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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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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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 [Abstract] [Full Text] [Related]
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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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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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 [Abstract] [Full Text] [Related] Page: [Next] [New Search]