Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Sergei I. Kutsev"'
Publikováno v:
Molecular Cytogenetics, Vol 15, Iss 1, Pp 1-11 (2022)
Abstract It is hard to believe that all the cells of a human brain share identical genomes. Indeed, single cell genetic studies have demonstrated intercellular genomic variability in the normal and diseased brain. Moreover, there is a growing amount
Externí odkaz:
https://doaj.org/article/4f0fba0c4d4a45bc929c2d56f729aa80
Autor:
Elizaveta S. Ershova, Ekaterina A. Savinova, Larisa V. Kameneva, Lev N. Porokhovnik, Roman V. Veiko, Tatiana A. Salimova, Vera L. Izhevskaya, Sergei I. Kutsev, Natalia N.Veiko, Svetlana V. Kostyuk
Publikováno v:
Frontiers in Bioscience-Landmark, Vol 28, Iss 8, p 191 (2023)
Background: The chromosome 1q12 region harbors the genome’s largest pericentromeric heterochromatin domain that includes tandemly repeated satellite III DNA [SatIII (1)]. Increased SatIII (1) copy numbers have been found in cultured human skin fibr
Externí odkaz:
https://doaj.org/article/790c0799b759468b8ed35e91c6f61f2a
Autor:
Elena I. Kondratyeva, Nuriniso D. Odinaeva, Leonid Ya Klimov, Nadeshda S. Podchernyaeva, Natalya I. Ilenkova, Svetlana V. Dolbnya, Elena K. Zhekaite, Victoria A. Kuryaninova, Yuliya V. Kotova, Margarita I. Tikhaya, Elena P. Shitkovskaya, Liubov V. Bychina, Tamara G. Drepa, Aisa E. Zodbinova, Yuliya L. Melyanovskaya, Nika V. Petrova, Elena V. Loshkova, Sergei I. Kutsev
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundJuvenile idiopathic arthritis (JIA) is a chronic autoimmune disease characterized by destructive and inflammatory damage to the joints. The aim in this study was to compare vitamin D levels between children and adolescents, 1–18 years of
Externí odkaz:
https://doaj.org/article/d39d1a95cdf1444780a67751f76a6569
Autor:
Kristina Mikhalchuk, Olga Shchagina, Alena Chukhrova, Viktoria Zabnenkova, Polina Chausova, Nina Ryadninskaya, Dmitry Vlodavets, Sergei I. Kutsev, Alexander Polyakov
Publikováno v:
International Journal of Neonatal Screening, Vol 9, Iss 2, p 29 (2023)
5q spinal muscular atrophy (5q SMA) is one of the most common autosomal recessive disorders in the Russian Federation. The first medication to treat 5q SMA was registered in the Russian Federation for treatment of all 5q SMA types in 2019, and the la
Externí odkaz:
https://doaj.org/article/5c5777e1a129498591976dfca2e76441
Autor:
Alexander A. Baranov, Leyla S. Namasova-Baranova, Tatyana E. Borovik, Tatyana V. Bushueva, Elena A. Vishneva, Oksana V. Globa, Nataliya V. Zhurkova, Elena Yu. Zakharova, Natal’ya G. Zvonkova, Lyudmila M. Kuzenkova, Sergei I. Kutsev, Svetlana V. Mikhailova, Ekaterina A. Nikolaeva, Petr V. Novikov, Alexander A. Pushkov, Kirill V. Savostianov, Liliya R. Selimzyanova
Publikováno v:
Педиатрическая фармакология, Vol 14, Iss 4, Pp 258-271 (2017)
Methylmalonic acidemia (aciduria) is an inherited metabolic disturbance from the group of organic acidemias (acidurias). The article presents etiopathogenetic, epidemiological, diagnostic, and therapeutic aspects of the problem. The possibilities of
Externí odkaz:
https://doaj.org/article/18a24263d84d41b39ff1b9cace018937
Publikováno v:
Cells, Vol 10, Iss 5, p 1256 (2021)
Chromosome instability (CIN) has been repeatedly associated with aging and progeroid phenotypes. Moreover, brain-specific CIN seems to be an important element of pathogenic cascades leading to neurodegeneration in late adulthood. Alternatively, CIN a
Externí odkaz:
https://doaj.org/article/64ed0b56dac54a0fa62a5f0532cab294
Autor:
Olga A. Simonova, Ekaterina B. Kuznetsova, Alexander S. Tanas, Viktoria V. Rudenko, Elena V. Poddubskaya, Tatiana V. Kekeeva, Ivan D. Trotsenko, Sergey S. Larin, Sergei I. Kutsev, Dmitry V. Zaletaev, Marina V. Nemtsova, Vladimir V. Strelnikov
Publikováno v:
Biomedicines, Vol 8, Iss 5, p 116 (2020)
Matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) substantially contribute to the regulation of intercellular interactions and thereby play a role in maintaining the tissue structure and function. We examined methylation of a subse
Externí odkaz:
https://doaj.org/article/3a12362de9774f44892d4de6c4804808
Publikováno v:
Cells
Cells, Vol 10, Iss 1256, p 1256 (2021)
Cells, Vol 10, Iss 1256, p 1256 (2021)
Chromosome instability (CIN) has been repeatedly associated with aging and progeroid phenotypes. Moreover, brain-specific CIN seems to be an important element of pathogenic cascades leading to neurodegeneration in late adulthood. Alternatively, CIN a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::129faeacd5e512bcbd20ac096a0a3240
http://europepmc.org/articles/PMC8161106
http://europepmc.org/articles/PMC8161106
Autor:
Ivan Y. Iourov, Svetlana G. Vorsanova, Oxana S Kurinnaia, Yuri B. Yurov, Sergei I. Kutsev, Kirill S. Vasin, Maria A Zelenova
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 8328, p 8328 (2020)
International Journal of Molecular Sciences
Volume 21
Issue 21
International Journal of Molecular Sciences
Volume 21
Issue 21
Mechanisms for somatic chromosomal mosaicism (SCM) and chromosomal instability (CIN) are not completely understood. During molecular karyotyping and bioinformatic analyses of children with neurodevelopmental disorders and congenital malformations (n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::470eb91f0e6342c9e3a478eb93ce281c
Autor:
Alice Krebsová, Svetlana G. Vorsanova, Milan Macek, Marina Machatkova, Martina Brouckova, Michael B. Petersen, Sergei I. Kutsev, Svetlana Arbuzova, Milada Matejckova, Roman Krejčí, Karl Sperling, Tatiana Zerova
Publikováno v:
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society. 53(3)
Study of parental/meiotic origin of free trisomy 21 in nuclear families from Russia (70 cases), Ukraine (32 cases), and 22 from Germany revealed maternal nondisjunction in 77.3% (Germany), 93.8% (Ukraine), and 91.4% (Russia), paternal origin in 13.6%
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccbdb0d713556938deee43bf9b2e5836
https://pubmed.ncbi.nlm.nih.gov/15750023
https://pubmed.ncbi.nlm.nih.gov/15750023