Papers associated with neural nucleus (and ctnnb1)

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	High variability of expression profiles of homeologous genes for Wnt, Hh, Notch, and Hippo signaling pathways in Xenopus laevis., Michiue T., Dev Biol. June 15, 2017; 426 (2): 270-290.
	Delamination of neural crest cells requires transient and reversible Wnt inhibition mediated by Dact1/2., Rabadán MA., Development. June 15, 2016; 143 (12): 2194-205.
	The cell proliferation antigen Ki-67 organises heterochromatin., Sobecki M., Elife. March 7, 2016; 5 e13722.
	The E3 ligase RNF43 inhibits Wnt signaling downstream of mutated β-catenin by sequestering TCF4 to the nuclear membrane., Loregger A., Sci Signal. September 8, 2015; 8 (393): ra90.
	JmjC Domain-containing Protein 6 (Jmjd6) Derepresses the Transcriptional Repressor Transcription Factor 7-like 1 (Tcf7l1) and Is Required for Body Axis Patterning during Xenopus Embryogenesis., Zhang X., J Biol Chem. August 14, 2015; 290 (33): 20273-83.
	Kdm2a/b Lysine Demethylases Regulate Canonical Wnt Signaling by Modulating the Stability of Nuclear β-Catenin., Lu L., Dev Cell. June 22, 2015; 33 (6): 660-74.
	The Tumor-Suppressor WWOX and HDAC3 Inhibit the Transcriptional Activity of the β-Catenin Coactivator BCL9-2 in Breast Cancer Cells., El-Hage P., Mol Cancer Res. May 1, 2015; 13 (5): 902-12.
	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.
	Isoquercitrin suppresses colon cancer cell growth in vitro by targeting the Wnt/β-catenin signaling pathway., Amado NG., J Biol Chem. December 19, 2014; 289 (51): 35456-67.
	Cell-autonomous signal transduction in the Xenopus egg Wnt/β-catenin pathway., Motomura E., Dev Growth Differ. December 1, 2014; 56 (9): 640-52.
	Casein kinase 1 α phosphorylates the Wnt regulator Jade-1 and modulates its activity., Borgal L., J Biol Chem. September 19, 2014; 289 (38): 26344-26356.
	Custos controls β-catenin to regulate head development during vertebrate embryogenesis., Komiya Y., Proc Natl Acad Sci U S A. September 9, 2014; 111 (36): 13099-104.
	In vivo collective cell migration requires an LPAR2-dependent increase in tissue fluidity., Kuriyama S., J Cell Biol. July 7, 2014; 206 (1): 113-27.
	Maternal syntabulin is required for dorsal axis formation and is a germ plasm component in Xenopus., Colozza G., Differentiation. July 1, 2014; 88 (1): 17-26.
	Anillin regulates cell-cell junction integrity by organizing junctional accumulation of Rho-GTP and actomyosin., Reyes CC., Curr Biol. June 2, 2014; 24 (11): 1263-70.
	IQGAP1 protein regulates nuclear localization of β-catenin via importin-β5 protein in Wnt signaling., Goto T., J Biol Chem. December 20, 2013; 288 (51): 36351-60.
	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.
	Par6b regulates the dynamics of apicobasal polarity during development of the stratified Xenopus epidermis., Wang S., PLoS One. October 8, 2013; 8 (10): e76854.
	Functional aspects of primary cilia in signaling, cell cycle and tumorigenesis., Basten SG., Cilia. April 29, 2013; 2 (1): 6.
	β-Catenin-independent activation of TCF1/LEF1 in human hematopoietic tumor cells through interaction with ATF2 transcription factors., Grumolato L., PLoS Genet. January 1, 2013; 9 (8): e1003603.
	Wnt/β-catenin and its diverse physiological cell signaling pathways in neurodegenerative and neuropsychiatric disorders., Al-Harthi L., J Neuroimmune Pharmacol. December 1, 2012; 7 (4): 725-30.
	Upon Wnt stimulation, Rac1 activation requires Rac1 and Vav2 binding to p120-catenin., Valls G., J Cell Sci. November 15, 2012; 125 (Pt 22): 5288-301.
	The many faces and functions of β-catenin., Valenta T., EMBO J. June 13, 2012; 31 (12): 2714-36.
	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.
	Maternal Wnt/β-catenin signaling coactivates transcription through NF-κB binding sites during Xenopus axis formation., Armstrong NJ., PLoS One. January 1, 2012; 7 (5): e36136.
	Cortical rotation and messenger RNA localization in Xenopus axis formation., Houston DW., Wiley Interdiscip Rev Dev Biol. January 1, 2012; 1 (3): 371-88.
	Wnt signaling meets internal dissent., Grove EA., Genes Dev. September 1, 2011; 25 (17): 1759-62.
	Functional analyses of vertebrate TCF proteins in C. elegans embryos., Robertson SM., Dev Biol. July 1, 2011; 355 (1): 115-23.
	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.
	Phosphorylation of TCF proteins by homeodomain-interacting protein kinase 2., Hikasa H., J Biol Chem. April 8, 2011; 286 (14): 12093-100.
	Wnt signaling requires sequestration of glycogen synthase kinase 3 inside multivesicular endosomes., Taelman VF., Cell. December 23, 2010; 143 (7): 1136-48.
	The tumor-associated EpCAM regulates morphogenetic movements through intracellular signaling., Maghzal N., J Cell Biol. November 1, 2010; 191 (3): 645-59.
	Collective chemotaxis requires contact-dependent cell polarity., Theveneau E., Dev Cell. July 20, 2010; 19 (1): 39-53.
	Homeodomain-interacting protein kinase 2 (HIPK2) targets beta-catenin for phosphorylation and proteasomal degradation., Kim EA., Biochem Biophys Res Commun. April 16, 2010; 394 (4): 966-71.
	Mutations in the human naked cuticle homolog NKD1 found in colorectal cancer alter Wnt/Dvl/beta-catenin signaling., Guo J., PLoS One. November 24, 2009; 4 (11): e7982.
	Requirement for Wnt and FGF signaling in Xenopus tadpole tail regeneration., Lin G., Dev Biol. April 15, 2008; 316 (2): 323-35.
	Silencing of Smed-betacatenin1 generates radial-like hypercephalized planarians., Iglesias M., Development. April 1, 2008; 135 (7): 1215-21.
	Intracellular expression profiles measured by real-time PCR tomography in the Xenopus laevis oocyte., Sindelka R., Nucleic Acids Res. February 1, 2008; 36 (2): 387-92.
	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.
	The Wnt-dependent signaling pathways as target in oncology drug discovery., Janssens N., Invest New Drugs. July 1, 2006; 24 (4): 263-80.
	TBX5 is required for embryonic cardiac cell cycle progression., Goetz SC., Development. July 1, 2006; 133 (13): 2575-84.
	HIC-5 is a novel repressor of lymphoid enhancer factor/T-cell factor-driven transcription., Ghogomu SM., J Biol Chem. January 20, 2006; 281 (3): 1755-64.
	Terminating Wnt signals: a novel nuclear export mechanism targets activated (beta)-catenin., Thorne ME., J Cell Biol. December 5, 2005; 171 (5): 761-3.
	RanBP3 enhances nuclear export of active (beta)-catenin independently of CRM1., Hendriksen J., J Cell Biol. December 5, 2005; 171 (5): 785-97.
	Germ-layer specification and control of cell growth by Ectodermin, a Smad4 ubiquitin ligase., Dupont S., Cell. April 8, 2005; 121 (1): 87-99.
	Nuclear localization is required for Dishevelled function in Wnt/beta-catenin signaling., Itoh K., J Biol. January 1, 2005; 4 (1): 3.
	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.
	Nuclear localization of Duplin, a beta-catenin-binding protein, is essential for its inhibitory activity on the Wnt signaling pathway., Kobayashi M., J Biol Chem. February 22, 2002; 277 (8): 5816-22.
	TGF-beta signalling pathways in early Xenopus development., Hill CS., Curr Opin Genet Dev. October 1, 2001; 11 (5): 533-40.
	Axis induction by wnt signaling: Target promoter responsiveness regulates competence., Darken RS., Dev Biol. June 1, 2001; 234 (1): 42-54.

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