Papers associated with central nervous system (and nodal3.1)

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	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 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.
	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.
	Notch destabilises maternal beta-catenin and restricts dorsal-anterior development in Xenopus., Acosta H., Development. June 1, 2011; 138 (12): 2567-79.
	An essential role of the cysteine-rich domain of FZD4 in Norrin/Wnt signaling and familial exudative vitreoretinopathy., Zhang K., J Biol Chem. March 25, 2011; 286 (12): 10210-5.
	Yes-associated protein 65 (YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone., Gee ST., PLoS One. January 1, 2011; 6 (6): e20309.
	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.
	beta-Catenin primes organizer gene expression by recruiting a histone H3 arginine 8 methyltransferase, Prmt2., Blythe SA., Dev Cell. August 17, 2010; 19 (2): 220-31.
	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.
	Early activation of FGF and nodal pathways mediates cardiac specification independently of Wnt/beta-catenin signaling., Samuel LJ., PLoS One. October 28, 2009; 4 (10): e7650.
	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.
	Vegetally localized Xenopus trim36 regulates cortical rotation and dorsal axis formation., Cuykendall TN., Development. September 1, 2009; 136 (18): 3057-65.
	Embryonic lethality of fortilin-null mutant mice by BMP-pathway overactivation., Koide Y., Biochim Biophys Acta. May 1, 2009; 1790 (5): 326-38.
	Effects of NR1 splicing on NR1/NR3B-type excitatory glycine receptors., Cavara NA., BMC Neurosci. April 6, 2009; 10 32.
	Lef1 plays a role in patterning the mesoderm and ectoderm in Xenopus tropicalis., Roel G., Int J Dev Biol. January 1, 2009; 53 (1): 81-9.
	Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1., Louie SH., PLoS One. January 1, 2009; 4 (2): e4310.
	IGFBP-4 is an inhibitor of canonical Wnt signalling required for cardiogenesis., Zhu W., Nature. July 17, 2008; 454 (7202): 345-9.
	LRP6 transduces a canonical Wnt signal independently of Axin degradation by inhibiting GSK3's phosphorylation of beta-catenin., Cselenyi CS., Proc Natl Acad Sci U S A. June 10, 2008; 105 (23): 8032-7.
	Lrig3 regulates neural crest formation in Xenopus by modulating Fgf and Wnt signaling pathways., Zhao H., Development. April 1, 2008; 135 (7): 1283-93.
	Long- and short-range signals control the dynamic expression of an animal hemisphere-specific gene in Xenopus., Mir A., Dev Biol. March 1, 2008; 315 (1): 161-72.
	Wise retained in the endoplasmic reticulum inhibits Wnt signaling by reducing cell surface LRP6., Guidato S., Dev Biol. October 15, 2007; 310 (2): 250-63.
	Beta-arrestin is a necessary component of Wnt/beta-catenin signaling in vitro and in vivo., Bryja V., Proc Natl Acad Sci U S A. April 17, 2007; 104 (16): 6690-5.
	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.
	Twisted gastrulation is required for forebrain specification and cooperates with Chordin to inhibit BMP signaling during X. tropicalis gastrulation., Wills A., Dev Biol. January 1, 2006; 289 (1): 166-78.
	Xenopus frizzled-4S, a splicing variant of Xfz4 is a context-dependent activator and inhibitor of Wnt/beta-catenin signaling., Swain RK., Cell Commun Signal. October 19, 2005; 3 12.
	Frodo proteins: modulators of Wnt signaling in vertebrate development., Brott BK., Differentiation. September 1, 2005; 73 (7): 323-9.
	XIC is required for Siamois activity and dorsoanterior development., Snider L., Mol Cell Biol. June 1, 2005; 25 (12): 5061-72.
	The NR3B subunit does not alter the anesthetic sensitivities of recombinant N-methyl-D-aspartate receptors., Yamakura T., Anesth Analg. June 1, 2005; 100 (6): 1687-1692.
	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.
	Exploration of the extracellular space by a large-scale secretion screen in the early Xenopus embryo., Pera EM., Int J Dev Biol. January 1, 2005; 49 (7): 781-96.
	New roles for FoxH1 in patterning the early embryo., Kofron M., Development. October 1, 2004; 131 (20): 5065-78.
	The involvement of Frodo in TCF-dependent signaling and neural tissue development., Hikasa H., Development. October 1, 2004; 131 (19): 4725-34.
	XSENP1, a novel sumo-specific protease in Xenopus, inhibits normal head formation by down-regulation of Wnt/beta-catenin signalling., Yukita A., Genes Cells. August 1, 2004; 9 (8): 723-36.
	Analysis of Spemann organizer formation in Xenopus embryos by cDNA macroarrays., Wessely O., Dev Biol. May 15, 2004; 269 (2): 552-66.
	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.
	Xenopus tropicalis nodal-related gene 3 regulates BMP signaling: an essential role for the pro-region., Haramoto Y., Dev Biol. January 1, 2004; 265 (1): 155-68.
	PP2A:B56epsilon is required for Wnt/beta-catenin signaling during embryonic development., Yang J., Development. December 1, 2003; 130 (23): 5569-78.
	Flamingo, a cadherin-type receptor involved in the Drosophila planar polarity pathway, can block signaling via the canonical wnt pathway in Xenopus laevis., Morgan R., Int J Dev Biol. May 1, 2003; 47 (4): 245-52.
	Regulation of nodal and BMP signaling by tomoregulin-1 (X7365) through novel mechanisms., Chang C., Dev Biol. March 1, 2003; 255 (1): 1-11.
	Xhex-expressing endodermal tissues are essential for anterior patterning in Xenopus., Smithers LE., Mech Dev. December 1, 2002; 119 (2): 191-200.
	The roles of three signaling pathways in the formation and function of the Spemann Organizer., Xanthos JB., Development. September 1, 2002; 129 (17): 4027-43.
	The Wnt/calcium pathway activates NF-AT and promotes ventral cell fate in Xenopus embryos., Saneyoshi T., Nature. May 16, 2002; 417 (6886): 295-9.
	The IGF pathway regulates head formation by inhibiting Wnt signaling in Xenopus., Richard-Parpaillon L., Dev Biol. April 15, 2002; 244 (2): 407-17.
	Excitatory glycine receptors containing the NR3 family of NMDA receptor subunits., Chatterton JE., Nature. February 14, 2002; 415 (6873): 793-8.
	The Wnt/beta-catenin pathway posteriorizes neural tissue in Xenopus by an indirect mechanism requiring FGF signalling., Domingos PM., Dev Biol. November 1, 2001; 239 (1): 148-60.
	Neural induction in the absence of mesoderm: beta-catenin-dependent expression of secreted BMP antagonists at the blastula stage in Xenopus., Wessely O., Dev Biol. June 1, 2001; 234 (1): 161-73.
	Axis induction by wnt signaling: Target promoter responsiveness regulates competence., Darken RS., Dev Biol. June 1, 2001; 234 (1): 42-54.
	foxD5a, a Xenopus winged helix gene, maintains an immature neural ectoderm via transcriptional repression that is dependent on the C-terminal domain., Sullivan SA., Dev Biol. April 15, 2001; 232 (2): 439-57.
	[Neural determination in Xenopus laevis embryos: control of early neural gene expression by calcium]., Leclerc C., J Soc Biol. January 1, 2001; 195 (3): 327-37.

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