Spina bifida and folate-related genes: a study of gene-gene interactions. (Q44103087)

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12 November 2019

title

Spina bifida and folate-related genes: a study of gene-gene interactions (English)

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12 November 2019

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6

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12 November 2019

2

Lorenzo D Botto

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12 November 2019

author name string

Raffaella de Franchis

1

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12 November 2019

Gianfranco Sebastio

3

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12 November 2019

Roberta Ricci

4

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12 November 2019

Achille Iolascon

5

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12 November 2019

Generoso Andria

7

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12 November 2019

Pierpaolo Mastroiacovo

8

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12 November 2019

language of work or name

English

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publication date

1 May 2002

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12 November 2019

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12 November 2019

volume

4

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12 November 2019

issue

3

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12 November 2019

page(s)

126-130

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https://scigraph.springernature.com/pub.10.1097/00125817-200205000-00005

12 November 2019

exact match

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

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

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Prevention of neural-tube defects with folic acid in China. China-U.S. Collaborative Project for Neural Tube Defect Prevention

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

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

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On extending the transmission/disequilibrium test (TDT).

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

21 January 2018

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

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Proportion of disease caused or prevented by a given exposure, trait or intervention

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The frequency of the methylenetetrahydrofolate reductase-gene mutation varies with age in the normal population

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A common mutation in the methylenetetrahydrofolate reductase gene (C677T) increases the risk for deep-vein thrombosis in patients with mutant factor V (factor V:Q506).

21 January 2018

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The VITA project: C677T mutation in the methylene-tetrahydrofolate reductase gene and risk of venous thromboembolism

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Common mutation in methylenetetrahydrofolate reductase. Correlation with homocysteine and other risk factors for vascular disease.

21 January 2018

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Evolving methods in genetic epidemiology. III. Gene-environment interaction in epidemiologic research

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Spatial and temporal expression of the cystathionine beta-synthase gene during early human development.

21 January 2018

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Influence of 699C-->T and 1080C-->T polymorphisms of the cystathionine beta-synthase gene on plasma homocysteine levels.

21 January 2018

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Relation between plasma homocysteine concentration, the 844ins68 variant of the cystathionine beta-synthase gene, and pyridoxal-5'-phosphate concentration.

21 January 2018

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World distribution of the T833C/844INS68 CBS in cis double mutation: a reliable anthropological marker

21 January 2018

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

21 January 2018

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

21 January 2018

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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.

21 January 2018

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21 January 2018

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

21 January 2018

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10.1097/00125817-200205000-00005

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12180146%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

12 November 2019

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1 reference