Ivan Y Iourov
Overview
Explore the profile of Ivan Y Iourov including associated specialties, affiliations and a list of published articles.
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67
Citations
1269
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Recent Articles
1.
Vorsanova S, Yurov Y, Iourov I
Methods Mol Biol
. 2024 Jun;
2825:239-246.
PMID: 38913313
Quantifying signals substantially increases the efficiency of fluorescence in situ hybridization (FISH). Quantitative FISH analysis or QFISHing may be useful for differentiation between chromosome loss and chromosomal associations, detection of...
2.
Iourov I, Vorsanova S, Yurov Y
Methods Mol Biol
. 2024 Jun;
2825:67-78.
PMID: 38913303
Somatic chromosomal mosaicism, chromosome instability, and cancer are intimately linked together. Addressing the role of somatic genome variations (encompassing chromosomal mosaicism and instability) in cancer yields paradoxical results. Firstly, somatic...
3.
Iourov I, Gerasimov A, Zelenova M, Ivanova N, Kurinnaia O, Zabrodskaya Y, et al.
Mol Cytogenet
. 2023 Jan;
16(1):1.
PMID: 36600272
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....
4.
Yurov Y, Vorsanova S, Iourov I
Methods Mol Biol
. 2022 Nov;
2561:191-204.
PMID: 36399271
Fluorescence in situ hybridization (FISH) is the method of choice for visualizing chromosomal DNA in post-mitotic cells. The availability of chromosome-enumeration (centromeric), site-specific, and multicolor-banding DNA probes offers opportunities to...
5.
6.
Iourov I, Vorsanova S, Kurinnaia O, Kutsev S, Yurov Y
Mol Cytogenet
. 2022 Oct;
15(1):45.
PMID: 36266706
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...
7.
8.
Iourov I, Vorsanova S
Front Aging Neurosci
. 2022 Mar;
14:786264.
PMID: 35309884
No abstract available.
9.
Vorsanova S, Demidova I, Kolotii A, Kurinnaia O, Kravets V, Soloviev I, et al.
Mol Cytogenet
. 2022 Mar;
15(1):8.
PMID: 35248137
Background: Klinefelter syndrome is a common chromosomal (aneuploidy) disorder associated with an extra X chromosome in males. Regardless of numerous studies dedicated to somatic gonosomal mosaicism, Klinefelter syndrome mosaicism (KSM)...
10.
Ivanov Y, Malsagova K, Goldaeva K, Pleshakova T, Shumov I, Galiullin R, et al.
Genes (Basel)
. 2022 Feb;
13(2).
PMID: 35205244
MicroRNAs (miRNAs), which represent short (20 to 22 nt) non-coding RNAs, were found to play a direct role in the development of autism in children. Herein, a highly sensitive "silicon-on-insulator"-based...