(Q74238328)

English

The allele frequency of mutations in four genes that confer enhanced susceptibility to venous thromboembolism in an unselected group of New York State newborns

scientific article published on 01 August 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:10963782%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

The allele frequency of mutations in four genes that confer enhanced susceptibility to venous thromboembolism in an unselected group of New York State newborns (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10963782%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

venous thromboembolism

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author name string

J M Conroy

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10963782%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

G Trivedi

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10963782%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

T Sovd

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10963782%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

M Caggana

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10963782%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

publication date

1 August 2000

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10963782%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Thrombosis Research

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10963782%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

99

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10963782%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10963782%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

317-324

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10963782%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

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

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Homocysteine metabolism in pregnancies complicated by neural-tube defects.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

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%2800%2900254-1

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%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

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%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic susceptibility to pregnancy-related venous thromboembolism: Roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

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%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Effect of the MTHFRC677T variant on risk of venous thromboembolism: interaction with factor V Leiden and prothrombin (F2G20210A) mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

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%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

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%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

A simplified procedure for developing multiplex PCRs

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevalence of the prothrombin 20210 G-to-A variant in blacks: infants, patients with venous thrombosis, patients with myocardial infarction, and control subjects

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

The 20210 G-->A mutation in the 3'-untranslated region of the prothrombin gene and the risk for arterial thrombotic disease

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Ethnic distribution of factor V Leiden in 4047 men and women. Implications for venous thromboembolism screening

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

The Arg506Gln mutation (FV Leiden) among a cohort of 4188 unselected Danish newborns

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

A racial difference in the prevalence of the Arg506-->Gln mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

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%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Inherited risk factors for thrombophilia among children with Legg-Calvé-Perthes disease

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

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%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Worldwide distribution of a common methylenetetrahydrofolate reductase mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Mortality risk in men is associated with a common mutation in the methylene-tetrahydrofolate reductase gene (MTHFR)

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

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%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Decreased proportion of female newborn infants homozygous for the 677 C-->T mutation in methylenetetrahydrofolate reductase

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

A prospective study of methylenetetrahydrofolate reductase and methionine synthase gene polymorphisms, and risk of colorectal adenoma

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

An unknown genetic defect increases venous thrombosis risk, through interaction with protein C deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Contribution of the glycoprotein Ia 807TT, methylene tetrahydrofolate reductase 677TT and prothrombin 20210GA genotypes to prothrombotic risk among factor V 1691GA (Leiden) carriers

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

The Risk of Recurrent Deep Venous Thrombosis among Heterozygous Carriers of Both Factor V Leiden and the G20210A Prothrombin Mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Additional genetic risk factors for venous thromboembolism in carriers of the factor V Leiden mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Single and combined prothrombotic factors in patients with idiopathic venous thromboembolism: prevalence and risk assessment

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

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%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

No evidence for an increased risk of venous thrombosis in patients with factor V Leiden by the homozygous 677 C to T mutation in the methylenetetrahydrofolate-reductase gene

1 reference

https://api.crossref.org/works/10.1016%2FS0049-3848%2800%2900254-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0049-3848(00)00254-1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10963782%20AND%20SRC:MED&resulttype=core&format=json

9 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:10963782%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

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