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Journal Abstract Search

208 related items for PubMed ID: 7561045

  • 1. Sand fly vector saliva selectively modulates macrophage functions that inhibit killing of Leishmania major and nitric oxide production.
    Hall LR, Titus RG.
    J Immunol; 1995 Oct 01; 155(7):3501-6. PubMed ID: 7561045
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  • 2. Phlebotomus papatasi sand fly salivary gland lysate down-regulates a Th1, but up-regulates a Th2, response in mice infected with Leishmania major.
    Mbow ML, Bleyenberg JA, Hall LR, Titus RG.
    J Immunol; 1998 Nov 15; 161(10):5571-7. PubMed ID: 9820534
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  • 3. Mice lacking the TNF receptor p55 fail to resolve lesions caused by infection with Leishmania major, but control parasite replication.
    Vieira LQ, Goldschmidt M, Nashleanas M, Pfeffer K, Mak T, Scott P.
    J Immunol; 1996 Jul 15; 157(2):827-35. PubMed ID: 8752935
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  • 4. Effects of anti-Leishmania monoclonal antibodies on the development of Leishmania major in Phlebotomus duboscqi (Diptera: Psychodidae).
    Anjili C, Langat B, Ngumbi P, Mbati PA, Githure J, Tonui WK.
    East Afr Med J; 2006 Feb 15; 83(2):72-8. PubMed ID: 16708877
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  • 5. Histologic characterization of experimental cutaneous leishmaniasis in mice infected with Leishmania braziliensis in the presence or absence of sand fly vector salivary gland lysate.
    Donnelly KB, Lima HC, Titus RG.
    J Parasitol; 1998 Feb 15; 84(1):97-103. PubMed ID: 9488345
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  • 12. Leishmania major-specific CD8+ T cells are inducers and targets of nitric oxide produced by parasitized macrophages.
    Stefani MM, Müller I, Louis JA.
    Eur J Immunol; 1994 Mar 15; 24(3):746-52. PubMed ID: 7510243
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  • 13. Adenosine, AMP, and protein phosphatase activity in sandfly saliva.
    Katz O, Waitumbi JN, Zer R, Warburg A.
    Am J Trop Med Hyg; 2000 Jan 15; 62(1):145-50. PubMed ID: 10761741
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  • 14. Immunological factors governing resistance and susceptibility of mice to Leishmania major infection.
    Aguilar-Torrentera F, Carlier Y.
    Rev Latinoam Microbiol; 2001 Jan 15; 43(3):135-42. PubMed ID: 17061500
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  • 15. Estimation of the minimum number of Leishmania major amastigotes required for infecting Phlebotomus duboscqi (Diptera: Psychodidae).
    Anjili C, Langat B, Lugalia R, Mwanyumba P, Ngumbi P, Mbati PA, Githure J, Tonui WK.
    East Afr Med J; 2006 Feb 15; 83(2):68-71. PubMed ID: 16708876
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  • 16. Leishmania antigens presented by GM-CSF-derived macrophages protect susceptible mice against challenge with Leishmania major.
    Doherty TM, Coffman RL.
    J Immunol; 1993 Jun 15; 150(12):5476-83. PubMed ID: 8515072
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  • 17. Persistence without pathology in phosphoglycan-deficient Leishmania major.
    Späth GF, Lye LF, Segawa H, Sacks DL, Turco SJ, Beverley SM.
    Science; 2003 Aug 29; 301(5637):1241-3. PubMed ID: 12947201
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  • 19. 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 29; 89(3):221-7. PubMed ID: 12541065
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  • 20. The protective effect against Leishmania infection conferred by sand fly bites is limited to short-term exposure.
    Rohoušová I, Hostomská J, Vlková M, Kobets T, Lipoldová M, Volf P.
    Int J Parasitol; 2011 Apr 29; 41(5):481-5. PubMed ID: 21310158
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