About: Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters’ cells and the fibrocytes, as the cause of nonsyndromic hearing loss

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About: Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters’ cells and the fibrocytes, as the cause of nonsyndromic hearing loss Goto Sponge NotDistinct Permalink

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scientific article published on October 24, 2003

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rdf:type	Item
description	article científic (ca) article scientific (oc) articol științific (ro) artigo científico (gl) artikulong pang-agham (tl) scienca artikolo (eo) teaduslik artikkel (et) tieteellinen artikkeli (fi) tudományos cikk (hu) vitenskapelig artikkel (nb) vitskapeleg artikkel (nn) επιστημονικό άρθρο (el) мақолаи илмӣ (tg) מאמר מדעי (he) სამეცნიერო სტატია (ka) บทความทางวิทยาศาสตร์ (th) artikel ilmiah (id) naučni članak (sr-el) мақолаи илмӣ (tg-cyrl) ശാസ്ത്ര പ്രബന്ധം (ml) artículu científicu espublizáu en 2003 (ast) سائنسی مضمون (ur) مقالهٔ علمی (fa) 2003 թվականին հրատարակված գիտական հոդված (hy) 2003 թուականին հրատարակուած գիտական յօդուած (hyw) مقالة علمية (نشرت عام 2003) (ar) maqolai ilmiy (tg-latn) ২০০৩-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ (bn) 2003년 논문 (ko) 2003 nî ê lūn-bûn (nan) 2003年の学術論文 (ja) 2003年学术文章 (zh-cn) 2003年学术文章 (zh-sg) 2003年学术文章 (zh-hans) 2003年学术文章 (wuu) 2003年学术文章 (zh-my) 2003年學術文章 (zh) 2003年學術文章 (zh-hk) 2003年學術文章 (zh-tw) 2003年學術文章 (zh-hant) 2003年學術文章 (yue) 2003年學術文章 (zh-mo) vetenskaplig artikel publicerad den 24 oktober 2003 (sv) научная статья опубликованная 24 октября 2003 г. (ru) научна статия, публикувана на 24 октомври 2003 г. (bg) 24 Ekim 2003'de yayımlanmış bilimsel makale (tr) научни чланак објављен 24. октобар 2003. (sr) научни чланак објављен 24. октобар 2003. (sr-ec) artículo científico publicado el 24 de octubre de 2003 (es) article scientifique publié le 24 octobre 2003 (fr) articolo scientifico pubblicato il 24 ottobre 2003 (it) artikull shkencor i botuar më 24 tetor 2003 (sq) artigo científico publicado em 24 de outubro de 2003 (pt) artigo científico publicado em 24 de outubro de 2003 (pt-br) scientific article published on 24 October 2003 (en-gb) scientific article published on October 24, 2003 (en) vedecký článok publikovaný 24. októbra 2003 (sk) vědecký článek publikovaný 24. října 2003 (cs) znanstveni članek objavljen 24. oktober 2003 (sl) videnskabelig artikel offentliggjort den 24. oktober 2003 (da) wetenschappelijk artikel gepubliceerd op 24 oktober 2003 (nl) mokslinis straipsnis, publikuotas 2003 m. spalio 24 d. (lt) bài báo khoa học xuất bản ngày 24 tháng 10, 2003 (vi) im 24. Oktober 2003 veröffentlichter wissenschaftlicher Artikel (de) наукова стаття, опублікована 24 жовтня 2003 (uk) artykuł naukowy opublikowany 24 października 2003 (pl)
publication date	wds:Q24298441-143261DB-5C2A-47A3-8F4B-7B08AF1AF81E wds:Q24298441-E7BF71C4-70B0-4097-8B1E-36823301539A
publication date	2003-01-01 00:00:00Z (xsd:dateTime) 2003-10-24 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q24298441-58375AC5-35F4-4D65-B560-E07B9ED61F5A
language of work or name	English
exact match	wds:Q24298441-2EA3219E-C629-4C78-A96A-FA2D2656357A
exact match	https://scigraph.springernature.com/pub.10.1007/s10038-003-0079-2
cites work	wds:Q24298441-200BC1F6-2328-4B98-A4EC-0CD01002565A wds:Q24298441-22E5E63E-928C-421E-90AB-B3C5F2D6F25F wds:Q24298441-336762B9-6D13-481A-A929-FAE96B1BBF0E wds:Q24298441-5A2F0D8F-EC9A-479F-94C4-3D4293885AD6 wds:Q24298441-5CFC49AF-81CD-4BAB-A850-AEDB20E31AD2 wds:Q24298441-5F0AB787-4B4F-48F1-961F-211BD5AB8B31 wds:Q24298441-753648A4-4233-4ED6-85F7-715E4E303F68 wds:Q24298441-87B8B611-5306-42D2-AB82-56753235CCC0 wds:Q24298441-9C9252AF-4BDC-4CC2-BD4D-3F65E2348163 wds:Q24298441-EF2686CE-41A0-4964-AF30-B01ED1BF0E1E wds:Q24298441-F20394CB-E0F0-4E30-87C8-C9991C0D45B1
cites work	A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues Identification of the gene responsible for gelatinous drop-like corneal dystrophy Isolation of 115 human chromosome 8-specific expressed-sequence tags by exon amplification Deafness and renal tubular acidosis in mice lacking the K-Cl co-transporter Kcc4. Supporting cells contribute to control of hearing sensitivity Expression of mRNA encoding extracellular matrix glycoproteins SPARC and SC1 is temporally and spatially regulated in the developing cochlea of the rat inner ear Development of endocochlear potential and compound action potential in the rat Mutations in the calcium-binding motifs of CDH23 and the 35delG mutation in GJB2 cause hearing loss in one family Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A-->G mitochondrial mutation. Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2
author name string	wds:Q24298441-1B4CCD07-505B-4064-AECF-20C073C68758 wds:Q24298441-201958B1-87BC-411A-8FEC-DA69212956EE wds:Q24298441-61CFF495-9D1E-4B5F-895B-8A405766CCBE

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