Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Krylova, Nadezhda"'
Autor:
Kiselev, Anton, Maretina, Marianna, Shtykalova, Sofia, Al-Hilal, Haya, Maslyanyuk, Natalia, Plokhih, Mariya, Serebryakova, Elena, Frolova, Marina, Shved, Natalia, Krylova, Nadezhda, Il'ina, Arina, Freund, Svetlana, Osinovskaya, Natalia, Sultanov, Iskender, Egorova, Anna, Lobenskaya, Anastasia, Koroteev, Alexander, Sosnina, Irina, Gorelik, Yulia, Bespalova, Olesya
Publikováno v:
International Journal of Neonatal Screening (IJNS); Mar2024, Vol. 10 Issue 1, p9, 11p
Akademický článek
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Autor:
Shuvaev Vyacheslav, Krylova Nadezhda
Publikováno v:
MATEC Web of Conferences, Vol 224, p 01052 (2018)
In work the questions of hardening of a surface layer of a detail by means of ultrasonic fluctuations are opened. The developed device for forming ultrasonic longitudinal-torsional oscillations is described, which makes it possible to substantially m
Externí odkaz:
https://doaj.org/article/9244f60427fb4a2fad3bfd3b4cd1fac5
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
Publikováno v:
Relevant lines of scientific research: theory and practice
Актуальные направления научных исследований: перспективы развития
Актуальные направления научных исследований: перспективы развития
В статье рассмотрены актуальные вопросы применения риск-ориентированного подхода. Проанализированы несовершенства и уязвимости нацио
Autor:
KRYLOVA, Nadezhda
This article focuses primarily on the photographic collection of the Police Department, currently hosted by the State Archive of the Russian Federation (GARF). Special attention is given to its isolation and new links, established by the archivists w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12d1ee3ede2b344b95dcdd91f1037018
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
Akademický článek
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Publikováno v:
Diffusion and Defect Data Part A: Defect and Diffusion Forum; November 2017, Vol. 380 Issue: 1 p98-106, 9p