Authors:
CORRADETTI R
LAARIS N
HANOUN N
LAPORTE AM
LEPOUL E
HAMON M
LANFUMEY L
Citation: R. Corradetti et al., ANTAGONIST PROPERTIES OF (-)-PINDOLOL AND WAY-100635 AT SOMATODENDRITIC AND POSTSYNAPTIC 5-HT1A RECEPTORS IN THE RAT-BRAIN, British Journal of Pharmacology, 123(3), 1998, pp. 449-462
Citation: E. Lepoul et al., FLUOXETINE-INDUCED DESENSITIZATION OF SOMATODENDRITIC 5-HT1A AUTORECEPTORS IS INDEPENDENT OF GLUCOCORTICOID(S), Synapse, 27(4), 1997, pp. 303-312
Citation: N. Laaris et al., STRESS-INDUCED ALTERATIONS OF SOMATODENDRITIC 5-HT1A AUTORECEPTOR SENSITIVITY IN THE RAT DORSAL RAPHE NUCLEUS - IN-VITRO ELECTROPHYSIOLOGICAL EVIDENCE, Fundamental and clinical pharmacology, 11(3), 1997, pp. 206-214
Authors:
LEPOUL E
BONI C
LAPORTE AM
LAARIS N
LANFUMEY L
HAMON M
Citation: E. Lepoul et al., FUNCTIONAL AND EXPRESSION CHANGES IN BRAIN 5-HT1A AND 5-HT1B RECEPTORS IN RATS TREATED CHRONICALLY WITH FLUOXETINE, Journal of neurochemistry, 69, 1997, pp. 116-116
Authors:
CORRADETTI R
LEPOUL E
LAARIS N
HAMON M
LANFUMEY L
Citation: R. Corradetti et al., ELECTROPHYSIOLOGICAL EFFECTS OF ETHOXYPHENYL)-1-PIPERAZINYL)ETHYL)-N-(2-PYRIDINYL) CYCLOHEXANE CARBOXAMIDE (WAY-100635) ON DORSAL RAPHE SEROTONERGIC NEURONS AND CA1 HIPPOCAMPAL PYRAMIDAL CELLS IN-VITRO, The Journal of pharmacology and experimental therapeutics, 278(2), 1996, pp. 679-688
Authors:
LANFUMEY L
CORRADETTI R
LAARIS N
LEPOUL E
HAMON M
Citation: L. Lanfumey et al., ELECTROPHYSIOLOGICAL EVIDENCE FOR THE ANTAGONIST ACTION OF WAY100635 AT BOTH PRESYNAPTIC AND POSTSYNAPTIC 5-HT1A RECEPTORS, Journal of neurochemistry, 66, 1996, pp. 37-37
Citation: N. Laaris et al., GLUCOCORTICOID RECEPTOR-MEDIATED INHIBITION BY CORTICOSTERONE OF 5-HT1A AUTORECEPTOR FUNCTIONING IN THE RAT DORSAL RAPHE NUCLEUS, Neuropharmacology, 34(9), 1995, pp. 1201-1210
Authors:
LEPOUL E
LAARIS N
DOUCET E
LAPORTE AM
HAMON M
LANFUMEY L
Citation: E. Lepoul et al., EARLY DESENSITIZATION OF SOMATO-DENDRITIC 5-HT1A AUTORECEPTORS IN RATS TREATED WITH FLUOXETINE OR PAROXETINE, Naunyn-Schmiedeberg's archives of pharmacology, 352(2), 1995, pp. 141-148