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European Journal of Pharmacology|October 15, 1982
U 43,465F: a benzodiazepine with antidepressant activity? Interaction with Ro 15-1788 and d,1-propranololM H Thiebot, L Doare, A J Puech, et al.
Journal of Psychopharmacology (Oxford, England)|January 1, 1997
Influence of anxiolytic drugs on the effects of specific serotonin reuptake inhibitors in the forced swimming test in miceM A Da-Rocha, A J Puech, M H Thiébot
Psychopharmacology|April 16, 1998
Involvement of central cannabinoid (CB1) receptors in the establishment of place conditioning in ratsF Chaperon, P Soubrié, A J Puech, et al.
European Psychiatry : the Journal of the Association of European Psychiatrists|August 25, 2009
Measures of anhedonia and hedonic responses to sucrose in depressive and schizophrenic patients in comparison with healthy subjectsI Berlin, L Givry-Steiner, Y Lecrubier, et al.
Nature|September 8, 1983
Identification of presynaptic serotonin autoreceptors using a new ligand: 3H-PATH Gozlan, S El Mestikawy, L Pichat, et al.
The Journal of Pharmacology and Experimental Therapeutics|March 1, 1989
Biochemical and electrophysiological evidence for an agonist action of CM 57493 at pre- and postsynaptic 5-hydroxytryptamine1A receptors in brainJ Adrien, L Lanfumey, H Gozlan, et al.
European Journal of Pharmacology|January 16, 1995
The selective 5-HT1A antagonist radioligand [3H]WAY 100635 labels both G-protein-coupled and free 5-HT1A receptors in rat brain membranesH Gozlan, S Thibault, A M Laporte, et al.
L'Encephale|December 1, 1991
[Preclinical pharmacology of amoxapine and amitriptyline. Implications of serotoninergic and opiodergic systems in their central effect in rats]H Gozlan, F Saddiki-Traki, N Merahi, et al.
Pflugers Archiv : European Journal of Physiology|August 1, 1991
Sleep changes induced by the local application of 5,7-dihydroxytryptamine into the nodose ganglia and aortic denervation in the ratH S Orer, N Merahi, A Nosjean, et al.
Neuroscience Letters|February 21, 1997
The calcium-dependent transient inactivation of recombinant NMDA receptor-channel does not involve the high affinity calmodulin binding site of the NR1 subunitA Rafiki, H Gozlan, Y Ben-Ari, et al.
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