Papers associated with tail region (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
	GSK3 Inhibits Macropinocytosis and Lysosomal Activity through the Wnt Destruction Complex Machinery., Albrecht LV., Cell Rep. July 28, 2020; 32 (4): 107973.
	Glycogen synthase kinase 3 controls migration of the neural crest lineage in mouse and Xenopus., Gonzalez Malagon SG., Nat Commun. March 19, 2018; 9 (1): 1126.
	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
	Involvement of JunB Proto-Oncogene in Tail Formation During Early Xenopus Embryogenesis., Yoshida H., Zoolog Sci. June 1, 2016; 33 (3): 282-9.
	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.
	GSK3 and Polo-like kinase regulate ADAM13 function during cranial neural crest cell migration., Abbruzzese G., Mol Biol Cell. December 15, 2014; 25 (25): 4072-82.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	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.
	Notch destabilises maternal beta-catenin and restricts dorsal-anterior development in Xenopus., Acosta H., Development. June 1, 2011; 138 (12): 2567-79.
	Early requirement of Hyaluronan for tail regeneration in Xenopus tadpoles., Contreras EG., Development. September 1, 2009; 136 (17): 2987-96.
	Mad is required for wingless signaling in wing development and segment patterning in Drosophila., Eivers E., PLoS One. August 6, 2009; 4 (8): e6543.
	Silencing of Smed-betacatenin1 generates radial-like hypercephalized planarians., Iglesias M., Development. April 1, 2008; 135 (7): 1215-21.
	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.
	Jun NH2-terminal kinase (JNK) prevents nuclear beta-catenin accumulation and regulates axis formation in Xenopus embryos., Liao G., Proc Natl Acad Sci U S A. October 31, 2006; 103 (44): 16313-8.
	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.
	Sox10 regulates the development of neural crest-derived melanocytes in Xenopus., Aoki Y., Dev Biol. July 1, 2003; 259 (1): 19-33.
	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.
	Domains of axin involved in protein-protein interactions, Wnt pathway inhibition, and intracellular localization., Fagotto F., J Cell Biol. May 17, 1999; 145 (4): 741-56.
	Xenopus axin interacts with glycogen synthase kinase-3 beta and is expressed in the anterior midbrain., Hedgepeth CM., Mech Dev. February 1, 1999; 80 (2): 147-51.

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