(Q57267273)

English

C677T (thermolabile alanine/valine) polymorphism in methylenetetrahydrofolate reductase (MTHFR): its frequency and impact on plasma homocysteine concentration in different European populations

scientific article published on 01 February 1998

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scholarly article

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10 November 2019

C677T (thermolabile alanine/valine) polymorphism in methylenetetrahydrofolate reductase (MTHFR): its frequency and impact on plasma homocysteine concentration in different European populations. EARS group (English)

1 reference

Europe PubMed Central

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10 November 2019

Vilmundur Gudnason

1

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10 November 2019

author name string

D Stansbie

2

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10 November 2019

J Scott

3

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10 November 2019

A Bowron

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10 November 2019

V Nicaud

5

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10 November 2019

S Humphries

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10 November 2019

publication date

1 February 1998

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10 November 2019

Atherosclerosis

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10 November 2019

136

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10 November 2019

347-354

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10 November 2019

2

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10 November 2019

The pathogenesis of coronary artery disease. A possible role for methionine metabolism

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Homocysteinemia, ischemic heart disease, and the carrier state for homocystinuria.

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Moderate homocysteinemia--a possible risk factor for arteriosclerotic cerebrovascular disease

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Heterozygosity for Homocystinuria in Premature Peripheral and Cerebral Occlusive Arterial Disease

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Protein-bound homocyst(e)ine. A possible risk factor for coronary artery disease

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Homocysteine and myocardial infarction

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Prevalence of hyperhomocyst(e)inemia in patients with peripheral arterial occlusive disease

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Plasma homocyst(e)ine levels in men with premature coronary artery disease

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Prevalence of familial hyperhomocyst(e)inemia in men with premature coronary artery disease

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Hyperhomocysteinemia: an independent risk factor for vascular disease

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A prospective study of plasma homocyst(e)ine and risk of myocardial infarction in US physicians

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Carotid artery intimal-medial wall thickening and plasma homocyst(e)ine in asymptomatic adults. The Atherosclerosis Risk in Communities Study

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Association between Plasma Homocysteine Concentrations and Extracranial Carotid-Artery Stenosis

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7 January 2021

Plasma homocyst(e)ine levels and graded risk for myocardial infarction: findings in two populations at contrasting risk for coronary heart disease

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7 January 2021

Serum total homocysteine and coronary heart disease

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Relation of serum homocysteine and lipoprotein(a) concentrations to atherosclerotic disease in a prospective Finnish population based study

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Genetic and nongenetic factors for moderate hyperhomocyst(e)inemia

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7 January 2021

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

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7 January 2021

Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.

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7 January 2021

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

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The common 'thermolabile' variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia

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7 January 2021

Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians

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7 January 2021

Genetic polymorphism of methylenetetrahydrofolate reductase and myocardial infarction. A case-control study

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Determinants and vitamin responsiveness of intermediate hyperhomocysteinemia (> or = 40 micromol/liter). The Hordaland Homocysteine Study

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7 January 2021

Thermolabile defect of methylenetetrahydrofolate reductase in coronary artery disease

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7 January 2021

Homocysteine and risk of premature coronary heart disease. Evidence for a common gene mutation

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7 January 2021

Common mutation in methylenetetrahydrofolate reductase. Correlation with homocysteine metabolism and late-onset vascular disease.

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7 January 2021

Distribution in healthy and coronary populations of the methylenetetrahydrofolate reductase (MTHFR) C677T mutation

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7 January 2021

Methylenetetrahydrofolate reductase gene and coronary artery disease

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7 January 2021

A common mutation in methylenetetrahydrofolate reductase gene is not a major risk of coronary artery disease or myocardial infarction.

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7 January 2021

The European Atherosclerosis Research Study (EARS): design and objectives

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

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Electrophoresis for genotyping: microtiter array diagonal gel electrophoresis on horizontal polyacrylamide gels, hydrolink, or agarose.

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7 January 2021

Inference of the strength of genotype-disease association from studies comparing offspring with and without parental history of disease

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Coffee consumption and plasma total homocysteine: The Hordaland Homocysteine Study

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Hyperhomocysteinaemia in stroke: prevalence, cause, and relationships to type of stroke and stroke risk factors

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Plasma sulfhydryl-containing amino acids in patients with cerebral infarction and in hypertensive subjects

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Prevalence of moderate hyperhomocysteinemia in patients with early-onset venous and arterial occlusive disease.

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Identifiers

10.1016/S0021-9150(97)00237-2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9543106%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9543106%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

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