Gene therapy for deafness: we can do more

IF 39.1 1区 生物学 Q1 GENETICS & HEREDITY Nature Reviews Genetics Pub Date : 2024-12-18 DOI:10.1038/s41576-024-00809-8
Yuxin Chen  (, ), Jiake Zhong  (, ), Yilai Shu  (, )
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Abstract

Challenges in the development of treatments for hereditary hearing loss include the exploration of the underlying pathological mechanisms, the comprehensive evaluation of safety and efficacy of gene therapies in clinical trials, the optimization of surgical approaches for drug delivery, and effective collaboration between industry and academia. Gene therapy for congenital deafness has made a breakthrough in recent clinical trials. However, more work is needed to develop successful treatments for hereditary hearing loss, as the authors argue in this Comment.
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耳聋的基因治疗:我们可以做得更多
遗传性听力损失治疗的发展面临的挑战包括探索潜在的病理机制,在临床试验中对基因治疗的安全性和有效性进行综合评估,优化手术给药方式,以及产业界和学术界的有效合作。基因治疗先天性耳聋在近期的临床试验中取得了突破性进展。然而,正如作者在这篇评论中所指出的那样,需要做更多的工作来开发成功的遗传性听力损失治疗方法。
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来源期刊
Nature Reviews Genetics
Nature Reviews Genetics 生物-遗传学
CiteScore
57.40
自引率
0.50%
发文量
113
审稿时长
6-12 weeks
期刊介绍: At Nature Reviews Genetics, our goal is to be the leading source of reviews and commentaries for the scientific communities we serve. We are dedicated to publishing authoritative articles that are easily accessible to our readers. We believe in enhancing our articles with clear and understandable figures, tables, and other display items. Our aim is to provide an unparalleled service to authors, referees, and readers, and we are committed to maximizing the usefulness and impact of each article we publish. Within our journal, we publish a range of content including Research Highlights, Comments, Reviews, and Perspectives that are relevant to geneticists and genomicists. With our broad scope, we ensure that the articles we publish reach the widest possible audience. As part of the Nature Reviews portfolio of journals, we strive to uphold the high standards and reputation associated with this esteemed collection of publications.
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