(Q43774489)

English

Gene polymorphisms of homocysteine metabolism-related enzymes in Chinese patients with occlusive coronary artery or cerebral vascular diseases

scientific article published in November 2001

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scholarly article

1 reference

Europe PubMed Central

26 November 2017

Gene polymorphisms of homocysteine metabolism-related enzymes in Chinese patients with occlusive coronary artery or cerebral vascular diseases (English)

1 reference

Europe PubMed Central

26 November 2017

author name string

Zhang G

1

1 reference

Europe PubMed Central

26 November 2017

Dai C

2

1 reference

Europe PubMed Central

26 November 2017

publication date

1 November 2001

1 reference

Europe PubMed Central

26 November 2017

Thrombosis Research

1 reference

Europe PubMed Central

26 November 2017

104

1 reference

Europe PubMed Central

26 November 2017

3

1 reference

Europe PubMed Central

26 November 2017

187-195

1 reference

Europe PubMed Central

26 November 2017

Homocysteine and atherothrombosis

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900352-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Relationship between homocysteine and thrombotic disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900352-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900352-8

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%2801%2900352-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Thermolabile methylenetetrahydrofolate reductase in coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900352-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900352-8

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

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900352-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900352-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Methylenetetrahydrofolate reductase gene and coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900352-8

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%2801%2900352-8

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%2801%2900352-8

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%2801%2900352-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900352-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Cloning, mapping and RNA analysis of the human methionine synthase gene

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900352-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Defects in human methionine synthase in cblG patients

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900352-8

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2801%2900352-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0049-3848(01)00352-8

1 reference

Europe PubMed Central

26 November 2017

1 reference

Europe PubMed Central

26 November 2017

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