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NLRP3 inflammasome activation in macrophage cell lines by prion protein fibrils as the source of IL-1β and neuronal toxicity

Prion diseases are fatal transmissible neurodegenerative diseases, characterized by aggregation of the pathological form of prion protein, spongiform degeneration, neuronal loss and activation of astrocytes and microglia. Microglia can clear prion plaques but on the other hand cause neuronal death v...

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Autors principals: Hafner-Bratkovič, Iva, Benčina, Mojca, Fitzgerald, Katherine A., Golenbock, Douglas, Jerala, Roman
Format: Artigo
Idioma:Inglês
Publicat: 2012
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3508391/
https://ncbi.nlm.nih.gov/pubmed/22926439
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00018-012-1140-0
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