Cochlin in normal middle ear and abnormal middle ear deposits in DFNA9 and Coch (G88E/G88E) mice. - Wikidata - awgldk - TriplyDB

Cochlin in normal middle ear and abnormal middle ear deposits in DFNA9 and Coch (G88E/G88E) mice.

Cochlin in normal middle ear and abnormal middle ear deposits in DFNA9 and Coch (G88E/G88E) mice.

http://www.wikidata.org/entity/Q35321185

about

Histopathology of the Human Inner Ear in the p.L114P COCH Mutation (DFNA9).Immunohistochemical techniques for the human inner ear.Novel COCH p.V123E Mutation, Causative of DFNA9 Sensorineural Hearing Loss and Vestibular Disorder, Shows Impaired Cochlin Post-Translational Cleavage and Secretion.

P2860

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P2860

Cochlin in normal middle ear and abnormal middle ear deposits in DFNA9 and Coch (G88E/G88E) mice.

http://www.wikidata.org/entity/Q35321185

description

2014 nî lūn-bûn

@nan

2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հուլիսին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Cochlin in normal middle ear a ...... NA9 and Coch (G88E/G88E) mice.

@ast

Cochlin in normal middle ear a ...... NA9 and Coch (G88E/G88E) mice.

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type

label

Cochlin in normal middle ear a ...... NA9 and Coch (G88E/G88E) mice.

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Cochlin in normal middle ear a ...... NA9 and Coch (G88E/G88E) mice.

@en

prefLabel

Cochlin in normal middle ear a ...... NA9 and Coch (G88E/G88E) mice.

@ast

Cochlin in normal middle ear a ...... NA9 and Coch (G88E/G88E) mice.

@en

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S10162-014-0481-9

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Cochlin in normal middle ear a ...... NA9 and Coch (G88E/G88E) mice.

@en

P2093

Anne B S Giersch

http://www.w3.org/2001/XMLSchema#string

Cheng Ai Ong

http://www.w3.org/2001/XMLSchema#string

Cynthia C Morton

http://www.w3.org/2001/XMLSchema#string

Jennifer T O'Malley

http://www.w3.org/2001/XMLSchema#string

Jun Shen

http://www.w3.org/2001/XMLSchema#string

Konstantina M Stankovic

http://www.w3.org/2001/XMLSchema#string

Nahid G Robertson

http://www.w3.org/2001/XMLSchema#string

P2860

NMR structure of the LCCL domain and implications for DFNA9 deafness disorder

Distribution and evolution of von Willebrand/integrin A domains: widely dispersed domains with roles in cell adhesion and elsewhere

Subcellular localisation, secretion, and post-translational processing of normal cochlin, and of mutants causing the sensorineural deafness and vestibular disorder, DFNA9

Cochlin, intraocular pressure regulation and mechanosensing

Crystal structure of the A domain from the alpha subunit of integrin CR3 (CD11b/CD18)

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

Role of the pro-inflammatory cytokines tumor necrosis factor-alpha, interleukin-1 beta, interleukin-6 and interleukin-8 in the pathogenesis of the otitis media with effusion

Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9

Autosomal dominant sensorineural hearing loss. Pedigrees, audiologic findings, and temporal bone findings in two kindreds

Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening

P2888

s10162-014-0481-9

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961-974

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scholarly article

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10.1007/S10162-014-0481-9

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6

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15

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2014-07-22T00:00:00Z

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264126185

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25049087

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