Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B. [electronic resource]
Producer: 20071025Description: 1316-26 p. digitalISSN:- 0016-5085
- Adaptor Proteins, Signal Transducing
- Adenosine Triphosphatases -- chemistry
- Binding Sites
- Carrier Proteins -- metabolism
- Cation Transport Proteins -- chemistry
- Cell Line, Tumor
- Copper -- metabolism
- Copper Transport Proteins
- Copper-Transporting ATPases
- Endoplasmic Reticulum -- metabolism
- Genetic Predisposition to Disease
- Hepatocytes -- enzymology
- Hepatolenticular Degeneration -- genetics
- Homeostasis
- Humans
- Metallochaperones
- Molecular Chaperones -- genetics
- Mutation
- Peptide Hydrolases -- metabolism
- Protein Binding
- Protein Structure, Tertiary
- Protein Transport
- RNA Interference
- RNA, Small Interfering -- metabolism
- Recombinant Fusion Proteins -- metabolism
- Transfection
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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