The molecular basis of the defect in phosphorylation of spectrin in human hereditary spherocytosis
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Biochemistry,Biophysics
Reference38 articles.
1. The abnormal phosphorylation of spectrin in human hereditary spherocytosis
2. Abnormal membrane protein of red blood cells in hereditary spherocytosis
3. Endogenous phosphorylation of membrane proteins in normal and in hereditary spherocytosis erythrocytes
4. Peptide mapping by limited proteolysis in sodium dodecyl sulfate and analysis by gel electrophoresis.
5. On the mechanism of ATP-induced shape changes in the human erythrocyte membranes: the role of ATP
Cited by 13 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Genetic Variants Affecting the Structure and Function of the Human Red Cell Membrane;Clinical Disorders of Membrane Transport Processes;1987
2. Clinical disorders of the red cell membrane skeleton;Critical Reviews in Oncology/Hematology;1986-01
3. Genetic Variants Affecting the Structure and Function of the Human Red Cell Membrane;Physiology of Membrane Disorders;1986
4. Hereditary Spherocytosis and Related Disorders;Clinics in Haematology;1985-02
5. Abnormal pattern of erythrocyte ageing in Hereditary Spherocytosis as shown by Percoll density gradient centrifugation;Clinica Chimica Acta;1984-09
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