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Microglia in prion diseases

Prion diseases are a group of progressive and fatal neurodegenerative disorders characterized by deposition of scrapie prion protein (PrP(Sc)) in the CNS. This deposition is accompanied by neuronal loss, spongiform change, astrogliosis, and conspicuous microglial activation. Here, we argue that micr...

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Detalhes bibliográficos
Publicado no:J Clin Invest
Main Authors: Aguzzi, Adriano, Zhu, Caihong
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5669569/
https://ncbi.nlm.nih.gov/pubmed/28714865
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI90605
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