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Journal Article
Szucs, P., Luz, L. L., Lima, D., & Safronov, B. V. (2010). Local axon collaterals of lamina I projection neurons in the spinal cord of young rats. Journal of Comparative Neurology, 518(14), 2645 - 2665.
Marques, O., Porto, G., Rêma, A., Faria, F., et al. (2016). Local iron homeostasis in the breast ductal carcinoma microenvironment. BMC Cancer, 16(1).
Vieira, C. P., Almeida, A., Dias, J. D., & Vieira, J. (2006). On the location of the gene(s) harbouring the advantageous variant that maintains the X/4 fusion of Drosophila americana. Genetical Research, 87(3), 163 - 174.
Alexandre, N., Amorim, I., Caseiro, A. R., Pereira, T., et al. (2016). Long term performance evaluation of small-diameter vascular grafts based on polyvinyl alcohol hydrogel and dextran and MSCs-based therapies using the ovine pre-clinical animal model. International Journal of Pharmaceutics, 513(1-2), 332 - 346.
Alexandre, N., Amorim, I., Caseiro, A. R., Pereira, T., et al. (2017). Long term performance evaluation of small-diameter vascular grafts based on polyvinyl alcohol hydrogel and dextran and MSCs-based therapies using the ovine pre-clinical animal model. International Journal of Pharmaceutics, 523(2), 515 - 530.
Harmatz, P., Giugliani, R., D. Schwartz, I. V., Guffon, N., et al. (2008). Long-term follow-up of endurance and safety outcomes during enzyme replacement therapy for mucopolysaccharidosis VI: Final results of three clinical studies of recombinant human N-acetylgalactosamine 4-sulfatase. Molecular Genetics and Metabolism, 94(4), 469 - 475.
Carvalho, M. F., Ferreira Jorge, R., Pacheco, C. C., de Marco, P., et al. (2006). Long-term performance and microbial dynamics of an up-flow fixed bed reactor established for the biodegradation of fluorobenzene. Applied Microbiology and Biotechnology, 71(4), 555 - 562.
Sereno, D., Vergnes, B., Mathieu-Daude, F., Cordeiro Da Silva, A., & Ouaissi, A. (2006). Looking for putative functions of the Leishmania cytosolic SIR2 deacetylase. Parasitology Research, 100(1), 1 - 9.
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.
Martin, E., Schüle, R., Smets, K., Rastetter, A., et al. (2013). Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia. American Journal of Human Genetics, 92(2), 238 - 244.
Seixas, A. I., Holmes, S. E., Takeshima, H., Pavlovich, A., et al. (2012). Loss of junctophilin-3 contributes to huntington disease-like 2 pathogenesis. Annals of Neurology, 71(2), 245 - 257.
Beirão, I., Moreira, L., Porto, G., Lobato, L., et al. (2008). Low erythropoietin production in familial amyloidosis TTR V30M is not related with renal congophilic amyloid deposition: A clinicopathologic study of twelve cases. Nephron - Clinical Practice, 109(2), c95 - c99.
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.
Cardoso, L., Lopes, A. P., Sherry, K., Schallig, H., & Solano-Gallego, L. (2010). Low seroprevalence of Leishmania infantum infection in cats from northern Portugal based on DAT and ELISA. Veterinary Parasitology, 174(1-2), 37 - 42.
Beirão, I., Almeida, S., Swinkels, D., Costa, P. M. P., et al. (2008). Low serum levels of prohepcidin, but not hepcidin-25, are related to anemia in familial amyloidosis TTR V30M. Blood Cells, Molecules, and Diseases, 41(2), 175 - 178.
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.
Valentim, A. M., Di Giminiani, P., Ribeiro, P. O., Rodrigues, P., et al. (2010). Lower isoflurane concentration affects spatial learning and neurodegeneration in adult mice compared with higher concentrations. Anesthesiology, 113(5), 1099 - 1108.
Sabet, C., Lecuit, M., Cabanes, D., Cossart, P., & Bierne, H. (2005). LPXTG protein InlJ, a newly identified internalin involved in Listeria monocytogenes virulence. Infection and Immunity, 73(10), 6912 - 6922.
Carvalho, F., Atilano, M. L., Pombinho, R., Covas, G., et al. (2015). L-Rhamnosylation of Listeria monocytogenes Wall Teichoic Acids Promotes Resistance to Antimicrobial Peptides by Delaying Interaction with the Membrane. PLoS Pathogens, 11(5).
Costa, M., Cruz, E., Oliveira, S., Benes, V., et al. (2015). Lymphocyte gene expression signatures from patients and mouse models of hereditary hemochromatosis reveal a function of hfe as a negative regulator of cd8+ t-Lymphocyte activation and differentiation in vivo. PLoS ONE, 10(4).
Ferraz, M. J., Marques, A. R. A., Gaspar, P., Mirzaian, M., et al. (2016). Lyso-glycosphingolipid abnormalities in different murine models of lysosomal storage disorders. Molecular Genetics and Metabolism, 117(2), 186 - 193.
Coutinho, M. F., Lacerda, L., Macedo-Ribeiro, S., Baptista, E., et al. (2012). Lysosomal multienzymatic complex-related diseases: A genetic study among Portuguese patients. Clinical Genetics, 81(4), 379 - 393.

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