These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

226 related articles for article (PubMed ID: 16314415)

  • 1. Annealing prion protein amyloid fibrils at high temperature results in extension of a proteinase K-resistant core.
    Bocharova OV; Makarava N; Breydo L; Anderson M; Salnikov VV; Baskakov IV
    J Biol Chem; 2006 Jan; 281(4):2373-9. PubMed ID: 16314415
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Two amyloid States of the prion protein display significantly different folding patterns.
    Ostapchenko VG; Sawaya MR; Makarava N; Savtchenko R; Nilsson KP; Eisenberg D; Baskakov IV
    J Mol Biol; 2010 Jul; 400(4):908-21. PubMed ID: 20553730
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pathway complexity of prion protein assembly into amyloid.
    Baskakov IV; Legname G; Baldwin MA; Prusiner SB; Cohen FE
    J Biol Chem; 2002 Jun; 277(24):21140-8. PubMed ID: 11912192
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Scrapie-infected cells, isolated prions, and recombinant prion protein: a comparative study.
    Kneipp J; Miller LM; Spassov S; Sokolowski F; Lasch P; Beekes M; Naumann D
    Biopolymers; 2004 May-Jun 5; 74(1-2):163-7. PubMed ID: 15137116
    [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 conversion of full-length mammalian prion protein produces amyloid form with physical properties of PrP(Sc).
    Bocharova OV; Breydo L; Parfenov AS; Salnikov VV; Baskakov IV
    J Mol Biol; 2005 Feb; 346(2):645-59. PubMed ID: 15670611
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dual nature of the infectious prion protein revealed by high pressure.
    Garcia AF; Heindl P; Voigt H; Büttner M; Butz P; Tauber N; Tauscher B; Pfaff E
    J Biol Chem; 2005 Mar; 280(11):9842-7. PubMed ID: 15598650
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An engineered PrPsc-like molecule from the chimera of mammalian prion protein and yeast Ure2p prion-inducing domain.
    Yin SM; Sy MS; Po T
    Acta Biochim Biophys Sin (Shanghai); 2004 Feb; 36(2):128-32. PubMed ID: 14970909
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Self-Replication of Prion Protein Fragment 89-230 Amyloid Fibrils Accelerated by Prion Protein Fragment 107-143 Aggregates.
    Sneideris T; Ziaunys M; Chu BK; Chen RP; Smirnovas V
    Int J Mol Sci; 2020 Oct; 21(19):. PubMed ID: 33049945
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prion protein amyloid formation under native-like conditions involves refolding of the C-terminal alpha-helical domain.
    Cobb NJ; Apetri AC; Surewicz WK
    J Biol Chem; 2008 Dec; 283(50):34704-11. PubMed ID: 18930924
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Conformational change, aggregation and fibril formation induced by detergent treatments of cellular prion protein.
    Xiong LW; Raymond LD; Hayes SF; Raymond GJ; Caughey B
    J Neurochem; 2001 Nov; 79(3):669-78. PubMed ID: 11701770
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Amyloid fibrils from the N-terminal prion protein fragment are infectious.
    Choi JK; Cali I; Surewicz K; Kong Q; Gambetti P; Surewicz WK
    Proc Natl Acad Sci U S A; 2016 Nov; 113(48):13851-13856. PubMed ID: 27849581
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Structural polymorphism in amyloids: new insights from studies with Y145Stop prion protein fibrils.
    Jones EM; Wu B; Surewicz K; Nadaud PS; Helmus JJ; Chen S; Jaroniec CP; Surewicz WK
    J Biol Chem; 2011 Dec; 286(49):42777-42784. PubMed ID: 22002245
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Conformational stability of PrP amyloid fibrils controls their smallest possible fragment size.
    Sun Y; Makarava N; Lee CI; Laksanalamai P; Robb FT; Baskakov IV
    J Mol Biol; 2008 Feb; 376(4):1155-67. PubMed ID: 18206163
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 44(48):15880-8. PubMed ID: 16313190
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Copper(II) inhibits in vitro conversion of prion protein into amyloid fibrils.
    Bocharova OV; Breydo L; Salnikov VV; Baskakov IV
    Biochemistry; 2005 May; 44(18):6776-87. PubMed ID: 15865423
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Conformational switching within individual amyloid fibrils.
    Makarava N; Ostapchenko VG; Savtchenko R; Baskakov IV
    J Biol Chem; 2009 May; 284(21):14386-95. PubMed ID: 19329794
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Fibril conformation as the basis of species- and strain-dependent seeding specificity of mammalian prion amyloids.
    Jones EM; Surewicz WK
    Cell; 2005 Apr; 121(1):63-72. PubMed ID: 15820679
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.