Silence of resident microglia in GPI anchorless prion disease and activation of microglia in Gerstma...
Silence of resident microglia in GPI anchorless prion disease and activation of microglia in Gerstmann-Straussler-Scheinker disease and sporadic Creutzfeldt-Jakob disease
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Oxford University Press
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Language
English
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Oxford University Press
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GPI anchorless prion diseases (GPIALPs) show numerous coarse prion protein (PrP) deposits in the CNS but neuropil spongiform changes are mild and the incidence of dementia is low. Here, we examined differences in resident microglial phenotypes between GPIALP (D178fs25) and the other prion diseases Gerstmann-Straussler-Scheinker (GSS) disease and sp...
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Full title
Silence of resident microglia in GPI anchorless prion disease and activation of microglia in Gerstmann-Straussler-Scheinker disease and sporadic Creutzfeldt-Jakob disease
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TN_cdi_gale_infotracmisc_A768425140
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A768425140
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ISSN
0022-3069
DOI
10.1093/jnen/nlac098
