PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
2752025-3	1989	Mg2+ forms crystalline complexes with saturated phosphatidylserines, such as DMPS, and probably with POPS.	Unithiol	77-81	mucin 7, secreted	Homo sapiens	0-3
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.	Unithiol	116-120	mucin 7, secreted	Homo sapiens	41-44
2898331-6	1988	Reduction of DMPS disulfide to DMPS also occurred in EDTA-Tris HCl (pH 9) containing glutathione disulfide and glutathione reductase.	Unithiol	13-17	glutathione-disulfide reductase	Gallus gallus	111-132
33113271-7	2020	GO analysis revealed that DMPs were significantly enriched in 540 GO terms, which included regulation of the differentiation of keratinocytes, T-helper cell differentiation, and alpha-beta T cell differentiation.	Unithiol	26-30	amyloid beta precursor protein	Homo sapiens	178-188
33279932-9	2021	The genes associated with top-ranked DMPs also included many genes involved in nervous system development, such as LIMK2 and TMOD2.	Unithiol	37-41	LIM domain kinase 2	Homo sapiens	115-120
33279932-9	2021	The genes associated with top-ranked DMPs also included many genes involved in nervous system development, such as LIMK2 and TMOD2.	Unithiol	37-41	tropomodulin 2	Homo sapiens	125-130
33113271-8	2020	Moreover, significant enrichment of KEGG pathways of the DMPs included mucin type O-glycan biosynthesis, focal adhesion, and the insulin signaling pathway.	Unithiol	57-61	LOC100508689	Homo sapiens	71-76
32233750-5	2020	Correlation between DNA methylation levels in DMPs and phospho-tau protein burden assessed by immunohistochemistry in the hippocampus was also determined.We found 4 DMPs showing higher levels of DNA methylation at early AD stages compared to controls, involving ELOVL2, GIT1/TP53I13 and the histone gene locus at chromosome 6.	Unithiol	165-169	ELOVL fatty acid elongase 2	Homo sapiens	262-268
32233750-5	2020	Correlation between DNA methylation levels in DMPs and phospho-tau protein burden assessed by immunohistochemistry in the hippocampus was also determined.We found 4 DMPs showing higher levels of DNA methylation at early AD stages compared to controls, involving ELOVL2, GIT1/TP53I13 and the histone gene locus at chromosome 6.	Unithiol	165-169	GIT ArfGAP 1	Homo sapiens	270-274
32233750-5	2020	Correlation between DNA methylation levels in DMPs and phospho-tau protein burden assessed by immunohistochemistry in the hippocampus was also determined.We found 4 DMPs showing higher levels of DNA methylation at early AD stages compared to controls, involving ELOVL2, GIT1/TP53I13 and the histone gene locus at chromosome 6.	Unithiol	165-169	tumor protein p53 inducible protein 13	Homo sapiens	275-282
32470185-11	2020	When DMRs and DMPs were annotated to genes, 3 genes associated with imprinting were found: IGF2, PRDM16, and CLF4/BRUNOL4.	Unithiol	14-18	insulin like growth factor 2	Homo sapiens	91-95
32470185-11	2020	When DMRs and DMPs were annotated to genes, 3 genes associated with imprinting were found: IGF2, PRDM16, and CLF4/BRUNOL4.	Unithiol	14-18	PR/SET domain 16	Homo sapiens	97-103
32470185-11	2020	When DMRs and DMPs were annotated to genes, 3 genes associated with imprinting were found: IGF2, PRDM16, and CLF4/BRUNOL4.	Unithiol	14-18	CUGBP Elav-like family member 4	Homo sapiens	114-121
31279243-8	2019	We further detected group-specific between-brain-region gene expression differences in ODC1, CALY, GALNT2, and GABRD, which contained significant between-brain-region DMPs.	Unithiol	167-171	ornithine decarboxylase 1	Homo sapiens	87-91
32736574-11	2020	For DMPs located in promoter CpG islands showing extreme hypermethylation, the candidate gene with the largest number of DMPs (n = 7) was mapped to HOXA5.	Unithiol	4-8	homeobox A5	Homo sapiens	148-153
32736574-11	2020	For DMPs located in promoter CpG islands showing extreme hypermethylation, the candidate gene with the largest number of DMPs (n = 7) was mapped to HOXA5.	Unithiol	121-125	homeobox A5	Homo sapiens	148-153
32117312-4	2020	Results: Analyses of these data revealed significantly more differentially methylated positions (DMPs) in CD4+ memory than in CD4+ naive T cells (904 vs. 19 DMPs) in RA patients compared to controls.	Unithiol	97-101	CD4 molecule	Homo sapiens	106-109
31279243-8	2019	We further detected group-specific between-brain-region gene expression differences in ODC1, CALY, GALNT2, and GABRD, which contained significant between-brain-region DMPs.	Unithiol	167-171	calcyon neuron specific vesicular protein	Homo sapiens	93-97
31279243-8	2019	We further detected group-specific between-brain-region gene expression differences in ODC1, CALY, GALNT2, and GABRD, which contained significant between-brain-region DMPs.	Unithiol	167-171	polypeptide N-acetylgalactosaminyltransferase 2	Homo sapiens	99-105
31279243-8	2019	We further detected group-specific between-brain-region gene expression differences in ODC1, CALY, GALNT2, and GABRD, which contained significant between-brain-region DMPs.	Unithiol	167-171	gamma-aminobutyric acid type A receptor subunit delta	Homo sapiens	111-116
28635014-5	2017	WHAT IS NEW AND CONCLUSION: Clinicians should keep in mind haemolysis as a potentially life-threatening side effect of DMPS in patients with G6PD.	Unithiol	119-123	glucose-6-phosphate dehydrogenase	Homo sapiens	141-145
30639570-6	2019	Ingenuity pathway analysis of 39 genes with DMPs for both CPSP and CASI revealed enrichment of several canonical pathways, including GABA receptor (P = .00016 for CPSP; P =.0008 for CASI) and dopamine-DARPP32 feedback in cyclic adenosine monophosphate (P = .004 for CPSP and P =.00003 for CASI) signaling.	Unithiol	44-48	GABA type A receptor-associated protein	Homo sapiens	133-146
30639570-6	2019	Ingenuity pathway analysis of 39 genes with DMPs for both CPSP and CASI revealed enrichment of several canonical pathways, including GABA receptor (P = .00016 for CPSP; P =.0008 for CASI) and dopamine-DARPP32 feedback in cyclic adenosine monophosphate (P = .004 for CPSP and P =.00003 for CASI) signaling.	Unithiol	44-48	protein phosphatase 1 regulatory inhibitor subunit 1B	Homo sapiens	201-208
31036381-12	2019	Furthermore, DMPs sensitized TRPV1 responses in mouse trigeminal neurons with greater activity seen with extracts from root dentin.	Unithiol	13-17	transient receptor potential cation channel, subfamily V, member 1	Mus musculus	29-34
29556023-3	2018	Using Illumina 450k arrays for 194 patients from The Cancer Genome Atlas, we identified two distinct DMPs by hierarchical clustering: DMP.1 and DMP.2.	Unithiol	101-105	dentin matrix acidic phosphoprotein 1	Homo sapiens	134-139
24530897-3	2014	P45 peptide showed lower surface activity and less extent of penetration into 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) and 1,2-dimyristoyl-sn-glycero-3-phospho-L-serine (DMPS) (3:2, mol/mol) lipid monolayers than P58 and P59.	Unithiol	180-184	nuclear factor, erythroid 2	Homo sapiens	0-3
26889208-11	2016	We also show that ERbeta is recruited to regions around hypermethylated DMPs.	Unithiol	72-76	estrogen receptor 2 (beta)	Mus musculus	18-24
26889208-12	2016	Finally, we demonstrate here that ERbeta interacts with TDG and that TDG binds ERbeta-dependently to hypermethylated DMPs.	Unithiol	117-121	thymine DNA glycosylase	Mus musculus	69-72
26889208-12	2016	Finally, we demonstrate here that ERbeta interacts with TDG and that TDG binds ERbeta-dependently to hypermethylated DMPs.	Unithiol	117-121	estrogen receptor 2 (beta)	Mus musculus	79-85
25918994-8	2015	Remarkably, one of these DMPs (cg01122889) was located in the WDR26 gene, the DNA sequence of which has been implicated in major depressive disorder from genome-wide association studies.	Unithiol	25-29	WD repeat domain 26	Homo sapiens	62-67
24929637-9	2014	RESULTS: Two reproducible depression-associated DMPs were identified, including the top-ranked DMP that was located within STK32C, which encodes a serine/threonine kinase, of unknown function.	Unithiol	48-52	serine/threonine kinase 32C	Homo sapiens	123-129
19806735-5	2009	The additional assessment of the stability of Hg2+-PCn complexes was achieved through ITC by using the therapeutic chelator sodium 2,3-dimercaptopropanesulfate (DMPS) over Hg2+-PCn systems.	Unithiol	161-165	polycystin 1, transient receptor potential channel interacting pseudogene 2	Homo sapiens	46-49
24562313-4	2014	In vitro, DMPs enhanced alkaline phosphatase activity and mineralization in BMMSCs cultures as well as increasing the expression of dentinogenic and osteogenic differentiation markers (including runt-related transcription factor 2, osterix, bone sialoprotein, dentin sialophosphoprotein and osteocalcin) at both transcript and protein levels, with 10 mug/mL DMPs being the optimal stimulatory concentration.	Unithiol	10-14	Sp7 transcription factor	Homo sapiens	232-239
24562313-5	2014	Expression of phosphor-ERK/phosphor-P38 in BMMSCs was up-regulated by DMPs and, in the presence of the ERK1/2- and p38-specific inhibitors, the differentiation of BMMSCs was inhibited.	Unithiol	70-74	mitogen-activated protein kinase 1	Homo sapiens	23-26
24562313-5	2014	Expression of phosphor-ERK/phosphor-P38 in BMMSCs was up-regulated by DMPs and, in the presence of the ERK1/2- and p38-specific inhibitors, the differentiation of BMMSCs was inhibited.	Unithiol	70-74	mitogen-activated protein kinase 1	Homo sapiens	36-39
24562313-5	2014	Expression of phosphor-ERK/phosphor-P38 in BMMSCs was up-regulated by DMPs and, in the presence of the ERK1/2- and p38-specific inhibitors, the differentiation of BMMSCs was inhibited.	Unithiol	70-74	mitogen-activated protein kinase 3	Homo sapiens	103-109
24562313-5	2014	Expression of phosphor-ERK/phosphor-P38 in BMMSCs was up-regulated by DMPs and, in the presence of the ERK1/2- and p38-specific inhibitors, the differentiation of BMMSCs was inhibited.	Unithiol	70-74	mitogen-activated protein kinase 1	Homo sapiens	115-118
24562313-6	2014	These data indicate that DMPs promote the dentinogenic/osteogenic differentiation of BMMSCs via the ERK/p38 MAPK pathways.	Unithiol	25-29	mitogen-activated protein kinase 1	Homo sapiens	100-103
24562313-6	2014	These data indicate that DMPs promote the dentinogenic/osteogenic differentiation of BMMSCs via the ERK/p38 MAPK pathways.	Unithiol	25-29	mitogen-activated protein kinase 1	Homo sapiens	104-107
24562313-6	2014	These data indicate that DMPs promote the dentinogenic/osteogenic differentiation of BMMSCs via the ERK/p38 MAPK pathways.	Unithiol	25-29	mitogen-activated protein kinase 3	Homo sapiens	108-112
19063911-0	2009	MRP2 involvement in renal proximal tubular elimination of methylmercury mediated by DMPS or DMSA.	Unithiol	84-88	ATP binding cassette subfamily C member 2	Rattus norvegicus	0-4
19063911-3	2009	In the present study, we extended our previous studies by testing the hypothesis that MRP2 mediates the secretion of DMPS or DMSA S-conjugates of CH(3)Hg(+).	Unithiol	117-121	ATP binding cassette subfamily C member 2	Rattus norvegicus	86-90
19063911-11	2009	Our findings in inside-out membrane vesicles prepared from hMRP2-transfected Sf9 cells show that uptake of DMPS and DMSA S-conjugates of CH(3)Hg(+) was greater in the vesicles containing hMRP2 than in control vesicles.	Unithiol	107-111	ATP binding cassette subfamily C member 2	Homo sapiens	59-64
19063911-11	2009	Our findings in inside-out membrane vesicles prepared from hMRP2-transfected Sf9 cells show that uptake of DMPS and DMSA S-conjugates of CH(3)Hg(+) was greater in the vesicles containing hMRP2 than in control vesicles.	Unithiol	107-111	ATP binding cassette subfamily C member 2	Homo sapiens	187-192
19063911-12	2009	Overall, these dispositional findings indicate that MRP2 does play a role in DMPS- and DMSA-mediated elimination of mercury from the kidney.	Unithiol	77-81	ATP binding cassette subfamily C member 2	Rattus norvegicus	52-56
17100619-6	2006	Another bioactive moiety of PGNs, diaminopimelic acid (DAP) containing desmuramylpeptides (DMPs), senses another intracellular receptor, NOD1.	Unithiol	91-95	nucleotide-binding oligomerization domain containing 1	Mus musculus	137-141
16850446-2	2006	An earlier study showed that DMPS increased the transport of insulin across porcine epidermis under electroporation by approximately fourfold.	Unithiol	29-33	insulin	Homo sapiens	61-68
16850446-4	2006	When electroosmosis was applied across the epidermis following electroporation with DMPS, the enhancement of insulin transport was approximately 18-fold over electroporation alone.	Unithiol	84-88	insulin	Homo sapiens	109-116
17100619-9	2006	In human monocytic cells, both MDP and DMPs exhibited definite activities; marked synergistic interleukin (IL)-8 secretion was induced by DMPs and MDP in combination with synthetic TLR agonists, and suppression of the mRNA expressions of NOD1 and NOD2, respectively, by RNA interference specifically inhibited synergistic IL-8 secretion.	Unithiol	39-43	C-X-C motif chemokine ligand 8	Homo sapiens	94-112
17100619-9	2006	In human monocytic cells, both MDP and DMPs exhibited definite activities; marked synergistic interleukin (IL)-8 secretion was induced by DMPs and MDP in combination with synthetic TLR agonists, and suppression of the mRNA expressions of NOD1 and NOD2, respectively, by RNA interference specifically inhibited synergistic IL-8 secretion.	Unithiol	39-43	nucleotide binding oligomerization domain containing 1	Homo sapiens	238-242
17100619-9	2006	In human monocytic cells, both MDP and DMPs exhibited definite activities; marked synergistic interleukin (IL)-8 secretion was induced by DMPs and MDP in combination with synthetic TLR agonists, and suppression of the mRNA expressions of NOD1 and NOD2, respectively, by RNA interference specifically inhibited synergistic IL-8 secretion.	Unithiol	39-43	nucleotide binding oligomerization domain containing 2	Homo sapiens	247-251
17100619-9	2006	In human monocytic cells, both MDP and DMPs exhibited definite activities; marked synergistic interleukin (IL)-8 secretion was induced by DMPs and MDP in combination with synthetic TLR agonists, and suppression of the mRNA expressions of NOD1 and NOD2, respectively, by RNA interference specifically inhibited synergistic IL-8 secretion.	Unithiol	39-43	C-X-C motif chemokine ligand 8	Homo sapiens	322-326
17100619-9	2006	In human monocytic cells, both MDP and DMPs exhibited definite activities; marked synergistic interleukin (IL)-8 secretion was induced by DMPs and MDP in combination with synthetic TLR agonists, and suppression of the mRNA expressions of NOD1 and NOD2, respectively, by RNA interference specifically inhibited synergistic IL-8 secretion.	Unithiol	138-142	C-X-C motif chemokine ligand 8	Homo sapiens	94-112
12237339-10	2002	These results indicate that the MeHg antidotes NAC and DMPS and their mercaptide complexes are transported by Oat1 but are comparatively poor substrates for Oat3.	Unithiol	55-59	solute carrier family 22 member 6	Rattus norvegicus	110-114
13129851-0	2004	Interaction of the metal chelator DMPS with OAT1 and OAT3 in intact isolated rabbit renal proximal tubules.	Unithiol	34-38	solute carrier family 22 member 6	Oryctolagus cuniculus	44-48
13129851-0	2004	Interaction of the metal chelator DMPS with OAT1 and OAT3 in intact isolated rabbit renal proximal tubules.	Unithiol	34-38	solute carrier family 22 member 8	Oryctolagus cuniculus	53-57
13129851-12	2004	This is the first evidence showing that both OAT1 and OAT3 can transport DMPS across the basolateral membrane of RPT.	Unithiol	73-77	solute carrier family 22 member 6	Oryctolagus cuniculus	45-49
13129851-12	2004	This is the first evidence showing that both OAT1 and OAT3 can transport DMPS across the basolateral membrane of RPT.	Unithiol	73-77	solute carrier family 22 member 8	Oryctolagus cuniculus	54-58
12391276-2	2002	To evaluate the involvement of the organic anion transporter 1 (OAT1) in the renal flux of DMPS, we examined the effect of DMPS on transport mediated by the rabbit ortholog of OAT1 and compared these characteristics with those observed in intact isolated rabbit proximal tubules.	Unithiol	91-95	solute carrier family 22 member 6	Oryctolagus cuniculus	35-62
12391276-2	2002	To evaluate the involvement of the organic anion transporter 1 (OAT1) in the renal flux of DMPS, we examined the effect of DMPS on transport mediated by the rabbit ortholog of OAT1 and compared these characteristics with those observed in intact isolated rabbit proximal tubules.	Unithiol	91-95	solute carrier family 22 member 6	Oryctolagus cuniculus	64-68
12391276-2	2002	To evaluate the involvement of the organic anion transporter 1 (OAT1) in the renal flux of DMPS, we examined the effect of DMPS on transport mediated by the rabbit ortholog of OAT1 and compared these characteristics with those observed in intact isolated rabbit proximal tubules.	Unithiol	123-127	solute carrier family 22 member 6	Oryctolagus cuniculus	176-180
12237339-4	2002	Xenopus laevis oocytes expressing rat Oat1 showed increased uptake of [(14)C]MeHg when complexed with either NAC or DMPS but not when complexed with L-cysteine, glutathione, dimercaptosuccinate, penicillamine, or gamma-glutamylcysteine.	Unithiol	116-120	solute carrier family 22 member 6	Rattus norvegicus	38-42
12237339-7	2002	Oat1-mediated uptake of [(14)C]MeHg-NAC and [(14)C]MeHg-DMPS was inhibited by prototypical substrates for Oat1, including p-aminohippurate (PAH), and was trans-stimulated when oocytes were preloaded with 2 mM glutarate but not glutamate.	Unithiol	56-60	solute carrier family 22 member 6	Rattus norvegicus	0-4
12237339-7	2002	Oat1-mediated uptake of [(14)C]MeHg-NAC and [(14)C]MeHg-DMPS was inhibited by prototypical substrates for Oat1, including p-aminohippurate (PAH), and was trans-stimulated when oocytes were preloaded with 2 mM glutarate but not glutamate.	Unithiol	56-60	solute carrier family 22 member 6	Rattus norvegicus	106-110
12237339-8	2002	Conversely, efflux of [(3)H]PAH from Oat1-expressing oocytes was trans-stimulated by glutarate, PAH, NAC, DMPS, MeHg-NAC, MeHg-DMPS, and a mercapturic acid, indicating that these are transported solutes.	Unithiol	106-110	solute carrier family 22 member 6	Rattus norvegicus	37-41
12237339-10	2002	These results indicate that the MeHg antidotes NAC and DMPS and their mercaptide complexes are transported by Oat1 but are comparatively poor substrates for Oat3.	Unithiol	55-59	solute carrier family 22 member 8	Rattus norvegicus	157-161
9929493-1	1999	Lipid activation of protein kinase C alpha (PKC alpha) was studied by using a model mixture containing 1, 2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC), 1, 2-dimyristoyl-sn-glycero-3-phosphoserine (DMPS), and 1, 2-dimyristoyl-sn-glycerol (1,2-DMG).	Unithiol	201-205	protein kinase C alpha	Homo sapiens	20-42
12100989-5	2002	In the current study, based on those earlier findings, the effect of 1,2-dimyristoyl-3-phosphatidylserine (DMPS) on the transdermal transport of insulin by electroporation was examined.	Unithiol	107-111	insulin	Homo sapiens	145-152
12100989-9	2002	Results show that when electroporation was carried out in the presence of DMPS, there was greater than 20-fold enhancement of insulin transport.	Unithiol	74-78	insulin	Homo sapiens	126-133
9929493-1	1999	Lipid activation of protein kinase C alpha (PKC alpha) was studied by using a model mixture containing 1, 2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC), 1, 2-dimyristoyl-sn-glycero-3-phosphoserine (DMPS), and 1, 2-dimyristoyl-sn-glycerol (1,2-DMG).	Unithiol	201-205	protein kinase C alpha	Homo sapiens	44-53
2177310-1	1990	Sodium dimercaptopropanesulphonate (DMPS) and sodium dimercaptosuccinate (DMS) were discovered to be effective antidotes for acute poisoning of insecticides SCD [sodium ammonium dimethyl-2-(propane-1,3-dithiosulfate) monohydrate], nereistoxin (4-N,N-dimethylamino-1,2-dithiolane) and cartap (dihydronereistoxin dicarbamate).	Unithiol	36-40	stearoyl-Coenzyme A desaturase 1	Mus musculus	157-160
8198824-12	1994	DMPS treatment, administered by intravenous and oral route, was shown to be an effective alternative for BAL in life-threatening mercuric chloride intoxication.	Unithiol	0-4	poly(ADP-ribose) polymerase family member 9	Homo sapiens	105-108
1664200-7	1991	Treatment with D-PEN, DMSA, DMPS, and bucillamine (1.2 mmol/kg) significantly prevented increases in the urinary excretion of protein, AST, and glucose and the BUN level after AuTM (0.026 mmol/kg) injection.	Unithiol	28-32	glutamic-oxaloacetic transaminase 2	Rattus norvegicus	135-138
9765315-7	1998	The urinary mercury greatly increased during those periods when DMPS was administered (1754, 314, and 173 microgram/24 h for the periods 1, 2 and 3, compared with 106, 48 and 53 microgram/24 h on the corresponding no-treatment periods).	Unithiol	64-68	period circadian regulator 2	Homo sapiens	129-147
2177310-5	1990	The therapeutic effect of DMPS was also demonstrated in SCD-poisoned conscious rabbits.	Unithiol	26-30	stearoyl-Coenzyme A desaturase 1	Mus musculus	56-59
2177310-6	1990	DMPS 62.5 mg/kg or DMS 500 mg/kg iv completely antagonized the neuromuscular blockade and respiratory depression caused by SCD, nereistoxin and cartap in anesthetized rabbits.	Unithiol	0-4	stearoyl-Coenzyme A desaturase 1	Mus musculus	123-126
2177310-2	1990	In mice, DMPS (250 mg/kg) or DMS (1000 mg/kg) ip 20 min before SCD increased LD50 of ig SCD from 97 to 374 or 251 mg/kg, respectively.	Unithiol	9-13	stearoyl-Coenzyme A desaturase 1	Mus musculus	88-91
32795589-5	2021	RESULTS: EWAS identified genes, including musashi RNA binding protein 2 (MSI2), associated with atopy, which contained enriched DMPs that that genetically affect atopy.	Unithiol	128-132	musashi RNA binding protein 2	Homo sapiens	42-71
32795589-5	2021	RESULTS: EWAS identified genes, including musashi RNA binding protein 2 (MSI2), associated with atopy, which contained enriched DMPs that that genetically affect atopy.	Unithiol	128-132	musashi RNA binding protein 2	Homo sapiens	73-77
32795589-7	2021	Regarding tissue eosinophilia, EWAS identified genes including CAMK1D with enriched DMPs directly contributing to tissue eosinophilia at the gene level.	Unithiol	84-88	calcium/calmodulin dependent protein kinase ID	Homo sapiens	63-69
34895303-10	2021	Seven of these DMPs (25%) could be allocated to a gene that was previously associated with cardiovascular diseases (HDAC4, IGF2BP3, CASZ1, SDK1, PCDHGA1, DIO3, PTPRN2).	Unithiol	15-19	histone deacetylase 4	Homo sapiens	116-121
33769968-8	2021	Functional analysis of genes with a minimum of two DMPs showed involvement in antigen binding, transcriptional regulation, cell adhesion, IFN-gamma pathway, type I IFN pathway, antigen presentation, EB virus infection, human T-lymphotropic virus type 1 virus infection, and metabolic disease-related pathways.	Unithiol	51-55	interferon gamma	Homo sapiens	138-147
33032082-7	2021	These novel DMPs were found to set off the release of higher levels of tumour necrosis factor alpha (TNF-alpha) than Murabutide, which is a well-known NOD2 agonist.	Unithiol	12-16	tumor necrosis factor	Homo sapiens	101-110
33032082-7	2021	These novel DMPs were found to set off the release of higher levels of tumour necrosis factor alpha (TNF-alpha) than Murabutide, which is a well-known NOD2 agonist.	Unithiol	12-16	nucleotide binding oligomerization domain containing 2	Homo sapiens	151-155
33032082-8	2021	Molecular docking studies indicate that all these DMPs bind well to NOD2 receptor with similar dock scores (binding energy) through a number of hydrogen bonding and hydrophobic/pi interactions with several crucial residues of the receptor.	Unithiol	50-54	nucleotide binding oligomerization domain containing 2	Homo sapiens	68-72
34895303-10	2021	Seven of these DMPs (25%) could be allocated to a gene that was previously associated with cardiovascular diseases (HDAC4, IGF2BP3, CASZ1, SDK1, PCDHGA1, DIO3, PTPRN2).	Unithiol	15-19	insulin like growth factor 2 mRNA binding protein 3	Homo sapiens	123-130
34895303-10	2021	Seven of these DMPs (25%) could be allocated to a gene that was previously associated with cardiovascular diseases (HDAC4, IGF2BP3, CASZ1, SDK1, PCDHGA1, DIO3, PTPRN2).	Unithiol	15-19	castor zinc finger 1	Homo sapiens	132-137
34895303-10	2021	Seven of these DMPs (25%) could be allocated to a gene that was previously associated with cardiovascular diseases (HDAC4, IGF2BP3, CASZ1, SDK1, PCDHGA1, DIO3, PTPRN2).	Unithiol	15-19	sidekick cell adhesion molecule 1	Homo sapiens	139-143
34895303-10	2021	Seven of these DMPs (25%) could be allocated to a gene that was previously associated with cardiovascular diseases (HDAC4, IGF2BP3, CASZ1, SDK1, PCDHGA1, DIO3, PTPRN2).	Unithiol	15-19	protocadherin gamma subfamily A, 1	Homo sapiens	145-152
34895303-10	2021	Seven of these DMPs (25%) could be allocated to a gene that was previously associated with cardiovascular diseases (HDAC4, IGF2BP3, CASZ1, SDK1, PCDHGA1, DIO3, PTPRN2).	Unithiol	15-19	iodothyronine deiodinase 3	Homo sapiens	154-158
34895303-10	2021	Seven of these DMPs (25%) could be allocated to a gene that was previously associated with cardiovascular diseases (HDAC4, IGF2BP3, CASZ1, SDK1, PCDHGA1, DIO3, PTPRN2).	Unithiol	15-19	protein tyrosine phosphatase receptor type N2	Homo sapiens	160-166
34117263-4	2021	We then used linear models to identify DMPs associated with CRP concentrations.	Unithiol	39-43	C-reactive protein	Homo sapiens	60-63
34098319-9	2021	Targeted deep bisulfite sequencing of eight DMPs (associated with three genes; CMIP, ST3GAL1 and DAPK3) in an independent PE cohort validated two DMPs in the CMIP gene.	Unithiol	146-150	c-Maf inducing protein	Homo sapiens	158-162
34117263-8	2021	We subsequently identified 14 novel DMPs associated with CRP.	Unithiol	36-40	C-reactive protein	Homo sapiens	57-60
35537341-4	2022	We found differentially methylated DNA positions (DMPs) and regions embedding DMPs associated with either disease status, C9ORF72 or FUS mutation status.	Unithiol	78-82	C9orf72-SMCR8 complex subunit	Homo sapiens	122-129
35537341-4	2022	We found differentially methylated DNA positions (DMPs) and regions embedding DMPs associated with either disease status, C9ORF72 or FUS mutation status.	Unithiol	78-82	FUS RNA binding protein	Homo sapiens	133-136
35537341-6	2022	Furthermore, we could demonstrate co-localization of DMPs with an ALS-associated GWAS region near the SCN7A/SCN9A and XIRP2 genes.	Unithiol	53-57	sodium voltage-gated channel alpha subunit 7	Homo sapiens	102-107
35537341-6	2022	Furthermore, we could demonstrate co-localization of DMPs with an ALS-associated GWAS region near the SCN7A/SCN9A and XIRP2 genes.	Unithiol	53-57	sodium voltage-gated channel alpha subunit 9	Homo sapiens	108-113
35537341-6	2022	Furthermore, we could demonstrate co-localization of DMPs with an ALS-associated GWAS region near the SCN7A/SCN9A and XIRP2 genes.	Unithiol	53-57	xin actin binding repeat containing 2	Homo sapiens	118-123
35256034-11	2022	DMPs in STXBP6, and PF4 DMR, mediated the association between the maternal intervention and the cognitive domain at 12 months of age.	Unithiol	0-4	syntaxin binding protein 6	Homo sapiens	8-14
35177097-8	2022	The small number of sex-specific DMPs that were affected by GAHT were those that become sex-specific during the lifetime, known as sex-and-age DMPs, including DMRs in PRR4 and VMP1 genes.	Unithiol	33-37	proline rich 4	Homo sapiens	167-171
35177097-8	2022	The small number of sex-specific DMPs that were affected by GAHT were those that become sex-specific during the lifetime, known as sex-and-age DMPs, including DMRs in PRR4 and VMP1 genes.	Unithiol	33-37	vacuole membrane protein 1	Homo sapiens	176-180
35177097-8	2022	The small number of sex-specific DMPs that were affected by GAHT were those that become sex-specific during the lifetime, known as sex-and-age DMPs, including DMRs in PRR4 and VMP1 genes.	Unithiol	143-147	proline rich 4	Homo sapiens	167-171
35177097-8	2022	The small number of sex-specific DMPs that were affected by GAHT were those that become sex-specific during the lifetime, known as sex-and-age DMPs, including DMRs in PRR4 and VMP1 genes.	Unithiol	143-147	vacuole membrane protein 1	Homo sapiens	176-180
35260870-4	2022	In this study, single-molecule Forster resonance energy transfer (smFRET) and fluorescence correlation spectroscopy (FCS) were applied to detect the conformational changes and intermolecular interactions of full-length Tau in the presence of different concentrations of 1,2-dimyristoyl-sn-glycero-3-phosphatidylserine (DMPS) vesicles.	Unithiol	319-323	microtubule associated protein tau	Homo sapiens	219-222
35260870-5	2022	The results show that the conformation of Tau becomes expanded with opening of the N-terminal and C-terminal domains of Tau upon binding to DMPS.	Unithiol	140-144	microtubule associated protein tau	Homo sapiens	42-45
35260870-5	2022	The results show that the conformation of Tau becomes expanded with opening of the N-terminal and C-terminal domains of Tau upon binding to DMPS.	Unithiol	140-144	microtubule associated protein tau	Homo sapiens	120-123
35260870-6	2022	At low DMPS concentrations, Tau forms oligomers with a partially extended conformation which facilitates the amyloid fibrillization process.	Unithiol	7-11	microtubule associated protein tau	Homo sapiens	28-31
35260870-7	2022	At high DMPS concentrations, Tau monomer binds to lipid membranes in a fully expanded conformation at low density thus inhibiting intermolecular aggregation.	Unithiol	8-12	microtubule associated protein tau	Homo sapiens	29-32