Zobrazeno 1 - 10
of 63
pro vyhledávání: '"Oleg S. Glotov"'
Autor:
Yulia S. Koshevaya, Mariia E. Turkunova, Anastasia O. Vechkasova, Elena A. Serebryakova, Maxim Yu. Donnikov, Svyatoslav I. Papanov, Alexander N. Chernov, Lev N. Kolbasin, Lyudmila V. Kovalenko, Andrey S. Glotov, Oleg S. Glotov
Publikováno v:
Current Issues in Molecular Biology, Vol 46, Iss 5, Pp 4106-4118 (2024)
Osteogenesis imperfecta (OI) is a group of inherited disorders of connective tissue that cause significant deformities and fragility in bones. Most cases of OI are associated with pathogenic variants in collagen type I genes and are characterized by
Externí odkaz:
https://doaj.org/article/c9c348e41fe94a8ca1e5079e95152198
Autor:
Evgeniia M. Maksiutenko, Valeriia Merkureva, Yury A. Barbitoff, Victoria V. Tsay, Mikhail V. Aseev, Andrey S. Glotov, Oleg S. Glotov
Publikováno v:
Physiological Reports, Vol 12, Iss 8, Pp n/a-n/a (2024)
Abstract Adaptation of humans to challenging environmental conditions, such as extreme temperature, malnutrition, or hypoxia, is an interesting phenomenon for both basic and applied research. Identification of the genetic factors contributing to huma
Externí odkaz:
https://doaj.org/article/1d731a852f9f4c87b42004487ddc58a9
Autor:
Maria V. Golubenko, Elena N. Pavlyukova, Ramil R. Salakhov, Oksana A. Makeeva, Konstantin V. Puzyrev, Oleg S. Glotov, Valery P. Puzyrev, Maria S. Nazarenko
Publikováno v:
Frontiers in Bioscience-Scholar, Vol 16, Iss 1, p 1 (2024)
Background: Hypertrophic cardiomyopathy is the most frequent autosomal dominant disease, yet due to genetic heterogeneity, incomplete penetrance, and phenotype variability, the prognosis of the disease course in pathogenic variant carriers remains an
Externí odkaz:
https://doaj.org/article/04fb8a3a8c6a467fbe527dddb81c2689
Autor:
Oleg V. Goloshchapov, Oksana B. Shchukina, Aleksey V. Kusakin, Viktoria V. Tsai, Roman S. Kalinin, Yury A. Eismont, Oleg S. Glotov, Alexei B. Chukhlovin
Publikováno v:
Pathogens, Vol 12, Iss 12, p 1438 (2023)
Inflammatory bowel diseases (IBD) and acute graft-versus-host disease (GVHD) are associated with persistent intestinal dysfunction preceded by gut bacterial dysbiosis. There are limited data on intestinal bacteriophages in these conditions. The aim o
Externí odkaz:
https://doaj.org/article/9f3cd899de294fc6a08a145f1e51bfeb
Autor:
Andrey S. Glotov, Vyacheslav B. Chernykh, Olga A. Solovova, Aleksander V. Polyakov, Maksim Yu. Donnikov, Ludmila V. Kovalenko, Yury A. Barbitoff, Yulia A. Nasykhova, Tatyana E. Lazareva, Oleg S. Glotov
Publikováno v:
Genes, Vol 15, Iss 1, p 45 (2023)
A male factor, commonly associated with poor semen quality, is revealed in about 50% of infertile couples. CFTR gene (Cystic Fibrosis Transmembrane Conduction Regulator) variants are one of the common genetic causes of azoospermia-related male infert
Externí odkaz:
https://doaj.org/article/2c596666a67148d288dbe7a6e76a7d88
Publikováno v:
Journal of Personalized Medicine, Vol 13, Iss 8, p 1236 (2023)
Today, whole-exome sequencing (WES) is used to conduct the massive screening of structural and regulatory genes in order to identify the allele frequencies of disease-associated polymorphisms in various populations and thus detect pathogenic genetic
Externí odkaz:
https://doaj.org/article/6b77f1553de14ad1b88d135c2a8700ae
Autor:
Alexei B. Chukhlovin, Vasilisa V. Dudurich, Aleksey V. Kusakin, Dmitry E. Polev, Ekaterina D. Ermachenko, Mikhail V. Aseev, Yuri A. Zakharov, Yuri A. Eismont, Lavrentii G. Danilov, Oleg S. Glotov
Publikováno v:
Microorganisms, Vol 11, Iss 7, p 1813 (2023)
Bacterial microbiota in stool may vary over a wide range, depending on age, nutrition, etc. The purpose of our work was to discriminate phyla and genera of intestinal bacteria and their biodiversity within a healthy population (North-Western Russia)
Externí odkaz:
https://doaj.org/article/7f7d2738ac2440ef9dbc2f21f406225c
Autor:
Anna Yu. Anisenkova, Svetlana V. Apalko, Zakhar P. Asaulenko, Alexander N. Bogdanov, Dmitry A. Vologzhanin, Evgenii Y. Garbuzov, Oleg S. Glotov, Tatyana A. Kamilova, Olga A. Klitsenko, Evdokiia M. Minina, Sergei V. Mosenko, Dmitry N. Khobotnikov, Sergey G. Sсherbak
Publikováno v:
Клиническая практика, Vol 12, Iss 1, Pp 5-15 (2021)
Background: According to WHO, as of March 31, 2021, 127 877 462 confirmed cases of the new COVID-19 coronavirus infection were registered in the world, including 2 796 561 deaths (WHO Coronavirus Disease). COVID-19 is characterized by a wide range of
Externí odkaz:
https://doaj.org/article/edbcf24a5b4c4822bd2d72c974def3ec
Autor:
Mariia E. Turkunova, Yury A. Barbitoff, Elena A. Serebryakova, Dmitrii E. Polev, Olga S. Berseneva, Elena B. Bashnina, Vladislav S. Baranov, Oleg S. Glotov, Andrey S. Glotov
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Introduction: Floating Harbor syndrome (FHS) is an extremely rare disorder, with slightly more than a hundred cases reported worldwide. FHS is caused by heterozygous mutations in the SRCAP gene; however, little is known about the pathogenesis of FHS
Externí odkaz:
https://doaj.org/article/315a146fb9c64f6f8b773c8657802a5f
Autor:
Aleksey V. Kusakin, Olga V. Goleva, Lavrentii G. Danilov, Andrey V. Krylov, Victoria V. Tsay, Roman S. Kalinin, Natalia S. Tian, Yuri A. Eismont, Anna L. Mukomolova, Alexei B. Chukhlovin, Aleksey S. Komissarov, Oleg S. Glotov
Publikováno v:
Genes, Vol 14, Iss 2, p 521 (2023)
Human herpes virus 6A (HHV-6A) is able to integrate into the telomeric and subtelomeric regions of human chromosomes representing chromosomally integrated HHV-6A (ciHHV-6A). The integration starts from the right direct repeat (DRR) region. It has bee
Externí odkaz:
https://doaj.org/article/6d9f25f18f3b42e38a31edcb71138523