Idea Proposed/Formulated by: Dr L Boominathan Ph.D.
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Citation: Boominathan, Therapeutic insights into the treatment of Sickle cell disease and β-thalassemias: C/EBPβ decreases sickling of erythrocytes via up regulation of fetal HbF, 27/September/2014, 05.59 am, Genome-2-Bio-Medicine Discovery center (GBMD), http://genomediscovery.org
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Significance: This study suggests that C/EBPβ, by regulating the expression of its target gene, it may increase the levels of HbF. Thus, pharmacological formulations encompassing “C/EBPβ activator” may be used to treat: (1) Sickle cell disease ; (2) β-thalassemias; and (3) disease conditions that has lower levels of HbF.
* Research cooperation