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Please use this identifier to cite or link to this item: http://dspace.bsu.edu.ru/handle/123456789/64201
Title: CRISPR/Cas9-generated mouse model with humanizing single-base substitution in the Gnao1 for safety studies of RNA therapeutics
Authors: Polikarpova, A. V.
Egorova, T. V.
Lunev, E. A.
Tsitrina, A. A.
Vassilieva, S. G.
Deykin, A. V.
Keywords: medicine
medical genetics
medical genomics
genetically modified mice
genome editing
CRISPR/Cas9
personalized medicine
GNAO1
encephalopathy
Issue Date: 2023
Citation: CRISPR/Cas9-generated mouse model with humanizing single-base substitution in the Gnao1 for safety studies of RNA therapeutics / A.V. Polikarpova, T.V. Egorova, E.A. Lunev [et al.] // Frontiers in Genome Editing. - 2023. - Vol.5.-Art. 1034720. - Doi: 10.3389/fgeed.2023.1034720.
Abstract: In this work, CRISPR/Cas9 technology was used to introduce a monobase substitution in exon 6 of the Gnao1 gene to replace the mouse triplet encoding Gly203 (GGG) with a codon used in the human gene (GGA)
URI: http://dspace.bsu.edu.ru/handle/123456789/64201
Appears in Collections:Статьи из периодических изданий и сборников (на иностранных языках) = Articles from periodicals and collections (in foreign languages)

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