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Results: 1-25 | 26-49 |
Results: 26-49/49
5-HT1B RECEPTOR ANTAGONIST PROPERTIES OF NOVEL ARYLPIPERAZIDE DERIVATIVES OF 1-NAPHTHYLPIPERAZINE
Authors: JORANDLEBRUN C PAUWELS PJ PALMIER C MORET C CHOPIN P PEREZ M MARIEN M HALAZY S
Citation: C. Jorandlebrun et al., 5-HT1B RECEPTOR ANTAGONIST PROPERTIES OF NOVEL ARYLPIPERAZIDE DERIVATIVES OF 1-NAPHTHYLPIPERAZINE, Journal of medicinal chemistry, 40(24), 1997, pp. 3974-3978
DIFFERENTIATION BETWEEN PARTIAL AGONISTS AND NEUTRAL 5-HT1B ANTAGONISTS BY CHEMICAL MODULATION OF PYL]-4-HYDROXY-N-[4-(PYRIDIN-4-YL)PHENYL]BENZAMIDE (GR-55562)
Authors: LAMOTHE M PAUWELS PJ BELLIARD K SCHAMBEL P HALAZY S
Citation: M. Lamothe et al., DIFFERENTIATION BETWEEN PARTIAL AGONISTS AND NEUTRAL 5-HT1B ANTAGONISTS BY CHEMICAL MODULATION OF PYL]-4-HYDROXY-N-[4-(PYRIDIN-4-YL)PHENYL]BENZAMIDE (GR-55562), Journal of medicinal chemistry, 40(22), 1997, pp. 3542-3550
RECOMBINANT H5-HT1B AND H5-HT1D RECEPTORS STABLY EXPRESSED IN C6 GLIOMA-CELLS ARE COUPLED TO CALCIUM-DEPENDENT POTASSIUM CHANNELS
Authors: LEGRAND B PAUWELS PJ PANISSIE A JOHN GW
Citation: B. Legrand et al., RECOMBINANT H5-HT1B AND H5-HT1D RECEPTORS STABLY EXPRESSED IN C6 GLIOMA-CELLS ARE COUPLED TO CALCIUM-DEPENDENT POTASSIUM CHANNELS, British Journal of Pharmacology, 122, 1997, pp. 253-253
RECOMBINANT SAPHENOUS-VEIN 5-HT1B RECEPTORS OF THE RABBIT - COMPARATIVE PHARMACOLOGY WITH HUMAN 5-HT1B RECEPTORS
Authors: WURCH T PALMIER C COLPAERT FC PAUWELS PJ
Citation: T. Wurch et al., RECOMBINANT SAPHENOUS-VEIN 5-HT1B RECEPTORS OF THE RABBIT - COMPARATIVE PHARMACOLOGY WITH HUMAN 5-HT1B RECEPTORS, British Journal of Pharmacology, 120(1), 1997, pp. 153-159
A 413 BP REGION UPSTREAM THE HUMAN 5-HT1A RECEPTOR GENE IS SUFFICIENTFOR ITS IN-VITRO EXPRESSION
Authors: WURCH T CHASTAGNIER C PALMIER C COLPAERT FC PAUWELS PJ
Citation: T. Wurch et al., A 413 BP REGION UPSTREAM THE HUMAN 5-HT1A RECEPTOR GENE IS SUFFICIENTFOR ITS IN-VITRO EXPRESSION, Neuroscience research communications, 19(2), 1996, pp. 75-82
MOLECULAR-CLONING AND IDENTIFICATION OF A RABBIT SAPHENOUS-VEIN 5-HT1D-BETA RECEPTOR GENE
Authors: WURCH T CATHALA C PALMIER C VALENTIN JP JOHN GW COLPAERT FC PAUWELS PJ
Citation: T. Wurch et al., MOLECULAR-CLONING AND IDENTIFICATION OF A RABBIT SAPHENOUS-VEIN 5-HT1D-BETA RECEPTOR GENE, Neuroscience research communications, 18(3), 1996, pp. 155-162
PROMOTION OF CELL-GROWTH BY STIMULATION OF CLONED HUMAN 5-HT1D RECEPTOR-SITES IN TRANSFECTED C6-GLIAL CELLS IS HIGHLY SENSITIVE TO INTRINSIC ACTIVITY AT 5-HT1D RECEPTORS
Authors: PAUWELS PJ WURCH T PALMIER C COLPAERT FC
Citation: Pj. Pauwels et al., PROMOTION OF CELL-GROWTH BY STIMULATION OF CLONED HUMAN 5-HT1D RECEPTOR-SITES IN TRANSFECTED C6-GLIAL CELLS IS HIGHLY SENSITIVE TO INTRINSIC ACTIVITY AT 5-HT1D RECEPTORS, Naunyn-Schmiedeberg's archives of pharmacology, 354(2), 1996, pp. 136-144
PHARMACOLOGY OF CLONED HUMAN 5-HT1D RECEPTOR-MEDIATED FUNCTIONAL-RESPONSES IN STABLY TRANSFECTED RAT C6-GLIAL CELL-LINES - FURTHER EVIDENCEDIFFERENTIATING HUMAN 5-HT1D AND 5-HT1B RECEPTORS
Authors: PAUWELS PJ PALMIER C WURCH T COLPAERT FC
Citation: Pj. Pauwels et al., PHARMACOLOGY OF CLONED HUMAN 5-HT1D RECEPTOR-MEDIATED FUNCTIONAL-RESPONSES IN STABLY TRANSFECTED RAT C6-GLIAL CELL-LINES - FURTHER EVIDENCEDIFFERENTIATING HUMAN 5-HT1D AND 5-HT1B RECEPTORS, Naunyn-Schmiedeberg's archives of pharmacology, 353(2), 1996, pp. 144-156
STIMULATION OF CLONED HUMAN SEROTONIN 5-HT1D-BETA RECEPTOR-SITES IN STABLY TRANSFECTED C6 GLIAL-CELLS PROMOTES CELL-GROWTH
Authors: PAUWELS PJ WURCH T AMOUREUX MC PALMIER C COLPAERT FC
Citation: Pj. Pauwels et al., STIMULATION OF CLONED HUMAN SEROTONIN 5-HT1D-BETA RECEPTOR-SITES IN STABLY TRANSFECTED C6 GLIAL-CELLS PROMOTES CELL-GROWTH, Journal of neurochemistry, 66(1), 1996, pp. 65-73
SEROTONIN DIMERS - APPLICATION OF THE BIVALENT LIGAND APPROACH TO THEDESIGN OF NEW POTENT AND SELECTIVE 5-HT1B 1D AGONISTS/
Authors: HALAZY S PEREZ M FOURRIER C PALLARD I PAUWELS PJ PALMIER C JOHN GW VALENTIN JP BONNAFOUS R MARTINEZ J
Citation: S. Halazy et al., SEROTONIN DIMERS - APPLICATION OF THE BIVALENT LIGAND APPROACH TO THEDESIGN OF NEW POTENT AND SELECTIVE 5-HT1B 1D AGONISTS/, Journal of medicinal chemistry, 39(25), 1996, pp. 4920-4927
STEREOSELECTIVITY OF 8-OH-DPAT ENANTIOMERS AT CLONED HUMAN 5-HT1D RECEPTOR-SITES
Authors: PAUWELS PJ COLPAERT FC
Citation: Pj. Pauwels et Fc. Colpaert, STEREOSELECTIVITY OF 8-OH-DPAT ENANTIOMERS AT CLONED HUMAN 5-HT1D RECEPTOR-SITES, European journal of pharmacology, 300(1-2), 1996, pp. 137-139
SELECTIVE ANTAGONISM OF HUMAN 5-HT1D AND 5-HT1B RECEPTOR-MEDIATED RESPONSES IN STABLY TRANSFECTED C6-GLIAL CELLS BY KETANSERIN AND GR-127,935
Authors: PAUWELS PJ COLPAERT FC
Citation: Pj. Pauwels et Fc. Colpaert, SELECTIVE ANTAGONISM OF HUMAN 5-HT1D AND 5-HT1B RECEPTOR-MEDIATED RESPONSES IN STABLY TRANSFECTED C6-GLIAL CELLS BY KETANSERIN AND GR-127,935, European journal of pharmacology, 300(1-2), 1996, pp. 141-145
FUNCTIONAL-EFFECTS OF THE 5-HT1D RECEPTOR ANTAGONIST GR-127,935 AT HUMAN 5-HT1D-ALPHA, 5-HT1D-BETA, 5-HT1A AND OPOSSUM 5-HT1B RECEPTORS
Authors: PAUWELS PJ PALMIER C
Citation: Pj. Pauwels et C. Palmier, FUNCTIONAL-EFFECTS OF THE 5-HT1D RECEPTOR ANTAGONIST GR-127,935 AT HUMAN 5-HT1D-ALPHA, 5-HT1D-BETA, 5-HT1A AND OPOSSUM 5-HT1B RECEPTORS, European journal of pharmacology. Molecular pharmacology section, 290(2), 1995, pp. 95-103
EXPRESSION OF HUMAN METALLOTHIONEIN-III CONFERS PROTECTION AGAINST SERUM-FREE EXPOSURE OF STABLY TRANSFECTED CHINESE-HAMSTER OVARY CHO-K1 CELLS
Authors: AMOUREUX MC WURCH T PAUWELS PJ
Citation: Mc. Amoureux et al., EXPRESSION OF HUMAN METALLOTHIONEIN-III CONFERS PROTECTION AGAINST SERUM-FREE EXPOSURE OF STABLY TRANSFECTED CHINESE-HAMSTER OVARY CHO-K1 CELLS, Neuroscience letters, 201(1), 1995, pp. 61-64
THE 5-HT1D RECEPTOR ANTAGONIST GR-127,935 IS AN AGONIST AT CLONED HUMAN 5-HT1D-ALPHA RECEPTOR-SITES
Authors: PAUWELS PJ COLPAERT FC
Citation: Pj. Pauwels et Fc. Colpaert, THE 5-HT1D RECEPTOR ANTAGONIST GR-127,935 IS AN AGONIST AT CLONED HUMAN 5-HT1D-ALPHA RECEPTOR-SITES, Neuropharmacology, 34(2), 1995, pp. 235-237
SYNTHESIS AND SEROTONERGIC ACTIVITY OF ARYLPIPERAZIDE DERIVATIVES OF SEROTONIN - POTENT AGONISTS FOR 5-HT1D RECEPTORS
Authors: PEREZ M FOURRIER C SIGOGNEAU I PAUWELS PJ PALMIER C JOHN GW VALENTIN JP HALAZY S
Citation: M. Perez et al., SYNTHESIS AND SEROTONERGIC ACTIVITY OF ARYLPIPERAZIDE DERIVATIVES OF SEROTONIN - POTENT AGONISTS FOR 5-HT1D RECEPTORS, Journal of medicinal chemistry, 38(18), 1995, pp. 3602-3607
DIFFERENTIATION BETWEEN PARTIAL AND SILENT 5-HT1D-BETA RECEPTOR ANTAGONISTS USING RAT C6-GLIAL AND CHINESE-HAMSTER OVARY CELL-LINES PERMANENTLY TRANSFECTED WITH A CLONED HUMAN 5-HT1D-BETA RECEPTOR GENE
Authors: PAUWELS PJ COLPAERT FC
Citation: Pj. Pauwels et Fc. Colpaert, DIFFERENTIATION BETWEEN PARTIAL AND SILENT 5-HT1D-BETA RECEPTOR ANTAGONISTS USING RAT C6-GLIAL AND CHINESE-HAMSTER OVARY CELL-LINES PERMANENTLY TRANSFECTED WITH A CLONED HUMAN 5-HT1D-BETA RECEPTOR GENE, Biochemical pharmacology, 50(10), 1995, pp. 1651-1658
MODULATION OF METALLOTHIONEIN-III MESSENGER-RNA CONTENT AND GROWTH-RATE OF RAT C6-GLIAL CELLS BY TRANSFECTION WITH HUMAN 5-HT1D RECEPTOR GENES
Authors: AMOUREUX MC WURCH T PAUWELS PJ
Citation: Mc. Amoureux et al., MODULATION OF METALLOTHIONEIN-III MESSENGER-RNA CONTENT AND GROWTH-RATE OF RAT C6-GLIAL CELLS BY TRANSFECTION WITH HUMAN 5-HT1D RECEPTOR GENES, Biochemical and biophysical research communications, 214(2), 1995, pp. 639-645
INHIBITION BY 5-HT OF FORSKOLIN-INDUCED CAMP FORMATION IN THE RENAL OPOSSUM EPITHELIAL-CELL LINE OK - MEDIATION OF A 5-HT1B LIKE RECEPTOR AND ANTAGONISM BY METHIOTHEPIN
Authors: PAUWELS PJ PALMIER C
Citation: Pj. Pauwels et C. Palmier, INHIBITION BY 5-HT OF FORSKOLIN-INDUCED CAMP FORMATION IN THE RENAL OPOSSUM EPITHELIAL-CELL LINE OK - MEDIATION OF A 5-HT1B LIKE RECEPTOR AND ANTAGONISM BY METHIOTHEPIN, Neuropharmacology, 33(1), 1994, pp. 67-75
DIFFERENTIAL FUNCTIONAL-ACTIVITY OF 5-HYDROXYTRYPTAMINE RECEPTOR LIGANDS AND BETA-ADRENERGIC-RECEPTOR ANTAGONISTS AT 5-HYDROXYTRYPTAMINE(1B) RECEPTOR-SITES IN CHINESE-HAMSTER LUNG FIBROBLASTS AND OPOSSUM RENALEPITHELIAL-CELLS
Authors: PAUWELS PJ PALMIER C
Citation: Pj. Pauwels et C. Palmier, DIFFERENTIAL FUNCTIONAL-ACTIVITY OF 5-HYDROXYTRYPTAMINE RECEPTOR LIGANDS AND BETA-ADRENERGIC-RECEPTOR ANTAGONISTS AT 5-HYDROXYTRYPTAMINE(1B) RECEPTOR-SITES IN CHINESE-HAMSTER LUNG FIBROBLASTS AND OPOSSUM RENALEPITHELIAL-CELLS, The Journal of pharmacology and experimental therapeutics, 270(3), 1994, pp. 938-945
IMPROVED SURVIVAL OF RAT-BRAIN NEURONS IN CULTURE BY FRONTAL-CORTEX BRAIN EXTRACT AND CEREBROSPINAL-FLUID OF PATIENTS WITH SENILE DEMENTIA OF ALZHEIMERS TYPE
Authors: PAUWELS PJ VANGOOL D
Citation: Pj. Pauwels et D. Vangool, IMPROVED SURVIVAL OF RAT-BRAIN NEURONS IN CULTURE BY FRONTAL-CORTEX BRAIN EXTRACT AND CEREBROSPINAL-FLUID OF PATIENTS WITH SENILE DEMENTIA OF ALZHEIMERS TYPE, Journal of neurochemistry, 61, 1993, pp. 190000173-190000173
TOWARDS AND IMPROVED SURVIVAL OF RAT-BRAIN NEURONS IN CULTURE BY CEREBROSPINAL-FLUID OF PATIENTS WITH SENILE DEMENTIA OF ALZHEIMERS TYPE
Authors: PAUWELS PJ VANASSOUW HP DERYCK M LEYSEN JE DOM R VANGOOL D
Citation: Pj. Pauwels et al., TOWARDS AND IMPROVED SURVIVAL OF RAT-BRAIN NEURONS IN CULTURE BY CEREBROSPINAL-FLUID OF PATIENTS WITH SENILE DEMENTIA OF ALZHEIMERS TYPE, Brain research, 610(1), 1993, pp. 8-15
IDENTIFICATION OF 5-HYDROXYTRYPTAMINE(10) BINDING-SITES IN SHEEP CAUDATE-NUCLEUS MEMBRANES
Authors: PAUWELS PJ PALMIER C BRILEY M
Citation: Pj. Pauwels et al., IDENTIFICATION OF 5-HYDROXYTRYPTAMINE(10) BINDING-SITES IN SHEEP CAUDATE-NUCLEUS MEMBRANES, Biochemical pharmacology, 46(3), 1993, pp. 535-538
INVITRO AND INVIVO RECEPTOR-BINDING AND EFFECTS ON MONOAMINE TURNOVERIN RAT-BRAIN REGIONS OF THE NOVEL ANTIPSYCHOTICS RISPERIDONE AND OCAPERIDONE
Authors: LEYSEN JE JANSSEN PMF GOMMEREN W WYNANTS J PAUWELS PJ JANSSEN PAJ
Citation: Je. Leysen et al., INVITRO AND INVIVO RECEPTOR-BINDING AND EFFECTS ON MONOAMINE TURNOVERIN RAT-BRAIN REGIONS OF THE NOVEL ANTIPSYCHOTICS RISPERIDONE AND OCAPERIDONE, Molecular pharmacology, 41(3), 1992, pp. 494-508
Risultati: 1-25 | 26-49 |