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Summary Anatomy Item Literature (1651) Expression Attributions Wiki
XB-ANAT-58

Papers associated with somite (and smad2)

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ZSWIM4 regulates embryonic patterning and BMP signaling by promoting nuclear Smad1 degradation., Wang C., EMBO Rep. February 1, 2024; 25 (2): 646-671.                                          


Prdm15 acts upstream of Wnt4 signaling in anterior neural development of Xenopus laevis., Saumweber E., Front Cell Dev Biol. January 1, 2024; 12 1316048.                            


Pinhead signaling regulates mesoderm heterogeneity via the FGF receptor-dependent pathway., Ossipova O., Development. September 11, 2020; 147 (17):                 


Pinhead signaling regulates mesoderm heterogeneity via FGF receptor-dependent pathway., Ossipova O., Development. January 1, 2020;                                       


Dual control of pcdh8l/PCNS expression and function in Xenopus laevis neural crest cells by adam13/33 via the transcription factors tfap2α and arid3a., Khedgikar V., Elife. August 22, 2017; 6                                                             


Similarity in gene-regulatory networks suggests that cancer cells share characteristics of embryonic neural cells., Zhang Z., J Biol Chem. August 4, 2017; 292 (31): 12842-12859.        


Dissecting BMP signaling input into the gene regulatory networks driving specification of the blood stem cell lineage., Kirmizitas A., Proc Natl Acad Sci U S A. June 6, 2017; 114 (23): 5814-5821.                    


Sox5 Is a DNA-binding cofactor for BMP R-Smads that directs target specificity during patterning of the early ectoderm., Nordin K., Dev Cell. November 10, 2014; 31 (3): 374-382.                              


Global identification of Smad2 and Eomesodermin targets in zebrafish identifies a conserved transcriptional network in mesendoderm and a novel role for Eomesodermin in repression of ectodermal gene expression., Nelson AC., BMC Biol. October 3, 2014; 12 81.            


Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.                                


RAB8B is required for activity and caveolar endocytosis of LRP6., Demir K., Cell Rep. September 26, 2013; 4 (6): 1224-34.                    


In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency., Gentsch GE., Cell Rep. September 26, 2013; 4 (6): 1185-96.                              


Lin28 proteins are required for germ layer specification in Xenopus., Faas L., Development. March 1, 2013; 140 (5): 976-86.                      


SNW1 is a critical regulator of spatial BMP activity, neural plate border formation, and neural crest specification in vertebrate embryos., Wu MY., PLoS Biol. February 15, 2011; 9 (2): e1000593.                              


TGF-beta signaling is required for multiple processes during Xenopus tail regeneration., Ho DM., Dev Biol. March 1, 2008; 315 (1): 203-16.                  


Coordination of cell polarity during Xenopus gastrulation., Shindo A., PLoS One. February 6, 2008; 3 (2): e1600.              


The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning., Sander V., EMBO J. June 20, 2007; 26 (12): 2955-65.              


Inhibitor-resistant type I receptors reveal specific requirements for TGF-beta signaling in vivo., Ho DM., Dev Biol. July 15, 2006; 295 (2): 730-42.            


Genomic profiling of mixer and Sox17beta targets during Xenopus endoderm development., Dickinson K., Dev Dyn. February 1, 2006; 235 (2): 368-81.                        


Vg 1 is an essential signaling molecule in Xenopus development., Birsoy B., Development. January 1, 2006; 133 (1): 15-20.    


New roles for FoxH1 in patterning the early embryo., Kofron M., Development. October 1, 2004; 131 (20): 5065-78.              


Lefty blocks a subset of TGFbeta signals by antagonizing EGF-CFC coreceptors., Cheng SK., PLoS Biol. February 1, 2004; 2 (2): E30.                  


Evidence for antagonism of BMP-4 signals by MAP kinase during Xenopus axis determination and neural specification., Sater AK., Differentiation. September 1, 2003; 71 (7): 434-44.                


Xenopus neurula left-right asymmetry is respeficied by microinjecting TGF-beta5 protein., Mogi K., Int J Dev Biol. February 1, 2003; 47 (1): 15-29.                  


The nodal target gene Xmenf is a component of an FGF-independent pathway of ventral mesoderm induction in Xenopus., Kumano G., Mech Dev. October 1, 2002; 118 (1-2): 45-56.    


The roles of three signaling pathways in the formation and function of the Spemann Organizer., Xanthos JB., Development. September 1, 2002; 129 (17): 4027-43.                  


Beta-catenin, MAPK and Smad signaling during early Xenopus development., Schohl A., Development. January 1, 2002; 129 (1): 37-52.                                                                                                      


Expression cloning of Xenopus Os4, an evolutionarily conserved gene, which induces mesoderm and dorsal axis., Zohn IE., Dev Biol. November 1, 2001; 239 (1): 118-31.                    


Activin A signaling directly activates Xenopus winged helix factors XFD-4/4', the orthologues to mammalian MFH-1., Köster M., Dev Genes Evol. June 1, 2000; 210 (6): 320-4.


Activation of Stat3 by cytokine receptor gp130 ventralizes Xenopus embryos independent of BMP-4., Nishinakamura R., Dev Biol. December 15, 1999; 216 (2): 481-90.              


Smad7 inhibits mesoderm formation and promotes neural cell fate in Xenopus embryos., Bhushan A., Dev Biol. August 15, 1998; 200 (2): 260-8.              


The Xenopus dorsalizing factor Gremlin identifies a novel family of secreted proteins that antagonize BMP activities., Hsu DR., Mol Cell. April 1, 1998; 1 (5): 673-83.                  

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