(Q44249445)

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

scientific article published in January 2003

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15 December 2019

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

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15 December 2019

Robert Curtis Ellison

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15 December 2019

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Rima Rozen

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15 December 2019

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Jacob Selhub

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15 December 2019

Andrew G. Bostom

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Andrew G Bostom

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15 December 2019

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Paul F Jacques

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15 December 2019

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Sharron Rich

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15 December 2019

John H Eckfeldt

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15 December 2019

Roy A Gravel

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15 December 2019

National Heart, Lung and Blood Institute, National Institutes of Health

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15 December 2019

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1 January 2003

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15 December 2019

Atherosclerosis

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15 December 2019

166

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15 December 2019

1

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15 December 2019

49-55

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15 December 2019

Homocysteine and cardiovascular disease

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900204-6

7 January 2021

A quantitative assessment of plasma homocysteine as a risk factor for vascular disease. Probable benefits of increasing folic acid intakes

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900204-6

7 January 2021

The pathogenesis of homocysteinemia: interruption of the coordinate regulation by S-adenosylmethionine of the remethylation and transsulfuration of homocysteine

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900204-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900204-6

7 January 2021

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%2FS0021-9150%2802%2900204-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900204-6

7 January 2021

Molecular cloning, expression and physical mapping of the human methionine synthase reductase gene

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900204-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900204-6

7 January 2021

A common polymorphism in methionine synthase reductase increases risk of premature coronary artery disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900204-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900204-6

7 January 2021

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%2FS0021-9150%2802%2900204-6

7 January 2021

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%2FS0021-9150%2802%2900204-6

7 January 2021

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%2FS0021-9150%2802%2900204-6

7 January 2021

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%2FS0021-9150%2802%2900204-6

7 January 2021

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

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0021-9150%2802%2900204-6

7 January 2021

Effect of heterozygosity for the methionine synthase 2756 A-->G mutation on the risk for recurrent cardiovascular events

1 reference

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7 January 2021

NHLBI Family Heart Study: objectives and design

1 reference

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7 January 2021

Determination of free and total homocysteine in human plasma by high-performance liquid chromatography with fluorescence detection

1 reference

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7 January 2021

Pyridoxal-5'-phosphate determination by a sensitive micromethod in human blood, urine and tissues; its relation to cystathioninuria in neuroblastoma and biliary atresia

1 reference

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7 January 2021

Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome

1 reference

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7 January 2021

Identifiers

10.1016/S0021-9150(02)00204-6

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12482550%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12482550%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

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