Papers associated with embryonic structure (and jup)

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	FAK is required for tension-dependent organization of collective cell movements in Xenopus mesendoderm., Bjerke MA., Dev Biol. October 15, 2014; 394 (2): 340-56.
	Genomic targets of Brachyury (T) in differentiating mouse embryonic stem cells., Evans AL., PLoS One. January 1, 2012; 7 (3): e33346.
	A Xenopus tribbles orthologue is required for the progression of mitosis and for development of the nervous system., Saka Y., Dev Biol. September 15, 2004; 273 (2): 210-25.
	Sox17 and beta-catenin cooperate to regulate the transcription of endodermal genes., Sinner D., Development. July 1, 2004; 131 (13): 3069-80.
	Plakoglobin is required for maintenance of the cortical actin skeleton in early Xenopus embryos and for cdc42-mediated wound healing., Kofron M., J Cell Biol. August 19, 2002; 158 (4): 695-708.
	Beta-catenin signaling activity dissected in the early Xenopus embryo: a novel antisense approach., Heasman J., Dev Biol. June 1, 2000; 222 (1): 124-34.
	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.
	Expression of the Armadillo family member p120cas1B in Xenopus embryos affects head differentiation but not axis formation., Geis K., Dev Genes Evol. January 1, 1998; 207 (7): 471-81.
	Cell type-specific desmosomal plaque proteins of the plakoglobin family: plakophilin 1 (band 6 protein)., Heid HW., Differentiation. December 1, 1994; 58 (2): 113-31.
	The armadillo homologs beta-catenin and plakoglobin are differentially expressed during early development of Xenopus laevis., DeMarais AA., Dev Biol. October 1, 1992; 153 (2): 337-46.

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