A human microglial cell model of autosomal recessive spastic ataxia of Charlevoix-Saguenay
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Elsevier BV
Reference25 articles.
1. Sacs knockout mice present pathophysiological defects underlying autosomal recessive spastic ataxia of Charlevoix-Saguenay;Larivière;Hum. Mol. Genet.,2015
2. The ataxia protein sacsin is a functional co-chaperone that protects against polyglutamine-expanded ataxin-1;Parfitt;Hum. Mol. Genet.,2009
3. Altered organization of the intermediate filament cytoskeleton and relocalization of proteostasis modulators in cells lacking the ataxia protein sacsin;Duncan;Hum. Mol. Genet.,2017
4. Sacsin, mutated in the ataxia ARSACS, regulates intermediate filament assembly and dynamics;Gentil;FASEB J.,2018
5. Sacsin deletion induces aggregation of glial intermediate filaments;Murtinheira;Cells,2022
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