Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing-Reference-Cited by-同舟云学术

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Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing

Published:2019 Issue:24 Volume:9 Page:7184-7199
ISSN:1838-7640
Container-title:Theranostics
language:en
Short-container-title:Theranostics

Author:

Kim Min-A,Kim Sung Huhn,Ryu Nari,Ma Ji-Hyun,Kim Ye-Ri,Jung Jinsei,Hsu Chuan-Jen,Choi Jae Young,Lee Kyu-Yup,Wangemann Philine,Bok Jinwoong,Kim Un-Kyung

Publisher

Ivyspring International Publisher

Subject

Pharmacology, Toxicology and Pharmaceutics (miscellaneous),Medicine (miscellaneous)

Cited by 40 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. In utero adeno-associated virus (AAV)-mediated gene delivery targeting sensory and supporting cells in the embryonic mouse inner ear;PLOS ONE;2024-07-19

2. In Utero Gene Therapy and its Application in Genetic Hearing Loss;Advanced Biology;2024-07-15

3. Low Efficiency of Homology-Independent Targeted Integration for CRISPR/Cas9 Correction in the Vicinity of SLC26A4 c.919–2A>G Variant;2024-06-20

4. In uteroadeno-associated virus (AAV)-mediated gene delivery targeting sensory and supporting cells in the embryonic mouse inner ear;2024-05-08

5. Chloride/Multiple Anion Exchanger SLC26A Family: Systemic Roles of SLC26A4 in Various Organs;International Journal of Molecular Sciences;2024-04-10

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