Loss of heterozygosity at chromosome 9p in ductal carcinoma in situ and invasive carcinoma of the breastMARSH, K. L; VARLEY, J. M.British journal of cancer. 1998, Vol 77, Num 9, pp 1439-1447, issn 0007-0920Article

Characterisation of a short, highly repeated and centromerically localised DNA sequence in crested and marbled newts of the genus TriturusVARLEY, J. M; MACGREGOR, H. C; BARNETT, L et al.Chromosoma (Berlin. Print). 1990, Vol 100, Num 1, pp 15-31, issn 0009-5915, 17 p.Article

Are there low-penetrance TP53 alleles? Evidence from childhood adrenocortical tumorsVARLEY, J. M; MCGOWN, G; THORNCROFT, M et al.American journal of human genetics. 1999, Vol 65, Num 4, pp 995-1006, issn 0002-9297Article

A detailed study of loss of heterozygosity on chromosome 17 in tumours from Li-Fraumeni patients carrying a mutation to the TP53 geneVARLEY, J. M; THORNCROFT, M; MCGOWN, G et al.Oncogene (Basingstoke). 1997, Vol 14, Num 7, pp 865-871, issn 0950-9232Article

Determination of the gene order of the three loci CD2, NGFB, and NRAS at human chromosome band 1p13 and refinement of their localisation at the subband level by fluorescence in situ hybridizationMITCHELL, E. L. D; JONES, D; WHITE, G. R. M et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 3-4, pp 183-185, issn 0301-0171Conference Paper

Loss of chromosome 17p13 sequences and mutation of p53 in human breast carcinomasVARLEY, J. M; BRAMMAR, W. J; LANE, D. P et al.Oncogene : (Basingstoke). 1991, Vol 6, Num 3, pp 413-421Article

A sequence previously identified as metastasis-related encodes an acidic ribosomal phosphoprotein, P2SHARP, M. G. F; ADAMS, S. M; ELVIN, P et al.British journal of cancer. 1990, Vol 61, Num 1, pp 83-88, issn 0007-0920, 6 p.Article

Engineered rat insulin I analogue having a B16 Tyr/Asp replacement exhibits unchanged susceptibility to cleavage by insulin proteinaseVARLEY, J. M; DAVIES, J. G; SHIRE, D et al.European journal of biochemistry (Print). 1988, Vol 171, Num 1-2, pp 351-354, issn 0014-2956Article

Delayed chromosome changes in gamma-irradiated normal and Li-Fraumeni fibroblastsBOYLE, J. M; SPREADBOROUGH, A. R; GREAVES, M. J et al.Radiation research. 2002, Vol 157, Num 2, pp 158-165, issn 0033-7587Article

Identification of a novel fusion gene involving hTAF_II68 and CHN from a t(9;17)(q22;q11.2) translocation in an extraskeletal myxoid chondrosarcomaATTWOOLL, C; TARIQ, M; HARRIS, M et al.Oncogene (Basingstoke). 1999, Vol 18, Num 52, pp 7599-7601, issn 0950-9232Article

Chromosome instability is a predominant trait of fibroblasts from Li-Fraumeni familiesBOYLE, J. M; MITCHELL, E. L. D; GREAVES, M. J et al.British journal of cancer. 1998, Vol 77, Num 12, pp 2181-2192, issn 0007-0920Article

Li-Fraumeni syndrome : a molecular and clinical reviewVARLEY, J. M; EVANS, D. G. R; BIRCH, J. M et al.British journal of cancer. 1997, Vol 76, Num 1, pp 1-14, issn 0007-0920Article

A novel deletion within exon 6 of TP53 in a family with Li-Fraumeni-like syndrome, and LOH in a benign lesion from a mutation carrierVARLEY, J. M; THORNCROFT, M; MCGOWN, G et al.Cancer genetics and cytogenetics. 1996, Vol 90, Num 1, pp 14-16, issn 0165-4608Article

Differential expression of translation-associated genes in benign and malignant human breast tumoursADAMS, S. M; SHARP, M. G. F; WALKER, R. A et al.British journal of cancer. 1992, Vol 65, Num 1, pp 65-71, issn 0007-0920Article

Isolation and characterization of a novel gene with differential expression in benign and malignant human breast tumoursADAMS, S. M; HELPS, N. R; SHARP, M. G. F et al.Human molecular genetics (Print). 1992, Vol 1, Num 2, pp 91-96, issn 0964-6906Article

Characterization of germline TP53 splicing mutations and their genetic and functional analysisVARLEY, J. M; ATTWOOLL, C; WHITE, G et al.Oncogene (Basingstoke). 2001, Vol 20, Num 21, pp 2647-2654, issn 0950-9232Article

Exclusion of the genes CDKN2 and PTEN as causative gene defects in Li-Fraumeni syndromeBURT, E. C; MCGOWN, G; THORNCROFT, M et al.British journal of cancer. 1999, Vol 80, Num 1-2, pp 9-10, issn 0007-0920Article

Highly consistent genetic alterations in childhood adrenocortical tumours detected by comparative genomic hybridizationJAMES, L. A; KELSEY, A. M; BIRCH, J. M et al.British journal of cancer. 1999, Vol 81, Num 2, pp 300-304, issn 0007-0920Article

Cancer phenotype correlates with constitutional TP53 genotype in families with the Li-Fraumeni syndromeBIRCH, J. M; BLAIR, V; KELSEY, A. M et al.Oncogene (Basingstoke). 1998, Vol 17, Num 9, pp 1061-1068, issn 0950-9232Article

Mutation of the TP53 gene and allelic imbalance at chromosome 17p13 in ductal carcinoma in situMUNN, K. E; WALKER, R. A; MENASCE, L et al.British journal of cancer. 1996, Vol 74, Num 10, pp 1578-1585, issn 0007-0920Article

Identification and cloning in yeast artificial chromosomes of a region of elevated loss of heterozygosity on chromosome 1p31.1 in human breast cancerHOGGARD, N; HEY, Y; BRINTNELL, B et al.Genomics (San Diego, Calif.). 1995, Vol 30, Num 2, pp 233-243, issn 0888-7543Article

An evaluation of immunoreactivity for c-erbB-2 protein as a marker of poor short-term prognosis in breast cancerWALKER, R. A; GULLICK, W. J; VARLEY, J. M et al.British journal of cancer. 1989, Vol 60, Num 3, pp 426-429, issn 0007-0920Article

Structural rearrangement of the retinoblastoma gene in human breast carcinomaT'ANG, A; VARLEY, J. M; SHIKHA CHAKRABORTY et al.Science (Washington, D.C.). 1988, Vol 242, Num 4876, pp 263-266, issn 0036-8075, 4 p.Article

Significance of intron 6 sequence variations in the TP53 gene in Li-Fraumeni syndromeVARLEY, J. M; MCGOWN, G; THORNCROFT, M et al.Cancer genetics and cytogenetics. 2001, Vol 129, Num 1, pp 85-87, issn 0165-4608Article

Radiation-induced G₁ arrest is not defective in fibroblasts from Li-Fraumeni families without TP53 mutationsBOYLE, J. M; GREAVES, M. J; CAMPLEJOHN, R. S et al.British journal of cancer. 1999, Vol 79, Num 11-12, pp 1657-1664, issn 0007-0920Article