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145 related items for PubMed ID: 16855791

  • 1. RNA and CuCl2 induced conformational changes of the recombinant ovine prion protein.
    Liu M, Yu S, Yang J, Yin X, Zhao D.
    Mol Cell Biochem; 2007 Jan; 294(1-2):197-203. PubMed ID: 16855791
    [Abstract] [Full Text] [Related]

  • 2. Copper induces increased beta-sheet content in the scrapie-susceptible ovine prion protein PrPVRQ compared with the resistant allelic variant PrPARR.
    Wong E, Thackray AM, Bujdoso R.
    Biochem J; 2004 May 15; 380(Pt 1):273-82. PubMed ID: 14969585
    [Abstract] [Full Text] [Related]

  • 3. Self-assembly of recombinant prion protein of 106 residues.
    Baskakov IV, Aagaard C, Mehlhorn I, Wille H, Groth D, Baldwin MA, Prusiner SB, Cohen FE.
    Biochemistry; 2000 Mar 14; 39(10):2792-804. PubMed ID: 10704232
    [Abstract] [Full Text] [Related]

  • 4. The stability and aggregation of ovine prion protein associated with classical and atypical scrapie correlates with the ease of unwinding of helix-2.
    Fitzmaurice TJ, Burke DF, Hopkins L, Yang S, Yu S, Sy MS, Thackray AM, Bujdoso R.
    Biochem J; 2008 Jan 15; 409(2):367-75. PubMed ID: 17931166
    [Abstract] [Full Text] [Related]

  • 5. Lipid interaction converts prion protein to a PrPSc-like proteinase K-resistant conformation under physiological conditions.
    Wang F, Yang F, Hu Y, Wang X, Wang X, Jin C, Ma J.
    Biochemistry; 2007 Jun 12; 46(23):7045-53. PubMed ID: 17503780
    [Abstract] [Full Text] [Related]

  • 6. On the mechanism of alpha-helix to beta-sheet transition in the recombinant prion protein.
    Morillas M, Vanik DL, Surewicz WK.
    Biochemistry; 2001 Jun 12; 40(23):6982-7. PubMed ID: 11389614
    [Abstract] [Full Text] [Related]

  • 7. Synthetic scrapie infectivity: interaction between recombinant PrP and scrapie brain-derived RNA.
    Simoneau S, Thomzig A, Ruchoux MM, Vignier N, Daus ML, Poleggi A, Lebon P, Freire S, Durand V, Graziano S, Galeno R, Cardone F, Comoy E, Pocchiari M, Beekes M, Deslys JP, Fournier JG.
    Virulence; 2015 Jun 12; 6(2):132-44. PubMed ID: 25585171
    [Abstract] [Full Text] [Related]

  • 8. Copper-induced structural changes in the ovine prion protein are influenced by a polymorphism at codon 112.
    Yang S, Thackray AM, Fitzmaurice TJ, Bujdoso R.
    Biochim Biophys Acta; 2008 Apr 12; 1784(4):683-92. PubMed ID: 18280261
    [Abstract] [Full Text] [Related]

  • 9. The H187R mutation of the human prion protein induces conversion of recombinant prion protein to the PrP(Sc)-like form.
    Hosszu LL, Tattum MH, Jones S, Trevitt CR, Wells MA, Waltho JP, Collinge J, Jackson GS, Clarke AR.
    Biochemistry; 2010 Oct 12; 49(40):8729-38. PubMed ID: 20718410
    [Abstract] [Full Text] [Related]

  • 10. Copper(II) inhibits in vitro conformational conversion of ovine prion protein triggered by low pH.
    Liu ML, Li YX, Zhou XM, Zhao DM.
    J Biochem; 2008 Mar 12; 143(3):333-7. PubMed ID: 18039688
    [Abstract] [Full Text] [Related]

  • 11. Cell Biology Approaches to Studying Prion Diseases.
    Priola SA.
    Methods Mol Biol; 2017 Mar 12; 1658():83-94. PubMed ID: 28861784
    [Abstract] [Full Text] [Related]

  • 12. A seven-residue deletion in PrP leads to generation of a spontaneous prion formed from C-terminal C1 fragment of PrP.
    Munoz-Montesino C, Larkem D, Barbereau C, Igel-Egalon A, Truchet S, Jacquet E, Nhiri N, Moudjou M, Sizun C, Rezaei H, Béringue V, Dron M.
    J Biol Chem; 2020 Oct 09; 295(41):14025-14039. PubMed ID: 32788216
    [Abstract] [Full Text] [Related]

  • 13. DNA converts cellular prion protein into the beta-sheet conformation and inhibits prion peptide aggregation.
    Cordeiro Y, Machado F, Juliano L, Juliano MA, Brentani RR, Foguel D, Silva JL.
    J Biol Chem; 2001 Dec 28; 276(52):49400-9. PubMed ID: 11604397
    [Abstract] [Full Text] [Related]

  • 14. In vitro conversion and seeded fibrillization of posttranslationally modified prion protein.
    Stöhr J, Elfrink K, Weinmann N, Wille H, Willbold D, Birkmann E, Riesner D.
    Biol Chem; 2011 May 28; 392(5):415-21. PubMed ID: 21476870
    [Abstract] [Full Text] [Related]

  • 15. Mapping the antigenicity of copper-treated cellular prion protein with the scrapie isoform.
    Wong BS, Li R, Sassoon J, Kang SC, Liu T, Pan T, Greenspan NS, Wisniewski T, Brown DR, Sy MS.
    Cell Mol Life Sci; 2003 Jun 28; 60(6):1224-34. PubMed ID: 12861388
    [Abstract] [Full Text] [Related]

  • 16. Cooperative binding of dominant-negative prion protein to kringle domains.
    Ryou C, Prusiner SB, Legname G.
    J Mol Biol; 2003 May 30; 329(2):323-33. PubMed ID: 12758079
    [Abstract] [Full Text] [Related]

  • 17. Expansion of the octarepeat domain alters the misfolding pathway but not the folding pathway of the prion protein.
    Leliveld SR, Stitz L, Korth C.
    Biochemistry; 2008 Jun 10; 47(23):6267-78. PubMed ID: 18473442
    [Abstract] [Full Text] [Related]

  • 18. Host Determinants of Prion Strain Diversity Independent of Prion Protein Genotype.
    Crowell J, Hughson A, Caughey B, Bessen RA.
    J Virol; 2015 Oct 10; 89(20):10427-41. PubMed ID: 26246570
    [Abstract] [Full Text] [Related]

  • 19. Prion protein aggregation and fibrillogenesis in vitro.
    Stöhr J.
    Subcell Biochem; 2012 Oct 10; 65():91-108. PubMed ID: 23225001
    [Abstract] [Full Text] [Related]

  • 20. Preventing misfolding of the prion protein by trimethylamine N-oxide.
    Bennion BJ, DeMarco ML, Daggett V.
    Biochemistry; 2004 Oct 19; 43(41):12955-63. PubMed ID: 15476389
    [Abstract] [Full Text] [Related]

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