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Summary Anatomy Item Literature (13) Expression Attributions Wiki
XB-ANAT-1632

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Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ., J Exp Zool B Mol Dev Evol. May 1, 2024; 342 (3): 212-240.            

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):                                               

Transplantation of Ears Provides Insights into Inner Ear Afferent Pathfinding Properties., Gordy C., Dev Neurobiol. November 1, 2018; 78 (11): 1064-1080.                  

Sonic hedgehog antagonists reduce size and alter patterning of the frog inner ear., Zarei S., Dev Neurobiol. December 1, 2017; 77 (12): 1385-1400.                

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.      

Opportunities and limits of the one gene approach: the ability of Atoh1 to differentiate and maintain hair cells depends on the molecular context., Jahan I., Front Cell Neurosci. February 5, 2015; 9 26.  

Embryological manipulations in the developing Xenopus inner ear reveal an intrinsic role for Wnt signaling in dorsal-ventral patterning., Forristall CA., Dev Dyn. October 1, 2014; 243 (10): 1262-74.            

Phylogenetic differences in calcium permeability of the auditory hair cell cholinergic nicotinic receptor., Lipovsek M., Proc Natl Acad Sci U S A. March 13, 2012; 109 (11): 4308-13.

Bisphenol A induces otolith malformations during vertebrate embryogenesis., Gibert Y., BMC Dev Biol. January 26, 2011; 11 4.            

Long-term consequences of Sox9 depletion on inner ear development., Park BY., Dev Dyn. April 1, 2010; 239 (4): 1102-12.          

Mutations of KCNJ10 together with mutations of SLC26A4 cause digenic nonsyndromic hearing loss associated with enlarged vestibular aqueduct syndrome., Yang T., Am J Hum Genet. May 1, 2009; 84 (5): 651-7.      

Origins of inner ear sensory organs revealed by fate map and time-lapse analyses., Kil SH., Dev Biol. May 15, 2001; 233 (2): 365-79.              

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