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CORC

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Recent Advancements in the Regeneration of Auditory Hair Cells and Hearing Restoration. 期刊论文
Frontiers in molecular neuroscience, 2017, 卷号: 10, 页码: 236
作者:  Mittal, Rahul;  Nguyen, Desiree;  Patel, Amit P.;  Debs, Luca H.;  Mittal, Jeenu
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/03
A comparison between systemic and intratympanic steroid therapies as initial therapy for idiopathic sudden sensorineural hearing loss: a meta-analysis 期刊论文
Acta oto-laryngologica, 2017, 卷号: 137, 期号: 6, 页码: 598-605
作者:  Qiang, Qingfen;  Wu, Xuewen;  Yang, Tao;  Yang, Chunguang;  Sun, Hong*
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/03
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
A mutation in SLC22A4 encoding an organic cation transporter expressed in the cochlea strial endothelium causes human recessive non-syndromic hearing loss DFNB60 期刊论文
Human Genetics, 2016, 卷号: 135, 期号: 5, 页码: 513-524
作者:  Ben Said, Mariem;  Grati, M'hamed;  Ishimoto, Takahiro;  Zou, Bing;  Chakchouk, Imen
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/03
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
Hearing loss in Waardenburg syndrome: a systematic review 期刊论文
Clinical Genetics, 2016, 卷号: 89, 期号: 4, 页码: 416-425
作者:  Song, J.;  Feng, Y.;  Acke, F. R.;  Coucke, P.;  Vleminckx, K.
收藏  |  浏览/下载：9/0  |  提交时间：2019/12/03
Prevalence of Mutations in GJB2, SLC26A4, and mtDNA in Children with Severe or Profound Sensorineural Hearing Loss in Southwestern China 期刊论文
Genetic Testing and Molecular Biomarkers., 2015, 卷号: 19, 期号: 1, 页码: 52-58
作者:  Qing, Jie;  Zhou, Yuan;  Lai, Ruosha;  Hu, Peng;  Ding, Yan
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/03
Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family 期刊论文
Journal of Human Genetics, 2015, 卷号: 60, 期号: 3, 页码: 119-126
作者:  Wang, Honghan;  Wang, Xinwei;  He, Chufeng;  Li, Haibo;  Qing, Jie
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/03
The application of genome editing in studying hearing loss 期刊论文
Hearing Research, 2015, 卷号: 327, 期号: Volume 327, 页码: 102-108
作者:  Zou, Bing;  Mittal, Rahul;  Grati, M'hamed;  Lu, Zhongmin;  Shu, Yilai
收藏  |  浏览/下载：9/0  |  提交时间：2019/12/03
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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