Papers associated with embryonic structure (and rab40b)

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	RARβ2 is required for vertebrate somitogenesis., Janesick A., Development. June 1, 2017; 144 (11): 1997-2008.
	A Retinoic Acid-Hedgehog Cascade Coordinates Mesoderm-Inducing Signals and Endoderm Competence during Lung Specification., Rankin SA, Rankin SA., Cell Rep. June 28, 2016; 16 (1): 66-78.
	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.
	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.
	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.
	Disruption of RAB40AL function leads to Martin--Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder., Bedoyan JK., J Med Genet. May 1, 2012; 49 (5): 332-40.
	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.
	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.
	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.
	Retinoid signaling can repress blastula Wnt signaling and impair dorsal development in Xenopus embryo., Li S., Differentiation. October 1, 2008; 76 (8): 897-907.
	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.
	Retinoic acid signalling is required for specification of pronephric cell fate., Cartry J., Dev Biol. November 1, 2006; 299 (1): 35-51.
	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.
	Active repression of RAR signaling is required for head formation., Koide T., Genes Dev. August 15, 2001; 15 (16): 2111-21.
	Molecular cloning of xSRC-3, a novel transcription coactivator from Xenopus, that is related to AIB1, p/CIP, and TIF2., Kim HJ., Mol Endocrinol. July 1, 1998; 12 (7): 1038-47.
	Xenopus hindbrain patterning requires retinoid signaling., Kolm PJ., Dev Biol. December 1, 1997; 192 (1): 1-16.
	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.
	The androgen receptor mRNA is up-regulated by testosterone in both the Harderian gland and thumb pad of the frog, Rana esculenta., Varriale B., J Steroid Biochem Mol Biol. December 1, 1994; 51 (5-6): 259-65.
	Regional specificity of RAR gamma isoforms in Xenopus development., Pfeffer PL., Mech Dev. February 1, 1994; 45 (2): 147-53.
	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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