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Journal Article
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.
Pinto, J. P., Ramos, P., & De Sousa, M. (2007). Overexpression of HFE in HepG2 cells reveals differences in intracellular distribution and co-localization of wt- and mutated forms. Blood Cells, Molecules, and Diseases, 39(1), 75 - 81.
Gardenghi, S., Marongiu, M. F., Ramos, P., Guy, E., et al. (2007). Ineffective erythropoiesis in β-thalassemia is characterized by increased iron absorption mediated by down-regulation of hepcidin and up-regulation of ferroportin. Blood, 109(11), 5027 - 5035.
Gardenghi, S., Ramos, P., Marongiu, M. F., Melchiori, L., et al. (2010). Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice. Journal of Clinical Investigation, 120(12), 4466 - 4477.
Ramos, P., Guy, E., Chen, N., Proenca, C. C., et al. (2011). Enhanced erythropoiesis in Hfe-KO mice indicates a role for Hfe in the modulation of erythroid iron homeostasis. Blood, 117(4), 1379 - 1389.
Libani, I. V., Guy, E. C., Melchiori, L., Schiro, R., et al. (2008). Decreased differentiation of erythroid cells exacerbates ineffective erythropoiesis in β-thalassemia. Blood, 112(3), 875 - 885.

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