Longitudinal gradients of KCNQ4 expression in spiral ganglion and cochlear hair cells correlate with progressive hearing loss in DFNA2. (Q33922424)

30 July 2017

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

1 reference

30 July 2017

1 reference

longitudinal gradient

1 reference

4

1 reference

30 July 2017

Beisel KW

1

1 reference

PubMed ID

11042367

30 July 2017

Nelson NC

series ordinal

2

1 reference

PubMed ID

11042367

30 July 2017

Delimont DC

series ordinal

3

1 reference

30 July 2017

1 October 2000

1 reference

30 July 2017

Molecular Brain Research

1 reference

30 July 2017

82

1 reference

30 July 2017

1-2

1 reference

30 July 2017

137-149

1 reference

Characterization of G-protein betagamma expression in inner ear.

30 July 2017

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

Response characteristics of mammalian cochlear hair cells

1 reference

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

7 January 2021

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

1 reference

7 January 2021

Developmental changes in the physiology of hair cells

1 reference

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

7 January 2021

Hair Cells in Mammalian Utricles

1 reference

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

7 January 2021

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

1 reference

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

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

1 reference

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

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.

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

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

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.

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

Multiple modes of inner hair cell stimulation.

1 reference

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

7 January 2021

Sodium current expression during postnatal development of rat outer hair cells

1 reference

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

7 January 2021

KCNE1 mutations cause jervell and Lange-Nielsen syndrome

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

Deafness genes: expressions of surprise

1 reference

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

7 January 2021

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

1 reference

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

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.

1 reference

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

1 reference

30 July 2017

1 reference

PubMed ID

11042367