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

Factor XII 46C --> T gene polymorphism in Chilean subjects with coronary artery disease and controls.

Medical principles and practice : international journal of the Kuwait University, Health Science Centre - 1 Jan 2009

Caamaño José, Jaramillo Priscilla C, Lanas Cecilia, Lanas Fernando, Salazar Luis A

Abstract excerpt

OBJECTIVE: To investigate the possible association between factor XII (F12) gene variant and the presence of coronary artery disease (CAD) in Chilean subjects. METHODS: A total of 112 unrelated patients with a diagnosis of CAD confirmed by angiography (33-74 years old) and 107 healthy controls (30-68 years old) were included in this study. PCR-RFLP was used to evaluate the 46C --> T polymorphism of the F12 gene....

Read the complete abstract on PubMed

Topics

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

Share to Blood Glucose
Share to Body Mass Index

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cardiovascular Diseases

Share to Coronary Artery Disease

Share to Factor XII

Share to Lipids

Share to Smoking

Source

Identifiers

PMID: 19204433
DOI: 10.1159/000189812

Genes

CAD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Factor XII 46C --> T gene polymorphism in Chilean subjects with coronary artery disease and controls.PMID 19204433Read ↗

Homozygosity of the T allele of the 46 C->T polymorphism in the F12 gene is a risk factor for ischemic stroke in the Spanish population.Semantic proximity Read ↗

FXII (46C-->T) polymorphism and in vivo generation of FXII activity--gene frequencies and relationship in patients with coronary artery disease.Semantic proximity Read ↗

Coagulation factor XII (FXII) activity, activated FXII, distribution of FXII C46T gene polymorphism and coronary risk.Semantic proximity Read ↗

Synergistic association between hypercholesterolemia and the C46T factor XII polymorphism for developing premature myocardial infarction.Semantic proximity Read ↗

Activated factor XII levels are dependent on factor XII 46C/T genotypes and factor XII zymogen levels, and are associated with vascular risk factors in patients and healthy subjects.Semantic proximity Read ↗

Association after linkage analysis indicates that homozygosity for the 46C-->T polymorphism in the F12 gene is a genetic risk factor for venous thrombosis.Semantic proximity Read ↗

Association of the factor XII 46C>T polymorphism with risk of coronary heart disease (CHD) in the WOSCOPS study.Semantic proximity Read ↗

Epidemiological and genetic associations of activated factor XII concentration with factor VII activity, fibrinopeptide A concentration, and risk of coronary heart disease in men.Semantic proximity Read ↗

Factor XII C46T gene polymorphism and the risk of cerebral venous thrombosis.Semantic proximity Read ↗

Activated factor XII levels and factor XII 46C>T genotype in relation to coronary artery calcification in patients with type 1 diabetes and healthy subjects.Semantic proximity Read ↗

Factor XIII Val34Leu variant protects against coronary artery diseaseSemantic proximity Read ↗

Correlation of von Willebrand factor gene polymorphism and coronary heart disease.Semantic proximity Read ↗

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