239 related articles for article (PubMed ID: 18418448)
1. Alteration of superoxide- and nitric oxide-mediated antimicrobial function of macrophages by in vivo cocaine exposure.
Tripathi AK; Rathi N; Suke SG; Banerjee BD; Ahmed RS; Mahajan P; Bhattacharya SK
Can J Physiol Pharmacol; 2008; 86(1-2):64-9. PubMed ID: 18418448
[TBL] [Abstract][Full Text] [Related]
2. Absence of complement receptor 3 results in reduced binding and ingestion of Mycobacterium tuberculosis but has no significant effect on the induction of reactive oxygen and nitrogen intermediates or on the survival of the bacteria in resident and interferon-gamma activated macrophages.
Rooyakkers AW; Stokes RW
Microb Pathog; 2005 Sep; 39(3):57-67. PubMed ID: 16084683
[TBL] [Abstract][Full Text] [Related]
3. Macrophage control of Brucella abortus: role of reactive oxygen intermediates and nitric oxide.
Jiang X; Leonard B; Benson R; Baldwin CL
Cell Immunol; 1993 Oct; 151(2):309-19. PubMed ID: 8402938
[TBL] [Abstract][Full Text] [Related]
4. Macrophage-derived superoxide is not required for nitric oxide mediated tumour cell killing by RAW 264 cells.
Fricker SP; Slade E; Powell NA
Anticancer Res; 1999; 19(1A):553-6. PubMed ID: 10226597
[TBL] [Abstract][Full Text] [Related]
5. Cyclosporin A-mediated killing of Leishmania major by macrophages is independent of reactive nitrogen and endogenous TNF-alpha and is not inhibited by IL-10 and 13.
Meissner U; Jüttner S; Röllinghoff M; Gessner A
Parasitol Res; 2003 Feb; 89(3):221-7. PubMed ID: 12541065
[TBL] [Abstract][Full Text] [Related]
6. Recombinant SSP4 protein from Trypanosoma cruzi amastigotes regulates nitric oxide production by macrophages.
Ramos-Ligonio A; López-Monteon A; Talamás-Rohana P; Rosales-Encina JL
Parasite Immunol; 2004 Oct; 26(10):409-18. PubMed ID: 15752118
[TBL] [Abstract][Full Text] [Related]
7. Changes in mechanisms of monocyte/macrophage-mediated cytotoxicity during culture. Reactive oxygen intermediates are involved in monocyte-mediated cytotoxicity, whereas reactive nitrogen intermediates are employed by macrophages in tumor cell killing.
Martin JH; Edwards SW
J Immunol; 1993 Apr; 150(8 Pt 1):3478-86. PubMed ID: 8385686
[TBL] [Abstract][Full Text] [Related]
8. Synergism in immunotoxicological effects due to repeated combined administration of arsenic and lead in mice.
Bishayi B; Sengupta M
Int Immunopharmacol; 2006 Mar; 6(3):454-64. PubMed ID: 16428081
[TBL] [Abstract][Full Text] [Related]
9. Rosmarinic acid inhibits the formation of reactive oxygen and nitrogen species in RAW264.7 macrophages.
Qiao S; Li W; Tsubouchi R; Haneda M; Murakami K; Takeuchi F; Nisimoto Y; Yoshino M
Free Radic Res; 2005 Sep; 39(9):995-1003. PubMed ID: 16087481
[TBL] [Abstract][Full Text] [Related]
10. iNOS-mediated generation of reactive oxygen and nitrogen species by biomaterial-adherent neutrophils.
Patel JD; Krupka T; Anderson JM
J Biomed Mater Res A; 2007 Feb; 80(2):381-90. PubMed ID: 17001645
[TBL] [Abstract][Full Text] [Related]
11. 3,4-dichloropropionaniline suppresses normal macrophage function.
Ustyugova IV; Frost LL; Van Dyke K; Brundage KM; Schafer R; Barnett JB
Toxicol Sci; 2007 Jun; 97(2):364-74. PubMed ID: 17355946
[TBL] [Abstract][Full Text] [Related]
12. Histone deacetylase inhibitors impair antibacterial defenses of macrophages.
Mombelli M; Lugrin J; Rubino I; Chanson AL; Giddey M; Calandra T; Roger T
J Infect Dis; 2011 Nov; 204(9):1367-74. PubMed ID: 21921209
[TBL] [Abstract][Full Text] [Related]
13. Pharmacological evaluation of anti-leishmanial activity by in vivo nitric oxide modulation in Balb/c mice infected with Leishmania major MRHO/IR/75/ER: an Iranian strain of cutaneous leishmaniasis.
Nahrevanian H; Farahmand M; Aghighi Z; Assmar M; Amirkhani A
Exp Parasitol; 2007 Jul; 116(3):233-40. PubMed ID: 17335813
[TBL] [Abstract][Full Text] [Related]
14. Gene targeting demonstrates that inducible nitric oxide synthase is not essential for resistance to oral candidiasis in mice, or for killing of Candida albicans by macrophages in vitro.
Farah CS; Saunus JM; Hu Y; Kazoullis A; Ashman RB
Oral Microbiol Immunol; 2009 Feb; 24(1):83-8. PubMed ID: 19121076
[TBL] [Abstract][Full Text] [Related]
15. Simultaneous increases in immune-competent cells and nitric oxide in the spleen during Plasmodium berghei infection in mice.
Nahrevanian H; Dascombe MJ
J Microbiol Immunol Infect; 2006 Feb; 39(1):11-7. PubMed ID: 16440118
[TBL] [Abstract][Full Text] [Related]
16. Real-time amperometric analysis of reactive oxygen and nitrogen species released by single immunostimulated macrophages.
Amatore C; Arbault S; Bouton C; Drapier JC; Ghandour H; Koh AC
Chembiochem; 2008 Jun; 9(9):1472-80. PubMed ID: 18491327
[TBL] [Abstract][Full Text] [Related]
17. Emergence of an effective adaptive cell mediated immune response to Mycobacterium leprae is not impaired in reactive oxygen intermediate-deficient mice.
Hagge DA; Marks VT; Ray NA; Dietrich MA; Kearney MT; Scollard DM; Krahenbuhl JL; Adams LB
FEMS Immunol Med Microbiol; 2007 Oct; 51(1):92-101. PubMed ID: 17645529
[TBL] [Abstract][Full Text] [Related]
18. Nitric oxide-mediated augmentation of neutrophil reactive oxygen and nitrogen species formation: Critical use of probes.
Kumar S; Patel S; Jyoti A; Keshari RS; Verma A; Barthwal MK; Dikshit M
Cytometry A; 2010 Nov; 77(11):1038-48. PubMed ID: 20886639
[TBL] [Abstract][Full Text] [Related]
19. Production of nitric oxide elevates nitrosothiol formation resulting in decreased glutathione in macrophages exposed to asbestos or asbestos substitutes.
Nishiike T; Nishimura Y; Wada Y; Iguchi H
Arch Toxicol; 2005 Feb; 79(2):83-9. PubMed ID: 15490125
[TBL] [Abstract][Full Text] [Related]
20. Oxidized low-density lipoprotein depletes PKCalpha and attenuates reactive oxygen species formation in monocytes/macrophages.
Köhl R; Preiss S; von Knethen A; Brüne B
Cardiovasc Res; 2006 Aug; 71(3):574-85. PubMed ID: 16843450
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
