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7 in total

1. Spectrin interactions with globin chains in the presence of phosphate metabolites and hydrogen peroxide: implications for thalassaemia.

Authors: Poppy Datta; Sudipa Chakrabarty; Amit Chakrabarty; Abhijit Chakrabarti
Journal: J Biosci Date: 2007-09 Impact factor: 1.826

2. Derangement of erythrocytic AE1 in beta-thalassemia by caspase 3: pathogenic mechanisms and implications in red blood cell senescence.

Authors: Silvana Ficarra; Ester Tellone; Bruno Giardina; Roberto Scatena; Annamaria Russo; Francesco Misiti; M Elisabetta Clementi; Deborah Colucci; Ersilia Bellocco; Giuseppina Laganà; Davide Barreca; Antonio Galtieri
Journal: J Membr Biol Date: 2009-02-24 Impact factor: 1.843

3. Oxidative effects of gemfibrozil on anion influx and metabolism in normal and Beta-thalassemic erythrocytes: physiological implications.

Authors: Ester Tellone; Silvana Ficarra; Bruno Giardina; Roberto Scatena; Annamaria Russo; M Elisabetta Clementi; Francesco Misiti; Ersilia Bellocco; Antonio Galtieri
Journal: J Membr Biol Date: 2008-09-29 Impact factor: 1.843

Cross-linking of red blood cell membrane proteins induced by oxidative stress in beta thalassemia.

1. Spectrin interactions with globin chains in the presence of phosphate metabolites and hydrogen peroxide: implications for thalassaemia.

2. Derangement of erythrocytic AE1 in beta-thalassemia by caspase 3: pathogenic mechanisms and implications in red blood cell senescence.

3. Oxidative effects of gemfibrozil on anion influx and metabolism in normal and Beta-thalassemic erythrocytes: physiological implications.

4. Effect of excess alpha-hemoglobin chains on cellular and membrane oxidation in model beta-thalassemic erythrocytes.

5. A study of spectrin and lipid peroxidation of red blood cell membrane in thalassaemia carrier.

6. Elution of antispectrin antibodies from red cells in homozygous beta-thalassaemia.

7. Differing erythrocyte membrane skeletal protein defects in alpha and beta thalassemia.