The neuroprotective agent sipatrigine (BW619C89) potently inhibits the human tandem pore-domain K + channels TREK-1 and TRAAK von Meadows, H.J., Chapman, C.G., Duckworth, D.M., Kelsell, R.E., Murdock, P.R., Nasir, S., Rennie, G., Randall, A.D.

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CuInSe2 semiconductor formation by laser annealing von Meadows, H.J., Regesch, D., Thevenin, M., Sendler, J., Schuler, T., Misra, S., Simonds, B.J., Scarpulla, M.A., Gerliz, V., Gütay, L., Guillot, J., Dale, P.J.

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Laser annealing of electrodeposited CuInSe2 semiconductor precursors: experiment and modeling von Meadows, HJ, Misra, S, Simonds, B J, Kurihara, M, Schuler, T, Reis-Adonis, V, Bhatia, A, Scarpulla, MA, Dale, P J

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Selective block of the human 2-P domain potassium channel, TASK-3, and the native leak potassium current, IKSO, by zinc von Clarke, Catherine E., Veale, Emma L., Green, Paula J., Meadows, Helen J., Mathie, Alistair

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Distribution and expression of TREK-1, a two-pore-domain potassium channel, in the adult rat CNS von Hervieu, G.J, Cluderay, J.E, Gray, C.W, Green, P.J, Ranson, J.L, Randall, A.D, Meadows, H.J

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Functional characterisation of human TASK-3, an acid-sensitive two-pore domain potassium channel von Meadows, H.J., Randall, A.D.

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Acute hypoxia occludes hTREK-1 modulation: re-evaluation of the potential role of tandem P domain K+ channels in central neuroprotection von Miller, P, Kemp, P J, Lewis, A, Chapman, C G, Meadows, H J, Peers, C

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Cloning, localisation and functional expression of the human orthologue of the TREK-1 potassium channel von Meadows, H J, Benham, C D, Cairns, W, Gloger, I, Jennings, C, Medhurst, A D, Murdock, P, Chapman, C G

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mGlu4 potentiation of K sub(2) sub(P)2.1 is dependant on C-terminal dephosphorylation von Cain, S M, Meadows, HJ, Dunlop, J, Bushell, T J

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Cloning, localisation and functional expression of the human orthologue of the TREK-1 potassium channel von Meadows, H.J., Benham, C.D., Cairns, W., Gloger, I., Jennings, C., Medhurst, A.D., Murdock, P., Chapman, C.G.

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Cloning, localisation and functional expression of a novel human, cerebellum specific, two pore domain potassium channel von Chapman, Conrad G., Meadows, Helen J., Godden, Rob J., Campbell, David A., Duckworth, Malcolm, Kelsell, Rosemary E., Murdock, Paul R., Randall, Andrew D., Rennie, Gillian I., Gloger, Israel S.

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SB-205384: a GABA(A) receptor modulator with novel mechanism of action that shows subunit selectivity von Meadows, H J, Kumar, C S, Pritchett, D B, Blackburn, T P, Benham, C D

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The neuroprotective agent sipatrigine (BW619C89) potently inhibits the human tandem pore-domain K super(+) channels TREK-1 and TRAAK von Meadows, HJ, Chapman, C G, Duckworth, D M, Kelsell, R E, Murdock, PR, Nasir, S, Rennie, G, Randall, AD

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SB-205384: a GABA sub(A) receptor modulator with novel mechanism of action that shows subunit selectivity von Meadows, HJ, Kumar, C S, Pritchett, D B, Blackburn, T P, Benham, C D

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Effect of SB‐205384 on the decay of GABA‐activated chloride currents in granule cells cultured from rat cerebellum von Meadows, H J, Harries, M H, Thompson, M, Benham, C D

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Site-specific splice variation of the human P2X sub(4) receptor von Carpenter, D, Meadows, HJ, Brough, S, Chapman, G, Clarke, C, Coldwell, M, Davis, R, Harrison, D, Meakin, J, McHale, M, Rice, SQJ, Tomlinson, W J, Wood, M, Sanger, G J

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