檢索結果 - Konrad Noben‐Trauth

  • Showing 1 - 7 results of 7
Refine Results
  1. 1
    Strain background effects and genetic modifiers of hearing in mice

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

    出版 2006
    獲取全文
    Revisão
    加到收藏夾
    Saved in:
  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 由 Konrad Noben‐Trauth, Qing Yin Zheng, Kenneth R. Johnson

    出版 2003
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  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 由 Michael North, Juergen K. Naggert, Yingzhuo Yan, Konrad Noben‐Trauth, Patsy M. Nishina

    出版 1997
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  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 由 Federica Di Palma, Inna A. Belyantseva, Hung J. Kim, Thomas Vogt, Bechara Kachar, Konrad Noben‐Trauth

    出版 2002
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  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 由 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

    出版 2008
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  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> 由 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

    出版 1998
    獲取全文
    Artigo
    加到收藏夾
    Saved in:
  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 由 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

    出版 2011
    獲取全文 獲取全文
    Artigo
    加到收藏夾
    Saved in:

檢索工具: