P. Chapman

发表

Diet and cancer prevention: the Concerted Action Polyp Prevention (CAPP) Studies

J. Mathers, J. Burn, D. Bishop, 1998, Proceedings of the Nutrition Society.

Tumor mapping in 2 large multigenerational families with CYLD mutations: implications for disease management and tumor induction.

A. Ashworth, J. Burn, A. Trainer, 2009, Archives of dermatology.

Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutations.

D. Bishop, R. Kolodner, J. Burn, 1994, Genomics.

Regionally clustered APC mutations are associated with a severe phenotype and occur at a high frequency in new mutation cases of adenomatous polyposis coli.

S. Gayther, D. Wells, J. Delhanty, 1994, Human molecular genetics.

Endoscopic screening and surgery for familial adenomatous polyposis: Dangerous delays

S. J. Mills, J. Burn, S. Mills, 1997, The British journal of surgery.

The protocol for a European double-blind trial of aspirin and resistant starch in familial adenomatous polyposis: the CAPP study. Concerted Action Polyposis Prevention.

J. Mathers, S. Bülow, J. Burn, 1995, European journal of cancer.

Germline rearrangement of MCC and APC detected by pulsed field gel electrophoresis and fluorescent in situ hybridization

S. Gayther, J. Burn, D. Wells, 1993, Annals of human genetics.

An intrachromosomal insertion causing 5q22 deletion and familial adenomatous polyposis coli in two generations.

D. Griffin, M. Bradburn, J. Delhanty, 1992, Journal of medical genetics.

Familial adenomatous polyposis: heterogeneity?

J. Burn, P. Chapman, 1994, American journal of human genetics.

Congenital hypertrophy of retinal pigment epithelium: a sign of familial adenomatous polyposis.

J. Burn, A. Gunn, W. Church, 1989, BMJ.

Clinical impact of colonoscopic screening in first‐degree relatives of patients with hereditary non‐polyposis colorectal cancer

D. Bishop, J. Burn, D. Bishop, 1995, The British journal of surgery.

Colonic fermentation of complex carbohydrates in patients with familial adenomatous polyposis.

J. Mathers, J. Burn, P. Chapman, 1993, Gut.

Genetic predictive testing for bowel cancer predisposition: the impact on the individual

J. Burn, P. Chapman, 1999, Cytogenetic and Genome Research.

Original Articles the Uk Northern Region Genetic Register for Familial Adenomatous Polyposis Coli: Use of Age of Onset, Congenital Hypertrophy of the Retinal Pigment Epithelium, and Dna Markers in Risk Calculations

J. Burn, F. Lalloo, J. Delhanty, 2022 .

adenomatous polyposis . carbohydrates in patients with familial Colonic fermentation of complex

D. Johnston, J. Mathers, J. Burn, 2006 .

Colonic epithelial cell proliferation in hereditary non-polyposis colorectal cancer

D. Appleton, D. Appleton, J. Mathers, 1998, Gut.

A Randomized Placebo-Controlled Prevention Trial of Aspirin and/or Resistant Starch in Young People with Familial Adenomatous Polyposis

D. Bishop, D. Evans, J. Mathers, 2011, Cancer Prevention Research.

Identification of the familial cylindromatosis tumour-suppressor gene

A. Ashworth, S. Seal, M. Stratton, 2000, Nature Genetics.

Familial cylindromatosis (turban tumour syndrome) gene localised to chromosome 16q12–q13: evidence for its role as a tumour suppressor gene

M. Stratton, R. Wooster, D. Easton, 1995, Nature Genetics.

Colonic crypt cell proliferation state assessed by whole crypt microdissection in sporadic neoplasia and familial adenomatous polyposis

S. J. Mills, J. Mathers, J. Burn, 2001, Gut.

The CHEK2 1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype.

J. Klijn, A. Hollestelle, M. Schutte, 2003, American journal of human genetics.

Linkage analysis in adenomatous polyposis coli: the use of four closely linked DNA probes in 20 UK families.

J. Attwood, J. Burn, M. Davis, 1991, Journal of medical genetics.

Genetic and functional studies of a germline TP53 splicing mutation in a Li–Fraumeni-like family

D. Evans, J. Varley, R. Reddel, 1998, Oncogene.

DNA markers in risk calculations . retinal pigment epithelium , and congenital hypertrophy of the polyposis coli : use of age of onset , register for familial adenomatous The UK Northern region genetic

J. Burn, F. Lalloo, J. Delhanty, 2004 .

Familial adenomatous polyposis.

J. Burn, P. Chapman, E. Eastham, 1994, Archives of disease in childhood.

Role of a regional register for familial adenomatous polyposis: Experience in the Northern Region

J. Burn, P. Chapman, M. Rhodes, 1991, The British journal of surgery.

Structure of the human MLH1 locus and analysis of a large hereditary nonpolyposis colorectal carcinoma kindred for mlh1 mutations.

R. Kolodner, J. Burn, M. Kane, 1995, Cancer research.

Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12–q13

S. Seal, M. Stratton, R. Siebert, 2000, Human Genetics.

The cylindromatosis gene (cyld1) on chromosome 16q may be the only tumour suppressor gene involved in the development of cylindromas.

M. Stratton, S. Lakhani, J. Burn, 1996, Oncogene.

Four novel germ-line mutations in the APC gene detected by heteroduplex analysis.

J. Burn, A. Curtis, T. Hamzehloei, 1994, Human molecular genetics.

Genetic linkage in Muir-Torre syndrome to the same chromosomal region as cancer family syndrome.

J. Burn, D. Bishop, V. Murday, 1994, European journal of cancer.

Histological detection of microadenomas in the diagnosis of familial adenomatous polyposis

N. Shepherd, J. Burn, P. Chapman, 1991, The British journal of surgery.

The genetic background of familial adenomatous polyposis. Linkage analysis, the APC gene identification and mutation screening.

J. Burn, A. Kartheuser, A. Curtis, 1995, Acta gastro-enterologica Belgica.

Human mismatch repair genes and their association with hereditary non-polyposis colon cancer.

R. Kolodner, J. Burn, M. Kane, 1994, Cold Spring Harbor symposia on quantitative biology.

Susceptibility markers in colorectal cancer.

J. Mathers, J. Burn, D. Bishop, 2001, IARC scientific publications.

Structure of the Human MLH 1 Locus and Analysis of a Large Hereditary Nonpolyposis Colorectal Carcinoma Kindred for mihi Mutations '

D. Bishop, R. Kolodner, J. Burn, 2006 .

Comparison of morbidity and function after colectomy with ileorectal anastomosis or restorative proctocolectomy for familial adenomatous polyposis

K. Neale, H. Bussey, R. Nicholls, 1991, The British journal of surgery.

Tumor mapping in 2 large multigenerational families with CYLD mutations: implications for disease management and tumor induction.

A. Ashworth, J. Burn, A. Trainer, 2009, Archives of dermatology.

A Randomized Placebo-Controlled Prevention Trial of Aspirin and/or Resistant Starch in Young People with Familial Adenomatous Polyposis

D. Bishop, J. Mathers, R. Fodde, 2011, Cancer Prevention Research.

The UK Northern region genetic register for familial adenomatous polyposis coli: use of age of onset, congenital hypertrophy of the retinal pigment epithelium, and DNA markers in risk calculations.

F. Lalloo, J. Delhanty, M. Cachón-González, 1991, Journal of medical genetics.

mlh 1 Mutations Hereditary Nonpolyposis Colorectal Carcinoma Kindred for Locus and Analysis of a Large MLH 1 Structure of the Human Updated

D. Bishop, R. Kolodner, J. Burn, 2006 .