Papers associated with regenerating tail (and smad1)

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	Noggin4 is a long-range inhibitor of Wnt8 signalling that regulates head development in Xenopus laevis., Eroshkin FM., Sci Rep. January 22, 2016; 6 23049.
	The Proto-oncogene Transcription Factor Ets1 Regulates Neural Crest Development through Histone Deacetylase 1 to Mediate Output of Bone Morphogenetic Protein Signaling., Wang C., J Biol Chem. September 4, 2015; 290 (36): 21925-38.
	Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
	Zygotic expression of Exostosin1 (Ext1) is required for BMP signaling and establishment of dorsal-ventral pattern in Xenopus., Shieh YE., Int J Dev Biol. January 1, 2014; 58 (1): 27-34.
	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.
	Origin of muscle satellite cells in the Xenopus embryo., Daughters RS., Development. March 1, 2011; 138 (5): 821-30.
	SNW1 is a critical regulator of spatial BMP activity, neural plate border formation, and neural crest specification in vertebrate embryos., Wu MY., PLoS Biol. February 15, 2011; 9 (2): e1000593.
	The role and regulation of GDF11 in Smad2 activation during tailbud formation in the Xenopus embryo., Ho DM., Mech Dev. January 1, 2010; 127 (9-12): 485-95.
	Bone morphogenetic protein 15 (BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis., Di Pasquale E., J Biol Chem. September 18, 2009; 284 (38): 26127-36.
	Mad is required for wingless signaling in wing development and segment patterning in Drosophila., Eivers E., PLoS One. August 6, 2009; 4 (8): e6543.
	TGF-beta signaling is required for multiple processes during Xenopus tail regeneration., Ho DM., Dev Biol. March 1, 2008; 315 (1): 203-16.
	The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning., Sander V., EMBO J. June 20, 2007; 26 (12): 2955-65.
	Dephosphorylation of the linker regions of Smad1 and Smad2/3 by small C-terminal domain phosphatases has distinct outcomes for bone morphogenetic protein and transforming growth factor-beta pathways., Sapkota G., J Biol Chem. December 29, 2006; 281 (52): 40412-9.
	Defining synphenotype groups in Xenopus tropicalis by use of antisense morpholino oligonucleotides., Rana AA., PLoS Genet. November 17, 2006; 2 (11): e193.
	BMP-3 is a novel inhibitor of both activin and BMP-4 signaling in Xenopus embryos., Gamer LW., Dev Biol. September 1, 2005; 285 (1): 156-68.
	Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos., Reversade B., Development. August 1, 2005; 132 (15): 3381-92.
	BMP4-dependent expression of Xenopus Grainyhead-like 1 is essential for epidermal differentiation., Tao J., Development. March 1, 2005; 132 (5): 1021-34.
	The POU factor Oct-25 regulates the Xvent-2B gene and counteracts terminal differentiation in Xenopus embryos., Cao Y, Cao Y., J Biol Chem. October 15, 2004; 279 (42): 43735-43.
	The role of BMP signaling in outgrowth and patterning of the Xenopus tail bud., Beck CW., Dev Biol. October 15, 2001; 238 (2): 303-14.
	Regulation of the mRNAs encoding proteins of the BMP signaling pathway during the maternal stages of Xenopus development., Fritz BR., Dev Biol. August 1, 2001; 236 (1): 230-43.
	FOG acts as a repressor of red blood cell development in Xenopus., Deconinck AE., Development. May 1, 2000; 127 (10): 2031-40.
	Characterization of zebrafish smad1, smad2 and smad5: the amino-terminus of smad1 and smad5 is required for specific function in the embryo., Müller F., Mech Dev. October 1, 1999; 88 (1): 73-88.
	Xenopus mothers against decapentaplegic is an embryonic ventralizing agent that acts downstream of the BMP-2/4 receptor., Thomsen GH., Development. August 1, 1996; 122 (8): 2359-66.

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