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 *

222 related articles for article (PubMed ID: 7494285)

  • 1. A single hamster PrP amino acid blocks conversion to protease-resistant PrP in scrapie-infected mouse neuroblastoma cells.
    Priola SA; Chesebro B
    J Virol; 1995 Dec; 69(12):7754-8. PubMed ID: 7494285
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Efficient conversion of normal prion protein (PrP) by abnormal hamster PrP is determined by homology at amino acid residue 155.
    Priola SA; Chabry J; Chan K
    J Virol; 2001 May; 75(10):4673-80. PubMed ID: 11312338
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Heterologous PrP molecules interfere with accumulation of protease-resistant PrP in scrapie-infected murine neuroblastoma cells.
    Priola SA; Caughey B; Race RE; Chesebro B
    J Virol; 1994 Aug; 68(8):4873-8. PubMed ID: 7913509
    [TBL] [Abstract][Full Text] [Related]  

  • 4. N-terminal truncation of prion protein affects both formation and conformation of abnormal protease-resistant prion protein generated in vitro.
    Lawson VA; Priola SA; Wehrly K; Chesebro B
    J Biol Chem; 2001 Sep; 276(38):35265-71. PubMed ID: 11466311
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Abnormal properties of prion protein with insertional mutations in different cell types.
    Priola SA; Chesebro B
    J Biol Chem; 1998 May; 273(19):11980-5. PubMed ID: 9565627
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Species specificity in the cell-free conversion of prion protein to protease-resistant forms: a model for the scrapie species barrier.
    Kocisko DA; Priola SA; Raymond GJ; Chesebro B; Lansbury PT; Caughey B
    Proc Natl Acad Sci U S A; 1995 Apr; 92(9):3923-7. PubMed ID: 7732006
    [TBL] [Abstract][Full Text] [Related]  

  • 7. N-terminal truncation of the scrapie-associated form of PrP by lysosomal protease(s): implications regarding the site of conversion of PrP to the protease-resistant state.
    Caughey B; Raymond GJ; Ernst D; Race RE
    J Virol; 1991 Dec; 65(12):6597-603. PubMed ID: 1682507
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Glycosylation influences cross-species formation of protease-resistant prion protein.
    Priola SA; Lawson VA
    EMBO J; 2001 Dec; 20(23):6692-9. PubMed ID: 11726505
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Deletion of beta-strand and alpha-helix secondary structure in normal prion protein inhibits formation of its protease-resistant isoform.
    Vorberg I; Chan K; Priola SA
    J Virol; 2001 Nov; 75(21):10024-32. PubMed ID: 11581371
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Inhibition of protease-resistant prion protein formation by porphyrins and phthalocyanines.
    Caughey WS; Raymond LD; Horiuchi M; Caughey B
    Proc Natl Acad Sci U S A; 1998 Oct; 95(21):12117-22. PubMed ID: 9770449
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Species-independent inhibition of abnormal prion protein (PrP) formation by a peptide containing a conserved PrP sequence.
    Chabry J; Priola SA; Wehrly K; Nishio J; Hope J; Chesebro B
    J Virol; 1999 Aug; 73(8):6245-50. PubMed ID: 10400714
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Specific binding of normal prion protein to the scrapie form via a localized domain initiates its conversion to the protease-resistant state.
    Horiuchi M; Caughey B
    EMBO J; 1999 Jun; 18(12):3193-203. PubMed ID: 10369660
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Interactions between heterologous forms of prion protein: binding, inhibition of conversion, and species barriers.
    Horiuchi M; Priola SA; Chabry J; Caughey B
    Proc Natl Acad Sci U S A; 2000 May; 97(11):5836-41. PubMed ID: 10811921
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prion protein and species barriers in the transmissible spongiform encephalopathies.
    Priola SA
    Biomed Pharmacother; 1999; 53(1):27-33. PubMed ID: 10221165
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cells expressing anchorless prion protein are resistant to scrapie infection.
    McNally KL; Ward AE; Priola SA
    J Virol; 2009 May; 83(9):4469-75. PubMed ID: 19225008
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A 60-kDa prion protein (PrP) with properties of both the normal and scrapie-associated forms of PrP.
    Priola SA; Caughey B; Wehrly K; Chesebro B
    J Biol Chem; 1995 Feb; 270(7):3299-305. PubMed ID: 7852415
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Flexible N-terminal region of prion protein influences conformation of protease-resistant prion protein isoforms associated with cross-species scrapie infection in vivo and in vitro.
    Lawson VA; Priola SA; Meade-White K; Lawson M; Chesebro B
    J Biol Chem; 2004 Apr; 279(14):13689-95. PubMed ID: 14736880
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Normal and scrapie-associated forms of prion protein differ in their sensitivities to phospholipase and proteases in intact neuroblastoma cells.
    Caughey B; Neary K; Buller R; Ernst D; Perry LL; Chesebro B; Race RE
    J Virol; 1990 Mar; 64(3):1093-101. PubMed ID: 1968104
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Scrapie susceptibility-linked polymorphisms modulate the in vitro conversion of sheep prion protein to protease-resistant forms.
    Bossers A; Belt PBGM ; Raymond GJ; Caughey B; de Vries R; Smits MA
    Proc Natl Acad Sci U S A; 1997 May; 94(10):4931-6. PubMed ID: 9144167
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Conversion of raft associated prion protein to the protease-resistant state requires insertion of PrP-res (PrP(Sc)) into contiguous membranes.
    Baron GS; Wehrly K; Dorward DW; Chesebro B; Caughey B
    EMBO J; 2002 Mar; 21(5):1031-40. PubMed ID: 11867531
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.