Expression of connexin 30 in the developing mouse cochlea.
Brain Res
; 898(2): 364-7, 2001 Apr 20.
Article
em En
| MEDLINE
| ID: mdl-11306024
Mutations in the GJB6 gene encoding connexin 30 (Cx30) can cause dominant forms of nonsyndromic deafness. By studying immunohistochemical localization of Cx30 in the mouse cochlea at different ages from 0 to 30 days after birth, we found that the expression of Cx30 is nearly the same as that of Cx26. These findings suggest that as well as Cx26, Cx30 may also contribute to the generation and maturation of endocochlear potential.
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Base de dados:
MEDLINE
Assunto principal:
Cóclea
/
Junções Comunicantes
/
Conexinas
/
Animais Recém-Nascidos
/
Camundongos Endogâmicos CBA
Tipo de estudo:
Etiology_studies
Idioma:
En
Revista:
Brain Res
Ano de publicação:
2001
Tipo de documento:
Article
País de afiliação:
Japão