Mazoyer S - Search Results

1

Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletions.

Puget N, Stoppa-Lyonnet D, Sinilnikova OM, Pagès S, Lynch HT, Lenoir GM, Mazoyer S. Puget N, et al. Among authors: mazoyer s. Cancer Res. 1999 Jan 15;59(2):455-61. Cancer Res. 1999. PMID: 9927062

2

Screening of inherited breast cancer with DNA markers.

Lalle P, Bignon YJ, Stoppa-Lyonnet D, Narod SA, Mazoyer S, Rio P, Courjal F, Bartholin P, Sobol H. Lalle P, et al. Among authors: mazoyer s. Lancet. 1993 May 29;341(8857):1422. Lancet. 1993. PMID: 8098837 No abstract available.

3

Two germ-line mutations affecting the same nucleotide at codon 257 of p53 gene, a rare site for mutations.

Mazoyer S, Lalle P, Moyret-Lalle C, Marçais C, Schraub S, Frappaz D, Sobol H, Ozturk M. Mazoyer S, et al. Oncogene. 1994 Apr;9(4):1237-9. Oncogene. 1994. PMID: 8134127

4

[Hereditary predisposition for cancer of the breast and the ovary].

Lalle P, Stoppa-Lyonnet D, Mazoyer S, Rio P, Girodet C, Hardouin A, Narod SA, Sobol H, Bignon YJ. Lalle P, et al. Among authors: mazoyer s. Bull Cancer. 1993 Oct;80(10):857-65. Bull Cancer. 1993. PMID: 8204923 French.

5

Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study.

Neuhausen SL, Mazoyer S, Friedman L, Stratton M, Offit K, Caligo A, Tomlinson G, Cannon-Albright L, Bishop T, Kelsell D, Solomon E, Weber B, Couch F, Struewing J, Tonin P, Durocher F, Narod S, Skolnick MH, Lenoir G, Serova O, Ponder B, Stoppa-Lyonnet D, Easton D, King MC, Goldgar DE. Neuhausen SL, et al. Among authors: mazoyer s. Am J Hum Genet. 1996 Feb;58(2):271-80. Am J Hum Genet. 1996. PMID: 8571953 Free PMC article.

6

A polymorphic stop codon in BRCA2.

Mazoyer S, Dunning AM, Serova O, Dearden J, Puget N, Healey CS, Gayther SA, Mangion J, Stratton MR, Lynch HT, Goldgar DE, Ponder BA, Lenoir GM. Mazoyer S, et al. Nat Genet. 1996 Nov;14(3):253-4. doi: 10.1038/ng1196-253. Nat Genet. 1996. PMID: 8896551 No abstract available.

7

A 1-kb Alu-mediated germ-line deletion removing BRCA1 exon 17.

Puget N, Torchard D, Serova-Sinilnikova OM, Lynch HT, Feunteun J, Lenoir GM, Mazoyer S. Puget N, et al. Among authors: mazoyer s. Cancer Res. 1997 Mar 1;57(5):828-31. Cancer Res. 1997. PMID: 9041180

8

Mutations in BRCA1 and BRCA2 in breast cancer families: are there more breast cancer-susceptibility genes?

Serova OM, Mazoyer S, Puget N, Dubois V, Tonin P, Shugart YY, Goldgar D, Narod SA, Lynch HT, Lenoir GM. Serova OM, et al. Among authors: mazoyer s. Am J Hum Genet. 1997 Mar;60(3):486-95. Am J Hum Genet. 1997. PMID: 9042907 Free PMC article.

9

BRCA2 mutations in hereditary breast and ovarian cancer in France.

Serova-Sinilnikova OM, Boutrand L, Stoppa-Lyonnet D, Bressac-de-Paillerets B, Dubois V, Lasset C, Janin N, Bignon YJ, Longy M, Maugard C, Lidereau R, Leroux D, Frebourg T, Mazoyer S, Lenoir GM. Serova-Sinilnikova OM, et al. Among authors: mazoyer s. Am J Hum Genet. 1997 May;60(5):1236-9. Am J Hum Genet. 1997. PMID: 9150172 Free PMC article. No abstract available.

10

A BRCA1 nonsense mutation causes exon skipping.

Mazoyer S, Puget N, Perrin-Vidoz L, Lynch HT, Serova-Sinilnikova OM, Lenoir GM. Mazoyer S, et al. Am J Hum Genet. 1998 Mar;62(3):713-5. doi: 10.1086/301768. Am J Hum Genet. 1998. PMID: 9497265 Free PMC article. No abstract available.

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