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Journal Abstract Search

363 related items for PubMed ID: 26864450

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  • 4. Virus Infection, Genetic Mutations, and Prion Infection in Prion Protein Conversion.
    Hara H, Sakaguchi S.
    Int J Mol Sci; 2021 Nov 18; 22(22):. PubMed ID: 34830321
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  • 5. The prion diseases.
    Brown K, Mastrianni JA.
    J Geriatr Psychiatry Neurol; 2010 Dec 18; 23(4):277-98. PubMed ID: 20938044
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  • 6. [A trend of molecular genetics on prion diseases and prion protein].
    Muramatsu Y, Shinagawa M.
    Nihon Rinsho; 1993 Sep 18; 51(9):2494-502. PubMed ID: 8411733
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  • 7. How an Infection of Sheep Revealed Prion Mechanisms in Alzheimer's Disease and Other Neurodegenerative Disorders.
    Carlson GA, Prusiner SB.
    Int J Mol Sci; 2021 May 04; 22(9):. PubMed ID: 34064393
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  • 8. Transgenic fatal familial insomnia mice indicate prion infectivity-independent mechanisms of pathogenesis and phenotypic expression of disease.
    Bouybayoune I, Mantovani S, Del Gallo F, Bertani I, Restelli E, Comerio L, Tapella L, Baracchi F, Fernández-Borges N, Mangieri M, Bisighini C, Beznoussenko GV, Paladini A, Balducci C, Micotti E, Forloni G, Castilla J, Fiordaliso F, Tagliavini F, Imeri L, Chiesa R.
    PLoS Pathog; 2015 Apr 04; 11(4):e1004796. PubMed ID: 25880443
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  • 9. Generation of a new infectious recombinant prion: a model to understand Gerstmann-Sträussler-Scheinker syndrome.
    Elezgarai SR, Fernández-Borges N, Eraña H, Sevillano AM, Charco JM, Harrathi C, Saá P, Gil D, Kong Q, Requena JR, Andréoletti O, Castilla J.
    Sci Rep; 2017 Aug 29; 7(1):9584. PubMed ID: 28851967
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  • 10. A New Transgenic Mouse Model of Gerstmann-Straussler-Scheinker Syndrome Caused by the A117V Mutation of PRNP.
    Yang W, Cook J, Rassbach B, Lemus A, DeArmond SJ, Mastrianni JA.
    J Neurosci; 2009 Aug 12; 29(32):10072-80. PubMed ID: 19675240
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  • 12. Experimental Models of Inherited PrP Prion Diseases.
    Watts JC, Prusiner SB.
    Cold Spring Harb Perspect Med; 2017 Nov 01; 7(11):. PubMed ID: 28096244
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  • 15. Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature.
    Takada LT, Kim MO, Cleveland RW, Wong K, Forner SA, Gala II, Fong JC, Geschwind MD.
    Am J Med Genet B Neuropsychiatr Genet; 2017 Jan 01; 174(1):36-69. PubMed ID: 27943639
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  • 17. Prion Mutations in Republic of Republic of Korea, China, and Japan.
    Kim DY, Shim KH, Bagyinszky E, An SSA.
    Int J Mol Sci; 2022 Dec 30; 24(1):. PubMed ID: 36614069
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  • 18. [Clinical characteristics and diagnostics of human spongiform encephalopathies: an update].
    Hermann P, Goebel S, Zerr I.
    Nervenarzt; 2024 Apr 30; 95(4):376-384. PubMed ID: 38503894
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  • 19. Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease.
    Zanusso G, Fiorini M, Ferrari S, Meade-White K, Barbieri I, Brocchi E, Ghetti B, Monaco S.
    J Biol Chem; 2014 Feb 21; 289(8):4870-81. PubMed ID: 24398683
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  • 20. Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification.
    Baiardi S, Rossi M, Mammana A, Appleby BS, Barria MA, Calì I, Gambetti P, Gelpi E, Giese A, Ghetti B, Herms J, Ladogana A, Mikol J, Pal S, Ritchie DL, Ruf V, Windl O, Capellari S, Parchi P.
    Acta Neuropathol; 2021 Oct 21; 142(4):707-728. PubMed ID: 34324063
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