BORDERLINE OVARIAN CANCER: PATIENTS' FEELING WITH RESPECT TO CONSERVING OR REMOVAL OF THE OTHER OVARY von Narayansingh, G V, Middlemiss, C F, Parkin, D E

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Temperature- and Pressure-Induced Proton Transfer in the 1:1 Adduct Formed between Squaric Acid and 4,4′-Bipyridine von Martins, David M. S, Middlemiss, Derek S, Pulham, Colin R, Wilson, Chick C, Weller, Mark T, Henry, Paul F, Shankland, Norman, Shankland, Kenneth, Marshall, William G, Ibberson, Richard M, Knight, Kevin, Moggach, Stephen, Brunelli, Michela, Morrison, Carole A

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The NEWTON-g Gravity Imager: Toward New Paradigms for Terrain Gravimetry von Carbone, D., Antoni-Micollier, L., Hammond, G., de Zeeuw - van Dalfsen, E., Rivalta, E., Bonadonna, C., Messina, A., Lautier-Gaud, J., Toland, K., Koymans, M., Anastasiou, K., Bramsiepe, S., Cannavò, F., Contrafatto, D., Frischknecht, C., Greco, F., Marocco, G., Middlemiss, R., Ménoret, V., Noack, A., Passarelli, L., Paul, D., Prasad, A., Siligato, G., Vermeulen, P.

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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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Trophic effects of purines in neurons and glial cells von Rathbone, M P, Middlemiss, P J, Gysbers, J W, Andrew, C, Herman, M A, Reed, J K, Ciccarelli, R, Di Iorio, P, Caciagli, F

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Fragment-based and structure-guided discovery of perforin inhibitors von Jose, Jiney, Law, Ruby H.P., Leung, Eleanor W.W., Wai, Dorothy C.C., Akhlaghi, Hedieh, Chandrashekaran, Indu R., Caradoc-Davies, Tom T., Voskoboinik, Ilia, Feutrill, John, Middlemiss, David, Jeevarajah, Devadharshini, Bashtannyk-Puhalovich, Tanya, Giddens, Anna C., Lee, Tet Woo, Jamieson, Stephen M.F., Trapani, Joseph A., Whisstock, James C., Spicer, Julie A., Norton, Raymond S.

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Characterization of SB‐271046: A potent, selective and orally active 5‐HT6 receptor antagonist von Routledge, Carol, Bromidge, Steven M, Moss, Stephen F, Price, Gary W, Hirst, Warren, Newman, Helen, Riley, Graham, Gager, Tracey, Stean, Tania, Upton, Neil, Clarke, Stephen E, Brown, Anthony M, Middlemiss, Derek N

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Characterization of [125I]‐SB‐258585 binding to human recombinant and native 5‐HT6 receptors in rat, pig and human brain tissue von Hirst, Warren D, Minton, Jayne A L, Bromidge, Steven M, Moss, Stephen F, Latter, Alison J, Riley, Graham, Routledge, Carol, Middlemiss, Derek N, Price, Gary W

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5-chloro-N-(4-methoxy-3-piperazin-1-yl-phenyl)-3-methyl-2-benzothiophenesulfonamide (SB-271046) : A potent, selective, and orally bioavailable 5-HT6 receptor antagonist von BROMIDGE, S. M, BROWN, A. M, MOSS, S. F, NEWMAN, H, RILEY, G, ROUTLEDGE, C, WYMAN, P, CLARKE, S. E, DODGSON, K, GAGER, T, GRASSAM, H. L, JEFFREY, P. M, JOINER, G. F, KING, F. D, MIDDLEMISS, D. N

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Implantation of a Slow Release Corticosterone Pellet Induces Long-Term Alterations in Serotonergic Neurochemistry in the Rat Brain von Bush, V. L., Middlemiss, D. N., Marsden, C. A., Fone, K. C. F.

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Indole-3-acetic Acid Antagonists of the Prostaglandin D 2 Receptor CRTH2 von Armer, Richard E., Ashton, Mark R., Boyd, Edward A., Brennan, Chris J., Brookfield, Frederick A., Gazi, Lucien, Gyles, Shân L., Hay, Philip A., Hunter, Michael G., Middlemiss, David, Whittaker, Mark, Xue, Luzheng, Pettipher, Roy

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Enhancement of 5-HT1B and 5-HT1D receptor antagonist effects on extracellular 5-HT levels in the guinea-pig brain following concurrent 5-HT1A or 5-HT re-uptake site blockade von ROBERTS, C, BOYD, D. F, MIDDLEMISS, D. N, ROUTLEDGE, C

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Spiropiperidines as high-affinity, selective .sigma. ligands von Chambers, Mark S, Baker, Raymond, Billington, David C, Knight, Anthony K, Middlemiss, D. N, Wong, Eric H. F

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Ait-082 and Methylprednisolone Singly, but Not in Combination, Enhance Functional and Histological Improvement after Acute Spinal Cord Injury in Rats von Jiang, S., Khan, M. I., Middlemiss, P. J., Lu, Y., Werstiuk, E. S., Crocker, C.E., Ciccarelli, R., Caciagli, F., Rathbone, M. P.

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Characterization of MDL 73005EF as a 5‐HT1A selective ligand and its effects in animal models of anxiety: comparison with buspirone, 8‐OH‐DPAT and diazepam von Moser, P.C., Tricklebank, M.D., Middlemiss, D.N., Mir, A.K., Hibert, M.F., Fozard, J.R.

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AIT-082 as a potential neuroprotective and regenerative agent in stroke and central nervous system injury von Rathbone, Michel P, Middlemiss, Pamela J, Crocker, Candice E, Glasky, Michelle S, Juurlink, Bernhard HJ, Ramirez, Julio J, Ciccarelli, Renata, Di Iorio, Patrizia, Caciagli, Francesco

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Pharmacological profile of GR117289 in vitro: a novel, potent and specific non‐peptide angiotensin AT1 receptor antagonist von Robertson, M.J., Barnes, J.C., Drew, G.M., Clark, K.L., Marshall, F.H., Michel, A., Middlemiss, D., Ross, B.C., Scopes, D., Dowle, M.D.

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Purine nucleosides protect injured neurons and stimulate neuronal regeneration by intracellular and membrane receptor-mediated mechanisms von Di Iorio, Patrizia, Caciagli, Francesco, Giuliani, Patricia, Ballerini, Patrizia, Ciccarelli, Renata, Sperling, Oded, Zoref-Shani, Esther, Benowitz, Larry, Traversa, Ugo, Bombi, Giulia, Florio, Tulio, Virgilio, Antonella, Andrew, Craig M., Crocker, Candice E., Werstiuk, Eva S., Middlemiss, Pamela J., Rathbone, Michel P.

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5-Chloro-N-(4-methoxy-3-piperazin-1-yl- phenyl)-3-methyl-2-benzothiophenesulfon- amide (SB-271046):  A Potent, Selective, and Orally Bioavailable 5-HT6 Receptor Antagonist von Bromidge, Steven M, Brown, Anthony M, Clarke, Stephen E, Dodgson, Kathy, Gager, Tracey, Grassam, Helen L, Jeffrey, Phil M, Joiner, Graham F, King, Frank D, Middlemiss, Derek N, Moss, Stephen F, Newman, Helen, Riley, Graham, Routledge, Carol, Wyman, Paul

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The trophic effects of purines and purinergic signaling in pathologic reactions of astrocytes von RATHBONE, M. P, MIDDLEMISS, P, ANDREW, C, CACIAGLI, F, CICCARELLI, R, DI IORIO, P, RONG HUANG

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