Inner ear localization of mRNA and protein products of COCH , mutated in the sensorineural deafness and vestibular disorder, DFNA9

By Robertson N.G.  

Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2493-2500

Oxford University Press

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A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction

By Robertson Nahid G.   Jones Sherri M.   Sivakumaran Theru A.   Giersch Anne B.S.   Jurado Sara A.   Call Linda M.   Miller Constance E.   Maison Stphane F.   Liberman M. Charles   Morton Cynthia C.  

Human Molecular Genetics, Vol. 17, Iss. 21, 2008-11 ,pp. : 3426-3434

Oxford University Press

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Proteomics, bioinformatics and targeted gene expression analysis reveals up-regulation of cochlin and identifies other potential biomarkers in the mouse model for deafness in usher syndrome type 1F

By Chance Mark R.   Chang Jinsook   Liu Shuqing   Gokulrangan Giridharan   Chen Daniel H.-C.   Lindsay Aaron   Geng Ruishuang   Zheng Qing Y.   Alagramam Kumar  

Human Molecular Genetics, Vol. 19, Iss. 8, 2010-04 ,pp. : 1515-1527

Oxford University Press

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An L1 element intronic insertion in the black-eyed white ( Mitf mi-bw ) gene: the loss of a single Mitf isoform responsible for the pigmentary defect and inner ear deafness

By Yajima Ichiro   Sato Shigeru   Kimura Takaharu   Yasumoto Ken-ichi  

Human Molecular Genetics, Vol. 8, Iss. 8, 1999-08 ,pp. : 1431-1441

Oxford University Press

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A Gene for a Dominant Form of Non-Syndromic Sensorineural Deafness ( DFNA11 ) Maps Within the Region Containing the DFNB2 Recessive Deafness Gene

By Tamagawa Yuya   Kitamura Ken   Ishida Takashi   Ishikawa Kazuhiro   Tanaka Hajime   Tsuji Shoji   Nishizawa Masatoyo  

Human Molecular Genetics, Vol. 5, Iss. 6, 1996-01 ,pp. : 849-852

Oxford University Press

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