250 related articles for article (PubMed ID: 7829969)
1. Macrophages derived from C3H/HeJ (Lpsd) mice respond to bacterial lipopolysaccharide by activating NF-kappa B.
Ding A; Hwang S; Lander HM; Xie QW
J Leukoc Biol; 1995 Jan; 57(1):174-9. PubMed ID: 7829969
[TBL] [Abstract][Full Text] [Related]
2. Paradoxical preservation of a lipopolysaccharide response in C3H/HeJ macrophages: induction of matrix metalloproteinase-9.
Jin F; Nathan CF; Ding A
J Immunol; 1999 Mar; 162(6):3596-600. PubMed ID: 10092819
[TBL] [Abstract][Full Text] [Related]
3. 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
[TBL] [Abstract][Full Text] [Related]
4. Endotoxin-induced early gene expression in C3H/HeJ (Lpsd) macrophages.
Manthey CL; Perera PY; Henricson BE; Hamilton TA; Qureshi N; Vogel SN
J Immunol; 1994 Sep; 153(6):2653-63. PubMed ID: 7521367
[TBL] [Abstract][Full Text] [Related]
5. Effects of different biological response modifiers on interferon expression in bacterial lipopolysaccharide (LPS)-responsive and LPS-hyporesponsive mouse peritoneal macrophages.
Di Marzio P; Gessani S; Locardi C; Borghi P; Baglioni C; Belardelli F
J Gen Virol; 1990 Nov; 71 ( Pt 11)():2585-91. PubMed ID: 1701475
[TBL] [Abstract][Full Text] [Related]
6. TNF-alpha gene expression in macrophages: regulation by NF-kappa B is independent of c-Jun or C/EBP beta.
Liu H; Sidiropoulos P; Song G; Pagliari LJ; Birrer MJ; Stein B; Anrather J; Pope RM
J Immunol; 2000 Apr; 164(8):4277-85. PubMed ID: 10754326
[TBL] [Abstract][Full Text] [Related]
7. Conserved kappa B element located downstream of the tumor necrosis factor alpha gene: distinct NF-kappa B binding pattern and enhancer activity in LPS activated murine macrophages.
Kuprash DV; Udalova IA; Turetskaya RL; Rice NR; Nedospasov SA
Oncogene; 1995 Jul; 11(1):97-106. PubMed ID: 7624137
[TBL] [Abstract][Full Text] [Related]
8. Toxoplasma gondii soluble antigen induces a subset of lipopolysaccharide-inducible genes and tyrosine phosphoproteins in peritoneal macrophages.
Li ZY; Manthey CL; Perera PY; Sher A; Vogel SN
Infect Immun; 1994 Aug; 62(8):3434-40. PubMed ID: 8039914
[TBL] [Abstract][Full Text] [Related]
9. Defective ceramide response in C3H/HeJ (Lpsd) macrophages.
Barber SA; Perera PY; Vogel SN
J Immunol; 1995 Sep; 155(5):2303-5. PubMed ID: 7650365
[TBL] [Abstract][Full Text] [Related]
10. Role of transcription factor NF-kappa B/Rel in induction of nitric oxide synthase.
Xie QW; Kashiwabara Y; Nathan C
J Biol Chem; 1994 Feb; 269(7):4705-8. PubMed ID: 7508926
[TBL] [Abstract][Full Text] [Related]
11. Differential activation of murine macrophages by angelan and LPS.
Jeon YJ; Han SB; Ahn KS; Kim HM
Immunopharmacology; 2000 Sep; 49(3):275-84. PubMed ID: 10996025
[TBL] [Abstract][Full Text] [Related]
12. Activation of NF-kappa B in murine macrophages by taxol.
Hwang S; Ding A
Cancer Biochem Biophys; 1995 Jan; 14(4):265-72. PubMed ID: 7767900
[TBL] [Abstract][Full Text] [Related]
13. Radicicol suppresses expression of inducible nitric-oxide synthase by blocking p38 kinase and nuclear factor-kappaB/Rel in lipopolysaccharide-stimulated macrophages.
Jeon YJ; Kim YK; Lee M; Park SM; Han SB; Kim HM
J Pharmacol Exp Ther; 2000 Aug; 294(2):548-54. PubMed ID: 10900231
[TBL] [Abstract][Full Text] [Related]
14. Susceptibility of lipopolysaccharide-responsive and -hyporesponsive ItyS Mice to infection with rough mutants of Salmonella typhimurium.
Mattsby-Baltzer I; Ahlström B; Edebo L; de Man P
Infect Immun; 1996 Apr; 64(4):1321-7. PubMed ID: 8606096
[TBL] [Abstract][Full Text] [Related]
15. Attenuation of inducible nitric oxide synthase gene expression by delta 9-tetrahydrocannabinol is mediated through the inhibition of nuclear factor- kappa B/Rel activation.
Jeon YJ; Yang KH; Pulaski JT; Kaminski NE
Mol Pharmacol; 1996 Aug; 50(2):334-41. PubMed ID: 8700141
[TBL] [Abstract][Full Text] [Related]
16. Two forms of NF-kappa B1 (p105/p50) in murine macrophages: differential regulation by lipopolysaccharide, interleukin-2, and interferon-gamma.
Brown MC; Tomaras GD; Vincenti MP; Taffet SM
J Interferon Cytokine Res; 1997 May; 17(5):295-306. PubMed ID: 9181468
[TBL] [Abstract][Full Text] [Related]
17. Detection and analysis of the 80-kd lipopolysaccharide receptor in macrophages derived from Lpsn and Lpsd mice.
Perera PY; Chan TY; Morrison DC; Vogel SN
J Leukoc Biol; 1992 May; 51(5):501-6. PubMed ID: 1376353
[TBL] [Abstract][Full Text] [Related]
18. Macrophage defect and inflammatory cell recruitment dysfunction in Salmonella susceptible C3H/HeJ mice.
Weinstein DL; Lissner CR; Swanson RN; O'Brien AD
Cell Immunol; 1986 Oct; 102(1):68-77. PubMed ID: 3542230
[TBL] [Abstract][Full Text] [Related]
19. 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; 141(12):4196-202. PubMed ID: 3143760
[TBL] [Abstract][Full Text] [Related]
20. Correlation between the lipopolysaccharide response of mice and the capacity of mouse peritoneal cells to transfer an antiviral state. Role of endogenous interferon.
Gessani S; Belardelli F; Borghi P; Boraschi D; Gresser I
J Immunol; 1987 Sep; 139(6):1991-8. PubMed ID: 3040861
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]