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,
2024.
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[2]
.
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.
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[3]
.
Tethered peptide activation mechanism of the adhesion GPCRs ADGRG2 and ADGRG4.
nature,
604,
771-778,
2022.
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[4]
.
Structure, function and pharmacology of human itch receptor complexes.
nature,
600,
164-,
2021.
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[5]
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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[6]
平玉奇.
Structural basis for the tethered peptide activation of adhesion GPCRs.
nature,
604,
763-770,
2022.
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[7]
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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[8]
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.
-
[9]
贺庆涛.
Structural studies of phosphorylation-dependent interactions between the V2R receptor and arrestin-2.
Nature Communications,
12,
2021.
-
[10]
平玉奇.
Structures of the glucocorticoid-bound adhesion receptor GPR97-G(o) complex.
Nature,
589,
620,
2021.
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[11]
肖鹏.
Ligand recognition and allosteric regulation of DRD1-Gs signaling complexes.
细胞,
184,
943,
2021.
-
[12]
徐云飞.
PTP-MEG2 regulates quantal size and fusion pore opening through two distinct structural bases and substrates.
EMBO Reports,
2021.
-
[13]
刘琪.
DeSiphering receptor core-induced and ligand-dependent conformational changes in arrestin via genetic encoded trimethylsilyl H-1-NMR probe.
Nature Communications,
11,
2020.
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[14]
卢志远.
Identification of HN252 as a potent inhibitor of protein phosphatase PPM1B.
journal of cellular and molecular medicine,
24,
13463,
2020.
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[15]
黄申明.
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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[16]
黄深明.
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,
5,
2020.
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[17]
杨帆.
Structural basis of GPBAR activation and bile acid recognition.
Nature,
587,
499,
2020.
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[18]
杨帆.
Structural basis of GPBAR activation and bile acid recognition.
Nature,
2020.
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[19]
梁啸.
Design, synthesis and biological evaluation of imidazolidine-2,4-dione and 2-thioxothiazolidin-4-one derivatives as lymphoid-specific tyrosine phosphatase inhibitors.
BIOORGANIC CHEMISTRY,
103,
2020.
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[20]
方浩 and 侯旭奔.
Design, synthesis and biological evaluation of imidazolidine-2,4-dione and 2-thioxothiazolidin-4-one derivatives as lymphoid-specific tyrosine phosphatase inhibitors.
Bioorg Chem.,
2020.
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