Gary L. Stiles
Affiliations: | Duke Medical School, Durham, NC, United States |
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Collaborators
Sign in to add collaborator| Kenneth A. Jacobson | collaborator | 1987-1999 | Duke Medical School |
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Publications
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| Ji XD, von Lubitz D, Olah ME, et al. (2024) Species Differences in Ligand Affinity at Central A-Adenosine Receptors. Drug Development Research. 33: 51-59 |
| Fredholm BB, Frenguelli BG, Hills R, et al. (2019) Adenosine receptors (version 2019.4) in the IUPHAR/BPS Guide to Pharmacology Database Iuphar/Bps Guide to Pharmacology Cite. 2019 |
| Ji XD, Stiles GL, Jacobson KA. (2012) [(3)H]XAC (xanthine amine congener) is a radioligand for A(2)-adenosine receptors in rabbit striatum. Neurochemistry International. 18: 207-13 |
| KARTON Y, JIANG J, JI X, et al. (2010) ChemInform Abstract: Synthesis and Biological Activities of Flavonoid Derivatives as A3 Adenosine Receptor Antagonists. Cheminform. 27: no-no |
| BARALDI PG, CACCIARI B, SPALLUTO G, et al. (2010) ChemInform Abstract: Novel N6-(Substituted-phenylcarbamoyl)adenosine-5′-uronamides as Potent Agonists for A3 Adenosine Receptors. Cheminform. 27: no-no |
| Olah ME, Stiles GL. (2000) The role of receptor structure in determining adenosine receptor activity. Pharmacology & Therapeutics. 85: 55-75 |
| Palmer TM, Stiles GL. (2000) Identification of Threonine Residues Controlling the Agonist-Dependent Phosphorylation and Desensitization of the Rat A3 Adenosine Receptor Molecular Pharmacology. 57: 539-545 |
| Palmer TM, Stiles GL. (1999) Stimulation of A(2A) adenosine receptor phosphorylation by protein kinase C activation: evidence for regulation by multiple protein kinase C isoforms. Biochemistry. 38: 14833-42 |
| Xie R, Li AH, Ji XD, et al. (1999) Selective A(3) adenosine receptor antagonists: water-soluble 3, 5-diacyl-1,2,4-trialkylpyridinium salts and their oxidative generation from dihydropyridine precursors. Journal of Medicinal Chemistry. 42: 4232-8 |
| Ren H, Stiles GL. (1999) Dexamethasone stimulates human A1 adenosine receptor (A1AR) gene expression through multiple regulatory sites in promoter B. Molecular Pharmacology. 55: 309-16 |