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Author Title [ Type(Desc)] Year
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Journal Article
França, M., Alberich-Bayarri, Á., Martí-Bonmatí, L., Oliveira, P., et al. (2017). Accurate simultaneous quantification of liver steatosis and iron overload in diffuse liver diseases with MRI. Abdominal Radiology, 42(5), 1434 - 1443.
Correia, A. P., Pinto, J. P., Dias, V., Mascarenhas, C., et al. (2009). CAT53 and HFE alleles in Alzheimer's disease: A putative protective role of the C282Y HFE mutation. Neuroscience Letters, 457(3), 129 - 132.
Cruz, E., Melo, G., Lacerda, R., Almeida, S., & Porto, G. (2006). The CD8+ T-lymphocyte profile as a modifier of iron overload in HFE hemochromatosis: An update of clinical and immunological data from 70 C282Y homozygous subjects. Blood Cells, Molecules, and Diseases, 37(1), 33 - 39.
Rodrigues, P., Lopes, C., Mascarenhas, C., Arosio, P., et al. (2006). Comparative study between Hfe-/- and β2m-/- mice: Progression with age of iron status and liver pathology. International Journal of Experimental Pathology, 87(4), 317 - 324.
Porto, G., Brissot, P., Swinkels, D. W., Zoller, H., et al. (2016). EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH). European Journal of Human Genetics, 24(4), 479 - 495.
Pinto, J. P., Ribeiro, S., Pontes, H., Thowfeequ, S., et al. (2008). Erythropoietin mediates hepcidin expression in hepatocytes through EPOR signaling and regulation of C/EBPα. Blood, 111(12), 5727 - 5733.
Beirão, I., Moreira, L., Barandela, T., Lobato, L., et al. (2010). Erythropoietin production by distal nephron in normal and familial amyloidotic adult human kidneys. Clinical Nephrology, 74(5), 327 - 335.
Crespo, T. C., Silva, B., Marques, L., Marcelino, E., et al. (2014). Genetic and biochemical markers in patients with Alzheimer's disease support a concerted systemic iron homeostasis dysregulation. Neurobiology of Aging, 35(4), 777 - 785.
Duarte, T. L., Caldas, C., Santos, A. G., Silva-Gomes, S., et al. (2017). Genetic disruption of NRF2 promotes the development of necroinflammation and liver fibrosis in a mouse model of HFE-hereditary hemochromatosis. Redox Biology, 11, 157 - 169.
Porto, G., Cruz, E., Miranda, H. P., Porto, B., et al. (2004). Growth hormone (GH)-induced reconstitution of CD8+ CD28+ T lymphocytes in a rare case of severe lymphopenia associated with Juvenile Haemochromatosis and Turner's syndrome. Clinical Endocrinology, 61(4), 437 - 440.
Neves, J. V., Olsson, I. A. S., Porto, G., & Rodrigues, P. N. (2010). Hemochromatosis and pregnancy: Iron stores in the Hfe-/- mouse are not reduced by multiple pregnancies. American Journal of Physiology - Gastrointestinal and Liver Physiology, 298(4), G525 - G529.
Pasricha, S. - R., Lim, P. J., Duarte, T. L., Casu, C., et al. (2017). Hepcidin is regulated by promoter-associated histone acetylation and HDAC3. Nature Communications, 8(1).
Pinto, J. P., Dias, V., Zoller, H., Porto, G., et al. (2010). Hepcidin messenger RNA expression in human lymphocytes. Immunology, 130(2), 217 - 230.
Cruz, E., Porto, G., Morais, S., Campos, M., & De Sousa, M. (2005). HFE mutations in the pathobiology of hemophilic arthropathy [1]. Blood, 105(8), 3381 - 3382.
Marques, O., Rosa, A., Leite, L., Faustino, P., et al. (2016). HFE Variants and the Expression of Iron-Related Proteins in Breast Cancer-Associated Lymphocytes and Macrophages. Cancer Microenvironment, 9(2-3), 85 - 91.
Nazareth, T., Sousa, C. A., Porto, G., Gonçalves, L., et al. (2015). Impact of a Dengue Outbreak Experience in the Preventive Perceptions of the Community from a Temperate Region: Madeira Island, Portugal. PLoS Neglected Tropical Diseases, 9(3).
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.
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, G., & De Sousa, M. (2007). Iron overload and immunity. World Journal of Gastroenterology, 13(35), 4707 - 4715.
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.
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.
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.
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., 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.

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