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CHEK2 1100delC mutation is frequent among Russian breast cancer patients.
Chekmariova EV, Sokolenko AP, Buslov KG, Iyevleva AG, Ulibina YM, Rozanov ME, Mitiushkina NV, Togo AV, Matsko DE, Voskresenskiy DA, Chagunava OL, Devilee P, Cornelisse C, Semiglazov VF, Imyanitov EN. Chekmariova EV, et al. Among authors: ulibina ym. Breast Cancer Res Treat. 2006 Nov;100(1):99-102. doi: 10.1007/s10549-006-9227-7. Epub 2006 Jun 7. Breast Cancer Res Treat. 2006. PMID: 16758118
High frequency of BRCA1 5382insC mutation in Russian breast cancer patients.
Sokolenko AP, Mitiushkina NV, Buslov KG, Bit-Sava EM, Iyevleva AG, Chekmariova EV, Kuligina ESh, Ulibina YM, Rozanov ME, Suspitsin EN, Matsko DE, Chagunava OL, Trofimov DY, Devilee P, Cornelisse C, Togo AV, Semiglazov VF, Imyanitov EN. Sokolenko AP, et al. Among authors: ulibina ym. Eur J Cancer. 2006 Jul;42(10):1380-4. doi: 10.1016/j.ejca.2006.01.050. Epub 2006 Jun 5. Eur J Cancer. 2006. PMID: 16737811
Combined CYP1A1/GSTM1 at-risk genotypes are overrepresented in squamous cell lung carcinoma patients but underrepresented in elderly tumor-free subjects.
Belogubova EV, Ulibina YM, Suvorova IK, Kuligina ESh, Karpova MB, Shutkin VA, Koloskov AV, Kuchinskiy AP, Togo AV, Hanson KP, Hirvonen A, Imyanitov EN. Belogubova EV, et al. Among authors: ulibina ym. J Cancer Res Clin Oncol. 2006 May;132(5):327-31. doi: 10.1007/s00432-005-0071-7. Epub 2006 Jan 14. J Cancer Res Clin Oncol. 2006. PMID: 16416283
Large family with both parents affected by distinct BRCA1 mutations: implications for genetic testing.
Sokolenko AP, Voskresenskiy DA, Iyevleva AG, Bit-Sava EM, Gutkina NI, Anisimenko MS, Yu Sherina N, Mitiushkina NV, Ulibina YM, Yatsuk OS, Zaitseva OA, Suspitsin EN, Togo AV, Pospelov VA, Kovalenko SP, Semiglazov VF, Imyanitov EN. Sokolenko AP, et al. Among authors: ulibina ym. Hered Cancer Clin Pract. 2009 Jan 26;7(1):2. doi: 10.1186/1897-4287-7-2. Hered Cancer Clin Pract. 2009. PMID: 19338681 Free PMC article.