机构

• 上海神经科学研究所 [8]
• 自动化研究所 [2]
• 上海生物化学与细胞生... [2]
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• OAI收割 [15]
• iSwitch采集 [1]

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• 期刊论文 [15]
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浏览/检索结果: 共16条，第1-10条 帮助 条数/页： 5101520253035404550556065707580859095100 排序方式： 请选择提交时间升序提交时间降序发表日期升序发表日期降序题名升序题名降序作者升序作者降序 EFTUD2 gene deficiency disrupts osteoblast maturation and inhibits chondrocyte differentiation via activation of the p53 signaling pathway 期刊论文  OAI收割 HUMAN GENOMICS, 2019, 卷号: 13, 期号: 1, 页码: - 作者:  Wu, J;  Yang, Y;  He, Y;  Li, Q;  Wang, X   |  收藏  |   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  |   De novo GLI3 mutation in esophageal atresia: Reproducing the phenotypic spectrum of Gli3 defects in murine models 期刊论文  OAI收割 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 收藏  |   Roles of intracellular fibroblast growth factors in neural development and functions 期刊论文  OAI收割 SCIENCE CHINA-LIFE SCIENCES, 2012, 卷号: 55, 期号: 12, 页码: 1038-1044 作者:   收藏  |   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  |   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  |   Roles of intracellular fibroblast growth factors in neural development and functions 期刊论文  OAI收割 SCIENCE CHINA-LIFE SCIENCES, 2012, 卷号: 55, 期号: 12, 页码: 1038-1044 作者:  Zhang, X;  Bao, L;  Yang, L;  Wu, QF;  Li, S 收藏  |   CDKL5, a Protein Associated with Rett Syndrome, Regulates Neuronal Morphogenesis via Rac1 Signaling 期刊论文  OAI收割 JOURNAL OF NEUROSCIENCE, 2010, 卷号: 30, 期号: 38, 页码: 12777-12786 作者:  Xiong, Zhi-Qi 收藏  |   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  |   An association study of the slc26a4 gene in children with mental retardation 期刊论文  iSwitch采集 Neuroscience letters, 2009, 卷号: 457, 期号: 3, 页码: 155-158 作者:  Li, Jun;  Zhang, Fuchang;  Gao, Jianjun;  Cai, Zhen;  Zhao, Qian 收藏  |