Papers associated with brain (and ctnnb1)

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	Genome-wide view of TGFβ/Foxh1 regulation of the early mesendoderm program., Chiu WT., Development. December 1, 2014; 141 (23): 4537-47.
	Fezf2 promotes neuronal differentiation through localised activation of Wnt/β-catenin signalling during forebrain development., Zhang S., Development. December 1, 2014; 141 (24): 4794-805.
	The conserved barH-like homeobox-2 gene barhl2 acts downstream of orthodentricle-2 and together with iroquois-3 in establishment of the caudal forebrain signaling center induced by Sonic Hedgehog., Juraver-Geslin HA., Dev Biol. December 1, 2014; 396 (1): 107-20.
	Neural transcription factors: from embryos to neural stem cells., Lee HK., Mol Cells. October 31, 2014; 37 (10): 705-12.
	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.
	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.
	The PDZ domain protein Mcc is a novel effector of non-canonical Wnt signaling during convergence and extension in zebrafish., Young T., Development. September 1, 2014; 141 (18): 3505-16.
	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.
	Role of Rab11 in planar cell polarity and apical constriction during vertebrate neural tube closure., Ossipova O., Nat Commun. May 13, 2014; 5 3734.
	PTK7 modulates Wnt signaling activity via LRP6., Bin-Nun N., Development. January 1, 2014; 141 (2): 410-21.
	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.
	Role of Sp5 as an essential early regulator of neural crest specification in xenopus., Park DS., Dev Dyn. December 1, 2013; 242 (12): 1382-94.
	A secreted splice variant of the Xenopus frizzled-4 receptor is a biphasic modulator of Wnt signalling., Gorny AK., Cell Commun Signal. November 19, 2013; 11 89.
	Par6b regulates the dynamics of apicobasal polarity during development of the stratified Xenopus epidermis., Wang S., PLoS One. October 8, 2013; 8 (10): e76854.
	RAB8B is required for activity and caveolar endocytosis of LRP6., Demir K., Cell Rep. September 26, 2013; 4 (6): 1224-34.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	Identification and characterization of a small-molecule inhibitor of Wnt signaling in glioblastoma cells., De Robertis A., Mol Cancer Ther. July 1, 2013; 12 (7): 1180-9.
	Neurulation and neurite extension require the zinc transporter ZIP12 (slc39a12)., Chowanadisai W., Proc Natl Acad Sci U S A. June 11, 2013; 110 (24): 9903-8.
	Different thresholds of Wnt-Frizzled 7 signaling coordinate proliferation, morphogenesis and fate of endoderm progenitor cells., Zhang Z., Dev Biol. June 1, 2013; 378 (1): 1-12.
	β-Arrestin 1 mediates non-canonical Wnt pathway to regulate convergent extension movements., Kim GH., Biochem Biophys Res Commun. May 31, 2013; 435 (2): 182-7.
	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.
	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.
	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.
	Subfunctionalization and neofunctionalization of vertebrate Lef/Tcf transcription factors., Klingel S., Dev Biol. August 1, 2012; 368 (1): 44-53.
	Suppression of Bmp4 signaling by the zinc-finger repressors Osr1 and Osr2 is required for Wnt/β-catenin-mediated lung specification in Xenopus., Rankin SA, Rankin SA., Development. August 1, 2012; 139 (16): 3010-20.
	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.
	Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/β-catenin signaling pathway., Fujimi TJ., Dev Biol. January 15, 2012; 361 (2): 220-31.
	Amer2 protein is a novel negative regulator of Wnt/β-catenin signaling involved in neuroectodermal patterning., Pfister AS., J Biol Chem. January 13, 2012; 287 (3): 1734-41.
	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.
	CRIM1 complexes with ß-catenin and cadherins, stabilizes cell-cell junctions and is critical for neural morphogenesis., Ponferrada VG., PLoS One. January 1, 2012; 7 (3): e32635.
	Maternal xNorrin, a canonical Wnt signaling agonist and TGF-β antagonist, controls early neuroectoderm specification in Xenopus., Xu S., PLoS Biol. January 1, 2012; 10 (3): e1001286.
	xCOUP-TF-B regulates xCyp26 transcription and modulates retinoic acid signaling for anterior neural patterning in Xenopus., Tanibe M., Int J Dev Biol. January 1, 2012; 56 (4): 239-44.
	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.
	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.
	Waif1/5T4 inhibits Wnt/β-catenin signaling and activates noncanonical Wnt pathways by modifying LRP6 subcellular localization., Kagermeier-Schenk B., Dev Cell. December 13, 2011; 21 (6): 1129-43.
	HESX1- and TCF3-mediated repression of Wnt/β-catenin targets is required for normal development of the anterior forebrain., Andoniadou CL., Development. November 1, 2011; 138 (22): 4931-42.
	Transcription factor Zic2 inhibits Wnt/β-catenin protein signaling., Pourebrahim R., J Biol Chem. October 28, 2011; 286 (43): 37732-40.
	The dual regulator Sufu integrates Hedgehog and Wnt signals in the early Xenopus embryo., Min TH., Dev Biol. October 1, 2011; 358 (1): 262-76.
	A novel mechanism for the transcriptional regulation of Wnt signaling in development., Vacik T., Genes Dev. September 1, 2011; 25 (17): 1783-95.
	Barhl2 limits growth of the diencephalic primordium through Caspase3 inhibition of beta-catenin activation., Juraver-Geslin HA., Proc Natl Acad Sci U S A. February 8, 2011; 108 (6): 2288-93.
	Different requirement for Wnt/β-catenin signaling in limb regeneration of larval and adult Xenopus., Yokoyama H., PLoS One. January 1, 2011; 6 (7): e21721.
	Regulation of TCF3 by Wnt-dependent phosphorylation during vertebrate axis specification., Hikasa H., Dev Cell. October 19, 2010; 19 (4): 521-32.
	Anterior neural development requires Del1, a matrix-associated protein that attenuates canonical Wnt signaling via the Ror2 pathway., Takai A., Development. October 1, 2010; 137 (19): 3293-302.
	Wnt/beta-catenin signaling is involved in the induction and maintenance of primitive hematopoiesis in the vertebrate embryo., Tran HT., Proc Natl Acad Sci U S A. September 14, 2010; 107 (37): 16160-5.
	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.
	Direct control of Hoxd1 and Irx3 expression by Wnt/beta-catenin signaling during anteroposterior patterning of the neural axis in Xenopus., Janssens S., Int J Dev Biol. January 1, 2010; 54 (10): 1435-42.
	Xenopus delta-catenin is essential in early embryogenesis and is functionally linked to cadherins and small GTPases., Gu D., J Cell Sci. November 15, 2009; 122 (Pt 22): 4049-61.
	Bone morphogenetic protein 15 (BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis., Di Pasquale E., J Biol Chem. September 18, 2009; 284 (38): 26127-36.
	Mad is required for wingless signaling in wing development and segment patterning in Drosophila., Eivers E., PLoS One. August 6, 2009; 4 (8): e6543.

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