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Mutational analysis of BRCA1 and BRCA2 and clinicopathologic analysis of ovarian cancer in 82 ovarian cancer families: two common founder mutations of BRCA1 in Japanese population.
Sekine M, Nagata H, Tsuji S, Hirai Y, Fujimoto S, Hatae M, Kobayashi I, Fujii T, Nagata I, Ushijima K, Obata K, Suzuki M, Yoshinaga M, Umesaki N, Satoh S, Enomoto T, Motoyama S, Tanaka K; Japanese Familial Ovarian Cancer Study Group. Sekine M, et al. Among authors: kobayashi i. Clin Cancer Res. 2001 Oct;7(10):3144-50. Clin Cancer Res. 2001. PMID: 11595708
Screening of BRCA1 mutation using immunohistochemical staining with C-terminal and N-terminal antibodies in familial ovarian cancers.
Kashima K, Oite T, Aoki Y, Takakuwa K, Aida H, Nagata H, Sekine M, Wu HJ, Hirai Y, Wada Y, Yamamoto K, Hasegawa K, Sonoda T, Maruo T, Nagata I, Ohno M, Suzuki M, Kobayashi I, Kuzuya K, Takahashi T, Torii Y, Tanaka K. Kashima K, et al. Among authors: kobayashi i. Jpn J Cancer Res. 2000 Apr;91(4):399-409. doi: 10.1111/j.1349-7006.2000.tb00959.x. Jpn J Cancer Res. 2000. PMID: 10804288 Free PMC article.
Localization of a novel susceptibility gene for familial ovarian cancer to chromosome 3p22-p25.
Sekine M, Nagata H, Tsuji S, Hirai Y, Fujimoto S, Hatae M, Kobayashi I, Fujii T, Nagata I, Ushijima K, Obata K, Suzuki M, Yoshinaga M, Umesaki N, Satoh S, Enomoto T, Motoyama S, Tanaka K; Japanese Familial Ovarian Cancer Study Group. Sekine M, et al. Among authors: kobayashi i. Hum Mol Genet. 2001 Jun 15;10(13):1421-9. doi: 10.1093/hmg/10.13.1421. Hum Mol Genet. 2001. PMID: 11440995
1,575 results