Cellular Aspects of Prion Replication In Vitro

Prion diseases or transmissible spongiform encephalopathies (TSEs) are fatal neurodegenerative disorders in mammals that are caused by unconventional agents predominantly composed of aggregated misfolded prion protein (PrP). Prions self-propagate by recruitment of host-encoded PrP into highly ordere...

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Detalles Bibliográficos
Autores principales: Grassmann, Andrea, Wolf, Hanna, Hofmann, Julia, Graham, James, Vorberg, Ina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3564126/
https://www.ncbi.nlm.nih.gov/pubmed/23340381
http://dx.doi.org/10.3390/v5010374

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3564126/
https://www.ncbi.nlm.nih.gov/pubmed/23340381
http://dx.doi.org/10.3390/v5010374

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