Congenital heart defects and genetic variants in the methylenetetrahydroflate reductase gene. - Wikidata - awgldk - TriplyDB

Congenital heart defects and genetic variants in the methylenetetrahydroflate reductase gene.

Congenital heart defects and genetic variants in the methylenetetrahydroflate reductase gene.

http://www.wikidata.org/entity/Q42914354

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Genetic epidemiology and nonsyndromic structural birth defects: from candidate genes to epigenetics Study on Environmental Causes and SNPs of MTHFR, MS and CBS Genes Related to Congenital Heart Disease 118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects Gene-gene interactions in the folate metabolic pathway and the risk of conotruncal heart defects Association of congenital cardiovascular malformations with 33 single nucleotide polymorphisms of selected cardiovascular disease-related genes Variants of folate metabolism genes and risk of left-sided cardiac defects.MTHFR polymorphisms in Puerto Rican children with isolated congenital heart disease and their mothers.Maternal folate-related gene environment interactions and congenital heart defects.Variants of folate metabolism genes and the risk of conotruncal cardiac defects.Association between MTHFR polymorphisms and congenital heart disease: a meta-analysis based on 9,329 cases and 15,076 controls.Association between selected folate pathway polymorphisms and nonsyndromic limb reduction defects: a case-parental analysis.MTHFR C677T polymorphism and risk of congenital heart defects: evidence from 29 case-control and TDT studies.A genetic association study detects haplotypes associated with obstructive heart defects NAT1, NOS3, and TYMS genotypes and the risk of conotruncal cardiac defects.Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: a report from the National Down Syndrome Project.Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.Meta analysis of the association between MTHFR C677T polymorphism and the risk of congenital heart defects.Role of folate-homocysteine pathway gene polymorphisms and nutritional cofactors in Down syndrome: A triad study.Risk of congenital heart defects is influenced by genetic variation in folate metabolism.MTHFR A1298C polymorphisms reduce the risk of congenital heart defects: a meta-analysis from 16 case-control studies.Association of SNPs in genes involved in folate metabolism with the risk of congenital heart disease.MTRR 66A>G polymorphism in relation to congenital heart defects.Urinary tract anomalies associated with MTHFR gene polymorphism C677T in girls.Risk factors and methylenetetrahydrofolate reductase gene in congenital heart disease.The A1298C Methylenetetrahydrofolate Reductase Gene Variant as a Susceptibility Gene for Non-Syndromic Conotruncal Heart Defects in an Indian Population.Obstructive heart defects associated with candidate genes, maternal obesity, and folic acid supplementation.

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Congenital heart defects and genetic variants in the methylenetetrahydroflate reductase gene.

http://www.wikidata.org/entity/Q42914354

description

2005 nî lūn-bûn

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2005年の論文

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2005年論文

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2005年論文

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2005年論文

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2005年論文

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2005年论文

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Congenital heart defects and g ...... etrahydroflate reductase gene.

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Congenital heart defects and g ...... etrahydroflate reductase gene.

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Congenital heart defects and g ...... etrahydroflate reductase gene.

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Congenital heart defects and g ...... etrahydroflate reductase gene.

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Congenital heart defects and g ...... etrahydroflate reductase gene.

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Journal of Medical Genetics

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Congenital heart defects and g ...... etrahydroflate reductase gene.

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A Parsian

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C A Hobbs

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J J Greenhaw

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S Jernigan

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P2860

Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida

The transmission/disequilibrium test: history, subdivision, and admixture

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting.

5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review.

On measures of gametic disequilibrium

Biological and clinical implications of the MTHFR C677T polymorphism.

Allowing for missing parents in genetic studies of case-parent triads

Folic acid, polymorphism of methyl-group metabolism genes, and DNA methylation in relation to GI carcinogenesis.

The National Birth Defects Prevention Study.

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