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5. The role of prion peptide structure and aggregation in toxicity and membrane binding. Rymer DL; Good TA J Neurochem; 2000 Dec; 75(6):2536-45. PubMed ID: 11080207 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. In vitro evaluation of the anti-prionic activity of newly synthesized congo red derivatives. Poli G; Ponti W; Carcassola G; Ceciliani F; Colombo L; Dall'Ara P; Gervasoni M; Giannino ML; Martino PA; Pollera C; Villa S; Salmona M Arzneimittelforschung; 2003; 53(12):875-88. PubMed ID: 14750496 [TBL] [Abstract][Full Text] [Related]
8. Conformational polymorphism of the amyloidogenic peptide homologous to residues 113-127 of the prion protein. Satheeshkumar KS; Jayakumar R Biophys J; 2003 Jul; 85(1):473-83. PubMed ID: 12829502 [TBL] [Abstract][Full Text] [Related]
9. Molecular determinants of the physicochemical properties of a critical prion protein region comprising residues 106-126. Salmona M; Malesani P; De Gioia L; Gorla S; Bruschi M; Molinari A; Della Vedova F; Pedrotti B; Marrari MA; Awan T; Bugiani O; Forloni G; Tagliavini F Biochem J; 1999 Aug; 342 ( Pt 1)(Pt 1):207-14. PubMed ID: 10432318 [TBL] [Abstract][Full Text] [Related]
10. A neurotoxic and gliotrophic fragment of the prion protein increases plasma membrane microviscosity. Salmona M; Forloni G; Diomede L; Algeri M; De Gioia L; Angeretti N; Giaccone G; Tagliavini F; Bugiani O Neurobiol Dis; 1997; 4(1):47-57. PubMed ID: 9258911 [TBL] [Abstract][Full Text] [Related]
11. The 118-135 peptide of the human prion protein forms amyloid fibrils and induces liposome fusion. Pillot T; Lins L; Goethals M; Vanloo B; Baert J; Vandekerckhove J; Rosseneu M; Brasseur R J Mol Biol; 1997 Dec; 274(3):381-93. PubMed ID: 9405147 [TBL] [Abstract][Full Text] [Related]
12. Molecular properties of complexes formed between the prion protein and synthetic peptides. Kaneko K; Wille H; Mehlhorn I; Zhang H; Ball H; Cohen FE; Baldwin MA; Prusiner SB J Mol Biol; 1997 Jul; 270(4):574-86. PubMed ID: 9245588 [TBL] [Abstract][Full Text] [Related]
13. Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitro. Tagliavini F; Prelli F; Verga L; Giaccone G; Sarma R; Gorevic P; Ghetti B; Passerini F; Ghibaudi E; Forloni G Proc Natl Acad Sci U S A; 1993 Oct; 90(20):9678-82. PubMed ID: 8105481 [TBL] [Abstract][Full Text] [Related]
14. Core structure of amyloid fibrils formed by residues 106-126 of the human prion protein. Walsh P; Simonetti K; Sharpe S Structure; 2009 Mar; 17(3):417-26. PubMed ID: 19278656 [TBL] [Abstract][Full Text] [Related]
15. A scrapie-like unfolding intermediate of the prion protein domain PrP(121-231) induced by acidic pH. Hornemann S; Glockshuber R Proc Natl Acad Sci U S A; 1998 May; 95(11):6010-4. PubMed ID: 9600908 [TBL] [Abstract][Full Text] [Related]