Результаты поиска - Konrad Noben‐Trauth

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  1. 1
    Strain background effects and genetic modifiers of hearing in mice

    Strain background effects and genetic modifiers of hearing in mice по Kenneth R. Johnson, Qing Yin Zheng, Konrad Noben‐Trauth

    Опубликовано 2006
    Полный текст
    Revisão
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  2. 2
    Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss

    Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss по Konrad Noben‐Trauth, Qing Yin Zheng, Kenneth R. Johnson

    Опубликовано 2003
    Полный текст
    Artigo
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  3. 3
    Molecular characterization of <i>TUB, TULP1</i> , and <i>TULP</i> 2, members of the novel tubby gene family and their possible relation to ocular diseases

    Molecular characterization of <i>TUB, TULP1</i> , and <i>TULP</i> 2, members of the novel tubby gene family and their possible relation to ocular diseases по Michael North, Juergen K. Naggert, Yingzhuo Yan, Konrad Noben‐Trauth, Patsy M. Nishina

    Опубликовано 1997
    Полный текст
    Artigo
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  4. 4
    Mutations in <i>Mcoln3</i> associated with deafness and pigmentation defects in varitint-waddler ( <i>Va</i> ) mice

    Mutations in <i>Mcoln3</i> associated with deafness and pigmentation defects in varitint-waddler ( <i>Va</i> ) mice по Federica Di Palma, Inna A. Belyantseva, Hung J. Kim, Thomas Vogt, Bechara Kachar, Konrad Noben‐Trauth

    Опубликовано 2002
    Полный текст
    Artigo
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  5. 5
    TRPML3 mutations cause impaired mechano‐electrical transduction and depolarization by an inward‐rectifier cation current in auditory hair cells of varitint‐waddler mice

    TRPML3 mutations cause impaired mechano‐electrical transduction and depolarization by an inward‐rectifier cation current in auditory hair cells of varitint‐waddler mice по Alexander F. J. van Aken, Margaret Atiba‐Davies, Walter Marcotti, Richard J. Goodyear, Jane E. Bryant, Guy P. Richardson, Konrad Noben‐Trauth, Corné J. Kros

    Опубликовано 2008
    Полный текст
    Artigo
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  6. 6
    Association of Unconventional Myosin <i>MYO15</i> Mutations with Human Nonsyndromic Deafness <i>DFNB3</i>

    Association of Unconventional Myosin <i>MYO15</i> Mutations with Human Nonsyndromic Deafness <i>DFNB3</i> по Aihui Wang, Yong Liang, Robert A. Fridell, Frank J. Probst, Edward R. Wilcox, Jeffrey W. Touchman, Cynthia C. Morton, Robert J. Morell, Konrad Noben‐Trauth, Sally A. Camper, Thomas B. Friedman

    Опубликовано 1998
    Полный текст
    Artigo
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  7. 7
    Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human

    Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human по Nikoletta Charizopoulou, Andrea Lelli, Margit Schraders, Kausik K. Ray, Michael S. Hildebrand, Arabandi Ramesh, C. R. Srikumari Srisailapathy, Jaap Oostrik, R.J.C. Admiraal, Harold R. Neely, Joseph R. Latoche, Richard J. Smith, John K. Northup, Hannie Kremer, Jeffrey R. Holt, Konrad Noben‐Trauth

    Опубликовано 2011
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    Artigo
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