Bevan S - Search Results

1

EXO1 variants occur commonly in normal population: evidence against a role in hereditary nonpolyposis colorectal cancer.

Jagmohan-Changur S, Poikonen T, Vilkki S, Launonen V, Wikman F, Orntoft TF, Møller P, Vasen H, Tops C, Kolodner RD, Mecklin JP, Järvinen H, Bevan S, Houlston RS, Aaltonen LA, Fodde R, Wijnen J, Karhu A. Jagmohan-Changur S, et al. Among authors: bevan s. Cancer Res. 2003 Jan 1;63(1):154-8. Cancer Res. 2003. PMID: 12517792

2

Mutations in the candidate tumour suppressor gene FLJ12973 on chromosome 15q15 are rare in colorectal cancer.

Fleischmann C, Bevan S, Neil JC, Terry A, Houlston RS. Fleischmann C, et al. Among authors: bevan s. Cancer Lett. 2003 Jun 30;196(1):65-7. doi: 10.1016/s0304-3835(03)00160-5. Cancer Lett. 2003. PMID: 12860291

3

CDX2 mutations do not account for juvenile polyposis or Peutz-Jeghers syndrome and occur infrequently in sporadic colorectal cancers.

Woodford-Richens KL, Halford S, Rowan A, Bevan S, Aaltonen LA, Wasan H, Bicknell D, Bodmer WF, Houlston RS, Tomlinson IP. Woodford-Richens KL, et al. Among authors: bevan s. Br J Cancer. 2001 May 18;84(10):1314-6. doi: 10.1054/bjoc.2001.1800. Br J Cancer. 2001. PMID: 11355940 Free PMC article.

4

Genetic predisposition to gastric cancer.

Bevan S, Houlston RS. Bevan S, et al. QJM. 1999 Jan;92(1):5-10. doi: 10.1093/qjmed/92.1.5. QJM. 1999. PMID: 10209666 Review. No abstract available.

5

Low frequency of germline E-cadherin mutations in familial and nonfamilial gastric cancer.

Stone J, Bevan S, Cunningham D, Hill A, Rahman N, Peto J, Marossy A, Houlston RS. Stone J, et al. Among authors: bevan s. Br J Cancer. 1999 Apr;79(11-12):1935-7. doi: 10.1038/sj.bjc.6690308. Br J Cancer. 1999. PMID: 10206317 Free PMC article.

6

Comprehensive analysis of SMAD4 mutations and protein expression in juvenile polyposis: evidence for a distinct genetic pathway and polyp morphology in SMAD4 mutation carriers.

Woodford-Richens KL, Rowan AJ, Poulsom R, Bevan S, Salovaara R, Aaltonen LA, Houlston RS, Wright NA, Tomlinson IP. Woodford-Richens KL, et al. Among authors: bevan s. Am J Pathol. 2001 Oct;159(4):1293-300. doi: 10.1016/S0002-9440(10)62516-3. Am J Pathol. 2001. PMID: 11583957 Free PMC article.

7

Relative power of linkage and transmission disequilibrium test strategies to detect non-HLA linked coeliac disease susceptibility genes.

Bevan S, Popat S, Houlston RS. Bevan S, et al. Gut. 1999 Nov;45(5):668-71. doi: 10.1136/gut.45.5.668. Gut. 1999. PMID: 10517901 Free PMC article.

8

Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer.

Tomlinson IP, Alam NA, Rowan AJ, Barclay E, Jaeger EE, Kelsell D, Leigh I, Gorman P, Lamlum H, Rahman S, Roylance RR, Olpin S, Bevan S, Barker K, Hearle N, Houlston RS, Kiuru M, Lehtonen R, Karhu A, Vilkki S, Laiho P, Eklund C, Vierimaa O, Aittomäki K, Hietala M, Sistonen P, Paetau A, Salovaara R, Herva R, Launonen V, Aaltonen LA; Multiple Leiomyoma Consortium. Tomlinson IP, et al. Among authors: bevan s. Nat Genet. 2002 Apr;30(4):406-10. doi: 10.1038/ng849. Epub 2002 Feb 25. Nat Genet. 2002. PMID: 11865300

9

Low frequency of somatic mutations in the FH/multiple cutaneous leiomyomatosis gene in sporadic leiomyosarcomas and uterine leiomyomas.

Barker KT, Bevan S, Wang R, Lu YJ, Flanagan AM, Bridge JA, Fisher C, Finlayson CJ, Shipley J, Houlston RS. Barker KT, et al. Among authors: bevan s. Br J Cancer. 2002 Aug 12;87(4):446-8. doi: 10.1038/sj.bjc.660502. Br J Cancer. 2002. PMID: 12177782 Free PMC article.

10

From linkage to genes : positional cloning.

Bevan S, Houlston RS. Bevan S, et al. Methods Mol Med. 2000;41:21-31. doi: 10.1385/1-59259-082-9:021. Methods Mol Med. 2000. PMID: 21374430

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