Kathy G. Sutton

Xention Discovery Ltd, Pampisford, England, United Kingdom 
drug discovery
"Kathy Sutton"
Mean distance: 15.83 (cluster 11)
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Ford J, Milnes J, Wettwer E, et al. (2013) Human electrophysiological and pharmacological properties of XEN-D0101: a novel atrial-selective Kv1.5/IKur inhibitor. Journal of Cardiovascular Pharmacology. 61: 408-15
Johnson DM, Garrett EM, Rutter R, et al. (2006) Functional mapping of the transient receptor potential vanilloid 1 intracellular binding site. Molecular Pharmacology. 70: 1005-12
Sutton KG, Garrett EM, Rutter AR, et al. (2005) Functional characterisation of the S512Y mutant vanilloid human TRPV1 receptor. British Journal of Pharmacology. 146: 702-11
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
Martin DJ, McClelland D, Herd MB, et al. (2002) Gabapentin-mediated inhibition of voltage-activated Ca2+ channel currents in cultured sensory neurones is dependent on culture conditions and channel subunit expression. Neuropharmacology. 42: 353-66
Sutton KG, Martin DJ, Pinnock RD, et al. (2002) Gabapentin inhibits high-threshold calcium channel currents in cultured rat dorsal root ganglion neurones. British Journal of Pharmacology. 135: 257-65
Santi CM, Cayabyab FS, Sutton KG, et al. (2002) Differential inhibition of T-type calcium channels by neuroleptics. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 22: 396-403
Sutton KG, Snutch TP. (2002) Gabapentin: A novel analgesic targeting voltage-gated calcium channels Drug Development Research. 54: 167-172
Snutch TP, Sutton KG, Zamponi GW. (2001) Voltage-dependent calcium channels--beyond dihydropyridine antagonists. Current Opinion in Pharmacology. 1: 11-6
McRory JE, Santi CM, Hamming KS, et al. (2001) Molecular and functional characterization of a family of rat brain T-type calcium channels. The Journal of Biological Chemistry. 276: 3999-4011
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