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Hyo Young Kim

Researcher at Korea Institute of Science and Technology

Publications -  22
Citations -  311

Hyo Young Kim is an academic researcher from Korea Institute of Science and Technology. The author has contributed to research in topics: Dehydrogenation & Catalysis. The author has an hindex of 7, co-authored 21 publications receiving 212 citations. Previous affiliations of Hyo Young Kim include Korea University.

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Self-assembled mirror DNA nanostructures for tumor-specific delivery of anticancer drugs

TL;DR: It is demonstrated that the mirror DNA nanostructures can deliver anticancer drugs selectively to tumors with enhanced cellular and tissue penetration and show greater anticancer effects as compared to that of conventional PEGylated liposomes.
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Discovery of a non-cationic cell penetrating peptide derived from membrane-interacting human proteins and its potential as a protein delivery carrier

TL;DR: The uptake mechanism, subcellular localization, and biophysical properties of the newly found CPP were investigated, verifying low cytotoxicity, long-term serum stability, and non-immunogenicity, and a potential use of the peptide as a carrier for the delivery of macromolecular cargos.
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Enhanced ammonia dehydrogenation over Ru/La(x)-Al2O3 (x=0-50 mol%): Structural and electronic effects of La doping

TL;DR: Ru (1.0% loaded)-based catalysts supported on La(x)-Al2O3 (x = 0, 1, 5, 10, and 50 moles) were synthesized and characterized by X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) measurement, X-Ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), scanning transmission electron microscope (STEM), and temperature programmed reduction (TPR) as mentioned in this paper.
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Influence of Cation Substitutions Based on ABO3 Perovskite Materials, Sr1–xYxTi1–yRuyO3−δ, on Ammonia Dehydrogenation

TL;DR: In this paper, a series of ABO3 perovskite materials were synthesized and tested for ammonia dehydrogenation, and the influence of A or B site substitution on the catalytic ammonia de-depletion activity was determined by varying the quantity of either A or b site cation, producing Sr1−xYxTi0.92Ru0.