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期
标题
作者
卷 18, 编号 4 (2023)
Study of the role of evolutionary new enhancers in the development of the corpus callosum
Kustova A., Celis Suescun J., Rybakova V., Tarabykin V.
PDF
(Rus)
卷 14, 编号 4 (2019)
Gene therapy approaches to the duchenne muscular dystrophy theatment
Zaynitdinova M., Smirnikhina S., Lavrov A., Eremin I., Pulin A.
PDF
(Rus)
卷 11, 编号 2 (2016)
Site-specific genome editing for hematopoetic stem cells transplantation-based gene therapy approaches
Lepik K., Popova M., Shakirova A., Sergeev V., Potter A., Barkhatov I., Fehse B., Afanasyev B.
PDF
(Rus)
卷 15, 编号 2 (2020)
Clinical trials for the treatment of hereditary diseases by genome editing
Slesarenko Y., Lavrov A., Smirnikhina S.
PDF
(Rus)
卷 11, 编号 2 (2016)
Application of CRISPR/Cas9 system for developing and studying cellular models of inherited disease
Valetdinova K.
PDF
(Rus)
卷 15, 编号 1 (2020)
Generation and characterization of human emryonic stem cells with increased expression of HIF-2a
Zhiven M., Zakharova I., Shevchenko A., Elisaphenko E., Orishchenko K., Zakian S.
PDF
(Rus)
卷 13, 编号 3 (2018)
Modern pathogenesis-based methods and development of new gene and cell-based methods for cystic fibrosis treatment
Smirnikhina S., Lavrov A.
PDF
(Rus)
卷 12, 编号 2 (2017)
Cellular models, genomic technologies and clinical practice: a synthesis of knowledge for the study of the mechanisms, diagnostics and treatment of Parkinson's disease
Kovalenko V., Khabarova E., Rzaev D., Medvedev S.
PDF
(Rus)
卷 11, 编号 2 (2016)
Genome editing on cell model of the genetic form of Parkinson's disease
Vetchinova A., Konovalova E., Volchkov P., Abramycheva N., Illarioshkin S.
PDF
(Rus)
卷 11, 编号 2 (2016)
Plakophilin-2 gene knockout using CRISPR/Cas9 system
Khudiakov A., Kostina D., Kostareva A., Malashicheva A.
PDF
(Rus)
卷 11, 编号 2 (2016)
Strategies to edit paralogous genes with CRISPR/Cas9
Nemudryi A., Malankhanova T., Malakhova A., Medvedev S., Zakian S.
PDF
(Rus)
卷 17, 编号 3 (2022)
Ekspressiya gena POU5F1 v rakovykh kletkakh myshi
Kuz'min A., Kudryashov V., Tomilin A.
PDF
(Rus)
卷 17, 编号 3 (2022)
Vliyanie mutatsii G2019S v kinaze LRRK2 na funktsional'noe sostoyanie mitokhondriy i mitofagiyu v izogennoy kletochnoy modeli bolezni Parkinsona
Kopylova I., Mayorova K., Vigont V., Grekhnev D., Bogomazova A., Lebedeva O., Lagar'kova M.
PDF
(Rus)
卷 17, 编号 3 (2022)
Ispol'zovanie genomnykh i kletochnykh tekhnologiy dlya vyyasneniya klinicheskogo znacheniya mutatsiy v genakh, assotsiirovannykh s gipertroficheskoy kardiomiopatiey
Dement'eva E., Pavlova S., Shul'gina A., Pronyaeva K., Zakiyan S.
PDF
(Rus)
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