Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
3R01HL048702-02S1
Application #
948100
Study Section
Allergy and Immunology Study Section (ALY)
Project Start
1993-12-01
Project End
1997-11-30
Budget Start
1994-12-01
Budget End
1995-11-30
Support Year
2
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Timblin, Greg A; Xie, Liangqi; Tjian, Robert et al. (2017) Dual Mechanism of Rag Gene Repression by c-Myb during Pre-B Cell Proliferation. Mol Cell Biol 37:
Vettermann, Christian; Timblin, Greg A; Lim, Vivian et al. (2015) The proximal J kappa germline-transcript promoter facilitates receptor editing through control of ordered recombination. PLoS One 10:e0113824
Chow, Kwan T; Schulz, Danae; McWhirter, Sarah M et al. (2013) Gfi1 and gfi1b repress rag transcription in plasmacytoid dendritic cells in vitro. PLoS One 8:e75891
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Chow, Kwan T; Timblin, Greg A; McWhirter, Sarah M et al. (2013) MK5 activates Rag transcription via Foxo1 in developing B cells. J Exp Med 210:1621-34
Schulz, Danae; Vassen, Lothar; Chow, Kwan T et al. (2012) Gfi1b negatively regulates Rag expression directly and via the repression of FoxO1. J Exp Med 209:187-99
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Guo, Chunguang; Yoon, Hye Suk; Franklin, Andrew et al. (2011) CTCF-binding elements mediate control of V(D)J recombination. Nature 477:424-30

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