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CORC

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Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature review. 期刊论文
Neuromuscular disorders : NMD, 2019, 卷号: 29, 期号: 4
作者:  Tian Wo-Tu;  Luan Xing-Hua;  Zhou Hai-Yan;  Zhang Chao;  Huang Xiao-Jun
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/06
lncRNA SLC16A1-AS1 as a novel prognostic biomarker in non-small cell lung cancer. 期刊论文
Journal of investigative medicine : the official publication of the American Federation for Clinical Research, 2019
作者:  Liu Hong Yue;  Lu Sheng Rong;  Guo Zi Han;  Zhang Zhi Sheng;  Ye Xuan
收藏  |  浏览/下载：21/0  |  提交时间：2019/12/06
A heterozygous mutation in GJA1 gene in Chinese family with serious erythrokeratodermia variabilis et progressive 期刊论文
CHINESE MEDICAL JOURNAL, 2019, 卷号: 132, 期号: 1
作者:  Guo, Bi-Rong;  Cai, Hai-Bin;  Zong, Wen-Kai;  Li, Cong-Sheng;  Liu, Li-Zhong
收藏  |  浏览/下载：9/0  |  提交时间：2019/12/06
CXCL16 Induces the Progression of Pulmonary Fibrosis through Promoting the Phosphorylation of STAT3 期刊论文
CANADIAN RESPIRATORY JOURNAL, 2019, 卷号: 2019
作者:  Zuo, Sheng;  Zhu, Zhen;  Liu, Yi;  Li, Hong;  Song, Shuang
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/06
The study of exercise tests in paroxysmal kinesigenic dyskinesia. 期刊论文
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, 2018, 卷号: 129, 期号: 11
作者:  Zhou Hai-Yan;  Zhan Fei-Xia;  Tian Wo-Tu;  Zhang Chao;  Wang Yan
收藏  |  浏览/下载：14/0  |  提交时间：2019/12/06
Cilia loss sensitizes cells to transformation by activating the mevalonate pathway 期刊论文
JOURNAL OF EXPERIMENTAL MEDICINE, 2018, 卷号: 215, 期号: 1
作者:  Deng, Yue-Zhen;  Cai, Zhen;  Shi, Shuo;  Jiang, Hao;  Shang, Yu-Rong
收藏  |  浏览/下载：8/0  |  提交时间：2019/12/06
A Randomized, Double-Blind, Multicenter, Placebo-Controlled Trial of Qi-Zhi-Wei-Tong Granules on Postprandial Distress Syndrome-Predominant Functional Dyspepsia 期刊论文
CHINESE MEDICAL JOURNAL, 2018, 卷号: 131, 期号: 13
作者:  Su, Qing;  Chen, Sheng-Liang;  Wang, Hua-Hong;  Liang, Lie-Xin;  Dai, Ning
收藏  |  浏览/下载：17/0  |  提交时间：2019/12/06
Progressive myoclonus epilepsy without renal failure in a Chinese family with a novel mutation in SCARB2 gene and literature 期刊论文
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2018, 卷号: 57
作者:  Tian, Wo-Tu;  Liu, Xiao-Li;  Xu, Yang-Qi;  Huang, Xiao-Jun;  Zhou, Hai-Yan
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/06
Gene expression profiling of brain metastatic cell from triple negative breast cancer: Understanding the molecular events 期刊论文
GENE, 2018, 卷号: 640
作者:  Zhou, Li;  Gao, Hong-Fang;  Liu, Ding-Sheng;  Feng, Jin-Yi;  Gao, Dan-Dan
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/06
GFI1 downregulation promotes inflammation-linked metastasis of colorectal cancer 期刊论文
CELL DEATH AND DIFFERENTIATION, 2017, 卷号: 24, 期号: 5
作者:  Xing, Wenjing;  Xiao, Yun;  Lu, Xinliang;  Zhu, Hongyan;  He, Xiangchuan
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/06

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