טוען...
Therapeutic levels of fetal hemoglobin in erythroid progeny of β-thalassemic CD34(+) cells after lentiviral vector-mediated gene transfer
β-Thalassemia major results from severely reduced or absent expression of the β-chain of adult hemoglobin (α(2)β(2);HbA). Increased levels of fetal hemoglobin (α(2)γ(2);HbF), such as occurs with hereditary persistence of HbF, ameliorate the severity of β-thalassemia, raising the potential for geneti...
שמור ב:
| Main Authors: | , , , , , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
American Society of Hematology
2011
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3062294/ https://ncbi.nlm.nih.gov/pubmed/21156846 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2010-08-300723 |
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