(Q44092037)

English

Factor V gene G1691A mutation, prothrombin gene G20210A mutation, and MTHFR gene C677T mutation are not risk factors for pulmonary thromboembolism in Chinese population

scientific article published in April 2002

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

Factor V gene G1691A mutation, prothrombin gene G20210A mutation, and MTHFR gene C677T mutation are not risk factors for pulmonary thromboembolism in Chinese population (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

pulmonary embolism

1 reference

based on heuristic

inferred from title

author name string

Yanhui Lu

1

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

Yanfen Zhao

2

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

Guozhang Liu

3

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

Xiaoling Wang

4

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

Zhihong Liu

5

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

Baiping Chen

6

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

Rutai Hui

7

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

publication date

1 April 2002

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Europe PubMed Central

PubMed publication ID

29 November 2017

number of pages

6

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inferred from page(s)

Thrombosis Research

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Europe PubMed Central

PubMed publication ID

29 November 2017

106

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Europe PubMed Central

PubMed publication ID

29 November 2017

1

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PubMed publication ID

29 November 2017

7-12

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2802%2900064-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutation in blood coagulation factor V associated with resistance to activated protein C.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2802%2900064-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Inherited Thrombophilic Risk Factors and Venous Thromboembolism

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2802%2900064-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevalence of the G1691A mutation in the factor V gene (factor V Leiden) and the G20210A prothrombin gene mutation in the Thai population

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2802%2900064-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Protein C and protein S deficiencies are the most important risk factors associated with thrombosis in Chinese venous thrombophilic patients in Taiwan

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2802%2900064-6

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%2802%2900064-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Relation of three genetic traits to venous thrombosis in an African-American population

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2802%2900064-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Low prevalence of activated protein C resistance and coagulation factor V Arg506 to Gln mutation among Korean patients with deep vein thrombosis

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2802%2900064-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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%2802%2900064-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Causes of venous thrombosis in fifty Chinese patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2802%2900064-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The prothrombin gene G20210A variant: prevalence in a U.K. anticoagulant clinic population

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2802%2900064-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Interaction of coagulation defects and cardiovascular risk factors: increased risk of myocardial infarction associated with factor V Leiden or prothrombin 20210A

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2802%2900064-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Prothrombin G20210A, factor V Leiden, and factor XIII Val34Leu: common mutations of blood coagulation factors and deep vein thrombosis in Austria

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2802%2900064-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The prothrombin 20210A allele and the factor V Leiden are associated with venous thrombosis but not with early coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2802%2900064-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The G20210A mutation of the prothrombin gene in patients with previous first episodes of deep-vein thrombosis: prevalence and association with factor V G1691A, methylenetetrahydrofolate reductase C677T and plasma prothrombin levels

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2802%2900064-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2802%2900064-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0049-3848(02)00064-6

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

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