Papers associated with bladder (and pdx1)

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	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.
	Prolonged FGF signaling is necessary for lung and liver induction in Xenopus., Shifley ET., BMC Dev Biol. September 18, 2012; 12 27.
	Homeoprotein hhex-induced conversion of intestinal to ventral pancreatic precursors results in the formation of giant pancreata in Xenopus embryos., Zhao H., Proc Natl Acad Sci U S A. May 29, 2012; 109 (22): 8594-9.
	Xenopus staufen2 is required for anterior endodermal organ formation., Bilogan CK., Genesis. March 1, 2012; 50 (3): 251-9.
	Functional analysis of Rfx6 and mutant variants associated with neonatal diabetes., Pearl EJ., Dev Biol. March 1, 2011; 351 (1): 135-45.
	Xenopus insm1 is essential for gastrointestinal and pancreatic endocrine cell development., Horb LD., Dev Dyn. October 1, 2009; 238 (10): 2505-10.
	Cell-autonomous and signal-dependent expression of liver and intestine marker genes in pluripotent precursor cells from Xenopus embryos., Chen Y, Chen Y., Mech Dev. March 1, 2003; 120 (3): 277-88.
	Downregulation of Hedgehog signaling is required for organogenesis of the small intestine in Xenopus., Zhang J., Dev Biol. January 1, 2001; 229 (1): 188-202.
	Development of the pancreas in Xenopus laevis., Kelly OG., Dev Dyn. August 1, 2000; 218 (4): 615-27.
	The Xenopus tadpole gut: fate maps and morphogenetic movements., Chalmers AD., Development. January 1, 2000; 127 (2): 381-92.
	Development of the gut in Xenopus laevis., Chalmers AD., Dev Dyn. August 1, 1998; 212 (4): 509-21.

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