A new mouse mutant of the Cdh23 gene with early-onset hearing loss facilitates evaluation of otoprotection drugs-Reference-Cited by-同舟云学术

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A new mouse mutant of the Cdh23 gene with early-onset hearing loss facilitates evaluation of otoprotection drugs

Published:2010-07-20 Issue:1 Volume:12 Page:30-44
ISSN:1470-269X
Container-title:The Pharmacogenomics Journal
language:en
Short-container-title:Pharmacogenomics J

Author:

Han F,Yu H,Tian C,Chen H E,Benedict-Alderfer C,Zheng Y,Wang Q,Han X,Zheng Q Y

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology,Genetics,Molecular Medicine

Link

http://www.nature.com/articles/tpj201060.pdf

Reference43 articles.

1. Di Palma F, Holme RH, Bryda EC, Belyantseva IA, Pellegrino R, Kachar B et al. Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D. Nat Genet 2001; 27: 103–107.

2. Di Palma F, Pellegrino R, Noben-Trauth K . Genomic structure, alternative splice forms and normal and mutant alleles of cadherin 23 (Cdh23). Gene 2001; 281: 31–41.

3. Siemens J, Lillo C, Dumont RA, Reynolds A, Williams DS, Gillespie PG et al. Cadherin 23 is a component of the tip link in hair-cell stereocilia. Nature 2004; 428: 950–955.

4. Noben-Trauth K, Zheng QY, Johnson KR . Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss. Nat Genet 2003; 35: 21–23.

5. Bolz H, von Brederlow B, Ramirez A, Bryda EC, Kutsche K, Nothwang HG et al. Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D. Nat Genet 2001; 27: 108–112.

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