Huntingtin Subcellular Localisation Is Regulated by Kinase Signalling Activity in the StHdhQ111 Model of HD.
Huntington's disease is a neurodegenerative disorder characterised primarily by motor abnormalities, and is caused by an expanded polyglutamine repeat in the huntingtin protein. Huntingtin dynamically shuttles between subcellular compartments, and the mutant huntingtin protein is mislocalised t...
Saved in:
| Main Authors: | Kathryn R Bowles, Simon P Brooks, Stephen B Dunnett, Lesley Jones |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science (PLoS)
2015-01-01
|
| Series: | PLoS ONE |
| Online Access: | https://doi.org/10.1371/journal.pone.0144864 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A Longitudinal Operant Assessment of Cognitive and Behavioural Changes in the HdhQ111 Mouse Model of Huntington's Disease.
by: Emma Yhnell, et al.
Published: (2016-01-01) -
Peripheral huntingtin silencing does not ameliorate central signs of disease in the B6.HttQ111/+ mouse model of Huntington's disease.
by: Sydney R Coffey, et al.
Published: (2017-01-01) -
Correlations of Behavioral Deficits with Brain Pathology Assessed through Longitudinal MRI and Histopathology in the HdhQ150/Q150 Mouse Model of Huntington's Disease.
by: Ivan Rattray, et al.
Published: (2017-01-01) -
UBL3 Interacts with PolyQ-Expanded Huntingtin Fragments and Modifies Their Intracellular Sorting
by: Soho Oyama, et al.
Published: (2024-10-01) -
The exergetic approach for the analysis of HDH desalination process using a pulverized column
by: Karima Larboui, et al.
Published: (2024-01-01)