Reducing erythroblast apoptosis in β-thalassemia via unfolded protein response (UPR) signaling
Author:
Funder
Faculty of Medicine Siriraj Hospital, Mahidol University
Publisher
Elsevier BV
Subject
General Medicine
Reference45 articles.
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3. Loss of alpha-hemoglobin-stabilizing protein impairs erythropoiesis and exacerbates beta-thalassemia;Kong;J Clin Invest,2004
4. The role of oxidant injury in the pathophysiology of human thalassemias;Schrier;Redox Rep,2003
5. Phosphoproteomic analysis of apoptotic hematopoietic stem cells from hemoglobin E/β-thalassemia;Ponnikorn;J Transl Med,2011
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