Papers associated with cardiac mesoderm (and ctnnb1)

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	G protein-coupled receptors Flop1 and Flop2 inhibit Wnt/β-catenin signaling and are essential for head formation in Xenopus., Miyagi A., Dev Biol. November 1, 2015; 407 (1): 131-44.
	Xenopus Pkdcc1 and Pkdcc2 Are Two New Tyrosine Kinases Involved in the Regulation of JNK Dependent Wnt/PCP Signaling Pathway., Vitorino M., PLoS One. August 13, 2015; 10 (8): e0135504.
	The extreme anterior domain is an essential craniofacial organizer acting through Kinin-Kallikrein signaling., Jacox L., Cell Rep. July 24, 2014; 8 (2): 596-609.
	Hhex and Cer1 mediate the Sox17 pathway for cardiac mesoderm formation in embryonic stem cells., Liu Y., Stem Cells. June 1, 2014; 32 (6): 1515-26.
	β-Arrestin 1 mediates non-canonical Wnt pathway to regulate convergent extension movements., Kim GH., Biochem Biophys Res Commun. May 31, 2013; 435 (2): 182-7.
	Retinoic acid-activated Ndrg1a represses Wnt/β-catenin signaling to allow Xenopus pancreas, oesophagus, stomach, and duodenum specification., Zhang T., PLoS One. May 15, 2013; 8 (5): e65058.
	sfrp1 promotes cardiomyocyte differentiation in Xenopus via negative-feedback regulation of Wnt signalling., Gibb N., Development. April 1, 2013; 140 (7): 1537-49.
	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.
	ATP4a is required for Wnt-dependent Foxj1 expression and leftward flow in Xenopus left-right development., Walentek P., Cell Rep. May 31, 2012; 1 (5): 516-27.
	Regulation of KCNQ1/KCNE1 by β-catenin., Wilmes J., Mol Membr Biol. January 1, 2012; 29 (3-4): 87-94.
	Strange as it may seem: the many links between Wnt signaling, planar cell polarity, and cilia., Wallingford JB., Genes Dev. February 1, 2011; 25 (3): 201-13.
	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.
	MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization., Suzuki M., Development. July 1, 2010; 137 (14): 2329-39.
	The extracellular domain of Lrp5/6 inhibits noncanonical Wnt signaling in vivo., Bryja V., Mol Biol Cell. February 1, 2009; 20 (3): 924-36.
	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.
	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.
	TBX5 is required for embryonic cardiac cell cycle progression., Goetz SC., Development. July 1, 2006; 133 (13): 2575-84.
	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.
	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.
	Beta-catenin, MAPK and Smad signaling during early Xenopus development., Schohl A., Development. January 1, 2002; 129 (1): 37-52.
	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.

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