Papers associated with tail (and not)

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	ARVCF catenin controls force production during vertebrate convergent extension., Huebner RJ., Dev Cell. May 9, 2022; 57 (9): 1119-1131.e5.
	Rab7 is required for mesoderm patterning and gastrulation in Xenopus., Kreis J., Biol Open. July 15, 2021; 10 (7):
	Furry is required for cell movements during gastrulation and functionally interacts with NDR1., Cervino AS., Sci Rep. March 23, 2021; 11 (1): 6607.
	Xenopus gpx3 Mediates Posterior Development by Regulating Cell Death during Embryogenesis., Lee H, Lee H., Antioxidants (Basel). December 12, 2020; 9 (12):
	Comprehensive RNA-Seq analysis of notochord-enriched genes induced during Xenopus tropicalis tail resorption., Nakajima K., Gen Comp Endocrinol. February 1, 2020; 287 113349.
	A unique role of thyroid hormone receptor β in regulating notochord resorption during Xenopus metamorphosis., Nakajima K., Gen Comp Endocrinol. June 1, 2019; 277 66-72.
	Shared evolutionary origin of vertebrate neural crest and cranial placodes., Horie R., Nature. August 1, 2018; 560 (7717): 228-232.
	Angiopoietin-like 4 Is a Wnt Signaling Antagonist that Promotes LRP6 Turnover., Kirsch N., Dev Cell. October 9, 2017; 43 (1): 71-82.e6.
	interleukin-11 induces and maintains progenitors of different cell lineages during Xenopus tadpole tail regeneration., Tsujioka H., Nat Commun. September 8, 2017; 8 (1): 495.
	FoxD1 protein interacts with Wnt and BMP signaling to differentially pattern mesoderm and neural tissue., Polevoy H., Int J Dev Biol. January 1, 2017; 61 (3-4-5): 293-302.
	Specification of anteroposterior axis by combinatorial signaling during Xenopus development., Carron C., Wiley Interdiscip Rev Dev Biol. January 1, 2016; 5 (2): 150-68.
	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.
	Active repression by RARγ signaling is required for vertebrate axial elongation., Janesick A., Development. June 1, 2014; 141 (11): 2260-70.
	High-resolution analysis of gene activity during the Xenopus mid-blastula transition., Collart C., Development. May 1, 2014; 141 (9): 1927-39.
	Zygotic expression of Exostosin1 (Ext1) is required for BMP signaling and establishment of dorsal-ventral pattern in Xenopus., Shieh YE., Int J Dev Biol. January 1, 2014; 58 (1): 27-34.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis., Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.
	Gastrulation and pre-gastrulation morphogenesis, inductions, and gene expression: similarities and dissimilarities between urodelean and anuran embryos., Kaneda T., Dev Biol. September 1, 2012; 369 (1): 1-18.
	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.
	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.
	Long-distance signals are required for morphogenesis of the regenerating Xenopus tadpole tail, as shown by femtosecond-laser ablation., Mondia JP., PLoS One. January 1, 2011; 6 (9): e24953.
	Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1., Louie SH., PLoS One. January 1, 2009; 4 (2): e4310.
	VegT, eFGF and Xbra cause overall posteriorization while Xwnt8 causes eye-level restricted posteriorization in synergy with chordin in early Xenopus development., Fujii H., Dev Growth Differ. March 1, 2008; 50 (3): 169-80.
	Evolution of axis specification mechanisms in jawed vertebrates: insights from a chondrichthyan., Coolen M., PLoS One. April 18, 2007; 2 (4): e374.
	Novel gene ashwin functions in Xenopus cell survival and anteroposterior patterning., Patil SS., Dev Dyn. July 1, 2006; 235 (7): 1895-907.
	XBtg2 is required for notochord differentiation during early Xenopus development., Sugimoto K., Dev Growth Differ. September 1, 2005; 47 (7): 435-43.
	JNK and ROKalpha function in the noncanonical Wnt/RhoA signaling pathway to regulate Xenopus convergent extension movements., Kim GH., Dev Dyn. April 1, 2005; 232 (4): 958-68.
	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.
	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.
	Xantivin suppresses the activity of EGF-CFC genes to regulate nodal signaling., Tanegashima K., Int J Dev Biol. June 1, 2004; 48 (4): 275-83.
	Chordin is required for the Spemann organizer transplantation phenomenon in Xenopus embryos., Oelgeschläger M., Dev Cell. February 1, 2003; 4 (2): 219-30.
	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.
	Calcium signaling during convergent extension in Xenopus., Wallingford JB., Curr Biol. May 1, 2001; 11 (9): 652-61.
	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.
	Xbra3 induces mesoderm and neural tissue in Xenopus laevis., Strong CF., Dev Biol. June 15, 2000; 222 (2): 405-19.
	The fate of cells in the tailbud of Xenopus laevis., Davis RL., Development. January 1, 2000; 127 (2): 255-67.
	Regulation of dorsal gene expression in Xenopus by the ventralizing homeodomain gene Vox., Melby AE., Dev Biol. July 15, 1999; 211 (2): 293-305.
	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.
	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.
	The Spemann organizer of Xenopus is patterned along its anteroposterior axis at the earliest gastrula stage., Zoltewicz JS., Dev Biol. December 15, 1997; 192 (2): 482-91.
	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.
	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.
	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.
	Drosophila short gastrulation induces an ectopic axis in Xenopus: evidence for conserved mechanisms of dorsal-ventral patterning., Schmidt J., Development. December 1, 1995; 121 (12): 4319-28.
	Tail bud determination in the vertebrate embryo., Tucker AS., Curr Biol. July 1, 1995; 5 (7): 807-13.
	Localized BMP-4 mediates dorsal/ventral patterning in the early Xenopus embryo., Schmidt JE., Dev Biol. May 1, 1995; 169 (1): 37-50.
	Xenopus chordin: a novel dorsalizing factor activated by organizer-specific homeobox genes., Sasai Y., Cell. December 2, 1994; 79 (5): 779-90.
	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.
	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.
	The evolution of vertebrate gastrulation., De Robertis EM., Dev Suppl. January 1, 1992; 117-24.

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