中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
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上海神经科学研究所 [3]
上海微系统与信息技术... [1]
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OAI收割 [5]
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期刊论文 [5]
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Intronic (TTTGA)(n) insertion in SAMD12 also causes familial cortical myoclonic tremor with epilepsy
期刊论文
OAI收割
MOVEMENT DISORDERS, 2019, 卷号: 34, 期号: 10, 页码: 1571-1576
作者:
Cen, Zhidong
;
Chen, You
;
Yang, Dehao
;
Chen, Si
;
Chen, Xinhui
  |  
收藏
  |  
浏览/下载:51/0
  |  
提交时间:2020/12/09
familial cortical myoclonic tremor with epilepsy
SAMD12
(TTTGA)(n) insertion
long-read sequencing
Molecular identity of axonal sodium channels in human cortical pyramidal cells
期刊论文
OAI收割
FRONTIERS IN CELLULAR NEUROSCIENCE, 2014, 卷号: 8, 期号: 1, 页码: 297-297
Tian, CP
;
Wang, KY
;
Ke, W
;
Guo, H
;
Shu, YS
收藏
  |  
浏览/下载:27/0
  |  
提交时间:2014/12/15
ACTION-POTENTIAL INITIATION
CEREBELLAR PURKINJE NEURONS
SEVERE MYOCLONIC EPILEPSY
KAINATE-INDUCED SEIZURES
CHANDELIER CELLS
CEREBRAL-CORTEX
VISUAL-CORTEX
IN-VIVO
MULTIPLE-SCLEROSIS
ABSENCE EPILEPSY
Action Potential Initiation in Neocortical Inhibitory Interneurons
期刊论文
OAI收割
PLOS BIOLOGY, 2014, 卷号: 12, 期号: 9, 页码: e1001944-e1001944
Li, T
;
Tian, CP
;
Scalmani, P
;
Frassoni, C
;
Mantegazza, M
;
Wang, YH
;
Yang, MP
;
Wu, S
;
Shu, YS
收藏
  |  
浏览/下载:35/0
  |  
提交时间:2014/12/15
CEREBELLAR PURKINJE NEURONS
NEONATAL-INFANTILE SEIZURES
SEVERE MYOCLONIC EPILEPSY
DE-NOVO MUTATIONS
SODIUM-CHANNEL
PYRAMIDAL NEURONS
GABAERGIC INTERNEURONS
DRAVET SYNDROME
ION CHANNELS
MOUSE MODEL
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:73/0
  |  
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
Detection of known base substitution mutations in human mitochondrial DNA of MERRF and MELAS by biochip technology
期刊论文
OAI收割
BIOSENSORS & BIOELECTRONICS, 2009, 卷号: 24, 期号: 8, 页码: 2371-2376
Du, WD
;
Li, W
;
Chen, G
;
Cao, HM
;
Tang, HY
;
Tang, XF
;
Jin, QH
;
Sun, ZW
;
Zhao, H
;
Zhou, WM
;
He, SM
;
Lv, YM
;
Zhao, JL
;
Zhang, XJ
收藏
  |  
浏览/下载:22/0
  |  
提交时间:2011/12/17
RAGGED-RED FIBERS
QUARTZ-CRYSTAL MICROBALANCE
TRNA(LYS) GENE
MYOCLONIC EPILEPSY
MTDNA MUTATION
RNALYS MUTATION
POINT MUTATION
DISORDERS
AMINOACYLATION
MICROARRAY