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

Papers associated with primary germ layer (and rab40b)

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Znf703 is a novel RA target in the neural plate border., Janesick A., Sci Rep. June 4, 2019; 9 (1): 8275.


Peroxiredoxin1, a novel regulator of pronephros development, influences retinoic acid and Wnt signaling by controlling ROS levels., Chae S., Sci Rep. August 21, 2017; 7 (1): 8874.                    


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.                                  


Zic1 controls placode progenitor formation non-cell autonomously by regulating retinoic acid production and transport., Jaurena MB., Nat Commun. June 23, 2015; 6 7476.            


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.                    


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.                


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.                          


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.              


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.        


Two isoforms of Xenopus retinoic acid receptor gamma 2 (B) exhibit differential expression and sensitivity to retinoic acid during embryogenesis., Crawford MJ., Dev Genet. January 1, 1995; 17 (4): 291-302.


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.          


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.


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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