Zobrazeno 1 - 10
of 22
pro vyhledávání: '"A.A. Anuchina"'
Publikováno v:
Molecular Biology Reports. 47:2371-2379
The majority of CRISPR-Cas9 methods for mutations correction are oriented on gene editing through homologous recombination that is normally restrained by non-homologous end joining (NHEJ). A recently identified protein TIRR can bind a 53BP1 protein,
Autor:
M.I. Yasinovskiy, A.A. Anuchina, Kirill D Ustinov, Alexander Lavrov, E. S. Voronina, V.Yu. Tabakov, S. A. Smirnikhina, Ekaterina Kondrateva, Elmira P. Adilgereeva, Elena Amelina
Publikováno v:
Siberian Medical Review. :95-101
Autor:
Kirill D Ustinov, Matvei I Yasinovsky, Ekaterina Kondrateva, Elmira P. Adilgereeva, Elena Amelina, Valentina D Yakushina, A.A. Anuchina, Vyacheslav Tabakov, Yana S Slesarenko, Angelina S Ershova, S. A. Smirnikhina, Alexander Lavrov, Milyausha Irshatovna Zaynitdinova, E. S. Voronina
Publikováno v:
PLoS ONE
PLoS ONE, Vol 15, Iss 11, p e0242094 (2020)
PLoS ONE, Vol 15, Iss 11, p e0242094 (2020)
Development of genome editing methods created new opportunities for the development of etiology-based therapies of hereditary diseases. Here, we demonstrate that CRISPR/Cas9 can correct p.F508del mutation in theCFTRgene in the CFTE29o- cells and indu
Autor:
A. V. Amelin, A.I. Zaitseva, K.V. Skorobogatykh, Julia Azimova, M.L. Kukushkin, O. I. Rudko, A.A. Anuchina, Z.G. Kokaeva, Elena Naumova, N.S. Kondratieva, E.A. Klimov
Publikováno v:
ZHurnal «Patologicheskaia fiziologiia i eksperimental`naia terapiia».
Перспективным в изучении биомаркеров мигрени может быть многолокусный анализ, в частности, анализ частот сочетанных генотипов. Цель ис
Autor:
S. A. Smirnikhina, Alexander Lavrov, A.A. Anuchina, Milyausha Irshatovna Zaynitdinova, Ekaterina Vladimirovna Kondratyeva
Publikováno v:
Medical news of the North Caucasus. 15
Publikováno v:
Human Genetics. 138:1-19
Despite the recent discover of genome-editing methods, today we can say these approaches have firmly entered our life. Two approaches-knocking out malfunctioning gene allele or correcting the mutation with precise knock-in-can be used in hereditary m
Autor:
Valentina D Yakushina, A.A. Anuchina, Elmira P. Adilgereeva, Alexander Lavrov, S. A. Smirnikhina, Konstantin S. Kochergin-Nikitsky
Publikováno v:
Bulletin of Russian State Medical University. :14-20
Publikováno v:
Molecular Biology Reports. 48:1033-1033
Autor:
Elena Naumova, G.R. Tabeeva, Natalia Kondratieva, K.V. Skorobogatykh, O. I. Rudko, E.A. Klimov, Z.G. Kokaeva, A.A. Anuchina, A.V. Sergeev, Julia Azimova
Publikováno v:
International Journal of Applied and Fundamental Research (Международный журнал прикладных и фундаментальных исследований). 2:258-262
Autor:
Matvey Yasinovsky, Elmira P. Adilgereeva, Konstantin S. Kochergin-Nikitsky, Kirill D Ustinov, Elena Amelina, A.A. Anuchina, I. Mozgovoy, M. Zainitdinova, Ekaterina Kondrateva, S. A. Smirnikhina, Alexander Lavrov
Publikováno v:
Journal of Cystic Fibrosis. 18:S39