Virally mediated Kcnq1 gene replacement therapy in the immature scala media restores hearing in a mouse model of human Jervell and Lange‐Nielsen deafness syndrome-Reference-Cited by-同舟云学术

Virally mediated Kcnq1 gene replacement therapy in the immature scala media restores hearing in a mouse model of human Jervell and Lange‐Nielsen deafness syndrome

Published:2015-06-17 Issue:8 Volume:7 Page:1077-1086
ISSN:1757-4676
Container-title:EMBO Molecular Medicine
language:en
Short-container-title:EMBO Mol Med

Author:

Chang Qing¹,Wang Jianjun¹,Li Qi¹²,Kim Yeunjung¹,Zhou Binfei¹,Wang Yunfeng³,Li Huawei³,Lin Xi³

Affiliation:

1. Department of Otolaryngology Emory University School of Medicine Atlanta GA USA

2. Department of Otolaryngology‐Head and Neck Surgery Nanfang Hospital of Southern Medical University Guangzhou China

3. Department of Otolaryngology Eye & ENT Hospital Fudan University Shanghai China

Funder

National Institute on Deafness and other Communication Disorders

National Science Foundation of China

973 Program

Publisher

EMBO

Subject

Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/emmm.201404929

Reference36 articles.

1. Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness

2. Restoration of Hearing in the VGLUT3 Knockout Mouse Using Virally Mediated Gene Therapy

3. Universal Real-Time PCR for the Detection and Quantification of Adeno-Associated Virus Serotype 2-Derived Inverted Terminal Repeat Sequences

4. Genomic advances for gene discovery in hereditary hearing loss

5. KvLQT1 and IsK (minK) proteins associate to form the IKS cardiac potassium current

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