Papers associated with early embryonic cell (and fgf8)

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	Enhanced sensitivity and stability in two-color in situ hybridization by means of a novel chromagenic substrate combination., Hurtado R., Dev Dyn. October 1, 2006; 235 (10): 2811-6.
	FGF is essential for both condensation and mesenchymal-epithelial transition stages of pronephric kidney tubule development., Urban AE., Dev Biol. September 1, 2006; 297 (1): 103-17.
	Conserved roles for Oct4 homologues in maintaining multipotency during early vertebrate development., Morrison GM., Development. May 1, 2006; 133 (10): 2011-22.
	FGF8 spliceforms mediate early mesoderm and posterior neural tissue formation in Xenopus., Fletcher RB., Development. May 1, 2006; 133 (9): 1703-14.
	Tes regulates neural crest migration and axial elongation in Xenopus., Dingwell KS., Dev Biol. May 1, 2006; 293 (1): 252-67.
	The doublesex-related gene, XDmrt4, is required for neurogenesis in the olfactory system., Huang X., Proc Natl Acad Sci U S A. August 9, 2005; 102 (32): 11349-54.
	Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos., Reversade B., Development. August 1, 2005; 132 (15): 3381-92.
	XTbx1 is a transcriptional activator involved in head and pharyngeal arch development in Xenopus laevis., Ataliotis P., Dev Dyn. April 1, 2005; 232 (4): 979-91.
	Conserved cross-interactions in Drosophila and Xenopus between Ras/MAPK signaling and the dual-specificity phosphatase MKP3., Gómez AR., Dev Dyn. March 1, 2005; 232 (3): 695-708.
	Msx1 and Pax3 cooperate to mediate FGF8 and WNT signals during Xenopus neural crest induction., Monsoro-Burq AH., Dev Cell. February 1, 2005; 8 (2): 167-78.
	Neural induction requires BMP inhibition only as a late step, and involves signals other than FGF and Wnt antagonists., Linker C., Development. November 1, 2004; 131 (22): 5671-81.
	R-Spondin2 is a secreted activator of Wnt/beta-catenin signaling and is required for Xenopus myogenesis., Kazanskaya O., Dev Cell. October 1, 2004; 7 (4): 525-34.
	Multiple points of interaction between retinoic acid and FGF signaling during embryonic axis formation., Shiotsugu J., Development. June 1, 2004; 131 (11): 2653-67.
	PP2A:B56epsilon is required for Wnt/beta-catenin signaling during embryonic development., Yang J., Development. December 1, 2003; 130 (23): 5569-78.
	Glypican 4 modulates FGF signalling and regulates dorsoventral forebrain patterning in Xenopus embryos., Galli A., Development. October 1, 2003; 130 (20): 4919-29.
	Neural crest induction by paraxial mesoderm in Xenopus embryos requires FGF signals., Monsoro-Burq AH., Development. July 1, 2003; 130 (14): 3111-24.
	Asymmetries in H+/K+-ATPase and cell membrane potentials comprise a very early step in left-right patterning., Levin M., Cell. October 4, 2002; 111 (1): 77-89.
	The homeoprotein Xiro1 is required for midbrain-hindbrain boundary formation., Glavic A., Development. April 1, 2002; 129 (7): 1609-21.
	The Wnt/beta-catenin pathway posteriorizes neural tissue in Xenopus by an indirect mechanism requiring FGF signalling., Domingos PM., Dev Biol. November 1, 2001; 239 (1): 148-60.
	Xenopus Sprouty2 inhibits FGF-mediated gastrulation movements but does not affect mesoderm induction and patterning., Nutt SL., Genes Dev. May 1, 2001; 15 (9): 1152-66.
	Cloning, expression and nuclear localization of human NPM3, a member of the nucleophosmin/nucleoplasmin family of nuclear chaperones., Shackleford GM., BMC Genomics. January 1, 2001; 2 8.

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