Papers associated with primary germ layer (and ctnnd1)

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	Modeling endoderm development and disease in Xenopus., Edwards NA., Curr Top Dev Biol. January 1, 2021; 145 61-90.
	Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome., Alharatani R., Hum Mol Genet. July 21, 2020; 29 (11): 1900-1921.
	The Lhx1-Ldb1 complex interacts with Furry to regulate microRNA expression during pronephric kidney development., Espiritu EB., Sci Rep. October 30, 2018; 8 (1): 16029.
	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.
	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.
	Plakophilin-3 catenin associates with the ETV1/ER81 transcription factor to positively modulate gene activity., Munoz WA., PLoS One. January 1, 2014; 9 (1): e86784.
	Par3 controls neural crest migration by promoting microtubule catastrophe during contact inhibition of locomotion., Moore R., Development. December 1, 2013; 140 (23): 4763-75.
	A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance., Livigni A., Curr Biol. November 18, 2013; 23 (22): 2233-2244.
	Plakophilin-3 is required for late embryonic amphibian development, exhibiting roles in ectodermal and neural tissues., Munoz WA., PLoS One. January 1, 2012; 7 (4): e34342.
	Kazrin, and its binding partners ARVCF- and delta-catenin, are required for Xenopus laevis craniofacial development., Cho K., Dev Dyn. December 1, 2011; 240 (12): 2601-12.
	Xenopus Kazrin interacts with ARVCF-catenin, spectrin and p190B RhoGAP, and modulates RhoA activity and epithelial integrity., Cho K., J Cell Sci. December 1, 2010; 123 (Pt 23): 4128-44.
	Collective chemotaxis requires contact-dependent cell polarity., Theveneau E., Dev Cell. July 20, 2010; 19 (1): 39-53.
	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.
	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.
	Inhibition of cell adhesion by xARVCF indicates a regulatory function at the plasma membrane., Reintsch WE., Dev Dyn. September 1, 2008; 237 (9): 2328-41.
	G-protein-coupled signals control cortical actin assembly by controlling cadherin expression in the early Xenopus embryo., Tao Q, Tao Q., Development. July 1, 2007; 134 (14): 2651-61.
	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.
	p120 catenin is required for morphogenetic movements involved in the formation of the eyes and the craniofacial skeleton in Xenopus., Ciesiolka M., J Cell Sci. August 15, 2004; 117 (Pt 18): 4325-39.
	Vertebrate development requires ARVCF and p120 catenins and their interplay with RhoA and Rac., Fang X., J Cell Biol. April 1, 2004; 165 (1): 87-98.
	Cadherin-mediated cell sorting not determined by binding or adhesion specificity., Niessen CM., J Cell Biol. January 21, 2002; 156 (2): 389-399.
	Xarvcf, Xenopus member of the p120 catenin subfamily associating with cadherin juxtamembrane region., Paulson AF., J Biol Chem. September 29, 2000; 275 (39): 30124-31.
	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.

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