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Summary Anatomy Item Literature (14955) Expression Attributions Wiki
XB-ANAT-468

Papers associated with whole organism (and mlc1)

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Ectoderm to mesoderm transition by down-regulation of actomyosin contractility., Kashkooli L., PLoS Biol. January 6, 2021; 19 (1): e3001060.                                            


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


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.              


Anillin regulates cell-cell junction integrity by organizing junctional accumulation of Rho-GTP and actomyosin., Reyes CC., Curr Biol. June 2, 2014; 24 (11): 1263-70.                


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.      


GlialCAM, a protein defective in a leukodystrophy, serves as a ClC-2 Cl(-) channel auxiliary subunit., Jeworutzki E., Neuron. March 8, 2012; 73 (5): 951-61.                


The tumor-associated EpCAM regulates morphogenetic movements through intracellular signaling., Maghzal N., J Cell Biol. November 1, 2010; 191 (3): 645-59.                


The involvement of lethal giant larvae and Wnt signaling in bottle cell formation in Xenopus embryos., Choi SC., Dev Biol. December 1, 2009; 336 (1): 68-75.      


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.                    


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.                      


Molecular pathogenesis of megalencephalic leukoencephalopathy with subcortical cysts: mutations in MLC1 cause folding defects., Duarri A., Hum Mol Genet. December 1, 2008; 17 (23): 3728-39.


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.            


Localization and functional analyses of the MLC1 protein involved in megalencephalic leukoencephalopathy with subcortical cysts., Teijido O., Hum Mol Genet. November 1, 2004; 13 (21): 2581-94.


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.    


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.                    


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


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.


The regulation of MyoD gene expression: conserved elements mediate expression in embryonic axial muscle., Asakura A., Dev Biol. October 1, 1995; 171 (2): 386-98.    


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.


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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