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Journal Abstract Search

63 related items for PubMed ID: 7684329

  • 1. Increased proliferative capacity of CD4+ and CD8+ T lymphocytes from mutant sphha/sphha mice is associated with increased IL-2 receptor expression.
    Maggio-Price L, Grossmann A, Shiota F, Engel D.
    Cell Immunol; 1993 May; 148(2):346-56. PubMed ID: 7684329
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  • 2. Maturational changes in CD4+ cell subsets and lymphokine production in BXSB mice.
    Chu EB, Ernst DN, Hobbs MV, Weigle WO.
    J Immunol; 1994 Apr 15; 152(8):4129-38. PubMed ID: 7511669
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  • 3. Differences in the expression profiles of CD45RB, Pgp-1, and 3G11 membrane antigens and in the patterns of lymphokine secretion by splenic CD4+ T cells from young and aged mice.
    Ernst DN, Hobbs MV, Torbett BE, Glasebrook AL, Rehse MA, Bottomly K, Hayakawa K, Hardy RR, Weigle WO.
    J Immunol; 1990 Sep 01; 145(5):1295-302. PubMed ID: 1974562
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  • 4. Direct effects of IL-10 on subsets of human CD4+ T cell clones and resting T cells. Specific inhibition of IL-2 production and proliferation.
    de Waal Malefyt R, Yssel H, de Vries JE.
    J Immunol; 1993 Jun 01; 150(11):4754-65. PubMed ID: 7684412
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  • 5. T cell deletion induced by chronic infection with mouse mammary tumor virus spares a CD25-positive, IL-10-producing T cell population with infectious capacity.
    Papiernik M, do Carmo Leite-de-MoraesM, Pontoux C, Joret AM, Rocha B, Penit C, Dy M.
    J Immunol; 1997 May 15; 158(10):4642-53. PubMed ID: 9144476
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  • 6. Distinct signal transduction in mouse CD4+ and CD8+ splenic T cells after CD28 receptor ligation.
    Abe R, Vandenberghe P, Craighead N, Smoot DS, Lee KP, June CH.
    J Immunol; 1995 Feb 01; 154(3):985-97. PubMed ID: 7822814
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  • 7. The expression of CD45RB on antigen-responsive CD4+ lymphocytes: mouse strain polymorphism and different responses to distinct antigens.
    Gahring LC, Ernst DN, Romball CG, Thoman ML, Torbett BE, Hobbs M, Weigle WO.
    Cell Immunol; 1993 May 01; 148(2):269-82. PubMed ID: 7684327
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  • 10. A distinct role for ICOS-mediated co-stimulatory signaling in CD4+ and CD8+ T cell subsets.
    Watanabe M, Hara Y, Tanabe K, Toma H, Abe R.
    Int Immunol; 2005 Mar 01; 17(3):269-78. PubMed ID: 15668466
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  • 11. Human gamma delta T cell subset-proliferative response to malarial antigen in vitro depends on CD4+ T cells or cytokines that signal through components of the IL-2R.
    Elloso MM, van der Heyde HC, Troutt A, Manning DD, Weidanz WP.
    J Immunol; 1996 Sep 01; 157(5):2096-102. PubMed ID: 8757332
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  • 12. Plasmodium yoelii in mice: antigen reactivity of CD4- and CD8-bearing T cells.
    Lucas B, Engel A, Camus D, Haque A.
    Cell Immunol; 1993 Aug 01; 150(1):59-71. PubMed ID: 8102089
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  • 13. Functional similarity and differences between selection-independent CD4-CD8- alphabeta T cells and positively selected CD8 T cells expressing the same TCR and the induction of anergy in CD4-CD8- alphabeta T cells in antigen-expressing mice.
    Caveno J, Zhang Y, Motyka B, Teh SJ, Teh HS.
    J Immunol; 1999 Aug 01; 163(3):1222-9. PubMed ID: 10415017
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  • 14. CD4+CD8- T cells are the effector cells in disease pathogenesis in the scurfy (sf) mouse.
    Blair PJ, Bultman SJ, Haas JC, Rouse BT, Wilkinson JE, Godfrey VL.
    J Immunol; 1994 Oct 15; 153(8):3764-74. PubMed ID: 7930593
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  • 17. CD8+ T-cell subsets defined by expression of CD45 isoforms differ in their capacity to produce IL-2, IFN-gamma and TNF-beta.
    Adamthwaite D, Cooley MA.
    Immunology; 1994 Feb 15; 81(2):253-60. PubMed ID: 7908892
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