| P2093 | author name string | Hiroshi Hibino | |
| | Yoshihisa Kurachi | |
| P2860 | cites work | KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness | Q22008780 |
| | A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome | Q24318498 |
| | Connexin mutations in X-linked Charcot-Marie-Tooth disease | Q24323296 |
| | Connexin 26 mutations in hereditary non-syndromic sensorineural deafness | Q28115871 |
| | Connexin-26 mutations in sporadic and inherited sensorineural deafness | Q28117673 |
| | Deafness and imbalance associated with inactivation of the secretory Na-K-2Cl co-transporter | Q28137646 |
| | Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss | Q28139583 |
| | Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus | Q28143612 |
| | Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness | Q28191572 |
| | K+ cycling and the endocochlear potential | Q28198160 |
| | Claudin-based barrier in simple and stratified cellular sheets | Q28201833 |
| | Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure | Q28203023 |
| | The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum | Q28205749 |
| | Barttin is a Cl- channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion | Q28209314 |
| | Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential | Q28218302 |
| | Expression patterns of claudins, tight junction adhesion molecules, in the inner ear | Q28236557 |
| | KCNE1 mutations cause jervell and Lange-Nielsen syndrome | Q28253362 |
| | How the ear's works work | Q28272150 |
| | Ion transport in guinea pig cochlea. I. Potassium and sodium transport | Q28275996 |
| | Expression of the gap-junction connexins 26 and 30 in the rat cochlea | Q28287580 |
| | Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis | Q28300307 |
| | Mice with altered KCNQ4 K+ channels implicate sensory outer hair cells in human progressive deafness | Q28594332 |
| | Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death | Q30578611 |
| | Hereditary motor and sensory neuropathy with agenesis of the corpus callosum | Q30808946 |
| | Dye-coupling of melanocytes with endothelial cells and pericytes in the cochlea of gerbils | Q32054738 |
| | Inner ear abnormalities in a Kcnq1 (Kvlqt1) knockout mouse: a model of Jervell and Lange-Nielsen syndrome | Q33215010 |
| | A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families | Q33864995 |
| | Deafness and renal tubular acidosis in mice lacking the K-Cl co-transporter Kcc4. | Q34125574 |
| | Molecular and cellular mechanisms of cardiac arrhythmias | Q34175373 |
| | Gap junctions between the supporting cells in some acoustico-vestibular receptors | Q34356503 |
| | Inner ear defects induced by null mutation of the isk gene | Q34412325 |
| | Immunohistochemical localization of the Na-K-Cl co-transporter (NKCC1) in the gerbil inner ear. | Q34430390 |
| | Potassium ion recycling pathway via gap junction systems in the mammalian cochlea and its interruption in hereditary nonsyndromic deafness | Q34505515 |
| | A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350) | Q35433462 |
| | Association of beta-catenin with the alpha-subunit of neuronal large-conductance Ca2+-activated K+ channels | Q35736357 |
| | Expression and functions of neuronal gap junctions | Q36058425 |
| | Deafness in Claudin 11-null mice reveals the critical contribution of basal cell tight junctions to stria vascularis function. | Q36191433 |
| | Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene | Q38970459 |
| | Loss of K-Cl co-transporter KCC3 causes deafness, neurodegeneration and reduced seizure threshold | Q39962346 |
| | Mechanism generating endocochlear potential: role played by intermediate cells in stria vascularis | Q40173673 |
| | Expression and functional phenotype of mouse ERG K+ channels in the inner ear: potential role in K+ regulation in the inner ear. | Q40370415 |
| | Na-K-Cl cotransporter expression in the developing and senescent gerbil cochlea. | Q40857559 |
| | The gap junction communication channel | Q40974984 |
| | Comparison of ion transport mechanisms between vestibular dark cells and strial marginal cells | Q41282690 |
| | Changes in cation contents of stria vascularis with ouabain and potassium-free perfusion | Q41634998 |
| | How hearing happens | Q41656220 |
| | Ion transport mechanisms responsible for K+ secretion and the transepithelial voltage across marginal cells of stria vascularis in vitro | Q41679999 |
| | Effects of barium and ion substitutions in artificial blood on endocochlear potential | Q42435626 |
| | Expression of gap junction protein connexin43 in the adult rat cochlea: comparison with connexin26. | Q42443122 |
| | Compartmentalization established by claudin-11-based tight junctions in stria vascularis is required for hearing through generation of endocochlear potential. | Q42468531 |
| | Novel structures in marginal and intermediate cells presumably relate to functions of apical versus basal strial strata | Q42473387 |
| | Differential expression of KCNQ4 in inner hair cells and sensory neurons is the basis of progressive high-frequency hearing loss. | Q42484960 |
| | Electrophysiological measurements of the stria vascularis potentials in vivo | Q42487624 |
| | Expression of alpha and beta subunit isoforms of Na,K-ATPase in the mouse inner ear and changes with mutations at the Wv or Sld loci | Q42492991 |
| | Electrochemical profiles for monovalent ions in the stria vascularis: cellular model of ion transport mechanisms | Q42498992 |
| | KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential | Q42515610 |
| | Reduction in the endocochlear potential caused by Cs(+) in the perilymph can be explained by the five-compartment model of the stria vascularis | Q42522324 |
| | The fine structure of spiral ligament cells relates to ion return to the stria and varies with place-frequency | Q42527121 |
| | A voltage- and Ca2+-dependent big conductance K channel in cochlear spiral ligament fibrocytes | Q42594859 |
| | Immunolocalization of voltage-gated potassium channel Kv3.1b subunit in the cochlea | Q43720243 |
| | The novel R75Q mutation in the GJB2 gene causes autosomal dominant hearing loss and palmoplantar keratoderma in a Turkish family | Q44173488 |
| | Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness | Q44201543 |
| | Expression of an inwardly rectifying K+ channel, Kir5.1, in specific types of fibrocytes in the cochlear lateral wall suggests its functional importance in the establishment of endocochlear potential | Q44747842 |
| | Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness | Q44884995 |
| | Endocochlear potential and endolymphatic K+ changes induced by gap junction blockers | Q45129623 |
| | Voltage-activated K channel in luminal membrane of marginal cells of stria vascularis dissected from guinea pig. | Q46786304 |
| | The cochlear potentials. I. The effect of ouabain on the cochlear potentials of the guinea pig. | Q46919314 |
| | Inwardly rectifying K+ currents in intermediate cells in the cochlea of gerbils: a possible contribution to the endocochlear potential | Q47876563 |
| | Connexin 26 gene linked to a dominant deafness | Q47991729 |
| | Distribution of Ca2+-activated K+ channel isoforms along the tonotopic gradient of the chicken's cochlea | Q48042092 |
| | Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans | Q48045551 |
| | A novel ATP-dependent inward rectifier potassium channel expressed predominantly in glial cells. | Q48072198 |
| | Altered cochlear fibrocytes in a mouse model of DFN3 nonsyndromic deafness. | Q48126240 |
| | Connexin mutations in deafness | Q48933412 |
| | High-throughput screening for GJB2 mutations--its clinical application to genetic testing in prelingual deafness screening for GJB2 mutations. | Q50487023 |
| | Mice lacking the basolateral Na-K-2Cl cotransporter have impaired epithelial chloride secretion and are profoundly deaf. | Q50499859 |
| | Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice. | Q50500527 |
| | Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma. | Q50502976 |
| | Differential distribution of Ca2+-activated K+ channel splice variants among hair cells along the tonotopic axis of the chick cochlea. | Q50507448 |
| | Distribution of immunoreactive Na+,K+-ATPase in gerbil cochlea. | Q50559424 |
| | Ion channels in basolateral membrane of marginal cells dissociated from gerbil stria vascularis. | Q52350052 |
| | Positive endocochlear potential: mechanism of production by marginal cells of stria vascularis. | Q53883513 |
| | Cellular localization of Na+, K+-ATPase in the mammalian cochlear duct: Significance for cochlear fluid balance | Q53933037 |
| | Transepithelial voltage and resistance of vestibular dark cell epithelium from the gerbil ampulla. | Q54215204 |
| | Evidence for a prostate cancer susceptibility locus on the X chromosome. | Q57274826 |
| | Effect of Ouabain on Cochlear Potentials and Endolymph Composition in Guinea Pigs | Q58280567 |
| | Resting Potentials Inside the Cochlear Partition of the Guinea Pig | Q59061801 |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 336-345 | |
| P577 | publication date | 2006-10-01 | |
| P1433 | published in | Physiology | Q1091804 |
| P1476 | title | Molecular and physiological bases of the K+ circulation in the mammalian inner ear. | |
| P478 | volume | 21 | |