McGown G - Search Results

1

Identification of a rare polymorphism in the human TP53 promoter.

Attwooll CL, McGown G, Thorncroft M, Stewart FJ, Birch JM, Varley JM. Attwooll CL, et al. Among authors: mcgown g. Cancer Genet Cytogenet. 2002 Jun;135(2):165-72. doi: 10.1016/s0165-4608(01)00649-5. Cancer Genet Cytogenet. 2002. PMID: 12127401

2

A previously undescribed mutation within the tetramerisation domain of TP53 in a family with Li-Fraumeni syndrome.

Varley JM, McGown G, Thorncroft M, Cochrane S, Morrison P, Woll P, Kelsey AM, Mitchell EL, Boyle J, Birch JM, Evans DG. Varley JM, et al. Among authors: mcgown g. Oncogene. 1996 Jun 6;12(11):2437-42. Oncogene. 1996. PMID: 8649785

3

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 carrier.

Varley JM, Thorncroft M, McGown G, Tricker K, Birch JM, Evans DG. Varley JM, et al. Among authors: mcgown g. Cancer Genet Cytogenet. 1996 Aug;90(1):14-6. doi: 10.1016/0165-4608(96)00059-3. Cancer Genet Cytogenet. 1996. PMID: 8780740

4

An extended Li-Fraumeni kindred with gastric carcinoma and a codon 175 mutation in TP53.

Varley JM, McGown G, Thorncroft M, Tricker KJ, Teare MD, Santibanez-Koref MF, Martin J, Birch JM, Evans DG. Varley JM, et al. Among authors: mcgown g. J Med Genet. 1995 Dec;32(12):942-5. doi: 10.1136/jmg.32.12.942. J Med Genet. 1995. PMID: 8825920 Free PMC article.

5

A detailed study of loss of heterozygosity on chromosome 17 in tumours from Li-Fraumeni patients carrying a mutation to the TP53 gene.

Varley JM, Thorncroft M, McGown G, Appleby J, Kelsey AM, Tricker KJ, Evans DG, Birch JM. Varley JM, et al. Among authors: mcgown g. Oncogene. 1997 Feb 20;14(7):865-71. doi: 10.1038/sj.onc.1201041. Oncogene. 1997. PMID: 9047394

6

Germ-line mutations of TP53 in Li-Fraumeni families: an extended study of 39 families.

Varley JM, McGown G, Thorncroft M, Santibanez-Koref MF, Kelsey AM, Tricker KJ, Evans DG, Birch JM. Varley JM, et al. Among authors: mcgown g. Cancer Res. 1997 Aug 1;57(15):3245-52. Cancer Res. 1997. PMID: 9242456

7

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

Varley JM, Chapman P, McGown G, Thorncroft M, White GR, Greaves MJ, Scott D, Spreadborough A, Tricker KJ, Birch JM, Evans DG, Reddel R, Camplejohn RS, Burn J, Boyle JM. Varley JM, et al. Among authors: mcgown g. Oncogene. 1998 Jun 25;16(25):3291-8. doi: 10.1038/sj.onc.1201878. Oncogene. 1998. PMID: 9681828

8

A novel TP53 splicing mutation in a Li-Fraumeni syndrome family: a patient with Wilms' tumour is not a mutation carrier.

Varley JM, McGown G, Thorncroft M, White GR, Tricker KJ, Kelsey AM, Birch JM, Evans DG. Varley JM, et al. Among authors: mcgown g. Br J Cancer. 1998 Oct;78(8):1081-3. doi: 10.1038/bjc.1998.631. Br J Cancer. 1998. PMID: 9792154 Free PMC article.

9

Exclusion of the genes CDKN2 and PTEN as causative gene defects in Li-Fraumeni syndrome.

Burt EC, McGown G, Thorncroft M, James LA, Birch JM, Varley JM. Burt EC, et al. Among authors: mcgown g. Br J Cancer. 1999 Apr;80(1-2):9-10. doi: 10.1038/sj.bjc.6690313. Br J Cancer. 1999. PMID: 10389970 Free PMC article.

10

Are there low-penetrance TP53 Alleles? evidence from childhood adrenocortical tumors.

Varley JM, McGown G, Thorncroft M, James LA, Margison GP, Forster G, Evans DG, Harris M, Kelsey AM, Birch JM. Varley JM, et al. Among authors: mcgown g. Am J Hum Genet. 1999 Oct;65(4):995-1006. doi: 10.1086/302575. Am J Hum Genet. 1999. PMID: 10486318 Free PMC article.

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