Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Elena V. Chekmariova"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a77c037911244a954bdd689bd1227eb7
https://doi.org/10.1016/j.ejca.2006.01.050
https://doi.org/10.1016/j.ejca.2006.01.050
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79cf2bfc46a647bda81991ffbf501a67
https://doi.org/10.1007/s10549-006-9227-7
https://doi.org/10.1007/s10549-006-9227-7
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d91e89dd1b0b49755e745fe5922b0e34
https://doi.org/10.1002/ijc.20765
https://doi.org/10.1002/ijc.20765
Autor:
Carl Blomqvist, Hanne Meijers-Heijerboer, Muhammad Usman Rashid, Laura J. van't Veer, Thilo Dörk, Alan Ashworth, Nichola Johnson, Outi Kilpivaara, Isabel dos Santos Silva, Julian Peto, Evgeny N. Imyanitov, Olivia Fletcher, Anna P. Sokolenko, Heli Nevanlinna, Christina Justenhoven, Annegien Broeks, Hiltrud Brauch, Marjanka K. Schmidt, Michael Bremer, Ute Hamann, Marijke Wasielewski, Kristiina Aittomäki, Elena V. Chekmariova
Publikováno v:
Cancer epidemiology, biomarkers & prevention, 18(1), 230-234. American Association for Cancer Research Inc.
If breast cancers arise independently in each breast the odds ratio (OR) for bilateral breast cancer for carriers of CHEK2*1100delC should be ∼5.5, the square of the reported OR for a first primary (OR, 2.34). In the subset of bilateral cases with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee67ac5d5f77035c7eaec16b0d2251de
https://europepmc.org/articles/PMC2727696/
https://europepmc.org/articles/PMC2727696/
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f3ab248b5b9bbf6bcd7d9164f1721e2
https://pubmed.ncbi.nlm.nih.gov/17333477
https://pubmed.ncbi.nlm.nih.gov/17333477
Autor:
Evgeny N. Imyanitov, Jos H.H. Thijssen, Anatolij Ju Kovalevskij, Anna P. Sokolenko, Dmitry A Vasilyev, Aglaya G. Iyevleva, Konstantin G. Buslov, Lev M Berstein, Sergei Maximov, Elena V. Chekmariova
Publikováno v:
Cancer letters. 207(2)
Excessive estrogenic influence is known to be associated with initiation/promotion of endometrial cancer (EC). Allelic polymorphisms of the genes involved in steroidogenesis/steroid metabolism may contribute to EC susceptibility. It is important to k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f14b0acb36ed17045d5324fcc2a956dd
https://pubmed.ncbi.nlm.nih.gov/15072828
https://pubmed.ncbi.nlm.nih.gov/15072828
Autor:
Svetlana N. Abysheva, Evgeny N. Suspitsin, Evgeny N. Imyanitov, Aglaya G. Iyevleva, Anna P. Sokolenko, Elena V. Chekmariova, Ekaterina Sh Kuligina
Publikováno v:
Cancer Research. 72:2597-2597
Major hereditary breast cancer (BC) genes, BRCA1 and BRCA2, contribute to no more than 20-25% of familial BC clustering; therefore the majority of BC-predisposing mutations remain to be identified. We have selected for the study 95 BC cases, which sh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47f0bf90873608a6666b21354897de06
https://doi.org/10.1158/1538-7445.am2012-2597
https://doi.org/10.1158/1538-7445.am2012-2597