Embryonic and fetal β-globin gene repression by the orphan nuclear receptors, TR2 and TR4-Reference-Cited by-同舟云学术

Embryonic and fetal β-globin gene repression by the orphan nuclear receptors, TR2 and TR4

Published:2007-04-12 Issue:9 Volume:26 Page:2295-2306
ISSN:0261-4189
Container-title:The EMBO Journal
language:
Short-container-title:EMBO J

Author:

Tanabe Osamu,McPhee David,Kobayashi Shoko,Shen Yannan,Brandt William,Jiang Xia,Campbell Andrew D,Chen Yei-Tsung,Chang Chawn shang,Yamamoto Masayuki,Tanimoto Keiji,Engel James Douglas

Publisher

Wiley

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience

Reference48 articles.

1. Human gamma- to beta-globin gene switching in transgenic mice.

2. A single point mutation is the cause of the Greek form of hereditary persistence of fetal haemoglobin

3. Synergistic regulation of human beta-globin gene switching by locus control region elements HS3 and HS4.

4. Hypersensitive Site 2 Specifies a Unique Function within the Human β-Globin Locus Control Region To Stimulate Globin Gene Transcription

5. Long-range chromatin regulatory interactions in vivo

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