Papers associated with sensory system (and fgf8)

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	FGF-8 is associated with anteroposterior patterning and limb regeneration in Xenopus., Christen B., Dev Biol. December 15, 1997; 192 (2): 455-66.
	A developmental pathway controlling outgrowth of the Xenopus tail bud., Beck CW., Development. April 1, 1999; 126 (8): 1611-20.
	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.
	Foregut endoderm is required at head process stages for anteriormost neural patterning in chick., Withington S., Development. February 1, 2001; 128 (3): 309-20.
	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.
	Otx2 can activate the isthmic organizer genetic network in the Xenopus embryo., Tour E., Mech Dev. January 1, 2002; 110 (1-2): 3-13.
	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.
	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.
	Glypican 4 modulates FGF signalling and regulates dorsoventral forebrain patterning in Xenopus embryos., Galli A., Development. October 1, 2003; 130 (20): 4919-29.
	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.
	Pbx genes are required in Xenopus lens development., Morgan R., Int J Dev Biol. September 1, 2004; 48 (7): 623-7.
	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.
	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.
	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.
	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.
	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.
	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.
	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.
	The zic1 gene is an activator of Wnt signaling., Merzdorf CS., Int J Dev Biol. January 1, 2006; 50 (7): 611-7.
	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.
	Tes regulates neural crest migration and axial elongation in Xenopus., Dingwell KS., Dev Biol. May 1, 2006; 293 (1): 252-67.
	Xenopus ADAMTS1 negatively modulates FGF signaling independent of its metalloprotease activity., Suga A., Dev Biol. July 1, 2006; 295 (1): 26-39.
	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.
	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.
	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.
	Expression of marker genes during early ear development in medaka., Hochmann S., Gene Expr Patterns. January 1, 2007; 7 (3): 355-62.
	The secreted serine protease xHtrA1 stimulates long-range FGF signaling in the early Xenopus embryo., Hou S., Dev Cell. August 1, 2007; 13 (2): 226-41.
	A ubiquitin-conjugating enzyme, ube2d3.2, regulates xMLK2 and pronephros formation in Xenopus., Jean S., Differentiation. April 1, 2008; 76 (4): 431-41.
	Lrig3 regulates neural crest formation in Xenopus by modulating Fgf and Wnt signaling pathways., Zhao H., Development. April 1, 2008; 135 (7): 1283-93.
	Mix.1/2-dependent control of FGF availability during gastrulation is essential for pronephros development in Xenopus., Colas A., Dev Biol. August 15, 2008; 320 (2): 351-65.
	Hindbrain-derived Wnt and Fgf signals cooperate to specify the otic placode in Xenopus., Park BY., Dev Biol. December 1, 2008; 324 (1): 108-21.
	FGF signalling during embryo development regulates cilia length in diverse epithelia., Neugebauer JM., Nature. April 2, 2009; 458 (7238): 651-4.
	Zebrafish gbx1 refines the midbrain-hindbrain boundary border and mediates the Wnt8 posteriorization signal., Rhinn M., Neural Dev. April 2, 2009; 4 12.
	Temporal and spatial expression of FGF ligands and receptors during Xenopus development., Lea R., Dev Dyn. June 1, 2009; 238 (6): 1467-79.
	The RNA-binding protein Mex3b has a fine-tuning system for mRNA regulation in early Xenopus development., Takada H., Development. July 1, 2009; 136 (14): 2413-22.
	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.
	Dynamic expression of axon guidance cues required for optic tract development is controlled by fibroblast growth factor signaling., Atkinson-Leadbeater K., J Neurosci. January 13, 2010; 30 (2): 685-93.
	Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2., Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.
	Microarray identification of novel downstream targets of FoxD4L1/D5, a critical component of the neural ectodermal transcriptional network., Yan B., Dev Dyn. December 1, 2010; 239 (12): 3467-80.
	Gadd45a and Gadd45g regulate neural development and exit from pluripotency in Xenopus., Kaufmann LT., Mech Dev. January 1, 2011; 128 (7-10): 401-11.
	Transdifferentiation from cornea to lens in Xenopus laevis depends on BMP signalling and involves upregulation of Wnt signalling., Day RC., BMC Dev Biol. January 26, 2011; 11 54.
	FGF signaling is required for lens regeneration in Xenopus laevis., Fukui L., Biol Bull. August 1, 2011; 221 (1): 137-45.
	Eukaryotic initiation factor 6 (eif6) overexpression affects eye development in Xenopus laevis., De Marco N., Differentiation. September 1, 2011; 82 (2): 108-15.
	HESX1- and TCF3-mediated repression of Wnt/β-catenin targets is required for normal development of the anterior forebrain., Andoniadou CL., Development. November 1, 2011; 138 (22): 4931-42.
	The forkhead transcription factor FoxB1 regulates the dorsal-ventral and anterior-posterior patterning of the ectoderm during early Xenopus embryogenesis., Takebayashi-Suzuki K., Dev Biol. December 1, 2011; 360 (1): 11-29.
	Regulation of XFGF8 gene expression through SRY (sex-determining region Y)-box 2 in developing Xenopus embryos., Kim YH., Reprod Fertil Dev. January 1, 2012; 24 (6): 769-77.
	Xaml1/Runx1 is required for the specification of Rohon-Beard sensory neurons in Xenopus., Park BY., Dev Biol. February 1, 2012; 362 (1): 65-75.
	RIPPLY3 is a retinoic acid-inducible repressor required for setting the borders of the pre-placodal ectoderm., Janesick A., Development. March 1, 2012; 139 (6): 1213-24.
	Transcription factors involved in lens development from the preplacodal ectoderm., Ogino H., Dev Biol. March 15, 2012; 363 (2): 333-47.
	Characterization and expressional analysis of Dleu7 during Xenopus tropicalis embryogenesis., Zhu X., Gene. November 1, 2012; 509 (1): 77-84.

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