Hearing consequences in Gjb2 knock-in mice: implications for human p.V37I mutation-Reference-Cited by-同舟云学术

Hearing consequences in Gjb2 knock-in mice: implications for human p.V37I mutation

Published:2019-09-27 Issue:18 Volume:11 Page:7416-7441
ISSN:1945-4589
Container-title:Aging
language:en
Short-container-title:Aging

Author:

Lin Xin¹²³,Li Gen¹²³,Zhang Yu¹²³,Zhao Jingjing¹²³,Lu Jiawen¹²³,Gao Yunge¹²³,Liu Huihui¹²³,Li Geng-Lin¹²³,Yang Tao¹²³,Song Lei¹²³,Wu Hao¹²³

Affiliation:

1. Department of Otolaryngology-Head and Neck Surgery, Shanghai Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200011, China

2. Ear Institute, Shanghai Jiao Tong University School of Medicine, Shanghai 200125, China

3. Shanghai Key Laboratory of Translational Medicine on Ear and Nose diseases, Shanghai 200125, China

Publisher

Impact Journals, LLC

Subject

Cell Biology,Aging

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1. Deficient Gap Junction Coupling in Two Common Hearing Loss-Related Variants of GJB2;Clinical and Experimental Otorhinolaryngology;2024-08-31

2. Assembly mechanisms of the neuronal gap junction channel connexin 36 elucidated by Cryo-EM;Archives of Biochemistry and Biophysics;2024-04

3. Interactions of genetic variations in FAS, GJB2 and PTPRN2 are associated with noise-induced hearing loss: a case-control study in China;BMC Medical Genomics;2024-01-11

4. Analysis of GJB2 gene mutations spectrum and the characteristics of individuals with c.109G>A in Western Guangdong;Molecular Genetics & Genomic Medicine;2023-04-18

5. Pathological mechanisms of connexin26-related hearing loss: Potassium recycling, ATP-calcium signaling, or energy supply?;Frontiers in Molecular Neuroscience;2022-09-15