Enhanced erythropoiesis in Hfe-KO mice indicates a role for Hfe in the modulation of erythroid iron homeostasis - Ramos, P.; Guy, E.; Chen, N.; Proenca, C.C.; Gardenghi, S.; Casu, C.; Follenzi, A.; Van Rooijen, N.; Grady, R.W.; De Sousa, M.; Rivella, S. (Blood, 2011)

Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice - Gardenghi, S.; Ramos, P.; Marongiu, M.F.; Melchiori, L.; Breda, L.; Guy, E.; Muirhead, K.; Rao, N.; Roy, C.N.; Andrews, N.C.; Nemeth, E.; Follenzi, A.; et al. (Journal of Clinical Investigation, 2010)

Decreased differentiation of erythroid cells exacerbates ineffective erythropoiesis in β-thalassemia - Libani, I.V.; Guy, E.C.; Melchiori, L.; Schiro, R.; Ramos, P.; Breda, L.; Scholzen, T.; Chadburn, A.; Liu, Y.; Kernbach, M.; Baron-Lühr, B.; Porotto, M.; et al. (Blood, 2008)

Protective role of calreticulin in HFE hemochromatosis - Pinto, J.P.; Ramos, P.; de Almeida, S.F.; Oliveira, S.; Breda, L.; Michalak, M.; Porto, G.; Rivella, S.; De Sousa, M. (Free Radical Biology and Medicine, 2008)

Ineffective erythropoiesis in β-thalassemia is characterized by increased iron absorption mediated by down-regulation of hepcidin and up-regulation of ferroportin - Gardenghi, S.; Marongiu, M.F.; Ramos, P.; Guy, E.; Breda, L.; Chadburn, A.; Liu, Y.; Amariglio, N.; Rechavi, G.; Rachmilewitz, E.A.; Breuer, W.; Cabantchik, Z.I.; et al. (Blood, 2007)

Overexpression of HFE in HepG2 cells reveals differences in intracellular distribution and co-localization of wt- and mutated forms - Pinto, J.P.; Ramos, P.; De Sousa, M. (Blood Cells, Molecules, and Diseases, 2007)