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T
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.
S
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.
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).
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.
P
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.
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.
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.
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.
O
França, M., Martí-Bonmatí, L., Silva, S., Oliveira, C., et al. (2017). Optimizing the management of hereditary haemochromatosis: The value of MRI R2* quantification to predict and monitor body iron stores. British Journal of Haematology.
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.
N
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., 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.
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.
L
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).
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.
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.
Marques, O., Porto, G., Rêma, A., Faria, F., et al. (2016). Local iron homeostasis in the breast ductal carcinoma microenvironment. BMC Cancer, 16(1).
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.
K
Beirão, I., Lobato, L., Costa, P. M., Fonseca, I., et al. (2004). Kidney and anemia in familial amyloidosis type I. Kidney international, 66(5), 2004 - 2009.
I
Freitas, M., Porto, G., Lima, J. L. F. C., & Fernandes, E. (2008). Isolation and activation of human neutrophils in vitro. The importance of the anticoagulant used during blood collection. Clinical Biochemistry, 41(7-8), 570 - 575.
Porto, G., & De Sousa, M. (2007). Iron overload and immunity. World Journal of Gastroenterology, 13(35), 4707 - 4715.
Cruz, E., Vieira, J., Gonçalves, R., Alves, H., et al. (2004). Involvement of the Major Histocompatibility Complex region in the regulation regulation of circulating CD8+ T-cell numbers in humans. Tissue Antigens, 64(1), 25 - 34.
Porto, B., Vieira, R., & Porto, G. (2009). Increased capacity of lymphocytes from hereditary hemochromatosis patients homozygous for the C282Y HFE mutation to respond to the genotoxic effect of diepoxybutane. Mutation Research - Genetic Toxicology and Environmental Mutagenesis, 673(1), 37 - 42.

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