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Author Title [ Type(Desc)] Year
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Journal Article
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.
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).
Cruz, E., Whittington, C., Krikler, S. H., Mascarenhas, C., et al. (2008). A new 500 kb haplotype associated with high CD8+ T-lymphocyte numbers predicts a less severe expression of hereditary hemochromatosis. BMC medical genetics, 9, 97.
Freitas, M., Gomes, A., Porto, G., & Fernandes, E. (2010). Nickel induces oxidative burst, NF-κB activation and interleukin-8 production in human neutrophils. Journal of Biological Inorganic Chemistry, 15(8), 1275 - 1283.
Roetto, A., & Porto, G. (2013). A novel mutation in the CUB sequence of matriptase-2 (TMPRSS6) is implicated in iron-resistant iron deficiency anaemia - response to Jaspers et al. British Journal of Haematology, 160(4), 566 - 567.
Freitas, M., Porto, G., Lima, J. L. F. C., & Fernandes, E. (2009). Optimization of experimental settings for the analysis of human neutrophils oxidative burst in vitro. Talanta, 78(4-5), 1476 - 1483.
Couto, D., Sousa, R., Andrade, L., Leander, M., et al. (2015). Polyacrylic acid coated and non-coated iron oxide nanoparticles are not genotoxic to human T lymphocytes. Toxicology Letters, 234(2), 67 - 73.
Bettencourt, B. F., Rocha, F. L., Alves, H., Amorim, R., et al. (2013). Protective effect of an ERAP1 haplotype in ankylosing spondylitis: Investigating non-MHC genes in HLA-B27-positive individuals. Rheumatology (United Kingdom), 52(12), 2168 - 2176.
Pinto, J. P., Ramos, P., de Almeida, S. F., Oliveira, S., et al. (2008). Protective role of calreticulin in HFE hemochromatosis. Free Radical Biology and Medicine, 44(1), 99 - 108.
Vieira, J., Cardoso, C. S., Pinto, J., Patil, K., et al. (2007). A putative gene located at the MHC class I region around the D6S105 marker contributes to the setting of CD8+ T-lymphocyte numbers in humans. International Journal of Immunogenetics, 34(5), 359 - 367.
Brandáo, M., Oliveira, J. C., Bravo, F., Reis, J., et al. (2005). The soluble transferrin receptor as a marker of iron homeostasis in normal subjects and in HFE-related hemochromatosis. Haematologica, 90(1), 31 - 37.
Nazareth, T., Teodósio, R., Porto, G., Gonçalves, L., et al. (2014). Strengthening the perception-assessment tools for dengue prevention: A cross-sectional survey in a temperate region Madeira, Portugal. BMC Public Health, 14(1).
Cruz, E., Vieira, J., Almeida, S., Lacerda, R., et al. (2006). A study of 82 extended HLA haplotypes in HFE-C282Y homozygous hemochromatosis subjects: Relationship to the genetic control of CD8+ T-lymphocyte numbers and severity of iron overload. BMC Medical Genetics, 7.
Pellegrino, R. M., Coutinho, M., D'Ascola, D., Lopes, A. M., et al. (2012). Two novel mutations in the tmprss6 gene associated with iron-refractory iron-deficiency anaemia (irida) and partial expression in the heterozygous form. British Journal of Haematology, 158(5), 668 - 672.

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