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131 related items for PubMed ID: 21214405

  • 1. Autophagy contributes to widespread neuronal degeneration in hamsters infected with the Echigo-1 strain of Creutzfeldt-Jakob disease and mice infected with the Fujisaki strain of Gerstmann-Sträussler-Scheinker (GSS) syndrome.
    Liberski PP, Sikorska B, Gibson P, Brown P.
    Ultrastruct Pathol; 2011 Feb; 35(1):31-6. PubMed ID: 21214405
    [Abstract] [Full Text] [Related]

  • 2. Robust autophagy in optic nerves of experimental Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker disease.
    Liberski PP, Gajos A, Bogucki A.
    Folia Neuropathol; 2017 Feb; 55(4):289-294. PubMed ID: 29363902
    [Abstract] [Full Text] [Related]

  • 3. Ultrastructural changes in the optic nerves of rodents with experimental Creutzfeldt-Jakob Disease (CJD), Gerstmann-Sträussler-Scheinker disease (GSS) or scrapie.
    Waliś A, Bratosiewicz J, Sikorska B, Brown P, Gajdusek DC, Liberski PP.
    J Comp Pathol; 2003 Feb; 129(2-3):213-25. PubMed ID: 12921728
    [Abstract] [Full Text] [Related]

  • 4. Autophagy is a part of ultrastructural synaptic pathology in Creutzfeldt-Jakob disease: a brain biopsy study.
    Sikorska B, Liberski PP, Giraud P, Kopp N, Brown P.
    Int J Biochem Cell Biol; 2004 Dec; 36(12):2563-73. PubMed ID: 15325593
    [Abstract] [Full Text] [Related]

  • 5. Neuronal cell death in transmissible spongiform encephalopathies (prion diseases) revisited: from apoptosis to autophagy.
    Liberski PP, Sikorska B, Bratosiewicz-Wasik J, Gajdusek DC, Brown P.
    Int J Biochem Cell Biol; 2004 Dec; 36(12):2473-90. PubMed ID: 15325586
    [Abstract] [Full Text] [Related]

  • 6. Echigo-1: a panencephalopathic strain of Creutzfeldt-Jakob disease. II. Ultrastructural studies in hamsters.
    Sikorska B, Hainfellner JA, Mori S, Bratosiewiczi J, Liberski PP, Budka H.
    Folia Neuropathol; 2004 Dec; 42 Suppl B():167-75. PubMed ID: 16903151
    [Abstract] [Full Text] [Related]

  • 7. Ultrastructural study of florid plaques in variant Creutzfeldt-Jakob disease: a comparison with amyloid plaques in kuru, sporadic Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker disease.
    Sikorska B, Liberski PP, Sobów T, Budka H, Ironside JW.
    Neuropathol Appl Neurobiol; 2009 Feb; 35(1):46-59. PubMed ID: 18513219
    [Abstract] [Full Text] [Related]

  • 8. [Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies. Part II].
    Zaborowski A.
    Psychiatr Pol; 2004 Feb; 38(2):297-309. PubMed ID: 15307294
    [Abstract] [Full Text] [Related]

  • 9. Experimental Creutzfeldt-Jakob disease: light microscopic, immunohistochemical and ultrastructural studies of the Fujisaki strain of Creutzfeldt-Jakob disease virus in NIH Swiss mice.
    Liberski PP, Yanagihara R, Gibbs CJ, Gajdusek DC.
    Neuropatol Pol; 1991 Feb; 29(1-2):1-17. PubMed ID: 1813811
    [Abstract] [Full Text] [Related]

  • 10. Fate of myelinated fibres in the optic nerves in experimental Creutzfeldt-Jakob disease in rodents: an ultrastructural study.
    Sikorska B, Waliś A, Bratosiewicz-Wasik J, Brown P, Liberski PP.
    Folia Neuropathol; 2004 Feb; 42(2):101-5. PubMed ID: 15266784
    [Abstract] [Full Text] [Related]

  • 11. Neuropathology of human prion diseases (spongiform encephalopathies).
    Kretzschmar HA.
    Dev Biol Stand; 1993 Feb; 80():71-90. PubMed ID: 8270118
    [Abstract] [Full Text] [Related]

  • 12. Prion protein (PrP) deposits in the tectum of experimental Gerstmann-Sträussler-Scheinker disease following intraocular inoculation.
    Liberski PP, Hainfellner JA, Sikorska B, Budka H.
    Folia Neuropathol; 2012 Feb; 50(1):85-8. PubMed ID: 22505367
    [Abstract] [Full Text] [Related]

  • 13. Immunolocalization of heparan sulfate proteoglycans to the prion protein amyloid plaques of Gerstmann-Straussler syndrome, Creutzfeldt-Jakob disease and scrapie.
    Snow AD, Wight TN, Nochlin D, Koike Y, Kimata K, DeArmond SJ, Prusiner SB.
    Lab Invest; 1990 Nov; 63(5):601-11. PubMed ID: 1977959
    [Abstract] [Full Text] [Related]

  • 14. Ultrastructural pathology of prion diseases revisited: brain biopsy studies.
    Liberski PP, Streichenberger N, Giraud P, Soutrenon M, Meyronnet D, Sikorska B, Kopp N.
    Neuropathol Appl Neurobiol; 2005 Feb; 31(1):88-96. PubMed ID: 15634235
    [Abstract] [Full Text] [Related]

  • 15. Cell death and autophagy in prion diseases (transmissible spongiform encephalopathies).
    Liberski PP, Brown DR, Sikorska B, Caughey B, Brown P.
    Folia Neuropathol; 2008 Feb; 46(1):1-25. PubMed ID: 18368623
    [Abstract] [Full Text] [Related]

  • 16. Scrg1 is induced in TSE and brain injuries, and associated with autophagy.
    Dron M, Bailly Y, Beringue V, Haeberlé AM, Griffond B, Risold PY, Tovey MG, Laude H, Dandoy-Dron F.
    Eur J Neurosci; 2005 Jul; 22(1):133-46. PubMed ID: 16029203
    [Abstract] [Full Text] [Related]

  • 17. Spongiform encephalopathy transmitted experimentally from Creutzfeldt-Jakob and familial Gerstmann-Sträussler-Scheinker diseases.
    Baker HF, Duchen LW, Jacobs JM, Ridley RM.
    Brain; 1990 Dec; 113 ( Pt 6)():1891-909. PubMed ID: 2276050
    [Abstract] [Full Text] [Related]

  • 18. [Creutzfeldt-Jakob disease and Gerstmann-Sträussler syndrome with reference to their differential diagnosis].
    Frýdl V, Závodská H.
    Zentralbl Pathol; 1991 Dec; 137(2):133-9. PubMed ID: 1911728
    [Abstract] [Full Text] [Related]

  • 19. Gerstmann-Sträussler-Scheinker disease: immunohistological and experimental studies.
    Tateishi J, Kitamoto T, Hashiguchi H, Shii H.
    Ann Neurol; 1988 Jul; 24(1):35-40. PubMed ID: 3046469
    [Abstract] [Full Text] [Related]

  • 20. [Gerstmann-Sträussler-Scheinker disease. Pathologal and genetic study].
    Genthon R, Gray F, Salama J, Duyckaerts C, Belin C, Brucher JM, Baron H, Delaporte P.
    Rev Neurol (Paris); 1992 Jul; 148(5):335-42. PubMed ID: 1448647
    [Abstract] [Full Text] [Related]

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