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

Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery disease.

Human molecular genetics - 15 Apr 2007

Baessler Andrea, Fischer Marcus, Mayer Bjoern, Koehler Martina, Wiedmann Silke, Stark Klaus, Doering Angela, Erdmann Jeanette, Riegger Guenter, Schunkert Heribert, Kwitek Anne E, Hengstenberg Christian

Abstract excerpt

Data from both experimental models and humans provide evidence that ghrelin and its receptor, the growth hormone secretagogue receptor (ghrelin receptor, GHSR), possess a variety of cardiovascular effects. Thus, we hypothesized that genetic variants within the ghrelin system (ligand ghrelin and i...

Read the complete abstract on PubMed

Topics

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

Share to Coronary Artery Disease
Share to Decision Trees

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Ghrelin

Share to Myocardial Infarction

Share to Peptide Hormones

Share to Receptors, G-Protein-Coupled

Share to Receptors, Ghrelin

Share to Siblings

Source

Identifiers

PMID: 17324965
DOI: 10.1093/hmg/ddm033

Genes

CAD
GHSR
GHRL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17324965-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery disease.PMID 17324965Read ↗

Association of the Ghrelin receptor gene region with left ventricular hypertrophy in the general population: results of the MONICA/KORA Augsburg Echocardiographic Substudy.Semantic proximity Read ↗

Genotypng:Genetic variation in coronary heart disease and myocardial infarction: methodological overview and clinical evidenceSemantic proximity Read ↗

Hypothesis-based analysis of gene-gene interactions and risk of myocardial infarction.Semantic proximity Read ↗

Polymorphisms in 33 inflammatory genes and risk of myocardial infarction--a system genetics approach.Semantic proximity Read ↗

Influence of ghrelin gene polymorphisms on hypertension and atherosclerotic disease.Semantic proximity Read ↗

Genetic linkage and association of the growth hormone secretagogue receptor (ghrelin receptor) gene in human obesity.Semantic proximity Read ↗

The association of ghrelin polymorphisms with coronary artery disease and ischemic chronic heart failure in an elderly Chinese population.Semantic proximity Read ↗

Association between ghrelin gene (Leu72Met) polymorphism and ghrelin serum level with coronary artery diseases.Semantic proximity Read ↗

The ABCG5/8 cholesterol transporter and myocardial infarction versus gallstone disease.Semantic proximity Read ↗

Familial predisposition and susceptibility to the effect of other risk factors for myocardial infarction.Semantic proximity Read ↗

Lack of association between a common polymorphism near the INSIG2 gene and BMI, myocardial infarction, and cardiovascular risk factors.Semantic proximity Read ↗

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