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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.
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.
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).
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).
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Marques, O., Porto, G., Rêma, A., Faria, F., et al. (2016). Local iron homeostasis in the breast ductal carcinoma microenvironment. BMC Cancer, 16(1).
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.
Martins, T. G., Gama, J. B., Fraga, A. G., Saraiva, M., et al. (2012). Local and regional re-establishment of cellular immunity during curative antibiotherapy of murine mycobacterium ulcerans infection. PLoS ONE, 7(2).
Carvalho, S., Barreira da Silva, R., Shawki, A., Castro, H., et al. (2015). LiZIP3 is a cellular zinc transporter that mediates the tightly regulated import of zinc in Leishmania infantum parasites. Molecular Microbiology, 96(3), 581 - 595.
Beirão, I., Lobato, L., Costa, P. M. P., Fonseca, I., et al. (2007). Liver transplantation and anemia in familial amyloidosis ATTR V30M. Amyloid, 14(1), 33 - 37.

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