Torthaí cuardaigh - 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 de réir Kenneth R. Johnson, Qing Yin Zheng, Konrad Noben‐Trauth

    Foilsithe / Cruthaithe 2006
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    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 de réir Konrad Noben‐Trauth, Qing Yin Zheng, Kenneth R. Johnson

    Foilsithe / Cruthaithe 2003
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    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 de réir Michael North, Juergen K. Naggert, Yingzhuo Yan, Konrad Noben‐Trauth, Patsy M. Nishina

    Foilsithe / Cruthaithe 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 de réir Federica Di Palma, Inna A. Belyantseva, Hung J. Kim, Thomas Vogt, Bechara Kachar, Konrad Noben‐Trauth

    Foilsithe / Cruthaithe 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 de réir 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

    Foilsithe / Cruthaithe 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> de réir 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

    Foilsithe / Cruthaithe 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 de réir 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

    Foilsithe / Cruthaithe 2011
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