(Q34139587)

31 July 2017

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title

A genetic approach to understanding auditory function (English)

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31 July 2017

Steel KP

1

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PubMed ID

11175778

31 July 2017

Kros CJ

series ordinal

2

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PubMed ID

11175778

31 July 2017

language of work or name

English

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publication date

1 February 2001

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31 July 2017

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31 July 2017

27

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31 July 2017

143-149

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31 July 2017

2

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https://scigraph.springernature.com/pub.10.1038/84758

31 July 2017

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cites work

Genes responsible for human hereditary deafness: symphony of a thousand

1 reference

7 January 2021

A type VII myosin encoded by the mouse deafness gene shaker-1

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7 January 2021

Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

1 reference

7 January 2021

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

1 reference

7 January 2021

Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development

1 reference

7 January 2021

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)

1 reference

7 January 2021

A targeted deletion in alpha-tectorin reveals that the tectorial membrane is required for the gain and timing of cochlear feedback.

1 reference

7 January 2021

Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

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7 January 2021

Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome.

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7 January 2021

Kinetics of the receptor current in bullfrog saccular hair cells.

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7 January 2021

Compliance of the hair bundle associated with gating of mechanoelectrical transduction channels in the bullfrog's saccular hair cell

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7 January 2021

Two mechanisms for transducer adaptation in vertebrate hair cells.

1 reference

7 January 2021

The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

1 reference

7 January 2021

Role of myosin VI in the differentiation of cochlear hair cells

1 reference

7 January 2021

Defective myosin VIIA gene responsible for Usher syndrome type 1B

1 reference

7 January 2021

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

1 reference

7 January 2021

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

1 reference

7 January 2021

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

1 reference

7 January 2021

Myosin VI is an actin-based motor that moves backwards

1 reference

7 January 2021

Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complex

1 reference

7 January 2021

A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C

1 reference

7 January 2021

A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene

1 reference

7 January 2021

The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene

1 reference

7 January 2021

The deaf jerker mouse has a mutation in the gene encoding the espin actin-bundling proteins of hair cell stereocilia and lacks espins.

1 reference

7 January 2021

Mechano-electrical transduction currents in isolated vestibular hair cells of the chick

1 reference

7 January 2021

Calcium permeation of the turtle hair cell mechanotransducer channel and its relation to the composition of endolymph

1 reference

7 January 2021

Plasma membrane Ca2+-ATPase extrudes Ca2+ from hair cell stereocilia

1 reference

7 January 2021

Mutations in a plasma membrane Ca2+-ATPase gene cause deafness in deafwaddler mice

1 reference

7 January 2021

Balance and hearing deficits in mice with a null mutation in the gene encoding plasma membrane Ca2+-ATPase isoform 2

1 reference

7 January 2021

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

1 reference

7 January 2021

Congenital deafness and sinoatrial node dysfunction in mice lacking class D L-type Ca2+ channels

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7 January 2021

A sugar transporter as a candidate for the outer hair cell motor.

1 reference

7 January 2021

Prestin is the motor protein of cochlear outer hair cells

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7 January 2021

Expression and localization of prestin and the sugar transporter GLUT-5 during development of electromotility in cochlear outer hair cells.

1 reference

7 January 2021

A Drosophila mechanosensory transduction channel

1 reference

7 January 2021

Targeted disruption of otog results in deafness and severe imbalance

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7 January 2021

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment

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7 January 2021

Strial dysfunction in mice with cochleo-saccular abnormalities

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7 January 2021

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7 January 2021

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

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7 January 2021

Vascular perfusion of the cochlea: Effect of potassium-free and rubidium-substituted media

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7 January 2021

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

1 reference

7 January 2021

Evidence for a medial K+ recycling pathway from inner hair cells.

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Neuronal KCNQ potassium channels: physiology and role in disease.

1 reference

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

7 January 2021

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

1 reference

7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

7 January 2021

Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Inner ear defects induced by null mutation of the isk gene

1 reference

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

7 January 2021

A new spontaneous mouse mutation in the Kcne1 gene

1 reference

7 January 2021

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

1 reference

7 January 2021

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

1 reference

7 January 2021

A mutation in PDS causes non-syndromic recessive deafness

1 reference

7 January 2021

Identifiers

DOI

10.1038/84758

1 reference

31 July 2017

1 reference

PubMed ID

11175778