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24. Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease. Zanusso G; Fiorini M; Ferrari S; Meade-White K; Barbieri I; Brocchi E; Ghetti B; Monaco S J Biol Chem; 2014 Feb; 289(8):4870-81. PubMed ID: 24398683 [TBL] [Abstract][Full Text] [Related]
25. 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]
26. Inherited prion disease A117V is not simply a proteinopathy but produces prions transmissible to transgenic mice expressing homologous prion protein. Asante EA; Linehan JM; Smidak M; Tomlinson A; Grimshaw A; Jeelani A; Jakubcova T; Hamdan S; Powell C; Brandner S; Wadsworth JD; Collinge J PLoS Pathog; 2013; 9(9):e1003643. PubMed ID: 24086135 [TBL] [Abstract][Full Text] [Related]
27. [Mechanisms of neuroinvasion by prions: molecular principles and present state of research]. Brandner S; Klein MA; Aguzzi A Schweiz Med Wochenschr; 2000 Mar; 130(12):435-42. PubMed ID: 10780058 [TBL] [Abstract][Full Text] [Related]
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29. The Ninth Datta Lecture. Molecular biology of transmissible spongiform encephalopathies. Weissmann C FEBS Lett; 1996 Jun; 389(1):3-11. PubMed ID: 8682199 [TBL] [Abstract][Full Text] [Related]