Published in Database (Oxford) on July 24, 2015
The 133-kDa N-terminal domain enables myosin 15 to maintain mechanotransducing stereocilia and is essential for hearing. Elife (2015) 0.90
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The zebrafish pinball wizard gene encodes WRB, a tail-anchored-protein receptor essential for inner-ear hair cells and retinal photoreceptors. J Physiol (2015) 0.77
A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60. Hum Genet (2016) 0.76
Assessment of the expression and role of the α1-nAChR subunit in efferent cholinergic function during the development of the mammalian cochlea. J Neurophysiol (2016) 0.76
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Sorting nexin 9 (SNX9) is not essential for development and auditory function in mice. Oncotarget (2016) 0.75
PSIP1/LEDGF: a new gene likely involved in sensorineural progressive hearing loss. Sci Rep (2015) 0.75
Global Analysis of Protein Expression of Inner Ear Hair Cells. J Neurosci (2016) 0.75
Harnessing Molecular Motors for Nanoscale Pulldown in Live Cells. Mol Biol Cell (2016) 0.75
DNA Methylation of a Novel PAK4 Locus Influences Ototoxicity Susceptibility following Cisplatin and Radiation Therapy for Pediatric Embryonal Tumors. Neuro Oncol (2017) 0.75
Angulin proteins ILDR1 and ILDR2 regulate alternative pre-mRNA splicing through binding to splicing factors TRA2A, TRA2B, or SRSF1. Sci Rep (2017) 0.75
Genome-wide identification and expression profiling of long non-coding RNAs in auditory and vestibular systems. Sci Rep (2017) 0.75
Wnt9a can influence cell fates and neural connectivity across the radial axis of the developing cochlea. J Neurosci (2017) 0.75
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A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C. Nat Genet (2000) 3.71
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Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48. Nat Genet (2012) 2.43
Molecular architecture of the chick vestibular hair bundle. Nat Neurosci (2013) 1.43
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The LINC complex is essential for hearing. J Clin Invest (2013) 1.22
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TBC1D24 mutation causes autosomal-dominant nonsyndromic hearing loss. Hum Mutat (2014) 1.05
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Barhl1 regulatory sequences required for cell-specific gene expression and autoregulation in the inner ear and central nervous system. Mol Cell Biol (2008) 1.00
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Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome. PLoS Genet (2015) 0.97
NeuroD factors regulate cell fate and neurite stratification in the developing retina. J Neurosci (2011) 0.97
Characterization of the transcriptome of nascent hair cells and identification of direct targets of the Atoh1 transcription factor. J Neurosci (2015) 0.95
USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1. J Hum Genet (2012) 0.92
Estrogen-related receptor gamma and hearing function: evidence of a role in humans and mice. Neurobiol Aging (2013) 0.91
A short splice form of Xin-actin binding repeat containing 2 (XIRP2) lacking the Xin repeats is required for maintenance of stereocilia morphology and hearing function. J Neurosci (2015) 0.91
Whole-exome sequencing and its impact in hereditary hearing loss. Genet Res (Camb) (2015) 0.91
A frameshift mutation in GRXCR2 causes recessively inherited hearing loss. Hum Mutat (2014) 0.90
C-MYC transcriptionally amplifies SOX2 target genes to regulate self-renewal in multipotent otic progenitor cells. Stem Cell Reports (2014) 0.89
The α1 subunit of nicotinic acetylcholine receptors in the inner ear: transcriptional regulation by ATOH1 and co-expression with the γ subunit in hair cells. J Neurochem (2007) 0.89
An alteration in ELMOD3, an Arl2 GTPase-activating protein, is associated with hearing impairment in humans. PLoS Genet (2013) 0.89
XIRP2, an actin-binding protein essential for inner ear hair-cell stereocilia. Cell Rep (2015) 0.87
Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish. Hum Mol Genet (2014) 0.87
Gene expression profiling identifies Hes6 as a transcriptional target of ATOH1 in cochlear hair cells. FEBS Lett (2007) 0.86
Slit/Robo signaling mediates spatial positioning of spiral ganglion neurons during development of cochlear innervation. J Neurosci (2013) 0.86
Diaphanous homolog 3 (Diap3) overexpression causes progressive hearing loss and inner hair cell defects in a transgenic mouse model of human deafness. PLoS One (2013) 0.86
Expression and replication studies to identify new candidate genes involved in normal hearing function. PLoS One (2014) 0.85
Next-generation sequencing of small RNAs from inner ear sensory epithelium identifies microRNAs and defines regulatory pathways. BMC Genomics (2014) 0.84
The function and molecular identity of inward rectifier channels in vestibular hair cells of the mouse inner ear. J Neurophysiol (2012) 0.82
Elongation factor 1 alpha1 and genes associated with Usher syndromes are downstream targets of GBX2. PLoS One (2012) 0.77