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Journal Abstract Search

268 related items for PubMed ID: 9405603

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  • 3. Guinea Pig Prion Protein Supports Rapid Propagation of Bovine Spongiform Encephalopathy and Variant Creutzfeldt-Jakob Disease Prions.
    Watts JC, Giles K, Saltzberg DJ, Dugger BN, Patel S, Oehler A, Bhardwaj S, Sali A, Prusiner SB.
    J Virol; 2016 Nov 01; 90(21):9558-9569. PubMed ID: 27440899
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  • 5. Measuring prions causing bovine spongiform encephalopathy or chronic wasting disease by immunoassays and transgenic mice.
    Safar JG, Scott M, Monaghan J, Deering C, Didorenko S, Vergara J, Ball H, Legname G, Leclerc E, Solforosi L, Serban H, Groth D, Burton DR, Prusiner SB, Williamson RA.
    Nat Biotechnol; 2002 Nov 01; 20(11):1147-50. PubMed ID: 12389035
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  • 7. Genetic and infectious prion diseases.
    Prusiner SB.
    Arch Neurol; 1993 Nov 01; 50(11):1129-53. PubMed ID: 8105771
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  • 8. 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 01; 92(1):. PubMed ID: 29046443
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  • 9. Molecular biology of prions causing infectious and genetic encephalopathies of humans as well as scrapie of sheep and BSE of cattle.
    Prusiner SB.
    Dev Biol Stand; 1991 Jan 01; 75():55-74. PubMed ID: 1686599
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  • 12. 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 01; 90(Pt 3):546-558. PubMed ID: 19218199
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  • 13. BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein.
    Asante EA, Linehan JM, Desbruslais M, Joiner S, Gowland I, Wood AL, Welch J, Hill AF, Lloyd SE, Wadsworth JD, Collinge J.
    EMBO J; 2002 Dec 02; 21(23):6358-66. PubMed ID: 12456643
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  • 14. Overexpression of chimaeric murine/ovine PrP (A136H154Q171) in transgenic mice facilitates transmission and differentiation of ruminant prions.
    Griffiths PC, Plater JM, Chave A, Jayasena D, Tout AC, Rice PB, Vickery CM, Spiropoulos J, Stack MJ, Windl O.
    J Gen Virol; 2013 Nov 02; 94(Pt 11):2577-2586. PubMed ID: 23761404
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  • 15. Increased expression of water channel aquaporin 1 and aquaporin 4 in Creutzfeldt-Jakob disease and in bovine spongiform encephalopathy-infected bovine-PrP transgenic mice.
    Rodríguez A, Pérez-Gracia E, Espinosa JC, Pumarola M, Torres JM, Ferrer I.
    Acta Neuropathol; 2006 Nov 02; 112(5):573-85. PubMed ID: 16871401
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  • 16. Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene.
    Korth C, Kaneko K, Groth D, Heye N, Telling G, Mastrianni J, Parchi P, Gambetti P, Will R, Ironside J, Heinrich C, Tremblay P, DeArmond SJ, Prusiner SB.
    Proc Natl Acad Sci U S A; 2003 Apr 15; 100(8):4784-9. PubMed ID: 12684540
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  • 17. Prion protein transgenes and the neuropathology in prion diseases.
    DeArmond SJ, Prusiner SB.
    Brain Pathol; 1995 Jan 15; 5(1):77-89. PubMed ID: 7767493
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  • 18. BSE: can we predict the future?
    Plum J.
    Bull Mem Acad R Med Belg; 1997 Jan 15; 152(6):264-73. PubMed ID: 9581370
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  • 19. A naturally occurring variant of the human prion protein completely prevents prion disease.
    Asante EA, Smidak M, Grimshaw A, Houghton R, Tomlinson A, Jeelani A, Jakubcova T, Hamdan S, Richard-Londt A, Linehan JM, Brandner S, Alpers M, Whitfield J, Mead S, Wadsworth JD, Collinge J.
    Nature; 2015 Jun 25; 522(7557):478-81. PubMed ID: 26061765
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  • 20. Insights into Mechanisms of Transmission and Pathogenesis from Transgenic Mouse Models of Prion Diseases.
    Moreno JA, Telling GC.
    Methods Mol Biol; 2017 Jun 25; 1658():219-252. PubMed ID: 28861793
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