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420 related items for PubMed ID: 299760

  • 21. Mitogenic activity of Actinomyces viscosus. I. Effects on murine B and T lymphocytes, and partial characterization.
    Engel D, Clagett J, Page R, Williams B.
    J Immunol; 1977 Apr; 118(4):1466-71. PubMed ID: 66295
    [Abstract] [Full Text] [Related]

  • 22. Calcium ionophore A23187 does not stimulate lipopolysaccharide nonresponsive C3H/HeJ peritoneal macrophages to produce interleukin 1.
    Shinomiya H, Nakano M.
    J Immunol; 1987 Oct 15; 139(8):2730-6. PubMed ID: 3116092
    [Abstract] [Full Text] [Related]

  • 23. Genetic and biochemical evidence for the involvement of a bacterial component in the mitogenic properties of polyribonucleotides on murine B lymphocytes.
    Kelly K, Watson J.
    J Immunol; 1979 Jun 15; 122(6):2304-8. PubMed ID: 312865
    [Abstract] [Full Text] [Related]

  • 24. Induction of phenotypic lymphocyte differentiation in LPS unresponsive mice by an LPS-induced serum factor and by lipid A-associated protein.
    Koenig S, Hoffmann MK, Thomas L.
    J Immunol; 1977 May 15; 118(5):1910-1. PubMed ID: 192800
    [Abstract] [Full Text] [Related]

  • 25. The activation of tumoricidal properties in macrophages of endotoxin responder and nonresponder mice by liposome-encapsulated immunomodulators.
    Fogler WE, Talmadge JE, Fidler IJ.
    J Reticuloendothel Soc; 1983 Mar 15; 33(3):165-74. PubMed ID: 6834360
    [Abstract] [Full Text] [Related]

  • 26. Murine immune responses to Salmonella lipopolysaccharide: oral administration of whole bacteria to C3H/HeJ mice induces secondary anti-LPS responses, especially of the IgA isotype.
    Jirillo E, Kiyono H, Michalek SM, McGhee JR.
    J Immunol; 1984 Apr 15; 132(4):1702-11. PubMed ID: 6366051
    [Abstract] [Full Text] [Related]

  • 27. Staphylococcal enterotoxin B induces hepatic injury and lethal shock in endotoxin-resistant C3H/HeJ mice despite a deficient macrophage response.
    Yasuda S, Nagaki M, Moriwaki H.
    J Endotoxin Res; 2002 Apr 15; 8(4):253-61. PubMed ID: 12230915
    [Abstract] [Full Text] [Related]

  • 28. Production of tumor necrosis factor by rIFN-gamma-primed C3H/HeJ (Lpsd) macrophages requires the presence of lipid A-associated proteins.
    Hogan MM, Vogel SN.
    J Immunol; 1988 Dec 15; 141(12):4196-202. PubMed ID: 3143760
    [Abstract] [Full Text] [Related]

  • 29. The lipid A moiety of Porphyromonas gingivalis lipopolysaccharide specifically mediates the activation of C3H/HeJ mice.
    Tanamoto K, Azumi S, Haishima Y, Kumada H, Umemoto T.
    J Immunol; 1997 May 01; 158(9):4430-6. PubMed ID: 9127008
    [Abstract] [Full Text] [Related]

  • 30. Lipid A-associated proteins provide an alternate "second signal" in the activation of recombinant interferon-gamma-primed, C3H/HeJ macrophages to a fully tumoricidal state.
    Hogan MM, Vogel SN.
    J Immunol; 1987 Dec 01; 139(11):3697-702. PubMed ID: 3119714
    [Abstract] [Full Text] [Related]

  • 31. Genetic control of B cell activation by bacterial lipopolysaccharide is mediated by multiple distinct genes or alleles.
    Glode LM, Rosenstreich DL.
    J Immunol; 1976 Dec 01; 117(6):2061-6. PubMed ID: 792337
    [Abstract] [Full Text] [Related]

  • 32. Genetical control of B-cell responses. III. Requirement for functional mitogenicity of the antigen in thymus-independent specific responses.
    Coutinho A, Gronowicz E.
    J Exp Med; 1975 Apr 01; 141(4):753-60. PubMed ID: 1092788
    [Abstract] [Full Text] [Related]

  • 33. Brucella abortus lipopolysaccharide is mitogenic for spleen cells of endotoxin-resistant C3H/HeJ mice.
    Moreno E, Berman DT.
    J Immunol; 1979 Dec 01; 123(6):2915-9. PubMed ID: 115923
    [Abstract] [Full Text] [Related]

  • 34. Role of acyl residues in polyclonal murine B cell activation by acylpoly(1,3)galactosides from Klebsiella pneumoniae.
    Hmama Z, Lina G, Normier G, Binz H, Revillard JP.
    J Immunol; 1993 Nov 15; 151(10):5440-9. PubMed ID: 8228237
    [Abstract] [Full Text] [Related]

  • 35. Restoration of LPS responsiveness of C3H/HeJ mouse lymphocytes by microinjection of cytoplasmic factor(s) from LPS-stimulated normal lymphocytes.
    Eda Y, Ohara J, Watanabe T.
    J Immunol; 1983 Sep 15; 131(3):1294-9. PubMed ID: 6604094
    [Abstract] [Full Text] [Related]

  • 36. Electrokinetic properties of splenic lymphocytes from the low-lipopolysaccharide responder C3H/Hej mice.
    Dumont F, Barrois R.
    Folia Biol (Praha); 1976 Sep 15; 12(3):145-50. PubMed ID: 1086804
    [Abstract] [Full Text] [Related]

  • 37. Correlation of the biologic responses of C3H/HEJ mice to endotoxin with the chemical and structural properties of the lipopolysaccharides from Pseudomonas aeruginosa and Escherichia coli.
    Pier GB, Markham RB, Eardley D.
    J Immunol; 1981 Jul 15; 127(1):184-91. PubMed ID: 6787121
    [Abstract] [Full Text] [Related]

  • 38. Relationship between immune system and gram-negative bacteria. IV. T lymphocytes from Lpsd mice possess binding site(s) for Rb Salmonella.
    Jirillo E, Antonaci S, Kiyono H, Michalek SM, McGhee JR.
    J Immunol; 1985 Nov 15; 135(5):3473-8. PubMed ID: 3876386
    [Abstract] [Full Text] [Related]

  • 39. Endotoxin-induced T lymphocyte proliferation.
    Vogel SN, Hilfiker ML, Caulfield MJ.
    J Immunol; 1983 Apr 15; 130(4):1774-9. PubMed ID: 6601137
    [Abstract] [Full Text] [Related]

  • 40. Genetic control of lymphocyte activation: lack of response to low doses of concanavalin A in lipopolysaccharide-nonresponder mice.
    Bick PH, Persson U, Smith E, Möller E, Hammarström L.
    J Exp Med; 1977 Oct 01; 146(4):1146-51. PubMed ID: 330792
    [Abstract] [Full Text] [Related]

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