Zobrazeno 1 - 10
of 215
pro vyhledávání: '"S A Mikhailova"'
Autor:
D. V. Martynov, T. T. Valiev, A. A. Odzharova, Yu. E. Ryabukhina, P. A. Zeynalova, S. N. Mikhailova
Publikováno v:
Онкогематология, Vol 19, Iss 3, Pp 199-205 (2024)
Plasmoblastic lymphoma is a rare, aggressive B-cell malignancy with poor long-term survival. Plasmoblastic lymphoma occurs most commonly in patients infected with human immunodeficiency virus (HIV), but cases associated with solid organ transplantati
Externí odkaz:
https://doaj.org/article/f08d87375c20415abe8eebc67d3b5594
Publikováno v:
RUDN Journal of Medicine, Vol 0, Iss S6, Pp 48-50 (2013)
Proton pump inhibitors are new most effective remedies for the treatment of gastric ulcer and duodenal ulcer. Analysis results of proton pump inhibitors assortment on the regional market are presented in the article.
Externí odkaz:
https://doaj.org/article/8c84fbc4a7b5401c8792b23935571020
Autor:
S. V. Mikhailova
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 27, Iss 6, Pp 684-693 (2023)
The review describes the main methods for assessing directional selection in human populations. These include bioinformatic analysis of DNA sequences via detection of linkage disequilibrium and of deviations from the random distribution of frequencie
Externí odkaz:
https://doaj.org/article/b5ed370901f945cbabe62144886ab1dc
Autor:
S. V. Mikhailova, D. E. Ivanoshchuk, P. S. Orlov, L. D. Latyntseva, E. V. Kashtanova, Ya. V. Polonskaya, Yu. I. Ragino, E. V. Shakhtshneider
Publikováno v:
Сибирский научный медицинский журнал, Vol 43, Iss 4, Pp 97-109 (2023)
Understanding the molecular mechanisms of atherosclerotic vascular lesions formation is necessary both for assessing the risks of cardiovascular diseases and for finding approaches to their therapy. The task remains relevant, despite the large number
Externí odkaz:
https://doaj.org/article/be3a3dc8ca524b2d87b367c32de1539d
Publikováno v:
Труды по прикладной ботанике, генетике и селекции, Vol 184, Iss 2, Pp 213-225 (2023)
Members of the Brassicaceae family are of great significance as weeds and invasive plants; they are one of the leading families of the alien fraction in the segetal floras of various regions of Russia. Among the cruciferous weeds growing over Russia,
Externí odkaz:
https://doaj.org/article/8775d01ef51e445eb16586ee71afa605
Autor:
T. A. Gremyakova, S. V. Artemyeva, N. D. Vashakmadze, I. P. Vitkovskaya, V. I. Guzeva, O. V. Guzeva, L. M. Kuzenkova, S. V. Mikhailova, L. P. Nazarenko, T. M. Pervunina, N. L. Pechatnikova, T. V. Podkletnova, G. E. Sakbaeva, A. A. Stepanov, V. M. Suslov, O. I. Gremyakova, N. I. Shakhovskaya, S. S. Nikitin
Publikováno v:
Нервно-мышечные болезни, Vol 12, Iss 2, Pp 10-18 (2022)
Duchenne muscular dystrophy (DMD) is a fatal neuromuscular disease due to a mutation in the gene encoding dystrophin synthesis. In patients, muscle damage and atrophy progresses, the ability to move independently decreases as well as respiratory and
Externí odkaz:
https://doaj.org/article/2d5cb1f3844a45cb95295db2a3337785
Autor:
E. Yu. Zakharova, S. V. Mikhailova, V. V. Zarubina, N. A. Krasnoshchekova, N. L. Pechatnikova, V. P. Vorontsova, D. I. Gribov, M. V. Zazivihina, А. N. Slatetskaya, M. V. Kurkina, P. V. Baranova, L. P. Nazarenko, S. А. Repina, L. R. Selimsyanova, N. D. Vashakmadse, T. V. Bushueva
Publikováno v:
Нервно-мышечные болезни, Vol 11, Iss 4, Pp 12-25 (2021)
Treatment of many of the diseases in the panel of expanded newborn screening includes dietary therapy. Glutaric aciduria type 1 (GA1) is a hereditary disorder caused by mutations in the gene GCDH, encoding glutaryl‑CoA dehydrogenase, an enzyme in t
Externí odkaz:
https://doaj.org/article/75dd2591077642beb4663d43ddbd4823
Autor:
V. V. Prokopenko, T. I. Kabakova, M. V. Chernikov, A. B. Goryachev, S. A. Mikhailova, O. I. Knysh
Publikováno v:
Фармация и фармакология (Пятигорск), Vol 9, Iss 5, Pp 400-409 (2021)
the aim. Focused on optimizing the assortment portfolio of pharmacy organizations and improving the process of drug supply to end-consumers, the aim of the study was to analyze the regional pharmaceutical market for antihistamines.Materials and metho
Externí odkaz:
https://doaj.org/article/1d3ff6eb65b24403bb4c955ce199e185
Autor:
S. V. Mikhailova, E. V. Saifullina, P. V. Baranova, V. P. Vorontsova, D. I. Gribov, M. V. Zhivihina, A. N. Slatetskaya, R. V. Magzhanov, V. A. Samokhvalov, M. N. Virtseva, L. P. Borscheva, E. E. Koh, M. V. Novikova, A. V. Abrukova, E. Yu. Belyashova, N. Yu. Gerasimenko, L. V. Guseva, Zh. V. Yukhimenko, N. V. Nikitina, T. I. Belyaeva, T. A. Shkurko, N. A. Pichkur, V. S. Kakaulina, N. L. Pechatnikova, N . A. Polyakova, S. A. Korostelev, D. V. Pyankov, I. V. Kanivets, N. A. Demina, E. Yu. Pyrkova, G. V. Baidakova, M. V. Kurkina, E. Yu. Zakharova
Publikováno v:
Нервно-мышечные болезни, Vol 11, Iss 2, Pp 61-79 (2021)
Background. Glutaric aciduria type 1 is an autosomal recessive disease caused by mutations in the GCDH gene, which encodes the enzyme glutaryl‑CoA dehydrogenase. Metabolic crisis in type 1 glutaric aciduria is an acute life‑threatening condition
Externí odkaz:
https://doaj.org/article/7260ea8a4de74abc9f7f0ad19298c84e
Publikováno v:
Вавиловский журнал генетики и селекции, Vol 25, Iss 3, Pp 301-309 (2021)
The innate Iнн\mmune system is the first to respond to invading pathogens. It is responsible for invader recognition, immune-cell recruitment, adaptive-immunity activation, and regulation of inflammation intensity. Previously, two single-nucleotide
Externí odkaz:
https://doaj.org/article/0198774aa51d44c7b53459bebeb888c1