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Ab initio simulations of Cu binding sites on the N-terminal region of prion protein

✍ Scribed by Sara Furlan; Giovanni La Penna; Francesco Guerrieri; Silvia Morante; Gian Carlo Rossi


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
498 KB
Volume
12
Category
Article
ISSN
1432-1327

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## Abstract Transmissible spongiform encephalopathies are a group of neurodegenerative disorders caused by a posttranslational, conformational change in the cellular isoform of the prion protein (PrP^C^) into an infectious, disease‐associated form (PrP^Sc^). Increasing evidence supports a role for