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