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Human Gene Therapy|April 2, 2011
Delivery of AAV2/9-microdystrophin genes incorporating helix 1 of the coiled-coil motif in the C-terminal domain of dystrophin improves muscle pathology and restores the level of α1-syntrophin and α-dystrobrevin in skeletal muscles of mdx miceTaeyoung Koo, Alberto Malerba, Takis Athanasopoulos, et al.Genome Research|February 24, 2018
CRISPR RNAs trigger innate immune responses in human cellsSojung Kim, Taeyoung Koo, Hyeon-Gun Jee, et al.Experimental & Molecular Medicine|January 31, 2023
Targeted dual base editing with Campylobacter jejuni Cas9 by single AAV-mediated deliveryJiyeon Kweon, An-Hee Jang, Eunji Kwon, et al.Genome Research|February 18, 2017
Genome surgery using Cas9 ribonucleoproteins for the treatment of age-related macular degenerationKyoungmi Kim, Sung Wook Park, Jin Hyoung Kim, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|May 7, 2018
Functional Rescue of Dystrophin Deficiency in Mice Caused by Frameshift Mutations Using Campylobacter jejuni Cas9Taeyoung Koo, Ngoc B Lu-Nguyen, Alberto Malerba, et al.Nature Communications|May 12, 2018
CRISPR-LbCpf1 prevents choroidal neovascularization in a mouse model of age-related macular degenerationTaeyoung Koo, Sung Wook Park, Dong Hyun Jo, et al.Nature Biotechnology|September 3, 2021
Efficient CRISPR editing with a hypercompact Cas12f1 and engineered guide RNAs delivered by adeno-associated virusDo Yon Kim, Jeong Mi Lee, Su Bin Moon, et al.Nature Biotechnology|April 28, 2018
Adenine base editing in mouse embryos and an adult mouse model of Duchenne muscular dystrophySeuk-Min Ryu, Taeyoung Koo, Kyoungmi Kim, et al.Human Gene Therapy|June 25, 2013
Gene correction of a duchenne muscular dystrophy mutation by meganuclease-enhanced exon knock-inLinda Popplewell, Taeyoung Koo, Xavier Leclerc, et al.Nature Communications|February 22, 2017
In vivo genome editing with a small Cas9 orthologue derived from Campylobacter jejuniEunji Kim, Taeyoung Koo, Sung Wook Park, et al.Pageof 4