Cargando…
RNA Interference Prevents Autosomal-Dominant Hearing Loss
Hearing impairment is the most common sensory deficit. It is frequently caused by the expression of an allele carrying a single dominant missense mutation. Herein, we show that a single intracochlear injection of an artificial microRNA carried in a viral vector can slow progression of hearing loss f...
Autores principales: | Shibata, Seiji B., Ranum, Paul T., Moteki, Hideaki, Pan, Bifeng, Goodwin, Alexander T., Goodman, Shawn S., Abbas, Paul J., Holt, Jeffrey R., Smith, Richard J.H. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4908151/ https://www.ncbi.nlm.nih.gov/pubmed/27236922 http://dx.doi.org/10.1016/j.ajhg.2016.03.028 |
Ejemplares similares
-
Mutation-agnostic RNA interference with engineered replacement rescues Tmc1-related hearing loss
por: Iwasa, Yoichiro, et al.
Publicado: (2022) -
The Prevalence and Clinical Characteristics of TECTA-Associated Autosomal Dominant Hearing Loss
por: Yasukawa, Rika, et al.
Publicado: (2019) -
Treatment of autosomal dominant hearing loss by in
vivo delivery of genome editing agents
por: Gao, Xue, et al.
Publicado: (2017) -
POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss
por: Kitano, Tomohiro, et al.
Publicado: (2017) -
Comprehensive Genetic Analysis of Japanese Autosomal Dominant Sensorineural Hearing Loss Patients
por: Iwasa, Yoh-ichiro, et al.
Publicado: (2016)