(Q44826641)

6 December 2017

title

Low erythrocyte folate status and polymorphic variation in folate-related genes are associated with risk of neural tube defect pregnancy (English)

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6 December 2017

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1

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6 December 2017

2

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6 December 2017

8

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6 December 2017

Alison J Laffling

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6 December 2017

Pat A Jonas

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6 December 2017

Terry Burgess

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6 December 2017

Keith Binks

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6 December 2017

E Janet Tawn

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6 December 2017

publication date

1 April 2004

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Molecular Genetics and Metabolism

6 December 2017

published in

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6 December 2017

volume

81

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6 December 2017

issue

4

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6 December 2017

page(s)

273-281

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Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group

6 December 2017

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Prevention of the First Occurrence of Neural-Tube Defects by Periconceptional Vitamin Supplementation

7 January 2021

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Altered folate and vitamin B12 metabolism in families with spina bifida offspring

7 January 2021

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Folate levels and neural tube defects. Implications for prevention

7 January 2021

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Polymorphisms of methylenetetrahydrofolate reductase and other enzymes: metabolic significance, risks and impact on folate requirement

7 January 2021

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Methylenetetrahydrofolate reductase polymorphism affects the change in homocysteine and folate concentrations resulting from low dose folic acid supplementation in women with unexplained recurrent miscarriages

7 January 2021

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A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.12.010

Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.12.010

A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida

7 January 2021

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A polymorphism (80G->A) in the reduced folate carrier gene and its associations with folate status and homocysteinemia

7 January 2021

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Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German population

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.12.010

Maternal periconceptional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifida

7 January 2021

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Gene-gene interaction between the cystathionine beta-synthase 31 base pair variable number of tandem repeats and the methylenetetrahydrofolate reductase 677C > T polymorphism on homocysteine levels and risk for neural tube defects

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.12.010

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

7 January 2021

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

7 January 2021

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Possible interaction of genotypes at cystathionine β-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects

7 January 2021

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Is mutated serine hydroxymethyltransferase (SHMT) involved in the etiology of neural tube defects?

7 January 2021

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The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.12.010

Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects

7 January 2021

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Is impaired folate absorption a factor in neural tube defects?

7 January 2021

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The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.12.010

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.12.010

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

7 January 2021

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Folic acid: nutritional biochemistry, molecular biology, and role in disease processes

7 January 2021

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The North Cumbria Community Genetics Project

7 January 2021

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A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

7 January 2021

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A common polymorphism in methionine synthase reductase increases risk of premature coronary artery disease.

7 January 2021

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Are common mutations of cystathionine beta-synthase involved in the aetiology of neural tube defects?

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.12.010

Susceptibility to spina bifida; an association study of five candidate genes

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.12.010

5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.12.010

The C677T mutation of the 5,10-methylenetetrahydrofolate reductase gene is a moderate risk factor for spina bifida in Italy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.12.010

Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.12.010

Methylenetetrahydrofolate reductase and neural tube defects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.12.010

An examination of polymorphic genes and folate metabolism in mothers affected by a spina bifida pregnancy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.12.010

Spina bifida and folate-related genes: a study of gene-gene interactions.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.12.010

A common mutation in the methylenetetrahydrofolate reductase gene is associated with an accumulation of formylated tetrahydrofolates in red blood cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2003.12.010

10.1016/J.YMGME.2003.12.010

7 January 2021

Identifiers

DOI

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6 December 2017

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