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

Mcp-1, eNOS, tPA and PAI-1 gene polymorphism and correlation of genotypes and phenotypes in hepatopulmonary syndrome.

Digestive diseases and sciences - 1 May 2008

Tumgor Gokhan, Berdeli Afig, Arikan Cigdem, Levent Ertürk, Aydogdu Sema

Abstract excerpt

AIM: The aim of this case-control study was to investigate both the distribution of MCP-1, eNOS, tPA and PAI-1 gene polymorphism and correlation of genotypes and phenotypes. METHOD: Between September 1997-January 2005, 20 patients with HPS (group 1) were compared with a group of cirrhotic patients (group 2, n = 19) as well as unrelated healthy controls (group 3, n = 59) in respect to MCP1, eNOS, tPA and PAI-1...

Read the complete abstract on PubMed

Topics

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

Share to Case-Control Studies
Share to Chemokine CCL2

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child, Preschool

Share to Infant

Share to Nitric Oxide Synthase Type III

Share to Plasminogen Activator Inhibitor 1

Share to Polymorphism, Restriction Fragment Length

Share to Tissue Plasminogen Activator

Source

Identifiers

PMID: 17934860
DOI: 10.1007/s10620-007-0002-3

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

Mcp-1, eNOS, tPA and PAI-1 gene polymorphism and correlation of genotypes and phenotypes in hepatopulmonary syndrome.PMID 17934860Read ↗

Genetic risk factors for hepatopulmonary syndrome in patients with advanced liver disease.Semantic proximity Read ↗

P-selectin gene polymorphism associates with pulmonary hypertension in congenital heart disease.Semantic proximity Read ↗

Functional variants of eNOS and iNOS genes have no relationship to the portal hypertension in patients with liver cirrhosis.Semantic proximity Read ↗

Combined platelet count with sCD163 and genetic variants optimizes esophageal varices prediction in cirrhotic patients.Semantic proximity Read ↗

The role of the eNOS G894T and T-786C gene polymorphism in the development of ascites in cirrhosis.Semantic proximity Read ↗

Study of the influence of heme oxygenase 1 gene single nucleotide polymorphism (rs2071746) on esophageal varices among patients with cirrhosis.Semantic proximity Read ↗

[The association between polymorphism of endothelial nitric oxide synthase gene and cirrhotic portal hypertension].Semantic proximity Read ↗

Genetic variants of endothelial nitric oxide synthase in patients with primary biliary cirrhosis: association with disease severity.Semantic proximity Read ↗

Association of arginine vasopressin receptor 1a gene polymorphisms with hepatorenal syndrome.Semantic proximity Read ↗

Characteristic genotypes of vascular endothelial growth factor are susceptible to ascites in patients with cirrhosis.Semantic proximity Read ↗

Variation at the Angiotensin-converting enzyme and endothelial nitric oxide synthase genes is associated with the risk of esophageal varices among patients with alcoholic cirrhosis.Semantic proximity Read ↗

Causes of portal venous thrombosis in cirrhotic patients: the role of genetic and acquired factors.Semantic proximity Read ↗

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