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- Publication Date2021-12 Mitochondrial DNA editing in mice with DddA-TALE fusion deaminases
- Publication Date2021-06 Off-the-Shelf, Immune-Compatible Human Embryonic Stem Cells Generated Via CRISPR-Mediated Genome Editing
- Publication Date2021-04 Base Editing in Progeria
- Publication Date2021-04 The efficacy of CRISPR-mediated cytosine base editing with the RPS5a promoter in Arabidopsis thaliana
- Publication Date2021-02 Adenine Base Editor Ribonucleoproteins Delivered by Lentivirus-Like Particles Show High On-Target Base Editing and Undetectable RNA Off-Target Activities
- Publication Date2021-02 Identifying genome-wide off-target sites of CRISPR RNA-guided nucleases and deaminases with Digenome-seq
- Publication Date2021-02 Small-molecule inhibitors of histone deacetylase improve CRISPR-based adenine base editing
- Publication Date2020-11 Highly Cited Researcher
- Publication Date2020-10 CRISPR-Cas12a with an oAd Induces Precise and Cancer-Specific Genomic Reprogramming of EGFR and Efficient Tumor Regression
- Publication Date2020-10 The road ahead in genetics and genomics
- Publication Date2020-08 Genome-wide specificity of dCpf1 cytidine base editors
- Publication Date2020-06 CRISPR-sub: Analysis of DNA substitution mutations caused by CRISPR-Cas9 in human cells
- Publication Date2020-05 Recent advances in genome editing of stem cells for drug discovery and therapeutic application
- Publication Date2020-05 Protein Kinase A Catalytic Subunit Is a Molecular Switch that Promotes the Pro-tumoral Function of Macrophages
- Publication Date2020-01 CRISPR/Cas9-mediated editing of 1-aminocyclopropane-1-carboxylate oxidase1 enhances Petunia flower longevity
- Publication Date2019-12 2019년 1 바이오분야 연구성과 및 뉴스 Top 5
- Publication Date2019-12 Generation of targeted homozygosity in the genome of human induced pluripotent stem cells
- Publication Date2019-11 Highly Cited Researcher
- Publication Date2019-10 A zero-background CRISPR binary vector system for construction of sgRNA libraries in plant functional genomics applications
- Publication Date2019-10 CRISPR-Cas9–mediated therapeutic editing of Rpe65 ameliorates the disease phenotypes in a mouse model of Leber congenital amaurosis
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