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Journal Article
Moniz, T., Nunes, A., Silva, A. M. G., Queirós, C., et al. (2013). Rhodamine labeling of 3-hydroxy-4-pyridinone iron chelators is an important contribution to target Mycobacterium avium infection. Journal of Inorganic Biochemistry, 121, 156 - 166.
Vale-Costa, S., Vale, N., Matos, J., Tomás, A., et al. (2012). Peptidomimetic and organometallic derivatives of primaquine active against Leishmania infantum. Antimicrobial Agents and Chemotherapy, 56(11), 5774 - 5781.
Vale-Costa, S., Costa-Gouveia, J., Pérez, B., Silva, T., et al. (2013). N-cinnamoylated aminoquinolines as promising antileishmanial agents. Antimicrobial Agents and Chemotherapy, 57(10), 5112 - 5115.
Rodrigues, P. N., Gomes, S. S., Neves, J. V., Gomes-Pereira, S., et al. (2011). Mycobacteria-induced anaemia revisited: A molecular approach reveals the involvement of NRAMP1 and lipocalin-2, but not of hepcidin. Immunobiology, 216(10), 1127 - 1134.
Gomes, M. S., Flórido, M., Cordeiro, J. V., Teixeira, C. M., et al. (2004). Limited role of the Toll-like receptor-2 in resistance to Mycobacterium avium. Immunology, 111(2), 179 - 185.
Silva, T., Moreira, A. C., Nazmi, K., Moniz, T., et al. (2017). Lactoferricin peptides increase macrophages' capacity to kill Mycobacterium avium. mSphere, 2(4).
Vale-Costa, S., Gomes-Pereira, S., Teixeira, C. M., Rosa, G., et al. (2013). Iron Overload Favors the Elimination of Leishmania infantum from Mouse Tissues through Interaction with Reactive Oxygen and Nitrogen Species. PLoS Neglected Tropical Diseases, 7(2).
Moniz, T., Leite, Â., Silva, T., Gameiro, P., et al. (2017). The influence of functional groups on the permeation and distribution of antimycobacterial rhodamine chelators. Journal of Inorganic Biochemistry, 175, 138 - 147.
Gomes-Pereira, S., Rodrigues, P. N., Appelberg, R., & Gomes, M. S. (2008). Increased susceptibility to Mycobacterium avium in hemochromatosis protein HFE-deficient mice. Infection and Immunity, 76(10), 4713 - 4719.
Silva, T., & Gomes, M. S. (2017). Immuno-stimulatory peptides as a potential adjunct therapy against intra-macrophagic pathogens. Molecules, 22(8).
Fernandes, S. S., Nunes, A., Gomes, A. R., de Castro, B., et al. (2010). Identification of a new hexadentate iron chelator capable of restricting the intramacrophagic growth of Mycobacterium avium. Microbes and Infection, 12(4), 287 - 294.
Moreira, A. C., Neves, J. V., Silva, T., Oliveira, P., et al. (2017). Hepcidin- (in)dependent mechanisms of iron metabolism regulation during infection by Listeria and Salmonella. Infection and Immunity, 85(9).
Silva-Gomes, S., Appelberg, R., Larsen, R., Soares, M. P., & Gomes, M. S. (2013). Heme catabolism by heme oxygenase-1 confers host resistance to Mycobacterium infection. Infection and Immunity, 81(7), 2536 - 2545.
Gomes, A. C., & Gomes, M. S. (2016). Hematopoietic niches, erythropoiesis and anemia of chronic infection. Experimental Hematology, 44(2), 85 - 91.
Neves, J. V., Ramos, M. F., Moreira, A. C., Silva, T., et al. (2017). Hamp1 but not Hamp2 regulates ferroportin in fish with two functionally distinct hepcidin types. Scientific Reports, 7(1).
Flórido, M., Gonçalves, A. S., Gomes, M. S., & Appelberg, R. (2004). CD40 is required for the optimal induction of protective immunity to Mycobacterium avium. Immunology, 111(3), 323 - 327.

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