中国科学院机构知识库网格系统: 检索

中国科学院机构知识库网格

Chinese Academy of Sciences Institutional Repositories Grid

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	Structural mechanism of the active bicarbonate transporter from cyanobacteria 期刊论文 OAI收割 NATURE PLANTS, 2019, 卷号: 5, 期号: 11, 页码: 1184-+ 作者: Wang, CC; Sun, B; Zhang, X; Huang, XW; Zhang, MH \| 收藏 \| 浏览/下载：50/0 \| 提交时间：2020/10/16 RENAL TUBULAR-ACIDOSIS STAS DOMAIN FUNCTIONAL-CHARACTERIZATION INCREASE PHOTOSYNTHESIS SULFATE TRANSPORTER ANION TRANSPORTERS CRYSTAL-STRUCTURE MUTATIONS MEMBRANE FAMILY
	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 \| 收藏 \| 浏览/下载：33/0 \| 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; Huang Jia; Liu Hongyan \| 收藏 \| 浏览/下载：21/0 \| 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