Risultati della ricerca - 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 di Kenneth R. Johnson, Qing Yin Zheng, Konrad Noben‐Trauth

    Pubblicazione 2006
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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 di Konrad Noben‐Trauth, Qing Yin Zheng, Kenneth R. Johnson

    Pubblicazione 2003
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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 di Michael North, Juergen K. Naggert, Yingzhuo Yan, Konrad Noben‐Trauth, Patsy M. Nishina

    Pubblicazione 1997
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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 di Federica Di Palma, Inna A. Belyantseva, Hung J. Kim, Thomas Vogt, Bechara Kachar, Konrad Noben‐Trauth

    Pubblicazione 2002
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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 di 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

    Pubblicazione 2008
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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> di 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

    Pubblicazione 1998
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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 di 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

    Pubblicazione 2011
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