Papers associated with central nervous system (and fgf8)

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	Expression of marker genes during early ear development in medaka., Hochmann S., Gene Expr Patterns. January 1, 2007; 7 (3): 355-62.
	Global analysis of gene expression in Xenopus hindlimbs during stage-dependent complete and incomplete regeneration., Grow M., Dev Dyn. October 1, 2006; 235 (10): 2667-85.
	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.
	Temporal requirement for bone morphogenetic proteins in regeneration of the tail and limb of Xenopus tadpoles., Beck CW., Mech Dev. September 1, 2006; 123 (9): 674-88.
	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.
	Xenopus Xotx2 and Drosophila otd share similar activities in anterior patterning of the frog embryo., Lunardi A., Dev Genes Evol. September 1, 2006; 216 (9): 511-21.
	Xenopus ADAMTS1 negatively modulates FGF signaling independent of its metalloprotease activity., Suga A., Dev Biol. July 1, 2006; 295 (1): 26-39.
	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.
	FGF8, Wnt8 and Myf5 are target genes of Tbx6 during anteroposterior specification in Xenopus embryo., Li HY., Dev Biol. February 15, 2006; 290 (2): 470-81.
	Ras-dva, a member of novel family of small GTPases, is required for the anterior ectoderm patterning in the Xenopus laevis embryo., Tereshina MB., Development. February 1, 2006; 133 (3): 485-94.
	The zic1 gene is an activator of Wnt signaling., Merzdorf CS., Int J Dev Biol. January 1, 2006; 50 (7): 611-7.
	Tissues and signals involved in the induction of placodal Six1 expression in Xenopus laevis., Ahrens K., Dev Biol. December 1, 2005; 288 (1): 40-59.
	Nerve-dependent and -independent events in blastema formation during Xenopus froglet limb regeneration., Suzuki M., Dev Biol. October 1, 2005; 286 (1): 361-75.
	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.
	Dorsoventral patterning of the Xenopus eye: a collaboration of Retinoid, Hedgehog and FGF receptor signaling., Lupo G., Development. April 1, 2005; 132 (7): 1737-48.
	Regulated expression pattern of gremlin during zebrafish development., Nicoli S., Gene Expr Patterns. April 1, 2005; 5 (4): 539-44.
	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.
	XPACE4 is a localized pro-protein convertase required for mesoderm induction and the cleavage of specific TGFbeta proteins in Xenopus development., Birsoy B., Development. February 1, 2005; 132 (3): 591-602.
	Insulin-like growth factor (IGF) signalling is required for early dorso-anterior development of the zebrafish embryo., Eivers E., Int J Dev Biol. December 1, 2004; 48 (10): 1131-40.
	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.
	New roles for FoxH1 in patterning the early embryo., Kofron M., Development. October 1, 2004; 131 (20): 5065-78.
	Pbx genes are required in Xenopus lens development., Morgan R., Int J Dev Biol. September 1, 2004; 48 (7): 623-7.
	Expression patterns of Xenopus FGF receptor-like 1/nou-darake in early Xenopus development resemble those of planarian nou-darake and Xenopus FGF8., Hayashi S., Dev Dyn. August 1, 2004; 230 (4): 700-7.
	Regulation of Otx2 expression and its functions in mouse epiblast and anterior neuroectoderm., Kurokawa D., Development. July 1, 2004; 131 (14): 3307-17.
	Multiple points of interaction between retinoic acid and FGF signaling during embryonic axis formation., Shiotsugu J., Development. June 1, 2004; 131 (11): 2653-67.
	Evolutionarily conserved expression pattern and trans-regulating activity of Xenopus p51/p63., Tomimori Y., Biochem Biophys Res Commun. January 9, 2004; 313 (2): 230-6.
	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.
	Cell fate specification and competence by Coco, a maternal BMP, TGFbeta and Wnt inhibitor., Bell E., Development. April 1, 2003; 130 (7): 1381-9.
	Induction and patterning of the telencephalon in Xenopus laevis., Lupo G., Development. December 1, 2002; 129 (23): 5421-36.
	Mouse GLI3 regulates Fgf8 expression and apoptosis in the developing neural tube, face, and limb bud., Aoto K., Dev Biol. November 15, 2002; 251 (2): 320-32.
	Isthmin is a novel secreted protein expressed as part of the Fgf-8 synexpression group in the Xenopus midbrain-hindbrain organizer., Pera EM., Mech Dev. August 1, 2002; 116 (1-2): 169-72.
	The role of the anterior neural ridge and Fgf-8 in early forebrain patterning and regionalization in Xenopus laevis., Eagleson GW., Comp Biochem Physiol B Biochem Mol Biol. May 1, 2002; 132 (1): 179-89.
	The homeoprotein Xiro1 is required for midbrain-hindbrain boundary formation., Glavic A., Development. April 1, 2002; 129 (7): 1609-21.
	Otx2 can activate the isthmic organizer genetic network in the Xenopus embryo., Tour E., Mech Dev. January 1, 2002; 110 (1-2): 3-13.
	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.
	Foregut endoderm is required at head process stages for anteriormost neural patterning in chick., Withington S., Development. February 1, 2001; 128 (3): 309-20.
	An epidermal signal regulates Lmx-1 expression and dorsal-ventral pattern during Xenopus limb regeneration., Matsuda H., Dev Biol. January 15, 2001; 229 (2): 351-62.
	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.
	Expression patterns of Fgf-8 during development and limb regeneration of the axolotl., Han MJ., Dev Dyn. January 1, 2001; 220 (1): 40-8.
	Mechanisms of left-right determination in vertebrates., Capdevila J., Cell. March 31, 2000; 101 (1): 9-21.
	Induction and differentiation of the zebrafish heart requires fibroblast growth factor 8 (fgf8/acerebellar)., Reifers F., Development. January 1, 2000; 127 (2): 225-35.
	The midbrain-hindbrain boundary genetic cascade is activated ectopically in the diencephalon in response to the widespread expression of one of its components, the medaka gene Ol-eng2., Ristoratore F., Development. September 1, 1999; 126 (17): 3769-79.

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