Rezultati pretrage - Konrad Noben‐Trauth

  • Prikaz rezultata 1 – 7 od 7
Detaljiziraj rezultate
  1. 1
    Strain background effects and genetic modifiers of hearing in mice

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

    Izdano 2006
    Preuzmi cijeli tekst
    Revisão
    Spremi u popis
    Spremljeno u:
  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 od Konrad Noben‐Trauth, Qing Yin Zheng, Kenneth R. Johnson

    Izdano 2003
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  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 od Michael North, Juergen K. Naggert, Yingzhuo Yan, Konrad Noben‐Trauth, Patsy M. Nishina

    Izdano 1997
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  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 od Federica Di Palma, Inna A. Belyantseva, Hung J. Kim, Thomas Vogt, Bechara Kachar, Konrad Noben‐Trauth

    Izdano 2002
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  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 od 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

    Izdano 2008
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  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> od 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

    Izdano 1998
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  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 od 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

    Izdano 2011
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:

Alati za pretragu: