The spectrin-actin junction of erythrocyte membrane skeletons
- 1 January 1989
- journal article
- review article
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Reviews on Biomembranes
- Vol. 988 (1) , 107-121
- https://doi.org/10.1016/0304-4157(89)90006-3
Abstract
No abstract availableKeywords
This publication has 136 references indexed in Scilit:
- Partial Ankyrin and Spectrin Deficiency in Severe, Atypical Hereditary SpherocytosisNew England Journal of Medicine, 1988
- Tropomyosin from human erythrocyte membrane polymerizes poorly but binds F-actin effectively in the presence and absence of spectrinBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1987
- Inheritance Pattern and Clinical Response to Splenectomy as a Reflection of Erythrocyte Spectrin Deficiency in Hereditary SpherocytosisNew England Journal of Medicine, 1986
- Molecular Basis of Hereditary Elliptocytosis Due to Protein 4.1 DeficiencyNew England Journal of Medicine, 1986
- A calmodulin and α-subunit binding domain in human erythrocyte spectrinBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1986
- Phorbol ester stimulates the phosphorylation of rabbit erythrocyte band 4.1Biochemical and Biophysical Research Communications, 1984
- A Genetic Defect in the Binding of Protein 4.1 to Spectrin in a Kindred with Hereditary SpherocytosisNew England Journal of Medicine, 1982
- Deficient Red-Cell Spectrin in Severe, Recessively Inherited SpherocytosisNew England Journal of Medicine, 1982
- Calmodulin-binding protein of erythrocyte cytoskeletonBiochemical and Biophysical Research Communications, 1981
- Relations of the spectrin complex of human erythrocyte membranes to the actomyosins of muscle cellBiochemistry, 1976