Papers associated with regenerating tail (and ctnnb1)

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	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.
	Early development of the neural plate: new roles for apoptosis and for one of its main effectors caspase-3., Juraver-Geslin HA., Genesis. February 1, 2015; 53 (2): 203-24.
	The PDZ domain protein Mcc is a novel effector of non-canonical Wnt signaling during convergence and extension in zebrafish., Young T., Development. September 1, 2014; 141 (18): 3505-16.
	In vivo collective cell migration requires an LPAR2-dependent increase in tissue fluidity., Kuriyama S., J Cell Biol. July 7, 2014; 206 (1): 113-27.
	Monensin Inhibits Canonical Wnt Signaling in Human Colorectal Cancer Cells and Suppresses Tumor Growth in Multiple Intestinal Neoplasia Mice., Tumova L., Mol Cancer Ther. April 1, 2014; .
	Loss of Xenopus cadherin-11 leads to increased Wnt/β-catenin signaling and up-regulation of target genes c-myc and cyclin D1 in neural crest., Koehler A., Dev Biol. November 1, 2013; 383 (1): 132-45.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	Injury-induced asymmetric cell death as a driving force for head regeneration in Hydra., Galliot B., Dev Genes Evol. March 1, 2013; 223 (1-2): 39-52.
	Amputation-induced reactive oxygen species are required for successful Xenopus tadpole tail regeneration., Love NR., Nat Cell Biol. February 1, 2013; 15 (2): 222-8.
	Imparting regenerative capacity to limbs by progenitor cell transplantation., Lin G., Dev Cell. January 14, 2013; 24 (1): 41-51.
	Transgenic analysis of signaling pathways required for Xenopus tadpole spinal cord and muscle regeneration., Lin G., Anat Rec (Hoboken). October 1, 2012; 295 (10): 1532-40.
	Wnt/β-catenin signaling requires interaction of the Dishevelled DEP domain and C terminus with a discontinuous motif in Frizzled., Tauriello DV., Proc Natl Acad Sci U S A. April 3, 2012; 109 (14): E812-20.
	Stimulation of HERG channel activity by β-catenin., Munoz C., PLoS One. January 1, 2012; 7 (8): e43353.
	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.
	[Between homeostasis and development, which strategies to regenerate?]., Galliot B., Biol Aujourdhui. January 1, 2011; 205 (2): 125-37.
	Identification of transmembrane protein 88 (TMEM88) as a dishevelled-binding protein., Lee HJ., J Biol Chem. December 31, 2010; 285 (53): 41549-56.
	The tumor-associated EpCAM regulates morphogenetic movements through intracellular signaling., Maghzal N., J Cell Biol. November 1, 2010; 191 (3): 645-59.
	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.
	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.
	Interactions between Sox9 and beta-catenin control chondrocyte differentiation., Akiyama H., Genes Dev. May 1, 2004; 18 (9): 1072-87.
	The role of maternal axin in patterning the Xenopus embryo., Kofron M., Dev Biol. September 1, 2001; 237 (1): 183-201.
	The juxtamembrane region of the cadherin cytoplasmic tail supports lateral clustering, adhesive strengthening, and interaction with p120ctn., Yap AS., J Cell Biol. May 4, 1998; 141 (3): 779-89.

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