GATA transcription factors in congenital heart defects: A Commentary on a novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect

[1] Gruber PJ(2004)Development gone awry: congenital heart disease Circ. Res. 94 273-283

[2] Epstein JA(2010)A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect Journal of Human Genetics 55 662-667

[3] Lin Xiaoping(2009)GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling Proc. Natl Acad. Sci. USA 106 13933-13938

[4] Huo Zhaoxia(1996)Roles of gastric GATA DNA-binding proteins J. Exp. Biol. 199 513-520

[5] Liu Xingyuan(2006)GATA-6 regulates semaphorin 3C and is required in cardiac neural crest for cardiovascular morphogenesis J. Clin. Invest. 116 929-939

[6] Zhang Yangyang(2003)Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome Trends Mol. Med. 9 383-389

[7] Li Li(2003)Tbx1 is regulated by tissue-specific forkhead proteins through a common Sonic hedgehog-responsive enhancer Genes Dev. 17 269-281

[8] Zhao Hong(2009)Molecular embryology for an understanding of congenital heart diseases Anat. Sci. Int. 84 88-94

[9] Yan Biao(2008)The del22q11.2 candidate gene Tbx1 controls regional outflow tract identity and coronary artery patterning Circ. Res. 103 142-148

[10] Liu Ying(undefined)undefined undefined undefined undefined-undefined

[1] Gruber PJ(2004)Development gone awry: congenital heart disease Circ. Res. 94 273-283

[2] Epstein JA(2010)A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect Journal of Human Genetics 55 662-667

[3] Lin Xiaoping(2009)GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling Proc. Natl Acad. Sci. USA 106 13933-13938

[4] Huo Zhaoxia(1996)Roles of gastric GATA DNA-binding proteins J. Exp. Biol. 199 513-520

[5] Liu Xingyuan(2006)GATA-6 regulates semaphorin 3C and is required in cardiac neural crest for cardiovascular morphogenesis J. Clin. Invest. 116 929-939

[6] Zhang Yangyang(2003)Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome Trends Mol. Med. 9 383-389

[7] Li Li(2003)Tbx1 is regulated by tissue-specific forkhead proteins through a common Sonic hedgehog-responsive enhancer Genes Dev. 17 269-281

[8] Zhao Hong(2009)Molecular embryology for an understanding of congenital heart diseases Anat. Sci. Int. 84 88-94

[9] Yan Biao(2008)The del22q11.2 candidate gene Tbx1 controls regional outflow tract identity and coronary artery patterning Circ. Res. 103 142-148

[10] Liu Ying(undefined)undefined undefined undefined undefined-undefined