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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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| Autores principales: | , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
MDPI
2013
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3564126/ https://ncbi.nlm.nih.gov/pubmed/23340381 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/v5010374 |
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