Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Mireille Meunier"'
Autor:
Mireille Meunier
Publikováno v:
Hegel. :309-315
Autor:
Pascal Chaillou, Mireille Meunier, Jean-Marie Miquet, Irène Mafhouz, Véronique Mary, Véronique Blanchard, Elisabeth Genet, Marie-Carmen Obinu, Agnès Hubert, Valérie Fauchey, Mati Lopez-Grancha, Nadine Michot, Stéphanie Eyquem
Publikováno v:
Alzheimer's & Dementia. 13
Autor:
Mireille Meunier, Saliha Moussaoui, Pierre Dubedat, Francoise Bordier, Assunta Imperato, Madeleine Coimbra, Alain Boireau
Publikováno v:
Annals of the New York Academy of Sciences. 893:254-257
Autor:
Jean Marie Miquet, Marie-Claude Burgevin, M. Daniel, C. Malgouris, Mireille Meunier, Francoise Bordier, Colette Peny, Gabrielle Durand, Adam Doble, Jean-Charles Blanchard, Alain Boireau, Thierry Chevet, Serge Mignani, Patrick Jimonet
Publikováno v:
European Journal of Pharmacology. 300:237-246
The NMDA antagonist and neuroprotective effects of RPR 104632 (2H-1,2,4-benzothiadiazine-1-dioxide-3-carboxylic acid), a new benzothiadiazine derivative, with affinity for the glycine site of the NMDA receptor-channel complex are described. RPR 10463
Publikováno v:
NeuroReport. 5:2157-2160
Superfusion of the rat striatum with 100 microM of 1-methyl-4-phenylpyridinium (MPP+) induced a 70-fold increase in dopamine (DA) release and a decrease in the extracellular levels of 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA)
Publikováno v:
European journal of pharmacology. 401(2)
RPR 118723 ((8-chloro-5-methyl-2,3-dioxo-1,4-dihydro-5H-indeno[1, 2-b]pyrazin-5-yl) acetic acid) was previously reported to exhibit potent affinity for the glycine site of the N-methyl-D-aspartate (NMDA) receptor-channel complex in the nanomolar rang
Publikováno v:
Neuroscience letters. 289(2)
We studied the effects of ebselen (a seleno-organic anti-oxidant), on the release of the apoptogenic factor, cytochrome c, in two different experimental situations damaging mitochondria: (1) Fe2+/citrate, known to induce lipid peroxidation consecutiv
Autor:
Patrick Jimonet, François Audiau, Michel Barreau, Jean-Charles Blanchard, Alain Boireau, Yvette Bour, Marie-Annick Coléno, Adam Doble, Gilles Doerflinger, Claudine Do Huu, Marie-Hélène Donat, Jean Marie Duchesne, Pierre Ganil, Claude Guérémy, Eliane Honoré, Bernard Just, Roselyne Kerphirique, Sylvie Gontier, Philippe Hubert, Pierre M. Laduron, Joseph Le Blevec, Mireille Meunier, Jean-Marie Miquet, Conception Nemecek, Martine Pasquet, Odile Piot, Jeremy Pratt, Jean Rataud, Michel Reibaud, Jean-Marie Stutzmann, Serge Mignani
Publikováno v:
Journal of medicinal chemistry. 42(15)
Two series of analogues of riluzole, a blocker of excitatory amino acid mediated neurotransmission, have been synthesized: monosubstituted 2-benzothiazolamines and 3-substituted derivatives. Of all the compounds prepared in the first series, only 2-b
Publikováno v:
The Journal of pharmacy and pharmacology. 50(11)
We have examined the effects of riluzole, a neuroprotective drug which stabilizes voltage-dependent sodium channels in their inactivated state and inhibits the release of glutamate in-vivo and in-vitro, on the release of newly taken up [3H]dopamine i
Publikováno v:
The Journal of pharmacy and pharmacology. 48(1)
3−Nitropropionic acid (3−NPA) is a metabolic poison that produces lesions of striatal intrinsic neurones such as γ-aminobutyric acid (GABA) neurones. This study was carried out to determine whether 3−NPA would impair the ability of striatal GA