Papers associated with otic vesicle (and actb)

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	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.
	Cilia-localized GID/CTLH ubiquitin ligase complex regulates protein homeostasis of sonic hedgehog signaling components., Hantel F., J Cell Sci. May 1, 2022; 135 (9):
	Spectrin βV adaptive mutations and changes in subcellular location correlate with emergence of hair cell electromotility in mammalians., Cortese M., Proc Natl Acad Sci U S A. February 21, 2017; 114 (8): 2054-2059.
	RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIM(®) genes for hereditary disorders of hearing and balance., Ramírez-Gordillo D., BMC Res Notes. November 18, 2015; 8 691.
	Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1., Bonnard C., Nat Genet. May 13, 2012; 44 (6): 709-13.
	The R109H variant of fascin-2, a developmentally regulated actin crosslinker in hair-cell stereocilia, underlies early-onset hearing loss of DBA/2J mice., Shin JB., J Neurosci. July 21, 2010; 30 (29): 9683-94.
	Myosin VI and VIIa distribution among inner ear epithelia in diverse fishes., Coffin AB., Hear Res. February 1, 2007; 224 (1-2): 15-26.
	Inner ear formation during the early larval development of Xenopus laevis., Quick QA., Dev Dyn. November 1, 2005; 234 (3): 791-801.
	Xenopus TRPN1 (NOMPC) localizes to microtubule-based cilia in epithelial cells, including inner-ear hair cells., Shin JB., Proc Natl Acad Sci U S A. August 30, 2005; 102 (35): 12572-7.
	Exploration of the extracellular space by a large-scale secretion screen in the early Xenopus embryo., Pera EM., Int J Dev Biol. January 1, 2005; 49 (7): 781-96.

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