Papers associated with upper blastopore lip (and post)

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	Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
	Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling., Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.
	The competence of marginal zone cells to become Spemann's organizer is controlled by Xcad2., Levy V., Dev Biol. August 1, 2002; 248 (1): 40-51.
	HNF1(beta) is required for mesoderm induction in the Xenopus embryo., Vignali R., Development. April 1, 2000; 127 (7): 1455-65.
	Spatial and temporal properties of ventral blood island induction in Xenopus laevis., Kumano G., Development. December 1, 1999; 126 (23): 5327-37.
	Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning., Gawantka V., Mech Dev. October 1, 1998; 77 (2): 95-141.
	Frzb, a secreted protein expressed in the Spemann organizer, binds and inhibits Wnt-8., Wang S., Cell. March 21, 1997; 88 (6): 757-66.
	eFGF, Xcad3 and Hox genes form a molecular pathway that establishes the anteroposterior axis in Xenopus., Pownall ME., Development. December 1, 1996; 122 (12): 3881-92.
	Expression of a dominant-negative Wnt blocks induction of MyoD in Xenopus embryos., Hoppler S., Genes Dev. November 1, 1996; 10 (21): 2805-17.
	Competition between noggin and bone morphogenetic protein 4 activities may regulate dorsalization during Xenopus development., Re'em-Kalma Y., Proc Natl Acad Sci U S A. December 19, 1995; 92 (26): 12141-5.

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