Papers associated with otic placode (and sox9)

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	Mapping single-cell atlases throughout Metazoa unravels cell type evolution., Tarashansky AJ., Elife. May 4, 2021; 10
	The ribosome biogenesis factor Nol11 is required for optimal rDNA transcription and craniofacial development in Xenopus., Griffin JN., PLoS Genet. March 10, 2015; 11 (3): e1005018.
	A novel function for Egr4 in posterior hindbrain development., Bae CJ., Sci Rep. January 12, 2015; 5 7750.
	SUMOylated SoxE factors recruit Grg4 and function as transcriptional repressors in the neural crest., Lee PC., J Cell Biol. September 3, 2012; 198 (5): 799-813.
	RIPPLY3 is a retinoic acid-inducible repressor required for setting the borders of the pre-placodal ectoderm., Janesick A., Development. March 1, 2012; 139 (6): 1213-24.
	V-ATPase-dependent ectodermal voltage and pH regionalization are required for craniofacial morphogenesis., Vandenberg LN., Dev Dyn. August 1, 2011; 240 (8): 1889-904.
	Cardiac neural crest is dispensable for outflow tract septation in Xenopus., Lee YH., Development. May 1, 2011; 138 (10): 2025-34.
	Long-term consequences of Sox9 depletion on inner ear development., Park BY., Dev Dyn. April 1, 2010; 239 (4): 1102-12.
	Genomic code for Sox10 activation reveals a key regulatory enhancer for cranial neural crest., Betancur P., Proc Natl Acad Sci U S A. February 23, 2010; 107 (8): 3570-5.
	CHD7 cooperates with PBAF to control multipotent neural crest formation., Bajpai R., Nature. February 18, 2010; 463 (7283): 958-62.
	Hindbrain-derived Wnt and Fgf signals cooperate to specify the otic placode in Xenopus., Park BY., Dev Biol. December 1, 2008; 324 (1): 108-21.
	Sox9 is required for invagination of the otic placode in mice., Barrionuevo F., Dev Biol. May 1, 2008; 317 (1): 213-24.
	An NF-kappaB and slug regulatory loop active in early vertebrate mesoderm., Zhang C., PLoS One. December 27, 2006; 1 e106.
	The role of Paraxial Protocadherin in Xenopus otic placode development., Hu RY., Biochem Biophys Res Commun. June 23, 2006; 345 (1): 239-47.
	SoxE factors function equivalently during neural crest and inner ear development and their activity is regulated by SUMOylation., Taylor KM., Dev Cell. November 1, 2005; 9 (5): 593-603.
	Xenopus Id3 is required downstream of Myc for the formation of multipotent neural crest progenitor cells., Light W., Development. April 1, 2005; 132 (8): 1831-41.
	A slug, a fox, a pair of sox: transcriptional responses to neural crest inducing signals., Heeg-Truesdell E., Birth Defects Res C Embryo Today. June 1, 2004; 72 (2): 124-39.
	Regulated gene expression of hyaluronan synthases during Xenopus laevis development., Nardini M., Gene Expr Patterns. May 1, 2004; 4 (3): 303-8.
	Specification of the otic placode depends on Sox9 function in Xenopus., Saint-Germain N., Development. April 1, 2004; 131 (8): 1755-63.
	Sox10 regulates the development of neural crest-derived melanocytes in Xenopus., Aoki Y., Dev Biol. July 1, 2003; 259 (1): 19-33.
	The transcription factor Sox9 is required for cranial neural crest development in Xenopus., Spokony RF., Development. January 1, 2002; 129 (2): 421-32.

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