×
Entrez Id:
4205
Gene Symbol:
MEF2A
MEF2A
0.100
GeneticVariation
disease
BEFREE
Myocyte Enhancer Factor-2A Gene Mutation and Coronary Artery Disease .
26415812
2015
×
Entrez Id:
4205
Gene Symbol:
MEF2A
MEF2A
0.100
GeneticVariation
disease
BEFREE
Association of MEF2A gene 3'UTR mutations with coronary artery disease .
26400337
2015
×
Entrez Id:
4205
Gene Symbol:
MEF2A
MEF2A
0.100
GeneticVariation
disease
BEFREE
MEF2A gene mutations and susceptibility to coronary artery disease in the Chinese population.
25366733
2014
×
Entrez Id:
4205
Gene Symbol:
MEF2A
MEF2A
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
×
Entrez Id:
4205
Gene Symbol:
MEF2A
MEF2A
0.100
Biomarker
disease
BEFREE
A study of the role of the Myocyte-specific Enhancer Factor-2A gene in coronary artery disease .
19782985
2010
×
Entrez Id:
4205
Gene Symbol:
MEF2A
MEF2A
0.100
GeneticVariation
disease
BEFREE
This finding raises the possibility that MEF2A variants may contribute to the risk of coronary artery disease .
19153100
2010
×
Entrez Id:
4205
Gene Symbol:
MEF2A
MEF2A
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
×
Entrez Id:
4205
Gene Symbol:
MEF2A
MEF2A
0.100
Biomarker
disease
BEFREE
However, the association of MEF2A with coronary artery disease /MI was not confirmed in other studies.
20031581
2009
×
Entrez Id:
4205
Gene Symbol:
MEF2A
MEF2A
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
×
Entrez Id:
4205
Gene Symbol:
MEF2A
MEF2A
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
×
Entrez Id:
4205
Gene Symbol:
MEF2A
MEF2A
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
×
Entrez Id:
4205
Gene Symbol:
MEF2A
MEF2A
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
×
Entrez Id:
4205
Gene Symbol:
MEF2A
MEF2A
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
×
Entrez Id:
4205
Gene Symbol:
MEF2A
MEF2A
0.100
GeneticVariation
disease
BEFREE
MEF2A sequence variants and coronary artery disease : a change of heart?
15841171
2005
×
Entrez Id:
4205
Gene Symbol:
MEF2A
MEF2A
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
×
Entrez Id:
4205
Gene Symbol:
MEF2A
MEF2A
0.100
GeneticVariation
disease
BEFREE
Transcription factor MEF2A mutations in patients with coronary artery disease .
15496429
2004
×
Entrez Id:
4205
Gene Symbol:
MEF2A
MEF2A
0.100
GeneticVariation
disease
BEFREE
Mutation of MEF2A in an inherited disorder with features of coronary artery disease .
14645853
2003