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CORC

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A de novo ANK1 mutation associated to hereditary spherocytosis: a case report 期刊论文
BMC PEDIATRICS, 2019, 卷号: 19
作者:  Huang, Ti-Long;  Sang, Bao-Hua;  Lei, Qing-Ling;  Song, Chun-Yan;  Lin, Yun-Bi
收藏  |  浏览/下载：26/0  |  提交时间：2019/12/04
Criteria and practical guidance for determination of brain death in adults (2nd edition) 期刊论文
CHINESE MEDICAL JOURNAL, 2019, 卷号: 132, 期号: 3
作者:  Qian, Su-Yun;  Cao, Bing-Zhen;  Cao, Jie;  Ding, Li;  Gao, Liang
收藏  |  浏览/下载：116/0  |  提交时间：2019/12/05
Novel mutations in ZP1, ZP2, and ZP3 cause female infertility due to abnormal zona pellucida formation 期刊论文
HUMAN GENETICS, 2019, 卷号: 138, 期号: 4
作者:  Sang, Qing;  Wang, Lei;  Fu, Jing;  Wang, Wenjing;  Zhao, Lin
收藏  |  浏览/下载：26/0  |  提交时间：2019/12/05
Concurrent chemoradiotherapy with/without induction chemotherapy in locoregionally advanced nasopharyngeal carcinoma: Long-term results of phase 3 randomized controlled trial 期刊论文
INTERNATIONAL JOURNAL OF CANCER, 2019, 卷号: 145, 期号: 1
作者:  Guo, Ying;  Chen, Yu-Ming;  Zhang, Fan;  Lin, Li;  Li, Wen-Fei
收藏  |  浏览/下载：33/0  |  提交时间：2019/12/05
A pannexin 1 channelopathy causes human oocyte death 期刊论文
SCIENCE TRANSLATIONAL MEDICINE, 2019, 卷号: 11, 期号: 485
作者:  Sang, Qing;  Zhang, Zhihua;  Shi, Juanzi;  Sun, Xiaoxi;  Li, Bin
收藏  |  浏览/下载：33/0  |  提交时间：2019/12/05
Propofol reduces synaptic strength by inhibiting sodium and calcium channels at nerve terminals 期刊论文
PROTEIN & CELL, 2019, 卷号: 10, 期号: 9
作者:  Liu, Qing-Zhuo;  Hao, Mei;  Zhou, Zi-Yang;  Ge, Jian-Long;  Wu, Yi-Chen
收藏  |  浏览/下载：13/0  |  提交时间：2019/12/05
What is the most relevent factor causing pain during ALA-PDT? A multi-center, open clinical pain score research trial of actinic keratosis, acne and condylomata acuminata 期刊论文
PHOTODIAGNOSIS AND PHOTODYNAMIC THERAPY, 2019, 卷号: 26
作者:  Zheng, Zhe;  Zhang, Ling-Lin;  Shi, Lei;  Zhang, Yun-Feng;  Wang, Bo
收藏  |  浏览/下载：33/0  |  提交时间：2019/12/05
Novel mutations in PATL2: expanding the mutational spectrum and corresponding phenotypic variability associated with female infertility 期刊论文
JOURNAL OF HUMAN GENETICS, 2019, 卷号: 64, 期号: 5
作者:  Wang, Lei;  Kuang, Yanping;  Li, Bin;  Sang, Qing;  Wu, Ling
收藏  |  浏览/下载：24/0  |  提交时间：2019/12/05
Mutations in NLRP2 and NLRP5 cause female infertility characterised by early embryonic arrest 期刊论文
JOURNAL OF MEDICAL GENETICS, 2019, 卷号: 56, 期号: 7
作者:  Mu, Jian;  Wang, Wenjing;  Chen, Biaobang;  Wu, Ling;  Li, Bin
收藏  |  浏览/下载：15/0  |  提交时间：2019/12/05
The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility 期刊论文
EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 卷号: 27, 期号: 2
作者:  Chen, Biaobang;  Wang, Wenjing;  Peng, Xiandong;  Jiang, Huafeng;  Zhang, Shaozhen
收藏  |  浏览/下载：25/0  |  提交时间：2019/12/05

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