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975 related items for PubMed ID: 9045912
1. MRL/lpr CD4- CD8- and CD8+ T cells, respectively, mediate Fas-dependent and perforin cytotoxic pathways. Benihoud K, Bonardelle D, Bobé P, Kiger N. Eur J Immunol; 1997 Feb; 27(2):415-20. PubMed ID: 9045912 [Abstract] [Full Text] [Related]
2. 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]
3. Origin of CD4-CD8-B220+ T cells in MRL-lpr/lpr mice. Clues from a T cell receptor beta transgenic mouse. Zhou T, Bluethmann H, Eldridge J, Berry K, Mountz JD. J Immunol; 1993 Apr 15; 150(8 Pt 1):3651-67. PubMed ID: 7682246 [Abstract] [Full Text] [Related]
4. B lymphocytes mediate Fas-dependent cytotoxicity in MRL/lpr mice. Bonardelle D, Benihoud K, Kiger N, Bobé P. J Leukoc Biol; 2005 Nov 15; 78(5):1052-9. PubMed ID: 16204618 [Abstract] [Full Text] [Related]
5. Identification of a population of CD4+ CTL that utilizes a perforin- rather than a Fas ligand-dependent cytotoxic mechanism. Williams NS, Engelhard VH. J Immunol; 1996 Jan 01; 156(1):153-9. PubMed ID: 8598456 [Abstract] [Full Text] [Related]
6. Differential expression of Fas and Fas ligand in acute and chronic graft-versus-host disease: up-regulation of Fas and Fas ligand requires CD8+ T cell activation and IFN-gamma production. Shustov A, Nguyen P, Finkelman F, Elkon KB, Via CS. J Immunol; 1998 Sep 15; 161(6):2848-55. PubMed ID: 9743345 [Abstract] [Full Text] [Related]
7. Human melanoma-reactive CD4+ and CD8+ CTL clones resist Fas ligand-induced apoptosis and use Fas/Fas ligand-independent mechanisms for tumor killing. Rivoltini L, Radrizzani M, Accornero P, Squarcina P, Chiodoni C, Mazzocchi A, Castelli C, Tarsini P, Viggiano V, Belli F, Colombo MP, Parmiani G. J Immunol; 1998 Aug 01; 161(3):1220-30. PubMed ID: 9686582 [Abstract] [Full Text] [Related]
8. Effector cells derived from host CD8 memory T cells mediate rapid resistance against minor histocompatibility antigen-mismatched allogeneic marrow grafts without participation of perforin, Fas ligand, and the simultaneous inhibition of 3 tumor necrosis factor family effector pathways. Zimmerman Z, Shatry A, Deyev V, Podack E, Mammolenti M, Blazar BR, Yagita H, Levy RB. Biol Blood Marrow Transplant; 2005 Aug 01; 11(8):576-86. PubMed ID: 16041307 [Abstract] [Full Text] [Related]
9. Elucidation of the protein kinase C-dependent apoptosis pathway in distinct subsets of T lymphocytes in MRL-lpr/lpr mice. Ohkusu K, Isobe K, Hidaka H, Nakashima I. Eur J Immunol; 1995 Nov 01; 25(11):3180-6. PubMed ID: 7489761 [Abstract] [Full Text] [Related]
10. Differential antitumor effects of administration of recombinant IL-18 or recombinant IL-12 are mediated primarily by Fas-Fas ligand- and perforin-induced tumor apoptosis, respectively. Hashimoto W, Osaki T, Okamura H, Robbins PD, Kurimoto M, Nagata S, Lotze MT, Tahara H. J Immunol; 1999 Jul 15; 163(2):583-9. PubMed ID: 10395644 [Abstract] [Full Text] [Related]
11. Cyclosporine-insensitive partial signaling and multiple roles of Ca2+ in Fas ligand-induced lysis. Rogers AM, Thilenius AR, Russell JH. J Immunol; 1997 Oct 01; 159(7):3140-7. PubMed ID: 9317111 [Abstract] [Full Text] [Related]
12. Perforin-dependent cytotoxic activity and lymphokine secretion by CD4+ T cells are regulated by CD8+ T cells. Williams NS, Engelhard VH. J Immunol; 1997 Sep 01; 159(5):2091-9. PubMed ID: 9278294 [Abstract] [Full Text] [Related]
13. Two types of anti-TL (thymus leukemia) CTL clones with distinct target specificities: differences in cytotoxic mechanisms and accessory molecule requirements. Tsujimura K, Takahashi T, Iwase S, Matsudaira Y, Kaneko Y, Yagita H, Obata Y. J Immunol; 1998 Jun 01; 160(11):5253-61. PubMed ID: 9605121 [Abstract] [Full Text] [Related]
14. 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]
15. Evidence of alternative or concomitant use of perforin- and Fas-dependent pathways in a T cell-mediated negative regulation of Ig production. Majlessi L, Bordenave G. J Immunol; 1999 Apr 15; 162(8):4391-8. PubMed ID: 10201974 [Abstract] [Full Text] [Related]
16. Evidence for the involvement of Fas ligand and perforin in the induction of vascular leak syndrome. Rafi AQ, Zeytun A, Bradley MJ, Sponenberg DP, Grayson RL, Nagarkatti M, Nagarkatti PS. J Immunol; 1998 Sep 15; 161(6):3077-86. PubMed ID: 9743374 [Abstract] [Full Text] [Related]
17. Tumor regression after adoptive transfer of effector T cells is independent of perforin or Fas ligand (APO-1L/CD95L). Winter H, Hu HM, Urba WJ, Fox BA. J Immunol; 1999 Oct 15; 163(8):4462-72. PubMed ID: 10510388 [Abstract] [Full Text] [Related]
18. 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]
19. Suppression of immune responses by CD8 cells. I. Superantigen-activated CD8 cells induce unidirectional Fas-mediated apoptosis of antigen-activated CD4 cells. Noble A, Pestano GA, Cantor H. J Immunol; 1998 Jan 15; 160(2):559-65. PubMed ID: 9551888 [Abstract] [Full Text] [Related]
20. Veto activity of activated bone marrow does not require perforin and Fas ligand. Chrobak P, Gress RE. Cell Immunol; 2001 Mar 15; 208(2):80-7. PubMed ID: 11333140 [Abstract] [Full Text] [Related] Page: [Next] [New Search]