GCN2 inhibition reduces mutant SOD1 clustering and toxicity and delays disease progression in an amyotrophic lateral sclerosis mouse model
Author
Date
2024-09-20Permanent link
https://hdl.handle.net/11351/12459DOI
10.1186/s40035-024-00441-w
ISSN
2047-9158
WOS
001317459900001
PMID
39304897
Keywords
Toxicity; Mouse model; Amyotrophic lateral sclerosisBibliographic citation
Ortiz DA, Peregrín N, Valencia M, Vinueza-Gavilanes R, Marín-Ordovas E, Ferrero R, et al. GCN2 inhibition reduces mutant SOD1 clustering and toxicity and delays disease progression in an amyotrophic lateral sclerosis mouse model. Transl Neurodegener. 2024 Sep 20;13:49.
Audience
Professionals
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- CEMCAT - Articles científics [161]
- VHIR - Articles científics [1750]
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