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Summary Anatomy Item Literature (3631) Expression Attributions Wiki
XB-ANAT-523

Papers associated with anterior (and mlc1)

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Otic Neurogenesis in Xenopus laevis: Proliferation, Differentiation, and the Role of Eya1., Almasoudi SH., Front Neuroanat. January 1, 2021; 15 722374.                                                    


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


EphA7 modulates apical constriction of hindbrain neuroepithelium during neurulation in Xenopus., Wang X., Biochem Biophys Res Commun. October 28, 2016; 479 (4): 759-765.        


Pax8 and Pax2 are specifically required at different steps of Xenopus pronephros development., Buisson I., Dev Biol. January 15, 2015; 397 (2): 175-90.                            


Variable combinations of specific ephrin ligand/Eph receptor pairs control embryonic tissue separation., Rohani N., PLoS Biol. September 23, 2014; 12 (9): e1001955.              


GEF-H1 functions in apical constriction and cell intercalations and is essential for vertebrate neural tube closure., Itoh K., J Cell Sci. June 1, 2014; 127 (Pt 11): 2542-53.              


The Xenopus homologue of Down syndrome critical region protein 6 drives dorsoanterior gene expression and embryonic axis formation by antagonising polycomb group proteins., Li HY., Development. December 1, 2013; 140 (24): 4903-13.                                


Vertebrate kidney tubules elongate using a planar cell polarity-dependent, rosette-based mechanism of convergent extension., Lienkamp SS., Nat Genet. December 1, 2012; 44 (12): 1382-7.      


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.                


Mad is required for wingless signaling in wing development and segment patterning in Drosophila., Eivers E., PLoS One. August 6, 2009; 4 (8): e6543.                    


Xenopus ADAM19 is involved in neural, neural crest and muscle development., Neuner R., Mech Dev. January 1, 2009; 126 (3-4): 240-55.                      


Redundancy and evolution of GATA factor requirements in development of the myocardium., Peterkin T., Dev Biol. November 15, 2007; 311 (2): 623-35.          


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


Conserved roles for Oct4 homologues in maintaining multipotency during early vertebrate development., Morrison GM., Development. May 1, 2006; 133 (10): 2011-22.                


The MLC1v gene provides a transgenic marker of myocardium formation within developing chambers of the Xenopus heart., Smith SJ., Dev Dyn. April 1, 2005; 232 (4): 1003-12.            


Connective-tissue growth factor modulates WNT signalling and interacts with the WNT receptor complex., Mercurio S., Development. May 1, 2004; 131 (9): 2137-47.                    


Induction of cardiomyocytes by GATA4 in Xenopus ectodermal explants., Latinkić BV., Development. August 1, 2003; 130 (16): 3865-76.              


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.    


An anterior signalling centre in Xenopus revealed by the homeobox gene XHex., Jones CM., Curr Biol. September 9, 1999; 9 (17): 946-54.              

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