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

Structural changes in exon 11 of MEF2A are not related to sporadic coronary artery disease in Han Chinese population.

European journal of clinical investigation - 1 Aug 2010

Dai Da-Peng, Zhou Xiao-Yang, Xiao Yao, Xu Feng, Sun Fu-Cheng, Ji Fu-Sui, Zhang Zhi-Xin, Hu Ji-Hong, Guo Jian, Zheng Jun-De, Dong Jia-Mei, Zhu Wei-Guo, Shen Yan, Qian Yi-Jian, He Qing, Cai Jian-Ping

Abstract excerpt

BACKGROUND: A mutation in MEF2A (myocyte enhancer factor-2A) had been reported to be the first gene linked directly to coronary artery disease (CAD). However, an opposing opinion was proposed recently that MEF2A mutations are not a common cause of sporadic CAD. In this study, we screened exon 11...

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to Coronary Artery Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Association Studies

Share to MADS Domain Proteins

Share to MEF2 Transcription Factors

Share to Myogenic Regulatory Factors

Share to Sequence Analysis, DNA

Source

Identifiers

PMID: 20546016
DOI: 10.1111/j.1365-2362.2010.02307.x

Genes

CAD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20546016-2026-09-02.2. 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 · 12 closest

Structural changes in exon 11 of MEF2A are not related to sporadic coronary artery disease in Han Chinese population.PMID 20546016Read ↗

Variants in exon 11 of MEF2A gene and coronary artery disease: evidence from a case-control study, systematic review, and meta-analysis.Semantic proximity Read ↗

MEF2A gene mutations and susceptibility to coronary artery disease in the Chinese population.Semantic proximity Read ↗

Novel 6-bp deletion in MEF2A linked to premature coronary artery disease in a large Chinese family.Semantic proximity Read ↗

Exon 11 deletion in the myocyte enhancer factor (MEF)2A and early onset coronary artery disease gene in a Sicilian family.Semantic proximity Read ↗

Relationship of the CAG repeat polymorphism of the MEF2A gene and coronary artery disease in a Chinese population.Semantic proximity Read ↗

MEF2A sequence variants and coronary artery disease: a change of heart?Semantic proximity Read ↗

A study of the role of the Myocyte-specific Enhancer Factor-2A gene in coronary artery disease.Semantic proximity Read ↗

[Study on novel mutations of MEF2A gene in Chinese patients with coronary artery disease].Semantic proximity Read ↗

MEF2A gene and susceptibility to coronary artery disease in the Chinese people.Semantic proximity Read ↗

Mutation of MEF2A in an inherited disorder with features of coronary artery disease.Semantic proximity Read ↗

Lack of MEF2A mutations in coronary artery disease.Semantic proximity Read ↗

CAG repeat polymorphism of the MEF2A gene is not associated with the risk of coronary artery disease among Taiwanese.Semantic proximity Read ↗

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