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PUBMED FOR HANDHELDS

Journal Abstract Search


372 related items for PubMed ID: 22349217

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  • 3. Mutations in cadherin 23 affect tip links in zebrafish sensory hair cells.
    Söllner C, Rauch GJ, Siemens J, Geisler R, Schuster SC, Müller U, Nicolson T, Tübingen 2000 Screen Consortium.
    Nature; 2004 Apr 29; 428(6986):955-9. PubMed ID: 15057246
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  • 5. Mutations in PMCA2 and hereditary deafness: a molecular analysis of the pump defect.
    Giacomello M, De Mario A, Lopreiato R, Primerano S, Campeol M, Brini M, Carafoli E.
    Cell Calcium; 2011 Dec 29; 50(6):569-76. PubMed ID: 22047666
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  • 6. Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells.
    Kazmierczak P, Sakaguchi H, Tokita J, Wilson-Kubalek EM, Milligan RA, Müller U, Kachar B.
    Nature; 2007 Sep 06; 449(7158):87-91. PubMed ID: 17805295
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  • 7. Nanomechanics of tip-link cadherins.
    Oroz J, Galera-Prat A, Hervás R, Valbuena A, Fernández-Bravo D, Carrión-Vázquez M.
    Sci Rep; 2019 Sep 16; 9(1):13306. PubMed ID: 31527607
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  • 8. The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing loss.
    Spiden SL, Bortolozzi M, Di Leva F, de Angelis MH, Fuchs H, Lim D, Ortolano S, Ingham NJ, Brini M, Carafoli E, Mammano F, Steel KP.
    PLoS Genet; 2008 Oct 16; 4(10):e1000238. PubMed ID: 18974863
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  • 9. Cadherin 23 is a component of the tip link in hair-cell stereocilia.
    Siemens J, Lillo C, Dumont RA, Reynolds A, Williams DS, Gillespie PG, Müller U.
    Nature; 2004 Apr 29; 428(6986):950-5. PubMed ID: 15057245
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  • 10. A functional study of plasma-membrane calcium-pump isoform 2 mutants causing digenic deafness.
    Ficarella R, Di Leva F, Bortolozzi M, Ortolano S, Donaudy F, Petrillo M, Melchionda S, Lelli A, Domi T, Fedrizzi L, Lim D, Shull GE, Gasparini P, Brini M, Mammano F, Carafoli E.
    Proc Natl Acad Sci U S A; 2007 Jan 30; 104(5):1516-21. PubMed ID: 17234811
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  • 11. Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells.
    Adato A, Lefèvre G, Delprat B, Michel V, Michalski N, Chardenoux S, Weil D, El-Amraoui A, Petit C.
    Hum Mol Genet; 2005 Dec 15; 14(24):3921-32. PubMed ID: 16301217
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  • 14. Stereocilia morphogenesis and maintenance through regulation of actin stability.
    McGrath J, Roy P, Perrin BJ.
    Semin Cell Dev Biol; 2017 May 15; 65():88-95. PubMed ID: 27565685
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  • 15. A new Atp2b2 deafwaddler allele, dfw(i5), interacts strongly with Cdh23 and other auditory modifiers.
    Watson CJ, Tempel BL.
    Hear Res; 2013 Oct 15; 304():41-8. PubMed ID: 23792079
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  • 16. Noddy, a mouse harboring a missense mutation in protocadherin-15, reveals the impact of disrupting a critical interaction site between tip-link cadherins in inner ear hair cells.
    Geng R, Sotomayor M, Kinder KJ, Gopal SR, Gerka-Stuyt J, Chen DH, Hardisty-Hughes RE, Ball G, Parker A, Gaudet R, Furness D, Brown SD, Corey DP, Alagramam KN.
    J Neurosci; 2013 Mar 06; 33(10):4395-404. PubMed ID: 23467356
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  • 17. Stereocilia defects in the sensory hair cells of the inner ear in mice deficient in integrin alpha8beta1.
    Littlewood Evans A, Müller U.
    Nat Genet; 2000 Apr 06; 24(4):424-8. PubMed ID: 10742111
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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 06; 135(8):1427-37. PubMed ID: 18339676
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  • 19. The composition and role of cross links in mechanoelectrical transduction in vertebrate sensory hair cells.
    Hackney CM, Furness DN.
    J Cell Sci; 2013 Apr 15; 126(Pt 8):1721-31. PubMed ID: 23641064
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  • 20. The tip-link molecular complex of the auditory mechano-electrical transduction machinery.
    Pepermans E, Petit C.
    Hear Res; 2015 Dec 15; 330(Pt A):10-7. PubMed ID: 26049141
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