Published in Genomics on June 01, 2004
Differential expression of genes within the cochlea as defined by a custom mouse inner ear microarray. J Assoc Res Otolaryngol (2005) 1.06
Ion channel gene expression in the inner ear. J Assoc Res Otolaryngol (2007) 1.01
NEIBank: genomics and bioinformatics resources for vision research. Mol Vis (2008) 0.99
Glucose transporter 5 is undetectable in outer hair cells and does not contribute to cochlear amplification. Brain Res (2008) 0.85
Identifying components of the hair-cell interactome involved in cochlear amplification. BMC Genomics (2009) 0.83
OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67). Orphanet J Rare Dis (2015) 0.81
Age-related changes in cochlear gene expression in normal and shaker 2 mice. J Assoc Res Otolaryngol (2006) 0.80
Synthesis of biotin-labeled RNA for gene expression measurements using oligonucleotide arrays. Methods Mol Biol (2009) 0.75
Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells. Nature (2007) 4.87
Determination of elastic moduli of thin layers of soft material using the atomic force microscope. Biophys J (2002) 4.71
Targeting a complex transcriptome: the construction of the mouse full-length cDNA encyclopedia. Genome Res (2003) 3.50
An actin molecular treadmill and myosins maintain stereocilia functional architecture and self-renewal. J Cell Biol (2004) 3.35
Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79. Am J Hum Genet (2010) 2.95
A role for actin arcs in the leading-edge advance of migrating cells. Nat Cell Biol (2011) 2.68
Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48. Nat Genet (2012) 2.43
The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15. J Neurosci (2006) 2.41
Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration. Hum Mol Genet (2003) 2.36
Review series: The cell biology of hearing. J Cell Biol (2010) 2.29
Stepwise morphological and functional maturation of mechanotransduction in rat outer hair cells. J Neurosci (2007) 2.28
Rapid renewal of auditory hair bundles. Nature (2002) 2.28
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23. Hum Mol Genet (2003) 2.14
Balancing selection maintains a form of ERAP2 that undergoes nonsense-mediated decay and affects antigen presentation. PLoS Genet (2010) 2.14
Genetic insights into the morphogenesis of inner ear hair cells. Nat Rev Genet (2004) 2.11
Tricellulin is a tight-junction protein necessary for hearing. Am J Hum Genet (2006) 2.05
Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice. Proc Natl Acad Sci U S A (2002) 2.03
Expression and function of FGF10 in mammalian inner ear development. Dev Dyn (2003) 1.95
Actin-bundling protein TRIOBP forms resilient rootlets of hair cell stereocilia essential for hearing. Cell (2010) 1.94
Role of membrane proteins in permeability barrier function: uroplakin ablation elevates urothelial permeability. Am J Physiol Renal Physiol (2002) 1.91
Deafness in Claudin 11-null mice reveals the critical contribution of basal cell tight junctions to stria vascularis function. J Neurosci (2004) 1.86
Myosin IIIa boosts elongation of stereocilia by transporting espin 1 to the plus ends of actin filaments. Nat Cell Biol (2009) 1.83
Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development. Dev Biol (2005) 1.82
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans. Nat Genet (2008) 1.78
Molecular remodeling of tip links underlies mechanosensory regeneration in auditory hair cells. PLoS Biol (2013) 1.77
A new compartment at stereocilia tips defined by spatial and temporal patterns of myosin IIIa expression. J Neurosci (2006) 1.73
Roles of uroplakins in plaque formation, umbrella cell enlargement, and urinary tract diseases. J Cell Biol (2004) 1.69
Bleaching/blinking assisted localization microscopy for superresolution imaging using standard fluorescent molecules. Proc Natl Acad Sci U S A (2011) 1.69
Deafness and stria vascularis defects in S1P2 receptor-null mice. J Biol Chem (2007) 1.66
Harmonin mutations cause mechanotransduction defects in cochlear hair cells. Neuron (2009) 1.63
Myosin VIIa and sans localization at stereocilia upper tip-link density implicates these Usher syndrome proteins in mechanotransduction. Proc Natl Acad Sci U S A (2011) 1.62
Regulation of stereocilia length by myosin XVa and whirlin depends on the actin-regulatory protein Eps8. Curr Biol (2011) 1.55
Dynamic length regulation of sensory stereocilia. Semin Cell Dev Biol (2008) 1.54
Strain background effects and genetic modifiers of hearing in mice. Brain Res (2006) 1.53
High-speed switchable lens enables the development of a volumetric stereoscopic display. Opt Express (2009) 1.51
Gene expression profile of the human trabecular meshwork: NEIBank sequence tag analysis. Invest Ophthalmol Vis Sci (2003) 1.48
Rapid turnover of stereocilia membrane proteins: evidence from the trafficking and mobility of plasma membrane Ca(2+)-ATPase 2. J Neurosci (2006) 1.47
Balanced levels of Espin are critical for stereociliary growth and length maintenance. Cell Motil Cytoskeleton (2005) 1.47
Distinct subdomain organization and molecular composition of a tight junction with adherens junction features. J Cell Sci (2006) 1.45
Mouse models of MYH9-related disease: mutations in nonmuscle myosin II-A. Blood (2011) 1.41
Defining the human macula transcriptome and candidate retinal disease genes using EyeSAGE. Invest Ophthalmol Vis Sci (2006) 1.41
A mouse model for nonsyndromic deafness (DFNB12) links hearing loss to defects in tip links of mechanosensory hair cells. Proc Natl Acad Sci U S A (2009) 1.39
Evidence and implications of inhomogeneity in tectorial membrane elasticity. Biophys J (2004) 1.36
When size matters: the dynamic regulation of stereocilia lengths. Curr Opin Cell Biol (2005) 1.36
Retinal parallel processors: more than 100 independent microcircuits operate within a single interneuron. Neuron (2010) 1.33
Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human. Nat Commun (2011) 1.33
Sharp Ca²⁺ nanodomains beneath the ribbon promote highly synchronous multivesicular release at hair cell synapses. J Neurosci (2011) 1.33
Differential expression of KCNQ4 in inner hair cells and sensory neurons is the basis of progressive high-frequency hearing loss. J Neurosci (2005) 1.32
TRPML3 mutations cause impaired mechano-electrical transduction and depolarization by an inward-rectifier cation current in auditory hair cells of varitint-waddler mice. J Physiol (2008) 1.30
NMII forms a contractile transcellular sarcomeric network to regulate apical cell junctions and tissue geometry. Curr Biol (2013) 1.29
Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in pendred syndrome. J Assoc Res Otolaryngol (2003) 1.27
The lacrimal gland transcriptome is an unusually rich source of rare and poorly characterized gene transcripts. Invest Ophthalmol Vis Sci (2005) 1.27
Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function. Hum Mutat (2008) 1.27
Regulation of PCDH15 function in mechanosensory hair cells by alternative splicing of the cytoplasmic domain. Development (2011) 1.27
Twinfilin 2 regulates actin filament lengths in cochlear stereocilia. J Neurosci (2009) 1.26
Dynamic compartmentalization of protein tyrosine phosphatase receptor Q at the proximal end of stereocilia: implication of myosin VI-based transport. Cell Motil Cytoskeleton (2008) 1.26
Expression of prestin, a membrane motor protein, in the mammalian auditory and vestibular periphery. Hear Res (2003) 1.24
SAP102 is a highly mobile MAGUK in spines. J Neurosci (2010) 1.22
Gene expression profile studies of human keratoconus cornea for NEIBank: a novel cornea-expressed gene and the absence of transcripts for aquaporin 5. Invest Ophthalmol Vis Sci (2005) 1.21
Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74. Am J Hum Genet (2010) 1.18
Retina-specific expression of 5A11/Basigin-2, a member of the immunoglobulin gene superfamily. Invest Ophthalmol Vis Sci (2003) 1.18
Protein localization by actin treadmilling and molecular motors regulates stereocilia shape and treadmilling rate. Biophys J (2008) 1.17
Auditory mechanotransduction in the absence of functional myosin-XVa. J Physiol (2006) 1.17
Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndrome. Am J Hum Genet (2009) 1.15
Signatures from tissue-specific MPSS libraries identify transcripts preferentially expressed in the mouse inner ear. Genomics (2006) 1.13
Mutation of the ATP-gated P2X(2) receptor leads to progressive hearing loss and increased susceptibility to noise. Proc Natl Acad Sci U S A (2013) 1.12
Tip links in hair cells: molecular composition and role in hearing loss. Curr Opin Otolaryngol Head Neck Surg (2009) 1.11
Mapping quantitative trait loci for hearing loss in Black Swiss mice. Hear Res (2006) 1.11
Expressed sequence tag analysis of zebrafish eye tissues for NEIBank. Mol Vis (2005) 1.10
CLAMP, a novel microtubule-associated protein with EB-type calponin homology. Cell Motil Cytoskeleton (2005) 1.09
Tricellulin deficiency affects tight junction architecture and cochlear hair cells. J Clin Invest (2013) 1.09
Solution structure of (gamma)S-crystallin by molecular fragment replacement NMR. Protein Sci (2005) 1.06
Differential expression of genes within the cochlea as defined by a custom mouse inner ear microarray. J Assoc Res Otolaryngol (2005) 1.06
Myosin IIIB uses an actin-binding motif in its espin-1 cargo to reach the tips of actin protrusions. Curr Biol (2012) 1.05
Localization of PDZD7 to the stereocilia ankle-link associates this scaffolding protein with the Usher syndrome protein network. J Neurosci (2012) 1.05
Have we found the tip link, transduction channel, and gating spring of the hair cell? Curr Opin Neurobiol (2005) 1.05
Sustained cadherin 23 expression in young and adult cochlea of normal and hearing-impaired mice. Hear Res (2005) 1.05
A novel bovine virus efficiently transduces inner ear neuroepithelial cells. Mol Ther (2005) 1.05
Determination of hair cell metabolic state in isolated cochlear preparations by two-photon microscopy. J Biomed Opt (2007) 1.04
Otopetrin 1 is required for otolith formation in the zebrafish Danio rerio. Dev Biol (2004) 1.03
Intermolecular autophosphorylation regulates myosin IIIa activity and localization in parallel actin bundles. J Biol Chem (2010) 1.03
Roles of alternative splicing in the functional properties of inner ear-specific KCNQ4 channels. J Biol Chem (2007) 1.02
NEIBank: genomics and bioinformatics resources for vision research. Mol Vis (2008) 0.99
Progressive hearing loss and gradual deterioration of sensory hair bundles in the ears of mice lacking the actin-binding protein Eps8L2. Proc Natl Acad Sci U S A (2013) 0.99
Regulation of outer hair cell cytoskeletal stiffness by intracellular Ca2+: underlying mechanism and implications for cochlear mechanics. Cell Calcium (2003) 0.98
Specific interaction between lens MIP/Aquaporin-0 and two members of the gamma-crystallin family. Mol Vis (2005) 0.97
A role for lengsin, a recruited enzyme, in terminal differentiation in the vertebrate lens. J Biol Chem (2008) 0.96
Developmental expression of Kcnq4 in vestibular neurons and neurosensory epithelia. Brain Res (2007) 0.95
Actin in hair cells and hearing loss. Hear Res (2011) 0.95
Changes in plasma membrane structure and electromotile properties in prestin deficient outer hair cells. Cytoskeleton (Hoboken) (2010) 0.95
A single destabilizing mutation (F9S) promotes concerted unfolding of an entire globular domain in gammaS-crystallin. J Mol Biol (2010) 0.95