Papers associated with ectoderm (and rab40b)

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	Using frogs faces to dissect the mechanisms underlying human orofacial defects., Dickinson AJ., Semin Cell Dev Biol. March 1, 2016; 51 54-63.
	The role of folate metabolism in orofacial development and clefting., Wahl SE., Dev Biol. September 1, 2015; 405 (1): 108-22.
	Heat shock 70-kDa protein 5 (Hspa5) is essential for pronephros formation by mediating retinoic acid signaling., Shi W., J Biol Chem. January 2, 2015; 290 (1): 577-89.
	Retinoic acid induced-1 (Rai1) regulates craniofacial and brain development in Xenopus., Tahir R., Mech Dev. August 1, 2014; 133 91-104.
	ERF and ETV3L are retinoic acid-inducible repressors required for primary neurogenesis., Janesick A., Development. August 1, 2013; 140 (15): 3095-106.
	Median facial clefts in Xenopus laevis: roles of retinoic acid signaling and homeobox genes., Kennedy AE., Dev Biol. May 1, 2012; 365 (1): 229-40.
	RIPPLY3 is a retinoic acid-inducible repressor required for setting the borders of the pre-placodal ectoderm., Janesick A., Development. March 1, 2012; 139 (6): 1213-24.
	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.
	Retinoid signalling is required for information transfer from mesoderm to neuroectoderm during gastrulation., Lloret-Vilaspasa F., Int J Dev Biol. January 1, 2010; 54 (4): 599-608.
	Developmental expression of retinoic acid receptors (RARs)., Dollé P., Nucl Recept Signal. May 12, 2009; 7 e006.
	A microarray screen for direct targets of Zic1 identifies an aquaporin gene, aqp-3b, expressed in the neural folds., Cornish EJ., Dev Dyn. May 1, 2009; 238 (5): 1179-94.
	Arsenic as an endocrine disruptor: arsenic disrupts retinoic acid receptor-and thyroid hormone receptor-mediated gene regulation and thyroid hormone-mediated amphibian tail metamorphosis., Davey JC., Environ Health Perspect. February 1, 2008; 116 (2): 165-72.
	Neofunctionalization in vertebrates: the example of retinoic acid receptors., Escriva H., PLoS Genet. July 1, 2006; 2 (7): e102.
	Global analysis of RAR-responsive genes in the Xenopus neurula using cDNA microarrays., Arima K., Dev Dyn. February 1, 2005; 232 (2): 414-31.
	The germ cell nuclear factor is required for retinoic acid signaling during Xenopus development., Barreto G., Mech Dev. April 1, 2003; 120 (4): 415-28.
	Active repression of RAR signaling is required for head formation., Koide T., Genes Dev. August 15, 2001; 15 (16): 2111-21.
	Xenopus hindbrain patterning requires retinoid signaling., Kolm PJ., Dev Biol. December 1, 1997; 192 (1): 1-16.
	Endogenous retinoic acid receptor (RAR)-retinoid X receptor (RXR) heterodimers are the major functional forms regulating retinoid-responsive elements in adult human keratinocytes. Binding of ligands to RAR only is sufficient for RAR-RXR heterodimers to confer ligand-dependent activation of hRAR beta 2/RARE (DR5)., Xiao JH., J Biol Chem. February 17, 1995; 270 (7): 3001-11.
	Characterization of cDNAs encoding the chick retinoic acid receptor gamma 2 and preferential distribution of retinoic acid receptor gamma transcripts during chick skin development., Michaille JJ., Dev Dyn. December 1, 1994; 201 (4): 334-43.
	The pattern of retinoic acid receptor gamma (RAR gamma) expression in normal development of Xenopus laevis and after manipulation of the main body axis., Ellinger-Ziegelbauer H., Mech Dev. April 1, 1993; 41 (1): 33-46.
	Two isoforms of retinoic acid receptor alpha expressed during Xenopus development respond to retinoic acid., Sharpe CR., Mech Dev. November 1, 1992; 39 (1-2): 81-93.

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