CORC

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CORC

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Effect of Microarc Oxidation-Treated Ti6Al4V Scaffold Following Low-Intensity Pulsed Ultrasound Stimulation on Osteogenic Cells in Vitro 期刊论文
ACS BIOMATERIALS SCIENCE & ENGINEERING, 2019, 卷号: 5, 期号: 2, 页码: 572-581
作者:  Chen, Jie;  Li, Jiongjiong;  Hu, Fu;  Zou, Qin;  Mei, Quanjing
收藏  |  浏览/下载：14/0  |  提交时间：2021/02/02
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
Identification of ANLN as a new likely pathogenic gene of branchio-otic syndrome in a three-generation Chinese family 期刊论文
MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 卷号: 7, 期号: 2
作者:  Deng, Lisha;  Liu, Yuanzhen;  Xia, Wenjun;  Hu, Jiongjiong;  Ma, Zhaoxin
收藏  |  浏览/下载：18/0  |  提交时间：2019/12/05
New role of LRP5, associated with nonsyndromic autosomal-recessive hereditary hearing loss (vol 38, pg 1421, 2017) 期刊论文
HUMAN MUTATION, 2018, 卷号: 39, 期号: 6
作者:  Xia, Wenjun;  Hu, Jiongjiong;  Liu, Fei;  Ma, Jing;  Sun, Shaoyang
收藏  |  浏览/下载：5/0  |  提交时间：2019/12/05
SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss 期刊论文
HUMAN MOLECULAR GENETICS, 2017, 卷号: 26, 期号: 2
作者:  Ma, Zhaoxin;  Xia, Wenjun;  Liu, Fei;  Ma, Jing;  Sun, Shaoyang
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/05
SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing loss. 期刊论文
Human molecular genetics, 2017, 卷号: 26, 期号: 16
作者:  Ma Zhaoxin;  Xia Wenjun;  Liu Fei;  Ma Jing;  Sun Shaoyang
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/05
New role of LRP5, associated with nonsyndromic autosomal-recessive hereditary hearing loss 期刊论文
HUMAN MUTATION, 2017, 卷号: 38, 期号: 10
作者:  Xia, Wenjun;  Hu, Jiongjiong;  Liu, Fei;  Ma, Jing;  Sun, Shaoyang
收藏  |  浏览/下载：5/0  |  提交时间：2019/12/05
Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing loss 期刊论文
JOURNAL OF TRANSLATIONAL MEDICINE, 2016, 卷号: 14
作者:  Hu, Jiongjiong;  Liu, Fei;  Xia, Wenjun;  Hao, Lili;  Lan, Jun
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/05
Solute Carrier Family 26 Member a2 (slc26a2) Regulates Otic Development and Hair Cell Survival in Zebrafish 期刊论文
PLOS ONE, 2015, 卷号: 10, 期号: 9
作者:  Liu, Fei;  Xia, Wenjun;  Hu, Jiongjiong;  Wang, Yingzhi;  Yang, Fan
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/19
Exome Sequencing Identifies a Mutation in EYA4 as a Novel Cause of Autosomal Dominant Non-Syndromic Hearing Loss 期刊论文
PLOS ONE, 2015, 卷号: 10, 期号: 5
作者:  Liu, Fei;  Hu, Jiongjiong;  Xia, Wenjun;  Hao, Lili;  Ma, Jing
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/19

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