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Citation: G. Drutel et al., Identification of rat H-3 receptor isoforms with different brain expression and signaling properties, MOLEC PHARM, 59(1), 2001, pp. 1-8
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Citation: P. Casarosa et al., Constitutive signaling of the human cytomegalovirus-encoded chemokine receptor US28, J BIOL CHEM, 276(2), 2001, pp. 1133-1137
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Citation: M. Hoffmann et al., Recombinant Semliki Forest virus for over-expression and pharmacological characterisation of the histamine H-2 receptor in mammalian cells, EUR J PHARM, 427(2), 2001, pp. 105-114
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Citation: M. Blomenrohr et al., Pivotal role for the cytoplasmic carboxyl-terminal tail of a nonmammalian gonadotropin-releasing hormone receptor in cell surface expression, ligand binding, and receptor phosphorylation and internalization. (vol 56, pg 1229, 1999), MOLEC PHARM, 57(1), 2000, pp. 211-211
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Citation: Ad. Windhorst et al., Characterization of the binding site of the histamine H-3 receptor. 2. Synthesis, in vitro pharmacology, and QSAR of a series of monosubstituted benzyl analogues of thioperamide, J MED CHEM, 43(9), 2000, pp. 1754-1761
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Citation: Ad. Windhorst et al., Radiosynthesis and biodistribution of I-123-labeled antagonists of the histamine H-3 receptor as potential SPECT ligands, NUCL MED BI, 26(6), 1999, pp. 651-659
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Citation: Ad. Windhorst et al., Evaluation of [F-18]VUF 5000 as a potential PET ligand for brain imaging of the histamine H-3 receptor, BIO MED CH, 7(9), 1999, pp. 1761-1767
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Menge, WMPB
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Citation: Ad. Windhorst et al., Synthesis, in vitro pharmacology and radiosynthesis of N-(cis-4-fluoromethylcyclohexyl)-4-(1(H)-imidazol-4-yl)piperidine-1-thiocarbonamide (VUF 5000), a potential pet ligand for the histamine H-3 receptor., J LABEL C R, 42(3), 1999, pp. 293-307
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Citation: Je. Ratsma et al., Platelet adenylyl cyclase activity as a biochemical trait marker for predisposition to alcoholism, ALC CLIN EX, 23(4), 1999, pp. 600-604