Potentiation of temozolomide-induced cytotoxicity: a comparative study of the biological effects of poly(ADP-ribose) polymerase inhibitors von Boulton, S, Pemberton, L C, Porteous, J K, Curtin, N J, Griffin, R J, Golding, B T, Durkacz, B W

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3-Aminobenzamide and/or O6-benzylguanine evaluated as an adjuvant to temozolomide or BCNU treatment in cell lines of variable mismatch repair status and O6-alkylguanine-DNA alkyltr... von WEDGE, S. R, PORTEOUS, J. K, NEWLANDS, E. S

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In vitro evaluation of temozolomide combined with X-irradiation von Wedge, Stephen R, Porteous, Julia K, Glaser, Mark G, Marcus, Kim, Newlands, Edward S

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Potentiation of temozolomide and BCNU cytotoxicity by O6-benzylguanine : a comparative study in vitro von WEDGE, S. R, PORTEOUS, J. K, MAY, B. L, NEWLANDS, E. S

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Effect of single and multiple administration of an O6-benzylguanine/temozolomide combination: an evaluation in a human melanoma xenograft model von WEDGE, S. R, PORTEOUS, J. K, NEWLANDS, E. S

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Potentiation of temozolomide and BCNU cytotoxicity by O(6)-benzylguanine: a comparative study in vitro von Wedge, S R, Porteus, J K, May, B L, Newlands, E S

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Effect of single and multiple administration of an O ? 6 -benzylguanine/temozolomide combination: an evaluation in a human melanoma xenograft model von Wedge, Stephen R., Porteous, Julia K., Newlands, E. S.

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Potentiation of temozolomide and BCNU cytotoxicity by O super(6)-benzylguanine: A comparative study in vitro von Wedge, SR, Porteous, J K, May, B L, Newlands, E S

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Potentiation of temozolomide-induced cytotoxicity : a comparative study of the biological effect of poly(ADP-ribose) polymerase inhibitors von BOULTON, S, PEMBERTON, L. C, PORTEOUS, J. K, CURTIN, N. J, GRIFFIN, R. J, GOLDING, B. T, DURKACZ, B. W

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The DISC locus in psychiatric illness von Chubb, J E, Bradshaw, N J, Soares, D C, Porteous, D J, Millar, J K

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Genome-wide association studies establish that human intelligence is highly heritable and polygenic von Davies, G, Tenesa, A, Payton, A, Yang, J, Harris, S E, Liewald, D, Ke, X, Le Hellard, S, Christoforou, A, Luciano, M, McGhee, K, Lopez, L, Gow, A J, Corley, J, Redmond, P, Fox, H C, Haggarty, P, Whalley, L J, McNeill, G, Goddard, M E, Espeseth, T, Lundervold, A J, Reinvang, I, Pickles, A, Steen, V M, Ollier, W, Porteous, D J, Horan, M, Starr, J M, Pendleton, N, Visscher, P M, Deary, I J

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Chronic pain, depression and cardiovascular disease linked through a shared genetic predisposition: Analysis of a family-based cohort and twin study von van Hecke, Oliver, Hocking, Lynne J, Torrance, Nicola, Campbell, Archie, Padmanabhan, Sandosh, Porteous, David J, McIntosh, Andrew M, Burri, Andrea V, Tanaka, Haruka, Williams, Frances M K, Smith, Blair H

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International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia von Faughnan, M E, Palda, V A, Garcia-Tsao, G, Geisthoff, U W, McDonald, J, Proctor, D D, Spears, J, Brown, D H, Buscarini, E, Chesnutt, M S, Cottin, V, Ganguly, A, Gossage, J R, Guttmacher, A E, Hyland, R H, Kennedy, S J, Korzenik, J, Mager, J J, Ozanne, A P, Piccirillo, J F, Picus, D, Plauchu, H, Porteous, M E M, Pyeritz, R E, Ross, D A, Sabba, C, Swanson, K, Terry, P, Wallace, M C, Westermann, C J J, White, R I, Young, L H, Zarrabeitia, R

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Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population von Clarke, T-K, Lupton, M K, Fernandez-Pujals, A M, Starr, J, Davies, G, Cox, S, Pattie, A, Liewald, D C, Hall, L S, MacIntyre, D J, Smith, B H, Hocking, L J, Padmanabhan, S, Thomson, P A, Hayward, C, Hansell, N K, Montgomery, G W, Medland, S E, Martin, N G, Wright, M J, Porteous, D J, Deary, I J, McIntosh, A M

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DISC1 as a genetic risk factor for schizophrenia and related major mental illness: response to Sullivan von Porteous, D J, Thomson, P A, Millar, J K, Evans, K L, Hennah, W, Soares, D C, McCarthy, S, McCombie, W R, Clapcote, S J, Korth, C, Brandon, N J, Sawa, A, Kamiya, A, Roder, J C, Lawrie, S M, McIntosh, A M, St Clair, D, Blackwood, D H

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Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112 117) von Clarke, T-K, Adams, M J, Davies, G, Howard, D M, Hall, L S, Padmanabhan, S, Murray, A D, Smith, B H, Campbell, A, Hayward, C, Porteous, D J, Deary, I J, McIntosh, A M

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Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP von Wigmore, EM, Hafferty, JD, Hall, LS, Howard, DM, Clarke, TK, Fabbri, C, Lewis, CM, Uher, R, Navrady, LB, Adams, MJ, Zeng, YN, Campbell, A, Gibson, J, Thomson, PA, Hayward, C, Smith, BH, Hocking, LJ, Padmanabhan, S, Deary, IJ, Porteous, DJ, Mors, O, Mattheisen, M, Nicodemus, KK, McIntosh, AM

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708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits von Thomson, P A, Parla, J S, McRae, A F, Kramer, M, Ramakrishnan, K, Yao, J, Soares, D C, McCarthy, S, Morris, S W, Cardone, L, Cass, S, Ghiban, E, Hennah, W, Evans, K L, Rebolini, D, Millar, J K, Harris, S E, Starr, J M, MacIntyre, D J, McIntosh, A M, Watson, J D, Deary, I J, Visscher, P M, Blackwood, D H, McCombie, W R, Porteous, D J

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Rethinking the genetic architecture of schizophrenia von Mitchell, K. J., Porteous, D. J.

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Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, p... von Burn, John, Sheth, Harsh, Elliott, Faye, Reed, Lynn, Macrae, Finlay, Mecklin, Jukka-Pekka, Möslein, Gabriela, McRonald, Fiona E, Bertario, Lucio, Evans, D Gareth, Gerdes, Anne-Marie, Ho, Judy W C, Lindblom, Annika, Morrison, Patrick J, Rashbass, Jem, Ramesar, Raj, Seppälä, Toni, Thomas, Huw J W, Pylvänäinen, Kirsi, Borthwick, Gillian M, Mathers, John C, Bishop, D Timothy, Boussioutas, Alex, Brewer, Carole, Cook, Jackie, Eccles, Diana, Ellis, Anthony, Hodgson, Shirley V, Lubinski, Jan, Maher, Eamonn R, Porteous, Mary EM, Sampson, Julian, Scott, Rodney J, Side, Lucy

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