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Journal Abstract Search

964 related items for PubMed ID: 19278656

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  • 24. A partially structured region of a largely unstructured protein, Plasmodium falciparum merozoite surface protein 2 (MSP2), forms amyloid-like fibrils.
    Yang X, Adda CG, Keizer DW, Murphy VJ, Rizkalla MM, Perugini MA, Jackson DC, Anders RF, Norton RS.
    J Pept Sci; 2007 Dec; 13(12):839-48. PubMed ID: 17883245
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  • 25. A cylinder-shaped double ribbon structure formed by an amyloid hairpin peptide derived from the beta-sheet of murine PrP: an X-ray and molecular dynamics simulation study.
    Croixmarie V, Briki F, David G, Coïc YM, Ovtracht L, Doucet J, Jamin N, Sanson A.
    J Struct Biol; 2005 Jun; 150(3):284-99. PubMed ID: 15890277
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  • 26. Methods for conversion of prion protein into amyloid fibrils.
    Breydo L, Makarava N, Baskakov IV.
    Methods Mol Biol; 2008 Jun; 459():105-15. PubMed ID: 18576151
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  • 27. Different structural stability and toxicity of PrP(ARR) and PrP(ARQ) sheep prion protein variants.
    Paludi D, Thellung S, Chiovitti K, Corsaro A, Villa V, Russo C, Ianieri A, Bertsch U, Kretzschmar HA, Aceto A, Florio T.
    J Neurochem; 2007 Dec; 103(6):2291-300. PubMed ID: 17919292
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  • 28. Structural diversity of the soluble trimers of the human amylin(20-29) peptide revealed by molecular dynamics simulations.
    Mo Y, Lu Y, Wei G, Derreumaux P.
    J Chem Phys; 2009 Mar 28; 130(12):125101. PubMed ID: 19334894
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  • 29. 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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  • 30. Assembly of natural and recombinant prion protein into fibrils.
    Leffers KW, Wille H, Stöhr J, Junger E, Prusiner SB, Riesner D.
    Biol Chem; 2005 Jun 30; 386(6):569-80. PubMed ID: 16006244
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  • 32. 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 Jun 30; 40(4):663-76. PubMed ID: 18023239
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  • 34. 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
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  • 37. Highly accelerated self-assembly and fibrillation of prion peptides on solid surfaces.
    Ku SH, Park CB.
    Langmuir; 2008 Dec 16; 24(24):13822-7. PubMed ID: 19053635
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  • 39. A structural core within apolipoprotein C-II amyloid fibrils identified using hydrogen exchange and proteolysis.
    Wilson LM, Mok YF, Binger KJ, Griffin MD, Mertens HD, Lin F, Wade JD, Gooley PR, Howlett GJ.
    J Mol Biol; 2007 Mar 09; 366(5):1639-51. PubMed ID: 17217959
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  • 40. Toward the molecular basis of inherited prion diseases: NMR structure of the human prion protein with V210I mutation.
    Biljan I, Ilc G, Giachin G, Raspadori A, Zhukov I, Plavec J, Legname G.
    J Mol Biol; 2011 Sep 30; 412(4):660-73. PubMed ID: 21839748
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