中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
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CAS IR Grid
机构
广州生物医药与健康研... [4]
上海神经科学研究所 [1]
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OAI收割 [5]
内容类型
期刊论文 [5]
发表日期
2016 [2]
2014 [2]
2010 [1]
学科主题
Psychiatry [2]
Science & ... [2]
Neuroscien... [1]
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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:32/0
  |  
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:17/0
  |  
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
Partial epilepsy with antecedent febrile seizures and seizure aggravation by antiepileptic drugs: Associated with loss of function of Na(v)1.1
期刊论文
OAI收割
EPILEPSIA, 2010, 卷号: 51, 期号: 9, 页码: 1669-1678
Liao, Wei-Ping
;
Shi, Yi-Wu
;
Long, Yue-Sheng
;
Zeng, Yang
;
Li, Tian
;
Yu, Mei-Juan
;
Su, Tao
;
Deng, Ping
;
Lei, Zhi-Gang
;
Xu, Shu-Jun
;
Deng, Wei-Yi
;
Liu, Xiao-Rong
;
Sun, Wei-Wen
;
Yi, Yong-Hong
;
Xu, Zao C.
;
Duan, Shumin
收藏
  |  
浏览/下载:52/0
  |  
提交时间:2012/07/13
SCN1A
Channelopathy
Partial epilepsy
Febrile seizures
Sodium channel
SEVERE MYOCLONIC EPILEPSY
NEURONAL SODIUM-CHANNEL
FAMILIAL HEMIPLEGIC MIGRAINE
TEMPORAL-LOBE EPILEPSY
GENERALIZED EPILEPSY
SCN1A MUTATIONS
NA+ CHANNEL
GENE SCN1A
INFANCY
PLUS