Genome editing approach for generation of isogenic cell lines modelling Huntington's disease in vitro
Malakhova A.A., Sorokin M.A., Sorokina A.E., Malankhanova T.B., Mazurok N.A., Medvedev S.P., Zakian S.M.
Gennaya inzheneriya mezenkhimnykh stvolovykh kletok (MSK) s tsel'yu uluchsheniya neyroprotektivnykh svoystv ikh sekretoma
Skryabina M.N., Dzhauari S.S., Primak A.L., Basalova N.A., Kulebyakina M.A., Popov V.S., Efimenko A.Y., Velichko A.Y., Tkachuk V.A., Karagyaur M.N.
Site-specific genome editing for hematopoetic stem cells transplantation-based gene therapy approaches
Lepik K.V., Popova M.O., Shakirova A.I., Sergeev V.S., Potter A.Y., Barkhatov I.M., Fehse B., Afanasyev B.V.
Legal boundaries of research to create inherited modifications of the human embryo genome in the people's Republic of China
Blinov A.G., Gerasimov A.M., Gerasimova E.A.
Genome editing on cell model of the genetic form of Parkinson's disease
Vetchinova A.S., Konovalova E.V., Volchkov P.Y., Abramycheva N.Y., Illarioshkin S.N.
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