The hairless gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor. [electronic resource]
Producer: 20011207Description: 2687-701 p. digitalISSN:- 0890-9369
- Amino Acid Sequence
- Blotting, Western
- Cell Nucleus -- ultrastructure
- Cells, Cultured
- DNA-Binding Proteins
- Fluorescent Antibody Technique
- Fungal Proteins -- metabolism
- Gene Expression
- Genetic Vectors
- Hair Diseases -- congenital
- Histone Deacetylases -- genetics
- Humans
- Molecular Sequence Data
- Mutagenesis, Site-Directed
- Mutation
- Nuclear Proteins -- genetics
- Nuclear Receptor Co-Repressor 1
- Promoter Regions, Genetic
- Proteins -- genetics
- Receptors, Thyroid Hormone -- metabolism
- Recombinant Fusion Proteins -- metabolism
- Repressor Proteins -- genetics
- Saccharomyces cerevisiae
- Saccharomyces cerevisiae Proteins
- Sequence Homology, Amino Acid
- Transcription Factors -- metabolism
- Two-Hybrid System Techniques
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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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