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Improved interfacial wetability in Cu/ZnO and its role in ZnO/Cu/ZnO sandwiched transparent electrodes 期刊论文
JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY, 2020, 卷号: 37, 页码: 123-127
作者:  Yu, Mingshi;  Wang, Guancheng;  Zhao, Rongrong;  Liu, Enze;  Chen, Tonglai
收藏  |  浏览/下载：126/0  |  提交时间：2021/02/02
Transparent electrodes  Interfacial wettability  UV treatment  Ultra-thin copper film  
Recognition of Early Paleozoic Magmatisms in the Supposed Proterozoic Basements of Zhalantun, Great Xing'an Range, NE China 期刊论文
ACTA GEOLOGICA SINICA-ENGLISH EDITION, 2019, 卷号: 93, 期号: 5, 页码: 1434-1455
作者:  Qin Tao;  Guo Rongrong;  Zang Yanqing;  Qian Cheng;  Wang Yan;  Si Qiuliang;  Sun Wei;  Ma Yongfei
收藏  |  浏览/下载：158/0  |  提交时间：2021/02/02
ASIAN OROGENIC BELT  ZIRCON U-PB  MESOZOIC VOLCANIC-ROCKS  I-TYPE GRANITES  LU-HF ISOTOPES  NEOARCHEAN SUBDUCTION  EASTERN MARGIN  CRUSTAL GROWTH  JURASSIC GRANITOIDS  TRIASSIC VOLCANISM  early Paleozoic magmatism  Xinghuadukou Group  Jiageda Formation  Zhalantun terrane  Great Xing'an Range  Central Asian Orogenic Belt  
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;  Gu Weiyue;  Zhang Xue
收藏  |  浏览/下载：149/0  |  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;  Gu Weiyue;  Zhang Xue
收藏  |  浏览/下载：144/0  |  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