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Summary Anatomy Item Literature (259) Expression Attributions Wiki
XB-ANAT-97

Papers associated with hyoid arch (and tbx2)

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Gli2 is required for the induction and migration of Xenopus laevis neural crest., Cerrizuela S., Mech Dev. December 1, 2018; 154 219-239.                      


A gene expression map of the larval Xenopus laevis head reveals developmental changes underlying the evolution of new skeletal elements., Square T., Dev Biol. January 15, 2015; 397 (2): 293-304.                                            


The extreme anterior domain is an essential craniofacial organizer acting through Kinin-Kallikrein signaling., Jacox L., Cell Rep. July 24, 2014; 8 (2): 596-609.                            


Developmental expression and role of Kinesin Eg5 during Xenopus laevis embryogenesis., Fernández JP., Dev Dyn. April 1, 2014; 243 (4): 527-40.              


Protonation controls ASIC1a activity via coordinated movements in multiple domains., Bonifacio G., J Gen Physiol. January 1, 2014; 143 (1): 105-18.                  


Characterization of the insulin-like growth factor binding protein family in Xenopus tropicalis., Haramoto Y., Int J Dev Biol. January 1, 2014; 58 (9): 705-11.                                            


A Rho GTPase signal treadmill backs a contractile array., Burkel BM., Dev Cell. August 14, 2012; 23 (2): 384-96.                        


A large scale screen for neural stem cell markers in Xenopus retina., Parain K., Dev Neurobiol. April 1, 2012; 72 (4): 491-506.                                                    


Identification and characterization of Xenopus kctd15, an ectodermal gene repressed by the FGF pathway., Takahashi C., Int J Dev Biol. January 1, 2012; 56 (5): 393-402.                  


Paraxial T-box genes, Tbx6 and Tbx1, are required for cranial chondrogenesis and myogenesis., Tazumi S., Dev Biol. October 15, 2010; 346 (2): 170-80.                                


Serotonin 2B receptor signaling is required for craniofacial morphogenesis and jaw joint formation in Xenopus., Reisoli E., Development. September 1, 2010; 137 (17): 2927-37.                            


Myosin-X is required for cranial neural crest cell migration in Xenopus laevis., Hwang YS., Dev Dyn. October 1, 2009; 238 (10): 2522-9.      


Runx2 is essential for larval hyobranchial cartilage formation in Xenopus laevis., Kerney R., Dev Dyn. June 1, 2007; 236 (6): 1650-62.                  


Regeneration of the amphibian retina: role of tissue interaction and related signaling molecules on RPE transdifferentiation., Araki M., Dev Growth Differ. February 1, 2007; 49 (2): 109-20.                


Hoxa2 knockdown in Xenopus results in hyoid to mandibular homeosis., Baltzinger M., Dev Dyn. December 1, 2005; 234 (4): 858-67.          


Phylogenetic footprinting and genome scanning identify vertebrate BMP response elements and new target genes., von Bubnoff A., Dev Biol. May 15, 2005; 281 (2): 210-26.                                                      


Mechanism of the voltage sensitivity of IRK1 inward-rectifier K+ channel block by the polyamine spermine., Shin HG., J Gen Physiol. April 1, 2005; 125 (4): 413-26.                      


Mechanism of rectification in inward-rectifier K+ channels., Guo D., J Gen Physiol. April 1, 2003; 121 (4): 261-75.                        


Chordin is required for the Spemann organizer transplantation phenomenon in Xenopus embryos., Oelgeschläger M., Dev Cell. February 1, 2003; 4 (2): 219-30.              


On the mechanism of MgATP-dependent gating of CFTR Cl- channels., Vergani P., J Gen Physiol. January 1, 2003; 121 (1): 17-36.                          


Drosophila Aurora A kinase is required to localize D-TACC to centrosomes and to regulate astral microtubules., Giet R., J Cell Biol. February 4, 2002; 156 (3): 437-51.                


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.            


Multiple isoforms of the high molecular weight microtubule associated protein XMAP215 are expressed during development in Xenopus., Becker BE., Cell Motil Cytoskeleton. December 1, 2000; 47 (4): 282-95.


Ectopic Hoxa2 induction after neural crest migration results in homeosis of jaw elements in Xenopus., Pasqualetti M., Development. December 1, 2000; 127 (24): 5367-78.          


The LIS1-related NUDF protein of Aspergillus nidulans interacts with the coiled-coil domain of the NUDE/RO11 protein., Efimov VP., J Cell Biol. August 7, 2000; 150 (3): 681-8.          


Xbra3 induces mesoderm and neural tissue in Xenopus laevis., Strong CF., Dev Biol. June 15, 2000; 222 (2): 405-19.                  


The expression pattern of thyroid hormone response genes in remodeling tadpole tissues defines distinct growth and resorption gene expression programs., Berry DL., Dev Biol. November 1, 1998; 203 (1): 24-35.                  


The chick Brachyury gene: developmental expression pattern and response to axial induction by localized activin., Kispert A., Dev Biol. April 1, 1995; 168 (2): 406-15.


Expression patterns of Hoxb genes in the Xenopus embryo suggest roles in anteroposterior specification of the hindbrain and in dorsoventral patterning of the mesoderm., Godsave S., Dev Biol. December 1, 1994; 166 (2): 465-76.              


Xl-fli, the Xenopus homologue of the fli-1 gene, is expressed during embryogenesis in a restricted pattern evocative of neural crest cell distribution., Meyer D., Mech Dev. December 1, 1993; 44 (2-3): 109-21.                    


Xenopus Distal-less related homeobox genes are expressed in the developing forebrain and are induced by planar signals., Papalopulu N., Development. March 1, 1993; 117 (3): 961-75.          

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