Papers associated with primary germ layer (and flrt3)

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	Tbx2 is required for the suppression of mesendoderm during early Xenopus development., Teegala S., Dev Dyn. July 1, 2018; 247 (7): 903-913.
	RAB8B is required for activity and caveolar endocytosis of LRP6., Demir K., Cell Rep. September 26, 2013; 4 (6): 1224-34.
	BMP signal attenuates FGF pathway in anteroposterior neural patterning., Cho GS., Biochem Biophys Res Commun. May 10, 2013; 434 (3): 509-15.
	A protocadherin-cadherin-FLRT3 complex controls cell adhesion and morphogenesis., Chen X., PLoS One. December 22, 2009; 4 (12): e8411.
	Unc5B interacts with FLRT3 and Rnd1 to modulate cell adhesion in Xenopus embryos., Karaulanov E., PLoS One. May 29, 2009; 4 (5): e5742.
	Ventral closure, headfold fusion and definitive endoderm migration defects in mouse embryos lacking the fibronectin leucine-rich transmembrane protein FLRT3., Maretto S., Dev Biol. June 1, 2008; 318 (1): 184-93.
	TGF-beta signaling-mediated morphogenesis: modulation of cell adhesion via cadherin endocytosis., Ogata S., Genes Dev. July 15, 2007; 21 (14): 1817-31.
	Regulated expression of FLRT genes implies a functional role in the regulation of FGF signalling during mouse development., Haines BP., Dev Biol. September 1, 2006; 297 (1): 14-25.
	Phylogenetic footprinting and genome scanning identify vertebrate BMP response elements and new target genes., von Bubnoff A., Dev Biol. May 15, 2005; 281 (2): 210-26.
	Microarray-based identification of VegT targets in Xenopus., Taverner NV., Mech Dev. March 1, 2005; 122 (3): 333-54.
	The transmembrane protein XFLRT3 forms a complex with FGF receptors and promotes FGF signalling., Böttcher RT., Nat Cell Biol. January 1, 2004; 6 (1): 38-44.

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