Functional Transcriptome Analysis in ARSACS KO Cell Model Reveals a Role of Sacsin in Autophagy

Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a rare early-onset neurological disease caused by mutations in SACS, which encodes sacsin. The complex architecture of sacsin suggests that it could be a key player in cellular protein quality control system. Molecular chaperones...

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Detalles Bibliográficos
Autores principales: Morani, Federica, Doccini, Stefano, Sirica, Roberto, Paterno, Marta, Pezzini, Francesco, Ricca, Ivana, Simonati, Alessandro, Delledonne, Massimo, Santorelli, Filippo Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6695435/
https://www.ncbi.nlm.nih.gov/pubmed/31417125
http://dx.doi.org/10.1038/s41598-019-48047-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6695435/
https://www.ncbi.nlm.nih.gov/pubmed/31417125
http://dx.doi.org/10.1038/s41598-019-48047-x

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