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

关键词：

D O I：

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学科分类号：

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.

引用

页码：635 / 643

页数：8

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