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Summary Anatomy Item Literature (14960) Expression Attributions Wiki
XB-ANAT-468

Papers associated with whole organism (and ctnnb1)

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Nectin-2 and N-cadherin interact through extracellular domains and induce apical accumulation of F-actin in apical constriction of Xenopus neural tube morphogenesis., Morita H., Development. April 1, 2010; 137 (8): 1315-25.                            

TMEPAI, a transmembrane TGF-beta-inducible protein, sequesters Smad proteins from active participation in TGF-beta signaling., Watanabe Y., Mol Cell. January 15, 2010; 37 (1): 123-34.                                      

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.            

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.            

A directional Wnt/beta-catenin-Sox2-proneural pathway regulates the transition from proliferation to differentiation in the Xenopus retina., Agathocleous M., Development. October 1, 2009; 136 (19): 3289-99.                          

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.                        

Mad is required for wingless signaling in wing development and segment patterning in Drosophila., Eivers E., PLoS One. August 6, 2009; 4 (8): e6543.                    

N- and E-cadherins in Xenopus are specifically required in the neural and non-neural ectoderm, respectively, for F-actin assembly and morphogenetic movements., Nandadasa S., Development. April 1, 2009; 136 (8): 1327-38.                      

The extracellular domain of Lrp5/6 inhibits noncanonical Wnt signaling in vivo., Bryja V., Mol Biol Cell. February 1, 2009; 20 (3): 924-36.        

Extracellular cleavage of cadherin-11 by ADAM metalloproteases is essential for Xenopus cranial neural crest cell migration., McCusker C., Mol Biol Cell. January 1, 2009; 20 (1): 78-89.                  

Inhibition of GSK3 phosphorylation of beta-catenin via phosphorylated PPPSPXS motifs of Wnt coreceptor LRP6., Wu G., PLoS One. January 1, 2009; 4 (3): e4926.              

Hindbrain-derived Wnt and Fgf signals cooperate to specify the otic placode in Xenopus., Park BY., 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., Development. December 1, 2008; 135 (23): 3903-10.          

Sfrp5 coordinates foregut specification and morphogenesis by antagonizing both canonical and noncanonical Wnt11 signaling., Li Y., Genes Dev. November 1, 2008; 22 (21): 3050-63.                        

Wnt5a and Wnt11 interact in a maternal Dkk1-regulated fashion to activate both canonical and non-canonical signaling in Xenopus axis formation., Cha SW., Development. November 1, 2008; 135 (22): 3719-29.        

Parathyroid hormone signaling through low-density lipoprotein-related protein 6., Wan M., Genes Dev. November 1, 2008; 22 (21): 2968-79.  

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.              

The functions and possible significance of Kremen as the gatekeeper of Wnt signalling in development and pathology., Nakamura T., J Cell Mol Med. April 1, 2008; 12 (2): 391-408.          

Long- and short-range signals control the dynamic expression of an animal hemisphere-specific gene in Xenopus., Mir A., Dev Biol. March 1, 2008; 315 (1): 161-72.            

Intracellular expression profiles measured by real-time PCR tomography in the Xenopus laevis oocyte., Sindelka R., Nucleic Acids Res. February 1, 2008; 36 (2): 387-92.        

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

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.

Sox17 and Sox4 differentially regulate beta-catenin/T-cell factor activity and proliferation of colon carcinoma cells., Sinner D., Mol Cell Biol. November 1, 2007; 27 (22): 7802-15.                

Multiscale computational analysis of Xenopus laevis morphogenesis reveals key insights of systems-level behavior., Robertson SH., BMC Syst Biol. October 22, 2007; 1 46.              

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.                

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

The Sox axis, Nodal signaling, and germ layer specification., Zhang C., Differentiation. July 1, 2007; 75 (6): 536-45.          

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

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

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., J Biol Chem. July 28, 2006; 281 (30): 20749-20760.                    

The Wnt-dependent signaling pathways as target in oncology drug discovery., Janssens N., Invest New Drugs. July 1, 2006; 24 (4): 263-80.        

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

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.                        

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

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.            

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

A cell cycle arrest is necessary for bottle cell formation in the early Xenopus gastrula: integrating cell shape change, local mitotic control and mesodermal patterning., Kurth T., Mech Dev. December 1, 2005; 122 (12): 1251-65.                  

Vezatin, a protein associated to adherens junctions, is required for mouse blastocyst morphogenesis., Hyenne V., Dev Biol. November 1, 2005; 287 (1): 180-91.        

Xenopus frizzled-4S, a splicing variant of Xfz4 is a context-dependent activator and inhibitor of Wnt/beta-catenin signaling., Swain RK., Cell Commun Signal. October 19, 2005; 3 12.          

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

beta-Catenin controls cell sorting at the notochord-somite boundary independently of cadherin-mediated adhesion., Reintsch WE., J Cell Biol. August 15, 2005; 170 (4): 675-86.              

xBtg-x regulates Wnt/beta-Catenin signaling during early Xenopus development., Wessely O., Dev Biol. July 1, 2005; 283 (1): 17-28.              

Kaiso/p120-catenin and TCF/beta-catenin complexes coordinately regulate canonical Wnt gene targets., Park JI., Dev Cell. June 1, 2005; 8 (6): 843-54.            

A vertebrate homolog of the cell cycle regulator Dbf4 is an inhibitor of Wnt signaling required for heart development., Brott BK., Dev Cell. May 1, 2005; 8 (5): 703-15.  

Germ-layer specification and control of cell growth by Ectodermin, a Smad4 ubiquitin ligase., Dupont S., Cell. April 8, 2005; 121 (1): 87-99.                                  

PR72, a novel regulator of Wnt signaling required for Naked cuticle function., Creyghton MP., Genes Dev. February 1, 2005; 19 (3): 376-86.            

XPACE4 is a localized pro-protein convertase required for mesoderm induction and the cleavage of specific TGFbeta proteins in Xenopus development., Birsoy B., Development. February 1, 2005; 132 (3): 591-602.                      

Nuclear localization is required for Dishevelled function in Wnt/beta-catenin signaling., Itoh K., J Biol. January 1, 2005; 4 (1): 3.                  

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

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