Papers associated with vestibuloauditory system (and dlx5)

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	In vitro modeling of cranial placode differentiation: Recent advances, challenges, and perspectives., Griffin C., Dev Biol. February 1, 2024; 506 20-30.
	The sulfotransferase XB5850668.L is required to apportion embryonic ectodermal domains., Marchak A., Dev Dyn. December 1, 2023; 252 (12): 1407-1427.
	Time-resolved quantitative proteomic analysis of the developing Xenopus otic vesicle reveals putative congenital hearing loss candidates., Baxi AB., iScience. September 15, 2023; 26 (9): 107665.
	Generation of a new six1-null line in Xenopus tropicalis for study of development and congenital disease., Coppenrath K., Genesis. December 1, 2021; 59 (12): e23453.
	Sobp modulates the transcriptional activation of Six1 target genes and is required during craniofacial development., Tavares ALP., Development. September 1, 2021; 148 (17):
	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):
	A Critical E-box in Barhl1 3' Enhancer Is Essential for Auditory Hair Cell Differentiation., Hou K., Cells. May 15, 2019; 8 (5):
	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.
	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.
	Early embryonic specification of vertebrate cranial placodes., Schlosser G., Wiley Interdiscip Rev Dev Biol. January 1, 2014; 3 (5): 349-63.
	Sox9 is required for invagination of the otic placode in mice., Barrionuevo F., Dev Biol. May 1, 2008; 317 (1): 213-24.
	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.
	Identification of novel genes affecting mesoderm formation and morphogenesis through an enhanced large scale functional screen in Xenopus., Chen JA., Mech Dev. March 1, 2005; 122 (3): 307-31.
	Expression cloning screening of a unique and full-length set of cDNA clones is an efficient method for identifying genes involved in Xenopus neurogenesis., Voigt J., Mech Dev. March 1, 2005; 122 (3): 289-306.
	Xenopus aristaless-related homeobox (xARX) gene product functions as both a transcriptional activator and repressor in forebrain development., Seufert DW., Dev Dyn. February 1, 2005; 232 (2): 313-24.
	A restrictive role for Hedgehog signalling during otic specification in Xenopus., Koebernick K., Dev Biol. August 15, 2003; 260 (2): 325-38.
	The Dlx5 homeobox gene is essential for vestibular morphogenesis in the mouse embryo through a BMP4-mediated pathway., Merlo GR., Dev Biol. August 1, 2002; 248 (1): 157-69.
	Misexpression of Polycomb-group proteins in Xenopus alters anterior neural development and represses neural target genes., Yoshitake Y., Dev Biol. November 15, 1999; 215 (2): 375-87.
	The Xenopus Emx genes identify presumptive dorsal telencephalon and are induced by head organizer signals., Pannese M., Mech Dev. April 1, 1998; 73 (1): 73-83.
	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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