The contribution of genes involved in potassium-recycling in the inner ear to noise-induced hearing loss (Q34545156)

2 August 2017

title

The contribution of genes involved in potassium-recycling in the inner ear to noise-induced hearing loss (English)

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2 August 2017

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Lut Van Laer

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2 August 2017

Per-Inge Carlsson

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2 August 2017

Natacha Ottschytsch

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2 August 2017

Marie-Louise Bondeson

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2 August 2017

Annelies Konings

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2 August 2017

Ann Vandevelde

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2 August 2017

Nele Dieltjens

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2 August 2017

Erik Fransen

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2 August 2017

Dirk Snyders

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2 August 2017

Erik Borg

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2 August 2017

Adam Raes

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2 August 2017

Guy Van Camp

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2 August 2017

publication date

1 August 2006

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2 August 2017

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2 August 2017

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2 August 2017

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2 August 2017

page(s)

786-795

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

2 August 2017

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RNA interference reveals that endogenous Xenopus MinK-related peptides govern mammalian K+ channel function in oocyte expression studies

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7 January 2021

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

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Maximum-likelihood estimation of haplotype frequencies in nuclear families

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A powerful strategy to account for multiple testing in the context of haplotype analysis

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ConSeq: the identification of functionally and structurally important residues in protein sequences

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The influence of genetic variation in oxidative stress genes on human noise susceptibility

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7 January 2021

Genotype transposer: automated genotype manipulation for linkage disequilibrium analysis

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Genetic basis for susceptibility to noise-induced hearing loss in mice

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

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

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Genetics of age-related hearing loss in mice. III. Susceptibility of inbred and F1 hybrid strains to noise-induced hearing loss

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

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Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

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Progressive hearing loss and increased susceptibility to noise-induced hearing loss in mice carrying a Cdh23 but not a Myo7a mutation

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7 January 2021

Effect of interaction between noise and toluene on auditory function in the rat.

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7 January 2021

DHPLC analysis of potassium ion channel genes in congenital long QT syndrome

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7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

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7 January 2021

Family-based association analysis with tightly linked markers

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7 January 2021

Deficiency in plasma membrane calcium ATPase isoform 2 increases susceptibility to noise-induced hearing loss in mice

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7 January 2021

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

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7 January 2021

Gating of shaker-type channels requires the flexibility of S6 caused by prolines

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7 January 2021

Combined effects of noise and styrene exposure on hearing function in the rat.

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Influence of genotype and age on acute acoustic trauma and recovery in CBA/Ca and C57BL/6J mice

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Connexin 31 (GJB3) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment

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7 January 2021

Genome-wide strategies for detecting multiple loci that influence complex diseases.

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7 January 2021

Structural determinants of KvLQT1 control by the KCNE family of proteins

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7 January 2021

KCNE1 binds to the KCNQ1 pore to regulate potassium channel activity

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7 January 2021

Noise-induced transient microlesions in the cell membranes of auditory hair cells

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7 January 2021

The future of association studies: gene-based analysis and replication

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7 January 2021

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

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7 January 2021

Targeted deletion of the cytosolic Cu/Zn-superoxide dismutase gene (Sod1) increases susceptibility to noise-induced hearing loss

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7 January 2021

Targeted mutation of the gene for cellular glutathione peroxidase (Gpx1) increases noise-induced hearing loss in mice

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7 January 2021

Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients

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7 January 2021

Are rare variants responsible for susceptibility to complex diseases?

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7 January 2021

Excitotoxicity, synaptic repair, and functional recovery in the mammalian cochlea: a review of recent findings

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7 January 2021

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

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7 January 2021

Antioxidant status and hearing function in noise-exposed workers

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7 January 2021

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

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7 January 2021

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

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7 January 2021

Proarrhythmic consequences of a KCNQ1 AKAP-binding domain mutation: computational models of whole cells and heterogeneous tissue.

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7 January 2021

KCNE1 mutations cause Jervell and Lange-Nielsen syndrome

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7 January 2021

How really rare are rare diseases?: the intriguing case of independent compound mutations in the long QT syndrome

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7 January 2021

Effects of coexposure to noise and mixture of organic solvents on hearing in dockyard workers

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7 January 2021

Mutations in the hminK gene cause long QT syndrome and suppress lKs function

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7 January 2021

Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss

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7 January 2021

STUDY OF NOISE AND HEARING IN JUTE WEAVING.

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7 January 2021

Exclusion of KCNE1 (IsK) as a Candidate Gene for Jervell and Lange-Nielsen Syndrome

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7 January 2021

Age and noise-induced hearing loss

1 reference

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7 January 2021

IsK and KvLQT1: Mutation in Either of the Two Subunits of the Slow Component of the Delayed Rectifier Potassium Channel Can Cause Jervell and Lange-Nielsen Syndrome

1 reference

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7 January 2021

K+ cycling and the endocochlear potential

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7 January 2021

Compound mutations: a common cause of severe long-QT syndrome

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7 January 2021

Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment

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7 January 2021

Identifiers

DOI

10.1002/HUMU.20360

1 reference

2 August 2017

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