Papers associated with optic vesicle (and gal.2)

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	RFX7 is required for the formation of cilia in the neural tube., Manojlovic Z., Mech Dev. May 1, 2014; 132 28-37.
	The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.
	Polycomb repressive complex PRC2 regulates Xenopus retina development downstream of Wnt/β-catenin signaling., Aldiri I., Development. July 1, 2013; 140 (14): 2867-78.
	Pax3 and Zic1 drive induction and differentiation of multipotent, migratory, and functional neural crest in Xenopus embryos., Milet C., Proc Natl Acad Sci U S A. April 2, 2013; 110 (14): 5528-33.
	Tet3 CXXC domain and dioxygenase activity cooperatively regulate key genes for Xenopus eye and neural development., Xu Y, Xu Y., Cell. December 7, 2012; 151 (6): 1200-13.
	Short chain dehydrogenase/reductase rdhe2 is a novel retinol dehydrogenase essential for frog embryonic development., Belyaeva OV., J Biol Chem. March 16, 2012; 287 (12): 9061-71.
	The RNA-binding protein XSeb4R regulates maternal Sox3 at the posttranscriptional level during maternal-zygotic transition in Xenopus., Bentaya S., Dev Biol. March 15, 2012; 363 (2): 362-72.
	Hyaluronan is required for cranial neural crest cells migration and craniofacial development., Casini P., Dev Dyn. February 1, 2012; 241 (2): 294-302.
	Transmembrane voltage potential controls embryonic eye patterning in Xenopus laevis., Pai VP., Development. January 1, 2012; 139 (2): 313-23.
	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.
	Bmp indicator mice reveal dynamic regulation of transcriptional response., Javier AL., PLoS One. January 1, 2012; 7 (9): e42566.
	V-ATPase-dependent ectodermal voltage and pH regionalization are required for craniofacial morphogenesis., Vandenberg LN., Dev Dyn. August 1, 2011; 240 (8): 1889-904.
	Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice., Rainger J., PLoS Genet. July 1, 2011; 7 (7): e1002114.
	Transmembrane potential of GlyCl-expressing instructor cells induces a neoplastic-like conversion of melanocytes via a serotonergic pathway., Blackiston D., Dis Model Mech. January 1, 2011; 4 (1): 67-85.
	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.
	Gadd45a and Gadd45g regulate neural development and exit from pluripotency in Xenopus., Kaufmann LT., Mech Dev. January 1, 2011; 128 (7-10): 401-11.
	The RNA-binding protein Xp54nrb isolated from a Ca²+-dependent screen is expressed in neural structures during Xenopus laevis development., Neant I., Int J Dev Biol. January 1, 2011; 55 (10-12): 923-31.
	Prohibitin1 acts as a neural crest specifier in Xenopus development by repressing the transcription factor E2F1., Schneider M., Development. December 1, 2010; 137 (23): 4073-81.
	Sumoylation controls retinal progenitor proliferation by repressing cell cycle exit in Xenopus laevis., Terada K., Dev Biol. November 1, 2010; 347 (1): 180-94.
	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.
	XPteg (Xenopus proximal tubules-expressed gene) is essential for pronephric mesoderm specification and tubulogenesis., Lee SJ., Mech Dev. January 1, 2010; 127 (1-2): 49-61.
	Involvement of an inner nuclear membrane protein, Nemp1, in Xenopus neural development through an interaction with the chromatin protein BAF., Mamada H., Dev Biol. March 15, 2009; 327 (2): 497-507.
	The role of Xenopus Rx-L in photoreceptor cell determination., Wu HY., Dev Biol. March 15, 2009; 327 (2): 352-65.
	Modulation of potassium channel function confers a hyperproliferative invasive phenotype on embryonic stem cells., Morokuma J., Proc Natl Acad Sci U S A. October 28, 2008; 105 (43): 16608-13.
	Expression cloning in Xenopus identifies RNA-binding proteins as regulators of embryogenesis and Rbmx as necessary for neural and muscle development., Dichmann DS., Dev Dyn. July 1, 2008; 237 (7): 1755-66.
	Pleiotropic effects in Eya3 knockout mice., Söker T., BMC Dev Biol. June 23, 2008; 8 118.
	The POU homeobox protein Oct-1 regulates radial glia formation downstream of Notch signaling., Kiyota T., Dev Biol. March 15, 2008; 315 (2): 579-92.
	Dicer inactivation causes heterochronic retinogenesis in Xenopus laevis., Decembrini S., Int J Dev Biol. January 1, 2008; 52 (8): 1099-103.
	Retinoic acid metabolizing factor xCyp26c is specifically expressed in neuroectoderm and regulates anterior neural patterning in Xenopus laevis., Tanibe M., Int J Dev Biol. January 1, 2008; 52 (7): 893-901.
	Xenopus galectin-VIa shows highly specific expression in cement glands and is regulated by canonical Wnt signaling., Michiue T., Gene Expr Patterns. October 1, 2007; 7 (8): 852-7.
	Ets-1 regulates radial glia formation during vertebrate embryogenesis., Kiyota T., Organogenesis. October 1, 2007; 3 (2): 93-101.
	Alterations of rx1 and pax6 expression levels at neural plate stages differentially affect the production of retinal cell types and maintenance of retinal stem cell qualities., Zaghloul NA., Dev Biol. June 1, 2007; 306 (1): 222-40.
	The competence of Xenopus blastomeres to produce neural and retinal progeny is repressed by two endo-mesoderm promoting pathways., Yan B., Dev Biol. May 1, 2007; 305 (1): 103-19.
	PP2A:B56epsilon is required for eye induction and eye field separation., Rorick AM., Dev Biol. February 15, 2007; 302 (2): 477-93.
	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.
	Smurf1 regulates neural patterning and folding in Xenopus embryos by antagonizing the BMP/Smad1 pathway., Alexandrova EM., Dev Biol. November 15, 2006; 299 (2): 398-410.
	Kermit 2/XGIPC, an IGF1 receptor interacting protein, is required for IGF signaling in Xenopus eye development., Wu J., Development. September 1, 2006; 133 (18): 3651-60.
	Metastasis-associated kinase modulates Wnt signaling to regulate brain patterning and morphogenesis., Kibardin A., Development. August 1, 2006; 133 (15): 2845-54.
	Nucleosome regulator Xhmgb3 is required for cell proliferation of the eye and brain as a downstream target of Xenopus rax/Rx1., Terada K., Dev Biol. March 15, 2006; 291 (2): 398-412.
	Dystroglycan is required for proper retinal layering., Lunardi A., Dev Biol. February 15, 2006; 290 (2): 411-20.
	Noelins modulate the timing of neuronal differentiation during development., Moreno TA., Dev Biol. December 15, 2005; 288 (2): 434-47.
	The assembly of POSH-JNK regulates Xenopus anterior neural development., Kim GH., Dev Biol. October 1, 2005; 286 (1): 256-69.
	Identification of shared transcriptional targets for the proneural bHLH factors Xath5 and XNeuroD., Logan MA., Dev Biol. September 15, 2005; 285 (2): 570-83.
	Dorsoventral patterning of the Xenopus eye: a collaboration of Retinoid, Hedgehog and FGF receptor signaling., Lupo G., Development. April 1, 2005; 132 (7): 1737-48.
	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.
	Olfactory and lens placode formation is controlled by the hedgehog-interacting protein (Xhip) in Xenopus., Cornesse Y., Dev Biol. January 15, 2005; 277 (2): 296-315.
	Xantivin suppresses the activity of EGF-CFC genes to regulate nodal signaling., Tanegashima K., Int J Dev Biol. June 1, 2004; 48 (4): 275-83.
	XIdax, an inhibitor of the canonical Wnt pathway, is required for anterior neural structure formation in Xenopus., Michiue T., Dev Dyn. May 1, 2004; 230 (1): 79-90.
	Evolution of neural precursor selection: functional divergence of proneural proteins., Quan XJ., Development. April 1, 2004; 131 (8): 1679-89.
	Morphogenetic movements underlying eye field formation require interactions between the FGF and ephrinB1 signaling pathways., Moore KB., Dev Cell. January 1, 2004; 6 (1): 55-67.

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