Accumulation of mutant huntingtin fragments in aggresome-like inclusion bodies as a result of insufficient protein degradation. [electronic resource]
Producer: 20010913Description: 1393-407 p. digitalISSN:- 1059-1524
- 14-3-3 Proteins
- Acetylcysteine -- analogs & derivatives
- Carrier Proteins -- metabolism
- Cell Line
- Cysteine Endopeptidases -- metabolism
- Cysteine Proteinase Inhibitors -- pharmacology
- Endoplasmic Reticulum Chaperone BiP
- Exons
- Heat-Shock Proteins
- Humans
- Huntingtin Protein
- Huntington Disease -- metabolism
- Immunoblotting
- Inclusion Bodies -- metabolism
- Membrane Proteins -- metabolism
- Microscopy, Fluorescence
- Models, Biological
- Molecular Chaperones -- metabolism
- Multienzyme Complexes -- antagonists & inhibitors
- Mutation
- Nerve Tissue Proteins -- genetics
- Nuclear Proteins -- genetics
- Peptide Fragments -- genetics
- Poly(A)-Binding Proteins
- Proteasome Endopeptidase Complex
- Proteins
- RNA-Binding Proteins -- metabolism
- Recombinant Fusion Proteins -- genetics
- Synucleins
- T-Cell Intracellular Antigen-1
- Transgenes
- Tyrosine 3-Monooxygenase -- metabolism
- Vimentin -- metabolism
- alpha-Synuclein
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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