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Pubmed for Handhelds

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Journal Abstract Search

87 related items for PubMed ID: 9390817

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  • 3. Mouse models to study inner ear development and hereditary hearing loss.
    Friedman LM, Dror AA, Avraham KB.
    Int J Dev Biol; 2007; 51(6-7):609-31. PubMed ID: 17891721
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  • 6. More deafness genes.
    Steel KP, Brown SD.
    Science; 1998 May 29; 280(5368):1403. PubMed ID: 9634418
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  • 8. The role of Pax2 in mouse inner ear development.
    Burton Q, Cole LK, Mulheisen M, Chang W, Wu DK.
    Dev Biol; 2004 Aug 01; 272(1):161-75. PubMed ID: 15242798
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  • 9. Unconventional myosins, the basis for deafness in mouse and man.
    Hasson T.
    Am J Hum Genet; 1997 Oct 01; 61(4):801-5. PubMed ID: 9382088
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  • 10. Genetics of deafness.
    Steel KP, Brown SD.
    Curr Opin Neurobiol; 1996 Aug 01; 6(4):520-5. PubMed ID: 8794099
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  • 11. The sex-linked fidget mutation abolishes Brn4/Pou3f4 gene expression in the embryonic inner ear.
    Phippard D, Boyd Y, Reed V, Fisher G, Masson WK, Evans EP, Saunders JC, Crenshaw EB.
    Hum Mol Genet; 2000 Jan 01; 9(1):79-85. PubMed ID: 10587581
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  • 15. Molecular mechanisms underlying inner ear patterning defects in kreisler mutants.
    Choo D, Ward J, Reece A, Dou H, Lin Z, Greinwald J.
    Dev Biol; 2006 Jan 15; 289(2):308-17. PubMed ID: 16325169
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  • 18. FGF receptor mutations: dimerization syndromes, cell growth suppression, and animal models.
    Kannan K, Givol D.
    IUBMB Life; 2000 Mar 15; 49(3):197-205. PubMed ID: 10868910
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