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Journal Abstract Search

175 related items for PubMed ID: 11041382

  • 1. Auditory and vestibular mouse mutants: models for human deafness.
    Ahituv N, Avraham KB.
    J Basic Clin Physiol Pharmacol; 2000; 11(3):181-91. PubMed ID: 11041382
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  • 2. Two deaf mice, two deaf mice..
    Heller S, Hudspeth AJ.
    Nat Med; 1998 May; 4(5):560-1. PubMed ID: 9585227
    [No Abstract] [Full Text] [Related]

  • 3. Late-onset hearing loss in a mouse model of DFN3 non-syndromic deafness: morphologic and immunohistochemical analyses.
    Xia AP, Kikuchi T, Minowa O, Katori Y, Oshima T, Noda T, Ikeda K.
    Hear Res; 2002 Apr; 166(1-2):150-8. PubMed ID: 12062767
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  • 4. Inner ear morphology is perturbed in two novel mouse models of recessive deafness.
    Miller KA, Williams LH, Rose E, Kuiper M, Dahl HH, Manji SS.
    PLoS One; 2012 Apr; 7(12):e51284. PubMed ID: 23251483
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  • 5. Mouse models to study inner ear development and hereditary hearing loss.
    Friedman LM, Dror AA, Avraham KB.
    Int J Dev Biol; 2007 Apr; 51(6-7):609-31. PubMed ID: 17891721
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  • 6. Hearing loss without overt metabolic acidosis in ATP6V1B1 deficient MRL mice, a new genetic model for non-syndromic deafness with enlarged vestibular aqueducts.
    Tian C, Gagnon LH, Longo-Guess C, Korstanje R, Sheehan SM, Ohlemiller KK, Schrader AD, Lett JM, Johnson KR.
    Hum Mol Genet; 2017 Oct 01; 26(19):3722-3735. PubMed ID: 28934385
    [Abstract] [Full Text] [Related]

  • 7. The Severity of Vestibular Dysfunction in Deafness as a Determinant of Comorbid Hyperactivity or Anxiety.
    Antoine MW, Vijayakumar S, McKeehan N, Jones SM, Hébert JM.
    J Neurosci; 2017 May 17; 37(20):5144-5154. PubMed ID: 28438970
    [Abstract] [Full Text] [Related]

  • 8. Paradigms and paradoxes: mouse (and human) models of genetic deafness.
    Hughes DC.
    Audiol Neurootol; 1997 May 17; 2(1-2):3-11. PubMed ID: 9390817
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  • 12. 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 17; 168():59-62. PubMed ID: 9153119
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  • 13. 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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  • 14. The role of mouse mutants in the identification of human hereditary hearing loss genes.
    Probst FJ, Camper SA.
    Hear Res; 1999 Apr 02; 130(1-2):1-6. PubMed ID: 10320095
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  • 18. The genetic bases for syndromic and nonsyndromic deafness among Jews.
    Ben-Yosef T, Friedman TB.
    Trends Mol Med; 2003 Nov 02; 9(11):496-502. PubMed ID: 14604828
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