×
Entrez Id:
10653
Gene Symbol:
SPINT2
SPINT2
0.300
Biomarker
disease
CTD_human
Functional analysis of a missense mutation in the serine protease inhibitor SPINT2 associated with congenital sodium diarrhea.
24722141
2014
×
Entrez Id:
5652
Gene Symbol:
PRSS8
PRSS8
0.300
Therapeutic
disease
CTD_human
Functional analysis of a missense mutation in the serine protease inhibitor SPINT2 associated with congenital sodium diarrhea.
24722141
2014
×
Entrez Id:
4524
Gene Symbol:
MTHFR
MTHFR
0.300
Biomarker
disease
CTD_human
Association of the maternal MTHFR C677T polymorphism with susceptibility to neural tube defects in offsprings: evidence from 25 case-control studies.
23056169
2012
×
Entrez Id:
10
Gene Symbol:
NAT2
NAT2
0.300
Biomarker
disease
CTD_human
Caffeine, selected metabolic gene variants, and risk for neural tube defects.
20641098
2010
×
Entrez Id:
1544
Gene Symbol:
CYP1A2
CYP1A2
0.300
Biomarker
disease
CTD_human
Caffeine, selected metabolic gene variants, and risk for neural tube defects.
20641098
2010
×
Entrez Id:
3630
Gene Symbol:
INS
INS
0.300
Therapeutic
disease
CTD_human
Arsenate-induced maternal glucose intolerance and neural tube defects in a mouse model.
19446573
2009
×
Entrez Id:
81839
Gene Symbol:
VANGL1
VANGL1
0.300
Biomarker
disease
CTD_human
Novel mutations in VANGL1 in neural tube defects.
19319979
2009
×
Entrez Id:
5697
Gene Symbol:
PYY
PYY
0.300
Biomarker
disease
CTD_human
Gastrointestinal hormones (anorexigenic peptide YY and orexigenic ghrelin) influence neural tube development.
17400914
2007
×
Entrez Id:
4886
Gene Symbol:
NPY1R
NPY1R
0.300
Biomarker
disease
CTD_human
Gastrointestinal hormones (anorexigenic peptide YY and orexigenic ghrelin) influence neural tube development.
17400914
2007
×
Entrez Id:
81839
Gene Symbol:
VANGL1
VANGL1
0.300
Biomarker
disease
CTD_human
Mutations in VANGL1 associated with neural-tube defects.
17409324
2007
×
Entrez Id:
51738
Gene Symbol:
GHRL
GHRL
0.300
Therapeutic
disease
CTD_human
Gastrointestinal hormones (anorexigenic peptide YY and orexigenic ghrelin) influence neural tube development.
17400914
2007
×
Entrez Id:
1437
Gene Symbol:
CSF2
CSF2
0.300
Therapeutic
disease
CTD_human
Valproic acid-induced fetal malformations are reduced by maternal immune stimulation with granulocyte-macrophage colony-stimulating factor or interferon-gamma.
17075842
2006
×
Entrez Id:
3458
Gene Symbol:
IFNG
IFNG
0.300
Therapeutic
disease
CTD_human
Valproic acid-induced fetal malformations are reduced by maternal immune stimulation with granulocyte-macrophage colony-stimulating factor or interferon-gamma.
17075842
2006
×
Entrez Id:
4522
Gene Symbol:
MTHFD1
MTHFD1
0.300
Biomarker
disease
CTD_human
Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population.
16552426
2006
×
Entrez Id:
635
Gene Symbol:
BHMT
BHMT
0.300
Biomarker
disease
CTD_human
Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions.
17035141
2006
×
Entrez Id:
2348
Gene Symbol:
FOLR1
FOLR1
0.300
Biomarker
disease
CTD_human
Role of Folbp1 in the regional regulation of apoptosis and cell proliferation in the developing neural tube and craniofacies.
15800851
2005
×
Entrez Id:
27443
Gene Symbol:
CECR2
CECR2
0.300
Biomarker
disease
CTD_human
CECR2, a protein involved in neurulation, forms a novel chromatin remodeling complex with SNF2L.
15640247
2005
×
Entrez Id:
2737
Gene Symbol:
GLI3
GLI3
0.300
Biomarker
disease
CTD_human
Exencephaly induction by valproic acid in the genetic polydactyly/arhinencephaly mouse, Pdn/Pdn.
16359493
2005
×
Entrez Id:
7546
Gene Symbol:
ZIC2
ZIC2
0.300
Biomarker
disease
CTD_human
Mouse Zic5 deficiency results in neural tube defects and hypoplasia of cephalic neural crest derivatives.
15136147
2004
×
Entrez Id:
85416
Gene Symbol:
ZIC5
ZIC5
0.300
Biomarker
disease
CTD_human
Mouse Zic5 deficiency results in neural tube defects and hypoplasia of cephalic neural crest derivatives.
15136147
2004
×
Entrez Id:
5077
Gene Symbol:
PAX3
PAX3
0.300
Biomarker
disease
CTD_human
Oxidant regulation of gene expression and neural tube development: Insights gained from diabetic pregnancy on molecular causes of neural tube defects.
12739027
2003
×
Entrez Id:
5077
Gene Symbol:
PAX3
PAX3
0.300
Therapeutic
disease
CTD_human
Oxidant regulation of gene expression and neural tube development: Insights gained from diabetic pregnancy on molecular causes of neural tube defects.
12739027
2003
×
Entrez Id:
5077
Gene Symbol:
PAX3
PAX3
0.300
Biomarker
disease
CTD_human
Effect of arsenite, maternal age, and embryonic sex on spina bifida, exencephaly, and resorption rates in the splotch mouse.
12854658
2003
×
Entrez Id:
5077
Gene Symbol:
PAX3
PAX3
0.300
Therapeutic
disease
CTD_human
Effect of arsenite, maternal age, and embryonic sex on spina bifida, exencephaly, and resorption rates in the splotch mouse.
12854658
2003
×
Entrez Id:
4522
Gene Symbol:
MTHFD1
MTHFD1
0.300
Biomarker
disease
CTD_human
A polymorphism, R653Q, in the trifunctional enzyme methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase/formyltetrahydrofolate synthetase is a maternal genetic risk factor for neural tube defects: report of the Birth Defects Research Group.
12384833
2002