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Aggregated, Wild-Type Prion Protein Causes Neurological Dysfunction and Synaptic Abnormalities

The neurotoxic forms of the prion protein (PrP) that cause neurodegeneration in prion diseases remain to be conclusively identified. Considerable evidence points to the importance of noninfectious oligomers of PrP in the pathogenic process. In this study, we describe lines of Tg(WT) transgenic mice...

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Detalhes bibliográficos
Main Authors: Chiesa, Roberto, Piccardo, Pedro, Biasini, Emiliano, Ghetti, Bernardino, Harris, David A.
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2646838/
https://ncbi.nlm.nih.gov/pubmed/19052217
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.3109-08.2008
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