Pathogenesis of Polyglutamine Diseases
Author:
Publisher
Wiley
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/9780470015902.a0021486
Reference56 articles.
1. Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death
2. Impairment of the Ubiquitin-Proteasome System by Protein Aggregation
3. Transcriptional Repression of PGC-1α by Mutant Huntingtin Leads to Mitochondrial Dysfunction and Neurodegeneration
4. Bergmann glia expression of polyglutamine-expanded ataxin-7 produces neurodegeneration by impairing glutamate transport
5. Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion
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