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TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations

Articolo
Data di Pubblicazione:
2015
Abstract:
Amyotrophic lateral sclerosis (ALS) is a devastating neurological disease with no effective treatment. We report the results of a moderate-scale sequencing study aimed at increasing the number of genes known to contribute to predisposition for ALS. We performed whole-exome sequencing of 2869 ALS patients and 6405 controls. Several known ALS genes were found to be associated, and TBK1 (the gene encoding TANK-binding kinase 1) was identified as an ALS gene. TBK1 is known to bind to and phosphorylate a number of proteins involved in innate immunity and autophagy, including optineurin (OPTN) and p62 (SQSTM1/sequestosome), both of which have also been implicated in ALS. These observations reveal a key role of the autophagic pathway in ALS and suggest specific targets for therapeutic intervention.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Neurology (clinical); Neurology
Elenco autori:
Pensato, Viviana; Tiloca, Cinzia; Corrado, Lucia; Bertolin, Cinzia; Sardone, Valentina; Del Bo, Roberto; Calini, Daniela; Mandrioli, Jessica; Lauria, Giuseppe; Mazzini, Letizia; Querin, Giorgia; Ceroni, Mauro; Cantello, Roberto; Corti, Stefania; Castellotti, Barbara; Soldà, Giulia; Duga, Stefano; Comi, Giacomo P.; Cereda, Cristina; Sorarù, Gianni; D’Alfonso, Sandra; Taroni, Franco; Shaw, Christopher E.; Landers, John E.; Ticozzi, Nicola; Ratti, Antonia; Gellera, Cinzia; Silani, Vincenzo
Link alla scheda completa:
https://iris.unipv.it/handle/11571/1105357
Pubblicato in:
JOURNAL OF NEUROLOGY
Journal
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