The rates of polymerization and depolymerization of sickle cell hemoglobin
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference22 articles.
1. Rheological Aspects of Sickle Cell Disease
2. Rate of Sickling of Red Cells during Deoxygenation of Blood from Persons with Various Sickling Disorders
3. The Sickle-Unsickle Cycle: A Cause of Cell Fragmentation Leading to Permanently Deformed Cells
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1. Impact of hemoglobin biophysical studies on molecular pathogenesis and drug therapy for sickle cell disease;Molecular Aspects of Medicine;2022-04
2. Hemoglobin S polymerization and sickle cell disease: A retrospective on the occasion of the 70th anniversary of Pauling'sSciencepaper;American Journal of Hematology;2019-12-31
3. High-throughput assessment of hemoglobin polymer in single red blood cells from sickle cell patients under controlled oxygen tension;Proceedings of the National Academy of Sciences;2019-11-25
4. Electrical Impedance Characterization of Erythrocyte Response to Cyclic Hypoxia in Sickle Cell Disease;ACS Sensors;2019-05-14
5. Identification of Aptamers That Bind to Sickle Hemoglobin and Inhibit Its Polymerization;Nucleic Acid Therapeutics;2017-12
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