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Journal Abstract Search

582 related items for PubMed ID: 12664293

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  • 2. Sheep-passaged bovine spongiform encephalopathy agent exhibits altered pathobiological properties in bovine-PrP transgenic mice.
    Espinosa JC, Andréoletti O, Castilla J, Herva ME, Morales M, Alamillo E, San-Segundo FD, Lacroux C, Lugan S, Salguero FJ, Langeveld J, Torres JM.
    J Virol; 2007 Jan; 81(2):835-43. PubMed ID: 17079295
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  • 3. Excretion of BSE and scrapie prions in stools from murine models.
    Maluquer de Motes C, Grassi J, Simon S, Herva ME, Torres JM, Pumarola M, Girones R.
    Vet Microbiol; 2008 Sep 18; 131(1-2):205-11. PubMed ID: 18395370
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  • 5. 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 Sep 18; 75():55-74. PubMed ID: 1686599
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  • 6. Transgenic mice expressing bovine PrP with a four extra repeat octapeptide insert mutation show a spontaneous, non-transmissible, neurodegenerative disease and an expedited course of BSE infection.
    Castilla J, Gutiérrez-Adán A, Brun A, Pintado B, Salguero FJ, Parra B, Segundo FD, Ramírez MA, Rábano A, Cano MJ, Torres JM.
    FEBS Lett; 2005 Nov 07; 579(27):6237-46. PubMed ID: 16253245
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  • 7. 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 07; 112(5):573-85. PubMed ID: 16871401
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  • 8. 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 07; 20(11):1147-50. PubMed ID: 12389035
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  • 13. L-type bovine spongiform encephalopathy in genetically susceptible and resistant sheep: changes in prion strain or phenotypic plasticity of the disease-associated prion protein?
    Nicot S, Bencsik A, Migliore S, Canal D, Leboidre M, Agrimi U, Nonno R, Baron T.
    J Infect Dis; 2014 Mar 07; 209(6):950-9. PubMed ID: 24218507
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  • 14. Molecular assessment of the potential transmissibilities of BSE and scrapie to humans.
    Raymond GJ, Hope J, Kocisko DA, Priola SA, Raymond LD, Bossers A, Ironside J, Will RG, Chen SG, Petersen RB, Gambetti P, Rubenstein R, Smits MA, Lansbury PT, Caughey B.
    Nature; 1997 Jul 17; 388(6639):285-8. PubMed ID: 9230438
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  • 15. Strain-specific proteolytic processing of the prion protein in prion diseases of ruminants transmitted in ovine transgenic mice.
    Nicot S, Baron TG.
    J Gen Virol; 2010 Feb 17; 91(Pt 2):570-4. PubMed ID: 19828761
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  • 17. Digestion and transportation of bovine spongiform encephalopathy-derived prion protein in the sheep intestine.
    Dagleish MP, Hamilton S, González L, Eaton SL, Steele P, Finlayson J, Sisó S, Pang Y, Sales J, Chianini F, Jeffrey M.
    J Gen Virol; 2010 Dec 17; 91(Pt 12):3116-23. PubMed ID: 20826616
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  • 19. BSE infection in bovine PrP transgenic mice leads to hyperphosphorylation of tau-protein.
    Bautista MJ, Gutiérrez J, Salguero FJ, Fernández de Marco MM, Romero-Trevejo JL, Gómez-Villamandos JC.
    Vet Microbiol; 2006 Jul 20; 115(4):293-301. PubMed ID: 16621340
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