Papers associated with fibroblast (and ncam1)

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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.
	Specific induction of cranial placode cells from Xenopus ectoderm by modulating the levels of BMP, Wnt and FGF signaling., Watanabe T., Genesis. October 1, 2014; .
	MRAS GTPase is a novel stemness marker that impacts mouse embryonic stem cell plasticity and Xenopus embryonic cell fate., Mathieu ME., Development. August 1, 2013; 140 (16): 3311-22.
	WNK4 is an essential effector of anterior formation in FGF signaling., Shimizu M., Genes Cells. June 1, 2013; 18 (6): 442-9.
	Neuronatin promotes neural lineage in ESCs via Ca(2+) signaling., Lin HH., Stem Cells. November 1, 2010; 28 (11): 1950-60.
	Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2., Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.
	Spinal cord is required for proper regeneration of the tail in Xenopus tadpoles., Taniguchi Y., Dev Growth Differ. February 1, 2008; 50 (2): 109-20.
	Vertebrate Ctr1 coordinates morphogenesis and progenitor cell fate and regulates embryonic stem cell differentiation., Haremaki T., Proc Natl Acad Sci U S A. July 17, 2007; 104 (29): 12029-34.
	Conditional BMP inhibition in Xenopus reveals stage-specific roles for BMPs in neural and neural crest induction., Wawersik S., Dev Biol. January 15, 2005; 277 (2): 425-42.
	Inhibition of FGF signaling causes expansion of the endoderm in Xenopus., Cha SW., Biochem Biophys Res Commun. February 27, 2004; 315 (1): 100-6.
	Essential role of the transcription factor Ets-2 in Xenopus early development., Kawachi K., J Biol Chem. February 14, 2003; 278 (7): 5473-7.
	Expression of scFv antibodies in Xenopus embryos to disrupt protein function: implications for large-scale evaluation of the embryonic proteome., Abler LL., Genesis. February 1, 2003; 35 (2): 107-13.
	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.
	Neuregulin induces the expression of mesodermal genes in the ectoderm of Xenopus laevis., Chung HG., Mol Cells. October 31, 1999; 9 (5): 497-503.
	derrière: a TGF-beta family member required for posterior development in Xenopus., Sun BI., Development. April 1, 1999; 126 (7): 1467-82.
	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.
	Xenopus Smad8 acts downstream of BMP-4 to modulate its activity during vertebrate embryonic patterning., Nakayama T., Development. March 1, 1998; 125 (5): 857-67.
	XBMPRII, a novel Xenopus type II receptor mediating BMP signaling in embryonic tissues., Frisch A., Development. February 1, 1998; 125 (3): 431-42.
	Essential role of heparan sulfates in axon navigation and targeting in the developing visual system., Walz A., Development. June 1, 1997; 124 (12): 2421-30.
	eFGF, Xcad3 and Hox genes form a molecular pathway that establishes the anteroposterior axis in Xenopus., Pownall ME., Development. December 1, 1996; 122 (12): 3881-92.
	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.
	A truncated activin receptor inhibits mesoderm induction and formation of axial structures in Xenopus embryos., Hemmati-Brivanlou A., Nature. October 15, 1992; 359 (6396): 609-14.
	Patterns of N-CAM expression during myogenesis in Xenopus laevis., Kay BK., Development. July 1, 1988; 103 (3): 463-71.

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