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Misfolding leads the way to unraveling signaling pathways in the pathophysiology of prion diseases

A misfolded version of the prion protein represents an essential component in the pathophysiology of fatal neurodegenerative prion diseases, which affect humans and animals alike. They may be of sporadic origin, acquired through exogenous introduction of infectious misfolded prion protein, or caused...

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Publicado en:Prion
Autores principales: Puig, Berta, Altmeppen, Hermann C., Glatzel, Markus
Formato: Artigo
Lenguaje:Inglês
Publicado: Taylor & Francis 2016
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5161300/
https://ncbi.nlm.nih.gov/pubmed/27870599
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19336896.2016.1244593
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