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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：4/0  |  提交时间：2023/12/13
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
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
Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China 期刊论文
ANNALS OF HUMAN GENETICS, 2017, 卷号: 81, 期号: 6, 页码: 258-266
作者:  Luo, Jianfen;  Bai, Xiaohui;  Zhang, Fengguo;  Xiao, Yun;  Gu, Lintao
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/12
Target sequencing of 307 deafness genes identifies candidate genes implicated in microtia 期刊论文
2017, 卷号: 8, 期号: 38, 页码: 63324-63332
作者:  Wang, Pu;  Fan, Xinmiao;  Wang, Yibei;  Fan, Yue;  Liu, Yaping
收藏  |  浏览/下载：6/0  |  提交时间：2020/01/03
Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness 期刊论文
FRONTIERS OF MEDICINE, 2016, 卷号: 10, 期号: 2
作者:  Xia, Wenjun
收藏  |  浏览/下载：9/0  |  提交时间：2019/12/05
A next-generation sequencing gene panel (MiamiOtoGenes) for comprehensive analysis of deafness genes 期刊论文
Hearing Research, 2016, 卷号: 333, 页码: 179-184
作者:  Tekin, Demet;  Yan, Denise;  Bademci, Guney;  Feng, Yong;  Guo, Shengru
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/03
Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay 期刊论文
BIOMED RESEARCH INTERNATIONAL, 2016
作者:  Zhang, Fengguo;  Xiao, Yun;  Xu, Lei;  Zhang, Xue;  Zhang, Guodong
收藏  |  浏览/下载：5/0  |  提交时间：2019/12/16
GJB2, SLC26A4, and mitochondrial DNA12S rRNA hot-spots in 156 subjects with non-syndromic hearing loss in Tengzhou, China 期刊论文
ACTA OTO-LARYNGOLOGICA, 2016, 卷号: 136, 期号: 8, 页码: 800-805
作者:  Ma, Yalin;  Xiao, Yun;  Bai, Xiaohui;  Zhang, Fengguo;  Zhang, Daogong
收藏  |  浏览/下载：5/0  |  提交时间：2019/12/16

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