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259 related items for PubMed ID: 3876285
1. Functional role of interleukin 1 in periodontal disease: induction of interleukin 1 production by Bacteroides gingivalis lipopolysaccharide in peritoneal macrophages from C3H/HeN and C3H/HeJ mice. Hanazawa S, Nakada K, Ohmori Y, Miyoshi T, Amano S, Kitano S. Infect Immun; 1985 Oct; 50(1):262-70. PubMed ID: 3876285 [Abstract] [Full Text] [Related]
2. 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]
3. 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]
4. Serological properties and immunobiological activities of lipopolysaccharides from black-pigmented and related oral Bacteroides species. Fujiwara T, Nishihara T, Koga T, Hamada S. J Gen Microbiol; 1988 Nov; 134(11):2867-76. PubMed ID: 3151207 [Abstract] [Full Text] [Related]
5. Lack of responsiveness of C3H/HeJ macrophages to lipopolysaccharide: the cellular basis of LPS-stimulated metabolism. Ryan JL, Glode LM, Rosenstreich DL. J Immunol; 1979 Mar; 122(3):932-5. PubMed ID: 376709 [Abstract] [Full Text] [Related]
9. Lipopolysaccharides (LPS) of oral black-pigmented bacteria induce tumor necrosis factor production by LPS-refractory C3H/HeJ macrophages in a way different from that of Salmonella LPS. Kirikae T, Nitta T, Kirikae F, Suda Y, Kusumoto S, Qureshi N, Nakano M. Infect Immun; 1999 Apr; 67(4):1736-42. PubMed ID: 10085012 [Abstract] [Full Text] [Related]
12. [Mitogenic activity of lipopolysaccharide from Bacteroides intermedius against C3H/HeJ mice spleen cells]. Yamamoto M, Ono K, Mochizuki S, Nishihara Y, Makimura M, Otake S. Nichidai Koko Kagaku; 1990 Sep; 16(3):332-9. PubMed ID: 2134944 [Abstract] [Full Text] [Related]
13. Biochemical and immunobiological properties of lipopolysaccharide (LPS) from Bacteroides gingivalis and comparison with LPS from Escherichia coli. Koga T, Nishihara T, Fujiwara T, Nisizawa T, Okahashi N, Noguchi T, Hamada S. Infect Immun; 1985 Mar; 47(3):638-47. PubMed ID: 3882561 [Abstract] [Full Text] [Related]
14. The induction of polyclonal B-cell activation and interleukin-1 production by the 75-kDa cell surface protein from Porphyromonas gingivalis in mice. Watanabe K, Kumada H, Yoshimura F, Umemoto T. Arch Oral Biol; 1996 Mar; 41(8-9):725-31. PubMed ID: 9022909 [Abstract] [Full Text] [Related]
15. Defective production of interleukin 6 by macrophages from C3H/HeJ mice: differential stimulation of interleukin 1 and interleukin 6 induction. Sarih M, Souvannavong V, Adam A. Immunol Lett; 1991 Sep; 30(1):69-74. PubMed ID: 1959943 [Abstract] [Full Text] [Related]
16. Bacteroides (Porphyromonas) gingivalis fimbriae activate mouse peritoneal macrophages and induce gene expression and production of interleukin-1. Hanazawa S, Murakami Y, Hirose K, Amano S, Ohmori Y, Higuchi H, Kitano S. Infect Immun; 1991 Jun; 59(6):1972-7. PubMed ID: 1709918 [Abstract] [Full Text] [Related]
17. 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]