Papers associated with plasma membrane (and ctnnb1)

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	The tyrosine Y2502.39 in Frizzled 4 defines a conserved motif important for structural integrity of the receptor and recruitment of Disheveled., Strakova K., Cell Signal. October 1, 2017; 38 85-96.
	Dual control of pcdh8l/PCNS expression and function in Xenopus laevis neural crest cells by adam13/33 via the transcription factors tfap2α and arid3a., Khedgikar V., Elife. August 22, 2017; 6
	Acetylcholinesterase plays a non-neuronal, non-esterase role in organogenesis., Pickett MA., Development. August 1, 2017; 144 (15): 2764-2770.
	Folate receptor 1 is necessary for neural plate cell apical constriction during Xenopus neural tube formation., Balashova OA., Development. April 15, 2017; 144 (8): 1518-1530.
	Cholesterol-rich membrane microdomains modulate Wnt/β-catenin morphogen gradient during Xenopus development., Reis AH., Mech Dev. November 1, 2016; 142 30-39.
	Phosphorylation-dependent ubiquitination of paraxial protocadherin (PAPC) controls gastrulation cell movements., Kai M., PLoS One. January 12, 2015; 10 (1): e0115111.
	Cell-autonomous signal transduction in the Xenopus egg Wnt/β-catenin pathway., Motomura E., Dev Growth Differ. December 1, 2014; 56 (9): 640-52.
	In vivo analysis of formation and endocytosis of the Wnt/β-catenin signaling complex in zebrafish embryos., Hagemann AI., J Cell Sci. September 15, 2014; 127 (Pt 18): 3970-82.
	β-Arrestin interacts with the beta/gamma subunits of trimeric G-proteins and dishevelled in the Wnt/Ca(2+) pathway in xenopus gastrulation., Seitz K., PLoS One. January 17, 2014; 9 (1): e87132.
	Syndecan-4 inhibits Wnt/β-catenin signaling through regulation of low-density-lipoprotein receptor-related protein (LRP6) and R-spondin 3., Astudillo P., Int J Biochem Cell Biol. January 1, 2014; 46 103-12.
	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.
	RAB8B is required for activity and caveolar endocytosis of LRP6., Demir K., Cell Rep. September 26, 2013; 4 (6): 1224-34.
	Lypd6 enhances Wnt/β-catenin signaling by promoting Lrp6 phosphorylation in raft plasma membrane domains., Özhan G., Dev Cell. August 26, 2013; 26 (4): 331-45.
	Wnt-11 and Fz7 reduce cell adhesion in convergent extension by sequestration of PAPC and C-cadherin., Kraft B., J Cell Biol. August 20, 2012; 198 (4): 695-709.
	Activation of voltage gated K⁺ channel Kv1.5 by β-catenin., Munoz C., Biochem Biophys Res Commun. January 13, 2012; 417 (2): 692-6.
	Mink1 regulates β-catenin-independent Wnt signaling via Prickle phosphorylation., Daulat AM., Mol Cell Biol. January 1, 2012; 32 (1): 173-85.
	Regulation of KCNQ1/KCNE1 by β-catenin., Wilmes J., Mol Membr Biol. January 1, 2012; 29 (3-4): 87-94.
	Stimulation of HERG channel activity by β-catenin., Munoz C., PLoS One. January 1, 2012; 7 (8): e43353.
	Differential role of Axin RGS domain function in Wnt signaling during anteroposterior patterning and maternal axis formation., Schneider PN., PLoS One. January 1, 2012; 7 (9): e44096.
	IGF-1 increases invasive potential of MCF 7 breast cancer cells and induces activation of latent TGF-β1 resulting in epithelial to mesenchymal transition., Walsh LA., Cell Commun Signal. May 2, 2011; 9 (1): 10.
	β-catenin is a molecular switch that regulates transition of cell-cell adhesion to fusion., Takezawa Y., Sci Rep. January 1, 2011; 1 68.
	Identification of transmembrane protein 88 (TMEM88) as a dishevelled-binding protein., Lee HJ., J Biol Chem. December 31, 2010; 285 (53): 41549-56.
	Stimulation of Na+/K+ ATPase activity and Na+ coupled glucose transport by β-catenin., Sopjani M., Biochem Biophys Res Commun. November 19, 2010; 402 (3): 467-70.
	WLS-dependent secretion of WNT3A requires Ser209 acylation and vacuolar acidification., Coombs GS., J Cell Sci. October 1, 2010; 123 (Pt 19): 3357-67.
	Nectin-2 and N-cadherin interact through extracellular domains and induce apical accumulation of F-actin in apical constriction of Xenopus neural tube morphogenesis., Morita H., Development. April 1, 2010; 137 (8): 1315-25.
	N- and E-cadherins in Xenopus are specifically required in the neural and non-neural ectoderm, respectively, for F-actin assembly and morphogenetic movements., Nandadasa S., Development. April 1, 2009; 136 (8): 1327-38.
	Jade-1 inhibits Wnt signalling by ubiquitylating beta-catenin and mediates Wnt pathway inhibition by pVHL., Chitalia VC., Nat Cell Biol. October 1, 2008; 10 (10): 1208-16.
	beta-Catenin controls cell sorting at the notochord-somite boundary independently of cadherin-mediated adhesion., Reintsch WE., J Cell Biol. August 15, 2005; 170 (4): 675-86.
	Nuclear localization is required for Dishevelled function in Wnt/beta-catenin signaling., Itoh K., J Biol. January 1, 2005; 4 (1): 3.
	The maternal Xenopus beta-catenin signaling pathway, activated by frizzled homologs, induces goosecoid in a cell non-autonomous manner., Brown JD., Dev Growth Differ. August 1, 2000; 42 (4): 347-57.
	The transcriptional coactivator CBP interacts with beta-catenin to activate gene expression., Takemaru KI., J Cell Biol. April 17, 2000; 149 (2): 249-54.
	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.
	Changes in the pattern of adherens junction-associated beta-catenin accompany morphogenesis in the sea urchin embryo., Miller JR., Dev Biol. December 15, 1997; 192 (2): 310-22.
	Analysis of the signaling activities of localization mutants of beta-catenin during axis specification in Xenopus., Miller JR., J Cell Biol. October 6, 1997; 139 (1): 229-43.
	Embryonic axis induction by the armadillo repeat domain of beta-catenin: evidence for intracellular signaling., Funayama N., J Cell Biol. March 1, 1995; 128 (5): 959-68.

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