Papers associated with fibroblast (and egr2)

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	Dusp1 modulates activin/smad2 mediated germ layer specification via FGF signal inhibition in Xenopus embryos., Umair Z., Anim Cells Syst (Seoul). November 27, 2020; 24 (6): 359-370.
	Coordinated regulation of the dorsal-ventral and anterior-posterior patterning of Xenopus embryos by the BTB/POZ zinc finger protein Zbtb14., Takebayashi-Suzuki K., Dev Growth Differ. April 1, 2018; 60 (3): 158-173.
	Temporally coordinated signals progressively pattern the anteroposterior and dorsoventral body axes., Tuazon FB., Semin Cell Dev Biol. June 1, 2015; 42 118-33.
	Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation., Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.
	Xenopus laevis FGF receptor substrate 3 (XFrs3) is important for eye development and mediates Pax6 expression in lens placode through its Shp2-binding sites., Kim YJ., Dev Biol. January 1, 2015; 397 (1): 129-39.
	Regulation of neurogenesis by Fgf8a requires Cdc42 signaling and a novel Cdc42 effector protein., Hulstrand AM., Dev Biol. October 15, 2013; 382 (2): 385-99.
	Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2., Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.
	Neural ectoderm-secreted FGF initiates the expression of Nkx2.5 in cardiac progenitors via a p38 MAPK/CREB pathway., Keren-Politansky A., Dev Biol. November 15, 2009; 335 (2): 374-84.
	Dazap2 is required for FGF-mediated posterior neural patterning, independent of Wnt and Cdx function., Roche DD., Dev Biol. September 1, 2009; 333 (1): 26-36.
	Xenopus SMOC-1 Inhibits bone morphogenetic protein signaling downstream of receptor binding and is essential for postgastrulation development in Xenopus., Thomas JT., J Biol Chem. July 10, 2009; 284 (28): 18994-9005.
	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.
	XMeis3 protein activity is required for proper hindbrain patterning in Xenopus laevis embryos., Dibner C., Development. September 1, 2001; 128 (18): 3415-26.
	Ras-mediated FGF signaling is required for the formation of posterior but not anterior neural tissue in Xenopus laevis., Ribisi S., Dev Biol. November 1, 2000; 227 (1): 183-96.
	Involvement of BMP-4/msx-1 and FGF pathways in neural induction in the Xenopus embryo., Ishimura A., Dev Growth Differ. August 1, 2000; 42 (4): 307-16.
	Signaling specificities of fibroblast growth factor receptors in early Xenopus embryo., Umbhauer M., J Cell Sci. August 1, 2000; 113 ( Pt 16) 2865-75.
	Xenopus nodal-related signaling is essential for mesendodermal patterning during early embryogenesis., Osada SI., Development. June 1, 1999; 126 (14): 3229-40.
	derrière: a TGF-beta family member required for posterior development in Xenopus., Sun BI., Development. April 1, 1999; 126 (7): 1467-82.
	FGF is required for posterior neural patterning but not for neural induction., Holowacz T., Dev Biol. January 15, 1999; 205 (2): 296-308.
	Anterior specification of embryonic ectoderm: the role of the Xenopus cement gland-specific gene XAG-2., Aberger F., Mech Dev. March 1, 1998; 72 (1-2): 115-30.
	XBMPRII, a novel Xenopus type II receptor mediating BMP signaling in embryonic tissues., Frisch A., Development. February 1, 1998; 125 (3): 431-42.
	Xenopus hindbrain patterning requires retinoid signaling., Kolm PJ., Dev Biol. December 1, 1997; 192 (1): 1-16.
	Fibroblast growth factor is a direct neural inducer, which combined with noggin generates anterior-posterior neural pattern., Lamb TM., Development. November 1, 1995; 121 (11): 3627-36.

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