Increase in Band 3 Density and Aggregation in Hereditary Spherocytosis
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference24 articles.
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2. Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis;Eber;Nat. Genet.,1996
3. Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8;Lux;Nature,1990
4. Mutations of the red blood cell membrane proteins: From clinical evaluation to detection of the underlying genetic defect;Palek;Blood,1992
5. Hereditary spherocytosis with Ankyrin Walsrode, a variant ankyrin with decreased affinity for band 3;Eber;Blood,1994
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1. Linkage of typically cytosolic peroxidases to erythrocyte membrane – A possible mechanism of protection in Hereditary Spherocytosis;Biochimica et Biophysica Acta (BBA) - Biomembranes;2020-03
2. Evaluation of Red Cell Membrane Cytoskeletal Disorders Using a Flow Cytometric Method in South Iran;Turkish Journal of Hematology;2014-03-01
3. Physiologically important secondary modifications of red cell membrane in hereditary spherocytosis-evidence for in vivo oxidation and lipid rafts protein variations;Blood Cells, Molecules, and Diseases;2007-05
4. Flow Cytometry as a Diagnostic Tool for Hereditary Spherocytosis;Acta Haematologica;2006
5. Hereditary spherocytosis—defects in proteins that connect the membrane skeleton to the lipid bilayer;Seminars in Hematology;2004-04
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