Papers associated with blastocoel (and ctnnb1)

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	Segregation of brain and organizer precursors is differentially regulated by Nodal signaling at blastula stage., Castro Colabianchi AM., Biol Open. February 25, 2021; 10 (2):
	Ectoderm to mesoderm transition by down-regulation of actomyosin contractility., Kashkooli L., PLoS Biol. January 6, 2021; 19 (1): e3001060.
	GSK3 Inhibits Macropinocytosis and Lysosomal Activity through the Wnt Destruction Complex Machinery., Albrecht LV., Cell Rep. July 28, 2020; 32 (4): 107973.
	Nucleotide receptor P2RY4 is required for head formation via induction and maintenance of head organizer in Xenopus laevis., Harata A., Dev Growth Differ. February 1, 2019; 61 (2): 186-197.
	Notch1 is asymmetrically distributed from the beginning of embryogenesis and controls the ventral center., Castro Colabianchi AM., Development. July 17, 2018; 145 (14):
	Roles for Xenopus aquaporin-3b (aqp3.L) during gastrulation: Fibrillar fibronectin and tissue boundary establishment in the dorsal margin., Forecki J., Dev Biol. January 1, 2018; 433 (1): 3-16.
	Roles of two types of heparan sulfate clusters in Wnt distribution and signaling in Xenopus., Mii Y., Nat Commun. December 7, 2017; 8 (1): 1973.
	Sorting at embryonic boundaries requires high heterotypic interfacial tension., Canty L., Nat Commun. July 31, 2017; 8 (1): 157.
	The phosphatase Pgam5 antagonizes Wnt/β-Catenin signaling in embryonic anterior-posterior axis patterning., Rauschenberger V., Development. June 15, 2017; 144 (12): 2234-2247.
	Brg1 chromatin remodeling ATPase balances germ layer patterning by amplifying the transcriptional burst at midblastula transition., Wagner G., PLoS Genet. May 12, 2017; 13 (5): e1006757.
	Leftward Flow Determines Laterality in Conjoined Twins., Tisler M., Curr Biol. February 20, 2017; 27 (4): 543-548.
	Apolipoprotein C-I mediates Wnt/Ctnnb1 signaling during neural border formation and is required for neural crest development., Yokota C., Int J Dev Biol. January 1, 2017; 61 (6-7): 415-425.
	Syndecan4 coordinates Wnt/JNK and BMP signaling to regulate foregut progenitor development., Zhang Z, Zhang Z., Dev Biol. August 1, 2016; 416 (1): 187-199.
	NF2/Merlin is required for the axial pattern formation in the Xenopus laevis embryo., Zhu X., Mech Dev. November 1, 2015; 138 Pt 3 305-12.
	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.
	FAK is required for tension-dependent organization of collective cell movements in Xenopus mesendoderm., Bjerke MA., Dev Biol. October 15, 2014; 394 (2): 340-56.
	Polarized Wnt signaling regulates ectodermal cell fate in Xenopus., Huang YL., Dev Cell. April 28, 2014; 29 (2): 250-7.
	Expression cloning of camelid nanobodies specific for Xenopus embryonic antigens., Itoh K., PLoS One. January 1, 2014; 9 (10): e107521.
	Nuclearization of β-catenin in ectodermal precursors confers organizer-like ability to induce endomesoderm and pattern a pluteus larva., Byrum CA., Evodevo. November 4, 2013; 4 (1): 31.
	ERK and phosphoinositide 3-kinase temporally coordinate different modes of actin-based motility during embryonic wound healing., Li J., J Cell Sci. November 1, 2013; 126 (Pt 21): 5005-17.
	Serotonin signaling is required for Wnt-dependent GRP specification and leftward flow in Xenopus., Beyer T., Curr Biol. January 10, 2012; 22 (1): 33-9.
	Sfrp5 coordinates foregut specification and morphogenesis by antagonizing both canonical and noncanonical Wnt11 signaling., Li Y., Genes Dev. November 1, 2008; 22 (21): 3050-63.
	A cell cycle arrest is necessary for bottle cell formation in the early Xenopus gastrula: integrating cell shape change, local mitotic control and mesodermal patterning., Kurth T., Mech Dev. December 1, 2005; 122 (12): 1251-65.
	Vezatin, a protein associated to adherens junctions, is required for mouse blastocyst morphogenesis., Hyenne V., Dev Biol. November 1, 2005; 287 (1): 180-91.
	XPACE4 is a localized pro-protein convertase required for mesoderm induction and the cleavage of specific TGFbeta proteins in Xenopus development., Birsoy B., Development. February 1, 2005; 132 (3): 591-602.
	Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus., Kuroda H., PLoS Biol. May 1, 2004; 2 (5): E92.
	Adhesive crosstalk in gastrulation., Montero JA., Dev Cell. August 1, 2003; 5 (2): 190-1.
	Beta-catenin, MAPK and Smad signaling during early Xenopus development., Schohl A., Development. January 1, 2002; 129 (1): 37-52.
	Timing of endogenous activin-like signals and regional specification of the Xenopus embryo., Lee MA., Development. August 1, 2001; 128 (15): 2939-52.
	Loss of cell adhesion in Xenopus laevis embryos mediated by the cytoplasmic domain of XLerk, an erythropoietin-producing hepatocellular ligand., Jones TL., Proc Natl Acad Sci U S A. January 20, 1998; 95 (2): 576-81.
	Antagonism of cell adhesion by an alpha-catenin mutant, and of the Wnt-signaling pathway by alpha-catenin in Xenopus embryos., Sehgal RN., J Cell Biol. November 17, 1997; 139 (4): 1033-46.
	XTcf-3 transcription factor mediates beta-catenin-induced axis formation in Xenopus embryos., Molenaar M., Cell. August 9, 1996; 86 (3): 391-9.
	Beta-catenin localization during Xenopus embryogenesis: accumulation at tissue and somite boundaries., Fagotto F., Development. December 1, 1994; 120 (12): 3667-79.
	Catenins in Xenopus embryogenesis and their relation to the cadherin-mediated cell-cell adhesion system., Schneider S., Development. June 1, 1993; 118 (2): 629-40.

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