Papers associated with tadpole (and not)

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	Tissue-specific expression of carbohydrate sulfotransferases drives keratan sulfate biosynthesis in the notochord and otic vesicles of Xenopus embryos., Yasuoka Y., Front Cell Dev Biol. January 1, 2023; 11 957805.
	ARVCF catenin controls force production during vertebrate convergent extension., Huebner RJ., Dev Cell. May 9, 2022; 57 (9): 1119-1131.e5.
	The tumor suppressor PTPRK promotes ZNRF3 internalization and is required for Wnt inhibition in the Spemann organizer., Chang LS., Elife. January 14, 2020; 9
	Modeling Bainbridge-Ropers Syndrome in Xenopus laevis Embryos., Lichtig H., Front Physiol. January 1, 2020; 11 75.
	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.
	Head formation requires Dishevelled degradation that is mediated by March2 in concert with Dapper1., Lee H, Lee H., Development. April 10, 2018; 145 (7):
	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.
	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.
	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.
	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.
	Anterior neural development requires Del1, a matrix-associated protein that attenuates canonical Wnt signaling via the Ror2 pathway., Takai A., Development. October 1, 2010; 137 (19): 3293-302.
	Identification and gastrointestinal expression of Xenopus laevis FoxF2., McLin VA., Int J Dev Biol. January 1, 2010; 54 (5): 919-24.
	The shroom family proteins play broad roles in the morphogenesis of thickened epithelial sheets., Lee C, Lee C, Lee C., Dev Dyn. June 1, 2009; 238 (6): 1480-91.
	Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1., Louie SH., PLoS One. January 1, 2009; 4 (2): e4310.
	Dkk3 is required for TGF-beta signaling during Xenopus mesoderm induction., Pinho S., Differentiation. December 1, 2007; 75 (10): 957-67.
	Inca: a novel p21-activated kinase-associated protein required for cranial neural crest development., Luo T., Development. April 1, 2007; 134 (7): 1279-89.
	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.
	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.
	Activin redux: specification of mesodermal pattern in Xenopus by graded concentrations of endogenous activin B., Piepenburg O., Development. October 1, 2004; 131 (20): 4977-86.
	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.
	Tumorhead, a Xenopus gene product that inhibits neural differentiation through regulation of proliferation., Wu CF., Development. September 1, 2001; 128 (17): 3381-93.
	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.
	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.
	XCtBP is a XTcf-3 co-repressor with roles throughout Xenopus development., Brannon M., Development. June 1, 1999; 126 (14): 3159-70.
	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.
	Mutant Vg1 ligands disrupt endoderm and mesoderm formation in Xenopus embryos., Joseph EM., Development. July 1, 1998; 125 (14): 2677-85.
	Vax1 is a novel homeobox-containing gene expressed in the developing anterior ventral forebrain., Hallonet M., Development. July 1, 1998; 125 (14): 2599-610.
	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.
	XIPOU 2 is a potential regulator of Spemann's Organizer., Witta SE., Development. March 1, 1997; 124 (6): 1179-89.
	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.
	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.
	Developmental expression of a neuron-specific beta-tubulin in frog (Xenopus laevis): a marker for growing axons during the embryonic period., Moody SA., J Comp Neurol. January 8, 1996; 364 (2): 219-30.
	Localized BMP-4 mediates dorsal/ventral patterning in the early Xenopus embryo., Schmidt JE., Dev Biol. May 1, 1995; 169 (1): 37-50.
	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.

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