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Proceedings of the National Academy of Sciences of the United States of America|September 1, 2009
Unexpected expression of alpha- and beta-globin in mesencephalic dopaminergic neurons and glial cellsMarta Biagioli, Milena Pinto, Daniela Cesselli, et al.Blood Advances|November 8, 2019
Cranberry A-type proanthocyanidins selectively target acute myeloid leukemia cellsLaura M Bystrom, Daniel P Bezerra, Hsiao-Ting Hsu, et al.Elife|May 18, 2021
The hepcidin regulator erythroferrone is a new member of the erythropoiesis-iron-bone circuitryMelanie Castro-Mollo, Sakshi Gera, Marc Ruiz-Martinez, et al.Plos One|April 6, 2012
Therapeutic hemoglobin levels after gene transfer in β-thalassemia mice and in hematopoietic cells of β-thalassemia and sickle cells disease patientsLaura Breda, Carla Casu, Sara Gardenghi, et al.Science (New York, N.Y.)|July 27, 2023
In vivo hematopoietic stem cell modification by mRNA deliveryLaura Breda, Tyler E Papp, Michael P Triebwasser, et al.Blood|February 3, 2017
Decreasing TfR1 expression reverses anemia and hepcidin suppression in β-thalassemic miceHuihui Li, Tenzin Choesang, Weili Bao, et al.Science Translational Medicine|October 20, 2021
DNA binding to TLR9 expressed by red blood cells promotes innate immune activation and anemiaL K Metthew Lam, Sophia Murphy, Dimitra Kokkinaki, et al.Blood|February 15, 2007
Ineffective erythropoiesis in beta-thalassemia is characterized by increased iron absorption mediated by down-regulation of hepcidin and up-regulation of ferroportinSara Gardenghi, Maria F Marongiu, Pedro Ramos, et al.The Journal of Clinical Investigation|November 25, 2010
Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic miceSara Gardenghi, Pedro Ramos, Maria Franca Marongiu, et al.Molecular Medicine (Cambridge, Mass.)|January 7, 2016
HMGB1 Mediates Anemia of Inflammation in Murine Sepsis SurvivorsSergio I Valdés-Ferrer, Julien Papoin, Meghan E Dancho, et al.Pageof 13