Electron microscopic evidence of impaired intramembrane particles and instability of the cytoskeletal network in band 4.2 deficiency in human red cells
Author:
Publisher
Wiley
Subject
Cell Biology,Structural Biology
Reference30 articles.
1. An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form of hereditary hemolytic anemia (protein 4.2NIPPON)
2. The preparation and chemical characteristics of hemoglobin-free ghosts of human erythrocytes
3. Distribution of glycophorin on the surface of human erythrocyte membranes and its association with intramembrane particles: An immunochemical and freeze-fracture study of normal and En(a−) erythrocytes
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1. Protein 4.2 : A complex linker;Blood Cells, Molecules, and Diseases;2009-05
2. Anchoring Proteins of the Erythrocyte Membrane;Protein Science Encyclopedia;2008-03-15
3. DNA Methylation in Promoter Regions of Red Cell Membrane Protein Genes in Healthy Individuals and Patients with Hereditary Membrane Disorders;International Journal of Hematology;2005-06-01
4. Hereditary Red Cell Membrane Disorders in Japan: Their Genotypic and Phenotypic Features in 1014 Cases Studied;Hematology;2001-01
5. Induction of Erythrocyte Protein 4.2 Gene Expression during Differentiation of Murine Erythroleukemia Cells;Genomics;1999-07
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