Papers associated with tail bud (and ctnnb1)

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	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.
	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.
	Beta-catenin localization during Xenopus embryogenesis: accumulation at tissue and somite boundaries., Fagotto F., Development. December 1, 1994; 120 (12): 3667-79.
	Misexpression of the catenin p120(ctn)1A perturbs Xenopus gastrulation but does not elicit Wnt-directed axis specification., Paulson AF., Dev Biol. March 15, 1999; 207 (2): 350-63.
	Anterior endomesoderm specification in Xenopus by Wnt/beta-catenin and TGF-beta signalling pathways., Zorn AM., Dev Biol. May 15, 1999; 209 (2): 282-97.
	Domains of axin involved in protein-protein interactions, Wnt pathway inhibition, and intracellular localization., Fagotto F., J Cell Biol. May 17, 1999; 145 (4): 741-56.
	XCtBP is a XTcf-3 co-repressor with roles throughout Xenopus development., Brannon M., Development. June 1, 1999; 126 (14): 3159-70.
	Regulation of Wnt signaling by Sox proteins: XSox17 alpha/beta and XSox3 physically interact with beta-catenin., Zorn AM., Mol Cell. October 1, 1999; 4 (4): 487-98.
	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.
	The maternal Xenopus beta-catenin signaling pathway, activated by frizzled homologs, induces goosecoid in a cell non-autonomous manner., Brown JD., Dev Growth Differ. August 1, 2000; 42 (4): 347-57.
	Beta-catenin, MAPK and Smad signaling during early Xenopus development., Schohl A., Development. January 1, 2002; 129 (1): 37-52.
	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.
	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.
	Interactions between Sox9 and beta-catenin control chondrocyte differentiation., Akiyama H., Genes Dev. May 1, 2004; 18 (9): 1072-87.
	XSENP1, a novel sumo-specific protease in Xenopus, inhibits normal head formation by down-regulation of Wnt/beta-catenin signalling., Yukita A., Genes Cells. August 1, 2004; 9 (8): 723-36.
	New roles for FoxH1 in patterning the early embryo., Kofron M., Development. October 1, 2004; 131 (20): 5065-78.
	Germ-layer specification and control of cell growth by Ectodermin, a Smad4 ubiquitin ligase., Dupont 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., Dev Cell. June 1, 2005; 8 (6): 843-54.
	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.
	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 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.
	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.
	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.
	Jun NH2-terminal kinase (JNK) prevents nuclear beta-catenin accumulation and regulates axis formation in Xenopus embryos., Liao G., Proc Natl Acad Sci U S A. October 31, 2006; 103 (44): 16313-8.
	IQGAP2 is required for the cadherin-mediated cell-to-cell adhesion in Xenopus laevis embryos., Yamashiro S., Dev Biol. August 15, 2007; 308 (2): 485-93.
	Silencing of Smed-betacatenin1 generates radial-like hypercephalized planarians., Iglesias M., Development. April 1, 2008; 135 (7): 1215-21.
	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.
	Fgf8a induces neural crest indirectly through the activation of Wnt8 in the paraxial mesoderm., Hong CS., Development. December 1, 2008; 135 (23): 3903-10.
	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.
	Mad is required for wingless signaling in wing development and segment patterning in Drosophila., Eivers E., PLoS One. August 6, 2009; 4 (8): e6543.
	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.
	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.
	Wnt/beta-catenin signaling is involved in the induction and maintenance of primitive hematopoiesis in the vertebrate embryo., Tran HT., Proc Natl Acad Sci U S A. September 14, 2010; 107 (37): 16160-5.
	Conservation and diversification of an ancestral chordate gene regulatory network for dorsoventral patterning., Kozmikova I., PLoS One. February 3, 2011; 6 (2): e14650.
	A gene regulatory network controlling hhex transcription in the anterior endoderm of the organizer., Rankin SA, Rankin SA., Dev Biol. March 15, 2011; 351 (2): 297-310.
	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.
	Waif1/5T4 inhibits Wnt/β-catenin signaling and activates noncanonical Wnt pathways by modifying LRP6 subcellular localization., Kagermeier-Schenk B., Dev Cell. December 13, 2011; 21 (6): 1129-43.
	Genomic targets of Brachyury (T) in differentiating mouse embryonic stem cells., Evans AL., PLoS One. January 1, 2012; 7 (3): e33346.
	Differential role of Axin RGS domain function in Wnt signaling during anteroposterior patterning and maternal axis formation., Schneider PN., PLoS One. January 1, 2012; 7 (9): e44096.
	Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/β-catenin signaling pathway., Fujimi TJ., Dev Biol. January 15, 2012; 361 (2): 220-31.
	Cadherin-dependent differential cell adhesion in Xenopus causes cell sorting in vitro but not in the embryo., Ninomiya H., J Cell Sci. April 15, 2012; 125 (Pt 8): 1877-83.
	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., Development. August 1, 2012; 139 (16): 3010-20.
	β-Catenin-independent activation of TCF1/LEF1 in human hematopoietic tumor cells through interaction with ATF2 transcription factors., Grumolato L., PLoS Genet. January 1, 2013; 9 (8): e1003603.
	Ptk7 promotes non-canonical Wnt/PCP-mediated morphogenesis and inhibits Wnt/β-catenin-dependent cell fate decisions during vertebrate development., Hayes M., Development. April 1, 2013; 140 (8): 1807-18.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	Par6b regulates the dynamics of apicobasal polarity during development of the stratified Xenopus epidermis., Wang S., PLoS One. October 8, 2013; 8 (10): e76854.
	A secreted splice variant of the Xenopus frizzled-4 receptor is a biphasic modulator of Wnt signalling., Gorny AK., Cell Commun Signal. November 19, 2013; 11 89.
	Maternal syntabulin is required for dorsal axis formation and is a germ plasm component in Xenopus., Colozza G., Differentiation. July 1, 2014; 88 (1): 17-26.
	FAK is required for tension-dependent organization of collective cell movements in Xenopus mesendoderm., Bjerke MA., Dev Biol. October 15, 2014; 394 (2): 340-56.

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