Stoppa-Lyonnet D - Search Results

1

Diagnostic strategy for analytical scanning of BRCA1 gene by fluorescence-assisted mismatch analysis using large, bifluorescently labeled amplicons.

Ricevuto E, Sobol H, Stoppa-Lyonnet D, Gulino A, Marchetti P, Ficorella C, Martinotti S, Meo T, Tosi M. Ricevuto E, et al. Clin Cancer Res. 2001 Jun;7(6):1638-46. Clin Cancer Res. 2001. PMID: 11410501

2

Recombinational biases in the rearranged C1-inhibitor genes of hereditary angioedema patients.

Stoppa-Lyonnet D, Duponchel C, Meo T, Laurent J, Carter PE, Arala-Chaves M, Cohen JH, Dewald G, Goetz J, Hauptmann G, et al. Stoppa-Lyonnet D, et al. Am J Hum Genet. 1991 Nov;49(5):1055-62. Am J Hum Genet. 1991. PMID: 1656734 Free PMC article.

3

Clusters of intragenic Alu repeats predispose the human C1 inhibitor locus to deleterious rearrangements.

Stoppa-Lyonnet D, Carter PE, Meo T, Tosi M. Stoppa-Lyonnet D, et al. Proc Natl Acad Sci U S A. 1990 Feb;87(4):1551-5. doi: 10.1073/pnas.87.4.1551. Proc Natl Acad Sci U S A. 1990. PMID: 2154751 Free PMC article.

4

Molecular defects of the C1-inhibitor gene in hereditary angioedema.

Tosi M, Stoppa-Lyonnet D, Carter P, Meo T. Tosi M, et al. Behring Inst Mitt. 1989 Jul;(84):173-9. Behring Inst Mitt. 1989. PMID: 2572212 Review.

5

Altered C1 inhibitor genes in type I hereditary angioedema.

Stoppa-Lyonnet D, Tosi M, Laurent J, Sobel A, Lagrue G, Meo T. Stoppa-Lyonnet D, et al. N Engl J Med. 1987 Jul 2;317(1):1-6. doi: 10.1056/NEJM198707023170101. N Engl J Med. 1987. PMID: 3587308

6

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. Lancet. 1993 May 29;341(8857):1422. Lancet. 1993. PMID: 8098837 No abstract available.

7

[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. Bull Cancer. 1993 Oct;80(10):857-65. Bull Cancer. 1993. PMID: 8204923 French.

8

Germ line mutation at BRCA1 affects the histoprognostic grade in hereditary breast cancer.

Eisinger F, Stoppa-Lyonnet D, Longy M, Kerangueven F, Noguchi T, Bailly C, Vincent-Salomon A, Jacquemier J, Birnbaum D, Sobol H. Eisinger F, et al. Cancer Res. 1996 Feb 1;56(3):471-4. Cancer Res. 1996. PMID: 8564955

9

Segregation of two BRCA1 mutations in a single family.

Stoppa-Lyonnet D, Fricker JP, Essioux L, Pages S, Limacher JM, Sobol H, Laurent-Puig P, Thomas G. Stoppa-Lyonnet D, et al. Am J Hum Genet. 1996 Aug;59(2):479-81. Am J Hum Genet. 1996. PMID: 8755940 Free PMC article. No abstract available.

10

Truncation at conserved terminal regions of BRCA1 protein is associated with highly proliferating hereditary breast cancers.

Sobol H, Stoppa-Lyonnet D, Bressac-de-Paillerets B, Peyrat JP, Kerangueven F, Janin N, Noguchi T, Eisinger F, Guinebretiere JM, Jacquemier J, Birnbaum D. Sobol H, et al. Cancer Res. 1996 Jul 15;56(14):3216-9. Cancer Res. 1996. PMID: 8764110

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