Papers associated with embryonic structure (and rara)

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	Retinoic acid-induced expression of Hnf1b and Fzd4 is required for pancreas development in Xenopus laevis., Gere-Becker MB., Development. June 8, 2018; 145 (12):
	A molecular atlas of the developing ectoderm defines neural, neural crest, placode, and nonneural progenitor identity in vertebrates., Plouhinec JL., PLoS Biol. October 19, 2017; 15 (10): e2004045.
	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.
	The role of folate metabolism in orofacial development and clefting., Wahl SE., Dev Biol. September 1, 2015; 405 (1): 108-22.
	The evolutionarily conserved transcription factor PRDM12 controls sensory neuron development and pain perception., Nagy V., Cell Cycle. January 1, 2015; 14 (12): 1799-808.
	Pax3 and Zic1 trigger the early neural crest gene regulatory network by the direct activation of multiple key neural crest specifiers., Plouhinec JL., Dev Biol. February 15, 2014; 386 (2): 461-72.
	ERF and ETV3L are retinoic acid-inducible repressors required for primary neurogenesis., Janesick A., Development. August 1, 2013; 140 (15): 3095-106.
	Developmental expression of retinoic acid receptors (RARs)., Dollé P., Nucl Recept Signal. May 12, 2009; 7 e006.
	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.
	Regulation of estrogen receptors in primary cultured hepatocytes of the amphibian Xenopus laevis as estrogenic biomarker and its application in environmental monitoring., Lutz I., Comp Biochem Physiol C Toxicol Pharmacol. August 1, 2005; 141 (4): 384-92.
	Global analysis of RAR-responsive genes in the Xenopus neurula using cDNA microarrays., Arima K., Dev Dyn. February 1, 2005; 232 (2): 414-31.
	Active repression of RAR signaling is required for head formation., Koide T., Genes Dev. August 15, 2001; 15 (16): 2111-21.
	The early expression control of Xepsin by nonaxial and planar posteriorizing signals in Xenopus epidermis., Yamada K., Dev Biol. October 15, 1999; 214 (2): 318-30.
	A Meis family protein caudalizes neural cell fates in Xenopus., Salzberg A., Mech Dev. January 1, 1999; 80 (1): 3-13.
	Mesoderm and endoderm differentiation in animal cap explants: identification of the HNF4-binding site as an activin A responsive element in the Xenopus HNF1alpha promoter., Weber H., Development. June 1, 1996; 122 (6): 1975-84.
	Cardiac troponin I is a heart-specific marker in the Xenopus embryo: expression during abnormal heart morphogenesis., Drysdale TA., Dev Biol. October 1, 1994; 165 (2): 432-41.
	Regional specificity of RAR gamma isoforms in Xenopus development., Pfeffer PL., Mech Dev. February 1, 1994; 45 (2): 147-53.
	Retinoic acid induces changes in the localization of homeobox proteins in the antero-posterior axis of Xenopus laevis embryos., López SL., Mech Dev. February 1, 1992; 36 (3): 153-64.

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