Papers associated with ventral (and myc)

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	Hes6 is required for MyoD induction during gastrulation., Murai K., Dev Biol. December 1, 2007; 312 (1): 61-76.
	Tsukushi modulates Xnr2, FGF and BMP signaling: regulation of Xenopus germ layer formation., Morris SA., PLoS One. October 10, 2007; 2 (10): e1004.
	XSUMO-1 is required for normal mesoderm induction and axis elongation during early Xenopus development., Yukita A., Dev Dyn. October 1, 2007; 236 (10): 2757-66.
	Targeting of retinal axons requires the metalloproteinase ADAM10., Chen YY., J Neurosci. August 1, 2007; 27 (31): 8448-56.
	Retinoic acid-inducible G protein-coupled receptors bind to frizzled receptors and may activate non-canonical Wnt signaling., Harada Y., Biochem Biophys Res Commun. July 13, 2007; 358 (4): 968-75.
	CVAK104 is a novel regulator of clathrin-mediated SNARE sorting., Borner GH., Traffic. July 1, 2007; 8 (7): 893-903.
	ANR5, an FGF target gene product, regulates gastrulation in Xenopus., Chung HA., Curr Biol. June 5, 2007; 17 (11): 932-9.
	Inca: a novel p21-activated kinase-associated protein required for cranial neural crest development., Luo T., Development. April 1, 2007; 134 (7): 1279-89.
	PP2A:B56epsilon is required for eye induction and eye field separation., Rorick AM., Dev Biol. February 15, 2007; 302 (2): 477-93.
	Wnt11/beta-catenin signaling in both oocytes and early embryos acts through LRP6-mediated regulation of axin., Kofron M., Development. February 1, 2007; 134 (3): 503-13.
	Negative regulation of Activin/Nodal signaling by SRF during Xenopus gastrulation., Yun CH., Development. February 1, 2007; 134 (4): 769-77.
	Xenopus glucose transporter 1 (xGLUT1) is required for gastrulation movement in Xenopus laevis., Suzawa K., Int J Dev Biol. January 1, 2007; 51 (3): 183-90.
	Functional analysis of Sox8 during neural crest development in Xenopus., O'Donnell M., Development. October 1, 2006; 133 (19): 3817-26.
	Tsukushi cooperates with VG1 to induce primitive streak and Hensen's node formation in the chick embryo., Ohta K., Development. October 1, 2006; 133 (19): 3777-86.
	Xenopus POU factors of subclass V inhibit activin/nodal signaling during gastrulation., Cao Y., Mech Dev. August 1, 2006; 123 (8): 614-25.
	Two distinct domains in pro-region of Nodal-related 3 are essential for BMP inhibition., Haramoto Y., Biochem Biophys Res Commun. July 28, 2006; 346 (2): 470-8.
	Novel gene ashwin functions in Xenopus cell survival and anteroposterior patterning., Patil SS., Dev Dyn. July 1, 2006; 235 (7): 1895-907.
	The RNA-binding protein, Vg1RBP, is required for pancreatic fate specification., Spagnoli FM., Dev Biol. April 15, 2006; 292 (2): 442-56.
	Mxi1 is essential for neurogenesis in Xenopus and acts by bridging the pan-neural and proneural genes., Klisch TJ., Dev Biol. April 15, 2006; 292 (2): 470-85.
	A requirement for NF-protocadherin and TAF1/Set in cell adhesion and neural tube formation., Rashid D., Dev Biol. March 1, 2006; 291 (1): 170-81.
	Xenopus apyrase (xapy), a secreted nucleotidase that is expressed during early development., Devader C., Gene. February 15, 2006; 367 135-41.
	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.
	Identification of TH-B, a new oligomeric variant of the Xenopus morphogenetic factor, tumorhead., Traverso EE., Int J Dev Biol. January 1, 2006; 50 (4): 423-7.
	The Vg1-related protein Gdf3 acts in a Nodal signaling pathway in the pre-gastrulation mouse embryo., Chen C., Development. January 1, 2006; 133 (2): 319-29.
	Noelins modulate the timing of neuronal differentiation during development., Moreno TA., Dev Biol. December 15, 2005; 288 (2): 434-47.
	RanBP3 enhances nuclear export of active (beta)-catenin independently of CRM1., Hendriksen J., J Cell Biol. December 5, 2005; 171 (5): 785-97.
	Role of crescent in convergent extension movements by modulating Wnt signaling in early Xenopus embryogenesis., Shibata M., Mech Dev. December 1, 2005; 122 (12): 1322-39.
	SOX7 and SOX18 are essential for cardiogenesis in Xenopus., Zhang C., Dev Dyn. December 1, 2005; 234 (4): 878-91.
	Xnr2 and Xnr5 unprocessed proteins inhibit Wnt signaling upstream of dishevelled., Onuma Y., Dev Dyn. December 1, 2005; 234 (4): 900-10.
	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.
	The novel Smad-interacting protein Smicl regulates Chordin expression in the Xenopus embryo., Collart C., Development. October 1, 2005; 132 (20): 4575-86.
	Novel Daple-like protein positively regulates both the Wnt/beta-catenin pathway and the Wnt/JNK pathway in Xenopus., Kobayashi H., Mech Dev. October 1, 2005; 122 (10): 1138-53.
	Reorganization of actin cytoskeleton by FRIED, a Frizzled-8 associated protein tyrosine phosphatase., Itoh K., Dev Dyn. September 1, 2005; 234 (1): 90-101.
	BMP-3 is a novel inhibitor of both activin and BMP-4 signaling in Xenopus embryos., Gamer LW., Dev Biol. September 1, 2005; 285 (1): 156-68.
	xBtg-x regulates Wnt/beta-Catenin signaling during early Xenopus development., Wessely O., Dev Biol. July 1, 2005; 283 (1): 17-28.
	Kaiso/p120-catenin and TCF/beta-catenin complexes coordinately regulate canonical Wnt gene targets., Park JI., Dev Cell. June 1, 2005; 8 (6): 843-54.
	Germ-layer specification and control of cell growth by Ectodermin, a Smad4 ubiquitin ligase., Dupont S., Cell. April 8, 2005; 121 (1): 87-99.
	Pontin and Reptin regulate cell proliferation in early Xenopus embryos in collaboration with c-Myc and Miz-1., Etard C., Mech Dev. April 1, 2005; 122 (4): 545-56.
	Xenopus ILK (integrin-linked kinase) is required for morphogenetic movements during gastrulation., Yasunaga T., Genes Cells. April 1, 2005; 10 (4): 369-79.
	Maternal wnt11 activates the canonical wnt signaling pathway required for axis formation in Xenopus embryos., Tao Q, Tao Q., Cell. March 25, 2005; 120 (6): 857-71.
	The Notch-target gene hairy2a impedes the involution of notochordal cells by promoting floor plate fates in Xenopus embryos., López SL., Development. March 1, 2005; 132 (5): 1035-46.
	The ARID domain protein dril1 is necessary for TGF(beta) signaling in Xenopus embryos., Callery EM., Dev Biol. February 15, 2005; 278 (2): 542-59.
	Identification of DRG family regulatory proteins (DFRPs): specific regulation of DRG1 and DRG2., Ishikawa K., Genes Cells. February 1, 2005; 10 (2): 139-50.
	Xenopus aristaless-related homeobox (xARX) gene product functions as both a transcriptional activator and repressor in forebrain development., Seufert DW., Dev Dyn. February 1, 2005; 232 (2): 313-24.
	Shisa promotes head formation through the inhibition of receptor protein maturation for the caudalizing factors, Wnt and FGF., Yamamoto A., Cell. January 28, 2005; 120 (2): 223-35.
	Nuclear localization is required for Dishevelled function in Wnt/beta-catenin signaling., Itoh K., J Biol. January 1, 2005; 4 (1): 3.
	MAB21L2, a vertebrate member of the Male-abnormal 21 family, modulates BMP signaling and interacts with SMAD1., Baldessari D., BMC Cell Biol. December 21, 2004; 5 (1): 48.
	Six1 promotes a placodal fate within the lateral neurogenic ectoderm by functioning as both a transcriptional activator and repressor., Brugmann SA., Development. December 1, 2004; 131 (23): 5871-81.
	Negative regulation of Smad2 by PIASy is required for proper Xenopus mesoderm formation., Daniels M., Development. November 1, 2004; 131 (22): 5613-26.
	XSIP1 is essential for early neural gene expression and neural differentiation by suppression of BMP signaling., Nitta KR., Dev Biol. November 1, 2004; 275 (1): 258-67.

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