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357 related items for PubMed ID: 15882574

  • 1. Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development.
    Lagziel A, Ahmed ZM, Schultz JM, Morell RJ, Belyantseva IA, Friedman TB.
    Dev Biol; 2005 Apr 15; 280(2):295-306. PubMed ID: 15882574
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  • 2. Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D.
    Di Palma F, Holme RH, Bryda EC, Belyantseva IA, Pellegrino R, Kachar B, Steel KP, Noben-Trauth K.
    Nat Genet; 2001 Jan 15; 27(1):103-7. PubMed ID: 11138008
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  • 3. Mutations in Cdh23 cause nonsyndromic hearing loss in waltzer mice.
    Wilson SM, Householder DB, Coppola V, Tessarollo L, Fritzsch B, Lee EC, Goss D, Carlson GA, Copeland NG, Jenkins NA.
    Genomics; 2001 Jun 01; 74(2):228-33. PubMed ID: 11386759
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  • 9. Characterization of a new allele of Ames waltzer generated by ENU mutagenesis.
    Washington JL, Pitts D, Wright CG, Erway LC, Davis RR, Alagramam K.
    Hear Res; 2005 Apr 01; 202(1-2):161-9. PubMed ID: 15811708
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  • 12. Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
    Bolz H, von Brederlow B, Ramírez A, Bryda EC, Kutsche K, Nothwang HG, Seeliger M, del C-Salcedó Cabrera M, Vila MC, Molina OP, Gal A, Kubisch C.
    Nat Genet; 2001 Jan 01; 27(1):108-12. PubMed ID: 11138009
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  • 13. Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells.
    El-Amraoui A, Petit C.
    J Cell Sci; 2005 Oct 15; 118(Pt 20):4593-603. PubMed ID: 16219682
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  • 14. Progression of inner ear pathology in Ames waltzer mice and the role of protocadherin 15 in hair cell development.
    Pawlowski KS, Kikkawa YS, Wright CG, Alagramam KN.
    J Assoc Res Otolaryngol; 2006 Jun 15; 7(2):83-94. PubMed ID: 16408167
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  • 15. A point mutation in a cadherin gene, Cdh23, causes deafness in a novel mutant, Waltzer mouse niigata.
    Wada T, Wakabayashi Y, Takahashi S, Ushiki T, Kikkawa Y, Yonekawa H, Kominami R.
    Biochem Biophys Res Commun; 2001 Apr 27; 283(1):113-7. PubMed ID: 11322776
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  • 16. A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.
    Verpy E, Leibovici M, Zwaenepoel I, Liu XZ, Gal A, Salem N, Mansour A, Blanchard S, Kobayashi I, Keats BJ, Slim R, Petit C.
    Nat Genet; 2000 Sep 27; 26(1):51-5. PubMed ID: 10973247
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  • 18. A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth.
    Lefèvre G, Michel V, Weil D, Lepelletier L, Bizard E, Wolfrum U, Hardelin JP, Petit C.
    Development; 2008 Apr 27; 135(8):1427-37. PubMed ID: 18339676
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