Search Results - "Voskresenskiy, Dmitry A."

Mixed epithelial/mesenchymal metaplastic carcinoma (carcinosarcoma) of the breast in BRCA1 carrier by Suspitsin, Evgeny N., Sokolenko, Anna P., Voskresenskiy, Dmitry A., Ivantsov, Alexandr O., Shelehova, Kseniya V., Klimashevskiy, Valery F., Matsko, Dmitry E., Semiglazov, Vladimir F., Imyanitov, Evgeny N.

“…This case report describes a 35-year-old woman who was diagnosed with mixed epithelial/mesenchymal metaplastic carcinoma (carcinosarcoma) of the breast…”
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Founder mutations in early-onset, familial and bilateral breast cancer patients from Russia by Sokolenko, Anna P, Rozanov, Maxim E, Mitiushkina, Natalia V, Sherina, Natalia Yu, Iyevleva, Aglaya G, Chekmariova, Elena V, Buslov, Konstantin G, Shilov, Evgeny S, Togo, Alexandr V, Bit-Sava, Elena M, Voskresenskiy, Dmitry A, Chagunava, Oleg L, Devilee, Peter, Cornelisse, Cees, Semiglazov, Vladimir F, Imyanitov, Evgeny N

“…Previous studies indicate that founder mutations may play a noticeable role in breast cancer (BC) predisposition in Russia. Here we performed a systematic…”
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Paired distribution of molecular subtypes in bilateral breast carcinomas by Russnes, Hege G, Kuligina, Ekatherina Sh, Suspitsin, Evgeny N, Voskresenskiy, Dmitry A, Jordanova, Ekaterina S, Cornelisse, Cees J, Borresen-Dale, Anne-Lise, Imyanitov, Evgeny N

“…The last decade has revealed fundamental new insight into the existence of intrinsic molecular subclasses of breast carcinomas. By using immunostaining on…”
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Non-founder BRCA1 mutations in Russian breast cancer patients by Iyevleva, Aglaya G, Suspitsin, Evgeny N, Kroeze, Karin, Gorodnova, Tatiana V, Sokolenko, Anna P, Buslov, Konstantin G, Voskresenskiy, Dmitry A, Togo, Alexandr V, Kovalenko, Sergey P, Stoep, Nienke van der, Devilee, Peter, Imyanitov, Evgeny N

“…Abstract A few founder BRCA1 mutations (5382insC, 4154delA, 185delAG) account for up to 15% of high-risk (young-onset or familial or bilateral) breast cancer…”
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Large family with both parents affected by distinct BRCA1 mutations: implications for genetic testing by Sokolenko, Anna P, Voskresenskiy, Dmitry A, Iyevleva, Aglaya G, Bit-Sava, Elena M, Gutkina, Nadezhda I, Anisimenko, Maxim S, Yu Sherina, Nathalia, Mitiushkina, Nathalia V, Ulibina, Yulia M, Yatsuk, Olga S, Zaitseva, Olga A, Suspitsin, Evgeny N, Togo, Alexandr V, Pospelov, Valery A, Kovalenko, Sergey P, Semiglazov, Vladimir F, Imyanitov, Evgeny N

“…Although the probability of both parents being affected by BRCA1 mutations is not negligible, such families have not been systematically described in the…”
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CHEK2 1100delC mutation is frequent among Russian breast cancer patients by Chekmariova, Elena V, Sokolenko, Anna P, Buslov, Konstantin G, Iyevleva, Aglaya G, Ulibina, Yulia M, Rozanov, Maxim E, Mitiushkina, Natalia V, Togo, Alexandr V, Matsko, Dmitry E, Voskresenskiy, Dmitry A, Chagunava, Oleg L, Devilee, Peter, Cornelisse, Cees, Semiglazov, Vladimir F, Imyanitov, Evgeny N

“…This study was aimed to assess the role of CHEK2 1100delC mutation in breast cancer (BC) predisposition in Russia. The 1100delC allele was detected in 14/660…”
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Distribution of Coding Apoptotic Gene Polymorphisms in Women with Extreme Phenotypes of Breast Cancer Predisposition and Tolerance by Ulybina, Yulia M, Kuligina, Ekatherina S, Mitiushkina, Nathalia V, Sherina, Nathalia Y, Baholdin, Dmitry V, Voskresenskiy, Dmitry A, Polyakov, Igor S, Togo, Alexandr V, Semiglazov, Vladimir F, Imyanitov, Evgeny N

“…Aims and background Comparison of subjects with extreme phenotypes of cancer susceptibility and tolerance allows to detect low-penetrance gene-disease…”
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Distribution of coding apoptotic gene polymorphisms in women with extreme phenotypes of breast cancer predisposition and tolerance by Ulybina, Yulia M, Kuligina, Ekatherina S, Mitiushkina, Nathalia V, Sherina, Nathalia Y, Baholdin, Dmitry V, Voskresenskiy, Dmitry A, Polyakov, Igor S, Togo, Alexandr V, Semiglazov, Vladimir F, Imyanitov, Evgeny N

“…AIMS AND BACKGROUNDComparison of subjects with extreme phenotypes of cancer susceptibility and tolerance allows to detect low-penetrance gene-disease…”
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CHEK2 1100delC mutation is frequent among Russian breast cancer patients by CHEKMARIOVA, Elena V, SOKOLENKO, Anna P, CHAGUNAVA, Oleg L, DEVILEE, Peter, CORNELISSE, Cees, SEMIGLAZOV, Vladimir F, IMYANITOV, Evgeny N, BUSLOV, Konstantin G, IYEVLEVA, Aglaya G, ULIBINA, Yulia M, ROZANOV, Maxim E, MITIUSHKINA, Natalia V, TOGO, Alexandr V, MATSKO, Dmitry E, VOSKRESENSKIY, Dmitry A

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