Papers associated with eye (and vax2)

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	Physiological effects of KDM5C on neural crest migration and eye formation during vertebrate development., Kim Y., Epigenetics Chromatin. December 6, 2018; 11 (1): 72.
	Nosip functions during vertebrate eye and cranial cartilage development., Flach H., Dev Dyn. September 1, 2018; 247 (9): 1070-1082.
	Dorsoventral patterning of the Xenopus eye involves differential temporal changes in the response of optic stalk and retinal progenitors to Hh signalling., Wang X., Neural Dev. March 20, 2015; 10 7.
	Fgfr signaling is required as the early eye field forms to promote later patterning and morphogenesis of the eye., Atkinson-Leadbeater K., Dev Dyn. May 1, 2014; .
	Bcl6a function is required during optic cup formation to prevent p53-dependent apoptosis and colobomata., Lee J., Hum Mol Genet. September 1, 2013; 22 (17): 3568-82.
	Identification and expression analysis of GPAT family genes during early development of Xenopus laevis., Bertolesi GE., Gene Expr Patterns. January 1, 2012; 12 (7-8): 219-27.
	A novel mechanism for the transcriptional regulation of Wnt signaling in development., Vacik T., Genes Dev. September 1, 2011; 25 (17): 1783-95.
	Peptidyl-prolyl cis-trans isomerase xFKBP1B induces ectopic secondary axis and is involved in eye formation during Xenopus embryogenesis., Terukina G., Dev Growth Differ. January 1, 2011; 53 (1): 55-68.
	Sonic hedgehog is involved in formation of the ventral optic cup by limiting Bmp4 expression to the dorsal domain., Zhao L., Mech Dev. January 1, 2010; 127 (1-2): 62-72.
	A role for Xvax2 in controlling proliferation of Xenopus ventral eye and brain progenitors., Liu M., Dev Dyn. November 1, 2008; 237 (11): 3387-93.
	Genetic analysis of metamorphic and premetamorphic Xenopus ciliary marginal zone., Casarosa S., Dev Dyn. June 1, 2005; 233 (2): 646-51.
	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.
	Tbx12 regulates eye development in Xenopus embryos., Carson CT., Biochem Biophys Res Commun. May 28, 2004; 318 (2): 485-9.
	Catalase and peroxiredoxin 5 protect Xenopus embryos against alcohol-induced ocular anomalies., Peng Y., Invest Ophthalmol Vis Sci. January 1, 2004; 45 (1): 23-9.
	Expression of recombinant XVAX2 peptide-104 of Xenopus laevis and preparation of the antibody., Liu Y., Protein Pept Lett. April 1, 2003; 10 (2): 213-9.
	A novel function for Hedgehog signalling in retinal pigment epithelium differentiation., Perron M., Development. April 1, 2003; 130 (8): 1565-77.
	Hedgehog signalling maintains the optic stalk-retinal interface through the regulation of Vax gene activity., Take-uchi M., Development. March 1, 2003; 130 (5): 955-68.
	Topographic mapping in dorsoventral axis of the Xenopus retinotectal system depends on signaling through ephrin-B ligands., Mann F., Neuron. August 1, 2002; 35 (3): 461-73.
	Axes establishment during eye morphogenesis in Xenopus by coordinate and antagonistic actions of BMP4, Shh, and RA., Sasagawa S., Genesis. June 1, 2002; 33 (2): 86-96.
	Vax2 inactivation in mouse determines alteration of the eye dorsal-ventral axis, misrouting of the optic fibres and eye coloboma., Barbieri AM., Development. February 1, 2002; 129 (3): 805-13.
	Expression of the Xvax2 gene demarcates presumptive ventral telencephalon and specific visual structures in Xenopus laevis., Liu Y., Mech Dev. January 1, 2001; 100 (1): 115-8.
	Homeobox genes in the genetic control of eye development., Lupo G., Int J Dev Biol. January 1, 2000; 44 (6): 627-36.
	A homeobox gene, vax2, controls the patterning of the eye dorsoventral axis., Barbieri AM., Proc Natl Acad Sci U S A. September 14, 1999; 96 (19): 10729-34.
	Expression of the Vax family homeobox genes suggests multiple roles in eye development., Ohsaki K., Genes Cells. May 1, 1999; 4 (5): 267-76.

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