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Journal Abstract Search

230 related items for PubMed ID: 7527440

  • 1. Characterization of a granule-independent lytic mechanism used by CTL hybridomas.
    Garner R, Helgason CD, Atkinson EA, Pinkoski MJ, Ostergaard HL, Sorensen O, Fu A, Lapchak PH, Rabinovitch A, McElhaney JE.
    J Immunol; 1994 Dec 15; 153(12):5413-21. PubMed ID: 7527440
    [Abstract] [Full Text] [Related]

  • 2. The role of the Fas lytic pathway in a perforin-less CTL hybridoma.
    Walsh CM, Glass AA, Chiu V, Clark WR.
    J Immunol; 1994 Sep 15; 153(6):2506-14. PubMed ID: 7521365
    [Abstract] [Full Text] [Related]

  • 3. Mechanism of lymphocyte-mediated cytolysis: functional cytolytic T cells lacking perforin and granzymes.
    Berke G, Rosen D, Ronen D.
    Immunology; 1993 Jan 15; 78(1):105-12. PubMed ID: 8436395
    [Abstract] [Full Text] [Related]

  • 4. Multiple cytolytic mechanisms displayed by activated human peripheral blood T cell subsets.
    Smyth MJ, Norihisa Y, Ortaldo JR.
    J Immunol; 1992 Jan 01; 148(1):55-62. PubMed ID: 1345790
    [Abstract] [Full Text] [Related]

  • 5. An anergic cytotoxic T lymphocyte clone exhibits granule exocytosis-mediated cytotoxicity.
    Kuwano K, Akashi A, Arai S.
    Cell Immunol; 1998 May 01; 185(2):114-22. PubMed ID: 9636689
    [Abstract] [Full Text] [Related]

  • 6. Highly lytic in vivo primed cytolytic T lymphocytes devoid of lytic granules and BLT-esterase activity acquire these constituents in the presence of T cell growth factors upon blast transformation in vitro.
    Berke G, Rosen D.
    J Immunol; 1988 Sep 01; 141(5):1429-36. PubMed ID: 3261748
    [Abstract] [Full Text] [Related]

  • 7. Inhibition of CPP32-like proteases prevents granzyme B- and Fas-, but not granzyme A-based cytotoxicity exerted by CTL clones.
    Anel A, Gamen S, Alava MA, Schmitt-Verhulst AM, Piñeiro A, Naval J.
    J Immunol; 1997 Mar 01; 158(5):1999-2006. PubMed ID: 9036942
    [Abstract] [Full Text] [Related]

  • 8. Concanamycin A, a powerful tool for characterization and estimation of contribution of perforin- and Fas-based lytic pathways in cell-mediated cytotoxicity.
    Kataoka T, Shinohara N, Takayama H, Takaku K, Kondo S, Yonehara S, Nagai K.
    J Immunol; 1996 May 15; 156(10):3678-86. PubMed ID: 8621902
    [Abstract] [Full Text] [Related]

  • 9. Involvement of granule proteins in T-cell-mediated cytolysis.
    Krähenbühl O, Tschopp J.
    Nat Immun Cell Growth Regul; 1990 May 15; 9(4):274-82. PubMed ID: 2215515
    [Abstract] [Full Text] [Related]

  • 10. The requirements for triggering of lysis by cytolytic T lymphocyte clones. II. Cyclosporin A inhibits TCR-mediated exocytosis by only selectively inhibits TCR-mediated lytic activity by cloned CTL.
    Lancki DW, Kaper BP, Fitch FW.
    J Immunol; 1989 Jan 15; 142(2):416-24. PubMed ID: 2492047
    [Abstract] [Full Text] [Related]

  • 11. Human purified protein derivative-specific CD4+ T cells use both CD95-dependent and CD95-independent cytolytic mechanisms.
    Lewinsohn DM, Bement TT, Xu J, Lynch DH, Grabstein KH, Reed SG, Alderson MR.
    J Immunol; 1998 Mar 01; 160(5):2374-9. PubMed ID: 9498779
    [Abstract] [Full Text] [Related]

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  • 13. Cytolytic T-cell cytotoxicity is mediated through perforin and Fas lytic pathways.
    Lowin B, Hahne M, Mattmann C, Tschopp J.
    Nature; 1994 Aug 25; 370(6491):650-2. PubMed ID: 7520535
    [Abstract] [Full Text] [Related]

  • 14. Independent roles of perforin, granzymes, and Fas in the control of Friend retrovirus infection.
    Zelinskyy G, Balkow S, Schimmer S, Schepers K, Simon MM, Dittmer U.
    Virology; 2004 Dec 20; 330(2):365-74. PubMed ID: 15567431
    [Abstract] [Full Text] [Related]

  • 15. Comparing the relative role of perforin/granzyme versus Fas/Fas ligand cytotoxic pathways in CD8+ T cell-mediated insulin-dependent diabetes mellitus.
    Kreuwel HT, Morgan DJ, Krahl T, Ko A, Sarvetnick N, Sherman LA.
    J Immunol; 1999 Oct 15; 163(8):4335-41. PubMed ID: 10510373
    [Abstract] [Full Text] [Related]

  • 16. An ovalbumin peptide-specific cytotoxic T cell clone with antigen self-presentation capacity uses two distinct mechanisms to kill target cells.
    Dick T, Reichmann G, Ebnet K, Simon MM, Dienes HP, Echternacher B, Krammer PH, Reske-Kunz AB.
    Cell Immunol; 1993 Dec 15; 152(2):333-47. PubMed ID: 8258142
    [Abstract] [Full Text] [Related]

  • 17. Perforin, Fas/Fas ligand, and TNF-alpha pathways as specific and bystander killing mechanisms of hepatitis C virus-specific human CTL.
    Ando K, Hiroishi K, Kaneko T, Moriyama T, Muto Y, Kayagaki N, Yagita H, Okumura K, Imawari M.
    J Immunol; 1997 Jun 01; 158(11):5283-91. PubMed ID: 9164947
    [Abstract] [Full Text] [Related]

  • 18. In vivo rejection of tumor cells dependent on CD8 cells that kill independently of perforin and FasL.
    Lee SH, Bar-Haim E, Machlenkin A, Goldberger O, Volovitz I, Vadai E, Tzehoval E, Eisenbach L.
    Cancer Gene Ther; 2004 Mar 01; 11(3):237-48. PubMed ID: 14739939
    [Abstract] [Full Text] [Related]

  • 19. Transfection of mouse cytotoxic T lymphocyte with an antisense granzyme A vector reduces lytic activity.
    Talento A, Nguyen M, Law S, Wu JK, Poe M, Blake JT, Patel M, Wu TJ, Manyak CL, Silberklang M.
    J Immunol; 1992 Dec 15; 149(12):4009-15. PubMed ID: 1460287
    [Abstract] [Full Text] [Related]

  • 20. Caspase dependence of target cell damage induced by cytotoxic lymphocytes.
    Sarin A, Haddad EK, Henkart PA.
    J Immunol; 1998 Sep 15; 161(6):2810-6. PubMed ID: 9743340
    [Abstract] [Full Text] [Related]

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