A study of membrane protein defects and α hemoglobin chains of red blood cells in human β thalassemia

This publication has 46 references indexed in Scilit:

• Crosslinking of isolated cytoskeletal proteins with hemoglobin: a possible damage inflicted to the red cell membrane
  Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1987
• Separation of red cell membrane proteins by urea‐Triton‐polyacrylamide gel electrophoresis in one‐ and two‐dimensional systems
  Electrophoresis, 1986
• Alterations in Membrane Protein and Phosphorylation Pattern in ?-Thalassemic Red Blood Cells
  Annals of the New York Academy of Sciences, 1985
• Partial deficiency of erythrocyte spectrin in hereditary spherocytosis
  Nature, 1985
• Evidence for Increased Proteolysis in Intact β Thalassemia Erythroid Cells
  Hemoglobin, 1981
• Red cell membrane abnormalities in β‐thalassaemia major
  FEBS Letters, 1980
• Polymerization of membrane components in aging red blood cells
  Biochemical and Biophysical Research Communications, 1980
• Cross‐linking of red blood cell membrane proteins induced by oxidative stress in β thalassemia
  FEBS Letters, 1978
• Globin Synthesis in Normal Human Bone Marrow
  British Journal of Haematology, 1976
• Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
  Nature, 1970