The pathology of inherited breast tumours

por Stratton, M
Publicado 2000

Absence of methylation of CpG dinucleotides within the promoter of the breast cancer susceptibility gene BRCA2 in normal tissues and in breast and ovarian cancers.

por Collins, N., Wooster, R., Stratton, M. R.
Publicado 1997

Promising agents for chemoprevention of skin cancer

por Stratton, S.P., Stratton, M.S., Alberts, D.S.
Publicado 2006

Structure of the met protein and variation of met protein kinase activity among human tumour cell lines.

por Tempest, P. R., Stratton, M. R., Cooper, C. S.
Publicado 1988

Modeling the evolution space of breakage fusion bridge cycles with a stochastic folding process

por Greenman, C. D., Cooke, S. L., Marshall, J., Stratton, M. R., Campbell, P. J.
Publicado 2015

A physical analysis of the Y chromosome shows no additional deletions, other than Gr/Gr, associated with testicular germ cell tumour

por Linger, R, Dudakia, D, Huddart, R, Easton, D, Bishop, D T, Stratton, M R, Rapley, E A
Publicado 2007

Clostridium difficile suppresses colonic vasoactive intestinal peptide associated with altered motility

por Nassif, A., Longo, W. E., Sexe, R., Stratton, M., Standeven, J., Vernava, A. M., Kaminski, D. L.
Publicado 1995

Loss of heterozygosity in sporadic breast tumours at the BRCA2 locus on chromosome 13q12-q13.

por Cleton-Jansen, A. M., Collins, N., Lakhani, S. R., Weissenbach, J., Devilee, P., Cornelisse, C. J., Stratton, M. R.
Publicado 1995

COSMIC 2005

por Forbes, S, Clements, J, Dawson, E, Bamford, S, Webb, T, Dogan, A, Flanagan, A, Teague, J, Wooster, R, Futreal, P A, Stratton, M R
Publicado 2006

The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website

por Bamford, S, Dawson, E, Forbes, S, Clements, J, Pettett, R, Dogan, A, Flanagan, A, Teague, J, Futreal, P A, Stratton, M R, Wooster, R
Publicado 2004

LKB1/KRAS mutant lung cancers constitute a genetic subset of NSCLC with increased sensitivity to MAPK and mTOR signalling inhibition

por Mahoney, C L, Choudhury, B, Davies, H, Edkins, S, Greenman, C, Haaften, G van, Mironenko, T, Santarius, T, Stevens, C, Stratton, M R, Futreal, P A
Publicado 2009

A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes

por Antoniou, A C, Pharoah, P D P, McMullan, G, Day, N E, Stratton, M R, Peto, J, Ponder, B J, Easton, D F
Publicado 2002

Structural alterations of the RB1 gene in human soft tissue tumours.

por Stratton, M. R., Williams, S., Fisher, C., Ball, A., Westbury, G., Gusterson, B. A., Fletcher, C. D., Knight, J. C., Fung, Y. K., Reeves, B. R.
Publicado 1989

Heterozygosity for mutations in the ataxia telangiectasia gene is not a major cause of radiotherapy complications in breast cancer patients.

por Shayeghi, M., Seal, S., Regan, J., Collins, N., Barfoot, R., Rahman, N., Ashton, A., Moohan, M., Wooster, R., Owen, R., Bliss, J. M., Stratton, M. R., Yarnold, J.
Publicado 1998

Testicular microlithiasis as a familial risk factor for testicular germ cell tumour

por Coffey, J, Huddart, R A, Elliott, F, Sohaib, S A, Parker, E, Dudakia, D, Pugh, J L, Easton, D F, Bishop, D T, Stratton, M R, Rapley, E A
Publicado 2007

HPC2/ELAC2 polymorphisms and prostate cancer risk: analysis by age of onset of disease

por Meitz, J C, Edwards, S M, Easton, D F, Murkin, A, Ardern-Jones, A, Jackson, R A, Williams, S, Dearnaley, D P, Stratton, M R, Houlston, R S, Eeles, R A
Publicado 2002

Lobular carcinoma in situ of the breast is not caused by constitutional mutations in the E-cadherin gene

por Rahman, N, Stone, J G, Coleman, G, Gusterson, B, Seal, S, Marossy, A, Lakhani, S R, Ward, A, Nash, A, McKinna, A, A'Hern, R, Stratton, M R, Houlston, R S
Publicado 2000

Screening for BRCA2 mutations in 81 Dutch breast–ovarian cancer families

por Peelen, T, Vliet, M van, Bosch, A, Bignell, G, Vasen, H F A, Klijn, J G M, Meijers-Heijboer, H, Stratton, M, Ommen, G-J B van, Cornelisse, C J, Devilee, P
Publicado 2000

A missense mutation in the BRCA2 gene in three siblings with ovarian cancer.

por Roth, S., Kristo, P., Auranen, A., Shayehgi, M., Seal, S., Collins, N., Barfoot, R., Rahman, N., Klemi, P. J., Grénman, S., Sarantaus, L., Nevanlinna, H., Butzow, R., Ashworth, A., Stratton, M. R., Aaltonen, L. A.
Publicado 1998

Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2

por Rapley, E A, Barfoot, R, Bonaïti-Pellié, C, Chompret, A, Foulkes, W, Perusinghe, N, Reeve, A, Royer-Pokora, B, Schumacher, V, Shelling, A, Skeen, J, Tourreil, S de, Weirich, A, Pritchard-Jones, K, Stratton, M R, Rahman, N
Publicado 2000