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Madureira, P., Andrade, E. B., Gama, B., Oliveira, L., et al. (2011). Inhibition of IL-10 production by maternal antibodies against group b streptococcus GAPDH confers immunity to offspring by favoring neutrophil recruitment. PLoS Pathogens, 7(11).
Madureira, P., Baptista, M., Vieira, M., Magalhães, V., et al. (2007). Streptococcus agalactiae GAPDH is a virulence-associated immunomodulatory protein. Journal of Immunology, 178(3), 1379 - 1387.
Madureira, P., Cunha, E. M., & Aguas, A. P. (2007). Acute depletion and recovery of peritoneal B-1 lymphocytes in BALB/c mice after a single injection of mercury chloride. Immunopharmacology and Immunotoxicology, 29(2), 311 - 322.
MacIel, P., Cruz, V. T., Constante, M., Iniesta, I., et al. (2005). Neuroferritinopathy: Missense mutation in FTL causing early-onset bilateral pallidal involvement. Neurology, 65(4), 603 - 605.
Machado, H., Lourenço, A., Carvalho, F., Cabanes, D., et al. (2013). The tat pathway is prevalent in Listeria monocytogenes lineage II and is not required for infection and spread in host cells. Journal of Molecular Microbiology and Biotechnology, 23(3), 209 - 218.
Machado, A., Tejera, E., Cruz-Monteagudo, M., & Rebelo, I. (2009). Application of desirability-based multi(bi)-objective optimization in the design of selective arylpiperazine derivates for the 5-HT1A serotonin receptor. European Journal of Medicinal Chemistry, 44(12), 5045 - 5054.
Machado, V. M., Morte, M. I., Carreira, B. P., Azevedo, M. M., et al. (2015). Involvement of calpains in adult neurogenesis: Implications for stroke. Frontiers in Cellular Neuroscience, 9(FEB).
de Macedo-Ribeiro, S., Renirie, R., Wever, R., & Messerschmidt, A. (2008). Crystal structure of a trapped phosphate intermediate in vanadium apochloroperoxidase catalyzing a dephosphorylation reaction. Biochemistry, 47(3), 929 - 934.
Macedo-Ribeiro, S., Almeida, C., Calisto, B. M., Friedrich, T., et al. (2008). Isolation, cloning and structural characterisation of boophilin, a multifunctional Kunitz-type proteinase inhibitor from the cattle tick. PLoS ONE, 3(2).
Macedo-Ribeiro, S., Cortes, L., MacIel, P., & Carvalho, A. L. (2009). Nucleocytoplasmic shuttling activity of ataxin-3. PLoS ONE, 4(6).
Macedo, J. C., Vaz, S., & Logarinho, E. (2017). Mitotic dysfunction associated with aging hallmarks. Advances in Experimental Medicine and Biology (Vol. 1002, pp. 153 - 188).
MacEdo, M. F., & De Sousa, M. (2008). Transferrin and the transferrin receptor: Of magic bullets and other concerns. Inflammation and Allergy - Drug Targets, 7(1), 41 - 52.
Macedo, M. E., Lima, M. J., Silva, A. O., Alcantara, P., et al. (2005). Prevalence, awareness, treatment and control of hypertension in Portugal: The PAP study. Journal of Hypertension, 23(9), 1661 - 1666.
Macedo, B., Magalhães, J., Batista, A. R., & Saraiva, M. J. (2010). Carvedilol treatment reduces transthyretin deposition in a familial amyloidotic polyneuropathy mouse model. Pharmacological Research, 62(6), 514 - 522.
MacEdo, M. F., De Sousa, M., Ned, R. M., Mascarenhas, C., et al. (2004). Transferrin is required for early T-cell differentiation. Immunology, 112(4), 543 - 549.
Macedo, B., Batista, A. R., Do Amaral, J. B., & Saraiva, M. J. (2007). Biomarkers in the assessment of therapies for familial amyloidotic polyneuropathy. Molecular Medicine, 13(11-12), 584 - 591.
MacEdo, M. F., Cruz, E., Lacerda, R., Porto, G., & De Sousa, M. (2005). Low serum transferrin levels in HFE C282Y homozygous subjects are associated with low CD8+ T lymphocyte numbers. Blood Cells, Molecules, and Diseases, 35(3), 319 - 325.
MacEdo, M. F., Quinta, R., Pereira, C. S., & Sa Miranda, M. C. (2012). Enzyme replacement therapy partially prevents invariant Natural Killer T cell deficiency in the Fabry disease mouse model. Molecular Genetics and Metabolism, 106(1), 83 - 91.
Macedo, B., Batista, A. R., Ferreira, N., Almeida, M. R., & Saraiva, M. J. (2008). Anti-apoptotic treatment reduces transthyretin deposition in a transgenic mouse model of Familial Amyloidotic Polyneuropathy. Biochimica et Biophysica Acta - Molecular Basis of Disease, 1782(9), 517 - 522.
MacEdo, M. F., Porto, G., Costa, M., Vieira, C. P., et al. (2010). Low numbers of CD8 + T lymphocytes in hereditary haemochromatosis are explained by a decrease of the most mature CD8 + effector memory T cells. Clinical and Experimental Immunology, 159(3), 363 - 371.


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