Papers associated with animal pole (and eomes)

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	A novel role for Ascl1 in the regulation of mesendoderm formation via HDAC-dependent antagonism of VegT., Gao L., Development. February 1, 2016; 143 (3): 492-503.
	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.
	Conservation and evolutionary divergence in the activity of receptor-regulated smads., Sorrentino GM., Evodevo. October 1, 2012; 3 (1): 22.
	Zygotic VegT is required for Xenopus paraxial mesoderm formation and is regulated by Nodal signaling and Eomesodermin., Fukuda M., Int J Dev Biol. January 1, 2010; 54 (1): 81-92.
	Vegetally localized Xenopus trim36 regulates cortical rotation and dorsal axis formation., Cuykendall TN., Development. September 1, 2009; 136 (18): 3057-65.
	The role of FGF signaling in the establishment and maintenance of mesodermal gene expression in Xenopus., Fletcher RB., Dev Dyn. May 1, 2008; 237 (5): 1243-54.
	PP2A:B56epsilon is required for eye induction and eye field separation., Rorick AM., Dev Biol. February 15, 2007; 302 (2): 477-93.
	Emilin1 links TGF-beta maturation to blood pressure homeostasis., Zacchigna L., Cell. March 10, 2006; 124 (5): 929-42.
	Twisted gastrulation is required for forebrain specification and cooperates with Chordin to inhibit BMP signaling during X. tropicalis gastrulation., Wills A., Dev Biol. January 1, 2006; 289 (1): 166-78.
	Germ-layer specification and control of cell growth by Ectodermin, a Smad4 ubiquitin ligase., Dupont S., Cell. April 8, 2005; 121 (1): 87-99.
	Endogenous Cerberus activity is required for anterior head specification in Xenopus., Silva AC., Development. October 1, 2003; 130 (20): 4943-53.
	Induction of cardiomyocytes by GATA4 in Xenopus ectodermal explants., Latinkić BV., Development. August 1, 2003; 130 (16): 3865-76.
	Redundant early and overlapping larval roles of Xsox17 subgroup genes in Xenopus endoderm development., Clements D., Mech Dev. March 1, 2003; 120 (3): 337-48.
	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.
	FGF signaling restricts the primary blood islands to ventral mesoderm., Kumano G., Dev Biol. December 15, 2000; 228 (2): 304-14.
	The bHLH class protein pMesogenin1 can specify paraxial mesoderm phenotypes., Yoon JK., Dev Biol. June 15, 2000; 222 (2): 376-91.
	In Xenopus embryos, BMP heterodimers are not required for mesoderm induction, but BMP activity is necessary for dorsal/ventral patterning., Eimon PM., Dev Biol. December 1, 1999; 216 (1): 29-40.
	Differential expression of VegT and Antipodean protein isoforms in Xenopus., Stennard F., Mech Dev. August 1, 1999; 86 (1-2): 87-98.
	derrière: a TGF-beta family member required for posterior development in Xenopus., Sun BI., Development. April 1, 1999; 126 (7): 1467-82.
	The Xenopus T-box gene, Antipodean, encodes a vegetally localised maternal mRNA and can trigger mesoderm formation., Stennard F., Development. December 1, 1996; 122 (12): 4179-88.
	An indelible lineage marker for Xenopus using a mutated green fluorescent protein., Zernicka-Goetz M., Development. December 1, 1996; 122 (12): 3719-24.

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