G A Kennett

发表

Single administration of 5-HT1A agonists decreases 5-HT1A presynaptic, but not postsynaptic receptor-mediated responses: relationship to antidepressant-like action.

G. Kennett, C. Dourish, G A Kennett, 1987, European journal of pharmacology.

5-Methyl-1-(3-pyridylcarbamoyl)-1,2,3,5-tetrahydropyrrolo[2,3-f]indole: a novel 5-HT2C/5-HT2B receptor antagonist with improved affinity, selectivity, and oral activity.

I. Forbes, P. Ham, T. Blackburn, 1995, Journal of medicinal chemistry.

A single dose of 8-OH-DPAT reduces raphe binding of [3H]8-OH-DPAT and increases the effect of raphe stimulation on 5-HT metabolism.

G. Kennett, G A Kennett, G Curzon, 1990, European journal of pharmacology.

Antidepressant-like action of 5-HT1A agonists and conventional antidepressants in an animal model of depression.

G. Kennett, C. Dourish, G A Kennett, 1987, European journal of pharmacology.

N-(1-methyl-5-indolyl)-N'-(3-pyridyl)urea hydrochloride: the first selective 5-HT1C receptor antagonist.

P. Ham, G. Kennett, M. Wood, 1993, Journal of medicinal chemistry.

Anxiogenic-like effects of mCPP and TFMPP in animal models are opposed by 5-HT1C receptor antagonists.

G. Kennett, P. Whitton, G A Kennett, 1989, European journal of pharmacology.

6-Chloro-5-methyl-1-[[2-[(2-methyl-3-pyridyl)oxy]-5-pyridyl]carbamoyl]- indoline (SB-242084): the first selective and brain penetrant 5-HT2C receptor antagonist.

F E Blaney, S. Bromidge, I. Forbes, 1997, Journal of medicinal chemistry.

Comparative effects of continuous infusion of mCPP, Ro 60‐0175 and d‐fenfluramine on food intake, water intake, body weight and locomotor activity in rats

G. Kennett, C. Dourish, G A Kennett, 2000, British journal of pharmacology.

Enhancement of some 5-HT-dependent behavioural responses following repeated immobilization in rats

G. Kennett, G A Kennett, G Curzon, 1985, Brain Research.