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

Pathway analysis using genome-wide association study data for coronary restenosis--a potential role for the PARVB gene.

PloS one - 1 Jan 2013

Verschuren Jeffrey J W, Trompet Stella, Sampietro M Lourdes, Heijmans Bastiaan T, Koch Werner, Kastrati Adnan, Houwing-Duistermaat Jeanine J, Slagboom P Eline, Quax Paul H A, Jukema J Wouter

Abstract excerpt

BACKGROUND: Coronary restenosis after percutaneous coronary intervention (PCI) still remains a significant limitation of the procedure. The causative mechanisms of restenosis have not yet been fully identified. The goal of the current study was to perform gene-set analysis of biological pathways related to inflammation, proliferation, vascular function and transcriptional regulation on coronary restenosis to...

Read the complete abstract on PubMed

Topics

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

Share to Actinin
Share to Coronary Restenosis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cytokines

Share to Endothelial Cells

Share to Endothelium, Vascular

Share to Extracellular Matrix

Share to Metabolic Networks and Pathways

Share to Software

Source

Open in PubMed Open full text

Identifiers

PMID: 23950981
DOI: 10.1371/journal.pone.0070676
PMCID: PMC3739784

Genes

PARVB

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

Pathway analysis using genome-wide association study data for coronary restenosis--a potential role for the PARVB gene.PMID 23950981Read ↗

Systematic testing of literature reported genetic variation associated with coronary restenosis: results of the GENDER Study.Semantic proximity Read ↗

A genome-wide association study identifies a region at chromosome 12 as a potential susceptibility locus for restenosis after percutaneous coronary intervention.Semantic proximity Read ↗

A systematic review and bioinformatic study on clinical, paraclinical, and genetic factors predisposing to stent restenosis following percutaneous coronary intervention.Semantic proximity Read ↗

Genetic Variants in PHACTR1 & LPL Mediate Restenosis Risk in Coronary Artery PatientsSemantic proximity Read ↗

Decoding Restenosis Risk After CABG: A Combined Transcriptomic and Mendelian Randomization AnalysisSemantic proximity Read ↗

Integrated Bioinformatics Analysis for Potential Target Genes of In-Stent RestenosisSemantic proximity Read ↗

Shared molecular pathways and gene networks for cardiovascular disease and type 2 diabetes mellitus in women across diverse ethnicities.Semantic proximity Read ↗

Integrative gene ontology and network analysis of coronary artery disease associated genes suggests potential role of ErbB pathway gene EGFR.Semantic proximity Read ↗

Genetic inflammatory factors predict restenosis after percutaneous coronary interventions.Semantic proximity Read ↗

Microarray Analysis Reveals the Potential Molecular Mechanism of Lp299v in Stable Coronary Atherosclerotic DiseaseSemantic proximity Read ↗

Vitamin D receptor: a new risk marker for clinical restenosis after percutaneous coronary intervention.Semantic proximity Read ↗

Potential molecular mechanisms of postoperative restenosis in lower extremity atherosclerotic occlusive diseaseSemantic proximity Read ↗

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