Papers associated with upper blastopore lip (and smad10)

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	The tumor suppressor Smad4/DPC4 is regulated by phosphorylations that integrate FGF, Wnt, and TGF-β signaling., Demagny H., Cell Rep. October 23, 2014; 9 (2): 688-700.
	Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
	Self-regulation of the head-inducing properties of the Spemann organizer., Inui M., Proc Natl Acad Sci U S A. September 18, 2012; 109 (38): 15354-9.
	Role of BMP, FGF, calcium signaling, and Zic proteins in vertebrate neuroectodermal differentiation., Aruga J., Neurochem Res. July 1, 2011; 36 (7): 1286-92.
	Dkk3 is required for TGF-beta signaling during Xenopus mesoderm induction., Pinho S., Differentiation. December 1, 2007; 75 (10): 957-67.
	Smad10 is required for formation of the frog nervous system., LeSueur JA., Dev Cell. June 1, 2002; 2 (6): 771-83.
	A novel Xenopus Smad-interacting forkhead transcription factor (XFast-3) cooperates with XFast-1 in regulating gastrulation movements., Howell M., Development. June 1, 2002; 129 (12): 2823-34.
	Expression cloning of Xenopus Os4, an evolutionarily conserved gene, which induces mesoderm and dorsal axis., Zohn IE., Dev Biol. November 1, 2001; 239 (1): 118-31.
	Interaction between Wnt and TGF-beta signalling pathways during formation of Spemann's organizer., Nishita M., Nature. February 17, 2000; 403 (6771): 781-5.
	Dominant-negative Smad2 mutants inhibit activin/Vg1 signaling and disrupt axis formation in Xenopus., Hoodless PA., Dev Biol. March 15, 1999; 207 (2): 364-79.
	Spemann organizer activity of Smad10., LeSueur JA., Development. January 1, 1999; 126 (1): 137-46.

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