Accès gratuit
| Numéro |
Med Sci (Paris)
Volume 21, Numéro 8-9, Août–Septembre 2005
|
|
|---|---|---|
| Page(s) | 737 - 740 | |
| Section | M/S revues | |
| DOI | https://doi.org/10.1051/medsci/2005218-9737 | |
| Publié en ligne | 15 août 2005 | |
- Petit C. Usher syndrome : from genetics to pathogenesis. Annu Rev Genomics Hum Genet 2001; 2 : 271–97. [Google Scholar]
- El-Amraoui A, Petit C. Usher I syndrome : unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells. J Cell Sci 2005 (sous presse). [Google Scholar]
- Weil D, El-Amraoui A, Masmoudi S, et al. Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin. Hum Mol Genet 2003; 12 : 463–71. [Google Scholar]
- Libby RT, Steel KP. Electroretinographic anomalies in mice with mutations in Myo7a, the gene involved in human Usher syndrome type 1B. Invest Ophthalmol Vis Sci 2001; 42 : 770–8. [Google Scholar]
- Holme RH, Steel KP. Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice. Hear Res 2002; 169 : 13–23. [Google Scholar]
- Hudspeth AJ, Choe Y, Mehta AD, Martin P. Putting ion channels to work : mechanoelectrical transduction, adaptation, and amplification by hair cells. Proc Natl Acad Sci USA 2000; 97 : 11765–72. [Google Scholar]
- Tilney LG, Tilney MS, DeRosier DJ. Actin filaments, stereocilia, and hair cells : how cells count and measure. Annu Rev Cell Biol 1992; 8 : 257–74. [Google Scholar]
- Goodyear RJ, Marcotti W, Kros CJ, Richardson GP. Development and properties of stereociliary link types in hair cells of the mouse cochlea. J Comp Neurol 2005; 485 : 75–85. [Google Scholar]
- Siemens J, Lillo C, Dumont RA, et al. Cadherin 23 is a component of the tip link in hair-cell stereocilia. Nature 2004; 428 : 950–5. [Google Scholar]
- Lagziel A, Ahmed ZM, Schultz JM, et al. Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development. Dev Biol 2005; 280 : 295–306. [Google Scholar]
- Michel V, Goodyear RJ, Weil D, et al. Cadherin 23 is a component of the sensory hair bundle’s transient lateral links in the developing cochlea. Dev Biol 2005; 280 : 281–94. [Google Scholar]
- Boëda B, El-Amraoui A, Bahloul A, et al. Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle. Embo J 2002; 21 : 6689–99. [Google Scholar]
- Bershadsky A. Magic touch : how does cell-cell adhesion trigger actin assembly ? Trends Cell Biol 2004; 14 : 589–93. [Google Scholar]
- Siemens J, Kazmierczak P, Reynolds A, et al. The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions. Proc Natl Acad Sci USA 2002; 99 : 14946–51 [Google Scholar]
- Adato A, Michel V, Kikkawa Y, et al. Interactions in the network of Usher syndrome type 1 proteins. Hum Mol Genet 2005; 14 : 347–56. [Google Scholar]
- Hung AY, Sheng M. PDZ domains : structural modules for protein complex assembly. J Biol Chem 2002; 277 : 5699–702. [Google Scholar]
- Kussel-Andermann P, El-Amraoui A, Safieddine S, et al. Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complex. EMBO J 2000; 19 : 6020–9. [Google Scholar]
- Self T, Mahony M, Fleming J, et al. Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells. Development 1998; 125 : 557–66. [Google Scholar]
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