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Summary Anatomy Item Literature (8570) Expression Attributions Wiki
XB-ANAT-506

Papers associated with embryonic structure (and tnni3)

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Liver Specification in the Absence of Cardiac Differentiation Revealed by Differential Sensitivity to Wnt/β Catenin Pathway Activation., Haworth K., Front Physiol. January 1, 2019; 10 155.              


Frizzled-7 is required for Xenopus heart development., Abu-Elmagd M., Biol Open. December 15, 2017; 6 (12): 1861-1868.            


Ventricular cell fate can be specified until the onset of myocardial differentiation., Caporilli S., Mech Dev. February 1, 2016; 139 31-41.                        


Nodal signalling in Xenopus: the role of Xnr5 in left/right asymmetry and heart development., Tadjuidje E., Open Biol. January 1, 2016; 6 (8):             


Direct nkx2-5 transcriptional repression of isl1 controls cardiomyocyte subtype identity., Dorn T., Stem Cells. April 1, 2015; 33 (4): 1113-29.              


Understanding early organogenesis using a simplified in situ hybridization protocol in Xenopus., Deimling SJ., J Vis Exp. January 12, 2015; (95): e51526.            


Xenopus Pkdcc1 and Pkdcc2 Are Two New Tyrosine Kinases Involved in the Regulation of JNK Dependent Wnt/PCP Signaling Pathway., Vitorino M., PLoS One. January 1, 2015; 10 (8): e0135504.                                    


Isolation and characterization of Xenopus soluble epoxide hydrolase., Purba ER., Biochim Biophys Acta. July 1, 2014; 1841 (7): 954-62.                    


Comparative analysis reveals distinct and overlapping functions of Mef2c and Mef2d during cardiogenesis in Xenopus laevis., Guo Y., PLoS One. January 1, 2014; 9 (1): e87294.                


sfrp1 promotes cardiomyocyte differentiation in Xenopus via negative-feedback regulation of Wnt signalling., Gibb N., Development. April 1, 2013; 140 (7): 1537-49.                                    


Prolonged FGF signaling is necessary for lung and liver induction in Xenopus., Shifley ET., BMC Dev Biol. December 17, 2012; 12 27.                      


Sizzled-tolloid interactions maintain foregut progenitors by regulating fibronectin-dependent BMP signaling., Kenny AP., Dev Cell. August 14, 2012; 23 (2): 292-304.                                


Suppression of Bmp4 signaling by the zinc-finger repressors Osr1 and Osr2 is required for Wnt/β-catenin-mediated lung specification in Xenopus., Rankin SA, Rankin SA., Development. August 1, 2012; 139 (16): 3010-20.                                                                                


An essential and highly conserved role for Zic3 in left-right patterning, gastrulation and convergent extension morphogenesis., Cast AE., Dev Biol. April 1, 2012; 364 (1): 22-31.            


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.  


Fgf is required to regulate anterior-posterior patterning in the Xenopus lateral plate mesoderm., Deimling SJ., Mech Dev. September 1, 2011; 128 (7-10): 327-41.                              


Early cardiac morphogenesis defects caused by loss of embryonic macrophage function in Xenopus., Smith SJ., Mech Dev. May 1, 2011; 128 (5-6): 303-15.                            


Claudin5 genes encoding tight junction proteins are required for Xenopus heart formation., Yamagishi M., Dev Growth Differ. September 1, 2010; 52 (7): 665-75.                        


Lymph heart musculature is under distinct developmental control from lymphatic endothelium., Peyrot SM., Dev Biol. March 15, 2010; 339 (2): 429-38.        


Neural ectoderm-secreted FGF initiates the expression of Nkx2.5 in cardiac progenitors via a p38 MAPK/CREB pathway., Keren-Politansky A., Dev Biol. November 15, 2009; 335 (2): 374-84.            


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.          


In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.                      


Shox2 is essential for the differentiation of cardiac pacemaker cells by repressing Nkx2-5., Espinoza-Lewis RA., Dev Biol. March 15, 2009; 327 (2): 376-85.      


Wnt6 signaling regulates heart muscle development during organogenesis., Lavery DL., Dev Biol. November 15, 2008; 323 (2): 177-88.            


Sfrp5 coordinates foregut specification and morphogenesis by antagonizing both canonical and noncanonical Wnt11 signaling., Li Y., Genes Dev. November 1, 2008; 22 (21): 3050-63.                        


GATA transcription factors integrate Wnt signalling during heart development., Afouda BA., Development. October 1, 2008; 135 (19): 3185-90.        


DM-GRASP/ALCAM/CD166 is required for cardiac morphogenesis and maintenance of cardiac identity in first heart field derived cells., Gessert S., Dev Biol. September 1, 2008; 321 (1): 150-61.            


Cardiac differentiation in Xenopus requires the cyclin-dependent kinase inhibitor, p27Xic1., Movassagh M., Cardiovasc Res. August 1, 2008; 79 (3): 436-47.                                


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


IGFBP-4 is an inhibitor of canonical Wnt signalling required for cardiogenesis., Zhu W., Nature. July 17, 2008; 454 (7202): 345-9.                        


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.                          


A crucial role of a high mobility group protein HMGA2 in cardiogenesis., Monzen K., Nat Cell Biol. May 1, 2008; 10 (5): 567-74.                  


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 amphibian second heart field: Xenopus islet-1 is required for cardiovascular development., Brade T., Dev Biol. November 15, 2007; 311 (2): 297-310.          


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


The left-right axis is regulated by the interplay of Coco, Xnr1 and derrière in Xenopus embryos., Vonica A., Dev Biol. March 1, 2007; 303 (1): 281-94.              


ADMP2 is essential for primitive blood and heart development in Xenopus., Kumano G., Dev Biol. November 15, 2006; 299 (2): 411-23.                


Xapelin and Xmsr are required for cardiovascular development in Xenopus laevis., Inui M., Dev Biol. October 1, 2006; 298 (1): 188-200.                


Characterization of myeloid cells derived from the anterior ventral mesoderm in the Xenopus laevis embryo., Tashiro S., Dev Growth Differ. October 1, 2006; 48 (8): 499-512.                    


Reduction of XNkx2-10 expression leads to anterior defects and malformation of the embryonic heart., Allen BG., Mech Dev. October 1, 2006; 123 (10): 719-29.          


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


Retinoic acid signaling is essential for formation of the heart tube in Xenopus., Collop AH., Dev Biol. March 1, 2006; 291 (1): 96-109.                  


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.            


Tbx5 and Tbx20 act synergistically to control vertebrate heart morphogenesis., Brown DD., Development. February 1, 2005; 132 (3): 553-63.                


Amphibian cardiac troponin I gene''s organization, developmental expression, and regulatory properties are different from its mammalian homologue., Warkman AS., Dev Dyn. February 1, 2004; 229 (2): 275-88.

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