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Defective organization of the erythroid cell membrane in a novel case of congenital anemia

  • Published:2003-01 Issue:1 Volume:30 Page:43-54
  • ISSN:1079-9796
  • Container-title:Blood Cells, Molecules, and Diseases
  • language:en
  • Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Antonelou Marianna H,Papassideri Issidora S,Karababa Fotini J,Stravopodis Dimitrios J,Loutradi Afroditi,Margaritis Lukas H

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference49 articles.

1. Electron microscopic and high resolution autoradiographic studies of the erythroblasts in hemoglobin-H disease;Wickramasinghe;Br. J. Haematol.,1980

2. Cellular and membrane properties of α and β thalassemic erythrocytes are different;Schrier;Blood,1989

3. Erythrokinetics in thalassemia. II. Studies in Lepore trait and hemoglobin H disease;Pearson;J. Lab. Clin. Med.,1962

4. Ferrokinetics in man;Finch;Medicine (Baltimore),1970

5. Cross-linking of red blood cell membrane proteins induced by oxidative stress in β-thalassemia;Kahane;FEBS Lett.,1978

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