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Journal Abstract Search

143 related items for PubMed ID: 8794099

  • 1. Genetics of deafness.
    Steel KP, Brown SD.
    Curr Opin Neurobiol; 1996 Aug; 6(4):520-5. PubMed ID: 8794099
    [Abstract] [Full Text] [Related]

  • 2. Unravelling the genetics of deafness.
    Steel KP, Mburu P, Gibson F, Walsh J, Varela A, Brown K, Self T, Mahony M, Fleming J, Pearce A, Harvey D, Cable J, Brown SD.
    Ann Otol Rhinol Laryngol Suppl; 1997 May; 168():59-62. PubMed ID: 9153119
    [Abstract] [Full Text] [Related]

  • 3. Mutations in the myosin VIIA gene cause non-syndromic recessive deafness.
    Liu XZ, Walsh J, Mburu P, Kendrick-Jones J, Cope MJ, Steel KP, Brown SD.
    Nat Genet; 1997 Jun; 16(2):188-90. PubMed ID: 9171832
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  • 5. Unconventional myosins, the basis for deafness in mouse and man.
    Hasson T.
    Am J Hum Genet; 1997 Oct; 61(4):801-5. PubMed ID: 9382088
    [No Abstract] [Full Text] [Related]

  • 6. A type VII myosin encoded by the mouse deafness gene shaker-1.
    Gibson F, Walsh J, Mburu P, Varela A, Brown KA, Antonio M, Beisel KW, Steel KP, Brown SD.
    Nature; 1995 Mar 02; 374(6517):62-4. PubMed ID: 7870172
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  • 7. Unconventional myosins and the genetics of hearing loss.
    Friedman TB, Sellers JR, Avraham KB.
    Am J Med Genet; 1999 Sep 24; 89(3):147-57. PubMed ID: 10704189
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  • 8. The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells.
    Avraham KB, Hasson T, Steel KP, Kingsley DM, Russell LB, Mooseker MS, Copeland NG, Jenkins NA.
    Nat Genet; 1995 Dec 24; 11(4):369-75. PubMed ID: 7493015
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  • 11. Auditory and vestibular mouse mutants: models for human deafness.
    Ahituv N, Avraham KB.
    J Basic Clin Physiol Pharmacol; 2000 Dec 24; 11(3):181-91. PubMed ID: 11041382
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  • 12. Myosins and deafness.
    Redowicz MJ.
    J Muscle Res Cell Motil; 1999 Apr 24; 20(3):241-8. PubMed ID: 10471988
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  • 14. Genes and deafness.
    Steel KP, Brown SD.
    Trends Genet; 1994 Dec 24; 10(12):428-35. PubMed ID: 7871592
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  • 16. Paradigms and paradoxes: mouse (and human) models of genetic deafness.
    Hughes DC.
    Audiol Neurootol; 1997 Dec 24; 2(1-2):3-11. PubMed ID: 9390817
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  • 17. The pathology of hereditary sensorineural hearing loss.
    Gacek R.
    Ann Otol Rhinol Laryngol; 1971 Apr 24; 80(2):289-98. PubMed ID: 5550782
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  • 18. Circling mouse: possible animal model for deafness.
    Lee JW, Lee EJ, Hong SH, Chung WH, Lee HT, Lee TW, Lee JR, Kim HT, Suh JG, Kim TY, Ryoo ZY.
    Comp Med; 2001 Dec 24; 51(6):550-4. PubMed ID: 11924819
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  • 19. A novel type of myosin encoded by the mouse deafness gene shaker-2.
    Wakabayashi Y, Takahashi Y, Kikkawa Y, Okano H, Mishima Y, Ushiki T, Yonekawa H, Kominami R.
    Biochem Biophys Res Commun; 1998 Jul 30; 248(3):655-9. PubMed ID: 9703981
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  • 20. Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice.
    Holme RH, Steel KP.
    Hear Res; 2002 Jul 30; 169(1-2):13-23. PubMed ID: 12121736
    [Abstract] [Full Text] [Related]

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