Therapeutic insights into the treatment of Sickle cell disease and β-thalassemias : Hepatitis B X-interacting protein (HBXIP) decreases sickling of erythrocytes via up regulation of fetal HbF, 22/September/2014, 09.01 am

Therapeutic insights into the treatment of Sickle cell disease and β-thalassemias : Hepatitis B X-interacting protein (HBXIP) decreases sickling of erythrocytes via up regulation of fetal HbF, 22/September/2014, 09.01 am

Therapeutic insights into the treatment of Sickle cell disease and β-thalassemias : Hepatitis B X-interacting protein (HBXIP) decreases sickling of erythrocytes via up regulation of fetal HbF, 22/September/2014, 09.01 am 150 150 Dr Boomi's Genom-2-Discovery Center

Idea Proposed/Formulated byDr L Boominathan Ph.D.

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CitationBoominathan, Therapeutic insights into the treatment of Sickle cell disease and β-thalassemias : Hepatitis B X-interacting protein (HBXIP) decreases sickling of erythrocytes via up regulation of fetal HbF, 22/September/2014, 09.01 am, Genome-2-Bio-Medicine Discovery center (GBMD), http://genomediscovery.org

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Significance: This study suggests that Hepatitis B X-interacting protein (HBXIP)by up regulating the expression of its target gene, it  may increase the levels of HbF.  Thus, pharmacological formulations encompassing “HBXIP activator” may be used to treat: (1) Sickle cell disease ;  (2) β-thalassemias; and (3) disease conditions that has lower levels of HbF

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