Zobrazeno 1 - 10
of 519
pro vyhledávání: '"V. Strelnikov"'
Autor:
K. E. Ponomarev, I. V. Strelnikov
Publikováno v:
Космические аппараты и технологии, Vol 7, Iss 2, Pp 126-131 (2023)
The possibility of using vibration technologies as an alternative to heat treatment, but having a shorter duration, low energy consumption, low capital costs and comparable efficiency, is substantiated. Priority areas of application of methods of vib
Externí odkaz:
https://doaj.org/article/a758e1a1e4cd4d4ba862751d9f75873d
Autor:
V. V. Berestov, K. Yu. Orlov, A. L. Krivoshapkin, N. V. Strelnikov, A. I. Somova, D. S. Kislitsin, A. V. Gorbatykh, P. O. Seleznev, T. S. Shayakhmetov, L. M. Kirillov
Publikováno v:
Сибирский научный медицинский журнал, Vol 41, Iss 4, Pp 40-47 (2021)
The necessity of quick surgical treatment of acute ruptured cerebral aneurysms was demonstrated in large studies by the ISAT and ISUIA, which also proved the advantage of the endovascular method over the surgical one. Ballonassistence is widely used
Externí odkaz:
https://doaj.org/article/b42f88ae592f416e92e87cec8f0496c1
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract The main types of thyroid neoplasms, follicular adenoma (FA), follicular thyroid carcinoma (FTC), classical and follicular variants of papillary carcinoma (clPTC and fvPTC), and anaplastic thyroid carcinoma (ATC), differ in prognosis, progre
Externí odkaz:
https://doaj.org/article/72b9d3fe521f46efad58e14192f452eb
Autor:
Vladimir V. Strelnikov, Ekaterina B. Kuznetsova, Alexander S. Tanas, Viktoria V. Rudenko, Alexey I. Kalinkin, Elena V. Poddubskaya, Tatiana V. Kekeeva, Galina G. Chesnokova, Ivan D. Trotsenko, Sergey S. Larin, Sergey I. Kutsev, Dmitry V. Zaletaev, Marina V. Nemtsova, Olga A. Simonova
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Abstract Cell transmembrane receptors and extracellular matrix components play a pivotal role in regulating cell activity and providing for the concerted integration of cells in the tissue structures. We have assessed DNA methylation in the promoter
Externí odkaz:
https://doaj.org/article/9674b2bcc0154773b10c7499d5ce84fc
Autor:
N. N. Mazurenko, I. V. Tsyganova, V. V. Strelnikov, A. V. Balbutsky, T. F. Malivanova, E. B. Kuznetsova, V. A. Draudin-Krilenko, O. V. Shangina, A. F. Mukeria, V. B. Matveev, D. G. Zaridze
Publikováno v:
Успехи молекулярной онкологии, Vol 7, Iss 3, Pp 48-57 (2020)
The VHL gene alterations are the early and characteristic feature of clear cell renal cell carcinoma (ccRCC). We have examined VHL mutations in sporadic 98 ccRCC cases to evaluate their localization in relation to functionally important motifs of the
Externí odkaz:
https://doaj.org/article/43a48e3e9d274851a601ba363f0cb505
Autor:
M. E. Ivanova, I. V. Zolnikova, I. E. Khatsenko, V. V. Strelnikov, F. A. Konovalov, E. R. Lozier, M. A. Ampleeva, A. V. Antonets, I. V. Kanivets, K. V. Gorgisheli, D. S. Atarshchikov, D. V. Pyankov, S. A. Korostelev, E. B. Kuznetsova, D. Bar, L. M. Balashova, Zh. M. Salmasi
Publikováno v:
Российский офтальмологический журнал, Vol 13, Iss 1, Pp 12-22 (2020)
Achromatopsia (ACHM) is a rare autosomal recessive disease. Its mutation spectrum is well described in other populations, but the data on ACHM prevalence and features in Russia are insufficient. Purpose. To describe clinically and genetically the Rus
Externí odkaz:
https://doaj.org/article/92260456696c478c91e15c42a02ce1d3
Autor:
E. L. Dadali, I. A. Akimova, F. A. Konovalov, P. A. Shatalov, A. Yu. Krasnenko, V. V. Strelnikov, M. A. Ampleeva
Publikováno v:
Русский журнал детской неврологии, Vol 14, Iss 3, Pp 28-36 (2020)
Early infantile epileptic encephalopathies (EIEE) are a group of disorders characterized by pharmacoresistant epileptic seizures manifesting in infancy and leading to psychomotor retardation. The most common genetic variant with X-linked dominant inh
Externí odkaz:
https://doaj.org/article/7d166f3ebe3242d7ac29da480525e283
Autor:
О. Е. Andreeva, V. О. Sigin, V. V. Strelnikov, A. S. Tanas, A. M. Scherbakov, M. A. Krasilnikov
Publikováno v:
Сибирский онкологический журнал, Vol 18, Iss 5, Pp 45-53 (2019)
Abstract Introduction. We have previously shown the feasibility of hormonal resistance horizontal distribution from cell to cell, with the joint cultivation of sensitive and resistant cells and/or through exosomes secreted by resistant cells. What is
Externí odkaz:
https://doaj.org/article/9729f0103a7845e3b9701d8f57c8986b
Autor:
N. L. Sheremet, I. G. Grushke, N. V. Zhorzholadze, I. A. Ronzina, A. A. Mikaelyan, S. A. Kurbatov, V. V. Kadyshev, K. I. Anoshkin, V. V. Strelnikov
Publikováno v:
Сибирский научный медицинский журнал, Vol 38, Iss 5, Pp 65-71 (2019)
Purpose of the study was to assess the spectrum of molecular genetic disorders and the variety of clinical forms in patients with Stargardt disease. Material and methods. 56 patients aged 15-44 years who had been diagnosed with Stargardt disease in a
Externí odkaz:
https://doaj.org/article/dd9051f9de144ecca4e63b03284bd4cb
Autor:
Dmitry S. Mikhaylenko, Alexey V. Klimov, Vsevolod B. Matveev, Svetlana I. Samoylova, Vladimir V. Strelnikov, Dmitry V. Zaletaev, Ludmila N. Lubchenko, Boris Y. Alekseev, Marina V. Nemtsova
Publikováno v:
Frontiers in Oncology, Vol 9 (2020)
Hereditary papillary renal carcinoma (HPRC) is a rare autosomal dominant disease characterized by the development of multiple papillary type I renal cell carcinomas. This hereditary kidney cancer form is caused by activating mutations in MET. Descrip
Externí odkaz:
https://doaj.org/article/2377b74b1e024c23b906cfc4a1da5af4