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Inchan Kwon

Researcher at Gwangju Institute of Science and Technology

Publications -  81
Citations -  1811

Inchan Kwon is an academic researcher from Gwangju Institute of Science and Technology. The author has contributed to research in topics: Amino acid & Human serum albumin. The author has an hindex of 22, co-authored 75 publications receiving 1511 citations. Previous affiliations of Inchan Kwon include LG Chem & University of California, Berkeley.

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Designer Gene Delivery Vectors: Molecular Engineering and Evolution of Adeno-Associated Viral Vectors for Enhanced Gene Transfer

TL;DR: Molecular engineering and directed evolution of AAV vectors offer promise for generating ‘designer’ gene delivery vectors with enhanced properties, particularly those based on AAV2, the best characterized AAV serotype.
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Breaking the degeneracy of the genetic code.

TL;DR: An E. coli strain co-transformed with ytRNAPheAAA and a mutant yeast phenylalanyl-tRNA synthetase is used to demonstrate efficient replacement of phenylalanine by L-3-(2-naphthyl)alanine (Nal) at UUU, but not at UUC codons.
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Improving cancer therapy through the nanomaterials-assisted alleviation of hypoxia.

TL;DR: An overview of the recent progress in the development of novel nanomaterials for the alleviation of hypoxic microenvironment is presented, with promising start in the early phase and expected to grow rapidly in the coming years.
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An evolved adeno-associated viral variant enhances gene delivery and gene targeting in neural stem cells.

TL;DR: This work applied directed evolution to create a "designer" AAV vector with enhanced delivery efficiency for neural stem cells (NSCs), and a novel AAV variant, carrying an insertion of a selected peptide sequence on the surface of the threefold spike within the heparin-binding site, emerged from this evolution.
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A Safe, Blood-Brain Barrier Permeable Triphenylmethane Dye Inhibits Amyloid-β Neurotoxicity by Generating Nontoxic Aggregates

TL;DR: It is demonstrated that BBG is an effective Aβ aggregation modulator, which reduces Aβ-associated cytotoxicity in a dose-dependent manner by promoting the formation of off-pathway, nontoxic aggregates and supports the hypothesis that generating nont toxic aggregates using small molecule modulators is aneffective strategy for reducing Aβ cytot toxicity.