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Jin-Soo Kim

Researcher at Seoul National University

Publications -  308
Citations -  26566

Jin-Soo Kim is an academic researcher from Seoul National University. The author has contributed to research in topics: CRISPR & Genome editing. The author has an hindex of 66, co-authored 264 publications receiving 21375 citations. Previous affiliations of Jin-Soo Kim include UPRRP College of Natural Sciences & Korea University of Science and Technology.

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kem mutations affect nuclear fusion in Saccharomyces cerevisiae.

TL;DR: Three genes of Saccharomyces cerevisiae are identified that enhance the nuclear fusion defect of kar1-1 yeast during conjugation and Mutant kem 1 strains are hypersensitive to benomyl, lose chromosomes at a rate 10-20-fold higher than KEM+ strains, and lose viability upon nitrogen starvation.
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Design of TATA box-binding protein/zinc finger fusions for targeted regulation of gene expression

TL;DR: A structure-based design strategy was used to construct a fusion protein, TBP/ZF, in which the three zinc fingers of Zif268 were linked to the COOH terminus of yeast TBP, which formed an extraordinarily stable complex when bound to the appropriate composite DNA site.
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Mechanism of Ribonuclease Cytotoxicity

TL;DR: Results suggest that dimeric BS-RNase enters cells by adsorptive rather than receptor-mediated endocytosis and then evades cytosolic ribonuclease inhibitor so as to degrade cellular RNA.
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Transcriptional Repression by Zinc Finger Peptides EXPLORING THE POTENTIAL FOR APPLICATIONS IN GENE THERAPY

TL;DR: It is found that the peptide containing the three zinc fingers of Zif268 could efficiently repress activated transcription when bound to a site near the TATA box (19-fold repression) or when Bound to a sites near the initiator element (18-fold repression).
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Zinc Finger Proteins as Designer Transcription Factors

TL;DR: This report uses a series of transient and stable transfection experiments to demonstrate that the expression of a target gene can be controlled by changing the in vivo concentration of designer zinc finger proteins in a dose-dependent manner and reports that designer zinc Finger proteins can access their binding sites integrated into the genome and function as potent transcription factors.