Ontology highlight
ABSTRACT:
SUBMITTER: Liu C
PROVIDER: S-EPMC9420823 | biostudies-literature | 2022 Aug
REPOSITORIES: biostudies-literature
Liu Chang C Luo Na N Zhao Bo B
Neuroscience 20220623
Recessive mutations in GRXCR2 cause deafness in both humans and mice. In Grxcr2 null hair cells, the sensory receptors for sound in the inner ear, stereocilia are disorganized. Reducing the expression of taperin, a protein that interacts with GRXCR2 at the base of stereocilia, corrects the morphological defects of stereocilia and restores hearing in Grxcr2 null mice. To further validate this finding, this study generated two novel taperin mutant mouse lines that exhibit progressive hearing loss. ...[more]