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浏览/检索结果: 共10条，第1-10条 帮助 限定条件 专题：暨南大学    第一署名单位    第一作者单位    通讯作者单位     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 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 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 Digoxin-induced anemia among patients with atrial fibrillation and heart failure: clinical data analysis and drug-gene interaction network 期刊论文 2017, 卷号: 8, 期号: 34, 页码: 57003 作者:  Lin, Yubi[1,2,3];  He, Siqi[1,2,3];  Feng, Ruiling[1,2,3];  Xu, Zhe[4];  Chen, Wanqun[5] 收藏  |  浏览/下载：10/0  |  提交时间：2019/12/06 Quest for Missing Proteins: Update 2015 on Chromosome-Centric Human Proteome Project 期刊论文 2015, 卷号: 14, 期号: [db:dc_citation_issue], 页码: 3415 作者:  Horvatovich, Peter[1];  Lundberg, Emma K.[2];  Chen, Yu-Ju[3];  Sung, Ting-Yi[4];  He, Fuchu[5] 收藏  |  浏览/下载：2/0  |  提交时间：2019/12/03 Omics Evidence: Single Nucleotide Variants Transmissions on Chromosome 20 in Liver Cancer Cell Lines 期刊论文 2014, 卷号: 13, 期号: [db:dc_citation_issue], 页码: 200 作者:  Wang, Quanhui[1,2];  Wen, Bo[2];  Wang, Tong[3];  Xu, Zhongwei[4];  Yin, Xuefei[5,6] 收藏  |  浏览/下载：6/0  |  提交时间：2019/12/03 Systematic Analyses of the Transcriptome, Translatome, and Proteome Provide a Global View and Potential Strategy for the C-HPP 期刊论文 2014, 卷号: 13, 期号: [db:dc_citation_issue], 页码: 38 作者:  Chang, Cheng[1];  Li, Liwei[1];  Zhang, Chengpu[1];  Wu, Songfeng[1];  Guo, Kun[2,3] 收藏  |  浏览/下载：7/0  |  提交时间：2019/12/03 Qualitative and Quantitative Expression Status of the Human Chromosome 20 Genes in Cancer Tissues and the Representative Cell Lines 期刊论文 2013, 卷号: 12, 期号: [db:dc_citation_issue], 页码: 151 作者:  Wang, Quanhui[1,2];  Wen, Bo[2];  Yan, Guangrong[3];  Wei, Junying[4,5];  Xie, Liqi[6,7] 收藏  |  浏览/下载：13/0  |  提交时间：2019/12/03 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 SCN5A Mutants Associated with Familial Cardiac Sodium Overlap Syndrome Characterized as Sick Sinus Syndrome, Atrial Fibrillation, Brugada Syndrome, and Progressive Conduction Disease 会议论文 Beijing, PEOPLES R CHINA, OCT 12-15, 2017 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：13/0  |  提交时间：2019/12/10 Digoxin-induced Anemia among Patients with Atrial Fibrillation and Heart Failure: Clinical Data Analysis and Drug-gene Interaction Network 会议论文 Beijing, PEOPLES R CHINA, OCT 12-15, 2017 作者:  Lin, Yubi[1,2,3,4,5,6];  Xue, Yumei[1,2,3,4,5];  He, Siqi[1,2,3,4,5,6];  Feng, Ruiling[1,2,3,4,5,6];  Xu, Zhe[7] 收藏  |  浏览/下载：6/0  |  提交时间：2019/12/23