Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association. (Q46567112)

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13 January 2020

title

Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association (English)

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2

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Valerie B O'Leary

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13 January 2020

Anne M. Molloy

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author name string

Faith Pangilinan

3

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13 January 2020

Peadar N Kirke

4

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13 January 2020

Christopher Cox

5

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Mary Conley

6

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13 January 2020

Kun Peng

8

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13 January 2020

Barry Shane

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John M Scott

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13 January 2020

Anne Parle-McDermott

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13 January 2020

Lawrence C Brody

13

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Members of the Birth Defects Research Group

14

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13 January 2020

Andrea Weiler

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publication date

17 March 2005

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Molecular Genetics and Metabolism

13 January 2020

published in

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volume

85

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issue

3

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page(s)

220-227

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Maternal hyperhomocysteinemia: a risk factor for neural-tube defects?

13 January 2020

cites work

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Structure-based perspectives on B12-dependent enzymes

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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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Differences in the efficiency of reductive activation of methionine synthase and exogenous electron acceptors between the common polymorphic variants of human methionine synthase reductase

7 January 2021

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

7 January 2021

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Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects

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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Methionine Synthase: High-Resolution Mapping of the Human Gene and Evaluation as a Candidate Locus for Neural Tube Defects

7 January 2021

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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

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Non-hierarchical logistic models and case-only designs for assessing susceptibility in population-based case-control studies

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Functionally null mutations in patients with the cblG-variant form of methionine synthase deficiency

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Targeted disruption of the methionine synthase gene in mice

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Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome

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MTRR and MTHFR polymorphism: link to Down syndrome?

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Methionine synthase (MTR) 2756 (A --> G) polymorphism, double heterozygosity methionine synthase 2756 AG/methionine synthase reductase (MTRR) 66 AG, and elevated homocysteinemia are three risk factors for having a child with Down syndrome

7 January 2021

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Common mutations at the homocysteine metabolism pathway and pediatric stroke

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Effects of polymorphisms of methionine synthase and methionine synthase reductase on total plasma homocysteine in the NHLBI Family Heart Study.

7 January 2021

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Methylenetetrahydrofolate reductase (MTHFR) 677C>T and methionine synthase reductase (MTRR) 66A>G polymorphisms: association with serum homocysteine and angiographic coronary artery disease in the era of flour products fortified with folic acid

7 January 2021

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

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