Found: 4
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Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31.
- Published in:
- Nature Genetics, 2003, v. 34, n. 4, p. 421, doi. 10.1038/ng1208
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- Publication type:
- Article
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D.
- Published in:
- Nature Genetics, 2001, v. 27, n. 1, p. 103, doi. 10.1038/83660
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- Publication type:
- Article
Elongation of hair cell stereocilia is defective in the mouse mutant whirler.
- Published in:
- Journal of Comparative Neurology, 2002, v. 450, n. 1, p. 94, doi. 10.1002/cne.10301
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- Publication type:
- Article
Progressive Hearing Loss and Increased Susceptibility to Noise-Induced Hearing Loss in Mice Carrying a Cdh23 but not a Myo7a Mutation.
- Published in:
- JARO - Journal of the Association for Research in Otolaryngology, 2004, v. 5, n. 1, p. 66, doi. 10.1007/s10162-003-4021-2
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- Publication type:
- Article