Compensatory increase in levels of beta minor globin in murine beta-thalassemia is under translational control.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
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2. Anemia, Ineffective Erythropoiesis, and Hepcidin: Interacting Factors in Abnormal Iron Metabolism Leading to Iron Overload in β-Thalassemia;Hematology/Oncology Clinics of North America;2010-12
3. Ineffective erythropoiesis in β-thalassemia is characterized by increased iron absorption mediated by down-regulation of hepcidin and up-regulation of ferroportin;Blood;2007-06-01
4. Effect of fetal hemoglobin-stimulating medicines on the interaction of DNA and protein of important erythroid regulatory elements;Biochemistry and Cell Biology;2003-08-01
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