Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Olga, Favorova"'
Autor:
Natalia Matveeva, Ivan Kiselev, Natalia Baulina, Ekaterina Semina, Viktor Kakotkin, Mikhail Agapov, Olga Kulakova, Olga Favorova
Publikováno v:
Frontiers in Aging Neuroscience, Vol 15 (2023)
The severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2) and the сoronavirus disease 2019 (COVID-19) have become a global health threat. At the height of the pandemic, major efforts were focused on reducing COVID-19-associated morbid
Externí odkaz:
https://doaj.org/article/13dcbabd14cf4ff485ded993db1bdcf3
Publikováno v:
Journal of Translational Medicine, Vol 18, Iss 1, Pp 1-11 (2020)
Abstract Background Myocardial infarction (MI) is one of the most severe manifestations of coronary artery disease (CAD) and the leading cause of death from non-infectious diseases worldwide. It is known that the central component of CAD pathogenesis
Externí odkaz:
https://doaj.org/article/11633c0e34ca4fc9a0c416d131cfa86d
Autor:
Ivan Kiselev, Maxim Kozin, Natalia Baulina, Maria Pisklova, Ludmila Danilova, Alexandr Zotov, Olga Chumakova, Dmitry Zateyshchikov, Olga Favorova
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 23, p 15280 (2022)
Hypertrophic cardiomyopathy (HCM) is the most common inherited heart disease; its pathogenesis is still being intensively studied to explain the reasons for the significant genetic and phenotypic heterogeneity of the disease. To search for new genes
Externí odkaz:
https://doaj.org/article/6b75a19631d5424fbd82dc5513da2c3a
Autor:
Boris Titov, Natalya Matveeva, Olga Kulakova, Natalia Baulina, Elizaveta Bazyleva, Grigory Kheymets, Anatolii Rogoza, Alexander Pevzner, Olga Favorova
Publikováno v:
Genes, Vol 13, Iss 9, p 1653 (2022)
Vasovagal syncope (VVS) is the most common cause of sudden loss of consciousness. VVS results from cerebral hypoperfusion, due to abnormal autonomic control of blood circulation, leading to arterial hypotension. It is a complex disease, and its devel
Externí odkaz:
https://doaj.org/article/40e66097240c428aa721704604d93066
Autor:
Natalia Baulina, Maria Pisklova, Ivan Kiselev, Olga Chumakova, Dmitry Zateyshchikov, Olga Favorova
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 7, p 3791 (2022)
Hypertrophic cardiomyopathy (HCM) is the most common inherited myocardial disease with significant genetic and phenotypic heterogeneity. To search for novel biomarkers, which could increase the accuracy of HCM diagnosis and improve understanding of i
Externí odkaz:
https://doaj.org/article/bc8a370e11d047e79216f8d04ec51ca7
Autor:
Azad Mamedov, Nadezhda Vorobyeva, Ioanna Filimonova, Maria Zakharova, Ivan Kiselev, Vitalina Bashinskaya, Natalia Baulina, Alexey Boyko, Alexander Favorov, Olga Kulakova, Rustam Ziganshin, Ivan Smirnov, Alina Poroshina, Igor Shilovskiy, Musa Khaitov, Yuri Sykulev, Olga Favorova, Valentin Vlassov, Alexander Gabibov, Alexey Belogurov
Publikováno v:
Frontiers in Immunology, Vol 10 (2020)
Risk of the development of multiple sclerosis (MS) is known to be increased in individuals bearing distinct class II human leukocyte antigen (HLA) variants, whereas some of them may have a protective effect. Here we analyzed distribution of a highly
Externí odkaz:
https://doaj.org/article/8c3a43fbbe5040a5b6fcdecb478f2687
Publikováno v:
Genes, Vol 12, Iss 12, p 2016 (2021)
Hypertrophic cardiomyopathy (HCM) is the most common hereditary heart disease. The wide spread of high-throughput sequencing casts doubt on its monogenic nature, suggesting the presence of mechanisms of HCM development independent from mutations in s
Externí odkaz:
https://doaj.org/article/9f729583678d4424a7b78824f7443bad
Publikováno v:
Biochemistry (Moscow). 87:832-838
Hypertrophic cardiomyopathy (HCM) is a hereditary heart disease caused by mutations in the sarcomere genes, which is accompanied by myocardial fibrosis leading to progressive heart failure and arrhythmias. Recent studies suggest that the HCM developm
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 19, p 10316 (2021)
Syncope, defined as a transient loss of consciousness caused by transient global cerebral hypoperfusion, affects 30–40% of humans during their lifetime. Vasovagal syncope (VVS) is the most common cause of syncope, the etiology of which is still unc
Externí odkaz:
https://doaj.org/article/285eee46d7804f81a8d3f29482574444
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 3, p 1346 (2021)
Multiple sclerosis (MS) is a chronic autoimmune neurodegenerative disease of the central nervous system that arises from interplay between non-genetic and genetic risk factors. The epigenetics functions as a link between these factors, affecting gene
Externí odkaz:
https://doaj.org/article/d0b3a4ff7ae349b59ed3cc294ca0ecc3