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Summary Anatomy Item Literature (1914) Expression Attributions Wiki
XB-ANAT-3755

Papers associated with rostral tuberal region (and tbx5)

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Carboxy terminus of GATA4 transcription factor is required for its cardiogenic activity and interaction with CDK4., Gallagher JM., Mech Dev. November 1, 2014; 134 31-41.            

Hhex and Cer1 mediate the Sox17 pathway for cardiac mesoderm formation in embryonic stem cells., Liu Y., Stem Cells. June 1, 2014; 32 (6): 1515-26.              

Cyclin D2 is a GATA4 cofactor in cardiogenesis., Yamak A., Proc Natl Acad Sci U S A. January 28, 2014; 111 (4): 1415-20.          

Zygotic expression of Exostosin1 (Ext1) is required for BMP signaling and establishment of dorsal-ventral pattern in Xenopus., Shieh YE., Int J Dev Biol. January 1, 2014; 58 (1): 27-34.          

Tcf21 regulates the specification and maturation of proepicardial cells., Tandon P., Development. June 1, 2013; 140 (11): 2409-21.                                

Microarray-based identification of Pitx3 targets during Xenopus embryogenesis., Hooker L., Dev Dyn. September 1, 2012; 241 (9): 1487-505.                          

Inhibition of heart formation by lithium is an indirect result of the disruption of tissue organization within the embryo., Martin LK., Dev Growth Differ. February 1, 2012; 54 (2): 153-66.                

Tbx5 overexpression favors a first heart field lineage in murine embryonic stem cells and in Xenopus laevis embryos., Herrmann F., Dev Dyn. December 1, 2011; 240 (12): 2634-45.  

The secreted integrin ligand nephronectin is necessary for forelimb formation in Xenopus tropicalis., Abu-Daya A., Dev Biol. January 15, 2011; 349 (2): 204-12.                                

Different requirement for Wnt/β-catenin signaling in limb regeneration of larval and adult Xenopus., Yokoyama H., PLoS One. January 1, 2011; 6 (7): e21721.                

Focal adhesion kinase is essential for cardiac looping and multichamber heart formation., Doherty JT., Genesis. August 1, 2010; 48 (8): 492-504.                  

Zygotic VegT is required for Xenopus paraxial mesoderm formation and is regulated by Nodal signaling and Eomesodermin., Fukuda M., Int J Dev Biol. January 1, 2010; 54 (1): 81-92.              

Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling., Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.                

Comparative gene expression analysis and fate mapping studies suggest an early segregation of cardiogenic lineages in Xenopus laevis., Gessert S., Dev Biol. October 15, 2009; 334 (2): 395-408.          

GATA4 and GATA5 are essential for heart and liver development in Xenopus embryos., Haworth KE., BMC Dev Biol. July 28, 2008; 8 74.                        

XHAPLN3 plays a key role in cardiogenesis by maintaining the hyaluronan matrix around heart anlage., Ito Y., Dev Biol. July 1, 2008; 319 (1): 34-45.                          

HIF-1alpha signaling upstream of NKX2.5 is required for cardiac development in Xenopus., Nagao K., J Biol Chem. April 25, 2008; 283 (17): 11841-9.                        

Vertebrate CASTOR is required for differentiation of cardiac precursor cells at the ventral midline., Christine KS., Dev Cell. April 1, 2008; 14 (4): 616-23.                                

The Gata5 target, TGIF2, defines the pancreatic region by modulating BMP signals within the endoderm., Spagnoli FM., Development. February 1, 2008; 135 (3): 451-61.                                                    

Multiple functions of Cerberus cooperate to induce heart downstream of Nodal., Foley AC., Dev Biol. March 1, 2007; 303 (1): 57-65.        

TBX5 is required for embryonic cardiac cell cycle progression., Goetz SC., Development. July 1, 2006; 133 (13): 2575-84.                

Xtbx6r, a novel T-box gene expressed in the paraxial mesoderm, has anterior neural-inducing activity., Yabe S., Int J Dev Biol. January 1, 2006; 50 (8): 681-9.                        

SOX7 and SOX18 are essential for cardiogenesis in Xenopus., Zhang C., Dev Dyn. December 1, 2005; 234 (4): 878-91.                    

Myocardin is sufficient and necessary for cardiac gene expression in Xenopus., Small EM., Development. March 1, 2005; 132 (5): 987-97.            

Heart induction by Wnt antagonists depends on the homeodomain transcription factor Hex., Foley AC., Genes Dev. February 1, 2005; 19 (3): 387-96.            

Cardiac T-box factor Tbx20 directly interacts with Nkx2-5, GATA4, and GATA5 in regulation of gene expression in the developing heart., Stennard FA., Dev Biol. October 15, 2003; 262 (2): 206-24.  

Amphibian in vitro heart induction: a simple and reliable model for the study of vertebrate cardiac development., Ariizumi T., Int J Dev Biol. September 1, 2003; 47 (6): 405-10.      

Endoderm specification and differentiation in Xenopus embryos., Horb ME., Dev Biol. August 15, 2001; 236 (2): 330-43.                

A role for BMP signalling in heart looping morphogenesis in Xenopus., Breckenridge RA., Dev Biol. April 1, 2001; 232 (1): 191-203.          

Wnt antagonism initiates cardiogenesis in Xenopus laevis., Schneider VA., Genes Dev. February 1, 2001; 15 (3): 304-15.        

Xbra3 induces mesoderm and neural tissue in Xenopus laevis., Strong CF., Dev Biol. June 15, 2000; 222 (2): 405-19.                  

Conserved and divergent expression of T-box genes Tbx2-Tbx5 in Xenopus., Takabatake Y., Mech Dev. March 1, 2000; 91 (1-2): 433-7.                            

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