Zobrazeno 1 - 10
of 38
pro vyhledávání: '"V V Ilinsky"'
Autor:
A. S. Boev, A. S. Rakitko, S. R. Usmanov, A. N. Kobzeva, I. V. Popov, V. V. Ilinsky, E. O. Kiktenko, A. K. Fedorov
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract Recent advances in DNA sequencing open prospects to make whole-genome analysis rapid and reliable, which is promising for various applications including personalized medicine. However, existing techniques for de novo genome assembly, which i
Externí odkaz:
https://doaj.org/article/cf61a08b80104c41b8c32113e6ff983b
Autor:
N G Neznanov, E D Kasyanov, A. S. Rakitko, V. V. Ilinsky, G. V. Rukavishnikov, A.B. Shmukler, Vera Golimbet, G. E. Mazo, A O Kibitov
Publikováno v:
Neuroscience and Behavioral Physiology. 51:1040-1049
Publikováno v:
Biophysics. 65:889-893
The MinION system (Oxford Nanopore Technologies, United Kingdom) was used to directly sequence genomic DNAs of two recombinant Escherichia coli strains. One strain carried a plasmid with the gene for M.HpaII DNA methyltransferase, which methylates th
Autor:
Olga A. Koksharova, T. R. Kravzova, I. V. Mosharova, A. U. Akulova, I. V. Lazebnaya, Oleg E. Lazebny, V. V. Ilinsky
Publikováno v:
Inland Water Biology. 13:178-185
Cultured hydrocarbon-oxidizing bacteria have been isolated for the first time from bacterioplankton in urban Lake Beloye (Moscow). The taxonomic positions of two bacterial strains (2012B and 2012C) isolated from this lake have been determined. Lipids
Autor:
P. A. Shatalov, V V Ilinsky, S. B. Artemieva, T. I. Baranich, A. Yu. Krasnenko, A. G. Kupriyanova, Natalia Vladimirovna Baryshnikova, Vladimir Sukhorukov, Anastasiya Aleksandrovna Kozina
Publikováno v:
TARGETED ONCOTHERAPY. :15-21
Congenital core myopathies are a clinically and genetically heterogenous group of congenital myopathies that share a specific histopathological feature: areas of reduced oxidative activity in muscle fibers. The relationship between clinical, genetic
Autor:
Torben Hansen, Thorkild I. A. Sørensen, V V Ilinsky, Dmitrii Borisevich, Alexander Rakitko, Theresia M. Schnurr, Lars Ängquist, Niels Grarup, Oluf Pedersen, Mette Aadahl, Line Engelbrechtsen
Publikováno v:
PLoS ONE, Vol 16, Iss 10, p e0258748 (2021)
Borisevich, D, Schnurr, T M, Engelbrechtsen, L, Rakitko, A, Ängquist, L, Ilinsky, V, Aadahl, M, Grarup, N, Pedersen, O, Sørensen, T I A & Hansen, T 2021, ' Non-linear interaction between physical activity and polygenic risk score of body mass index in Danish and Russian populations ', PLoS ONE, vol. 16, no. 10, e0258748 . https://doi.org/10.1371/journal.pone.0258748
PLoS ONE
PLoS ONE, Vol 16, Iss 10 (2021)
Borisevich, D, Schnurr, T M, Engelbrechtsen, L, Rakitko, A, Ängquist, L, Ilinsky, V, Aadahl, M, Grarup, N, Pedersen, O, Sørensen, T I A & Hansen, T 2021, ' Non-linear interaction between physical activity and polygenic risk score of body mass index in Danish and Russian populations ', PLoS ONE, vol. 16, no. 10, e0258748 . https://doi.org/10.1371/journal.pone.0258748
PLoS ONE
PLoS ONE, Vol 16, Iss 10 (2021)
Body mass index (BMI) is a highly heritable polygenic trait. It is also affected by various environmental and behavioral risk factors. We used a BMI polygenic risk score (PRS) to study the interplay between the genetic and environmental factors defin
Autor:
V V Ilinsky, Tatiana A. Gurbich
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-7 (2020)
Scientific Reports
Scientific Reports
Copy-number variants (CNVs) are an important part of human genetic variation. They can be benign or can play a role in human disease by creating dosage imbalances and disrupting genes and regulatory elements. Accurate identification and clinical anno
Autor:
I. D. Fedonyuk, I. F. Stetsenko, V V Ilinsky, E. I. Surkova, Elena Grigorievna Okuneva, A. A. Kholin, Nikolay Plotnikov, Olesia Igorevna Klimchuk, Natalia Vladimirovna Baryshnikova, Anna Krasnenko, Anastasiya Aleksandrovna Kozina, E S Il'ina
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)
Background Epilepsy with intellectual disability limited to females (Epileptic encephalopathy, early infantile, 9; EIEE9) is a rare early infantile epileptic encephalopathy characterized by an unusual X-linked inheritance: females with heterozygous m
Autor:
G E Mazo, Alexander Rakitko, N. G. Neznanov, A.A. Kibitov, V V Ilinsky, G V Rukavishnikov, A O Kibitov, E D Kasyanov, KA Kozlova
One of the most promising areas of research into the biological underpinnings of depression is genetic studies. However, the absence of generally accepted phenotyping methods leads to the difficulties in generalizing their results due to the heteroge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a3ca4f39c67355321112938f2728ebc
https://doi.org/10.1101/2020.10.16.20213843
https://doi.org/10.1101/2020.10.16.20213843
Autor:
V V Ilinsky, Sergey Evfratov, Gennady V. Khvorykh, Vera Belova, Denis V. Rebrikov, Alexander Rakitko, Daria Plakhina, Dmitriy Korostin, Kirill Tsukanov, Alexander Konoplyannikov
Publikováno v:
Genes
Volume 11
Issue 6
Genes, Vol 11, Iss 590, p 590 (2020)
Volume 11
Issue 6
Genes, Vol 11, Iss 590, p 590 (2020)
Non-invasive prenatal testing (NIPT) for aneuploidy on Chromosomes 21 (T21), 18 (T18) and 13 (T13) is actively used in clinical practice around the world. One of the limitations of the wider implementation of this test is the high cost of the analysi