xiaopeng 山东大学主页平台管理系统--Home

- 中文

肖鹏

Professor

Name (Simplified Chinese):肖鹏

Name (Pinyin):xiaopeng

Date of Employment:2012-07-16

School/Department:基础医学院

Gender:Male

Status:Employed

Whether on the job:1

Academic Honor:

Honors and Titles:

Current position: Home >> Scientific Research >> Paper Publications

[1] . Differential contributions of G protein- or arrestin subtype-mediated signalling underlie urocortin . BRITISH JOURNAL OF PHARMACOLOGY, 2600, 2024.
[2] . Single hormone or synthetic agonist induces Gs/Gi coupling selectivity of EP receptors via distinct . Proceedings of the National Academy of Sciences of the United States of America, 2023.
[3] . DeSiphering receptor core-induced and ligand dependent conformational changes in Arrestin via geneti. NATURE COMMUNICATIONS, 2020.
[4] . Tethered peptide activation mechanism of the adhesion GPCRs ADGRG2 and ADGRG4. Nature, 2022.
[5] . Structural studies of phosphorylation-dependent interactions between the V2R receptor and Arrestin-2. NATURE COMMUNICATIONS, 2022.
[6] . Unsaturated bond recognition leads to biased signal in a fatty acid receptor. science, 380, 2023.
[7] . Structural basis of signaling of cannabinoids receptors: paving a way for rational drug design in co. SIGNAL TRANSDUCTION AND TARGETED THERAPY, 2020.
[8] . Gut microbial metabolite facilitates colorectal cancer development via ferroptosis inhibition. NATURE CELL BIOLOGY, 26, 124-137, 2024.
[9] . Differential contributions of G protein- or arrestin subtype-mediated signalling underlie urocortin . BRITISH JOURNAL OF PHARMACOLOGY, 2024.
[10] . Progesterone activates GPR126 to promote breast cancer development via the Gi pathway. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2022.
[11] . Tethered peptide activation mechanism of the adhesion GPCRs ADGRG2 and ADGRG4. nature, 604, 771-778, 2022.
[12] . Structure, function and pharmacology of human itch receptor complexes. nature, 600, 164-, 2021.
[13] 安文涛. Progesterone activates GPR126 to promote breast cancer development via the Gi pathway. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF T, 119, e2117004119, 2022.
[14] 平玉奇. Structural basis for the tethered peptide activation of adhesion GPCRs. nature, 604, 763-770, 2022.
[15] 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.
[16] 屈昌秀. Ligand recognition, unconventional activation, and G protein coupling of the prostaglandin E-2 recep. 科学前沿, 7, 2021.
[17] 贺庆涛. Structural studies of phosphorylation-dependent interactions between the V2R receptor and arrestin-2. NATURE COMMUNICATIONS, 12, 2021.
[18] 平玉奇. Structures of the glucocorticoid-bound adhesion receptor GPR97-G(o) complex. Nature, 589, 620, 2021.
[19] 肖鹏. Ligand recognition and allosteric regulation of DRD1-Gs signaling complexes. 细胞, 184, 943, 2021.
[20] 徐云飞. PTP-MEG2 regulates quantal size and fusion pore opening through two distinct structural bases and su. EMBO Reports, 2021.

total67 1/4

firstpreviousnext last Page