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184 related items for PubMed ID: 22811758

  • 1. Calcium binding promotes prion protein fragment 90-231 conformational change toward a membrane destabilizing and cytotoxic structure.
    Sorrentino S, Bucciarelli T, Corsaro A, Tosatto A, Thellung S, Villa V, Schininà ME, Maras B, Galeno R, Scotti L, Creati F, Marrone A, Re N, Aceto A, Florio T, Mazzanti M.
    PLoS One; 2012; 7(7):e38314. PubMed ID: 22811758
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  • 2. High hydrophobic amino acid exposure is responsible of the neurotoxic effects induced by E200K or D202N disease-related mutations of the human prion protein.
    Corsaro A, Thellung S, Bucciarelli T, Scotti L, Chiovitti K, Villa V, D'Arrigo C, Aceto A, Florio T.
    Int J Biochem Cell Biol; 2011 Mar; 43(3):372-82. PubMed ID: 21094273
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  • 3. Intracellular mechanisms mediating the neuronal death and astrogliosis induced by the prion protein fragment 106-126.
    Thellung S, Florio T, Corsaro A, Arena S, Merlino M, Salmona M, Tagliavini F, Bugiani O, Forloni G, Schettini G.
    Int J Dev Neurosci; 2000 Mar; 18(4-5):481-92. PubMed ID: 10817932
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  • 4. The interaction of humic substances with the human prion protein fragment 90-231 affects its protease K resistance and cell internalization.
    Corsaro A, Anselmi C, Polano M, Aceto A, Florio T, De Nobili M.
    J Biol Regul Homeost Agents; 2010 Mar; 24(1):27-39. PubMed ID: 20385069
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  • 5. Copper modulation of ion channels of PrP[106-126] mutant prion peptide fragments.
    Kourie JI, Kenna BL, Tew D, Jobling MF, Curtain CC, Masters CL, Barnham KJ, Cappai R.
    J Membr Biol; 2003 May 01; 193(1):35-45. PubMed ID: 12879164
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  • 6. The toxicity of prion protein fragment PrP(106-126) is not mediated by membrane permeabilization as shown by a M112W substitution.
    Henriques ST, Pattenden LK, Aguilar MI, Castanho MA.
    Biochemistry; 2009 May 19; 48(19):4198-208. PubMed ID: 19301918
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  • 9. Mechanisms of prion-induced modifications in membrane transport properties: implications for signal transduction and neurotoxicity.
    Kourie JI.
    Chem Biol Interact; 2001 Oct 25; 138(1):1-26. PubMed ID: 11640912
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  • 11. Recombinant human prion protein fragment 90-231, a useful model to study prion neurotoxicity.
    Corsaro A, Thellung S, Villa V, Nizzari M, Aceto A, Florio T.
    OMICS; 2012 Oct 25; 16(1-2):50-9. PubMed ID: 22321015
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  • 12. NMR solution structure of the human prion protein.
    Zahn R, Liu A, Lührs T, Riek R, von Schroetter C, López García F, Billeter M, Calzolai L, Wider G, Wüthrich K.
    Proc Natl Acad Sci U S A; 2000 Jan 04; 97(1):145-50. PubMed ID: 10618385
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  • 13. The pathological prion protein forms ionic conductance in lipid bilayer.
    Paulis D, Maras B, Schininà ME, di Francesco L, Principe S, Galeno R, Abdel-Haq H, Cardone F, Florio T, Pocchiari M, Mazzanti M.
    Neurochem Int; 2011 Aug 04; 59(2):168-74. PubMed ID: 21683106
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  • 14. Neurotoxic prion protein (PrP) fragment 106-126 requires the N-terminal half of the hydrophobic region of PrP in the PrP-deficient neuronal cell line.
    Sakudo A, Nakamura I, Lee DC, Saeki K, Ikuta K, Onodera T.
    Protein Pept Lett; 2007 Aug 04; 14(1):1-6. PubMed ID: 17266643
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  • 15. Tetracycline affects abnormal properties of synthetic PrP peptides and PrP(Sc) in vitro.
    Tagliavini F, Forloni G, Colombo L, Rossi G, Girola L, Canciani B, Angeretti N, Giampaolo L, Peressini E, Awan T, De Gioia L, Ragg E, Bugiani O, Salmona M.
    J Mol Biol; 2000 Jul 28; 300(5):1309-22. PubMed ID: 10903871
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  • 20. Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible.
    Donne DG, Viles JH, Groth D, Mehlhorn I, James TL, Cohen FE, Prusiner SB, Wright PE, Dyson HJ.
    Proc Natl Acad Sci U S A; 1997 Dec 09; 94(25):13452-7. PubMed ID: 9391046
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