Papers associated with anatomical space (and ctnnb1)

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	Competence for neural crest induction is controlled by hydrostatic pressure through Yap., Alasaadi DN., Nat Cell Biol. March 18, 2024;
	R-Spondin 2 governs Xenopus left-right body axis formation by establishing an FGF signaling gradient., Lee H, Lee H., Nat Commun. February 2, 2024; 15 (1): 1003.
	Mink1 regulates spemann organizer cell fate in the xenopus gastrula via Hmga2., Colleluori V., Dev Biol. March 1, 2023; 495 42-53.
	Dorsal lip maturation and initial archenteron extension depend on Wnt11 family ligands., Van Itallie ES., Dev Biol. January 1, 2023; 493 67-79.
	Rab7 is required for mesoderm patterning and gastrulation in Xenopus., Kreis J., Biol Open. July 15, 2021; 10 (7):
	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.
	Desmoplakin is required for epidermal integrity and morphogenesis in the Xenopus laevis embryo., Bharathan NK., Dev Biol. June 15, 2019; 450 (2): 115-131.
	The Wnt inhibitor Dkk1 is required for maintaining the normal cardiac differentiation program in Xenopus laevis., Guo Y., Dev Biol. May 1, 2019; 449 (1): 1-13.
	Modeling congenital kidney diseases in Xenopus laevis., Blackburn ATM., Dis Model Mech. April 9, 2019; 12 (4):
	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):
	Role of the visual experience-dependent nascent proteome in neuronal plasticity., Liu HH., Elife. February 7, 2018; 7
	RAPGEF5 Regulates Nuclear Translocation of β-Catenin., Griffin JN., Dev Cell. January 22, 2018; 44 (2): 248-260.e4.
	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.
	Similarity in gene-regulatory networks suggests that cancer cells share characteristics of embryonic neural cells., Zhang Z., J Biol Chem. August 4, 2017; 292 (31): 12842-12859.
	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.
	Spatiotemporally Controlled Mechanical Cues Drive Progenitor Mesenchymal-to-Epithelial Transition Enabling Proper Heart Formation and Function., Jackson TR., Curr Biol. May 8, 2017; 27 (9): 1326-1335.
	The CapZ interacting protein Rcsd1 is required for cardiogenesis downstream of Wnt11a in Xenopus laevis., Hempel A., Dev Biol. April 1, 2017; 424 (1): 28-39.
	Leftward Flow Determines Laterality in Conjoined Twins., Tisler M., Curr Biol. February 20, 2017; 27 (4): 543-548.
	Leptin Induces Mitosis and Activates the Canonical Wnt/β-Catenin Signaling Pathway in Neurogenic Regions of Xenopus Tadpole Brain., Bender MC., Front Endocrinol (Lausanne). January 1, 2017; 8 99.
	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.
	G protein-coupled receptors Flop1 and Flop2 inhibit Wnt/β-catenin signaling and are essential for head formation in Xenopus., Miyagi A., Dev Biol. November 1, 2015; 407 (1): 131-44.
	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.
	ATP4 and ciliation in the neuroectoderm and endoderm of Xenopus embryos and tadpoles., Walentek P., Data Brief. April 20, 2015; 4 22-31.
	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.
	The extreme anterior domain is an essential craniofacial organizer acting through Kinin-Kallikrein signaling., Jacox L., Cell Rep. July 24, 2014; 8 (2): 596-609.
	The Wnt/JNK signaling target gene alcam is required for embryonic kidney development., Cizelsky W., Development. May 1, 2014; 141 (10): 2064-74.
	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.
	FAK transduces extracellular forces that orient the mitotic spindle and control tissue morphogenesis., Petridou NI., Nat Commun. January 1, 2014; 5 5240.
	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.
	Retinoic acid-activated Ndrg1a represses Wnt/β-catenin signaling to allow Xenopus pancreas, oesophagus, stomach, and duodenum specification., Zhang T., PLoS One. May 15, 2013; 8 (5): e65058.
	Vertebrate kidney tubules elongate using a planar cell polarity-dependent, rosette-based mechanism of convergent extension., Lienkamp SS., Nat Genet. December 1, 2012; 44 (12): 1382-7.
	ATP4a is required for Wnt-dependent Foxj1 expression and leftward flow in Xenopus left-right development., Walentek P., Cell Rep. May 31, 2012; 1 (5): 516-27.
	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.
	Expression analysis of epb41l4a during Xenopus laevis embryogenesis., Guo Y., Dev Genes Evol. June 1, 2011; 221 (2): 113-9.
	Expression of Wnt signaling components during Xenopus pronephros development., Zhang B., PLoS One. January 1, 2011; 6 (10): e26533.
	MID1 and MID2 are required for Xenopus neural tube closure through the regulation of microtubule organization., Suzuki M., Development. July 1, 2010; 137 (14): 2329-39.
	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.
	The functions and possible significance of Kremen as the gatekeeper of Wnt signalling in development and pathology., Nakamura T., J Cell Mol Med. April 1, 2008; 12 (2): 391-408.
	TBX5 is required for embryonic cardiac cell cycle progression., Goetz SC., Development. July 1, 2006; 133 (13): 2575-84.
	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.

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