Published in Curr Biol on July 09, 2002
Life cycle of connexins in health and disease. Biochem J (2006) 3.44
Notch inhibition induces cochlear hair cell regeneration and recovery of hearing after acoustic trauma. Neuron (2013) 2.90
Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential. J Physiol (2006) 2.68
Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome. PLoS Genet (2009) 2.14
Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study. Am J Hum Genet (2003) 1.79
Inner ear drug delivery for auditory applications. Adv Drug Deliv Rev (2008) 1.51
Connexins: a myriad of functions extending beyond assembly of gap junction channels. Cell Commun Signal (2009) 1.49
Differentially altered Ca2+ regulation and Ca2+ permeability in Cx26 hemichannels formed by the A40V and G45E mutations that cause keratitis ichthyosis deafness syndrome. J Gen Physiol (2010) 1.45
Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness. Proc Natl Acad Sci U S A (2007) 1.44
Gap junctions and cochlear homeostasis. J Membr Biol (2006) 1.41
Connexin30 deficiency causes instrastrial fluid-blood barrier disruption within the cochlear stria vascularis. Proc Natl Acad Sci U S A (2007) 1.41
Gap-junction channels dysfunction in deafness and hearing loss. Antioxid Redox Signal (2009) 1.39
Gap junction-mediated intercellular biochemical coupling in cochlear supporting cells is required for normal cochlear functions. Proc Natl Acad Sci U S A (2005) 1.39
Connexin26 is responsible for anionic molecule permeability in the cochlea for intercellular signalling and metabolic communications. Eur J Neurosci (2005) 1.36
A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice. Proc Natl Acad Sci U S A (2005) 1.34
The role of connexins in ear and skin physiology - functional insights from disease-associated mutations. Biochim Biophys Acta (2012) 1.34
Endocochlear potential depends on Cl- channels: mechanism underlying deafness in Bartter syndrome IV. EMBO J (2008) 1.33
Targeted connexin26 ablation arrests postnatal development of the organ of Corti. Biochem Biophys Res Commun (2009) 1.32
Distinct and gradient distributions of connexin26 and connexin30 in the cochlear sensory epithelium of guinea pigs. J Comp Neurol (2006) 1.30
Paracrine signaling through plasma membrane hemichannels. Biochim Biophys Acta (2012) 1.28
Connexin30 null and conditional connexin26 null mice display distinct pattern and time course of cellular degeneration in the cochlea. J Comp Neurol (2009) 1.25
Diverse deafness mechanisms of connexin mutations revealed by studies using in vitro approaches and mouse models. Brain Res (2009) 1.20
Potassium ion movement in the inner ear: insights from genetic disease and mouse models. Physiology (Bethesda) (2009) 1.18
Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing loss. Hum Genet (2004) 1.17
Gap junction mediated intercellular metabolite transfer in the cochlea is compromised in connexin30 null mice. PLoS One (2008) 1.16
Pathogenetic role of the deafness-related M34T mutation of Cx26. Hum Mol Genet (2006) 1.14
Coordinated control of connexin 26 and connexin 30 at the regulatory and functional level in the inner ear. Proc Natl Acad Sci U S A (2008) 1.11
Recent findings and emerging questions in cochlear noise injury. Hear Res (2008) 1.10
The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice. Hum Mol Genet (2010) 1.07
Properties of connexin26 hemichannels expressed in Xenopus oocytes. Cell Mol Neurobiol (2004) 1.07
What's new in ion transports in the cochlea? Pflugers Arch (2006) 1.03
Inner ear supporting cells: rethinking the silent majority. Semin Cell Dev Biol (2013) 1.01
Active cochlear amplification is dependent on supporting cell gap junctions. Nat Commun (2013) 1.00
Cell degeneration is not a primary causer for Connexin26 (GJB2) deficiency associated hearing loss. Neurosci Lett (2012) 1.00
Orphan glutamate receptor delta1 subunit required for high-frequency hearing. Mol Cell Biol (2007) 1.00
ATP-mediated cell-cell signaling in the organ of Corti: the role of connexin channels. Purinergic Signal (2010) 1.00
Post-translational modifications of connexin26 revealed by mass spectrometry. Biochem J (2009) 1.00
Virally expressed connexin26 restores gap junction function in the cochlea of conditional Gjb2 knockout mice. Gene Ther (2013) 0.99
Three-dimensional current flow in a large-scale model of the cochlea and the mechanism of amplification of sound. J R Soc Interface (2009) 0.99
Mice lacking ganglioside GM3 synthase exhibit complete hearing loss due to selective degeneration of the organ of Corti. Proc Natl Acad Sci U S A (2009) 0.98
Cochleosaccular dysplasia associated with a connexin 26 mutation in keratitis-ichthyosis-deafness syndrome. Laryngoscope (2006) 0.97
Gap junctions in inherited human disease. Pflugers Arch (2010) 0.97
Deafness induced by Connexin 26 (GJB2) deficiency is not determined by endocochlear potential (EP) reduction but is associated with cochlear developmental disorders. Biochem Biophys Res Commun (2014) 0.97
Cellular and Deafness Mechanisms Underlying Connexin Mutation-Induced Hearing Loss - A Common Hereditary Deafness. Front Cell Neurosci (2015) 0.97
Human hereditary hearing impairment: mouse models can help to solve the puzzle. Hum Genet (2008) 0.96
Analysis of four connexin26 mutant gap junctions and hemichannels reveals variations in hexamer stability. Biophys J (2010) 0.96
Dominant connexin26 mutants associated with human hearing loss have trans-dominant effects on connexin30. Neurobiol Dis (2010) 0.96
Connexin26 (GJB2) deficiency reduces active cochlear amplification leading to late-onset hearing loss. Neuroscience (2014) 0.92
Dominant Cx26 mutants associated with hearing loss have dominant-negative effects on wild type Cx26. Mol Cell Neurosci (2010) 0.92
Genetics of hearing and deafness. Anat Rec (Hoboken) (2012) 0.91
Selective ablation of pillar and deiters' cells severely affects cochlear postnatal development and hearing in mice. J Neurosci (2013) 0.90
Audiologic phenotype and progression in GJB2 (Connexin 26) hearing loss. Arch Otolaryngol Head Neck Surg (2010) 0.90
BAAV mediated GJB2 gene transfer restores gap junction coupling in cochlear organotypic cultures from deaf Cx26Sox10Cre mice. PLoS One (2011) 0.90
Conditional gene expression in the mouse inner ear using Cre-loxP. J Assoc Res Otolaryngol (2012) 0.89
Possible role of gap junction intercellular channels and connexin 43 in satellite glial cells (SGCs) for preservation of human spiral ganglion neurons : A comparative study with clinical implications. Cell Tissue Res (2013) 0.87
Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing loss. PLoS Genet (2014) 0.87
How do taste cells lacking synapses mediate neurotransmission? CALHM1, a voltage-gated ATP channel. Bioessays (2013) 0.86
The Membrane Properties of Cochlear Root Cells are Consistent with Roles in Potassium Recirculation and Spatial Buffering. J Assoc Res Otolaryngol (2010) 0.86
EKV mutant connexin 31 associated cell death is mediated by ER stress. Hum Mol Genet (2009) 0.86
Aberrant Cx26 hemichannels and keratitis-ichthyosis-deafness syndrome: insights into syndromic hearing loss. Front Cell Neurosci (2014) 0.86
Connexin 26 null mice exhibit spiral ganglion degeneration that can be blocked by BDNF gene therapy. Hear Res (2013) 0.86
Viral vector tropism for supporting cells in the developing murine cochlea. Hear Res (2011) 0.85
Reduced phosphatidylinositol 4,5-bisphosphate synthesis impairs inner ear Ca2+ signaling and high-frequency hearing acquisition. Proc Natl Acad Sci U S A (2012) 0.85
Surgical method for virally mediated gene delivery to the mouse inner ear through the round window membrane. J Vis Exp (2015) 0.85
Inner ear gene transfection in neonatal mice using adeno-associated viral vector: a comparison of two approaches. PLoS One (2012) 0.84
Conditional and inducible gene recombineering in the mouse inner ear. Brain Res (2006) 0.84
Pannexins are new molecular candidates for assembling gap junctions in the cochlea. Neuroreport (2008) 0.84
ILDR1 deficiency causes degeneration of cochlear outer hair cells and disrupts the structure of the organ of Corti: a mouse model for human DFNB42. Biol Open (2015) 0.84
Early developmental expression of connexin26 in the cochlea contributes to its dominate functional role in the cochlear gap junctions. Biochem Biophys Res Commun (2011) 0.83
Regulation of cellular function by connexin hemichannels. Int J Biochem Mol Biol (2011) 0.83
Mouse otocyst transuterine gene transfer restores hearing in mice with connexin 30 deletion-associated hearing loss. Mol Ther (2013) 0.83
Audiological and electrocochleography findings in hearing-impaired children with connexin 26 mutations and otoacoustic emissions. Eur Arch Otorhinolaryngol (2007) 0.82
Calcium signaling in the cochlea - Molecular mechanisms and physiopathological implications. Cell Commun Signal (2012) 0.82
Strategies for developing novel therapeutics for sensorineural hearing loss. Front Pharmacol (2014) 0.82
Analysis of connexin subunits required for the survival of vestibular hair cells. J Comp Neurol (2007) 0.81
Phenotypic variability in gap junction syndromic skin disorders: experience from KID and Clouston syndromes' clinical diagnostics. J Appl Genet (2015) 0.81
Connexins and gap junctions in the inner ear--it's not just about K⁺ recycling. Cell Tissue Res (2014) 0.80
Connexin26 expression in brain parenchymal cells demonstrated by targeted connexin ablation in transgenic mice. Eur J Neurosci (2011) 0.80
The Genetics of Deafness in Domestic Animals. Front Vet Sci (2015) 0.80
Genetics of auditory mechano-electrical transduction. Pflugers Arch (2014) 0.79
Vestibular dysfunction in DFNB1 deafness. Am J Med Genet A (2011) 0.79
Reduced Connexin26 in the Mature Cochlea Increases Susceptibility to Noise-Induced Hearing Lossin Mice. Int J Mol Sci (2016) 0.79
Ultrastructural pathological changes in the cochlear cells of connexin 26 conditional knockout mice. Mol Med Rep (2013) 0.79
A mouse model for degeneration of the spiral ligament. J Assoc Res Otolaryngol (2009) 0.78
Mice with conditional deletion of Cx26 exhibit no vestibular phenotype despite secondary loss of Cx30 in the vestibular end organs. Hear Res (2015) 0.78
Development of the stria vascularis and potassium regulation in the human fetal cochlea: Insights into hereditary sensorineural hearing loss. Dev Neurobiol (2015) 0.78
Heptanol application to the mouse round window: a model for studying cochlear lateral wall regeneration. Otolaryngol Head Neck Surg (2014) 0.78
Potential treatments for genetic hearing loss in humans: current conundrums. Gene Ther (2015) 0.78
Hypothesis of K(+)-Recycling Defect Is Not a Primary Deafness Mechanism for Cx26 (GJB2) Deficiency. Front Mol Neurosci (2017) 0.77
Do cell junction protein mutations cause an airway phenotype in mice or humans? Am J Respir Cell Mol Biol (2011) 0.77
Trafficking abnormality and ER stress underlie functional deficiency of hearing impairment-associated connexin-31 mutants. Protein Cell (2010) 0.77
Reduced electromotility of outer hair cells associated with connexin-related forms of deafness: an in silico study of a cochlear network mechanism. J Assoc Res Otolaryngol (2010) 0.77
Hearing loss in syndromic craniosynostoses: introduction and consideration of mechanisms. Am J Audiol (2014) 0.77
Pannexin 1 deficiency can induce hearing loss. Biochem Biophys Res Commun (2015) 0.77
Mammary gland specific knockdown of the physiological surge in Cx26 during lactation retains normal mammary gland development and function. PLoS One (2014) 0.76
Progressive age-dependence and frequency difference in the effect of gap junctions on active cochlear amplification and hearing. Biochem Biophys Res Commun (2017) 0.76
Human diseases associated with connexin mutations. Biochim Biophys Acta (2017) 0.75
ATP-sensitive K(+) channels (Kir6.1/SUR1) regulate gap junctional coupling in cochlear-supporting cells. Pflugers Arch (2016) 0.75
Connexinopathies: a structural and functional glimpse. BMC Cell Biol (2016) 0.75
Characterization of a knock-in mouse model of the homozygous p.V37I variant in Gjb2. Sci Rep (2016) 0.75
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature (1997) 6.89
The active cochlea. J Neurosci (1992) 4.37
Unconventional myosins in inner-ear sensory epithelia. J Cell Biol (1997) 3.64
Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans. Hum Mol Genet (1997) 3.39
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene. Hum Mol Genet (1997) 3.26
Glutamate toxicity in a neuronal cell line involves inhibition of cystine transport leading to oxidative stress. Neuron (1989) 3.06
Molecular genetics of hearing loss. Annu Rev Genet (2001) 2.69
The regulation of reactive oxygen species production during programmed cell death. J Cell Biol (1998) 2.62
Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis. Anat Embryol (Berl) (1995) 2.47
Cholinergic synaptic inhibition of inner hair cells in the neonatal mammalian cochlea. Science (2000) 2.21
Neurotransmitters and neuromodulators of the mammalian cochlea. Physiol Rev (1993) 1.93
Non-vesicular release of glutamate from glial cells by reversed electrogenic glutamate uptake. Nature (1990) 1.91
Stria vascularis as source of endocochlear potential. J Neurophysiol (1959) 1.88
Oxidative stress induces a form of programmed cell death with characteristics of both apoptosis and necrosis in neuronal cells. J Neurochem (1998) 1.72
Effect of absence of cochlear outer hair cells on behavioural auditory threshold. Nature (1975) 1.63
Otogelin: a glycoprotein specific to the acellular membranes of the inner ear. Proc Natl Acad Sci U S A (1997) 1.60
Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells. Hum Mol Genet (1996) 1.59
Expression of the gap-junction connexins 26 and 30 in the rat cochlea. Cell Tissue Res (1998) 1.58
Ion transport mechanisms responsible for K+ secretion and the transepithelial voltage across marginal cells of stria vascularis in vitro. Hear Res (1995) 1.54
Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins. Hum Mutat (2000) 1.49
Transplacental uptake of glucose is decreased in embryonic lethal connexin26-deficient mice. J Cell Biol (1998) 1.49
Outer hair cell loss and supporting cell expansion following chronic gentamicin treatment. Hear Res (1985) 1.31
Exacerbation of noise-induced hearing loss in mice lacking the glutamate transporter GLAST. J Neurosci (2000) 1.28
Development of endocochlear potential and its negative component in mouse cochlea. Hear Res (1995) 1.28
Evidence for a medial K+ recycling pathway from inner hair cells. Hear Res (1998) 1.24
Spatiotemporal expression of otogelin in the developing and adult mouse inner ear. Hear Res (2001) 1.18
Immunocytochemical localization of a high-affinity glutamate-aspartate transporter, GLAST, in the rat and guinea-pig cochlea. Eur J Neurosci (1997) 1.12
Mapping the distribution of outer hair cell voltage-dependent conductances by electrical amputation. Biophys J (1997) 1.10
Organization of cell junctions and cytoskeleton in the reticular lamina in normal and ototoxically damaged organ of Corti. Hear Res (1997) 1.09
Intracellular recordings from supporting cells in the guinea pig cochlea: DC potentials. J Neurophysiol (1990) 0.98
Expression of connexin 26 and Na,K-ATPase in the developing mouse cochlear lateral wall: functional implications. Brain Res (1999) 0.97
Gap junction systems in the rat vestibular labyrinth: immunohistochemical and ultrastructural analysis. Acta Otolaryngol (1994) 0.95
Ontogenetic approach to inner and outer hair cell function. Hear Res (1980) 0.91
Immunolocalization of connexin 26 in the developing mouse cochlea. Brain Res Brain Res Rev (2000) 0.87
Effects of kanamycin sulfate on cochlear potentials and potassium ion permeability through the cochlear partitions. ORL J Otorhinolaryngol Relat Spec (1987) 0.81
Androgen receptor regulates a distinct transcription program in androgen-independent prostate cancer. Cell (2009) 7.09
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome. Nat Genet (2003) 4.44
A family cluster of infections by a newly recognized bunyavirus in eastern China, 2007: further evidence of person-to-person transmission. Clin Infect Dis (2011) 3.91
Ciliary proteins link basal body polarization to planar cell polarity regulation. Nat Genet (2007) 3.79
Changes in hippocampal connectivity in the early stages of Alzheimer's disease: evidence from resting state fMRI. Neuroimage (2006) 3.77
Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse. Cell (2006) 3.71
Gap junctions and the connexin protein family. Cardiovasc Res (2004) 3.66
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. Nat Genet (2010) 3.63
Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle. EMBO J (2002) 3.53
Astroglial metabolic networks sustain hippocampal synaptic transmission. Science (2008) 3.49
Engraftment of connexin 43-expressing cells prevents post-infarct arrhythmia. Nature (2007) 3.46
A gene expression atlas of the model legume Medicago truncatula. Plant J (2008) 3.38
Defining the roles of the periplasmic chaperones SurA, Skp, and DegP in Escherichia coli. Genes Dev (2007) 3.24
Metabolic inhibition induces opening of unapposed connexin 43 gap junction hemichannels and reduces gap junctional communication in cortical astrocytes in culture. Proc Natl Acad Sci U S A (2001) 3.17
Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2. PLoS Genet (2006) 3.16
Lipoprotein SmpA is a component of the YaeT complex that assembles outer membrane proteins in Escherichia coli. Proc Natl Acad Sci U S A (2007) 3.09
Imaging of Plasmodium liver stages to drive next-generation antimalarial drug discovery. Science (2011) 3.07
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31. Nat Genet (2003) 2.98
Expression and functions of neuronal gap junctions. Nat Rev Neurosci (2005) 2.91
The impact of astrocytic gap junctional coupling on potassium buffering in the hippocampus. J Neurosci (2006) 2.85
Platelet glycoprotein Ibalpha forms catch bonds with human WT vWF but not with type 2B von Willebrand disease vWF. J Clin Invest (2008) 2.43
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes. Proc Natl Acad Sci U S A (2004) 2.41
MtHAP2-1 is a key transcriptional regulator of symbiotic nodule development regulated by microRNA169 in Medicago truncatula. Genes Dev (2006) 2.41
Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells. Hum Mol Genet (2005) 2.38
Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin. Hum Mol Genet (2003) 2.37
Inhibition of breast cancer metastasis by selective synthetic polypeptide against CXCR4. Cancer Res (2004) 2.31
Loss of connexin36 channels alters beta-cell coupling, islet synchronization of glucose-induced Ca2+ and insulin oscillations, and basal insulin release. Diabetes (2005) 2.24
Slow conduction and enhanced anisotropy increase the propensity for ventricular tachyarrhythmias in adult mice with induced deletion of connexin43. Circulation (2004) 2.23
An automatic valuation system in the human brain: evidence from functional neuroimaging. Neuron (2009) 2.20
Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential. Hum Mol Genet (2003) 2.17
Interactions in the network of Usher syndrome type 1 proteins. Hum Mol Genet (2004) 2.16
A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth. Development (2008) 2.09
KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential. Am J Physiol Cell Physiol (2002) 2.08
Low peak bone mass and attenuated anabolic response to parathyroid hormone in mice with an osteoblast-specific deletion of connexin43. J Cell Sci (2006) 2.06
Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning. J Neurosci (2007) 2.05
Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly. Hum Mol Genet (2004) 2.04
Global changes in transcription orchestrate metabolic differentiation during symbiotic nitrogen fixation in Lotus japonicus. Plant J (2004) 1.99
Functional network disruption in the degenerative dementias. Lancet Neurol (2011) 1.98
Genomic analysis of the immune gene repertoire of amphioxus reveals extraordinary innate complexity and diversity. Genome Res (2008) 1.92
Remorin, a solanaceae protein resident in membrane rafts and plasmodesmata, impairs potato virus X movement. Plant Cell (2009) 1.91
Coregistered tomographic x-ray and optical breast imaging: initial results. J Biomed Opt (2005) 1.89
Deafness in Claudin 11-null mice reveals the critical contribution of basal cell tight junctions to stria vascularis function. J Neurosci (2004) 1.86
Probing the barrier function of the outer membrane with chemical conditionality. ACS Chem Biol (2006) 1.86
Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cells. Dev Biol (2005) 1.84
Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells. J Cell Sci (2005) 1.84
Loss of cochlear HCO3- secretion causes deafness via endolymphatic acidification and inhibition of Ca2+ reabsorption in a Pendred syndrome mouse model. Am J Physiol Renal Physiol (2007) 1.83
Connexin hemichannel-mediated CO2-dependent release of ATP in the medulla oblongata contributes to central respiratory chemosensitivity. J Physiol (2010) 1.81
Structural basis of substrate discrimination and integrin binding by autotaxin. Nat Struct Mol Biol (2011) 1.81
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss. Hum Mol Genet (2003) 1.80
Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study. Am J Hum Genet (2003) 1.79
How the genetics of deafness illuminates auditory physiology. Annu Rev Physiol (2011) 1.78
An update on connexin genes and their nomenclature in mouse and man. Cell Commun Adhes (2003) 1.77
Association between point-of-care CRP testing and antibiotic prescribing in respiratory tract infections: a systematic review and meta-analysis of primary care studies. Br J Gen Pract (2013) 1.75
Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model. BMC Med (2004) 1.74
Control of exocytosis by synaptotagmins and otoferlin in auditory hair cells. J Neurosci (2010) 1.72
Cardiomyocyte-restricted deletion of connexin43 during mouse development. J Mol Cell Cardiol (2006) 1.70
Reliability analysis of a smartphone-aided measurement method for the Cobb angle of scoliosis. J Spinal Disord Tech (2012) 1.69
SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations. Eur J Hum Genet (2006) 1.69
Tomographic optical breast imaging guided by three-dimensional mammography. Appl Opt (2003) 1.69
Role of olivary electrical coupling in cerebellar motor learning. Neuron (2008) 1.67
Impairment of SLC17A8 encoding vesicular glutamate transporter-3, VGLUT3, underlies nonsyndromic deafness DFNA25 and inner hair cell dysfunction in null mice. Am J Hum Genet (2008) 1.65
Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22. Proc Natl Acad Sci U S A (2002) 1.65
Self-doped Ti3+ enhanced photocatalyst for hydrogen production under visible light. J Am Chem Soc (2010) 1.63
Connexin 43 enhances the adhesivity and mediates the invasion of malignant glioma cells. J Neurosci (2002) 1.62
A remorin protein interacts with symbiotic receptors and regulates bacterial infection. Proc Natl Acad Sci U S A (2010) 1.61
The conditional connexin43G138R mouse mutant represents a new model of hereditary oculodentodigital dysplasia in humans. Hum Mol Genet (2007) 1.61
Environmental and antigen receptor-derived signals support sustained surveillance of the lungs by pathogen-specific cytotoxic T lymphocytes. J Virol (2011) 1.61
Recruitment of an area involved in eye movements during mental arithmetic. Science (2009) 1.61
Accelerated hippocampal spreading depression and enhanced locomotory activity in mice with astrocyte-directed inactivation of connexin43. J Neurosci (2003) 1.59
Adult ceramide synthase 2 (CERS2)-deficient mice exhibit myelin sheath defects, cerebellar degeneration, and hepatocarcinomas. J Biol Chem (2009) 1.58
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis. Orphanet J Rare Dis (2011) 1.57
Neutrophil migration across tight junctions is mediated by adhesive interactions between epithelial coxsackie and adenovirus receptor and a junctional adhesion molecule-like protein on neutrophils. Mol Biol Cell (2005) 1.57
Functional significance of channels and transporters expressed in the inner ear and kidney. Am J Physiol Cell Physiol (2007) 1.57
A central role of connexin 43 in hypoxic preconditioning. J Neurosci (2008) 1.56
Developmental expression of solute carrier family 26A member 4 (SLC26A4/pendrin) during amelogenesis in developing rodent teeth. Eur J Oral Sci (2011) 1.55
Functional properties of mouse connexin30.2 expressed in the conduction system of the heart. Circ Res (2005) 1.54
Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome. Am J Hum Genet (2007) 1.52
Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy. Nat Genet (2006) 1.51
Connexin43 interacts with NOV: a possible mechanism for negative regulation of cell growth in choriocarcinoma cells. J Biol Chem (2004) 1.50
Microarray-based comparison of three amplification methods for nanogram amounts of total RNA. Am J Physiol Cell Physiol (2004) 1.50
Increasing structure dimensionality of copper(I) complexes by varying the flexible thioether ligand geometry and counteranions. Inorg Chem (2006) 1.49
Physiology, pharmacology and plasticity at the inner hair cell synaptic complex. Hear Res (2006) 1.48