Characterization of a new allele of Ames waltzer generated by ENU mutagenesis
- 30 April 2005
- journal article
- Published by Elsevier in Hearing Research
- Vol. 202 (1-2) , 161-169
- https://doi.org/10.1016/j.heares.2004.09.014
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23Human Molecular Genetics, 2003
- Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1FHuman Molecular Genetics, 2001
- 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
- Severe vestibular and auditory impairment in three alleles of Ames waltzer ( av ) miceHearing Research, 2000
- Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzerHearing Research, 2000
- Planar polarity: Out of joint?Current Biology, 2000
- Planar polarization of Drosophila and vertebrate epitheliaCurrent Opinion in Cell Biology, 1997
- Genetics of age-related hearing loss in mice. III. Susceptibility of inbred and F1 hybrid strains to noise-induced hearing lossHearing Research, 1996
- Genetics of age-related hearing loss in mice: I. Inbred and F1 hybrid strainsHearing Research, 1993