[47] Methods for the study of sickling and hemoglobin S gelation
Author:
Publisher
Elsevier
Reference95 articles.
1. Studies on Abnormal Hemoglobins
2. Properties of sickle-cell haemoglobin
3. Conformational requirements for the polymerization of hemoglobin S: Studies of mixed liganded hybrids
4. Ligand binding and the gelation of sickle cell hemoglobin
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1. Dalcetrapib and reduced glutathione effect on hemoglobin S polymerization studied by NMR;Research on Biomedical Engineering;2022-06-18
2. MR Relaxation Studies of Hemoglobin Aggregation Process in Sickle Cell Disease: Application for Diagnostics and Therapeutics;Applied Magnetic Resonance;2018-12-05
3. Polymerization of Hemoglobin S;Journal of Biological Chemistry;1995-08
4. Mild sickle cell anemia associated with alpha globin mutant alpha montgomery;The American Journal of Medicine;1989-01
5. Membrane expansion as a mechanism explaining the antisickling action of ticlopidine observed in vitro;American Journal of Hematology;1985-02
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