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Journal Abstract Search

419 related items for PubMed ID: 25495404

  • 1. 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; 8(4):286-95. PubMed ID: 25495404
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Creutzfeldt-Jakob disease, prion protein gene codon 129VV, and a novel PrPSc type in a young British woman.
    Mead S, Joiner S, Desbruslais M, Beck JA, O'Donoghue M, Lantos P, Wadsworth JD, Collinge J.
    Arch Neurol; 2007 Dec 01; 64(12):1780-4. PubMed ID: 18071044
    [Abstract] [Full Text] [Related]

  • 5. The French surveillance network of Creutzfeldt-Jakob disease. Epidemiological data in France and worldwide.
    Brandel JP, Peckeu L, Haïk S.
    Transfus Clin Biol; 2013 Sep 01; 20(4):395-7. PubMed ID: 23587616
    [Abstract] [Full Text] [Related]

  • 6. Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.
    Mead S, Poulter M, Uphill J, Beck J, Whitfield J, Webb TE, Campbell T, Adamson G, Deriziotis P, Tabrizi SJ, Hummerich H, Verzilli C, Alpers MP, Whittaker JC, Collinge J.
    Lancet Neurol; 2009 Jan 01; 8(1):57-66. PubMed ID: 19081515
    [Abstract] [Full Text] [Related]

  • 7. Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion.
    Llewelyn CA, Hewitt PE, Knight RS, Amar K, Cousens S, Mackenzie J, Will RG.
    Lancet; 2004 Feb 07; 363(9407):417-21. PubMed ID: 14962520
    [Abstract] [Full Text] [Related]

  • 8. Experimental sheep BSE prions generate the vCJD phenotype when serially passaged in transgenic mice expressing human prion protein.
    Joiner S, Asante EA, Linehan JM, Brock L, Brandner S, Bellworthy SJ, Simmons MM, Hope J, Collinge J, Wadsworth JDF.
    J Neurol Sci; 2018 Mar 15; 386():4-11. PubMed ID: 29406965
    [Abstract] [Full Text] [Related]

  • 9. Dissociation of pathological and molecular phenotype of variant Creutzfeldt-Jakob disease in transgenic human prion protein 129 heterozygous mice.
    Asante EA, Linehan JM, Gowland I, Joiner S, Fox K, Cooper S, Osiguwa O, Gorry M, Welch J, Houghton R, Desbruslais M, Brandner S, Wadsworth JD, Collinge J.
    Proc Natl Acad Sci U S A; 2006 Jul 11; 103(28):10759-64. PubMed ID: 16809423
    [Abstract] [Full Text] [Related]

  • 10. 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 11; 23(9):1522-1530. PubMed ID: 28820136
    [Abstract] [Full Text] [Related]

  • 11. Neuropathology and molecular biology of variant Creutzfeldt-Jakob disease.
    Ironside JW, Head MW.
    Curr Top Microbiol Immunol; 2004 Sep 11; 284():133-59. PubMed ID: 15148991
    [Abstract] [Full Text] [Related]

  • 12. 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
    [Abstract] [Full Text] [Related]

  • 13. Human prion diseases: surgical lessons learned from iatrogenic prion transmission.
    Bonda DJ, Manjila S, Mehndiratta P, Khan F, Miller BR, Onwuzulike K, Puoti G, Cohen ML, Schonberger LB, Cali I.
    Neurosurg Focus; 2016 Jul 02; 41(1):E10. PubMed ID: 27364252
    [Abstract] [Full Text] [Related]

  • 14. Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt-Jakob disease.
    Bishop MT, Diack AB, Ritchie DL, Ironside JW, Will RG, Manson JC.
    Brain; 2013 Apr 02; 136(Pt 4):1139-45. PubMed ID: 23449776
    [Abstract] [Full Text] [Related]

  • 15. Variant Creutzfeldt-Jakob disease: an update.
    Ironside JW.
    Folia Neuropathol; 2012 Apr 02; 50(1):50-6. PubMed ID: 22505363
    [Abstract] [Full Text] [Related]

  • 16. Strain-specific viral properties of variant Creutzfeldt-Jakob disease (vCJD) are encoded by the agent and not by host prion protein.
    Manuelidis L, Liu Y, Mullins B.
    J Cell Biochem; 2009 Feb 01; 106(2):220-31. PubMed ID: 19097123
    [Abstract] [Full Text] [Related]

  • 17. Variant Creutzfeldt-Jakob disease strain is identical in individuals of two PRNP codon 129 genotypes.
    Diack AB, Boyle A, Plinston C, Hunt E, Bishop MT, Will RG, Manson JC.
    Brain; 2019 May 01; 142(5):1416-1428. PubMed ID: 30938429
    [Abstract] [Full Text] [Related]

  • 18. PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism.
    Bishop MT, Pennington C, Heath CA, Will RG, Knight RS.
    BMC Med Genet; 2009 Dec 26; 10():146. PubMed ID: 20035629
    [Abstract] [Full Text] [Related]

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  • 20. Rapid amplification of prions from variant Creutzfeldt-Jakob disease cerebrospinal fluid.
    Barria MA, Lee A, Green AJ, Knight R, Head MW.
    J Pathol Clin Res; 2018 Apr 26; 4(2):86-92. PubMed ID: 29665324
    [Abstract] [Full Text] [Related]

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