Papers associated with otic vesicle (and sox9)

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	The sulfotransferase XB5850668.L is required to apportion embryonic ectodermal domains., Marchak A., Dev Dyn. December 1, 2023; 252 (12): 1407-1427.
	Phenotype-genotype relationships in Xenopus sox9 crispants provide insights into campomelic dysplasia and vertebrate jaw evolution., Hossain N., Dev Growth Differ. October 1, 2023; 65 (8): 481-497.
	Influence of Sox protein SUMOylation on neural development and regeneration., Chang KC., Neural Regen Res. March 1, 2022; 17 (3): 477-481.
	Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development., Shah AM., Dis Model Mech. March 3, 2020; 13 (3):
	Six1 and Irx1 have reciprocal interactions during cranial placode and otic vesicle formation., Sullivan CH., Dev Biol. February 1, 2019; 446 (1): 68-79.
	Pa2G4 is a novel Six1 co-factor that is required for neural crest and otic development., Neilson KM., Dev Biol. January 15, 2017; 421 (2): 171-182.
	Sf3b4-depleted Xenopus embryos: A model to study the pathogenesis of craniofacial defects in Nager syndrome., Devotta A., Dev Biol. July 15, 2016; 415 (2): 371-382.
	Hmga2 is required for neural crest cell specification in Xenopus laevis., Macrì S., Dev Biol. March 1, 2016; 411 (1): 25-37.
	A novel function for Egr4 in posterior hindbrain development., Bae CJ., Sci Rep. January 12, 2015; 5 7750.
	Temporal and spatial expression analysis of peripheral myelin protein 22 (Pmp22) in developing Xenopus., Tae HJ., Gene Expr Patterns. January 1, 2015; 17 (1): 26-30.
	Identification of distal enhancers for Six2 expression in pronephros., Suzuki N., Int J Dev Biol. January 1, 2015; 59 (4-6): 241-6.
	Chibby functions in Xenopus ciliary assembly, embryonic development, and the regulation of gene expression., Shi J., Dev Biol. November 15, 2014; 395 (2): 287-98.
	Par3 controls neural crest migration by promoting microtubule catastrophe during contact inhibition of locomotion., Moore R., Development. December 1, 2013; 140 (23): 4763-75.
	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.
	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.
	The protein kinase MLTK regulates chondrogenesis by inducing the transcription factor Sox6., Suzuki T., Development. August 1, 2012; 139 (16): 2988-98.
	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.
	The LIM adaptor protein LMO4 is an essential regulator of neural crest development., Ochoa SD., Dev Biol. January 15, 2012; 361 (2): 313-25.
	Mustn1 is essential for craniofacial chondrogenesis during Xenopus development., Gersch RP., Gene Expr Patterns. January 1, 2012; 12 (3-4): 145-53.
	V-ATPase-dependent ectodermal voltage and pH regionalization are required for craniofacial morphogenesis., Vandenberg LN., Dev Dyn. August 1, 2011; 240 (8): 1889-904.
	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.
	Regulatory elements of Xenopus col2a1 drive cartilaginous gene expression in transgenic frogs., Kerney R., Int J Dev Biol. January 1, 2010; 54 (1): 141-50.
	Involvement of Neptune in induction of the hatching gland and neural crest in the Xenopus embryo., Kurauchi T., Differentiation. January 1, 2010; 79 (4-5): 251-9.
	Myosin-X is required for cranial neural crest cell migration in Xenopus laevis., Hwang YS., Dev Dyn. October 1, 2009; 238 (10): 2522-9.
	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.
	A new role for the Endothelin-1/Endothelin-A receptor signaling during early neural crest specification., Bonano M., Dev Biol. November 1, 2008; 323 (1): 114-29.
	Sox9 is required for invagination of the otic placode in mice., Barrionuevo F., Dev Biol. May 1, 2008; 317 (1): 213-24.
	Inca: a novel p21-activated kinase-associated protein required for cranial neural crest development., Luo T., Development. April 1, 2007; 134 (7): 1279-89.
	Functional analysis of Sox8 during neural crest development in Xenopus., O'Donnell M., Development. October 1, 2006; 133 (19): 3817-26.
	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.
	Maternal Xenopus Zic2 negatively regulates Nodal-related gene expression during anteroposterior patterning., Houston DW., Development. November 1, 2005; 132 (21): 4845-55.
	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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