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495 related items for PubMed ID: 7537297

  • 1. In CD8+ T cell-deficient lpr/lpr mice, CD4+B220+ and CD4+B220- T cells replace B220+ double-negative T cells as the predominant populations in enlarged lymph nodes.
    Giese T, Davidson WF.
    J Immunol; 1995 May 15; 154(10):4986-95. PubMed ID: 7537297
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  • 2. Evidence for early onset, polyclonal activation of T cell subsets in mice homozygous for lpr.
    Giese T, Davidson WF.
    J Immunol; 1992 Nov 01; 149(9):3097-106. PubMed ID: 1383337
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  • 3. Chronic treatment of C3H-lpr/lpr and C3H-gld/gld mice with anti-CD8 monoclonal antibody prevents the accumulation of double negative T cells but not autoantibody production.
    Giese T, Davidson WF.
    J Immunol; 1994 Feb 15; 152(4):2000-10. PubMed ID: 8120404
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  • 4. Functionally anergic lpr and gld B220+ T cell receptor (TCR)-alpha/beta+ double-negative T cells express CD28 and respond to costimulation with phorbol myristate acetate and antibodies to CD28 and the TCR.
    Giese T, Allison JP, Davidson WF.
    J Immunol; 1993 Jul 15; 151(2):597-609. PubMed ID: 7687618
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  • 5. Evidence for the existence of two parallel differentiation pathways in the thymus of MRL lpr/lpr mice.
    Matsuzaki Y, Pannetien C, Kanagawa O, Gachelin G, Nakauchi H.
    J Immunol; 1992 Aug 01; 149(3):1069-74. PubMed ID: 1378863
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  • 6. 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
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  • 7. Cytokine secretion by C3H-lpr and -gld T cells. Hypersecretion of IFN-gamma and tumor necrosis factor-alpha by stimulated CD4+ T cells.
    Davidson WF, Calkins C, Hügins A, Giese T, Holmes KL.
    J Immunol; 1991 Jun 15; 146(12):4138-48. PubMed ID: 1674953
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  • 8. Intestinal intraepithelial lymphocyte T cells are resistant to lpr gene-induced T cell abnormalities.
    Aicher WK, Fujihashi K, Taguchi T, McGhee JR, Yamamoto M, Eldridge JH, Gay S, Kiyono H.
    Eur J Immunol; 1992 Jan 15; 22(1):137-45. PubMed ID: 1346108
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  • 13. CD2 expression correlates with proliferative capacity of alpha beta + or gamma delta + CD4-CD8- T cells in lpr mice.
    Budd RC, Russell JQ, van Houten N, Cooper SM, Yagita H, Wolfe J.
    J Immunol; 1992 Feb 15; 148(4):1055-64. PubMed ID: 1346621
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  • 14. The accumulation of B220+ CD4- CD8- (DN) T cells in C3H-lpr/lpr mice is not accelerated by the stimulation of CD8+ T cells or B220+ DN T cells with staphylococcal enterotoxin B and occurs independently of V beta 8+ T cells.
    Giese T, Davidson WF.
    Int Immunol; 1995 Aug 15; 7(8):1213-23. PubMed ID: 7495728
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  • 15. Selection of the T cell receptor repertoire in Lpr mice.
    Herron LR, Eisenberg RA, Roper E, Kakkanaiah VN, Cohen PL, Kotzin BL.
    J Immunol; 1993 Oct 01; 151(7):3450-9. PubMed ID: 8376785
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  • 17. Inhibition of abnormal T cell development and autoimmunity in gld mice by transgenic T cell receptor beta chain.
    Yui K, Bhandoola A, Radic MZ, Komori S, Katsumata M, Greene MI.
    Eur J Immunol; 1992 Jul 01; 22(7):1693-700. PubMed ID: 1385574
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  • 18. A model for the origin of TCR-alphabeta+ CD4-CD8- B220+ cells based on high affinity TCR signals.
    Mixter PF, Russell JQ, Morrissette GJ, Charland C, Aleman-Hoey D, Budd RC.
    J Immunol; 1999 May 15; 162(10):5747-56. PubMed ID: 10229807
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  • 19. Influence of the lpr environment on the lymph node cell phenotypes in C57BL/6 nubg and nulpr chimeras.
    Tiberghien F, Ceredig R, Loor F.
    Immunology; 1994 Dec 15; 83(4):552-61. PubMed ID: 7875735
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