Mutation of MEF2A in an inherited disorder with features of coronary artery disease. [electronic resource]
Producer: 20031218Description: 1578-81 p. digitalISSN:- 1095-9203
- 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
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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