Une famille chimique originale de tranquillisants: les cyclopyrrolones = A new class of anxiolytic agents: cyclopyrrolonesBLANCHARD, J. C; COTREL, C.L' Actualité chimique (Paris. 1973). 1983, Num 9, pp 37-46, issn 0151-9093Article

Autoradiographic distribution of [³H]-suriclone binding sites in the rat brainMALGOURIS, C; PERROT, F; DUPUIS, M et al.Drug development research. 1995, Vol 34, Num 4, pp 336-343, issn 0272-4391Article

A role for nitric oxide in long-term potentiationBON, C; BÖHME, G. A; DOBLE, A et al.European journal of neuroscience (Print). 1992, Vol 4, Num 5, pp 420-424, issn 0953-816XArticle

Neuroprotective actions of riluzole in rodent models of global and focal cerebral ischaemiaPRATT, J; RATAUD, J; BARDOT, F et al.Neuroscience letters. 1992, Vol 140, Num 2, pp 225-230, issn 0304-3940Article

Riluzole, a novel antiglutamate, prevents memory loss and hippocampal neuronal damage in ischemic gerbilsMALGOURIS, C; BARDOT, F; DANIEL, M et al.The Journal of neuroscience. 1989, Vol 9, Num 11, pp 3720-3727, issn 0270-6474, 8 p.Article

Riluzole series. Synthesis and in vivo antiglutamate activity of 6-substituted-2-benzothiazolamines and 3-substituted-2-imino-benzothiazolinesJIMONET, P; AUDIAU, F; DONAT, M.-H et al.Journal of medicinal chemistry (Print). 1999, Vol 42, Num 15, pp 2828-2843, issn 0022-2623Article

Molecular cloning, functional expression, pharmacological characterization and chromosomal localization of the human metabotropic glutamate receptor type 3EMILE, L; MERCKEN, L; APIOU, F et al.Neuropharmacology. 1996, Vol 35, Num 5, pp 523-530, issn 0028-3908Article

Comparative behavioural profile of centrally administered tachykinin NK₁, NK₂ and NK₃ receptor agonists in the guinea-pigPIOT, O; BETSCHART, J; GRALL, I et al.British journal of pharmacology. 1995, Vol 116, Num 5, pp 2496-2502, issn 0007-1188Article

Measurement of nerve growth factor-like immunoreactivity in human brain using an anti-mouse-NGF enzyme immunoassayBERTRAND, P; ROGER, O; HOULGATTE, R et al.Neurochemistry international. 1992, Vol 20, Num 2, pp 215-218, issn 0197-0186Article

Electrophysiological studies with new CCK analogs: correlation with binding affinity on B-type receptorsBÖHME, G. A; DURIEUX, C; STUTZMANN, J.-M et al.Peptides (New York, NY. 1980). 1989, Vol 10, Num 2, pp 407-414, issn 0196-9781Article

Effect of non-NMDA receptor modulators on [³H]dopamine release from rat mesencephalic cells in primary culturePETITET, F; BLANCHARD, J.-C; DOBLE, A et al.Journal of neurochemistry. 1995, Vol 64, Num 3, pp 1410-1412, issn 0022-3042Article

New indole derivatives as potent and selective serotonin uptake inhibitorsMALLERON, J.-L; GUEREMY, C; BETSCHART, J et al.Journal of medicinal chemistry (Print). 1993, Vol 36, Num 9, pp 1194-1202, issn 0022-2623Article

A rapid filtration assay for the glycine binding site on the NMDA receptor in rat cortical membranes using [³D]dichlorokynurenic acidCANTON, T; DOBLE, A; MIQUET, J.-M et al.Journal of pharmacy and pharmacology. 1992, Vol 44, Num 10, pp 812-816, issn 0022-3573Article

RP 62203, a 5-hydroxytryptamine₂ antagonist, enhances deep NREM sleep in ratsSTUTZMANN, J.-M; EON, B; LUCAS, M et al.Sleep (New York, NY). 1992, Vol 15, Num 2, pp 119-124, issn 0161-8105Article

The trophic effect of β-amyloid 25-35 peptide is not mediated by NK₁ or bombesin receptorsBURGEVIN, M.-C; DANIEL, N; DOBLE, A et al.Neuroreport (Oxford). 1992, Vol 3, Num 12, pp 1131-1134, issn 0959-4965Article

RP 67580, un antagoniste, non peptidique, puissant et sélectif de la substance P = RP 67580, a potent and selective non-peptide substance P antagonisteGARRET, C; CARRUETTE, A; FARDIN, V et al.Comptes rendus de l'Académie des sciences. Série 3, Sciences de la vie. 1992, Vol 314, Num 5, pp 199-204, issn 0764-4469Article

Enzyme-resistant CCK analogs with high affinities for central receptorsCHARPENTIER, B; DURIEUX, C; PELAPRAT, D et al.Peptides (New York, NY. 1980). 1988, Vol 9, Num 4, pp 835-841, issn 0196-9781Article

Neuroprotective effects of RPR 104632, a novel antagonist at the glycine site of the NMDA receptor, in vitroBOIREAU, A; MALGOURIS, C; JIMONET, P et al.European journal of pharmacology. 1996, Vol 300, Num 3, pp 237-246, issn 0014-2999Article

The naphtosultam derivative RP 62203 (fananserin) has high affinity for the dopamine D₄ receptorHEUILLET, E; PETITET, F; MIGNAMI, S et al.European journal of pharmacology. 1996, Vol 314, Num 1-2, pp 229-233, issn 0014-2999Article

Effects of complete and partial lesions of the dopaminergic mesotelencephalic system on skilled forelimb use in the ratBARNEOUD, P; PARMENTIER, S; MAZADIER, M et al.Neuroscience. 1995, Vol 67, Num 4, pp 837-848, issn 0306-4522Article

Possible involvement of nitric oxide in long-term potentiationBOHME, G. A; BON, C; STUTZMAN, J.-M et al.European journal of pharmacology. 1991, Vol 199, Num 3, pp 379-381, issn 0014-2999, 3 p.Article

Pharmacological properties of a potent and selective nonpeptide substance P antagonistGARRET, C; CARRUETTE, A; FARDIN, V et al.Proceedings of the National Academy of Sciences of the United States of America. 1991, Vol 88, Num 22, pp 10208-10212, issn 0027-8424Article

Développement d'analogues sélectifs de la cholécystokinine pour la caractérisation biochimique et pharmacologique des sites de liaison centraux = Development of selective CCK-related compounds as probes for biochemical and pharmacological characterization of CCK binding sites heterogeneityROQUES, B. P; CHARPENTIER, B; MARSEIGNE, I et al.Entretiens du Carla (Les). 1990, Vol 8, pp 219-226, 8 p.Article

Effects of ICV administration of neurotensin and analogs on EEG in ratsCASTEL, M.-N; STUTZMANN, J.-M; LUCAS, M et al.Peptides (New York, NY. 1980). 1989, Vol 10, Num 1, pp 95-101, issn 0196-9781Article

Proconflict and electrocorticographic effects of drugs modulating GABAergic neurotransmissionSTUTZMANN, J.-M; BOHME, G. A; COCHON, M et al.Psychopharmacologia. 1987, Vol 91, Num 1, pp 74-79, issn 0033-3158Article