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138 related items for PubMed ID: 15649429

  • 1. Prion protein with Y145STOP mutation induces mitochondria-mediated apoptosis and PrP-containing deposits in vitro.
    Hachiya NS, Watanabe K, Kawabata MY, Jozuka A, Kozuka Y, Sakasegawa Y, Kaneko K.
    Biochem Biophys Res Commun; 2005 Feb 18; 327(3):894-9. PubMed ID: 15649429
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  • 2. Mitochondrial localization of cellular prion protein (PrPC) invokes neuronal apoptosis in aged transgenic mice overexpressing PrPC.
    Hachiya NS, Yamada M, Watanabe K, Jozuka A, Ohkubo T, Sano K, Takeuchi Y, Kozuka Y, Sakasegawa Y, Kaneko K.
    Neurosci Lett; 2005 Feb 10; 374(2):98-103. PubMed ID: 15644272
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  • 3. An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques.
    Kitamoto T, Iizuka R, Tateishi J.
    Biochem Biophys Res Commun; 1993 Apr 30; 192(2):525-31. PubMed ID: 8097911
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  • 4. Species-specific anti-apoptotic activity of cellular prion protein in a mouse PrP-deficient neuronal cell line transfected with mouse, hamster, and bovine Prnp.
    Wu G, Nakajima K, Takeyama N, Yukawa M, Taniuchi Y, Sakudo A, Onodera T.
    Neurosci Lett; 2008 Nov 28; 446(1):11-5. PubMed ID: 18809465
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  • 5. Aggregation/fibrillogenesis of recombinant human prion protein and Gerstmann-Sträussler-Scheinker disease peptides in the presence of metal ions.
    Ricchelli F, Buggio R, Drago D, Salmona M, Forloni G, Negro A, Tognon G, Zatta P.
    Biochemistry; 2006 May 30; 45(21):6724-32. PubMed ID: 16716083
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  • 6. Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.
    Hsiao K, Dlouhy SR, Farlow MR, Cass C, Da Costa M, Conneally PM, Hodes ME, Ghetti B, Prusiner SB.
    Nat Genet; 1992 Apr 30; 1(1):68-71. PubMed ID: 1363810
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  • 8. Gerstmann-Sträussler-Scheinker: a new phenotype with 'curly' PrP deposits.
    Colucci M, Moleres FJ, Xie ZL, Ray-Chaudhury A, Gutti S, Butefisch CM, Cervenakova L, Wang W, Goldfarb LG, Kong Q, Ghetti B, Chen SG, Gambetti P.
    J Neuropathol Exp Neurol; 2006 Jul 30; 65(7):642-51. PubMed ID: 16825951
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  • 10. A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient.
    Jansen C, Parchi P, Capellari S, Strammiello R, Dopper EG, van Swieten JC, Kamphorst W, Rozemuller AJ.
    J Neuropathol Exp Neurol; 2011 Aug 30; 70(8):698-702. PubMed ID: 21760536
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  • 11. The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease.
    Di Fede G, Giaccone G, Limido L, Mangieri M, Suardi S, Puoti G, Morbin M, Mazzoleni G, Ghetti B, Tagliavini F.
    J Neuropathol Exp Neurol; 2007 Feb 30; 66(2):124-30. PubMed ID: 17278997
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  • 13. Neuropathological features of a case with schizophrenia and prion protein gene P102L mutation before onset of Gerstmann-Sträussler-Scheinker disease.
    Sasaki K, Doh-ura K, Furuta A, Nakashima S, Morisada Y, Tateishi J, Iwaki T.
    Acta Neuropathol; 2003 Jul 30; 106(1):92-6. PubMed ID: 12682740
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  • 16. Novel localization of OCTN1, an organic cation/carnitine transporter, to mammalian mitochondria.
    Lamhonwah AM, Tein I.
    Biochem Biophys Res Commun; 2006 Jul 14; 345(4):1315-25. PubMed ID: 16729965
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  • 18. [A case of variant Gerstmann-Sträussler-Scheinker disease with the mutation of codon P105L].
    Kubo M, Nishimura T, Shikata E, Kokubun Y, Takasu T.
    Rinsho Shinkeigaku; 1995 Aug 14; 35(8):873-7. PubMed ID: 8665729
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  • 19. Loss of anti-Bax function in Gerstmann-Sträussler-Scheinker syndrome-associated prion protein mutants.
    Jodoin J, Misiewicz M, Makhijani P, Giannopoulos PN, Hammond J, Goodyer CG, LeBlanc AC.
    PLoS One; 2009 Aug 14; 4(8):e6647. PubMed ID: 19680558
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  • 20. A novel PRNP Y218N mutation in Gerstmann-Sträussler-Scheinker disease with neurofibrillary degeneration.
    Alzualde A, Indakoetxea B, Ferrer I, Moreno F, Barandiaran M, Gorostidi A, Estanga A, Ruiz I, Calero M, van Leeuwen FW, Atares B, Juste R, Rodriguez-Martínez AB, López de Munain A.
    J Neuropathol Exp Neurol; 2010 Aug 14; 69(8):789-800. PubMed ID: 20613639
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