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12. Prion Protein Devoid of the Octapeptide Repeat Region Delays Bovine Spongiform Encephalopathy Pathogenesis in Mice. Hara H; Miyata H; Das NR; Chida J; Yoshimochi T; Uchiyama K; Watanabe H; Kondoh G; Yokoyama T; Sakaguchi S J Virol; 2018 Jan; 92(1):. PubMed ID: 29046443 [TBL] [Abstract][Full Text] [Related]
13. Prion encephalopathies of animals and humans. Prusiner SB Dev Biol Stand; 1993; 80():31-44. PubMed ID: 8270114 [TBL] [Abstract][Full Text] [Related]
14. [Genetic background of human prion diseases]. Kovács GG Ideggyogy Sz; 2007 Nov; 60(11-12):438-46. PubMed ID: 18198790 [TBL] [Abstract][Full Text] [Related]
15. Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1. Mead S; Mahal SP; Beck J; Campbell T; Farrall M; Fisher E; Collinge J Am J Hum Genet; 2001 Dec; 69(6):1225-35. PubMed ID: 11704923 [TBL] [Abstract][Full Text] [Related]
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17. Transgenic mouse models expressing human and macaque prion protein exhibit similar prion susceptibility on a strain-dependent manner. Espinosa JC; Comoy EE; Marin-Moreno A; Aguilar-Calvo P; Birling MC; Pitarch JL; Deslys JP; Torres JM Sci Rep; 2019 Oct; 9(1):15699. PubMed ID: 31666632 [TBL] [Abstract][Full Text] [Related]
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