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

A nonsynonymous variant I248L of the adenosine A3 receptor is associated with coronary heart disease in a Latvian population.

DNA and cell biology - 1 Nov 2011

Peculis Raitis, Latkovskis Gustavs, Tarasova Linda, Pirags Valdis, Erglis Andrejs, Klovins Janis

Abstract excerpt

Adenosine plays an important part in the cardiac response to ischemia and reperfusion. The human adenosine receptor A3 (A3R), along with other adenosine receptors, is involved in mediation of those effects. The aim of the study was to ascertain whether the nonsynonymous single-nucleotide polymorphism (SNP) I248L (reference SNP ID: rs35511654) located in the A3R gene is associated with coronary heart disease...

Read the complete abstract on PubMed

Topics

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

Share to Alleles

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Cohort Studies

Share to Coronary Disease

Share to Databases, Genetic

Share to Latvia

Share to Polymorphism, Single Nucleotide

Source

Identifiers

PMID: 21675873
DOI: 10.1089/dna.2011.1230

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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

A nonsynonymous variant I248L of the adenosine A3 receptor is associated with coronary heart disease in a Latvian population.PMID 21675873Read ↗

Analysis on the polymorphisms of site RS4977574, and RS1333045 in region 9p21 and the susceptibility of coronary heart disease in Chinese population.Semantic proximity Read ↗

The association between the single-nucleotide polymorphism of site rs1333040 in region 9p21 and the risk of coronary heart disease in Chinese population.Semantic proximity Read ↗

Polymorphisms in adenosine receptor genes are associated with infarct size in patients with ischemic cardiomyopathy.Semantic proximity Read ↗

Genetic variation in ABCA1 predicts ischemic heart disease in the general population.Semantic proximity Read ↗

Association of the L3MBTL3 rs1125970 and rs4897367 Gene Polymorphisms With Coronary Heart Disease Susceptibility in the Chinese Population: A Case-Control Study.Semantic proximity Read ↗

Increased Risk of CHD in the Presence of rs7865618 (A allele): Tehran Lipid and Glucose Study.Semantic proximity Read ↗

ABCA1 rs4149313 polymorphism and susceptibility to coronary heart disease: a meta-analysis.Semantic proximity Read ↗

Association Between rs2200733 Polymorphism on Chromosome 4q25 and Atrial Fibrillation in a Greek Population.Semantic proximity Read ↗

The rs1892818 polymorphism of ADRB3 is associated with coronary artery disease in a Han populationSemantic proximity Read ↗

Ethnic differences in the linkage disequilibrium and distribution of single-nucleotide polymorphisms in 35 candidate genes for cardiovascular diseases.Semantic proximity Read ↗

Association of single nucleotide polymorphism rs6903956 on chromosome 6p24.1 with coronary artery disease and lipid levels in different ethnic groups of the Singaporean population.Semantic proximity Read ↗

Evaluation of the participation of ABCA1 transporter in epicardial and mediastinal adipose tissue from patients with coronary artery disease.Semantic proximity Read ↗

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