(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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Molecular genetic analysis of the gene encoding the trifunctional enzyme MTHFD (methylenetetrahydrofolate-dehydrogenase, methenyltetrahydrofolate-cyclohydrolase, formyltetrahydrofolate synthetase) in patients with neural tube 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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Polymorphism of the methionine synthase gene : association with homocysteine metabolism and late-onset vascular diseases in the Japanese population

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

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

21 January 2018

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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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21 January 2018

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21 January 2018

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

21 January 2018

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

Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial and conotruncal heart defects

21 January 2018

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21 January 2018

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

Variation and expression of dihydrofolate reductase (DHFR) in relation to spina bifida

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

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

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

21 January 2018

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

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

21 January 2018

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

Associations between polymorphisms within the thymidylate synthase gene and spina bifida

21 January 2018

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

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

21 January 2018

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

Transcobalamin C776G genotype modifies the association between vitamin B12 and homocysteine in older Hispanics

21 January 2018

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

Transcobalamin II 775G>C polymorphism and indices of vitamin B12 status in healthy older adults

21 January 2018

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

Single nucleotide polymorphisms in the transcobalamin gene: relationship with transcobalamin concentrations and risk for neural tube defects

21 January 2018

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

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

21 January 2018

1 reference

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

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

1 reference

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

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

1 reference

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

1 reference

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

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

1 reference

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

1 reference

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

Cancer chemoprevention mechanisms mediated through the Keap1-Nrf2 pathway

21 January 2018

1 reference

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

1 reference

26 March 2018