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上海神经科学研究所 [5]
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学科主题:Biochemistry & Molecular Biology
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SUMOylation of MeCP2 is essential for transcriptional repression and hippocampal synapse development
期刊论文
JOURNAL OF NEUROCHEMISTRY, 2014, 卷号: 128, 期号: 6, 页码: 798-806
Cheng, J
;
Huang, M
;
Zhu, Y
;
Xin, YJ
;
Zhao, YK
;
Huang, J
;
Yu, JX
;
Zhou, WH
;
Qiu, ZL
收藏
  |  
浏览/下载:29/0
  |  
提交时间:2014/07/30
RETT-SYNDROME
BDNF TRANSCRIPTION
NERVOUS-SYSTEM
PHOSPHORYLATION
CHROMATIN
SUMO
EXPRESSION
De novo GLI3 mutation in esophageal atresia: Reproducing the phenotypic spectrum of Gli3 defects in murine models
期刊论文
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2014, 卷号: 1842, 期号: 9, 页码: 1755-1761
Yang, L
;
Shen, C
;
Mei, M
;
Zhan, GD
;
Zhao, YK
;
Wang, HJ
;
Huang, GY
;
Qiu, ZL
;
Lu, WN
;
Zhou, WH
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  |  
浏览/下载:39/0
  |  
提交时间:2014/12/15
PALLISTER-HALL-SYNDROME
TRACHEOESOPHAGEAL FISTULA
MENTAL-RETARDATION
COPY NUMBER
GENE
FEATURES
CANCER
MICRODELETION
ASSOCIATION
ANOMALIES
Action Potential Initiation in Neocortical Inhibitory Interneurons
期刊论文
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
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  |  
浏览/下载:25/0
  |  
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
The Epigenetic Switches for Neural Development and Psychiatric Disorders
期刊论文
JOURNAL OF GENETICS AND GENOMICS, 2013, 卷号: 40, 期号: 7, 页码: 339-346
Lv, JW
;
Xin, YJ
;
Zhou, WH
;
Qiu, ZL
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  |  
浏览/下载:14/0
  |  
提交时间:2013/11/06
REGULATES MEMORY FORMATION
ACTIVE DNA DEMETHYLATION
RETT-SYNDROME
ADULT NEUROGENESIS
GENE-EXPRESSION
MOUSE MODEL
SYNAPTIC PLASTICITY
BDNF TRANSCRIPTION
DENDRITIC GROWTH
VISUAL-CORTEX
The Role of Calcium-Dependent Gene Expression in Autism Spectrum Disorders: Lessons from MeCP2, Ube3a and Beyond
期刊论文
NEUROSIGNALS, 2010, 卷号: 18, 期号: 2, 页码: 72-81
作者:
Qiu, Zilong
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浏览/下载:25/0
  |  
提交时间:2012/07/13
Calcium
Transcription
MeCP2
Copy number variations
SPINOCEREBELLAR ATAXIA TYPE-1
UBIQUITIN-PROTEIN LIGASE
COPY NUMBER VARIATION
RETT-SYNDROME
MOUSE MODEL
ANGELMAN-SYNDROME
TRANSCRIPTIONAL REPRESSION
INTERSTITIAL DELETION
SYNAPTIC-TRANSMISSION
NEUROLOGICAL DISEASE
Application of methyl parathion hydrolase (MPH) as a labeling enzyme
期刊论文
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2008, 卷号: 390, 期号: 8, 页码: 2133-2140
Yang, Wei
;
Zhou, YaFeng
;
Dai, HePing
;
Bi, Lijun
;
毕利军
;
Zhang, ZhiPing
;
Zhang, XiaoHua
;
Leng, Yan
;
Zhang, Xianen
;
张先恩
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  |  
浏览/下载:10/0
  |  
提交时间:2013/12/25
methyl parathion hydrolase
labeling enzyme
single-chain variable fragment
fusion protein
white spot syndrome virus
Studies on nitric oxide synthase activity in haemocytes of shrimps Fenneropenaeus chinensis and Marsupenaeus japonicus after white spot syndrome virus infection
期刊论文
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2006, 卷号: 14, 期号: 3, 页码: 219-227
作者:
Jiang, GJ
;
Yu, RC
;
Zhou, MJ
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  |  
浏览/下载:11/0
  |  
提交时间:2010/12/24
Fenneropenaeus Chinensis (Osbeck)
Marsupenaeus Japonicus (Bate)
White Spot Syndrome Virus
Nitric Oxide Synthase
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