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Inner ear cell therapy targeting hereditary deafness by activation of stem cell homing factors

Congenital deafness affects about 1 in 1000 children and more than half of them have a genetic background such as Connexin26 (CX26) gene mutation. Inner ear cell therapy for sensorineural hearing loss has been expected to be an effective therapy for hereditary deafness. Previously, we developed a no...

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Detalles Bibliográficos
Autor principal: Kamiya, Kazusaku
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307216/
https://www.ncbi.nlm.nih.gov/pubmed/25674062
http://dx.doi.org/10.3389/fphar.2015.00002

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