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3. Mutant PrPSc conformers induced by a synthetic peptide and several prion strains. Tremblay P; Ball HL; Kaneko K; Groth D; Hegde RS; Cohen FE; DeArmond SJ; Prusiner SB; Safar JG J Virol; 2004 Feb; 78(4):2088-99. PubMed ID: 14747574 [TBL] [Abstract][Full Text] [Related]
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8. A New Transgenic Mouse Model of Gerstmann-Straussler-Scheinker Syndrome Caused by the A117V Mutation of PRNP. Yang W; Cook J; Rassbach B; Lemus A; DeArmond SJ; Mastrianni JA J Neurosci; 2009 Aug; 29(32):10072-80. PubMed ID: 19675240 [TBL] [Abstract][Full Text] [Related]
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11. Dominant-negative inhibition of prion replication in transgenic mice. Perrier V; Kaneko K; Safar J; Vergara J; Tremblay P; DeArmond SJ; Cohen FE; Prusiner SB; Wallace AC Proc Natl Acad Sci U S A; 2002 Oct; 99(20):13079-84. PubMed ID: 12271119 [TBL] [Abstract][Full Text] [Related]
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15. Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein. Telling GC; Scott M; Mastrianni J; Gabizon R; Torchia M; Cohen FE; DeArmond SJ; Prusiner SB Cell; 1995 Oct; 83(1):79-90. PubMed ID: 7553876 [TBL] [Abstract][Full Text] [Related]
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20. Hyperphosphorylated tau deposition parallels prion protein burden in a case of Gerstmann-Sträussler-Scheinker syndrome P102L mutation complicated with dementia. Ishizawa K; Komori T; Shimazu T; Yamamoto T; Kitamoto T; Shimazu K; Hirose T Acta Neuropathol; 2002 Oct; 104(4):342-50. PubMed ID: 12200619 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]