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Variable tau accumulation in murine models with abnormal prion protein deposits

The conversion of cellular prion protein (PrP) into a misfolded isoform is central to the development of prion diseases. However, the heterogeneous phenotypes observed in prion disease may be linked with the presence of other misfolded proteins in the brain. While hyperphosphorylated tau (p.tau) is...

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Detalles Bibliográficos
Autores principales: Piccardo, Pedro, King, Declan, Brown, Deborah, Barron, Rona M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381323/
https://www.ncbi.nlm.nih.gov/pubmed/29246602
http://dx.doi.org/10.1016/j.jns.2017.10.040