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8. Role of prion protein glycosylation in replication of human prions by protein misfolding cyclic amplification. Camacho MV; Telling G; Kong Q; Gambetti P; Notari S Lab Invest; 2019 Nov; 99(11):1741-1748. PubMed ID: 31249376 [TBL] [Abstract][Full Text] [Related]
9. Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins. Asante EA; Gowland I; Grimshaw A; Linehan JM; Smidak M; Houghton R; Osiguwa O; Tomlinson A; Joiner S; Brandner S; Wadsworth JDF; Collinge J J Gen Virol; 2009 Mar; 90(Pt 3):546-558. PubMed ID: 19218199 [TBL] [Abstract][Full Text] [Related]
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19. Absence of Evidence for a Causal Link between Bovine Spongiform Encephalopathy Strain Variant L-BSE and Known Forms of Sporadic Creutzfeldt-Jakob Disease in Human PrP Transgenic Mice. Jaumain E; Quadrio I; Herzog L; Reine F; Rezaei H; Andréoletti O; Laude H; Perret-Liaudet A; Haïk S; Béringue V J Virol; 2016 Dec; 90(23):10867-10874. PubMed ID: 27681129 [TBL] [Abstract][Full Text] [Related]
20. Artificial strain of human prions created in vitro. Kim C; Xiao X; Chen S; Haldiman T; Smirnovas V; Kofskey D; Warren M; Surewicz K; Maurer NR; Kong Q; Surewicz W; Safar JG Nat Commun; 2018 Jun; 9(1):2166. PubMed ID: 29867164 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]