(Q55042537)

16 June 2018

meta-analysis

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title

The methionine synthase reductase 66A>G polymorphism is a maternal risk factor for spina bifida. (English)

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16 June 2018

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7

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16 June 2018

Lydia A Afman

3

object named as

Lydia A Afman

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16 June 2018

author name string

Ivon J M van der Linden

1

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16 June 2018

Martin den Heijer

2

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16 June 2018

Henkjan Gellekink

4

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16 June 2018

Sita H H M Vermeulen

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16 June 2018

Leo A J Kluijtmans

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16 June 2018

publication date

6 October 2006

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16 June 2018

Journal of Molecular Medicine

published in

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16 June 2018

volume

84

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16 June 2018

issue

12

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16 June 2018

page(s)

1047-1054

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16 June 2018

https://scigraph.springernature.com/pub.10.1007/s00109-006-0093-x

exact match

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cites work

Hyperhomocysteinemia: a risk factor for ischemic stroke in children.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00109-006-0093-X

Human methionine synthase reductase, a soluble P-450 reductase-like dual flavoprotein, is sufficient for NADPH-dependent methionine synthase activation

21 January 2018

1 reference

12 December 2020

Methionine synthase reductase MTRR 66A > G has no effect on total homocysteine, folate, and Vitamin B12 concentrations in renal transplant patients

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12 December 2020

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

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12 December 2020

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

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12 December 2020

Possible prevention of neural-tube defects by periconceptional vitamin supplementation

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects

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12 December 2020

Accurate and rapid "multiplex heteroduplexing" method for genotyping key enzymes involved in folate/homocysteine metabolism

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12 December 2020

Three different methods for the determination of total homocysteine in plasma

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12 December 2020

Sensitivity of serum methylmalonic acid and total homocysteine determinations for diagnosing cobalamin and folate deficiencies

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Polymorphisms of the 5,10-methylenetetrahydrofolate and the methionine synthase reductase genes as independent risk factors for spina bifida

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12 December 2020

Is hyperhomocysteinaemia a risk factor for recurrent venous thrombosis?

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12 December 2020

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

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12 December 2020

Sequence analysis of the coding region of human methionine synthase: relevance to hyperhomocysteinaemia in neural-tube defects and vascular disease

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12 December 2020

Mutation incidence in folate metabolism genes and regulatory genes in Polish families with neural tube defects

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Impact of Violations and Deviations in Hardy-Weinberg Equilibrium on Postulated Gene-Disease Associations

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12 December 2020

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

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12 December 2020

Gene-gene interaction in folate-related genes and risk of neural tube defects in a UK population

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12 December 2020

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

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12 December 2020

Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria

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12 December 2020

Methylmalonic acid: a test whose time has come?

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12 December 2020

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

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12 December 2020

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

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12 December 2020

Methionine and neural tube closure in cultured rat embryos: morphological and biochemical analyses

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12 December 2020

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

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12 December 2020

10.1007/S00109-006-0093-X

Identifiers

DOI

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16 June 2018

Dimensions Publication ID

1044912362

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16 June 2018