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- W2136825909 endingPage "8669" @default.
- W2136825909 startingPage "8648" @default.
- W2136825909 abstract "In several neurodegenerative diseases, such as Parkinson, Alzheimer's, Huntington, and prion diseases, the deposition of aggregated misfolded proteins is believed to be responsible for the neurotoxicity that characterizes these diseases. Prion protein (PrP), the protein responsible of prion diseases, has been deeply studied for the peculiar feature of its misfolded oligomers that are able to propagate within affected brains, inducing the conversion of the natively folded PrP into the pathological conformation. In this review, we summarize the available experimental evidence concerning the relationship between aggregation status of misfolded PrP and neuronal death in the course of prion diseases. In particular, we describe the main findings resulting from the use of different synthetic (mainly PrP106-126) and recombinant PrP-derived peptides, as far as mechanisms of aggregation and amyloid formation, and how these different spatial conformations can affect neuronal death. In particular, most data support the involvement of non-fibrillar oligomers rather than actual amyloid fibers as the determinant of neuronal death." @default.
- W2136825909 created "2016-06-24" @default.
- W2136825909 creator A5004141549 @default.
- W2136825909 creator A5017546293 @default.
- W2136825909 creator A5019847626 @default.
- W2136825909 creator A5035985266 @default.
- W2136825909 creator A5055369359 @default.
- W2136825909 date "2012-07-11" @default.
- W2136825909 modified "2023-10-06" @default.
- W2136825909 title "Role of Prion Protein Aggregation in Neurotoxicity" @default.
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