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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：28/0  |  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
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
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
大脑海氏回的结构、功能连接及其遗传基础 学位论文
博士, 北京: 中国科学院心理研究所, 2015
作者:  蔡丹超
收藏  |  浏览/下载：347/0  |  提交时间：2016/04/13
A study of deafness-related genetic mutations as a basis for strategies to prevent hereditary hearing loss in Hebei, China 期刊论文
Intractable & Rare Diseases Research, 2015, 卷号: Vol.4 No.3, 页码: 131–138
作者:  Junzhen Zhu;  Qinying Cao;  Ning Zhang;  Jun Ge;  Donglan Sun
收藏  |  浏览/下载：2/0  |  提交时间：2019/03/26
First healthy baby born after PGD (preimplantation genetic diagnosis) - noninvasive haplotype screening in couples both carrying deafness gene GJB2 mutation 会议论文
31st Annual Meeting of the European-Society-of-Human-Reproduction-and-Embryology (ESHRE), JUN 14-17, 2015
作者:  Chen, Z.;  Gao, Y.;  Huang, S.;  Yan, J.;  Li, J.
收藏  |  浏览/下载：11/0  |  提交时间：2019/12/31
A genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus 期刊论文
GENES BRAIN AND BEHAVIOR, 2014, 卷号: 13, 期号: 7, 页码: 675-685
作者:  Cai, D. -C.;  Fonteijn, H.;  Guadalupe, T.;  Zwiers, M.;  Wittfeld, K.
收藏  |  浏览/下载：20/0  |  提交时间：2015/09/09
Whole-Exome Sequencing to Decipher the Genetic Heterogeneity of Hearing Loss in a Chinese Family with Deaf by Deaf Mating 期刊论文
PLOS ONE, 2014, 卷号: 9, 期号: 10, 页码: e109178
作者:  Qing, Jie;  Yan, Denise;  Zhou, Yuan;  Liu, Qiong;  Wu, Weijing
收藏  |  浏览/下载：10/0  |  提交时间：2019/12/03

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