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CORC

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EAT-2 attenuates C. elegans development via metabolic remodeling in a chemically defined food environment 期刊论文
CELLULAR AND MOLECULAR LIFE SCIENCES, 2023, 卷号: 80, 期号: 8, 页码: 18
作者:  Cao, Xuwen;  Xie, Yusu;  Yang, Hanwen;  Sun, Peiqi;  Xue, Beining
收藏  |  浏览/下载：5/0  |  提交时间：2023/12/13
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
A novel mutation of the PAX3 gene in a Chinese family with Waardenburg syndrome type I 期刊论文
MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 卷号: 7, 期号: 7
作者:  Zhang, Yu;  Ma, Jing;  Lin, Ken;  Jiang, Hong-chao;  Yang, Yanli
收藏  |  浏览/下载：17/0  |  提交时间：2019/12/04
A novel dominant mutation in the SOX10 gene in a Chinese family with Waardenburg syndrome type II 期刊论文
MOLECULAR MEDICINE REPORTS, 2019, 卷号: 19, 期号: 3
作者:  Ma, Jing;  Zhang, Zhen;  Jiang, Hong-Chao;  Sun, Hao;  Ming, Cheng
收藏  |  浏览/下载：15/0  |  提交时间：2019/12/04
Mutations in TOP2B cause autosomal-dominant hereditary hearing loss via inhibition of the PI3K-Akt signalling pathway 期刊论文
FEBS LETTERS, 2019, 卷号: 593, 期号: 15
作者:  Xia, Wenjun;  Hu, Jiongjiong;  Ma, Jing;  Huang, Jianbo;  Jing, Tianrui
收藏  |  浏览/下载：31/0  |  提交时间：2019/12/05
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
Critical role of spectrin in hearing development and deafness 期刊论文
Science Advances, 2019, 卷号: Vol.5 No.4
作者:  Liu, Y.;  Qi, J.;  Chen, X.;  Tang, M.;  Chu, C.
收藏  |  浏览/下载：4/0  |  提交时间：2019/11/21
Age-associated variation in the expression and function of TMEM16A calcium-activated chloride channels in the cochlear stria vascularis of guinea pigs 期刊论文
MOLECULAR MEDICINE REPORTS, 2019, 卷号: 20, 期号: 2
作者:  Zhou, Ying;  Song, Jia;  Wang, Yan-Ping;  Zhang, Ai-Mei;  Tan, Chao-Yang
收藏  |  浏览/下载：29/0  |  提交时间：2019/12/06
G59S mutation in the GJB2 gene in a Chinese family with classic Vohwinkel syndrome 期刊论文
JOURNAL OF DERMATOLOGY, 2019, 卷号: Vol.46 No.2, 页码: 154-157
作者:  Xie, Ming-xing;  Yang, Wei-ping;  Luo, Hao-jie;  Ismail, Ferina;  Hao, Yang-yang
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/17
The mitochondrial transfer RNAAsp A7551G mutation may contribute to the clinical expression of deafness associated with the A1555G mutation in a pedigree with hearing impairment 期刊论文
Molecular Medicine Reports, 2019, 卷号: Vol.19 No.3, 页码: 1797-1802
作者:  Jing Zhang;  Bo Lu;  Wei-Wei Xia;  Bin Fang;  Xiao-Xia Ding
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/17

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