Noguchi T - Search Results

1

First large rearrangement in the MUTYH gene and attenuated familial adenomatous polyposis syndrome.

Rouleau E, Zattara H, Lefol C, Noguchi T, Briaux A, Buecher B, Bourdon V, Sobol H, Lidereau R, Olschwang S. Rouleau E, et al. Among authors: noguchi t. Clin Genet. 2011 Sep;80(3):301-3. doi: 10.1111/j.1399-0004.2011.01699.x. Clin Genet. 2011. PMID: 21815886 No abstract available.

2

Familial hematological malignancies: ASXL1 gene investigation.

Hamadou WS, Abed RE, Besbes S, Bourdon V, Fabre A, Youssef YB, Laatiri MA, Eisinger F, Mari V, Gesta P, Dreyfus H, Bonadona V, Dugast C, Zattara H, Faivre L, Jemni SY, Noguchi T, Khélif A, Sobol H, Soua Z. Hamadou WS, et al. Among authors: noguchi t. Clin Transl Oncol. 2016 Apr;18(4):385-90. doi: 10.1007/s12094-015-1379-7. Epub 2015 Aug 19. Clin Transl Oncol. 2016. PMID: 26286068

3

Three novel BRCA2 germline mutations (1864 delT, 6132 del4, 8208 del5) detected in breast cancer families identified in the south of France.

Noguchi T, Sauvan R, Moyal-Amsellem N, Boubli L, Eisinger F, Birnbaum D, Sobol H. Noguchi T, et al. Hum Mutat. 2001 Feb;17(2):155. doi: 10.1002/1098-1004(200102)17:2<155::AID-HUMU14>3.0.CO;2-F. Hum Mutat. 2001. PMID: 11180605 No abstract available.

4

Novel indications for BRCA1 screening using individual clinical and morphological features.

Eisinger F, Noguès C, Guinebretière JM, Peyrat JP, Bardou VJ, Noguchi T, Vennin P, Sauvan R, Lidereau R, Birnbaum D, Jacquemier J, Sobol H. Eisinger F, et al. Among authors: noguchi t. Int J Cancer. 1999 Jun 21;84(3):263-7. doi: 10.1002/(sici)1097-0215(19990621)84:3<263::aid-ijc11>3.0.co;2-g. Int J Cancer. 1999. PMID: 10371344

5

Three novel BRCA1 germline mutations (1104delAA, 1276delTT, 3747delGA) detected in breast/ovarian cancer families identified in the south of France.

Sauvan R, Noguchi T, Moyal-Amsellem N, Serin D, Eisinger F, Birnbaum D, Sobol H. Sauvan R, et al. Among authors: noguchi t. Hum Mutat. 2001 Feb;17(2):154. doi: 10.1002/1098-1004(200102)17:2<154::AID-HUMU13>3.0.CO;2-L. Hum Mutat. 2001. PMID: 11180604 No abstract available.

6

A novel germline in frame deletion (4128del3) of the BRCA2 gene detected in a breast/ovarian cancer family with fallopian tube and brain tumors identified in the north of France.

Demange L, Noguchi T, Sauvan R, Moyal-Amsellem N, Birnbaum D, Eisinger F, Sobol H. Demange L, et al. Among authors: noguchi t. Hum Mutat. 2001 Feb;17(2):155. doi: 10.1002/1098-1004(200102)17:2<155::AID-HUMU15>3.0.CO;2-C. Hum Mutat. 2001. PMID: 11180606 No abstract available.

7

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: noguchi t. Fam Cancer. 2009;8(4):581-4. doi: 10.1007/s10689-009-9289-x. Fam Cancer. 2009. PMID: 19731081

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

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: noguchi t. 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: noguchi t. Ann Endocrinol (Paris). 1998;59(6):459-64. Ann Endocrinol (Paris). 1998. PMID: 10189988 Review. French.

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