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Species differences in ligand affinity at central A3-adenosine receptorsXIAO-DUO JI; VON LUBITZ, D; OLAH, M. E et al.Drug development research. 1994, Vol 33, Num 1, pp 51-59, issn 0272-4391Article

A role for central A3-adenosine receptors : mediation of behavioral depressant effectsJACOBSON, K. A; NIKODIJEVIC, O; DAN SHI et al.FEBS letters. 1993, Vol 336, Num 1, pp 57-60, issn 0014-5793Article

Pharmacological characterization of novel A3 adenosine receptor-selective antagonistsJACOBSON, K. A; PARK, K.-S; JIANG, J.-L et al.Neuropharmacology. 1997, Vol 36, Num 9, pp 1157-1165, issn 0028-3908Conference Paper

Structure-activity relationships of N6-benzyladenosine-5'-uronamides as A3-selective adenosine agonistsGALLO-RODRIGUEZ, C; XIAO-DUO JI; STILES, G. L et al.Journal of medicinal chemistry (Print). 1994, Vol 37, Num 5, pp 636-646, issn 0022-2623Article

Molecular cloning and characterization of an adenosine receptor : the A3 adenosine receptorQUN-YONG ZHOU; CHUANYU LI; OLAH, M. E et al.Proceedings of the National Academy of Sciences of the United States of America. 1992, Vol 89, Num 16, pp 7432-7436, issn 0027-8424Article

Selective as adenosine receptor antagonists : Water-soluble 3,5-diacyl-1,2,4-trialkylpyridinium salts and their oxidative generation from dihydropyridine precursorsRONGYUAN XIE; LI, A.-H; JI, X.-D et al.Journal of medicinal chemistry (Print). 1999, Vol 42, Num 20, pp 4232-4238, issn 0022-2623Article

Structure-activity relationships of 9-alkyladenine and ribose-modified adenosine derivatives at rat A3 adenosine receptorsJACOBSON, K. A; SIDDIQI, S. M; OLAH, M. E et al.Journal of medicinal chemistry (Print). 1995, Vol 38, Num 10, pp 1720-1735, issn 0022-2623Article

Structure-activity relationships of 1,3-dialkylxanthine derivatives at rat A3 adenosine receptorsHEA OK KIM; XIAO-DUO JI; MELMAN, N et al.Journal of medicinal chemistry (Print). 1994, Vol 37, Num 20, pp 3373-3382, issn 0022-2623Article

Adenosine receptorsOLAH, M. E; STILES, G. L.Annual review of physiology. 1992, Vol 54, pp 211-225, issn 0066-4278Article

Distinct pathways of desensitization of A1- and A2-adenosine receptors in DDT1MF-2 cellsVICKRAM RAMKUMAR; OLAH, M. E; JACOBSON, K. A et al.Molecular pharmacology. 1991, Vol 40, Num 5, pp 639-647, issn 0026-895XArticle

Purification and characterization of bovine cerebral cortex A1 adenosine receptorOLAH, M. E; JACOBSON, K. A; STILES, G. L et al.Archives of biochemistry and biophysics (Print). 1990, Vol 283, Num 2, pp 440-446, issn 0003-9861, 7 p.Article

Differential effects of calcium channel blockade and intracellular calcium antagonism on endothelium-dependent responses of the rat aorta to drugsOLAH, M. E; RAHWAN, R. G.Pharmacology. 1988, Vol 37, Num 5, pp 305-320, issn 0031-7012Article

Novel N6-(substituted-phenylcarbamoyl)adenosine-5'-uronamides as potent agonists for A3 adenosine receptorsBARALDI, P. G; CACCIARI, B; SPALLUTO, G et al.Journal of medicinal chemistry (Print). 1996, Vol 39, Num 3, pp 802-806, issn 0022-2623Article

Synthesis and biological activities of flavonoid derivatives as A3 adenosine receptor antagonistsKARTON, Y; JIANG, J.-L; JI, X.-D et al.Journal of medicinal chemistry (Print). 1996, Vol 39, Num 12, pp 2293-2301, issn 0022-2623Article

125I-4-aminobenzyl-5'-N-methylcarboxamidoadenosine, a high affinity radioligand for the rat A3 adenosine receptorOLAH, M. E; GALLO-RODRIGUEZ, C; JACOBSON, K. A et al.Molecular pharmacology. 1994, Vol 45, Num 5, pp 978-982, issn 0026-895XArticle

2-Substitution of N6-benzyladenosine-5'-uronamides enhances selectivity for A3 adenosine receptorsKIM, H. O; XIAO-DUO JI; SIDDIQI, S. M et al.Journal of medicinal chemistry (Print). 1994, Vol 37, Num 21, pp 3614-3621, issn 0022-2623Article

Age-related changes in responsiveness of the rat aorta to depolarizing and receptor-mediated contractile stimuli and to calcium antagonismOLAH, M. E; RHAWAN, R. G.Pharmacology. 1987, Vol 35, Num 3, pp 163-173, issn 0031-7012Article

Interaction of 1,4-dihydropyridine and pyridine derivatives with adenosine receptors : Selectivity for A3 receptorsVAN RHEE, A. M; JIANG, J.-L; MELMAN, N et al.Journal of medicinal chemistry (Print). 1996, Vol 39, Num 15, pp 2980-2989, issn 0022-2623Article

Search for new purine- and ribose-modified adenosine analogues as selective agonists and antagonists at adenosine receptorsSIDDIQI, S. M; JACOBSON, K. A; STILES, G. L et al.Journal of medicinal chemistry (Print). 1995, Vol 38, Num 7, pp 1174-1188, issn 0022-2623Article

Identification of an adenosine receptor domain specifically involved in binding of 5'-substituted adenosine agonistsOLAH, M. E; JACOBSON, K. A; STILES, G. L et al.The Journal of biological chemistry (Print). 1994, Vol 269, Num 27, pp 18016-18020, issn 0021-9258Article

Selective ligands for rat A3 adenosine receptors : structure-activity relationships of 1,3-dialkylxanthine 7-riboside derivativesHEA OK KIM; XIAO-DUO JI; MELMAN, N et al.Journal of medicinal chemistry (Print). 1994, Vol 37, Num 23, pp 4020-4030, issn 0022-2623Article

Molecular characterization of A1 and A2a adenosine receptorsJACOBSON, K. A; VAN GALEN, P. J. M; XIAO-DUO JI et al.Drug development research. 1993, Vol 28, Num 3, pp 226-231, issn 0272-4391Article

Cloning, expression, and characterization of the unique bovine A1 adenosine receptor : studies on the ligand binding site by site-directed mutagenesisOLAH, M. E; HONGZU REN; OSTROWSKI, J et al.The Journal of biological chemistry (Print). 1992, Vol 267, Num 15, pp 10764-10770, issn 0021-9258Article

Affinity chromatography of the bovine cerebral cortex A2 adenosine receptorOLAH, M. E; JACOBSON, K. A; STILES, G. L et al.FEBS letters. 1989, Vol 257, Num 2, pp 292-296, issn 0014-5793Article

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