Papers associated with embryonic structure (and gsk3b)

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	Lysosomes are required for early dorsal signaling in the Xenopus embryo., Tejeda-Muñoz N., Proc Natl Acad Sci U S A. April 26, 2022; 119 (17): e2201008119.
	Establishing embryonic territories in the context of Wnt signaling., Velloso I., Int J Dev Biol. January 1, 2021; 65 (4-5-6): 227-233.
	TMEM79/MATTRIN defines a pathway for Frizzled regulation and is required for Xenopus embryogenesis., Chen M., Elife. September 14, 2020; 9
	PAWS1 controls Wnt signalling through association with casein kinase 1α., Bozatzi P., EMBO Rep. April 1, 2018; 19 (4):
	RAPGEF5 Regulates Nuclear Translocation of β-Catenin., Griffin JN., Dev Cell. January 22, 2018; 44 (2): 248-260.e4.
	The RNF146 E3 ubiquitin ligase is required for the control of Wnt signaling and body pattern formation in Xenopus., Zhu X., Mech Dev. October 1, 2017; 147 28-36.
	Lineage commitment of embryonic cells involves MEK1-dependent clearance of pluripotency regulator Ventx2., Scerbo P., Elife. June 27, 2017; 6
	Capsaicin inhibits the Wnt/β-catenin signaling pathway by down-regulating PP2A., Park DS., Biochem Biophys Res Commun. September 9, 2016; 478 (1): 455-461.
	Gtpbp2 is a positive regulator of Wnt signaling and maintains low levels of the Wnt negative regulator Axin., Gillis WQ., Cell Commun Signal. August 2, 2016; 14 (1): 15.
	Involvement of JunB Proto-Oncogene in Tail Formation During Early Xenopus Embryogenesis., Yoshida H., Zoolog Sci. June 1, 2016; 33 (3): 282-9.
	Spatial and temporal aspects of Wnt signaling and planar cell polarity during vertebrate embryonic development., Sokol SY., Semin Cell Dev Biol. June 1, 2015; 42 78-85.
	Early development of the neural plate: new roles for apoptosis and for one of its main effectors caspase-3., Juraver-Geslin HA., Genesis. February 1, 2015; 53 (2): 203-24.
	Phosphorylation-dependent ubiquitination of paraxial protocadherin (PAPC) controls gastrulation cell movements., Kai M., PLoS One. January 12, 2015; 10 (1): e0115111.
	The tumor suppressor Smad4/DPC4 is regulated by phosphorylations that integrate FGF, Wnt, and TGF-β signaling., Demagny H., Cell Rep. October 23, 2014; 9 (2): 688-700.
	Cholesterol selectively activates canonical Wnt signalling over non-canonical Wnt signalling., Sheng R., Nat Commun. July 15, 2014; 5 4393.
	Role of Sp5 as an essential early regulator of neural crest specification in xenopus., Park DS., Dev Dyn. December 1, 2013; 242 (12): 1382-94.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	Different thresholds of Wnt-Frizzled 7 signaling coordinate proliferation, morphogenesis and fate of endoderm progenitor cells., Zhang Z., Dev Biol. June 1, 2013; 378 (1): 1-12.
	Conservation and evolutionary divergence in the activity of receptor-regulated smads., Sorrentino GM., Evodevo. October 1, 2012; 3 (1): 22.
	Inhibition of heart formation by lithium is an indirect result of the disruption of tissue organization within the embryo., Martin LK., Dev Growth Differ. February 1, 2012; 54 (2): 153-66.
	Cortical rotation and messenger RNA localization in Xenopus axis formation., Houston DW., Wiley Interdiscip Rev Dev Biol. January 1, 2012; 1 (3): 371-88.
	Canonical WNT signaling enhances stem cell expression in the developing heart without a corresponding inhibition of cardiogenic differentiation., Martin LK., Stem Cells Dev. November 1, 2011; 20 (11): 1973-83.
	A novel mechanism for the transcriptional regulation of Wnt signaling in development., Vacik T., Genes Dev. September 1, 2011; 25 (17): 1783-95.
	Notch destabilises maternal beta-catenin and restricts dorsal-anterior development in Xenopus., Acosta H., Development. June 1, 2011; 138 (12): 2567-79.
	Different requirement for Wnt/β-catenin signaling in limb regeneration of larval and adult Xenopus., Yokoyama H., PLoS One. January 1, 2011; 6 (7): e21721.
	Systematic discovery of nonobvious human disease models through orthologous phenotypes., McGary KL., Proc Natl Acad Sci U S A. April 6, 2010; 107 (14): 6544-9.
	Differential requirements of BMP and Wnt signalling during gastrulation and neurulation define two steps in neural crest induction., Steventon B., Development. March 1, 2009; 136 (5): 771-9.
	Integrating patterning signals: Wnt/GSK3 regulates the duration of the BMP/Smad1 signal., Fuentealba LC., Cell. November 30, 2007; 131 (5): 980-93.
	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.
	The zic1 gene is an activator of Wnt signaling., Merzdorf CS., Int J Dev Biol. January 1, 2006; 50 (7): 611-7.
	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.
	Heart induction by Wnt antagonists depends on the homeodomain transcription factor Hex., Foley AC., Genes Dev. February 1, 2005; 19 (3): 387-96.
	PR72, a novel regulator of Wnt signaling required for Naked cuticle function., Creyghton MP., Genes Dev. February 1, 2005; 19 (3): 376-86.
	Move it or lose it: axis specification in Xenopus., Weaver C., Development. August 1, 2004; 131 (15): 3491-9.
	GBP binds kinesin light chain and translocates during cortical rotation in Xenopus eggs., Weaver C., Development. November 1, 2003; 130 (22): 5425-36.
	Sox10 regulates the development of neural crest-derived melanocytes in Xenopus., Aoki Y., Dev Biol. July 1, 2003; 259 (1): 19-33.
	Neural crest induction by paraxial mesoderm in Xenopus embryos requires FGF signals., Monsoro-Burq AH., Development. July 1, 2003; 130 (14): 3111-24.
	Glycogen synthase kinase-3 beta mutagenesis identifies a common binding domain for GBP and Axin., Ferkey DM., J Biol Chem. May 3, 2002; 277 (18): 16147-52.
	Wnt antagonism initiates cardiogenesis in Xenopus laevis., Schneider VA., Genes Dev. February 1, 2001; 15 (3): 304-15.
	Cloning, expression and nuclear localization of human NPM3, a member of the nucleophosmin/nucleoplasmin family of nuclear chaperones., Shackleford GM., BMC Genomics. January 1, 2001; 2 8.
	Control of beta-catenin signaling in tumor development., Behrens J., Ann N Y Acad Sci. June 1, 2000; 910 21-33; discussion 33-5.
	The putative wnt receptor Xenopus frizzled-7 functions upstream of beta-catenin in vertebrate dorsoventral mesoderm patterning., Sumanas S., Development. May 1, 2000; 127 (9): 1981-90.
	Primary neuronal differentiation in Xenopus embryos is linked to the beta(3) subunit of the sodium pump., Messenger NJ., Dev Biol. April 15, 2000; 220 (2): 168-82.
	Wnt signaling in Xenopus embryos inhibits bmp4 expression and activates neural development., Baker JC., Genes Dev. December 1, 1999; 13 (23): 3149-59.
	Keeping a close eye on Wnt-1/wg signaling in Xenopus., Gradl D., Mech Dev. August 1, 1999; 86 (1-2): 3-15.
	Establishment of the dorsal-ventral axis in Xenopus embryos coincides with the dorsal enrichment of dishevelled that is dependent on cortical rotation., Miller JR., J Cell Biol. July 26, 1999; 146 (2): 427-37.
	Dishevelled: at the crossroads of divergent intracellular signaling pathways., Boutros M., Mech Dev. May 1, 1999; 83 (1-2): 27-37.
	Negative regulation of axis formation and Wnt signaling in Xenopus embryos by the F-box/WD40 protein beta TrCP., Lagna G., Mech Dev. January 1, 1999; 80 (1): 101-6.
	Nuclear glycogen and glycogen synthase kinase 3., Ragano-Caracciolo M., Biochem Biophys Res Commun. August 19, 1998; 249 (2): 422-7.
	GSK3beta/shaggy mediates patterning along the animal-vegetal axis of the sea urchin embryo., Emily-Fenouil F., Development. July 1, 1998; 125 (13): 2489-98.

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