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Molecular Therapy : the Journal of the American Society of Gene Therapy|April 6, 2021
CRISPR technologies for the treatment of Duchenne muscular dystrophyEunyoung Choi, Taeyoung KooArchives of Pharmacal Research|June 24, 2021
Recent advances in CRISPR technologies for genome editingMyeonghoon Song, Taeyoung KooBriefings in Functional Genomics|August 27, 2016
Therapeutic applications of CRISPR RNA-guided genome editingTaeyoung Koo, Jin-Soo KimHuman Gene Therapy|March 26, 2013
Clinical trials using antisense oligonucleotides in duchenne muscular dystrophyTaeyoung Koo, Matthew J WoodCancer Gene Therapy|September 19, 2025
Gene editing in cancer therapy: overcoming drug resistance and enhancing precision medicineHyeonjeong Park, Suyeun Yu, Taeyoung KooMolecules and Cells|May 20, 2015
Measuring and Reducing Off-Target Activities of Programmable Nucleases Including CRISPR-Cas9Taeyoung Koo, Jungjoon Lee, Jin-Soo KimGene Therapy|November 12, 2025
Therapeutic in vivo genome editing: innovations and challenges in rAAV vector-based CRISPR deliveryJin-Seok Gil, Soyeon Lee, Taeyoung KooHuman Gene Therapy|November 7, 2013
Triple trans-splicing adeno-associated virus vectors capable of transferring the coding sequence for full-length dystrophin protein into dystrophic miceTaeyoung Koo, Linda Popplewell, Takis Athanasopoulos, et al.Methods in Molecular Biology (Clifton, N.J.)|October 29, 2011
Gene therapy in skeletal muscle mediated by adeno-associated virus vectorsChunping Qiao, Taeyoung Koo, Juan Li, et al.Molecular Therapy. Nucleic Acids|October 17, 2022
Expanded targeting scope of LbCas12a variants allows editing of multiple oncogenic mutationsEunyoung Choi, Hye-Yeon Hwang, Eunji Kwon, et al.Pageof 4