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Author Title [ Type(Desc)] Year
Filters: Author is Oliveira, L.  [Clear All Filters]
Journal Article
Domingues, R. G., Lago-Baldaia, I., Pereira-Castro, I., Fachini, J. M., et al. (2016). CD5 expression is regulated during human T-cell activation by alternative polyadenylation, PTBP1, and miR-204. European Journal of Immunology, 46(6), 1490 - 1503.
Oliveira, L., Correia, A., Cristina Costa, A., Guerra-Gomes, S., et al. (2015). Deficits in Endogenous Adenosine Formation by Ecto-5′-Nucleotidase/CD73 Impair Neuromuscular Transmission and Immune Competence in Experimental Autoimmune Myasthenia Gravis. Mediators of Inflammation, 2015.
Oliveira, L., Madureira, P., Andrade, E. B., Bouaboud, A., et al. (2012). Group B streptococcus GAPDH is released upon cell lysis, associates with bacterial surface, and induces apoptosis in murine macrophages. PLoS ONE, 7(1).
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).
Oliveira, L., & Carmo, A. M. (2017). Response: Commentary: the scavenger receptor SSc5D physically interacts with bacteria through the SrCr-containing n-terminal domain. Frontiers in Immunology, 8(AUG).
Pereira, C. B., Bocková, M., Santos, R. F., Santos, A. M., et al. (2016). The scavenger receptor SSc5D physically interacts with bacteria through the SRCR-containing N-terminal domain. Frontiers in Immunology, 7(OCT).
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.
Andrade, E. B., Alves, J., Madureira, P., Oliveira, L., et al. (2013). TLR2-induced IL-10 production impairs neutrophil recruitment to infected tissues during neonatal bacterial sepsis. Journal of Immunology, 191(9), 4759 - 4768.
Santos, R. F., Oliveira, L., & Carmo, A. M. (2016). Tuning T cell activation: The function of CD6 at the immunological synapse and in T cell responses. Current Drug Targets, 17(6), 630 - 639.

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