Papers associated with neurogenic placode (and bmp4)

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	Differential requirement of bone morphogenetic protein receptors Ia (ALK3) and Ib (ALK6) in early embryonic patterning and neural crest development., Schille C., BMC Dev Biol. January 19, 2016; 16 1.
	Functional analysis of Hairy genes in Xenopus neural crest initial specification and cell migration., Vega-López GA., Dev Dyn. August 1, 2015; 244 (8): 988-1013.
	The requirement of histone modification by PRDM12 and Kdm4a for the development of pre-placodal ectoderm and neural crest in Xenopus., Matsukawa S., Dev Biol. March 1, 2015; 399 (1): 164-176.
	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; .
	Semicircular canal morphogenesis in the zebrafish inner ear requires the function of gpr126 (lauscher), an adhesion class G protein-coupled receptor gene., Geng FS., Development. November 1, 2013; 140 (21): 4362-74.
	Transcription factors involved in lens development from the preplacodal ectoderm., Ogino H., Dev Biol. March 15, 2012; 363 (2): 333-47.
	Williams Syndrome Transcription Factor is critical for neural crest cell function in Xenopus laevis., Barnett C., Mech Dev. January 1, 2012; 129 (9-12): 324-38.
	Bmp indicator mice reveal dynamic regulation of transcriptional response., Javier AL., PLoS One. January 1, 2012; 7 (9): e42566.
	Novel functions of Noggin proteins: inhibition of Activin/Nodal and Wnt signaling., Bayramov AV., Development. December 1, 2011; 138 (24): 5345-56.
	Bisphenol A induces otolith malformations during vertebrate embryogenesis., Gibert Y., BMC Dev Biol. January 26, 2011; 11 4.
	Microarray identification of novel downstream targets of FoxD4L1/D5, a critical component of the neural ectodermal transcriptional network., Yan B., Dev Dyn. December 1, 2010; 239 (12): 3467-80.
	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.
	Neural crest migration requires the activity of the extracellular sulphatases XtSulf1 and XtSulf2., Guiral EC., Dev Biol. May 15, 2010; 341 (2): 375-88.
	Long-term consequences of Sox9 depletion on inner ear development., Park BY., Dev Dyn. April 1, 2010; 239 (4): 1102-12.
	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.
	Vestigial like gene family expression in Xenopus: common and divergent features with other vertebrates., Faucheux C., Int J Dev Biol. January 1, 2010; 54 (8-9): 1375-82.
	LIMK1 acts downstream of BMP signaling in developing retinal ganglion cell axons but not dendrites., Hocking JC., Dev Biol. June 15, 2009; 330 (2): 273-85.
	DM-GRASP/ALCAM/CD166 is required for cardiac morphogenesis and maintenance of cardiac identity in first heart field derived cells., Gessert S., Dev Biol. September 1, 2008; 321 (1): 150-61.
	Extracellular regulation of developmental cell signaling by XtSulf1., Freeman SD., Dev Biol. August 15, 2008; 320 (2): 436-45.
	Requirement for Wnt and FGF signaling in Xenopus tadpole tail regeneration., Lin G., Dev Biol. April 15, 2008; 316 (2): 323-35.
	Expression of Bmp ligands and receptors in the developing Xenopus retina., Hocking JC., Int J Dev Biol. January 1, 2007; 51 (2): 161-5.
	Novel gene ashwin functions in Xenopus cell survival and anteroposterior patterning., Patil SS., Dev Dyn. July 1, 2006; 235 (7): 1895-907.
	RE-1 silencer of transcription/neural restrictive silencer factor modulates ectodermal patterning during Xenopus development., Olguín P., J Neurosci. March 8, 2006; 26 (10): 2820-9.
	The zic1 gene is an activator of Wnt signaling., Merzdorf CS., Int J Dev Biol. January 1, 2006; 50 (7): 611-7.
	Tsukushi controls ectodermal patterning and neural crest specification in Xenopus by direct regulation of BMP4 and X-delta-1 activity., Kuriyama S., Development. January 1, 2006; 133 (1): 75-88.
	Tissues and signals involved in the induction of placodal Six1 expression in Xenopus laevis., Ahrens K., Dev Biol. December 1, 2005; 288 (1): 40-59.
	Xnr2 and Xnr5 unprocessed proteins inhibit Wnt signaling upstream of dishevelled., Onuma Y., Dev Dyn. December 1, 2005; 234 (4): 900-10.
	An essential role of Xenopus Foxi1a for ventral specification of the cephalic ectoderm during gastrulation., Matsuo-Takasaki M., Development. September 1, 2005; 132 (17): 3885-94.
	An atlas of differential gene expression during early Xenopus embryogenesis., Pollet N., Mech Dev. March 1, 2005; 122 (3): 365-439.
	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.
	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.
	dlx3b and dlx4b function in the development of Rohon-Beard sensory neurons and trigeminal placode in the zebrafish neurula., Kaji T., Dev Biol. December 15, 2004; 276 (2): 523-40.
	Pbx genes are required in Xenopus lens development., Morgan R., Int J Dev Biol. September 1, 2004; 48 (7): 623-7.
	Specification of the otic placode depends on Sox9 function in Xenopus., Saint-Germain N., Development. April 1, 2004; 131 (8): 1755-63.
	Regulation of vertebrate eye development by Rx genes., Bailey TJ., Int J Dev Biol. January 1, 2004; 48 (8-9): 761-70.
	Cloning and characterization of Xenopus Id4 reveals differing roles for Id genes., Liu KJ, Liu KJ., Dev Biol. December 15, 2003; 264 (2): 339-51.
	Xenopus X-box binding protein 1, a leucine zipper transcription factor, is involved in the BMP signaling pathway., Zhao H., Dev Biol. May 15, 2003; 257 (2): 278-91.
	The Dlx5 homeobox gene is essential for vestibular morphogenesis in the mouse embryo through a BMP4-mediated pathway., Merlo GR., Dev Biol. August 1, 2002; 248 (1): 157-69.
	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.
	The Xiro-repressed gene CoREST is expressed in Xenopus neural territories., de la Calle-Mustienes E., Mech Dev. January 1, 2002; 110 (1-2): 209-11.
	Transcription factors of the anterior neural plate alter cell movements of epidermal progenitors to specify a retinal fate., Kenyon KL., Dev Biol. December 1, 2001; 240 (1): 77-91.
	Transgenic Xenopus embryos reveal that anterior neural development requires continued suppression of BMP signaling after gastrulation., Hartley KO., Dev Biol. October 1, 2001; 238 (1): 168-84.
	Origins of inner ear sensory organs revealed by fate map and time-lapse analyses., Kil SH., Dev Biol. May 15, 2001; 233 (2): 365-79.
	Activation of Stat3 by cytokine receptor gp130 ventralizes Xenopus embryos independent of BMP-4., Nishinakamura R., Dev Biol. December 15, 1999; 216 (2): 481-90.
	Animal-vegetal asymmetries influence the earliest steps in retina fate commitment in Xenopus., Moore KB., Dev Biol. August 1, 1999; 212 (1): 25-41.
	Xenopus GDF6, a new antagonist of noggin and a partner of BMPs., Chang C., Development. August 1, 1999; 126 (15): 3347-57.
	Geminin, a neuralizing molecule that demarcates the future neural plate at the onset of gastrulation., Kroll KL., Development. August 1, 1998; 125 (16): 3247-58.
	Xenopus Smad8 acts downstream of BMP-4 to modulate its activity during vertebrate embryonic patterning., Nakayama T., Development. March 1, 1998; 125 (5): 857-67.
	A Xenopus gene, Xbr-1, defines a novel class of homeobox genes and is expressed in the dorsal ciliary margin of the eye., Papalopulu N., Dev Biol. February 25, 1996; 174 (1): 104-14.

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