Association of SNPs in genes involved in folate metabolism with the risk of congenital heart disease. (Q50967534)

26 March 2018

title

Association of SNPs in genes involved in folate metabolism with the risk of congenital heart disease. (English)

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26 March 2018

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Benjing Wang

1

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26 March 2018

Minjuan Liu

2

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26 March 2018

Wenhua Yan

3

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26 March 2018

Jun Mao

4

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26 March 2018

Dong Jiang

5

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26 March 2018

Hong Li

6

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26 March 2018

Ying Chen

7

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26 March 2018

publication date

10 June 2013

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26 March 2018

Journal of Maternal-Fetal and Neonatal Medicine

published in

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26 March 2018

volume

26

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26 March 2018

issue

18

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26 March 2018

page(s)

1768-1777

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26 March 2018

The changing epidemiology of congenital heart disease

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Association between 5,10-Methylenetetrahydrofolate Reductase C677T and A1298C Polymorphisms and Conotruncal Heart Defects

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The MTHFD1 p.Arg653Gln variant alters enzyme function and increases risk for congenital heart defects

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A Polymorphism, R653Q, in the Trifunctional Enzyme Methylenetetrahydrofolate Dehydrogenase/Methenyltetrahydrofolate Cyclohydrolase/Formyltetrahydrofolate Synthetase Is a Maternal Genetic Risk Factor for Neural Tube Defects

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Influence of a methionine synthase (D919G) polymorphism on plasma homocysteine and folate levels and relation to risk of myocardial infarction

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Transcobalamin and methionine synthase reductase mutated polymorphisms aggravate the risk of neural tube defects in humans

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The reduced folate carrier (SLC19A1) c.80G>A polymorphism is associated with red cell folate concentrations among women

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Evaluation of genetic variants in the reduced folate carrier and in glutamate carboxypeptidase II for spina bifida risk

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Association of reduced folate carrier gene polymorphism and maternal folic acid use with neural tube defects

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Correlation of polymorphism of MTHFRs and RFC-1 genes with neural tube defects in China

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Reduced folate carrier polymorphism (80A-->G) and neural tube defects

21 January 2018

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Reduced-folate carrier (RFC) is expressed in placenta and yolk sac, as well as in cells of the developing forebrain, hindbrain, neural tube, craniofacial region, eye, limb buds and heart

21 January 2018

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Intron 1 and the 5'-flanking region of the human thymidylate synthase gene as a regulatory determinant of growth-dependent expression

21 January 2018

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Genetic polymorphisms of the TYMS gene are not associated with congenital cardiac septal defects in a Han Chinese population

21 January 2018

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Thymidylate synthase: a novel genetic determinant of plasma homocysteine and folate levels

21 January 2018

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Distribution of mutations in human thymidylate synthase yielding resistance to 5-fluorodeoxyuridine

21 January 2018

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21 January 2018

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NAT1, NOS3, and TYMS genotypes and the risk of conotruncal cardiac defects.

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Polymorphisms in genes related to folate and cobalamin metabolism and the associations with complex birth defects

21 January 2018

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Study of four genes belonging to the folate pathway: transcobalamin 2 is involved in the onset of non-syndromic cleft lip with or without cleft palate.

21 January 2018

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Glutathione S-transferase omega genes in Alzheimer and Parkinson disease risk, age-at-diagnosis and brain gene expression: an association study with mechanistic implications

21 January 2018

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https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Characterization of the human Omega class glutathione transferase genes and associated polymorphisms

21 January 2018

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Characterization of the monomethylarsonate reductase and dehydroascorbate reductase activities of Omega class glutathione transferase variants: implications for arsenic metabolism and the age-at-onset of Alzheimer's and Parkinson's diseases

21 January 2018

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https://api.crossref.org/works/10.3109%2F14767058.2013.799648

NFE2L2 gene mutation in male Japanese squamous cell carcinoma of the lung

21 January 2018

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Cancer chemoprevention mechanisms mediated through the Keap1-Nrf2 pathway

21 January 2018

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https://api.crossref.org/works/10.3109%2F14767058.2013.799648

New 19 bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR): A risk factor for spina bifida acting in mothers during pregnancy?

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish population

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F14767058.2013.799648

10.3109/14767058.2013.799648

21 January 2018

Identifiers

DOI

1 reference

26 March 2018

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26 March 2018