Fatal Transmissible Amyloid Encephalopathy: A New Type of Prion Disease Associated with Lack of Prion Protein Membrane Anchoring

Prion diseases are fatal neurodegenerative diseases of humans and animals characterized by gray matter spongiosis and accumulation of aggregated, misfolded, protease-resistant prion protein (PrPres). PrPres can be deposited in brain in an amyloid-form and/or non-amyloid form, and is derived from hos...

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Detalles Bibliográficos
Autores principales: Chesebro, Bruce, Race, Brent, Meade-White, Kimberly, LaCasse, Rachel, Race, Richard, Klingeborn, Mikael, Striebel, James, Dorward, David, McGovern, Gillian, Jeffrey, Martin
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2832701/
https://www.ncbi.nlm.nih.gov/pubmed/20221436
http://dx.doi.org/10.1371/journal.ppat.1000800

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2832701/
https://www.ncbi.nlm.nih.gov/pubmed/20221436
http://dx.doi.org/10.1371/journal.ppat.1000800

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