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The American Journal of Clinical Nutrition|June 9, 2017
Cholecystokinin responsiveness varies across the population dependent on metabolic phenotypeAditya J Desai, Maoqing Dong, Blake T Langlais, et al.
Molecular Endocrinology (Baltimore, Md.)|October 31, 2002
Interaction among four residues distributed through the secretin pharmacophore and a focused region of the secretin receptor amino terminusMaoqing Dong, Mengwei Zang, Delia I Pinon, et al.
Molecular Pharmacology|August 24, 2004
Key differences in molecular complexes of the cholecystokinin receptor with structurally related peptide agonist, partial agonist, and antagonistSonnet J H Arlander, Maoqing Dong, Xi-Qin Ding, et al.
The Journal of Biological Chemistry|September 23, 2003
Spatial approximation between two residues in the mid-region of secretin and the amino terminus of its receptor. Incorporation of seven sets of such constraints into a three-dimensional model of the agonist-bound secretin receptorMaoqing Dong, Zhijun Li, Mengwei Zang, et al.
Cellular Signalling|October 29, 2002
Forskolin suppresses insulin gene transcription in islet beta-cells through a protein kinase A-independent pathwayWei-Qun Ding, Maoqing Dong, Dora Ninova, et al.
Biochemistry|March 11, 2011
Importance of each residue within secretin for receptor binding and biological activityMaoqing Dong, Angela Le, Jerez A Te, et al.
Biochemistry|December 6, 2006
Transmembrane segment peptides can disrupt cholecystokinin receptor oligomerization without affecting receptor functionKaleeckal G Harikumar, Maoqing Dong, Zhijie Cheng, et al.
Journal of the American Chemical Society|September 7, 2017
Spirohexene-Tetrazine Ligation Enables Bioorthogonal Labeling of Class B G Protein-Coupled Receptors in Live CellsCarlo P Ramil, Maoqing Dong, Peng An, et al.
Molecular Pharmacology|May 10, 2008
Spatial approximation between secretin residue five and the third extracellular loop of its receptor provides new insight into the molecular basis of natural agonist bindingMaoqing Dong, Polo C-H Lam, Delia I Pinon, et al.
The Journal of Biological Chemistry|September 11, 2007
Fluorescence resonance energy transfer analysis of secretin docking to its receptor: mapping distances between residues distributed throughout the ligand pharmacophore and distinct receptor residuesKaleeckal G Harikumar, Polo C-H Lam, Maoqing Dong, et al.
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