136 related articles for article (PubMed ID: 9195875)
1. Kinetics and mechanism of amyloid formation by the prion protein H1 peptide as determined by time-dependent ESR.
Lundberg KM; Stenland CJ; Cohen FE; Prusiner SB; Millhauser GL
Chem Biol; 1997 May; 4(5):345-55. PubMed ID: 9195875
[TBL] [Abstract][Full Text] [Related]
2. Location of the cross-β structure in prion fibrils: A search by seeding and electron spin resonance spectroscopy.
Chu BK; Tsai RF; Hung CL; Kuo YH; Chen EH; Chiang YW; Chan SI; Chen RP
Protein Sci; 2022 Jun; 31(6):e4326. PubMed ID: 35634767
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Conformational plasticity of the Gerstmann-Sträussler-Scheinker disease peptide as indicated by its multiple aggregation pathways.
Natalello A; Prokorov VV; Tagliavini F; Morbin M; Forloni G; Beeg M; Manzoni C; Colombo L; Gobbi M; Salmona M; Doglia SM
J Mol Biol; 2008 Sep; 381(5):1349-61. PubMed ID: 18619462
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Quantitative analysis of spin exchange interactions to identify β strand and turn regions in Ure2 prion domain fibrils with site-directed spin labeling.
Ngo S; Chiang V; Guo Z
J Struct Biol; 2012 Nov; 180(2):374-81. PubMed ID: 22967940
[TBL] [Abstract][Full Text] [Related]
7. X-ray diffraction analysis of scrapie prion: intermediate and folded structures in a peptide containing two putative alpha-helices.
Inouye H; Kirschner DA
J Mol Biol; 1997 May; 268(2):375-89. PubMed ID: 9159477
[TBL] [Abstract][Full Text] [Related]
8. Critical region for amyloid fibril formation of mouse prion protein: unusual amyloidogenic properties of the helix 2 peptide.
Yamaguchi K; Matsumoto T; Kuwata K
Biochemistry; 2008 Dec; 47(50):13242-51. PubMed ID: 19053276
[TBL] [Abstract][Full Text] [Related]
9. Dissection of conformational conversion events during prion amyloid fibril formation using hydrogen exchange and mass spectrometry.
Singh J; Udgaonkar JB
J Mol Biol; 2013 Sep; 425(18):3510-21. PubMed ID: 23811055
[TBL] [Abstract][Full Text] [Related]
10. Structures of amyloid fibrils formed by the prion protein derived peptides PrP(244-249) and PrP(245-250).
Yau J; Sharpe S
J Struct Biol; 2012 Nov; 180(2):290-302. PubMed ID: 22929126
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. The role of hydrophobic interactions in amyloidogenesis: example of prion-related polypeptides.
Tcherkasskaya O; Sanders W; Chynwat V; Davidson EA; Orser CS
J Biomol Struct Dyn; 2003 Dec; 21(3):353-65. PubMed ID: 14616031
[TBL] [Abstract][Full Text] [Related]
13. High pressure induces scrapie-like prion protein misfolding and amyloid fibril formation.
Torrent J; Alvarez-Martinez MT; Harricane MC; Heitz F; Liautard JP; Balny C; Lange R
Biochemistry; 2004 Jun; 43(22):7162-70. PubMed ID: 15170353
[TBL] [Abstract][Full Text] [Related]
14. Evidence for stepwise formation of amyloid fibrils by the mouse prion protein.
Jain S; Udgaonkar JB
J Mol Biol; 2008 Oct; 382(5):1228-41. PubMed ID: 18687339
[TBL] [Abstract][Full Text] [Related]
15. Predicted alpha-helical regions of the prion protein when synthesized as peptides form amyloid.
Gasset M; Baldwin MA; Lloyd DH; Gabriel JM; Holtzman DM; Cohen F; Fletterick R; Prusiner SB
Proc Natl Acad Sci U S A; 1992 Nov; 89(22):10940-4. PubMed ID: 1438300
[TBL] [Abstract][Full Text] [Related]
16. 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; 9(11):e113238. PubMed ID: 25401497
[TBL] [Abstract][Full Text] [Related]
17. Mechanisms of prion protein assembly into amyloid.
Stöhr J; Weinmann N; Wille H; Kaimann T; Nagel-Steger L; Birkmann E; Panza G; Prusiner SB; Eigen M; Riesner D
Proc Natl Acad Sci U S A; 2008 Feb; 105(7):2409-14. PubMed ID: 18268326
[TBL] [Abstract][Full Text] [Related]
18. Diversity of kinetic pathways in amyloid fibril formation.
Bellesia G; Shea JE
J Chem Phys; 2009 Sep; 131(11):111102. PubMed ID: 19778093
[TBL] [Abstract][Full Text] [Related]
19. The N-terminal region of non-A beta component of Alzheimer's disease amyloid is responsible for its tendency to assume beta-sheet and aggregate to form fibrils.
El-Agnaf OM; Bodles AM; Guthrie DJ; Harriott P; Irvine GB
Eur J Biochem; 1998 Nov; 258(1):157-63. PubMed ID: 9851705
[TBL] [Abstract][Full Text] [Related]
20. Prion protein peptides induce alpha-helix to beta-sheet conformational transitions.
Nguyen J; Baldwin MA; Cohen FE; Prusiner SB
Biochemistry; 1995 Apr; 34(13):4186-92. PubMed ID: 7703230
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]