-0	2009	Robust Au-PEG/PS microbeads as optically stable platforms for SERS.	Phosphorus	14-16	seryl-tRNA synthetase 2, mitochondrial	Homo sapiens	62-66
21583030-1	2009	In the title complex, [CoPd(2)(C(3)H(5))(2)(C(8)H(11))Cl(2)(C(40)H(30)P(2))] CH(2)Cl(2), the Co(I) atom is sandwiched between the cyclo-penta-dienyl and cyclo-butadiene rings.	Phosphorus	25-26	mitochondrially encoded cytochrome c oxidase I	Homo sapiens	93-98
18639247-6	2009	TG down-regulates p-beta-catenin (S33/S37/T41) and promotes translocation of beta-catenin into the nucleus.	Phosphorus	18-19	catenin beta 1	Homo sapiens	20-32
19152834-10	2009	They further suggest that the inhibitory effect of noradrenaline on PS may be due to the A1/C1, A2 and to a lesser degree to A5 neurons but not from those of the LC as previously hypothesized.	Phosphorus	68-70	UDP glucuronosyltransferase family 1 member A6	Rattus norvegicus	89-98
19269482-6	2009	The average recovery of these phosphorus compounds was 94+/-11% for the DIW matrix and 90+/-12% for the ASW matrix.	Phosphorus	30-40	chromosome 2 open reading frame 49	Homo sapiens	104-107
19233920-10	2009	In patients with PHPT, serum phosphorus was negatively correlated with plasma PAI-1 Ag levels and PAI-1/t-PA ratio (r: -0.453, P&lt;0.05; r: -0.580, P&lt;0.01 respectively).	Phosphorus	29-39	serpin family E member 1	Homo sapiens	78-83
19233920-10	2009	In patients with PHPT, serum phosphorus was negatively correlated with plasma PAI-1 Ag levels and PAI-1/t-PA ratio (r: -0.453, P&lt;0.05; r: -0.580, P&lt;0.01 respectively).	Phosphorus	29-39	serpin family E member 1	Homo sapiens	98-103
19429241-1	2009	We have previously shown that benzo[a]pyrene (B[a]P) administrated at extremely low dose can cause weight gain in mice and that the increase in adipose tissue mass is due to inhibition of beta-adrenergic stimulation of lipolysis.	Phosphorus	50-51	WD and tetratricopeptide repeats 1	Mus musculus	144-151
19233920-10	2009	In patients with PHPT, serum phosphorus was negatively correlated with plasma PAI-1 Ag levels and PAI-1/t-PA ratio (r: -0.453, P&lt;0.05; r: -0.580, P&lt;0.01 respectively).	Phosphorus	29-39	plasminogen activator, tissue type	Homo sapiens	104-108
19233920-11	2009	There was a positive correlation between Cl/P ratio and plasma PAI-1 levels and PAI-1/t-PA ratio (r: 0.434, P&lt;0.05; r: 0.528, P&lt;0.05 respectively).	Phosphorus	44-45	serpin family E member 1	Homo sapiens	63-68
19233920-11	2009	There was a positive correlation between Cl/P ratio and plasma PAI-1 levels and PAI-1/t-PA ratio (r: 0.434, P&lt;0.05; r: 0.528, P&lt;0.05 respectively).	Phosphorus	44-45	serpin family E member 1	Homo sapiens	80-85
19233920-11	2009	There was a positive correlation between Cl/P ratio and plasma PAI-1 levels and PAI-1/t-PA ratio (r: 0.434, P&lt;0.05; r: 0.528, P&lt;0.05 respectively).	Phosphorus	44-45	plasminogen activator, tissue type	Homo sapiens	86-90
19075196-0	2009	Phosphorus overload and PTH induce aortic expression of Runx2 in experimental uraemia.	Phosphorus	0-10	RUNX family transcription factor 2	Homo sapiens	56-61
19289643-7	2009	Sulfaphenazole (P&lt;0.01) blunted bradykinin-induced but not acetylcholine-induced tPA release in both groups.	Phosphorus	16-17	kininogen 1	Homo sapiens	35-45
19595143-4	2009	RESULTS: A mutation (A239G) in the exon 1 of the Nkx2.5 was identified in 3 of 90 normal control subjects and 12 of 99 CHD patients, including 3 of 24 with VSD, 7 of 35 with ASD, 1 of 13 with PS and 1 of 21 with PDA.	Phosphorus	192-194	NK2 homeobox 5	Homo sapiens	49-55
19129257-0	2009	Regulation of PTH mRNA stability by the calcimimetic R568 and the phosphorus binder lanthanum carbonate in CKD.	Phosphorus	66-76	parathyroid hormone	Rattus norvegicus	14-17
19129257-2	2009	PTH gene expression is reduced by the calcimimetic R568 and the oral phosphorus binder lanthanum carbonate (La).	Phosphorus	69-79	parathyroid hormone	Rattus norvegicus	0-3
19129257-10	2009	Therefore, the calcimimetic R568 and correction of serum phosphorus by La determine PTH mRNA stability through KSRP-mediated recruitment of a degradation complex to the PTH mRNA, thereby decreasing PTH expression.	Phosphorus	57-67	parathyroid hormone	Rattus norvegicus	84-87
19129257-10	2009	Therefore, the calcimimetic R568 and correction of serum phosphorus by La determine PTH mRNA stability through KSRP-mediated recruitment of a degradation complex to the PTH mRNA, thereby decreasing PTH expression.	Phosphorus	57-67	KH-type splicing regulatory protein	Rattus norvegicus	111-115
19129257-10	2009	Therefore, the calcimimetic R568 and correction of serum phosphorus by La determine PTH mRNA stability through KSRP-mediated recruitment of a degradation complex to the PTH mRNA, thereby decreasing PTH expression.	Phosphorus	57-67	parathyroid hormone	Rattus norvegicus	169-172
19129257-10	2009	Therefore, the calcimimetic R568 and correction of serum phosphorus by La determine PTH mRNA stability through KSRP-mediated recruitment of a degradation complex to the PTH mRNA, thereby decreasing PTH expression.	Phosphorus	57-67	parathyroid hormone	Rattus norvegicus	169-172
19048631-8	2009	The strongest association in our data (between fetal FOLH1 and CPO, P=0.0008) is not in agreement with epidemiologic evidence that folic acid reduces the risk of CL/P in these data, not CPO.	Phosphorus	64-65	folate hydrolase 1	Homo sapiens	53-58
18936979-6	2009	The GFR levels correlated positively with hemoglobin/hematocrit and calcium levels and negatively with phosphorus and parathyroid hormone (PTH) levels (P &lt; 0.05).	Phosphorus	103-113	Rap guanine nucleotide exchange factor 5	Homo sapiens	4-7
19246988-4	2009	7SK RNA is released from P-TEFb/HEXIM/7SK complexes upon an arrest in transcription and physiological stimulations such as cardiac hypertrophy, leading to P-TEFb activation.	Phosphorus	25-26	RNA component of 7SK nuclear ribonucleoprotein	Homo sapiens	0-3
19246988-4	2009	7SK RNA is released from P-TEFb/HEXIM/7SK complexes upon an arrest in transcription and physiological stimulations such as cardiac hypertrophy, leading to P-TEFb activation.	Phosphorus	25-26	RNA component of 7SK nuclear ribonucleoprotein	Homo sapiens	38-41
19268585-0	2009	Exploring the pharmacokinetic properties of phosphorus-containing selective HDAC 1 and 2 inhibitors (SHI-1:2).	Phosphorus	44-54	histone deacetylase 1	Mus musculus	76-88
19112160-4	2009	Phosphorus-31 magnetic resonance spectroscopy ((31)P-MRS) was used to noninvasively monitor the intracellular concentrations of phosphocreatine ([PCr]) and inorganic phosphate ([P(i)]) as well as intracellular pH (pH(i)) status during exercise in WRM and Con.	Phosphorus	0-10	glucose-6-phosphate isomerase	Homo sapiens	214-219
19436134-3	2009	FGF23 is a circulating factor that regulates renal phosphorus reabsorption and 1 alpha-hydroxylase activity.	Phosphorus	51-61	fibroblast growth factor 23	Rattus norvegicus	0-5
19436134-12	2009	These results might be a result of the mechanisms of FGF23 such as phosphaturic activity and lowering the level of 1,25(OH)(2)D. In conclusion, mutant FGF23 prevented the progression of chronic renal failure by regulating serum phosphorus but aggravated renal osteodystrophy from the lowered levels of 1,25(OH)(2)D.	Phosphorus	228-238	fibroblast growth factor 23	Rattus norvegicus	53-58
19436134-12	2009	These results might be a result of the mechanisms of FGF23 such as phosphaturic activity and lowering the level of 1,25(OH)(2)D. In conclusion, mutant FGF23 prevented the progression of chronic renal failure by regulating serum phosphorus but aggravated renal osteodystrophy from the lowered levels of 1,25(OH)(2)D.	Phosphorus	228-238	fibroblast growth factor 23	Rattus norvegicus	151-156
19135230-0	2009	Atmospheric metal and phosphorus concentrations, inputs, and their biogeochemical significances in the Japan/East Sea.	Phosphorus	22-32	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	114-117
19030908-13	2009	The effects on calcium and phosphorus excretion were mainly due to the group supplemented with Ca + ITF + CPP.	Phosphorus	27-37	trefoil factor 3	Homo sapiens	100-103
19182781-10	2009	Thus heterotrophic bacteria, which compete with phytoplankton for nutrients in oligotrophic regions like the Sargasso Sea, appear to have a biochemical phosphorus requirement that phytoplankton avoid by using substitute lipids.	Phosphorus	152-162	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	118-121
19167798-11	2009	In multivariate logistic regression, higher calcium-phosphorus product was associated with lower serum fetuin A level (odds ratio, 0.96; 95% confidence interval [CI], 0.93 to 1.00; P = 0.02).	Phosphorus	52-62	alpha 2-HS glycoprotein	Homo sapiens	103-111
19402492-4	2009	Being the efficient electron acceptor, NO3(-) or O2 supplying SBRs removed phosphorus smoothly and comparatively, in viewpoint of stiochoimetry and constitution of functional bacteria.	Phosphorus	75-85	NBL1, DAN family BMP antagonist	Homo sapiens	39-42
19402492-7	2009	And facultative PAO of PON and PONn were found as the main contributors for the phosphorus removal.	Phosphorus	80-90	paraoxonase 1	Homo sapiens	23-26
18683894-7	2009	Comparison of cleft subphenotypes with tooth agenesis and controls revealed borderline associations for CDH1 (p = .008) and AXIN2 (p = .01) with unilateral right CL/P with tooth agenesis.	Phosphorus	165-166	axin 2	Homo sapiens	124-129
18683894-8	2009	CONCLUSIONS: We observed only borderline results for the association of AXIN2 and CDH1 with CL/P with and without tooth agenesis.	Phosphorus	95-96	axin 2	Homo sapiens	72-77
18683894-8	2009	CONCLUSIONS: We observed only borderline results for the association of AXIN2 and CDH1 with CL/P with and without tooth agenesis.	Phosphorus	95-96	cadherin 1	Homo sapiens	82-86
18683894-7	2009	Comparison of cleft subphenotypes with tooth agenesis and controls revealed borderline associations for CDH1 (p = .008) and AXIN2 (p = .01) with unilateral right CL/P with tooth agenesis.	Phosphorus	165-166	cadherin 1	Homo sapiens	104-108
19090655-4	2009	The two series of (POSS-M)p-(x/y) molecules are different in hydrophobic-hydrophilic balance of their terminal groups, with x and y respectively referring to the molar percent of -OCONH-C(18)H(37) tails and -OH for p = 1 and the percent of -OCONH-C(18)H(37) tails and -OCO-C(6)H(4)COOH terminal groups for p = 2.	Phosphorus	26-27	crystallin gamma F, pseudogene	Homo sapiens	215-220
19040196-3	2009	N-vinylazoles-based hexa-coordinated phosphorus compounds have been synthesized for the first time.	Phosphorus	37-47	hexosaminidase subunit alpha	Homo sapiens	20-24
19382473-3	2009	The effect of TSN in different concentrations on calcineurin (CaN) activity was detected by enzyme reaction phosphorus measurement; the CaN mRNA expression was detected by RT-PCR; and the expression of proliferating cell nuclear antigen (PCNA) were observed by immunocytochemical method.	Phosphorus	108-118	translin	Rattus norvegicus	14-17
19022365-8	2009	Mechanistic studies indicate that B[a]P-induced transcriptional activation of MMP-3 is not mediated by AP-1, NF-kappaB.	Phosphorus	38-39	matrix metallopeptidase 3	Rattus norvegicus	78-83
19690405-9	2009	In stepwise multiple regression analyses, age, phosphorus and high-sensitivity C-reactive protein were independent predictors of IL-6 (R(2) = 0.466, p &lt; 0.0001).	Phosphorus	47-57	interleukin 6	Homo sapiens	129-133
19101228-8	2009	In conclusion, African-American patients who were undergoing long-term hemodialysis and with good phosphorus control exhibited a strong inverse correlation between fetuin-A level and CACS that was independent of age.	Phosphorus	98-108	alpha 2-HS glycoprotein	Homo sapiens	164-172
18990420-4	2009	For initial solution pH&gt;6.5, the phosphorus removal through struvite precipitation could be improved by increasing the airflow rate up to 25 L min(-1), or by increasing the initial pH for higher airflow rates.	Phosphorus	36-46	CD59 molecule (CD59 blood group)	Homo sapiens	146-152
19119171-9	2009	Furthermore, AXIN2, a gene that when mutated increases susceptibility to colon cancer, also is associated with CL/P.	Phosphorus	114-115	axin 2	Homo sapiens	13-18
19739148-5	2009	The Lewis acid mediated/catalyzed additions and substitutions, to form sp3-carbon-phosphorus bonds including an asymmetric reaction, are described.	Phosphorus	82-92	Sp3 transcription factor	Homo sapiens	71-74
19290408-1	2009	OBJECTIVE: Hyperparathyroidism is a generalized alteration of calcium, phosphorus and bone metabolism due to an increased secretion of parathyroid hormone (PTH).	Phosphorus	71-81	parathyroid hormone	Homo sapiens	135-154
18854401-1	2009	CONTEXT: Previous studies have suggested a regulatory relationship between serum phosphorus, vitamin D, and fibroblast growth factor 23 (FGF23), a hormone that promotes renal excretion of phosphate.	Phosphorus	81-91	fibroblast growth factor 23	Homo sapiens	108-135
18854401-1	2009	CONTEXT: Previous studies have suggested a regulatory relationship between serum phosphorus, vitamin D, and fibroblast growth factor 23 (FGF23), a hormone that promotes renal excretion of phosphate.	Phosphorus	81-91	fibroblast growth factor 23	Homo sapiens	137-142
19229118-9	2009	CONCLUSIONS: BCL3 appears to influence risk of CL/P through a parent-of-origin effect with excess maternal transmission.	Phosphorus	50-51	BCL3 transcription coactivator	Homo sapiens	13-17
19619031-2	2009	We found that individual phosphorus efflux rate (Q the rate at which excreted and unassimilated P was egested in frass, mgP/day) was related to larval mass (M, mg dry) and environmental temperature (T,K) as Q = e(14.69) M(1.00)e(-0.54/kT), where K is Boltzmann"s constant (8.62 x 10(-5) eV/K, 1 eV = 1.60 x 10-19J).	Phosphorus	25-35	matrix Gla protein	Homo sapiens	120-123
19492925-2	2009	Inositol phosphoglycan P-type (P-IPG), a second messenger of insulin, was reported to negatively correlate with the degree of insulin resistance in non-pregnant diabetic subjects.	Phosphorus	23-24	insulin	Homo sapiens	61-68
19492925-2	2009	Inositol phosphoglycan P-type (P-IPG), a second messenger of insulin, was reported to negatively correlate with the degree of insulin resistance in non-pregnant diabetic subjects.	Phosphorus	23-24	insulin	Homo sapiens	126-133
19155602-2	2009	Studies using (31)-phosphorus magnetic resonance spectroscopy ((31)P-MRS) have shown that phosphocreatine (PCr) and muscle pH (pHi) are significantly decreased in patients with COPD during mild exercise, suggesting the early activation of anaerobic glycolysis in their muscles.	Phosphorus	19-29	glucose-6-phosphate isomerase	Homo sapiens	127-130
19121771-10	2009	Finally, klotho extends life span via several mechanisms, including the reduction of calcitriol synthesis, serum calcium, and phosphorus levels; the induction of insulin resistance; and by increasing the resistance to oxidative stress.	Phosphorus	126-136	klotho	Homo sapiens	9-15
19365139-1	2009	BACKGROUND/AIMS: The calcimimetic cinacalcet (Mimpara/Sensipar) simultaneously lowers parathyroid hormone (PTH), phosphorus (P) and calcium (Ca) levels in patients with secondary hyperparathyroidism.	Phosphorus	107-108	parathyroid hormone	Homo sapiens	86-105
19185780-4	2009	We demonstrate herein that dietary supplementation with a mixture of ALA, ALCAR, GPC, DHA, and PS reduced reactive oxygen species in normal mice by 57% and prevented the increase in reactive oxygen species normally observed in mice lacking murine ApoE when maintained on a vitamin-free, iron-enriched, oxidative-challenge diet.	Phosphorus	95-97	apolipoprotein E	Mus musculus	247-251
19396314-1	2009	The mechanism of regulation of Parathyroid hormone (PTH) is complex, and diverse factors are involved: the fundamental ones are calcium, calcitriol and phosphorus.	Phosphorus	152-162	parathyroid hormone	Homo sapiens	31-50
19396314-1	2009	The mechanism of regulation of Parathyroid hormone (PTH) is complex, and diverse factors are involved: the fundamental ones are calcium, calcitriol and phosphorus.	Phosphorus	152-162	parathyroid hormone	Homo sapiens	52-55
19081473-15	2009	Inhibiting the generation of reactive oxygen species with N-acetylcysteine and of epidermal growth factor receptor with AG1478 inhibited PDK1 activation in response to S-1-P.	Phosphorus	171-173	epidermal growth factor receptor	Mus musculus	82-114
19081473-15	2009	Inhibiting the generation of reactive oxygen species with N-acetylcysteine and of epidermal growth factor receptor with AG1478 inhibited PDK1 activation in response to S-1-P.	Phosphorus	171-173	pyruvate dehydrogenase kinase, isoenzyme 1	Mus musculus	137-141
19002333-0	2008	A mechanistic study of the C-P bond cleavage reaction of 1,2-(PH2)2-C6H4 with nBuLi/Sb(NMe2)3.	Phosphorus	29-30	NME/NM23 nucleoside diphosphate kinase 2	Homo sapiens	87-91
19182340-4	2009	The phosphorus removal depending on the adsorption to sand in the reed-bed filter was, however, the lowest in the extremely shallow SSF although the volumetric removal efficiency was much higher compared with other SSF.	Phosphorus	4-14	peter pan homolog	Homo sapiens	132-135
19182340-4	2009	The phosphorus removal depending on the adsorption to sand in the reed-bed filter was, however, the lowest in the extremely shallow SSF although the volumetric removal efficiency was much higher compared with other SSF.	Phosphorus	4-14	peter pan homolog	Homo sapiens	215-218
19007158-10	2008	Monosubstituted [M(N)(PS)Cl(PPh(3))] species bearing the substitution-inert [M(N)(PS)](+) moieties act as suitable building blocks proposed for the construction of new classes of dissymmetrical nitrido compounds with potential application in the development of essential and target specific (99m)Tc and (188)Re radiopharmaceuticals for imaging and therapy, respectively.	Phosphorus	21-25	protein phosphatase 4 catalytic subunit	Homo sapiens	28-34
18921987-1	2008	Photochemical properties of p-phenylphenacyl derivatives (PP-X) having C-halide, C-S, and C-O bonds in the lowest (T 1) and higher (T n ) triplet excited states were investigated in solution by using single-color and stepwise two-color two-laser flash photolysis techniques.	Phosphorus	14-15	protein phosphatase 4 catalytic subunit	Homo sapiens	58-62
19034326-8	2008	New available vitamin D receptor activators with lower effect in serum phosphorus are available.	Phosphorus	71-81	vitamin D receptor	Homo sapiens	14-32
18929386-6	2008	Energy dispersive X-ray analysis showed the SRB-PP contained elements such as sulphur, iron, calcium and phosphorus.	Phosphorus	105-115	chaperonin containing TCP1 subunit 4	Homo sapiens	44-47
18784085-4	2008	Furthermore, protein S specifically and saturably altered the fluorescence anisotropy of PC/PS-bound active site-labeled LWB-FPR-fXa(i) (Kd = 33 nm) and was photocross-linked to PC/PS-bound LWB-FPR-fXa(i) analog, independently confirming the above results.	Phosphorus	92-94	coagulation factor X	Homo sapiens	129-132
18784085-4	2008	Furthermore, protein S specifically and saturably altered the fluorescence anisotropy of PC/PS-bound active site-labeled LWB-FPR-fXa(i) (Kd = 33 nm) and was photocross-linked to PC/PS-bound LWB-FPR-fXa(i) analog, independently confirming the above results.	Phosphorus	92-94	coagulation factor X	Homo sapiens	198-201
19032923-2	2008	Phosphate, the principal form in which phosphorus is found in the body, is regulated by the complex interplay of the hormones parathyroid hormone (PTH), calcitriol (1,25[OH](2) vitamin D(3)), and fibroblast growth factor 23 (FGF23).	Phosphorus	39-49	parathyroid hormone	Homo sapiens	126-145
19032923-2	2008	Phosphate, the principal form in which phosphorus is found in the body, is regulated by the complex interplay of the hormones parathyroid hormone (PTH), calcitriol (1,25[OH](2) vitamin D(3)), and fibroblast growth factor 23 (FGF23).	Phosphorus	39-49	parathyroid hormone	Homo sapiens	147-150
18975951-10	2008	Mass spectrometric analysis of the aged tabun-inhibited hBChE showed that both the dimethylamine and ethoxy side chains were missing from the phosphorus.	Phosphorus	142-152	butyrylcholinesterase	Homo sapiens	56-61
19138996-7	2008	The formation of B(a)P-induced DNA adducts in MSK-Leuk1 cells was inhibited by 17-AAG, celastrol, and alpha-naphthoflavone, a known AhR antagonist.	Phosphorus	21-22	aryl hydrocarbon receptor	Homo sapiens	132-135
18931726-3	2008	In addition to the P-atom, the MOP class uses the pi-electrons of the naphthyl group, not attached to the phosphorus atom, to form a 4e chelate ligand.	Phosphorus	106-116	opioid receptor mu 1	Homo sapiens	31-34
18485119-9	2008	RESULTS: After OCT-LAR therapy, hypercalcaemia and hypercalciuria normalized in 75% and 62.5% of patients, respectively, and serum phosphorus and renal threshold phosphate significantly increased.	Phosphorus	131-141	plexin A2	Homo sapiens	15-18
18484067-10	2008	In patients with PHPT, we showed a positive correlation between urinary phosphorus excretion and factors VIII, IX, and X (r: 0.572, p&lt;0.01; r: 0.543, p&lt;0.01; r: 0.532, p&lt;0.01, respectively).	Phosphorus	72-82	cytochrome c oxidase subunit 8A	Homo sapiens	105-109
19106513-5	2008	Eleven days following the administration of docetaxel: 30 mg/m2 and nedaplatin: 30 mg/m2, the patient developed TLS (serum creatinine: 8.57 mg/dL, uric acid: 11.0 mg/dL, serum potassium: 6.3 mEq/L, serum phosphorus: 7.18 mg/dL).	Phosphorus	204-214	FUS RNA binding protein	Homo sapiens	112-115
18811154-1	2008	The reaction of [(p-cym)Ru(bpy)Cl](+) (p-cym = eta(6)-p-cymene; bpy = 2,2"-bipyridine) with SCN(-) gives a mixture of the linkage isomers [(p-cym)Ru(bpy)(SCN)](+) and [(p-cym)Ru(bpy)(NCS)](+).	Phosphorus	18-20	endothelin receptor type A	Homo sapiens	47-50
18778104-4	2008	The reaction, which is strongly influenced by steric and stereoelectronic effects, permits in some cases the transformation of alpha-D-Hex p-(1--&gt;4)-D-Hex p into beta-L-Hex p-(1--&gt;4)-D-Hex p disaccharides in a single step with high diastereoselectivity.	Phosphorus	83-84	hematopoietically expressed homeobox	Homo sapiens	135-138
18778104-4	2008	The reaction, which is strongly influenced by steric and stereoelectronic effects, permits in some cases the transformation of alpha-D-Hex p-(1--&gt;4)-D-Hex p into beta-L-Hex p-(1--&gt;4)-D-Hex p disaccharides in a single step with high diastereoselectivity.	Phosphorus	83-84	hematopoietically expressed homeobox	Homo sapiens	154-157
18778104-4	2008	The reaction, which is strongly influenced by steric and stereoelectronic effects, permits in some cases the transformation of alpha-D-Hex p-(1--&gt;4)-D-Hex p into beta-L-Hex p-(1--&gt;4)-D-Hex p disaccharides in a single step with high diastereoselectivity.	Phosphorus	83-84	hematopoietically expressed homeobox	Homo sapiens	154-157
18778104-4	2008	The reaction, which is strongly influenced by steric and stereoelectronic effects, permits in some cases the transformation of alpha-D-Hex p-(1--&gt;4)-D-Hex p into beta-L-Hex p-(1--&gt;4)-D-Hex p disaccharides in a single step with high diastereoselectivity.	Phosphorus	83-84	hematopoietically expressed homeobox	Homo sapiens	154-157
18842502-12	2008	The blood diamine oxidase level before and after gallstone formation in the PS group was 2.6333+/-0.8037 U/ml and 3.3642+/-0.9545 U/ml, respectively (P&lt;0.05).	Phosphorus	76-78	amine oxidase copper containing 1	Homo sapiens	10-25
18583400-3	2008	This binding is decreased in glands from calcium-depleted or experimental chronic kidney failure rats in which PTH mRNA is more stable compared to parathyroid glands from control and phosphorus-depleted rats in which PTH mRNA is less stable.	Phosphorus	183-193	parathyroid hormone	Rattus norvegicus	111-114
18583400-3	2008	This binding is decreased in glands from calcium-depleted or experimental chronic kidney failure rats in which PTH mRNA is more stable compared to parathyroid glands from control and phosphorus-depleted rats in which PTH mRNA is less stable.	Phosphorus	183-193	parathyroid hormone	Rattus norvegicus	217-220
18583400-7	2008	Therefore, calcium or phosphorus depletion, as well as chronic kidney failure, regulate the interaction of KSRP and AUF1 with PTH mRNA and its half-life.	Phosphorus	22-32	KH-type splicing regulatory protein	Rattus norvegicus	107-111
18583400-7	2008	Therefore, calcium or phosphorus depletion, as well as chronic kidney failure, regulate the interaction of KSRP and AUF1 with PTH mRNA and its half-life.	Phosphorus	22-32	heterogeneous nuclear ribonucleoprotein D	Rattus norvegicus	116-120
18583400-7	2008	Therefore, calcium or phosphorus depletion, as well as chronic kidney failure, regulate the interaction of KSRP and AUF1 with PTH mRNA and its half-life.	Phosphorus	22-32	parathyroid hormone	Rattus norvegicus	126-129
18998031-1	2008	OBJECTIVE: Hyperparathyroidism is a generalized alteration of calcium, phosphorus and bone metabolism due to an increased secretion of parathyroid hormone (PTH).	Phosphorus	71-81	parathyroid hormone	Homo sapiens	135-154
18314179-11	2008	PS instillation damaged the urothelium layer of heparin sulfate and syndecan-4 seen in the control animals.	Phosphorus	0-2	syndecan 4	Rattus norvegicus	68-78
18826853-4	2008	RESULTS: With similar phosphorus control, Stx was associated with numerically higher serum calcium levels at most visits.	Phosphorus	22-32	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	Homo sapiens	42-45
18826853-13	2008	CONCLUSION: These findings show that similar phosphorus control with Stx and LC results in higher bone turnover after 1 year and higher bone volume after 2 years with LC.	Phosphorus	45-55	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	Homo sapiens	69-72
18363643-8	2008	The calcification score, decreased expression of alpha-SMA and upregulation of OP were positively correlated with older age, serum calcium, serum phosphorus and calcium x phosphorus product (P &lt; 0.01).	Phosphorus	146-156	secreted phosphoprotein 1	Homo sapiens	79-81
18363643-8	2008	The calcification score, decreased expression of alpha-SMA and upregulation of OP were positively correlated with older age, serum calcium, serum phosphorus and calcium x phosphorus product (P &lt; 0.01).	Phosphorus	171-181	secreted phosphoprotein 1	Homo sapiens	79-81
18357615-3	2008	This study examines the association between markers in RUNX2 and isolated, nonsyndromic CL/P using a case-parent trio design, while considering parent-of-origin effects.	Phosphorus	91-92	RUNX family transcription factor 2	Homo sapiens	55-60
18562187-7	2008	The high bulk and tap densities of PS coupled with their good flowability offer a unique possibility of the starches being used as filler in capsule formulations.	Phosphorus	35-37	nuclear RNA export factor 1	Homo sapiens	18-21
18357615-10	2008	Thus, RUNX2 appears to influence risk of CL/P through a parent-of-origin effect with excess maternal transmission.	Phosphorus	44-45	RUNX family transcription factor 2	Homo sapiens	6-11
18640939-1	2008	PURPOSE: We hypothesized that common polymorphisms in excision repair cross-complementation group 1 (ERCC1), involved in nucleotide excision repair of platinum-induced damage, would be associated with progression-free survival (PFS) and overall survival (OS) in women with optimally resected, stage III epithelial ovarian cancer (EOC) treated with cisplatin and paclitaxel (C+P).	Phosphorus	0-1	ERCC excision repair 1, endonuclease non-catalytic subunit	Homo sapiens	101-106
18752451-0	2008	p.Ala546 &gt; Asp and p.Arg555 &gt; Trp mutations of TGFBI gene and their clinical manifestations in two large Chinese families with granular corneal dystrophy type I.	Phosphorus	0-1	transforming growth factor beta induced	Homo sapiens	53-58
18627046-0	2008	Matrix extracellular phosphoglycoprotein (MEPE) correlates with serum phosphorus prior to and during octreotide treatment and following excisional surgery in hypophosphatemic linear sebaceous nevus syndrome.	Phosphorus	70-80	matrix extracellular phosphoglycoprotein	Homo sapiens	0-40
18627046-0	2008	Matrix extracellular phosphoglycoprotein (MEPE) correlates with serum phosphorus prior to and during octreotide treatment and following excisional surgery in hypophosphatemic linear sebaceous nevus syndrome.	Phosphorus	70-80	matrix extracellular phosphoglycoprotein	Homo sapiens	42-46
18687639-9	2008	Future studies might investigate whether FGF-23 is a potential biomarker that can be used to guide strategies for the management of phosphorus balance in patients with chronic kidney disease.	Phosphorus	132-142	fibroblast growth factor 23	Homo sapiens	41-47
18604532-4	2008	We found that PHO mutants expressing PHO84 and PHO5, even under high-P conditions, could take up phosphorus at twice the rate of the wild-type strain.	Phosphorus	97-107	phosphate transporter PHO84	Saccharomyces cerevisiae S288C	37-42
18604532-4	2008	We found that PHO mutants expressing PHO84 and PHO5, even under high-P conditions, could take up phosphorus at twice the rate of the wild-type strain.	Phosphorus	97-107	acid phosphatase PHO5	Saccharomyces cerevisiae S288C	47-51
18616248-6	2008	Variation of the phosphorus substituents exerts a marked effect on the P...O distance, with electron-withdrawing groups favoring a covalent interaction [P...O 1.97 A for PR3 = PPh(catechyl)] and electron-donating groups favoring a weak interaction [P...O 3.92 A for PR3 = PPh3].	Phosphorus	17-27	proteinase 3	Homo sapiens	170-173
18616248-6	2008	Variation of the phosphorus substituents exerts a marked effect on the P...O distance, with electron-withdrawing groups favoring a covalent interaction [P...O 1.97 A for PR3 = PPh(catechyl)] and electron-donating groups favoring a weak interaction [P...O 3.92 A for PR3 = PPh3].	Phosphorus	17-27	proteinase 3	Homo sapiens	266-269
18616248-6	2008	Variation of the phosphorus substituents exerts a marked effect on the P...O distance, with electron-withdrawing groups favoring a covalent interaction [P...O 1.97 A for PR3 = PPh(catechyl)] and electron-donating groups favoring a weak interaction [P...O 3.92 A for PR3 = PPh3].	Phosphorus	17-27	caveolin 1	Homo sapiens	272-276
18093595-4	2008	RESULTS: Phosphorus levels were significantly associated with age, female gender, diabetes mellitus, hypertension, hypercholesterolemia and fibrinogen levels (p &lt; 0.0001 for each), but not with estimated glomerular filtration rate (eGFR).	Phosphorus	9-19	fibrinogen beta chain	Homo sapiens	140-150
18544081-6	2008	The compound (p-coumaric acid) inhibited alpha-MSH-stimulated cellular melanogenesis more effectively than arbutin or other structurally similar compounds including 3-(4-hydroxyphenyl) propionic acid, cinnamic acid and caffeic acid.	Phosphorus	7-8	pro-opiomelanocortin-alpha	Mus musculus	41-50
18613280-6	2008	In both modes, the dissociations are essentially losses of ROH, and of phosphorus-containing species (HPO2, ROP(OH)2 and ROPO(OH)2), where R=H, C6H5, or CH3OC6H5.	Phosphorus	71-81	growth factor, augmenter of liver regeneration	Homo sapiens	102-106
18591743-14	2008	How does the Fgf23/alpha-Kl system regulate phosphorus homeostasis?How are serum concentrations of Ca(2 + ) and phosphate mutually regulated?	Phosphorus	44-54	fibroblast growth factor 23	Mus musculus	13-18
18591743-14	2008	How does the Fgf23/alpha-Kl system regulate phosphorus homeostasis?How are serum concentrations of Ca(2 + ) and phosphate mutually regulated?	Phosphorus	44-54	klotho	Mus musculus	19-27
18474869-7	2008	B[a]P-7,8-trans-dihydrodiol produced DNA strand breaks in the hOGG1-coupled comet assay as well as 8-oxo-dGuo (as measured by LC-ESI/MRM/MS) and was enhanced by a catechol O-methyl transferase (COMT) inhibitor, suggesting that COMT protects against o-quinone-mediated redox cycling.	Phosphorus	4-5	8-oxoguanine DNA glycosylase	Homo sapiens	62-67
18460448-2	2008	Structure-activity studies show that the p-bromo (DIM-C-pPhBr) and p-fluoro (DIM-C-pPhF) analogs, which exhibit minimal activation of Nur77 and PPARgamma, induce expression of CCAAT/enhancer-binding protein homologous protein (CHOP/GADD153) in colon cancer cells.	Phosphorus	41-42	peroxisome proliferator activated receptor gamma	Homo sapiens	144-153
18460448-2	2008	Structure-activity studies show that the p-bromo (DIM-C-pPhBr) and p-fluoro (DIM-C-pPhF) analogs, which exhibit minimal activation of Nur77 and PPARgamma, induce expression of CCAAT/enhancer-binding protein homologous protein (CHOP/GADD153) in colon cancer cells.	Phosphorus	41-42	DNA damage inducible transcript 3	Homo sapiens	176-225
18460448-2	2008	Structure-activity studies show that the p-bromo (DIM-C-pPhBr) and p-fluoro (DIM-C-pPhF) analogs, which exhibit minimal activation of Nur77 and PPARgamma, induce expression of CCAAT/enhancer-binding protein homologous protein (CHOP/GADD153) in colon cancer cells.	Phosphorus	41-42	DNA damage inducible transcript 3	Homo sapiens	227-231
18460448-2	2008	Structure-activity studies show that the p-bromo (DIM-C-pPhBr) and p-fluoro (DIM-C-pPhF) analogs, which exhibit minimal activation of Nur77 and PPARgamma, induce expression of CCAAT/enhancer-binding protein homologous protein (CHOP/GADD153) in colon cancer cells.	Phosphorus	41-42	DNA damage inducible transcript 3	Homo sapiens	232-239
18417722-4	2008	These changes, however, did not lead to matrix mineralization until the phosphorus concentration of the media was increased; phosphorus stimulated expression of osterix, a second critical osteoblast transcription factor.	Phosphorus	125-135	Sp7 transcription factor	Homo sapiens	161-168
18518338-0	2008	Spin echoes in the charge transport through phosphorus donors in silicon.	Phosphorus	44-54	spindlin 1	Homo sapiens	0-4
18518338-1	2008	The electrical detection of spin echoes via echo tomography is used to observe coherent processes associated with the electrical readout of the spin state of phosphorus donor electrons in silicon near a SiO2 interface.	Phosphorus	158-168	spindlin 1	Homo sapiens	28-32
18518338-1	2008	The electrical detection of spin echoes via echo tomography is used to observe coherent processes associated with the electrical readout of the spin state of phosphorus donor electrons in silicon near a SiO2 interface.	Phosphorus	158-168	spindlin 1	Homo sapiens	144-148
18452350-1	2008	OBJECTIVE: The 677C--&gt;T allele in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene has been implicated in the etiology of nonsyndromic cleft lip and palate (CL/P).	Phosphorus	172-173	methylenetetrahydrofolate reductase	Homo sapiens	41-81
18261183-3	2008	The aim of this study was to evaluate the role of two polymorphisms of the methylenetetrahydrofolate dehydrogenase 1 (MTHFD1) gene, the A1958G and the G401A variants, on the risk of CL/P in the Italian population.	Phosphorus	185-186	methylenetetrahydrofolate dehydrogenase, cyclohydrolase and formyltetrahydrofolate synthetase 1	Homo sapiens	75-116
18261183-3	2008	The aim of this study was to evaluate the role of two polymorphisms of the methylenetetrahydrofolate dehydrogenase 1 (MTHFD1) gene, the A1958G and the G401A variants, on the risk of CL/P in the Italian population.	Phosphorus	185-186	methylenetetrahydrofolate dehydrogenase, cyclohydrolase and formyltetrahydrofolate synthetase 1	Homo sapiens	118-124
18452350-1	2008	OBJECTIVE: The 677C--&gt;T allele in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene has been implicated in the etiology of nonsyndromic cleft lip and palate (CL/P).	Phosphorus	172-173	methylenetetrahydrofolate reductase	Homo sapiens	83-88
18393496-5	2008	In addition, AFM images show the presence inside each object of all the branching points which appear as white harder zones regularly distributed in the less dense and softer PS matrix.	Phosphorus	175-177	afamin	Homo sapiens	13-16
18624196-8	2008	The NAP has positive correlation with c(EPC) and the trend is that the sediment with higher NAP easily desorbs phosphorus to the water, contrarily the sediment with lower NAP easily adsorbs phosphorus.	Phosphorus	111-121	catenin beta like 1	Homo sapiens	4-7
18624196-8	2008	The NAP has positive correlation with c(EPC) and the trend is that the sediment with higher NAP easily desorbs phosphorus to the water, contrarily the sediment with lower NAP easily adsorbs phosphorus.	Phosphorus	111-121	catenin beta like 1	Homo sapiens	92-95
18624196-8	2008	The NAP has positive correlation with c(EPC) and the trend is that the sediment with higher NAP easily desorbs phosphorus to the water, contrarily the sediment with lower NAP easily adsorbs phosphorus.	Phosphorus	111-121	catenin beta like 1	Homo sapiens	92-95
18624196-8	2008	The NAP has positive correlation with c(EPC) and the trend is that the sediment with higher NAP easily desorbs phosphorus to the water, contrarily the sediment with lower NAP easily adsorbs phosphorus.	Phosphorus	190-200	catenin beta like 1	Homo sapiens	4-7
17966119-9	2008	P was the most effective inhibitor of IL-8 release; IL-8 was significantly decreased after exposure to un, tri, tetra and penta but significantly increased after JP-8 exposure compared with controls.	Phosphorus	0-1	C-X-C motif chemokine ligand 8	Homo sapiens	38-42
17943415-7	2008	The HAp spheroids were 5 microm in size with a Ca/P ratio of 1.68 which was close to bone-like apatite (1.67).	Phosphorus	50-51	reticulon 3	Homo sapiens	4-7
18186025-5	2008	The calculated binding constants of the MARCKS(151-175) peptide and a series of related peptides to mixed PC/PS/PIP2 membranes are in satisfactory agreement with in vitro experiments.	Phosphorus	109-111	myristoylated alanine rich protein kinase C substrate	Homo sapiens	40-46
17963236-6	2008	In agreement with experimental data, MD simulations revealed that the catalytic attack distance between the 3-OH of the primer and the phosphorus in complexes containing Be2+ instead of Mg2+ at site A was above 4.5 A.	Phosphorus	135-145	mucin 7, secreted	Homo sapiens	186-189
18331026-6	2008	PhN3 reacts fast, via several intermediates detected below 0 degrees C, to finally release N2 and form a CoI product where one phosphorus has been oxidized, PN(P=NPh)Co.	Phosphorus	127-137	mitochondrially encoded cytochrome c oxidase I	Homo sapiens	105-108
18481421-4	2008	The expressions of JNK and c-jun mRNA were elevated with increased concentration of p,p"-DDE, with significant differences between the control and the case groups (P &lt; 0.05), and they were also significantly upregulated in the beta-BHC and p,p"-DDE + beta-BHC groups in a dose-dependent manner.	Phosphorus	164-165	mitogen-activated protein kinase 8	Rattus norvegicus	19-22
18393760-6	2008	As shown by both methods, APE1 binds with the highest efficiency to DNA substrate containing 5 -sugar phosphate group in the nick/gap, whereas DNA polymerase beta binds to DNA duplex with a mononucleotide gap flanked by the 5 -p group.	Phosphorus	102-103	apurinic/apyrimidinic endodeoxyribonuclease 1	Homo sapiens	26-30
18290647-3	2008	We show that the enzyme MccB, encoded by the MccC7 gene cluster, is responsible for formation of the N-P bond in MccC7.	Phosphorus	103-104	MccB	Escherichia coli	24-28
18006320-1	2008	Stereoselective reductive metabolism of various p-substituted acetophenone derivatives was studied using isolated rat liver 3alpha-hydroxysteroid dehydrogenase (3alpha-HSD).	Phosphorus	48-49	aldo-keto reductase family 1, member C14	Rattus norvegicus	124-159
18039685-1	2008	The stimulatory effects of SH (sulfatide and heparin) and two phospholipids (PI and PS) on autophosphorylation of GSK-3beta and the GSK-3beta-mediated phosphorylation of myelin basic protein (MBP) and two synthetic MBP peptides (M86 and M156) were comparatively examined in vitro.	Phosphorus	84-86	glycogen synthase kinase 3 beta	Homo sapiens	114-123
18039685-1	2008	The stimulatory effects of SH (sulfatide and heparin) and two phospholipids (PI and PS) on autophosphorylation of GSK-3beta and the GSK-3beta-mediated phosphorylation of myelin basic protein (MBP) and two synthetic MBP peptides (M86 and M156) were comparatively examined in vitro.	Phosphorus	84-86	glycogen synthase kinase 3 beta	Homo sapiens	132-141
18094166-4	2008	For example, the Pro-Thr/Ser-Ala-Pro [P(T/S)AP] motif of HIV-1 Gag interacts directly with Tsg101, a component of the endosomal sorting complex required for transport I (ESCRT-I).	Phosphorus	17-18	Pr55(Gag)	Human immunodeficiency virus 1	63-66
18203168-8	2008	We found a reduced risk of CL/P with mothers who carried the CBS C699T variant (rs234706); relative risk was 0.94 with one copy of the T allele (95% CI 0.63-1.4) and 0.50 (95% CI 0.26-0.96) with two copies (P = 0.008).	Phosphorus	30-31	cystathionine beta-synthase	Homo sapiens	61-64
18248363-11	2008	Consistently, electron probe micro-analysis verified sporadic distributions of higher or lower concentrations of calcium and phosphorus in each trabecule of the klotho(-/-)mice.	Phosphorus	125-135	klotho	Mus musculus	161-167
18309349-2	2008	Most clinicians rely on surrogate markers, mainly serum parathyroid hormone and total alkaline phosphatases, in association with serum calcium and phosphorus.	Phosphorus	147-157	parathyroid hormone	Homo sapiens	56-75
18056998-7	2008	Atypical PE and PS species were rapidly remodeled at both sn1 and sn2 position, yielding a molecular species profile similar to that the endogenous PE and PS.	Phosphorus	16-18	solute carrier family 38 member 3	Homo sapiens	58-61
18056998-7	2008	Atypical PE and PS species were rapidly remodeled at both sn1 and sn2 position, yielding a molecular species profile similar to that the endogenous PE and PS.	Phosphorus	16-18	solute carrier family 38 member 5	Homo sapiens	66-69
18006320-1	2008	Stereoselective reductive metabolism of various p-substituted acetophenone derivatives was studied using isolated rat liver 3alpha-hydroxysteroid dehydrogenase (3alpha-HSD).	Phosphorus	48-49	aldo-keto reductase family 1, member C14	Rattus norvegicus	161-171
18046316-5	2008	NaPiIIc colocalizes with both NHERF1 and NHERF3 in brush-border membranes of rats fed either a low- or high-phosphorus diet.	Phosphorus	108-118	solute carrier family 34 member 3	Rattus norvegicus	0-7
18161971-4	2008	The sigma3-P,(NH)2,S- and sigma3-P,N2,S-hybrids react with Pd(OAc)2 and Pd(dba)2, respectively, to afford the same Pd(II)-P,N2,S-hybrid complex, in which the calixphyrin platform is regarded as a dianionic ligand.	Phosphorus	10-12	DBA2	Homo sapiens	72-80
18441928-3	2008	The efficiency of calcite barrier to control phosphorus release from sediments will increase with the increment of Ca2+ concentration of overlying water and barrier thickness.	Phosphorus	45-55	carbonic anhydrase 2	Homo sapiens	115-118
18371709-5	2008	Phosphorus sorption by the resin decreased with increasing Cl(-) concentrations until there was a 100% decrease at 300mgL(-1) Cl(-) when the P concentration of the test solution was 2mgL(-1) and a 92% reduction at 700mgL(-1) Cl(-) when the P concentration of the test solution was 0.2mgL(-1).	Phosphorus	0-10	LLGL scribble cell polarity complex component 1	Homo sapiens	118-124
18211269-3	2008	This is true for enhanced biological phosphorus removal (EBPR), an environmental process that results in the enrichment of the polyphosphate-accumulating organism Accumulibacter spp.	Phosphorus	37-47	histocompatibility minor 13	Homo sapiens	178-181
18238737-14	2008	Early detection of elevated PTH levels with appropriate intervention using active vitamin D therapy, even in the absence of elevated serum phosphorus and reduced serum calcium, is critical.	Phosphorus	139-149	parathyroid hormone	Homo sapiens	28-31
18441928-5	2008	When the Ca2+ concentration of overlying water increased from 1 mmol/L to 5 mmol/L, the phosphorus concentration was reduced by about 36% in the 72nd day.	Phosphorus	88-98	carbonic anhydrase 2	Homo sapiens	9-12
18368510-4	2008	We have reviewed novel data linking fibroblast growth factor 23 (FGF-23) to phosphorus and vitamin D homeostasis.	Phosphorus	76-86	fibroblast growth factor 23	Homo sapiens	36-63
18368510-4	2008	We have reviewed novel data linking fibroblast growth factor 23 (FGF-23) to phosphorus and vitamin D homeostasis.	Phosphorus	76-86	fibroblast growth factor 23	Homo sapiens	65-71
18089450-4	2008	A pivotal role in the inhibition of calcium x phosphorus (Ca x P) precipitation is played by fetuin-A, a circulating plasma glycoprotein.	Phosphorus	46-56	alpha 2-HS glycoprotein	Homo sapiens	93-101
18552353-5	2008	In contrast, when supplied with limiting N and limiting phosphorus (Pi), the nla mutants accumulated abundant anthocyanins and did not show the N limitation-induced early senescence phenotype.	Phosphorus	56-66	SPX (SYG1/Pho81/XPR1) domain-containing protein	Arabidopsis thaliana	77-80
18603618-3	2008	myo-inositol-6-phosphate (InsP(6) or phytic acid) is the predominant form of phosphorus found in seeds and accumulates as a consequence of MIPS action.	Phosphorus	77-87	myo-inositol-1-phosphate synthase 1	Arabidopsis thaliana	139-143
18089450-4	2008	A pivotal role in the inhibition of calcium x phosphorus (Ca x P) precipitation is played by fetuin-A, a circulating plasma glycoprotein.	Phosphorus	63-64	alpha 2-HS glycoprotein	Homo sapiens	93-101
19050760-10	2008	CONCLUSIONS/SIGNIFICANCE: GPRC6A(-/-) mice have a metabolic syndrome characterized by defective osteoblast-mediated bone mineralization, abnormal renal handling of calcium and phosphorus, fatty liver, glucose intolerance and disordered steroidogenesis.	Phosphorus	176-186	G protein-coupled receptor, family C, group 6, member A	Mus musculus	26-32
25983953-4	2008	Recent studies have demonstrated that use of calcimimetics that reduce PTH secretion by increasing the sensitivity of the parathyroid gland calcium-sensing receptor to circulating calcium allow improved control of serum PTH, calcium, phosphorus and calcium-phosphorus product.	Phosphorus	257-267	parathyroid hormone	Homo sapiens	71-74
18000714-0	2008	Phosphorus-31 two-dimensional chemical shift imaging in the myocardium of patients with late onset of Friedreich ataxia.	Phosphorus	0-13	frataxin	Homo sapiens	102-119
19029723-6	2008	Phosphorus balances at a testfield situated in a polder area typical for the central Spreewald region point out that hydrological and consequently hydraulic conditions are the key factors for the phosphorus sink or source behaviour.	Phosphorus	196-206	tribbles pseudokinase 3	Homo sapiens	207-211
18587195-2	2008	These households cause larger phosphorus flows to the Baltic Sea than the 1.8 million people connected to four advanced large-scale treatment plants in the same region.	Phosphorus	30-40	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	61-64
17699549-0	2007	Fibroblast growth factor 23 impairs phosphorus and vitamin D metabolism in vivo and suppresses 25-hydroxyvitamin D-1alpha-hydroxylase expression in vitro.	Phosphorus	36-46	fibroblast growth factor 23	Mus musculus	0-27
18026594-2	2007	Bis(trichlorostannyl) compounds Ru(SnCl3)2(N-N)P2 [N-N = bpy, P = P(OEt)3 3a, PPh(OEt)2 3b; N-N = 1,10-phenanthroline (phen), P = P(OEt)3 4] were also prepared by reacting [RuCl(N-N)P3]BPh4 precursors with SnCl2.2H2O in ethanol.	Phosphorus	47-48	enolase 1	Homo sapiens	78-81
17985877-2	2007	The quantum mechanically derived molecular electrostatic potential minimum (Vmin) of a PR3 ligand at the phosphorus lone pair region provides a direct measure of the total electronic (Eeff) and steric effects (Seff) of the ligand.	Phosphorus	105-115	proteinase 3	Homo sapiens	87-90
17985877-5	2007	The Vmin of the ONIOM-optimized PR3 at the phosphorus lone-pair region thus provides the quantification of the steric effect as Seff = Vmin(PH3)-Vmin(ONIOM_PR3).	Phosphorus	43-53	proteinase 3	Homo sapiens	32-35
17985877-5	2007	The Vmin of the ONIOM-optimized PR3 at the phosphorus lone-pair region thus provides the quantification of the steric effect as Seff = Vmin(PH3)-Vmin(ONIOM_PR3).	Phosphorus	43-53	proteinase 3	Homo sapiens	156-159
17525976-3	2007	Reports have shown an association of a serotonin-2A receptor (HTR2A) gene T102C polymorphism with AD + P and with depression during AD.	Phosphorus	103-104	5-hydroxytryptamine receptor 2A	Homo sapiens	39-60
17525976-3	2007	Reports have shown an association of a serotonin-2A receptor (HTR2A) gene T102C polymorphism with AD + P and with depression during AD.	Phosphorus	103-104	5-hydroxytryptamine receptor 2A	Homo sapiens	62-67
17937438-8	2007	Our data suggest that an unidentified CL/P gene, or a non-coding IRF6 regulatory element in this linkage interval may have caused CL/P in this family.	Phosphorus	133-134	interferon regulatory factor 6	Homo sapiens	65-69
17715259-0	2007	Elevated phosphorus modulates vitamin D receptor-mediated gene expression in human vascular smooth muscle cells.	Phosphorus	9-19	vitamin D receptor	Homo sapiens	30-48
19029723-3	2008	With its dense network of impounded waterways and a forced tendency of sedimentation of soluble reactive phosphorus adsorbed to large amounts of FeOH/FeOOH available from mining water and groundwater discharges the 320 km2 region is favoured to accumulate large amounts of total phosphorus (TR) and thus act as an effective phosphorus sink.	Phosphorus	105-115	tribbles pseudokinase 3	Homo sapiens	335-339
19029723-3	2008	With its dense network of impounded waterways and a forced tendency of sedimentation of soluble reactive phosphorus adsorbed to large amounts of FeOH/FeOOH available from mining water and groundwater discharges the 320 km2 region is favoured to accumulate large amounts of total phosphorus (TR) and thus act as an effective phosphorus sink.	Phosphorus	279-289	tribbles pseudokinase 3	Homo sapiens	335-339
18031033-4	2007	The two PR3 (R = Ph, Me) or DMSO ligands are trans to each other with P/S-Os-P/S angles of approximately 177 degrees .	Phosphorus	17-18	proteinase 3	Homo sapiens	8-11
17726161-4	2007	T cells from patients with APS responded to beta(2)GPI/PS in the presence of immunoglobulin G (IgG) anti-beta(2)GPI antibodies derived from APS plasma, and this response was completely inhibited either by the depletion of monocytes or by the addition of anti-FcgammaRI antibody.	Phosphorus	28-30	apolipoprotein H	Homo sapiens	44-54
17726161-4	2007	T cells from patients with APS responded to beta(2)GPI/PS in the presence of immunoglobulin G (IgG) anti-beta(2)GPI antibodies derived from APS plasma, and this response was completely inhibited either by the depletion of monocytes or by the addition of anti-FcgammaRI antibody.	Phosphorus	28-30	apolipoprotein H	Homo sapiens	105-115
17889392-10	2007	Furthermore, the knockout of PA2384 also resulted in an altered expression of genes involved in electron transfer, central metabolism, phosphorus starvation and translation.	Phosphorus	135-145	hypothetical protein	Pseudomonas aeruginosa PAO1	29-35
17948256-6	2007	Elemental analysis of calcium, phosphorus, and iron revealed changes in -/- incisors consistent with GnRH-1 affecting movement of minerals into the dental matrix.	Phosphorus	31-41	gonadotropin releasing hormone 1	Mus musculus	101-107
17662338-1	2007	In most studies on phosphorus- and glycogen-accumulating organisms (PAO and GAO), pH was controlled constantly throughout the entire anaerobic and aerobic periods, and acetic acid was used as the carbon source.	Phosphorus	19-29	spermine oxidase	Homo sapiens	68-71
17942777-3	2007	In normal animals and humans, factors such as phosphorus and vitamin D modify the basal parathyroid hormone level and the maximal parathyroid hormone response to hypocalcemia.	Phosphorus	46-56	parathyroid hormone	Homo sapiens	88-107
17942777-3	2007	In normal animals and humans, factors such as phosphorus and vitamin D modify the basal parathyroid hormone level and the maximal parathyroid hormone response to hypocalcemia.	Phosphorus	46-56	parathyroid hormone	Homo sapiens	130-149
18047119-1	2007	The present research describes synthesis of highly sinterable, nano-sized hydroxyapatite (HAp) powders using a wet chemical route with recycled eggshell and phosphoric acid as calcium and phosphorous sources.	Phosphorus	188-199	reticulon 3	Homo sapiens	90-93
18299713-0	2007	High-phosphorus diet induces osteopontin expression of renal tubules in rats.	Phosphorus	5-15	secreted phosphoprotein 1	Rattus norvegicus	29-40
18299713-3	2007	Based on these observations, we speculated that the osteopontin play an important role in the formation of the Ca deposits induced by high-P diet.	Phosphorus	139-140	secreted phosphoprotein 1	Rattus norvegicus	52-63
18299713-9	2007	These results suggest that high-P diet induces osteopontin expression in the renal tubules.	Phosphorus	32-33	secreted phosphoprotein 1	Rattus norvegicus	47-58
18299713-10	2007	Moreover, our results suggest that increase in osteopontin expression in the renal tubules is presumably involved in the formation of Ca deposits induced by high-P diet.	Phosphorus	162-163	secreted phosphoprotein 1	Rattus norvegicus	47-58
18047119-6	2007	The Ca/P ratio for stoichiometric composition of HAp was controlled by adjustment of the mixing ratio.	Phosphorus	7-8	reticulon 3	Homo sapiens	49-52
17711412-3	2007	Molecular genetic manipulation of AVP1 expression in Arabidopsis, tomato and rice results in plants that outperform controls when challenged with limited phosphorus.	Phosphorus	154-164	Inorganic H pyrophosphatase family protein	Arabidopsis thaliana	34-38
17925876-2	2007	A new eco-evolutionary hypothesis (the "Growth Rate Hypothesis", GRH) proposes that tumors have elevated phosphorus (P) demands due to increased allocation to P-rich nucleic acids, especially ribosomal RNA, to meet the protein synthesis demands of accelerated proliferation.	Phosphorus	105-115	gonadotropin releasing hormone 1	Homo sapiens	65-68
17914842-0	2007	Mechanism of SN2 disulfide bond cleavage by phosphorus nucleophiles.	Phosphorus	44-54	solute carrier family 38 member 5	Homo sapiens	13-16
17892282-7	2007	Evidence is presented for greater M-P sigma bonding effects on coordination of the PC3 phosphorus of P(CH2NR)3P (R = Me, Ph) than are present in PMe3 analogues of group 6B metal carbonyls.	Phosphorus	87-97	chromobox 8	Homo sapiens	83-86
17524547-11	2007	Furthermore, Anc2-Cyc1(His6)p may be an useful molecular tool to investigate in vivo interactions between components of the respiratory chain complexes such as COX and the proteins implicated in ATP biogenesis, such as the ATP/ADP carrier.	Phosphorus	27-29	ADP/ATP carrier protein PET9	Saccharomyces cerevisiae S288C	13-17
17976086-7	2007	The intact PTH concentration in patients with normal phosphorus and calcium concentration was in the reference range (60-180 pg/ml) in about 50% of the patients, high (&gt;180 pg/ml) in 35%, low (&lt;60 pg/ml) in 10% during the study periods.	Phosphorus	53-63	parathyroid hormone	Homo sapiens	11-14
17851519-3	2007	In 1946, Wheeler speculated that two Ps atoms may combine to form the di-positronium molecule (Ps2), with a binding energy of 0.4 eV.	Phosphorus	37-39	taste 2 receptor member 64 pseudogene	Homo sapiens	95-98
17785425-5	2007	p-nitrophenyl phosphonate-conjugated fluorochromes, including the very bright and stable quantum dots, bound efficiently and specifically to LFA-1/cutinase.	Phosphorus	0-2	integrin subunit alpha L	Homo sapiens	141-155
17598127-4	2007	Since phosphorus is one of the essential macronutrients for plants, we examined its role in the regulation of the expression of 14-3-3 isoforms belonging to epsilon (GRF9, GRF10, GRF11, GRF13) and non-epsilon (GRF1, GRF3, GRF6, GRF8) groups.	Phosphorus	6-16	general regulatory factor 9	Arabidopsis thaliana	166-170
17598127-4	2007	Since phosphorus is one of the essential macronutrients for plants, we examined its role in the regulation of the expression of 14-3-3 isoforms belonging to epsilon (GRF9, GRF10, GRF11, GRF13) and non-epsilon (GRF1, GRF3, GRF6, GRF8) groups.	Phosphorus	6-16	general regulatory factor 11	Arabidopsis thaliana	179-184
17524547-11	2007	Furthermore, Anc2-Cyc1(His6)p may be an useful molecular tool to investigate in vivo interactions between components of the respiratory chain complexes such as COX and the proteins implicated in ATP biogenesis, such as the ATP/ADP carrier.	Phosphorus	27-29	cytochrome c isoform 1	Saccharomyces cerevisiae S288C	18-22
17826950-5	2007	In contrast, beta(2)GPI complexes with oxLDL or PS-liposomes were transported into the lysosome.	Phosphorus	48-50	apolipoprotein H	Mus musculus	13-23
17547401-4	2007	Nonsymmetrically substituted derivatives of 1,2-diphosphonium cations enable the direct observation of 1J(PAPB) coupling constants for two tetracoordinate phosphorus centers.	Phosphorus	155-165	GLI family zinc finger 3	Homo sapiens	106-110
17111159-10	2007	Our results indicate that intensive nutritional therapy and phosphorus control aiming to keep PTH within the normal range prevents further loss of HtSDS in short children on dialysis.	Phosphorus	60-70	parathyroid hormone	Homo sapiens	94-97
17655364-1	2007	The reaction of alkynes 1 with CO and pyridin-2-ylmethylamine (2) in the presence of Rh4(CO)12/P(OEt)3 results in the incorporation of two molecules of CO leading to maleimide derivatives 3.	Phosphorus	95-96	Rh blood group D antigen	Homo sapiens	85-88
17918144-1	2007	Even though there are some functional similarities between the aged kidney and the chronically damaged one, such as the reduction in glomerular filtration rate and in the sodium-water reabsorption capability, there are many physiological differences between these two groups, as is the case of erythropoietin, urea, potassium, calcium, phosphorus and magnesium renal handling.	Phosphorus	336-346	erythropoietin	Homo sapiens	294-308
17713618-4	2007	The observed ranking of binding interaction of the tested EDCs with ER-beta is diethylstilbestrol (DES) &gt; 17-beta-estradiol &gt; 17-alpha-estradiol &gt; 2-OH-estrone &gt; bisphenol A &gt; p,p"-dichlorodiphenyldichloroethylene (p,p"-DDE) with measurements exhibiting intra-day RSDs of about 3%.	Phosphorus	137-138	estrogen receptor 2	Homo sapiens	68-75
17893770-5	2007	The reaction of (Me(2)N)(3)P with IBr forms [(Me(2)N)(3)PBr]I, which when recrystallised from chlorinated solvents forms [(Me(2)N)(3)PCl(0.5)Br(0.5)]I.	Phosphorus	26-28	translocator protein	Homo sapiens	56-59
17585033-0	2007	Supplemental Escherichia coli phytase and strontium enhance bone strength of young pigs fed a phosphorus-adequate diet.	Phosphorus	94-104	putative glycerophosphoryl diester phosphodiesterase	Glycine max	30-37
17520123-1	2007	The Hint-1 hydrolase assisted cleavage of the P-N bond in adenosine-5"-O-[N-(tryptophanylamide)]phosphoramidothioate proceeds with retention of configuration at the phosphorus atom which is consistent with the formation of a covalent enzyme-substrate complex.	Phosphorus	165-175	histidine triad nucleotide binding protein 1	Homo sapiens	4-10
17674741-2	2007	Results show that nitrogen and phosphorus surplus in China are 640 x 10(4) t and 98 x 10(4) t respectively, and nitrogen and phosphorus surplus intensity in China are 16.56 kg/hm2 and 2.53 kg/hm2 respectively.	Phosphorus	125-135	cholinergic receptor muscarinic 2	Homo sapiens	176-185
17433523-5	2007	While alpha-naphtoflavone (alpha-NF) and ellipticine suppressed B[a]P-induced CYP1A1 activation as well as apoptosis, the 2,3",4,5"-tetramethoxystilbene (TMS) and pyrene, known CYP1B1 inhibitors, failed to inhibit apoptosis.	Phosphorus	68-69	cytochrome P450, family 1, subfamily a, polypeptide 1	Mus musculus	78-84
26627440-4	2007	A very low rotational barrier of 0.17 kcal/mol (BP86) and 0.64 kcal/mol (MP2) was calculated for the arene rotation in [(eta(6)-C6H6)Ru(en)(Cl)](+) (3) allowing complexes containing arenes with bulky side chains like p-cymene to minimize steric interactions with, e.g., DNA by simple arene rotation.	Phosphorus	164-165	tryptase pseudogene 1	Homo sapiens	73-76
17502528-6	2007	In multivariable analyses and adjusting for established risk factors and additionally for glomerular filtration rate and for hemoglobin, serum albumin, proteinuria, and C-reactive protein levels, a higher level of serum phosphorus was associated with an increased CVD risk in a continuous fashion (adjusted hazard ratio per increment of milligrams per deciliter, 1.31; 95% confidence interval, 1.05-1.63; P=.02; P value for trend across quartiles = .004).	Phosphorus	220-230	C-reactive protein	Homo sapiens	169-187
17384007-4	2007	We observed a strong positive association between L:P ratio and blood lactate in non-PDH CLA, whereas this association was weak in PDH-D CLA.	Phosphorus	52-53	pyruvate dehydrogenase phosphatase catalytic subunit 1	Homo sapiens	85-88
17471006-7	2007	Under these circumstances, the regulation of PTH is limited by the range of target values for serum phosphorus and calcium.	Phosphorus	100-110	parathyroid hormone	Homo sapiens	45-48
17461764-9	2007	An extremely low concentration of cisplatin in addition to Ps-S-Oligos further up-regulated p53 activity, provoking massive apoptotic induction.	Phosphorus	59-63	tumor protein p53	Homo sapiens	92-95
17506310-0	2007	[Regulation of phosphorus-vitamin D metabolism by FGF23].	Phosphorus	15-25	fibroblast growth factor 23	Homo sapiens	50-55
17536604-10	2007	Compared to the PS group, protein levels of SERCA2 significantly decreased and NCX1 increased in the CHF-C group.	Phosphorus	16-18	ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2	Rattus norvegicus	44-50
17910410-16	2007	Pre-dialysis age (p &lt; 0.05), peritonitis rate (p &lt; 0.05), and serum phosphorus at the end of follow-up (p &lt; 0.05) were associated with technique failure in univariate analysis, while in multivariate analysis, only pre-dialysis age (RR 1.07, p = 0.001) and peritonitis rate (RR 481, p &lt; 0.0001) were technique failure predictors.	Phosphorus	74-84	ribonucleotide reductase catalytic subunit M1	Homo sapiens	241-245
16962227-9	2007	Final docked energies predicted correctly the relative order of the inhibition potency of compounds (except in the case of Py-4-CH(3)) as well as the most probable orientation of the best reactivator, Py-4-Br, which can result in an attack on the phosphorus atom of the tabun-phosphorylated human AChE.	Phosphorus	247-257	acetylcholinesterase (Cartwright blood group)	Homo sapiens	297-301
17346756-0	2007	Seasonal and tidal variability of phosphorus along a salinity gradient in the heavily polluted estuarine system of Santos/Sao Vicente - Sao Paulo, Brazil.	Phosphorus	34-44	solute carrier family 4 member 1 (Diego blood group)	Homo sapiens	122-125
17699419-12	2007	Severe periodontitis was associated with low serum albumin (odds ratio 8.20; 95% confidence interval 1.61 to 41.82; P = 0.01) compared with individuals without severe periodontitis disease after adjustment for age, gender, race, diabetes, hypertension, body mass index, smoking, study site, total cholesterol, serum calcium, serum phosphorus, and normalized protein catabolic rate.	Phosphorus	331-341	albumin	Homo sapiens	51-58
17355433-6	2007	Under other stress conditions including low phosphorus nutrient, drought and high temperature, the nla mutant did not show this early senescence phenotype, but closely resembled the wild type in growth and development.	Phosphorus	44-54	SPX (SYG1/Pho81/XPR1) domain-containing protein	Arabidopsis thaliana	99-102
17258455-0	2007	Discovery of novel phosphorus-containing steroids as selective glucocorticoid receptor antagonist.	Phosphorus	19-29	nuclear receptor subfamily 3, group C, member 1	Rattus norvegicus	63-86
17258455-2	2007	For glucocorticoid receptor (GR) program, we sought an unexplored, synthetically accessible phosphorus-containing steroidal mimetic of mifepristone, suitable for parallel synthesis of analogues.	Phosphorus	92-102	nuclear receptor subfamily 3, group C, member 1	Rattus norvegicus	4-27
17258455-2	2007	For glucocorticoid receptor (GR) program, we sought an unexplored, synthetically accessible phosphorus-containing steroidal mimetic of mifepristone, suitable for parallel synthesis of analogues.	Phosphorus	92-102	nuclear receptor subfamily 3, group C, member 1	Rattus norvegicus	29-31
17298091-5	2007	Through the nucleophilic attack, the oximate first binds to the sarin-AChE adduct to form a relatively stable phosphorus complex.	Phosphorus	110-120	acetylcholinesterase (Cartwright blood group)	Homo sapiens	70-74
17289767-9	2007	Wound fluid was harvested every hour for a total follow up of 3 h. RESULTS: P-novispirin G10 demonstrated broad-spectrum antimicrobial activity with moderate haemolytic and cytotoxic activities compared with protegrin-1.	Phosphorus	76-77	BUD31 homolog	Homo sapiens	89-92
17541996-6	2007	The high electrophilicity of the phosphorus center in [Et4C4P]+, combined with strong pi-pi interactions between the ring and the incoming and outgoing phenyl groups of PPh3, favours the SN2-type over the SN1-type pathway in [Et4C4P(PPh3)]+.	Phosphorus	33-43	protein phosphatase 4 catalytic subunit	Homo sapiens	169-173
17352436-2	2007	Their structures and the influence of their ligands (phosphorus and nitrogen atoms directly bonded to the Ga(8) moieties) are discussed on the basis of DFT calculations, providing an insight into a probable mechanism for insertion reactions between GaX and GaX(3) species that lead to a reaction cascade via halides like Ga(2)X(4) and Ga(5)X(7) to Ga(8)X(10) and Ga(8)X(12) (2-), respectively.	Phosphorus	53-63	mesenchyme homeobox 2	Homo sapiens	249-252
17072757-1	2007	In this study, we examined the cellular content of the insulin receptor substrate (IRS)-1, the levels of phosphorylated tyrosine (pY) and serine (pS) residues in IRS-1, and the glucose transporters GLUT-1 and GLUT-4 in primary cultured rat skeletal myocytes treated with the glucocorticoid, dexamethasone.	Phosphorus	146-148	insulin receptor substrate 1	Rattus norvegicus	162-167
17071095-2	2007	One means of reducing PS-complex activity entails decreasing the levels of one or more of its components, such as nicastrin, which is fundamental to its assembly.	Phosphorus	22-24	nicastrin	Mus musculus	114-123
17209608-4	2007	The morphologies seen in PS-rich blends (networklike rings) are consistent with a recent study of a nonamphiphilic polyhedral oligomeric silsesquioxane (POSS), octaisobutyl-POSS, blended with amphiphilic poly(dimethylsiloxane), suggesting that the nonamphiphilic PS aggregates at the A/W interface produce domains with dipole densities that differ from that of pure PCL.	Phosphorus	25-27	PHD finger protein 1	Homo sapiens	366-369
17215179-2	2007	The ingestion of 4% phytosterols-containing diacylglycerol (PS/DAG) decreases serum total cholesterol and low density lipoprotein cholesterol (LDL-C) concentrations in adults.	Phosphorus	60-62	component of oligomeric golgi complex 2	Homo sapiens	143-148
17541996-6	2007	The high electrophilicity of the phosphorus center in [Et4C4P]+, combined with strong pi-pi interactions between the ring and the incoming and outgoing phenyl groups of PPh3, favours the SN2-type over the SN1-type pathway in [Et4C4P(PPh3)]+.	Phosphorus	33-43	protein phosphatase 4 catalytic subunit	Homo sapiens	233-237
17338295-6	2006	XPS spectra of HAp treated with 4-MET also disclosed the surface to be enriched in calcium and decreased in phosphorus, indicating that phosphorus was extracted at a relatively higher rate than calcium.	Phosphorus	108-118	reticulon 3	Homo sapiens	15-18
17994578-2	2007	We compared liver expression of the VKORC1 gene, which encodes a protein of the vitamin K 2,3-epoxide reductase complex, the NQO1 gene, which encodes a NAD(P)H quinone dehydrogenase and the Calumenin gene between bromadiolone-resistant and anticoagulant-susceptible rats upon saline and bromadiolone administration.	Phosphorus	155-158	NAD(P)H quinone dehydrogenase 1	Rattus norvegicus	125-129
17654321-1	2007	BACKGROUND: In hemodialysis patients, the relationships between serum PTH and phosphorus levels and mortality are debated because both high and low turnover bone diseases increase the risk of vascular calcifications.	Phosphorus	78-88	parathyroid hormone	Homo sapiens	70-73
17425085-9	2007	When flushed with tap water, nitrogen and phosphorus were retained by the vegetated mesocosms, but leached from the non-vegetated mesocosms.	Phosphorus	42-52	nuclear RNA export factor 1	Homo sapiens	18-21
17128984-7	2006	Overall, these findings suggest that PKCalpha undergoes a isozyme-specific interaction with membrane-bound Cdc42 to form a PKCalpha-Cdc42 complex, which possesses a membrane-binding affinity that is reduced relative to that of the individual components due to competition between Cdc42 and PS/Ca2+ for binding to PKCalpha.	Phosphorus	290-292	protein kinase C alpha	Homo sapiens	37-45
17128984-7	2006	Overall, these findings suggest that PKCalpha undergoes a isozyme-specific interaction with membrane-bound Cdc42 to form a PKCalpha-Cdc42 complex, which possesses a membrane-binding affinity that is reduced relative to that of the individual components due to competition between Cdc42 and PS/Ca2+ for binding to PKCalpha.	Phosphorus	290-292	cell division cycle 42	Homo sapiens	107-112
17128984-7	2006	Overall, these findings suggest that PKCalpha undergoes a isozyme-specific interaction with membrane-bound Cdc42 to form a PKCalpha-Cdc42 complex, which possesses a membrane-binding affinity that is reduced relative to that of the individual components due to competition between Cdc42 and PS/Ca2+ for binding to PKCalpha.	Phosphorus	290-292	protein kinase C alpha	Homo sapiens	123-131
17128984-7	2006	Overall, these findings suggest that PKCalpha undergoes a isozyme-specific interaction with membrane-bound Cdc42 to form a PKCalpha-Cdc42 complex, which possesses a membrane-binding affinity that is reduced relative to that of the individual components due to competition between Cdc42 and PS/Ca2+ for binding to PKCalpha.	Phosphorus	290-292	cell division cycle 42	Homo sapiens	132-137
17128984-7	2006	Overall, these findings suggest that PKCalpha undergoes a isozyme-specific interaction with membrane-bound Cdc42 to form a PKCalpha-Cdc42 complex, which possesses a membrane-binding affinity that is reduced relative to that of the individual components due to competition between Cdc42 and PS/Ca2+ for binding to PKCalpha.	Phosphorus	290-292	cell division cycle 42	Homo sapiens	132-137
17128984-7	2006	Overall, these findings suggest that PKCalpha undergoes a isozyme-specific interaction with membrane-bound Cdc42 to form a PKCalpha-Cdc42 complex, which possesses a membrane-binding affinity that is reduced relative to that of the individual components due to competition between Cdc42 and PS/Ca2+ for binding to PKCalpha.	Phosphorus	290-292	protein kinase C alpha	Homo sapiens	123-131
17117074-3	2006	One month later, she received a second intravenous phosphorus-32 treatment of 3.5 mCi.	Phosphorus	51-61	multiciliate differentiation and DNA synthesis associated cell cycle protein	Mus musculus	82-85
16924500-3	2006	Previous studies have shown that GIT1 expression is regulated by inorganic phosphate (P(i)) availability through the transcription factors Pho2p and Pho4p.	Phosphorus	0-1	Git1p	Saccharomyces cerevisiae S288C	33-37
16924500-3	2006	Previous studies have shown that GIT1 expression is regulated by inorganic phosphate (P(i)) availability through the transcription factors Pho2p and Pho4p.	Phosphorus	0-1	Pho2p	Saccharomyces cerevisiae S288C	139-144
16924500-3	2006	Previous studies have shown that GIT1 expression is regulated by inorganic phosphate (P(i)) availability through the transcription factors Pho2p and Pho4p.	Phosphorus	0-1	phosphate-sensing transcription factor PHO4	Saccharomyces cerevisiae S288C	149-154
17338295-6	2006	XPS spectra of HAp treated with 4-MET also disclosed the surface to be enriched in calcium and decreased in phosphorus, indicating that phosphorus was extracted at a relatively higher rate than calcium.	Phosphorus	136-146	reticulon 3	Homo sapiens	15-18
17044716-2	2006	In the phosphorus(III) systems, the P-diphenyl substituted compounds are observed as only one isomer, shown by NMR spectroscopy to be the E(syn)-(alpha) configuration.	Phosphorus	7-17	synemin	Homo sapiens	140-143
17123251-9	2006	A slight but significant correlation was detected between i-Ca and serum phosphorus concentration (r = -.284; P = .022), as well as between serum t-Ca and i-Ca concentration (r = .497; P &lt; .0001).	Phosphorus	73-83	calcium voltage-gated channel subunit alpha1 C	Canis lupus familiaris	58-62
17088965-0	2006	A series of complexes of the phosphorus-based TTF ligand o-P2 with the metal ions Fe(II), Co(II), Ni(II), Pd(II), Pt(II), and Ag(I).	Phosphorus	29-39	ras homolog family member H	Homo sapiens	46-49
17088965-0	2006	A series of complexes of the phosphorus-based TTF ligand o-P2 with the metal ions Fe(II), Co(II), Ni(II), Pd(II), Pt(II), and Ag(I).	Phosphorus	29-39	bone morphogenetic protein 8b	Homo sapiens	57-61
17010989-6	2006	Replacement of serines-23/24 (PKA sites) with alanine prevented cross-phosphorylation of these sites, reduced (32)P-incorporation into cTnI by half and resulted in myofilament Ca(2+) sensitization rather than desensitization in response to PKC-betaII.	Phosphorus	30-31	troponin I, cardiac 3	Mus musculus	135-139
16934845-0	2006	Novel phosphorus-containing 17beta-side chain mifepristone analogues as progesterone receptor antagonists.	Phosphorus	6-16	progesterone receptor	Rattus norvegicus	72-93
16934845-1	2006	A novel series of steroidal compounds were designed and synthesized with various phosphorus-containing groups on the 17beta-side chain as progesterone receptor antagonists.	Phosphorus	81-91	progesterone receptor	Rattus norvegicus	138-159
17167206-0	2006	[Adaptive changes in activity of tonoplast H(+)-ATPase from the roots of tomato seedlings under phosphorus starvation].	Phosphorus	96-106	plasma membrane ATPase 1	Solanum lycopersicum	43-54
17167206-4	2006	The tonoplast H(+)-ATPase activity in the roots of tomato seedlings increased under phosphorus starvation and reached maximum values under the starvation for 7 days, while the activity of the control changed little.	Phosphorus	84-94	plasma membrane ATPase 1	Solanum lycopersicum	14-25
17167206-5	2006	Kinetic analysis of tonoplast H(+)-ATPase showed that phosphorus starvation significantly lowered the K(m) value, but had no significant effect on the V(max) value of the enzyme.	Phosphorus	54-64	plasma membrane ATPase 1	Solanum lycopersicum	30-41
16904338-6	2006	Path B mostly proceeds via phenyl migration from the triphenylphosphine ligand to the palladium center by cleavage of the phosphorus-phenyl bond to give a palladium-phenyl intermediate, and subsequent reductive elimination of the intermediate to yield a product ion [PPh4]+.	Phosphorus	122-132	potassium two pore domain channel subfamily K member 3	Homo sapiens	267-271
17044716-2	2006	In the phosphorus(III) systems, the P-diphenyl substituted compounds are observed as only one isomer, shown by NMR spectroscopy to be the E(syn)-(alpha) configuration.	Phosphorus	36-37	synemin	Homo sapiens	140-143
16806946-0	2006	New progesterone receptor antagonists: phosphorus-containing 11beta-aryl-substituted steroids.	Phosphorus	39-49	progesterone receptor	Homo sapiens	4-25
16945340-9	2006	This new analog is one of the most potent non-phosphorus-containing Grb2-SH2 antagonists reported to date.	Phosphorus	46-56	growth factor receptor bound protein 2	Homo sapiens	68-72
16458958-1	2006	Cystic endometrial hyperplasia-pyometra (CEH-P) complex is a progesterone-dependent disease that requires medical treatment in bitches intended for breeding.	Phosphorus	45-46	epoxide hydrolase 2	Homo sapiens	41-44
16980611-5	2006	When the P-TEFb-dependent HEXIM1 expression markedly increased as the treatment continued, the abundant HEXIM1 pushed the P-TEFb equilibrium back toward the 7SK/HEXIM1-bound state.	Phosphorus	9-10	HEXIM P-TEFb complex subunit 1	Homo sapiens	26-32
16980611-5	2006	When the P-TEFb-dependent HEXIM1 expression markedly increased as the treatment continued, the abundant HEXIM1 pushed the P-TEFb equilibrium back toward the 7SK/HEXIM1-bound state.	Phosphorus	9-10	HEXIM P-TEFb complex subunit 1	Homo sapiens	104-110
16980611-5	2006	When the P-TEFb-dependent HEXIM1 expression markedly increased as the treatment continued, the abundant HEXIM1 pushed the P-TEFb equilibrium back toward the 7SK/HEXIM1-bound state.	Phosphorus	9-10	HEXIM P-TEFb complex subunit 1	Homo sapiens	104-110
16891548-8	2006	Disruption of both PLD zeta1 and PLD zeta2 function resulted in a smaller decrease in phosphatidylcholine and a smaller increase in digalactosyldiacylglycerol in phosphorus-starved roots.	Phosphorus	162-172	phospholipase D P1	Arabidopsis thaliana	19-42
17014551-7	2006	RESULTS: There was a significant direct or positive correlation at the 0.01 levels between dry weight, age, intact parathyroid hormone level (PTH), and serum phosphorus and EPO dose.	Phosphorus	158-168	erythropoietin	Homo sapiens	173-176
17014551-9	2006	There was significant colinearity between serum phosphorus and PTH but serum phosphorus showed a more significant correlation with EPO overall.	Phosphorus	77-87	erythropoietin	Homo sapiens	131-134
17014551-10	2006	Stepwise regression analysis for covariance revealed that phosphorus remained significantly correlated with EPO resistance after the removal of the effect of PTH while PTH lost its significance after the effect of phosphorus was removed.	Phosphorus	58-68	erythropoietin	Homo sapiens	108-111
16956297-3	2006	Bisphosphonates, pyrophosphate analogues in which the oxygen bridge between the two phosphorus atoms has been replaced by a carbon substituted with different side chains, are able to inhibit the FPPS enzyme.	Phosphorus	84-94	farnesyl diphosphate synthase	Homo sapiens	195-199
31627640-7	2006	Significant changes were observed in biochemical parameters during the performed therapy: the decrease in the levels of total cholesterol and low-density lipoproteins, which suggests the antiatherogenic effect of GH therapy on lipid metabolism; a significant increase in the level of calcium and phosphorus, the activity of alkaline phosphatase, which is 3.5 times greater than the normal values, which indicate the acceleration of bone metabolic processes.	Phosphorus	296-306	growth hormone 1	Homo sapiens	213-215
16925861-1	2006	Ca and P are both essential nutrients for bone and are known to affect one of the most important regulators of bone metabolism, parathyroid hormone (PTH).	Phosphorus	7-8	parathyroid hormone	Homo sapiens	128-147
16866508-1	2006	The acyclic tetraphosphorus dication [Ph3P-PPh-PPh-PPh3]2+ has been formed by the reductive coupling of [Ph3P-PPhCl]+, providing a new synthetic method for the systematic development of catena-phosphorus cations.	Phosphorus	17-27	enolase 1	Homo sapiens	43-46
16866508-1	2006	The acyclic tetraphosphorus dication [Ph3P-PPh-PPh-PPh3]2+ has been formed by the reductive coupling of [Ph3P-PPhCl]+, providing a new synthetic method for the systematic development of catena-phosphorus cations.	Phosphorus	17-27	enolase 1	Homo sapiens	47-50
17117292-2	2006	Additionally, the PTH prompts an increase in urinary excretion of phosphorus and bicarbonate, seeking a larger quantity of free calcium available in circulation.	Phosphorus	66-76	parathyroid hormone	Homo sapiens	18-21
16554319-7	2006	The annualized change of the square root-transformed CAC score positively correlated with the time-integrated levels of C-reactive protein (R = 0.521, P = 0.001), phosphorus (R = 0.433, P = 0.005) and calcium x phosphorus product (R = 0.394, P = 0.012), but did not correlate with the levels of fetuin-A or lipid parameters.	Phosphorus	211-221	C-reactive protein	Homo sapiens	120-138
17402501-1	2006	HYPOTHESIS: Increasing levels of dietary calcium (Ca) and phosphorous (P) might have a negative impact on parathyroid hormone (PTH) response and result in a more pronounced hypocalcaemia during high-speed exercise in horses.	Phosphorus	58-69	parathyroid hormone	Equus caballus	106-125
17402501-1	2006	HYPOTHESIS: Increasing levels of dietary calcium (Ca) and phosphorous (P) might have a negative impact on parathyroid hormone (PTH) response and result in a more pronounced hypocalcaemia during high-speed exercise in horses.	Phosphorus	2-3	parathyroid hormone	Equus caballus	106-125
16603671-7	2006	When aortic rings from normal rats or a primary culture of human coronary artery smooth muscle cells were treated with phosphorus or vitamin D analogs in vitro, high phosphorus induced calcium accumulation and/or 45Ca uptake in a dose- or time-dependent manner, whereas vitamin D analogs including 1alpha(OH)D2 up to 100 nM had no significant effect despite the presence of a functional vitamin D receptor.	Phosphorus	119-129	vitamin D receptor	Homo sapiens	387-405
16603671-7	2006	When aortic rings from normal rats or a primary culture of human coronary artery smooth muscle cells were treated with phosphorus or vitamin D analogs in vitro, high phosphorus induced calcium accumulation and/or 45Ca uptake in a dose- or time-dependent manner, whereas vitamin D analogs including 1alpha(OH)D2 up to 100 nM had no significant effect despite the presence of a functional vitamin D receptor.	Phosphorus	166-176	vitamin D receptor	Homo sapiens	387-405
16721748-6	2006	The stimulatory effects of B[a]P on expression of these genes were abrogated by cotreatment with the AhR antagonist flavonoid, alpha-napthoflavone (ANF).	Phosphorus	31-32	aryl hydrocarbon receptor	Homo sapiens	101-104
16735491-1	2006	CONTEXT: Fibroblast growth factor 23 (FGF-23) is important in the regulation of phosphorus and vitamin D metabolism.	Phosphorus	80-90	fibroblast growth factor 23	Homo sapiens	9-36
16735491-1	2006	CONTEXT: Fibroblast growth factor 23 (FGF-23) is important in the regulation of phosphorus and vitamin D metabolism.	Phosphorus	80-90	fibroblast growth factor 23	Homo sapiens	38-44
16735491-3	2006	Conversely, states of absent or biologically inactive circulating FGF-23 are associated with increased serum phosphorus and 1,25(OH)(2)D concentrations.	Phosphorus	109-119	fibroblast growth factor 23	Homo sapiens	66-72
16735491-5	2006	OBJECTIVE: We sought to determine whether serum FGF-23 concentration is regulated by dietary phosphorus and thereby mediates the physiological response of serum 1,25(OH)(2)D to changes in dietary phosphorus.	Phosphorus	93-103	fibroblast growth factor 23	Homo sapiens	48-54
16735491-5	2006	OBJECTIVE: We sought to determine whether serum FGF-23 concentration is regulated by dietary phosphorus and thereby mediates the physiological response of serum 1,25(OH)(2)D to changes in dietary phosphorus.	Phosphorus	196-206	fibroblast growth factor 23	Homo sapiens	48-54
16735491-10	2006	RESULTS: Serum FGF-23 concentrations decreased significantly from 30.7 +/- 8.7 pg/ml during phosphorus supplementation to 19.6 +/- 7.0 pg/ml during phosphorus restriction.	Phosphorus	92-102	fibroblast growth factor 23	Homo sapiens	15-21
16735491-10	2006	RESULTS: Serum FGF-23 concentrations decreased significantly from 30.7 +/- 8.7 pg/ml during phosphorus supplementation to 19.6 +/- 7.0 pg/ml during phosphorus restriction.	Phosphorus	148-158	fibroblast growth factor 23	Homo sapiens	15-21
16735491-13	2006	CONCLUSIONS: We conclude that in healthy men, changes in dietary phosphorus within the physiological range of intakes regulate serum FGF-23 concentrations and suggest that dietary phosphorus regulation of 1,25(OH)(2)D production is mediated, at least in part, by changes in circulating FGF-23.	Phosphorus	65-75	fibroblast growth factor 23	Homo sapiens	133-139
16735491-13	2006	CONCLUSIONS: We conclude that in healthy men, changes in dietary phosphorus within the physiological range of intakes regulate serum FGF-23 concentrations and suggest that dietary phosphorus regulation of 1,25(OH)(2)D production is mediated, at least in part, by changes in circulating FGF-23.	Phosphorus	180-190	fibroblast growth factor 23	Homo sapiens	286-292
16405955-3	2006	Drinking-WTRs can be obtained free-of-charge from drinking-water treatment plants, and they have been successfully used to reduce soluble phosphorus (P) concentrations in poorly P-sorbing soils.	Phosphorus	138-148	WTRS	Homo sapiens	9-13
16711707-4	2006	Exposure of 5a or 5b to NaN(SiMe3)2 generated the corresponding (COD)M(kappa2-C,S-1-iPr2P(S)-2-NMe2-(C1-indenyl)) complex (M = Rh, 6a, 70%; M = Ir, 6b, 86%) in which the metal is incorporated into an M-C-P-S ring via coordination to the indenyl ring in an eta1-fashion, as well as to sulfur.	Phosphorus	85-86	NME/NM23 nucleoside diphosphate kinase 2	Homo sapiens	95-99
16794064-2	2006	(Reports, 12 August 2005, p. 1068) reported that in situ mesoscale phosphorus enrichment of the eastern Mediterranean Sea altered selected biological parameters and concluded that the added phosphorus was rapidly transferred from bacteria to mesozooplankton.	Phosphorus	67-77	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	118-121
16794064-2	2006	(Reports, 12 August 2005, p. 1068) reported that in situ mesoscale phosphorus enrichment of the eastern Mediterranean Sea altered selected biological parameters and concluded that the added phosphorus was rapidly transferred from bacteria to mesozooplankton.	Phosphorus	190-200	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	118-121
16787855-0	2006	Phytase effects on the efficiency of utilisation and blood concentrations of phosphorus and calcium in Pekin ducks.	Phosphorus	77-87	phytase	Zea mays	0-7
16817793-6	2006	Between the low-serum phosphorus (&lt;6 mg/dL) group and high-serum phosphorus (&gt; or =6 mg/dL) group, significant differences were detected in the expression of OPN (P = 0.0049) and the levels of BUN (P = 0.0005), serum phosphorus (P &lt; 0.0001) and calcium x phosphorus products (P &lt; 0.0001).	Phosphorus	22-32	secreted phosphoprotein 1	Homo sapiens	164-167
16817793-6	2006	Between the low-serum phosphorus (&lt;6 mg/dL) group and high-serum phosphorus (&gt; or =6 mg/dL) group, significant differences were detected in the expression of OPN (P = 0.0049) and the levels of BUN (P = 0.0005), serum phosphorus (P &lt; 0.0001) and calcium x phosphorus products (P &lt; 0.0001).	Phosphorus	68-78	secreted phosphoprotein 1	Homo sapiens	164-167
16817793-6	2006	Between the low-serum phosphorus (&lt;6 mg/dL) group and high-serum phosphorus (&gt; or =6 mg/dL) group, significant differences were detected in the expression of OPN (P = 0.0049) and the levels of BUN (P = 0.0005), serum phosphorus (P &lt; 0.0001) and calcium x phosphorus products (P &lt; 0.0001).	Phosphorus	68-78	secreted phosphoprotein 1	Homo sapiens	164-167
16817793-6	2006	Between the low-serum phosphorus (&lt;6 mg/dL) group and high-serum phosphorus (&gt; or =6 mg/dL) group, significant differences were detected in the expression of OPN (P = 0.0049) and the levels of BUN (P = 0.0005), serum phosphorus (P &lt; 0.0001) and calcium x phosphorus products (P &lt; 0.0001).	Phosphorus	68-78	secreted phosphoprotein 1	Homo sapiens	164-167
16817793-7	2006	Moreover, between the low-BUN (&lt;70 mg/dL, N = 19) group and high-BUN (&gt; or =70 mg/dL) group, significant differences were detected in the expression of OPN (P = 0.0039) and the levels of BUN (P = 0.0002), serum phosphorus (P = 0.0002) and calcium x phosphorus products (P = 0.0003).	Phosphorus	217-227	secreted phosphoprotein 1	Homo sapiens	158-161
16817793-7	2006	Moreover, between the low-BUN (&lt;70 mg/dL, N = 19) group and high-BUN (&gt; or =70 mg/dL) group, significant differences were detected in the expression of OPN (P = 0.0039) and the levels of BUN (P = 0.0002), serum phosphorus (P = 0.0002) and calcium x phosphorus products (P = 0.0003).	Phosphorus	255-265	secreted phosphoprotein 1	Homo sapiens	158-161
16711707-4	2006	Exposure of 5a or 5b to NaN(SiMe3)2 generated the corresponding (COD)M(kappa2-C,S-1-iPr2P(S)-2-NMe2-(C1-indenyl)) complex (M = Rh, 6a, 70%; M = Ir, 6b, 86%) in which the metal is incorporated into an M-C-P-S ring via coordination to the indenyl ring in an eta1-fashion, as well as to sulfur.	Phosphorus	85-86	secreted phosphoprotein 1	Homo sapiens	256-260
16641675-2	2006	Here, we report that aging nuclear vitamin D receptor knockout mice demonstrate a symmetric thalamic calcification with numerous Ca/P-containing laminated bodies.	Phosphorus	132-133	vitamin D (1,25-dihydroxyvitamin D3) receptor	Mus musculus	35-53
16649796-1	2006	The chemically active phosphorus surface sites defined as PO(x), PO(x)H, and PO(x)H2, where x = 1, 2, or 3, and the bulk phosphorus groups of PO4(3-) at synthetic carbonate-free fluorapatite (Ca5(PO4)3F) have been studied by means of single-pulse 1H,31P, and 31P CP MAS NMR.	Phosphorus	22-32	proline dehydrogenase 1	Homo sapiens	58-63
16671751-3	2006	In an earlier work we have measured the proximity of the lysine (K6) side chain in an SN-15 peptide fragment of the salivary protein statherin adsorbed to the Phosphorus-rich surface of HAP using solid-state NMR recoupling experiments.	Phosphorus	159-169	statherin	Homo sapiens	133-142
16563169-2	2006	Causative mutations in the transcription factor IRF6 have also been identified in two allelic CL/P syndromes and common polymorphisms in the same gene are significantly associated with non-syndromal CL/P in different populations.	Phosphorus	97-98	interferon regulatory factor 6	Homo sapiens	48-52
16669977-7	2006	Serum phosphorus concentration was higher in patients on sevelamer hydrochloride compared to CCB 2.10 +/- 0.87 versus 1.74 +/- 0.28 mmol/L (P = 0.0013), as was the Ca-P product 4.97 +/- 0.94 mmol2L2 (62.1 +/- 11.8 mg2/dL2) versus 3.97 +/- 1.18 mmol2/L2 (49.7 +/- 14.7 mg2/dL2), P = 0.0009).	Phosphorus	6-16	l(1)L2	Drosophila melanogaster	218-221
16669977-7	2006	Serum phosphorus concentration was higher in patients on sevelamer hydrochloride compared to CCB 2.10 +/- 0.87 versus 1.74 +/- 0.28 mmol/L (P = 0.0013), as was the Ca-P product 4.97 +/- 0.94 mmol2L2 (62.1 +/- 11.8 mg2/dL2) versus 3.97 +/- 1.18 mmol2/L2 (49.7 +/- 14.7 mg2/dL2), P = 0.0009).	Phosphorus	6-16	l(1)L2	Drosophila melanogaster	196-198
16669977-7	2006	Serum phosphorus concentration was higher in patients on sevelamer hydrochloride compared to CCB 2.10 +/- 0.87 versus 1.74 +/- 0.28 mmol/L (P = 0.0013), as was the Ca-P product 4.97 +/- 0.94 mmol2L2 (62.1 +/- 11.8 mg2/dL2) versus 3.97 +/- 1.18 mmol2/L2 (49.7 +/- 14.7 mg2/dL2), P = 0.0009).	Phosphorus	6-16	l(1)L2	Drosophila melanogaster	272-275
16734088-8	2006	Time from admission to initiation of subcutaneous insulin therapy was correlated with lower serum potassium concentration (P = .0056), lower serum phosphorus concentration (P = .0043), abnormally high white blood cell count (P = .0060), large base deficit (P = .0015), and low venous pH (P &lt; .001).	Phosphorus	147-157	insulin	Canis lupus familiaris	50-57
16848114-7	2006	There was a positive correlation between serum phosphorus (P) and OC (r=0.394, p=0.031), alkaline phosphatase (ALP) and OC (r=0.520, p=0.003), and parathyroid hormone (PTH) and OC (r=0.441, p=0.017), whereas no correlation was found between OC and calcium (Ca) and OC and magnesium (Mg).	Phosphorus	47-57	bone gamma-carboxyglutamate protein	Homo sapiens	66-68
16497488-1	2006	Altered high energy and membrane metabolism, measured with phosphorus magnetic resonance spectroscopy (31P-MRS), has been inconsistently reported in schizophrenic patients in several anatomical brain regions implicated in the pathophysiology of this illness, with little attention to the effects of brain tissue type on the results.	Phosphorus	59-69	MROS	Homo sapiens	107-110
16526755-1	2006	Para- and meta-isomers of center-to-edge phosphorus(V) porphyrin heterodimers (p- and m-Pm-PCl2) composed of a phosphorus(V) tetraphenylporphyrin (P) and a phosphorus(V) tetrakis(4-methoxyphenyl)porphyrin (Pm) were synthesized to investigate the geometry and solvent-polarity dependences of the relaxation dynamics of the lowest singlet excited state (S1) of the porphyrin dimer.	Phosphorus	111-121	metal response element binding transcription factor 2	Homo sapiens	91-95
16526755-1	2006	Para- and meta-isomers of center-to-edge phosphorus(V) porphyrin heterodimers (p- and m-Pm-PCl2) composed of a phosphorus(V) tetraphenylporphyrin (P) and a phosphorus(V) tetrakis(4-methoxyphenyl)porphyrin (Pm) were synthesized to investigate the geometry and solvent-polarity dependences of the relaxation dynamics of the lowest singlet excited state (S1) of the porphyrin dimer.	Phosphorus	111-121	metal response element binding transcription factor 2	Homo sapiens	91-95
16506768-4	2006	Use of PCy(3) or P[(4-MeO)C(6)H(4)](3) as the ligand for Pd leads to syn-addition of the arene and the oxygen atom across the double bond, whereas use of (+/-)-BINAP or DPP-benzene affords products that result from anti-addition.	Phosphorus	7-8	synemin	Homo sapiens	69-72
16542086-2	2006	From phenomenological point of view, the mutual relationships between the characteristic PALS temperatures, the glass temperature TgPALS, and the crossover temperatures Tb1L and Tb2L on the ortho-positronium (o-Ps) lifetime versus the temperature plot, have been discussed with respect to the characteristic DS temperatures, the glass temperature TgDS and the dynamic crossover temperature TBST, concerning the crossover behavior of primary alpha-relaxation times.	Phosphorus	210-213	TDP-glucose 4,6-dehydratase	Homo sapiens	347-351
16555680-3	2006	CKD patients encounter a much higher risk of cardiovascular disease than do members of the general public, and recent clinical observations have shown that VDR activator therapy provides survival benefit for CKD patients in the rank order of paricalcitol &gt; calcitriol &gt; no VDR activator therapy, independent of parathyroid hormone, phosphorus and calcium.	Phosphorus	338-348	vitamin D receptor	Homo sapiens	156-159
16402222-9	2006	The presence of multiple sequences with a high similarity to phyS in aquatic environmental samples and the widespread occurrence of the Shewanella species in nature suggest that the beta-propeller phytase family is the major class of phytases in the aquatic environment, and that it may play an important role in the recycling of phosphorus.	Phosphorus	330-340	phytase	Shewanella oneidensis MR-1	61-65
16470748-7	2006	Our finding suggests that TCN2 is involved in causing CL/P.	Phosphorus	57-58	transcobalamin 2	Homo sapiens	26-30
16405724-5	2006	Phosphorus magnetic resonance spectroscopy from the medial gastrocnemius muscle was used to calculate free Mg2+ from the concentrations and chemical shifts of Pi, PCr, and beta ATP peaks.	Phosphorus	0-10	mucin 7, secreted	Homo sapiens	107-110
16443695-0	2006	Characterization of low phosphorus insensitive mutants reveals a crosstalk between low phosphorus-induced determinate root development and the activation of genes involved in the adaptation of Arabidopsis to phosphorus deficiency.	Phosphorus	24-34	induced by phosphate starvation1	Arabidopsis thaliana	98-105
16443695-0	2006	Characterization of low phosphorus insensitive mutants reveals a crosstalk between low phosphorus-induced determinate root development and the activation of genes involved in the adaptation of Arabidopsis to phosphorus deficiency.	Phosphorus	87-97	induced by phosphate starvation1	Arabidopsis thaliana	98-105
16448181-7	2006	These findings suggest that oligophosphopeptides from hen egg yolk phosvitin possess novel antioxidative activity against oxidative stress in intestinal epithelial cells and that phosphorus and peptide structure seem to have a key role in the activity.	Phosphorus	179-189	casein kinase 2 beta	Homo sapiens	67-76
16395276-0	2006	Effect of manipulating serum phosphorus with phosphate binder on circulating PTH and FGF23 in renal failure rats.	Phosphorus	29-39	parathyroid hormone	Rattus norvegicus	77-80
16395276-0	2006	Effect of manipulating serum phosphorus with phosphate binder on circulating PTH and FGF23 in renal failure rats.	Phosphorus	29-39	fibroblast growth factor 23	Rattus norvegicus	85-90
16395276-1	2006	Phosphorus directly controls parathyroid hormone (PTH) synthesis and secretion.	Phosphorus	0-10	parathyroid hormone	Rattus norvegicus	29-48
16395276-1	2006	Phosphorus directly controls parathyroid hormone (PTH) synthesis and secretion.	Phosphorus	0-10	parathyroid hormone	Rattus norvegicus	50-53
16395276-3	2006	We proposed that changes in serum PTH and FGF23 levels might be associated with changes in serum phosphorus levels caused by the phosphate binder sevelamer hydrochloride (sevelamer, i.e. crosslinked poly[allylamine hydrochloride]).	Phosphorus	97-107	parathyroid hormone	Rattus norvegicus	34-37
16395276-3	2006	We proposed that changes in serum PTH and FGF23 levels might be associated with changes in serum phosphorus levels caused by the phosphate binder sevelamer hydrochloride (sevelamer, i.e. crosslinked poly[allylamine hydrochloride]).	Phosphorus	97-107	fibroblast growth factor 23	Rattus norvegicus	42-47
16395276-10	2006	However, the changes in serum FGF23 levels began after the onset of changes in serum phosphorus and PTH levels.	Phosphorus	85-95	fibroblast growth factor 23	Rattus norvegicus	30-35
16395276-11	2006	In conclusion, circulating PTH, and FGF23 levels can be promptly manipulated through the control of serum phosphorus levels.	Phosphorus	106-116	parathyroid hormone	Rattus norvegicus	27-30
16395276-11	2006	In conclusion, circulating PTH, and FGF23 levels can be promptly manipulated through the control of serum phosphorus levels.	Phosphorus	106-116	fibroblast growth factor 23	Rattus norvegicus	36-41
16568023-1	2006	Primary hyperparathyroidism is a clinical condition related to an excessive and abnormally regulated secretion of parathyroid hormone (PTH) from the parathyroid glands which is responsible for an alteration of the calcium and phosphorus metabolism.	Phosphorus	226-236	parathyroid hormone	Homo sapiens	114-133
16495674-0	2006	Effects of lowering food intake by high phosphorus diet on parathyroid hormone actions and kidney mineral concentration in rats.	Phosphorus	40-50	parathyroid hormone	Rattus norvegicus	59-78
17366841-14	2006	Moreover, we studied the association of isolated CL/P with the IRF6 locus using two variants in a set of 195 patients from Belgium.	Phosphorus	52-53	interferon regulatory factor 6	Homo sapiens	63-67
16055523-7	2006	Pretreatment of cells with the NAD(P)H oxidase inhibitor diphenyleneiodonium chloride or with the superoxide scavenger 4,5-dihydroxy-1,3-benzene-disulfonic acid did not affect the ANG II-induced NIE.	Phosphorus	0-1	angiotensinogen	Rattus norvegicus	180-186
17366841-16	2006	This suggests that IRF6 also contributes to the occurrence of sporadic, isolated CL/P, even if no mutation in the gene can be identified in such patients.	Phosphorus	84-85	interferon regulatory factor 6	Homo sapiens	19-23
16636542-0	2006	The relationship between plasma BNP level and the myocardial phosphocreatine/adenosine triphosphate ratio determined by phosphorus-31 magnetic resonance spectroscopy in patients with dilated cardiomyopathy.	Phosphorus	120-130	natriuretic peptide B	Homo sapiens	32-35
16636542-1	2006	The purpose of this study was to evaluate the correlation between the plasma B-type natriuretic peptide (BNP) level and the myocardial phosphocreatine/adenosine triphosphate ratio determined using rapid phosphorus-31 magnetic resonance spectroscopy (31P-MRS) in patients with dilated cardiomyopathy (DCM).	Phosphorus	203-213	natriuretic peptide B	Homo sapiens	77-103
16636542-1	2006	The purpose of this study was to evaluate the correlation between the plasma B-type natriuretic peptide (BNP) level and the myocardial phosphocreatine/adenosine triphosphate ratio determined using rapid phosphorus-31 magnetic resonance spectroscopy (31P-MRS) in patients with dilated cardiomyopathy (DCM).	Phosphorus	203-213	natriuretic peptide B	Homo sapiens	105-108
16331108-2	2006	OBJECTIVE: To test the hypothesis that central effects of Ang II are mediated by reduced nicotinamide adenine dinucleotide phosphate [NAD(P)H]-oxidase-dependent production of superoxide in the hypothalamus.	Phosphorus	137-140	angiotensinogen	Rattus norvegicus	58-64
16400166-1	2006	The Chlamydomonas reinhardtii transcription factor PSR1 is required for the control of activities involved in scavenging phosphate from the environment during periods of phosphorus limitation.	Phosphorus	170-180	uncharacterized protein	Chlamydomonas reinhardtii	51-55
16400166-3	2006	A comparison of gene expression patterns using microarray analyses and quantitative PCRs with wild-type and psr1 mutant cells deprived of phosphorus has revealed that PSR1 also controls genes encoding proteins with potential "electron valve" functions--these proteins can serve as alternative electron acceptors that help prevent photodamage caused by overexcitation of the photosynthetic electron transport system.	Phosphorus	138-148	uncharacterized protein	Chlamydomonas reinhardtii	108-112
16400166-3	2006	A comparison of gene expression patterns using microarray analyses and quantitative PCRs with wild-type and psr1 mutant cells deprived of phosphorus has revealed that PSR1 also controls genes encoding proteins with potential "electron valve" functions--these proteins can serve as alternative electron acceptors that help prevent photodamage caused by overexcitation of the photosynthetic electron transport system.	Phosphorus	138-148	uncharacterized protein	Chlamydomonas reinhardtii	167-171
16400166-4	2006	In accordance with this finding, phosphorus-starved psr1 mutants die when subjected to elevated light intensities; at these intensities, the wild-type cells still exhibit rapid growth.	Phosphorus	33-43	uncharacterized protein	Chlamydomonas reinhardtii	52-56
16400166-6	2006	Surprisingly, phosphorus-deficient psr1 cells (but not wild-type cells) also display expression patterns associated with specific responses to sulfur deprivation, suggesting a hitherto unsuspected link between the signal transduction pathways involved in controlling phosphorus and sulfur starvation responses.	Phosphorus	14-24	uncharacterized protein	Chlamydomonas reinhardtii	35-39
16400166-7	2006	Together, these results demonstrate that PSR1 is critical for the survival of cells under conditions of suboptimal phosphorus availability and that it plays a key role in controlling both scavenging responses and the ability of the cell to manage excess absorbed excitation energy.	Phosphorus	115-125	uncharacterized protein	Chlamydomonas reinhardtii	41-45
16868704-2	2006	Parathyroid hormone (PTH) levels are affected by calcium, vitamin D, and phosphorus.	Phosphorus	73-83	parathyroid hormone	Homo sapiens	0-19
16868704-2	2006	Parathyroid hormone (PTH) levels are affected by calcium, vitamin D, and phosphorus.	Phosphorus	73-83	parathyroid hormone	Homo sapiens	21-24
16547127-0	2006	Root plasma membrane H+-ATPase is involved in the adaptation of soybean to phosphorus starvation.	Phosphorus	75-85	plasma membrane ATPase 4	Glycine max	21-30
16375584-9	2006	Serum phosphorus concentration was a significant correlate of triglyceride (r = 0.199, p &lt; or =0.001) and Lp(a) (r = 0.129, p &lt; or =0.04).	Phosphorus	6-16	lipoprotein(a)	Homo sapiens	109-114
16441824-2	2006	Calcimimetics are a new class of drugs approved in the European Community and the United States by the Food and Drug Administration that were designed to suppress parathyroid hormone (PTH) levels with a simultaneous reduction in serum calcium and phosphorus levels, and calcium phosphorus product (Ca x P).	Phosphorus	184-185	parathyroid hormone	Homo sapiens	163-182
16247549-3	2006	We first searched for mutations in these genes among 112 CL/P and 16 CPO patients, and found a heterozygous missense mutation (640A &gt; G, S214G) in exon 3 of PAX9 in two sibs with CL/P and their phenotypically normal mother from a Japanese family.	Phosphorus	60-61	paired box 9	Homo sapiens	160-164
16247549-3	2006	We first searched for mutations in these genes among 112 CL/P and 16 CPO patients, and found a heterozygous missense mutation (640A &gt; G, S214G) in exon 3 of PAX9 in two sibs with CL/P and their phenotypically normal mother from a Japanese family.	Phosphorus	70-71	paired box 9	Homo sapiens	160-164
16735562-1	2006	Low temperature radioluminescence spectra of LiF, variously co-doped with Mg, Cu and P, show highly unusual temperature dependencies which resemble thermoluminescence data.	Phosphorus	85-86	LIF interleukin 6 family cytokine	Homo sapiens	45-48
16868654-1	2006	Previous studies observed that MSX1 mutations could contribute to nonsyndromic cleft lip with or without cleft palate (CL/P) in some populations.	Phosphorus	0-1	msh homeobox 1	Homo sapiens	31-35
16868654-3	2006	We investigated whether MSX1 mutations also contribute to nonsyndromic CL/P in the Thai population.	Phosphorus	74-75	msh homeobox 1	Homo sapiens	24-28
16691036-5	2006	RESULTS: Plasma FGF-23 correlated with creatinine clearance (r2 = -0.584, p &lt; 0.0001) and plasma phosphorus (r2 = 0.347, p &lt; 0.001) in CKD patients and with plasma phosphorus (r2 = 0.448, p &lt; 0.001) in end-stage renal disease patients.	Phosphorus	170-180	fibroblast growth factor 23	Homo sapiens	16-22
16691036-8	2006	In patients with post-transplant hypophosphatemia, FGF-23 levels correlated inversely with plasma phosphorus (r2 = 0.661, p &lt; 0.05).	Phosphorus	98-108	fibroblast growth factor 23	Homo sapiens	51-57
16691036-10	2006	CONCLUSIONS: In CKD, FGF-23 levels rose with decreasing creatinine clearance rates and increasing plasma phosphorus levels, and rapidly decreased post-transplantation suggesting FGF-23 is cleared by the kidney.	Phosphorus	105-115	fibroblast growth factor 23	Homo sapiens	21-27
16260911-2	2005	Twelve weeks after initiating a tenofovir-containing HAART regimen, a high urine-beta 2 microglobulin level was observed in 12 out of 17 patients, the percentage of tubular reabsorption of phosphate decreased from 96.0 to 91.1% and alkaline phosphatase increased from 294 to 365 U/l, whereas serum creatinine and phosphorus remained largely unchanged.	Phosphorus	313-323	beta-2-microglobulin	Homo sapiens	81-101
16557497-3	2006	The most widely accepted pathway involves cytochrome-P450 (CYP) 1A1- and/or 1B1-mediated formation of B[a]P-7,8-oxide, which undergoes epoxide hydrolase-mediated metabolism to the proximate carcinogen B[a]P-7,8-dihydro-7,8-diol.	Phosphorus	53-54	olfactory receptor family 1 subfamily B member 1	Homo sapiens	73-79
16260018-6	2006	At 8 h after initial dosing, brain cholinesterase inhibition was significantly greater in the C/P group (59%) compared to the P/C group (28%).	Phosphorus	96-97	butyrylcholinesterase	Rattus norvegicus	35-49
16260018-6	2006	At 8 h after initial dosing, brain cholinesterase inhibition was significantly greater in the C/P group (59%) compared to the P/C group (28%).	Phosphorus	126-127	butyrylcholinesterase	Rattus norvegicus	35-49
16841742-4	2006	Anoxic phosphorus assimilation rate could reach 10.44 mgP/gSS.h and the percentage of anoxic phosphorus assimilation amount was more than 97% with continuous feed mode.	Phosphorus	7-17	matrix Gla protein	Homo sapiens	54-57
16841742-4	2006	Anoxic phosphorus assimilation rate could reach 10.44 mgP/gSS.h and the percentage of anoxic phosphorus assimilation amount was more than 97% with continuous feed mode.	Phosphorus	7-17	glutathione synthetase	Homo sapiens	58-61
16269583-5	2005	There was some evidence for higher risk of CL/P with maternal periconceptional smoking in infants with an NOS3 -922G allele (for homozygotes, OR = 2.5, 95% CI: 1.2, 5.6) but not in those with an 894T allele.	Phosphorus	46-47	nitric oxide synthase 3	Homo sapiens	106-110
16322323-4	2005	It is now evident that cPAcP functions as a neutral protein tyrosine phosphatase (PTP) in prostate cancer cells and dephosphorylates HER-2/ErbB-2/Neu (HER-2: human epidermal growth factor receptor-2) at the phosphotyrosine (p-Tyr) residues.	Phosphorus	52-53	protein tyrosine phosphatase non-receptor type 22	Homo sapiens	82-85
17373206-3	2005	It results from an imbalance in the interaction between calcium, phosphorus, vitamin D and parathyroid hormone (PTH).	Phosphorus	65-75	parathyroid hormone	Homo sapiens	91-110
16123154-1	2005	Fibroblast growth factor-23 (FGF-23) is a novel circulating peptide that regulates phosphorus (Pi) and vitamin D metabolism, but the mechanisms by which circulating FGF-23 itself is regulated are unknown.	Phosphorus	83-93	fibroblast growth factor 23	Mus musculus	0-27
16123154-1	2005	Fibroblast growth factor-23 (FGF-23) is a novel circulating peptide that regulates phosphorus (Pi) and vitamin D metabolism, but the mechanisms by which circulating FGF-23 itself is regulated are unknown.	Phosphorus	83-93	fibroblast growth factor 23	Mus musculus	29-35
15998841-7	2005	Thus enhanced parathyroid TGF-alpha/EGFR expression, self-upregulation, and growth signals occur early in kidney disease, are aggravated by low-Ca and high-P intake, and constitute the main pathogenic mechanism of the severity of parathyroid hyperplasia.	Phosphorus	156-157	epidermal growth factor receptor	Rattus norvegicus	36-40
16248661-1	2005	White phosphorus (P(4)) reacts with three-coordinate molybdenum(III) trisamides or molybdaziridine hydride complexes to produce either bridging or terminal phosphide (P(3)(-)) species, depending upon the ancillary ligand steric demands.	Phosphorus	0-16	solute carrier family 10 member 4	Homo sapiens	18-22
16248661-1	2005	White phosphorus (P(4)) reacts with three-coordinate molybdenum(III) trisamides or molybdaziridine hydride complexes to produce either bridging or terminal phosphide (P(3)(-)) species, depending upon the ancillary ligand steric demands.	Phosphorus	0-16	solute carrier family 10 member 3	Homo sapiens	167-171
16248661-3	2005	Thermochemical measurements together with computational analysis rule out simple P-atom abstraction from P(4) as a step in the phosphorus activation mechanism.	Phosphorus	127-137	solute carrier family 10 member 4	Homo sapiens	105-109
15998841-7	2005	Thus enhanced parathyroid TGF-alpha/EGFR expression, self-upregulation, and growth signals occur early in kidney disease, are aggravated by low-Ca and high-P intake, and constitute the main pathogenic mechanism of the severity of parathyroid hyperplasia.	Phosphorus	156-157	transforming growth factor alpha	Rattus norvegicus	26-35
15975090-5	2005	Previously, we demonstrated that the protein, ubiquilin-1, interacts both in vivo and in vitro with PS and that overexpression of ubiquilin-1 or -2 leads to increased accumulation of full-length PS proteins.	Phosphorus	100-102	ubiquilin 1	Homo sapiens	46-57
15975090-5	2005	Previously, we demonstrated that the protein, ubiquilin-1, interacts both in vivo and in vitro with PS and that overexpression of ubiquilin-1 or -2 leads to increased accumulation of full-length PS proteins.	Phosphorus	100-102	ubiquilin 1	Homo sapiens	130-147
16277767-0	2005	High-phosphorus diet stimulates receptor activator of nuclear factor-kappaB ligand mRNA expression by increasing parathyroid hormone secretion in rats.	Phosphorus	5-15	TNF superfamily member 11	Rattus norvegicus	32-82
16358222-0	2005	The klotho gene: a gene predominantly expressed in the kidney is a fundamental regulator of aging and calcium/phosphorus metabolism.	Phosphorus	110-120	klotho	Homo sapiens	4-10
16120820-5	2005	Treatment with sulfatase resulted in recovery of this peak as p-cresol, confirming its identity.	Phosphorus	54-55	arylsulfatase family member H	Homo sapiens	15-24
16132054-10	2005	This result, with previous studies performed in the United States and Italy, shows for the first time the implication of IRF6 in isolated CL/P in northern Europe.	Phosphorus	141-142	interferon regulatory factor 6	Homo sapiens	121-125
16358222-4	2005	Klotho plays a critical role in the regulation of calcium and phosphorus homeostasis by negatively regulating active vitamin D synthesis.	Phosphorus	62-72	klotho	Homo sapiens	0-6
16268954-9	2005	Also, serum phosphorus level was significantly decreased on the first (P &lt; 0.05) and third (P &lt; 0.001) days of ACTH challenge but remained unaffected after the cessation of ACTH treatment.	Phosphorus	12-22	proopiomelanocortin	Homo sapiens	117-121
16268954-9	2005	Also, serum phosphorus level was significantly decreased on the first (P &lt; 0.05) and third (P &lt; 0.001) days of ACTH challenge but remained unaffected after the cessation of ACTH treatment.	Phosphorus	12-22	proopiomelanocortin	Homo sapiens	179-183
16221819-3	2005	Because internal phosphorus release from the bottom sediments is comparatively low and external phosphorus loading to the Salton Sea is high, reduction of tributary phosphorus is expected to reduce algal blooms, increase dissolved oxygen, and reduce odors.	Phosphorus	96-106	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	129-132
16091995-7	2005	In situ rat liver perfusion studies showed that the only rate process for the disposition of [(3)H]PA in the liver inhibited by L-FABP antisera was that for influx, as defined by PS, and that it reduced PS in the perfused liver by 42%.	Phosphorus	179-181	fatty acid binding protein 1	Rattus norvegicus	128-134
16221819-3	2005	Because internal phosphorus release from the bottom sediments is comparatively low and external phosphorus loading to the Salton Sea is high, reduction of tributary phosphorus is expected to reduce algal blooms, increase dissolved oxygen, and reduce odors.	Phosphorus	96-106	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	129-132
16165154-2	2005	We report here two crystal forms of a complex between the Grb2 SH2 domain and a potent non-phosphorus-containing macrocyclic peptide mimetic that exhibits significant anti-proliferative effects against erbB-2-dependent breast cancers.	Phosphorus	91-101	growth factor receptor bound protein 2	Homo sapiens	58-62
16165154-2	2005	We report here two crystal forms of a complex between the Grb2 SH2 domain and a potent non-phosphorus-containing macrocyclic peptide mimetic that exhibits significant anti-proliferative effects against erbB-2-dependent breast cancers.	Phosphorus	91-101	erb-b2 receptor tyrosine kinase 2	Homo sapiens	202-208
16222095-0	2005	[The structure and phosphorus or potassium deficiency induced expression of a calmodulin-like protein gene in Arabidopsis].	Phosphorus	19-29	calmodulin-like protein	Arabidopsis thaliana	78-101
15899935-6	2005	Adjusting for CRP and calcium x phosphorus product, every 0.01 g/l increase in serum fetuin-A remained independently associated with a 6% decrease in the risk of valvular calcification (95% confidence intervals, 0.90-0.99; P = 0.028).	Phosphorus	32-42	alpha 2-HS glycoprotein	Homo sapiens	85-93
16272627-1	2005	Phosphorus directly controls parathyroid hormone (PTH) synthesis and secretion.	Phosphorus	0-10	parathyroid hormone	Rattus norvegicus	29-48
16117800-5	2005	DB[a,l]P-induced early preneoplastic cell proliferation correlated with H-ras and specific G1 cyclin expression.	Phosphorus	6-8	Harvey rat sarcoma virus oncogene	Mus musculus	72-77
15972241-1	2005	The release kinetics of recombinant human bone morphogenetic protein-2 (rhBMP-2) loaded poly(dl-lactic-co-glycolic acid)/calcium phosphate cement (PLGA/Ca-P cement) composites were studied in vivo.	Phosphorus	76-77	bone morphogenetic protein 2	Homo sapiens	42-70
16114795-3	2005	We report the case of a 49-year-old woman on hemodialysis with chronic HCV infection who developed significant decrease in serum calcium (Ca) and phosphorus (P) levels accompanied by relative hypoparathyroidism while being under treatment with alpha-IFN.	Phosphorus	158-159	interferon alpha 1	Homo sapiens	250-253
15962968-0	2005	Synthesis, structure, and stereochemistry of trinuclear metal complexes formed from the phosphorus-based achiral tripodal ligand {P(S)[N(Me)N=CHC6H4-o-OH]3} (LH3): luminescent properties of L2Cd3 x 2H2O.	Phosphorus	88-98	procollagen-lysine,2-oxoglutarate 5-dioxygenase 3	Homo sapiens	158-161
16018650-0	2005	P(i-BuNCH2CH2)3N: an efficient promoter for the nucleophilic aromatic substitution reaction of aryl fluorides with aryl TBDMS (or TMS) ethers.	Phosphorus	0-1	PYD and CARD domain containing	Homo sapiens	130-133
16164192-11	2005	Ca and P levels were increased significantly because of the medicinal action of OCT.	Phosphorus	7-8	plexin A2	Homo sapiens	80-83
15855166-11	2005	Our data suggest a model where HIV-1 Tat competes with Hexim1 for cyclin T1 binding, thus releasing P-TEFb from the inactive complex to stimulate the transcription of HIV-1 gene expression.	Phosphorus	100-101	HEXIM P-TEFb complex subunit 1	Homo sapiens	55-61
15855166-11	2005	Our data suggest a model where HIV-1 Tat competes with Hexim1 for cyclin T1 binding, thus releasing P-TEFb from the inactive complex to stimulate the transcription of HIV-1 gene expression.	Phosphorus	100-101	proliferating cell nuclear antigen	Homo sapiens	66-72
15994871-1	2005	BACKGROUND: Previous data have shown an association between DNA sequence variants in the IRF6 gene and an increased risk of non-syndromic cleft lip with or without cleft palate (CL/P) in some populations.	Phosphorus	12-13	interferon regulatory factor 6	Homo sapiens	89-93
15994871-8	2005	The IRF6 820G-->A was responsible for 16.7% of the genetic contribution to CL/P.	Phosphorus	78-79	interferon regulatory factor 6	Homo sapiens	4-8
15994871-9	2005	CONCLUSIONS: The findings confirm that IRF6 820G-->A is associated with CL/P.	Phosphorus	75-76	interferon regulatory factor 6	Homo sapiens	39-43
15976027-7	2005	Our studies demonstrate that normal phosphorus levels are required for growth plate maturation and implicate a critical role for phosphate-regulated apoptosis of hypertrophic chondrocytes via activation of the caspase-9-mediated mitochondrial pathway.	Phosphorus	36-46	caspase 9	Mus musculus	210-219
15946641-10	2005	The phosphorus on adjacent site G2pA3 is in B(II) conformation and hence a distinct pattern of B(I) and B(II) conformations is induced and stabilized.	Phosphorus	4-14	calcium voltage-gated channel subunit alpha1 E	Homo sapiens	95-109
15909042-3	2005	The solution NMR spectroscopic and X-ray crystallographic studies are indicative of a trigonal bipyramidal geometry for these aluminium complexes in which the amino nitrogen atom is trans to the phosphorus donor of the [PNN]- ligand.	Phosphorus	195-205	pinin, desmosome associated protein	Homo sapiens	220-223
15899134-12	2005	In CHF-C group, the left ventricular mRNA of NCX1 and PLB were significantly upregulated in comparing with PS group (RNCX1/beta-Actin: 0.51 +/- 0.12 vs 0.19 +/- 0.06, P &lt; 0.01; RPLB/beta-Actin: 0.26 +/- 0.12 vs 0.20 +/- 0.08, P &lt; 0.05), while SERCA2 mRNA was downregulated (0.48 +/- 0.10 vs 0.80 +/- 0.11, P &lt; 0.01).	Phosphorus	107-109	solute carrier family 8 member A1	Rattus norvegicus	45-49
15933779-5	2005	ACE measurements in the plasma of 80 healthy patients with Hip-His-Leu and with Abz-FRK(Dnp)P-OH correlated closely (r = 0.90, P &lt; 0.001).	Phosphorus	92-93	angiotensin I converting enzyme	Homo sapiens	0-3
16124641-2	2005	METHOD: The expression of EBV LMP2A was detected in the specimens of 40 patients with NPC and 38 cases with nasopharyngeal inflammation by S-P immunohistochemical methods.	Phosphorus	139-142	LMP2A	Human gammaherpesvirus 4	30-35
15899134-12	2005	In CHF-C group, the left ventricular mRNA of NCX1 and PLB were significantly upregulated in comparing with PS group (RNCX1/beta-Actin: 0.51 +/- 0.12 vs 0.19 +/- 0.06, P &lt; 0.01; RPLB/beta-Actin: 0.26 +/- 0.12 vs 0.20 +/- 0.08, P &lt; 0.05), while SERCA2 mRNA was downregulated (0.48 +/- 0.10 vs 0.80 +/- 0.11, P &lt; 0.01).	Phosphorus	107-109	phospholamban	Rattus norvegicus	54-57
15784719-9	2005	Blocking IL-11 signaling reduced RLX+P- or PGE(2)+P-induced decidualization, suggesting that RLX and PGE(2) act via IL-11.	Phosphorus	37-38	interleukin 11	Homo sapiens	9-14
16053783-10	2005	In CHF - C and CHF - T group, the protein levels of NCX(1) were 1.141 +/- 0.047 and 1.074 +/- 0.081 times PS group, respectively (both P &lt; 0.05), and SERCA(2) protein levels were respectively 0.803 +/- 0.100 and 0.893 +/- 0.084 times as high as in PS group (both P &lt; 0.05).	Phosphorus	106-108	solute carrier family 8 member A1	Rattus norvegicus	52-58
15899134-13	2005	The mRNA levels of NCX1 and SERCA2 in CHF-T group were between the CHF-C and PS group, and the differences of the latter two groups were significant (all P &lt; 0.05).	Phosphorus	77-79	solute carrier family 8 member A1	Rattus norvegicus	19-23
15899134-13	2005	The mRNA levels of NCX1 and SERCA2 in CHF-T group were between the CHF-C and PS group, and the differences of the latter two groups were significant (all P &lt; 0.05).	Phosphorus	77-79	ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2	Rattus norvegicus	28-34
15899134-12	2005	In CHF-C group, the left ventricular mRNA of NCX1 and PLB were significantly upregulated in comparing with PS group (RNCX1/beta-Actin: 0.51 +/- 0.12 vs 0.19 +/- 0.06, P &lt; 0.01; RPLB/beta-Actin: 0.26 +/- 0.12 vs 0.20 +/- 0.08, P &lt; 0.05), while SERCA2 mRNA was downregulated (0.48 +/- 0.10 vs 0.80 +/- 0.11, P &lt; 0.01).	Phosphorus	107-109	actin, beta	Rattus norvegicus	123-133
15899134-14	2005	In CHF-C and CHF-T groups, the protein expression of NCX1 were 1.141 +/- 0.047 and 1.074 +/- 0.081 times of that in PS group respectively (both P &lt; 0.05), and SERCA2 protein levels were 0.803 +/- 0.100 and 0.893 +/- 0.084 times of that in PS group respectively (both P &lt; 0.05).	Phosphorus	116-118	solute carrier family 8 member A1	Rattus norvegicus	53-57
15899134-14	2005	In CHF-C and CHF-T groups, the protein expression of NCX1 were 1.141 +/- 0.047 and 1.074 +/- 0.081 times of that in PS group respectively (both P &lt; 0.05), and SERCA2 protein levels were 0.803 +/- 0.100 and 0.893 +/- 0.084 times of that in PS group respectively (both P &lt; 0.05).	Phosphorus	242-244	solute carrier family 8 member A1	Rattus norvegicus	53-57
15870290-2	2005	Here, we show that bone marrow macrophages of SHIP(-/-) animals have elevated levels of phosphatidylinositol 3,4,5-trisphosphate [PI (3,4,5)P(3)] and displayed higher and more prolonged chemotactic responses to macrophage colony-stimulating factor (M-CSF) and elevated levels of F-actin relative to wild-type macrophages.	Phosphorus	49-50	colony stimulating factor 1	Homo sapiens	211-247
15870290-2	2005	Here, we show that bone marrow macrophages of SHIP(-/-) animals have elevated levels of phosphatidylinositol 3,4,5-trisphosphate [PI (3,4,5)P(3)] and displayed higher and more prolonged chemotactic responses to macrophage colony-stimulating factor (M-CSF) and elevated levels of F-actin relative to wild-type macrophages.	Phosphorus	49-50	colony stimulating factor 1	Homo sapiens	249-254
15785941-13	2005	There was a direct relationship between serum phosphorus concentration and the percentage change in PTH from baseline in both the calcitriol group (r=0.46; P&lt;0.0001) and the placebo group (r=0.21; P=0.0005).	Phosphorus	46-56	parathyroid hormone	Homo sapiens	100-103
15846431-1	2005	The reductive coupling of the bridging phosphide and the adjacent [sigma]-alkynyl moieties in [Pt2(mu-P(t)Bu2){mu,eta1:eta2-C(Ph)CH2}(C[triple bond]C-Ph)(CO)(P(t)Bu2H)(Br)] is promoted by bromide abstraction and is reversed by adding N(n)Bu4Br.	Phosphorus	95-96	secreted phosphoprotein 1	Homo sapiens	114-118
15846431-1	2005	The reductive coupling of the bridging phosphide and the adjacent [sigma]-alkynyl moieties in [Pt2(mu-P(t)Bu2){mu,eta1:eta2-C(Ph)CH2}(C[triple bond]C-Ph)(CO)(P(t)Bu2H)(Br)] is promoted by bromide abstraction and is reversed by adding N(n)Bu4Br.	Phosphorus	95-96	DNA polymerase iota	Homo sapiens	119-123
15740037-1	2005	The effects of soil and foliar phosphorus supplementation on the activities and levels of superoxide dismutase (SOD), guaiacol peroxidase (POX), and ascorbate peroxidase (APX) in tomato fruits were evaluated by determining enzyme activities and isoenzyme analysis.	Phosphorus	31-41	cytosolic ascorbate peroxidase 2	Solanum lycopersicum	149-169
15755664-4	2005	Additionally, cathepsin B exhibits chiral selectivity at the phosphorus center.	Phosphorus	61-71	cathepsin B	Homo sapiens	14-25
15637092-4	2005	The biological relevance of B[a]P and 7,8-diol-B[a]P redistribution by antibody was demonstrated by reversion of B[a]P-induced inhibition of proliferation of human peripheral blood lymphocytes and by inhibition of CYP 1A1 induction in HepG2 cells.	Phosphorus	32-33	cytochrome P450 family 1 subfamily A member 1	Homo sapiens	214-221
15736953-7	2005	Both A-Raf and Raf-1 were found to bind to 3-, 4-, and 5-monophosphorylated phosphoinositides [PI(3)P, PI(4)P, and PI(5)P] as well as phosphatidylinositol 3,5-bisphosphate [PI(3,5)P(2)].	Phosphorus	99-101	A-Raf proto-oncogene, serine/threonine kinase	Homo sapiens	5-10
15736953-7	2005	Both A-Raf and Raf-1 were found to bind to 3-, 4-, and 5-monophosphorylated phosphoinositides [PI(3)P, PI(4)P, and PI(5)P] as well as phosphatidylinositol 3,5-bisphosphate [PI(3,5)P(2)].	Phosphorus	99-101	Raf-1 proto-oncogene, serine/threonine kinase	Homo sapiens	15-20
15531762-8	2005	Serum FGF-23 had a strong correlation with serum inorganic phosphorus controlled by dietary phosphorus in 5/6 nephrectomized rats.	Phosphorus	59-69	fibroblast growth factor 23	Rattus norvegicus	6-12
15716346-4	2005	Nestin cre; Bmpr1a mutants had completely penetrant, bilateral CL/P with arrested tooth formation.	Phosphorus	66-67	bone morphogenetic protein receptor, type 1A	Mus musculus	12-18
16004330-1	2005	A new method to assess phosphorus bioavailability in the sediments and soils was developed by using a homemade iron oxide/ cellulose acetate membrane(FeO/CAM).	Phosphorus	23-33	calmodulin 3	Homo sapiens	154-157
15698460-6	2005	The adjusted rate of parathyroidectomy varied 4-fold across the DOPPS countries, and was significantly associated with baseline concentrations of phosphorus (RR 1.17, P &lt; 0.0001), calcium (RR 1.58, P &lt; 0.0001), calcium-phosphorus product (RR 1.11, P &lt; 0.0001), PTH (RR 1.07, P &lt; 0.0001), and dialysate calcium concentration (RR 0.57, P= 0.03).	Phosphorus	146-156	ribonucleotide reductase catalytic subunit M1	Homo sapiens	158-162
15613480-4	2005	The early embryonic lethality of PS1 and PS2 double knock-out (PS1/2 null) mice prevents the evaluation of physiological roles of PS.	Phosphorus	33-35	presenilin 1	Mus musculus	63-68
15691756-2	2005	(2005) show that N-WASP activation of actin-related protein2/3 (Arp2/3) is ultrasensitive to PI(4,5)P(2) concentration.	Phosphorus	99-101	WASP like actin nucleation promoting factor	Homo sapiens	17-23
15691756-2	2005	(2005) show that N-WASP activation of actin-related protein2/3 (Arp2/3) is ultrasensitive to PI(4,5)P(2) concentration.	Phosphorus	99-101	actin related protein 2	Homo sapiens	38-62
15691756-2	2005	(2005) show that N-WASP activation of actin-related protein2/3 (Arp2/3) is ultrasensitive to PI(4,5)P(2) concentration.	Phosphorus	99-101	actin related protein 2	Homo sapiens	64-70
15514034-7	2005	Mice with genetic deletion of the calcineurin Abeta gene had markedly increased PTH mRNA levels that were still regulated by low calcium and phosphorus diets.	Phosphorus	141-151	parathyroid hormone	Mus musculus	80-83
15900896-2	2005	The milk from cows infected with subclinical mastitis revealed a significant decrease in potassium (P &lt; 0.001) and a significant increase in sodium and phosphorus content (P &lt; 0.01).	Phosphorus	155-165	Weaning weight-maternal milk	Bos taurus	4-8
15698460-5	2005	Cardiovascular mortality was significantly associated with the serum concentrations of phosphorus (RR 1.09, P &lt; 0.0001), calcium (RR 1.14, P &lt; 0.0001), calcium-phosphorus product (RR 1.05, P &lt; 0.0001), and PTH (RR 1.02, P= 0.03).	Phosphorus	87-97	ribonucleotide reductase catalytic subunit M1	Homo sapiens	99-103
15540112-0	2005	Viable, apoptotic and necrotic monocytes expose phosphatidylserine: cooperative binding of the ligand Annexin V to dying but not viable cells and implications for PS-dependent clearance.	Phosphorus	163-165	annexin A5	Homo sapiens	102-111
15536160-17	2005	We suggest that PS is a more sensitive marker for insulin resistance during hyperinsulinemia than limb flow.	Phosphorus	16-18	insulin	Homo sapiens	50-57
15692183-0	2005	[The effects of phosphorus, glucose and cytokinin on SEN1 gene expression in Arabidopsis].	Phosphorus	16-26	splicing endonuclease 1	Arabidopsis thaliana	53-57
15531762-0	2005	Circulating FGF-23 is regulated by 1alpha,25-dihydroxyvitamin D3 and phosphorus in vivo.	Phosphorus	69-79	fibroblast growth factor 23	Rattus norvegicus	12-18
15531762-11	2005	Taken together, this shows that both serum phosphorus and 1alpha,25(OH)(2)D(3) regulate circulating FGF-23 independent of each other.	Phosphorus	43-53	fibroblast growth factor 23	Rattus norvegicus	100-106
15598562-3	2005	A molecular modeling (docking) study showed that the p-MeSO2NH group present in (Z)-8d inserts deep inside the 2 degrees-pocket of the COX-2 binding site, it undergoes a hydrophobic interaction with Ala516 and Gly519, and one of the O-atoms of the MeSO2 group participates in a weak hydrogen bonding interaction with the NH2 of Arg513 (distance= 3.85 angstroms).	Phosphorus	53-54	prostaglandin-endoperoxide synthase 2	Homo sapiens	135-140
15558496-3	2005	Mutations in the gene for interferon regulatory factor 6 (IRF6) have been shown to be the cause of Van der Woude syndrome, a dominant disorder that has CL/P as a common feature.	Phosphorus	155-156	interferon regulatory factor 6	Homo sapiens	26-56
15719058-7	2005	On the basis of this finding, we identify P-TEFb-dependent cellular promoters that also recruit TBP in the absence of TAFs.	Phosphorus	42-43	TATA-box binding protein	Homo sapiens	96-99
16839095-3	2005	The syn form has a symmetry plane (C(s)() symmetry) where the lone electron pair of phosphorus points toward the double bonds.	Phosphorus	84-94	synemin	Homo sapiens	4-7
15558496-3	2005	Mutations in the gene for interferon regulatory factor 6 (IRF6) have been shown to be the cause of Van der Woude syndrome, a dominant disorder that has CL/P as a common feature.	Phosphorus	155-156	interferon regulatory factor 6	Homo sapiens	58-62
15354199-12	2005	The change in PTH concentration was negatively correlated with changes in ionized calcium concentration (r=-0.75, P=0.02) and positively correlated with changes in serum phosphorus (r=0.71, P=0.03) only in the LPD group.	Phosphorus	170-180	parathyroid hormone	Homo sapiens	14-17
15668496-9	2005	IGF-I was positively associated with intakes of protein, magnesium, zinc, calcium, potassium, and phosphorus, and IGFBP-3 was positively associated with energy.	Phosphorus	98-108	insulin like growth factor 1	Homo sapiens	0-5
15668496-10	2005	The IGF-I/IGFBP-3 ratio was positively associated with intakes of protein, zinc, and phosphorus.	Phosphorus	85-95	insulin like growth factor 1	Homo sapiens	4-9
15668496-10	2005	The IGF-I/IGFBP-3 ratio was positively associated with intakes of protein, zinc, and phosphorus.	Phosphorus	85-95	insulin like growth factor binding protein 3	Homo sapiens	10-17
16086235-8	2005	Our data demonstrate that B[a]P-induced changes in invasion are mediated through augmented COX-II expression and PGE(2) production involving an AhR regulated pathway.	Phosphorus	30-31	aryl hydrocarbon receptor	Homo sapiens	144-147
15917991-5	2005	MCP-1-stimulated A7r5 migration was completely blocked by the NAD(P)H oxidase inhibitor, diphenylene iodonium (DPI), and dose-dependently inhibited by polyethylene glycol-conjugated superoxide dismutase (PEG-SOD), suggesting a role for reactive oxygen species (ROS) in this process.	Phosphorus	66-68	C-C motif chemokine ligand 2	Rattus norvegicus	0-5
15632449-7	2005	The Mramp-KO phagosome showed a significant increase of P, Ca, Mn, Fe and Zn concentrations between 1 and 24 h after infection, while the concentrations of K and Ni decreased.	Phosphorus	56-57	divalent metal cation transporter MntH	Mycobacterium tuberculosis H37Rv	4-9
15757719-10	2005	PIP is the dominant form of phosphorus in river water, but leaves the estuary more evenly distributed between all forms.	Phosphorus	28-38	prolactin induced protein	Homo sapiens	0-3
16114688-5	2005	The removed sludge of AP1 and AP2 was characterized as rich sludge in volatile solids and with low stabilization, there was a great accumulation of the total phosphorus in the sludge of AP2.	Phosphorus	158-168	JunB proto-oncogene, AP-1 transcription factor subunit	Homo sapiens	22-25
15540261-1	2004	The magnetic interaction and spin transfer via phosphorus have been investigated for the tri-tert-butylaminoxyl para-substituted triphenylphosphine oxide.	Phosphorus	47-57	spindlin 1	Homo sapiens	29-33
15540261-6	2004	These techniques established in particular that spin density is located at the phosphorus (rho=-15x10(-3) au), that its sign is in line with the sign alternation principle and that its magnitude is in the order of that found on the aromatic C atoms of the molecule.	Phosphorus	79-89	spindlin 1	Homo sapiens	48-52
16114688-5	2005	The removed sludge of AP1 and AP2 was characterized as rich sludge in volatile solids and with low stabilization, there was a great accumulation of the total phosphorus in the sludge of AP2.	Phosphorus	158-168	transcription factor AP-2 alpha	Homo sapiens	30-33
16042245-11	2005	The apparent progressive slowing of the MRP removal rate throughout the treatment of the five batches may have implications for the sustainable use of this technology for phosphorus control.	Phosphorus	171-181	ATP binding cassette subfamily C member 1	Homo sapiens	40-43
16114688-5	2005	The removed sludge of AP1 and AP2 was characterized as rich sludge in volatile solids and with low stabilization, there was a great accumulation of the total phosphorus in the sludge of AP2.	Phosphorus	158-168	transcription factor AP-2 alpha	Homo sapiens	186-189
15581351-5	2004	We investigated the ability of human Arf1.GDP (Arf1.GDP) to bind myo-inositol (1,4,5)-trisphosphate (I(1,4,5)P(3)), the soluble headgroup for PI(4,5)P(2), and a short acyl-chain soluble PI(4,5)P(2) analogue using heteronuclear single quantum coherence (HSQC)-based NMR techniques.	Phosphorus	108-110	ADP ribosylation factor 1	Homo sapiens	37-41
15581351-5	2004	We investigated the ability of human Arf1.GDP (Arf1.GDP) to bind myo-inositol (1,4,5)-trisphosphate (I(1,4,5)P(3)), the soluble headgroup for PI(4,5)P(2), and a short acyl-chain soluble PI(4,5)P(2) analogue using heteronuclear single quantum coherence (HSQC)-based NMR techniques.	Phosphorus	108-110	ADP ribosylation factor 1	Homo sapiens	47-51
15618618-1	2004	This study investigates the phosphorus (P) homeostasis in the process of an altered parathyroid hormone (PTH) action in the kidney of rats fed a high P diet.	Phosphorus	28-38	parathyroid hormone	Rattus norvegicus	84-103
15618618-0	2004	Decreased mRNA expression of the PTH/PTHrP receptor and type II sodium-dependent phosphate transporter in the kidney of rats fed a high phosphorus diet accompanied with a decrease in serum calcium concentration.	Phosphorus	136-146	parathyroid hormone	Rattus norvegicus	33-36
15669316-5	2004	Phosphorus sorption maxima for both Fe- and Al-based WTRs exceeded 9100 mg of P kg(-1) and required a greater specific surface area (SSA) than would be available based on BET-N2 calculations.	Phosphorus	0-10	delta/notch like EGF repeat containing	Homo sapiens	171-174
15618618-0	2004	Decreased mRNA expression of the PTH/PTHrP receptor and type II sodium-dependent phosphate transporter in the kidney of rats fed a high phosphorus diet accompanied with a decrease in serum calcium concentration.	Phosphorus	136-146	parathyroid hormone-like hormone	Rattus norvegicus	37-42
15618618-1	2004	This study investigates the phosphorus (P) homeostasis in the process of an altered parathyroid hormone (PTH) action in the kidney of rats fed a high P diet.	Phosphorus	28-38	parathyroid hormone	Rattus norvegicus	105-108
15595334-10	2004	CONCLUSION: Parathyroid hormone is the major regulator of serum phosphorus concentrations in patients with primary hyperparathyroidism.	Phosphorus	64-74	parathyroid hormone	Homo sapiens	12-31
15590969-2	2004	In normal individuals, circulating serum-levels of MEPE are tightly correlated with serum-phosphorus, parathyroid hormone (PTH) and bone mineral density (BMD).	Phosphorus	90-100	matrix extracellular phosphoglycoprotein with ASARM motif (bone)	Mus musculus	51-55
15557261-5	2004	A putative orientation for the phosphorylcholine head group of the ASM substrate, sphingomyelin (SM), was made based on the predicted catalysis of the phosphorus-oxygen bond in the active site of ASM and on a structural comparison of the PAP-phosphate complex to the C-reactive protein-phosphorylcholine complex.	Phosphorus	151-161	sphingomyelin phosphodiesterase 1	Homo sapiens	67-70
15557261-5	2004	A putative orientation for the phosphorylcholine head group of the ASM substrate, sphingomyelin (SM), was made based on the predicted catalysis of the phosphorus-oxygen bond in the active site of ASM and on a structural comparison of the PAP-phosphate complex to the C-reactive protein-phosphorylcholine complex.	Phosphorus	151-161	sphingomyelin phosphodiesterase 1	Homo sapiens	196-199
25175613-12	2004	Genetic polymorphism of CYP2E1 and ALDH2 did not affect urinary methylhippuric acid level in the exposed group (p&amp;gt; 0.05).	Phosphorus	8-9	cytochrome P450 family 2 subfamily E member 1	Homo sapiens	24-30
15663548-11	2004	As in the case of PTH, calcium and phosphorus showed dose-dependent increases.	Phosphorus	35-45	parathyroid hormone	Homo sapiens	18-21
15505825-2	2004	We used phosphorus magnetic resonance spectroscopy to assess calf muscle oxidative metabolism in six patients from two unrelated families carrying the c.2708-2711delTTAG deletion in exon 27 of the OPA1 gene.	Phosphorus	8-18	OPA1 mitochondrial dynamin like GTPase	Homo sapiens	197-201
15297370-1	2004	Several members of the P450 family, including cytochrome P450 1B1 (CYP1B1), can convert tobacco smoke (TS) procarcinogens, including benzo[a]pyrene (B[a]P), to carcinogenic intermediates.	Phosphorus	23-24	cytochrome P450 family 1 subfamily B member 1	Homo sapiens	67-73
15390134-2	2004	The single-crystal X-ray structure of the complexed 1,7-methano-3-phospha[11]annulene (6 c) shows a syn-W(CO)5 group at the exo bent phosphorus.	Phosphorus	133-143	synemin	Homo sapiens	100-103
15533211-7	2004	But in 9 families with left and bilateral CL/P, two-point Zmax for APOC2[AC1/AC2] was 1.701 and multi-point Zmax at APOC2 locus was 1.909.	Phosphorus	45-46	apolipoprotein C2	Homo sapiens	67-72
15533211-7	2004	But in 9 families with left and bilateral CL/P, two-point Zmax for APOC2[AC1/AC2] was 1.701 and multi-point Zmax at APOC2 locus was 1.909.	Phosphorus	45-46	long intergenic non-protein coding RNA 1587	Homo sapiens	73-76
15533211-7	2004	But in 9 families with left and bilateral CL/P, two-point Zmax for APOC2[AC1/AC2] was 1.701 and multi-point Zmax at APOC2 locus was 1.909.	Phosphorus	45-46	adenylate cyclase 2	Homo sapiens	77-80
15456534-3	2004	Activity of PKC and PKA were assayed by transferring phosphorus (32P) into substrate after treatment with IFN-gamma 1000 kU/L at 10, 30, 60, and 120 min.	Phosphorus	53-63	proline rich transmembrane protein 2	Homo sapiens	12-15
15294912-7	2004	Immunohistochemistry for Akt-p-Ser473 revealed a low level of this active kinase in Min/+ and WT enterocytes and its strong presence in tumors.	Phosphorus	29-30	thymoma viral proto-oncogene 1	Mus musculus	25-28
15504146-2	2004	In the present study, we have examined the effect of a low protein, low phosphorus diet on circulating levels of leptin, tumour necrosis factor (TNF)-alpha, and insulin in patients with CRF.	Phosphorus	72-82	leptin	Homo sapiens	113-119
15169678-7	2004	Energy-filtering EM demonstrated that CCT-alpha bound to phosphorus-rich (phospholipid) structures in the glycogen.	Phosphorus	57-67	phosphate cytidylyltransferase 1, choline, alpha isoform	Mus musculus	38-47
16701529-0	2004	Influence of nitrate and COD on phosphorus, nitrogen and dinitrotoluene (DNT) removals under batch anaerobic and anoxic conditions.	Phosphorus	32-42	small nuclear ribonucleoprotein polypeptides B and B1	Homo sapiens	25-28
15333644-7	2004	External phosphorus markedly affected influx: roots averaged 5, 16, and 34 pmol P min(-1) in the apical 20 mm when exposed to 1, 5, and 10 microM P solutions, respectively.	Phosphorus	9-19	CD59 molecule (CD59 blood group)	Homo sapiens	82-88
15516868-4	2004	The APTT was prolonged on the PU-C-H and PU-P-H, suggesting the binding of immobilized heparin to the antithrombin III.	Phosphorus	5-6	serpin family C member 1	Homo sapiens	102-118
15528855-9	2004	As with the PKC activity, inhibition by sphingosine of phosphorylation of the 56-kDa protein and 36-kDa annexin I was reversed by the excess addition of PS, but not by OAG or Ca2+.	Phosphorus	153-155	annexin A1	Bos taurus	104-113
15504146-8	2004	CONCLUSIONS: A low protein, low phosphorus diet reduces TNF-alpha and leptin levels in plasma.	Phosphorus	32-42	tumor necrosis factor	Homo sapiens	56-65
15504146-8	2004	CONCLUSIONS: A low protein, low phosphorus diet reduces TNF-alpha and leptin levels in plasma.	Phosphorus	32-42	leptin	Homo sapiens	70-76
15332221-6	2004	RESULTS: Preoperative FGF-23 levels correlated positively with phosphorus (P &lt; 0.05), calcium-phosphorus product (Ca x P; P &lt; 0.0005), and PTH values (P &lt; 0.05).	Phosphorus	63-73	fibroblast growth factor 23	Homo sapiens	22-28
15466235-6	2004	In vesicle-binding assays, PATL1 bound to specific phosphoinositides, important regulators of membrane trafficking, with a preference for phosphatidylinositol(5)P, phosphatidylinositol(4,5)P(2), and phosphatidylinositol(3)P. Taken together, these findings suggest a role for PATL1 in membrane-trafficking events associated with cell-plate expansion or maturation and point to the involvement of phosphoinositides in cell-plate biogenesis.	Phosphorus	160-162	PATELLIN 1	Arabidopsis thaliana	27-32
15514862-6	2004	The chemical components analysis showed that the Ca/P ratio of TCP/HA coating was lower than that of HA coating.	Phosphorus	52-53	serine peptidase inhibitor Kazal type 1	Homo sapiens	63-66
15308378-2	2004	Coculture of mouse splenic adherent cells with ovalbumin (OVA)-specific Th1 clone (42-6A) cells in the presence of PS-liposomes encapsulating OVA resulted in high levels of IL-12 and IFN-gamma productions compared with those of positively charged or neutral liposomes.	Phosphorus	115-117	interferon gamma	Mus musculus	183-192
15332221-9	2004	Furthermore, FGF-23 levels days 1 and 3 correlated linearly with serum phosphorus (P &lt; 0.05; P &lt; 0.005, respectively) and Ca x P values (P &lt; 0.01; P &lt; 0.0001, respectively).	Phosphorus	71-81	fibroblast growth factor 23	Homo sapiens	13-19
15332221-10	2004	CONCLUSION: FGF-23 levels correlate positively with serum phosphorus, Ca x P, and PTH values in patients with advanced secondary hyperparathyroidism.	Phosphorus	58-68	fibroblast growth factor 23	Homo sapiens	12-18
15332221-10	2004	CONCLUSION: FGF-23 levels correlate positively with serum phosphorus, Ca x P, and PTH values in patients with advanced secondary hyperparathyroidism.	Phosphorus	75-76	fibroblast growth factor 23	Homo sapiens	12-18
15356053-1	2004	The Identification and characterization of FGF-23 has provided an opportunity to gain new insight into phosphorus metabolism.	Phosphorus	103-113	fibroblast growth factor 23	Homo sapiens	43-49
15356053-2	2004	Circulating FGF-23 promotes renal excretion of phosphorus, and FGF-23 is measurable in the serum of normal subjects.	Phosphorus	47-57	fibroblast growth factor 23	Homo sapiens	12-18
15356053-10	2004	In conclusion, serum FGF-23 levels are elevated in patients with hyperphosphatemia and chronic hypoparathyroidism, suggesting a feedback system in which serum FGF-23 responds to serum phosphorus and regulates it.	Phosphorus	184-194	fibroblast growth factor 23	Homo sapiens	21-27
15356053-10	2004	In conclusion, serum FGF-23 levels are elevated in patients with hyperphosphatemia and chronic hypoparathyroidism, suggesting a feedback system in which serum FGF-23 responds to serum phosphorus and regulates it.	Phosphorus	184-194	fibroblast growth factor 23	Homo sapiens	159-165
15461740-2	2004	Data from the literature show that the majority of dialysis patients treated with traditional calcium-containing phosphorus binders and vitamin D or vitamin D analogue preparations have serum parathyroid hormone (PTH), calcium, and phosphorus levels outside these strict K/DOQI target ranges.	Phosphorus	113-123	parathyroid hormone	Homo sapiens	192-211
15197152-1	2004	BACKGROUND: We previously reported that 20% of women with chest pain but without obstructive coronary artery disease (CAD) had stress-induced reduction in myocardial phosphocreatine-adenosine triphosphate ratio by phosphorus-31 nuclear magnetic resonance spectroscopy (abnormal MRS), consistent with myocardial ischemia.	Phosphorus	214-224	MROS	Homo sapiens	278-281
15292364-0	2004	Serum levels of matrix extracellular phosphoglycoprotein (MEPE) in normal humans correlate with serum phosphorus, parathyroid hormone and bone mineral density.	Phosphorus	102-112	matrix extracellular phosphoglycoprotein	Homo sapiens	16-56
15292364-0	2004	Serum levels of matrix extracellular phosphoglycoprotein (MEPE) in normal humans correlate with serum phosphorus, parathyroid hormone and bone mineral density.	Phosphorus	102-112	matrix extracellular phosphoglycoprotein	Homo sapiens	58-62
15292364-5	2004	MEPE levels were also significantly correlated with serum phosphorus and parathyroid hormone (PTH).	Phosphorus	58-68	matrix extracellular phosphoglycoprotein	Homo sapiens	0-4
15260685-0	2004	Phosphorus hyperfine structure in the electronic spectrum of the HPCl free radical.	Phosphorus	0-10	2-hydroxyacyl-CoA lyase 1	Homo sapiens	65-69
15314220-6	2004	(131)I-P-GUS was transported across the BBB after i.v.	Phosphorus	7-8	glucuronidase, beta	Mus musculus	9-12
15254624-2	2004	Reagent, based on the novel phosphorus heterocycle 1,1,3,3-tetraphenyl-2-oxa-1,3-diphospholanium bis(trifluoromethanesulfonate), was found to be a useful reagent for ester and amide formation.	Phosphorus	28-38	OXA1L mitochondrial inner membrane protein	Homo sapiens	73-78
15222785-1	2004	OBJECTIVE: Transforming growth factor-alpha (TGFA) was the first gene suggested to be associated with nonsyndromic cleft lip, cleft palate, or both (CL/ P).	Phosphorus	153-154	tumor necrosis factor	Homo sapiens	11-43
15222785-1	2004	OBJECTIVE: Transforming growth factor-alpha (TGFA) was the first gene suggested to be associated with nonsyndromic cleft lip, cleft palate, or both (CL/ P).	Phosphorus	153-154	transforming growth factor alpha	Homo sapiens	45-49
15222785-8	2004	RESULTS: The TGFA genotype distribution was very similar in patients with CL/P ascertained in the three different regions of Brazil.	Phosphorus	77-78	transforming growth factor alpha	Homo sapiens	13-17
15199292-8	2004	Bone morphogenetic protein 7 is broadly efficacious in renal osteodystrophy, and importantly increases the skeletal deposition of ingested phosphorus and calcium, improving ion homeostasis in chronic kidney disease.	Phosphorus	139-149	bone morphogenetic protein 7	Homo sapiens	0-28
15054400-1	2004	The 677 C --&gt; T polymorphism in the 5-10 methylenetetrahydrofolate reductase (MTHFR) gene has been associated with nonsyndromic cleft lip with or without cleft palate (CL/P) in some populations, but not others.	Phosphorus	174-175	methylenetetrahydrofolate reductase	Homo sapiens	81-86
15182206-4	2004	The mechanism is inspired by the chain-fold similarities of Fhit to galactose-1-phosphate uridylyltransferase, which functions by an analogous mechanism, and the observation of overall retention in configuration at phosphorus in the action of Fhit (Abend, A., Garrison, P. N., Barnes, L. D., and Frey, P. A.	Phosphorus	215-225	galactose-1-phosphate uridylyltransferase	Homo sapiens	68-109
15024017-5	2004	Guided by x-ray crystallography, molecular modeling, and enzyme kinetic analyses with wild type and mutant PTPs, we describe the development of a general, low molecular weight, non-peptide, non-phosphorus PTP inhibitor into an inhibitor that displays more than 100-fold selectivity for PTPbeta over PTP1B.	Phosphorus	194-204	6-pyruvoyltetrahydropterin synthase	Homo sapiens	107-111
15024017-5	2004	Guided by x-ray crystallography, molecular modeling, and enzyme kinetic analyses with wild type and mutant PTPs, we describe the development of a general, low molecular weight, non-peptide, non-phosphorus PTP inhibitor into an inhibitor that displays more than 100-fold selectivity for PTPbeta over PTP1B.	Phosphorus	194-204	protein tyrosine phosphatase receptor type U	Homo sapiens	107-110
15024017-5	2004	Guided by x-ray crystallography, molecular modeling, and enzyme kinetic analyses with wild type and mutant PTPs, we describe the development of a general, low molecular weight, non-peptide, non-phosphorus PTP inhibitor into an inhibitor that displays more than 100-fold selectivity for PTPbeta over PTP1B.	Phosphorus	194-204	protein tyrosine phosphatase non-receptor type 1	Homo sapiens	299-304
15182206-4	2004	The mechanism is inspired by the chain-fold similarities of Fhit to galactose-1-phosphate uridylyltransferase, which functions by an analogous mechanism, and the observation of overall retention in configuration at phosphorus in the action of Fhit (Abend, A., Garrison, P. N., Barnes, L. D., and Frey, P. A.	Phosphorus	215-225	fragile histidine triad diadenosine triphosphatase	Homo sapiens	243-247
15086913-9	2004	IGF-I protein and IGF binding protein-3 staining were diminished in both Nx groups without changes in the IGF-I receptor expression; the decline in IGF-I protein expression was much lower in the Nx-phosphorus group.	Phosphorus	198-208	insulin-like growth factor 1	Rattus norvegicus	0-5
15189355-7	2004	Interestingly, these immature Nct variants selectively bound to APH-1, suggesting a stable Nct/APH-1 interaction independent of PS and PEN-2.	Phosphorus	128-130	aph-1 homolog A, gamma-secretase subunit	Homo sapiens	64-69
15189355-9	2004	Taken together, our findings suggest that immature Nct can stably interact with APH-1 to form a potential scaffold for binding of PS and PEN-2.	Phosphorus	130-132	aph-1 homolog A, gamma-secretase subunit	Homo sapiens	80-85
15169877-1	2004	The HEXIM1 protein inhibits the kinase activity of P-TEFb (CDK9/cyclin T) to suppress RNA polymerase II transcriptional elongation in a process that specifically requires the 7SK snRNA, which mediates the interaction of HEXIM1 with P-TEFb.	Phosphorus	51-52	HEXIM P-TEFb complex subunit 1	Homo sapiens	4-10
15169877-1	2004	The HEXIM1 protein inhibits the kinase activity of P-TEFb (CDK9/cyclin T) to suppress RNA polymerase II transcriptional elongation in a process that specifically requires the 7SK snRNA, which mediates the interaction of HEXIM1 with P-TEFb.	Phosphorus	51-52	cyclin dependent kinase 9	Homo sapiens	59-63
15169877-1	2004	The HEXIM1 protein inhibits the kinase activity of P-TEFb (CDK9/cyclin T) to suppress RNA polymerase II transcriptional elongation in a process that specifically requires the 7SK snRNA, which mediates the interaction of HEXIM1 with P-TEFb.	Phosphorus	51-52	HEXIM P-TEFb complex subunit 1	Homo sapiens	220-226
15139762-6	2004	Detailed studies demonstrated that the inhibitory effect against BChE is dependent on the nucleoside analogue, the substitution pattern of the cycloSal-moiety, and particularly on the stereochemistry at the phosphorus atom.	Phosphorus	207-217	butyrylcholinesterase	Homo sapiens	65-69
15118109-2	2004	Mice carrying a spontaneous mutation, Dancer (Dc), exhibit CL/P in homozygotes and show significantly increased susceptibility to CL/P in heterozygotes [Deol, M. S. &amp; Lane, P. W. (1966) J. Embryol.	Phosphorus	62-63	T-box 10	Mus musculus	38-44
15118109-2	2004	Mice carrying a spontaneous mutation, Dancer (Dc), exhibit CL/P in homozygotes and show significantly increased susceptibility to CL/P in heterozygotes [Deol, M. S. &amp; Lane, P. W. (1966) J. Embryol.	Phosphorus	62-63	T-box 10	Mus musculus	46-48
15118109-2	2004	Mice carrying a spontaneous mutation, Dancer (Dc), exhibit CL/P in homozygotes and show significantly increased susceptibility to CL/P in heterozygotes [Deol, M. S. &amp; Lane, P. W. (1966) J. Embryol.	Phosphorus	133-134	T-box 10	Mus musculus	38-44
15118109-2	2004	Mice carrying a spontaneous mutation, Dancer (Dc), exhibit CL/P in homozygotes and show significantly increased susceptibility to CL/P in heterozygotes [Deol, M. S. &amp; Lane, P. W. (1966) J. Embryol.	Phosphorus	133-134	T-box 10	Mus musculus	46-48
15577030-4	2004	Dietary phosphorus should be restricted when the serum levels of i-PTH are elevated above target range of CKD stage.	Phosphorus	8-18	parathyroid hormone	Homo sapiens	67-70
15225829-5	2004	At early stages of renal failure, vitamin D therapy efficiently counteracts uremia- and high phosphorus-induced hyperplasia by inhibiting the increases in parathyroid-TGFalpha/EGFR co-expression.	Phosphorus	93-103	transforming growth factor alpha	Homo sapiens	167-175
15225829-5	2004	At early stages of renal failure, vitamin D therapy efficiently counteracts uremia- and high phosphorus-induced hyperplasia by inhibiting the increases in parathyroid-TGFalpha/EGFR co-expression.	Phosphorus	93-103	epidermal growth factor receptor	Homo sapiens	176-180
15165541-15	2004	The use of drugs did not differ in the two groups, except for lower intake of phosphorus binders and antihypertensive drugs among RLS patients.	Phosphorus	78-88	RLS1	Homo sapiens	130-133
15056012-0	2004	Macrocyclization in the design of non-phosphorus-containing Grb2 SH2 domain-binding ligands.	Phosphorus	38-48	growth factor receptor bound protein 2	Homo sapiens	60-64
14557885-6	2004	Hypoxia (H+P) per se, compared to C+P, induced a significant increase in %GSSG (5.68 vs. 1.14%), TBARS (436.7 vs. 227.9 nM), NAG (4.49 vs. 3.35 U/mg) and HSP70 (178.7 vs. 100%).	Phosphorus	11-12	O-GlcNAcase	Mus musculus	125-128
15003013-2	2004	Temperature-responsive poly(N-isopropylacrylamide-co-2-carboxyisopropylacrylamide) (P(IPAAm-co-CIPAAm)) copolymer grafted onto tissue culture grade polystyrene (TCPS) dishes permits RGDS immobilization.	Phosphorus	84-86	ral guanine nucleotide dissociation stimulator	Homo sapiens	182-186
14557885-6	2004	Hypoxia (H+P) per se, compared to C+P, induced a significant increase in %GSSG (5.68 vs. 1.14%), TBARS (436.7 vs. 227.9 nM), NAG (4.49 vs. 3.35 U/mg) and HSP70 (178.7 vs. 100%).	Phosphorus	11-12	heat shock protein 1B	Mus musculus	154-159
15228213-6	2004	The dietary intakes of Ca, Mg and P ranged from 4.83-23.58, 2.44-7.83 and 13.46-45.69 mg/ kg BW/d, respectively.	Phosphorus	34-35	SMU1 DNA replication regulator and spliceosomal factor	Homo sapiens	93-97
14977836-2	2004	To gain insight into possible roles for P-Ser(118)-ERalpha in human breast cancer in vivo.	Phosphorus	40-41	estrogen receptor 1	Homo sapiens	51-58
14977836-3	2004	EXPERIMENTAL DESIGN: A specific antibody for P-Ser(118)-ERalpha was validated for immunohistochemistry (IHC), and Western blot analysis confirmed IHC results.	Phosphorus	2-3	estrogen receptor 1	Homo sapiens	56-63
15065894-7	2004	In normal perilesional skin, OCT identifies epidermal and dermal structure; PS-OCT identified dermal birefringence.	Phosphorus	76-78	plexin A2	Homo sapiens	79-82
14755461-12	2004	Previous studies have also found linkage of NS CL/P to 4q31 and 6p23.	Phosphorus	0-1	nescient helix-loop-helix 1	Homo sapiens	44-49
15630249-1	2004	To determine the parathyroid hormone (PTH) action on kidney and bone by high phosphorus (P) diet, this study investigated PTH/PTH-related peptide (PTHrP) receptor mRNA expression in 6-week-old parathyroidectomized (PTX) rats received constant amount of PTH.	Phosphorus	77-87	parathyroid hormone	Rattus norvegicus	17-36
14964364-2	2004	The degree of phosphorus saturation (DPS), which relates a measure of P already adsorbed by a soil to its P adsorption capacity, could be a good indicator of that soil"s P release capability.	Phosphorus	14-24	decaprenyl diphosphate synthase subunit 1	Homo sapiens	37-40
15268792-4	2004	Milk is a source of calcium, phosphorus, zinc, magnesium and vitamin B2 and B12.	Phosphorus	29-39	Weaning weight-maternal milk	Bos taurus	0-4
14745193-1	2004	In this study, we ascertained whether the parathyroid hormone (PTH) dominantly regulated the effects of high phosphorus (P) intakes on urinary excretion of P and bone metabolism in rats.	Phosphorus	109-119	parathyroid hormone	Rattus norvegicus	42-61
14765820-0	2004	Effect of dietary phosphorus on performance of lactating dairy cows: milk production and cow health.	Phosphorus	18-28	Weaning weight-maternal milk	Bos taurus	69-73
15139213-5	2004	The pool of elements was 78.483 kg.hm-2 N, 3.843 kg.hm-2 P, 48.205 kg.hm-2 K, 23.115 kg.hm-2 Ca, 13.157 kg.hm-2 Na, 30.554 kg.hm-2 Fe, 2.113 kg.hm-2 Mn and 27.513 kg.hm-2 Mg.	Phosphorus	57-58	cholinergic receptor muscarinic 2	Homo sapiens	52-56
15283317-9	2004	There was a significant decrease in the average PTH levels (pre 234.9 +/- 285 vs. post 174 +/- 174 p&lt; 0.0001) PTH&gt;300 pg/ml (pre 23.7% vs. post 16.4% p&lt;0.001) calcium levels (pre 10.02 +/- 0.99 vs. 9.83 +/- 0.88 p&lt;0.001), phosphorus (pre 5.50 +/- 1.55 vs. post 5.01 +/- 1.47 p&lt;0.001) as well as serum calcium levels &gt;11 mg/dl (pre 14.6% vs. post 11% p&lt;0.001) and phosphorus &gt;6 g/dl (pre 34% post 21.5% p&lt;0.001).	Phosphorus	234-244	parathyroid hormone	Homo sapiens	48-51
15283317-9	2004	There was a significant decrease in the average PTH levels (pre 234.9 +/- 285 vs. post 174 +/- 174 p&lt; 0.0001) PTH&gt;300 pg/ml (pre 23.7% vs. post 16.4% p&lt;0.001) calcium levels (pre 10.02 +/- 0.99 vs. 9.83 +/- 0.88 p&lt;0.001), phosphorus (pre 5.50 +/- 1.55 vs. post 5.01 +/- 1.47 p&lt;0.001) as well as serum calcium levels &gt;11 mg/dl (pre 14.6% vs. post 11% p&lt;0.001) and phosphorus &gt;6 g/dl (pre 34% post 21.5% p&lt;0.001).	Phosphorus	384-394	parathyroid hormone	Homo sapiens	48-51
14681835-10	2004	However, in carriers of the Ala allele the association of P:S ratio with fasting insulin was modified by activity level (interaction P = 0.038).	Phosphorus	58-59	insulin	Homo sapiens	81-88
15139213-5	2004	The pool of elements was 78.483 kg.hm-2 N, 3.843 kg.hm-2 P, 48.205 kg.hm-2 K, 23.115 kg.hm-2 Ca, 13.157 kg.hm-2 Na, 30.554 kg.hm-2 Fe, 2.113 kg.hm-2 Mn and 27.513 kg.hm-2 Mg.	Phosphorus	57-58	cholinergic receptor muscarinic 2	Homo sapiens	52-56
15139213-5	2004	The pool of elements was 78.483 kg.hm-2 N, 3.843 kg.hm-2 P, 48.205 kg.hm-2 K, 23.115 kg.hm-2 Ca, 13.157 kg.hm-2 Na, 30.554 kg.hm-2 Fe, 2.113 kg.hm-2 Mn and 27.513 kg.hm-2 Mg.	Phosphorus	57-58	cholinergic receptor muscarinic 2	Homo sapiens	52-56
15139213-5	2004	The pool of elements was 78.483 kg.hm-2 N, 3.843 kg.hm-2 P, 48.205 kg.hm-2 K, 23.115 kg.hm-2 Ca, 13.157 kg.hm-2 Na, 30.554 kg.hm-2 Fe, 2.113 kg.hm-2 Mn and 27.513 kg.hm-2 Mg.	Phosphorus	57-58	cholinergic receptor muscarinic 2	Homo sapiens	52-56
15139213-5	2004	The pool of elements was 78.483 kg.hm-2 N, 3.843 kg.hm-2 P, 48.205 kg.hm-2 K, 23.115 kg.hm-2 Ca, 13.157 kg.hm-2 Na, 30.554 kg.hm-2 Fe, 2.113 kg.hm-2 Mn and 27.513 kg.hm-2 Mg.	Phosphorus	57-58	cholinergic receptor muscarinic 2	Homo sapiens	52-56
15139213-5	2004	The pool of elements was 78.483 kg.hm-2 N, 3.843 kg.hm-2 P, 48.205 kg.hm-2 K, 23.115 kg.hm-2 Ca, 13.157 kg.hm-2 Na, 30.554 kg.hm-2 Fe, 2.113 kg.hm-2 Mn and 27.513 kg.hm-2 Mg.	Phosphorus	57-58	cholinergic receptor muscarinic 2	Homo sapiens	52-56
15139213-5	2004	The pool of elements was 78.483 kg.hm-2 N, 3.843 kg.hm-2 P, 48.205 kg.hm-2 K, 23.115 kg.hm-2 Ca, 13.157 kg.hm-2 Na, 30.554 kg.hm-2 Fe, 2.113 kg.hm-2 Mn and 27.513 kg.hm-2 Mg.	Phosphorus	57-58	cholinergic receptor muscarinic 2	Homo sapiens	52-56
14972007-15	2003	Non-significant increases in phosphorus levels were observed in the NaP group.	Phosphorus	29-39	catenin beta like 1	Homo sapiens	68-71
14613129-1	2003	Thermal reaction of white phosphorus with [(triphos)RhH(3)] (1) in THF affords [(triphos)Rh(eta(1):eta(2)-P(4)H)] (2), triphos=MeC(CH(2)PPh(2))(3).	Phosphorus	20-36	C-C motif chemokine ligand 28	Homo sapiens	127-130
14623063-8	2003	The values of circulating OPG also correlated significantly with those of serum calcium (Ca) and phosphorus (P) (r = 0.65 and 0.72, P &lt; 0.01).	Phosphorus	97-107	TNF receptor superfamily member 11b	Homo sapiens	26-29
14599789-8	2003	However, the IFN-beta promoter was not activated in cells that were first preinfected for 1 h with rSV5-WT and then subsequently infected with rSV5-P/V-CPI-.	Phosphorus	148-149	interferon beta 1	Homo sapiens	13-21
14511659-5	2003	On the other hand, treatment of klotho mice with low phosphorus diet results in partial decrease in STC2 gene expression with normalization of hyperphosphatemia.	Phosphorus	53-63	klotho	Mus musculus	32-38
14529268-8	2003	In this report, we have performed a kinetic study with dog and human gastric lipases (DGL and HGL, respectively) using several phosphonate inhibitors by varying the absolute configuration of the phosphorus atom and the chain length of the alkyl/alkoxy substituents.	Phosphorus	195-205	lipase F, gastric type	Homo sapiens	69-97
14568069-1	2003	myo-Inositol-1,2,3,4,5,6-hexakisphosphate (Ins P(6)) was first described as an abundant form of phosphorus in plant seeds and other plant tissues and dubbed "phytic acid".	Phosphorus	96-106	S100 calcium binding protein A12	Homo sapiens	47-51
14511659-5	2003	On the other hand, treatment of klotho mice with low phosphorus diet results in partial decrease in STC2 gene expression with normalization of hyperphosphatemia.	Phosphorus	53-63	stanniocalcin 2	Mus musculus	100-104
12816744-1	2003	Mammalian type II sodium-phosphate cotransporter (NaPi-II) and inorganic phosphate uptake stimulator (PiUS) genes are upregulated by dietary phosphorus (P) restriction to increase intestinal and renal P transport, but little is known about NaPi-II and PiUS regulation in other vertebrates.	Phosphorus	141-151	inositol hexakisphosphate kinase 2	Oncorhynchus mykiss	102-106
14520624-6	2003	Intact parathyroid hormone (PTH) levels decreased significantly after treatment (from 950.5 +/- 448.1 to 532.0 +/- 393.2 pg/mL [ng/L], P &lt; 0.05), and the serum calcium and phosphorus levels as well as all bone metabolic parameters had improved.	Phosphorus	175-185	parathyroid hormone	Homo sapiens	7-26
12816744-1	2003	Mammalian type II sodium-phosphate cotransporter (NaPi-II) and inorganic phosphate uptake stimulator (PiUS) genes are upregulated by dietary phosphorus (P) restriction to increase intestinal and renal P transport, but little is known about NaPi-II and PiUS regulation in other vertebrates.	Phosphorus	141-151	inositol hexakisphosphate kinase 2	Oncorhynchus mykiss	252-256
15012693-5	2003	To prevent hypercalcemia, non-calcium containing phosphorus binder (sevelamer hydrochloride) and vitamin D analogues, which suppress PTH secretion with minimum calcemic action, have been developed.	Phosphorus	49-59	parathyroid hormone	Homo sapiens	133-136
14580347-4	2003	P-TEFb was inhibited by the HEXIM1 protein in a process that specifically required 7SK for mediating the HEXIM1:P-TEFb interaction.	Phosphorus	0-1	HEXIM P-TEFb complex subunit 1	Homo sapiens	28-34
14580347-4	2003	P-TEFb was inhibited by the HEXIM1 protein in a process that specifically required 7SK for mediating the HEXIM1:P-TEFb interaction.	Phosphorus	0-1	HEXIM P-TEFb complex subunit 1	Homo sapiens	105-111
14733418-9	2003	There was a significant positive correlation between changes of phosphorus and PTH-1-84 (tau=0.48; p=0.007) or PTH-7-84 concentration (tau=0.43; p=0.02).	Phosphorus	64-74	parathyroid hormone	Homo sapiens	79-82
14499533-10	2003	The AAPBe concentrations are linearly correlated with the concentrations of suspended sediment, particulate organic carbon, particulate nitrogen, particulate phosphorus, and the AAP for several transition metals (Al, Co, Cr, Fe, Mn, Ni and Y), and the lanthanides.	Phosphorus	158-168	serpin family F member 2	Homo sapiens	4-7
14604115-3	2003	CZE of serum Tf was carefully evaluated using the P/ACE MDQ with fused-silica capillaries of 50 microm I.D.	Phosphorus	50-51	transferrin	Homo sapiens	13-15
12878216-0	2003	Structural basis for a non-phosphorus-containing cyclic peptide binding to Grb2-SH2 domain with high affinity.	Phosphorus	27-37	growth factor receptor bound protein 2	Homo sapiens	75-79
12878216-4	2003	To understand the structural basis for the high-affinity binding of these novel non-phosphorus-containing inhibitors to the Grb2-SH2 domain, we extensively studied herein the unique functional requirements of the acidic side chain in Tyr-2 position due to the absence of the phosphate group in these non-phosphorylated peptides.	Phosphorus	84-94	growth factor receptor bound protein 2	Homo sapiens	124-128
12875848-0	2003	The course of phosphorus in the reaction of N-acetyl-L-glutamate kinase, determined from the structures of crystalline complexes, including a complex with an AlF(4)(-) transition state mimic.	Phosphorus	14-24	N-acetyl-alpha-glucosaminidase	Homo sapiens	44-64
12874449-5	2003	It was independent of the conserved canonical PKC consensus sites in hOAT1, however, and was unaffected by agents that destabilize actin filaments or microtubules, which altered baseline hOAT1-mediated p-aminohippurate uptake activity in oocytes.	Phosphorus	11-12	solute carrier family 22 member 6	Homo sapiens	69-74
12874449-5	2003	It was independent of the conserved canonical PKC consensus sites in hOAT1, however, and was unaffected by agents that destabilize actin filaments or microtubules, which altered baseline hOAT1-mediated p-aminohippurate uptake activity in oocytes.	Phosphorus	11-12	solute carrier family 22 member 6	Homo sapiens	187-192
12869701-2	2003	One mechanism for RNA cleavage involves internal phosphoester transfer, wherein the 2"-oxygen atom carries out an SN2-like nucleophilic attack on the adjacent phosphorus center (transesterification).	Phosphorus	159-169	solute carrier family 38 member 5	Homo sapiens	114-117
12834739-7	2003	This observation suggested that in addition to the two well-accepted groups of phosphorus removal bacteria (one can only utilize oxygen to take up phosphorus, P(O), while the other can use both oxygen and nitrate, P(ON)), a new group of phosphorus removal bacteria, P(ON(n)), which could use oxygen, nitrate or nitrite to take up phosphorus was identified.	Phosphorus	79-89	paraoxonase 1	Homo sapiens	214-219
12834739-7	2003	This observation suggested that in addition to the two well-accepted groups of phosphorus removal bacteria (one can only utilize oxygen to take up phosphorus, P(O), while the other can use both oxygen and nitrate, P(ON)), a new group of phosphorus removal bacteria, P(ON(n)), which could use oxygen, nitrate or nitrite to take up phosphorus was identified.	Phosphorus	147-157	paraoxonase 1	Homo sapiens	214-219
12781187-2	2003	(S)-Isomer at the phosphorus atom (7b) displayed potent inhibition for TACE, while selectivity sparing MMP-1, -3, and -9.	Phosphorus	18-28	ADAM metallopeptidase domain 17	Homo sapiens	71-75
12854831-0	2003	Dietary calcium and phosphorus ratio regulates bone mineralization and turnover in vitamin D receptor knockout mice by affecting intestinal calcium and phosphorus absorption.	Phosphorus	20-30	vitamin D (1,25-dihydroxyvitamin D3) receptor	Mus musculus	83-101
12854831-0	2003	Dietary calcium and phosphorus ratio regulates bone mineralization and turnover in vitamin D receptor knockout mice by affecting intestinal calcium and phosphorus absorption.	Phosphorus	152-162	vitamin D (1,25-dihydroxyvitamin D3) receptor	Mus musculus	83-101
12854832-10	2003	There was a strong inverse correlation between FGF23 and serum phosphorus (r = -0.60) and calcium and phosphorus (Ca x P) product (r = -0.65) in XLH, and a strong positive relationship between FGF23 and Pi (r = 0.50) and Ca x P product (r = 0.62) in ESRD.	Phosphorus	63-73	fibroblast growth factor 23	Homo sapiens	47-52
12702726-5	2003	In intact cells, the Sec14 domain is responsible for localization of PTP-MEG2 to the perinuclear region, and uploading of PS into the cell membrane causes translocation of PTP-MEG2 to the plasma membrane.	Phosphorus	122-124	protein tyrosine phosphatase non-receptor type 9	Homo sapiens	172-180
12753275-8	2003	The second-generation calcimimetic, AMG 073, having a better pharmacokinetic profile, appears to be effective and safe for the treatment of secondary hyperparathyroidism, suppressing PTH levels while simultaneously reducing serum phosphorus levels and the calcium x phosphorus product.	Phosphorus	230-240	amelogenin X-linked	Homo sapiens	36-39
12866877-5	2003	The optimal gas flows established for the detection of sulfur and phosphorus are in the range of 4 mL min(-1) of oxygen and 9 to 13 mL min(-1) of hydrogen.	Phosphorus	66-76	CD59 molecule (CD59 blood group)	Homo sapiens	102-108
12771309-9	2003	There was also a strong correlation between the maximal PTG area and serum PTH concentration, and between PCNA-positive cells and the maximal PTG area, as well as between serum phosphorus concentration and PCNA-positive cells.	Phosphorus	177-187	proliferating cell nuclear antigen	Rattus norvegicus	206-210
12771940-6	2003	(32)Phosphorus labeling showed that ARHI is maintained in a constitutively activated GTP-bound state in resting cells, possibly because of impaired GTPase activity.	Phosphorus	4-14	DIRAS family GTPase 3	Homo sapiens	36-40
12560222-3	2003	The thiol agent p-chloromercuribenzene sulfonic acid (pCMBS) and the active metabolites from antiplatelet drugs, clopidogrel and CS-747, inactivate the P2Y(12) receptor and are predicted to interact with the extracellular cysteine residues on the P2Y(12) receptor.	Phosphorus	16-17	purinergic receptor P2Y12	Homo sapiens	152-159
12560222-3	2003	The thiol agent p-chloromercuribenzene sulfonic acid (pCMBS) and the active metabolites from antiplatelet drugs, clopidogrel and CS-747, inactivate the P2Y(12) receptor and are predicted to interact with the extracellular cysteine residues on the P2Y(12) receptor.	Phosphorus	16-17	purinergic receptor P2Y12	Homo sapiens	247-254
12742022-10	2003	It was therefore concluded that the tetrahedral geometry of gamma-phosphate (or its analogs) and the inter-atomic distance ( approximately 1.6A) between phosphorus (vanadium, or metal atom) and oxygen (or fluorine) are both important for inducing the allosteric transition of GroEL, leading to the high selectivity of GroEL for ATP about ligand adenine nucleotides, which function as the preferred allosteric ligand.	Phosphorus	153-163	heat shock protein family D (Hsp60) member 1	Homo sapiens	276-281
12742022-10	2003	It was therefore concluded that the tetrahedral geometry of gamma-phosphate (or its analogs) and the inter-atomic distance ( approximately 1.6A) between phosphorus (vanadium, or metal atom) and oxygen (or fluorine) are both important for inducing the allosteric transition of GroEL, leading to the high selectivity of GroEL for ATP about ligand adenine nucleotides, which function as the preferred allosteric ligand.	Phosphorus	153-163	heat shock protein family D (Hsp60) member 1	Homo sapiens	318-323
12739956-3	2003	With excess of CsF, P-Cl bonds of 5 were found to undergo fluorination leading to the formation of 2, which transformed to spirocyclic compound 3.	Phosphorus	20-21	colony stimulating factor 2	Homo sapiens	15-18
12719236-5	2003	(31)P-NMR of lipid bilayers composed of MSI-78 and 1-palmitoyl-2-oleoyl-phosphatidylethanolamine demonstrated that the peptide inhibited the fluid lamellar to inverted hexagonal phase transition of 1-palmitoyl-2-oleoyl-phosphatidylethanolamine, supporting the DSC results, and the peptide did not induce the formation of nonlamellar phases, even at very high peptide concentrations (15 mol %).	Phosphorus	3-5	RB binding protein 4, chromatin remodeling factor	Homo sapiens	40-43
12699926-6	2003	An eastward geographic trend of increasing ratios of alpha/beta-HCH, gamma/beta-HCH, p,p"-DDT/p,p"-DDE and PCB-180/28 was observed.	Phosphorus	18-19	pyruvate carboxylase	Homo sapiens	107-110
12666070-6	2003	In multivariate analyses, low hemoglobin levels, high serum phosphorus levels, high anxiety levels, and a great degree of emotion-oriented coping were independently related to the presence of RLS in uremic patients on HD therapy, with statistical significance (P &lt; 0.05).	Phosphorus	60-70	RLS1	Homo sapiens	192-195
12689675-0	2003	Correction of the abnormal mineral ion homeostasis with a high-calcium, high-phosphorus, high-lactose diet rescues the PDDR phenotype of mice deficient for the 25-hydroxyvitamin D-1alpha-hydroxylase (CYP27B1).	Phosphorus	77-87	cytochrome P450, family 27, subfamily b, polypeptide 1	Mus musculus	119-123
12689675-3	2003	The bone phenotype of VDR-ablated mice can be completely rescued by feeding the animals with a high-calcium, high-phosphorus, high-lactose diet.	Phosphorus	114-124	vitamin D (1,25-dihydroxyvitamin D3) receptor	Mus musculus	22-25
12538645-8	2003	These different sensitivities to S"-P" interactions show that Pr3 and NE are not interchangeable enzymes despite their similar P(1) specificity.	Phosphorus	33-37	proteinase 3	Homo sapiens	62-65
12606410-8	2003	The nitric oxide-mediated increase of P-Thr-Glu-Tyr-P involved protein Tyr kinase, MEK or MEK-like kinase, and protein kinase C but not protein kinase A.	Phosphorus	38-39	mitogen-activated protein kinase kinase 7	Homo sapiens	83-86
12606410-8	2003	The nitric oxide-mediated increase of P-Thr-Glu-Tyr-P involved protein Tyr kinase, MEK or MEK-like kinase, and protein kinase C but not protein kinase A.	Phosphorus	38-39	mitogen-activated protein kinase kinase 7	Homo sapiens	90-93
12676605-8	2003	The order of their binding potencies to hAR was CNP &gt; o,p-DDT = p,p-DDE = CNP-amino &gt; vinclozolin, and that of their binding potencies to hER alpha was o,p-DDT &gt; CNP-amino &gt; p,p-DDT = CNP.	Phosphorus	27-28	lymphatic vessel endothelial hyaluronan receptor 1	Homo sapiens	40-43
12676605-8	2003	The order of their binding potencies to hAR was CNP &gt; o,p-DDT = p,p-DDE = CNP-amino &gt; vinclozolin, and that of their binding potencies to hER alpha was o,p-DDT &gt; CNP-amino &gt; p,p-DDT = CNP.	Phosphorus	27-28	2',3'-cyclic nucleotide 3' phosphodiesterase	Homo sapiens	48-51
12631346-7	2003	RESULTS: In SNX animals with moderate renal failure serum phosphorus concentrations were higher than in sham-operated controls on low phosphorus diet (1.7 +/- 0.37 mmol/L) and were significantly higher in SNX + high phosphorus diet (2.33 +/- 0.23 mmol/L) compared to SNX + low phosphorus diet (1.95 +/- 0.32 mmol/L; P &lt; 0.05).	Phosphorus	58-68	annexin A7	Homo sapiens	12-15
12631346-7	2003	RESULTS: In SNX animals with moderate renal failure serum phosphorus concentrations were higher than in sham-operated controls on low phosphorus diet (1.7 +/- 0.37 mmol/L) and were significantly higher in SNX + high phosphorus diet (2.33 +/- 0.23 mmol/L) compared to SNX + low phosphorus diet (1.95 +/- 0.32 mmol/L; P &lt; 0.05).	Phosphorus	58-68	annexin A7	Homo sapiens	205-208
12631346-7	2003	RESULTS: In SNX animals with moderate renal failure serum phosphorus concentrations were higher than in sham-operated controls on low phosphorus diet (1.7 +/- 0.37 mmol/L) and were significantly higher in SNX + high phosphorus diet (2.33 +/- 0.23 mmol/L) compared to SNX + low phosphorus diet (1.95 +/- 0.32 mmol/L; P &lt; 0.05).	Phosphorus	58-68	annexin A7	Homo sapiens	205-208
12631346-7	2003	RESULTS: In SNX animals with moderate renal failure serum phosphorus concentrations were higher than in sham-operated controls on low phosphorus diet (1.7 +/- 0.37 mmol/L) and were significantly higher in SNX + high phosphorus diet (2.33 +/- 0.23 mmol/L) compared to SNX + low phosphorus diet (1.95 +/- 0.32 mmol/L; P &lt; 0.05).	Phosphorus	134-144	annexin A7	Homo sapiens	12-15
12631346-7	2003	RESULTS: In SNX animals with moderate renal failure serum phosphorus concentrations were higher than in sham-operated controls on low phosphorus diet (1.7 +/- 0.37 mmol/L) and were significantly higher in SNX + high phosphorus diet (2.33 +/- 0.23 mmol/L) compared to SNX + low phosphorus diet (1.95 +/- 0.32 mmol/L; P &lt; 0.05).	Phosphorus	134-144	annexin A7	Homo sapiens	12-15
12631346-7	2003	RESULTS: In SNX animals with moderate renal failure serum phosphorus concentrations were higher than in sham-operated controls on low phosphorus diet (1.7 +/- 0.37 mmol/L) and were significantly higher in SNX + high phosphorus diet (2.33 +/- 0.23 mmol/L) compared to SNX + low phosphorus diet (1.95 +/- 0.32 mmol/L; P &lt; 0.05).	Phosphorus	134-144	annexin A7	Homo sapiens	12-15
12612963-4	2003	To prevent hypercalcemia, non-calcium-containing phosphorus binders and vitamin D analogues, which suppress parathyroid hormone (PTH) secretion with minimum calcemic action, have been developed.	Phosphorus	49-59	parathyroid hormone	Homo sapiens	108-127
12515807-4	2003	To test this idea we raised an antibody against the phospho-peptide RARTSpSFAEP, where pS is a phospho-serine corresponding to the glycogen synthase kinase 3alpha Ser-21 sequence.	Phosphorus	73-75	glycogen synthase kinase 3 alpha	Homo sapiens	131-162
12848293-8	2003	The in vitro interaction between Raf-1 and membrane was affected not only by the PS content but also by the fatty acyl composition in PS.	Phosphorus	81-83	v-raf-leukemia viral oncogene 1	Mus musculus	33-38
12848293-9	2003	The reduction of PS concentration as well as the substitution of 18:0,22:6 with 16:0,18:1 in the liposome considerably reduced the interaction with Raf-1.	Phosphorus	17-19	v-raf-leukemia viral oncogene 1	Mus musculus	148-153
12595492-8	2003	Calcium x phosphorus levels decreased by 7.9% in AMG 073 patients compared with an increase of 11.3% in placebo patients (P = 0.013).	Phosphorus	10-20	amelogenin X-linked	Homo sapiens	49-52
12598567-3	2003	Three PEPC genes (Nsppc1-3) from the C(3) plant Nicotiana sylvestris were used to investigate their roles and regulation in a C(3) plant, and their regulation by phosphorus depletion in particular.	Phosphorus	162-172	phosphoenolpyruvate carboxylase	Nicotiana tabacum	6-10
12598567-4	2003	First, the induction of PEPC by phosphorus depletion was confirmed.	Phosphorus	32-42	phosphoenolpyruvate carboxylase	Nicotiana tabacum	24-28
12595492-10	2003	In this study, the calcimimetic AMG 073 at doses up to 100 mg for 18 wk provided a safe and effective means to attain significant reductions in PTH and calcium x phosphorus levels in ESRD patients.	Phosphorus	162-172	amelogenin X-linked	Homo sapiens	32-35
12582016-4	2003	In this generally well-nourished population of middle-aged to elderly men, plasma IGF-I and IGF-I:IGF-binding protein-3 molar ratio tended to increase with higher intake of protein and minerals, including potassium, zinc, magnesium, calcium, and phosphorus.	Phosphorus	246-256	insulin like growth factor 1	Homo sapiens	92-119
12515474-2	2003	Primary alkyl, secondary alkyl, and substituted aromatic substituents were successfully introduced at the phosphorus center, along with ferrocenyl and phenyl groups, generating phosphines of the general structure FcP(Ph)(R) (Fc = ferrocenyl, R = aryl, alkyl).	Phosphorus	106-116	FCP1	Homo sapiens	213-216
12580320-2	2003	The aim of the present study was to determine whether in vivo phosphorus-31 magnetic resonance spectroscopy (31P MRS) accurately assesses the severity of liver damage and is of prognostic value in a D-galactosamine (D-galN)-induced model of acute liver failure.	Phosphorus	62-72	galanin and GMAP prepropeptide	Rattus norvegicus	218-222
12419819-2	2003	The hFGF23 mutants (R176Q, R179Q, and R179W) markedly reduced serum phosphorus (6.2-6.9 mg/dl) compared with the plasmid MOCK (8.5 mg/dl).	Phosphorus	68-78	fibroblast growth factor 23	Homo sapiens	4-10
12472790-10	2003	Patients receiving AMG 073 had an 11.9% decrease in calcium x phosphorus compared with a 10.9% increase in the placebo group (P &lt; 0.001).	Phosphorus	62-72	amelogenin X-linked	Homo sapiens	19-22
12833164-8	2003	The reason for the greater synthesis of PS may be the higher level of expression of PSS1 in immature oocytes.	Phosphorus	40-42	phosphatidylserine synthase 1	Homo sapiens	84-88
12485945-5	2003	The 453 base pairs PCR product was hybridized with specific internal oligonucleotide probes for CYP3A4 or CYP3A7 end labeled with (32)P gamma-ATP.	Phosphorus	19-20	cytochrome P450 family 3 subfamily A member 4	Homo sapiens	96-102
12485945-5	2003	The 453 base pairs PCR product was hybridized with specific internal oligonucleotide probes for CYP3A4 or CYP3A7 end labeled with (32)P gamma-ATP.	Phosphorus	19-20	cytochrome P450 family 3 subfamily A member 7	Homo sapiens	106-112
14690021-1	2003	In the middle of the last century in the case of many river basins, it became obvious that the targets of the Helsinki-Commission (HELCOM) concerning a 50% reduction of nitrogen and phosphorus inputs to the Baltic Sea had not been reached.	Phosphorus	182-192	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	214-217
12778857-8	2003	The low phosphorus diet (Group I) resulted in a significant decrease in PTH levels (81.3 +/- 35 vs 71 +/- 39 pg/ml, p &lt; 0.05) and significant increase in calcitriol levels (22.4 +/- 4.4 vs 33.4 +/- 7.5 pg/ml, p &lt; 0.05).	Phosphorus	8-18	parathyroid hormone	Homo sapiens	72-75
12542939-4	2002	In this study we examined the reduced modulus; hardness; and mineral-to-matrix, crystallinity, carbonate-to-mineral, and calcium-to-phosphorus ratios of mineral formed by bFGF-treated rat-derived bone marrow stromal cells in vitro.	Phosphorus	132-142	fibroblast growth factor 2	Rattus norvegicus	171-175
12845234-11	2003	Stepwise multivariate analysis revealed that serum levels of CAP were significantly determined by serum levels of Ca, P, Alb, and oral dosage of vitamin D (F ratio = 18.81, adjusted r(2) = 0.302).	Phosphorus	63-64	albumin	Homo sapiens	121-124
12475228-4	2002	From structure-activity studies, we show that chirality at the phosphorus atom, hydrophobicity, basicity, size, and charge all influence the ability of a compound to inhibit estrone sulfatase activity.	Phosphorus	63-73	steroid sulfatase	Homo sapiens	174-191
12388558-3	2002	The Ser(P)/Thr-Pro moiety exists in the two distinct cis and trans conformations and their conversion is catalyzed specifically by the prolyl isomerase Pin1.	Phosphorus	7-10	peptidylprolyl cis/trans isomerase, NIMA-interacting 1	Homo sapiens	152-156
12778857-2	2003	The aim of this study was to evaluate the effect of dietary phosphorus restriction versus calcium carbonate treatment for one month on PTH and calcitriol levels in patients with mild renal failure.	Phosphorus	60-70	parathyroid hormone	Homo sapiens	135-138
28443771-9	2003	Bombesin stimulated gastrin decreased from 49 (40-62) pmol/L before to 36 (33-59) pmol/L (P &amp;lt; 0.005) 2 weeks after infliximab.	Phosphorus	90-91	gastrin releasing peptide	Homo sapiens	0-8
28443771-9	2003	Bombesin stimulated gastrin decreased from 49 (40-62) pmol/L before to 36 (33-59) pmol/L (P &amp;lt; 0.005) 2 weeks after infliximab.	Phosphorus	90-91	gastrin	Homo sapiens	20-27
12502069-3	2003	Despite the species alteration, the phosphorus contents of the PAOs appeared to be steady within 0.182-0.308 mg/mg VSS(PAO) regardless of the temperature level.	Phosphorus	36-46	spermine oxidase	Homo sapiens	63-66
12502069-4	2003	The initial specific phosphorus release rates, which are solely due to the PAOs activities, increased with the temperature from 37.5-55.9 to 51.8-61.3, 52.0-76.9, 147.2-210.3, and 374.2-756.3 mgP/gmVSS(PAO) h, at 20.0 degrees C, 25.0 degrees C, 30.0 degrees C, 32.5 degrees C, and 35.0 degrees C, respectively.	Phosphorus	21-31	matrix Gla protein	Homo sapiens	192-195
12502069-4	2003	The initial specific phosphorus release rates, which are solely due to the PAOs activities, increased with the temperature from 37.5-55.9 to 51.8-61.3, 52.0-76.9, 147.2-210.3, and 374.2-756.3 mgP/gmVSS(PAO) h, at 20.0 degrees C, 25.0 degrees C, 30.0 degrees C, 32.5 degrees C, and 35.0 degrees C, respectively.	Phosphorus	21-31	spermine oxidase	Homo sapiens	75-78
12447926-5	2002	pH(i) was calculated using phosphorus-31 MR spectroscopy and lactate/creatine was measured using proton MRS.	Phosphorus	27-37	glucose-6-phosphate isomerase	Homo sapiens	0-5
12371973-0	2002	Phosphorus and uremic serum up-regulate osteopontin expression in vascular smooth muscle cells.	Phosphorus	0-10	secreted phosphoprotein 1	Homo sapiens	40-51
12401218-1	2002	The lack of phosphorus in the nutrient medium increased the expression of rab18, an abscisic acid (ABA)-responsive gene, in leaves of Arabidopsis thaliana.	Phosphorus	12-22	RAB GTPASE HOMOLOG B18	Arabidopsis thaliana	74-79
12414116-2	2002	Phosphorylated form of PTEN (p-PTEN) is a key survival factor relating PI3K-Akt pathway and their downstream effectors.	Phosphorus	4-5	phosphatase and tensin homolog	Rattus norvegicus	23-27
12414116-2	2002	Phosphorylated form of PTEN (p-PTEN) is a key survival factor relating PI3K-Akt pathway and their downstream effectors.	Phosphorus	4-5	phosphatase and tensin homolog	Rattus norvegicus	31-35
12412801-3	2002	In this study, we compared serum phosphorus (sPi) levels to histomorphometric findings in 27 iliac bone samples from 23 children and adolescents (aged 4.2-16.4 years) with polyostotic FD.	Phosphorus	33-43	chromogranin A	Homo sapiens	45-48
12431122-5	2002	The rearrangement of both anti- and syn-2-vinylphosphiranes occurs in a concerted pericyclic manner with inversion of configuration at the migrating phosphorus, requiring, respectively, 29.3 and 36.7 kcal/mol, much in contrast to the 44.6 kcal/mol demanding diradical-like process for the hydrocarbon analogue.	Phosphorus	149-159	synapsin II	Homo sapiens	36-41
12431122-6	2002	Epimerization at the phosphorus center (syn right arrow over left arrow anti) requires approximately 32.0 kcal/mol and occurs in a single step, reflecting a diradical-like ring opening-ring closure process that can occur in both a clockwise and counterclockwise fashion.	Phosphorus	21-31	synemin	Homo sapiens	40-43
12425634-0	2002	Peculiar antiaromatic inorganic molecules of tetrapnictogen in Na+Pn4- (Pn = P, As, Sb) and important consequences for hydrocarbons.	Phosphorus	0-1	sodium voltage-gated channel alpha subunit 8	Homo sapiens	66-69
12226754-8	2002	This is due to the Taxol-mediated reactivation of RelA through phosphorylation and degradation of IkappaBbeta and the re-expression of NF-kappaB regulated bcl-xl gene in these cancer cells as ectopic expression of the bcl-xl gene confers resistance to Taxol-induced apoptosis in PS-341 sensitized cells.	Phosphorus	279-281	RELA proto-oncogene, NF-kB subunit	Homo sapiens	50-54
12418664-5	2002	The estuary was a source for dissolved phosphorus to the sea.	Phosphorus	39-49	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	57-60
12376803-2	2002	Several advances have been made in the understanding of the pathogenesis of secondary hyperparathyroidism, particularly the critical roles of calcium, phosphorus, and vitamin D in promoting excess parathyroid hormone (PTH) synthesis and secretion, and parathyroid gland hyperplasia in renal failure.	Phosphorus	151-161	parathyroid hormone	Homo sapiens	197-216
12357766-1	2002	The luminescence lifetime of TbL2 with a pendant 15-crown-5 increased by 65% to 2.95 ms with an [Na+] concentration of 0.13 M in aqueous solution; the maximum amplification of the luminescence intensity of TbL1 containing aza-15-crown-5 reached a factor of 47 upon addition of the aromatic antenna p-chlorobenzoate 1.	Phosphorus	41-42	transducin beta like 2	Homo sapiens	29-33
12226754-8	2002	This is due to the Taxol-mediated reactivation of RelA through phosphorylation and degradation of IkappaBbeta and the re-expression of NF-kappaB regulated bcl-xl gene in these cancer cells as ectopic expression of the bcl-xl gene confers resistance to Taxol-induced apoptosis in PS-341 sensitized cells.	Phosphorus	279-281	nuclear factor kappa B subunit 1	Homo sapiens	135-144
12226754-8	2002	This is due to the Taxol-mediated reactivation of RelA through phosphorylation and degradation of IkappaBbeta and the re-expression of NF-kappaB regulated bcl-xl gene in these cancer cells as ectopic expression of the bcl-xl gene confers resistance to Taxol-induced apoptosis in PS-341 sensitized cells.	Phosphorus	279-281	BCL2 like 1	Homo sapiens	155-161
12362891-6	2002	Klotho plays a critical role for the regulation of calcium and phosphorus homeostasis by negatively regulating the synthesis of active Vitamin D.	Phosphorus	63-73	klotho	Mus musculus	0-6
12271625-0	2002	Unusual properties of the first copper complex containing a pi(eta 2)-coordinated phosphorus-carbon double bond moiety.	Phosphorus	82-92	DNA polymerase iota	Homo sapiens	63-68
12196103-2	2002	14-3-3 proteins bind phosphoserine-phosphorylated ligands, such as the Raf-1 kinase and Bad, through recognition of the phosphorylated consensus motif, RSXpSXP (where pS is phosphoserine).	Phosphorus	155-157	BCL2 associated agonist of cell death	Homo sapiens	71-91
15775406-4	2002	Klotho plays a critical role for the regulation of calcium and phosphorus homeostasis by negatively regulating the synthesis of active vitamin D.	Phosphorus	63-73	klotho	Mus musculus	0-6
12074251-4	2002	RESULTS: Mean net absorption of phosphorus was 60.3% (+/- 18.1) for data set 1 and 53.0% (+/-9.4) for data set 2.	Phosphorus	32-42	SET domain containing 2, histone lysine methyltransferase	Homo sapiens	107-112
12203199-3	2002	In recent decades, our understanding of the complex interactions between calcium, phosphorus, vitamin D, and parathyroid hormone (PTH) has increased, resulting in a rational approach to therapy in which vitamin D analogs have become an essential component.	Phosphorus	82-92	parathyroid hormone	Homo sapiens	109-128
12203199-3	2002	In recent decades, our understanding of the complex interactions between calcium, phosphorus, vitamin D, and parathyroid hormone (PTH) has increased, resulting in a rational approach to therapy in which vitamin D analogs have become an essential component.	Phosphorus	82-92	parathyroid hormone	Homo sapiens	130-133
12089348-7	2002	Feeding of a diet high in calcium, phosphorus, and lactose normalized blood calcium and serum PTH levels, but revealed a profound renal calcium leak in normocalcemic homozygous mutants.	Phosphorus	35-45	parathyroid hormone	Mus musculus	94-97
12071854-6	2002	This suggests that MDR1 Pgp transports endogenous PS, the lipid exhibiting the most pronounced transverse asymmetry in the plasma membrane.	Phosphorus	50-52	ATP binding cassette subfamily B member 1	Homo sapiens	19-23
12071854-6	2002	This suggests that MDR1 Pgp transports endogenous PS, the lipid exhibiting the most pronounced transverse asymmetry in the plasma membrane.	Phosphorus	50-52	phosphoglycolate phosphatase	Homo sapiens	24-27
11914953-4	2002	Caspase-3 was activated and induced internucleosomal DNA fragmentation and externalization of PS residues.	Phosphorus	94-96	caspase 3	Homo sapiens	0-9
11872748-5	2002	Our studies demonstrate that PS-1145 and PS-341 block TNFalpha-induced NF-kappaB activation in a dose- and time-dependent fashion in MM cells through inhibition of IkappaBalpha phosphorylation and degradation of IkappaBalpha, respectively.	Phosphorus	29-31	tumor necrosis factor	Homo sapiens	54-62
11872748-5	2002	Our studies demonstrate that PS-1145 and PS-341 block TNFalpha-induced NF-kappaB activation in a dose- and time-dependent fashion in MM cells through inhibition of IkappaBalpha phosphorylation and degradation of IkappaBalpha, respectively.	Phosphorus	29-31	nuclear factor kappa B subunit 1	Homo sapiens	71-80
11872748-5	2002	Our studies demonstrate that PS-1145 and PS-341 block TNFalpha-induced NF-kappaB activation in a dose- and time-dependent fashion in MM cells through inhibition of IkappaBalpha phosphorylation and degradation of IkappaBalpha, respectively.	Phosphorus	29-31	NFKB inhibitor alpha	Homo sapiens	164-176
11872748-5	2002	Our studies demonstrate that PS-1145 and PS-341 block TNFalpha-induced NF-kappaB activation in a dose- and time-dependent fashion in MM cells through inhibition of IkappaBalpha phosphorylation and degradation of IkappaBalpha, respectively.	Phosphorus	29-31	NFKB inhibitor alpha	Homo sapiens	212-224
12145936-0	2002	[Effect of the COD and total phosphorus concentration on biological phosphorus removal supplied with acetate as a sole carbon source].	Phosphorus	68-78	small nuclear ribonucleoprotein polypeptides B and B1	Homo sapiens	15-18
12145936-3	2002	The results indicated that when COD &lt; 600 mg.L-1 the phosphorus removal increased with the increase of COD/TP; and this removal increased obviously when COD/TP &lt; 50 but not when COD/TP &gt; 50.	Phosphorus	56-66	small nuclear ribonucleoprotein polypeptides B and B1	Homo sapiens	32-35
12145936-3	2002	The results indicated that when COD &lt; 600 mg.L-1 the phosphorus removal increased with the increase of COD/TP; and this removal increased obviously when COD/TP &lt; 50 but not when COD/TP &gt; 50.	Phosphorus	56-66	small nuclear ribonucleoprotein polypeptides B and B1	Homo sapiens	106-109
12145936-3	2002	The results indicated that when COD &lt; 600 mg.L-1 the phosphorus removal increased with the increase of COD/TP; and this removal increased obviously when COD/TP &lt; 50 but not when COD/TP &gt; 50.	Phosphorus	56-66	small nuclear ribonucleoprotein polypeptides B and B1	Homo sapiens	106-109
12145936-3	2002	The results indicated that when COD &lt; 600 mg.L-1 the phosphorus removal increased with the increase of COD/TP; and this removal increased obviously when COD/TP &lt; 50 but not when COD/TP &gt; 50.	Phosphorus	56-66	small nuclear ribonucleoprotein polypeptides B and B1	Homo sapiens	106-109
12145936-4	2002	The phosphorus removal descended at high acetate concentration (COD &gt; 600 mg.L-1) and broke down when COD &gt; 1000 mg.L-1.	Phosphorus	4-14	small nuclear ribonucleoprotein polypeptides B and B1	Homo sapiens	64-67
12145936-4	2002	The phosphorus removal descended at high acetate concentration (COD &gt; 600 mg.L-1) and broke down when COD &gt; 1000 mg.L-1.	Phosphorus	4-14	small nuclear ribonucleoprotein polypeptides B and B1	Homo sapiens	105-108
11996885-4	2002	With both cell lines, the drug induces cell cycle perturbations (G2/M arrest) and triggers apoptosis as revealed by the externalization of Annexin V-targeted PS residues at the periphery of the cells.	Phosphorus	158-160	annexin A5	Homo sapiens	139-148
11814461-4	2002	METHODS: Activities of GALC towards galactosylceramide (GC) and galactosylsphingosine (psychosine; PS) were determined in white blood cells and cultured fibroblasts derived from GLD patients and controls using tritium-labelled natural substrates.	Phosphorus	99-101	galactosylceramidase	Homo sapiens	23-27
11788345-1	2002	The function of creatine kinase (CK) and its effect on phosphorus metabolites was studied in livers of transgenic mice expressing human ubiquitous mitochondrial CK (CK-Mit) and rat brain CK (CK-B) isoenzymes and their combination.	Phosphorus	55-65	creatine kinase, brain	Mus musculus	33-35
11902787-5	2002	The phosphorus removal rate with various calcium concentrations and pHs could be predicted from high relationships between residual phosphorus concentration and pH (after reaction).	Phosphorus	4-14	pterin-4 alpha-carbinolamine dehydratase 1	Bos taurus	68-71
11902787-5	2002	The phosphorus removal rate with various calcium concentrations and pHs could be predicted from high relationships between residual phosphorus concentration and pH (after reaction).	Phosphorus	132-142	pterin-4 alpha-carbinolamine dehydratase 1	Bos taurus	68-71
11796525-8	2002	Klotho protein may participate in calcium and phosphorus homeostasis via the regulation of the 1,25-(OH)2D signaling pathway.	Phosphorus	46-56	klotho	Mus musculus	0-6
11863555-9	2002	The results for the material with the less abundant PCL block are explained as a result of the confinement in nanotubes of PCL surrounded by PB embedded in a vitreous PS matrix.	Phosphorus	167-169	PHD finger protein 1	Homo sapiens	52-55
12055341-4	2002	Both P450C1 and P450C24 are highly regulated enzymes whose differential expression is controlled in response to numerous cellular modulatory agents such as parathyroid hormone (PTH), calcitonin, interferon gamma, calcium, phosphorus, and pituitary hormones as well as the secosteroid hormone 1,25VD.	Phosphorus	222-232	cytochrome P450 family 27 subfamily B member 1	Homo sapiens	5-11
11857093-2	2002	We hypothesized that the retention of Ca (calcium) and P (phosphorus) would be improved by an E2 and Prog replacement.	Phosphorus	55-56	cystatin 12, pseudogene	Homo sapiens	94-105
11857093-2	2002	We hypothesized that the retention of Ca (calcium) and P (phosphorus) would be improved by an E2 and Prog replacement.	Phosphorus	58-68	cystatin 12, pseudogene	Homo sapiens	94-105
11790118-15	2002	We conclude that PS-containing membranes regulate prothrombin activation by factor X(a) mainly via interaction of individual PS molecules with factor X(a).	Phosphorus	17-19	coagulation factor II, thrombin	Homo sapiens	50-61
11810291-5	2002	Interestingly, a significant LD between GABRB3 and CL/P was obtained ( P-value=0.008 in the allele-wise analysis for multiallelic markers), suggesting that the GABRB3 gene is involved in this congenital disease.	Phosphorus	54-55	gamma-aminobutyric acid (GABA) A receptor, subunit beta 3	Mus musculus	40-46
11810291-8	2002	Exclusion of the GAD1 gene, which encodes the GABA-producing enzyme, in CL/P pathogenesis was obtained in our study.	Phosphorus	75-76	glutamate decarboxylase 1	Mus musculus	17-21
11810291-5	2002	Interestingly, a significant LD between GABRB3 and CL/P was obtained ( P-value=0.008 in the allele-wise analysis for multiallelic markers), suggesting that the GABRB3 gene is involved in this congenital disease.	Phosphorus	54-55	gamma-aminobutyric acid (GABA) A receptor, subunit beta 3	Mus musculus	160-166
12077491-10	2002	Patients with fDH had higher serum phosphorus levels (1.99 vs. 1.79 mmol, p &lt; 0.005).	Phosphorus	35-45	alcohol dehydrogenase 5 (class III), chi polypeptide	Homo sapiens	14-17
12077491-12	2002	In multivariate analysis, significant independent predictors of fDH were older age (OR = 1.04 [1.02-1.07]), lack of glomerulonephritis as renal diagnosis (2.63 [1.18-5.87]), high phosphorus levels (5.0 [2.45-10.0]), lack of use of Ca-channel blockers (2.09 [1.12-3.91]), and the use of nitrates (2.38 [1.24-4.55]).	Phosphorus	179-189	alcohol dehydrogenase 5 (class III), chi polypeptide	Homo sapiens	64-67
11737585-1	2001	BACKGROUND: High dietary phosphorus (P) worsens uremia-induced parathyroid (PT) hyperplasia through increases in the growth promoter transforming growth factor-alpha (TGF-alpha).	Phosphorus	25-35	transforming growth factor alpha	Rattus norvegicus	133-165
11984634-0	2002	Longitudinal and vertical trends of bacterial limitation by phosphorus and carbon in the Mediterranean Sea.	Phosphorus	60-70	S13 erythroblastosis (avian) oncogene homolog	Homo sapiens	103-106
12541610-3	2002	Results showed that micro-phase separation of PS-PEO-PS had a greater influence on crystallization of PEO molecule-chain.	Phosphorus	46-48	twinkle mtDNA helicase	Homo sapiens	49-52
12541610-3	2002	Results showed that micro-phase separation of PS-PEO-PS had a greater influence on crystallization of PEO molecule-chain.	Phosphorus	46-48	twinkle mtDNA helicase	Homo sapiens	102-105
11728974-7	2001	For HD patients, age and months on HD at enrollment were associated inversely with PTH level, whereas black race, creatinine, and phosphorus were associated directly with PTH.	Phosphorus	130-140	parathyroid hormone	Homo sapiens	171-174
11728974-8	2001	For PD patients, age, diabetes, and months on PD at enrollment were inverse predictors, whereas black race, albumin, creatinine, and phosphorus were associated positively with PTH.	Phosphorus	133-143	parathyroid hormone	Homo sapiens	176-179
12043849-6	2001	METHODS: G protein functional measurements coupled to beta-adrenergic, muscarinic, and dopamine receptors were undertaken through bacterial toxin sensitive, agonist enhanced [3H]-Gpp(NH)p binding capacity, substantiated by quantitative measures of Gs alpha, Gi alpha, and G beta subunit proteins through immunoblot analysis in mononuclear leukocytes obtained from patients with schizophrenia under haloperidol, or clozapine treatments in comparison with untreated patients with schizophrenia and healthy volunteers.	Phosphorus	11-12	GNAS complex locus	Homo sapiens	248-256
11739863-0	2001	The progression of aging in klotho mutant mice can be modified by dietary phosphorus and zinc.	Phosphorus	74-84	klotho	Mus musculus	28-34
11739863-2	2001	We have now found two key substances, phosphorus and zinc, which affect the appearance of klotho phenotypes.	Phosphorus	38-48	klotho	Mus musculus	90-96
11739863-3	2001	Klotho mutant homozygotes fed nonpurified diet with a phosphorus concentration of 1.03 g/100 g showed typical klotho phenotypes.	Phosphorus	54-64	klotho	Mus musculus	0-6
11739863-3	2001	Klotho mutant homozygotes fed nonpurified diet with a phosphorus concentration of 1.03 g/100 g showed typical klotho phenotypes.	Phosphorus	54-64	klotho	Mus musculus	110-116
11739863-4	2001	However, most of the klotho phenotypes no longer appeared in male homozygotes fed a 0.4 g/100 g phosphorus diet.	Phosphorus	96-106	klotho	Mus musculus	21-27
11739863-7	2001	On the other hand, female klotho mice required supplementation of 0.25 g/100 g zinc orotate to the 0.4 g/100 g phosphorus diet to be rescued.	Phosphorus	111-121	klotho	Mus musculus	26-32
11739863-9	2001	Wild-type (C3H/He) mice fed 1.5 or 1.0 g/100 g phosphorus diets had lower klotho protein expression in the kidneys than those fed a 0.4 g/100 g phosphorus diet (Kruskal-Wallis test, P &lt; 0.05).	Phosphorus	47-57	klotho	Mus musculus	74-80
11739863-10	2001	These results indicate that dietary phosphorus and zinc modulate the phenotypes of klotho mice, and that klotho expression in the kidneys is regulated not only in klotho mutant mice, but also in wild-type mice.	Phosphorus	36-46	klotho	Mus musculus	83-89
12474461-8	2002	In questionable cases if the level of total lipid phosphorus is greater than 21.36 (M P/L (M + 26, there will be 98.3% probability for no tuberculosis in such a patient.	Phosphorus	50-60	MPL proto-oncogene, thrombopoietin receptor	Homo sapiens	84-89
12382869-5	2002	This research concludes that phosphorus inclusions are formed and a valence change of the Cu ions occurs after annealing above 270 degrees C, which degrades the TL sensitivity of LiF:Mg,Cu,P phosphors.	Phosphorus	29-39	LIF interleukin 6 family cytokine	Homo sapiens	179-182
11737585-1	2001	BACKGROUND: High dietary phosphorus (P) worsens uremia-induced parathyroid (PT) hyperplasia through increases in the growth promoter transforming growth factor-alpha (TGF-alpha).	Phosphorus	25-35	transforming growth factor alpha	Rattus norvegicus	167-176
11595617-0	2001	Influence of a low calcium and phosphorus diet on the anabolic effect of human parathyroid hormone (1-38) in female rats.	Phosphorus	31-41	parathyroid hormone	Homo sapiens	79-98
11504728-5	2001	Stoichiometric amounts of P(i) and Dol-P are formed during the enzymatic reaction indicating that Cwh8p cleaves the anhydride linkage in Dol-P-P.	Phosphorus	26-27	dolichyldiphosphatase	Saccharomyces cerevisiae S288C	98-103
11675637-1	2001	Post-exercise recovery of intracellular pH (pH(i)) assessed using phosphorus magnetic resonance spectroscopy has not been previously evaluated in its entirety due to its complex time-course and missing data points resulting from a transient loss of inorganic phosphate signal.	Phosphorus	66-76	glucose-6-phosphate isomerase	Homo sapiens	44-49
11776435-3	2001	The phosphate group was determined to be at C-23 by HMBC between phosphorus and H-23.	Phosphorus	65-75	nucleolin	Homo sapiens	44-48
15775644-0	2001	[The regulation of vitamin D metabolism and PTH secretion by phosphorus].	Phosphorus	61-71	parathyroid hormone	Homo sapiens	44-47
15775644-2	2001	Also, the serum level of phosphorus is known to change according to the level of calcium and to regulate the vitamin D and PTH.	Phosphorus	25-35	parathyroid hormone	Homo sapiens	123-126
15775644-4	2001	Furthermore, the direct effect of phosphorus in PTH synthesis is being elucidated in recent reports.	Phosphorus	34-44	parathyroid hormone	Homo sapiens	48-51
15775644-5	2001	In this paper, we summarized the regulation of vitamin D and PTH by phosphorus.	Phosphorus	68-78	parathyroid hormone	Homo sapiens	61-64
11453739-7	2001	For methamidophos, we show that phosphylation of AChE involves elimination of the thiomethyl moiety and that the spontaneous reactivation of the resulting organophosphate adduct generates the phosphorus free AChE active site Ser-peptide.	Phosphorus	192-202	acetylcholinesterase (Cartwright blood group)	Homo sapiens	208-212
11668218-8	2001	The CYP2C9-mediated production of (S)-p-HPPH represented the major metabolic pathway of phenytoin biotransformation as its excretion accounted for 95.6 + 0.9% of "total" p-HPPH excretion over the 96 h collection interval.	Phosphorus	34-39	cytochrome P450 family 2 subfamily C member 9	Homo sapiens	4-10
11522872-9	2001	Serum phosphorus levels positively correlated well with serum PTH levels and maximal PTG area.	Phosphorus	6-16	parathyroid hormone	Rattus norvegicus	62-65
11522872-12	2001	The correlation analysis suggests that reduced serum phosphorus levels contributed to the suppression of PTG hyperplasia and resulted in the reduction of PTH levels in this animal model after the sevelamer treatment.	Phosphorus	53-63	parathyroid hormone	Rattus norvegicus	154-157
11505053-1	2001	BACKGROUND: In vivo phosphorus magnetic resonance spectroscopy (31P MRS) at a magnetic field strength of 1.5 T allows measurement of fairly mobile membrane phospholipids in the human brain.	Phosphorus	20-30	MROS	Homo sapiens	68-71
11522087-13	2001	CONCLUSIONS: BsmI polymorphism of the VDR gene induces differences on the response to a single bolus of calcitriol independently of calcium and phosphorus.	Phosphorus	144-154	vitamin D receptor	Homo sapiens	38-41
11702418-4	2001	Milk-protein based infant formulas showed for both manufacturers higher dialysis percentage (%) of phosphorus and zinc than the soy-protein based formulas.	Phosphorus	99-109	Weaning weight-maternal milk	Bos taurus	0-4
11493008-0	2001	Inhibition of human alpha-thrombin by a phosphonate tripeptide proceeds via a metastable pentacoordinated phosphorus intermediate.	Phosphorus	106-116	coagulation factor II, thrombin	Homo sapiens	26-34
11493008-1	2001	X-ray crystallographic studies of human alpha-thrombin with a novel synthetic inhibitor, an acyl (alpha-aminoalkyl)phosphonate, reveal the existence of a pentacovalent phosphorus intermediate state.	Phosphorus	168-178	coagulation factor II, thrombin	Homo sapiens	46-54
11493008-5	2001	In the first structure, a water molecule, made nucleophilic by coordination to His57 of alpha-thrombin, is bonded to the pentacoordinated phosphorus atom.	Phosphorus	138-148	coagulation factor II, thrombin	Homo sapiens	94-102
11508330-9	2001	PTH alone significantly increased serum Ca, P, Mg, and osteocalcin concentrations, although it had no effect on bone mineral balance.	Phosphorus	0-1	bone gamma-carboxyglutamate protein	Rattus norvegicus	55-66
11426974-8	2001	E(2) at 10 microM downregulated iNOS expression and significantly reduced NO production in HOC-7 cells, while 10 microM P(4) or 10 microM E + P increased iNOS expression and NO production.	Phosphorus	140-143	nitric oxide synthase 2	Homo sapiens	154-158
11499657-0	2001	Parathyroid hormone changes during phosphorus load in patients with chronic renal insufficiency with low serum parathyroid hormone or adynamic bone disease.	Phosphorus	35-45	parathyroid hormone	Homo sapiens	0-19
11499657-0	2001	Parathyroid hormone changes during phosphorus load in patients with chronic renal insufficiency with low serum parathyroid hormone or adynamic bone disease.	Phosphorus	35-45	parathyroid hormone	Homo sapiens	111-130
11499657-2	2001	Many clinical and therapeutic conditions have been associated with ABD, and recently, a low phosphorus intake accompanied by low serum concentration of phosphorus and PTH has been described.	Phosphorus	92-102	parathyroid hormone	Homo sapiens	167-170
11499657-3	2001	AIM: To evaluate the parathyroid gland response of chronic renal insufficiency patients (CRI) with low serum PTH or ABD to a phosphorus load.	Phosphorus	125-135	parathyroid hormone	Homo sapiens	109-112
11499657-5	2001	RESULTS: Serum intact PTH increased significantly only after 1 g of phosphorus (58.5 to 83 ng/l) with a median percent increase of 72%.	Phosphorus	68-78	parathyroid hormone	Homo sapiens	22-25
11499657-9	2001	Changes in PTH were inversely correlated with changes in serum ionized calcium (r = -0.54, p &lt; 0.05) and the final PTH concentrations were positively correlated with changes in serum phosphorus (r= 0.52, p &lt; 0.05).	Phosphorus	186-196	parathyroid hormone	Homo sapiens	118-121
11499657-10	2001	CONCLUSIONS: The parathyroid glands of chronic renal insufficiency patients with "relative hypoparathyroidism" or ABD responded to a phosphorus load with an increase in serum PTH levels.	Phosphorus	133-143	parathyroid hormone	Homo sapiens	175-178
11331006-1	2001	Phosphatidylinositol-specific phospholipase C (PI-PLC) catalyzes the cleavage of the P-O bond in phosphatidylinositol via intramolecular nucleophilic attack of the 2-hydroxyl group of inositol on the phosphorus atom.	Phosphorus	200-210	phospholipase C beta 1	Homo sapiens	0-45
11278981-1	2001	The ptxD gene from Pseudomonas stutzeri WM88 encoding the novel phosphorus oxidizing enzyme NAD:phosphite oxidoreductase (trivial name phosphite dehydrogenase, PtxD) was cloned into an expression vector and overproduced in Escherichia coli.	Phosphorus	64-74	oxidoreductase	Pseudomonas stutzeri	106-120
11457248-0	2001	Ag(P4)2(+): the first homoleptic metal-phosphorus cation.	Phosphorus	39-49	solute carrier family 10 member 4	Homo sapiens	0-5
11423575-2	2001	19-Nor-1,25-(OH)(2)D(2) is approximately 10 times less active than 1,25-(OH)(2)D(3) in promoting bone resorption, which accounts in part for the low potency of this analog in increasing serum calcium and phosphorus.	Phosphorus	204-214	nuclear receptor subfamily 4 group A member 3	Homo sapiens	3-8
11410147-6	2001	We show that the high HBD is a result of food quantity effects and that the low HBD is a result of food quality effects, which are maintained by phosphorus limitation in the predator.	Phosphorus	145-155	HBD	Homo sapiens	80-83
11331006-1	2001	Phosphatidylinositol-specific phospholipase C (PI-PLC) catalyzes the cleavage of the P-O bond in phosphatidylinositol via intramolecular nucleophilic attack of the 2-hydroxyl group of inositol on the phosphorus atom.	Phosphorus	200-210	phospholipase C beta 1	Homo sapiens	47-53
11278862-5	2001	The work described herein has focused on the Lck SH2 domain, which binds the consensus peptide acetyl-Tyr(P)-Glu-Glu-Ile-amide with a K(D) of 1.3 micrometer.	Phosphorus	106-108	LCK proto-oncogene, Src family tyrosine kinase	Homo sapiens	45-48
11154690-0	2001	Mechanistic inferences from the crystal structure of fumarylacetoacetate hydrolase with a bound phosphorus-based inhibitor.	Phosphorus	96-106	fumarylacetoacetate hydrolase	Homo sapiens	53-82
11145967-7	2001	Therefore, it is likely that P-TEFb participates in regulation of elongation by RNA Pol II by phosphorylation of its substrates, hSPT5 and the CTD of RNA Pol II, in a CAK-independent manner.	Phosphorus	29-30	SPT5 homolog, DSIF elongation factor subunit	Homo sapiens	129-134
11388474-3	2001	As indicators of the proximal tubular function, the N-acetyl-beta-D-glucosaminidase activity in urine and the urinary beta2-microglobulin excretion were significantly increased in those rats fed on the high-phosphorus diet containing K5P3O10.	Phosphorus	207-217	beta-2 microglobulin	Rattus norvegicus	118-137
11312743-3	2001	Density functional theory calculations on simplified models of 4, 5, and related radicals were performed and revealed that spin polarization effects and the nature of the substituents on phosphorus have significant effects on the structures and spin distributions of these radicals.	Phosphorus	187-197	spindlin 1	Homo sapiens	123-127
11312743-3	2001	Density functional theory calculations on simplified models of 4, 5, and related radicals were performed and revealed that spin polarization effects and the nature of the substituents on phosphorus have significant effects on the structures and spin distributions of these radicals.	Phosphorus	187-197	spindlin 1	Homo sapiens	245-249
11323770-2	2001	MR-spectroscopy (MRS) records protons from tissue chemicals other than water, intrinsic phosphorus containing metabolites, sodium, potassium, carbon, nitrogen, and fluorine.	Phosphorus	88-98	sterile alpha motif domain containing 11	Mus musculus	17-20
11393310-6	2001	The calcium concentration in the kidney was significantly increased with age, but the copper and phosphorus concentrations significantly decreased with age in SAMP1 and SAMR1.	Phosphorus	97-107	transmembrane protein 201	Mus musculus	159-164
11701096-7	2001	CONCLUSIONS: The best Fhit inhibitors obtained to date separate two or more 5"-O-phosphoromonothioadenosyl moieties with as many bond lengths as in AppppA, maintain oxygen at the location of the alpha-beta bridging oxygen, and replace carbon for the beta phosphorus.	Phosphorus	255-265	fragile histidine triad diadenosine triphosphatase	Homo sapiens	22-26
11330911-3	2001	The reaction between the isomeric carborane arachno-4,5-C2B7H13 (4) and PCl3 in dichloromethane in the presence of PS gave the asymmetrical isomer, nido-7,8,9,10-P2C2B7H, (5).	Phosphorus	115-117	PHD finger protein 19	Homo sapiens	72-76
11238186-6	2001	Km values for all metabolites with CYP1A1.2 were generally significantly lower than with wild-type enzyme (e.g. B[a]P-7,8-diol formation: 13.8 microM for wild-type, 3.5 microM for CYP1A1.2 and 7.7 microM for CYP1A1.4).	Phosphorus	37-38	cytochrome P450 family 1 subfamily A member 1	Homo sapiens	180-186
11238186-6	2001	Km values for all metabolites with CYP1A1.2 were generally significantly lower than with wild-type enzyme (e.g. B[a]P-7,8-diol formation: 13.8 microM for wild-type, 3.5 microM for CYP1A1.2 and 7.7 microM for CYP1A1.4).	Phosphorus	37-38	cytochrome P450 family 1 subfamily A member 1	Homo sapiens	180-186
11277180-10	2001	Higher IL-6 and IL-8 levels were directly associated with lower phosphorus levels.	Phosphorus	64-74	interleukin 6	Homo sapiens	7-11
11277180-10	2001	Higher IL-6 and IL-8 levels were directly associated with lower phosphorus levels.	Phosphorus	64-74	C-X-C motif chemokine ligand 8	Homo sapiens	16-20
11158862-4	2001	High dietary phosphorus (P), independent of calcium and calcitriol, further enhances uremia-induced PTG hyperplasia and PTH synthesis and secretion, the latter by posttranscriptional mechanisms.	Phosphorus	13-23	parathyroid hormone	Homo sapiens	120-123
11258813-6	2001	The ratio of DOC to TFP (C:P) influenced the fate of PO4 in the water, implying that DOC was forming complexes with phosphorus.	Phosphorus	116-126	inhibitor of carbonic anhydrase pseudogene	Homo sapiens	20-23
11145614-0	2001	Dietary phosphorus restriction reverses the impaired bone mineralization in vitamin D receptor knockout mice.	Phosphorus	8-18	vitamin D (1,25-dihydroxyvitamin D3) receptor	Mus musculus	76-94
11145614-3	2001	Normalization of impaired mineral homeostasis in VDR KO mice fed a diet supplemented with high concentrations of calcium (2%) and phosphorus (1.25%) is reported to reverse the malformation of bone and the growth retardation as well.	Phosphorus	130-140	vitamin D (1,25-dihydroxyvitamin D3) receptor	Mus musculus	49-52
11145614-6	2001	We report here that feeding a diet supplemented with a restricted amount of phosphorus (0.25%) and a normal amount of calcium (0.5%) for 4 weeks reverses the growth retardation and the impaired mineralization in VDR KO mice, as does a high-calcium and high-phosphorus diet (Ca: 2%; P: 1.25%).	Phosphorus	76-86	vitamin D (1,25-dihydroxyvitamin D3) receptor	Mus musculus	212-215
11174029-12	2001	Pneumonia is believed to have caused local synthesis of parathyroid hormone-related protein that, along with high calcium x phosphorus product, contributed to calcium deposition.	Phosphorus	124-134	parathyroid hormone like hormone	Homo sapiens	56-91
11922476-2	2001	X-ray photoelectron spectra of the surface of the HAp-deposited film showed the presence of calcium and phosphorus of a suitable peak ratio for HAp formation.	Phosphorus	104-114	reticulon 3	Homo sapiens	50-53
11922476-2	2001	X-ray photoelectron spectra of the surface of the HAp-deposited film showed the presence of calcium and phosphorus of a suitable peak ratio for HAp formation.	Phosphorus	104-114	reticulon 3	Homo sapiens	144-147
11588892-1	2001	Monoclonal antibody (MAb) 1-7-1 against 3-methylcholanthrene (MC)-induced forms of cytochrome P-450 (CYP) was used to characterize benzo[a]pyrene (B[a]P) metabolism in rat liver and extrahepatic tissues and its modulation by phenolic antioxidants, propyl and octyl gallates.	Phosphorus	94-95	cytochrome P450, family 2, subfamily g, polypeptide 1	Rattus norvegicus	101-104
11575087-1	2001	This papers describes the behaviour of wetlands as a post-treatment unit for anaerobically treated sewage for the removal of organic matter, suspended solids, nutrients (nitrogen and phosphorus) and faecal coliforms.	Phosphorus	183-193	solute carrier family 35 member G1	Homo sapiens	53-57
11208041-3	2001	Two of these hormones, parathyroid hormone (PTH) and calcitriol (the active form of vitamin D), interact in multiple tissues in the body to regulate the flux of calcium and phosphorus between extra- and intracellular compartments.	Phosphorus	173-183	parathyroid hormone	Homo sapiens	23-42
11208041-3	2001	Two of these hormones, parathyroid hormone (PTH) and calcitriol (the active form of vitamin D), interact in multiple tissues in the body to regulate the flux of calcium and phosphorus between extra- and intracellular compartments.	Phosphorus	173-183	parathyroid hormone	Homo sapiens	44-47
11208041-4	2001	Changes in the concentration of PTH and vitamin D, or the interaction of these with other factors, lead to the aberrant regulation of calcium and phosphorus.	Phosphorus	146-156	parathyroid hormone	Homo sapiens	32-35
11381902-3	2001	It was observed that, 10 mg/L of NO3-N suppressed phosphorus release during the feed and mix phases.	Phosphorus	50-60	NBL1, DAN family BMP antagonist	Homo sapiens	33-36
11303783-3	2000	To clarify the mechanism(s) by which PS facilitates Notch signaling, we examined human Jagged-2-dependent metabolism and activity of a chimeric full-length Notchl-GFP molecule expressed in fibroblasts with heterozygous, or homozygous deletions of PS1.	Phosphorus	37-39	notch receptor 1	Homo sapiens	52-57
11066054-10	2000	Bacterial/fungal infections were slightly less frequent in the G-CSF group with CAV (P = 0.11) but not with P/VP.	Phosphorus	85-86	colony stimulating factor 3	Homo sapiens	63-68
11066054-10	2000	Bacterial/fungal infections were slightly less frequent in the G-CSF group with CAV (P = 0.11) but not with P/VP.	Phosphorus	85-86	caveolin 2	Homo sapiens	80-83
11146319-0	2000	Chronic phosphorus supplementation decreases the expression of renal PTH/PTHrP receptor mRNA in rats.	Phosphorus	8-18	parathyroid hormone-like hormone	Rattus norvegicus	73-78
11146319-1	2000	Dietary intake of high levels of phosphorus is known to increase serum levels of parathyroid hormone (PTH); however, how this increased serum PTH affects the action of PTH in major target tissues, particularly by kidney, remains unknown.	Phosphorus	33-43	parathyroid hormone	Rattus norvegicus	81-100
11193397-1	2000	To find whether a high phosphorus (P) diet stimulate the secretion of PTH, a high-P diet was fed to rats and an increase in serum P levels has occurred.	Phosphorus	23-33	parathyroid hormone	Rattus norvegicus	70-73