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Microglia in Prion Diseases: Angels or Demons?
Prion diseases are rare transmissible neurodegenerative disorders caused by the accumulation of a misfolded isoform (PrP(Sc)) of the cellular prion protein (PrP(C)) in the central nervous system (CNS). Neuropathological hallmarks of prion diseases are neuronal loss, astrogliosis, and enhanced microg...
Guardado en:
| Publicado en: | Int J Mol Sci |
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| Autores principales: | , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
MDPI
2020
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7589037/ https://ncbi.nlm.nih.gov/pubmed/33092220 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21207765 |
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