KLF1 directly activates expression of the novel fetal globin repressor ZBTB7A/LRF in erythroid cells
Abstract: Genes encoding the human β-like hemoglobin proteins undergo a developmental switch from fetal γ-globin to adult β-globin expression around the time of birth. β-hemoglobinopathies, such as sickle-cell disease and β-thalassemia, result from mutations affecting the adult β-globin gene. The on...
Main Authors: | , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2017-04-01
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Series: | Blood Advances |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2473952920301737 |