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CCDC40 mutation as a cause of primary ciliary dyskinesia: a case report and review of literature 期刊论文
2016, 卷号: 10, 期号: [db:dc_citation_issue], 页码: 614
作者:  Sui, Weiguo[1];  Hou, Xianliang[1,2];  Che, Wenti[1];  Ou, Minglin[1];  Sun, Guoping[3]
收藏  |  浏览/下载:3/0  |  提交时间:2019/12/03
Study on 3 '-UTR length polymorphism in peripheral blood mononuclear cells of uremia patient 期刊论文
2016, 卷号: 38, 期号: 1, 页码: 96
作者:  Sui, Weiguo[1];  Zheng, Can[1];  Yang, Ming[1];  Ou, Minglin[1];  Chen, Jiejing[1]
收藏  |  浏览/下载:13/0  |  提交时间:2019/12/10
Whole-genome re-sequencing for the identification of high contribution susceptibility gene variants in patients with type 2 diabetes 期刊论文
2016, 卷号: 13, 期号: 5, 页码: 3735
作者:  Sun, Xiaojuan[1,2];  Sui, Weiguo[3,4];  Wang, Xiaobing[2];  Hou, Xianliang[3,4];  Ou, Minglin[3,4]
收藏  |  浏览/下载:17/0  |  提交时间:2019/12/10
Whole-genome resequencing of 100 healthy individuals using DNA pooling 期刊论文
2016, 卷号: 12, 期号: 5, 页码: 3143
作者:  Wang, Xiaobin[1,2];  Sui, Weiguo[2,3];  Wu, Weiqing[4];  Hou, Xianliang[2,3,5];  Ou, Minglin[2,3]
收藏  |  浏览/下载:4/0  |  提交时间:2019/12/17
Basic research and clinical application of immune repertoire sequencing 期刊论文
2016, 卷号: 9, 期号: 10, 页码: 18868
作者:  Hou, Xianliang[1];  Chen, Jianing[1];  Wang, Lin[1];  Dai, Yong[2];  Diao, Hongyan[1]
收藏  |  浏览/下载:2/0  |  提交时间:2019/12/23
High Throughput Sequencing of T Cell Antigen Receptors Reveals a Conserved TCR Repertoire 期刊论文
2016, 卷号: 95, 期号: 10
作者:  Hou, Xianliang[1];  Lu, Chong[1];  Chen, Sisi[2];  Xie, Qian[1];  Cui, Guangying[1]
收藏  |  浏览/下载:2/0  |  提交时间:2019/12/06
T cell repertoire following kidney transplantation revealed by high-throughput sequencing 期刊论文
2016, 卷号: 39, 页码: 34
作者:  Lai, Liusheng[1];  Wang, Lei[1];  Chen, Huaizhou[2];  Zhang, Jiaxing[1];  Yan, Qiang[1]
收藏  |  浏览/下载:5/0  |  提交时间:2019/12/06
Analysis of the Repertoire Features of TCR Beta Chain CDR3 in Human by High-Throughput Sequencing 期刊论文
2016, 卷号: 39, 期号: 2, 页码: 651
作者:  Hou, Xianliang[1];  Wang, Mingbang[2];  Lu, Chong[1];  Xie, Qian[1];  Cui, Guangying[1]
收藏  |  浏览/下载:9/0  |  提交时间:2019/12/06
ARHGAP4 mutated in a Chinese intellectually challenged family 期刊论文
2016, 卷号: 578, 期号: 2, 页码: 205
作者:  Liu, Fuhua[1,2];  Guo, Hui[3];  Ou, Minglin[1];  Hou, Xianliang[1];  Sun, Guoping[4]
收藏  |  浏览/下载:5/0  |  提交时间:2019/12/06


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