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Production of beta-globin and adult hemoglobin following G418 treatment of erythroid precursor cells from homozygous beta039 thalassemia patients
American Journal of Hematology, 10/09/09
Salvatori F et al. – This study strongly suggests that ribosomal readthrough should be considered a strategy for developing experimental strategies for the treatment of beta0–thalassemia caused by stop codon mutations.
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Unpredictability of iv Busulfan pharmacokinetics in children undergoing hematopoietic stem cell transplant for advanced beta thalassemia: Limited toxicity with a dose adjustment policy
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Today in Basic Science/Genetics...keeping you current
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Melanoma-associated fibroblasts modulate NK cell phenotype and antitumor cytotoxicity
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A gene expression signature that predicts the therapeutic response of the basal-like breast cancer to neoadjuvant chemotherapy
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