Papers associated with notochord (and smad2)

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	ZSWIM4 regulates embryonic patterning and BMP signaling by promoting nuclear Smad1 degradation., Wang C., EMBO Rep. February 1, 2024; 25 (2): 646-671.
	Segregation of brain and organizer precursors is differentially regulated by Nodal signaling at blastula stage., Castro Colabianchi AM., Biol Open. February 25, 2021; 10 (2):
	Pinhead signaling regulates mesoderm heterogeneity via the FGF receptor-dependent pathway., Ossipova O., Development. September 11, 2020; 147 (17):
	Pinhead signaling regulates mesoderm heterogeneity via FGF receptor-dependent pathway., Ossipova O., Development. January 1, 2020;
	A transgenic reporter under control of an es1 promoter/enhancer marks wound epidermis and apical epithelial cap during tail regeneration in Xenopus laevis tadpole., Sato K., Dev Biol. January 15, 2018; 433 (2): 404-415.
	Similarity in gene-regulatory networks suggests that cancer cells share characteristics of embryonic neural cells., Zhang Z., J Biol Chem. August 4, 2017; 292 (31): 12842-12859.
	Dissecting BMP signaling input into the gene regulatory networks driving specification of the blood stem cell lineage., Kirmizitas A., Proc Natl Acad Sci U S A. June 6, 2017; 114 (23): 5814-5821.
	The serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation., Acosta H., Development. March 15, 2015; 142 (6): 1146-58.
	E2a is necessary for Smad2/3-dependent transcription and the direct repression of lefty during gastrulation., Wills AE., Dev Cell. February 9, 2015; 32 (3): 345-57.
	In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency., Gentsch GE., Cell Rep. September 26, 2013; 4 (6): 1185-96.
	Lin28 proteins are required for germ layer specification in Xenopus., Faas L., Development. March 1, 2013; 140 (5): 976-86.
	mNanog possesses dorsal mesoderm-inducing ability by modulating both BMP and Activin/nodal signaling in Xenopus ectodermal cells., Miyazaki A., PLoS One. January 1, 2012; 7 (10): e46630.
	Regulation of TGF-(beta) signalling by N-acetylgalactosaminyltransferase-like 1., Herr P., Development. May 1, 2008; 135 (10): 1813-22.
	TGF-beta signaling is required for multiple processes during Xenopus tail regeneration., Ho DM., Dev Biol. March 1, 2008; 315 (1): 203-16.
	Coordination of cell polarity during Xenopus gastrulation., Shindo A., PLoS One. February 6, 2008; 3 (2): e1600.
	Dkk3 is required for TGF-beta signaling during Xenopus mesoderm induction., Pinho S., Differentiation. December 1, 2007; 75 (10): 957-67.
	Neural induction requires continued suppression of both Smad1 and Smad2 signals during gastrulation., Chang C., Development. November 1, 2007; 134 (21): 3861-72.
	FoxD3 regulation of Nodal in the Spemann organizer is essential for Xenopus dorsal mesoderm development., Steiner AB., Development. December 1, 2006; 133 (24): 4827-38.
	Vg 1 is an essential signaling molecule in Xenopus development., Birsoy B., Development. January 1, 2006; 133 (1): 15-20.
	Notch signaling modulates the nuclear localization of carboxy-terminal-phosphorylated smad2 and controls the competence of ectodermal cells for activin A., Abe T., Mech Dev. May 1, 2005; 122 (5): 671-80.
	XPACE4 is a localized pro-protein convertase required for mesoderm induction and the cleavage of specific TGFbeta proteins in Xenopus development., Birsoy B., Development. February 1, 2005; 132 (3): 591-602.
	Lefty blocks a subset of TGFbeta signals by antagonizing EGF-CFC coreceptors., Cheng SK., PLoS Biol. February 1, 2004; 2 (2): E30.
	The nodal target gene Xmenf is a component of an FGF-independent pathway of ventral mesoderm induction in Xenopus., Kumano G., Mech Dev. October 1, 2002; 118 (1-2): 45-56.
	The roles of three signaling pathways in the formation and function of the Spemann Organizer., Xanthos JB., Development. September 1, 2002; 129 (17): 4027-43.
	Beta-catenin, MAPK and Smad signaling during early Xenopus development., Schohl A., Development. January 1, 2002; 129 (1): 37-52.
	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.
	Xenopus Smad3 is specifically expressed in the chordoneural hinge, notochord and in the endocardium of the developing heart., Howell M., Mech Dev. June 1, 2001; 104 (1-2): 147-50.
	Mesendoderm induction and reversal of left-right pattern by mouse Gdf1, a Vg1-related gene., Wall NA., Dev Biol. November 15, 2000; 227 (2): 495-509.
	Gli2 functions in FGF signaling during antero-posterior patterning., Brewster R., Development. October 1, 2000; 127 (20): 4395-405.
	Fast1 is required for the development of dorsal axial structures in zebrafish., Sirotkin HI., Curr Biol. September 7, 2000; 10 (17): 1051-4.
	Homeodomain and winged-helix transcription factors recruit activated Smads to distinct promoter elements via a common Smad interaction motif., Germain S., Genes Dev. February 15, 2000; 14 (4): 435-51.
	Activation of Stat3 by cytokine receptor gp130 ventralizes Xenopus embryos independent of BMP-4., Nishinakamura R., Dev Biol. December 15, 1999; 216 (2): 481-90.
	A mouse homologue of FAST-1 transduces TGF beta superfamily signals and is expressed during early embryogenesis., Weisberg E., Mech Dev. December 1, 1998; 79 (1-2): 17-27.
	Smad7 inhibits mesoderm formation and promotes neural cell fate in Xenopus embryos., Bhushan A., Dev Biol. August 15, 1998; 200 (2): 260-8.
	The Xenopus dorsalizing factor Gremlin identifies a novel family of secreted proteins that antagonize BMP activities., Hsu DR., Mol Cell. April 1, 1998; 1 (5): 673-83.

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