Ontology highlight
ABSTRACT:
SUBMITTER: Zhou XX
PROVIDER: S-EPMC4813165 | biostudies-literature | 2016 Feb
REPOSITORIES: biostudies-literature
Zhou Xing-Xing XX Chen Sen S Xie Le L Ji Yu-Zi YZ Wu Xia X Wang Wen-Wen WW Yang Qi Q Yu Jin-Tao JT Sun Yu Y Lin Xi X Kong Wei-Jia WJ
International journal of molecular sciences 20160226 3
Connexin26 (Cx26, encoded by GJB2) mutations are the most common cause of non-syndromic deafness. GJB2 is thought to be involved in noise-induced hearing loss (NIHL). However, the role of Cx26 in NIHL is still obscure. To explore the association between Cx26 and NIHL, we established a Cx26 knockdown (KD) mouse model by conditional knockdown of Cx26 at postnatal day 18 (P18), and then we observed the auditory threshold and morphologic changes in these mice with or without noise exposure. The Cx26 ...[more]