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

Polymorphism on chromosome 9p21.3 contributes to early-onset and severity of coronary artery disease in non-diabetic and type 2 diabetic patients.

Chinese medical journal - 1 Jan 2011

Wang Wei, Peng Wen-Hui, Lu Lin, Zhang Rui-Yan, Zhang Qi, Wang Ling-Jie, Chen Qiu-Jing, Shen Wei-Feng

Abstract excerpt

BACKGROUND: Susceptibility to coronary artery disease (CAD) and diabetes is encoded by distinct, tightly-linked single nucleotide polymorphisms on chromosome 9p21. This study aimed to examine the association of variant rs1333049 on chromosome 9p21.3 with early-onset and severity of CAD in Chinese patients with and without type 2 diabetes, and to determine the possible impact of rs1333049 on glucose metabolism and...

Read the complete abstract on PubMed

Topics

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

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to C-Reactive Protein
Share to Chromosomes, Human, Pair 9
Share to Coronary Angiography
Share to Coronary Artery Disease
Share to Glycated Hemoglobin
Share to Interleukin-6
Share to Multivariate Analysis
Share to Tumor Necrosis Factor-alpha

Source

Identifiers

PMID: 21362310
DOI: 10.3901/jme.2011.08.066

Genes

CAD

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

Polymorphism on chromosome 9p21.3 contributes to early-onset and severity of coronary artery disease in non-diabetic and type 2 diabetic patients.PMID 21362310Read ↗

The same chromosome 9p21.3 locus is associated with type 2 diabetes and coronary artery disease in a Chinese Han population.Semantic proximity Read ↗

Evaluation of association between common genetic variants on chromosome 9p21 and coronary artery disease in Turkish population.Semantic proximity Read ↗

Chromosome 9p21.3 polymorphism in a Chinese Han population is associated with angiographic coronary plaque progression in non-diabetic but not in type 2 diabetic patients.Semantic proximity Read ↗

Association between 1p13 polymorphisms and peripheral arterial disease in a Chinese population with diabetes.Semantic proximity Read ↗

Association Study of rs1333040 and rs1004638 Polymorphisms in the 9p21 Locus with Coronary Artery Disease in Southwest of Iran.Semantic proximity Read ↗

Association of the single nucleotide polymorphism in chromosome 9p21 and chromosome 9q33 with coronary artery disease in Chinese population.Semantic proximity Read ↗

Variants in 9p21 Predicts Severity of Coronary Artery Disease in a Chinese Han Population.Semantic proximity Read ↗

Association between rs3088440 (G > A) polymorphism at 9p21.3 locus with the occurrence and severity of coronary artery disease in an Iranian 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 ↗

Genetic variants in PCSK1 gene are associated with the risk of coronary artery disease in type 2 diabetes in a Chinese Han population: a case control study.Semantic proximity Read ↗

Variant on 9p21 is strongly associated with coronary artery disease but lacks association with myocardial infarction and disease severity in a population in Western India.Semantic proximity Read ↗

Association between 9p21.3 genomic markers and coronary artery disease in East Asians: a meta-analysis involving 9,813 cases and 10,710 controls.Semantic proximity Read ↗

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