Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

G20210A Prothrombin gene variant in Turkish patients with angiographically documented coronary artery disease.

Journal of thrombosis and thrombolysis - 1 Dec 2007

Gundogdu Fuat, Gurlertop Yekta, Pirim Ibrahim, Arslan Sakir, Ikbal Mevlut, Islamoglu Yahya, Aksoy Hulya, Senocak Huseyin

Abstract excerpt

BACKGROUND: G-->A substitution at position 20210A in the 3'-untranslated region in prothrombin gene is associated with raised plasma prothrombin. G20210A prothrombin variant has been associated with high prothrombin levels and an increased risk of venous thrombosis. To determine the prevalence of the G20210A prothrombin variant among Turkish and to evaluate the potential relevance of this variant to Turkish...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Coronary Angiography

Share to Coronary Artery Disease

Share to Polymorphism, Single Nucleotide

Share to Prevalence

Share to Prothrombin

Share to Turkey

Source

Identifiers

PMID: 17334933
DOI: 10.1007/s11239-007-0019-7

Genes

CAD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

G20210A Prothrombin gene variant in Turkish patients with angiographically documented coronary artery disease.PMID 17334933Read ↗

G20210A prothrombin gene polymorphism and prothrombin activity in subjects with or without angiographically documented coronary artery disease.Semantic proximity Read ↗

Prevalence of the 20210 G-->A prothrombin variant and its association with coronary artery disease in a Middle Eastern Arab population.Semantic proximity Read ↗

G20210A prothrombin gene polymorphism and coronary ischaemic syndromes: a phenotype-specific meta-analysis of 12 034 subjects.Semantic proximity Read ↗

Prevalence of the prothrombin gene variant 20210 G --> A among patients with myocardial infarction.Semantic proximity Read ↗

Prevalence of the G20210A polymorphism in the 3'-untranslated region of the prothrombin gene in different human populations.Semantic proximity Read ↗

Association Between the G20210A Polymorphism of Prothrombin Gene and Myocardial Infarction in Tunisian Population.Semantic proximity Read ↗

Prothrombin gene G20210-->A transition is a risk factor for cerebral venous thrombosis.Semantic proximity Read ↗

Increased prevalence of a polymorphism in the gene coding for human prothrombin in patients with coronary heart disease.Semantic proximity Read ↗

Varied association of prothrombin G20210A polymorphism with coronary artery disease susceptibility in different ethnic groups: evidence from 15,041 cases and 21,507 controls.Semantic proximity Read ↗

Increased prevalence of the G20210A prothrombin gene variant in acute coronary syndromes without metabolic or acquired risk factors or with limited extent of disease.Semantic proximity Read ↗

Prothrombin 20210GA and factor V Leiden mutations in patients less than 55 years old with myocardial infarction.Semantic proximity Read ↗

G20210A prothrombin gene variant and clinical outcome in patients with a first acute coronary syndrome.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.