Ulrich Schwabe

1983-1988 Pharmacology University of Heidelberg, Germany, Heidelberg, Baden-Württemberg, Germany 
"Ulrich Schwabe"
Mean distance: 14.87 (cluster 6)
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Lorenzen A, Beukers MW, van der Graaf PH, et al. (2002) Modulation of agonist responses at the A(1) adenosine receptor by an irreversible antagonist, receptor-G protein uncoupling and by the G protein activation state. Biochemical Pharmacology. 64: 1251-65
Lorenzen A, Stannek C, Burmeister A, et al. (2002) G protein-coupled receptor for nicotinic acid in mouse macrophages. Biochemical Pharmacology. 64: 645-8
Lorenzen A, Stannek C, Lang H, et al. (2001) Characterization of a G protein-coupled receptor for nicotinic acid. Molecular Pharmacology. 59: 349-57
Lorenzen A, Guerra L, Campi F, et al. (2000) Thermodynamically distinct high and low affinity states of the A(1) adenosine receptor induced by G protein coupling and guanine nucleotide ligation states of G proteins. British Journal of Pharmacology. 130: 595-604
Kull B, Arslan G, Nilsson C, et al. (1999) Differences in the order of potency for agonists but not antagonists at human and rat adenosine A2A receptors. Biochemical Pharmacology. 57: 65-75
Lorenzen A, Lang H, Schwabe U. (1998) Activation of various subtypes of G-protein alpha subunits by partial agonists of the adenosine A1 receptor. Biochemical Pharmacology. 56: 1287-93
Lorenzen A, Engelhardt J, Kerst B, et al. (1998) Heterogeneous forms of adenotin-1 of different subcellular localization. Biochemical Pharmacology. 55: 455-64
Holschbach MH, Fein T, Krummeich C, et al. (1998) A1 adenosine receptor antagonists as ligands for positron emission tomography (PET) and single-photon emission tomography (SPET). Journal of Medicinal Chemistry. 41: 555-63
Lorenzen A, Sebastião AM, Sellink A, et al. (1997) Biological activities of N6,C8-disubstituted adenosine derivatives as partial agonists at rat brain adenosine A1 receptors. European Journal of Pharmacology. 334: 299-307
Fredholm BB, Abbracchio MP, Burnstock G, et al. (1997) Towards a revised nomenclature for P1 and P2 receptors. Trends in Pharmacological Sciences. 18: 79-82
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