TSH Receptor Reduces Hemoglobin S Polymerization and Increases Deformability and Adhesion of Sickle Erythrocytes

<div>Scheme showing the importance of TSH in HbS polymerization, adhesion of erythrocyte to thrombospondin, and deformability of erythrocytes from patients with sickle cell disease.</div>

Anemia

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Figure 5

Figure 5: TSH Receptor Reduces Hemoglobin S Polymerization and Increases Deformability and Adhesion of Sickle Erythrocytes 