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Summary Anatomy Item Literature (553) Expression Attributions Wiki
XB-ANAT-33

Papers associated with cement gland (and ctnnb1)

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


The RNF146 E3 ubiquitin ligase is required for the control of Wnt signaling and body pattern formation in Xenopus., Zhu X., Mech Dev. October 1, 2017; 147 28-36.              


Genome-wide analysis of dorsal and ventral transcriptomes of the Xenopus laevis gastrula., Ding Y., Dev Biol. June 15, 2017; 426 (2): 176-187.                                  


G protein-coupled receptors Flop1 and Flop2 inhibit Wnt/β-catenin signaling and are essential for head formation in Xenopus., Miyagi A., Dev Biol. November 1, 2015; 407 (1): 131-44.                                          


Sebox regulates mesoderm formation in early amphibian embryos., Chen G., Dev Dyn. November 1, 2015; 244 (11): 1415-26.              


Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation., Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.                                  


Custos controls β-catenin to regulate head development during vertebrate embryogenesis., Komiya Y., Proc Natl Acad Sci U S A. September 9, 2014; 111 (36): 13099-104.                                


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.                            


The dual regulator Sufu integrates Hedgehog and Wnt signals in the early Xenopus embryo., Min TH., Dev Biol. October 1, 2011; 358 (1): 262-76.                            


Barhl2 limits growth of the diencephalic primordium through Caspase3 inhibition of beta-catenin activation., Juraver-Geslin HA., Proc Natl Acad Sci U S A. February 8, 2011; 108 (6): 2288-93.                    


Regulation of TCF3 by Wnt-dependent phosphorylation during vertebrate axis specification., Hikasa H., Dev Cell. October 19, 2010; 19 (4): 521-32.        


Anterior neural development requires Del1, a matrix-associated protein that attenuates canonical Wnt signaling via the Ror2 pathway., Takai A., Development. October 1, 2010; 137 (19): 3293-302.            


MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization., Suzuki M., Development. July 1, 2010; 137 (14): 2329-39.                                                      


Mutations in the human naked cuticle homolog NKD1 found in colorectal cancer alter Wnt/Dvl/beta-catenin signaling., Guo J., PLoS One. November 24, 2009; 4 (11): e7982.            


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.            


Wise retained in the endoplasmic reticulum inhibits Wnt signaling by reducing cell surface LRP6., Guidato S., Dev Biol. October 15, 2007; 310 (2): 250-63.                


Vg1 has specific processing requirements that restrict its action to body axis patterning centers., Thomas JT., Dev Biol. October 1, 2007; 310 (1): 129-39.          


The MRH protein Erlectin is a member of the endoplasmic reticulum synexpression group and functions in N-glycan recognition., Cruciat CM., J Biol Chem. May 5, 2006; 281 (18): 12986-93.                        


HIC-5 is a novel repressor of lymphoid enhancer factor/T-cell factor-driven transcription., Ghogomu SM., J Biol Chem. January 20, 2006; 281 (3): 1755-64.            


RanBP3 enhances nuclear export of active (beta)-catenin independently of CRM1., Hendriksen J., J Cell Biol. December 5, 2005; 171 (5): 785-97.                  


Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus., Kuroda H., PLoS Biol. May 1, 2004; 2 (5): E92.                


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.                  


Endostatin is a potential inhibitor of Wnt signaling., Hanai J., J Cell Biol. August 5, 2002; 158 (3): 529-39.            


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


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.              


Beta-catenin signaling activity dissected in the early Xenopus embryo: a novel antisense approach., Heasman J., Dev Biol. June 1, 2000; 222 (1): 124-34.        


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.              


A role for Siamois in Spemann organizer formation., Fan MJ., Development. July 1, 1997; 124 (13): 2581-9.              


Activation of the Wnt signaling pathway: a molecular mechanism for lithium action., Hedgepeth CM., Dev Biol. May 1, 1997; 185 (1): 82-91.          


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


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


Catenins in Xenopus embryogenesis and their relation to the cadherin-mediated cell-cell adhesion system., Schneider S., Development. June 1, 1993; 118 (2): 629-40.                    


The armadillo homologs beta-catenin and plakoglobin are differentially expressed during early development of Xenopus laevis., DeMarais AA., Dev Biol. October 1, 1992; 153 (2): 337-46.          

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