Papers associated with tail bud (and not)

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	Induction of the Xenopus organizer: expression and regulation of Xnot, a novel FGF and activin-regulated homeo box gene., von Dassow G., Genes Dev. March 1, 1993; 7 (3): 355-66.
	Tail formation as a continuation of gastrulation: the multiple cell populations of the Xenopus tailbud derive from the late blastopore lip., Gont LK., Development. December 1, 1993; 119 (4): 991-1004.
	On the function of BMP-4 in patterning the marginal zone of the Xenopus embryo., Fainsod A., EMBO J. November 1, 1994; 13 (21): 5015-25.
	Localized BMP-4 mediates dorsal/ventral patterning in the early Xenopus embryo., Schmidt JE., Dev Biol. May 1, 1995; 169 (1): 37-50.
	Tail bud determination in the vertebrate embryo., Tucker AS., Curr Biol. July 1, 1995; 5 (7): 807-13.
	Bone morphogenetic protein-4 (BMP-4) acts during gastrula stages to cause ventralization of Xenopus embryos., Jones CM., Development. May 1, 1996; 122 (5): 1545-54.
	Regulation of dorsal-ventral patterning: the ventralizing effects of the novel Xenopus homeobox gene Vox., Schmidt JE., Development. June 1, 1996; 122 (6): 1711-21.
	Role of notochord in specification of cardiac left-right orientation in zebrafish and Xenopus., Danos MC., Dev Biol. July 10, 1996; 177 (1): 96-103.
	The Xvent-2 homeobox gene is part of the BMP-4 signalling pathway controlling [correction of controling] dorsoventral patterning of Xenopus mesoderm., Onichtchouk D., Development. October 1, 1996; 122 (10): 3045-53.
	Differential activation of the clustered homeobox genes CNOT2 and CNOT1 during notogenesis in the chick., Stein S., Dev Biol. December 15, 1996; 180 (2): 519-33.
	XIPOU 2 is a potential regulator of Spemann's Organizer., Witta SE., Development. March 1, 1997; 124 (6): 1179-89.
	The KH domain protein encoded by quaking functions as a dimer and is essential for notochord development in Xenopus embryos., Zorn AM., Genes Dev. September 1, 1997; 11 (17): 2176-90.
	Analysis of the developing Xenopus tail bud reveals separate phases of gene expression during determination and outgrowth., Beck CW., Mech Dev. March 1, 1998; 72 (1-2): 41-52.
	Gene expression screening in Xenopus identifies molecular pathways, predicts gene function and provides a global view of embryonic patterning., Gawantka V., Mech Dev. October 1, 1998; 77 (2): 95-141.
	The role of paraxial protocadherin in selective adhesion and cell movements of the mesoderm during Xenopus gastrulation., Kim SH., Development. December 1, 1998; 125 (23): 4681-90.
	FGF is required for posterior neural patterning but not for neural induction., Holowacz T., Dev Biol. January 15, 1999; 205 (2): 296-308.
	Regulation of BMP signaling by the BMP1/TLD-related metalloprotease, SpAN., Wardle FC., Dev Biol. February 1, 1999; 206 (1): 63-72.
	Misexpression of the catenin p120(ctn)1A perturbs Xenopus gastrulation but does not elicit Wnt-directed axis specification., Paulson AF., Dev Biol. March 15, 1999; 207 (2): 350-63.
	derrière: a TGF-beta family member required for posterior development in Xenopus., Sun BI., Development. April 1, 1999; 126 (7): 1467-82.
	XCtBP is a XTcf-3 co-repressor with roles throughout Xenopus development., Brannon M., Development. June 1, 1999; 126 (14): 3159-70.
	The early expression control of Xepsin by nonaxial and planar posteriorizing signals in Xenopus epidermis., Yamada K., Dev Biol. October 15, 1999; 214 (2): 318-30.
	The fate of cells in the tailbud of Xenopus laevis., Davis RL., Development. January 1, 2000; 127 (2): 255-67.
	HNF1(beta) is required for mesoderm induction in the Xenopus embryo., Vignali R., Development. April 1, 2000; 127 (7): 1455-65.
	Xenopus kielin: A dorsalizing factor containing multiple chordin-type repeats secreted from the embryonic midline., Matsui M., Proc Natl Acad Sci U S A. May 9, 2000; 97 (10): 5291-6.
	A direct screen for secreted proteins in Xenopus embryos identifies distinct activities for the Wnt antagonists Crescent and Frzb-1., Pera EM., Mech Dev. September 1, 2000; 96 (2): 183-95.
	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.
	Tumorhead, a Xenopus gene product that inhibits neural differentiation through regulation of proliferation., Wu CF., Development. September 1, 2001; 128 (17): 3381-93.
	Siamois functions in the early blastula to induce Spemann's organiser., Kodjabachian L., Mech Dev. October 1, 2001; 108 (1-2): 71-9.
	Xenopus Cdc42 regulates convergent extension movements during gastrulation through Wnt/Ca2+ signaling pathway., Choi SC., Dev Biol. April 15, 2002; 244 (2): 342-57.
	Xolloid-related: a novel BMP1/Tolloid-related metalloprotease is expressed during early Xenopus development., Dale L., Mech Dev. December 1, 2002; 119 (2): 177-90.
	Activation of Gbetagamma signaling downstream of Wnt-11/Xfz7 regulates Cdc42 activity during Xenopus gastrulation., Penzo-Mendèz A., Dev Biol. May 15, 2003; 257 (2): 302-14.
	Selective degradation of excess Ldb1 by Rnf12/RLIM confers proper Ldb1 expression levels and Xlim-1/Ldb1 stoichiometry in Xenopus organizer functions., Hiratani I., Development. September 1, 2003; 130 (17): 4161-75.
	Screening of FGF target genes in Xenopus by microarray: temporal dissection of the signalling pathway using a chemical inhibitor., Chung HA., Genes Cells. August 1, 2004; 9 (8): 749-61.
	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.
	Regional requirements for Dishevelled signaling during Xenopus gastrulation: separable effects on blastopore closure, mesendoderm internalization and archenteron formation., Ewald AJ., Development. December 1, 2004; 131 (24): 6195-209.
	Sequences downstream of the bHLH domain of the Xenopus hairy-related transcription factor-1 act as an extended dimerization domain that contributes to the selection of the partners., Taelman V., Dev Biol. December 1, 2004; 276 (1): 47-63.
	XBtg2 is required for notochord differentiation during early Xenopus development., Sugimoto K., Dev Growth Differ. September 1, 2005; 47 (7): 435-43.
	Msx1 and Msx2 have shared essential functions in neural crest but may be dispensable in epidermis and axis formation in Xenopus., Khadka D., Int J Dev Biol. January 1, 2006; 50 (5): 499-502.
	A novel Cripto-related protein reveals an essential role for EGF-CFCs in Nodal signalling in Xenopus embryos., Dorey K., Dev Biol. April 15, 2006; 292 (2): 303-16.
	Novel gene ashwin functions in Xenopus cell survival and anteroposterior patterning., Patil SS., Dev Dyn. July 1, 2006; 235 (7): 1895-907.
	TGF-beta signaling-mediated morphogenesis: modulation of cell adhesion via cadherin endocytosis., Ogata S., Genes Dev. July 15, 2007; 21 (14): 1817-31.
	Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1., Louie SH., PLoS One. January 1, 2009; 4 (2): e4310.
	Bestrophin genes are expressed in Xenopus development., Onuma Y., Biochem Biophys Res Commun. July 3, 2009; 384 (3): 290-5.
	Identification and gastrointestinal expression of Xenopus laevis FoxF2., McLin VA., Int J Dev Biol. January 1, 2010; 54 (5): 919-24.
	Distinct Xenopus Nodal ligands sequentially induce mesendoderm and control gastrulation movements in parallel to the Wnt/PCP pathway., Luxardi G., Development. February 1, 2010; 137 (3): 417-26.
	SNW1 is a critical regulator of spatial BMP activity, neural plate border formation, and neural crest specification in vertebrate embryos., Wu MY., PLoS Biol. February 15, 2011; 9 (2): e1000593.
	A revised model of Xenopus dorsal midline development: differential and separable requirements for Notch and Shh signaling., Peyrot SM., Dev Biol. April 15, 2011; 352 (2): 254-66.
	Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/β-catenin signaling pathway., Fujimi TJ., Dev Biol. January 15, 2012; 361 (2): 220-31.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	Active repression by RARγ signaling is required for vertebrate axial elongation., Janesick A., Development. June 1, 2014; 141 (11): 2260-70.

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