Base-editing-mediated dissection of a γ-globin cis-regulatory element for the therapeutic reactivation of fetal hemoglobin expression | Nature Communications
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Editing a γ-globin repressor binding site restores fetal hemoglobin synthesis and corrects the sickle cell disease phenotype | Science Advances
The β-Thalassemias | NEJM
Neither DNA hypomethylation nor changes in the kinetics of erythroid differentiation explain 5-azacytidine's ability to induce human fetal hemoglobin - ScienceDirect
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PDF) Perspectives and challenges to discovering hemoglobin-inducing agents in Sickle Cell Disease
Glutathione Reductase-Catalyzed Cascade of Redox Reactions To Bioactivate Potent Antimalarial 1,4-Naphthoquinones – A New Strategy to Combat Malarial Parasites | Journal of the American Chemical Society
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PDF) EHA Research Roadmap on Hemoglobinopathies and Thalassemia: An Update
Sotatercept, a novel transforming growth factor β ligand trap, improves anemia in β-thalassemia: a phase II, open-label, dose-finding study | Haematologica
Editing a γ-globin repressor binding site restores fetal hemoglobin synthesis and corrects the sickle cell disease phenotype | Science Advances
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Long-term outcomes of lentiviral gene therapy for the β-hemoglobinopathies: the HGB-205 trial | Nature Medicine
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Sotatercept, a novel transforming growth factor β ligand trap, improves anemia in β-thalassemia: a phase II, open-label, dose-finding study | Haematologica
Linear and nonlinear optical properties of human hemoglobin - ScienceDirect
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