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Summary Anatomy Item Literature (4274) Expression Attributions Wiki
XB-ANAT-170

Papers associated with muscle (and ctnnb1)

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TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa., Bocquet B., JCI Insight. November 8, 2023; 8 (21):                                               


Cannabinoid Receptor Type 1 regulates growth cone filopodia and axon dispersion in the optic tract of Xenopus laevis tadpoles., Elul T., Eur J Neurosci. February 1, 2022; 55 (4): 989-1001.


CRISPR-SID: Identifying EZH2 as a druggable target for desmoid tumors via in vivo dependency mapping., Naert T., Proc Natl Acad Sci U S A. November 23, 2021; 118 (47):                             


Maternal pluripotency factors initiate extensive chromatin remodelling to predefine first response to inductive signals., Gentsch GE., Nat Commun. September 19, 2019; 10 (1): 4269.                                        


The Wnt inhibitor Dkk1 is required for maintaining the normal cardiac differentiation program in Xenopus laevis., Guo Y., Dev Biol. May 1, 2019; 449 (1): 1-13.                                  


Liver Specification in the Absence of Cardiac Differentiation Revealed by Differential Sensitivity to Wnt/β Catenin Pathway Activation., Haworth K., Front Physiol. January 1, 2019; 10 155.              


Using Zebrafish to Study Collective Cell Migration in Development and Disease., Olson HM., Front Cell Dev Biol. January 1, 2018; 6 83.            


Angiopoietin-like 4 Is a Wnt Signaling Antagonist that Promotes LRP6 Turnover., Kirsch N., Dev Cell. October 9, 2017; 43 (1): 71-82.e6.                                


Brg1 chromatin remodeling ATPase balances germ layer patterning by amplifying the transcriptional burst at midblastula transition., Wagner G., PLoS Genet. May 12, 2017; 13 (5): e1006757.                                    


Spatiotemporally Controlled Mechanical Cues Drive Progenitor Mesenchymal-to-Epithelial Transition Enabling Proper Heart Formation and Function., Jackson TR., Curr Biol. May 8, 2017; 27 (9): 1326-1335.                            


The CapZ interacting protein Rcsd1 is required for cardiogenesis downstream of Wnt11a in Xenopus laevis., Hempel A., Dev Biol. April 1, 2017; 424 (1): 28-39.                                  


Genome evolution in the allotetraploid frog Xenopus laevis., Session AM., Nature. October 20, 2016; 538 (7625): 336-343.                              


Structure and functional properties of Norrin mimic Wnt for signalling with Frizzled4, Lrp5/6, and proteoglycan., Chang TH., Elife. July 9, 2015; 4                               


Klhl31 attenuates β-catenin dependent Wnt signaling and regulates embryo myogenesis., Abou-Elhamd A., Dev Biol. June 1, 2015; 402 (1): 61-71.              


Cell-autonomous signal transduction in the Xenopus egg Wnt/β-catenin pathway., Motomura E., Dev Growth Differ. December 1, 2014; 56 (9): 640-52.                                


The PDZ domain protein Mcc is a novel effector of non-canonical Wnt signaling during convergence and extension in zebrafish., Young T., Development. September 1, 2014; 141 (18): 3505-16.        


The extreme anterior domain is an essential craniofacial organizer acting through Kinin-Kallikrein signaling., Jacox L., Cell Rep. July 24, 2014; 8 (2): 596-609.                            


Hhex and Cer1 mediate the Sox17 pathway for cardiac mesoderm formation in embryonic stem cells., Liu Y., Stem Cells. June 1, 2014; 32 (6): 1515-26.              


Wnt signaling and cell-matrix adhesion., Astudillo P., Curr Mol Med. February 1, 2014; 14 (2): 209-20.


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


Neurulation and neurite extension require the zinc transporter ZIP12 (slc39a12)., Chowanadisai W., Proc Natl Acad Sci U S A. June 11, 2013; 110 (24): 9903-8.                


sfrp1 promotes cardiomyocyte differentiation in Xenopus via negative-feedback regulation of Wnt signalling., Gibb N., Development. April 1, 2013; 140 (7): 1537-49.                                    


Connective tissue cells, but not muscle cells, are involved in establishing the proximo-distal outcome of limb regeneration in the axolotl., Nacu E., Development. February 1, 2013; 140 (3): 513-8.


Imparting regenerative capacity to limbs by progenitor cell transplantation., Lin G., Dev Cell. January 14, 2013; 24 (1): 41-51.                          


Transgenic analysis of signaling pathways required for Xenopus tadpole spinal cord and muscle regeneration., Lin G., Anat Rec (Hoboken). October 1, 2012; 295 (10): 1532-40.


Activation of voltage gated K⁺ channel Kv1.5 by β-catenin., Munoz C., Biochem Biophys Res Commun. January 13, 2012; 417 (2): 692-6.


A photoactivatable small-molecule inhibitor for light-controlled spatiotemporal regulation of Rho kinase in live embryos., Morckel AR., Development. January 1, 2012; 139 (2): 437-42.        


Maternal xNorrin, a canonical Wnt signaling agonist and TGF-β antagonist, controls early neuroectoderm specification in Xenopus., Xu S., PLoS Biol. January 1, 2012; 10 (3): e1001286.                                    


WNT-3A modulates articular chondrocyte phenotype by activating both canonical and noncanonical pathways., Nalesso G., J Cell Biol. May 2, 2011; 193 (3): 551-64.              


Xenopus delta-catenin is essential in early embryogenesis and is functionally linked to cadherins and small GTPases., Gu D., J Cell Sci. November 15, 2009; 122 (Pt 22): 4049-61.            


Bone morphogenetic protein 15 (BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis., Di Pasquale E., J Biol Chem. September 18, 2009; 284 (38): 26127-36.                        


Retinoid signaling can repress blastula Wnt signaling and impair dorsal development in Xenopus embryo., Li S., Differentiation. October 1, 2008; 76 (8): 897-907.            


Requirement for Wnt and FGF signaling in Xenopus tadpole tail regeneration., Lin G., Dev Biol. April 15, 2008; 316 (2): 323-35.              


Silencing of Smed-betacatenin1 generates radial-like hypercephalized planarians., Iglesias M., Development. April 1, 2008; 135 (7): 1215-21.  


Embryonic cells depleted of beta-catenin remain competent to differentiate into dorsal mesodermal derivatives., Chu FH., Dev Dyn. November 1, 2007; 236 (11): 3007-19.


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


The LIM-only protein FHL2 interacts with beta-catenin and promotes differentiation of mouse myoblasts., Martin B., J Cell Biol. October 14, 2002; 159 (1): 113-22.                  


The Wnt/beta-catenin pathway posteriorizes neural tissue in Xenopus by an indirect mechanism requiring FGF signalling., Domingos PM., Dev Biol. November 1, 2001; 239 (1): 148-60.              


Axis induction by wnt signaling: Target promoter responsiveness regulates competence., Darken RS., Dev Biol. June 1, 2001; 234 (1): 42-54.            


Wnt signaling in Xenopus embryos inhibits bmp4 expression and activates neural development., Baker JC., Genes Dev. December 1, 1999; 13 (23): 3149-59.              


Sizzled: a secreted Xwnt8 antagonist expressed in the ventral marginal zone of Xenopus embryos., Salic AN., Development. December 1, 1997; 124 (23): 4739-48.              


Analysis of Dishevelled signalling pathways during Xenopus development., Sokol SY., Curr Biol. November 1, 1996; 6 (11): 1456-67.                  


Maternal beta-catenin establishes a 'dorsal signal' in early Xenopus embryos., Wylie C., Development. October 1, 1996; 122 (10): 2987-96.              


Beta-catenin localization during Xenopus embryogenesis: accumulation at tissue and somite boundaries., Fagotto F., Development. December 1, 1994; 120 (12): 3667-79.                  

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