Papers associated with posterior (and rab40b)

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	Alteration of the Retinoid Acid-CBP Signaling Pathway in Neural Crest Induction Contributes to Enteric Nervous System Disorder., Li C., Front Pediatr. December 3, 2018; 6 382.
	RARβ2 is required for vertebrate somitogenesis., Janesick A., Development. June 1, 2017; 144 (11): 1997-2008.
	Zic1 controls placode progenitor formation non-cell autonomously by regulating retinoic acid production and transport., Jaurena MB., Nat Commun. June 23, 2015; 6 7476.
	Active repression by RARγ signaling is required for vertebrate axial elongation., Janesick A., Development. June 1, 2014; 141 (11): 2260-70.
	ERF and ETV3L are retinoic acid-inducible repressors required for primary neurogenesis., Janesick A., Development. August 1, 2013; 140 (15): 3095-106.
	Chemical activation of RARβ induces post-embryonically bilateral limb duplication during Xenopus limb regeneration., Cuervo R., Sci Rep. January 1, 2013; 3 1886.
	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.
	Analyzing the function of a hox gene: an evolutionary approach., Michaut L., Dev Growth Differ. December 1, 2011; 53 (9): 982-93.
	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.
	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.
	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.
	Spatiotemporal retinoid-X receptor activation detected in live vertebrate embryos., Luria A., Proc Natl Acad Sci U S A. June 15, 2004; 101 (24): 8987-92.
	Multiple points of interaction between retinoic acid and FGF signaling during embryonic axis formation., Shiotsugu J., Development. June 1, 2004; 131 (11): 2653-67.
	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.
	Inhibition of retinoic acid receptor-mediated signalling alters positional identity in the developing hindbrain., van der Wees J., Development. February 1, 1998; 125 (3): 545-56.
	Xenopus hindbrain patterning requires retinoid signaling., Kolm PJ., Dev Biol. December 1, 1997; 192 (1): 1-16.
	Retinoid X receptor-selective ligands produce malformations in Xenopus embryos., Minucci S., Proc Natl Acad Sci U S A. March 5, 1996; 93 (5): 1803-7.
	Retinoic acid receptors and nuclear orphan receptors in the development of Xenopus laevis., Dreyer C., Int J Dev Biol. February 1, 1996; 40 (1): 255-62.
	Regional specificity of RAR gamma isoforms in Xenopus development., Pfeffer PL., Mech Dev. February 1, 1994; 45 (2): 147-53.
	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.
	A retinoic acid receptor expressed in the early development of Xenopus laevis., Ellinger-Ziegelbauer H., Genes Dev. January 1, 1991; 5 (1): 94-104.

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