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2015
De Paula Costa Monteiro, I., Madureira, P., De Vasconscelos, A., Humberto Pozza, D., & De Mello, R. A. (2015). Targeting HER family in HER2-positive metastatic breast cancer: Potential biomarkers and novel targeted therapies. Pharmacogenomics, 16(3), 257 - 271.
Canhão, H., Rodrigues, A. M., Santos, M. J., Carmona-Fernandes, D., et al. (2015). TRAF1/C5 but not PTPRC variants are potential predictors of rheumatoid arthritis response to anti-tumor necrosis factor therapy. BioMed Research International, 2015.
Canhão, H., Rodrigues, A. M., Santos, M. J., Carmona-Fernandes, D., et al. (2015). TRAF1/C5 but not PTPRC variants are potential predictors of rheumatoid arthritis response to anti-tumor necrosis factor therapy. BioMed Research International, 2015.
Sousa, R. G., Esteves, T., Rocha, S., Figueiredo, F., et al. (2015). Transfer learning for the recognition of immunogold particles in TEM imaging. Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics) (Vol. 9094, pp. 374 - 384).
Appelberg, R., Moreira, D., Barreira-Silva, P., Borges, M., et al. (2015). The Warburg effect in mycobacterial granulomas is dependent on the recruitment and activation of macrophages by interferon-γ. Immunology, 145(4), 498 - 507.
2014
Dias, A. M., Dourado, J., Lago, P., Cabral, J., et al. (2014). Dysregulation of T cell receptor N-glycosylation: A molecular mechanism involved in ulcerative colitis. Human Molecular Genetics, 23(9), 2416 - 2427.
Dias, A. M., Dourado, J., Lago, P., Cabral, J., et al. (2014). Dysregulation of T cell receptor N-glycosylation: A molecular mechanism involved in ulcerative colitis. Human Molecular Genetics, 23(9), 2416 - 2427.
Dias, A. M., Dourado, J., Lago, P., Cabral, J., et al. (2014). Dysregulation of T cell receptor N-glycosylation: A molecular mechanism involved in ulcerative colitis. Human Molecular Genetics, 23(9), 2416 - 2427.
Nischwitz, S., Faber, H., Sämann, P. G., Domingues, H. S., et al. (2014). Interferon β-1a reduces increased interleukin-16 levels in multiple sclerosis patients. Acta Neurologica Scandinavica, 130(1), 46 - 52.
Esteves, T., Durr, A., Mundwiller, E., Loureiro, J. L., et al. (2014). Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia. American Journal of Human Genetics, 94(2), 268 - 277.
Esteves, T., Durr, A., Mundwiller, E., Loureiro, J. L., et al. (2014). Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia. American Journal of Human Genetics, 94(2), 268 - 277.
Esteves, T., Durr, A., Mundwiller, E., Loureiro, J. L., et al. (2014). Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia. American Journal of Human Genetics, 94(2), 268 - 277.
Esteves, T., Durr, A., Mundwiller, E., Loureiro, J. L., et al. (2014). Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia. American Journal of Human Genetics, 94(2), 268 - 277.
Esteves, T., Durr, A., Mundwiller, E., Loureiro, J. L., et al. (2014). Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia. American Journal of Human Genetics, 94(2), 268 - 277.
Esteves, T., Durr, A., Mundwiller, E., Loureiro, J. L., et al. (2014). Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia. American Journal of Human Genetics, 94(2), 268 - 277.
Da Silva, T. F., Eira, J., Lopes, A. T., Malheiro, A. R., et al. (2014). Peripheral nervous system plasmalogens regulate Schwann cell differentiation and myelination. Journal of Clinical Investigation, 124(6), 2560 - 2570.
Montani, L., Buerki-Thurnherr, T., de Faria, J. P., Pereira, J. A., et al. (2014). Profilin 1 is required for peripheral nervous system myelination. Development (Cambridge), 141(7), 1553 - 1561.
Ferreirinha, P., Dias, J., Correia, A., Pérez-Cabezas, B., et al. (2014). Protective effect of intranasal immunization with Neospora caninum membrane antigens against murine neosporosis established through the gastrointestinal tract. Immunology, 141(2), 256 - 267.
Rieder, F., de Bruyn, J. R., Pham, B. T., Katsanos, K., et al. (2014). Results of the 4th Scientific Workshop of the ECCO (Group II): Markers of intestinal fibrosis in inflammatory bowel disease. Journal of Crohn's and Colitis.
2013
Boukhris, A., Schule, R., Loureiro, J. L., Lourenço, C. M., et al. (2013). Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia. American Journal of Human Genetics, 93(1), 118 - 123.
Boukhris, A., Schule, R., Loureiro, J. L., Lourenço, C. M., et al. (2013). Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia. American Journal of Human Genetics, 93(1), 118 - 123.
Boukhris, A., Schule, R., Loureiro, J. L., Lourenço, C. M., et al. (2013). Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia. American Journal of Human Genetics, 93(1), 118 - 123.
Boukhris, A., Schule, R., Loureiro, J. L., Lourenço, C. M., et al. (2013). Alteration of ganglioside biosynthesis responsible for complex hereditary spastic paraplegia. American Journal of Human Genetics, 93(1), 118 - 123.
Leão, P. N., Costa, M., Ramos, V., Pereira, A. R., et al. (2013). Antitumor Activity of Hierridin B, a Cyanobacterial Secondary Metabolite Found in both Filamentous and Unicellular Marine Strains. PLoS ONE, 8(7).
Pereira, S. B., Mota, R., Santos, C. L., De Philippis, R., & Tamagnini, P. (2013). Assembly and export of extracellular polymeric substances (EPS) in cyanobacteria. A phylogenomic approach. Advances in Botanical Research (Vol. 65, pp. 235 - 279).

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