Different tau fibril types reduce prion level in chronically and de novo infected cells

Neurodegenerative diseases are often characterized by the codeposition of different amyloidogenic proteins, normally defining distinct proteinopathies. An example is represented by prion diseases, where the classical deposition of the aberrant conformational isoform of the prion protein (PrP(Sc)) ca...

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Detalles Bibliográficos
Autores principales: Celauro, Luigi, Burato, Anna, Zattoni, Marco, De Cecco, Elena, Fantuz, Marco, Cazzaniga, Federico Angelo, Bistaffa, Edoardo, Moda, Fabio, Legname, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2023
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10432985/
https://www.ncbi.nlm.nih.gov/pubmed/37454740
http://dx.doi.org/10.1016/j.jbc.2023.105054

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10432985/
https://www.ncbi.nlm.nih.gov/pubmed/37454740
http://dx.doi.org/10.1016/j.jbc.2023.105054

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