Seal S - Search Results

1

Consistent loss of the wild type allele in breast cancers from a family linked to the BRCA2 gene on chromosome 13q12-13.

Collins N, McManus R, Wooster R, Mangion J, Seal S, Lakhani SR, Ormiston W, Daly PA, Ford D, Easton DF, et al. Collins N, et al. Among authors: seal s. Oncogene. 1995 Apr 20;10(8):1673-5. Oncogene. 1995. PMID: 7731724

2

Familial male breast cancer is not linked to the BRCA1 locus on chromosome 17q.

Stratton MR, Ford D, Neuhasen S, Seal S, Wooster R, Friedman LS, King MC, Egilsson V, Devilee P, McManus R, et al. Stratton MR, et al. Among authors: seal s. Nat Genet. 1994 May;7(1):103-7. doi: 10.1038/ng0594-103. Nat Genet. 1994. PMID: 8075631

3

Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.

Wooster R, Neuhausen SL, Mangion J, Quirk Y, Ford D, Collins N, Nguyen K, Seal S, Tran T, Averill D, et al. Wooster R, et al. Among authors: seal s. Science. 1994 Sep 30;265(5181):2088-90. doi: 10.1126/science.8091231. Science. 1994. PMID: 8091231

4

Identification of the breast cancer susceptibility gene BRCA2.

Wooster R, Bignell G, Lancaster J, Swift S, Seal S, Mangion J, Collins N, Gregory S, Gumbs C, Micklem G. Wooster R, et al. Among authors: seal s. Nature. 1995 Dec 21-28;378(6559):789-92. doi: 10.1038/378789a0. Nature. 1995. PMID: 8524414

5

BRCA2 mutations in primary breast and ovarian cancers.

Lancaster JM, Wooster R, Mangion J, Phelan CM, Cochran C, Gumbs C, Seal S, Barfoot R, Collins N, Bignell G, Patel S, Hamoudi R, Larsson C, Wiseman RW, Berchuck A, Iglehart JD, Marks JR, Ashworth A, Stratton MR, Futreal PA. Lancaster JM, et al. Among authors: seal s. Nat Genet. 1996 Jun;13(2):238-40. doi: 10.1038/ng0696-238. Nat Genet. 1996. PMID: 8640235

6

Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer.

Peto J, Collins N, Barfoot R, Seal S, Warren W, Rahman N, Easton DF, Evans C, Deacon J, Stratton MR. Peto J, et al. Among authors: seal s. J Natl Cancer Inst. 1999 Jun 2;91(11):943-9. doi: 10.1093/jnci/91.11.943. J Natl Cancer Inst. 1999. PMID: 10359546

7

Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22.

Rahman N, Teare MD, Seal S, Renard H, Mangion J, Cour C, Thompson D, Shugart Y, Eccles D, Devilee P, Meijers H, Nathanson KL, Neuhausen SL, Weber B, Chang-Claude J, Easton DF, Goldgar D, Stratton MR. Rahman N, et al. Among authors: seal s. Oncogene. 2000 Aug 24;19(36):4170-3. doi: 10.1038/sj.onc.1203735. Oncogene. 2000. PMID: 10962578

8

Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene.

Gayther SA, Mangion J, Russell P, Seal S, Barfoot R, Ponder BA, Stratton MR, Easton D. Gayther SA, et al. Among authors: seal s. Nat Genet. 1997 Jan;15(1):103-5. doi: 10.1038/ng0197-103. Nat Genet. 1997. PMID: 8988179

9

Low frequency of somatic mutations in the LKB1/Peutz-Jeghers syndrome gene in sporadic breast cancer.

Bignell GR, Barfoot R, Seal S, Collins N, Warren W, Stratton MR. Bignell GR, et al. Among authors: seal s. Cancer Res. 1998 Apr 1;58(7):1384-6. Cancer Res. 1998. PMID: 9537235

10

Heterozygosity for mutations in the ataxia telangiectasia gene is not a major cause of radiotherapy complications in breast cancer patients.

Shayeghi M, Seal S, Regan J, Collins N, Barfoot R, Rahman N, Ashton A, Moohan M, Wooster R, Owen R, Bliss JM, Stratton MR, Yarnold J. Shayeghi M, et al. Among authors: seal s. Br J Cancer. 1998 Oct;78(7):922-7. doi: 10.1038/bjc.1998.602. Br J Cancer. 1998. PMID: 9764584 Free PMC article. Clinical Trial.

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