Jacquemier J - Search Results

1

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. Among authors: jacquemier j. Cancer Res. 1996 Jul 15;56(14):3216-9. Cancer Res. 1996. PMID: 8764110

2

Major improvement in the efficacy of BRCA1 mutation screening using morphoclinical features of breast cancer.

Lidereau R, Eisinger F, Champème MH, Noguès C, Bièche I, Birnbaum D, Pallud C, Jacquemier J, Sobol H. Lidereau R, et al. Among authors: jacquemier j. Cancer Res. 2000 Mar 1;60(5):1206-10. Cancer Res. 2000. PMID: 10728676

3

PS2 expression in BRCA1-associated breast cancers.

Charafe-Jauffre E, Eisinger F, Mathoulin-Portier MP, Sobol H, Jacquemier J. Charafe-Jauffre E, et al. Among authors: jacquemier j. Anticancer Res. 2001 Jul-Aug;21(4B):2877-81. Anticancer Res. 2001. PMID: 11712780

4

BRCA1-p53 relationship in hereditary breast cancer.

Sobol H, Stoppalyonnet D, Bressacdepaillerets B, Peyrat J, Guinebretiere J, Jacquemier J, Eisinger F, Birnbaum D. Sobol H, et al. Among authors: jacquemier j. Int J Oncol. 1997 Feb;10(2):349-53. doi: 10.3892/ijo.10.2.349. Int J Oncol. 1997. PMID: 21533383

5

Patterns of loss of heterozygosity at loci from chromosome arm 13q suggests a possible involvement of BRCA2 in sporadic breast tumors.

Kerangueven F, Allione F, Noguchi T, Adélaïde J, Sobol H, Jacquemier J, Birnbaum D. Kerangueven F, et al. Among authors: jacquemier j. Genes Chromosomes Cancer. 1995 Aug;13(4):291-4. doi: 10.1002/gcc.2870130410. Genes Chromosomes Cancer. 1995. PMID: 7547638

6

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. Among authors: jacquemier j. Cancer Res. 1996 Feb 1;56(3):471-4. Cancer Res. 1996. PMID: 8564955

7

Loss of heterozygosity in human breast carcinomas in the ataxia telangiectasia, Cowden disease and BRCA1 gene regions.

Kerangueven F, Eisinger F, Noguchi T, Allione F, Wargniez V, Eng C, Padberg G, Theillet C, Jacquemier J, Longy M, Sobol H, Birnbaum D. Kerangueven F, et al. Among authors: jacquemier j. Oncogene. 1997 Jan 23;14(3):339-47. doi: 10.1038/sj.onc.1200818. Oncogene. 1997. PMID: 9018120 Free article.

8

Genome-wide search for loss of heterozygosity shows extensive genetic diversity of human breast carcinomas.

Kerangueven F, Noguchi T, Coulier F, Allione F, Wargniez V, Simony-Lafontaine J, Longy M, Jacquemier J, Sobol H, Eisinger F, Birnbaum D. Kerangueven F, et al. Among authors: jacquemier j. Cancer Res. 1997 Dec 15;57(24):5469-74. Cancer Res. 1997. PMID: 9407952

9

Mutations at BRCA1: the medullary breast carcinoma revisited.

Eisinger F, Jacquemier J, Charpin C, Stoppa-Lyonnet D, Bressac-de Paillerets B, Peyrat JP, Longy M, Guinebretière JM, Sauvan R, Noguchi T, Birnbaum D, Sobol H. Eisinger F, et al. Among authors: jacquemier j. Cancer Res. 1998 Apr 15;58(8):1588-92. Cancer Res. 1998. PMID: 9563465

10

[Impact of recent oncogenetic progress on the management of high risk breast cancer patients: the example of BRCA1 and BRCA2 genes].

Sobol H, Eisinger F, Sauvan R, Noguchi T, Jacquemier J, Birnbaum D. Sobol H, et al. Among authors: jacquemier j. Ann Endocrinol (Paris). 1998;59(6):459-64. Ann Endocrinol (Paris). 1998. PMID: 10189988 Review. French.

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