These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
343 related articles for article (PubMed ID: 8788530)
1. Electrophysiological, biochemical, neurohormonal and behavioural studies with WAY-100635, a potent, selective and silent 5-HT1A receptor antagonist. Fletcher A; Forster EA; Bill DJ; Brown G; Cliffe IA; Hartley JE; Jones DE; McLenachan A; Stanhope KJ; Critchley DJ; Childs KJ; Middlefell VC; Lanfumey L; Corradetti R; Laporte AM; Gozlan H; Hamon M; Dourish CT Behav Brain Res; 1996; 73(1-2):337-53. PubMed ID: 8788530 [TBL] [Abstract][Full Text] [Related]
2. A pharmacological profile of the selective silent 5-HT1A receptor antagonist, WAY-100635. Forster EA; Cliffe IA; Bill DJ; Dover GM; Jones D; Reilly Y; Fletcher A Eur J Pharmacol; 1995 Jul; 281(1):81-8. PubMed ID: 8566121 [TBL] [Abstract][Full Text] [Related]
3. The selective 5-HT1A antagonist radioligand [3H]WAY 100635 labels both G-protein-coupled and free 5-HT1A receptors in rat brain membranes. Gozlan H; Thibault S; Laporte AM; Lima L; Hamon M Eur J Pharmacol; 1995 Jan; 288(2):173-86. PubMed ID: 7720779 [TBL] [Abstract][Full Text] [Related]
4. Antagonist properties of (-)-pindolol and WAY 100635 at somatodendritic and postsynaptic 5-HT1A receptors in the rat brain. Corradetti R; Laaris N; Hanoun N; Laporte AM; Le Poul E; Hamon M; Lanfumey L Br J Pharmacol; 1998 Feb; 123(3):449-62. PubMed ID: 9504386 [TBL] [Abstract][Full Text] [Related]
5. Characterization of the aminomethylchroman derivative BAY x 3702 as a highly potent 5-hydroxytryptamine1A receptor agonist. De Vry J; Schohe-Loop R; Heine HG; Greuel JM; Mauler F; Schmidt B; Sommermeyer H; Glaser T J Pharmacol Exp Ther; 1998 Mar; 284(3):1082-94. PubMed ID: 9495870 [TBL] [Abstract][Full Text] [Related]
6. Electrophysiological effects of WAY 100635, a new 5-HT1A receptor antagonist, on dorsal raphe nucleus serotoninergic neurones and CA1 pyramidal cells in vitro. Corradetti R; Pugliese AM; Le Poul E; Laaris N; Hamon M; Lanfumey L Acta Physiol Hung; 1996; 84(4):407-9. PubMed ID: 9328615 [TBL] [Abstract][Full Text] [Related]
7. Labelling of recombinant human and native rat serotonin 5-HT1A receptors by a novel, selective radioligand, [3H]-S 15535: definition of its binding profile using agonists, antagonists and inverse agonists. Newman-Tancredi A; Verrièle L; Chaput C; Millan MJ Naunyn Schmiedebergs Arch Pharmacol; 1998 Mar; 357(3):205-17. PubMed ID: 9550290 [TBL] [Abstract][Full Text] [Related]
8. Characterization of 4-(2-hydroxyphenyl)-1-[2'-[N-(2''-pyridinyl)-p-fluorobenzamido]ethyl]piperazine (p-DMPPF) as a new potent 5-HT1A antagonist. Defraiteur C; Plenevaux A; Scuvée-Moreau J; Rouchet N; Goblet D; Luxen A; Seutin V Br J Pharmacol; 2007 Nov; 152(6):952-8. PubMed ID: 17704821 [TBL] [Abstract][Full Text] [Related]
9. Quantitative autoradiographic characterisation of the binding of [3H]WAY-100635, a selective 5-HT1A receptor antagonist. Khawaja X Brain Res; 1995 Mar; 673(2):217-25. PubMed ID: 7606435 [TBL] [Abstract][Full Text] [Related]
10. Characterization of 5-hydroxytryptamine1A properties of flesinoxan: in vivo electrophysiology and hypothermia study. Hadrava V; Blier P; Dennis T; Ortemann C; de Montigny C Neuropharmacology; 1995 Oct; 34(10):1311-26. PubMed ID: 8570029 [TBL] [Abstract][Full Text] [Related]
11. Inhibition of 8-OH-DPAT-induced elevation of plasma corticotrophin by the 5-HT1A receptor antagonist WAY100635. Critchley DJ; Childs KJ; Middlefell VC; Dourish CT Eur J Pharmacol; 1994 Oct; 264(1):95-7. PubMed ID: 7828650 [TBL] [Abstract][Full Text] [Related]
12. Biochemical, electrophysiological and neurohormonal studies with B-20991, a selective 5-HT1A receptor agonist. Caicoya AG; Beneytez ME; Delgado M; Manzanares J; López-Rodríguez ML; Benhamu B; Morcillo MJ; Pozo MA; Rubia FJ; Fuentes JA Pharmacology; 2001 May; 62(4):234-42. PubMed ID: 11360001 [TBL] [Abstract][Full Text] [Related]
13. WAY-100635 inhibits 8-OH-DPAT-stimulated oxytocin, ACTH and corticosterone, but not prolactin secretion. Vicentic A; Li Q; Battaglia G; Van de Kar LD Eur J Pharmacol; 1998 Apr; 346(2-3):261-6. PubMed ID: 9652368 [TBL] [Abstract][Full Text] [Related]
14. Two selective 5-HT1A receptor antagonists, WAY-100 635 and NDL-249, stimulate locomotion in rats acclimatised to their environment and alter their behaviour: a behavioural analysis. Jackson DM; Wallsten CE; Jerning E; Hu PS; Deveney AM Psychopharmacology (Berl); 1998 Oct; 139(4):300-10. PubMed ID: 9809851 [TBL] [Abstract][Full Text] [Related]
15. Further assessment of the antagonist properties of the novel and selective 5-HT1A receptor ligands (+)-WAY 100 135 and SDZ 216-525. Lanfumey L; Haj-Dahmane S; Hamon M Eur J Pharmacol; 1993 Nov; 249(1):25-35. PubMed ID: 8282017 [TBL] [Abstract][Full Text] [Related]
16. Selective antiaggressive effects of alnespirone in resident-intruder test are mediated via 5-hydroxytryptamine1A receptors: A comparative pharmacological study with 8-hydroxy-2-dipropylaminotetralin, ipsapirone, buspirone, eltoprazine, and WAY-100635. de Boer SF; Lesourd M; Mocaer E; Koolhaas JM J Pharmacol Exp Ther; 1999 Mar; 288(3):1125-33. PubMed ID: 10027850 [TBL] [Abstract][Full Text] [Related]
17. Interactions of lesopitron (E-4424) with central 5-HT1A receptors: in vitro and in vivo studies in the rat. Haj-Dahmane S; Jolas T; Laporte AM; Gozlan H; Farré AJ; Hamon M; Lanfumey L Eur J Pharmacol; 1994 Apr; 255(1-3):185-96. PubMed ID: 8026543 [TBL] [Abstract][Full Text] [Related]
18. Electrophysiological effects of N-(2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl)-N-(2-pyridinyl) cyclohexane carboxamide (WAY 100635) on dorsal raphe serotonergic neurons and CA1 hippocampal pyramidal cells in vitro. Corradetti R; Le Poul E; Laaris N; Hamon M; Lanfumey L J Pharmacol Exp Ther; 1996 Aug; 278(2):679-88. PubMed ID: 8768719 [TBL] [Abstract][Full Text] [Related]
19. Role of the medial prefrontal cortex in 5-HT1A receptor-induced inhibition of 5-HT neuronal activity in the rat. Hajós M; Hajós-Korcsok E; Sharp T Br J Pharmacol; 1999 Apr; 126(8):1741-50. PubMed ID: 10372816 [TBL] [Abstract][Full Text] [Related]
20. Evaluation of [O-methyl-3H]WAY-100635 as an in vivo radioligand for 5-HT1A receptors in rat brain. Hume SP; Ashworth S; Opacka-Juffry J; Ahier RG; Lammertsma AA; Pike VW; Cliffe IA; Fletcher A; White AC Eur J Pharmacol; 1994 Dec; 271(2-3):515-23. PubMed ID: 7705452 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]