Papers associated with tail bud (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.
	Role of fibroblast growth factor during early midbrain development in Xenopus., Riou JF., Mech Dev. November 1, 1998; 78 (1-2): 3-15.
	A developmental pathway controlling outgrowth of the Xenopus tail bud., Beck CW., Development. April 1, 1999; 126 (8): 1611-20.
	Expression patterns of Fgf-8 during development and limb regeneration of the axolotl., Han MJ., Dev Dyn. January 1, 2001; 220 (1): 40-8.
	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.
	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.
	Asymmetries in H+/K+-ATPase and cell membrane potentials comprise a very early step in left-right patterning., Levin M., Cell. October 4, 2002; 111 (1): 77-89.
	Glypican 4 modulates FGF signalling and regulates dorsoventral forebrain patterning in Xenopus embryos., Galli A., Development. October 1, 2003; 130 (20): 4919-29.
	The transmembrane protein XFLRT3 forms a complex with FGF receptors and promotes FGF signalling., Böttcher RT., Nat Cell Biol. January 1, 2004; 6 (1): 38-44.
	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.
	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.
	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.
	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.
	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.
	Sirenomelia in Bmp7 and Tsg compound mutant mice: requirement for Bmp signaling in the development of ventral posterior mesoderm., Zakin L., Development. May 1, 2005; 132 (10): 2489-99.
	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.
	Vg 1 is an essential signaling molecule in Xenopus development., Birsoy B., Development. January 1, 2006; 133 (1): 15-20.
	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.
	Limb regeneration in Xenopus laevis froglet., Suzuki M, Suzuki M., ScientificWorldJournal. May 12, 2006; 6 Suppl 1 26-37.
	Xenopus ADAMTS1 negatively modulates FGF signaling independent of its metalloprotease activity., Suga A., Dev Biol. July 1, 2006; 295 (1): 26-39.
	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.
	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.
	FoxI1e activates ectoderm formation and controls cell position in the Xenopus blastula., Mir A., Development. February 1, 2007; 134 (4): 779-88.
	The activity of Pax3 and Zic1 regulates three distinct cell fates at the neural plate border., Hong CS., Mol Biol Cell. June 1, 2007; 18 (6): 2192-202.
	The homeodomain factor Xanf represses expression of genes in the presumptive rostral forebrain that specify more caudal brain regions., Ermakova GV., Dev Biol. July 15, 2007; 307 (2): 483-97.
	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.
	The role of FoxC1 in early Xenopus development., Cha JY., Dev Dyn. October 1, 2007; 236 (10): 2731-41.
	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.
	Hairy2-Id3 interactions play an essential role in Xenopus neural crest progenitor specification., Nichane M., Dev Biol. October 15, 2008; 322 (2): 355-67.
	Fgf8a induces neural crest indirectly through the activation of Wnt8 in the paraxial mesoderm., Hong CS., Development. December 1, 2008; 135 (23): 3903-10.
	The roles of the FGF signal in zebrafish embryos analyzed using constitutive activation and dominant-negative suppression of different FGF receptors., Ota S., Mech Dev. January 1, 2009; 126 (1-2): 1-17.
	The Xenopus Bowline/Ripply family proteins negatively regulate the transcriptional activity of T-box transcription factors., Hitachi K., Int J Dev Biol. January 1, 2009; 53 (4): 631-9.
	Characterisation of the fibroblast growth factor dependent transcriptome in early development., Branney PA., PLoS One. January 1, 2009; 4 (3): e4951.
	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.
	A divergent Tbx6-related gene and Tbx6 are both required for neural crest and intermediate mesoderm development in Xenopus., Callery EM., Dev Biol. April 1, 2010; 340 (1): 75-87.
	The Pax3 and Pax7 paralogs cooperate in neural and neural crest patterning using distinct molecular mechanisms, in Xenopus laevis embryos., Maczkowiak F., Dev Biol. April 15, 2010; 340 (2): 381-96.
	Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2., Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.
	Characterisation of a new regulator of BDNF signalling, Sprouty3, involved in axonal morphogenesis in vivo., Panagiotaki N., Development. December 1, 2010; 137 (23): 4005-15.
	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.

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