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CORC

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Truncated Epithelial Sodium Channel β Subunit Responsible for Liddle Syndrome in a Chinese Family 期刊论文
2019, 页码: 1-8
作者:  Fan Peng;  Lu Chao-Xia;  Yang Kun-Qi;  Lu Pei-Pei;  Hao Su-Fang
收藏  |  浏览/下载：28/0  |  提交时间：2020/01/03
Hypertension and brachydactyly syndrome associated with vertebral artery malformation caused by a PDE3A missense mutation 期刊论文
2019
作者:  Fan Peng;  Zhang Di;  Yang Kun-Qi;  Zhang Qiong-Yu;  Luo Fang
收藏  |  浏览/下载：36/0  |  提交时间：2020/01/03
Tuberculosis infection and lung adenocarcinoma: Mendelian randomization and pathway analysis of genome-wide association study data from never-smoking Asian women 期刊论文
2019
作者:  Wong Jason Y Y;  Zhang Han;  Hsiung Chao A;  Shiraishi Kouya;  Yu Kai
收藏  |  浏览/下载：100/0  |  提交时间：2020/01/03
Criteria and practical guidance for determination of brain death in adults (2nd edition) 期刊论文
2019, 卷号: 132, 期号: 3, 页码: 329-335
作者:  Cao, Bing-Zhen;  Cao, Jie;  Ding, Li;  Gao, Liang;  Guo, Tao
收藏  |  浏览/下载：97/0  |  提交时间：2020/01/03
The differences in the esophageal motility between liquid and solid bolus swallows: A multicenter high-resolution manometry study in Chinese asymptomatic volunteers 期刊论文
2019, 卷号: 31, 期号: 6, 页码: e13574
作者:  Xiang, Xuelian;  Wang, Ao;  Tu, Lei;  Xie, Xiaoping;  Ke, Meiyun
收藏  |  浏览/下载：32/0  |  提交时间：2020/01/03
Efficacy and safety of ranibizumab 0.5 mg in Chinese patients with visual impairment due to diabetic macular edema: results from the 12-month REFINE study 期刊论文
2019, 卷号: 257, 期号: 3, 页码: 529-541
作者:  Li, Xiaoxin;  Dai, Hong;  Li, Xiaorong;  Han, Mei;  Li, Jun
收藏  |  浏览/下载：166/0  |  提交时间：2020/01/03
A Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with Normokalemia 期刊论文
2019, 卷号: 32, 期号: 8, 页码: 752-758
作者:  Fan Peng;  Zhao Yu-Mo;  Zhang Di;  Liao Ying;  Yang Kun-Qi
收藏  |  浏览/下载：10/0  |  提交时间：2020/01/03
mTOR-dependent upregulation of xCT blocks melanin synthesis and promotes tumorigenesis 期刊论文
2019, 卷号: 26, 期号: 10, 页码: 2015-2028
作者:  Li Chunjia;  Chen Hongyu;  Lan Zhou;  He Shaozong;  Chen Rongrong
收藏  |  浏览/下载：13/0  |  提交时间：2020/01/03
Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome 期刊论文
2018, 卷号: 40, 期号: 2, 页码: 107-111
作者:  Yang, Kun-Qi;  Lu, Chao-Xia;  Fan, Peng;  Zhang, Ying;  Meng, Xu
收藏  |  浏览/下载：3/0  |  提交时间：2020/01/03
Liddle syndrome misdiagnosed as primary aldosteronism resulting from a novel frameshift mutation of SCNN1B 期刊论文
2018, 卷号: 7, 期号: 12, 页码: 1528-1534
作者:  Fan, Peng;  Lu, Chao-Xia;  Zhang, Di;  Yang, Kun-Qi;  Lu, Pei-Pei
收藏  |  浏览/下载：4/0  |  提交时间：2020/01/03

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