5World Health Organization Consultation.WHO infection control guidelines for transmissible spongiform encephalopathies[R].Geneva:World Health Organization,1999.
6Fornai F,Ferrucci M,Gesi M,et al.A hypothesis on prion disorders:are infectious,inherited,and sporadic causes so distinct?[J].Brain Res Bull,2006,69(2):95-100.
7Ma J,Lindquist S.Wild-type PrP and a mutant associated with prion disease are subject to retrograde transport and proteasome degradation[J].Proc Nail Acad Sci USA,2001,98(26):14955-14960.
8Kristiansen M,Deriziotis P,Dimcheff DE,et al.Disease-associated prion protein oligomers inhibit the 26S protea-some[J].Mol Cell,2007,26(2):175-188.
10Polymenidou M,Stoeck K,Glatzel M,et al.Coexistence of multiple PrPSc types in individuals with CreutzfeldtJakob disease[J].Lancet Neurol,2005,4(12):805-814.
