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Transgenic mice recapitulate the phenotypic heterogeneity of genetic prion diseases without developing prion infectivity: Role of intracellular PrP retention in neurotoxicity

Genetic prion diseases are degenerative brain disorders caused by mutations in the gene encoding the prion protein (PrP). Different PrP mutations cause different diseases, including Creutzfeldt-Jakob disease (CJD), Gerstmann-Sträussler-Scheinker (GSS) syndrome and fatal familial insomnia (FFI). The...

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Detaylı Bibliyografya
Yayımlandı:Prion
Asıl Yazarlar: Chiesa, Roberto, Restelli, Elena, Comerio, Liliana, Del Gallo, Federico, Imeri, Luca
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Taylor & Francis 2016
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4981194/
https://ncbi.nlm.nih.gov/pubmed/26864450
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19336896.2016.1139276
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