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303 related items for PubMed ID: 15882412

  • 1. LmxPK4, a mitogen-activated protein kinase kinase homologue of Leishmania mexicana with a potential role in parasite differentiation.
    Kuhn D, Wiese M.
    Mol Microbiol; 2005 Jun; 56(5):1169-82. PubMed ID: 15882412
    [Abstract] [Full Text] [Related]

  • 2. The Leishmania mexicana A600 genes are functionally required for amastigote replication.
    Murray AS, Lynn MA, McMaster WR.
    Mol Biochem Parasitol; 2010 Aug; 172(2):80-9. PubMed ID: 20307588
    [Abstract] [Full Text] [Related]

  • 3. Leishmania: overexpression and comparative structural analysis of the stage-regulated meta 1 gene.
    Uliana SR, Goyal N, Freymüller E, Smith DF.
    Exp Parasitol; 1999 Jul; 92(3):183-91. PubMed ID: 10403759
    [Abstract] [Full Text] [Related]

  • 4. A mitogen-activated protein (MAP) kinase homologue of Leishmania mexicana is essential for parasite survival in the infected host.
    Wiese M.
    EMBO J; 1998 May 01; 17(9):2619-28. PubMed ID: 9564044
    [Abstract] [Full Text] [Related]

  • 5. Leishmania major CorA-like magnesium transporters play a critical role in parasite development and virulence.
    Zhu Y, Davis A, Smith BJ, Curtis J, Handman E.
    Int J Parasitol; 2009 May 01; 39(6):713-23. PubMed ID: 19136005
    [Abstract] [Full Text] [Related]

  • 6. LmxMPK9, a mitogen-activated protein kinase homologue affects flagellar length in Leishmania mexicana.
    Bengs F, Scholz A, Kuhn D, Wiese M.
    Mol Microbiol; 2005 Mar 01; 55(5):1606-15. PubMed ID: 15720564
    [Abstract] [Full Text] [Related]

  • 7. Interacting protein kinases involved in the regulation of flagellar length.
    Erdmann M, Scholz A, Melzer IM, Schmetz C, Wiese M.
    Mol Biol Cell; 2006 Apr 01; 17(4):2035-45. PubMed ID: 16467378
    [Abstract] [Full Text] [Related]

  • 8. LmxMPK4, an essential mitogen-activated protein kinase of Leishmania mexicana is phosphorylated and activated by the STE7-like protein kinase LmxMKK5.
    John von Freyend S, Rosenqvist H, Fink A, Melzer IM, Clos J, Jensen ON, Wiese M.
    Int J Parasitol; 2010 Jul 01; 40(8):969-78. PubMed ID: 20178803
    [Abstract] [Full Text] [Related]

  • 9. Involvement of a Leishmania thymidine kinase in flagellum formation, promastigote shape and growth as well as virulence.
    Thiel M, Harder S, Wiese M, Kroemer M, Bruchhaus I.
    Mol Biochem Parasitol; 2008 Apr 01; 158(2):152-62. PubMed ID: 18222009
    [Abstract] [Full Text] [Related]

  • 10. Disruption of mannose activation in Leishmania mexicana: GDP-mannose pyrophosphorylase is required for virulence, but not for viability.
    Garami A, Ilg T.
    EMBO J; 2001 Jul 16; 20(14):3657-66. PubMed ID: 11447107
    [Abstract] [Full Text] [Related]

  • 11. Deletion of the gene for the membrane-bound acid phosphatase of Leishmania mexicana.
    Benzel I, Weise F, Wiese M.
    Mol Biochem Parasitol; 2000 Nov 16; 111(1):77-86. PubMed ID: 11087918
    [Abstract] [Full Text] [Related]

  • 12. Glycosylation defects and virulence phenotypes of Leishmania mexicana phosphomannomutase and dolicholphosphate-mannose synthase gene deletion mutants.
    Garami A, Mehlert A, Ilg T.
    Mol Cell Biol; 2001 Dec 16; 21(23):8168-83. PubMed ID: 11689705
    [Abstract] [Full Text] [Related]

  • 13. Sir2-Related Protein 1 from Leishmania amazonensis is a glycosylated NAD+-dependent deacetylase.
    Fessel MR, Lira CB, Giorgio S, Ramos CH, Cano MI.
    Parasitology; 2011 Sep 16; 138(10):1245-58. PubMed ID: 21819639
    [Abstract] [Full Text] [Related]

  • 14. Leishmania mexicana: identification of genes that are preferentially expressed in amastigotes.
    Bellatin JA, Murray AS, Zhao M, McMaster WR.
    Exp Parasitol; 2002 Jan 16; 100(1):44-53. PubMed ID: 11971653
    [Abstract] [Full Text] [Related]

  • 15. Over-expression of Leishmania major MAP kinases reveals stage-specific induction of phosphotransferase activity.
    Morales MA, Renaud O, Faigle W, Shorte SL, Späth GF.
    Int J Parasitol; 2007 Sep 16; 37(11):1187-99. PubMed ID: 17481635
    [Abstract] [Full Text] [Related]

  • 16. Lipophosphoglycan is not required for infection of macrophages or mice by Leishmania mexicana.
    Ilg T.
    EMBO J; 2000 May 02; 19(9):1953-62. PubMed ID: 10790362
    [Abstract] [Full Text] [Related]

  • 17. Pathogenicity and protective immunogenicity of cysteine proteinase-deficient mutants of Leishmania mexicana in non-murine models.
    Saravia NG, Escorcia B, Osorio Y, Valderrama L, Brooks D, Arteaga L, Coombs G, Mottram J, Travi BL.
    Vaccine; 2006 May 08; 24(19):4247-59. PubMed ID: 16216395
    [Abstract] [Full Text] [Related]

  • 18. Cysteine peptidases as virulence factors of Leishmania.
    Mottram JC, Coombs GH, Alexander J.
    Curr Opin Microbiol; 2004 Aug 08; 7(4):375-81. PubMed ID: 15358255
    [Abstract] [Full Text] [Related]

  • 19. Acute cysticercosis favours rapid and more severe lesions caused by Leishmania major and Leishmania mexicana infection, a role for alternatively activated macrophages.
    Rodríguez-Sosa M, Rivera-Montoya I, Espinoza A, Romero-Grijalva M, López-Flores R, González J, Terrazas LI.
    Cell Immunol; 2006 Aug 08; 242(2):61-71. PubMed ID: 17118349
    [Abstract] [Full Text] [Related]

  • 20. Genetic background influences immune responses and disease outcome of cutaneous L. mexicana infection in mice.
    Rosas LE, Keiser T, Barbi J, Satoskar AA, Septer A, Kaczmarek J, Lezama-Davila CM, Satoskar AR.
    Int Immunol; 2005 Oct 08; 17(10):1347-57. PubMed ID: 16141242
    [Abstract] [Full Text] [Related]

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