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Molecular mechanisms underlying function of hair bundle: study on genetic deafness in mouse models / 生理学报
Acta Physiologica Sinica ; (6): 481-488, 2012.
Artigo em Chinês | WPRIM | ID: wpr-333175
ABSTRACT
Although the basic principles for the function of peripheral auditory system have been known for many years, the molecular mechanisms which affect deafness are not clear. In recent years, the study of hereditary deafness associated mouse models has revealed the molecular basis which is related with the formation and function of the hair bundle and the mechanosensory organelle of hair cell. This review focused on the role of protein network, which is formed by the proteins encoded by the Usher syndrome type 1 genes, in hair-bundle development and mechanotransducer channel gating. And the review also showed how the stereocilia rootlets contribute to the hair bundle's mechanical properties and how the hair bundle produces suppressive masking. Finally, the review revealed multiple roles of the tectorial membrane and extracellular matrix in the hair bundles stimulating in the cochlea.
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Patologia / Fisiologia / Cóclea / Mecanotransdução Celular / Modelos Animais de Doenças / Síndromes de Usher / Matriz Extracelular / Genética / Células Ciliadas Auditivas / Perda Auditiva Neurossensorial Limite: Animais / Humanos Idioma: Chinês Revista: Acta Physiologica Sinica Ano de publicação: 2012 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Patologia / Fisiologia / Cóclea / Mecanotransdução Celular / Modelos Animais de Doenças / Síndromes de Usher / Matriz Extracelular / Genética / Células Ciliadas Auditivas / Perda Auditiva Neurossensorial Limite: Animais / Humanos Idioma: Chinês Revista: Acta Physiologica Sinica Ano de publicação: 2012 Tipo de documento: Artigo