Papers associated with animal cap (and fgf2)

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	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.
	PV.1 induced by FGF-Xbra functions as a repressor of neurogenesis in Xenopus embryos., Yoon J., BMB Rep. December 1, 2014; 47 (12): 673-8.
	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.
	Comparative Functional Analysis of ZFP36 Genes during Xenopus Development., Tréguer K., PLoS One. January 1, 2013; 8 (1): e54550.
	TAK1 promotes BMP4/Smad1 signaling via inhibition of erk MAPK: a new link in the FGF/BMP regulatory network., Liu C., Differentiation. April 1, 2012; 83 (4): 210-9.
	Inhibition of FGF signaling converts dorsal mesoderm to ventral mesoderm in early Xenopus embryos., Lee SY., Differentiation. September 1, 2011; 82 (2): 99-107.
	Anterior neural development requires Del1, a matrix-associated protein that attenuates canonical Wnt signaling via the Ror2 pathway., Takai A., Development. October 1, 2010; 137 (19): 3293-302.
	Vestigial like gene family expression in Xenopus: common and divergent features with other vertebrates., Faucheux C., Int J Dev Biol. January 1, 2010; 54 (8-9): 1375-82.
	Xmc mediates Xctr1-independent morphogenesis in Xenopus laevis., Haremaki T., Dev Dyn. September 1, 2009; 238 (9): 2382-7.
	A role for Syndecan-4 in neural induction involving ERK- and PKC-dependent pathways., Kuriyama S., Development. February 1, 2009; 136 (4): 575-84.
	Lrig3 regulates neural crest formation in Xenopus by modulating Fgf and Wnt signaling pathways., Zhao H., Development. April 1, 2008; 135 (7): 1283-93.
	Mouse homologues of Shisa antagonistic to Wnt and Fgf signalings., Furushima K., Dev Biol. June 15, 2007; 306 (2): 480-92.
	Differential expression of two TEF-1 (TEAD) genes during Xenopus laevis development and in response to inducing factors., Naye F., Int J Dev Biol. January 1, 2007; 51 (8): 745-52.
	Shisa2 promotes the maturation of somitic precursors and transition to the segmental fate in Xenopus embryos., Nagano T., Development. December 1, 2006; 133 (23): 4643-54.
	Cold-inducible RNA binding protein is required for the expression of adhesion molecules and embryonic cell movement in Xenopus laevis., Peng Y., Biochem Biophys Res Commun. May 26, 2006; 344 (1): 416-24.
	BMP-3 is a novel inhibitor of both activin and BMP-4 signaling in Xenopus embryos., Gamer LW., Dev Biol. September 1, 2005; 285 (1): 156-68.
	FGF signal regulates gastrulation cell movements and morphology through its target NRH., Chung HA., Dev Biol. June 1, 2005; 282 (1): 95-110.
	FGF signal interpretation is directed by Sprouty and Spred proteins during mesoderm formation., Sivak JM., Dev Cell. May 1, 2005; 8 (5): 689-701.
	Shisa promotes head formation through the inhibition of receptor protein maturation for the caudalizing factors, Wnt and FGF., Yamamoto A., Cell. January 28, 2005; 120 (2): 223-35.
	Control of embryonic Xenopus morphogenesis by a Ral-GDS/Xral branch of the Ras signalling pathway., Lebreton S., J Cell Sci. November 15, 2003; 116 (Pt 22): 4651-62.
	Neural crest induction by paraxial mesoderm in Xenopus embryos requires FGF signals., Monsoro-Burq AH., Development. July 1, 2003; 130 (14): 3111-24.
	Isolation and growth factor inducibility of the Xenopus laevis Lmx1b gene., Haldin CE., Int J Dev Biol. May 1, 2003; 47 (4): 253-62.
	Using Xenopus as a model system for an undergraduate laboratory course in vertebrate development at the University of Bordeaux, France., Olive M., Int J Dev Biol. January 1, 2003; 47 (2-3): 153-60.
	Induction and patterning of the telencephalon in Xenopus laevis., Lupo G., Development. December 1, 2002; 129 (23): 5421-36.
	Common and distinct signals specify the distribution of blood and vascular cell lineages in Xenopus laevis embryos., Iraha F., Dev Growth Differ. October 1, 2002; 44 (5): 395-407.
	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.
	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.
	Participation of transcription elongation factor XSII-K1 in mesoderm-derived tissue development in Xenopus laevis., Taira Y., J Biol Chem. October 13, 2000; 275 (41): 32011-5.
	FOG acts as a repressor of red blood cell development in Xenopus., Deconinck AE., Development. May 1, 2000; 127 (10): 2031-40.
	Expression pattern of BXR suggests a role for benzoate ligand-mediated signalling in hatching gland function., Heath LA., Int J Dev Biol. January 1, 2000; 44 (1): 141-4.
	Blood cell induction in Xenopus animal cap explants: effects of fibroblast growth factor, bone morphogenetic proteins, and activin., Miyanaga Y., Dev Genes Evol. February 1, 1999; 209 (2): 69-76.
	The Xenopus Ets transcription factor XER81 is a target of the FGF signaling pathway., Münchberg SR., Mech Dev. January 1, 1999; 80 (1): 53-65.
	Patterns and control of cell motility in the Xenopus gastrula., Wacker S., Development. May 1, 1998; 125 (10): 1931-42.
	Xenopus eHAND: a marker for the developing cardiovascular system of the embryo that is regulated by bone morphogenetic proteins., Sparrow DB., Mech Dev. February 1, 1998; 71 (1-2): 151-63.
	Cloning and expression pattern of Xenopus prx-1 (Xprx-1) during embryonic development., Takahashi S., Dev Growth Differ. February 1, 1998; 40 (1): 97-104.
	Neural induction and patterning by fibroblast growth factor, notochord and somite tissue in Xenopus., Barnett MW., Dev Growth Differ. February 1, 1998; 40 (1): 47-57.
	Xenopus Zic-related-1 and Sox-2, two factors induced by chordin, have distinct activities in the initiation of neural induction., Mizuseki K., Development. February 1, 1998; 125 (4): 579-87.
	Loss of cell adhesion in Xenopus laevis embryos mediated by the cytoplasmic domain of XLerk, an erythropoietin-producing hepatocellular ligand., Jones TL., Proc Natl Acad Sci U S A. January 20, 1998; 95 (2): 576-81.
	Mesoderm induction by heterodimeric AP-1 (c-Jun and c-Fos) and its involvement in mesoderm formation through the embryonic fibroblast growth factor/Xbra autocatalytic loop during the early development of Xenopus embryos., Kim J., J Biol Chem. January 16, 1998; 273 (3): 1542-50.
	Regulation of SPARC expression during early Xenopus development: evolutionary divergence and conservation of DNA regulatory elements between amphibians and mammals., Damjanovski S., Dev Genes Evol. January 1, 1998; 207 (7): 453-61.
	Involvement of NF-kappaB associated proteins in FGF-mediated mesoderm induction., Beck CW., Int J Dev Biol. January 1, 1998; 42 (1): 67-77.
	Wnt and FGF pathways cooperatively pattern anteroposterior neural ectoderm in Xenopus., McGrew LL., Mech Dev. December 1, 1997; 69 (1-2): 105-14.
	Xenopus Pax-2 displays multiple splice forms during embryogenesis and pronephric kidney development., Heller N., Mech Dev. December 1, 1997; 69 (1-2): 83-104.
	Studies on the role of fibroblast growth factor signaling in neurogenesis using conjugated/aged animal caps and dorsal ectoderm-grafted embryos., Xu RH., J Neurosci. September 15, 1997; 17 (18): 6892-8.
	Frzb, a secreted protein expressed in the Spemann organizer, binds and inhibits Wnt-8., Wang S., Cell. March 21, 1997; 88 (6): 757-66.
	Neural induction and patterning in embryos deficient in FGF signaling., Godsave SF., Int J Dev Biol. February 1, 1997; 41 (1): 57-65.
	A Xenopus type I activin receptor mediates mesodermal but not neural specification during embryogenesis., Chang C., Development. February 1, 1997; 124 (4): 827-37.
	The Xenopus T-box gene, Antipodean, encodes a vegetally localised maternal mRNA and can trigger mesoderm formation., Stennard F., Development. December 1, 1996; 122 (12): 4179-88.
	Regulated expression of the retinoblastoma gene product by fibroblast growth factor but not by activin during mesoderm induction in Xenopus., Greenland J., Dev Genes Evol. December 1, 1996; 206 (5): 333-6.
	The homeobox gene Siamois is a target of the Wnt dorsalisation pathway and triggers organiser activity in the absence of mesoderm., Carnac G., Development. October 1, 1996; 122 (10): 3055-65.

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