These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 304417)

  • 21. Cellular requirements for lipopolysaccharide adjuvanticity. A role for both T lymphocytes and macrophages for in vitro responses to particulate antigens.
    McGhee JR; Farrar JJ; Michalek SM; Mergenhagen SE; Rosenstreich DL
    J Exp Med; 1979 Apr; 149(4):793-807. PubMed ID: 372482
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Biological effects of Escherichia coli lipopolysaccharide (LPS) in vivo. II. Selection in the mouse thymus of PHA- and con A-responsive cells.
    Adorini L; Ruco L; Uccini S; De Franceschi GS; Baroni CD; Doria G
    Immunology; 1976 Aug; 31(2):225-32. PubMed ID: 783042
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Modification of lipopolysaccharide non-responder cells in low cell density culture.
    Ishizaka S
    Immunol Lett; 1983 Jun; 6(6):343-50. PubMed ID: 6195102
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The effects of LPS on the cellular composition of the splenic white pulp in responder C3H/He and non-responder C3H/HeJ mice.
    Groeneveld PH; Koopman G; van Rooijen N
    Virchows Arch B Cell Pathol Incl Mol Pathol; 1985; 49(2):183-93. PubMed ID: 2866627
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Macrophage stimulation by bacterial lipopolysaccharides. III. Selective unresponsiveness of C3H/HeJ macrophages to the lipid A differentiation signal.
    Doe WF; Henson PM
    J Immunol; 1979 Nov; 123(5):2304-10. PubMed ID: 385780
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Comparison of thymocyte and T lymphocyte gangliosides from C3H/HeN and C3H/HeJ mice.
    Yohe HC; Cuny CL; Berenson CS; Ryan JL
    J Leukoc Biol; 1988 Dec; 44(6):521-8. PubMed ID: 3264007
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Lipopolysaccharide nonresponder cells: the C3H/HeJ defect.
    Sultzer BM; Castagna R; Bandekar J; Wong P
    Immunobiology; 1993 Apr; 187(3-5):257-71. PubMed ID: 8330899
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Endotoxin-induced interferon-gamma production in culture cells derived from BCG-infected C3H/HeJ mice.
    Matsumura H; Nakano M
    J Immunol; 1988 Jan; 140(2):494-500. PubMed ID: 3121747
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Partial restoration of the lipopolysaccharide-induced proliferative response in splenic B cells from C3H/HeJ mice.
    Kuus-Reichel K; Ulevitch RJ
    J Immunol; 1986 Jul; 137(2):472-7. PubMed ID: 3487572
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Action of endotoxin on lymphoid cells.
    Rosenstreich DL; Glode LM; Mergenhagen SE
    J Infect Dis; 1977 Aug; 136 Suppl():S239-45. PubMed ID: 302290
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Genetic control of responses to bacterial lipopolysaccharides in mice. I. Evidence for a single gene that influences mitogenic and immunogenic respones to lipopolysaccharides.
    Watson J; Riblet R
    J Exp Med; 1974 Nov; 140(5):1147-61. PubMed ID: 4138849
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The membrane potential of lymphocytes changes only in response to specific stimulation.
    Kiefer H; Schulze R
    Biosci Rep; 1982 Aug; 2(8):583-8. PubMed ID: 7139073
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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; 33(3):165-74. PubMed ID: 6834360
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Isolation of a lipid A bound polypeptide responsible for "LPS-initiated" mitogenesis of C3H/HeJ spleen cells.
    Morrison DC; Betz SJ; Jacobs DM
    J Exp Med; 1976 Sep; 144(3):840-6. PubMed ID: 182900
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Structural and genetic basis of the in vivo immune response to TNP-LPS.
    Jacobs DM
    J Immunol; 1975 Oct; 115(4):988-92. PubMed ID: 1100725
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mitogenic response of C3H/HeJ mouse lymphocytes to polyanionic polysaccharides obtained from Bordetella pertussis endotoxin and from other bacterial species.
    Girard R; Chaby R; Bordenave G
    Infect Immun; 1981 Jan; 31(1):122-8. PubMed ID: 6260659
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Con-A-activated T cells secrete factors with polyclonal B-cell-activating properties.
    Primi D; Hammarström L; Möller G; Smith CI; Uhr J
    Scand J Immunol; 1979; 9(5):467-75. PubMed ID: 88758
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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; 117(6):2061-6. PubMed ID: 792337
    [TBL] [Abstract][Full Text] [Related]  

  • 40. C3H/HeJ mice are refractory to lipopolysaccharide in the brain.
    Johnson RW; Gheusi G; Segreti S; Dantzer R; Kelley KW
    Brain Res; 1997 Mar; 752(1-2):219-26. PubMed ID: 9106460
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.