中国科学院机构知识库网格系统: 检索

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	Metal telluride nanosheets by scalable solid lithiation and exfoliation 期刊论文 OAI收割 NATURE, 2024, 卷号: 628, 期号: 8007, 页码: 15 作者: Zhang, Liangzhu; Yang, Zixuan; Feng, Shun; Guo, Zhuobin; Jia, Qingchao \| 收藏 \| 浏览/下载：2/0 \| 提交时间：2025/04/27
	Metal telluride nanosheets by scalable solid lithiation and exfoliation 期刊论文 OAI收割 NATURE, 2024, 卷号: 628, 期号: 8007, 页码: 15 作者: Zhang, Liangzhu; Yang, Zixuan; Feng, Shun; Guo, Zhuobin; Jia, Qingchao \| 收藏 \| 浏览/下载：1/0 \| 提交时间：2025/04/27
	Shape-tailorable high-energy asymmetric micro-supercapacitors based on plasma reduced and nitrogen-doped graphene oxide and MoO2 nanoparticles 期刊论文 OAI收割 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：105/0 \| 提交时间：2019/12/02
	Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis 期刊论文 OAI收割 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：48/0 \| 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 OAI收割 SCIENCE CHINA-LIFE SCIENCES, 2018, 卷号: 61, 期号: 8, 页码: 947-953 作者: Wang Rongrong; Yang Shuanghao; Xu Ming \| 收藏 \| 浏览/下载：38/0 \| 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