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Summary Anatomy Item Literature (7318) Expression Attributions Wiki
XB-ANAT-489

Papers associated with trunk (and mlc1)

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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.                            


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.                


N- and E-cadherins in Xenopus are specifically required in the neural and non-neural ectoderm, respectively, for F-actin assembly and morphogenetic movements., Nandadasa S., Development. April 1, 2009; 136 (8): 1327-38.                      


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


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


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.              


Phorbol esters increase MLC phosphorylation and actin remodeling in bovine lung endothelium without increased contraction., Bogatcheva NV., Am J Physiol Lung Cell Mol Physiol. August 1, 2003; 285 (2): L415-26.


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.    


The small muscle-specific protein Csl modifies cell shape and promotes myocyte fusion in an insulin-like growth factor 1-dependent manner., Palmer S., J Cell Biol. May 28, 2001; 153 (5): 985-98.                    


CARP, a cardiac ankyrin repeat protein, is downstream in the Nkx2-5 homeobox gene pathway., Zou Y., Development. February 1, 1997; 124 (4): 793-804.


Expression of cardiac muscle markers in rat myocyte cell lines., Engelmann GL., Mol Cell Biochem. April 1, 1996; 157 (1-2): 87-91.


EFIA/YB-1 is a component of cardiac HF-1A binding activity and positively regulates transcription of the myosin light-chain 2v gene., Zou Y., Mol Cell Biol. June 1, 1995; 15 (6): 2972-82.


Induction of T cell differentiation in early-thymectomized Xenopus by grafting adult thymuses from either MHC-matched or from partially or totally MHC-mismatched donors., Nagata S., Thymus. January 1, 1984; 6 (1-2): 89-103.


Monoclonal anti-IgM can separate T cell from B cell proliferative responses in the frog, Xenopus laevis., Bleicher PA., J Immunol. October 1, 1981; 127 (4): 1549-55.

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