Papers associated with otic vesicle (and tubb2b)

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	The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in Xenopus embryos., Willsey HR., Development. June 22, 2020; 147 (21):
	Six1 and Irx1 have reciprocal interactions during cranial placode and otic vesicle formation., Sullivan CH., Dev Biol. February 1, 2019; 446 (1): 68-79.
	Hmga2 is required for neural crest cell specification in Xenopus laevis., Macrì S., Dev Biol. March 1, 2016; 411 (1): 25-37.
	The serpin PN1 is a feedback regulator of FGF signaling in germ layer and primary axis formation., Acosta H., Development. March 15, 2015; 142 (6): 1146-58.
	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.
	Sp8 regulates inner ear development., Chung HA., Proc Natl Acad Sci U S A. April 29, 2014; 111 (17): 6329-34.
	Xenopus laevis nucleotide binding protein 1 (xNubp1) is important for convergent extension movements and controls ciliogenesis via regulation of the actin cytoskeleton., Ioannou A., Dev Biol. August 15, 2013; 380 (2): 243-58.
	Yes-associated protein 65 (YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone., Gee ST., PLoS One. January 1, 2011; 6 (6): e20309.
	The Xenopus Irx genes are essential for neural patterning and define the border between prethalamus and thalamus through mutual antagonism with the anterior repressors Fezf and Arx., Rodríguez-Seguel E., Dev Biol. May 15, 2009; 329 (2): 258-68.
	Two Hoxc6 transcripts are differentially expressed and regulate primary neurogenesis in Xenopus laevis., Bardine N., Dev Dyn. March 1, 2009; 238 (3): 755-65.
	BDNF promotes target innervation of Xenopus mandibular trigeminal axons in vivo., Huang JK., BMC Dev Biol. May 31, 2007; 7 59.
	Novel gene ashwin functions in Xenopus cell survival and anteroposterior patterning., Patil SS., Dev Dyn. July 1, 2006; 235 (7): 1895-907.
	Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus., Kuroda H., PLoS Biol. May 1, 2004; 2 (5): E92.
	Depletion of the cell-cycle inhibitor p27(Xic1) impairs neuronal differentiation and increases the number of ElrC(+) progenitor cells in Xenopus tropicalis., Carruthers S., Mech Dev. May 1, 2003; 120 (5): 607-16.
	The E3 ubiquitin ligase GREUL1 anteriorizes ectoderm during Xenopus development., Borchers AG., Dev Biol. November 15, 2002; 251 (2): 395-408.
	Hes6 acts in a positive feedback loop with the neurogenins to promote neuronal differentiation., Koyano-Nakagawa N., Development. October 1, 2000; 127 (19): 4203-16.
	Primary neuronal differentiation in Xenopus embryos is linked to the beta(3) subunit of the sodium pump., Messenger NJ., Dev Biol. April 15, 2000; 220 (2): 168-82.
	The control of Xenopus embryonic primary neurogenesis is mediated by retinoid signalling in the neurectoderm., Sharpe C., Mech Dev. March 1, 2000; 91 (1-2): 69-80.
	Geminin, a neuralizing molecule that demarcates the future neural plate at the onset of gastrulation., Kroll KL., Development. August 1, 1998; 125 (16): 3247-58.
	XATH-1, a vertebrate homolog of Drosophila atonal, induces a neuronal differentiation within ectodermal progenitors., Kim P., Dev Biol. July 1, 1997; 187 (1): 1-12.
	A role for Xenopus Gli-type zinc finger proteins in the early embryonic patterning of mesoderm and neuroectoderm., Marine JC., Mech Dev. May 1, 1997; 63 (2): 211-25.
	X-MyT1, a Xenopus C2HC-type zinc finger protein with a regulatory function in neuronal differentiation., Bellefroid EJ., Cell. December 27, 1996; 87 (7): 1191-202.
	Overexpression of a cellular retinoic acid binding protein (xCRABP) causes anteroposterior defects in developing Xenopus embryos., Dekker EJ., Development. April 1, 1994; 120 (4): 973-85.

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