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Summary Anatomy Item Literature (2349) Expression Attributions Wiki
XB-ANAT-4083

Papers associated with tadpole (and foxg1)

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The Secreted Protein Disulfide Isomerase Ag1 Lost by Ancestors of Poorly Regenerating Vertebrates Is Required for Xenopus laevis Tail Regeneration., Ivanova AS., Front Cell Dev Biol. January 1, 2021; 9 738940.                  


R-spondins are BMP receptor antagonists in Xenopus early embryonic development., Lee H, Lee H., Nat Commun. November 4, 2020; 11 (1): 5570.                                            


DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain., Kyono Y., Dev Biol. June 15, 2020; 462 (2): 180-196.                                                    


The tumor suppressor PTPRK promotes ZNRF3 internalization and is required for Wnt inhibition in the Spemann organizer., Chang LS., Elife. January 14, 2020; 9                                                                                               


Modeling Bainbridge-Ropers Syndrome in Xenopus laevis Embryos., Lichtig H., Front Physiol. January 1, 2020; 11 75.                    


HCN2 Channel-Induced Rescue of Brain Teratogenesis via Local and Long-Range Bioelectric Repair., Pai VP., Front Cell Neurosci. January 1, 2020; 14 136.                      


Bioinformatics Screening of Genes Specific for Well-Regenerating Vertebrates Reveals c-answer, a Regulator of Brain Development and Regeneration., Korotkova DD., Cell Rep. October 22, 2019; 29 (4): 1027-1040.e6.                              


Head formation requires Dishevelled degradation that is mediated by March2 in concert with Dapper1., Lee H, Lee H., Development. April 10, 2018; 145 (7):               


HCN2 Rescues brain defects by enforcing endogenous voltage pre-patterns., Pai VP., Nat Commun. March 8, 2018; 9 (1): 998.                        


Gene expression of the two developmentally regulated dermatan sulfate epimerases in the Xenopus embryo., Gouignard N., PLoS One. January 18, 2018; 13 (1): e0191751.                                                          


Tbx2 regulates anterior neural specification by repressing FGF signaling pathway., Cho GS., Dev Biol. January 15, 2017; 421 (2): 183-193.              


Tbx3 represses bmp4 expression and, with Pax6, is required and sufficient for retina formation., Motahari Z., Development. October 1, 2016; 143 (19): 3560-3572.                                      


Noggin4 is a long-range inhibitor of Wnt8 signalling that regulates head development in Xenopus laevis., Eroshkin FM., Sci Rep. January 22, 2016; 6 23049.                                                            


The small leucine-rich repeat secreted protein Asporin induces eyes in Xenopus embryos through the IGF signalling pathway., Luehders K., Development. October 1, 2015; 142 (19): 3351-61.                              


Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation., Zhang X., Dev Cell. March 23, 2015; 32 (6): 719-30.                                  


The serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation., Acosta H., Development. March 15, 2015; 142 (6): 1146-58.                                    


Endogenous gradients of resting potential instructively pattern embryonic neural tissue via Notch signaling and regulation of proliferation., Pai VP., J Neurosci. March 11, 2015; 35 (10): 4366-85.                    


Xenopus laevis FGF receptor substrate 3 (XFrs3) is important for eye development and mediates Pax6 expression in lens placode through its Shp2-binding sites., Kim YJ., Dev Biol. January 1, 2015; 397 (1): 129-39.                                          


Xenopus mutant reveals necessity of rax for specifying the eye field which otherwise forms tissue with telencephalic and diencephalic character., Fish MB., Dev Biol. November 15, 2014; 395 (2): 317-330.                  


Cholesterol selectively activates canonical Wnt signalling over non-canonical Wnt signalling., Sheng R., Nat Commun. July 15, 2014; 5 4393.              


Ras-dva1 small GTPase regulates telencephalon development in Xenopus laevis embryos by controlling Fgf8 and Agr signaling at the anterior border of the neural plate., Tereshina MB., Biol Open. March 15, 2014; 3 (3): 192-203.                        


Role of Sp5 as an essential early regulator of neural crest specification in xenopus., Park DS., Dev Dyn. December 1, 2013; 242 (12): 1382-94.                


The Xenopus doublesex-related gene Dmrt5 is required for olfactory placode neurogenesis., Parlier D., Dev Biol. January 1, 2013; 373 (1): 39-52.                              


Maternal xNorrin, a canonical Wnt signaling agonist and TGF-β antagonist, controls early neuroectoderm specification in Xenopus., Xu S., PLoS Biol. January 1, 2012; 10 (3): e1001286.                                    


xCOUP-TF-B regulates xCyp26 transcription and modulates retinoic acid signaling for anterior neural patterning in Xenopus., Tanibe M., Int J Dev Biol. January 1, 2012; 56 (4): 239-44.            


Novel functions of Noggin proteins: inhibition of Activin/Nodal and Wnt signaling., Bayramov AV., Development. December 1, 2011; 138 (24): 5345-56.              


The dual regulator Sufu integrates Hedgehog and Wnt signals in the early Xenopus embryo., Min TH., Dev Biol. October 1, 2011; 358 (1): 262-76.                            


Anterior neural development requires Del1, a matrix-associated protein that attenuates canonical Wnt signaling via the Ror2 pathway., Takai A., Development. October 1, 2010; 137 (19): 3293-302.            


A non-enzymatic function of 17beta-hydroxysteroid dehydrogenase type 10 is required for mitochondrial integrity and cell survival., Rauschenberger K., EMBO Mol Med. February 1, 2010; 2 (2): 51-62.                        


In vitro organogenesis from undifferentiated cells in Xenopus., Asashima M., Dev Dyn. June 1, 2009; 238 (6): 1309-20.                      


Retinol dehydrogenase 10 is a feedback regulator of retinoic acid signalling during axis formation and patterning of the central nervous system., Strate I., Development. February 1, 2009; 136 (3): 461-72.                


The secreted serine protease xHtrA1 stimulates long-range FGF signaling in the early Xenopus embryo., Hou S., Dev Cell. August 1, 2007; 13 (2): 226-41.                      


The homeodomain factor Xanf represses expression of genes in the presumptive rostral forebrain that specify more caudal brain regions., Ermakova GV., Dev Biol. July 15, 2007; 307 (2): 483-97.        


Kermit 2/XGIPC, an IGF1 receptor interacting protein, is required for IGF signaling in Xenopus eye development., Wu J., Development. September 1, 2006; 133 (18): 3651-60.          


Xenopus aristaless-related homeobox (xARX) gene product functions as both a transcriptional activator and repressor in forebrain development., Seufert DW., Dev Dyn. February 1, 2005; 232 (2): 313-24.                  


Of Fox and Frogs: Fox (fork head/winged helix) transcription factors in Xenopus development., Pohl BS., Gene. January 3, 2005; 344 21-32.      


Xantivin suppresses the activity of EGF-CFC genes to regulate nodal signaling., Tanegashima K., Int J Dev Biol. June 1, 2004; 48 (4): 275-83.          


Regulation of vertebrate eye development by Rx genes., Bailey TJ., Int J Dev Biol. January 1, 2004; 48 (8-9): 761-70.    


Xhex-expressing endodermal tissues are essential for anterior patterning in Xenopus., Smithers LE., Mech Dev. December 1, 2002; 119 (2): 191-200.            


Expression of the Xvax2 gene demarcates presumptive ventral telencephalon and specific visual structures in Xenopus laevis., Liu Y., Mech Dev. January 1, 2001; 100 (1): 115-8.                


Distinct effects of XBF-1 in regulating the cell cycle inhibitor p27(XIC1) and imparting a neural fate., Hardcastle Z., Development. March 1, 2000; 127 (6): 1303-14.                  


XBF-1, a winged helix transcription factor with dual activity, has a role in positioning neurogenesis in Xenopus competent ectoderm., Bourguignon C., Development. December 1, 1998; 125 (24): 4889-900.                  

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