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5. Disease-associated F198S mutation increases the propensity of the recombinant prion protein for conformational conversion to scrapie-like form. Vanik DL; Surewicz WK J Biol Chem; 2002 Dec; 277(50):49065-70. PubMed ID: 12372829 [TBL] [Abstract][Full Text] [Related]
6. Globular domain of the prion protein needs to be unlocked by domain swapping to support prion protein conversion. Hafner-Bratkovic I; Bester R; Pristovsek P; Gaedtke L; Veranic P; Gaspersic J; Mancek-Keber M; Avbelj M; Polymenidou M; Julius C; Aguzzi A; Vorberg I; Jerala R J Biol Chem; 2011 Apr; 286(14):12149-56. PubMed ID: 21324909 [TBL] [Abstract][Full Text] [Related]
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8. Autocatalytic conversion of recombinant prion proteins displays a species barrier. Baskakov IV J Biol Chem; 2004 Feb; 279(9):7671-7. PubMed ID: 14668351 [TBL] [Abstract][Full Text] [Related]
9. 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; 40(4):663-76. PubMed ID: 18023239 [TBL] [Abstract][Full Text] [Related]
10. Assemblages of prion fragments: novel model systems for understanding amyloid toxicity. Satheeshkumar KS; Murali J; Jayakumar R J Struct Biol; 2004 Nov; 148(2):176-93. PubMed ID: 15477098 [TBL] [Abstract][Full Text] [Related]
11. Formation of soluble oligomers and amyloid fibrils with physical properties of the scrapie isoform of the prion protein from the C-terminal domain of recombinant murine prion protein mPrP-(121-231). Martins SM; Frosoni DJ; Martinez AM; De Felice FG; Ferreira ST J Biol Chem; 2006 Sep; 281(36):26121-8. PubMed ID: 16844683 [TBL] [Abstract][Full Text] [Related]
12. Shaking alone induces de novo conversion of recombinant prion proteins to β-sheet rich oligomers and fibrils. Ladner-Keay CL; Griffith BJ; Wishart DS PLoS One; 2014; 9(6):e98753. PubMed ID: 24892647 [TBL] [Abstract][Full Text] [Related]
13. Generic amyloidogenicity of mammalian prion proteins from species susceptible and resistant to prions. Nyström S; Hammarström P Sci Rep; 2015 May; 5():10101. PubMed ID: 25960067 [TBL] [Abstract][Full Text] [Related]
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15. Amyloid nucleation and hierarchical assembly of Ure2p fibrils. Role of asparagine/glutamine repeat and nonrepeat regions of the prion domains. Jiang Y; Li H; Zhu L; Zhou JM; Perrett S J Biol Chem; 2004 Jan; 279(5):3361-9. PubMed ID: 14610069 [TBL] [Abstract][Full Text] [Related]
16. Octapeptide repeat insertions increase the rate of protease-resistant prion protein formation. Moore RA; Herzog C; Errett J; Kocisko DA; Arnold KM; Hayes SF; Priola SA Protein Sci; 2006 Mar; 15(3):609-19. PubMed ID: 16452616 [TBL] [Abstract][Full Text] [Related]
17. Y145Stop is sufficient to induce de novo generation prions using protein misfolding cyclic amplification. Abdallah A; Wang P; Richt JA; Sreevatsan S Prion; 2012; 6(1):81-8. PubMed ID: 22453182 [TBL] [Abstract][Full Text] [Related]
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20. Amyloid fibrils of human prion protein are spun and woven from morphologically disordered aggregates. Almstedt K; Nyström S; Nilsson KP; Hammarström P Prion; 2009; 3(4):224-35. PubMed ID: 19923901 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]