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Results: 1-15 |
Results: 15
New halogenated [C-11]WAY analogues, [C-11]6FPWAY and [C-11]6BPWAY - Radiosynthesis and assessment as radioligands for the study of brain 5-HT1A receptors in living monkey
Authors: Sandell, J Halldin, C Pike, VW Chou, YH Varnas, K Hall, H Marchais, S Nowicki, B Wikstrom, HV Swahn, CG Farde, L
Citation: J. Sandell et al., New halogenated [C-11]WAY analogues, [C-11]6FPWAY and [C-11]6BPWAY - Radiosynthesis and assessment as radioligands for the study of brain 5-HT1A receptors in living monkey, NUCL MED BI, 28(2), 2001, pp. 177-185
Antipsychotic drugs classified by their effects on the release of dopamineand noradrenaline in the prefrontal cortex and striatum
Authors: Westerink, BHC Kawahara, Y De Boer, P Geels, C De Vries, JB Wikstrom, HV Van Kalkeren, A Van Vliet, B Kruse, CG Long, SK
Citation: Bhc. Westerink et al., Antipsychotic drugs classified by their effects on the release of dopamineand noradrenaline in the prefrontal cortex and striatum, EUR J PHARM, 412(2), 2001, pp. 127-138
Is the beneficial antidepressant effect of coadministration of pindolol really due to somatodendritic autoreceptor antagonism?
Authors: Cremers, TIFH Wiersma, LJ Bosker, FJ den Boer, JA Westerink, BHC Wikstrom, HV
Citation: Tifh. Cremers et al., Is the beneficial antidepressant effect of coadministration of pindolol really due to somatodendritic autoreceptor antagonism?, BIOL PSYCHI, 50(1), 2001, pp. 13-21
Ion-pair formation of hydroquinine by chromatography
Authors: Marchais, S Vermeulen, ES Semple, G Sundell, S Wikstrom, HV
Citation: S. Marchais et al., Ion-pair formation of hydroquinine by chromatography, ANALYT CHIM, 426(1), 2001, pp. 85-93
In vitro mimicry of metabolic oxidation reactions by electrochemistry/massspectrometry
Authors: Jurva, U Wikstrom, HV Bruins, AP
Citation: U. Jurva et al., In vitro mimicry of metabolic oxidation reactions by electrochemistry/massspectrometry, RAP C MASS, 14(6), 2000, pp. 529-533
Synthesis and in vitro and in vivo functional studies of ortho-substitutedphenylpiperazine and N-substituted 4-N-(o-methoxyphenyl)aminopiperidine analogues of WAY100635
Authors: Mensonides-Harsema, MM Liao, Y Bottcher, H Bartoszyk, GD Greiner, HE Harting, J de Boer, P Wikstrom, HV
Citation: Mm. Mensonides-harsema et al., Synthesis and in vitro and in vivo functional studies of ortho-substitutedphenylpiperazine and N-substituted 4-N-(o-methoxyphenyl)aminopiperidine analogues of WAY100635, J MED CHEM, 43(3), 2000, pp. 432-439
Desensitisation of 5-HT autoreceptors upon pharmacokinetically monitored chronic treatment with citalopram
Authors: Cremers, TIFH Spoelstra, EN de Boer, P Bosker, FJ Mork, A den Boer, JA Westerink, BHC Wikstrom, HV
Citation: Tifh. Cremers et al., Desensitisation of 5-HT autoreceptors upon pharmacokinetically monitored chronic treatment with citalopram, EUR J PHARM, 397(2-3), 2000, pp. 351-357
Augmentation with a 5-HT1A but not a 5-HT1B receptor antagonist criticallydepends on the dose of citalopram
Authors: Cremers, TIFH de Boer, P Liao, Y Bosker, FJ den Boer, JA Westerink, BHC Wikstrom, HV
Citation: Tifh. Cremers et al., Augmentation with a 5-HT1A but not a 5-HT1B receptor antagonist criticallydepends on the dose of citalopram, EUR J PHARM, 397(1), 2000, pp. 63-74
Thiophene analogs of naphthoxazines and 2-aminotetralins: bioisosteres with improved relative oral bioavailability, as compared to 5-OH-DPAT
Authors: Rodenhuis, N Timmerman, W Wikstrom, HV Dijkstra, D
Citation: N. Rodenhuis et al., Thiophene analogs of naphthoxazines and 2-aminotetralins: bioisosteres with improved relative oral bioavailability, as compared to 5-OH-DPAT, EUR J PHARM, 394(2-3), 2000, pp. 255-263
Dopamine D-2 activity of R-(-)-apomorphine and selected analogs: a microdialysis study
Authors: Rodenhuis, N Dijkstra, D de Boer, P Vermeulen, ES Timmerman, W Wikstrom, HV
Citation: N. Rodenhuis et al., Dopamine D-2 activity of R-(-)-apomorphine and selected analogs: a microdialysis study, EUR J PHARM, 387(1), 2000, pp. 39-45
Molecular modeling of the dopamine D-2 and serotonin 5-HT1A receptor binding modes of the enantiomers of 5-OMe-BPAT
Authors: Homan, EJ Wikstrom, HV Grol, CJ
Citation: Ej. Homan et al., Molecular modeling of the dopamine D-2 and serotonin 5-HT1A receptor binding modes of the enantiomers of 5-OMe-BPAT, BIO MED CH, 7(9), 1999, pp. 1805-1820
Synthesis and pharmacology of the enantiomers of the potential atypical antipsychotic agents 5-OMe-BPAT and 5-OMe-(2,6-di-OMe)-BPAT
Authors: Homan, EJ Copinga, S Unelius, L Jackson, DM Wikstrom, HV Grol, CJ
Citation: Ej. Homan et al., Synthesis and pharmacology of the enantiomers of the potential atypical antipsychotic agents 5-OMe-BPAT and 5-OMe-(2,6-di-OMe)-BPAT, BIO MED CH, 7(7), 1999, pp. 1263-1271
Structural analogues of 5-OMe-BPAT: Synthesis and interactions with dopamine D-2, D-3, and serotonin 5-HT1A receptors
Authors: Homan, EJ Kroodsma, E Copinga, S Unelius, L Mohell, N Wikstrom, HV Grol, CJ
Citation: Ej. Homan et al., Structural analogues of 5-OMe-BPAT: Synthesis and interactions with dopamine D-2, D-3, and serotonin 5-HT1A receptors, BIO MED CH, 7(6), 1999, pp. 1111-1121
C5-substituted derivatives of 5-OMe-BPAT: Synthesis and interactions with dopamine D-2 and serotonin 5-HT1A receptors
Authors: Homan, EJ Tulp, MTM Nilsson, JE Wikstrom, HV Grol, CJ
Citation: Ej. Homan et al., C5-substituted derivatives of 5-OMe-BPAT: Synthesis and interactions with dopamine D-2 and serotonin 5-HT1A receptors, BIO MED CH, 7(11), 1999, pp. 2541-2548
2-aminotetralin-derived substituted benzamides with mixed dopamine D-2, D-3, and serotonin 5-HT1A receptor binding properties: A novel class of potential atypical antipsychotic agents
Authors: Homan, EJ Copinga, S Elfstrom, L van der Veen, T Hallema, JP Mohell, N Unelius, L Johansson, R Wikstrom, HV Grol, CJ
Citation: Ej. Homan et al., 2-aminotetralin-derived substituted benzamides with mixed dopamine D-2, D-3, and serotonin 5-HT1A receptor binding properties: A novel class of potential atypical antipsychotic agents, BIO MED CH, 6(11), 1998, pp. 2111-2126
Risultati: 1-15 |