AON-based degradation of c.151C>T mutant COCH transcripts associated with dominantly inherited hearing impairment DFNA9
Author:
Funder
Foundation Fighting Blindness Inc
ZonMw
Publisher
Elsevier BV
Subject
Drug Discovery,Molecular Medicine
Reference42 articles.
1. Cochlin immunostaining of inner ear pathologic deposits and proteomic analysis in DFNA9 deafness and vestibular dysfunction;Robertson;Hum. Mol. Genet.,2006
2. Cross-sectional analysis of hearing threshold in relation to age in a large family with cochleovestibular impairment thoroughly genotyped for DFNA9/COCH;Bom;Ann. Otol. Rhinol. Laryngol.,2003
3. Does Otovestibular Loss in the Autosomal Dominant Disorder DFNA9 Have an Impact of on Cognition? A Systematic Review;De Belder;Front. Neurosci.,2018
4. Novel COCH mutation in a family with autosomal dominant late onset sensorineural hearing impairment and tinnitus;Gallant;Am. J. Otolaryngol.,2013
5. Cleaved Cochlin Sequesters Pseudomonas aeruginosa and Activates Innate Immunity in the Inner Ear;Jung;Cell Host Microbe,2019
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2. Interaural and sex differences in the natural evolution of hearing levels in pre-symptomatic and symptomatic carriers of the p.Pro51Ser variant in the COCH gene;Scientific Reports;2024-01-02
3. Recent Therapeutic Progress and Future Perspectives for the Treatment of Hearing Loss;Biomedicines;2023-12-18
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5. Altering gene expression using antisense oligonucleotide therapy for hearing loss;Hearing Research;2022-12
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