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上海神经科学研究所 [10]
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期刊论文 [10]
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2016 [1]
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Reciprocal regulation of autism-related genes MeCP2 and PTEN via microRNAs
期刊论文
SCIENTIFIC REPORTS, 2016, 卷号: 6, 页码: 20392
作者:
Lyu, JW
;
Yuan, B
;
Cheng, TL
;
Qiu, ZL
;
Zhou, WH
收藏
  |  
浏览/下载:53/0
  |  
提交时间:2016/09/14
RETT-SYNDROME
BDNF TRANSCRIPTION
DENDRITIC GROWTH
MOUSE MODEL
EXPRESSION
BRAIN
PHOSPHORYLATION
TUMORIGENESIS
MIR-17-92
CANCER
MeCP2 Suppresses Nuclear MicroRNA Processing and Dendritic Growth by Regulating the DGCR8/Drosha Complex
期刊论文
DEVELOPMENTAL CELL, 2014, 卷号: 28, 期号: 5, 页码: 547-560
Cheng, TL
;
Wang, ZZ
;
Liao, QM
;
Zhu, Y
;
Zhou, WH
;
Xu, WQ
;
Qiu, ZL
收藏
  |  
浏览/下载:52/0
  |  
提交时间:2014/07/30
CPG-BINDING PROTEIN-2
RETT-SYNDROME
DEPENDENT PHOSPHORYLATION
MICROPROCESSOR COMPLEX
CHROMOSOMAL PROTEIN
BDNF TRANSCRIPTION
MOUSE MODEL
DROSHA
BRAIN
EXPRESSION
Generation of a monkey with MECP2 mutations by TALEN-based gene targeting
期刊论文
NEUROSCIENCE BULLETIN, 2014, 卷号: 30, 期号: 3, 页码: 381-386
Liu, Z
;
Zhou, X
;
Zhu, Y
;
Chen, ZF
;
Yu, B
;
Wang, Y
;
Zhang, CC
;
Nie, YH
;
Sang, X
;
Cai, YJ
;
Zhang, YF
;
Zhang, C
;
Zhou, WH
;
Sun, Q
;
Qiu, ZL
收藏
  |  
浏览/下载:23/0
  |  
提交时间:2014/07/30
CPG-BINDING PROTEIN-2
ONE-STEP GENERATION
CYNOMOLGUS MONKEY
RETT-SYNDROME
MICE
CHROMATIN
MOUSE
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
Conditional deletion of Mecp2 in parvalbumin-expressing GABAergic cells results in the absence of critical period plasticity
期刊论文
NATURE COMMUNICATIONS, 2014, 卷号: 5, 期号: 1, 页码: 5036-5036
He, LJ
;
Liu, N
;
Cheng, TL
;
Chen, XJ
;
Li, YD
;
Shu, YS
;
Qiu, ZL
;
Zhang, XH
收藏
  |  
浏览/下载:34/0
  |  
提交时间:2014/12/15
PRIMARY VISUAL-CORTEX
EXPERIENCE-DEPENDENT PLASTICITY
CPG-BINDING PROTEIN-2
RETT-SYNDROME
MOUSE MODEL
RECEPTIVE-FIELDS
CORTICAL PLASTICITY
OCULAR DOMINANCE
MUTANT MICE
INTERNEURONS
MeCP2: multifaceted roles in gene regulation and neural development
期刊论文
NEUROSCIENCE BULLETIN, 2014, 卷号: 30, 期号: 4, 页码: 601-609
Cheng, TL
;
Qiu, ZL
收藏
  |  
浏览/下载:14/0
  |  
提交时间:2014/12/15
CPG-BINDING PROTEIN
RETT-SYNDROME PHENOTYPES
DNA METHYLATION
MOUSE MODEL
TRANSCRIPTIONAL REPRESSION
DEPENDENT PHOSPHORYLATION
CHROMOSOMAL PROTEIN
BDNF TRANSCRIPTION
DENDRITIC GROWTH
NONCODING RNAS
A case report of Chinese brothers with inherited MECP2-containing duplication: autism and intellectual disability, but not seizures or respiratory infections
期刊论文
BMC MEDICAL GENETICS, 2012, 卷号: 13, 期号: Aug, 页码: -75
Xu, X
;
Xu, Q
;
Zhang, Y
;
Zhang, XD
;
Cheng, TL
;
Wu, BB
;
Ding, YH
;
Lu, P
;
Zheng, JJ
;
Zhang, M
;
Qiu, ZL
;
Yu, X
收藏
  |  
浏览/下载:24/0
  |  
提交时间:2013/06/04
SEVERE MENTAL-RETARDATION
CREATINE TRANSPORTER DEFICIENCY
CPG-BINDING PROTEIN-2
GENE COPY NUMBER
RETT-SYNDROME
MECP2 GENE
NEUROLOGICAL SYMPTOMS
RECURRENT INFECTIONS
XQ28
DISORDER
The Rett Syndrome Protein MeCP2 Regulates Synaptic Scaling
期刊论文
JOURNAL OF NEUROSCIENCE, 2012, 卷号: 32, 期号: 3, 页码: 989-994
作者:
Qiu, Zilong
收藏
  |  
浏览/下载:19/0
  |  
提交时间:2012/07/13
CPG-BINDING PROTEIN-2
AMPA RECEPTOR
HIPPOCAMPAL-NEURONS
SUBUNIT
EXPRESSION
EXCITATION
SYNAPSES
GENE
CDKL5, a Protein Associated with Rett Syndrome, Regulates Neuronal Morphogenesis via Rac1 Signaling
期刊论文
JOURNAL OF NEUROSCIENCE, 2010, 卷号: 30, 期号: 38, 页码: 12777-12786
作者:
Xiong, Zhi-Qi
收藏
  |  
浏览/下载:41/0
  |  
提交时间:2012/07/13
SEVERE MENTAL-RETARDATION
EARLY-ONSET SEIZURES
INFANTILE SPASMS
RHO-GTPASES
MECP2 GENE
HISTONE DEACETYLASE
ACTIN CYTOSKELETON
MUTATIONS
GROWTH
EXPRESSION
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
收藏
  |  
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
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