Zobrazeno 1 - 10
of 245
pro vyhledávání: '"Matsko De"'
Autor:
Matsko Mv, Evgeny N. Imyanitov, A. A. Zrelov, Malik Tastanbekov, S. S. Skliar, A. O. Baksheeva, A. Yu. Ulitin, Matsko De
Publikováno v:
Translational Medicine. 5:44-52
Background. Gemistocytic astrocytomas (GA) are a variant of diffuse astrocytomas GII (WHO, 2016), which is characterized by a shorter overall survival of patients than diffuse astrocytoma. The role of vascular endothelial growth factor (VEGF) gene ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5851b2cd864a478adec5eb7a4097505d
https://doi.org/10.18705/2311-4495-2018-5-1-44-52
https://doi.org/10.18705/2311-4495-2018-5-1-44-52
Autor:
Vitaly V Egorenkov, Marina V Matsko, Aglaya G. Iyevleva, Valery A Kheinstein, Ksenya V. Shelekhova, Anastasia M. Konstantinova, Evgeny N. Imyanitov, Matsko De
Publikováno v:
International Journal of Surgical Pathology. 26:364-369
Primary extraspinal myxopapillary ependymoma (MPE) is an exceptionally rare lesion that is mainly located in the subcutaneous sacrococcygeal region. We describe the first case of MPE that presented as an intramuscular tumor mass located in the lumbar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb46b2a54b3386590f372fb3208b76da
https://doi.org/10.1177/1066896917748195
https://doi.org/10.1177/1066896917748195
Autor:
Viktor I. Novik, Natalia V. Mitiushkina, Alexandr V. Togo, Aglaya G. Iyevleva, A. Poltoratskiy, Alexandr O. Ivantsov, Igor S. Polyakov, Sergey V. Orlov, Matsko De, Evgeny N. Imyanitov
Publikováno v:
Cancer Cytopathology. 121:370-376
BACKGROUND Although the molecular analysis of epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) in archived lung cancer tissues is relatively well established, the genetic testing of cytological material has not yet become
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b39b87930251dd8cfd973a73c02deffe
https://doi.org/10.1002/cncy.21281
https://doi.org/10.1002/cncy.21281
High prevalence and breast cancer predisposing role of the BLM c.1642 C>T (Q548X) mutation in Russia
Autor:
Alexey Larionov, Werner Pfeifer, Sergey G. Kuznetsov, Alexandr O. Ivantsov, Matsko De, Nathalia V. Mitiushkina, Elena V. Preobrazhenskaya, Dmitry V Voskresenskiy, Aglaya G. Iyevleva, Evgeny N. Imyanitov, Ekatherina Sh. Kuligina, Alexandr V. Togo, Evgeny N. Suspitsin, Anna P. Sokolenko, Georgy D Dolmatov, Turkevich Ea, Svetlana N. Abysheva, Iduna Fichtner, Elena M. Bit-Sava, Antonis C. Antoniou, Tatiana V. Gorodnova, Vladimir Semiglazov
Publikováno v:
International Journal of Cancer. 130:2867-2873
The BLM gene belongs to the RecQ helicase family and has been implicated in the maintenance of genomic stability. Its homozygous germline inactivation causes Bloom syndrome, a severe genetic disorder characterized by growth retardation, impaired fert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6f931b7e4c697b5c9fc64d441a7648b
https://doi.org/10.1002/ijc.26342
https://doi.org/10.1002/ijc.26342
Autor:
Nathalia Yu. Sherina, Igor I. Semionov, Vladimir M. Moiseyenko, Alexandr V. Togo, Ekatherina Sh. Kuligina, Pavel I. Krzhivitskiy, Anna P. Sokolenko, Aglaya G. Iyevleva, Madina M. Gergova, Nikita V. Brezhnev, Svetlana Protsenko, Eduard D. Gershveld, Matsko De, Marina A. Hudyakova, Sergey Ya Maximov, Oksana S Lobeiko, Evgeny N. Imyanitov, Evgeny N. Suspitsin
Publikováno v:
Cancer Genetics and Cytogenetics. 197:91-94
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d87bece0c0037b6f9c62e8c8c54d7f26
https://doi.org/10.1016/j.cancergencyto.2009.10.003
https://doi.org/10.1016/j.cancergencyto.2009.10.003
Autor:
Alexandr O. Ivantsov, Vladimir M. Moiseyenko, Evgeny N. Imyanitov, Igor I. Semionov, Aglaya G. Iyevleva, Valentin V. Anisimov, Stepan M. Yargnian, Evgeny Levchenko, Matsko De
Publikováno v:
Onkologie. 32:674-677
Non-small cell lung carcinomas (NSCLC) carrying a mutation in the epidermal growth factor receptor (EGFR) gene show unprecedented sensitivity to gefitinib or erlotinib.We present the follow-up data of 2 EGFR mutation-positive stage IV NSCLC patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6693cffb5d2a702c9904ed2e2cff768f
https://doi.org/10.1159/000242220
https://doi.org/10.1159/000242220
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:
Alexandr A. Bessonov, Olga A. Zaitseva, Anna P. Sokolenko, Alexandr V. Togo, Evgeny N. Imyanitov, Tatiana Yu. Semiglazova, Olga N. Potapova, Sergey A. Laptiev, Alexandr O. Ivantsov, Matsko De, Werner Pfeifer, Olga S. Yatsuk
Publikováno v:
Breast cancer research and treatment. 148(3)
Breast carcinomas caused by inheritance of cancer-predisposing germ-line mutations have specific bioclinical features. This study aimed to analyze the efficacy of conventional cytotoxic treatment in BRCA1 and CHEK2 mutation carriers and non-carriers.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7009c0d5d0c8052e3b8e385721e6d626
https://pubmed.ncbi.nlm.nih.gov/25414026
https://pubmed.ncbi.nlm.nih.gov/25414026