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浏览/检索结果: 共5条，第1-5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 An integration-free iPSC line (SDQLCHi012-A) derived from a patient with inflammatory bowel disease- 28 carrying compound heterozygote mutations in IL10RA gene 期刊论文 Stem Cell Research, 2019, 卷号: 41 作者:  Ma Y.;  Zhang H.;  Zhang S.;  Dong R.;  Yang X. 收藏  |  浏览/下载：5/0  |  提交时间：2019/12/11 A Brugada syndrome proband with compound heterozygote SCN5A mutations identified from a Chinese family in Singapore 期刊论文 EUROPACE, 2016, 卷号: 18, 期号: 6 作者:  Tan, Boon Yew;  Yong, Rita Yu Yin;  Barajas-Martinez, Hector;  Dumaine, Robert;  Chew, Ying Xia 收藏  |  浏览/下载：2/0  |  提交时间：2019/12/05 Brugada syndrome  Channelopathy  SCN5A  Nav1.5  Compound heterozygote   Marked Alteration of Rosuvastatin Pharmacokinetics in Healthy Chinese with ABCG2 34G > A and 421C > A Homozygote or Compound Heterozygote 期刊论文 The Journal of pharmacology and experimental therapeutics, 2015, 卷号: 354, 期号: 3, 页码: 310-315 作者:  Wan, Zirui;  Wang, Guo*;  Li, Tailin;  Xu, Biaobo;  Pei, Qi 收藏  |  浏览/下载：5/0  |  提交时间：2019/12/03 Marked Alteration of Rosuvastatin Pharmacokinetics in Healthy Chinese with ABCG2 34G > A and 421C > A Homozygote or Compound Heterozygote 期刊论文 The Journal of pharmacology and experimental therapeutics, 2015, 卷号: 354, 期号: 3, 页码: 310-315 作者:  Wan, Zirui;  Wang, Guo*;  Li, Tailin;  Xu, Biaobo;  Pei, Qi 收藏  |  浏览/下载：11/0  |  提交时间：2019/12/27 Novel mutations of SLC26A4 in Chinese patients with nonsyndromic hearing loss 期刊论文 ACTA OTO-LARYNGOLOGICA, 2013, 卷号: 133, 期号: 8 作者:  Yao, Gendong;  Chen, Dingli;  Wang, Huijun;  Li, Shouxia;  Zhang, Jin 收藏  |  浏览/下载：4/0  |  提交时间：2019/12/19 Sanger sequencing  pathogenic  heterogeneity  compound heterozygote