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Journal Abstract Search

169 related items for PubMed ID: 9382088

  • 1. 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]

  • 2. DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15.
    Friedman TB, Hinnant JT, Fridell RA, Wilcox ER, Raphael Y, Camper SA.
    Adv Otorhinolaryngol; 2000 Oct; 56():131-44. PubMed ID: 10868225
    [No Abstract] [Full Text] [Related]

  • 3. Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.
    Probst FJ, Fridell RA, Raphael Y, Saunders TL, Wang A, Liang Y, Morell RJ, Touchman JW, Lyons RH, Noben-Trauth K, Friedman TB, Camper SA.
    Science; 1998 May 29; 280(5368):1444-7. PubMed ID: 9603735
    [Abstract] [Full Text] [Related]

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  • 6. Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.
    Wang A, Liang Y, Fridell RA, Probst FJ, Wilcox ER, Touchman JW, Morton CC, Morell RJ, Noben-Trauth K, Camper SA, Friedman TB.
    Science; 1998 May 29; 280(5368):1447-51. PubMed ID: 9603736
    [Abstract] [Full Text] [Related]

  • 7. Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2.
    Liang Y, Wang A, Belyantseva IA, Anderson DW, Probst FJ, Barber TD, Miller W, Touchman JW, Jin L, Sullivan SL, Sellers JR, Camper SA, Lloyd RV, Kachar B, Friedman TB, Fridell RA.
    Genomics; 1999 Nov 01; 61(3):243-58. PubMed ID: 10552926
    [Abstract] [Full Text] [Related]

  • 8. MYO1F as a candidate gene for nonsyndromic deafness, DFNB15.
    Chen AH, Stephan DA, Hasson T, Fukushima K, Nelissen CM, Chen AF, Jun AI, Ramesh A, Van Camp G, Smith RJ.
    Arch Otolaryngol Head Neck Surg; 2001 Aug 01; 127(8):921-5. PubMed ID: 11493199
    [Abstract] [Full Text] [Related]

  • 9. Similarities between mice and humans with hereditary deafness.
    Steel KP.
    Ann N Y Acad Sci; 1991 Aug 01; 630():68-79. PubMed ID: 1952625
    [No Abstract] [Full Text] [Related]

  • 10. Paradigms and paradoxes: mouse (and human) models of genetic deafness.
    Hughes DC.
    Audiol Neurootol; 1997 Aug 01; 2(1-2):3-11. PubMed ID: 9390817
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. The architecture of hearing.
    Pennisi E.
    Science; 1997 Nov 14; 278(5341):1223-4. PubMed ID: 9411747
    [No Abstract] [Full Text] [Related]

  • 13. 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
    [Abstract] [Full Text] [Related]

  • 14. Mouse models for Usher syndrome 1B.
    Lillo C, Kitamoto J, Liu X, Quint E, Steel KP, Williams DS.
    Adv Exp Med Biol; 2003 Jul 30; 533():143-50. PubMed ID: 15180258
    [Abstract] [Full Text] [Related]

  • 15. Deaf and dizzy mice with mutated myosin motors.
    Gillespie PG.
    Nat Med; 1996 Jan 30; 2(1):27-9. PubMed ID: 8564830
    [No Abstract] [Full Text] [Related]

  • 16. Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
    Riazuddin S, Nazli S, Ahmed ZM, Yang Y, Zulfiqar F, Shaikh RS, Zafar AU, Khan SN, Sabar F, Javid FT, Wilcox ER, Tsilou E, Boger ET, Sellers JR, Belyantseva IA, Riazuddin S, Friedman TB.
    Hum Mutat; 2008 Apr 30; 29(4):502-11. PubMed ID: 18181211
    [Abstract] [Full Text] [Related]

  • 17. 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
    [Abstract] [Full Text] [Related]

  • 18. Fine mapping of the circling (cir) gene on the distal portion of mouse chromosome 9.
    Cho KI, Lee JW, Kim KS, Lee EJ, Suh JG, Lee HJ, Kim HT, Hong SH, Chung WH, Chang KT, Hyun BH, Oh YS, Ryoo ZY.
    Comp Med; 2003 Dec 02; 53(6):642-8. PubMed ID: 14727813
    [Abstract] [Full Text] [Related]

  • 19. 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 02; 11(4):369-75. PubMed ID: 7493015
    [Abstract] [Full Text] [Related]

  • 20. Mapping of unconventional myosins in mouse and human.
    Hasson T, Skowron JF, Gilbert DJ, Avraham KB, Perry WL, Bement WM, Anderson BL, Sherr EH, Chen ZY, Greene LA, Ward DC, Corey DP, Mooseker MS, Copeland NG, Jenkins NA.
    Genomics; 1996 Sep 15; 36(3):431-9. PubMed ID: 8884266
    [Abstract] [Full Text] [Related]

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