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成果统计

合作作者[TOP 5]

  • 水雯箐

    合作成果数：23

  • Raymond C. Stevens

    合作成果数：5

  • 叶娜

    合作成果数：5

  • 秦姗姗

    合作成果数：4

  • 辛晔

    合作成果数：4
张冰洁 副研究员
所在学院： iHuman研究所
职务： 副研究员
研究方向：
备注： --
张冰洁

科研成果

23 11324 683 347 0 9
Items Views Downloads TC[WOS] TC[CSCD] H-index
排序方式：
 [1] Yue, Xiaolei.,Peng, Li.,Liu, Shenhui.,Zhang, Bingjie.,Zhang, Xiaodan.,...&Hua, Tian.(2025).Structural basis of stepwise proton sensing-mediated GPCR activation.CELL RESEARCH.浏览/下载:55/3; 被引[WOS]:0; IF:28.1/36.4评论推荐收藏
 [2] Zhang, Bingjie.,Ge, Wei.,Ma, Mengna.,Li, Shanshan.,Yu, Jie.,...&Shui, Wenqing.(2025).Post-translational modifications orchestrate the intrinsic signaling bias of GPR52.NATURE CHEMICAL BIOLOGY.浏览/下载:50/2; 被引[WOS]:0; IF:12.9/14.7评论推荐收藏
 [3] Dang, Ting.,Yu, Jie.,Cao, Zhihe.,Zhang, Bingjie.,Li, Shanshan.,...&Shui, Wenqing.(2025).Endogenous cell membrane interactome mapping for the GLP-1 receptor in different cell types.NATURE CHEMICAL BIOLOGY,21,256-267.浏览/下载:461/31; 被引[WOS]:4; IF:12.9/14.7评论推荐收藏
 [4] 叶娜,水雯箐,镇学初,等. 阿朴菲衍生物及其制备方法和应用. 2023-09-12.浏览/下载:499/1评论推荐收藏
 [5] 叶娜,水雯箐,李婉婉,等. Α-色烯螺哌啶类化合物在制备5-羟色胺2c受体激动剂中的应用. 2023-09-08.浏览/下载:502/1评论推荐收藏
 [6] Yuan, Shijia.,Xia, Lisha.,Wang, Chenxi.,Wu, Fan.,Zhang, Bingjie.,...&Shui, Wenqing.(2023).Conformational Dynamics of the Activated GLP-1 Receptor-Gs Complex Revealed by Cross-Linking Mass Spectrometry and Integrative Structure Modeling.ACS CENTRAL SCIENCE,9(5),992-1007.浏览/下载:576/5; 被引[WOS]:10; IF:12.7/15.8评论推荐收藏
 [7] Xin, Ye.,Liu, Shuo.,Liu, Yan.,Qian, Zhen.,Liu, Hongyue.,...&Shui, Wenqing.(2023).Affinity selection of double-click triazole libraries for rapid discovery of allosteric modulators for GLP-1 receptor.PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,120(11),e2220767120.浏览/下载:643/4; 被引[WOS]:8; IF:9.4/10.8评论推荐收藏
 [8] 叶娜,水雯箐,秦望智,等. 阿朴菲衍生物及其制备方法和应用. 2022-09-27.浏览/下载:364/0评论推荐收藏
 [9] 叶娜,水雯箐,李婉婉,等. Α-色烯螺哌啶类化合物在制备5-羟色胺2c受体激动剂中的应用. 2022-09-20.浏览/下载:310/0评论推荐收藏
 [10] Mao, Qi.,Zhang, Bingjie.,Tian, Sheng.,Qin, Wangzhi.,Chen, Jiaojiao.,...&Ye, Na.(2022).Structural optimizations and bioevaluation of N-H aporphine analogues as Gq-biased and selective serotonin 5-HT2C receptor agonists.BIOORGANIC CHEMISTRY,123.浏览/下载:283/2; 被引[WOS]:3; IF:4.5/4.7评论推荐收藏