Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Konstantin G, Buslov"'
Autor:
Tatiana V. Gorodnova, Peter Devilee, Evgeny N. Imyanitov, Aglaya G. Iyevleva, Karin Kroeze, Nienke van der Stoep, Konstantin G. Buslov, Alexandr V. Togo, Evgeny N. Suspitsin, Sergey P. Kovalenko, Anna P. Sokolenko, Dmitry A. Voskresenskiy
Publikováno v:
Cancer Letters, 298(2), 258-263
A few founder BRCA1 mutations (5382insC 4154delA 185delAG) account for up to 15% of high-risk (young-onset or familial or bilateral) breast cancer (BC) cases in Russia The impact of non founder BRCA1 mutations in this country is less studied in parti
Autor:
Cees J. Cornelisse, Evgeny N. Imyanitov, Oleg L. Chagunava, Ekatherina Sh. Kuligina, Dmitry Yu. Trofimov, Matsko De, Vladimir Semiglazov, Peter Devilee, Natalia V. Mitiushkina, Aglaya G. Iyevleva, Elena M. Bit-Sava, Yulia M. Ulibina, Anna P. Sokolenko, Elena V. Chekmariova, Alexandr V. Togo, Konstantin G. Buslov, Maxim E. Rozanov, Evgeny N. Suspitsin
Publikováno v:
European Journal of Cancer. 42:1380-1384
BRCA1 5382insC variant was repeatedly detected in Jewish breast cancer (BC) families residing in USA and Israel as well as in non-Jewish familial BC patients from Poland, Latvia, Hungary, Russia and some other European countries. However, the distrib
Autor:
Vladimir Semiglazov, Evgeny N. Imyanitov, Anna P. Sokolenko, Dmitry A. Voskresenskiy, Matsko De, Yulia M. Ulibina, Natalia V. Mitiushkina, Maxim E. Rozanov, Aglaya G. Iyevleva, Oleg L. Chagunava, Peter Devilee, Alexandr V. Togo, Konstantin G. Buslov, Elena V. Chekmariova, Cees J. Cornelisse
Publikováno v:
Breast Cancer Research and Treatment. 100:99-102
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 (2.1%) unilateral BC cases and in 8/155 (5.2%) patients with the bilateral form of the disea
Autor:
Anna P. Sokolenko, Evgeny N. Suspitsin, Cees J. Cornelisse, Elena M. Bit-Sava, Peter Devilee, Oleg L. Chagunava, Yulia R. Lazareva, Vladimir Semiglazov, Konstantin G. Buslov, Matsko De, Evgeny N. Imyanitov, Turkevich Ea, Aglaya G. Iyevleva, Alexandr V. Togo, Kaido P. Hanson, Ekatherina Sh. Kuligina, Elena V. Chekmariova
Publikováno v:
International Journal of Cancer. 114:585-589
The gene for Nijmegen chromosomal breakage syndrome (NBS1) plays a role in a variety of processes protecting chromosomal stability. Recently, it was suggested in a Polish case-control study that the founder hypomorphic mutation in NBS1, 657del5, whic
Autor:
Vera B. Gamajunova, Evgeniya V. Belogubova, Alexandr V. Togo, Maria B. Karpova, Konstantin G. Buslov, Anatolij Ju Kovalevskij, Lev M. Berstein, Evgeny N. Imyanitov, Irina G. Kovalenko, Ekatherina Sh. Kuligina, Oleg N Volkov
Publikováno v:
Cancer Letters. 180:47-53
Initiation and/or promotion of endometrial cancer is known to be associated with estrogen and androgen (androstenedione) excess as well as with hyperinsulinemia/insulin resistance. It is possible that some allelic polymorphisms of the genes involved
Autor:
Alexey Samtsov, Alexandr V. Moshkalov, Alexandr V. Togo, Konstantin G. Buslov, Kaido P. Hanson, Ekatherina Sh. Kuligina, Vladislav R. Hairutdinov, Evgeny N. Imyanitov, Natalia V. Mitiushkina, Evgeny N. Suspitsin
Publikováno v:
Journal of Dermatological Science. 37:185-187
Autor:
Konstantin G. Buslov, Vladimir M. Moiseyenko, Aglaya G. Iyevleva, Alexandr V. Togo, Matsko De, Evgeny N. Imyanitov, Vasily P. Filimonenko
Publikováno v:
Onkologie. 30(6)
Measurement of intratumoral expression of dihydropyrimidine dehydrogenase (DPD) and thymidylate synthase (TS) may have some value in predicting the response to fluoropyrimidine-containing therapy. Patients and Methods: We attempted to validate this a
Autor:
Natalia V. Mitiushkina, Alexandr V. Togo, Evgeny N. Imyanitov, Konstantin G. Buslov, Anna P. Sokolenko, Dmitry A. Voskresenskiy, Elena M. Bit-Sava, Elena V. Chekmariova, Vladimir Semiglazov, Aglaya G. Iyevleva, E. S. Shilov, Maxim E. Rozanov, Cees J. Cornelisse, Natalia Yu. Sherina, Oleg L. Chagunava, Peter Devilee
Publikováno v:
Familial cancer. 6(3)
Previous studies indicate that founder mutations may play a noticeable role in breast cancer (BC) predisposition in Russia. Here we performed a systematic analysis of eight recurrent mutations in 302 BC cases (St.-Petersburg, Russia), which were sele
Autor:
Konstantin G. Buslov, Evgeny N. Imyanitov, Evgeny N. Suspitsin, Olga A. Zaitseva, Maxim Yu. Grigoriev, Ekatherina Sh. Kuligina, Alexandr V. Togo, Yulia R. Lazareva, Olga S. Yatsuk
Publikováno v:
Journal of cancer research and clinical oncology. 133(1)
High-frequency microsatellite instability (MSI-H) occurs frequently in colorectal cancers and some other tumor types, but is very uncommon in breast cancer. In the earlier study devoted to microsatellite analysis of allelic imbalances, the authors ac
Autor:
Vladislav R, Hairutdinov, Alexandr V, Moshkalov, Alexey V, Samtsov, Konstantin G, Buslov, Ekatherina Sh, Kuligina, Natalia V, Mitiushkina, Evgeny N, Suspitsin, Alexandr V, Togo, Kaido P, Hanson, Evgeny N, Imyanitov
Publikováno v:
Journal of dermatological science. 37(3)