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Journal Abstract Search

295 related items for PubMed ID: 18071044

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  • 3. Neuropathology and molecular biology of variant Creutzfeldt-Jakob disease.
    Ironside JW, Head MW.
    Curr Top Microbiol Immunol; 2004; 284():133-59. PubMed ID: 15148991
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  • 7. Characterization of variant Creutzfeldt-Jakob disease prions in prion protein-humanized mice carrying distinct codon 129 genotypes.
    Takeuchi A, Kobayashi A, Ironside JW, Mohri S, Kitamoto T.
    J Biol Chem; 2013 Jul 26; 288(30):21659-66. PubMed ID: 23792955
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  • 9. Prion Strain Characterization of a Novel Subtype of Creutzfeldt-Jakob Disease.
    Galeno R, Di Bari MA, Nonno R, Cardone F, Sbriccoli M, Graziano S, Ingrosso L, Fiorini M, Valanzano A, Pasini G, Poleggi A, Vinci R, Ladogana A, Puopolo M, Monaco S, Agrimi U, Zanusso G, Pocchiari M.
    J Virol; 2017 Jun 01; 91(11):. PubMed ID: 28298604
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  • 12. Protective Effect of Val129-PrP against Bovine Spongiform Encephalopathy but not Variant Creutzfeldt-Jakob Disease.
    Fernández-Borges N, Espinosa JC, Marín-Moreno A, Aguilar-Calvo P, Asante EA, Kitamoto T, Mohri S, Andréoletti O, Torres JM.
    Emerg Infect Dis; 2017 Sep 01; 23(9):1522-1530. PubMed ID: 28820136
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  • 13. Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics.
    Cali I, Castellani R, Alshekhlee A, Cohen Y, Blevins J, Yuan J, Langeveld JP, Parchi P, Safar JG, Zou WQ, Gambetti P.
    Brain; 2009 Oct 01; 132(Pt 10):2643-58. PubMed ID: 19734292
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  • 14. Variant CJD. 18 years of research and surveillance.
    Diack AB, Head MW, McCutcheon S, Boyle A, Knight R, Ironside JW, Manson JC, Will RG.
    Prion; 2014 Oct 01; 8(4):286-95. PubMed ID: 25495404
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  • 15. Cross-sequence transmission of sporadic Creutzfeldt-Jakob disease creates a new prion strain.
    Kobayashi A, Asano M, Mohri S, Kitamoto T.
    J Biol Chem; 2007 Oct 12; 282(41):30022-8. PubMed ID: 17709374
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  • 16. Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD.
    Pastore M, Chin SS, Bell KL, Dong Z, Yang Q, Yang L, Yuan J, Chen SG, Gambetti P, Zou WQ.
    Am J Pathol; 2005 Dec 12; 167(6):1729-38. PubMed ID: 16314483
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  • 17. Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
    Schmitz M, Lüllmann K, Zafar S, Ebert E, Wohlhage M, Oikonomou P, Schlomm M, Mitrova E, Beekes M, Zerr I.
    Neurobiol Aging; 2014 May 12; 35(5):1177-88. PubMed ID: 24360565
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  • 18. 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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  • 19. Sporadic Creutzfeldt-Jakob disease VM1: phenotypic and molecular characterization of a novel subtype of human prion disease.
    Gelpi E, Baiardi S, Nos C, Dellavalle S, Aldecoa I, Ruiz-Garcia R, Ispierto L, Escudero D, Casado V, Barranco E, Boltes A, Molina-Porcel L, Bargalló N, Rossi M, Mammana A, Tiple D, Vaianella L, Stoegmann E, Simonitsch-Klupp I, Kasprian G, Klotz S, Höftberger R, Budka H, Kovacs GG, Ferrer I, Capellari S, Sanchez-Valle R, Parchi P.
    Acta Neuropathol Commun; 2022 Aug 17; 10(1):114. PubMed ID: 35978418
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  • 20. 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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