Papers associated with whole organism (and smad6)

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	Patterning of the Vertebrate Head in Time and Space by BMP Signaling., Zhu K., J Dev Biol. July 3, 2023; 11 (3):
	Identification and validation of candidate risk genes in endocytic vesicular trafficking associated with esophageal atresia and tracheoesophageal fistulas., Zhong G., HGG Adv. July 14, 2022; 3 (3): 100107.
	HMCES modulates the transcriptional regulation of nodal/activin and BMP signaling in mESCs., Liang T., Cell Rep. July 12, 2022; 40 (2): 111038.
	Axis Patterning by BMPs: Cnidarian Network Reveals Evolutionary Constraints., Genikhovich G., Cell Rep. March 17, 2015; 10 (10): 1646-1654.
	USP15 targets ALK3/BMPR1A for deubiquitylation to enhance bone morphogenetic protein signalling., Herhaus L., Open Biol. May 1, 2014; 4 (5): 140065.
	Role of BMP, FGF, calcium signaling, and Zic proteins in vertebrate neuroectodermal differentiation., Aruga J., Neurochem Res. July 1, 2011; 36 (7): 1286-92.
	Negative feedback in the bone morphogenetic protein 4 (BMP4) synexpression group governs its dynamic signaling range and canalizes development., Paulsen M., Proc Natl Acad Sci U S A. June 21, 2011; 108 (25): 10202-7.
	Expression cloning of Xenopus zygote arrest 2 (Xzar2) as a novel epidermalization-promoting factor in early embryos of Xenopus laevis., Nakajima Y., Genes Cells. May 1, 2009; 14 (5): 583-95.
	The secreted EGF-Discoidin factor xDel1 is essential for dorsal development of the Xenopus embryo., Arakawa A., Dev Biol. June 1, 2007; 306 (1): 160-9.
	Defining synphenotype groups in Xenopus tropicalis by use of antisense morpholino oligonucleotides., Rana AA., PLoS Genet. November 17, 2006; 2 (11): e193.
	Temporal analysis of the early BMP functions identifies distinct anti-organizer and mesoderm patterning phases., Marom K., Dev Biol. June 15, 2005; 282 (2): 442-54.
	Neural induction in Xenopus requires early FGF signalling in addition to BMP inhibition., Delaune E., Development. January 1, 2005; 132 (2): 299-310.
	A new role for BMP5 during limb development acting through the synergic activation of Smad and MAPK pathways., Zuzarte-Luís V., Dev Biol. August 1, 2004; 272 (1): 39-52.
	TGF-beta signalling pathways in early Xenopus development., Hill CS., Curr Opin Genet Dev. October 1, 2001; 11 (5): 533-40.
	Human truncated Smad 6 (Smad 6s) inhibits the BMP pathway in Xenopus laevis., Krishnan P., Dev Growth Differ. April 1, 2001; 43 (2): 115-32.
	Bone morphogenetic protein function is required for terminal differentiation of the heart but not for early expression of cardiac marker genes., Walters MJ., Mech Dev. February 1, 2001; 100 (2): 263-73.
	The Xvex-1 antimorph reveals the temporal competence for organizer formation and an early role for ventral homeobox genes., Shapira E., Mech Dev. January 1, 2000; 90 (1): 77-87.
	Evidence for a role of Smad6 in chick cardiac development., Yamada M., Dev Biol. November 1, 1999; 215 (1): 48-61.
	Smad6 functions as an intracellular antagonist of some TGF-beta family members during Xenopus embryogenesis., Nakayama T., Genes Cells. June 1, 1998; 3 (6): 387-94.
	Xenopus Smad7 inhibits both the activin and BMP pathways and acts as a neural inducer., Casellas R., Dev Biol. June 1, 1998; 198 (1): 1-12.
	Smad6 inhibits BMP/Smad1 signaling by specifically competing with the Smad4 tumor suppressor., Hata A., Genes Dev. January 15, 1998; 12 (2): 186-97.

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