Guy R. Seabrook
Affiliations: | 1987-1989 | Molecular & Cellular Pharmacology | University of Miami School of Medicine, Miami, FL, United States |
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Parents
Sign in to add mentorDavid J. Adams | post-doc | 1987-1989 | University of Miami School of Medicine |
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Publications
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Seabrook GR, Sutton KG, Jarolimek W, et al. (2002) Functional properties of the high-affinity TRPV1 (VR1) vanilloid receptor antagonist (4-hydroxy-5-iodo-3-methoxyphenylacetate ester) iodo-resiniferatoxin. The Journal of Pharmacology and Experimental Therapeutics. 303: 1052-60 |
Maubach KA, Martin K, Smith DW, et al. (2001) Substance P stimulates inhibitory synaptic transmission in the guinea pig basolateral amygdala in vitro Neuropharmacology. 40: 806-817 |
Kuenzi FM, Fitzjohn SM, Morton RA, et al. (2000) Reduced long-term potentiation in hippocampal slices prepared using sucrose-based artificial cerebrospinal fluid. Journal of Neuroscience Methods. 100: 117-22 |
Seabrook GR, Easter A, Dawson GR, et al. (1997) Modulation of long-term potentiation in CA1 region of mouse hippocampal brain slices by GABAA receptor benzodiazepine site ligands. Neuropharmacology. 36: 823-30 |
Caeser M, Seabrook GR, Kemp JA. (1993) Block of voltage-dependent sodium currents by the substance P receptor antagonist (+/-)-CP-96,345 in neurones cultured from rat cortex. British Journal of Pharmacology. 109: 918-24 |
Seabrook GR, Howson W, Lacey MG. (1991) Subpopulations of GABA-mediated synaptic potentials in slices of rat dorsal striatum are differentially modulated by presynaptic GABAB receptors. Brain Research. 562: 332-4 |
Seabrook GR, Fieber LA, Adams DJ. (1990) Neurotransmission in neonatal rat cardiac ganglion in situ. The American Journal of Physiology. 259: H997-1005 |
Seabrook GR, Howson W, Lacey MG. (1990) Electrophysiological characterization of potent agonists and antagonists at pre- and postsynaptic GABAB receptors on neurones in rat brain slices. British Journal of Pharmacology. 101: 949-57 |
Seabrook GR, Adams DJ. (1989) Inhibition of neurally-evoked transmitter release by calcium channel antagonists in rat parasympathetic ganglia. British Journal of Pharmacology. 97: 1125-36 |