机构

• 上海神经科学研究所 [4]
• 生物物理研究所 [1]
• 上海生物化学与细胞生... [1]

采集方式

• OAI收割 [6]

内容类型

• 期刊论文 [6]

发表日期

• 2018 [1]
• 2012 [2]
• 2010 [1]
• 2009 [1]
• 2007 [1]

学科主题

• Neuroscien... [2]
• Cell Biolo... [1]
• Genetics &... [1]
• Science & ... [1]

筛选

浏览/检索结果: 共6条，第1-6条 帮助 条数/页： 5101520253035404550556065707580859095100 排序方式： 请选择题名升序题名降序提交时间升序提交时间降序作者升序作者降序发表日期升序发表日期降序 Phf8 histone demethylase deficiency causes cognitive impairments through the mTOR pathway 期刊论文  OAI收割 NATURE COMMUNICATIONS, 2018, 卷号: 9, 期号: 1, 页码: 114 作者:  Chen, Xuemei;  Wang, Shuai;  Zhou, Ying;  Han, Yanfei;  Li, Shengtian   |  收藏  |  浏览/下载：55/0  |  提交时间：2019/04/28 Linked Mental-retardation  Cleft lip/Cleft Palate  Synaptic Plasticity  Protein-synthesis  Cell-cycle  Gene  Mutations  Memory  Identification  Differentiation   High Proportion of 22q13 Deletions and SHANK3 Mutations in Chinese Patients with Intellectual Disability 期刊论文  OAI收割 PLOS ONE, 2012, 卷号: 7, 期号: 4, 页码: -e34739 Gong, XH; Jiang, YW; Zhang, X; An, Y; Zhang, J; Wu, Y; Wang, JM; Sun, YF; Liu, YY; Gao, XW; Shen, YP; Wu, XR; Qiu, ZL; Jin, L; Wu, BL; Wang, HY 收藏  |  浏览/下载：31/0  |  提交时间：2013/06/04 SCAFFOLDING PROTEIN SHANK3  COPY NUMBER VARIATION  MENTAL-RETARDATION  CONGENITAL-ANOMALIES  LEARNING-DISABILITY  GENE-EXPRESSION  ARRAY CGH  DELAY   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  OAI收割 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：32/0  |  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   Structural insights into a novel histone demethylase PHF8 期刊论文  OAI收割 CELL RESEARCH, 2010, 卷号: 20, 期号: 2, 页码: 166-173 Yu, Lin; Wang, Yang; Huang, Shuo; Wang, Jianjun; Deng, Zengqin; Zhang, Qi; Wu, Wei; Zhang, Xingliang; Liu, Zhao; Gong, Weimin; 龚为民; Chen, Zhongzhou 收藏  |  浏览/下载：29/0  |  提交时间：2013/12/24 PHF8 (PHD finger protein 8)  histone demethylase  chromatin modification  methylated H3K9  crystal structure  X-linked mental retardation (XLMR)  facial anomalies   Limbic Epileptogenesis in a Mouse Model of Fragile X Syndrome 期刊论文  OAI收割 CEREBRAL CORTEX, 2009, 卷号: 19, 期号: 7, 页码: 1504-1514 作者:  Xiong, Zhi-Qi 收藏  |  浏览/下载：28/0  |  提交时间：2012/07/13 epilepsy  FMRP  kindling  mGluR5  mossy fiber sprouting  NMDA  MENTAL-RETARDATION PROTEIN  METABOTROPIC GLUTAMATE-RECEPTOR  SELECTIVE RNA-BINDING  LONG-TERM DEPRESSION  KINDLING MODEL  MESSENGER-RNAS  ELECTRICAL STIMULATION  KNOCKOUT MICE  EEG FINDINGS  EPILEPSY   Phenylalanine activates the mitochondria-mediated apoptosis through the RhoA/Rho-associated kinase pathway in cortical neurons 期刊论文  OAI收割 EUROPEAN JOURNAL OF NEUROSCIENCE, 2007, 卷号: 25, 期号: 5, 页码: 1341-1348 Zhang, Yongjun; Gu, Xuefan; Yuan, Xiaobing 收藏  |  浏览/下载：25/0  |  提交时间：2012/07/23 apoptosis  phenylalanine  phenylketonuria  RhoA  Rho-associated kinase  LINKED MENTAL-RETARDATION  RHO-ASSOCIATED KINASE  SPINAL-CORD-INJURY  HIPPOCAMPAL-NEURONS  SIGNALING PATHWAYS  MYOSIN PHOSPHATASE  ENDOTHELIAL-CELLS  ENERGY-METABOLISM  PROTEIN-KINASE  EMBRYONIC RAT