教授
性别：男
在职信息：在职
所在单位：基础医学院
入职时间：2012-07-16
访问量：
最后更新时间：..
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[1]
.
Differential contributions of G protein- or arrestin subtype-mediated signalling underlie urocortin 3-induced somatostatin secretion in pancreatic δ cells.
BRITISH JOURNAL OF PHARMACOLOGY,
2600,
2024.
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[2]
.
Single hormone or synthetic agonist induces Gs/Gi coupling selectivity of EP receptors via distinct binding modes and propagating paths.
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 genetic encoded trimethylsilyl 1H-NMR probe.
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.
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[7]
.
Structural basis of signaling of cannabinoids receptors: paving a way for rational drug design in controling mutiple neurological and immune diseases.
SIGNAL TRANSDUCTION AND TARGETED THERAPY,
2020.
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[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 3-induced somatostatin secretion in pancreatic δ cells.
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.
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[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.
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[14]
平玉奇.
Structural basis for the tethered peptide activation of adhesion GPCRs.
nature,
604,
763-770,
2022.
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[15]
孙玉静.
Optimization of a peptide ligand for the adhesion GPCR ADGRG2 provides a potent tool to explore receptor biology.
JOURNAL OF BIOLOGICAL CHEMISTRY,
296,
2021.
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[16]
屈昌秀.
Ligand recognition, unconventional activation, and G protein coupling of the prostaglandin E-2 receptor EP2 subtype.
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.
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[19]
肖鹏.
Ligand recognition and allosteric regulation of DRD1-Gs signaling complexes.
细胞,
184,
943,
2021.
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[20]
徐云飞.
PTP-MEG2 regulates quantal size and fusion pore opening through two distinct structural bases and substrates.
EMBO Reports,
2021.
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