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性别:女
在职信息:在职
所在单位:基础医学院
入职时间:2009-11-10
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[21] 孙玉静. Optimization of a peptide ligand for the adhesion GPCR ADGRG2 provides a potent tool to explore rece. JOURNAL OF BIOLOGICAL CHEMISTRY, 296, 2021.
[22] 屈昌秀. Ligand recognition, unconventional activation, and G protein coupling of the prostaglandin E-2 recep. 科学前沿, 7, 2021.
[23] 贺庆涛. Structural studies of phosphorylation-dependent interactions between the V2R receptor and arrestin-2. NATURE COMMUNICATIONS, 12, 2021.
[24] 平玉奇. Structures of the glucocorticoid-bound adhesion receptor GPR97-G(o) complex. Nature, 589, 620, 2021.
[25] 肖鹏. Ligand recognition and allosteric regulation of DRD1-Gs signaling complexes. 细胞, 184, 943, 2021.
[26] 徐云飞. PTP-MEG2 regulates quantal size and fusion pore opening through two distinct structural bases and su. EMBO Reports, 2021.
[27] 林婧宇. An ionic lock and a hydrophobic zipper mediate the coupling between an insect pheromone receptor BmO. J Biol Chem., 2021.
[28] 卢志远. Identification of HN252 as a potent inhibitor of protein phosphatase PPM1B. journal of cellular and molecular medicine, 24, 13463, 2020.
[29] 蒲泽青. NR4A1 counteracts JNK activation incurred by ER stress or ROS in pancreatic beta-cells for protectio. journal of cellular and molecular medicine, 24, 14171, 2020.
[30] Zhao, Shuai. Cell active and functionally-relevant small-molecule agonists of calcitonin receptor. BIOORGANIC CHEMISTRY, 96, 2020.
[31] 付艺. Elevation of JAML Promotes Diabetic Kidney Disease by Modulating Podocyte Lipid Metabolism. CELL METABOLISM, 32, 2020.
[32] 杨帆. Structural basis of GPBAR activation and bile acid recognition. Nature, 587, 499, 2020.
[33] 刘琪. DeSiphering receptor core-induced and ligand-dependent conformational changes in arrestin via geneti. NATURE COMMUNICATIONS, 11, 2020.
[34] 杨帆. Structural basis of GPBAR activation and bile acid recognition. Nature, 2020.
[35] 林婧宇. In vitro expansion of pancreatic islet clusters facilitated by hormones and chemicals. CELL DISCOVERY, 6, 2020.
[36] Zhang, Daolai. Function and therapeutic potential of G protein-coupled receptors in epididymis. BRITISH JOURNAL OF PHARMACOLOGY, 177, 5489, 2020.
[37] Huang, Shen-Ming. Genetically Encoded Fluorescent Amino Acid for Monitoring Protein Interactions through FRET. ANALYTICAL CHEMISTRY, 91, 14936, 2019.
[38] Dolatabad, Meisam Rostaminasab. Crystal structure and catalytic activity of the PPM1K N94K mutant. Journal of Neurochemistry, 148, 550, 2019.
[39] Park, Ji Young. Structural Mechanism of the Arrestin-3/JNK3 Interaction. STRUCTURE, 27, 1162, 2019.
[40] 李康帅. Identification and structure-function analyses of an allosteric inhibitor of the tyrosine phosphatas. 294, 8653, 2019.
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