Papers associated with marginal zone (and tbx5)

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	Tbx5 is essential for heart development., Horb ME., Development. April 1, 1999; 126 (8): 1739-51.
	Xbra3 induces mesoderm and neural tissue in Xenopus laevis., Strong CF., Dev Biol. June 15, 2000; 222 (2): 405-19.
	Wnt antagonism initiates cardiogenesis in Xenopus laevis., Schneider VA., Genes Dev. February 1, 2001; 15 (3): 304-15.
	Endoderm specification and differentiation in Xenopus embryos., Horb ME., Dev Biol. August 15, 2001; 236 (2): 330-43.
	Heart induction by Wnt antagonists depends on the homeodomain transcription factor Hex., Foley AC., Genes Dev. February 1, 2005; 19 (3): 387-96.
	SOX7 and SOX18 are essential for cardiogenesis in Xenopus., Zhang C., Dev Dyn. December 1, 2005; 234 (4): 878-91.
	Xtbx6r, a novel T-box gene expressed in the paraxial mesoderm, has anterior neural-inducing activity., Yabe S., Int J Dev Biol. January 1, 2006; 50 (8): 681-9.
	Developmental expression patterns of Tbx1, Tbx2, Tbx5, and Tbx20 in Xenopus tropicalis., Showell C., Dev Dyn. June 1, 2006; 235 (6): 1623-30.
	Multiple functions of Cerberus cooperate to induce heart downstream of Nodal., Foley AC., Dev Biol. March 1, 2007; 303 (1): 57-65.
	The Gata5 target, TGIF2, defines the pancreatic region by modulating BMP signals within the endoderm., Spagnoli FM., Development. February 1, 2008; 135 (3): 451-61.
	GATA4 and GATA5 are essential for heart and liver development in Xenopus embryos., Haworth KE., BMC Dev Biol. July 28, 2008; 8 74.
	Coordinating the timing of cardiac precursor development during gastrulation: a new role for Notch signaling., Miazga CM., Dev Biol. September 15, 2009; 333 (2): 285-96.
	Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling., Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.
	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.
	Shox2 mediates Tbx5 activity by regulating Bmp4 in the pacemaker region of the developing heart., Puskaric S., Hum Mol Genet. December 1, 2010; 19 (23): 4625-33.
	Early cardiac morphogenesis defects caused by loss of embryonic macrophage function in Xenopus., Smith SJ., Mech Dev. January 1, 2011; 128 (5-6): 303-15.
	Cardiac neural crest is dispensable for outflow tract septation in Xenopus., Lee YH., Development. May 1, 2011; 138 (10): 2025-34.
	Canonical WNT signaling enhances stem cell expression in the developing heart without a corresponding inhibition of cardiogenic differentiation., Martin LK., Stem Cells Dev. November 1, 2011; 20 (11): 1973-83.
	Inhibition of heart formation by lithium is an indirect result of the disruption of tissue organization within the embryo., Martin LK., Dev Growth Differ. February 1, 2012; 54 (2): 153-66.
	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.
	Dorsoventral patterning of the Xenopus eye involves differential temporal changes in the response of optic stalk and retinal progenitors to Hh signalling., Wang X., Neural Dev. March 20, 2015; 10 7.

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