The ARSACS disease protein sacsin controls lysosomal positioning and reformation by regulating microtubule dynamics
Author:
Funder
ALS Society of Canada
Canadian Institutes of Health Research
Fonds de Recherche du Québec - Santé
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference38 articles.
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2. ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF;Engert;Nat. Genet.,2000
3. ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia;Vermeer;Neurogenetics,2008
4. Autosomal recessive spastic ataxia of charlevoix saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum;Synofzik;Orphanet J. Rare Dis.,2013
5. The ataxia protein sacsin is a functional co-chaperone that protects against polyglutamine-expanded ataxin-1;Parfitt;Hum. Mol. Genet.,2009
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2. HDAC inhibitor SAHA resolved intermediate filament bundling and defective autophagy caused by the lack of sacsin in ARSACS.;2024-08-17
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