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Linear and nonlinear optical properties of human hemoglobin - ScienceDirect
Neither DNA hypomethylation nor changes in the kinetics of erythroid differentiation explain 5-azacytidine's ability to induce human fetal hemoglobin - ScienceDirect
PDF) EHA Research Roadmap on Hemoglobinopathies and Thalassemia: An Update
Editing a γ-globin repressor binding site restores fetal hemoglobin synthesis and corrects the sickle cell disease phenotype | Science Advances
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Iron deficiency screening is a key issue in chronic inflammatory diseases: A call to action - Cacoub - Journal of Internal Medicine - Wiley Online Library
Editing a γ-globin repressor binding site restores fetal hemoglobin synthesis and corrects the sickle cell disease phenotype | Science Advances
Butyrate Trialsa - CAPPELLINI - 1998 - Annals of the New York Academy of Sciences - Wiley Online Library
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
Synthesis and evaluation of resveratrol derivatives as fetal hemoglobin inducers - ScienceDirect
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The β-Thalassemias | NEJM
Sotatercept, a novel transforming growth factor β ligand trap, improves anemia in β-thalassemia: a phase II, open-label, dose-finding study | Haematologica
PDF) Haemoglobin changes and risk of anaemia following treatment for uncomplicated falciparum malaria in sub-Saharan Africa
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Long-term outcomes of lentiviral gene therapy for the β-hemoglobinopathies: the HGB-205 trial | Nature Medicine
GranTorino HB Lounge Chair by Poltrona Frau - Switch Modern
Base-editing-mediated dissection of a γ-globin cis-regulatory element for the therapeutic reactivation of fetal hemoglobin expression | Nature Communications
Cappellini - 6 vintage design items
PDF) Perspectives and challenges to discovering hemoglobin-inducing agents in Sickle Cell Disease
