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浏览/检索结果: 共11条，第1-10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 A Bivalent Securinine Compound SN3-L6 Induces Neuronal Differentiation via Translational Upregulation of Neurogenic Transcription Factors 期刊论文 2018, 卷号: 9 作者:  Liao, Yumei[1,2];  Zhuang, Xiaoji[1,2];  Huang, Xiaojie[1,2];  Peng, Yinghui[1,2];  Ma, Xuanyue[1,2] 收藏  |  浏览/下载：24/0  |  提交时间：2019/12/10 Case report of familial sudden cardiac death caused by a DSG2 p.F531C mutation as genetic background when carrying with heterozygous KCNE5 p.D92E/E93X mutation 期刊论文 2018, 卷号: 19 作者:  Lin, Yubi[1,2];  Huang, Jiana[1,3];  He, Siqi[1,3];  Feng, Ruiling[1,3];  Zhong, ZhiAn[2] 收藏  |  浏览/下载：6/0  |  提交时间：2019/12/17 Whole exome sequencing identified a pathogenic mutation in RYR2 in a Chinese family with unexplained sudden death 期刊论文 2018, 卷号: 51, 期号: 2, 页码: 309 作者:  Lin, Yubi[1];  He, Siqi[1,2];  Liao, Zili[1];  Feng, Ruiling[1,2];  Liu, Ruilin[3] 收藏  |  浏览/下载：10/0  |  提交时间：2019/12/17 Whole Genome Sequence Identified a Rare Homozygous Pathogenic Mutation of the DSG2 Gene in a Familial Arrhythmogenic Cardiomyopathy Involving Both Ventricles 期刊论文 2017, 卷号: 138, 期号: 1, 页码: 41 作者:  Lin, Yubi[1,2];  Zhang, Qianhuan[1];  Zhong, Zhi An[1];  Xu, Zhe[3];  He, Siqi[1,2] 收藏  |  浏览/下载：17/0  |  提交时间：2019/12/06 7-(4-Hydroxyphenyl)-1-phenyl-4E-hepten-3-one, a Diarylheptanoid from Alpinia officinarum, Protects Neurons against Amyloid-beta Induced Toxicity 期刊论文 2016, 卷号: 39, 期号: 12, 页码: 1961 作者:  Huang, Xiaojie[1];  Tang, Genyun[1,2];  Liao, Yumei[1];  Zhuang, Xiaoji[1];  Dong, Xiao[1] 收藏  |  浏览/下载：4/0  |  提交时间：2019/12/06 Effects of Maternal and Fetal Characteristics on Cell-Free Fetal DNA Fraction in Maternal Plasma 期刊论文 REPRODUCTIVE SCIENCES, 2015, 卷号: 22, 页码: 1429-1435 作者:  Zhou, Yi[1];  Zhu, Zhongyi[2];  Gao, Ya[2];  Yuan, Yuying[2];  Guo, Yulai[2] 收藏  |  浏览/下载：18/0  |  提交时间：2019/04/25 fetal fraction  gestational age  body mass index  preexisting hypertension  twin pregnancy  multiples of the median   Familial Sudden Cardiac Death Caused by DSG2 Mutation as Genetic Backgrounds: Whole Exome Sequencing and Valid Therapy of Catheter Ablation (CPCI-S收录) 会议 作者:  Lin, Yubi[1,2,3,4,5,6,7];  Zhang, Qianhuan[1,2,3,4,5,6];  Chen, Jia[8];  Feng, Ruiling[1,2,3,4,5,6,7];  He, Siqi[1,2,3,4,5,6,7] 收藏  |  浏览/下载：8/0  |  提交时间：2019/04/11 Whole Exome Sequencing Identified a Pathogenic Mutation in RYR2 in a Chinese Family with Unexplained Sudden Death (CPCI-S收录) 会议 作者:  Lin, Yubi[1,2,3,4,5,6];  Liao, Zili[1,2,3,4,5];  He, Siqi[1,2,3,4,5,6];  Liu, Ruilin[7];  Peng, Yongzheng[8] 收藏  |  浏览/下载：2/0  |  提交时间：2019/04/11 SCN5A Mutants Associated with Familial Cardiac Sodium Overlap Syndrome Characterized as Sick Sinus Syndrome, Atrial Fibrillation, Brugada Syn (CPCI-S收录) 会议 作者:  Lin, Yubi[1,2];  Deng, Chunyu[1,2];  Zhan, XianZhang[1,2];  Xu, Zhe[3];  Zhu, Jiening[1,2] 收藏  |  浏览/下载：11/0  |  提交时间：2019/04/11 Whole Exome Sequencing Identified a Pathogenic Mutation in RYR2 in a Chinese Family with Unexplained Sudden Death 会议论文 Beijing, PEOPLES R CHINA, OCT 12-15, 2017 作者:  Lin, Yubi[1,2,3,4,5,6];  Liao, Zili[1,2,3,4,5];  He, Siqi[1,2,3,4,5,6];  Liu, Ruilin[7];  Peng, Yongzheng[8] 收藏  |  浏览/下载：7/0  |  提交时间：2019/12/13