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浏览/检索结果: 共7条，第1-7条 帮助 限定条件 发表日期：2019     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 Reduced default mode network functional connectivity in patients with recurrent major depressive disorder 期刊论文 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2019, 卷号: 116, 期号: 18, 页码: 9078-9083 作者:  Yan, Chao-Gan;  Chen, Xiao;  Li, Le;  Castellanos, Francisco Xavier;  Bai, Tong-Jian 收藏  |  浏览/下载：180/0  |  提交时间：2019/06/03 default mode network  functional connectivity  major depressive disorder  resting-state fMRI  REST-meta-MDD   Reduced default mode network functional connectivity in patients with recurrent major depressive disorder 期刊论文 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2019, 卷号: 116, 期号: 18 作者:  Yan, Chao-Gan;  Chen, Xiao;  Li, Le;  Castellanos, Francisco Xavier;  Bai, Tong-Jian 收藏  |  浏览/下载：99/0  |  提交时间：2019/12/04 default mode network  functional connectivity  major depressive disorder  resting-state fMRI  REST-meta-MDD   NR2F2 loss-of-function mutation is responsible for congenital bicuspid aortic valve 期刊论文 INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2019, 卷号: 43, 期号: 4 作者:  Wang, Juan;  Abhinav, Pradhan;  Xu, Ying-Jia;  Li, Ruo-Gu;  Zhang, Min 收藏  |  浏览/下载：54/0  |  提交时间：2019/12/05 congenital heart disease  bicuspid aortic valve  genetics  transcription factor  nuclear receptor subfamily 2 group F member 2  reporter gene assay   Identification and Functional Characterization of an ISL1 Mutation Predisposing to Dilated Cardiomyopathy 期刊论文 JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH, 2019, 卷号: 12, 期号: 3 作者:  Xu, Ying-Jia;  Wang, Zhang-Sheng;  Yang, Chen-Xi;  Di, Ruo-Min;  Qiao, Qi 收藏  |  浏览/下载：79/0  |  提交时间：2019/12/05 Dilated cardiomyopathy  Genetics  Transcription factor  ISL1  Reporter gene assay   ISL1 loss-of-function mutation contributes to congenital heart defects 期刊论文 HEART AND VESSELS, 2019, 卷号: 34, 期号: 4 作者:  Ma, Lan;  Wang, Juan;  Li, Li;  Qiao, Qi;  Di, Ruo-Min 收藏  |  浏览/下载：25/0  |  提交时间：2019/12/05 Congenital heart defect  Patent ductus arteriosus  Molecular genetics  Transcription factor  ISL1  Reporter gene assay   Reduced default mode network functional connectivity in patients with recurrent major depressive disorder 期刊论文 Proceedings of the National Academy of Sciences of the United States of America, 2019, 卷号: 116, 期号: 18, 页码: 9078-9083 作者:  Yan, Chao-Gan*;  Chen, Xiao;  Li, Le;  Castellanos, Francisco Xavier;  Bai, Tong-Jian 收藏  |  浏览/下载：71/0  |  提交时间：2019/12/03 REST-meta-MDD  default mode network  functional connectivity  major depressive disorder  resting-state fMRI   Reduced default mode network functional connectivity in patients with recurrent major depressive disorder 期刊论文 2019, 卷号: 116, 期号: 18, 页码: 9078-9083 作者:  Yan, Chao-Gan;  Chen, Xiao;  Li, Le;  Castellanos, Francisco Xavier;  Bai, Tong-Jian 收藏  |  浏览/下载：41/0  |  提交时间：2020/01/03 default mode network  functional connectivity  major depressive disorder  resting-state fMRI  REST-meta-MDD