(Q46567112)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15979034%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

title

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

1 reference

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13 January 2020

2

1 reference

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13 January 2020

Valerie B O'Leary

1

1 reference

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13 January 2020

Anne M. Molloy

12

1 reference

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13 January 2020

author name string

Faith Pangilinan

3

1 reference

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13 January 2020

Peadar N Kirke

4

1 reference

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13 January 2020

Christopher Cox

5

1 reference

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13 January 2020

Mary Conley

6

1 reference

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13 January 2020

Kun Peng

8

1 reference

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13 January 2020

Barry Shane

9

1 reference

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13 January 2020

John M Scott

10

1 reference

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13 January 2020

Anne Parle-McDermott

11

1 reference

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13 January 2020

Lawrence C Brody

13

1 reference

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13 January 2020

Members of the Birth Defects Research Group

14

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13 January 2020

Andrea Weiler

7

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13 January 2020

publication date

17 March 2005

1 reference

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Molecular Genetics and Metabolism

13 January 2020

published in

1 reference

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13 January 2020

volume

85

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13 January 2020

issue

3

1 reference

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13 January 2020

page(s)

220-227

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15979034%20AND%20SRC:MED&resulttype=core&format=json

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

13 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

Homocysteine metabolism in pregnancies complicated by neural-tube defects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

Structure-based perspectives on B12-dependent enzymes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

Targeted disruption of the methionine synthase gene in mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

MTRR and MTHFR polymorphism: link to Down syndrome?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

Common mutations at the homocysteine metabolism pathway and pediatric stroke

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2005.02.003