Zobrazeno 1 - 10
of 56
pro vyhledávání: '"N. A. Oparina"'
Publikováno v:
Онкогематология, Vol 0, Iss 4, Pp 36-38 (2022)
Clinical efficiency of Dacogen (inhibitor of DNA hypermethylation) in 16 patients with MDS is presented. Bone marrow cytogenetic studies were performed in 6 patients; the detected chromosome aberrations included 5q deletion in 1 patient, X monosomy i
Externí odkaz:
https://doaj.org/article/97419dbb66be459c8485286dab601154
Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 48, Iss 4, Pp 271-279 (2020)
The 5p inverted duplication deletion syndrome, also known as inv dup del 5p, is a rare genetic disorder with a prevalence of below 1:1 000 000, whose underlying abnormality lies in a segmental trisomy and simultaneous segmental monosomy of the short
Externí odkaz:
https://doaj.org/article/b039bc28506f49d7827c388640776e57
Autor:
Lyubov Samsonova, Vyacheslav B. Chernykh, O. Yu. Latyshev, N. Yu. Raygorodskaya, E. A. Volodko, N. V. Oparina, S. A. Suyazova
Publikováno v:
Russian Journal of Genetics. 57:1312-1321
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0c6dcf266719fa25e478443722ad82a
https://doi.org/10.1134/s1022795421110107
https://doi.org/10.1134/s1022795421110107
Autor:
E. R. Tchartchan, S. A. Abugov, R. S. Polyakov, E. V. Zaklyazminskaya, V. A. Rumyantseva, V. V. Khovrin, A. A. Skvortsov, M. N. Kabanova, Z. R. Khatchatryan, N. V. Oparina
Publikováno v:
Российский кардиологический журнал, Vol 0, Iss 5, Pp 111-117 (2015)
Shereshevsky-Turner syndrome — is chromosome anomaly, the monosomia by X-chromosome (cariotype 45, X0) that has prevalence 1:2000-1:2500 newborn girls. It is well known that these patients very often have cardiovascular pathology. Aortic aneurysm i
Externí odkaz:
https://doaj.org/article/78475614e8c94c5ea737b40181d12b05
Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 48, Iss 4, Pp 271-279 (2020)
The 5p inverted duplication deletion syndrome, also known as inv dup del 5p, is a rare genetic disorder with a prevalence of below 1:1 000 000, whose underlying abnormality lies in a segmental trisomy and simultaneous segmental monosomy of the short
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ee4bcfd2781a7e1bd47213d981462bb
https://doi.org/10.18786/2072-0505-2020-48-025
https://doi.org/10.18786/2072-0505-2020-48-025
Publikováno v:
Proceedings of the International Scientific Conference “Smart Nations: Global Trends In The Digital Economy” ISBN: 9783030948696
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93a77ffd2a2b08da0ca72f85d33fb591
https://doi.org/10.1007/978-3-030-94870-2_37
https://doi.org/10.1007/978-3-030-94870-2_37
Publikováno v:
Russian Journal of Genetics. 53:982-987
We studied genome distribution of single-nucleotide polymorphisms (SNP) associated with development of multiple sclerosis and identified genome segments enriched in such polymorphisms. Some SNPs observed in identified segments are also local or dista
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63098d6ea15c8733445e27221796b596
https://doi.org/10.1134/s1022795417090058
https://doi.org/10.1134/s1022795417090058
Autor:
E. S. Kuznetsova, O. L. Zinovieva, N. Yu. Oparina, M. M. Prokofjeva, P. V. Spirin, I. A. Favorskaya, I. B. Zborovskaya, N. A. Lisitsyn, V. S. Prassolov, T. D. Mashkova
Publikováno v:
Molecular Biology. 50:220-229
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba4b8858c1e2a9eee99be4949da3638b
https://doi.org/10.1134/s0026893316020138
https://doi.org/10.1134/s0026893316020138
Autor:
E. S. Kuznetsova, O. L. Zinovieva, N. Yu. Oparina, M. M. Prokofjeva, P. V. Spirin, I. A. Favorskaya, I. B. Zborovskaya, N. A. Lisitsyn, V. S. Prassolov, T. D. Mashkova
Publikováno v:
Молекулярная биология. 50:255-265
Retinoids are signaling molecules that control a wide variety of cellular processes and possess antitumor activity. This work presents a comprehensive description of changes in the expression of 23 genes that regulate retinoid metabolism and signalin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f57970f68f7800c995152fe791cc236
https://doi.org/10.7868/s0026898416020130
https://doi.org/10.7868/s0026898416020130
Autor:
N. Yu. Oparina, A. V. Snezhkina, A. F. Sadritdinova, V. A. Veselovskii, A. A. Dmitriev, V. N. Senchenko, N. V. Mel’nikova, A. S. Speranskaya, M. V. Darii, O. A. Stepanov, I. M. Barkhatov, A. V. Kudryavtseva
Publikováno v:
Russian Journal of Genetics. 49:707-716
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c04be1f720333b808939edbe0cbf4a93
https://doi.org/10.1134/s1022795413050104
https://doi.org/10.1134/s1022795413050104