The Ubiquitin-Proteasome Pathway in Huntington's Disease
The accumulation of mutant protein is a common feature of neurodegenerative disease. In Huntington's disease, a polyglutamine expansion in the huntingtin protein triggers neuronal toxicity. Accompanying neuronal death, mutant huntingtin aggregates in large macromolecular structures called inclu...
Saved in:
| Main Authors: | Siddhartha Mitra, Steven Finkbeiner |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wiley
2008-01-01
|
| Series: | The Scientific World Journal |
| Online Access: | http://dx.doi.org/10.1100/tsw.2008.60 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
The Ubiquitin-Proteasome System in Huntington’s Disease: Are Proteasomes Impaired, Initiators of Disease, or Coming to the Rescue?
by: Sabine Schipper-Krom, et al.
Published: (2012-01-01) -
The ubiquitin-proteasome system in circadian regulation
by: Kara M. Costanzo, et al.
Published: (2025-08-01) -
Regulation of STIM1 and SOCE by the ubiquitin-proteasome system (UPS).
by: Jeffrey M Keil, et al.
Published: (2010-10-01) -
Reduced Levels of Proteasome Products in a Mouse Striatal Cell Model of Huntington's Disease.
by: Sayani Dasgupta, et al.
Published: (2015-01-01) -
S-Nitrosation and Ubiquitin-Proteasome System Interplay in Neuromuscular Disorders
by: Salvatore Rizza, et al.
Published: (2014-01-01)