Papers associated with blastopore (and epha4)

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	Retinoic Acid is Required for Normal Morphogenetic Movements During Gastrulation., Gur M., Front Cell Dev Biol. January 1, 2022; 10 857230.
	Sorting at embryonic boundaries requires high heterotypic interfacial tension., Canty L., Nat Commun. July 31, 2017; 8 (1): 157.
	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.
	EphA4-dependent Brachyury expression is required for dorsal mesoderm involution in the Xenopus gastrula., Evren S., Development. October 1, 2014; 141 (19): 3649-61.
	Cloning and spatiotemporal expression of RIC-8 in Xenopus embryogenesis., Maldonado-Agurto R., Gene Expr Patterns. October 1, 2011; 11 (7): 401-8.
	The involvement of Eph-Ephrin signaling in tissue separation and convergence during Xenopus gastrulation movements., Park EC., Dev Biol. February 15, 2011; 350 (2): 441-50.
	FGF8 spliceforms mediate early mesoderm and posterior neural tissue formation in Xenopus., Fletcher RB., Development. May 1, 2006; 133 (9): 1703-14.
	Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning., Gawantka V., Mech Dev. October 1, 1998; 77 (2): 95-141.
	Neural induction in whole chick embryo cultures by FGF., Alvarez IS., Dev Biol. July 1, 1998; 199 (1): 42-54.
	Tail formation as a continuation of gastrulation: the multiple cell populations of the Xenopus tailbud derive from the late blastopore lip., Gont LK., Development. December 1, 1993; 119 (4): 991-1004.

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