Sobol H - Search Results

1

Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-year medical genetics service to French patients with FAP.

Lagarde A, Rouleau E, Ferrari A, Noguchi T, Qiu J, Briaux A, Bourdon V, Rémy V, Gaildrat P, Adélaïde J, Birnbaum D, Lidereau R, Sobol H, Olschwang S. Lagarde A, et al. Among authors: sobol h. J Med Genet. 2010 Oct;47(10):721-2. doi: 10.1136/jmg.2010.078964. Epub 2010 Aug 3. J Med Genet. 2010. PMID: 20685668 Free article.

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

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.

4

[Genetics and cancer of the breast].

Sobol H, Bignon YJ, Eisinger F, Birnbaum D, Fervers B. Sobol H, et al. Ann Chir. 1994;48(4):303-8. Ann Chir. 1994. PMID: 8085754 Review. French.

5

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

6

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

7

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

8

Attitudes towards cancer predictive testing and transmission of information to the family.

Julian-Reynier C, Eisinger F, Vennin P, Chabal F, Aurran Y, Noguès C, Bignon YJ, Machelard-Roumagnac M, Maugard-Louboutin C, Serin D, Blanc B, Orsoni P, Sobol H. Julian-Reynier C, et al. Among authors: sobol h. J Med Genet. 1996 Sep;33(9):731-6. doi: 10.1136/jmg.33.9.731. J Med Genet. 1996. PMID: 8880571 Free PMC article.

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 Free article. French. No abstract available.

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