CORC

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CORC

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Identification of Two Missense Mutations in DUOX1 (p.R1307Q) and DUOXA1 (p.R56W) That Can Cause Congenital Hypothyroidism Through Impairing H2O2 Generation 期刊论文
2019, 卷号: 10, 页码: 526
作者:  Liu, Shiguo;  Han, Wenxiu;  Zang, Yucui;  Zang, Hongwei;  Wang, Fang
收藏  |  浏览/下载：10/0  |  提交时间：2020/01/03
Neuroendocrine carcinoma in the extrahepatic biliary tract A case report and literature review 期刊论文
2018, 卷号: 97, 期号: 29
作者:  Zhang, Liang;  Wan, DaLong;  Bao, Li;  Chen, Qing;  Xie, HaiYang
收藏  |  浏览/下载：3/0  |  提交时间：2020/01/03
Three-dimensional printing assisted transcatheter closure of atrial septal defect with deficient posterior-inferior rim 期刊论文
2018, 卷号: 92, 期号: 7, 页码: 1309-1314
作者:  Yan, Chaowu;  Wang, Cheng;  Pan, Xiangbin;  Li, Shiguo;  Song, Huijun
收藏  |  浏览/下载：8/0  |  提交时间：2020/01/03
Genetic and functional analysis of two missense DUOX2 mutations in congenital hypothyroidism and goiter 期刊论文
2018, 卷号: 9, 期号: 4, 页码: 4366-4374
作者:  Liu, Shiguo;  Zhang, Wenhui;  Zhang, Liqin;  Zou, Hui;  Lu, Kunna
收藏  |  浏览/下载：2/0  |  提交时间：2020/01/03
The Subjective Quality of Life in Young People With Tourette Syndrome in China 期刊论文
2017, 卷号: 21, 期号: 5, 页码: 426-432
作者:  Liu Shiguo;  Zheng Lanlan;  Zheng Xueping;  Zhang Xinhua;  Yi Mingji
收藏  |  浏览/下载：5/0  |  提交时间：2020/01/04
Lack of genetic association of 5-HTR2A 102 T/C and-1438A/G polymorphisms with Tourette syndrome in a family-based association study in a Chinese Han population 期刊论文
2016, 卷号: 8, 期号: 1, 页码: 87-91
作者:  Xu, Longqiang;  Zheng, Lanlan;  Ma, Jianhua;  Su, Nailun;  Liu, Yujun
收藏  |  浏览/下载：2/0  |  提交时间：2020/01/04
Autophagy protects cardiomyocytes from the myocardial ischaemia-reperfusion injury through the clearance of CLP36 期刊论文
2016, 卷号: 6, 期号: 8
作者:  Li, Shiguo;  Liu, Chao;  Gu, Lei;  Wang, Lina;  Shang, Yongliang
收藏  |  浏览/下载：3/0  |  提交时间：2020/01/04
An association study between DLGAP1 rs11081062 and EFNA5 rs26728 polymorphisms with obsessive-compulsive disorder in a Chinese Han population 期刊论文
2015, 卷号: 11, 页码: 897-905
作者:  Li, Jiang;  Cui, Jiajia;  Wang, Xiuhai;  Ma, Jianhua;  Niu, Haitao
收藏  |  浏览/下载：2/0  |  提交时间：2020/01/13
Family-based association study between monoamine oxidase A (MAOA) gene promoter VNTR polymorphism and Tourette's syndrome in Chinese Han population 期刊论文
2015, 卷号: 21, 期号: 1, 页码: 106-108
作者:  Liu, Shiguo;  Wang, Xueqin;  Xu, Longqiang;  Zheng, Lanlan;  Ge, Yinlin
收藏  |  浏览/下载：3/0  |  提交时间：2020/01/13
MAOA  VNTR  TDT  TS  
Do obsessive-compulsive disorder and Tourette syndrome share a common susceptibility gene? An association study of the BDNF Val66Met polymorphism in the Chinese Han population 期刊论文
2015, 卷号: 16, 期号: 8, 页码: 602-609
作者:  Liu, Shiguo;  Cui, Jiajia;  Niu, Zhaoyuan;  Yi, Mingji;  Zhang, Xinhua
收藏  |  浏览/下载：10/0  |  提交时间：2020/01/13

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