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Journal Abstract Search

243 related items for PubMed ID: 7913762

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. PrP-deficient mice are resistant to scrapie.
    Weissmann C, Büeler H, Fischer M, Sailer A, Aguzzi A, Aguet M.
    Ann N Y Acad Sci; 1994 Jun 06; 724():235-40. PubMed ID: 8030944
    [Abstract] [Full Text] [Related]

  • 3. Mice devoid of PrP are resistant to scrapie.
    Büeler H, Aguzzi A, Sailer A, Greiner RA, Autenried P, Aguet M, Weissmann C.
    Cell; 1993 Jul 02; 73(7):1339-47. PubMed ID: 8100741
    [Abstract] [Full Text] [Related]

  • 4. Prion encephalopathies of animals and humans.
    Prusiner SB.
    Dev Biol Stand; 1993 Jul 02; 80():31-44. PubMed ID: 8270114
    [Abstract] [Full Text] [Related]

  • 5. Genetics of prion diseases and prion diversity in mice.
    Carlson GA, DeArmond SJ, Torchia M, Westaway D, Prusiner SB.
    Philos Trans R Soc Lond B Biol Sci; 1994 Mar 29; 343(1306):363-9. PubMed ID: 7913753
    [Abstract] [Full Text] [Related]

  • 6. The use of transgenic mice in the investigation of transmissible spongiform encephalopathies.
    Weissmann C, Fischer M, Raeber A, Büeler H, Sailer A, Shmerling D, Rülicke T, Brandner S, Aguzzi A.
    Rev Sci Tech; 1998 Apr 29; 17(1):278-90. PubMed ID: 9638817
    [Abstract] [Full Text] [Related]

  • 7. High prion and PrPSc levels but delayed onset of disease in scrapie-inoculated mice heterozygous for a disrupted PrP gene.
    Büeler H, Raeber A, Sailer A, Fischer M, Aguzzi A, Weissmann C.
    Mol Med; 1994 Nov 29; 1(1):19-30. PubMed ID: 8790598
    [Abstract] [Full Text] [Related]

  • 8. Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies.
    Prusiner SB, Groth D, Serban A, Koehler R, Foster D, Torchia M, Burton D, Yang SL, DeArmond SJ.
    Proc Natl Acad Sci U S A; 1993 Nov 15; 90(22):10608-12. PubMed ID: 7902565
    [Abstract] [Full Text] [Related]

  • 9. The Ninth Datta Lecture. Molecular biology of transmissible spongiform encephalopathies.
    Weissmann C.
    FEBS Lett; 1996 Jun 24; 389(1):3-11. PubMed ID: 8682199
    [Abstract] [Full Text] [Related]

  • 10. Normal host prion protein necessary for scrapie-induced neurotoxicity.
    Brandner S, Isenmann S, Raeber A, Fischer M, Sailer A, Kobayashi Y, Marino S, Weissmann C, Aguzzi A.
    Nature; 1996 Jan 25; 379(6563):339-43. PubMed ID: 8552188
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. Propagation of prions with artificial properties in transgenic mice expressing chimeric PrP genes.
    Scott M, Groth D, Foster D, Torchia M, Yang SL, DeArmond SJ, Prusiner SB.
    Cell; 1993 Jun 04; 73(5):979-88. PubMed ID: 8098995
    [Abstract] [Full Text] [Related]

  • 13. Astrocyte-specific expression of hamster prion protein (PrP) renders PrP knockout mice susceptible to hamster scrapie.
    Raeber AJ, Race RE, Brandner S, Priola SA, Sailer A, Bessen RA, Mucke L, Manson J, Aguzzi A, Oldstone MB, Weissmann C, Chesebro B.
    EMBO J; 1997 Oct 15; 16(20):6057-65. PubMed ID: 9321385
    [Abstract] [Full Text] [Related]

  • 14. Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein.
    Büeler H, Fischer M, Lang Y, Bluethmann H, Lipp HP, DeArmond SJ, Prusiner SB, Aguet M, Weissmann C.
    Nature; 1992 Apr 16; 356(6370):577-82. PubMed ID: 1373228
    [Abstract] [Full Text] [Related]

  • 15. Mouse-adapted sporadic human Creutzfeldt-Jakob disease prions propagate in cell culture.
    Lawson VA, Vella LJ, Stewart JD, Sharples RA, Klemm H, Machalek DM, Masters CL, Cappai R, Collins SJ, Hill AF.
    Int J Biochem Cell Biol; 2008 Apr 16; 40(12):2793-801. PubMed ID: 18590830
    [Abstract] [Full Text] [Related]

  • 16. PrP-expressing tissue required for transfer of scrapie infectivity from spleen to brain.
    Blättler T, Brandner S, Raeber AJ, Klein MA, Voigtländer T, Weissmann C, Aguzzi A.
    Nature; 1997 Sep 04; 389(6646):69-73. PubMed ID: 9288968
    [Abstract] [Full Text] [Related]

  • 17. Prion isolate specified allotypic interactions between the cellular and scrapie prion proteins in congenic and transgenic mice.
    Carlson GA, Ebeling C, Yang SL, Telling G, Torchia M, Groth D, Westaway D, DeArmond SJ, Prusiner SB.
    Proc Natl Acad Sci U S A; 1994 Jun 07; 91(12):5690-4. PubMed ID: 7911243
    [Abstract] [Full Text] [Related]

  • 18. 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 01; 99(20):13079-84. PubMed ID: 12271119
    [Abstract] [Full Text] [Related]

  • 19. Foreign PrP expression and scrapie infection in tissue culture cell lines.
    Chesebro B, Wehrly K, Caughey B, Nishio J, Ernst D, Race R.
    Dev Biol Stand; 1993 Oct 01; 80():131-40. PubMed ID: 8270103
    [Abstract] [Full Text] [Related]

  • 20. Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques.
    Scott M, Foster D, Mirenda C, Serban D, Coufal F, Wälchli M, Torchia M, Groth D, Carlson G, DeArmond SJ, Westaway D, Prusiner SB.
    Cell; 1989 Dec 01; 59(5):847-57. PubMed ID: 2574076
    [Abstract] [Full Text] [Related]

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