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Summary Anatomy Item Literature (3673) Expression Attributions Wiki
XB-ANAT-490

Papers associated with tail (and egr2)

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The complete dorsal structure is formed from only the blastocoel roof of Xenopus blastula: insight into the gastrulation movement evolutionarily conserved among chordates., Sato Y., Dev Genes Evol. June 1, 2023; 233 (1): 1-12.                


Functions of block of proliferation 1 during anterior development in Xenopus laevis., Gärtner C., PLoS One. August 2, 2022; 17 (8): e0273507.                        


Lysosomes are required for early dorsal signaling in the Xenopus embryo., Tejeda-Muñoz N., Proc Natl Acad Sci U S A. April 26, 2022; 119 (17): e2201008119.                          


Bighead is a Wnt antagonist secreted by the Xenopus Spemann organizer that promotes Lrp6 endocytosis., Ding Y., Proc Natl Acad Sci U S A. September 25, 2018; 115 (39): E9135-E9144.                    


FoxD1 protein interacts with Wnt and BMP signaling to differentially pattern mesoderm and neural tissue., Polevoy H., Int J Dev Biol. January 1, 2017; 61 (3-4-5): 293-302.              


The positive transcriptional elongation factor (P-TEFb) is required for neural crest specification., Hatch VL., Dev Biol. August 15, 2016; 416 (2): 361-72.                                    


Prdm12 specifies V1 interneurons through cross-repressive interactions with Dbx1 and Nkx6 genes in Xenopus., Thélie A., Development. October 1, 2015; 142 (19): 3416-28.                                    


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.                                  


An essential role for LPA signalling in telencephalon development., Geach TJ., Development. February 1, 2014; 141 (4): 940-9.                            


Loss of Xenopus cadherin-11 leads to increased Wnt/β-catenin signaling and up-regulation of target genes c-myc and cyclin D1 in neural crest., Koehler A., Dev Biol. November 1, 2013; 383 (1): 132-45.                        


The Xenopus Tgfbi is required for embryogenesis through regulation of canonical Wnt signalling., Wang F., Dev Biol. July 1, 2013; 379 (1): 16-27.                            


An intact brachyury function is necessary to prevent spurious axial development in Xenopus laevis., Aguirre CE., PLoS One. January 1, 2013; 8 (1): e54777.                                      


Kcnh1 voltage-gated potassium channels are essential for early zebrafish development., Stengel R., J Biol Chem. October 12, 2012; 287 (42): 35565-35575.            


Self-regulation of the head-inducing properties of the Spemann organizer., Inui M., Proc Natl Acad Sci U S A. September 18, 2012; 109 (38): 15354-9.                            


Short chain dehydrogenase/reductase rdhe2 is a novel retinol dehydrogenase essential for frog embryonic development., Belyaeva OV., J Biol Chem. March 16, 2012; 287 (12): 9061-71.              


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.                            


xCITED2 Induces Neural Genes in Animal Cap Explants of Xenopus Embryos., Yoon J., Exp Neurobiol. September 1, 2011; 20 (3): 123-9.        


Focal adhesion kinase protein regulates Wnt3a gene expression to control cell fate specification in the developing neural plate., Fonar Y., Mol Biol Cell. July 1, 2011; 22 (13): 2409-21.                  


Rab3d is required for Xenopus anterior neurulation by regulating Noggin secretion., Kim H., Dev Dyn. June 1, 2011; 240 (6): 1430-9.              


Activity of the RhoU/Wrch1 GTPase is critical for cranial neural crest cell migration., Fort P., Dev Biol. February 15, 2011; 350 (2): 451-63.                      


A divergent Tbx6-related gene and Tbx6 are both required for neural crest and intermediate mesoderm development in Xenopus., Callery EM., Dev Biol. April 1, 2010; 340 (1): 75-87.                


Mad is required for wingless signaling in wing development and segment patterning in Drosophila., Eivers E., PLoS One. August 6, 2009; 4 (8): e6543.                    


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.                


VegT, eFGF and Xbra cause overall posteriorization while Xwnt8 causes eye-level restricted posteriorization in synergy with chordin in early Xenopus development., Fujii H., Dev Growth Differ. March 1, 2008; 50 (3): 169-80.                  


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 opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning., Sander V., EMBO J. June 20, 2007; 26 (12): 2955-65.              


Cholesterol homeostasis in development: the role of Xenopus 7-dehydrocholesterol reductase (Xdhcr7) in neural development., Tadjuidje E., Dev Dyn. August 1, 2006; 235 (8): 2095-110.                          


Novel gene ashwin functions in Xenopus cell survival and anteroposterior patterning., Patil SS., Dev Dyn. July 1, 2006; 235 (7): 1895-907.                            


FGF8 spliceforms mediate early mesoderm and posterior neural tissue formation in Xenopus., Fletcher RB., Development. May 1, 2006; 133 (9): 1703-14.            


Tes regulates neural crest migration and axial elongation in Xenopus., Dingwell KS., Dev Biol. May 1, 2006; 293 (1): 252-67.                          


Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos., Reversade B., Development. August 1, 2005; 132 (15): 3381-92.            


Conserved cross-interactions in Drosophila and Xenopus between Ras/MAPK signaling and the dual-specificity phosphatase MKP3., Gómez AR., Dev Dyn. March 1, 2005; 232 (3): 695-708.            


Shisa promotes head formation through the inhibition of receptor protein maturation for the caudalizing factors, Wnt and FGF., Yamamoto A., Cell. January 28, 2005; 120 (2): 223-35.                      


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.          


Morphogenetic movements underlying eye field formation require interactions between the FGF and ephrinB1 signaling pathways., Moore KB., Dev Cell. January 1, 2004; 6 (1): 55-67.                


Twisted gastrulation loss-of-function analyses support its role as a BMP inhibitor during early Xenopus embryogenesis., Blitz IL., Development. October 1, 2003; 130 (20): 4975-88.              


Xolloid-related: a novel BMP1/Tolloid-related metalloprotease is expressed during early Xenopus development., Dale L., Mech Dev. December 1, 2002; 119 (2): 177-90.      


Anteroposterior patterning in Xenopus embryos: egg fragment assay system reveals a synergy of dorsalizing and posteriorizing embryonic domains., Fujii H., Dev Biol. December 1, 2002; 252 (1): 15-30.


Molecular cloning and characterization of dullard: a novel gene required for neural development., Satow R., Biochem Biophys Res Commun. July 5, 2002; 295 (1): 85-91.                  


XSPR-1 and XSPR-2, novel Sp1 related zinc finger containing genes, are dynamically expressed during Xenopus embryogenesis., Ossipova O., Mech Dev. July 1, 2002; 115 (1-2): 117-22.        


Proteolytic cleavage of Chordin as a switch for the dual activities of Twisted gastrulation in BMP signaling., Larraín J., Development. November 1, 2001; 128 (22): 4439-47.    


Xenopus Dishevelled signaling regulates both neural and mesodermal convergent extension: parallel forces elongating the body axis., Wallingford JB., Development. July 1, 2001; 128 (13): 2581-92.  


foxD5a, a Xenopus winged helix gene, maintains an immature neural ectoderm via transcriptional repression that is dependent on the C-terminal domain., Sullivan SA., Dev Biol. April 15, 2001; 232 (2): 439-57.            


Functional characterization and genetic mapping of alk8., Payne TL., Mech Dev. February 1, 2001; 100 (2): 275-89.          


A study of Xlim1 function in the Spemann-Mangold organizer., Kodjabachian L., Int J Dev Biol. January 1, 2001; 45 (1): 209-18.            


Different activities of the frizzled-related proteins frzb2 and sizzled2 during Xenopus anteroposterior patterning., Bradley L., Dev Biol. November 1, 2000; 227 (1): 118-32.                    


Characterization of a subfamily of related winged helix genes, XFD-12/12'/12" (XFLIP), during Xenopus embryogenesis., Sölter M., Mech Dev. December 1, 1999; 89 (1-2): 161-5.                  


Evidence for non-axial A/P patterning in the nonneural ectoderm of Xenopus and zebrafish pregastrula embryos., Read EM., Int J Dev Biol. September 1, 1998; 42 (6): 763-74.    


Xenopus hindbrain patterning requires retinoid signaling., Kolm PJ., Dev Biol. December 1, 1997; 192 (1): 1-16.              

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