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Autor:
Stefano Thellung, Tullio Florio, Valentina Villa, Alessandro Corsaro, Sara Arena, Carolina Amico, Mauro Robello, Mario Salmona, Gianluigi Forloni, Orso Bugiani, Fabrizio Tagliavini, Gennaro Schettini
Publikováno v:
Neurobiology of Disease, Vol 7, Iss 4, Pp 299-309 (2000)
Prion diseases are neurodegenerative pathologies characterized by the accumulation, in the brain, of altered forms of the prion protein (PrP), named PrPSc. A synthetic peptide homologous to residues 106–126 of PrP (PrP106–126) was reported to mai
Externí odkaz:
https://doaj.org/article/8728751c620e4e1389c4298e7b8af311
