CORC

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CORC

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The mechanoelectrical transducer channel is not required for regulation of cochlear blood flow during loud sound exposure in mice 期刊论文
SCIENTIFIC REPORTS, 2020, 卷号: 10, 期号: 1
作者:  Burwood, George W. S.;  Dziennis, Suzan;  Wilson, Teresa;  Foster, Sarah;  Zhang, Yuan
收藏  |  浏览/下载：29/0  |  提交时间：2020/12/16
Diagnosis, Intervention, and Prevention of Genetic Hearing Loss 期刊论文
HEARING LOSS: MECHANISMS, PREVENTION AND CURE, 2019, 卷号: 1130
作者:  Yang, Tao;  Guo, Luo;  Wang, Longhao;  Yu, Xiaoyu
收藏  |  浏览/下载：12/0  |  提交时间：2019/12/05
Identification of causative variants in patients with non-syndromic hearing loss in the Minnan region, China by targeted next-generation sequencing 期刊论文
ACTA OTO-LARYNGOLOGICA, 2019, 卷号: 139, 期号: 3
作者:  Han, Peng;  Wu, Xiaohui;  Gao, Xingqiang;  Zhou, Yulin
收藏  |  浏览/下载：19/0  |  提交时间：2019/12/05
Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China 期刊论文
2019, 卷号: 105, 期号: 4, 页码: 803-812
作者:  Dai Pu;  Huang Li-Hui;  Wang Guo-Jian;  Gao Xue;  Qu Chun-Yan
收藏  |  浏览/下载：37/0  |  提交时间：2020/01/03
Clinical and genetic features of eight Chinese autosomal-dominant optic atrophy pedigrees with six novel OPA1 pathogenic variants 期刊论文
2018, 卷号: 39, 期号: 5, 页码: 569-576
作者:  Li, Huajin;  Jones, Evan M.;  Li, Hui;  Yang, Lizhu;  Sun, Zixi
收藏  |  浏览/下载：8/0  |  提交时间：2020/01/03
ADOA  hearing loss  NGS  OPA1  
Genetic screening revealed usher syndrome in a paediatric Chinese patient 期刊论文
Hearing, Balance and Communication, 2017, 卷号: 15, 期号: 2, 页码: 1-9
作者:  Qu C.;  Liang F.;  Long Q.;  Zhao M.;  Shang H.
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/11
Genetic screening revealed usher syndrome in a paediatric Chinese patient 期刊论文
2017, 卷号: 15, 期号: 2, 页码: 98-106
作者:  Qu Chunyan;  Liang Fenghe;  Long Qin;  Zhao Min;  Shang Haiqiong
收藏  |  浏览/下载：2/0  |  提交时间：2020/01/04
Transmembrane channel-like (tmc) gene regulates Drosophila larval locomotion 期刊论文
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2016, 卷号: 113, 期号: 26, 页码: 7243-7248
作者:  Guo, YM;  Wang, YP;  Zhang, W;  Meltzer, S;  Zanini, D
收藏  |  浏览/下载：93/0  |  提交时间：2016/09/14
Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents 期刊论文
Human Genetics, 2016, 卷号: 135, 期号: 8, 页码: 953-961
作者:  Yan, Denise;  Tekin, Demet;  Bademci, Guney;  Foster, Joseph, II;  Cengiz, F. Basak
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/03
Deafness genes in families with non-syndromic hearing loss in Shandong, China: a genetic study 会议论文
Lancet-Chinese-Academy-of-Medical-Sciences (CAMS) Health Summit, OCT 30-31, 2016
作者:  Bai, Xiaohui;  Xu, Lei;  Zhang, Fengguo;  Xiao, Yun;  Li, Jianfeng
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/31

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