(Q73461278)

English

The prevalence of C677T mutation in the methylenetetrahydrofolate reductase gene and its association with venous thrombophilia in Taiwanese Chinese

scientific article published on 01 February 2000

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10680639%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

The prevalence of C677T mutation in the methylenetetrahydrofolate reductase gene and its association with venous thrombophilia in Taiwanese Chinese (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10680639%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

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author name string

J S Lin

1

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Europe PubMed Central

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4 November 2019

M C Shen

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10680639%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

W Tsai

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10680639%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

B Lin

4

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Europe PubMed Central

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4 November 2019

publication date

1 February 2000

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4 November 2019

Thrombosis Research

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10680639%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

97

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Europe PubMed Central

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4 November 2019

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10680639%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

89-94

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10680639%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

High prevalence of antithrombin III, protein C and protein S deficiency, but no factor V Leiden mutation in venous thrombophilic Chinese patients in Taiwan

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900160-7

7 January 2021

based on heuristic

inferred from DOI database lookup

The G1691A mutation of the coagulation factor V gene (factor V Leiden) is rare in Chinese: an analysis of 618 individuals

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900160-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Hyperhomocysteinemia: an independent risk factor for vascular disease

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900160-7

7 January 2021

based on heuristic

inferred from DOI database lookup

A prospective study of plasma homocyst(e)ine and risk of ischemic stroke

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900160-7

7 January 2021

based on heuristic

inferred from DOI database lookup

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%2FS0049-3848%2899%2900160-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Hyperhomocysteinemia as a risk factor for deep-vein thrombosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900160-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Is hyperhomocysteinaemia a risk factor for recurrent venous thrombosis?

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900160-7

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%2899%2900160-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Myocardial infarction in young women in relation to plasma total homocysteine, folate, and a common variant in the methylenetetrahydrofolate reductase gene

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900160-7

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900160-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900160-7

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900160-7

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900160-7

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%2899%2900160-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Heterogeneity in world distribution of the thermolabile C677T mutation in 5,10-methylenetetrahydrofolate reductase.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900160-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Methylenetetrahydrofolate reductase gene polymorphism and ischemic stroke in Japanese

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900160-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0049-3848(99)00160-7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10680639%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10680639%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

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