Impairment of T Cell Development in <i>δ</i> <i>EF1</i> Mutant Mice
Yujiro Higashi(Aichi Human Service Center), Hisato Kondoh(The University of Osaka), Tsuyoshi Takagi(The University of Osaka), Hiroki Moribe(The University of Osaka), Kiyoshi Kawakami(Jichi Medical University), Hitoshi Kikutani(Immune Regulation (United Kingdom)), Ryohei Sekido(Jichi Medical University)
Cited by 151
Related Papers
Mice Lacking Zfhx1b, the Gene That Codes for Smad-Interacting Protein-1, Reveal a Role for Multiple Neural Crest Cell Defects in the Etiology of Hirschsprung Disease–Mental Retardation Syndrome
|The American Journal of Human Genetics|2003|308
Zeb1 links epithelial-mesenchymal transition and cellular senescence
|Development|2008|302
δEF1, a zinc finger and homeodomain transcription factor, is required for skeleton patterning in multiple lineages
|Development|1998|298
Transcriptional repressor ZEB2 promotes terminal differentiation of CD8+ effector and memory T cell populations during infection
|The Journal of Experimental Medicine|2015|258