Science, medicine, and the future: New interventions in hearing impairment. - Wikidata - wikimedia - TriplyDB

Science, medicine, and the future: New interventions in hearing impairment.

Science, medicine, and the future: New interventions in hearing impairment.

http://www.wikidata.org/entity/Q33800062

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Functional analysis and regulation of purified connexin hemichannels Neonatal screening for hearing impairment.Potentiation of Chemical Ototoxicity by Noise.Mitochondrial rRNA and tRNA and hearing function.Prevalence of permanent childhood hearing impairment in the United Kingdom and implications for universal neonatal hearing screening: questionnaire based ascertainment study.Community-based infant hearing screening for early detection of permanent hearing loss in Lagos, Nigeria: a cross-sectional study.Idiopathic sensorineural hearing loss is associated with endothelial dysfunction.Self-reported hearing difficulty and hearing impairment in Japanese people living in a community.

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P2860

Science, medicine, and the future: New interventions in hearing impairment.

http://www.wikidata.org/entity/Q33800062

description

2000 nî lūn-bûn

@nan

2000 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի մարտին հրատարակված գիտական հոդված

@hy

2000年の論文

@ja

2000年論文

@yue

2000年論文

@zh-hant

2000年論文

@zh-hk

2000年論文

@zh-mo

2000年論文

@zh-tw

2000年论文

@wuu

name

Science, medicine, and the future: New interventions in hearing impairment.

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Science, medicine, and the future: New interventions in hearing impairment.

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Science, medicine, and the future: New interventions in hearing impairment.

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Science, medicine, and the future: New interventions in hearing impairment.

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Science, medicine, and the future: New interventions in hearing impairment.

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Science, medicine, and the future: New interventions in hearing impairment.

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P2860

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

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

Connexin-26 mutations in sporadic and inherited sensorineural deafness

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

Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

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

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

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

Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells

Role of myosin VI in the differentiation of cochlear hair cells

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