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Neuroscience|October 27, 2012
The low-frequency blood oxygenation level-dependent functional connectivity signature of the hippocampal-prefrontal network in the rat brainA J Schwarz, N Gass, A Sartorius, et al.
British Journal of Pharmacology|September 1, 1995
RS-45041-190: a selective, high-affinity ligand for I2 imidazoline receptorsC M Brown, A C MacKinnon, W S Redfern, et al.
Journal of Medicinal Chemistry|February 1, 1990
1,9-Alkano-bridged 2,3,4,5-tetrahydro-1H-3-benzazepines with affinity for the alpha 2-adrenoceptor and the 5-HT1A receptorR D Clark, K K Weinhardt, J Berger, et al.
Neuropharmacology|April 1, 1997
SB 242084, a selective and brain penetrant 5-HT2C receptor antagonistG A Kennett, M D Wood, F Bright, et al.
Neuroscience|September 21, 2000
The expression of GABA(B1) and GABA(B2) receptor subunits in the cNS differs from that in peripheral tissuesA R Calver, A D Medhurst, M J Robbins, et al.
Neuropharmacology|August 8, 2001
SB-243213; a selective 5-HT2C receptor inverse agonist with improved anxiolytic profile: lack of tolerance and withdrawal anxietyM D Wood, C Reavill, B Trail, et al.
Molecular Psychiatry|June 27, 2012
Regulation of AMPA receptor surface trafficking and synaptic plasticity by a cognitive enhancer and antidepressant moleculeH Zhang, L-A Etherington, A-S Hafner, et al.
Journal of Medicinal Chemistry|February 1, 1991
Structure-affinity relationships of 12-sulfonyl derivatives of 5,8,8a,9,10,11,12,12a,13,13a-decahydro-6H-isoquino[2,1-g][1 ,6] naphthyridines at alpha-adrenoceptorsR D Clark, D B Repke, J Berger, et al.
The Journal of Pharmacology and Experimental Therapeutics|July 1, 1997
S 15535, a novel benzodioxopiperazine ligand of serotonin (5-HT)1A receptors: II. Modulation of hippocampal serotonin release in relation to potential anxiolytic propertiesM J Millan, S Hjorth, R Samanin, et al.
Journal of Medicinal Chemistry|July 31, 1998
4H-1,2,4-Pyridothiadiazine 1,1-dioxides and 2,3-dihydro-4H-1,2, 4-pyridothiadiazine 1,1-dioxides chemically related to diazoxide and cyclothiazide as powerful positive allosteric modulators of (R/S)-2-amino-3-(3-hydroxy-5-methylisoxazol-4-yl)propionic acid receptors: design, synthesis, pharmacology, and structure-activity relationshipsB Pirotte, T Podona, O Diouf, et al.
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