Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Kirill S. Vasin"'
Autor:
Ivan Y. Iourov, Alexandr P. Gerasimov, Maria A. Zelenova, Natalya E. Ivanova, Oksana S. Kurinnaia, Yulia M. Zabrodskaya, Irina A. Demidova, Evgeny R. Barantsevich, Kirill S. Vasin, Alexey D. Kolotii, Vseslav V. Ushanov, Darya A. Sitovskaya, Timur B.-A. Lobzhanidze, Maria E. Iuditskaia, Nikita S. Iakushev, Muslim M. Zhumatov, Svetlana G. Vorsanova, Konstantin A. Samochernyh
Publikováno v:
Molecular Cytogenetics, Vol 16, Iss 1, Pp 1-18 (2023)
Abstract Molecular cytogenetic and cytogenomic studies have made a contribution to genetics of epilepsy. However, current genomic research of this devastative condition is generally focused on the molecular genetic aspects (i.e. gene hunting, detecti
Externí odkaz:
https://doaj.org/article/95d9c24d4b984991baed1086afb6fe00
Autor:
Kirill S. Vasin, Svetlana G. Vorsanova, Yuri B. Yurov, Alexey D. Kolotii, I.V. Soloviev, Victor S. Kravets, Ivan Y. Iourov, Demidova Ia
Publikováno v:
RESEARCH RESULTS IN BIOMEDICINE. 7:257-271
Chromosome 18p deletion syndrome (18p-) is associated with a loss of chromosomal material of the short arm (partial monosomy); however, the whole short arm is lost in the majority of cases. The frequency of 18p- syndrome is 1:60000. The syndrome is c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9a1dec7e12cd4944e273c1e9d393182
https://doi.org/10.18413/2658-6533-2021-7-3-0-5
https://doi.org/10.18413/2658-6533-2021-7-3-0-5
Autor:
Kurinnaia Os, Svetlana G. Vorsanova, Yuri B. Yurov, Maria A Zelenova, Ivan Y. Iourov, Kirill S. Vasin
Publikováno v:
Молекулярная биология. 55:42-53
Each neuron has 100-10000 connections (synapses) with other neural cells, therefore genome pathologies affecting a small proportion of brain cells are capable of causing dysfunction of the entire central nervous system (CNS). Recently, genome and chr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24fae2d6b03e96cd17d9d97658b2f358
https://doi.org/10.31857/s0026898421010158
https://doi.org/10.31857/s0026898421010158
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:
Maria I. Yablonskaya, Marina A. Bulatnikova, Vasilii O. Sharonin, Maria A Zelenova, Alexey D. Kolotii, Yuri B. Yurov, Svetlana G. Vorsanova, Demidova Ia, Kirill S. Vasin, Oksana S. Kurinnaia, Victor S. Kravets, Victoria Y. Voinova, Ivan Y. Iourov
Publikováno v:
Research Results in Biomedicine. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f9a06b59670bb44b6fd5d83b732a4a4
https://doi.org/10.18413/2658-6533-2020-6-2-0-3
https://doi.org/10.18413/2658-6533-2020-6-2-0-3
Autor:
Svetlana G. Vorsanova, Oksana S. Kurinnaia, Victoria Y. Voinova, Marina A. Bulatnikova, Ivan Y. Iourov, Kirill S. Vasin, Victor S. Kravets, Yuri B. Yurov, Vasiliy O. Sharonin, Maria A Zelenova, Demidova Ia, Alexey D. Kolotii, Sergey V. Bochenkov
Publikováno v:
Research Results in Biomedicine. 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d70d08ee3a77e7ea6474a0fe44b7c62
https://doi.org/10.18413/2658-6533-2019-5-4-0-4
https://doi.org/10.18413/2658-6533-2019-5-4-0-4
Autor:
Maria A Zelenova, Kurinnaia Os, Kirill S. Vasin, A.A. Kharlamova, S.I. Kutsev, I.A. Demidova, I. Y. Iourov, Yu. B. Yurov, Svetlana G. Vorsanova
Publikováno v:
Современные проблемы науки и образования (Modern Problems of Science and Education). :74-74
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f615ad92c822a34a37cff1c907224dd0
https://doi.org/10.17513/spno.30817
https://doi.org/10.17513/spno.30817
Autor:
I.Y. Yurov, O.S. Kurinnaya, A.D. Kolotiy, I.A. Demidova, V.S. Lashkov, Yu. B. Yurov, Kirill S. Vasin, Svetlana G. Vorsanova, Maria A Zelenova, V.S. Kravets
Publikováno v:
Современные проблемы науки и образования (Modern Problems of Science and Education). :142-142
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::127097cc09780df8db54f6189d73dd3c
https://doi.org/10.17513/spno.30679
https://doi.org/10.17513/spno.30679
Autor:
S. A. Korostelev, Svetlana G. Vorsanova, Kirill S. Vasin, Maria A Zelenova, Yu. B. Yurov, Ivan Y. Iourov, Kurinnaia Os
Publikováno v:
Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova. 119:91
Long continuous stretches of homozygosity (LCSH) are regularly detected in studies using molecular karyotyping (SNP array). Despite this type of variation being able to provide meaningful data on the parents' kinship, uniparental disomy and chromosom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e700b022d74001b9e24c81c4fc69da62
https://doi.org/10.17116/jnevro201911905191
https://doi.org/10.17116/jnevro201911905191
Autor:
Maria A Zelenova, Sergei A. Korostelev, Yuri B. Yurov, Svetlana G. Vorsanova, Kirill S. Vasin, Ivan Y. Iourov, Kurinnaia Os
Publikováno v:
Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova. 116:50
To analyze structural variations in the genome in children with autism and intellectual disability.Using high-resolution karyotyping (AffymetrixCytoScan HD Array) and original bioinformatic technology, 200 children with autism and intellectual disabi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdc661884968f339cc699e5f400e26b6
https://doi.org/10.17116/jnevro20161167150-54
https://doi.org/10.17116/jnevro20161167150-54