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Cellular prion protein: A co-receptor mediating neuronal cofilin-actin rod formation induced by β-amyloid and proinflammatory cytokines

Increasing evidence suggests that proteins exhibiting “prion-like” behavior cause distinct neurodegenerative diseases, including inherited, sporadic and acquired types. The conversion of cellular prion protein (PrP(C)) to its infectious protease resistant counterpart (PrP(Res)) is the essential feat...

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Dades bibliogràfiques
Publicat a:Prion
Autors principals: Walsh, Keifer P, Kuhn, Thomas B, Bamburg, James R
Format: Artigo
Idioma:Inglês
Publicat: Taylor & Francis 2014
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4601493/
https://ncbi.nlm.nih.gov/pubmed/25426519
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/pri.35504
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