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Summary Anatomy Item Literature (2419) Expression Attributions Wiki
XB-ANAT-28

Papers associated with epidermis (and dkk1)

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The early dorsal signal in vertebrate embryos requires endolysosomal membrane trafficking., Azbazdar Y., Bioessays. January 1, 2024; 46 (1): e2300179.                            


Evo-Devo of Urbilateria and its larval forms., De Robertis EM., Dev Biol. July 1, 2022; 487 10-20.        


Secreted inhibitors drive the loss of regeneration competence in Xenopus limbs., Aztekin C., Development. June 1, 2021; 148 (11):                                             


Establishing embryonic territories in the context of Wnt signaling., Velloso I., Int J Dev Biol. January 1, 2021; 65 (4-5-6): 227-233.      


TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis., Chen M., Elife. September 14, 2020; 9                                                                                           


ΔN-Tp63 Mediates Wnt/β-Catenin-Induced Inhibition of Differentiation in Basal Stem Cells of Mucociliary Epithelia., Haas M., Cell Rep. September 24, 2019; 28 (13): 3338-3352.e6.                              


Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis., Ding Y., Proc Natl Acad Sci U S A. September 25, 2018; 115 (39): E9135-E9144.                    


Dkk2 promotes neural crest specification by activating Wnt/β-catenin signaling in a GSK3β independent manner., Devotta A., Elife. July 23, 2018; 7                             


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


Identifying domains of EFHC1 involved in ciliary localization, ciliogenesis, and the regulation of Wnt signaling., Zhao Y., Dev Biol. March 15, 2016; 411 (2): 257-265.                      


ATP4a is required for development and function of the Xenopus mucociliary epidermis - a potential model to study proton pump inhibitor-associated pneumonia., Walentek P., Dev Biol. December 15, 2015; 408 (2): 292-304.                                


The serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation., Acosta H., Development. March 15, 2015; 142 (6): 1146-58.                                    


Pax8 and Pax2 are specifically required at different steps of Xenopus pronephros development., Buisson I., Dev Biol. January 15, 2015; 397 (2): 175-90.                            


Transcriptional regulators in the Hippo signaling pathway control organ growth in Xenopus tadpole tail regeneration., Hayashi S., Dev Biol. December 1, 2014; 396 (1): 31-41.                      


Chibby functions in Xenopus ciliary assembly, embryonic development, and the regulation of gene expression., Shi J., Dev Biol. November 15, 2014; 395 (2): 287-98.                    


Developmental mechanisms directing early anterior forebrain specification in vertebrates., Andoniadou CL., Cell Mol Life Sci. October 1, 2013; 70 (20): 3739-52.        


Early neural crest induction requires an initial inhibition of Wnt signals., Steventon B., Dev Biol. May 1, 2012; 365 (1): 196-207.              


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.                              


Different requirement for Wnt/β-catenin signaling in limb regeneration of larval and adult Xenopus., Yokoyama H., PLoS One. January 1, 2011; 6 (7): e21721.                


Integrating patterning signals: Wnt/GSK3 regulates the duration of the BMP/Smad1 signal., Fuentealba LC., Cell. November 30, 2007; 131 (5): 980-93.      


Neural crests are actively precluded from the anterior neural fold by a novel inhibitory mechanism dependent on Dickkopf1 secreted by the prechordal mesoderm., Carmona-Fontaine C., Dev Biol. September 15, 2007; 309 (2): 208-21.              


Characterization of myeloid cells derived from the anterior ventral mesoderm in the Xenopus laevis embryo., Tashiro S., Dev Growth Differ. October 1, 2006; 48 (8): 499-512.                    


FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development., Urban AE., Dev Biol. September 1, 2006; 297 (1): 103-17.                    


An essential role of Xenopus Foxi1a for ventral specification of the cephalic ectoderm during gastrulation., Matsuo-Takasaki M., Development. September 1, 2005; 132 (17): 3885-94.                      


Neural induction in Xenopus requires early FGF signalling in addition to BMP inhibition., Delaune E., Development. January 1, 2005; 132 (2): 299-310.                    


Selective degradation of excess Ldb1 by Rnf12/RLIM confers proper Ldb1 expression levels and Xlim-1/Ldb1 stoichiometry in Xenopus organizer functions., Hiratani I., Development. September 1, 2003; 130 (17): 4161-75.                    


Neural induction in the absence of mesoderm: beta-catenin-dependent expression of secreted BMP antagonists at the blastula stage in Xenopus., Wessely O., Dev Biol. June 1, 2001; 234 (1): 161-73.              


A study of Xlim1 function in the Spemann-Mangold organizer., Kodjabachian L., Int J Dev Biol. January 1, 2001; 45 (1): 209-18.            


Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning., Gawantka V., Mech Dev. October 1, 1998; 77 (2): 95-141.                                                            

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