Papers associated with rostral tuberal region (and lrp6)

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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.
	Isoquercitrin suppresses colon cancer cell growth in vitro by targeting the Wnt/β-catenin signaling pathway., Amado NG., J Biol Chem. December 19, 2014; 289 (51): 35456-67.
	RAB8B is required for activity and caveolar endocytosis of LRP6., Demir K., Cell Rep. September 26, 2013; 4 (6): 1224-34.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	Role of the Rap2/TNIK kinase pathway in regulation of LRP6 stability for Wnt signaling., Park DS., Biochem Biophys Res Commun. June 28, 2013; 436 (2): 338-43.
	Essential role of AWP1 in neural crest specification in Xenopus., Seo JH., Int J Dev Biol. January 1, 2013; 57 (11-12): 829-36.
	Tiki1 is required for head formation via Wnt cleavage-oxidation and inactivation., Zhang X., Cell. June 22, 2012; 149 (7): 1565-77.
	Maternal xNorrin, a canonical Wnt signaling agonist and TGF-β antagonist, controls early neuroectoderm specification in Xenopus., Xu S., PLoS Biol. January 1, 2012; 10 (3): e1001286.
	Macrophage Wnt7b is critical for kidney repair and regeneration., Lin SL., Proc Natl Acad Sci U S A. March 2, 2010; 107 (9): 4194-9.
	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.
	Kremen is required for neural crest induction in Xenopus and promotes LRP6-mediated Wnt signaling., Hassler C., Development. December 1, 2007; 134 (23): 4255-63.
	Integrating patterning signals: Wnt/GSK3 regulates the duration of the BMP/Smad1 signal., Fuentealba LC., Cell. November 30, 2007; 131 (5): 980-93.
	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.
	Mouse homologues of Shisa antagonistic to Wnt and Fgf signalings., Furushima K., Dev Biol. June 15, 2007; 306 (2): 480-92.
	Beta-arrestin is a necessary component of Wnt/beta-catenin signaling in vitro and in vivo., Bryja V., Proc Natl Acad Sci U S A. April 17, 2007; 104 (16): 6690-5.
	Wnt11/beta-catenin signaling in both oocytes and early embryos acts through LRP6-mediated regulation of axin., Kofron M., Development. February 1, 2007; 134 (3): 503-13.
	Shisa2 promotes the maturation of somitic precursors and transition to the segmental fate in Xenopus embryos., Nagano T., Development. December 1, 2006; 133 (23): 4643-54.
	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.
	Connective-tissue growth factor modulates WNT signalling and interacts with the WNT receptor complex., Mercurio S., Development. May 1, 2004; 131 (9): 2137-47.
	Wise, a context-dependent activator and inhibitor of Wnt signalling., Itasaki N., Development. September 1, 2003; 130 (18): 4295-305.
	Kremen proteins interact with Dickkopf1 to regulate anteroposterior CNS patterning., Davidson G., Development. December 1, 2002; 129 (24): 5587-96.

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