(Q33681688)

28 July 2017

title

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

1 reference

28 July 2017

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R de Franchis

1

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28 July 2017

A Buoninconti

2

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28 July 2017

C Mandato

3

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28 July 2017

A Pepe

4

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28 July 2017

M P Sperandeo

5

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28 July 2017

R Del Gado

6

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28 July 2017

V Capra

7

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28 July 2017

E Salvaggio

8

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28 July 2017

G Andria

9

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28 July 2017

P Mastroiacovo

10

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28 July 2017

language of work or name

English

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publication date

1 December 1998

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

35

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28 July 2017

issue

12

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28 July 2017

page(s)

1009-1013

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

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051513

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051513

The role of vitamins in the pathogenesis and treatment of hyperhomocyst(e)inaemia

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051513

Folic acid and neural tube defects: the current evidence and implications for prevention

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051513

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051513

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051513

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051513

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051513

A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051513

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051513

Homocysteine metabolism in pregnancies complicated by neural-tube defects.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051513

Homocysteine increases as folate decreases in plasma of healthy men during short-term dietary folate and methyl group restriction

30 October 2018

1 reference

12 December 2020

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

1 reference

12 December 2020

Endogenous synthesis of galactose in normal men and patients with hereditary galactosaemia

1 reference

12 December 2020

Is mutated MTHFR a risk factor for neural tube defects?

1 reference

12 December 2020

Methylenetetrahydrofolate reductase and neural tube defects

1 reference

12 December 2020

Factor V Leiden, C > T MTHFR polymorphism and genetic susceptibility to preeclampsia

1 reference

12 December 2020

High frequency of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in Northern Italy

1 reference

12 December 2020

MTHFR 677C-->T mutation, folate intake, neural-tube defect, and risk of cardiovascular disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Elevated plasma total homocysteine and C677T mutation of the methylenetetrahydrofolate reductase gene in patients with spina bifida

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.35.12.1009

1 reference

release_i7l2tkv5bfcv7ofg7igmfn4sne

28 July 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/i7l2tkv5bfcv7ofg7igmfn4sne

24 November 2022

mapped directly with Wikidata item

PMC publication ID

1051513

1 reference

28 July 2017

1 reference