A global network of transcription factors, involving E2A, EBF1 and Foxo1, that orchestrates B cell fate

被引:0
作者
Yin C Lin
Suchit Jhunjhunwala
Christopher Benner
Sven Heinz
Eva Welinder
Robert Mansson
Mikael Sigvardsson
James Hagman
Celso A Espinoza
Janusz Dutkowski
Trey Ideker
Christopher K Glass
Cornelis Murre
机构
[1] University of California,Department of Molecular Biology
[2] San Diego,Department of Cellular and Molecular Medicine
[3] University of California,Department for Biomedicine and Surgery
[4] San Diego,Integrated Department of Immunology
[5] Center for Stem Cell Biology and Cell Therapy,Department of Bioengineering and Department of Cellular and Molecular Medicine
[6] Lund University,undefined
[7] Lund,undefined
[8] Linkoping University,undefined
[9] Linkoping,undefined
[10] National Jewish Health,undefined
[11] Ludwig Institute for Cancer Research,undefined
[12] University of California,undefined
[13] San Diego,undefined
[14] University of California,undefined
[15] San Diego,undefined
[16] The Institute for Genomic Medicine,undefined
[17] University of California,undefined
[18] San Diego,undefined
来源
Nature Immunology | 2010年 / 11卷
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摘要
Lineage specification and development require a hierarchy of transcription factors. Murre and colleagues have compiled a genome-wide set of cis-acting targets centered on E2A, EBF1 and Foxo1 that govern early B cell development.
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页码:635 / 643
页数:8
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