Zobrazeno 1 - 10
of 69
pro vyhledávání: '"E A Dunaeva"'
Autor:
N. V. Vlasenko, T. A. Loscutova, K. O. Mironov, A. S. Esman, E. A. Dunaeva, T. A. Semenenko, D. B. Dubodelov, M. I. Korabelnikova, Z. B. Ponezheva, V. V. Makashova, K. G. Omarova, A. V. Sacuk, G. G. Solopova, S. N. Kuzin, V. G. Akimkin
Publikováno v:
Эпидемиология и вакцинопрофилактика, Vol 22, Iss 2, Pp 55-65 (2023)
Relevance. The identification of determinants of the human genome, such as single nucleotide polymorphisms (SNPs), in association with various disease patterns, including infectious diseases, is one of the most actively developing areas of scientific
Externí odkaz:
https://doaj.org/article/f745bad8240b41f6be99a852c36b2e88
Autor:
T. N. Subbotina, I. E. Maslyukova, K. S. Semashchenko, G. A. Khodos, D. V. Kurochkin, A. A. Shalyova, M. A. Mikhalev, E. V. Vasiliev, M. G. Osadchaya, E. A. Dunaeva, A. S. Esman, K. O. Mironov
Publikováno v:
Онкогематология, Vol 18, Iss 1, Pp 63-75 (2023)
Background. The development of myelofibrosis (MF) is driven by complex molecular genetic events that include driver somatic mutations responsible for the constitutive activation of the JAK/STAT signaling pathway (JAK2, CALR, and MPL), additional muta
Externí odkaz:
https://doaj.org/article/271d47d097ae4504ac8bd87fab744cd1
Autor:
N. V. Vlasenko, N. S. Churilova, T. A. Loskutova, K. O. Mironov, A. S. Esman, E. A. Dunaeva, T. A. Semenenko, Z. S. Rodionova, I. G. Nikitin, A. V. Tutelian, S. N. Kuzin, V. G. Akimkin
Publikováno v:
Журнал микробиологии, эпидемиологии и иммунобиологии, Vol 99, Iss 2, Pp 149-159 (2022)
Introduction. Hepatitis B retains the status of socially significant infection and remains a major health problem worldwide, including the Russian Federation. The improvement of the effectiveness of the current complex of preventive measures, especia
Externí odkaz:
https://doaj.org/article/c53ef1c9d8f44287b4e899b3e624b20a
Autor:
T. N. Subbotina, I. E. Maslyukova, D. V. Kurochkin, M. A. Mikhalev, M. G. Osadchaya, V. A. Khorzhevskiy, T. A. Garkusha, E. A. Dunaeva, K. O. Mironov
Publikováno v:
Онкогематология, Vol 17, Iss 2, Pp 30-35 (2022)
JAK2 mutations can be associated with any phenotypic form of chronic myeloproliferative neoplasia, while MPL and CALR mutations occur, as a rule, in cases of essential thrombocythemia and primary myelofibrosis and they are not observed in polycythemi
Externí odkaz:
https://doaj.org/article/47182056f2d748148f454fefc5457c9c
Autor:
O. P. Dribnokhodova, E. A. Dunaeva, G. V. Leshkina, E. A. Yarygina, A. Yu. Bukharina, Ya. A. Voiciehovskaya, E. V. Borisova, S. K. Bormotova, A. I. Daoud, V. N. Khlavich, K. O. Mironov
Publikováno v:
Сибирский онкологический журнал, Vol 20, Iss 5, Pp 75-83 (2021)
Introduction. Detection of somatic mutations in the BRAF gene can be used in clinical oncology to clarify the diagnosis, select therapy and assess the prognosis of the disease. Pyrosequencing technology makes it possible to identify both already know
Externí odkaz:
https://doaj.org/article/c9a2a247394241b89a9ae6d39e726c46
Autor:
T. N. Subbotina, D. V. Kurochkin, I. E. Maslyukova, A. S. Khazieva, E. V. Vasiliev, M. A. Mikhalev, E. A. Dunaeva, K. O. Mironov
Publikováno v:
Онкогематология, Vol 16, Iss 2, Pp 48-55 (2021)
Background. In accordance with the World health organization clinical guidelines, the analysis of somatic mutations in the CALR gene, as well as mutations in the JAK2 and MPL genes, are included in the list of criteria for the Ph-myeloproliferative n
Externí odkaz:
https://doaj.org/article/43c934e311f744ed94dab242733f6db9
Autor:
T. N. Subbotina, I. E. Maslyukova, A. A. Faleeva, P. A. Nikolaeva, A. S. Khazieva, E. A. Dunaeva, K. O. Mironov, L. B. Polushkina, I. S. Martynkevich, S. V. Vereshchagina, B. V. Barankin
Publikováno v:
Онкогематология, Vol 15, Iss 2, Pp 85-91 (2020)
Background. There are problems related to both quantitative assessment of an allele burden level of a mutant gene and interpretation of results in DNA samples with the burden level of the mutant allele less than 15–20 %, when using Sanger sequencin
Externí odkaz:
https://doaj.org/article/bc3b0376a2864fffaa914ecdf25e92fa
Autor:
L. I. Melnikova, L. Yu. Ilchenko, E. A. Dunaeva, M. V. Kozitsyna, O. P. Dribnokhodova, K. O. Mironov
Publikováno v:
Архивъ внутренней медицины, Vol 9, Iss 6, Pp 475-482 (2019)
Relevance. Gilbert’s syndrome (GS) is a disease with an autosomal recessive type of inheritance caused by either impaired expression of the UGT1A1 gene, which encodes the isoform of the uridine-5-diphosphate glucuronosyltransferase (UDP-GTA1), or s
Externí odkaz:
https://doaj.org/article/619d874e4e5e4775ae4a72bf3b5c03ba
Autor:
E. V. DUNAEVA
Publikováno v:
Контуры глобальных трансформаций: политика, экономика, право, Vol 11, Iss 4, Pp 169-189 (2018)
The article is devoted to the role of Shiite clergy in the Islamic revolution and in the political life of Islamic Republic of Iran. The author attempts to analize the possibilities of the Islamic regime’s survival in the context of modernizing soc
Externí odkaz:
https://doaj.org/article/94b9de22011442a581c82b996a1cafb0
Autor:
I. А. Olkhovskiy, M. A. Stolyar, Yu. Yu. Komarovskiy, A. S. Gorbenko, V. I. Korchagin, E. A. Dunaeva, K. O. Mironov, V. I. Bakhtina, T. I. Olkhovik, E. V. Vasiliev, M. A. Mikhalev
Publikováno v:
Russian journal of hematology and transfusiology. 67:377-387
Introduction. Haplotype JAK2 46/1 is associated with more frequent development of Ph-negative myeloproliferative neoplasms (MPN) and with an increased detection rate of the JAK2 V617F mutation. At the same time, the molecular mechanisms of such assoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f77c73190051f30e010f0b9a114adb70
https://doi.org/10.35754/0234-5730-2022-67-3-377-387
https://doi.org/10.35754/0234-5730-2022-67-3-377-387