BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

72 related articles for article (PubMed ID: 8913775)

  • 21. Microglial cells qualify as the stimulators of unprimed CD4+ and CD8+ T lymphocytes in the central nervous system.
    Cash E; Rott O
    Clin Exp Immunol; 1994 Nov; 98(2):313-8. PubMed ID: 7955538
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Direct activation of innate and antigen-presenting functions of microglia following infection with Theiler's virus.
    Olson JK; Girvin AM; Miller SD
    J Virol; 2001 Oct; 75(20):9780-9. PubMed ID: 11559811
    [TBL] [Abstract][Full Text] [Related]  

  • 23. CD28, IL-2-independent costimulatory pathways for CD8 T lymphocyte activation.
    Sepulveda H; Cerwenka A; Morgan T; Dutton RW
    J Immunol; 1999 Aug; 163(3):1133-42. PubMed ID: 10415007
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A subset of mouse splenic macrophages can constitutively present alloantigen directly to CD8+ T cells.
    McCormack JM; Sun D; Walker WS
    J Immunol; 1991 Jul; 147(2):421-7. PubMed ID: 1677021
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Purified MHC class I and peptide complexes activate naive CD8+ T cells independently of the CD28/B7 and LFA-1/ICAM-1 costimulatory interactions.
    Goldstein JS; Chen T; Brunswick M; Mostowsky H; Kozlowski S
    J Immunol; 1998 Apr; 160(7):3180-7. PubMed ID: 9531273
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Proliferation of human T lymphocytes induced with superantigens is not dependent on costimulation by the CD28 counter-receptor B7.
    Damle NK; Klussman K; Leytze G; Linsley PS
    J Immunol; 1993 Feb; 150(3):726-35. PubMed ID: 7678619
    [TBL] [Abstract][Full Text] [Related]  

  • 27. CTLA-4 and CD28 mRNA are coexpressed in most T cells after activation. Expression of CTLA-4 and CD28 mRNA does not correlate with the pattern of lymphokine production.
    Freeman GJ; Lombard DB; Gimmi CD; Brod SA; Lee K; Laning JC; Hafler DA; Dorf ME; Gray GS; Reiser H
    J Immunol; 1992 Dec; 149(12):3795-801. PubMed ID: 1281186
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Costimulatory effect of IL-12 on the activation of naive, memory CD4+ T cells, and Th1 clone.
    Kato T; Morokata T; Igarashi O; Yee ST; Inobe M; Uede T; Azuma M; Okumura K; Nariuchi H
    Cell Immunol; 1997 Feb; 176(1):50-8. PubMed ID: 9070317
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The B7/BB1 antigen provides one of several costimulatory signals for the activation of CD4+ T lymphocytes by human blood dendritic cells in vitro.
    Young JW; Koulova L; Soergel SA; Clark EA; Steinman RM; Dupont B
    J Clin Invest; 1992 Jul; 90(1):229-37. PubMed ID: 1378854
    [TBL] [Abstract][Full Text] [Related]  

  • 30. CD80 (B7) and CD86 (B70) provide similar costimulatory signals for T cell proliferation, cytokine production, and generation of CTL.
    Lanier LL; O'Fallon S; Somoza C; Phillips JH; Linsley PS; Okumura K; Ito D; Azuma M
    J Immunol; 1995 Jan; 154(1):97-105. PubMed ID: 7527824
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Heterogeneity of mouse brain macrophages in alloantigen presentation to naive CD8+ T cells as revealed by a panel of microglial cell lines.
    Askew D; Havenith CE; Walker WS
    Immunobiology; 1996 Oct; 195(4-5):417-30. PubMed ID: 8933148
    [No Abstract]   [Full Text] [Related]  

  • 32. Expression of costimulatory molecules in the bovine corpus luteum.
    Cannon MJ; Davis JS; Pate JL
    Reprod Biol Endocrinol; 2007 Jan; 5():5. PubMed ID: 17266770
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Regulation of CD80/B7-1 and CD86/B7-2 molecule expression in human primary acute myeloid leukemia and their role in allogenic immune recognition.
    Costello RT; Mallet F; Sainty D; Maraninchi D; Gastaut JA; Olive D
    Eur J Immunol; 1998 Jan; 28(1):90-103. PubMed ID: 9485189
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Major histocompatibility antigen class II expressing resting porcine T lymphocytes are potent antigen-presenting cells in mixed leukocyte culture.
    Saalmüller A; Maurer S
    Immunobiology; 1994 Feb; 190(1-2):23-34. PubMed ID: 8082885
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Neonatal and adult microglia cross-present exogenous antigens.
    Beauvillain C; Donnou S; Jarry U; Scotet M; Gascan H; Delneste Y; Guermonprez P; Jeannin P; Couez D
    Glia; 2008 Jan; 56(1):69-77. PubMed ID: 17932942
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Separate precursor cells for macrophages and microglia in mouse brain: immunophenotypic and immunoregulatory properties of the progeny.
    Walker WS
    J Neuroimmunol; 1999 Feb; 94(1-2):127-33. PubMed ID: 10376945
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Regional oral tolerance in transgenic 2C mice.
    Margenthaler JA; Flye MW
    Surgery; 2005 Aug; 138(2):141-9. PubMed ID: 16153420
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Psoriatic skin-derived dendritic cell function is inhibited by exogenous IL-10. Differential modulation of B7-1 (CD80) and B7-2 (CD86) expression.
    Mitra RS; Judge TA; Nestle FO; Turka LA; Nickoloff BJ
    J Immunol; 1995 Mar; 154(6):2668-77. PubMed ID: 7533180
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Inhibition of alloantigen-primed memory CD4+ and CD8+ T cells by hematopoietic chimerism in mice.
    Lan T; Chen J; Xia J; Wang Y; Xie B; Wang F; Qi Z
    Scand J Immunol; 2010 Aug; 72(2):86-93. PubMed ID: 20618766
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification and characterization of intestinal Peyer's patch interferon-alpha producing (plasmacytoid) dendritic cells.
    Castellaneta A; Abe M; Morelli AE; Thomson AW
    Hum Immunol; 2004 Feb; 65(2):104-13. PubMed ID: 14969765
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.