MEF2CGATA4

Seiichiro Honda1, Taketaro Sadahiro2, Yuto Abe1

  • 1Department of Cardiology, Institute of Medicine, University of Tsukuba, 1-1-1 Tennoudai, Tsukuba City, Ibaraki, 305-8575, Japan.

概括

优化心脏重编程因子MEF2C,GATA4和TBX5 (MGT) 通过删除非必不可少的域显著增强诱导心肌细胞 (iCM) 的产生. 这种缩短的MGT序列提高了效率,并可能促进再生医学应用.