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Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice.
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Current approaches for Usher syndrome disease models and developing therapies.
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Outcomes of cochlear implants in patients with mutations: a clinical study.
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Mechanobiology in cellular, molecular, and tissue adaptation.
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Cochlear Implantation Outcomes in Genotyped Subjects with Sensorineural Hearing Loss.
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Select autosomal dominant DFNA11 deafness variants activate Myo7A targeting in epithelial cells.
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1
Fast adaptation in vestibular hair cells requires myosin-1c activity.
Neuron. 2005 Aug 18;47(4):541-53. doi: 10.1016/j.neuron.2005.07.024.
2
Sustained cadherin 23 expression in young and adult cochlea of normal and hearing-impaired mice.
Hear Res. 2005 Oct;208(1-2):114-21. doi: 10.1016/j.heares.2005.05.008. Epub 2005 Jul 6.
3
Characterization of vestibular dysfunction in the mouse model for Usher syndrome 1F.
J Assoc Res Otolaryngol. 2005 Jun;6(2):106-18. doi: 10.1007/s10162-004-5032-3. Epub 2005 Jun 10.
7
Development and properties of stereociliary link types in hair cells of the mouse cochlea.
J Comp Neurol. 2005 Apr 25;485(1):75-85. doi: 10.1002/cne.20513.
8
Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia.
Nat Cell Biol. 2005 Feb;7(2):148-56. doi: 10.1038/ncb1219. Epub 2005 Jan 16.
9
Interactions in the network of Usher syndrome type 1 proteins.
Hum Mol Genet. 2005 Feb 1;14(3):347-56. doi: 10.1093/hmg/ddi031. Epub 2004 Dec 8.
10
Mutant analysis reveals whirlin as a dynamic organizer in the growing hair cell stereocilium.
Hum Mol Genet. 2005 Feb 1;14(3):391-400. doi: 10.1093/hmg/ddi035. Epub 2004 Dec 8.

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