The endogenous lipid anandamide is a full agonist at the human vanilloid receptor (hVR1) von Smart, D, Gunthorpe, M J, Jerman, J C, Nasir, S, Gray, J, Muir, A I, Chambers, J K, Randall, A D, Davis, J B

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TRPV3 is a temperature-sensitive vanilloid receptor-like protein von Davis, J. B, Smith, G. D, Gunthorpe, M. J, Kelsell, R. E, Hayes, P. D, Reilly, P, Facer, P, Wright, J. E, Jerman, J. C, Walhin, J.-P, Ooi, L, Egerton, J, Charles, K. J, Smart, D, Randall, A. D, Anand, P

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SB‐334867‐A: the first selective orexin‐1 receptor antagonist von Smart, D, Sabido‐David, C, Brough, S J, Jewitt, F, Johns, A, Porter, R A, Jerman, J C

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Ethanol elicits and potentiates nociceptor responses via the vanilloid receptor-1 von Davis, J B, Trevisani, M, Smart, D, Gunthorpe, M J, Tognetto, M, Barbieri, M, Campi, B, Amadesi, S, Gray, J, Jerman, J C, Brough, S J, Owen, D, Smith, G D, Randall, A D, Harrison, S, Bianchi, A, Geppetti, P

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Ethanol elicits and potentiates nociceptor responses via the vanilloid receptor-1 von Trevisani, M, Smart, D, Gunthorpe, MJ, Tognetto, M, Barbieri, M, Campi, B, Amadesi, S, Gray, J, Jerman, J C, Brough, S J, Owen, D, Smith, G D, Randall, AD, Davis, J B

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Identification and characterisation of SB-366791, a potent and selective vanilloid receptor (VR1/TRPV1) antagonist von Gunthorpe, M.J., Rami, H.K., Jerman, J.C., Smart, D., Gill, C.H., Soffin, E.M., Luis Hannan, S., Lappin, S.C., Egerton, J., Smith, G.D., Worby, A., Howett, L., Owen, D., Nasir, S., Davies, C.H., Thompson, M., Wyman, P.A., Randall, A.D., Davis, J.B.

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Characterization using FLIPR of rat vanilloid receptor (rVR1) pharmacology von Jerman, J C, Brough, S J, Prinjha, R, Harries, M H, Davis, J B, Smart, D

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Characterization of recombinant human orexin receptor pharmacology in a Chinese hamster ovary cell‐line using FLIPR von Smart, D, Jerman, J C, Brough, S J, Rushton, S L, Murdock, P R, Jewitt, F, Elshourbagy, N A, Ellis, C E, Middlemiss, D N, Brown, F

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Anandamide: an endogenous activator of the vanilloid receptor von Smart, Darren, Jerman, Jeffery C

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Orexinergic neurons and barbiturate anesthesia von Kushikata, T, Hirota, K, Yoshida, H, Kudo, M, Lambert, D.G, Smart, D, Jerman, J.C, Matsuki, A

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Comparison of effects of anandamide at recombinant and endogenous rat vanilloid receptors von Jerman, J.C., Gray, J., Brough, S.J., Ooi, L., Owen, D., Davis, J.B., Smart, D.

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Activation of TRPV4 Channels (hVRL-2/mTRP12) by Phorbol Derivatives von Watanabe, Hiroyuki, Davis, John B., Smart, Darren, Jerman, Jeff C., Smith, Graham D., Hayes, Phil, Vriens, Joris, Cairns, William, Wissenbach, Ullrich, Prenen, Jean, Flockerzi, Veit, Droogmans, Guy, Benham, Christopher D., Nilius, Bernd

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Nonlinear regression using spreadsheets von Bowen, W.P., Jerman, J.C.

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The hypocretins are weak agonists at recombinant human orexin‐1 and orexin‐2 receptors von Smart, D, Jerman, J C, Brough, S J, Neville, W A, Jewitt, F, Porter, R A

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Cannabinoid activation of recombinant and endogenous vanilloid receptors von Ralevic, Vera, Kendall, David A., Jerman, Jeffrey C., Middlemiss, Derek N., Smart, Darren

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Discovery of SB-705498: A potent, selective and orally bioavailable TRPV1 antagonist suitable for clinical development von Rami, Harshad K., Thompson, Mervyn, Stemp, Geoffrey, Fell, Steve, Jerman, Jeffrey C., Stevens, Alexander J., Smart, Darren, Sargent, Becky, Sanderson, Dominic, Randall, Andrew D., Gunthorpe, Martin J., Davis, John B.

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1,3-Biarylureas as selective non-peptide antagonists of the orexin-1 receptor von PORTER, Roderick A, CHAN, Wai N, JEWITT, A. Frances, JEFFREY, Phillip, AUSTIN, Nigel, COULTON, Steven, JOHNS, Amanda, HADLEY, Michael S, WIDDOWSON, Katherine, JERMAN, Jeffrey C, BROUGH, Stephen J, COLDWELL, Martyn, SMART, Darren

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Synthesis of Novel trans-4-(Substituted-benzamido)-3,4-dihydro-2H-benzo[b]pyran-3-ol Derivatives as Potential Anticonvulsant Agents with a Distinctive Binding Profile von Chan, Wai N, Evans, John M, Hadley, Michael S, Herdon, Hugh J, Jerman, Jeffrey C, Morgan, Helen K. A, Stean, Tania O, Thompson, Mervyn, Upton, Neil, Vong, Antonio K

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Identification of (-)-cis-6-acetyl-4S-(3-chloro-4-fluoro-benzoylamino)-3,4-dihydro-2,2-dimethyl-2H-benzo[b]pyran-3S-ol as a potential antimigraine agent von CHAN, W. N, EVANS, J. M, HADLEY, M. S, HERDON, H. J, JERMAN, J. C, PARSONS, A. A, READ, S. J, STEAN, T. O, THOMPSON, M, UPTON, N

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Pharmacological characterisation of human 5-HT2 receptor subtypes von JERMAN, Jeffrey C, BROUGH, Stephen J, GAGER, Tracey, WOOD, Martyn, COLDWELL, Martyn C, SMART, Darren, MIDDLEMISS, Derek N

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