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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 Correlating Oxygen Species with Product Selectivity for Dehydrogenation of Butane over Titanium Mixed Oxide Catalysts 期刊论文 INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2020, 卷号: 59, 期号: 1, 页码: 71-80 作者:  Shao, Mingyuan;  Hu, Chaoquan;  Sun, Jiahan;  Xu, Shuanghao;  Xiang, Maoqiao 收藏  |  浏览/下载：2/0  |  提交时间：2020/03/24 The role of hydrogen coverage and location in 1,3-butadiene hydrogenation over Pt/SiO2 期刊论文 REACTION CHEMISTRY & ENGINEERING, 2020, 卷号: 5, 期号: 1, 页码: 87-100 作者:  Hu, Chaoquan;  Shao, Mingyuan;  Xiang, Maoqiao;  Li, Shaofu;  Xu, Shuanghao 收藏  |  浏览/下载：5/0  |  提交时间：2020/03/24 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