Published in Brain Res Mol Brain Res on July 05, 2004
Prestin-based outer hair cell motility is necessary for mammalian cochlear amplification. Neuron (2008) 2.98
The role of inherited TPMT and COMT genetic variation in cisplatin-induced ototoxicity in children with cancer. Clin Pharmacol Ther (2013) 2.40
Cochlear function in Prestin knockout mice. J Physiol (2004) 1.83
Essential role of retinoblastoma protein in mammalian hair cell development and hearing. Proc Natl Acad Sci U S A (2006) 1.78
Cochlear amplification, outer hair cells and prestin. Curr Opin Neurobiol (2008) 1.69
Prestin and the cochlear amplifier. J Physiol (2006) 1.48
The hearing gene Prestin reunites echolocating bats. Proc Natl Acad Sci U S A (2008) 1.44
Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation. Dis Model Mech (2010) 1.40
Otoacoustic emissions without somatic motility: can stereocilia mechanics drive the mammalian cochlea? J Acoust Soc Am (2004) 1.40
Rapid cell-cycle reentry and cell death after acute inactivation of the retinoblastoma gene product in postnatal cochlear hair cells. Proc Natl Acad Sci U S A (2008) 1.21
Prestin-based outer hair cell electromotility in knockin mice does not appear to adjust the operating point of a cilia-based amplifier. Proc Natl Acad Sci U S A (2007) 1.20
In vivo proliferation of postmitotic cochlear supporting cells by acute ablation of the retinoblastoma protein in neonatal mice. J Neurosci (2010) 1.17
Developmental expression of the outer hair cell motor prestin in the mouse. J Membr Biol (2007) 1.16
Slc26a9 is inhibited by the R-region of the cystic fibrosis transmembrane conductance regulator via the STAS domain. J Biol Chem (2009) 1.08
Using the cochlear microphonic as a tool to evaluate cochlear function in mouse models of hearing. J Assoc Res Otolaryngol (2010) 1.07
Hearing loss and hair cell death in mice given the cholesterol-chelating agent hydroxypropyl-β-cyclodextrin. PLoS One (2012) 1.03
High frequency of the IVS2-2A>G DNA sequence variation in SLC26A5, encoding the cochlear motor protein prestin, precludes its involvement in hereditary hearing loss. BMC Med Genet (2005) 1.03
Somatic motility and hair bundle mechanics, are both necessary for cochlear amplification? Hear Res (2010) 0.94
Genetics of hearing and deafness. Anat Rec (Hoboken) (2012) 0.91
Vacuolization and alterations of lysosomal membrane proteins in cochlear marginal cells contribute to hearing loss in neuraminidase 1-deficient mice. Biochim Biophys Acta (2009) 0.86
Outer hair cell-specific prestin-CreERT2 knockin mouse lines. Genesis (2012) 0.86
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
Auditory hair cell-specific deletion of p27Kip1 in postnatal mice promotes cell-autonomous generation of new hair cells and normal hearing. J Neurosci (2014) 0.83
Prestin shows divergent evolution between constant frequency echolocating bats. J Mol Evol (2011) 0.83
Normal hearing sensitivity at low-to-middle frequencies with 34% prestin-charge density. PLoS One (2012) 0.82
Cell cycle regulation in hair cell development and regeneration in the mouse cochlea. Cell Cycle (2008) 0.82
A chimera analysis of prestin knock-out mice. J Neurosci (2009) 0.81
Outer Hair Cell Lateral Wall Structure Constrains the Mobility of Plasma Membrane Proteins. PLoS Genet (2015) 0.79
Susceptibility of outer hair cells to cholesterol chelator 2-hydroxypropyl-β-cyclodextrine is prestin-dependent. Sci Rep (2016) 0.78
Prestin-Dependence of Outer Hair Cell Survival and Partial Rescue of Outer Hair Cell Loss in PrestinV499G/Y501H Knockin Mice. PLoS One (2015) 0.77
Interaction between the motor protein prestin and the transporter protein VAPA. Biochim Biophys Acta (2010) 0.77
The R130S mutation significantly affects the function of prestin, the outer hair cell motor protein. J Mol Med (Berl) (2016) 0.76
Abnormal mRNA splicing but normal auditory brainstem response (ABR) in mice with the prestin (SLC26A5) IVS2-2A>G mutation. Mutat Res (2016) 0.75
Reduction in noise-induced functional loss of the cochleae in mice with pre-existing cochlear dysfunction due to genetic interference of prestin. PLoS One (2014) 0.75
Hearing Loss Controlled by Optogenetic Stimulation of Nonexcitable Nonglial Cells in the Cochlea of the Inner Ear. Front Mol Neurosci (2017) 0.75
Symbiotic gut microbes modulate human metabolic phenotypes. Proc Natl Acad Sci U S A (2008) 6.42
Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier. Nature (2002) 5.54
Elastic fiber homeostasis requires lysyl oxidase-like 1 protein. Nat Genet (2004) 3.83
Prestin-based outer hair cell motility is necessary for mammalian cochlear amplification. Neuron (2008) 2.98
A review of current large-scale mouse knockout efforts. Genesis (2010) 2.10
Purkinje cell degeneration (pcd) phenotypes caused by mutations in the axotomy-induced gene, Nna1. Science (2002) 1.90
Prestin's role in cochlear frequency tuning and transmission of mechanical responses to neural excitation. Curr Biol (2008) 1.85
Fructose-induced hypertension: essential role of chloride and fructose absorbing transporters PAT1 and Glut5. Kidney Int (2008) 1.80
The retinitis pigmentosa 1 protein is a photoreceptor microtubule-associated protein. J Neurosci (2004) 1.68
Identification and subcellular localization of the RP1 protein in human and mouse photoreceptors. Invest Ophthalmol Vis Sci (2002) 1.58
Expression profile of embryonic stem cell-associated genes Oct4, Sox2 and Nanog in human gliomas. Histopathology (2011) 1.55
Wnt signaling induces proliferation of sensory precursors in the postnatal mouse cochlea. Proc Natl Acad Sci U S A (2012) 1.54
Efferent protection from acoustic injury is mediated via alpha9 nicotinic acetylcholine receptors on outer hair cells. J Neurosci (2002) 1.54
Essential role of cleavage of Polycystin-1 at G protein-coupled receptor proteolytic site for kidney tubular structure. Proc Natl Acad Sci U S A (2007) 1.52
Age-dependent in vivo conversion of mouse cochlear pillar and Deiters' cells to immature hair cells by Atoh1 ectopic expression. J Neurosci (2012) 1.51
Progressive photoreceptor degeneration, outer segment dysplasia, and rhodopsin mislocalization in mice with targeted disruption of the retinitis pigmentosa-1 (Rp1) gene. Proc Natl Acad Sci U S A (2002) 1.51
A comparative study: Early results and complications of percutaneous and surgical closure of ventricular septal defect. Cardiology (2009) 1.47
The ciliary rootlet maintains long-term stability of sensory cilia. Mol Cell Biol (2005) 1.43
Otoacoustic emissions without somatic motility: can stereocilia mechanics drive the mammalian cochlea? J Acoust Soc Am (2004) 1.40
Spontaneous hair cell regeneration in the neonatal mouse cochlea in vivo. Development (2014) 1.27
Epidermal wound repair is regulated by the planar cell polarity signaling pathway. Dev Cell (2010) 1.25
Slc2a5 (Glut5) is essential for the absorption of fructose in the intestine and generation of fructose-induced hypertension. J Biol Chem (2008) 1.25
Rapid cell-cycle reentry and cell death after acute inactivation of the retinoblastoma gene product in postnatal cochlear hair cells. Proc Natl Acad Sci U S A (2008) 1.21
Prestin-based outer hair cell electromotility in knockin mice does not appear to adjust the operating point of a cilia-based amplifier. Proc Natl Acad Sci U S A (2007) 1.20
Inducible Cre recombinase activity in mouse cerebellar granule cell precursors and inner ear hair cells. Dev Dyn (2006) 1.20
In vivo proliferation of postmitotic cochlear supporting cells by acute ablation of the retinoblastoma protein in neonatal mice. J Neurosci (2010) 1.17
Pathogenesis of persistent hyperplastic primary vitreous in mice lacking the arf tumor suppressor gene. Invest Ophthalmol Vis Sci (2004) 1.17
Vacuolar H+-ATPase binding to microfilaments: regulation in response to phosphatidylinositol 3-kinase activity and detailed characterization of the actin-binding site in subunit B. J Biol Chem (2003) 1.16
In vivo proliferative regeneration of balance hair cells in newborn mice. J Neurosci (2012) 1.10
Identification of 17 hearing impaired mouse strains in the TMGC ENU-mutagenesis screen. Hear Res (2006) 1.09
Actin-related protein 2/3 complex is required for actin ring formation. J Bone Miner Res (2003) 1.07
Dynamic expression pattern of Sonic hedgehog in developing cochlear spiral ganglion neurons. Dev Dyn (2010) 1.04
Prestin-prestin and prestin-GLUT5 interactions in HEK293T cells. Dev Neurobiol (2007) 1.02
Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear hair cells. EMBO Mol Med (2009) 1.01
Transcatheter device closure of perimembranous ventricular septal defects: mid-term outcomes. Eur Heart J (2010) 1.00
Orphan glutamate receptor delta1 subunit required for high-frequency hearing. Mol Cell Biol (2007) 1.00
Targeting hearing genes in mice. Brain Res Mol Brain Res (2004) 0.97
Essential and synergistic roles of RP1 and RP1L1 in rod photoreceptor axoneme and retinitis pigmentosa. J Neurosci (2009) 0.97
4-[(E)-(2-Methoxy-phen-yl)imino-meth-yl]-N,N-dimethyl-aniline. Acta Crystallogr Sect E Struct Rep Online (2010) 0.96
In vivo Notch reactivation in differentiating cochlear hair cells induces Sox2 and Prox1 expression but does not disrupt hair cell maturation. Dev Dyn (2012) 0.95
Calcium hydroxide reduces lipopolysaccharide-stimulated osteoclast formation. Oral Surg Oral Med Oral Pathol Oral Radiol Endod (2003) 0.95
Changes in plasma membrane structure and electromotile properties in prestin deficient outer hair cells. Cytoskeleton (Hoboken) (2010) 0.95
Regulation of p27Kip1 by Sox2 maintains quiescence of inner pillar cells in the murine auditory sensory epithelium. J Neurosci (2012) 0.95
The role of prestin in the generation of electrically evoked otoacoustic emissions in mice. J Neurophysiol (2008) 0.94
Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene. Mol Vis (2003) 0.93
Overactivation of Notch1 signaling induces ectopic hair cells in the mouse inner ear in an age-dependent manner. PLoS One (2012) 0.93
FCHSD1 and FCHSD2 are expressed in hair cell stereocilia and cuticular plate and regulate actin polymerization in vitro. PLoS One (2013) 0.91
Gene expression profiles of mouse retinas during the second and third postnatal weeks. Brain Res (2006) 0.91
Selective ablation of pillar and deiters' cells severely affects cochlear postnatal development and hearing in mice. J Neurosci (2013) 0.90
Enoxacin directly inhibits osteoclastogenesis without inducing apoptosis. J Biol Chem (2012) 0.89
Postnatal development, maturation and aging in the mouse cochlea and their effects on hair cell regeneration. Hear Res (2012) 0.89
Conditional gene expression in the mouse inner ear using Cre-loxP. J Assoc Res Otolaryngol (2012) 0.89
Creation of a transgenic mouse for hair-cell gene targeting by using a modified bacterial artificial chromosome containing Prestin. Dev Dyn (2004) 0.88
Polycystin-1 is required for stereocilia structure but not for mechanotransduction in inner ear hair cells. J Neurosci (2011) 0.88
Deafness in TRbeta mutants is caused by malformation of the tectorial membrane. J Neurosci (2009) 0.88
Overexpression of SK2 channels enhances efferent suppression of cochlear responses without enhancing noise resistance. J Neurophysiol (2007) 0.87
Vacuolization and alterations of lysosomal membrane proteins in cochlear marginal cells contribute to hearing loss in neuraminidase 1-deficient mice. Biochim Biophys Acta (2009) 0.86
The practical use of Cre and loxP technologies in mouse auditory research. Methods Mol Biol (2009) 0.86
A chemical small molecule induces mouse embryonic stem cell differentiation into functional vascular endothelial cells via Hmbox1. Stem Cells Dev (2012) 0.86
Changes of gut bacteria and immune parameters in liver transplant recipients. Hepatobiliary Pancreat Dis Int (2012) 0.86
Impaired stria vascularis in the inner ear of apolipoprotein E gene knockout mice. ORL J Otorhinolaryngol Relat Spec (2008) 0.86
Outer hair cell-specific prestin-CreERT2 knockin mouse lines. Genesis (2012) 0.86
Propolis inhibits osteoclast maturation. Dent Traumatol (2009) 0.86
Assessment of the fecal lactobacilli population in patients with hepatitis B virus-related decompensated cirrhosis and hepatitis B cirrhosis treated with liver transplant. Microb Ecol (2011) 0.86
Endovascular stent-graft treatment of thoracic aortic dissection. Interact Cardiovasc Thorac Surg (2006) 0.85
Transcriptional profiling identifies upregulated genes following induction of epithelial-mesenchymal transition in squamous carcinoma cells. Exp Cell Res (2011) 0.85
PTEN regulation of the proliferation and differentiation of auditory progenitors through the PTEN/PI3K/Akt-signaling pathway in mice. Neuroreport (2014) 0.85
Glucose transporter 5 is undetectable in outer hair cells and does not contribute to cochlear amplification. Brain Res (2008) 0.85
In vivo visualization of Notch1 proteolysis reveals the heterogeneity of Notch1 signaling activity in the mouse cochlea. PLoS One (2013) 0.84
Conditional and inducible gene recombineering in the mouse inner ear. Brain Res (2006) 0.84
Distinct gene expression profiles and reduced JNK signaling in retinitis pigmentosa caused by RP1 mutations. Hum Mol Genet (2005) 0.84
Absence of hearing loss in a mouse model for DFNA17 and MYH9-related disease: the use of public gene-targeted ES cell resources. Brain Res (2006) 0.84
Prestin links extrinsic tuning to neural excitation in the mammalian cochlea. Curr Biol (2011) 0.83
Endonasal endoscopic repair of cerebrospinal fluid rhinorrhea in a series of 69 patients. Br J Neurosurg (2010) 0.83
Studying inner ear protein-protein interactions using FRET and FLIM. Brain Res (2006) 0.83
[Identification of novel mutations in the phenylalanine hydroxylase gene of classical phenylketonuria]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi (2005) 0.83
(E)-2-[2-(4-Chloro-benzyl-idene)hydrazin-1-yl]-4-{[3-(dimethyl-aza-nium-yl)prop-yl]amino}-quinazolin-1-ium bis-(perchlorate). Acta Crystallogr Sect E Struct Rep Online (2012) 0.82
Acute interactions between intestinal sugar and calcium transport in vitro. Am J Physiol Gastrointest Liver Physiol (2013) 0.82
Cell cycle regulation in hair cell development and regeneration in the mouse cochlea. Cell Cycle (2008) 0.82
Interactions between vacuolar H+-ATPases and microfilaments in osteoclasts. J Bioenerg Biomembr (2005) 0.82
Normal hearing sensitivity at low-to-middle frequencies with 34% prestin-charge density. PLoS One (2012) 0.82
Fast colloidal synthesis of scalable Mo-rich hierarchical ultrathin MoSe(2-x) nanosheets for high-performance hydrogen evolution. Nanoscale (2014) 0.81
[Antitumor activities of kushen flavonoids in vivo and in vitro]. Zhong Xi Yi Jie He Xue Bao (2008) 0.81
Inner hair cell Cre-expressing transgenic mouse. Genesis (2004) 0.81
1,10-Phenanthroline promotes copper complexes into tumor cells and induces apoptosis by inhibiting the proteasome activity. J Biol Inorg Chem (2012) 0.80
The synergistic effect of peptidoglycan and lipopolysaccaride on osteoclast formation. Oral Surg Oral Med Oral Pathol Oral Radiol Endod (2003) 0.79
Granulocyte colony-stimulating factor improves neuron survival in experimental spinal cord injury by regulating nucleophosmin-1 expression. J Neurosci Res (2014) 0.79