Zobrazeno 1 - 10
of 23
pro vyhledávání: '"A. S. Kolobkov"'
Autor:
Maryam B. Khadzhieva, Alesya S. Gracheva, Olesya B. Belopolskaya, Dmitry S. Kolobkov, Darya A. Kashatnikova, Ivan V. Redkin, Artem N. Kuzovlev, Andrey V. Grechko, Lyubov E. Salnikova
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Rare variants affecting host defense against pathogens may be involved in COVID-19 severity, but most rare variants are not expected to have a major impact on the course of COVID-19. We hypothesized that the accumulation of weak effects of many rare
Externí odkaz:
https://doaj.org/article/6c5a8d79b5684c93910fc6a79f42a04b
Autor:
Maryam B. Khadzhieva, Dmitry S. Kolobkov, Darya A. Kashatnikova, Alesya S. Gracheva, Ivan V. Redkin, Artem N. Kuzovlev, Lyubov E. Salnikova
Publikováno v:
Biomolecules, Vol 13, Iss 9, p 1380 (2023)
The development of severe COVID-19, which is a complex multisystem disease, is thought to be associated with many genes whose action is modulated by numerous environmental and genetic factors. In this study, we focused on the ideas of the omnigenic m
Externí odkaz:
https://doaj.org/article/db0727a1864a4da29f46b2640cb60311
Publikováno v:
Voprosy Materialovedeniya. :67-78
The article describes the stage-by-stage development of Russian aramid fibers. The differences between the third generation of Rusar NT fibers and CBM and Ruslan fibers are described. In this work, we studied the resistance of a structural organoplas
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
Abstract Pelvic organ prolapse (POP) is a highly disabling condition common for a vast number of women worldwide. To contribute to existing knowledge in POP pathogenesis, we performed a systematic review of expression studies on both specific gene an
Externí odkaz:
https://doaj.org/article/21e8d92602404051b5c18bd13883e3e9
Publikováno v:
Human Genetics. 140:1379-1393
Primary immunodeficiencies (PID) are a diverse group of genetic disorders caused by inadequate development and function of immune system. Identifying genetic etiology is important for genetic counselling and treatment decisions. Clinical relevance of
Autor:
Dmitry S. Kolobkov, Darya A. Sviridova, Serikbai K. Abilev, Artem N. Kuzovlev, Lyubov E. Salnikova
Publikováno v:
Genes; Volume 13; Issue 7; Pages: 1168
Results of expression studies can be useful to clarify the genotype-phenotype relationship. However, according to data from recent literature, there is a large group of genes that are revealed as differentially expressed (DE) in many studies, regardl
Autor:
Artem Kuzovlev, Sal'nikova Le, Maryam B. Khadzhieva, S. K. Abilev, Dmitry S. Kolobkov, Alesya S. Gracheva
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-14 (2020)
Scientific Reports
Scientific Reports
Dysregulation in cytokine production has been linked to the pathogenesis of various immune-mediated traits, in which genetic variability contributes to the etiopathogenesis. GWA studies have identified many genetic variants in or near cytokine genes,
Autor:
A. S. Kolobkov, S. S. Malakhovskii
Publikováno v:
Fibre Chemistry. 52:1-5
The general development and current state of technology for producing carbon fibers is considered. The potential of improving the performance of carbon fibers and the promising areas of development of technologies for the production of carbon fiber m
Autor:
Darya A. Kashatnikova, Maryam B. Khadzhieva, Dmitry S. Kolobkov, Olesya B. Belopolskaya, Tamara V. Smelaya, Alesya S. Gracheva, Ekaterina V. Kalinina, Sergey S. Larin, Artem N. Kuzovlev, Lyubov E. Salnikova
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 17; Pages: 9896
Pneumonia is an acute infectious disease with high morbidity and mortality rates. Pneumonia’s development, severity and outcome depend on age, comorbidities and the host immune response. In this study, we combined theoretical and experimental inves
Publikováno v:
Human genetics. 140(9)
Primary immunodeficiencies (PID) are a diverse group of genetic disorders caused by inadequate development and function of immune system. Identifying genetic etiology is important for genetic counselling and treatment decisions. Clinical relevance of