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Journal Abstract Search


879 related items for PubMed ID: 7767493

  • 1. Prion protein transgenes and the neuropathology in prion diseases.
    DeArmond SJ, Prusiner SB.
    Brain Pathol; 1995 Jan; 5(1):77-89. PubMed ID: 7767493
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  • 3. Prion encephalopathies of animals and humans.
    Prusiner SB.
    Dev Biol Stand; 1993 Jan; 80():31-44. PubMed ID: 8270114
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  • 4. Molecular biology and genetics of prion diseases.
    Prusiner SB.
    Philos Trans R Soc Lond B Biol Sci; 1994 Mar 29; 343(1306):447-63. PubMed ID: 7913765
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  • 5. Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein.
    Telling GC, Scott M, Hsiao KK, Foster D, Yang SL, Torchia M, Sidle KC, Collinge J, DeArmond SJ, Prusiner SB.
    Proc Natl Acad Sci U S A; 1994 Oct 11; 91(21):9936-40. PubMed ID: 7937921
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  • 6. 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 Oct 11; 75():55-74. PubMed ID: 1686599
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  • 7. 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 06; 83(1):79-90. PubMed ID: 7553876
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  • 8. Biology and genetics of prion diseases.
    Prusiner SB.
    Annu Rev Microbiol; 1994 Oct 06; 48():655-86. PubMed ID: 7826022
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  • 9. 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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  • 10. Towards authentic transgenic mouse models of heritable PrP prion diseases.
    Watts JC, Giles K, Bourkas ME, Patel S, Oehler A, Gavidia M, Bhardwaj S, Lee J, Prusiner SB.
    Acta Neuropathol; 2016 Oct 15; 132(4):593-610. PubMed ID: 27350609
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  • 13. 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 15; 78(4):2088-99. PubMed ID: 14747574
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  • 15. The role of PrP in health and disease.
    Flechsig E, Weissmann C.
    Curr Mol Med; 2004 Jun 15; 4(4):337-53. PubMed ID: 15354865
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  • 17. Pathogenic mutations within the hydrophobic domain of the prion protein lead to the formation of protease-sensitive prion species with increased lethality.
    Coleman BM, Harrison CF, Guo B, Masters CL, Barnham KJ, Lawson VA, Hill AF.
    J Virol; 2014 Mar 15; 88(5):2690-703. PubMed ID: 24352465
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  • 18. The neuropathological phenotype in transgenic mice expressing different prion protein constructs.
    DeArmond SJ, Yang SL, Cayetano-Canlas J, Groth D, Prusiner SB.
    Philos Trans R Soc Lond B Biol Sci; 1994 Mar 29; 343(1306):415-23. PubMed ID: 7913760
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  • 20. Susceptibility of transgenic mice expressing chimeric sheep, bovine and human PrP genes to sheep scrapie.
    Gombojav A, Shimauchi I, Horiuchi M, Ishiguro N, Shinagawa M, Kitamoto T, Miyoshi I, Mohri S, Takata M.
    J Vet Med Sci; 2003 Mar 29; 65(3):341-7. PubMed ID: 12679564
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