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Prion Diseases: From Protein to Cell Pathology

Prion diseases or transmissible spongiform encephalopathies are fatal neurodegenerative conditions in humans and animals that originate spontaneously, genetically or by infection. Conformational change of the normal (cellular) form of prion protein (PrP(c)) to a pathological, disease-associated form...

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Detalhes bibliográficos
Main Authors: Kovacs, Gabor G., Budka, Herbert
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Investigative Pathology 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2258253/
https://ncbi.nlm.nih.gov/pubmed/18245809
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/ajpath.2008.070442
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