Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (82) GO Terms (4) Nucleotides (465) Proteins (43) Interactants (691) Wiki
XB--989282

Papers associated with myh4 (and morpholino)



Limit to papers also referencing gene:
Show all myh4 papers

Results 1 - 15 of 15 results

Page(s): 1

Sort Newest To Oldest Sort Oldest To Newest

The alternative splicing regulator Tra2b is required for somitogenesis and regulates splicing of an inhibitory Wnt11b isoform., Dichmann DS, Walentek P, Harland RM., Cell Rep. February 3, 2015; 10 (4): 527-36.                    


The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F, Hu W, Xian J, Ohnuma S, Brenton JD., Dev Biol. July 1, 2013; 379 (1): 16-27.                            


Spindle position in symmetric cell divisions during epiboly is controlled by opposing and dynamic apicobasal forces., Woolner S, Papalopulu N., Dev Cell. April 17, 2012; 22 (4): 775-87.                                          


Mef2d acts upstream of muscle identity genes and couples lateral myogenesis to dermomyotome formation in Xenopus laevis., Della Gaspera B, Armand AS, Lecolle S, Charbonnier F, Chanoine C., PLoS One. January 1, 2012; 7 (12): e52359.                  


Focal adhesion kinase is essential for cardiac looping and multichamber heart formation., Doherty JT, Conlon FL, Mack CP, Taylor JM., Genesis. August 1, 2010; 48 (8): 492-504.                  


Absence of heartbeat in the Xenopus tropicalis mutation muzak is caused by a nonsense mutation in cardiac myosin myh6., Abu-Daya A, Sater AK, Wells DE, Mohun TJ, Zimmerman LB., Dev Biol. December 1, 2009; 336 (1): 20-9.            


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


Morphogenetic movements driving neural tube closure in Xenopus require myosin IIB., Rolo A, Skoglund P, Keller R., Dev Biol. March 15, 2009; 327 (2): 327-38.    


Loss of REEP4 causes paralysis of the Xenopus embryo., Argasinska J, Rana AA, Gilchrist MJ, Lachani K, Young A, Smith JC., Int J Dev Biol. January 1, 2009; 53 (1): 37-43.          


A role of D domain-related proteins in differentiation and migration of embryonic cells in Xenopus laevis., Shibata T, Takahashi Y, Tasaki J, Saito Y, Izutsu Y, Maéno M., Mech Dev. March 1, 2008; 125 (3-4): 284-98.                            


Myoskeletin, a factor related to Myocardin, is expressed in somites and required for hypaxial muscle formation in Xenopus., Zhao H, Rebbert ML, Dawid IB., Int J Dev Biol. January 1, 2007; 51 (4): 315-20.              


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


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


SOX7 and SOX18 are essential for cardiogenesis in Xenopus., Zhang C, Basta T, Klymkowsky MW., Dev Dyn. December 1, 2005; 234 (4): 878-91.                    


Inhibition of the cell cycle is required for convergent extension of the paraxial mesoderm during Xenopus neurulation., Leise WF, Mueller PR., Development. April 1, 2004; 131 (8): 1703-15.              

Page(s): 1