(Q33922424)

30 July 2017

title

Longitudinal gradients of KCNQ4 expression in spiral ganglion and cochlear hair cells correlate with progressive hearing loss in DFNA2. (English)

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30 July 2017

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longitudinal gradient

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4

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30 July 2017

Beisel KW

1

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30 July 2017

Nelson NC

series ordinal

2

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30 July 2017

Delimont DC

series ordinal

3

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30 July 2017

publication date

1 October 2000

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30 July 2017

published in

Molecular Brain Research

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30 July 2017

volume

82

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30 July 2017

issue

1-2

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30 July 2017

page(s)

137-149

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Characterization of G-protein betagamma expression in inner ear.

30 July 2017

cites work

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Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.

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Response characteristics of mammalian cochlear hair cells

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Developmental changes in the physiology of hair cells

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Hair Cells in Mammalian Utricles

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Limiting dynamics of high-frequency electromechanical transduction of outer hair cells

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7 January 2021

Pathology of the ear in the cardio-auditory syndrome of Jervell and Lange-Nielsen. Report of a third case with an appendix on possible linkage with the Rh blood group locus

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Development and maintenance of ear innervation and function: lessons from mutations in mouse and man.

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Developmental evolutionary biology of the vertebrate ear: conserving mechanoelectric transduction and developmental pathways in diverging morphologies

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Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

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7 January 2021

An ATP-dependent inwardly rectifying potassium channel, KAB-2 (Kir4. 1), in cochlear stria vascularis of inner ear: its specific subcellular localization and correlation with the formation of endocochlear potential.

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7 January 2021

Ionic currents of outer hair cells isolated from the guinea-pig cochlea

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7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

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7 January 2021

KCNQ4, a K+ channel mutated in a form of dominant deafness, is expressed in the inner ear and the central auditory pathway.

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7 January 2021

Expression of a potassium current in inner hair cells during development of hearing 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

Non-syndromic autosomal dominant sensorineural hearing loss: a new field of research

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7 January 2021

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

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7 January 2021

Molecular cloning and functional expression of KCNQ5, a potassium channel subunit that may contribute to neuronal M-current diversity

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7 January 2021

Patch clamped responses from outer hair cells in the intact adult organ of Corti

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7 January 2021

Developmental expression of the potassium current IK,n contributes to maturation of mouse outer hair cells.

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7 January 2021

Inherited nonsyndromic hearing loss. An audiovestibular study in a large family with autosomal dominant progressive hearing loss related to DFNA2.

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7 January 2021

Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias

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7 January 2021

Expression of Delta1 and Serrate1 (Jagged1) in the mouse inner ear

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7 January 2021

Multiple modes of inner hair cell stimulation.

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7 January 2021

Sodium current expression during postnatal development of rat outer hair cells

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7 January 2021

KCNE1 mutations cause jervell and Lange-Nielsen syndrome

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7 January 2021

KCNQ5, a novel potassium channel broadly expressed in brain, mediates M-type currents

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7 January 2021

Deafness genes: expressions of surprise

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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

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

https://api.crossref.org/works/10.1016%2FS0169-328X%2800%2900204-7

7 January 2021

Eight potassium channel families revealed by the C. elegans genome project

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https://api.crossref.org/works/10.1016%2FS0169-328X%2800%2900204-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2800%2900204-7

7 January 2021

Auditory collusion and a coupled couple of outer hair cells

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2800%2900204-7

7 January 2021

Visualization of alpha9 acetylcholine receptor expression in hair cells of transgenic mice containing a modified bacterial artificial chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2800%2900204-7

7 January 2021

10.1016/S0169-328X(00)00204-7

Identifiers

DOI

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30 July 2017

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