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CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation 期刊论文  OAI收割
TRANSLATIONAL PSYCHIATRY, 2016, 卷号: 6
Liu, J.; Gao, C.; Chen, W.; Ma, W.; Li, X.; Shi, Y.; Zhang, H.; Zhang, L.; Long, Y.; Xu, H.; Guo, X.; Deng, S.; Yan, X.; Yu, D.; Pan, G.; Chen, Y.; Lai, L.; Liao, W.; Li, Z.
收藏  |  浏览/下载:31/0  |  提交时间:2016/12/16
CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation 期刊论文  OAI收割
TRANSLATIONAL PSYCHIATRY, 2016, 卷号: 6
作者:  
Li, Z.;  Liu, J.;  Gao, C.;  Chen, W.;  Ma, W.
  |  收藏  |  浏览/下载:16/0  |  提交时间:2018/12/13
Generation of the SCN1A epilepsy mutation in hiPS cells using the TALEN technique 期刊论文  OAI收割
SCIENTIFIC REPORTS, 2014, 卷号: 4
作者:  
Li, Zhiyuan;  Chen, Yonglong;  Chen, Wanjuan;  Liu, Jingxin;  Zhang, Longmei
  |  收藏  |  浏览/下载:16/0  |  提交时间:2018/12/13
Generation of the SCN1A epilepsy mutation in hiPS cells using the TALEN technique 期刊论文  OAI收割
SCIENTIFIC REPORTS, 2014, 卷号: 4
Chen, Wanjuan; Liu, Jingxin; Zhang, Longmei; Xu, Huijuan; Guo, Xiaogang; Deng, Sihao; Liu, Lipeng; Yu, Daiguan; Chen, Yonglong; Li, Zhiyuan
收藏  |  浏览/下载:25/0  |  提交时间:2016/12/16