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浏览/检索结果: 共5条，第1-5条 帮助 已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择发表日期升序发表日期降序提交时间升序提交时间降序题名升序题名降序作者升序作者降序 Shape-tailorable high-energy asymmetric micro-supercapacitors based on plasma reduced and nitrogen-doped graphene oxide and MoO2 nanoparticles 期刊论文 JOURNAL OF MATERIALS CHEMISTRY A, 2019, 卷号: 7, 期号: 23, 页码: 14328-14336 作者:  Zhang, Liangzhu;  Chen, Zhiqiang;  Zheng, Shuanghao;  Qin, Si;  Wang, Jiemin 收藏  |  浏览/下载：71/0  |  提交时间：2019/12/02 Conductive Microporous Covalent Triazine-Based Framework for High-Performance Electrochemical Capacitive Energy Storage 期刊论文 ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2018, 卷号: 57, 期号: 27, 页码: 7992-7996 作者:  Li, Yajuan;  Zheng, Shuanghao;  Liu, Xue;  Li, Pan;  Sun, Lei 收藏  |  浏览/下载：6/0  |  提交时间：2019/12/11 covalent organic frameworks  electrode materials  energy storage  microporous materials  supercapacitors   Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis 期刊论文 2018, 卷号: 61, 期号: 8, 页码: 947-953 作者:  Wang, Rongrong;  Yang, Shuanghao;  Xu, Ming;  Huang, Jia;  Liu, Hongyan 收藏  |  浏览/下载：5/0  |  提交时间：2020/01/03 hereditary spherocytosis  mutation  ANK1  SPTB  SLC4A1  whole-exome sequencing   Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis 期刊论文 SCIENCE CHINA-LIFE SCIENCES, 2018, 卷号: 61, 期号: 8, 页码: 947-953 作者:  Wang Rongrong;  Yang Shuanghao;  Xu Ming;  Huang Jia;  Liu Hongyan 收藏  |  浏览/下载：63/0  |  提交时间：2021/02/02 RED-CELL MEMBRANE  HEMATOLOGICALLY IMPORTANT MUTATIONS  RENAL TUBULAR-ACIDOSIS  HEMOLYTIC-ANEMIA  BETA-SPECTRIN  CYTOPLASMIC DOMAIN  BAND-3 DEFICIENCY  DISORDERS  ANKYRIN  VARIANTS  hereditary spherocytosis  mutation  ANK1  SPTB  SLC4A1  whole-exome sequencing   Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis 期刊论文 SCIENCE CHINA-LIFE SCIENCES, 2018, 卷号: 61, 期号: 8, 页码: 947-953 作者:  Wang Rongrong;  Yang Shuanghao;  Xu Ming;  Huang Jia;  Liu Hongyan 收藏  |  浏览/下载：6/0  |  提交时间：2021/02/02 RED-CELL MEMBRANE  HEMATOLOGICALLY IMPORTANT MUTATIONS  RENAL TUBULAR-ACIDOSIS  HEMOLYTIC-ANEMIA  BETA-SPECTRIN  CYTOPLASMIC DOMAIN  BAND-3 DEFICIENCY  DISORDERS  ANKYRIN  VARIANTS  hereditary spherocytosis  mutation  ANK1  SPTB  SLC4A1  whole-exome sequencing