Prion Protein Accumulation in Lipid Rafts of Mouse Aging Brain

The cellular form of the prion protein (PrP(C)) is a normal constituent of neuronal cell membranes. The protein misfolding causes rare neurodegenerative disorders known as transmissible spongiform encephalopathies or prion diseases. These maladies can be sporadic, genetic or infectious. Sporadic pri...

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Detalles Bibliográficos
Autores principales: Agostini, Federica, Dotti, Carlos G., Pérez-Cañamás, Azucena, Ledesma, Maria Dolores, Benetti, Federico, Legname, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3769255/
https://www.ncbi.nlm.nih.gov/pubmed/24040215
http://dx.doi.org/10.1371/journal.pone.0074244

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3769255/
https://www.ncbi.nlm.nih.gov/pubmed/24040215
http://dx.doi.org/10.1371/journal.pone.0074244

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