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

Genetic susceptibility to deep venous thromboembolism: the roles of inherited thrombophilia polymorphisms.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Apr 2016

Bargahi Nasrin, Ghorbian Saeid, Zonouzi Ali Akbar Poursadegh, Zonouzi Ahmad Poursadegh

Abstract excerpt

Recently much attention has been paid to the possibly considerable role of the thrombophilic gene polymorphisms in the pathogenesis of deep venous thromboembolism (DVT). However, the reported results are controversial. Hence, this study aimed to disclose the association between factor VII (FVII) 10976G/A, angiotensin-converting enzyme (ACE; intron 16 I/D), glycoprotein Ia (GPIa) 807C/T, tissue-type plasminogen...

Read the complete abstract on PubMed

Topics

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

Share to Integrin alpha2
Share to Factor VII

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lipoproteins

Share to Peptidyl-Dipeptidase A

Share to Plasminogen Activator Inhibitor 1

Share to Thrombophilia

Share to Tissue Plasminogen Activator

Share to Venous Thromboembolism

Source

Identifiers

PMID: 27023879
DOI: 10.1097/MBC.0000000000000430

Genes

ACE

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

Genetic susceptibility to deep venous thromboembolism: the roles of inherited thrombophilia polymorphisms.PMID 27023879Read ↗

A preliminary study of inherited thrombophilic risk factors in different clinical manifestations of venous thromboembolism in central Iran.Semantic proximity Read ↗

ACE DD genotype: an independent predisposition factor to venous thromboembolism.Semantic proximity Read ↗

Prevalence of factor V leiden, MTHFR C677T and MTHFR A1298C polymorphisms in patients with deep vein thrombosis in Central Iran.Semantic proximity Read ↗

Gene polymorphisms implicated in influencing susceptibility to venous and arterial thromboembolism: frequency distribution in a healthy German population.Semantic proximity Read ↗

Polymorphisms and mutations in vWF and ADAMTS13 genes and their correlation with plasma levels of FVIII and vWF in patients with deep venous thrombosis.Semantic proximity Read ↗

Thrombophilic Gene Mutations in Relation to Different Manifestations of Venous Thromboembolism: A Single Tertiary Center Study.Semantic proximity Read ↗

A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis.Semantic proximity Read ↗

Influence of tissue factor polymorphisms (603A>G and 5466A>G) on plasma tissue factor levels and their impact on deep vein thrombosis risk in young Indian population.Semantic proximity Read ↗

Endothelial cell protein C receptor gene 6936A/G and 4678G/C polymorphisms as risk factors for deep venous thrombosis.Semantic proximity Read ↗

Deep venous thrombosis and thrombophilic mutations in western Iran: association with factor V Leiden.Semantic proximity Read ↗

The PAI-1 gene 4G/5G polymorphism and deep vein thrombosis in patients with inherited thrombophilia.Semantic proximity Read ↗

Molecular analysis of prothrombotic gene variants in venous thrombotic diseases. Different risk factors in different sex and clinical forms.Semantic proximity Read ↗

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