Stratton MR - Search Results

1

Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.

Tarpey P, Thomas S, Sarvananthan N, Mallya U, Lisgo S, Talbot CJ, Roberts EO, Awan M, Surendran M, McLean RJ, Reinecke RD, Langmann A, Lindner S, Koch M, Jain S, Woodruff G, Gale RP, Bastawrous A, Degg C, Droutsas K, Asproudis I, Zubcov AA, Pieh C, Veal CD, Machado RD, Backhouse OC, Baumber L, Constantinescu CS, Brodsky MC, Hunter DG, Hertle RW, Read RJ, Edkins S, O'Meara S, Parker A, Stevens C, Teague J, Wooster R, Futreal PA, Trembath RC, Stratton MR, Raymond FL, Gottlob I. Tarpey P, et al. Among authors: stratton mr. Nat Genet. 2006 Nov;38(11):1242-4. doi: 10.1038/ng1893. Epub 2006 Oct 1. Nat Genet. 2006. PMID: 17013395 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

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

4

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.

5

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. Nat Genet. 1994 May;7(1):103-7. doi: 10.1038/ng0594-103. Nat Genet. 1994. PMID: 8075631

6

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

7

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

8

Hereditary predisposition to breast cancer.

Stratton MR, Wooster R. Stratton MR, et al. Curr Opin Genet Dev. 1996 Feb;6(1):93-7. doi: 10.1016/s0959-437x(96)90017-9. Curr Opin Genet Dev. 1996. PMID: 8791478 Review.

9

The BRC repeats are conserved in mammalian BRCA2 proteins.

Bignell G, Micklem G, Stratton MR, Ashworth A, Wooster R. Bignell G, et al. Among authors: stratton mr. Hum Mol Genet. 1997 Jan;6(1):53-8. doi: 10.1093/hmg/6.1.53. Hum Mol Genet. 1997. PMID: 9002670

10

Cloning, chromosomal mapping and expression pattern of the mouse Brca2 gene.

Connor F, Smith A, Wooster R, Stratton M, Dixon A, Campbell E, Tait TM, Freeman T, Ashworth A. Connor F, et al. Hum Mol Genet. 1997 Feb;6(2):291-300. doi: 10.1093/hmg/6.2.291. Hum Mol Genet. 1997. PMID: 9063750

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