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2. Effects of BCL11A Shmir-Induced Post-Transcriptional Silencing on Hemoglobin Polymer Inhibition in Single Red Blood Cells at Physiologic Oxygen Tension

4. An irradiated marrow niche reveals a small non-collagenous protein mediator of homing, dermatopontin

5. MetAP2 inhibition modifies hemoglobin S to delay polymerization and improves blood flow in sickle cell disease

6. Robust Pre-Clinical Results and Large-Scale Manufacturing Process for Edit-301: An Autologous Cell Therapy for the Potential Treatment of SCD

9. Validation of BCL11A As Therapeutic Target in Sickle Cell Disease: Results from the Adult Cohort of a Pilot/Feasibility Gene Therapy Trial Inducing Sustained Expression of Fetal Hemoglobin Using Post-Transcriptional Gene Silencing

10. MetAP2 Inhibition Modifies Hemoglobin S (HbS) to Delay Polymerization and Improve Blood Flow in Sickle Cell Disease

12. An irradiated marrow niche reveals a small noncollagenous protein mediator of homing, dermatopontin.

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