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浏览/检索结果: 共13条，第1-10条 帮助 已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 TNF-alpha inhibits the migration of oral squamous cancer cells mediated by miR-765-EMP3-p66Shc axis 期刊论文 CELLULAR SIGNALLING, 2017, 卷号: 34, 页码: 102-109 作者:  Zheng, Zhichao[1];  Luan, Xiuwen[2];  Zha, Jun[1];  Li, Zhengmao[1];  Wu, Lihong[1] 收藏  |  浏览/下载：10/0  |  提交时间：2019/04/24 TNF-alpha  MiR-765  EMP3  p66Shc  Migration  Oral squamous cancer cell   Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family 期刊论文 Journal of Human Genetics, 2015, 卷号: 60, 期号: 3, 页码: 119-126 作者:  Wang, Honghan;  Wang, Xinwei;  He, Chufeng;  Li, Haibo;  Qing, Jie 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/03 Mutations of P4HA2 encoding prolyl 4-hydroxylase 2 are associated with nonsyndromic high myopia 期刊论文 Genetics in Medicine, 2015, 卷号: 17, 期号: 4, 页码: 300-306 作者:  Guo, Hui;  Tong, Ping;  Liu, Yanling;  Xia, Lu;  Wang, Tianyun 收藏  |  浏览/下载：8/0  |  提交时间：2019/12/03 collagen hydroxylation  high myopia  P4HA2  whole-exome sequencing   MSX2 mediates entry of human pluripotent stem cells into mesendoderm by simultaneously suppressing SOX2 and activating NODAL signaling 期刊论文 2015, 卷号: 25, 期号: 12, 页码: 1314-1332 作者:  Wu, Qingqing;  Zhang, Leisheng;  Su, Pei;  Lei, Xiaohua;  Liu, Xin 收藏  |  浏览/下载：2/0  |  提交时间：2020/01/13 MSX2  hPSC  SOX2  NODAL  mesendoderm   Whole exome sequencing identifies a novel EMD mutation in a Chinese family with dilated cardiomyopathy 期刊论文 BMC MEDICAL GENETICS, 2014, 卷号: 15 作者:  Si, Dayong;  Zhang, Mingqiu;  Chen, Jia;  Zheng, Yu;  Jiao, Haixu 收藏  |  浏览/下载：7/0  |  提交时间：2019/12/05 Dilated cardiomyopathy  Emery-Dreifuss muscular dystrophy  EMD gene  Novel mutation  Whole exome sequencing   Whole exome sequencing identifies a novel EMD mutation in a Chinese family with dilated cardiomyopathy 期刊论文 BMC Medical Genetics, 2014, 卷号: 15, 期号: 1, 页码: 77- 作者:  Zhang, Mingqiu;  Chen, Jia;  Si, Dayong;  Zheng, Yu;  Jiao, Haixu 收藏  |  浏览/下载：6/0  |  提交时间：2019/12/03 Dilated cardiomyopathy  EMD gene  Emery-Dreifuss muscular dystrophy  Novel mutation  Whole exome sequencing   SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia 期刊论文 Journal of Medical Genetics, 2014, 卷号: 51, 期号: 8, 页码: 518-525 作者:  Guo, Hui;  Jin, Xuemin;  Zhu, Tengfei;  Wang, Tianyun;  Tong, Ping 收藏  |  浏览/下载：4/0  |  提交时间：2019/12/03 Genetics  Genome-wide  Linkage  Myopia   Novel mutations in the SOX10 gene in the first two Chinese cases of type IV Waardenburg syndrome 期刊论文 Biochemical and Biophysical Research Communications, 2011, 卷号: 408, 期号: 4, 页码: 620-624 作者:  Jiang, Lu;  Chen, Hongsheng;  Jiang, Wen;  Hu, Zhengmao;  Mei, Lingyun 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/03 Shah-Waardenburg syndrome  SOX10 gene  Hirschsprung disease   Design and Study of Heavy Tipper Multistage Hydraulic Cylinder Based on CAD/CAE 会议论文 International Conference on Manufacturing Engineering and Automation, DEC 07-09, 2010 作者:  Sui, Xiuhua;  Miao, Dejun;  Feng, Zhengmao 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/31 Heavy tipper  Hydraulic cylinder  CAD  Finite element analysis   Design and Analysis of Automatic Cutting Robot for Vertical-pull Glass Pipe 会议论文 International Conference on Manufacturing Engineering and Automation, DEC 07-09, 2010 作者:  Sui, Xiuhua;  Miao, Dejun;  Feng, Zhengmao 收藏  |  浏览/下载：5/0  |  提交时间：2019/12/31 Vertical-pull  Cutting robot  Design  Stability