BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

287 related articles for article (PubMed ID: 30336980)

  • 1. A valine-to-lysine substitution at position 210 induces structural conversion of prion protein into a β-sheet rich oligomer.
    Kakuda K; Yamaguchi KI; Kuwata K; Honda R
    Biochem Biophys Res Commun; 2018 Nov; 506(1):81-86. PubMed ID: 30336980
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Residue-specific mobility changes in soluble oligomers of the prion protein define regions involved in aggregation.
    Glaves JP; Ladner-Keay CL; Bjorndahl TC; Wishart DS; Sykes BD
    Biochim Biophys Acta Proteins Proteom; 2018 Sep; 1866(9):982-988. PubMed ID: 29935976
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 412(4):660-73. PubMed ID: 21839748
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A Promising Antiprion Trimethoxychalcone Binds to the Globular Domain of the Cellular Prion Protein and Changes Its Cellular Location.
    Ferreira NC; Ascari LM; Hughson AG; Cavalheiro GR; Góes CF; Fernandes PN; Hollister JR; da Conceição RA; Silva DS; Souza AMT; Barbosa MLC; Lara FA; Martins RAP; Caughey B; Cordeiro Y
    Antimicrob Agents Chemother; 2018 Feb; 62(2):. PubMed ID: 29133563
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Atomic insights into the effects of pathological mutants through the disruption of hydrophobic core in the prion protein.
    Lee J; Chang I; Yu W
    Sci Rep; 2019 Dec; 9(1):19144. PubMed ID: 31844149
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Method for Folding of Recombinant Prion Protein to Soluble β-Sheet Secondary Structure.
    Ellett LJ
    Methods Mol Biol; 2017; 1658():23-26. PubMed ID: 28861779
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9.
    Eraña H; Fernández-Borges N; Elezgarai SR; Harrathi C; Charco JM; Chianini F; Dagleish MP; Ortega G; Millet Ó; Castilla J
    J Virol; 2017 Dec; 91(24):. PubMed ID: 28978705
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Proline and lysine residues provide modulatory switches in amyloid formation: Insights from prion protein.
    Kraus A
    Prion; 2016; 10(1):57-62. PubMed ID: 26864641
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Thermodynamic characterization for the denatured state of bovine prion protein and the BSE Associated variant E211K.
    Hwang S; Nicholson EM
    Prion; 2018; 12(5-6):301-309. PubMed ID: 30354921
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evidence for a central role of PrP helix 2 in the nucleation of amyloid fibrils.
    Honda R; Kuwata K
    FASEB J; 2018 Jul; 32(7):3641-3652. PubMed ID: 29401635
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Biochemical Analysis of Interaction between Kringle Domains of Plasminogen and Prion Proteins with Q167R Mutation.
    Lee J; Lee BW; Kang HE; Choe KK; Kwon M; Ryou C
    J Microbiol Biotechnol; 2017 May; 27(5):1023-1031. PubMed ID: 28274104
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The G127V variant of the prion protein interferes with dimer formation in vitro but not in cellulo.
    Sangeetham SB; Engelke AD; Fodor E; Krausz SL; Tatzelt J; Welker E
    Sci Rep; 2021 Feb; 11(1):3116. PubMed ID: 33542378
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Analysis of Prion Protein Conformation Using Circular Dichroism Spectroscopy.
    Ellett LJ; Johanssen VA
    Methods Mol Biol; 2017; 1658():27-34. PubMed ID: 28861780
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Disassociation of β1-α1-β2 from the α2-α3 domain of prion protein (PrP) is a prerequisite for the conformational conversion of PrP
    Chandrasekaran P; Santosh Kumar C; Rangachari K; Sekar K
    Int J Biol Macromol; 2019 Sep; 136():368-376. PubMed ID: 31207327
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The role of the unusual threonine string in the conversion of prion protein.
    Abskharon R; Wang F; Vander Stel KJ; Sinniah K; Ma J
    Sci Rep; 2016 Dec; 6():38877. PubMed ID: 27982059
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.