CORC

在结果中检索

CORC

浏览/检索结果: 共13条，第1-10条 帮助

限定条件                
已选(0)清除 条数/页：   排序方式：
Elongator promotes the migration and invasion of hepatocellular carcinoma cell by the phosphorylation of AKT 期刊论文
INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES, 2018, 卷号: 14, 期号: 5
作者:  Xu, Yi;  Zhou, Wei;  Ji, Yuan;  Shen, Jian;  Zhu, Xiaxia
收藏  |  浏览/下载：6/0  |  提交时间：2019/12/05
Independent of EPR Effect: A Smart Delivery Nanosystem for Tracking and Treatment of Nonvascularized Intra-Abdominal Metastases 期刊论文
ADVANCED FUNCTIONAL MATERIALS, 2018, 卷号: 28, 期号: 50
作者:  Yuan, Wei;  Peng, Juanjuan;  Chen, Rui;  Yang, Liqiang;  Tham, Huijun Phoebe
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/05
A novel ZIC3 gene mutation identified in patients with heterotaxy and congenital heart disease 期刊论文
SCIENTIFIC REPORTS, 2018, 卷号: 8
作者:  Li, Shuolin;  Liu, Sida;  Chen, Weicheng;  Yuan, Yuan;  Gu, Ruoyi
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/05
A genome-wide association study identifies six novel risk loci for primary biliary cholangitis 期刊论文
NATURE COMMUNICATIONS, 2017, 卷号: 8
作者:  Huang, Lihua;  Qing, Zhuye;  Wu, Jianfang;  Huang, Qinghai;  Han, Junhai
收藏  |  浏览/下载：29/0  |  提交时间：2019/12/05
Pedigree-based Analysis of Inherited and Noninherited Risk Factors of Congenital Heart Defects 期刊论文
EARLY HUMAN DEVELOPMENT, 2015, 卷号: 91, 期号: 12
作者:  Yuan, Yuan;  Chen, Weicheng;  Ma, Xiaojing;  Wang, Huijun;  Yan, Weili
收藏  |  浏览/下载：5/0  |  提交时间：2019/12/19
Quantitative Proteomic Analysis of Serum from Pregnant Women Carrying a Fetus with Conotruncal Heart Defect Using Isobaric Tags for Relative and Absolute Quantitation (iTRAQ) Labeling 期刊论文
PLOS ONE, 2014, 卷号: 9, 期号: 11
作者:  Zhang, Ying;  Kang, Yuan;  Zhou, Qiongjie;  Zhou, Jizi;  Wang, Huijun
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/19
De novo mutation in ATP6V1B2 impairs lysosome acidification and causes dominant deafness-onychodystrophy syndrome 期刊论文
CELL RESEARCH, 2014, 卷号: 24, 期号: 11
作者:  Yuan, Yongyi;  Zhang, Jianguo;  Chang, Qing;  Zeng, Jin;  Xin, Feng
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/19
Promoter Methylation and Expression of the VANGL2 Gene in the Myocardium of Pediatric Patients with Tetralogy of Fallot 期刊论文
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY, 2014, 卷号: 100, 期号: 12
作者:  Yuan, Yuan;  Gao, Yan;  Wang, Huijun;  Ma, Xiaojing;  Ma, Duan
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/19
The relationship between neuroticism, major depressive disorder and comorbid disorders in Chinese women 期刊论文
JOURNAL OF AFFECTIVE DISORDERS, 2011, 卷号: 135, 期号: 1-3
作者:  Xia, Jing;  He, Qiang;  Li, Yihan;  Xie, Dong;  Zhu, Suoyu
收藏  |  浏览/下载：3/0  |  提交时间：2019/12/19
Functional Mutation of SMAC/DIABLO, Encoding a Mitochondrial Proapoptotic Protein, Causes Human Progressive Hearing Loss DFNA64 期刊论文
AMERICAN JOURNAL OF HUMAN GENETICS, 2011, 卷号: 89, 期号: 1
作者:  Cheng, Jing;  Zhu, Yuhua;  He, Sudan;  Lu, Yanping;  Chen, Jing
收藏  |  浏览/下载：5/0  |  提交时间：2019/12/19

©版权所有 ©2017 CSpace - Powered by CSpace