Molecular and physiological bases of the K+ circulation in the mammalian inner ear. (Q36600743)

15 August 2017

1 reference

title

Molecular and physiological bases of the K+ circulation in the mammalian inner ear. (English)

1 reference

15 August 2017

Hiroshi Hibino

1

1 reference

PubMed ID

16990454

15 August 2017

Yoshihisa Kurachi

series ordinal

2

1 reference

PubMed ID

16990454

15 August 2017

language of work or name

1 reference

1 October 2006

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15 August 2017

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15 August 2017

21

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15 August 2017

336-345

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Differential expression of KCNQ4 in inner hair cells and sensory neurons is the basis of progressive high-frequency hearing loss.

15 August 2017

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Connexin mutations in X-linked Charcot-Marie-Tooth disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Deafness and renal tubular acidosis in mice lacking the K-Cl co-transporter Kcc4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Loss of K-Cl co-transporter KCC3 causes deafness, neurodegeneration and reduced seizure threshold

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Immunohistochemical localization of the Na-K-Cl co-transporter (NKCC1) in the gerbil inner ear.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Deafness and imbalance associated with inactivation of the secretory Na-K-2Cl co-transporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Connexin 26 gene linked to a dominant deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Hereditary motor and sensory neuropathy with agenesis of the corpus callosum

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Barttin is a Cl- channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Connexin-26 mutations in sporadic and inherited sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Mice lacking the basolateral Na-K-2Cl cotransporter have impaired epithelial chloride secretion and are profoundly deaf.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Deafness in Claudin 11-null mice reveals the critical contribution of basal cell tight junctions to stria vascularis function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Gap junctions between the supporting cells in some acoustico-vestibular receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350)

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

21 January 2018

How the ear's works work

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Electrochemical profiles for monovalent ions in the stria vascularis: cellular model of ion transport mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Reduction in the endocochlear potential caused by Cs(+) in the perilymph can be explained by the five-compartment model of the stria vascularis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Molecular and cellular mechanisms of cardiac arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Cellular localization of Na+, K+-ATPase in the mammalian cochlear duct: Significance for cochlear fluid balance

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Mice with altered KCNQ4 K+ channels implicate sensory outer hair cells in human progressive deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Potassium ion recycling pathway via gap junction systems in the mammalian cochlea and its interruption in hereditary nonsyndromic deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Compartmentalization established by claudin-11-based tight junctions in stria vascularis is required for hearing through generation of endocochlear potential.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Expression patterns of claudins, tight junction adhesion molecules, in the inner ear

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Ion transport in guinea pig cochlea. I. Potassium and sodium transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

The cochlear potentials. I. The effect of ouabain on the cochlear potentials of the guinea pig.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

The gap junction communication channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Expression of the gap-junction connexins 26 and 30 in the rat cochlea

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Association of beta-catenin with the alpha-subunit of neuronal large-conductance Ca2+-activated K+ channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

A voltage- and Ca2+-dependent big conductance K channel in cochlear spiral ligament fibrocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Transepithelial voltage and resistance of vestibular dark cell epithelium from the gerbil ampulla.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Changes in cation contents of stria vascularis with ouabain and potassium-free perfusion

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Effects of barium and ion substitutions in artificial blood on endocochlear potential

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Electrophysiological measurements of the stria vascularis potentials in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Altered cochlear fibrocytes in a mouse model of DFN3 nonsyndromic deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Differential distribution of Ca2+-activated K+ channel splice variants among hair cells along the tonotopic axis of the chick cochlea.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Expression and functional phenotype of mouse ERG K+ channels in the inner ear: potential role in K+ regulation in the inner ear.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Positive endocochlear potential: mechanism of production by marginal cells of stria vascularis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Inner ear abnormalities in a Kcnq1 (Kvlqt1) knockout mouse: a model of Jervell and Lange-Nielsen syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Distribution of Ca2+-activated K+ channel isoforms along the tonotopic gradient of the chicken's cochlea.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Na-K-Cl cotransporter expression in the developing and senescent gerbil cochlea.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Distribution of immunoreactive Na+,K+-ATPase in gerbil cochlea.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

KCNE1 mutations cause jervell and Lange-Nielsen syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Immunolocalization of voltage-gated potassium channel Kv3.1b subunit in the cochlea

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Expression and functions of neuronal gap junctions

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

The fine structure of spiral ligament cells relates to ion return to the stria and varies with place-frequency

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Novel structures in marginal and intermediate cells presumably relate to functions of apical versus basal strial strata

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

High-throughput screening for GJB2 mutations--its clinical application to genetic testing in prelingual deafness screening for GJB2 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Voltage-activated K channel in luminal membrane of marginal cells of stria vascularis dissected from guinea pig.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Endocochlear potential and endolymphatic K+ changes induced by gap junction blockers

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Expression of gap junction protein connexin43 in the adult rat cochlea: comparison with connexin26.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Dye-coupling of melanocytes with endothelial cells and pericytes in the cochlea of gerbils

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Inwardly rectifying K+ currents in intermediate cells in the cochlea of gerbils: a possible contribution to the endocochlear potential.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Mechanism generating endocochlear potential: role played by intermediate cells in stria vascularis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Ion channels in basolateral membrane of marginal cells dissociated from gerbil stria vascularis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

A novel ATP-dependent inward rectifier potassium channel expressed predominantly in glial cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Claudin-based barrier in simple and stratified cellular sheets

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

The novel R75Q mutation in the GJB2 gene causes autosomal dominant hearing loss and palmoplantar keratoderma in a Turkish family

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Inner ear defects induced by null mutation of the isk gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Comparison of ion transport mechanisms between vestibular dark cells and strial marginal cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

K+ cycling and the endocochlear potential

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Ion transport mechanisms responsible for K+ secretion and the transepithelial voltage across marginal cells of stria vascularis in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Connexin mutations in deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Evidence for a prostate cancer susceptibility locus on the X chromosome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Effect of Ouabain on Cochlear Potentials and Endolymph Composition in Guinea Pigs

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

Resting Potentials Inside the Cochlear Partition of the Guinea Pig

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOL.00023.2006

10.1152/PHYSIOL.00023.2006

21 January 2018

Identifiers

DOI

1 reference

15 August 2017

1 reference

PubMed ID

16990454