(Q73521051)

English

Common C677T polymorphism in the methylenetetrahydrofolate reductase gene increases the risk for deep vein thrombosis in patients with predisposition of thrombophilia

scientific article published on 01 April 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:10706928%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Common C677T polymorphism in the methylenetetrahydrofolate reductase gene increases the risk for deep vein thrombosis in patients with predisposition of thrombophilia (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10706928%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

deep vein thrombosis

1 reference

based on heuristic

inferred from title

author name string

H Fujimura

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10706928%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

T Kawasaki

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10706928%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

T Sakata

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10706928%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

H Ariyoshi

4

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10706928%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

H Kato

5

1 reference

Europe PubMed Central

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4 November 2019

M Monden

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10706928%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

T Miyata

7

1 reference

Europe PubMed Central

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4 November 2019

publication date

1 April 2000

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10706928%20AND%20SRC:MED&resulttype=core&format=json

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:10706928%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

98

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Europe PubMed Central

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4 November 2019

1

1 reference

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4 November 2019

1-8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10706928%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

Hyperhomocyst(e)inemia as a risk factor for occlusive vascular disease

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Homocyst(e)ine: an important risk factor for atherosclerotic vascular disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

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%2900231-5

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

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%2900231-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Hyperhomocyst(e)inemia is a risk factor for arterial endothelial dysfunction in humans.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Plasma homocysteine levels and mortality in patients with coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

7 January 2021

based on heuristic

inferred from DOI database lookup

High prevalence of hyperhomocyst(e)inemia in patients with juvenile venous thrombosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

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%2900231-5

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%2900231-5

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%2900231-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Plasma homocysteine levels in patients with deep venous thrombosis

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

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%2900231-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

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%2900231-5

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%2899%2900231-5

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%2899%2900231-5

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%2899%2900231-5

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%2900231-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Interrelation of hyperhomocyst(e)inemia, factor V Leiden, and risk of future venous thromboembolism

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

7 January 2021

based on heuristic

inferred from DOI database lookup

A common mutation in the methylenetetrahydrofolate reductase gene (C677T) increases the risk for deep-vein thrombosis in patients with mutant factor V (factor V:Q506).

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Hyperhomocyst(e)inemia and a common methylenetetrahydrofolate reductase mutation (Ala223Val MTHFR) in patients with inherited thrombophilic coagulation defects.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

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%2899%2900231-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Frequencies of prothrombin 20210 G-->A mutation may be different among races--studies on Japanese populations with various forms of thrombotic disorders and healthy subjects.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

7 January 2021

based on heuristic

inferred from DOI database lookup

The prothrombin gene G20210A mutation is not found among Japanese patients with deep vein thrombosis and healthy individuals

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Absence of thrombosis in subjects with heterozygous protein C deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevalence of antithrombin deficiency in the healthy population.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2899%2900231-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0049-3848(99)00231-5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10706928%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:10706928%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

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