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Blood|May 16, 2008
Decreased differentiation of erythroid cells exacerbates ineffective erythropoiesis in beta-thalassemiaIlaria V Libani, Ella C Guy, Luca Melchiori, et al.
Blood|June 20, 2020
Correcting β-thalassemia by combined therapies that restrict iron and modulate erythropoietin activityCarla Casu, Mariateresa Pettinato, Alison Liu, et al.
Haematologica|May 28, 2017
Recommendations regarding splenectomy in hereditary hemolytic anemiasAchille Iolascon, Immacolata Andolfo, Wilma Barcellini, et al.
Communications Biology|May 4, 2021
Pleckstrin-2 is essential for erythropoiesis in β-thalassemic mice, reducing apoptosis and enhancing enucleationMaria Feola, Andrea Zamperone, Daniel Moskop, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 30, 2021
Lentiviral vector ALS20 yields high hemoglobin levels with low genomic integrations for treatment of beta-globinopathiesLaura Breda, Valentina Ghiaccio, Naoto Tanaka, et al.
Blood|July 1, 2024
Use of HSC-targeted LNP to generate a mouse model of lethal α-thalassemia and treatment via lentiviral gene therapyMaxwell E Chappell, Laura Breda, Lucas Tricoli, et al.
Nature Communications|September 3, 2017
Hepcidin is regulated by promoter-associated histone acetylation and HDAC3Sant-Rayn Pasricha, Pei Jin Lim, Tiago L Duarte, et al.
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