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

Higher frequency of rs4977574 (the G Allele) on chromosome 9p21.3 in patients with myocardial infarction as revealed by PCR-RFLP analysis.

The Tohoku journal of experimental medicine - 1 Jul 2013

Sakalar Cagri, Gurbuz Esra, Kalay Nihat, Kaya Mehmet Gungor

Abstract excerpt

Single Nucleotide Polymorphisms (SNPs) can genetically predispose individuals for certain diseases and therefore are of clinical significance. Myocardial infarction (MI) was investigated in large genetic association studies revealing novel SNPs associated with MI. rs4977574 is a non-protein coding SNP (A>G) that is located in proximity of cyclin-dependent kinase inhibitor 2A and B genes on chromosome 9p21.3....

Topics

Join the communities discussing this publication.

Chromosomes, Human, Pair 9
DNA, Intergenic
DNA Primers
Myocardial Infarction

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Polymerase Chain Reaction

Polymorphism, Restriction Fragment Length

Sequence Analysis, DNA

Source

Identifiers

PMID: 23856978
DOI: 10.1620/tjem.230.171

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Higher frequency of rs4977574 (the G Allele) on chromosome 9p21.3 in patients with myocardial infarction as revealed by PCR-RFLP analysis.PMID 23856978Read ↗

Genetic Variant rs10757278 on Chromosome 9p21 Contributes to Myocardial Infarction Susceptibility.Semantic proximity Read ↗

Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population.Semantic proximity Read ↗

A common variant on chromosome 9p21 affects the risk of myocardial infarction.Semantic proximity Read ↗

Genetics of myocardial infarction: a progress reportSemantic proximity Read ↗

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 ↗

Interaction of type 2 diabetes mellitus with chromosome 9p21 rs10757274 polymorphism on the risk of myocardial infarction: a case-control study in Chinese population.Semantic proximity Read ↗

Association of Common Variants of APOE, CETP, and the 9p21.3 Chromosomal Region with the Risk of Myocardial Infarction: A Prospective Study.Semantic proximity Read ↗

The Correlation Between 9p21 Chromosome rs4977574 Polymorphism Genotypes and the Development of Coronary Artery Heart Disease.Semantic proximity Read ↗

The chromosome 9p21 region and myocardial infarction in a European population.Semantic proximity Read ↗

Association of MIR-499a expression and seed region variant (rs3746444) with cardiovascular disease in Egyptian patients.Semantic proximity Read ↗

[Evaluation of association between 9 genetic polymorphism and myocardial infarction in the Siberian population].Semantic proximity Read ↗

[Association between gene polymorphisms and myocardial infarction in Han Chinese of Yunnan province].Semantic proximity Read ↗

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