Hydroxyl radical generation in β-thalassemic red blood cells
- 31 March 1995
- journal article
- research article
- Published by Elsevier in Free Radical Biology & Medicine
- Vol. 18 (3) , 611-615
- https://doi.org/10.1016/0891-5849(94)00160-l
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Nonrandom association of free iron with membranes of sickle and beta- thalassemic erythrocytesBlood, 1993
- Effect of excess alpha-hemoglobin chains on cellular and membrane oxidation in model beta-thalassemic erythrocytes.Journal of Clinical Investigation, 1993
- Primaquine-induced superoxde production by β-thalassemic red blood cellsBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1992
- Hydroxyl radical formation by sickle erythrocyte membranes: role of pathologic iron deposits and cytoplasmic reducing agentsBlood, 1991
- Fate of α‐Hemoglobin Chains and Erythrocyte Defects in β‐ThalassemiaaAnnals of the New York Academy of Sciences, 1990
- Oxidative damage to human red cells induced by copper and iron complexes in the presence of ascorbateBiochimica et Biophysica Acta (BBA) - Molecular Cell Research, 1989
- Studies of ascorbate-dependent, iron-catalyzed lipid peroxidationArchives of Biochemistry and Biophysics, 1989
- Aromatic hydroxylation as a potential measure of hydroxyl-radical formation in vivo. Identification of hydroxylated derivatives of salicylate in human body fluidsBiochemical Journal, 1986
- Lipid membrane peroxidation in beta-thalassemia majorBlood, 1976
- Formation of Superoxide in the Autoxidation of the Isolated alpha and beta Chains of Human Hemoglobin and Its Involvement in Hemichrome PrecipitationEuropean Journal of Biochemistry, 1975