(Q33650503)

28 July 2017

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title

Deafness genes: expressions of surprise (English)

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28 July 2017

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Steel KP

1

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28 July 2017

Bussoli TJ

series ordinal

2

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28 July 2017

publication date

1 June 1999

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28 July 2017

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28 July 2017

volume

15

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28 July 2017

issue

6

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28 July 2017

page(s)

207-211

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Genetic epidemiology of hearing impairment

28 July 2017

cites work

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7 January 2021

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The gene for an inherited form of deafness maps to chromosome 5q31

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7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

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7 January 2021

Connexin-26 mutations in sporadic and inherited sensorineural deafness

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7 January 2021

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

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7 January 2021

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

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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

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

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7 January 2021

Cellular localization of rat Isk protein in the stria vascularis by immunohistochemical observation

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7 January 2021

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

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7 January 2021

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction

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7 January 2021

Human cochlear expressed sequence tags provide insight into cochlear gene expression and identify candidate genes for deafness

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7 January 2021

Unconventional myosins in inner-ear sensory epithelia

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7 January 2021

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

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7 January 2021

Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous

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7 January 2021

Changes in the subcellular localization of the Brn4 gene product precede mesenchymal remodeling of the otic capsule

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7 January 2021

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

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7 January 2021

The mouse tectorins. Modular matrix proteins of the inner ear homologous to components of the sperm-egg adhesion system

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7 January 2021

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

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7 January 2021

Nonsyndromic hearing impairment is associated with a mutation in DFNA5

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7 January 2021

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

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7 January 2021

A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family

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7 January 2021

Pax-3, a novel murine DNA binding protein expressed during early neurogenesis.

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7 January 2021

Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein

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7 January 2021

Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model

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7 January 2021

Cloning and functional expression of human cDNA for the ETB endothelin receptor

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7 January 2021

Immunoreactivity of endothelins and endothelin receptor in the stria vascularis of the mouse cochlea

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7 January 2021

The site of action of neuronal acidic fibroblast growth factor is the organ of Corti of the rat cochlea

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7 January 2021

Positional cloning of a gene involved in the pathogenesis of Treacher Collins syndrome. The Treacher Collins Syndrome Collaborative Group

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7 January 2021

Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.

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7 January 2021

Ultrastructural, physiological, and molecular defects in the inner ear of a gene-knockout mouse model for autosomal Alport syndrome

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7 January 2021

Expression and localization of COL2A1 mRNA and type II collagen in human fetal cochlea.

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7 January 2021

A novel X-linked gene, DDP, shows mutations in families with deafness (DFN-1), dystonia, mental deficiency and blindness

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901753-9

7 January 2021

The fundamental and medical impacts of recent progress in research on hereditary hearing loss.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901753-9

7 January 2021

Hear come more genes!

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https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901753-9

7 January 2021

10.1016/S0168-9525(99)01753-9

Identifiers

DOI

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28 July 2017

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