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Summary Expression Phenotypes Gene Literature (522) GO Terms (40) Nucleotides (1106) Proteins (68) Interactants (2006) Wiki
XB--487199

Papers associated with ctnnb1 (and morpholino)



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


Multiple interactions between maternally-activated signalling pathways control Xenopus nodal-related genes., Rex M, Hilton E, Old R., Int J Dev Biol. March 1, 2002; 46 (2): 217-26.


The roles of three signaling pathways in the formation and function of the Spemann Organizer., Xanthos JB, Kofron M, Tao Q, Tao Q, Schaible K, Wylie C, Heasman J., Development. September 1, 2002; 129 (17): 4027-43.                  


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


Negative regulation of Smad2 by PIASy is required for proper Xenopus mesoderm formation., Daniels M, Shimizu K, Zorn AM, Ohnuma S., Development. November 1, 2004; 131 (22): 5613-26.                                


Germ-layer specification and control of cell growth by Ectodermin, a Smad4 ubiquitin ligase., Dupont S, Zacchigna L, Cordenonsi M, Soligo S, Adorno M, Rugge M, Piccolo S., Cell. April 8, 2005; 121 (1): 87-99.                                  


Kaiso/p120-catenin and TCF/beta-catenin complexes coordinately regulate canonical Wnt gene targets., Park JI, Kim SW, Lyons JP, Ji H, Nguyen TT, Cho K, Barton MC, Deroo T, Vleminckx K, Vleminckx K, Moon RT, McCrea PD., Dev Cell. June 1, 2005; 8 (6): 843-54.            


xBtg-x regulates Wnt/beta-Catenin signaling during early Xenopus development., Wessely O, Kim JI, Tran U, Fuentealba L, De Robertis EM., Dev Biol. July 1, 2005; 283 (1): 17-28.              


Frodo proteins: modulators of Wnt signaling in vertebrate development., Brott BK, Sokol SY., Differentiation. September 1, 2005; 73 (7): 323-9.      


Vezatin, a protein associated to adherens junctions, is required for mouse blastocyst morphogenesis., Hyenne V, Louvet-Vallée S, El-Amraoui A, Petit C, Maro B, Simmler MC., Dev Biol. November 1, 2005; 287 (1): 180-91.        


Tcf- and Vent-binding sites regulate neural-specific geminin expression in the gastrula embryo., Taylor JJ, Wang T, Kroll KL., Dev Biol. January 15, 2006; 289 (2): 494-506.                


A requirement for NF-protocadherin and TAF1/Set in cell adhesion and neural tube formation., Rashid D, Newell K, Shama L, Bradley R., Dev Biol. March 1, 2006; 291 (1): 170-81.                    


A requirement for NF-protocadherin and TAF1/Set in cell adhesion and neural tube formation., Rashid D, Newell K, Shama L, Bradley R., Dev Biol. March 1, 2006; 291 (1): 170-81.                    


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


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


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


NARF, an nemo-like kinase (NLK)-associated ring finger protein regulates the ubiquitylation and degradation of T cell factor/lymphoid enhancer factor (TCF/LEF)., Yamada M, Ohnishi J, Ohkawara B, Iemura S, Satoh K, Hyodo-Miura J, Kawachi K, Natsume T, Shibuya H., J Biol Chem. July 28, 2006; 281 (30): 20749-20760.                    


Slug stability is dynamically regulated during neural crest development by the F-box protein Ppa., Vernon AE, LaBonne C., Development. September 1, 2006; 133 (17): 3359-70.                


Jun NH2-terminal kinase (JNK) prevents nuclear beta-catenin accumulation and regulates axis formation in Xenopus embryos., Liao G, Tao Q, Tao Q, Kofron M, Chen JS, Schloemer A, Davis RJ, Hsieh JC, Wylie C, Heasman J, Kuan CY., Proc Natl Acad Sci U S A. October 31, 2006; 103 (44): 16313-8.                    


Dickkopf-1 regulates gastrulation movements by coordinated modulation of Wnt/beta catenin and Wnt/PCP activities, through interaction with the Dally-like homolog Knypek., Caneparo L, Huang YL, Staudt N, Tada M, Ahrendt R, Kazanskaya O, Niehrs C, Houart C., Genes Dev. February 15, 2007; 21 (4): 465-80.


Two oppositely localised frizzled RNAs as axis determinants in a cnidarian embryo., Momose T, Houliston E., PLoS Biol. April 1, 2007; 5 (4): e70.                


IQGAP2 is required for the cadherin-mediated cell-to-cell adhesion in Xenopus laevis embryos., Yamashiro S, Abe H, Mabuchi I., Dev Biol. August 15, 2007; 308 (2): 485-93.            


Integrin alpha5 is required for somite rotation and boundary formation in Xenopus., Kragtorp KA, Miller JR., Dev Dyn. September 1, 2007; 236 (9): 2713-20.  


Embryonic cells depleted of beta-catenin remain competent to differentiate into dorsal mesodermal derivatives., Chu FH, Afonin B, Gustin JK, Bost A, Sanchez M, Domingo CR., Dev Dyn. November 1, 2007; 236 (11): 3007-19.


Expression of Siamois and Twin in the blastula Chordin/Noggin signaling center is required for brain formation in Xenopus laevis embryos., Ishibashi H, Matsumura N, Hanafusa H, Matsumoto K, De Robertis EM, Kuroda H., Mech Dev. January 1, 2008; 125 (1-2): 58-66.              


Nucleoredoxin regulates the Wnt/planar cell polarity pathway in Xenopus., Funato Y, Michiue T, Terabayashi T, Yukita A, Danno H, Asashima M, Miki H., Genes Cells. September 1, 2008; 13 (9): 965-75.            


Hindbrain-derived Wnt and Fgf signals cooperate to specify the otic placode in Xenopus., Park BY, Saint-Jeannet JP., Dev Biol. December 1, 2008; 324 (1): 108-21.      


Fgf8a induces neural crest indirectly through the activation of Wnt8 in the paraxial mesoderm., Hong CS, Park BY, Saint-Jeannet JP., Development. December 1, 2008; 135 (23): 3903-10.          


The extracellular domain of Lrp5/6 inhibits noncanonical Wnt signaling in vivo., Bryja V, Andersson ER, Schambony A, Esner M, Bryjová L, Biris KK, Hall AC, Kraft B, Cajanek L, Yamaguchi TP, Buckingham M, Arenas E., Mol Biol Cell. February 1, 2009; 20 (3): 924-36.        


Mad is required for wingless signaling in wing development and segment patterning in Drosophila., Eivers E, Fuentealba LC, Sander V, Clemens JC, Hartnett L, De Robertis EM., PLoS One. August 6, 2009; 4 (8): e6543.                    


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


Xenopus delta-catenin is essential in early embryogenesis and is functionally linked to cadherins and small GTPases., Gu D, Sater AK, Ji H, Cho K, Clark M, Stratton SA, Barton MC, Lu Q, McCrea PD., J Cell Sci. November 15, 2009; 122 (Pt 22): 4049-61.            


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


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


Collective chemotaxis requires contact-dependent cell polarity., Theveneau E, Marchant L, Kuriyama S, Gull M, Moepps B, Parsons M, Mayor R., Dev Cell. July 20, 2010; 19 (1): 39-53.                


Collective chemotaxis requires contact-dependent cell polarity., Theveneau E, Marchant L, Kuriyama S, Gull M, Moepps B, Parsons M, Mayor R., Dev Cell. July 20, 2010; 19 (1): 39-53.                


Wnt/beta-catenin signaling is involved in the induction and maintenance of primitive hematopoiesis in the vertebrate embryo., Tran HT, Sekkali B, Van Imschoot G, Janssens S, Vleminckx K, Vleminckx K., Proc Natl Acad Sci U S A. September 14, 2010; 107 (37): 16160-5.                                                


Wnt signaling requires sequestration of glycogen synthase kinase 3 inside multivesicular endosomes., Taelman VF, Dobrowolski R, Plouhinec JL, Fuentealba LC, Vorwald PP, Gumper I, Sabatini DD, De Robertis EM., Cell. December 23, 2010; 143 (7): 1136-48.        


A gene regulatory network controlling hhex transcription in the anterior endoderm of the organizer., Rankin SA, Rankin SA, Kormish J, Kofron M, Jegga A, Zorn AM., Dev Biol. March 15, 2011; 351 (2): 297-310.                            


A novel mechanism for the transcriptional regulation of Wnt signaling in development., Vacik T, Stubbs JL, Lemke G., Genes Dev. September 1, 2011; 25 (17): 1783-95.      


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


Transcription factor Zic2 inhibits Wnt/β-catenin protein signaling., Pourebrahim R, Houtmeyers R, Ghogomu S, Janssens S, Thelie A, Tran HT, Langenberg T, Vleminckx K, Vleminckx K, Bellefroid E, Cassiman JJ, Tejpar S., J Biol Chem. October 28, 2011; 286 (43): 37732-40.          


HESX1- and TCF3-mediated repression of Wnt/β-catenin targets is required for normal development of the anterior forebrain., Andoniadou CL, Signore M, Young RM, Gaston-Massuet C, Wilson SW, Fuchs E, Martinez-Barbera JP., Development. November 1, 2011; 138 (22): 4931-42.


CRIM1 complexes with ß-catenin and cadherins, stabilizes cell-cell junctions and is critical for neural morphogenesis., Ponferrada VG, Fan J, Vallance JE, Hu S, Mamedova A, Rankin SA, Kofron M, Zorn AM, Hegde RS, Lang RA., PLoS One. January 1, 2012; 7 (3): e32635.                        


CRIM1 complexes with ß-catenin and cadherins, stabilizes cell-cell junctions and is critical for neural morphogenesis., Ponferrada VG, Fan J, Vallance JE, Hu S, Mamedova A, Rankin SA, Kofron M, Zorn AM, Hegde RS, Lang RA., PLoS One. January 1, 2012; 7 (3): e32635.                        


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


Serotonin signaling is required for Wnt-dependent GRP specification and leftward flow in Xenopus., Beyer T, Danilchik M, Thumberger T, Vick P, Tisler M, Schneider I, Bogusch S, Andre P, Ulmer B, Walentek P, Niesler B, Blum M, Schweickert A., Curr Biol. January 10, 2012; 22 (1): 33-9.                


Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/β-catenin signaling pathway., Fujimi TJ, Hatayama M, Aruga J., Dev Biol. January 15, 2012; 361 (2): 220-31.                          


Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/β-catenin signaling pathway., Fujimi TJ, Hatayama M, Aruga J., Dev Biol. January 15, 2012; 361 (2): 220-31.                          


ATP4a is required for Wnt-dependent Foxj1 expression and leftward flow in Xenopus left-right development., Walentek P, Beyer T, Thumberger T, Schweickert A, Blum M., Cell Rep. May 31, 2012; 1 (5): 516-27.                              


Subfunctionalization and neofunctionalization of vertebrate Lef/Tcf transcription factors., Klingel S, Morath I, Strietz J, Menzel K, Holstein TW, Gradl D., Dev Biol. August 1, 2012; 368 (1): 44-53.              


Suppression of Bmp4 signaling by the zinc-finger repressors Osr1 and Osr2 is required for Wnt/β-catenin-mediated lung specification in Xenopus., Rankin SA, Rankin SA, Gallas AL, Neto A, Gómez-Skarmeta JL, Zorn AM., Development. August 1, 2012; 139 (16): 3010-20.                                                                                


Wnt-11 and Fz7 reduce cell adhesion in convergent extension by sequestration of PAPC and C-cadherin., Kraft B, Berger CD, Wallkamm V, Steinbeisser H, Wedlich D., J Cell Biol. August 20, 2012; 198 (4): 695-709.                  


Upon Wnt stimulation, Rac1 activation requires Rac1 and Vav2 binding to p120-catenin., Valls G, Codina M, Miller RK, Del Valle-Pérez B, Vinyoles M, Caelles C, McCrea PD, García de Herreros A, Duñach M., J Cell Sci. November 15, 2012; 125 (Pt 22): 5288-301.                


The Wnt signaling mediator tcf1 is required for expression of foxd3 during Xenopus gastrulation., Janssens S, Van Den Broek O, Davenport IR, Akkers RC, Liu F, Veenstra GJ, Hoppler S, Vleminckx K, Vleminckx K, Destrée O., Int J Dev Biol. January 1, 2013; 57 (1): 49-54.    


Amputation-induced reactive oxygen species are required for successful Xenopus tadpole tail regeneration., Love NR, Chen Y, Ishibashi S, Kritsiligkou P, Lea R, Koh Y, Gallop JL, Dorey K, Amaya E., Nat Cell Biol. February 1, 2013; 15 (2): 222-8.        

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