PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
21672148-8	2011	In vivo rapamycin treatment induced higher degree of RICTOR and AKT Ser(473) expression directly correlating with long-term rapamycin exposure, FE(PO4) and HOMA index.	po4	147-150	RPTOR independent companion of MTOR complex 2	Homo sapiens	53-59
27877452-13	2011	Laboratory studies confirm that a small amount of PO4 in solution (>30 muM) can significantly inhibit the transformation of MHC.	po4	50-53	latexin	Homo sapiens	74-77
22007384-0	2011	[Preparation and luminescence characteristics of white-light emitting Ca9.95-xNa0.75K0.25(PO4)7: Eu0.05(2+), Mn(x)2+ phosphors].	po4	90-93	carbonic anhydrase 9	Homo sapiens	70-73
21037382-7	2010	In the process of degeneration of elastin polypentapeptide structure in elastin can be easily conbined to Ca(2+), elastin-Ca(2+) complex is neutralized by PO4(2-) and calcium phosphate is accumulated in degenerated elastin.	po4	155-158	elastin	Homo sapiens	34-41
21037382-7	2010	In the process of degeneration of elastin polypentapeptide structure in elastin can be easily conbined to Ca(2+), elastin-Ca(2+) complex is neutralized by PO4(2-) and calcium phosphate is accumulated in degenerated elastin.	po4	155-158	elastin	Homo sapiens	72-79
21037382-7	2010	In the process of degeneration of elastin polypentapeptide structure in elastin can be easily conbined to Ca(2+), elastin-Ca(2+) complex is neutralized by PO4(2-) and calcium phosphate is accumulated in degenerated elastin.	po4	155-158	elastin	Homo sapiens	72-79
21037382-7	2010	In the process of degeneration of elastin polypentapeptide structure in elastin can be easily conbined to Ca(2+), elastin-Ca(2+) complex is neutralized by PO4(2-) and calcium phosphate is accumulated in degenerated elastin.	po4	155-158	elastin	Homo sapiens	72-79
19387319-11	2009	I-FGF-23 decreased to its nadir of 7.8 +/- 6.9 pg/mL (P < 0.001) on po day 3 and was correlated with PO4 levels on po days 0, 3, 5, and 7 (P < 0.001).	po4	104-107	fibroblast growth factor 23	Homo sapiens	2-8
20584882-5	2010	When sporozoites are injected into the mammalian host, an eIF2alpha phosphatase removes the PO4 from eIF2alpha-P, and the repression of translation is alleviated to permit their transformation into liver stages.	po4	92-95	eukaryotic translation initiation factor 2A	Homo sapiens	58-67
20584882-5	2010	When sporozoites are injected into the mammalian host, an eIF2alpha phosphatase removes the PO4 from eIF2alpha-P, and the repression of translation is alleviated to permit their transformation into liver stages.	po4	92-95	eukaryotic translation initiation factor 2A	Homo sapiens	101-110
19036652-0	2009	Effect of silicon content on the sintering and biological behaviour of Ca10(PO4)(6-x)(SiO4)x(OH)(2-x) ceramics.	po4	76-79	carbonic anhydrase 10	Homo sapiens	71-75
19036652-1	2009	Silicated hydroxyapatite powders (Ca10(PO4)(6-x)(SiO4)x(OH)(2-x); Si(x)HA) were synthesized using a wet precipitation method.	po4	39-42	carbonic anhydrase 10	Homo sapiens	34-38
19432338-3	2009	After stopping PAFC (Al2 O3 : 10.8%, Fe2 O3: 1.8%) addition, COD removal efficiency is achieved at about 50%, and removal rates of PO4(3-) and TP gradually decline.	po4	131-134	PAFC	Homo sapiens	15-19
18303779-13	2007	RESULTS: The result at 3 months after surgery was frequency 2x/week within 10/30 minutes after self administrated ACE (PO4 + 100ml saline) with very occasional soilage.	po4	119-122	angiotensin I converting enzyme	Homo sapiens	114-117
18986671-4	2008	Oxidation of TCEP results in both H+ and Cl(-) release, while the TBP mineralization pathway results in CO2, H2O, H+, and PO4(3-).	po4	122-125	TATA-box binding protein	Homo sapiens	66-69
15917335-8	2005	Increased Fe(PO4) was associated with decreased eGFR, and both increased FGF-23 and PTH were independently associated with increased Fe(PO4).	po4	136-139	fibroblast growth factor 23	Homo sapiens	73-79
17359508-8	2007	A high FGF-23(post) level was independently associated with a high FE(PO4).	po4	70-73	fibroblast growth factor 23	Homo sapiens	7-13
17388516-8	2007	The Asp4 side chain thus regulates efficiency of the electrostatic binding between the peptide N-terminal NH3(+) and the lipid headgroup PO4(-).	po4	137-140	napsin A aspartic peptidase	Homo sapiens	4-8
16428247-8	2006	The plant ligase, like yeast Trl1 but unlike T4 RNA ligase 1, requires a 2"-PO4 end for tRNA splicing in vivo.	po4	76-79	tRNA ligase	Saccharomyces cerevisiae S288C	29-33
15961223-7	2005	The co-presence of silicate or phosphate with each of the organic species enhanced As(V) extraction in the order SiO3(2-)>PO4(3-).	po4	125-128	SRC proto-oncogene, non-receptor tyrosine kinase	Homo sapiens	83-88
16055687-11	2005	While the ionome of cax1 and cax3 lines were modestly perturbed, the cax1/cax3 lines displayed increased PO4(3-), Mn2+, and Zn2+ and decreased Ca2+ and Mg2+ in shoot tissue.	po4	105-108	cation exchanger 1	Arabidopsis thaliana	69-73
16055687-11	2005	While the ionome of cax1 and cax3 lines were modestly perturbed, the cax1/cax3 lines displayed increased PO4(3-), Mn2+, and Zn2+ and decreased Ca2+ and Mg2+ in shoot tissue.	po4	105-108	cation exchanger 3	Arabidopsis thaliana	74-78
15917335-10	2005	It is concluded that FGF-23 levels increase early in CKD before the development of serum mineral abnormalities and are independently associated with serum phosphate, Fe(PO4), and calcitriol deficiency.	po4	169-172	fibroblast growth factor 23	Homo sapiens	21-27
17915758-3	2007	The concentration of ions in samples showed a general pattern as SO4(2-) > NO3- > Cl- > PO4(2-) > F- for anions and Na+ > Ca2+ > NH4+ > Mg2+ > K+ for cations.	po4	97-100	NBL1, DAN family BMP antagonist	Homo sapiens	78-81
15917335-8	2005	Increased Fe(PO4) was associated with decreased eGFR, and both increased FGF-23 and PTH were independently associated with increased Fe(PO4).	po4	136-139	parathyroid hormone	Homo sapiens	84-87
15643055-7	2005	Downregulation of PKC by prolonged exposure to PMA (100 nM; 24 h) completely inhibited thrombin-stimulated increases in arachidonic acid release (7.1 +/- 0.6 to 0.5 +/- 0.1%) and lysoplasmenylcholine production (2.0 +/- 0.1 to 0.2 +/- 0.1 nmol PO4/mg of protein).	po4	244-247	coagulation factor II, thrombin	Homo sapiens	87-95
12613005-8	2003	The Ca x phosphorus (PO4) product decreased from 85 mg2/dL2 (6.80 mmol2/L2) and remained less than 55 mg2/dL2 (4.4 mmol2/L2) throughout the patient"s course on DNHD.	po4	21-24	l(1)L2	Drosophila melanogaster	56-59
15643055-3	2005	Thrombin stimulation resulted in a decrease in arachidonylated plasmenylcholine (2.7 +/- 0.1 vs. 5.3 +/- 0.4 nmol PO4/mg of protein) and plasmenylethanolamine (7.5 +/- 1.0 vs. 12.0 +/- 0.9 nmol PO4/mg of protein).	po4	114-117	coagulation factor II, thrombin	Homo sapiens	0-8
15643055-3	2005	Thrombin stimulation resulted in a decrease in arachidonylated plasmenylcholine (2.7 +/- 0.1 vs. 5.3 +/- 0.4 nmol PO4/mg of protein) and plasmenylethanolamine (7.5 +/- 1.0 vs. 12.0 +/- 0.9 nmol PO4/mg of protein).	po4	194-197	coagulation factor II, thrombin	Homo sapiens	0-8
15712160-4	2005	RESULTS: Data revealed that the hydrolytic activity of F0F1-ATPase increases significantly in patients with probable AD (41.7+/-4.3 nmol PO4 min-1[mg protein]-1, n=29) as compared to the control subjects (29.1+/-1.9 nmol PO4 min-1 [mg protein]-1, n=29).	po4	137-140	ATP synthase F1 subunit epsilon	Homo sapiens	55-66
15712160-4	2005	RESULTS: Data revealed that the hydrolytic activity of F0F1-ATPase increases significantly in patients with probable AD (41.7+/-4.3 nmol PO4 min-1[mg protein]-1, n=29) as compared to the control subjects (29.1+/-1.9 nmol PO4 min-1 [mg protein]-1, n=29).	po4	221-224	ATP synthase F1 subunit epsilon	Homo sapiens	55-66
15473549-2	2004	The HNO3 reacts with silicates and possibly PO4(3-) species, releasing Al, Fe, nutrient base cations and H2PO4-, and is transformed into NO3-.	po4	44-47	NBL1, DAN family BMP antagonist	Homo sapiens	5-8
12672655-4	2003	Here we show that erythrocytes have Li-activated PO4 transport that behaves as if it is mediated by the Na-PO4 cotransporter (hBNP1) and provide evidence that this Na/Li-PO4 cotransporter is also the mechanism for Na/Li exchange.	po4	49-52	solute carrier family 17 member 4	Homo sapiens	104-124
12613005-8	2003	The Ca x phosphorus (PO4) product decreased from 85 mg2/dL2 (6.80 mmol2/L2) and remained less than 55 mg2/dL2 (4.4 mmol2/L2) throughout the patient"s course on DNHD.	po4	21-24	l(1)L2	Drosophila melanogaster	57-59
12613005-8	2003	The Ca x phosphorus (PO4) product decreased from 85 mg2/dL2 (6.80 mmol2/L2) and remained less than 55 mg2/dL2 (4.4 mmol2/L2) throughout the patient"s course on DNHD.	po4	21-24	l(1)L2	Drosophila melanogaster	106-109
12613005-8	2003	The Ca x phosphorus (PO4) product decreased from 85 mg2/dL2 (6.80 mmol2/L2) and remained less than 55 mg2/dL2 (4.4 mmol2/L2) throughout the patient"s course on DNHD.	po4	21-24	l(1)L2	Drosophila melanogaster	72-74
11532115-3	2001	We tested the hypothesis that a circulating serum factor [non-parathyroid hormone (non-PTH)], which operates during chronic renal failure (CRF) to maintain phosphate (Pi) homeostasis, can increase fractional excretion of Pi (FE(PO4)) in normal functioning kidney grafts during the early post-transplant period, thereby causing phosphaturia and hypophosphatemia.	po4	228-231	parathyroid hormone	Homo sapiens	87-90
12777712-0	2003	Rat polymerase beta gapped DNA interactions: antagonistic effects of the 5" terminal PO4 - group and magnesium on the enzyme binding to the gapped DNAs with different ssDNA gaps.	po4	85-88	DNA polymerase beta	Rattus norvegicus	4-19
11900549-1	2002	The catalytic activity of adenosine kinase (AK) from mammalian sources has previously been shown to exhibit a marked dependency upon the presence of pentavalent ions (PVI), such as phosphate (PO4), arsenate, or vanadate.	po4	192-195	adenosine kinase	Homo sapiens	26-42
11900549-1	2002	The catalytic activity of adenosine kinase (AK) from mammalian sources has previously been shown to exhibit a marked dependency upon the presence of pentavalent ions (PVI), such as phosphate (PO4), arsenate, or vanadate.	po4	192-195	adenosine kinase	Homo sapiens	44-46
11900549-6	2002	The N and E of this motif make close contacts with Mg2+ and PO4 ions in the crystal structures of AK and bacterial ribokinase (another PfkB member which shows PVI dependency), implicating these residues in their binding.	po4	60-63	adenosine kinase	Homo sapiens	98-100
11937868-3	2002	The bone mineral idealized as calcium hydroxyapatite, Ca10 (PO4)(6)(OH)2, is a carbonatehydroxyapatite, approximated by the formula: (Ca,X)(10)(PO4,HPO4,CO3)(6)(OH,Y)2, where X are cations (magnesium, sodium, strontium ions) that can substitute for the calcium ions, and Y are anions (chloride or fluoride ions) that can substitute for the hydroxyl group.	po4	60-63	carbonic anhydrase 10	Homo sapiens	54-58
11900549-12	2002	These observations support the view that N239 and E242 play an important role in the binding of PO4 and Mg2+ ions required for the catalytic activity of adenosine kinase.	po4	96-99	adenosine kinase	Homo sapiens	153-169
11532115-16	2001	CONCLUSION: A non-PTH circulating serum factor (possibly phosphatonin) that increases FE(PO4) during CRF is also responsible for phosphaturia and hypophosphatemia in the early period following successful kidney transplantation.	po4	89-92	parathyroid hormone	Homo sapiens	18-21
11341286-7	2001	The major nutrients in all the four seasons were found in the magnitude of SiO3 > NO3 > PO4 in all the stations, and thus, support the presence of rich diatoms and dinoflagellates than other phytoplankton groups.	po4	94-97	NBL1, DAN family BMP antagonist	Homo sapiens	85-88
11922476-1	2001	A poly(vinyl alcohol) (PVA)-coating on polyethylene films, prepared by repetitive adsorption/drying in an aqueous PVA solution, accelerated hydroxyapatite (HAp) deposition by an altemate soaking in aqueous solutions containing Ca2+ and PO4(3-) ions.	po4	236-239	reticulon 3	Homo sapiens	156-159
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.	po4	53-56	inhibitor of carbonic anhydrase pseudogene	Homo sapiens	20-23
10340593-5	1999	In contrast, plasma concentrations of Ca and PO4 during amylin infusion were reduced by 18 and 30%, respectively, relative to saline infusion.	po4	45-48	islet amyloid polypeptide	Rattus norvegicus	56-62
10381152-13	1999	GH further increased serum 1,25(OH)2D and the systemic calcium load, which account for the suppression of parathyroid hormone (PTH) despite renal PO4 retention and correction of hypophosphatemia.	po4	146-149	growth hormone 1	Homo sapiens	0-2
10340593-9	1999	Mammary blood flow (measured with a transit-time blood flow probe) increased up to 26% during amylin infusion, although this effect lasted only for the first 3 h. In conclusion, amylin increased plasma concentrations of glucose and NEFA, and mammary blood flow, while decreasing plasma concentrations of Ca and PO4.	po4	311-314	islet amyloid polypeptide	Rattus norvegicus	178-184
10370058-9	1999	CFTR in Calu-3 cells also conducts physiologically relevant anions, but not ATP, PO4 or SO4.	po4	81-84	CF transmembrane conductance regulator	Homo sapiens	0-4
10194441-6	1999	As predicted by its sequence, PSP was detected predominantly in the platelet cytosol and was phosphorylated in vitro by protein kinase C (PKC), a secretion-linked kinase, incorporating 0.87 +/- 0.11 mol of PO4 per mole of protein.	po4	206-209	syntaxin binding protein 3	Homo sapiens	30-33
10194441-6	1999	As predicted by its sequence, PSP was detected predominantly in the platelet cytosol and was phosphorylated in vitro by protein kinase C (PKC), a secretion-linked kinase, incorporating 0.87 +/- 0.11 mol of PO4 per mole of protein.	po4	206-209	proline rich transmembrane protein 2	Homo sapiens	120-136
10194441-6	1999	As predicted by its sequence, PSP was detected predominantly in the platelet cytosol and was phosphorylated in vitro by protein kinase C (PKC), a secretion-linked kinase, incorporating 0.87 +/- 0.11 mol of PO4 per mole of protein.	po4	206-209	proline rich transmembrane protein 2	Homo sapiens	138-141
10047984-4	1998	gamma-PAK phosphorylated endothelial cell myosin II to 0.85 +/- 0.02 mol PO4 per mol RLC.	po4	73-76	p21 (RAC1) activated kinase 2	Homo sapiens	0-9
9531176-16	1998	Those in the highest quintile of the Ca x PO4 product (>72 mg2/dL2) had a relative mortality risk of 1.34 relative to those with products of 42 to 52 mg2/dL2.	po4	42-45	l(1)L2	Drosophila melanogaster	66-69
9432113-3	1998	The MLCK activity (nanomoles/min/mg) was determined by the incorporation of [32P]PO4(-3) to the 20-kD smooth muscle myosin light chains and the MLCP activity by assaying for the dephosphorylation of the 20-kD myosin light chain (MLCP-light chain) and heavy meromyosin (MLCP-HMM).	po4	81-84	myosin light chain kinase, smooth muscle	Ovis aries	4-8
9530108-2	1998	The initial rate of 32PO4 influx had saturation kinetics for external Na and PO4 with K1/2Na of 128 mM (PO4 = 0.1 mM) and K1/2PO4 of 0.084 mM (extracellular Na = 143 mM) in sham- and NaPi-3-transfected cells expressing the transporter.	po4	22-25	keratin 1	Homo sapiens	122-129
9530108-2	1998	The initial rate of 32PO4 influx had saturation kinetics for external Na and PO4 with K1/2Na of 128 mM (PO4 = 0.1 mM) and K1/2PO4 of 0.084 mM (extracellular Na = 143 mM) in sham- and NaPi-3-transfected cells expressing the transporter.	po4	22-25	solute carrier family 34 member 1	Homo sapiens	183-189
9530108-2	1998	The initial rate of 32PO4 influx had saturation kinetics for external Na and PO4 with K1/2Na of 128 mM (PO4 = 0.1 mM) and K1/2PO4 of 0.084 mM (extracellular Na = 143 mM) in sham- and NaPi-3-transfected cells expressing the transporter.	po4	77-80	keratin 1	Homo sapiens	122-129
9530108-2	1998	The initial rate of 32PO4 influx had saturation kinetics for external Na and PO4 with K1/2Na of 128 mM (PO4 = 0.1 mM) and K1/2PO4 of 0.084 mM (extracellular Na = 143 mM) in sham- and NaPi-3-transfected cells expressing the transporter.	po4	77-80	solute carrier family 34 member 1	Homo sapiens	183-189
10022752-2	1998	Increasing concentration of Tris-HCl (Tris) and sodium phosphate (PO4) buffers differentially affected MDZ 1"-OH and MDZ 4-OH formation rates and had a different effect on MDZ metabolism mediated by microsomes containing CYP3A4 versus CYP3A4 and CYP3A5.	po4	66-69	cytochrome P450 family 3 subfamily A member 4	Homo sapiens	221-227
10022752-2	1998	Increasing concentration of Tris-HCl (Tris) and sodium phosphate (PO4) buffers differentially affected MDZ 1"-OH and MDZ 4-OH formation rates and had a different effect on MDZ metabolism mediated by microsomes containing CYP3A4 versus CYP3A4 and CYP3A5.	po4	66-69	cytochrome P450 family 3 subfamily A member 4	Homo sapiens	235-241
10022752-2	1998	Increasing concentration of Tris-HCl (Tris) and sodium phosphate (PO4) buffers differentially affected MDZ 1"-OH and MDZ 4-OH formation rates and had a different effect on MDZ metabolism mediated by microsomes containing CYP3A4 versus CYP3A4 and CYP3A5.	po4	66-69	cytochrome P450 family 3 subfamily A member 5	Homo sapiens	246-252
9182531-2	1997	Addition of forskolin or prostaglandin E1, agents known to elevate platelet cAMP and calcium efflux, to platelets pre-labeled with [32P]PO4 resulted in the direct phosphorylation of platelet PMCA.	po4	136-139	ATPase plasma membrane Ca2+ transporting 2	Homo sapiens	191-195
9374484-6	1997	Also, PI-3,4-(PO4)2, PI-3,4,5-(PO4)3, and PI-4,5-(PO4)2 directly stimulated enzyme activity and autophosphoralytion in control PKC-zeta immunoprecipitates to levels observed in insulin-treated PKC-zeta immunoprecipitates.	po4	14-17	protein kinase C, zeta	Rattus norvegicus	127-135
9374484-6	1997	Also, PI-3,4-(PO4)2, PI-3,4,5-(PO4)3, and PI-4,5-(PO4)2 directly stimulated enzyme activity and autophosphoralytion in control PKC-zeta immunoprecipitates to levels observed in insulin-treated PKC-zeta immunoprecipitates.	po4	14-17	protein kinase C, zeta	Rattus norvegicus	193-201
8993337-6	1997	We previously reported the identification of four phosphorylation sites in chicken progesterone receptor using oviduct tissue minces labeled with [32P]PO4 under nonequilibrium conditions.	po4	151-154	progesterone receptor	Gallus gallus	83-104
8751832-6	1996	1774 cells from PO4 and NH4Cl groups showed significant increases in intracellular IL-1 alpha following treatment with LPS.	po4	16-19	interleukin 1 alpha	Mus musculus	83-93
8841118-6	1996	Intermolecular contacts between the DNA and the 8-kDa domain of a symmetry-related pol beta molecule reveal a plausible binding site on the 8-kDa domain for the downstream oligonucleotide of a gapped-DNA substrate; in addition to a lysine-rich binding pocket that accommodates a 5"-PO4 end group, the 8-kDa domain also contains a newly discovered helix-hairpin-helix (HhH) motif that binds to DNA in the same way as does a structurally and sequentially homologous HhH motif in the 31-kDa domain.	po4	282-285	DNA polymerase beta	Homo sapiens	83-91
8530412-3	1995	Metabolic labeling of stably transfected hEK-293 and AtT-20 cells showed that [32P]PO4(3-) was efficiently incorporated into Ser and Thr residues of membrane PAM but not into soluble PAM.	po4	83-86	peptidylglycine alpha-amidating monooxygenase	Homo sapiens	158-161
8621419-3	1996	This led to the recovery of dephosphorylated tau from the NT2N cells as monitored by a relative increase in the electrophoretic mobility of tau and an increase in the turnover of [32P]PO4-labeled tau.	po4	184-187	microtubule associated protein tau	Homo sapiens	45-48
7713808-0	1995	Effect of aging on beta 2-adrenergic receptor-stimulated flux of K+, PO4, FFA, and glycerol in human forearms.	po4	69-72	adrenoceptor beta 2	Homo sapiens	19-45
7642584-7	1995	Phosphoamino acid analysis of a series of mutants in which an individual serine residue was replaced by a threonine residue indicates that the C5aR undergoes C5a-dependent phosphorylation to the maximal stoichiometry of 6 mol of PO4/mol of receptor at Ser314, Ser317, Ser327, Ser332, Ser334, and Ser338.	po4	229-232	complement C5a receptor 1	Homo sapiens	143-147
7642584-7	1995	Phosphoamino acid analysis of a series of mutants in which an individual serine residue was replaced by a threonine residue indicates that the C5aR undergoes C5a-dependent phosphorylation to the maximal stoichiometry of 6 mol of PO4/mol of receptor at Ser314, Ser317, Ser327, Ser332, Ser334, and Ser338.	po4	229-232	complement C5a receptor 1	Homo sapiens	143-146
8195113-3	1994	TRAP also partially dephosphorylated metabolically [32P]PO4-labeled OPN as well as BSP, whereas comparable amounts of either alkaline phosphatase or prostatic acid phosphatase, at their respective pH optima, were ineffective, indicating a certain preference of TRAP for these phosphoprotein substrates.	po4	56-59	secreted phosphoprotein 1	Homo sapiens	68-71
7929059-7	1994	The attachment of these glycans to the polypeptide backbone via the linkage, Man alpha 1-PO4-Ser, is suggested by: 1) the finding that more than 60% of the serine residues in the polypeptide are phosphorylated and 2) the resistance of the phosphoserine residues to alkaline phosphatase digestion unless the sAP was first treated with either mild acid (to release all glycans) or jack bean alpha-mannosidase (to release neutral mannose glycans).	po4	89-92	adrenoceptor alpha 1D	Homo sapiens	81-88
7929059-7	1994	The attachment of these glycans to the polypeptide backbone via the linkage, Man alpha 1-PO4-Ser, is suggested by: 1) the finding that more than 60% of the serine residues in the polypeptide are phosphorylated and 2) the resistance of the phosphoserine residues to alkaline phosphatase digestion unless the sAP was first treated with either mild acid (to release all glycans) or jack bean alpha-mannosidase (to release neutral mannose glycans).	po4	89-92	SH2 domain containing 1A	Homo sapiens	307-310
7929067-13	1994	The interaction between ribBP and the 95-kDa receptor and/or VTG requires Ca2+ and PO4(3-).	po4	83-86	riboflavin binding protein	Gallus gallus	24-29
7929067-13	1994	The interaction between ribBP and the 95-kDa receptor and/or VTG requires Ca2+ and PO4(3-).	po4	83-86	vitellogenin 2	Gallus gallus	61-64
8026463-3	1994	Two very polar [3H]mannose-labeled glycolipids named CP1 and CP2 qualified as GPI precursor lipids since their carbohydrate head group, Man alpha 1,2(X-->PO4-->6)Man alpha 1,2Man alpha 1,6Man alpha-GlcN-inositol (with X most likely being ethanolamine) comprises the core structure which is common to all GPI anchors described so far.	po4	157-160	ceruloplasmin	Homo sapiens	61-64
2537487-8	1989	It is concluded that PTH probably regulates the PO4 transport through the placenta syncytio-trophoblast cell through cAMP mediation.	po4	48-51	parathyroid hormone	Homo sapiens	21-24
8144611-9	1994	We have produced recombinant p18 in bacterial cells and shown that it can be phosphorylated in vitro by purified p34cdc2 kinase with a stoichiometry of 0.86 mol of PO4/mol of substrate.	po4	164-167	H3 histone pseudogene 12	Homo sapiens	29-32
8144611-9	1994	We have produced recombinant p18 in bacterial cells and shown that it can be phosphorylated in vitro by purified p34cdc2 kinase with a stoichiometry of 0.86 mol of PO4/mol of substrate.	po4	164-167	cyclin dependent kinase 1	Homo sapiens	113-120
1451221-5	1992	Urine flow, Na and PO4 excretion increased following the administration of nicardipine or hANP.	po4	19-22	natriuretic peptide A	Homo sapiens	90-94
1818761-1	1991	The hydrolytic conversion of a solid amorphous calcium phosphate of empirical formula Ca9 (PO4)6 to a poorly crystalline apatitic phase, under conditions where Ca2+ and PO4(3-) were conserved, was studied by means of solid-state magic-angle sample spinning 31P-NMR (nuclear magnetic resonance).	po4	91-94	carbonic anhydrase 9	Homo sapiens	86-89
1654804-6	1991	Upon stimulation, dibutryl cAMP-differentiated U937 cells labeled with alkylacyl-[32P]GPC produce [32P]PO4 but not [32P]phosphocholine.	po4	103-106	glycophorin C (Gerbich blood group)	Homo sapiens	86-89
1654804-7	1991	Furthermore, when these cells were labeled in alkylacyl-GPC by incubation with [3H]alkyllyso-GPC and then stimulated, [3H]alkylacyl-glycerol ([3H]alkylacyl-Gro) is produced with a time-course similar to that of [32P]PO4 formation and coincident with the decline in alkylacyl-GP accumulation.	po4	216-219	glycophorin C (Gerbich blood group)	Homo sapiens	56-59
1654804-8	1991	These results demonstrate that alkylacyl-GP formed by PLD is dephosphorylated by phosphatidate phosphohydrolase to produce PO4 and alkylacyl-Gro.	po4	123-126	glycosylphosphatidylinositol specific phospholipase D1	Homo sapiens	54-57
1850997-2	1991	Sequential analysis of the purified phosphopeptides demonstrated that the sites are -Thr-Arg-Thr-Tyr-Ser(PO4)38-Leu-Gly-Ser-Ala- and -Val-Arg-Leu-Leu-Gln-Asp-Ser(PO4)82-Val-Asp-, which are located within the amino-terminal head domain of vimentin.	po4	105-108	vimentin	Homo sapiens	238-246
1850997-2	1991	Sequential analysis of the purified phosphopeptides demonstrated that the sites are -Thr-Arg-Thr-Tyr-Ser(PO4)38-Leu-Gly-Ser-Ala- and -Val-Arg-Leu-Leu-Gln-Asp-Ser(PO4)82-Val-Asp-, which are located within the amino-terminal head domain of vimentin.	po4	162-165	vimentin	Homo sapiens	238-246
2307846-8	1990	Upon C5a stimulation, neutrophils labeled with 3H and 32P also produce 1-O-[3H]alkyl-diglyceride [( 3H]alkyl-DG) and [32P]orthophosphate [( 32P]PO4), but not [32P]phosphocholine.	po4	144-147	complement C5a receptor 1	Homo sapiens	5-8
33944567-0	2021	Energetic Stability and Its Role in the Mechanism of Ionic Transport in NASICON-Type Solid-State Electrolyte Li1+xAlxTi2-x(PO4)3.	po4	123-126	transglutaminase 1	Homo sapiens	109-112
34885388-0	2021	Growth and Optical Properties of the Whole System of Li(Mn1-x,Nix)PO4 (0 <= x <= 0.5) Single Crystals.	po4	66-69	BCL2 interacting protein 3 like	Homo sapiens	62-65
34961041-5	2021	Here, we exposed Arabidopsis thaliana (Arabidopsis) transformant lines which harbor molecular modifications to the miR396 and miR399 expression modules to phosphate (PO4) starvation.	po4	166-169	MIR399f	Arabidopsis thaliana	126-132
34961041-6	2021	We show that molecular alteration of either miR396 or miR399 abundance afforded the Arabidopsis transformant lines different degrees of tolerance to PO4 starvation.	po4	149-152	MIR399f	Arabidopsis thaliana	54-60
34677913-5	2021	Also, morphological degradations such as micro-cracking or amorphization of surface are significantly suppressed by the presence of Ca4.67 Li0.33 (PO4 )3 (OH) layer on the Li(Ni0.8 Co0.15 Al0.05 )O2 , of which the Ca4.67 Li0.33 (PO4 )3 (OH) is transformed to CaF2 via Ca4.67 Li0.33 (PO4 )3 F during the long term cycles reacting with HF in electrolyte.	po4	283-286	carbonic anhydrase 4	Homo sapiens	132-135
34677913-5	2021	Also, morphological degradations such as micro-cracking or amorphization of surface are significantly suppressed by the presence of Ca4.67 Li0.33 (PO4 )3 (OH) layer on the Li(Ni0.8 Co0.15 Al0.05 )O2 , of which the Ca4.67 Li0.33 (PO4 )3 (OH) is transformed to CaF2 via Ca4.67 Li0.33 (PO4 )3 F during the long term cycles reacting with HF in electrolyte.	po4	283-286	carbonic anhydrase 4	Homo sapiens	214-217
34677913-5	2021	Also, morphological degradations such as micro-cracking or amorphization of surface are significantly suppressed by the presence of Ca4.67 Li0.33 (PO4 )3 (OH) layer on the Li(Ni0.8 Co0.15 Al0.05 )O2 , of which the Ca4.67 Li0.33 (PO4 )3 (OH) is transformed to CaF2 via Ca4.67 Li0.33 (PO4 )3 F during the long term cycles reacting with HF in electrolyte.	po4	283-286	CCR4-NOT transcription complex subunit 8	Homo sapiens	259-263
34677913-5	2021	Also, morphological degradations such as micro-cracking or amorphization of surface are significantly suppressed by the presence of Ca4.67 Li0.33 (PO4 )3 (OH) layer on the Li(Ni0.8 Co0.15 Al0.05 )O2 , of which the Ca4.67 Li0.33 (PO4 )3 (OH) is transformed to CaF2 via Ca4.67 Li0.33 (PO4 )3 F during the long term cycles reacting with HF in electrolyte.	po4	283-286	carbonic anhydrase 4	Homo sapiens	268-271
34677913-7	2021	Therefore, the stable Ca4.67 Li0.33 (PO4 )3 F and CaF2 layers play a pivotal role to protect the Li(Ni0.8 Co0.15 Al0.05 )O2 with ultra-long cycling stability.	po4	37-40	carbonic anhydrase 4	Homo sapiens	22-25
34555892-3	2021	Based on the temperature-dependent PL analysis of K3Lu(PO4)2:Pr3+, we find that Pr3+ ions occupy the noninversion sites (Cs) in the two low-temperature phases but preferentially enter into the inversion ones (C3i) in phase III.	po4	55-58	proteinase 3	Homo sapiens	61-64
34555892-3	2021	Based on the temperature-dependent PL analysis of K3Lu(PO4)2:Pr3+, we find that Pr3+ ions occupy the noninversion sites (Cs) in the two low-temperature phases but preferentially enter into the inversion ones (C3i) in phase III.	po4	55-58	proteinase 3	Homo sapiens	80-83
34555892-5	2021	To enhance the room-temperature PL property of K3Lu(PO4)2:Pr3+, a polymorphous adjustment strategy was proposed by the use of the ion-doping method.	po4	52-55	proteinase 3	Homo sapiens	58-61
34557008-3	2021	This study aims to compare the levels of blood biomarkers, specifically, calcium (Ca), vitamin D, and phosphate (PO4), and their association with parathyroid hormone (PTH) levels pre- and post-bariatric surgery.	po4	113-116	parathyroid hormone	Homo sapiens	146-165
33835608-6	2021	RESULTS: The mean delta18 O value of the new BOKU Ag3 PO4 comparison material on the VSMOW-SLAP scale is 13.71 % and the combined uncertainty is estimated as +- 0.34 %.	po4	54-57	anterior gradient 3, protein disulphide isomerase family member	Homo sapiens	50-53
35489146-9	2022	Both NO3N (160 muM) and PO4 (7.5 muM) were significantly elevated after the fires (~15-22x; P = 0.01), with maximum monthly loads of 0.82 and 0.14 kg ha-1 respectively.	po4	24-27	keratin 31	Homo sapiens	150-154
35294795-0	2022	Stabilizing the Li1.3Al0.3Ti1.7(PO4)3 Li Interface for High Efficiency and Long Lifespan Quasi-Solid-State Lithium Metal Batteries.	po4	32-35	transglutaminase 1	Homo sapiens	16-19
35297444-0	2022	Influence of TiIV substitution on the properties of a Li1.5Al0.5Ge1.5(PO4)3 nanofiber-based solid electrolyte.	po4	70-73	transglutaminase 1	Homo sapiens	54-57
35133813-3	2022	Herein, We synthesized a series of beta-Ca3(PO4)2-type Ca8ZnGa(1-x)Lax(PO4)7:Eu2+ solid solution phosphors by design.	po4	71-74	small nucleolar RNA, H/ACA box 3A	Homo sapiens	35-43
35133813-3	2022	Herein, We synthesized a series of beta-Ca3(PO4)2-type Ca8ZnGa(1-x)Lax(PO4)7:Eu2+ solid solution phosphors by design.	po4	71-74	lymphocyte transmembrane adaptor 1	Homo sapiens	67-70
35073485-2	2022	Herein, we develop a whitlockite-type NIR phosphor Sr9Sc(PO4)7:Cr3+ with an emission centered at 860 nm and full width at half-maximum of 147 nm.	po4	57-60	teratocarcinoma-derived growth factor 1 pseudogene 3	Homo sapiens	63-66
2706740-4	1989	The maximal velocities for TPA-stimulated epidermal PKC activity in CD-1, DBA/2 and C57BL/6 were 0.28, 0.29 and 0.27 nmol PO4-histone/mg 10(5)g protein/min, respectively.	po4	122-125	CD1 antigen complex	Mus musculus	68-72
2546843-4	1989	Increasing the insulin concentration from 0 to 10(-5) M resulted in a dose-dependent inhibition of phosphate uptake with half-maximal effect at 1.1 x 10(-9) M. The hormone decreased PO4 transport by decreasing the affinity of the carrier for the substrate (Km = 0.180 +/- 0.010 mM and 0.215 +/- 0.015 mM in absence and presence of 10(-6) M insulin respectively, P less than 0.05).	po4	182-185	insulin	Homo sapiens	15-22
2546843-4	1989	Increasing the insulin concentration from 0 to 10(-5) M resulted in a dose-dependent inhibition of phosphate uptake with half-maximal effect at 1.1 x 10(-9) M. The hormone decreased PO4 transport by decreasing the affinity of the carrier for the substrate (Km = 0.180 +/- 0.010 mM and 0.215 +/- 0.015 mM in absence and presence of 10(-6) M insulin respectively, P less than 0.05).	po4	182-185	insulin	Homo sapiens	340-347
2546843-6	1989	It is therefore assumed that receptor phosphorylation, which needs the presence of Mn2+, is an intermediate step of insulin action on PO4 uptake by the subsequently isolated brush border membranes.	po4	134-137	insulin	Homo sapiens	116-123
2537487-0	1989	Effect of parathyroid hormone on PO4 transport through the human placenta microvilli.	po4	33-36	parathyroid hormone	Homo sapiens	10-29
2537487-2	1989	In this study, we investigated whether PTH, the main hormone regulating PO4 transport in the kidney and gut, has a similar role in the placenta.	po4	72-75	parathyroid hormone	Homo sapiens	39-42
2537487-6	1989	Increasing concentrations of di-butyryl cAMP from 0 to 10(-3) M significantly decreased the PO4 uptake from 0.29 +/- 0.02 to 0.22 +/- 0.01 pmol/micrograms/20 s. Similarly, incubation of the placental tissue with PTH resulted in a comparable decrease in the PO4 uptake by the corresponding brush border membrane vesicles.	po4	92-95	parathyroid hormone	Homo sapiens	212-215
8197398-4	1994	and an inhaled beta 2-agonist (albuterol) both increased the normal morning-till-noon serum concentration difference (mean +/- SEM, mmol l-1) in PO4 (from -0.13 +/- 0.04 to - 0.23 +/- 0.03 and -0.23 +/- 0.04, respectively) and reduced the normal increase in serum-K (from 0.25 +/- 0.07 to 0.06 +/- 0.08 and -0.13 +/- 0.09, respectively).	po4	145-148	potassium calcium-activated channel subfamily M regulatory beta subunit 2	Homo sapiens	15-21
1431688-16	1992	All three doses of EGF induced polydipsic and diuretic responses in ewes, and infusions of 5-10 micrograms EGF/kg liveweight per day affected renal excretion of Ca2+, Na+ and PO4(3-).	po4	175-178	epidermal growth factor	Homo sapiens	107-110
1501405-2	1992	Ca2+ uptake increased by 50% in rPT incubated in zero PO4 medium as compared to control (2.6 +/- 0.1 vs. 3.9 +/- 0.19, P less than 0.001) and LDH release increased 2.5-fold from 14.2 +/- 0.6 to 31.6 +/- 1.6%, P less than 0.001.	po4	54-57	magnesium transporter MRS2	Rattus norvegicus	32-35
1501405-6	1992	PO4-depleted rPT, LDH release was diminished significantly by glycine treatment (31.0 +/- 0.9 vs. 15.5 +/- 1.6%, P less than 0.001) or acidosis (30.3 +/- 0.04 vs. 19.2 +/- 0.9%, P less than 0.01).	po4	0-3	magnesium transporter MRS2	Rattus norvegicus	13-16
2280412-4	1990	However, a small amount of phosphate (17%) was detected in a light chain peptide phosphorylated by protein kinase C. Endothelin-1 also stimulated phosphorylation of the thin filament protein, caldesmon, (from 0.35 mol PO4/mol caldesmon to 0.52 mol PO4/mol).	po4	218-221	endothelin 1	Homo sapiens	117-129
2280412-4	1990	However, a small amount of phosphate (17%) was detected in a light chain peptide phosphorylated by protein kinase C. Endothelin-1 also stimulated phosphorylation of the thin filament protein, caldesmon, (from 0.35 mol PO4/mol caldesmon to 0.52 mol PO4/mol).	po4	248-251	endothelin 1	Homo sapiens	117-129
33778959-6	2021	This analysis showed that the levels of VTC1 and VTC4 transcripts were strongly reduced at 5 and 24 h after the addition of PO4 3- to the cells, although polyP granules were continuously synthesized during this 24 h period.	po4	124-127	uncharacterized protein	Chlamydomonas reinhardtii	40-44
34677913-3	2021	To verify the availability of hydroxyapatite as a surface protection material, lithium-doped hydroxyapatite, Ca4.67 Li0.33 (PO4 )3 (OH), is formed with  10-nm layer after reacting with residual lithium compounds on Li(Ni0.8 Co0.15 Al0.05 )O2 , which spontaneously results in dramatic reduction of surface lithium residues to 2879 ppm from 22364 ppm.	po4	124-127	carbonic anhydrase 4	Homo sapiens	109-112
34677913-4	2021	The Ca4.67 Li0.33 (PO4 )3 (OH)-modified Li(Ni0.8 Co0.15 Al0.05 )O2 electrode provides ultra-long term cycling stability, enabling 1000 cycles retaining 66.3% of its initial capacity.	po4	19-22	carbonic anhydrase 4	Homo sapiens	4-7
34677913-5	2021	Also, morphological degradations such as micro-cracking or amorphization of surface are significantly suppressed by the presence of Ca4.67 Li0.33 (PO4 )3 (OH) layer on the Li(Ni0.8 Co0.15 Al0.05 )O2 , of which the Ca4.67 Li0.33 (PO4 )3 (OH) is transformed to CaF2 via Ca4.67 Li0.33 (PO4 )3 F during the long term cycles reacting with HF in electrolyte.	po4	147-150	carbonic anhydrase 4	Homo sapiens	132-135
34677913-5	2021	Also, morphological degradations such as micro-cracking or amorphization of surface are significantly suppressed by the presence of Ca4.67 Li0.33 (PO4 )3 (OH) layer on the Li(Ni0.8 Co0.15 Al0.05 )O2 , of which the Ca4.67 Li0.33 (PO4 )3 (OH) is transformed to CaF2 via Ca4.67 Li0.33 (PO4 )3 F during the long term cycles reacting with HF in electrolyte.	po4	147-150	carbonic anhydrase 4	Homo sapiens	214-217
34677913-5	2021	Also, morphological degradations such as micro-cracking or amorphization of surface are significantly suppressed by the presence of Ca4.67 Li0.33 (PO4 )3 (OH) layer on the Li(Ni0.8 Co0.15 Al0.05 )O2 , of which the Ca4.67 Li0.33 (PO4 )3 (OH) is transformed to CaF2 via Ca4.67 Li0.33 (PO4 )3 F during the long term cycles reacting with HF in electrolyte.	po4	147-150	CCR4-NOT transcription complex subunit 8	Homo sapiens	259-263
34677913-5	2021	Also, morphological degradations such as micro-cracking or amorphization of surface are significantly suppressed by the presence of Ca4.67 Li0.33 (PO4 )3 (OH) layer on the Li(Ni0.8 Co0.15 Al0.05 )O2 , of which the Ca4.67 Li0.33 (PO4 )3 (OH) is transformed to CaF2 via Ca4.67 Li0.33 (PO4 )3 F during the long term cycles reacting with HF in electrolyte.	po4	147-150	carbonic anhydrase 4	Homo sapiens	268-271
34677913-5	2021	Also, morphological degradations such as micro-cracking or amorphization of surface are significantly suppressed by the presence of Ca4.67 Li0.33 (PO4 )3 (OH) layer on the Li(Ni0.8 Co0.15 Al0.05 )O2 , of which the Ca4.67 Li0.33 (PO4 )3 (OH) is transformed to CaF2 via Ca4.67 Li0.33 (PO4 )3 F during the long term cycles reacting with HF in electrolyte.	po4	229-232	carbonic anhydrase 4	Homo sapiens	132-135
34677913-5	2021	Also, morphological degradations such as micro-cracking or amorphization of surface are significantly suppressed by the presence of Ca4.67 Li0.33 (PO4 )3 (OH) layer on the Li(Ni0.8 Co0.15 Al0.05 )O2 , of which the Ca4.67 Li0.33 (PO4 )3 (OH) is transformed to CaF2 via Ca4.67 Li0.33 (PO4 )3 F during the long term cycles reacting with HF in electrolyte.	po4	229-232	carbonic anhydrase 4	Homo sapiens	214-217
34677913-5	2021	Also, morphological degradations such as micro-cracking or amorphization of surface are significantly suppressed by the presence of Ca4.67 Li0.33 (PO4 )3 (OH) layer on the Li(Ni0.8 Co0.15 Al0.05 )O2 , of which the Ca4.67 Li0.33 (PO4 )3 (OH) is transformed to CaF2 via Ca4.67 Li0.33 (PO4 )3 F during the long term cycles reacting with HF in electrolyte.	po4	229-232	CCR4-NOT transcription complex subunit 8	Homo sapiens	259-263
34677913-5	2021	Also, morphological degradations such as micro-cracking or amorphization of surface are significantly suppressed by the presence of Ca4.67 Li0.33 (PO4 )3 (OH) layer on the Li(Ni0.8 Co0.15 Al0.05 )O2 , of which the Ca4.67 Li0.33 (PO4 )3 (OH) is transformed to CaF2 via Ca4.67 Li0.33 (PO4 )3 F during the long term cycles reacting with HF in electrolyte.	po4	229-232	carbonic anhydrase 4	Homo sapiens	268-271
34831136-6	2021	PFKFB3 synthesizes F2,6P2 through the phosphorylation of F6P with a donated PO4 group from ATP and has the highest kinase activity of all PFKFB isoenzymes.	po4	76-79	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3	Homo sapiens	0-6
34606719-0	2021	Reaction of Li1.3Al0.3Ti1.7(PO4)3 and LiNi0.6Co0.2Mn0.2O2 in Co-Sintered Composite Cathodes for Solid-State Batteries.	po4	28-31	transglutaminase 1	Homo sapiens	12-15
35174991-7	2022	A simultaneous formation of Na5 V2 (PO4 )3 phase in the anode and NaV2 (PO4 )3 phase in the cathode is revealed by synchrotron-based X-ray diffraction and X-ray absorption spectroscopy.	po4	72-75	neuron navigator 2	Homo sapiens	66-70
3552262-6	1987	In contrast, sheetlike lamellipodia were formed in EGF-treated cells by the addition of K+ or PO4(3-) to the NaCl solution or by the addition of PO4(3-) to the LiCl solution.	po4	94-97	epidermal growth factor	Homo sapiens	51-54
3257964-6	1988	Thiophosphorylated LC20 could be subsequently phosphorylated at a threonine residue to a stoichiometry of 1.7 mol of PO4/mol of LC20 by incubation in the presence of MgATP, calcium, and calmodulin.	po4	117-120	myosin light chain 9	Homo sapiens	19-23
2971667-7	1988	In the presence of saturating tropomyosin, a 2-fold difference in Vmax was measured: phosphorylated, aortic, 0.119 +/- 0.009 versus stomach, 0.239 +/- 0.012 mumol of PO4 liberated/min/mg of myosin; nonphosphorylated, aortic, 0.065 +/- 0.004 versus stomach, 0.123 +/- 0.004 mumol of PO4 liberated/min/mg of myosin.	po4	166-169	myosin heavy chain 14	Homo sapiens	35-41
2971667-7	1988	In the presence of saturating tropomyosin, a 2-fold difference in Vmax was measured: phosphorylated, aortic, 0.119 +/- 0.009 versus stomach, 0.239 +/- 0.012 mumol of PO4 liberated/min/mg of myosin; nonphosphorylated, aortic, 0.065 +/- 0.004 versus stomach, 0.123 +/- 0.004 mumol of PO4 liberated/min/mg of myosin.	po4	282-285	myosin heavy chain 14	Homo sapiens	35-41
3339007-3	1988	In solution, each kinase catalyzed the incorporation of 1-4 mol of PO4/mol of band 4.1.	po4	67-70	erythrocyte membrane protein band 4.1	Homo sapiens	78-86
3339007-6	1988	Phosphorylation of band 4.1 by each kinase for increasing time periods enabled us to demonstrate an approximately linear inverse relationship between PO4 incorporation into band 4.1 and spectrin binding.	po4	150-153	erythrocyte membrane protein band 4.1	Homo sapiens	19-27
3339007-6	1988	Phosphorylation of band 4.1 by each kinase for increasing time periods enabled us to demonstrate an approximately linear inverse relationship between PO4 incorporation into band 4.1 and spectrin binding.	po4	150-153	erythrocyte membrane protein band 4.1	Homo sapiens	173-181
3285297-5	1988	In contrast, P74raf, which was detected into a spontaneously transformed 3T3 (R+/Cl 3) cell line and may represent the full-length gene product of c-raf, appeared to incorporate [32P]PO4 less efficiently in vivo and exhibited a barely detectable associated kinase activity in only half of the experiments.	po4	183-186	v-raf-leukemia viral oncogene 1	Mus musculus	147-152
3593411-6	1987	In primary hepatocyte cultures, CCl4, DCE, and PE exposure increased the activity of phosphorylase a at 5 min from 39 +/- 2 to 130 +/- 12, 80 +/- 13, and 97 +/- 10 nmoles PO4(3-)/mg protein/min respectively.	po4	171-174	C-C motif chemokine ligand 4	Rattus norvegicus	32-36
3552262-6	1987	In contrast, sheetlike lamellipodia were formed in EGF-treated cells by the addition of K+ or PO4(3-) to the NaCl solution or by the addition of PO4(3-) to the LiCl solution.	po4	145-148	epidermal growth factor	Homo sapiens	51-54
3552262-7	1987	These findings indicate that Li+, K+, PO4(3-) and vanadate are involved in the processes of EGF-induced morphological changes.	po4	38-41	epidermal growth factor	Homo sapiens	92-95
6294112-10	1983	In intact cells incubated with [32P]PO4, PTH stimulated most noticeably the phosphorylation of the 35,000-dalton protein.	po4	36-39	parathyroid hormone	Gallus gallus	41-44
6499771-7	1984	Fractional excretion of PO4 rose from 1.58 +/- 0.6% to 29.5 +/- 2.5% with active PTH and from 1.4 +/- 0.4% to 5.7 +/- 1% with oxidized PTH.	po4	24-27	parathyroid hormone	Canis lupus familiaris	81-84
6499771-7	1984	Fractional excretion of PO4 rose from 1.58 +/- 0.6% to 29.5 +/- 2.5% with active PTH and from 1.4 +/- 0.4% to 5.7 +/- 1% with oxidized PTH.	po4	24-27	parathyroid hormone	Canis lupus familiaris	135-138
6597316-10	1984	In the PST, PTH (1 microgram/ml) inhibited Jv and Jl-b PO4 by 34 and 20%, respectively (P less than 0.01).	po4	55-58	parathyroid hormone	Oryctolagus cuniculus	12-15
6465346-2	1984	Subsequent parathyroid hormone (PTH) infusion caused net PO4 secretion.	po4	57-60	parathyroid hormone	Gallus gallus	11-30
6321942-5	1984	Both phosphatidic acid (PA) and 1,2-diacylglycerol levels increased in response to TRH in [32P]PO4- and [3H]glycerol-labeled GH3 cells.	po4	95-98	thyrotropin releasing hormone	Rattus norvegicus	83-86
6971290-4	1981	In fetal human bone, the level of BGP (grams of BGP/mol of bone PO4) rises from 5% of the adult level at 10 weeks gestational age to the adult level at 15 weeks.	po4	64-67	bone gamma-carboxyglutamate protein	Homo sapiens	34-37
6282142-12	1982	Our findings on cAMP are most compatible with the hypothesis that biochemical events beyond cAMP generation mediate both the phosphaturia of NH4Cl and its ability to restore PTH sensitivity in PO4 deprivation.	po4	193-196	parathyroid hormone	Rattus norvegicus	174-177
7067299-4	1982	The Ca:PO4 ratio in the mitochondria of bone lining cells rises slightly with a small dose of parathyroid hormone and is reduced with a small dose of calcitonin.	po4	7-10	parathyroid hormone	Rattus norvegicus	94-113
7067299-4	1982	The Ca:PO4 ratio in the mitochondria of bone lining cells rises slightly with a small dose of parathyroid hormone and is reduced with a small dose of calcitonin.	po4	7-10	calcitonin-related polypeptide alpha	Rattus norvegicus	150-160
6293671-2	1982	Kept wet at room temperature, this phosphate is hydrolyzed according to the reaction PO4(3-) + H2O leads to HPO4(2-) + OH-; a tricalcium orthophosphate series is then formed, its general formula is Ca9 (HPO4)x (PO4)6-x (OH)x, O less than or equal to x less than or equal to 1.	po4	85-88	carbonic anhydrase 9	Homo sapiens	198-201
6971290-4	1981	In fetal human bone, the level of BGP (grams of BGP/mol of bone PO4) rises from 5% of the adult level at 10 weeks gestational age to the adult level at 15 weeks.	po4	64-67	bone gamma-carboxyglutamate protein	Homo sapiens	48-51
7356023-3	1980	In the presence of a constant infusion of parathyroid hormone (PTH) the drug caused a greater degree of natriuresis, calciuria, and bicarbonaturia and a significant increase in %E of PO4 (from 7.4 +/- 1.6 to 20.0 +/- 2.1, P less than 0.05).	po4	183-186	parathyroid hormone	Canis lupus familiaris	42-61
7016738-7	1981	Adsorption of fibrinogen was accomplished using a 0.05 M phosphate/0.2 M NaCl/0.02% NaN3/pH 7.0 buffer system followed by elution with 0.05 M PO4/1 M NaCl/0.02% NaN3 to remove non specifically bound components.	po4	142-145	fibrinogen beta chain	Homo sapiens	14-24
6247419-9	1980	Extrapolation of the relation to the lowest Ca sensitivity observed gives a stoichiometry of about 0.8 mol PO4 per mol TNI.	po4	107-110	troponin I3, cardiac type	Rattus norvegicus	119-122
484524-5	1979	By contrast, other factors must play a dominant role in regulating net intestinal PO4 and Mg absorption.	po4	82-85	solute carrier family 6 member 2	Homo sapiens	67-70
33070860-1	2020	Alkaline phosphatase (ALP), which converts the phosphate group (-PO4) in the substrate to the hydroxyl group (-OH), is a useful tool in the biological analysis, a good indicator of dissolved inorganic phosphorus levels and an important biomarker for several diseases.	po4	65-68	alkaline phosphatase, placental	Homo sapiens	0-20
850143-0	1977	Effect of acetazolamide and parathyroid hormone on HCO3 and PO4 excretion.	po4	60-63	parathyroid hormone	Canis lupus familiaris	28-47
6048324-2	1967	The control of Ca2 plus and PO4-3 minus exchange by univalent CATION Ca2 plus substitution at the hydroxyapatite crystal surface.	po4	28-31	carbonic anhydrase 2	Homo sapiens	69-72
33396498-1	2020	In Arabidopsis thaliana (Arabidopsis), the microRNA399 (miR399)/PHOSPHATE2 (PHO2) expression module is central to the response of Arabidopsis to phosphate (PO4) stress.	po4	156-159	MIR399f	Arabidopsis thaliana	43-54
33396498-1	2020	In Arabidopsis thaliana (Arabidopsis), the microRNA399 (miR399)/PHOSPHATE2 (PHO2) expression module is central to the response of Arabidopsis to phosphate (PO4) stress.	po4	156-159	MIR399f	Arabidopsis thaliana	56-62
33396498-1	2020	In Arabidopsis thaliana (Arabidopsis), the microRNA399 (miR399)/PHOSPHATE2 (PHO2) expression module is central to the response of Arabidopsis to phosphate (PO4) stress.	po4	156-159	phosphate 2	Arabidopsis thaliana	64-74
33396498-1	2020	In Arabidopsis thaliana (Arabidopsis), the microRNA399 (miR399)/PHOSPHATE2 (PHO2) expression module is central to the response of Arabidopsis to phosphate (PO4) stress.	po4	156-159	phosphate 2	Arabidopsis thaliana	76-80
33453600-2	2021	Benefitting from highly condensed and flexible framework structure of beta-Ca3(PO4)2-type compounds, we have successfully prepared three different kinds of novel high color purity red-emitting phosphors Sr19Mg2(PO4)14: Re3+ (Re3+= Eu3+, Sm3+, Pr3+) by using traditional sintering method.	po4	79-82	small nucleolar RNA, H/ACA box 3A	Homo sapiens	70-78
33641329-0	2021	Color-Tunable Persistent Luminescence of Ca10M(PO4)7:Eu2+ (M = Li, Na, and K) with a beta-Ca3(PO4)2-Type Structure.	po4	47-50	small nucleolar RNA, H/ACA box 3A	Homo sapiens	85-93
33641329-2	2021	Herein, the persistent luminescence (PersL) properties of Eu2+-doped Ca10M(PO4)7 phosphors with a beta-Ca3(PO4)2-type structure are reported.	po4	75-78	small nucleolar RNA, H/ACA box 3A	Homo sapiens	98-106
33257245-0	2021	Controllable luminescence and efficient energy transfer investigation of a novel white light emission phosphor Ca19Na2Mg(PO4)14: Dy3+, Tm3+ with high thermal stability.	po4	121-124	tropomyosin 3	Homo sapiens	135-138
33257245-9	2021	Moreover, CNMP: Dy3+, Tm3+ exhibites a high thermal stability and the emission intensity still keeps 84% of the initial intensity of Dy3+ at 230  C. These outstanding properties show that Ca19Na2Mg(PO4)14: Dy3+, Tm3+ have great advantages and potentiality for applying in solid state lighting.	po4	198-201	tropomyosin 3	Homo sapiens	22-25
33257245-9	2021	Moreover, CNMP: Dy3+, Tm3+ exhibites a high thermal stability and the emission intensity still keeps 84% of the initial intensity of Dy3+ at 230  C. These outstanding properties show that Ca19Na2Mg(PO4)14: Dy3+, Tm3+ have great advantages and potentiality for applying in solid state lighting.	po4	198-201	tropomyosin 3	Homo sapiens	212-215
33644700-2	2021	Herein, we present work on the conceptually interesting NASICON-type all-solid-state battery LiM2(PO4)3, using M = Ti in the cathode, M = Zr in the electrolyte, and a Li metal anode.	po4	98-101	lens intrinsic membrane protein 2	Homo sapiens	93-97
33070860-1	2020	Alkaline phosphatase (ALP), which converts the phosphate group (-PO4) in the substrate to the hydroxyl group (-OH), is a useful tool in the biological analysis, a good indicator of dissolved inorganic phosphorus levels and an important biomarker for several diseases.	po4	65-68	alkaline phosphatase, placental	Homo sapiens	22-25
33070860-2	2020	In conventional designs for ALP detection, both the interferent with a -PO4 and the target with a -OH will go into the sensing path and give out the undesired background and the desired signal respectively.	po4	72-75	alkaline phosphatase, placental	Homo sapiens	28-31
32678403-0	2020	Sulfur doped Li1.3Al0.3Ti1.7(PO4)3 solid electrolytes with enhanced ionic conductivity and a reduced activation energy barrier.	po4	29-32	transglutaminase 1	Homo sapiens	13-16
32893499-2	2020	In this work, phosphate ion (PO4 3- )-doped SnS2 (P-SnS2 ) nanoflake arrays on conductive TiC/C backbone are reported to form high-quality P-SnS2 @TiC/C arrays via a hydrothermal-chemical vapor deposition method.	po4	29-32	sodium voltage-gated channel alpha subunit 11	Homo sapiens	44-48
32893499-2	2020	In this work, phosphate ion (PO4 3- )-doped SnS2 (P-SnS2 ) nanoflake arrays on conductive TiC/C backbone are reported to form high-quality P-SnS2 @TiC/C arrays via a hydrothermal-chemical vapor deposition method.	po4	29-32	sodium voltage-gated channel alpha subunit 11	Homo sapiens	50-56
32893499-2	2020	In this work, phosphate ion (PO4 3- )-doped SnS2 (P-SnS2 ) nanoflake arrays on conductive TiC/C backbone are reported to form high-quality P-SnS2 @TiC/C arrays via a hydrothermal-chemical vapor deposition method.	po4	29-32	aryl hydrocarbon receptor nuclear translocator like	Homo sapiens	90-93
32893499-2	2020	In this work, phosphate ion (PO4 3- )-doped SnS2 (P-SnS2 ) nanoflake arrays on conductive TiC/C backbone are reported to form high-quality P-SnS2 @TiC/C arrays via a hydrothermal-chemical vapor deposition method.	po4	29-32	sodium voltage-gated channel alpha subunit 11	Homo sapiens	52-56
32893499-2	2020	In this work, phosphate ion (PO4 3- )-doped SnS2 (P-SnS2 ) nanoflake arrays on conductive TiC/C backbone are reported to form high-quality P-SnS2 @TiC/C arrays via a hydrothermal-chemical vapor deposition method.	po4	29-32	aryl hydrocarbon receptor nuclear translocator like	Homo sapiens	147-150
32893499-3	2020	By virtue of the synergistic effect between PO4 3- doping and conductive network of TiC/C arrays, enhanced electronic conductivity and enlarged interlayer spacing are realized in the designed P-SnS2 @TiC/C arrays.	po4	44-47	aryl hydrocarbon receptor nuclear translocator like	Homo sapiens	84-87
32893499-3	2020	By virtue of the synergistic effect between PO4 3- doping and conductive network of TiC/C arrays, enhanced electronic conductivity and enlarged interlayer spacing are realized in the designed P-SnS2 @TiC/C arrays.	po4	44-47	sodium voltage-gated channel alpha subunit 11	Homo sapiens	194-198
32893499-3	2020	By virtue of the synergistic effect between PO4 3- doping and conductive network of TiC/C arrays, enhanced electronic conductivity and enlarged interlayer spacing are realized in the designed P-SnS2 @TiC/C arrays.	po4	44-47	aryl hydrocarbon receptor nuclear translocator like	Homo sapiens	200-203
32974302-5	2020	Fmoc-FFpY peptides (F: phenylalanine; Y: tyrosine; p: PO4 2-) are dephosphorylated enzymatically into Fmoc-FFY by action of alkaline phosphatase functionalized silica nanoparticles (NPs@AP), previously deposited on a surface.	po4	54-57	AT695_RS04080	Staphylococcus aureus	124-144
32786252-3	2020	Herein, a new electrolyte additive copper fluoride (CuF2) is used in liquid electrolyte to construct a stable interphase between Li1.5Al0.5Ge1.5(PO4)3 (LAGP) SSE and Li metal for a quasi-solid-state Li-S battery.	po4	145-148	transglutaminase 1	Homo sapiens	129-132
32939306-0	2020	Synthesis, crystal structure determination of a novel phosphate Ag1.64Zn1.64Fe1.36(PO4)3 with an alluaudite-like structure.	po4	83-86	thioredoxin domain containing 12	Homo sapiens	64-67
32939306-1	2020	Single crystals of Ag1.64Zn1.64Fe1.36(PO4)3 [silver zinc iron phosphate (1.64/1.64/1.36/3)] have been synthesized by a conventional solid-state reaction and structurally characterized by single-crystal X-ray diffraction.	po4	38-41	thioredoxin domain containing 12	Homo sapiens	19-22
32409050-4	2020	The Mg2.75Sr0.25(PO4)2 bioceramic had the most desirable overall performance, as reflected by considerably high compressive strength, enhanced in vitro osteogenesis and inhibited osteoclastic activities.	po4	17-20	mucin 7, secreted	Homo sapiens	4-7
32409050-5	2020	Therefore, the Mg2.75Sr0.25(PO4)2 bioceramic is considered a promising biomaterial for osteoporotic bone regeneration.	po4	28-31	mucin 7, secreted	Homo sapiens	15-18
31932322-1	2020	The enzyme Tpt1 removes an internal RNA 2"-PO4 via a two-step reaction in which: (i) the 2"-PO4 attacks NAD+ to form an RNA-2"-phospho-(ADP-ribose) intermediate and nicotinamide; and (ii) transesterification of the ADP-ribose O2"" to the RNA 2"-phosphodiester yields 2"-OH RNA and ADP-ribose-1"",2""-cyclic phosphate.	po4	43-46	tumor protein, translationally-controlled 1	Homo sapiens	11-15
32268605-3	2020	The dense Li1.1Y0.1Zr1.9(PO4)3 pellet prepared by hot-pressing shows a high Li-ion conductivity of 9 x 10-5 S cm-1, which is two orders of magnitude higher than that of LiZr2(PO4)3.	po4	25-28	transglutaminase 1	Homo sapiens	10-13
31019096-3	2019	An attractive prospect is that Tpt1 enzymes might catalyze reactions other than internal RNA 2"-PO4 removal, via their unique NAD+-dependent transferase mechanism.	po4	96-99	tumor protein, translationally-controlled 1	Homo sapiens	31-35
31029349-1	2019	Hydroxyapatite (Ca10(PO4)6(OH)2, HAP1) an immensely favoured biomaterial in the medical industry, is known for its extensive applications in orthopaedics and dentistry because of its bioactivity and osteoconductivity.	po4	21-24	huntingtin associated protein 1	Homo sapiens	33-37
28747359-5	2017	The model predicts that large perturbations in PTH or vitamin D3 synthesis have a greater impact on the plasma concentration of Ca2+ ([Ca2+]p) than on that of PO4 ([PO4]p); due to negative feedback loops, [PO4]p does not consistently increase when the production rate of PTH or vitamin D3 is decreased.	po4	165-168	parathyroid hormone	Rattus norvegicus	47-50
30916953-0	2019	Tuning of the Compositions and Multiple Activator Sites toward Single-Phased White Emission in (Ca9- xSr x)MgK(PO4)7:Eu2+ Phosphors for Solid-State Lighting.	po4	111-114	carbonic anhydrase 9	Homo sapiens	96-99
31182610-5	2019	Here, we show that deletion of the neurotrophin brain-derived neurotrophic factor (BDNF)-dependent GR-phosphorylation (PO4) sites impairs long-term memory retention and maintenance of newly formed postsynaptic dendritic spines in the mouse cortex after motor skills training.	po4	119-122	brain derived neurotrophic factor	Mus musculus	83-87
31182610-6	2019	Chronic stress and the BDNF polymorphism Val66Met disrupt the BDNF-dependent GR-PO4 pathway necessary for preserving training-induced spines and previously acquired memories.	po4	80-83	brain derived neurotrophic factor	Mus musculus	23-27
31182610-6	2019	Chronic stress and the BDNF polymorphism Val66Met disrupt the BDNF-dependent GR-PO4 pathway necessary for preserving training-induced spines and previously acquired memories.	po4	80-83	brain derived neurotrophic factor	Mus musculus	62-66
31182610-7	2019	Conversely, enrichment living promotes spine formation but fails to salvage training-related spines in mice lacking BDNF-dependent GR-PO4 sites, suggesting it is essential for spine consolidation and memory retention.	po4	134-137	brain derived neurotrophic factor	Mus musculus	116-120
31086001-4	2019	PHO2 is itself under tight regulation by the PO4 responsive microRNA (miRNA), miR399.	po4	45-48	phosphate 2	Arabidopsis thaliana	0-4
31086001-4	2019	PHO2 is itself under tight regulation by the PO4 responsive microRNA (miRNA), miR399.	po4	45-48	MIR399f	Arabidopsis thaliana	78-84
31086001-6	2019	Here, we assessed the requirement of DRB1, DRB2 and DRB4 to regulate the miR399/PHO2 expression module under PO4 starvations conditions.	po4	109-112	dsRNA-binding domain-like superfamily protein	Arabidopsis thaliana	37-41
31086001-6	2019	Here, we assessed the requirement of DRB1, DRB2 and DRB4 to regulate the miR399/PHO2 expression module under PO4 starvations conditions.	po4	109-112	double-stranded-RNA-binding protein 4	Arabidopsis thaliana	52-56
31086001-6	2019	Here, we assessed the requirement of DRB1, DRB2 and DRB4 to regulate the miR399/PHO2 expression module under PO4 starvations conditions.	po4	109-112	MIR399f	Arabidopsis thaliana	73-79
31086001-6	2019	Here, we assessed the requirement of DRB1, DRB2 and DRB4 to regulate the miR399/PHO2 expression module under PO4 starvations conditions.	po4	109-112	phosphate 2	Arabidopsis thaliana	80-84
32187608-2	2019	We aimed to evaluate age- and pregnancy-related changes in MEPE and FGF-23 levels and their correlations with calcium (Ca)-phosphate (PO4) metabolism.	po4	134-137	matrix extracellular phosphoglycoprotein	Homo sapiens	59-63
32187608-2	2019	We aimed to evaluate age- and pregnancy-related changes in MEPE and FGF-23 levels and their correlations with calcium (Ca)-phosphate (PO4) metabolism.	po4	134-137	fibroblast growth factor 23	Homo sapiens	68-74
32187608-11	2019	MEPE was positively correlated with S-Ca, S-PO4 and TmPO4/GFR and negatively correlated with PTH, IGF-1, and IGFBP-3.	po4	44-47	matrix extracellular phosphoglycoprotein	Homo sapiens	0-4
30351061-9	2018	From this, the crystal structures of CBP xF: yBi3+ ( y = 0.05, 0.15; x = 0-3) has been inferred to transform from Ca5(BO3)3F (ISCD-65763) to Ca5(PO4)3F (ISCD-30261), and then to Ca5(PO4)3F (ISCD-9444) with x increasing.	po4	145-148	CREB binding protein	Homo sapiens	37-40
29846115-10	2018	Furthermore, PTH is predicted to exert an indirect impact on PO4 reabsorption via its inhibitory action on NHE3.	po4	61-64	solute carrier family 9 member A3	Rattus norvegicus	107-111
30150536-11	2018	The sealant formulation with NACP at 20% displayed desirable mechanical performance and ideal flow and handling properties, and also showed high levels of long-term Ca and PO4 ion release and excellent recharge capabilities.	po4	172-175	synuclein alpha	Homo sapiens	29-33
28747359-4	2017	Our results suggest that the Ca and PO4 homeostatic systems are robust enough to handle small perturbations in the production rate of either PTH or vitamin D3.	po4	36-39	parathyroid hormone	Rattus norvegicus	141-144
28747359-5	2017	The model predicts that large perturbations in PTH or vitamin D3 synthesis have a greater impact on the plasma concentration of Ca2+ ([Ca2+]p) than on that of PO4 ([PO4]p); due to negative feedback loops, [PO4]p does not consistently increase when the production rate of PTH or vitamin D3 is decreased.	po4	159-162	parathyroid hormone	Rattus norvegicus	47-50
28747359-5	2017	The model predicts that large perturbations in PTH or vitamin D3 synthesis have a greater impact on the plasma concentration of Ca2+ ([Ca2+]p) than on that of PO4 ([PO4]p); due to negative feedback loops, [PO4]p does not consistently increase when the production rate of PTH or vitamin D3 is decreased.	po4	165-168	parathyroid hormone	Rattus norvegicus	47-50
28936578-8	2017	The common presence of NO3 in waters of the phreatic zone of the Czestochowa Upland, an area developed in an agricultural direction, is documented by, inter alia, the exploitation of intakes supplying the city of Czestochowa (10-57 mg dm-3, 2011) and crenological studies from 2008 to 2015 (NO3, 2-58 mg dm-3), at simultaneously low phosphate concentrations (PO4, 0.02-0.24 mg dm-3).	po4	359-362	NBL1, DAN family BMP antagonist	Homo sapiens	23-26
28960575-2	2017	Here, mesoporous Na3 V2 (PO4 )3 /C (NVP/C) spheres have been synthesized through a facile spray-drying-annealing method, and their electrochemically desodiated phase NaV2 (PO4 )3 /C (ED-NVP/C) has been investigated as an intercalation host for Mg2+ ions.	po4	25-28	neuron navigator 2	Homo sapiens	166-170
28287220-0	2017	A NaV3(PO4)3@C hierarchical nanofiber in high alignment: exploring a novel high-performance anode for aqueous rechargeable sodium batteries.	po4	7-10	neuron navigator 3	Homo sapiens	2-6
28471641-5	2017	In addition, combined with the typical Na3V2(PO4)3 cathode to constitute full SIBs, the assembled FTO CNT//Na3V2(PO4)3 batteries are also demonstrated with superior rate capability and a long cycle life.	po4	45-48	FTO alpha-ketoglutarate dependent dioxygenase	Homo sapiens	98-101
28471641-5	2017	In addition, combined with the typical Na3V2(PO4)3 cathode to constitute full SIBs, the assembled FTO CNT//Na3V2(PO4)3 batteries are also demonstrated with superior rate capability and a long cycle life.	po4	113-116	FTO alpha-ketoglutarate dependent dioxygenase	Homo sapiens	98-101
31457522-6	2017	All three complexes exhibit a mu4:eta1:eta1:eta1:eta1 bridging mode of the PO4 3-/HPO4 2-/AsO4 3- groups, with each bridging among four metal ions.	po4	75-78	secreted phosphoprotein 1	Homo sapiens	34-38
31457522-6	2017	All three complexes exhibit a mu4:eta1:eta1:eta1:eta1 bridging mode of the PO4 3-/HPO4 2-/AsO4 3- groups, with each bridging among four metal ions.	po4	75-78	secreted phosphoprotein 1	Homo sapiens	39-43
31457522-6	2017	All three complexes exhibit a mu4:eta1:eta1:eta1:eta1 bridging mode of the PO4 3-/HPO4 2-/AsO4 3- groups, with each bridging among four metal ions.	po4	75-78	secreted phosphoprotein 1	Homo sapiens	39-43
31457522-6	2017	All three complexes exhibit a mu4:eta1:eta1:eta1:eta1 bridging mode of the PO4 3-/HPO4 2-/AsO4 3- groups, with each bridging among four metal ions.	po4	75-78	secreted phosphoprotein 1	Homo sapiens	39-43
28287220-4	2017	For the first time, its sodium intercalation mechanism in an aqueous electrolyte is explored, and moreover, the well-aligned NaV3(PO4)3@porous carbon nanofiber is constructed to fulfil its full potential.	po4	130-133	neuron navigator 3	Homo sapiens	125-129
28287220-5	2017	Based on the reversible phase transformation and 3D open framework, the NaV3(PO4)3 is demonstrated to be reliable in the aqueous electrolyte.	po4	77-80	neuron navigator 3	Homo sapiens	72-76
27749988-0	2016	Correlation between the O 2p Orbital and Redox Reaction in LiMn0.6 Fe0.4 PO4 Nanowires Studied by Soft X-ray Absorption.	po4	73-76	immunoglobulin kappa variable 1D-39	Homo sapiens	24-28
27859382-11	2017	Hypotonic stress response and morphology were less and p-selectin (CD62P) binding was greater in -Ca/-PO4 PLT aliquots.	po4	102-105	selectin P	Homo sapiens	55-65
27859382-11	2017	Hypotonic stress response and morphology were less and p-selectin (CD62P) binding was greater in -Ca/-PO4 PLT aliquots.	po4	102-105	selectin P	Homo sapiens	67-72
27859382-13	2017	Phosphorylation of p38 mitogen-activated protein kinase (MAPK) was greater in -Ca and -Ca/-PO4 PLT aliquots during storage.	po4	91-94	mitogen-activated protein kinase 14	Homo sapiens	19-55
28098285-2	2017	Herein we report on the discovery of a novel anhydrous non-centrosymmetric alkali fluorinated borophosphate KB(PO4)F (KBPF) featuring a cut-off wavelength of less than 200 nm and a large second-harmonic generation (SHG) effect similar to KH2PO4 (KDP), hence representing a new promising deep-ultraviolet NLO material.	po4	111-114	WNK lysine deficient protein kinase 1	Homo sapiens	246-249
28944060-4	2017	Co-precipitation yielded HAp with higher selenite contents than sorption and the stoichiometry of HAp richest in selenite was represented as Ca9.75(PO4)5.75(SeO3)0.25(OH)1.75.	po4	148-151	retinoic acid receptor, beta	Mus musculus	98-101
27749037-0	2016	Incorporation of Thorium in the Zircon Structure Type through the Th1-xErx(SiO4)1-x(PO4)x Thorite-Xenotime Solid Solution.	po4	84-87	negative elongation factor complex member C/D	Homo sapiens	66-69
26207797-7	2016	Baseline hydrolytic activity of the F0F1-ATPase enzyme increased in the three study groups vs. normal values (184.50 +- 7.84 nmol PO4), placebo, 304.12 +- 22.83 nmol PO4 (P &lt; 0.002); ubiquinone, 312.41 +- 25.63 nmol PO4 (P &lt; 0.009); and combined therapy, 371.28 +- 33.50 nmol PO4 (P &lt; 0.002).	po4	130-133	ATP synthase F1 subunit epsilon	Homo sapiens	36-47
27711630-0	2016	Crystal structure, luminescence properties, energy transfer and thermal properties of a novel color-tunable, white light-emitting phosphor Ca9-x-yCe(PO4)7:xEu2+,yMn2.	po4	149-152	carbonic anhydrase 9	Homo sapiens	139-142
27294328-11	2016	When PTH was increasing, the strongest cross-correlation was with Ca(2+) at 0 lags (3.5 min) (r = -0.902 to -0.950); during recovery, the strongest cross-correlation was with PO4 at 0 lags (8 min) (r = 0.987-0.995).	po4	175-178	parathyroid hormone	Homo sapiens	5-8
27294328-12	2016	CONCLUSIONS: PTH secretion during exercise and recovery is controlled by a combination of changes in Ca(2+) and PO4 in men.	po4	112-115	parathyroid hormone	Homo sapiens	13-16
27409598-1	2016	In this study, a simple and amplified colorimetric assay is developed for the detection of the enzymatic activity of glucose oxidase (GOx) based on in situ formation of a photoswitchable oxidase mimetic of PO4(3-)-capped CdS quantum dots (QDs).	po4	206-209	hydroxyacid oxidase 1	Homo sapiens	117-132
27409598-1	2016	In this study, a simple and amplified colorimetric assay is developed for the detection of the enzymatic activity of glucose oxidase (GOx) based on in situ formation of a photoswitchable oxidase mimetic of PO4(3-)-capped CdS quantum dots (QDs).	po4	206-209	hydroxyacid oxidase 1	Homo sapiens	134-137
27409598-2	2016	GOx catalyzes the oxidation of 1-thio-beta-d-glucose to give 1-thio-beta-d-gluconic acid which spontaneously hydrolyzes to beta-d-gluconic acid and H2S; the generated H2S instantly reacts with Cd(2+) in the presence of Na3PO4 to give PO4(3-)-stabilized CdS QDs in situ.	po4	222-225	hydroxyacid oxidase 1	Homo sapiens	0-3
26207797-7	2016	Baseline hydrolytic activity of the F0F1-ATPase enzyme increased in the three study groups vs. normal values (184.50 +- 7.84 nmol PO4), placebo, 304.12 +- 22.83 nmol PO4 (P &lt; 0.002); ubiquinone, 312.41 +- 25.63 nmol PO4 (P &lt; 0.009); and combined therapy, 371.28 +- 33.50 nmol PO4 (P &lt; 0.002).	po4	166-169	ATP synthase F1 subunit epsilon	Homo sapiens	36-47
26207797-7	2016	Baseline hydrolytic activity of the F0F1-ATPase enzyme increased in the three study groups vs. normal values (184.50 +- 7.84 nmol PO4), placebo, 304.12 +- 22.83 nmol PO4 (P &lt; 0.002); ubiquinone, 312.41 +- 25.63 nmol PO4 (P &lt; 0.009); and combined therapy, 371.28 +- 33.50 nmol PO4 (P &lt; 0.002).	po4	166-169	ATP synthase F1 subunit epsilon	Homo sapiens	36-47
26207797-7	2016	Baseline hydrolytic activity of the F0F1-ATPase enzyme increased in the three study groups vs. normal values (184.50 +- 7.84 nmol PO4), placebo, 304.12 +- 22.83 nmol PO4 (P &lt; 0.002); ubiquinone, 312.41 +- 25.63 nmol PO4 (P &lt; 0.009); and combined therapy, 371.28 +- 33.50 nmol PO4 (P &lt; 0.002).	po4	166-169	ATP synthase F1 subunit epsilon	Homo sapiens	36-47
26531710-4	2016	At laboratory scale, As and Sb release was much higher under reducing conditions (up to 138 and 1 mug L(-1), respectively) compared to oxic conditions (up to 6 and 0.5 mug L(-1), respectively) and was enhanced by NO3 (-) and PO4 (3-) addition (increased by a factor of 2.3 for As and 1.6 for Sb).	po4	225-228	NBL1, DAN family BMP antagonist	Homo sapiens	213-216
25491819-4	2014	At 160 C, further hydrolysis reactions of urea and HPO4(2-) ions resulted in the generation of ample OH(-) and PO4(3-) ions, which provided a high chemical potential for the dissolution of Y-HAp and recrystallization of HAp and YPO4.	po4	52-55	reticulon 3	Homo sapiens	191-194
26734506-11	2015	Finally, using vacuum infiltration, we were able quantify induction of phospholipase D activity after AvrRpm1 recognition in leaves labeled with (33)PO4.	po4	149-152	phospholipase D delta	Arabidopsis thaliana	71-86
26373081-0	2015	Synthesis and Luminescence Properties of Blue Na(Sr0.97-xCa(x))PO4:0.03Eu2+ Phosphors for White Light Emitting Diode Applications.	po4	63-66	X chromosome controlling element	Homo sapiens	56-59
25090980-6	2015	The results showed that hexagonal-shaped gamma-MnS with a diameter of 2-3 mum and a thickness of 200-300 nm was obtained by biosynthesis at 0.014 g/L PO4(3-) dose and pH 5.8.	po4	150-153	glycophorin E (MNS blood group)	Homo sapiens	47-50
26827953-3	2016	1,25D/VDR signaling exerts feedback control of Ca/PO4 via regulation of FGF23, klotho, and CYP24A1 to prevent age-related, ectopic calcification, fibrosis, and associated pathologies.	po4	50-53	vitamin D receptor	Homo sapiens	6-9
25830567-1	2015	Stanniocalcin (STC), a glycoprotein hormone, is expressed in a wide variety of tissues to regulate Ca2+ and PO4- homeostasis.	po4	108-111	stanniocalcin 1	Homo sapiens	0-13
25830567-1	2015	Stanniocalcin (STC), a glycoprotein hormone, is expressed in a wide variety of tissues to regulate Ca2+ and PO4- homeostasis.	po4	108-111	stanniocalcin 1	Homo sapiens	15-18
25491819-5	2014	Finally, HAp tubes were formed in situ on Y-HAp according to the Kirkendall effect as a result of the difference of diffusion rate of cations (Ca(2+) ions, outward and slow) and anions (OH(-) and PO4(3-) ions, inward and fast).	po4	196-199	reticulon 3	Homo sapiens	9-12
25491819-4	2014	At 160 C, further hydrolysis reactions of urea and HPO4(2-) ions resulted in the generation of ample OH(-) and PO4(3-) ions, which provided a high chemical potential for the dissolution of Y-HAp and recrystallization of HAp and YPO4.	po4	52-55	reticulon 3	Homo sapiens	220-223
24317266-0	2014	A study of the phosphate mineral kapundaite NaCa(Fe3+)4(PO4)4(OH)3 5(H2O) using SEM/EDX and vibrational spectroscopic methods.	po4	56-59	nascent polypeptide associated complex subunit alpha	Homo sapiens	44-48
25157844-7	2014	In comparison with other nucleases, the AtBFN2/ligand-free and AtBFN2/PO4 models suggest a similar, previously proposed, catalytic mechanism.	po4	70-73	endonuclease 2	Arabidopsis thaliana	40-46
25157844-7	2014	In comparison with other nucleases, the AtBFN2/ligand-free and AtBFN2/PO4 models suggest a similar, previously proposed, catalytic mechanism.	po4	70-73	endonuclease 2	Arabidopsis thaliana	63-69
23493873-6	2013	More importantly, Ca(2+) ions are found to form ionic bridges to associate negatively charged residues of p3 with anionic headgroups of the lipid bilayer, resulting in Abeta-Ca(2+)-PO4(-) complexes.	po4	181-184	amyloid beta precursor protein	Homo sapiens	168-173
24310914-5	2014	The FTIR signal confirms the presence of isolated PO4 tetrahedron groups connected to different cations in PANK glass.	po4	50-53	pantothenate kinase 1	Homo sapiens	107-111
24125760-8	2014	CONCLUSIONS: Insulin resistant CKD patients demonstrated higher FGF-23 levels, and increased CAC, while PO4 levels remained normal, suggesting a potential link between insulin resistance and PO4 homeostasis in CKD.	po4	191-194	insulin	Homo sapiens	13-20
24125760-8	2014	CONCLUSIONS: Insulin resistant CKD patients demonstrated higher FGF-23 levels, and increased CAC, while PO4 levels remained normal, suggesting a potential link between insulin resistance and PO4 homeostasis in CKD.	po4	191-194	insulin	Homo sapiens	168-175
23904617-6	2013	Notch in conjunction with PKC activity upregulates the level of a hyperphosphorylated form of CREB (hyper-PO4 CREB) and triggers its ultradian oscillation, both of which are linked to LTM formation.	po4	106-109	Notch	Drosophila melanogaster	0-5
23904617-6	2013	Notch in conjunction with PKC activity upregulates the level of a hyperphosphorylated form of CREB (hyper-PO4 CREB) and triggers its ultradian oscillation, both of which are linked to LTM formation.	po4	106-109	cAMP responsive element binding protein 1	Homo sapiens	94-98
23904617-6	2013	Notch in conjunction with PKC activity upregulates the level of a hyperphosphorylated form of CREB (hyper-PO4 CREB) and triggers its ultradian oscillation, both of which are linked to LTM formation.	po4	106-109	cAMP responsive element binding protein 1	Homo sapiens	110-114
23904617-7	2013	One of the sites that is phosphorylated in hyper-PO4 CREB is serine 231, which is the functional equivalent of mammalian CREB serine 133, the phosphorylation of which is an important regulator of CREB functions.	po4	49-52	cAMP responsive element binding protein 1	Homo sapiens	53-57
23904617-7	2013	One of the sites that is phosphorylated in hyper-PO4 CREB is serine 231, which is the functional equivalent of mammalian CREB serine 133, the phosphorylation of which is an important regulator of CREB functions.	po4	49-52	cAMP responsive element binding protein 1	Homo sapiens	121-125
23904617-7	2013	One of the sites that is phosphorylated in hyper-PO4 CREB is serine 231, which is the functional equivalent of mammalian CREB serine 133, the phosphorylation of which is an important regulator of CREB functions.	po4	49-52	cAMP responsive element binding protein 1	Homo sapiens	121-125
23467180-4	2013	High riverine concentrations of nitrate (NO3; up to 220 muM) and phosphate (PO4; up to 3.7 muM) mainly originated from agricultural fertilizer input.	po4	76-79	latexin	Homo sapiens	91-94
23274254-0	2013	A vibrational spectroscopic study of the phosphate mineral zanazziite - Ca2(MgFe2+)(MgFe2+Al)4Be4(PO4)6.6(H2O).	po4	98-101	carbonic anhydrase 2	Homo sapiens	72-75
21984410-2	2012	Powder X-ray diffraction (XRD) analysis demonstrated that the Sr3.5Y6.5O2(PO4)1.5(SiO4)4.5 host had a hexagonal crystal structure in the space group P6(3) /m and unit cell parameters a = 9.418 A, c = 6.900 A.	po4	74-77	tumor protein p63	Homo sapiens	149-154
22609717-7	2012	The mMR was able to remove on average 50% of NH4, 75% of NO2, 35% of NO3 and 60% of PO4 consistently from the MBR effluent under the conditions tested.	po4	84-87	ATPase, class II, type 9B	Mus musculus	4-7