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Summary Anatomy Item Literature (1716) Expression Attributions Wiki
XB-ANAT-106

Papers associated with tail bud (and myh6)

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A systemic cell cycle block impacts stage-specific histone modification profiles during Xenopus embryogenesis., Pokrovsky D., PLoS Biol. September 1, 2021; 19 (9): e3001377.                        


Loss of function of Kmt2d, a gene mutated in Kabuki syndrome, affects heart development in Xenopus laevis., Schwenty-Lara J., Dev Dyn. June 1, 2019; 248 (6): 465-476.                  


Innate Immune Response and Off-Target Mis-splicing Are Common Morpholino-Induced Side Effects in Xenopus., Gentsch GE., Dev Cell. March 12, 2018; 44 (5): 597-610.e10.                                            


Id genes are essential for early heart formation., Cunningham TJ., Genes Dev. July 1, 2017; 31 (13): 1325-1338.                


Molecular model for force production and transmission during vertebrate gastrulation., Pfister K., Development. February 15, 2016; 143 (4): 715-27.              


A thioredoxin fold protein Sh3bgr regulates Enah and is necessary for proper sarcomere formation., Jang DG., Dev Biol. September 1, 2015; 405 (1): 1-9.                                    


The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.                            


Developmental expression and cardiac transcriptional regulation of Myh7b, a third myosin heavy chain in the vertebrate heart., Warkman AS., Cytoskeleton (Hoboken). May 1, 2012; 69 (5): 324-35.  


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.                            


Notch activates Wnt-4 signalling to control medio-lateral patterning of the pronephros., Naylor RW., Development. November 1, 2009; 136 (21): 3585-95.                                  


Normal levels of p27 are necessary for somite segmentation and determining pronephric organ size., Naylor RW., Organogenesis. October 1, 2009; 5 (4): 201-10.                                          


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


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.            


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.                                


A role of D domain-related proteins in differentiation and migration of embryonic cells in Xenopus laevis., Shibata T., Mech Dev. January 1, 2008; 125 (3-4): 284-98.                            


The cdx genes and retinoic acid control the positioning and segmentation of the zebrafish pronephros., Wingert RA., PLoS Genet. October 1, 2007; 3 (10): 1922-38.                


Xtn3 is a developmentally expressed cardiac and skeletal muscle-specific novex-3 titin isoform., Brown DD., Gene Expr Patterns. October 1, 2006; 6 (8): 913-8.          


p38 MAP kinase regulates the expression of XMyf5 and affects distinct myogenic programs during Xenopus development., Keren A., Dev Biol. December 1, 2005; 288 (1): 73-86.              


Xenopus bagpipe-related gene, koza, may play a role in regulation of cell proliferation., Newman CS., Dev Dyn. December 1, 2002; 225 (4): 571-80.    


Cardiac myosin heavy chain expression during heart development in Xenopus laevis., Cox WG., Differentiation. April 1, 1995; 58 (4): 269-80.                


Induction of cardiac muscle differentiation in isolated animal pole explants of Xenopus laevis embryos., Logan M., Development. July 1, 1993; 118 (3): 865-75.              

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