(Q44533816)

English

The 2756A>G variant in the gene encoding methionine synthase: its relation with plasma homocysteine levels and risk of coronary heart disease in a Dutch case-control study

scientific article published in May 2003

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

The 2756A>G variant in the gene encoding methionine synthase: its relation with plasma homocysteine levels and risk of coronary heart disease in a Dutch case-control study (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

1 reference

based on heuristic

inferred from title

coronary artery disease

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based on heuristic

inferred from title

4

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PubMed publication ID

3 December 2017

author name string

Mariska Klerk

1

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Karin J A Lievers

2

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Leo A J Kluijtmans

3

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Martin den Heijer

5

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Evert G Schouten

6

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Frans J Kok

7

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Petra Verhoef

8

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

publication date

1 May 2003

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Thrombosis Research

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

110

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3 December 2017

2-3

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Europe PubMed Central

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3 December 2017

87-91

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Methylenetetrahydrofolate reductase and methionine synthase: biochemistry and molecular biology

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

The controversy over homocysteine and cardiovascular risk

1 reference

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7 January 2021

based on heuristic

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Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease: the result of a meta-analysis

1 reference

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7 January 2021

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MTHFR 677C-->T polymorphism and risk of coronary heart disease: a meta-analysis.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2803%2900341-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2803%2900341-4

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2803%2900341-4

7 January 2021

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Human methionine synthase. cDNA cloning, gene localization, and expression

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

The 677C-->T mutation in the methylenetetrahydrofolate reductase gene: associations with plasma total homocysteine levels and risk of coronary atherosclerotic disease.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Is hyperhomocysteinaemia a risk factor for recurrent venous thrombosis?

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Three different methods for the determination of total homocysteine in plasma

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Methionine synthase D919G polymorphism is a significant but modest determinant of circulating homocysteine concentrations

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Polymorphism of the methionine synthase gene : association with homocysteine metabolism and late-onset vascular diseases in the Japanese population

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2803%2900341-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic defects as important factors for moderate hyperhomocysteinemia

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2803%2900341-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Relationship between total plasma homocysteine, polymorphisms of homocysteine metabolism related enzymes, risk factors and coronary artery disease in the Australian hospital-based population

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2803%2900341-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic causes of mild hyperhomocysteinemia in patients with premature occlusive coronary artery diseases.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2803%2900341-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Polygenic influence on plasma homocysteine: association of two prevalent mutations, the 844ins68 of cystathionine beta-synthase and A(2756)G of methionine synthase, with lowered plasma homocysteine levels.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2803%2900341-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Influence of a methionine synthase (D919G) polymorphism on plasma homocysteine and folate levels and relation to risk of myocardial infarction

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2803%2900341-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Altered folate metabolism and disposition in mothers affected by a spina bifida pregnancy: influence of 677c --> t methylenetetrahydrofolate reductase and 2756a --> g methionine synthase genotypes.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2803%2900341-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Vitamins B6, B12, and folate: association with plasma total homocysteine and risk of coronary atherosclerosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2803%2900341-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Homocysteine metabolism and risk of myocardial infarction: relation with vitamins B6, B12, and folate.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2803%2900341-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Low circulating folate and vitamin B6 concentrations: risk factors for stroke, peripheral vascular disease, and coronary artery disease. European COMAC Group

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2803%2900341-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Prospective study of coronary heart disease incidence in relation to fasting total homocysteine, related genetic polymorphisms, and B vitamins: the Atherosclerosis Risk in Communities (ARIC) study.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2803%2900341-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Plasma homocyst(e)ine, folate, and vitamin B-12 concentrations and risk for early-onset coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2803%2900341-4

7 January 2021

based on heuristic

inferred from DOI database lookup

The association of vitamin b 12 and folate blood levels with mortality and cardiovascular morbidity incidence in the old old: the Bronx aging study

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2803%2900341-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0049-3848(03)00341-4

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

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