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

Identification of gene variants associated with hypoxia pathway in acute coronary syndrome: a pilot study.

Molecular biology reports - 1 Dec 2014

Gokkusu Cahide, Cakmakoglu Bedia, Cincin Zeynep Birsu, Karaagac Mehmet, Emet Samim, Tamer Sule, Umman Berrin

Abstract excerpt

Hypoxic condition is known to play an important role in the development of acute coronary syndrome (ACS) and understanding mechanism of hypoxic effects is essential to develop new treatment strategies for ACS. Based on the phenotypic features of cardiovascular diseases, it is claimed that genetic factors play an important role in the development genome-wide association studies have been studied to clarify the...

Read the complete abstract on PubMed

Topics

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

Share to Acute Coronary Syndrome
Share to Aged

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genome-Wide Association Study

Share to Hypoxia

Share to Pilot Projects

Share to Poly-ADP-Ribose Binding Proteins

Share to Polymorphism, Single Nucleotide

Share to Vascular Endothelial Growth Factor A

Source

Identifiers

PMID: 25234649
DOI: 10.1007/s11033-014-3703-7

Genes

PIAS4
VEGFA

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

Identification of gene variants associated with hypoxia pathway in acute coronary syndrome: a pilot study.PMID 25234649Read ↗

Identification of gene variants related to the nitric oxide pathway in patients with acute coronary syndrome.Semantic proximity Read ↗

Pathway-Specific Polygenic Risk Scores Identify Obstructive Sleep Apnea-Related Pathways Differentially Moderating Genetic Susceptibility to Coronary Artery Disease.Semantic proximity Read ↗

SCD leads to the development and progression of acute myocardial infarction through the AMPK signaling pathwaySemantic proximity Read ↗

Pathway-specific Polygenic Risk Scores (PRS) identify OSA-related pathways differentially moderating genetic susceptibility to CADSemantic proximity Read ↗

Hypoxia-induced signaling in the cardiovascular system: pathogenesis and therapeutic targetsSemantic proximity Read ↗

Identifying key genes associated with acute myocardial infarctionSemantic proximity Read ↗

Integrative Analysis of Key Candidate Genes and Signaling Pathways in Acute Coronary Syndrome Related to Obstructive Sleep Apnea by bioinformaticsSemantic proximity Read ↗

Integrative analysis of key candidate genes and signaling pathways in acute coronary syndrome related to obstructive sleep apnea by bioinformatics.Semantic proximity Read ↗

The Interplay of Hypoxia Signaling on Mitochondrial Dysfunction and Inflammation in Cardiovascular Diseases and Cancer: From Molecular Mechanisms to Therapeutic ApproachesSemantic proximity Read ↗

Hypoxia-inducible factor-1α polymorphisms link to coronary artery collateral development and clinical presentation of coronary artery disease.Semantic proximity Read ↗

Missense Variants in Hypoxia-Induced VEGFA/VEGFR2 Signaling Predict the Outcome of Large Artery Atherosclerotic Stroke.Semantic proximity Read ↗

Further evidence for the contribution of the vascular endothelial growth factor gene in coronary artery disease susceptibility.Semantic proximity Read ↗

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