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Research Square|May 20, 2024
Biopreservation and Reversal of Oxidative Injury During Blood Storage by a Novel Curcumin-based Gel FormulationWayne Hicks, Sirsendu Jana, Tigist Kassa, et al.
The Journal of Biological Chemistry|January 12, 2019
Substitutions in the β subunits of sickle-cell hemoglobin improve oxidative stability and increase the delay time of sickle-cell fiber formationFantao Meng, Tigist Kassa, Michael Brad Strader, et al.
The Journal of Biological Chemistry|September 24, 2015
Sickle Cell Hemoglobin in the Ferryl State Promotes βCys-93 Oxidation and Mitochondrial Dysfunction in Epithelial Lung Cells (E10)Tigist Kassa, Sirsendu Jana, Michael Brad Strader, et al.
Bioconjugate Chemistry|March 24, 2018
Comprehensive Biochemical and Biophysical Characterization of Hemoglobin-Based Oxygen Carrier Therapeutics: All HBOCs Are Not Created EquallyFantao Meng, Tigist Kassa, Sirsendu Jana, et al.
Redox Biology|March 21, 2016
Oxidative instability of hemoglobin E (β26 Glu→Lys) is increased in the presence of free α subunits and reversed by α-hemoglobin stabilizing protein (AHSP): Relevance to HbE/β-thalassemiaMichael Brad Strader, Tigist Kassa, Fantao Meng, et al.
The Journal of Biological Chemistry|June 19, 2014
Post-translational transformation of methionine to aspartate is catalyzed by heme iron and driven by peroxide: a novel subunit-specific mechanism in hemoglobinMichael Brad Strader, Wayne A Hicks, Tigist Kassa, et al.
JCI Insight|November 3, 2018
Hemoglobin oxidation-dependent reactions promote interactions with band 3 and oxidative changes in sickle cell-derived microparticlesSirsendu Jana, Michael Brad Strader, Fantao Meng, et al.
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