期刊
BLOOD
卷 107, 期 2, 页码 435-443出版社
AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2005-05-2113
关键词
-
类别
资金
- NHLBI NIH HHS [HL-59887] Funding Source: Medline
- NIDDK NIH HHS [DK-56635, DK-07373] Funding Source: Medline
The human globin genes are among the most extensively characterized in the human genome, yet the details of the molecular events regulating normal human hemoglobin switching and the potential reactivation of fetal hemoglobin in adult hematopoietic cells remain elusive. Recent discoveries demonstrate physical interactions between the beta locus control region and the downstream structural gamma-and beta-globin genes, and with transcription factors and chromatin remodeling complexes. These interactions all play roles in globin gene expression and globin switching at the human beta-globin locus. If the molecular events in hemoglobin switching were better understood and fetal hemoglobin could be more fully reactivated in adult cells, the insights obtained might lead to new approaches to the therapy of sickle cell disease and beta thalassemia by identifying specific new targets for molecular therapies.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据