Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Maximov Sergey"'
Publikováno v:
E3S Web of Conferences, Vol 164, p 03046 (2020)
The article presents the results of research in the field of ensuring the performance of complex technical objects on the example of transport and technological machines (TTM), which include transport equipment, as well as technological machines (exc
Externí odkaz:
https://doaj.org/article/938588a99a454b2d900d610382a92b1a
Publikováno v:
E3S Web of Conferences, Vol 210, p 13030 (2020)
The Russian competition law does not include the definition of the concept of collective dominance, and the notion of this institution itself contains many gaps. The indicated disadvantages of statutory regulation and simplified approaches of the Fed
Externí odkaz:
https://doaj.org/article/4f1e5bb541e74c048fd95b1124c9918a
Autor:
Krylova Nadezhda, Ponomariova Daria N, Sherina Natalia, Ogorodnikova Natalia, Logvinov Denis A, Porhanova Natalia V, Lobeiko Oksana S, Urmancheyeva Adel F, Maximov Sergey, Togo Alexandr V, Suspitsin Evgeny N, Imyanitov Evgeny N
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 5, Iss 3, Pp 153-156 (2007)
Abstract BRCA1 and BRCA2 germ-line mutations occur in a significant number of unselected ovarian cancer (OC) patients, thus making a noticeable contribution to OC morbidity. It is of interest whether CHEK2, which is frequently regarded as a third bre
Externí odkaz:
https://doaj.org/article/6fde968f46e443e7b3507c375317fd89
Autor:
Krylova Nadezhda, Lobeiko Oksana S, Sokolenko Anna P, Iyevleva Aglaya G, Rozanov Maxim E, Mitiushkina Natalia V, Gergova Madina M, Porhanova Tatiana V, Urmancheyeva Adel F, Maximov Sergey, Togo Alexandr V, Imyanitov Evgeny N
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 4, Iss 4, Pp 193-196 (2006)
Abstract The BRCA1 4153delA allele is frequently referred to as the Russian founder mutation, as it was initially detected in several cancer families from Moscow. Our earlier studies have demonstrated 1% occurrence of BRCA1 4153delA heterozygosity in
Externí odkaz:
https://doaj.org/article/59f420f9b52041e888275da6e8cbb3b8
Autor:
Suspitsin Evgeny N, Sherina Nathalia, Ponomariova Daria N, Sokolenko Anna P, Iyevleva Aglaya G, Gorodnova Tatyana V, Zaitseva Olga A, Yatsuk Olga S, Togo Alexandr V, Tkachenko Nathalia N, Shiyanov Grigory A, Lobeiko Oksana S, Krylova Nadezhda, Matsko Dmitry E, Maximov Sergey, Urmancheyeva Adel F, Porhanova Nathalia V, Imyanitov Evgeny N
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 7, Iss 1, p 5 (2009)
Abstract Background A significant portion of ovarian cancer (OC) cases is caused by germ-line mutations in BRCA1 or BRCA2 genes. BRCA testing is cheap in populations with founder effect and therefore recommended for all patients with OC diagnosis. Re
Externí odkaz:
https://doaj.org/article/bdf87e8757ba49f0a03bbb28c435b737
Autor:
Chubenko, Eugene B., Maximov, Sergey E., Bui, Cong Doan, Pham, Van Tung, Borisenko, Victor E.
Publikováno v:
In Materialia May 2023 28
Akademický článek
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Autor:
Gorodnova, Tatiana V., Sokolenko, Anna P., Ivantsov, Alexandr O., Iyevleva, Aglaya G., Suspitsin, Evgeny N., Aleksakhina, Svetlana N., Yanus, Grigory A., Togo, Alexandr V., Maximov, Sergey Ya., Imyanitov, Evgeny N. *
Publikováno v:
In Cancer Letters 28 December 2015 369(2):363-367
Akademický článek
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