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

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

Thrombosis research - 15 Sept 1997

Watzke H H, Schüttrumpf J, Graf S, Huber K, Panzer S

Abstract excerpt

A number of genetic risk factors for the development of coronary heart disease has been identified in the past. Some of these represent polymorphisms in genes of proteins which are associated with the process of blood clotting. We investigated the distribution of a recently described G/A polymorphism in the 3'untranslated region of the human prothrombin gene (nt 20210) in 98 patients (19 female age: 53 + 12 SD...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Alleles
Share to DNA

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Frequency

Share to Genotype

Share to Heterozygote

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 9330434
DOI: 10.1016/s0049-3848(97)00181-3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Increased prevalence of a polymorphism in the gene coding for human prothrombin in patients with coronary heart disease.PMID 9330434Read ↗

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

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

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

The 20210 G → A mutation in the 3′‐untranslated region of the prothrombin gene and the risk for arterial thrombotic diseaseSemantic proximity Read ↗

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

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

Hematological risk factors for coronary heart disease.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 ↗

No association between the 20210 G/A prothrombin gene mutation and premature coronary artery disease.Semantic proximity Read ↗

The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease.Semantic proximity Read ↗

[Gene polymorphisms of hemostasis and coronary risk].Semantic proximity Read ↗

Coagulation Factors II, V, VII, and X, Prothrombin Gene 20210G→A Transition, and Factor V Leiden in Coronary Artery DiseaseSemantic proximity Read ↗

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