BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

103 related articles for article (PubMed ID: 15031284)

  • 21. 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]  

  • 22. 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]  

  • 23. Cell Biology of Prion Protein.
    Sarnataro D; Pepe A; Zurzolo C
    Prog Mol Biol Transl Sci; 2017; 150():57-82. PubMed ID: 28838675
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A role for His155 in binding of human prion peptide144-167 to immobilised prion protein.
    Hesp JR; Raven ND; Sutton JM
    Biochem Biophys Res Commun; 2007 Oct; 362(3):695-9. PubMed ID: 17761148
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Aggregation and fibrillization of prions in lipid membranes.
    Kazlauskaite J; Pinheiro TJ
    Biochem Soc Symp; 2005; (72):211-22. PubMed ID: 15649144
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prion protein-related proteins from zebrafish are complex glycosylated and contain a glycosylphosphatidylinositol anchor.
    Miesbauer M; Bamme T; Riemer C; Oidtmann B; Winklhofer KF; Baier M; Tatzelt J
    Biochem Biophys Res Commun; 2006 Mar; 341(1):218-24. PubMed ID: 16414019
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. Structural dependence of the cellular isoform of prion protein on solvent: spectroscopic characterization of an intermediate conformation.
    Pergami P; Bramanti E; Ascoli GA
    Biochem Biophys Res Commun; 1999 Nov; 264(3):972-8. PubMed ID: 10544040
    [TBL] [Abstract][Full Text] [Related]  

  • 30. PrP Knockout Cells Expressing Transmembrane PrP Resist Prion Infection.
    Marshall KE; Hughson A; Vascellari S; Priola SA; Sakudo A; Onodera T; Baron GS
    J Virol; 2017 Jan; 91(2):. PubMed ID: 27847358
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Functionally relevant domains of the prion protein identified in vivo.
    Baumann F; Pahnke J; Radovanovic I; Rülicke T; Bremer J; Tolnay M; Aguzzi A
    PLoS One; 2009 Sep; 4(9):e6707. PubMed ID: 19738901
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Seeded conversion of recombinant prion protein to a disulfide-bonded oligomer by a reduction-oxidation process.
    Lee S; Eisenberg D
    Nat Struct Biol; 2003 Sep; 10(9):725-30. PubMed ID: 12897768
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Membrane interactions and conformational preferences of human and avian prion N-terminal tandem repeats: the role of copper(II) ions, pH, and membrane mimicking environments.
    Di Natale G; Pappalardo G; Milardi D; Sciacca MF; Attanasio F; La Mendola D; Rizzarelli E
    J Phys Chem B; 2010 Nov; 114(43):13830-8. PubMed ID: 20936829
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. In vitro amplification of scrapie and chronic wasting disease PrP(res) using baculovirus-expressed recombinant PrP as substrate.
    Faburay B; Tark D; Kanthasamy AG; Richt JA
    Prion; 2014; 8(6):393-403. PubMed ID: 25495764
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Binding of prion protein to lipid membranes and implications for prion conversion.
    Sanghera N; Pinheiro TJ
    J Mol Biol; 2002 Feb; 315(5):1241-56. PubMed ID: 11827491
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Studies on the putative interactions between the organophosphorus insecticide Phosmet and recombinant mouse PrP and its implication in the BSE epidemic.
    Shaw I; Berry C; Lane E; Fitzmaurice P; Clarke D; Holden A
    Vet Res Commun; 2002 Jun; 26(4):263-71. PubMed ID: 12184497
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The effect of disease-associated mutations on the folding pathway of human prion protein.
    Apetri AC; Surewicz K; Surewicz WK
    J Biol Chem; 2004 Apr; 279(17):18008-14. PubMed ID: 14761942
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Folding and intrinsic stability of deletion variants of PrP(121-231), the folded C-terminal domain of the prion protein.
    Eberl H; Glockshuber R
    Biophys Chem; 2002 May; 96(2-3):293-303. PubMed ID: 12034448
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Recombinant human prion protein fragment 90-231, a useful model to study prion neurotoxicity.
    Corsaro A; Thellung S; Villa V; Nizzari M; Aceto A; Florio T
    OMICS; 2012; 16(1-2):50-9. PubMed ID: 22321015
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.