Regulatory characterisation of the schizophrenia-associated CACNA1C proximal promoter and the potential role for the transcription factor EZH2 in schizophrenia aetiology von Billingsley, Kimberley J., Manca, Maurizio, Gianfrancesco, Olympia, Collier, David A., Sharp, Helen, Bubb, Vivien J., Quinn, John P.

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A Dopamine Transporter Gene Functional Variant Associated with Cocaine Abuse in a Brazilian Sample von Guindalini, Camila, Howard, Mark, Haddley, Kate, Laranjeira, Ronaldo, Collier, David, Ammar, Nik, Craig, Ian, O'Gara, Colin, Bubb, Vivian J., Greenwood, Tiffany, Kelsoe, John, Asherson, Phil, Murray, Robin M., Castelo, Adauto, Quinn, John P., Vallada, Homero, Breen, Gerome

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Kirsten ras mutations in patients with colorectal cancer: the 'RASCAL II' study von ANDREYEV, H. J. N, NORMAN, A. R, BERANEK, M, JANDIK, P, BENAMOUZIG, R, JULLIAN, E, LAURENT-PUIG, P, OLSCHWANG, S, MULLER, O, HOFFMANN, I, RABES, H. M, ZIETZ, C, CUNNINGHAM, D, TROUNGOS, C, VALAVANIS, C, YUEN, S. T, HO, J. W. C, CROKE, C. T, O'DONOGHUE, D. P, GIARETTI, W, RAPALLO, A, RUSSO, A, BAZAN, V, OATES, J, TANAKA, M, OMURA, K, AZUMA, T, OHKUSA, T, FUJIMORI, T, ONO, Y, PAULY, M, FABER, C, GLAESENER, R, DE GOEIJ, Afpm, DIX, B. R, ARENDS, J. W, ANDERSEN, S. N, LÖVIG, T, BREIVIK, J, GAUDERNACK, G, CLAUSEN, O. P. F, DE ANGELIS, P, MELING, G. I, ROGNUM, T. O, SMITH, R, LACOPETTA, B. J, GOH, H-S, FONT, A, ROSELL, R, SUN, X. F, ZHANG, H, BENHATTAR, J, LOSI, L, LEE, J. Q, WANG, S. T, YOUNG, J, WALSH, T, WARD, R, HAWKINS, N

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Polymorphism in serotonin transporter gene associated with susceptibility to major depression von Ogilvie, A.D, Battersby, S, Fink, G, Harmar, A.J, Goodwin, G.M, Bubb, V.J, Dale Smith, C.A

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The serotonin transporter intronic VNTR enhancer correlated with a predisposition to affective disorders has distinct regulatory elements within the domain based on the primary DNA... von Lovejoy, E. A., Scott, A. C., Fiskerstrand, C. E., Bubb, V. J., Quinn, J. P.

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YB-1 and CTCF Differentially Regulate the 5-HTT Polymorphic Intron 2 Enhancer Which Predisposes to a Variety of Neurological Disorders von Klenova, Elena, Scott, Alison C, Roberts, Julian, Shamsuddin, Shaharum, Lovejoy, Elizabeth A, Bergmann, Stephan, Bubb, Vivien J, Royer, Hans-Dieter, Quinn, John P

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The human papillomavirus type 6 and 16 E5 proteins are membrane-associated proteins which associate with the 16-kilodalton pore-forming protein von CONRAD, M, BUBB, V. J, SCHLEGEL, R

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Abstract P2-06-03: A Polymorphic AAAG Repeat in the Estrogen Receptor-Related-Gamma Gene May Represent a Breast Cancer Predisposition Biomarker von Garner, HR, McCormick, JF, Li, L-S, McIver, LJ, Bubb, VJ, George, AC, Boothman, DA, Quinn, JP, Galindo, C.

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Apoptosis and carcinogenesis von Wyllie, A H, Bellamy, C O, Bubb, V J, Clarke, A R, Corbet, S, Curtis, L, Harrison, D J, Hooper, M L, Toft, N, Webb, S, Bird, C C

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Evidence for an age‐related influence of microsatellite instability on colorectal cancer survival von Farrington, Susan M., McKinley, Aileen J., Carothers, Andrew D., Cunningham, Christopher, Bubb, Vivien J., Sharp, Linda, Wyllie, Andrew H., Dunlop, Malcolm G.

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Dysregulated expression of β-catenin marks early neoplastic change in Apc mutant mice, but not all lesions arising in Msh2 deficient mice von KONGKANUNTN, R, BUBB, V. J, SANSOM, O. J, WYLLIE, A. H, HARRISON, D. J, CLARKE, A. R

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Neuron restrictive silencer factor as a modulator of neuropeptide gene expression von Quinn, J.P, Bubb, V.J, Marshall-Jones, Z.V, Coulson, J.M

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Adenomatous polyposis coli (APC), β-catenin, and cadherin are expressed in human bone and cartilage von Monaghan, H, Bubb, V J, Sirimujalin, R, Millward-Sadler, S J, Salter, D M

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APC EXPRESSION IN NORMAL HUMAN TISSUES von MIDGLEY, CAROL A., WHITE, SUSAN, HOWITT, RACHEL, SAVE, VICKI, DUNLOP, MALCOLM G., HALL, PETER A., LANE, DAVID P., WYLLIE, ANDREW H., BUBB, VIVIEN J.

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The pattern of K-ras mutation in pulmonary adenocarcinoma defines a new pathway of tumour development in the human lung von COOPER, C. A, CAREY, F. A, BUBB, V. J, LAMB, D, KERR, K. M, WYLLIE, A. H

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Genome-Wide Analysis of Structural Variants in Parkinson Disease von Billingsley, KJ, Ding, J, Jerez, PA, Illarionova, A, Levine, K, Grenn, FP, Makarious, MB, Moore, A, Vitale, D, Reed, X, Hernandez, D, Torkamani, A, Ryten, M, Hardy, J, Chia, R, Scholz, SW, Traynor, BJ, Dalgard, CL, Ehrlich, DJ, Tanaka, T, Ferrucci, L, Beach, TG, Serrano, GE, Quinn, JP, Bubb, VJ, Collins, RL, Zhao, X, Walker, M, Pierce-Hoffman, E, Brand, H, Talkowski, ME, Casey, B, Cookson, MR, Markham, A, Nalls, MA, Mahmoud, M, Sedlazeck, FJ, Blauwendraat, C, Gibbs, JR, Singleton, AB

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LOSS OF HETEROZYGOSITY AT 5q21 IN NON-SMALL CELL LUNG CANCER: A FREQUENT EVENT BUT WITHOUT EVIDENCE OF APC MUTATION von COOPER, CINDY A., BUBB, VIVIEN J., SMITHSON, NICOLA, CARTER, ROBERT L., GLEDHILL, SARAH, LAMB, DAVID, WYLLIE, ANDREW H., CAREY, FRANCIS A.

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Germline APC mutation (Gln1317) in a cancer-prone family that does not result in familial adenomatous polyposis von White, Susan, Bubb, Vivien J., Wyllie, Andrew H.

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Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset von Billingsley, KJ, Barbosa, IA, Bandrés-Ciga, S, Quinn, JP, Bubb, VJ, Deshpande, C, Botia, JA, Reynolds, RH, Zhang, D, Simpson, MA, Blauwendraat, C, Gan-Or, Z, Gibbs, JR, Nalls, MA, Singleton, A, International Parkinson’s Disease Genomics Consortium (IPDGC), Ryten, M, Koks, S

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Loss of heterozygosity of MCC is not associated with mutation of the retained allele in sporadic colorectal cancer von Curtis, Lucy J., Bubb, Vivien J., Gledhlll, Sarah, Morris, Robert G., Bird, Colin C., Wyllle, Andrew H.

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