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Intracellular mechanisms mediating the neuronal death and astrogliosis induced by the prion protein fragment 106–126

✍ Scribed by Stefano Thellung; Tullio Florio; Alessandro Corsaro; Sara Arena; Massimo Merlino; Mario Salmona; Fabrizio Tagliavini; Orso Bugiani; Gianluigi Forloni; Gennaro Schettini


Book ID
117563426
Publisher
Elsevier Science
Year
2000
Tongue
English
Weight
631 KB
Volume
18
Category
Article
ISSN
0736-5748

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## Abstract A synthetic peptide corresponding to the 106–126 amyloidogenic region of the cellular human prion protein (PrP^c^) is useful for in vitro study of prion‐induced neuronal cell death. The aim of the present work was to examine the implication of the cellular prion protein in the toxicity

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The prion diseases are transmissible neurodegenerative pathologies characterized by the accumulation of altered forms of the prion protein (PrP), termed PrP Sc , in the brain. Previous studies have shown that a synthetic peptide homologous to residues 106-126 of PrP (PrP 106-126) maintains many char