BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 9383432)

  • 1. Theoretical studies of sequence effects on the conformational properties of a fragment of the prion protein: implications for scrapie formation.
    Kazmirski SL; Alonso DO; Cohen FE; Prusiner SB; Daggett V
    Chem Biol; 1995 May; 2(5):305-15. PubMed ID: 9383432
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Abnormalities in stress proteins in prion diseases.
    Tatzelt J; Voellmy R; Welch WJ
    Cell Mol Neurobiol; 1998 Dec; 18(6):721-9. PubMed ID: 9876878
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic and infectious prion diseases.
    Prusiner SB
    Arch Neurol; 1993 Nov; 50(11):1129-53. PubMed ID: 8105771
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A synthetic peptide initiates Gerstmann-Sträussler-Scheinker (GSS) disease in transgenic mice.
    Kaneko K; Ball HL; Wille H; Zhang H; Groth D; Torchia M; Tremblay P; Safar J; Prusiner SB; DeArmond SJ; Baldwin MA; Cohen FE
    J Mol Biol; 2000 Jan; 295(4):997-1007. PubMed ID: 10656806
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [A trend of molecular genetics on prion diseases and prion protein].
    Muramatsu Y; Shinagawa M
    Nihon Rinsho; 1993 Sep; 51(9):2494-502. PubMed ID: 8411733
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prion encephalopathies of animals and humans.
    Prusiner SB
    Dev Biol Stand; 1993; 80():31-44. PubMed ID: 8270114
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoform.
    Kaneko K; Peretz D; Pan KM; Blochberger TC; Wille H; Gabizon R; Griffith OH; Cohen FE; Baldwin MA; Prusiner SB
    Proc Natl Acad Sci U S A; 1995 Nov; 92(24):11160-4. PubMed ID: 7479957
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prions mediated neurodegenerative disorders.
    Huang WJ; Chen WW; Zhang X
    Eur Rev Med Pharmacol Sci; 2015 Nov; 19(21):4028-34. PubMed ID: 26592824
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular biology and genetics of prion diseases.
    Prusiner SB
    Philos Trans R Soc Lond B Biol Sci; 1994 Mar; 343(1306):447-63. PubMed ID: 7913765
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prion protein amyloidosis.
    Ghetti B; Piccardo P; Frangione B; Bugiani O; Giaccone G; Young K; Prelli F; Farlow MR; Dlouhy SR; Tagliavini F
    Brain Pathol; 1996 Apr; 6(2):127-45. PubMed ID: 8737929
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Comparative computational analysis of prion proteins reveals two fragments with unusual structural properties and a pattern of increase in hydrophobicity associated with disease-promoting mutations.
    Kuznetsov IB; Rackovsky S
    Protein Sci; 2004 Dec; 13(12):3230-44. PubMed ID: 15557265
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Insight into the PrPC-->PrPSc conversion from the structures of antibody-bound ovine prion scrapie-susceptibility variants.
    Eghiaian F; Grosclaude J; Lesceu S; Debey P; Doublet B; Tréguer E; Rezaei H; Knossow M
    Proc Natl Acad Sci U S A; 2004 Jul; 101(28):10254-9. PubMed ID: 15240887
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Integrity of H1 helix in prion protein revealed by molecular dynamic simulations to be especially vulnerable to changes in the relative orientation of H1 and its S1 flank.
    Tseng CY; Yu CP; Lee HC
    Eur Biophys J; 2009 Jun; 38(5):601-11. PubMed ID: 19229533
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Biology and genetics of prion diseases.
    Prusiner SB
    Annu Rev Microbiol; 1994; 48():655-86. PubMed ID: 7826022
    [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]  

  • 16. The role of electrostatic interaction in triggering the unraveling of stable helix 1 in normal prion protein. A molecular dynamics simulation investigation.
    Ji HF; Zhang HY; Shen L
    J Biomol Struct Dyn; 2005 Apr; 22(5):563-70. PubMed ID: 15702928
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular origin of Gerstmann-Sträussler-Scheinker syndrome: insight from computer simulation of an amyloidogenic prion peptide.
    Daidone I; Di Nola A; Smith JC
    Biophys J; 2011 Jun; 100(12):3000-7. PubMed ID: 21689534
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Nucleation-dependent conformational conversion of the Y145Stop variant of human prion protein: structural clues for prion propagation.
    Kundu B; Maiti NR; Jones EM; Surewicz KA; Vanik DL; Surewicz WK
    Proc Natl Acad Sci U S A; 2003 Oct; 100(21):12069-74. PubMed ID: 14519851
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Computational studies on prion proteins: effect of Ala(117)-->Val mutation.
    Okimoto N; Yamanaka K; Suenaga A; Hata M; Hoshino T
    Biophys J; 2002 May; 82(5):2746-57. PubMed ID: 11964260
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Scrapie prions: a three-dimensional model of an infectious fragment.
    Huang Z; Prusiner SB; Cohen FE
    Fold Des; 1996; 1(1):13-9. PubMed ID: 9079359
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.