Papers associated with mesoderm (and cdh2)

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	Gli2 is required for the induction and migration of Xenopus laevis neural crest., Cerrizuela S., Mech Dev. December 1, 2018; 154 219-239.
	Cadherins function during the collective cell migration of Xenopus Cranial Neural Crest cells: revisiting the role of E-cadherin., Cousin H., Mech Dev. December 1, 2017; 148 79-88.
	PFKFB4 control of AKT signaling is essential for premigratory and migratory neural crest formation., Figueiredo AL., Development. November 15, 2017; 144 (22): 4183-4194.
	Similarity in gene-regulatory networks suggests that cancer cells share characteristics of embryonic neural cells., Zhang Z., J Biol Chem. August 4, 2017; 292 (31): 12842-12859.
	E-cadherin is required for cranial neural crest migration in Xenopus laevis., Huang C., Dev Biol. March 15, 2016; 411 (2): 159-171.
	Cadherin Switch during EMT in Neural Crest Cells Leads to Contact Inhibition of Locomotion via Repolarization of Forces., Scarpa E., Dev Cell. August 24, 2015; 34 (4): 421-34.
	Cell movements of the deep layer of non-neural ectoderm underlie complete neural tube closure in Xenopus., Morita H., Development. April 1, 2012; 139 (8): 1417-26.
	IGF-1 increases invasive potential of MCF 7 breast cancer cells and induces activation of latent TGF-β1 resulting in epithelial to mesenchymal transition., Walsh LA., Cell Commun Signal. May 2, 2011; 9 (1): 10.
	Lhx1 is required for specification of the renal progenitor cell field., Cirio MC., PLoS One. April 15, 2011; 6 (4): e18858.
	SNW1 is a critical regulator of spatial BMP activity, neural plate border formation, and neural crest specification in vertebrate embryos., Wu MY., PLoS Biol. February 15, 2011; 9 (2): e1000593.
	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.
	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.
	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.
	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.
	Sox9 is required for invagination of the otic placode in mice., Barrionuevo F., Dev Biol. May 1, 2008; 317 (1): 213-24.
	Xenopus cadherin-11 (Xcadherin-11) expression requires the Wg/Wnt signal., Hadeball B., Mech Dev. March 1, 1998; 72 (1-2): 101-13.
	Cadherin-mediated cell interactions are necessary for the activation of MyoD in Xenopus mesoderm., Holt CE., Proc Natl Acad Sci U S A. November 8, 1994; 91 (23): 10844-8.
	Structure and distribution of N-cadherin in developing zebrafish embryos: morphogenetic effects of ectopic over-expression., Bitzur S., Dev Dyn. October 1, 1994; 201 (2): 121-36.
	Expression of an extracellular deletion of Xotch diverts cell fate in Xenopus embryos., Coffman CR., Cell. May 21, 1993; 73 (4): 659-71.
	N-cadherin transcripts in Xenopus laevis from early tailbud to tadpole., Simonneau L., Dev Dyn. August 1, 1992; 194 (4): 247-60.

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