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Summary Anatomy Item Literature (98) Expression Attributions Wiki
XB-ANAT-1575

Papers associated with rhombomere R3 (and myc)

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PTK7 modulates Wnt signaling activity via LRP6., Bin-Nun N., Development. January 1, 2014; 141 (2): 410-21.              


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.                


Calponin 2 acts as an effector of noncanonical Wnt-mediated cell polarization during neural crest cell migration., Ulmer B., Cell Rep. March 28, 2013; 3 (3): 615-21.              


Xenopus HJURP and condensin II are required for CENP-A assembly., Bernad R., J Cell Biol. February 21, 2011; 192 (4): 569-82.              


The Pax3 and Pax7 paralogs cooperate in neural and neural crest patterning using distinct molecular mechanisms, in Xenopus laevis embryos., Maczkowiak F., Dev Biol. April 15, 2010; 340 (2): 381-96.                                                    


Eya1 and Six1 promote neurogenesis in the cranial placodes in a SoxB1-dependent fashion., Schlosser G., Dev Biol. August 1, 2008; 320 (1): 199-214.                  


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


Autoregulation of canonical Wnt signaling controls midbrain development., Kunz M., Dev Biol. September 15, 2004; 273 (2): 390-401.          


N- and C-terminal domains of beta-catenin, respectively, are required to initiate and shape axon arbors of retinal ganglion cells in vivo., Elul TM., J Neurosci. July 23, 2003; 23 (16): 6567-75.          


Xenopus X-box binding protein 1, a leucine zipper transcription factor, is involved in the BMP signaling pathway., Zhao H., Dev Biol. May 15, 2003; 257 (2): 278-91.          


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.            

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