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Summary Anatomy Item Literature (102) Expression Attributions Wiki
XB-ANAT-328

Papers associated with endocardial tube (and tnni3)

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


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


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


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


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


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.          


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.            


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


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.                


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.          


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


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


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


Regulation of heart size in Xenopus laevis., Garriock RJ., Differentiation. October 1, 2003; 71 (8): 506-15.            


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


BMP signaling is required for heart formation in vertebrates., Shi Y, Shi Y., Dev Biol. August 15, 2000; 224 (2): 226-37.          


The lefty-related factor Xatv acts as a feedback inhibitor of nodal signaling in mesoderm induction and L-R axis development in xenopus., Cheng AM., Development. March 1, 2000; 127 (5): 1049-61.                


The homeobox gene Pitx2: mediator of asymmetric left-right signaling in vertebrate heart and gut looping., Campione M., Development. March 1, 1999; 126 (6): 1225-34.            


Tinman function is essential for vertebrate heart development: elimination of cardiac differentiation by dominant inhibitory mutants of the tinman-related genes, XNkx2-3 and XNkx2-5., Grow MW., Dev Biol. December 1, 1998; 204 (1): 187-96.      


Vertebrate tinman homologues XNkx2-3 and XNkx2-5 are required for heart formation in a functionally redundant manner., Fu Y., Development. November 1, 1998; 125 (22): 4439-49.            


Retinoic acid can block differentiation of the myocardium after heart specification., Drysdale TA., Dev Biol. August 15, 1997; 188 (2): 205-15.          

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