Mutation of MEF2A in an inherited disorder with features of coronary artery disease.

Wang, Lejin

Mutation of MEF2A in an inherited disorder with features of coronary artery disease. [electronic resource] - Science (New York, N.Y.) Nov 2003 - 1578-81 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

1095-9203

10.1126/science.1088477 doi


Aged
Amino Acid Sequence
Animals
Arteries--metabolism
Base Sequence
Cell Nucleus--metabolism
Chromosomes, Human, Pair 15--genetics
Coronary Artery Disease--genetics
Coronary Vessels--metabolism
DNA-Binding Proteins--chemistry
Dimerization
Endothelium, Vascular--metabolism
Erythroid-Specific DNA-Binding Factors
Female
Fluorescent Antibody Technique
GATA1 Transcription Factor
Gene Expression
Genes, Dominant
Genetic Linkage
Genetic Markers
Genetic Predisposition to Disease
Humans
MADS Domain Proteins
MEF2 Transcription Factors
Male
Middle Aged
Molecular Sequence Data
Muscle, Smooth--cytology
Myocardial Infarction--genetics
Myogenic Regulatory Factors
Pedigree
Protein Binding
Protein Conformation
Protein Structure, Tertiary
Protein Transport
Rats
Risk Factors
Sequence Deletion
Signal Transduction
Transcription Factors--chemistry
Transcriptional Activation