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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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Foilsithe in: | J Clin Invest |
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Main Authors: | , |
Formáid: | Artigo |
Teanga: | Inglês |
Foilsithe: |
American Society for Clinical Investigation
2017
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Ábhair: | |
Rochtain Ar Líne: | 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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