Sobol H - Search Results

1

Sublocalization of smallest common regions of deletion on chromosome 17q12-q23 in sporadic primary breast-tumors.

Champeme M, Mazoyer S, Stoppalyonnet D, Bieche I, Ithier G, Sobol H, Nogues C, Lidereau R. Champeme M, et al. Among authors: sobol h. Oncol Rep. 1995 Sep;2(5):825-31. doi: 10.3892/or.2.5.825. Oncol Rep. 1995. PMID: 21597825

2

Genetic heterogeneity of early-onset familial breast cancer.

Sobol H, Mazoyer S, Narod SA, Smith SA, Black DM, Kerbrat P, Jamot B, Solomon E, Ponder BA, Guerin D. Sobol H, et al. Hum Genet. 1992 Jun;89(4):381-3. doi: 10.1007/BF00194307. Hum Genet. 1992. PMID: 1352270

3

Linkage analysis of 19 French breast cancer families, with five chromosome 17q markers.

Mazoyer S, Lalle P, Narod SA, Bignon YJ, Courjal F, Jamot B, Dutrillaux B, Stoppa-Lyonnett D, Sobol H. Mazoyer S, et al. Among authors: sobol h. Am J Hum Genet. 1993 Apr;52(4):754-60. Am J Hum Genet. 1993. PMID: 8096359 Free PMC article.

4

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

5

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. Among authors: sobol h. Oncogene. 1994 Apr;9(4):1237-9. Oncogene. 1994. PMID: 8134127

6

Familial ovarian carcinoma: pedigree studies and preliminary results from linkage analysis.

Sobol H, Mazoyer S, Smith SA, Lyonnet D, Bignon YJ, Narod SA, Ardoin A, Biron P, Bobin JY, Bremond A, et al. Sobol H, et al. Bull Cancer. 1993 Feb;80(2):121-34. Bull Cancer. 1993. PMID: 8173163

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

9

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

10

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: sobol h. Cancer Res. 1998 Apr 15;58(8):1588-92. Cancer Res. 1998. PMID: 9563465

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