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Journal Abstract Search


134 related items for PubMed ID: 1320591

  • 21. Modulatory effect of glucans on the functional and biochemical activities of guinea-pig macrophages.
    Ferencík M, Kotulová D, Masler L, Bergendi L, Sandula J, Stefanovic J.
    Methods Find Exp Clin Pharmacol; 1986 Mar; 8(3):163-6. PubMed ID: 3012227
    [Abstract] [Full Text] [Related]

  • 22. Production of prostaglandin E2 and interleukin 1 by mouse peritoneal macrophages stimulated with beta-1,3-D-glucan derivatized plastic beads.
    Rasmussen LT, Lipsky PE, Seljelid R.
    Scand J Immunol; 1987 Dec; 26(6):731-6. PubMed ID: 3501158
    [Abstract] [Full Text] [Related]

  • 23. Endotoxin tolerance from lipopolysaccharide pretreatment induces nuclear factor-kappaB alterations not present in C3H/HeJ mice.
    West MA, Clair L, Kraatz J, Rodriguez JL.
    J Trauma; 2000 Aug; 49(2):298-305. PubMed ID: 10963543
    [Abstract] [Full Text] [Related]

  • 24. Defective tumoricidal capacity of macrophages from C3H/HeJ mice.
    Ruco LP, Meltzer MS.
    J Immunol; 1978 Jan; 120(1):329-34. PubMed ID: 627723
    [Abstract] [Full Text] [Related]

  • 25. Comparative effects of soluble and particulate glucans on survival in irradiated mice.
    Patchen ML, MacVittie TJ.
    J Biol Response Mod; 1986 Feb; 5(1):45-60. PubMed ID: 3958754
    [Abstract] [Full Text] [Related]

  • 26. Temporal sequence of pulmonary cytokine gene expression in response to endotoxin in C3H/HeN endotoxin-sensitive and C3H/HeJ endotoxin-resistant mice.
    Nill MR, Oberyszyn TM, Ross MS, Oberyszyn AS, Robertson FM.
    J Leukoc Biol; 1995 Nov; 58(5):563-74. PubMed ID: 7595058
    [Abstract] [Full Text] [Related]

  • 27. LPS regulation of the immune response: separate mechanisms for murine B cell activation by lipid A (direct) and polysaccharide (macrophage-dependent) derived from Bacteroides LPS.
    Williamson SI, Wannemuehler MJ, Jirillo E, Pritchard DG, Michalek SM, McGhee JR.
    J Immunol; 1984 Nov; 133(5):2294-300. PubMed ID: 6332842
    [Abstract] [Full Text] [Related]

  • 28. Effects of particulate and soluble (1-3)-beta-glucans on Ca2+ influx in NR8383 alveolar macrophages.
    Mörk AC, Helmke RJ, Martinez JR, Michalek MT, Patchen ML, Zhang GH.
    Immunopharmacology; 1998 Jul; 40(1):77-89. PubMed ID: 9776481
    [Abstract] [Full Text] [Related]

  • 29. Stimulation of splenocytes in C3H/HeJ mice with Porphyromonas gingivalis lipid A in comparison with enterobacterial lipid A.
    Ogawa T, Shimauchi H, Uchida H, Mori Y.
    Immunobiology; 1996 Jul; 196(4):399-414. PubMed ID: 9061380
    [Abstract] [Full Text] [Related]

  • 30. 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; 132(4):1702-11. PubMed ID: 6366051
    [Abstract] [Full Text] [Related]

  • 31. Endogenous interferon production by endotoxin-responsive macrophages provides an autostimulatory differentiation signal.
    Vogel SN, Fertsch D.
    Infect Immun; 1984 Aug; 45(2):417-23. PubMed ID: 6378797
    [Abstract] [Full Text] [Related]

  • 32. Refractoriness to migration inhibitory factor of macrophages of LPS nonresponder mouse strains.
    Tagliabue A, McCoy JL, Herberman RB.
    J Immunol; 1978 Oct; 121(4):1223-6. PubMed ID: 359704
    [Abstract] [Full Text] [Related]

  • 33. Differential expression of inducible nitric oxide synthase gene by alveolar and peritoneal macrophages in lipopolysaccharide-hyporesponsive C3H/HeJ mice.
    Wang MJ, Jeng KC, Shih PC.
    Immunology; 1999 Dec; 98(4):497-503. PubMed ID: 10594680
    [Abstract] [Full Text] [Related]

  • 34. Quantitative aspects of lipopolysaccharide and cytokine requirements to generate nitric oxide in macrophages from LPS-hyporesponsive (Lps(d)) C3H/HeJ mice.
    Kmonícková E, Zídek Z.
    Folia Microbiol (Praha); 2004 Dec; 49(6):737-44. PubMed ID: 15881412
    [Abstract] [Full Text] [Related]

  • 35. Response of C3H/HeJ and C3H/HeN mice and their peritoneal macrophages to the toxicity of Chlamydia psittaci elementary bodies.
    Ivins BE, Wyrick PB.
    Infect Immun; 1978 Nov; 22(2):620-2. PubMed ID: 730377
    [Abstract] [Full Text] [Related]

  • 36. Difference in susceptibility to gram-negative urinary tract infection between C3H/HeJ and C3H/HeN mice.
    Hagberg L, Hull R, Hull S, McGhee JR, Michalek SM, Svanborg Edén C.
    Infect Immun; 1984 Dec; 46(3):839-44. PubMed ID: 6389367
    [Abstract] [Full Text] [Related]

  • 37. LPS regulation of the immune response: Bacteroides endotoxin induces mitogenic, polyclonal, and antibody responses in classical LPS responsive but not C3H/HeJ mice.
    Wannemuehler MJ, Michalek SM, Jirillo E, Williamson SI, Hirasawa M, McGhee JR.
    J Immunol; 1984 Jul; 133(1):299-305. PubMed ID: 6202784
    [Abstract] [Full Text] [Related]

  • 38. Hemopoietic effects of intravenous soluble glucan administration.
    Patchen ML, MacVittie TJ.
    J Immunopharmacol; 1986 Jul; 8(3):407-25. PubMed ID: 3760593
    [Abstract] [Full Text] [Related]

  • 39. Effects of various inhibitors of arachidonic acid oxygenation on macrophage superoxide release and tumoricidal activity.
    Schultz RM, Nanda SK, Altom MG.
    J Immunol; 1985 Sep; 135(3):2040-4. PubMed ID: 2991375
    [Abstract] [Full Text] [Related]

  • 40. Bacterial lipopolysaccharides, phorbol myristate acetate, and zymosan induce the myristoylation of specific macrophage proteins.
    Aderem AA, Keum MM, Pure E, Cohn ZA.
    Proc Natl Acad Sci U S A; 1986 Aug; 83(16):5817-21. PubMed ID: 3461461
    [Abstract] [Full Text] [Related]


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