Kelsey A - Search Results

1

Pediatric intracranial clear cell meningioma associated with a germline mutation of SMARCE1: a novel case.

Raffalli-Ebezant H, Rutherford SA, Stivaros S, Kelsey A, Smith M, Evans DG, Kilday JP. Raffalli-Ebezant H, et al. Among authors: kelsey a. Childs Nerv Syst. 2015 Mar;31(3):441-7. doi: 10.1007/s00381-014-2558-5. Epub 2014 Sep 24. Childs Nerv Syst. 2015. PMID: 25249420

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: kelsey am. Oncogene. 1996 Jun 6;12(11):2437-42. Oncogene. 1996. PMID: 8649785

3

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: kelsey am. Oncogene. 1997 Feb 20;14(7):865-71. doi: 10.1038/sj.onc.1201041. Oncogene. 1997. PMID: 9047394

4

The gene for the naevoid basal cell carcinoma syndrome acts as a tumour-suppressor gene in medulloblastoma.

Cowan R, Hoban P, Kelsey A, Birch JM, Gattamaneni R, Evans DG. Cowan R, et al. Among authors: kelsey a. Br J Cancer. 1997;76(2):141-5. doi: 10.1038/bjc.1997.354. Br J Cancer. 1997. PMID: 9231911 Free PMC article.

5

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: kelsey am. Cancer Res. 1997 Aug 1;57(15):3245-52. Cancer Res. 1997. PMID: 9242456

6

Cancer phenotype correlates with constitutional TP53 genotype in families with the Li-Fraumeni syndrome.

Birch JM, Blair V, Kelsey AM, Evans DG, Harris M, Tricker KJ, Varley JM. Birch JM, et al. Among authors: kelsey am. Oncogene. 1998 Sep 3;17(9):1061-8. doi: 10.1038/sj.onc.1202033. Oncogene. 1998. PMID: 9764816

7

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: kelsey am. Br J Cancer. 1998 Oct;78(8):1081-3. doi: 10.1038/bjc.1998.631. Br J Cancer. 1998. PMID: 9792154 Free PMC article.

8

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: kelsey am. Am J Hum Genet. 1999 Oct;65(4):995-1006. doi: 10.1086/302575. Am J Hum Genet. 1999. PMID: 10486318 Free PMC article.

9

Relative frequency and morphology of cancers in carriers of germline TP53 mutations.

Birch JM, Alston RD, McNally RJ, Evans DG, Kelsey AM, Harris M, Eden OB, Varley JM. Birch JM, et al. Among authors: kelsey am. Oncogene. 2001 Aug 2;20(34):4621-8. doi: 10.1038/sj.onc.1204621. Oncogene. 2001. PMID: 11498785

10

Isolated intracranial Rosai-Dorfman disease mimicking meningioma in a child.

Griffiths SJ, Tang W, Parameswaran R, Kelsey A, West CG. Griffiths SJ, et al. Among authors: kelsey a. Br J Neurosurg. 2004 Jun;18(3):293-7. doi: 10.1080/02688690410001732788. Br J Neurosurg. 2004. PMID: 15327236 Review.

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