|
Coronary heart disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Myocyte Enhancer Factor-2A Gene Mutation and Coronary Artery Disease.
|
26415812 |
2015 |
|
Coronary heart disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Association of MEF2A gene 3'UTR mutations with coronary artery disease.
|
26400337 |
2015 |
|
Coronary heart disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
MEF2A gene mutations and susceptibility to coronary artery disease in the Chinese population.
|
25366733 |
2014 |
|
Coronary heart disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Variants in exon 11 of MEF2A gene and coronary artery disease: evidence from a case-control study, systematic review, and meta-analysis.
|
22363637 |
2012 |
|
Coronary heart disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
A study of the role of the Myocyte-specific Enhancer Factor-2A gene in coronary artery disease.
|
19782985 |
2010 |
|
Coronary heart disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
This finding raises the possibility that MEF2A variants may contribute to the risk of coronary artery disease.
|
19153100 |
2010 |
|
Coronary heart disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Structural changes in exon 11 of MEF2A are not related to sporadic coronary artery disease in Han Chinese population.
|
20546016 |
2010 |
|
Coronary heart disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
However, the association of MEF2A with coronary artery disease/MI was not confirmed in other studies.
|
20031581 |
2009 |
|
Coronary heart disease
|
0.100 |
GeneticVariation
|
disease |
LHGDN |
Relationship of the CAG repeat polymorphism of the MEF2A gene and coronary artery disease in a Chinese population.
|
17579569 |
2007 |
|
Coronary heart disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Relationship of the CAG repeat polymorphism of the MEF2A gene and coronary artery disease in a Chinese population.
|
17579569 |
2007 |
|
Coronary heart disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Polymorphisms in myocyte enhancer factor 2A, a transcription factor, tumor necrosis factor (ligand) superfamily, member 4, the OX40 ligand, and proprotein convertase subtilisin/kexin type 9, which affect low-density lipoprotein levels, have all been associated with an altered risk of coronary artery disease and myocardial infarction.
|
16943719 |
2006 |
|
Coronary heart disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
Positional cloning based on genome-wide linkage analysis with large families identified the first non - lipid-related disease-causing gene, MEF2A (encoding a transcriptional factor), for coronary artery disease and myocardiaI infarction.
|
15861005 |
2005 |
|
Coronary heart disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Recently, a mutation in the human MEF2A gene was reported to be responsible for an autosomal dominant form of coronary artery disease, so the purpose of the present study was to assess the significance of MEF2A mutations in Japanese subjects with myocardial infarction (MI).
|
16195615 |
2005 |
|
Coronary heart disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
MEF2A sequence variants and coronary artery disease: a change of heart?
|
15841171 |
2005 |
|
Coronary heart disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
However, we did identify the 21-bp MEF2A coding sequence deletion originally implicated in adCAD1 in 1 of 300 elderly control subjects without CAD.
|
15841183 |
2005 |
|
Coronary heart disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Transcription factor MEF2A mutations in patients with coronary artery disease.
|
15496429 |
2004 |
|
Coronary heart disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Mutation of MEF2A in an inherited disorder with features of coronary artery disease.
|
14645853 |
2003 |