Abstract
Recent research has identified ER stress as a major mechanism implicated in cytotoxicity in many neurodegenerative diseases, among them Huntington's disease. This genetic disorder is of late-onset, progressive and fatal, affecting cognition and movement. There is presently no cure nor any effective therapy for the disease. This review focuses on recent findings that shed light on the mechanisms of the advent and development of ER stress in Huntington's disease and on its implications, highlighting possible therapeutic avenues that are being or could be explored.
| Original language | English |
|---|---|
| Pages (from-to) | 94-106 |
| Number of pages | 13 |
| Journal | Endoplasmic Reticulum Stress in Diseases |
| Volume | 2 |
| Issue number | 1 |
| DOIs | |
| State | Published - 15 Jul 2015 |
Keywords
- ER-associated degradation
- Huntington
- conformational disease
- neurodegenerative disease
- protein aggregation
- protein misfolding
- unfolded protein response
All Science Journal Classification (ASJC) codes
- Medicine (miscellaneous)
- Cell Biology
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