The β-hemoglobinopathies, which include β-thalassemia and sickle cell disease, are among the most prevalent monogenic disorders worldwide. β-thalassemia is caused by more than 200 mutations in the HBB globin gene, which encodes the beta subunit of the most common form of adult hemoglobin, HbA.…
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Πέμπτη 19 Απριλίου 2018
Gene Therapy in Patients with Transfusion-Dependent β-Thalassemia
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This protocol presents an in vitro live-imaging phagocytosis assay to measure the phagocytic capacity of astrocytes. Purified rat astrocyt...
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Association française pour l'étude du cancer [Imatinib in the treatment of chronic myeloid leukemia in Morocco]. Related Articles [Im...
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Measuring alterations in metabolic rates is central to understanding the progression of various diseases and aging. Here, we present a nov...
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