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浏览/检索结果: 共4条，第1-4条 帮助 已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 Shank3 mutations enhance early neural responses to deviant tones in dogs 期刊论文 CEREBRAL CORTEX, 2023, 页码: 12 作者:  Wu, Liang;  Mei, Shuting;  Yu, Shan;  Han, Shihui;  Zhang, Yong Q. 收藏  |  浏览/下载：5/0  |  提交时间：2023/11/17 auditory processing  autism  dog  electrocorticogram  Shank3   Genetic variants in the transcription regulatory region of MEGF10 are associated with autism in Chinese Han population 期刊论文 SCIENTIFIC REPORTS, 2017 Wu, Zhiliu; Qin, Jian; You, Yang; Ma, Yuanlin; Jia, Meixiang; Wang, Linyan; Lu, Tianlan; Yue, Weihua; Ruan, Yanyan; Zhang, Dai; Li, Jun; Wang, Lifang 收藏  |  浏览/下载：123/0  |  提交时间：2017/12/03 SCAFFOLDING PROTEIN SHANK3  CELL CORPSE ENGULFMENT  COPY NUMBER VARIATION  DE-NOVO MUTATIONS  SPECTRUM DISORDERS  SCHIZOPHRENIA  EXPRESSION  BRAIN  NEUROLIGINS  ASTROCYTES   Schizophrenia Related Variants in CACNA1C also Confer Risk of Autism 期刊论文 PLOS ONE, 2015 Li, Jun; Zhao, Linnan; You, Yang; Lu, Tianlan; Jia, Meixiang; Yu, Hao; Ruan, Yanyan; Yue, Weihua; Liu, Jing; Lu, Lin; Zhang, Dai; Wang, Lifang 收藏  |  浏览/下载：6/0  |  提交时间：2017/12/03 GENOME-WIDE ASSOCIATION  SCAFFOLDING PROTEIN SHANK3  COMMON GENETIC-VARIANTS  DE-NOVO MUTATIONS  BIPOLAR DISORDER  SPECTRUM DISORDERS  ASPERGER-SYNDROME  SUBUNIT GENE  COPY NUMBER  CONNECTIVITY   High Proportion of 22q13 Deletions and SHANK3 Mutations in Chinese Patients with Intellectual Disability 期刊论文 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：19/0  |  提交时间：2013/06/04 SCAFFOLDING PROTEIN SHANK3  COPY NUMBER VARIATION  MENTAL-RETARDATION  CONGENITAL-ANOMALIES  LEARNING-DISABILITY  GENE-EXPRESSION  ARRAY CGH  DELAY