Risk of Transmissibility From Neurodegenerative Disease-Associated Proteins: Experimental Knowns and Unknowns

Recent studies in animal models demonstrate that certain misfolded proteins associated with neurodegenerative diseases can support templated misfolding of cognate native proteins, to propagate across neural systems, and to therefore have some of the properties of classical prion diseases like Creutz...

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Detalles Bibliográficos
Autores principales: Asher, David M, Belay, Ermias, Bigio, Eileen, Brandner, Sebastian, Brubaker, Scott A, Caughey, Byron, Clark, Brychan, Damon, Inger, Diamond, Marc, Freund, Michelle, Hyman, Bradley T, Jucker, Mathias, Keene, C Dirk, Lieberman, Andrew P, Mackiewicz, Miroslaw, Montine, Thomas J, Morgello, Susan, Phelps, Creighton, Safar, Jiri, Schneider, Julie A, Schonberger, Lawrence B, Sigurdson, Christina, Silverberg, Nina, Trojanowski, John Q, Frosch, Matthew P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577514/
https://www.ncbi.nlm.nih.gov/pubmed/33000167
http://dx.doi.org/10.1093/jnen/nlaa109

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577514/
https://www.ncbi.nlm.nih.gov/pubmed/33000167
http://dx.doi.org/10.1093/jnen/nlaa109

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