about
Blocking angiogenesis and tumorigenesis with GFA-116, a synthetic molecule that inhibits binding of vascular endothelial growth factor to its receptor.Artificial neural network models for prediction of intestinal permeability of oligopeptides.Extracellular transglutaminase 2 is catalytically inactive, but is transiently activated upon tissue injury.Artificial neural network study on organ-targeting peptides.Crystallization and preliminary X-ray crystallographic studies of the N-terminal domain of human ribosomal protein L7a (RPL7a).Discovery of piperidinyl aminopyrimidine derivatives as IKK-2 inhibitors.Inhibition of genotoxic stress induced apoptosis by novel TAT-fused peptides targeting PIDDosome.Chemistry and biology of dihydroisoxazole derivatives: selective inhibitors of human transglutaminase 2.Acylideneoxoindoles: a new class of reversible inhibitors of human transglutaminase 2.Catalytic nickel nanoparticles embedded in a mesoporous metal-organic framework.Cyclic ketals of tartaric acid: simple and tunable reagents for the determination of the absolute configuration of primary amines.Rigid macrocyclic triamides as anion receptors: anion-dependent binding stoichiometries and 1H chemical shift changes.Synthesis and evaluation of oxime derivatives as modulators for amyloid beta-induced mitochondrial dysfunction.Tissue transglutaminase 2 inhibition promotes cell death and chemosensitivity in glioblastomas.Synthesis and biological evaluation of 2-(arylethynyl)quinoline derivatives as mGluR5 antagonists for the treatment of neuropathic pain.Transglutaminase 2 inhibitor, KCC009, disrupts fibronectin assembly in the extracellular matrix and sensitizes orthotopic glioblastomas to chemotherapy.Selective anion binding by a macrocycle with convergent hydrogen bonding functionality.Aminoindanol-based chiral derivatizing agents for the determination of the absolute configuration of carboxylic acids.N-(2-Nitrophenyl)proline: an intramolecular hydrogen bond forming reagent for the determination of the absolute configuration of primary amines.Crystal structure and guest uptake of a mesoporous metal-organic framework containing cages of 3.9 and 4.7 nm in diameter.Synthesis and Photoluminescent Properties of New Aza-Indenofluorene DerivativesPalladium Nanoparticle Catalyzed Conversion of Iron Nanoparticles into Diameter- and Length-Controlled Fe2P NanorodsPharmacologic transglutaminase inhibition attenuates drug-primed liver hypertrophy but not Mallory body formationA Dual Channel Fluorescence Chemosensor for Anions Involving Intermolecular Excited State Proton Transfer We thank the National Institutes of Health for financial support of this work
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Q33203015-CFAE506B-6A0B-4A52-BA7B-33A56A291794Q33290486-ED0DA972-CE18-44AF-B557-6ADB74831039Q33325485-E876F849-627B-4148-9473-A4BF24B24392Q33519580-AF6BDB63-2553-4900-8A23-1CF93B826296Q34823974-D532F669-021A-427C-B74A-85508B3BBFC7Q38475062-BC87EC68-924A-40A0-A0B2-BCF1DF3CE543Q39447673-1884BD3C-FDEA-4FBD-B6DF-B3889FC8B504Q40430886-2FA1CCA5-C85B-4C52-BA94-ED0C47387337Q41888707-0B8E30DE-B054-4A22-940A-30A09A5A5A06Q43105190-9CE9C548-899E-42B2-9393-28463CE5F3FCQ43186015-4B67D5A2-3ADE-4339-B682-4DDD4B5B09F4Q44554773-EBCEFB2B-C757-4F8E-B56B-CFC219D1EED3Q45828915-EC39CB8B-5491-4C7C-808B-A21B1A85BF7DQ46709549-35188EE7-4894-4CA8-94B5-C6ABB5E17426Q48203375-3E449886-7A15-4F68-A815-7D8CEEBC95D8Q48372615-295FF943-3D03-466D-98FB-11D630BABDE9Q49310698-85A83FAC-DD17-4EBF-A38E-0463BCEF45A2Q53362470-BE8976EA-CE94-4A35-B557-91E1DAFD529BQ53467587-CFB1C944-61AA-491A-BCC7-CC0C88874D54Q53565127-8C1B7801-89DD-40E0-AE90-3F416353D9C3Q58059635-EF3B8C44-0782-458F-B1C3-E5BF52EDD1A0Q58059715-2EF93827-9632-46CC-89CA-D6323FF0ABF0Q58059793-C2D2738B-C50B-4FCA-848A-736F754DAFF5Q74826418-9584B917-65C0-434D-BA11-BE536729A682
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Kihang Choi
@ast
Kihang Choi
@en
Kihang Choi
@es
Kihang Choi
@sl
type
label
Kihang Choi
@ast
Kihang Choi
@en
Kihang Choi
@es
Kihang Choi
@sl
prefLabel
Kihang Choi
@ast
Kihang Choi
@en
Kihang Choi
@es
Kihang Choi
@sl
P106
P1153
15759043900
P31
P496
0000-0001-5196-4107