Zobrazeno 1 - 10
of 118
pro vyhledávání: '"Oleg L. Serov"'
Autor:
Sergey V. Guselnikov, Konstantin O. Baranov, Sergey V. Kulemzin, Tatyana N. Belovezhets, Anton N. Chikaev, Svetlana V. Murasheva, Olga Y. Volkova, Ludmila V. Mechetina, Alexander M. Najakshin, Nikolai A. Chikaev, Pavel P. Solodkov, Maria V. Sergeeva, Alexander V. Smirnov, Irina A. Serova, Oleg L. Serov, Alexander G. Markhaev, Yulia V. Kononova, Alexander Y. Alekseev, Marina A. Gulyaeva, Daria M. Danilenko, Nariman R. Battulin, Alexander M. Shestopalov, Alexander V. Taranin
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
The COVID-19 pandemic has uncovered the high genetic variability of the SARS-CoV-2 virus and its ability to evade the immune responses that were induced by earlier viral variants. Only a few monoclonal antibodies that have been reported to date are c
Externí odkaz:
https://doaj.org/article/6da10109f6fb4cc2aa3729d2219d4170
Publikováno v:
BMC Genetics, Vol 18, Iss S1, Pp 53-60 (2017)
Abstract Background Copy Number Variation (CNV) of the human CNTN6 gene (encoding the contactin-6 protein), caused by deletions or duplications, is responsible for severe neurodevelopmental impairments, often in combination with facial dysmorphias. C
Externí odkaz:
https://doaj.org/article/25b9ea4c2d1447f9a79654b205f36546
Autor:
Vicente J.F. Freitas, Irina A. Serova, Lyudmila E. Andreeva, Guennadi A. Dvoryanchikov, Edilson S. Lopes-Jr., Dárcio I.A. Teixeira, Luciene P.B. Dias, Suely R.G. Avelar, Raylene R. Moura, Luciana M. Melo, Alexsandra F. Pereira, João B. Cajazeiras, Maria L.L. Andrade, Karlliely C. Almeida, Francisco C. Sousa, Antonio C.C. Carvalho, Oleg L. Serov
Publikováno v:
Anais da Academia Brasileira de Ciências, Vol 79, Iss 4, Pp 585-592 (2007)
In order to produce transgenic goats with hG-CSF, a total of 24 adult Saanen and 48 adult undefined breed goats were used as donors and recipients, respectively. Donors were estrus-synchronized with vaginal sponges and superovulated by a treatment wi
Externí odkaz:
https://doaj.org/article/c98869ed48b642719820a5d704f0a18a
Publikováno v:
Anais da Academia Brasileira de Ciências, Vol 72, Iss 3, Pp 389-398 (2000)
The review is concerned with a progress in genetic modification of a mammalian genome in vitro and in vivo at chromosomal level. Recently three new approaches for the chromosome biotechnology have been developed: Using Cre/loxP-system a researcher is
Externí odkaz:
https://doaj.org/article/2bc07b82979b49f183e4b2c48f0e07d4
Autor:
Veniamin S. Fishman, S. A. Vasilyev, Oleg L. Serov, A. V. Vertinsky, Igor N. Lebedev, Evgeniia Sukhikh, A. A. Murashkina, Leonid Sukhikh, R. R. Savchenko
Publikováno v:
Russian Journal of Genetics. 57:856-862
The effect of knockout and overexpression of the ADAMTS1 on the radiation-induced response in HeLa cell line was analyzed. The cell line with the ADAMTS1 gene knockout was created using the CRISPR/Cas9 genome editing technology. The ADAMTS1 gene over
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::531f7583d64b1c1f5f5d3b3bfac60c56
https://doi.org/10.1134/s1022795421070127
https://doi.org/10.1134/s1022795421070127
Autor:
Inna E. Pristyazhnyuk, A.G. Menzorov, S. A. Vasilyev, T. V. Nikitina, Oleg L. Serov, A.A. Khabarova, M.E. Lopatkina, D. A. Fedotov, I. N. Lebedev, Yu. A. Minina, Yu.S. Yakovleva, A. A. Kashevarova, M.M. Gridina
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
Scientific Reports
Scientific Reports
Human ring chromosomes are often unstable during mitosis, and daughter cells can be partially or completely aneuploid. We studied the mitotic stability of four ring chromosomes, 8, 13, 18, and 22, in long-term cultures of skin fibroblasts and induced
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c929ddd066e7e0234cca2bec400f58d0
https://doaj.org/article/fc412a934b244d68a001677be77b2118
https://doaj.org/article/fc412a934b244d68a001677be77b2118
Autor:
Inna E. Pristyazhnyuk, Veniamin S. Fishman, Roman V. Mungalov, Natalia Alenina, Aleksei G. Menzorov, Michael Bader, N. M. Matveeva, Nikolai B. Rubtsov, Konstantin E. Orishchenko, Elena A. Kizilova, Anastasia A. Shevtsova, Oleg L. Serov
Publikováno v:
Journal of Cellular Biochemistry. 120:17208-17218
Neuronal tracing is a modern technology that is based on the expression of fluorescent proteins under the control of cell type-specific promoters. However, random genomic integration of the reporter construct often leads to incorrect spatial and temp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::437fa279d9855c016e32bfb173f24d4a
https://doi.org/10.1002/jcb.28981
https://doi.org/10.1002/jcb.28981
Autor:
M.M. Gridina, Inna E. Pristyazhnyuk, Igor N. Lebedev, Yu.S. Yakovleva, S. A. Vasilyev, T.V. Nikitina, M.E. Lopatkina, A.G. Menzorov, Oleg L. Serov, A. A. Kashevarova, A.A. Khabarova
Publikováno v:
Stem Cell Research, Vol 33, Iss, Pp 260-264 (2018)
Skin fibroblasts from a patient with neurodevelopmental and speech delay, anxiety disorder, macrocephaly, microorchidism, multiple anomalies of internal organs and ring chromosome 13 were reprogrammed into induced pluripotent stem cells (iPSCs) to ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edc6c986fcb67a7907f98a43e5ed5c24
https://doi.org/10.1016/j.scr.2018.11.009
https://doi.org/10.1016/j.scr.2018.11.009
Autor:
Igor N. Lebedev, A. A. Kashevarova, D. A. Fedotov, Yu.S. Yakovleva, M.E. Lopatkina, P.A. Orlova, T.V. Nikitina, Lyudmila P. Nazarenko, Oleg L. Serov, M.M. Gridina, S. A. Vasilyev, J.M. Minina, L.I. Mikhailik
Publikováno v:
Stem Cell Research, Vol 49, Iss, Pp 102024-(2020)
Ring chromosomes are structural aberrations commonly associated with disease phenotype. We consider necessary to create the iPSCs with a ring chromosome 8, which can be used for disease modeling and related research. The ICGi025-A iPSCs line was obta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3347f46d6e7b0553f2135e2baedc70ce
http://www.sciencedirect.com/science/article/pii/S1873506120303251
http://www.sciencedirect.com/science/article/pii/S1873506120303251
Autor:
P.A. Orlova, T.V. Nikitina, Inna E. Pristyazhnyuk, Lyudmila P. Nazarenko, Igor N. Lebedev, Oleg L. Serov, A.A. Khabarova, A. A. Kashevarova, M.E. Lopatkina, Elena O. Belyaeva, N.N. Sukhanova
Publikováno v:
Stem Cell Research, Vol 49, Iss, Pp 102076-(2020)
Ring chromosome 18 is a rare chromosomal disorders that usually originate de novo and correlate with clinical manifestation: developmental delay as well as microcephaly, brain and ocular malformations, hypotonia and skeletal abnormalities. We generat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51610e04eb18c9583fd7ea328f63b865
http://www.sciencedirect.com/science/article/pii/S1873506120303779
http://www.sciencedirect.com/science/article/pii/S1873506120303779