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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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Bibliografische gegevens
Gepubliceerd in:Prion
Hoofdauteurs: Puig, Berta, Altmeppen, Hermann C., Glatzel, Markus
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Taylor & Francis 2016
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Online toegang: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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