Sobol H - Search Results

1

Molecular study of CEBPA in familial hematological malignancies.

El Abed R, Bourdon V, Huiart L, Eisinger F, Khelif A, Frenay M, Gesta P, Demange L, Dreyfus H, Bonadona V, Dugast C, Zattara H, Faivre L, Noguchi T, Sauvan R, Soua Z, Sobol H. El Abed R, et al. Among authors: sobol h. Fam Cancer. 2009;8(4):581-4. doi: 10.1007/s10689-009-9289-x. Fam Cancer. 2009. PMID: 19731081

2

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: sobol h. Genes Chromosomes Cancer. 1995 Aug;13(4):291-4. doi: 10.1002/gcc.2870130410. Genes Chromosomes Cancer. 1995. PMID: 7547638

3

[Genetics and screening perspectives in subjects at risk].

Eisinger F, Seitz JF, Sobol H. Eisinger F, et al. Among authors: sobol h. Ann Gastroenterol Hepatol (Paris). 1995 Mar-Apr;31(2):78-81. Ann Gastroenterol Hepatol (Paris). 1995. PMID: 7618847 Review. French. No abstract available.

4

Histoprognostic grade in BRCA1-associated breast cancer.

Jacquemier J, Eisinger F, Birnbaum D, Sobol H. Jacquemier J, et al. Among authors: sobol h. Lancet. 1995 Jun 10;345(8963):1503. doi: 10.1016/s0140-6736(95)91060-3. Lancet. 1995. PMID: 7769911 No abstract available.

5

Evidence for a third breast-cancer susceptibility gene.

Sobol H, Birnbaum D, Eisinger F. Sobol H, et al. Lancet. 1994 Oct 22;344(8930):1151-2. doi: 10.1016/s0140-6736(94)90655-6. Lancet. 1994. PMID: 7934505 No abstract available.

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

7

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

8

Integrated map of the chromosome 8p12-p21 region, a region involved in human cancers and Werner syndrome.

Imbert A, Chaffanet M, Essioux L, Noguchi T, Adélaïde J, Kerangueven F, Le Paslier D, Bonaïti-Pellié C, Sobol H, Birnbaum D, Pébusque MJ. Imbert A, et al. Among authors: sobol h. Genomics. 1996 Feb 15;32(1):29-38. doi: 10.1006/geno.1996.0073. Genomics. 1996. PMID: 8786118

9

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: sobol h. Oncogene. 1997 Jan 23;14(3):339-47. doi: 10.1038/sj.onc.1200818. Oncogene. 1997. PMID: 9018120 Free article.

10

[Molecular typing of tumors: possibilities and problems].

Birnbaum D, Penault-Llorca F, Eisinger F, Sobol H. Birnbaum D, et al. Among authors: sobol h. Bull Cancer. 1997 Aug;84(8):835-6. Bull Cancer. 1997. PMID: 9339191 French. No abstract available.

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