Relationship between the GSTM1 genetic polymorphism and susceptibility to bladder, breast and colon cancer von Zhong, S., Wyllie, A.H., Barnes, D., Wolf, C.R., Spurr, N.K.

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Plectin deficiency results in muscular dystrophy with epidermolysis bullosa von Leigh, I.M, Bryant, S.P, Milana, G, Kirtschig, G, Pulkkinen, L, Smith, F.J.D, McLean, W.H.I, Eady, R.A.J, Spurr, N.K, Owaribe, K, McMillan, J.R, Lane, E.B, Geddes, J.F, de Bono, A.G, Uitto, J, Wiche, G, Kelsell, D.P, Rugg, E.L

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Multifactorial Analysis of Differences Between Sporadic Breast Cancers and Cancers Involving BRCA1 and BRCA2 Mutations von Lakhani, Sunil R., Jacquemier, Jocelyne, Sloane, John P., Gusterson, Barry A., Anderson, Thomas J., van de Vijver, Marc J., Farid, Linda M., Venter, Deon, Antoniou, Antonios, Storfer-Isser, Amy, Smyth, Elizabeth, Steel, C. Michael, Haites, Neva, Scott, Rodney J., Goldgar, David, Neuhausen, Susan, Daly, Peter A., Ormiston, Wilma, McManus, Ross, Scherneck, Siegfried, Ponder, Bruce A. J., Ford, Debbie, Peto, Julian, Stoppa-Lyonnet, Dominique, Bignon, Yves-Jean, Struewing, Jeffery P., Spurr, Nigel K., Bishop, D. Timothy, Klijn, J. G. M., Devilee, Peter, Cornelisse, Cees J., Lasset, Christine, Lenoir, Gilbert, Barkardottir, Rosa Bjork, Egilsson, Valgardur, Hamann, Ute, Chang-Claude, Jenny, Sobol, Hagay, Weber, Barbara, Stratton, Michael R., Easton, Douglas F.

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Mutation and expression analysis of the putative prostate tumour-suppressor gene PTEN von GRAY, I. C, STEWART, L. M. D, PHILLIPS, S. M. A, HAMILTON, J. A, GRAY, N. E, WATSON, G. J, SPURR, N. K, SNARY, D

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A Gilbert's syndrome UGT1A1 variant confers susceptibility to tranilast-induced hyperbilirubinemia von Danoff, T M, Campbell, D A, McCarthy, L C, Lewis, K F, Repasch, M H, Saunders, A M, Spurr, N K, Purvis, I J, Roses, A D, Xu, C-F

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Germline Mutations of the CDKN2 Gene in UK Melanoma Families von Harland, Mark, Meloni, Rolando, Gruis, Nelleke, Pinney, Elizabeth, Brookes, Sharon, Spurr, Nigel K., Frischauf, Anna-Marie, Bataille, Veronique, Peters, Gordon, Cuzick, Jack, Selby, Peter, Bishop, D. Timothy, Bishop, Julia Newton

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A first-generation whole genome-radiation hybrid map spanning the mouse genome von McCarthy, L C, Terrett, J, Davis, M E, Knights, C J, Smith, A L, Critcher, R, Schmitt, K, Hudson, J, Spurr, N K, Goodfellow, P N

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Loss of the chromosomal region 10q23-25 in prostate cancer von GRAY, I. C, PHILLIPS, S. M. A, LEE, S. J, NEOPTOLEMOS, J. P, WEISSENBACH, J, SPURR, N. K

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Chromosomal localization of human genes for arylamine N-acetyltransferase von HICKMAN, D, RISCH, A, BUCKLE, V, SPURR, N. K, JEREMIAH, S. J, MCCARTHY, A, SIM, E

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SIMPLE REPEAT SEQUENCES ON THE HUMAN Y-CHROMOSOME ARE EQUALLY POLYMORPHIC AS THEIR AUTOSOMAL COUNTERPARTS von ROEWER, L, ARNEMANN, J, SPURR, NK, GRZESCHIK, KH, EPPLEN, JT

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Abnormal expression of wild type p53 protein in normal cells of a cancer family patient von Barnes, D.M., Gillett, C.E., Bobrow, L.G., Hanby, A.M., Mohammed, S., Hodgson, S., Leigh, I.M., Purkis, T., MacGeoch, C., Spurr, N.K., Bartek, J., Vojtesek, B., Picksley, S.M., Lane, D.P.

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The Lutheran Blood Group Glycoprotein, Another Member of the Immunoglobulin Superfamily, is Widely Expressed in Human Tissues and is Developmentally Regulated in Human Liver von Parsons, S. F., Mallinson, G., Holmes, C. H., Houlihan, J. M., Simpson, K. L., Mawby, W. J., Spurr, N. K., Warne, D., Barclay, A. N., Anstee, D. J.

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Localization of the gene for familial adenomatous polyposis on chromosome 5 von Bodmer, W. F, Bailey, C. J, Bodmer, J, Bussey, H. J. R, Ellis, A, Gorman, P, Lucibello, F. C, Murday, V. A, Rider, S. H, Scambler, P, Sheer, D, Solomon, E, Spurr, N. K

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Identification of the primary gene defect at the cytochrome P450 CYP2D locus von GOUGH, A. C, MILES, J. S, SPURR, N. K, MOSS, J. E, GAEDIGK, A, EICHELBAUM, M, WOLF, C. R

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ISOLATION OF CDNA CLONES FOR A 50-KDA GLYCOPROTEIN OF THE HUMAN ERYTHROCYTE-MEMBRANE ASSOCIATED WITH RH (RHESUS) BLOOD-GROUP ANTIGEN EXPRESSION von RIDGWELL, K, SPURR, NK, LAGUDA, B, MACGEOCH, C, AVENT, ND, TANNER, MJA

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A 2.4-Megabase Physical Map Spanning the CYP2C Gene Cluster on Chromosome 10q24 von Gray, Ian C., Nobile, Carlo, Muresu, Rosella, Ford, Sally, Spurr, Nigel K.

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Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy von ISAACS, A. M, DAVIES, K. E, FISHER, E. M. C, BOUZYK, M. M, POTTER, A, MASIH, M, WALSH, F. S, SIMS, M. A, DONCASTER, K. E, PARSONS, C. A, MARTIN, J, BROWN, S. D. M, HUNTER, A. J, RASTAN, S, SPURR, N. K, GRAY, L. C, NOLAN, P. M, VIZOR, L, PETERS, J, GALE, D. G, KELSELL, D. P, LATHAM, I. D, CHASE, J. M

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Single nucleotide polymorphisms as tools in human genetics von Gray, I C, Campbell, D A, Spurr, N K

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An autosomal transcript in skeletal muscle with homology to dystrophin von Love, Donald R, Hill, Diane F, Dickson, George, Spurr, Nigel K, Byth, Barbara C, Marsden, Rosalind F, Walsh, Frank S, Edwards, Yvonne H, Davies, Kay E

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Glutathione S-transferase mu locus: use of genotyping and phenotyping assays to assess association with lung cancer susceptibility von Zhong, Shan, Howie, A. Forbes, Ketterer, Brian, Taylor, John, Hayes, John D., Beckett, Geoffrey J., Wathen, Christopher G., Wolf, C.Roland, Spurr, Nigel K.

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