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Journal Abstract Search

296 related items for PubMed ID: 18576151

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  • 4. Copper(II) inhibits in vitro conversion of prion protein into amyloid fibrils.
    Bocharova OV, Breydo L, Salnikov VV, Baskakov IV.
    Biochemistry; 2005 May 10; 44(18):6776-87. PubMed ID: 15865423
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  • 6. Core structure of amyloid fibrils formed by residues 106-126 of the human prion protein.
    Walsh P, Simonetti K, Sharpe S.
    Structure; 2009 Mar 11; 17(3):417-26. PubMed ID: 19278656
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  • 7. Amyloid formation by recombinant full-length prion proteins in phospholipid bicelle solutions.
    Lührs T, Zahn R, Wüthrich K.
    J Mol Biol; 2006 Mar 31; 357(3):833-41. PubMed ID: 16466741
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  • 8. Amyloids, prions and the inherent infectious nature of misfolded protein aggregates.
    Soto C, Estrada L, Castilla J.
    Trends Biochem Sci; 2006 Mar 31; 31(3):150-5. PubMed ID: 16473510
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  • 9. Methionine oxidation interferes with conversion of the prion protein into the fibrillar proteinase K-resistant conformation.
    Breydo L, Bocharova OV, Makarava N, Salnikov VV, Anderson M, Baskakov IV.
    Biochemistry; 2005 Nov 29; 44(47):15534-43. PubMed ID: 16300402
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  • 10. 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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  • 11. Identification and characterization of a spontaneously aggregating amyloid-forming variant of human PrP((90-231)) through phage-display screening of variants randomized between residues 101 and 112.
    Verma A, Sharma S, Ganguly NK, Majumdar S, Guptasarma P, Luthra-Guptasarma M.
    Int J Biochem Cell Biol; 2008 Jul 28; 40(4):663-76. PubMed ID: 18023239
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  • 15. Semiautomated cell-free conversion of prion protein: applications for high-throughput screening of potential antiprion drugs.
    Breydo L, Bocharova OV, Baskakov IV.
    Anal Biochem; 2005 Apr 01; 339(1):165-73. PubMed ID: 15766724
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  • 16. Polymorphism at residue 129 modulates the conformational conversion of the D178N variant of human prion protein 90-231.
    Apetri AC, Vanik DL, Surewicz WK.
    Biochemistry; 2005 Dec 06; 44(48):15880-8. PubMed ID: 16313190
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  • 17. Prion Protein Prolines 102 and 105 and the Surrounding Lysine Cluster Impede Amyloid Formation.
    Kraus A, Anson KJ, Raymond LD, Martens C, Groveman BR, Dorward DW, Caughey B.
    J Biol Chem; 2015 Aug 28; 290(35):21510-22. PubMed ID: 26175152
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  • 19. How does domain replacement affect fibril formation of the rabbit/human prion proteins.
    Yan X, Huang JJ, Zhou Z, Chen J, Liang Y.
    PLoS One; 2014 Aug 28; 9(11):e113238. PubMed ID: 25401497
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  • 20. Rapid formation of amyloid from alpha-monomeric recombinant human PrP in vitro.
    Tahiri-Alaoui A, James W.
    Protein Sci; 2005 Apr 28; 14(4):942-7. PubMed ID: 15741327
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