Elongation of hair cell stereocilia is defective in the mouse mutant whirler
- 9 July 2002
- journal article
- research article
- Published by Wiley in Journal of Comparative Neurology
- Vol. 450 (1), 94-102
- https://doi.org/10.1002/cne.10301
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1FAmerican Journal of Human Genetics, 2001
- The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin geneNature Genetics, 2001
- Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1DNature Genetics, 2001
- Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1DNature Genetics, 2001
- Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23American Journal of Human Genetics, 2001
- Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzerHearing Research, 2000
- The motor and tail regions of myosin XV are critical for normal structure and function of auditory and vestibular hair cellsHuman Molecular Genetics, 2000
- A comprehensive genetic map of the mouse genomeNature, 1996
- The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cellsNature Genetics, 1995
- Linkage Analysis of the whirler Deafness Gene on Mouse Chromosome 4Genomics, 1994