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Rapamycin reduces neuronal mutant huntingtin aggregation and ameliorates locomotor performance in Drosophila
Huntington’s disease (HD) is a neurodegenerative disease characterized by movement and cognitive dysfunction. HD is caused by a CAG expansion in exon 1 of the HTT gene that leads to a polyglutamine (PQ) repeat in the huntingtin protein, which aggregates in the brain and periphery. Previously, we use...
Autores principales: | Roth, Jonathan R., de Moraes, Ruan Carlos Macedo, Xu, Brittney P., Crawley, Savannah R., Khan, Malghalara A., Melkani, Girish C. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562706/ https://www.ncbi.nlm.nih.gov/pubmed/37823007 http://dx.doi.org/10.3389/fnagi.2023.1223911 |
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