中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
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浏览/检索结果: 共7条,第1-7条 帮助

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RIPK3 Mediates Necroptosis during Embryonic Development and Postnatal Inflammation in Fadd-Deficient Mice 期刊论文  OAI收割
CELL REPORTS, 2017, 卷号: 19, 期号: 4, 页码: 798-808
作者:  
Zhao, Qun;  Yu, XianJun;  Zhang, HaiWei;  Liu, YongBo;  Zhang, XiXi
  |  收藏  |  浏览/下载:31/0  |  提交时间:2020/12/09
RIP1 kinase activity-dependent roles in embryonic development of Fadd-deficient mice 期刊论文  OAI收割
CELL DEATH AND DIFFERENTIATION, 2017, 卷号: 24, 期号: 8, 页码: 1459-1469
作者:  
Liu, Yongbo;  Fan, Cunxian;  Yu, Xianjun;  Wu, Xiaoxia;  Zhang, Xixi
  |  收藏  |  浏览/下载:36/0  |  提交时间:2020/12/09
Whole-exome sequencing reveals a novel frameshift mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in the Indian population 期刊论文  OAI收割
JOURNAL OF HUMAN GENETICS, 2015, 卷号: 60, 期号: 10, 页码: 625-630
作者:  
Zhou, Yu;  Saikia, Bibhuti B.;  Jiang, Zhilin;  Zhu, Xiong;  Liu, Yuqing
收藏  |  浏览/下载:47/0  |  提交时间:2016/12/22
Tertiary amine mediated aerobic oxidation of sulfides into sulfoxides by visible-light photoredox catalysis on TiO2 期刊论文  OAI收割
CHEMICAL SCIENCE, 2015, 卷号: 6, 期号: 8, 页码: 5000-5005
作者:  
Lang, Xianjun;  Hao, Wei;  Leow, Wan Ru;  Li, Shuzhou;  Zhao, Jincai
收藏  |  浏览/下载:30/0  |  提交时间:2015/10/27
Exome Sequencing Analysis Identifies Compound Heterozygous Mutation in ABCA4 in a Chinese Family with Stargardt Disease 期刊论文  OAI收割
PLOS ONE, 2014, 卷号: 9, 期号: 3, 页码: e91962(1-8)
Zhou, Yu; Tao, Siyu; Chen, Hui; Huang, Lulin; Zhu, Xiong; Li, Youping; Wang, Zhili; Lin, He; Hao, Fang; Yang, Zhenglin; Wang, Liya; Zhu, Xianjun
收藏  |  浏览/下载:41/0  |  提交时间:2016/01/07
Experimental Study of Ultralight (< 300 kg/m(3)) Foamed Concrete 期刊论文  OAI收割
ADVANCES IN MATERIALS SCIENCE AND ENGINEERING, 2014, 页码: -
作者:  
Wang, Xu;  Tan, Xianjun T;  Chen, Weizhong;  Hao, Yingge
  |  收藏  |  浏览/下载:22/0  |  提交时间:2018/06/05
一维声波方程声阻抗反演问题的稳定性分析 期刊论文  OAI收割
计算物理, 1998, 卷号: 000, 期号: 005, 页码: 559
作者:  
朱本仁;  郝现军;  张关泉
  |  收藏  |  浏览/下载:11/0  |  提交时间:2020/01/10