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128 related items for PubMed ID: 12130636

  • 1. Changes in the glycosylation pattern of prion protein in murine scrapie. Implications for the mechanism of neurodegeneration in prion diseases.
    Russelakis-Carneiro M, Saborio GP, Anderes L, Soto C.
    J Biol Chem; 2002 Sep 27; 277(39):36872-7. PubMed ID: 12130636
    [Abstract] [Full Text] [Related]

  • 2. Prion replication alters the distribution of synaptophysin and caveolin 1 in neuronal lipid rafts.
    Russelakis-Carneiro M, Hetz C, Maundrell K, Soto C.
    Am J Pathol; 2004 Nov 27; 165(5):1839-48. PubMed ID: 15509552
    [Abstract] [Full Text] [Related]

  • 3. Mouse-adapted scrapie strains 139A and ME7 overcome species barrier to induce experimental scrapie in hamsters and changed their pathogenic features.
    Shi Q, Zhang BY, Gao C, Zhang J, Jiang HY, Chen C, Han J, Dong XP.
    Virol J; 2012 Mar 09; 9():63. PubMed ID: 22400710
    [Abstract] [Full Text] [Related]

  • 4. Scrapie infection in experimental rodents and SMB-S15 cells decreased the brain endogenous levels and activities of Sirt1.
    Wang J, Zhang J, Shi Q, Zhang BY, Chen C, Chen LN, Sun J, Wang H, Xiao K, Dong XP.
    J Mol Neurosci; 2015 Apr 09; 55(4):1022-30. PubMed ID: 25391763
    [Abstract] [Full Text] [Related]

  • 5. Glycosylation deficiency at either one of the two glycan attachment sites of cellular prion protein preserves susceptibility to bovine spongiform encephalopathy and scrapie infections.
    Neuendorf E, Weber A, Saalmueller A, Schatzl H, Reifenberg K, Pfaff E, Groschup MH.
    J Biol Chem; 2004 Dec 17; 279(51):53306-16. PubMed ID: 15448157
    [Abstract] [Full Text] [Related]

  • 6. Changes in the localization of brain prion proteins during scrapie infection.
    DeArmond SJ, Mobley WC, DeMott DL, Barry RA, Beckstead JH, Prusiner SB.
    Neurology; 1987 Aug 17; 37(8):1271-80. PubMed ID: 3112607
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  • 7. Differences in proteinase K resistance and neuronal deposition of abnormal prion proteins characterize bovine spongiform encephalopathy (BSE) and scrapie strains.
    Kuczius T, Groschup MH.
    Mol Med; 1999 Jun 17; 5(6):406-18. PubMed ID: 10415165
    [Abstract] [Full Text] [Related]

  • 8. Propagation of prion strains through specific conformers of the prion protein.
    Scott MR, Groth D, Tatzelt J, Torchia M, Tremblay P, DeArmond SJ, Prusiner SB.
    J Virol; 1997 Dec 17; 71(12):9032-44. PubMed ID: 9371560
    [Abstract] [Full Text] [Related]

  • 9. Scrapie pathogenesis in brain and retina: effects of prion protein expression in neurons and astrocytes.
    Chesebro B, Race R, Kercher L.
    J Neurovirol; 2005 Oct 17; 11(5):476-80. PubMed ID: 16287689
    [Abstract] [Full Text] [Related]

  • 10. Characteristics of prion protein (PrP(Sc)) in the brains of hamsters inoculated serially with a mouse-passaged scrapie strain.
    Kimura K, Kubo M, Yokoyama T.
    J Comp Pathol; 2000 Oct 17; 122(2-3):123-30. PubMed ID: 10684681
    [Abstract] [Full Text] [Related]

  • 11. Successive passaging of the scrapie strains, ME7-ha and 139A-ha, generated by the interspecies transmission of mouse-adapted strains into hamsters markedly shortens the incubation times, but maintains their molecular and pathological properties.
    Shi Q, Xiao K, Zhang BY, Zhang XM, Chen LN, Chen C, Gao C, Dong XP.
    Int J Mol Med; 2015 Apr 17; 35(4):1138-46. PubMed ID: 25683243
    [Abstract] [Full Text] [Related]

  • 12. Protein Misfolding Cyclic Amplification Cross-Species Products of Mouse-Adapted Scrapie Strain 139A and Hamster-Adapted Scrapie Strain 263K with Brain and Muscle Tissues of Opposite Animals Generate Infectious Prions.
    Gao C, Han J, Zhang J, Wei J, Zhang BY, Tian C, Zhang J, Shi Q, Dong XP.
    Mol Neurobiol; 2017 Jul 17; 54(5):3771-3782. PubMed ID: 27259989
    [Abstract] [Full Text] [Related]

  • 13. Differences between the prion protein and its homolog Doppel: a partially structured state with implications for scrapie formation.
    Nicholson EM, Mo H, Prusiner SB, Cohen FE, Marqusee S.
    J Mol Biol; 2002 Feb 22; 316(3):807-15. PubMed ID: 11866533
    [Abstract] [Full Text] [Related]

  • 14. Effect of transition metals (Mn, Cu, Fe) and deoxycholic acid (DA) on the conversion of PrPC to PrPres.
    Kim NH, Choi JK, Jeong BH, Kim JI, Kwon MS, Carp RI, Kim YS.
    FASEB J; 2005 May 22; 19(7):783-5. PubMed ID: 15758042
    [Abstract] [Full Text] [Related]

  • 15. Re-transmissibility of mouse-adapted ME7 scrapie strain to ovine PrP transgenic mice.
    Babalola JA, Kim JM, Lee YJ, Park JH, Choi HS, Choi YG, Choi EK, Kim YS.
    J Vet Sci; 2019 Mar 22; 20(2):e8. PubMed ID: 30944531
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  • 19. Evidence for co-infection of ovine prion strains in classical scrapie isolates.
    Thackray AM, Lockey R, Beck KE, Spiropoulos J, Bujdoso R.
    J Comp Pathol; 2012 Mar 22; 147(2-3):316-29. PubMed ID: 22522075
    [Abstract] [Full Text] [Related]

  • 20. Scrapie-specific neuronal lesions are independent of neuronal PrP expression.
    Jeffrey M, Goodsir CM, Race RE, Chesebro B.
    Ann Neurol; 2004 Jun 22; 55(6):781-92. PubMed ID: 15174012
    [Abstract] [Full Text] [Related]

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