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Summary Anatomy Item Literature (6278) Expression Attributions Wiki
XB-ANAT-475

Papers associated with primary germ layer (and rara)

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Retinoic acid control of pax8 during renal specification of Xenopus pronephros involves hox and meis3., Durant-Vesga J., Dev Biol. January 1, 2023; 493 17-28.


Characterising open chromatin in chick embryos identifies cis-regulatory elements important for paraxial mesoderm formation and axis extension., Mok GF., Nat Commun. February 19, 2021; 12 (1): 1157.              


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.                                            


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.                  


Global analysis of RAR-responsive genes in the Xenopus neurula using cDNA microarrays., Arima K., Dev Dyn. February 1, 2005; 232 (2): 414-31.                          


Identification of 3,4-didehydroretinal isomers in the Xenopus tadpole tail fin containing photosensitive melanophores., Okano K., Zoolog Sci. February 1, 2002; 19 (2): 191-5.


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.              


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.


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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