Stratton MR - Search Results

1

Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus.

Raymond FL, Tarpey PS, Edkins S, Tofts C, O'Meara S, Teague J, Butler A, Stevens C, Barthorpe S, Buck G, Cole J, Dicks E, Gray K, Halliday K, Hills K, Hinton J, Jones D, Menzies A, Perry J, Raine K, Shepherd R, Small A, Varian J, Widaa S, Mallya U, Moon J, Luo Y, Shaw M, Boyle J, Kerr B, Turner G, Quarrell O, Cole T, Easton DF, Wooster R, Bobrow M, Schwartz CE, Gecz J, Stratton MR, Futreal PA. Raymond FL, et al. Among authors: stratton mr. Am J Hum Genet. 2007 May;80(5):982-7. doi: 10.1086/513609. Epub 2007 Mar 20. Am J Hum Genet. 2007. PMID: 17436253 Free PMC article.

2

A germline mutation in the androgen receptor gene in two brothers with breast cancer and Reifenstein syndrome.

Wooster R, Mangion J, Eeles R, Smith S, Dowsett M, Averill D, Barrett-Lee P, Easton DF, Ponder BA, Stratton MR. Wooster R, et al. Among authors: stratton mr. Nat Genet. 1992 Oct;2(2):132-4. doi: 10.1038/ng1092-132. Nat Genet. 1992. PMID: 1303262

3

Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype-phenotype correlation.

Gayther SA, Warren W, Mazoyer S, Russell PA, Harrington PA, Chiano M, Seal S, Hamoudi R, van Rensburg EJ, Dunning AM, Love R, Evans G, Easton D, Clayton D, Stratton MR, Ponder BA. Gayther SA, et al. Among authors: stratton mr. Nat Genet. 1995 Dec;11(4):428-33. doi: 10.1038/ng1295-428. Nat Genet. 1995. PMID: 7493024

4

Familial cylindromatosis (turban tumour syndrome) gene localised to chromosome 16q12-q13: evidence for its role as a tumour suppressor gene.

Biggs PJ, Wooster R, Ford D, Chapman P, Mangion J, Quirk Y, Easton DF, Burn J, Stratton MR. Biggs PJ, et al. Among authors: stratton mr. Nat Genet. 1995 Dec;11(4):441-3. doi: 10.1038/ng1295-441. Nat Genet. 1995. PMID: 7493027

5

Localisation of the breast-ovarian cancer susceptibility gene (BRCA1) on 17q12-21 to an interval of < or = 1 cM.

Smith SA, DiCioccio RA, Struewing JP, Easton DF, Gallion HH, Albertsen H, Mazoyer S, Johansson B, Steichen-Gersdorf E, Stratton M, et al. Smith SA, et al. Genes Chromosomes Cancer. 1994 May;10(1):71-6. doi: 10.1002/gcc.2870100112. Genes Chromosomes Cancer. 1994. PMID: 7519878

6

Breast cancer susceptibility: a complex disease unravels.

Wooster R, Stratton MR. Wooster R, et al. Among authors: stratton mr. Trends Genet. 1995 Jan;11(1):3-5. doi: 10.1016/s0168-9525(00)88974-x. Trends Genet. 1995. PMID: 7900193 Review. No abstract available.

7

Familial cancer syndromes.

Eng C, Stratton M, Ponder B, Murday V, Easton D, Sacks N, Watson M, Eeles R. Eng C, et al. Lancet. 1994 Mar 19;343(8899):709-13. doi: 10.1016/s0140-6736(94)91585-7. Lancet. 1994. PMID: 7907684 No abstract available.

8

Absence of linkage to the ataxia telangiectasia locus in familial breast cancer.

Wooster R, Ford D, Mangion J, Ponder BA, Peto J, Easton DF, Stratton MR. Wooster R, et al. Among authors: stratton mr. Hum Genet. 1993 Aug;92(1):91-4. doi: 10.1007/BF00216153. Hum Genet. 1993. PMID: 8365732

9

Genetic heterogeneity and localization of a familial breast-ovarian cancer gene on chromosome 17q12-q21.

Smith SA, Easton DF, Ford D, Peto J, Anderson K, Averill D, Stratton M, Ponder M, Pye C, Ponder BA. Smith SA, et al. Am J Hum Genet. 1993 Apr;52(4):767-76. Am J Hum Genet. 1993. PMID: 8460642 Free PMC article.

10

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: stratton mr. Nat Genet. 1996 Jun;13(2):238-40. doi: 10.1038/ng0696-238. Nat Genet. 1996. PMID: 8640235

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