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Heterodimers of nanoparticles: formation at a liquid-liquid interface and particle-specific surface modification by functional moleculesElectron transport across glycerol monooleate bilayer lipid membranes facilitated by magnesium etiochlorinpi cation radicals of ferrous and free base isobacteriochlorins: Models for siroheme and sirohydrochlorin.The role of subcellular localization in initiation of apoptosis by photodynamic therapy.Photodynamic therapy-mediated modulation of inflammatory cytokine production by Epstein-Barr virus-infected nasopharyngeal carcinoma cells.Role of mitogen-activated protein kinase in Zn-BC-AM PDT-induced apoptosis in nasopharyngeal carcinoma cells.Targeted inhibition of the EGFR pathways enhances Zn-BC-AM PDT-induced apoptosis in well-differentiated nasopharyngeal carcinoma cells.Apoptosis and expression of cytokines triggered by pyropheophorbide-a methyl ester-mediated photodynamic therapy in nasopharyngeal carcinoma cells.Evidence that heme d1 is a 1,3-porphyrindione.A bulky bis-pocket manganese(V)-oxo corrole complex: observation of oxygen atom transfer between triply bonded Mn(V)[triple bond]O and alkene.Cyclophane porphyrin.Microemulsion and micellar electrokinetic chromatography of Hematoporphyrin D: a starting material of hematoporphyrin derivative.Investigation of solvent effects in capillary electrophoresis for the separation of biological porphyrin methyl esters.High catalytic activities of artificial peroxidases based on supramolecular hydrogels that contain heme models.Hydrocarbon oxidation by beta-halogenated dioxoruthenium(VI) porphyrin complexes: effect of reduction potential (RuVI/V) and C-H bond-dissociation energy on rate constants.A new iso-amyl benzothiazolyl sulfoxide as an extractant for palladium and the crystal structure of its palladium (II) complex.Fast atom bombardment mass spectrometry of high-molecular-weight fraction of porphyrin-based photodynamic therapy drugs.Proximal base influence on the binding of oxygen and carbon monoxide to heme.Solution behavior of a synthetic myoglobin active site.Involvement of both endoplasmic reticulum and mitochondria in photokilling of nasopharyngeal carcinoma cells by the photosensitizer Zn-BC-AM.Multifunctional divalent vancomycin: the fluorescent imaging and photodynamic antimicrobial properties for drug resistant bacteria.Resonance Raman detection of Fe-CO stretching and Fe-C-O bending vibrations in sterically hindered carbonmonoxy "strapped hemes". A structural probe of Fe-C-O distortion.Synthesis of Octafluoroporphyrin.Simple dioxygen heme complexes formed in N,N-dimethylformamide.The active site structure of E. coli HPII catalase. Evidence favoring coordination of a tyrosinate proximal ligand to the chlorin iron.A Supramolecular-Hydrogel-Encapsulated Hemin as an Artificial Enzyme to Mimic PeroxidaseUsing enzymatic reactions to enhance the photodynamic therapy effect of porphyrin dityrosine phosphatesSynthesis and cellular uptake of porphyrin decorated iron oxide nanoparticles—a potential candidate for bimodal anticancer therapyHorseradish peroxidase. XXXVII. Compound I formation from reconstituted enzyme lacking free carboxyl groups as heme side chainsLetter: Coordination of myoglobin active site models in aqueous solution as studied by kinetic methodsLetter: Ferrous porphyrin-mercaptide complexes. Models for reduced cytochrome P-450Letter: Oxygen binding to mercaptide-heme complexes. Models for reduced cytochrome P-450Oxygen binding to ferrous heme alpha and a synthetic analogStacked double-macrocyclic ligands. 1. synthesis of a 'crowned' porphyrinPhotosensitization by synthetic diporphyrins and dichlorins in vivo and in vitroResonance Raman spectra of the II-cation radicals of copper, cobalt, and nickel methyloctaethylchlorins: vibrational characteristics of chlorophyll modelsModelling heme d1. The spectral properties of copper(II) porphyrindionesSolvent effects on reversible formation and oxidative stability of heme-oxygen complexesChemistry of hematoporphyrin-derived photosensitizersA convenient photochemical method for reduction of ferric hemes
P50
Q28301024-820D62BC-7334-4830-B286-479D9793EEBEQ34252089-04DD1D93-1707-4798-AC96-BEF205B09A47Q35357534-D6A25001-C96B-4534-87A2-384C37A04CBBQ36058055-08E781C0-4D98-426D-AACD-A8BCBFC9516DQ39026506-9B2696EC-58A4-4276-B886-23FE082B02B2Q39717681-8390FF55-47A3-411B-BFCD-CC2BB2D83A88Q39789471-241B96A4-DEE6-402A-87BA-EEAA1AFA87E5Q40203201-2DF77087-CDB3-4E68-AB50-4F0C3A98643EQ42224136-B56A5FE5-B66E-48B0-95AC-686441BA63BFQ43279690-30AEB982-FB36-43EA-BF77-4FA6168747FBQ43896076-1BAEEACE-337F-4416-8A5F-0DACC9583600Q45237191-4A2C3B97-B4FA-4870-858A-E5EBDB337FBCQ46634471-58416128-D510-47C1-87CD-418D598E407EQ46655271-03242168-35C2-4B49-94A1-94B88CEB509EQ46704131-7665E81F-0C11-4B9D-80A4-9B9802ACAB91Q46897081-5B9930EC-CA84-461C-B782-8C99423EB9EDQ47183237-59841D0B-E194-43E2-9873-397D9A8922B8Q47906088-9CD45AFB-55DD-42C0-B45D-27012C8EA37FQ47970949-2D789842-3388-4D49-8D4E-13980FE5DFA8Q50781537-E8725CBB-4E5B-4BD0-8885-F2099E2CF558Q51630639-44DE642F-8D6F-40EB-A2B5-7E66DAD2C36AQ52702130-4D9DD91A-A998-4FE6-BC15-691D2BD12508Q53625052-3EA2AD93-E619-4F14-9ED3-03AE2A4053A1Q54196504-04D5594E-0D61-42A2-9377-EDAD80509D14Q54687477-92F3C1C4-9829-44DB-8F38-BF08FB01AA9EQ59279628-B46A1112-65FE-497D-9C5E-3C286405BE49Q59279656-F5D4927F-06CA-4FCA-9DC0-EDCD85B0A52DQ59279660-50C2B90D-FD54-4C6D-B425-7D157F0A8CB2Q66970874-346FF35F-2A43-4E80-A8B2-10B24E905D8EQ67250720-55284F97-D3DF-48ED-9F25-6804DD701DF5Q67250727-12CC2388-5A0C-4142-90ED-A86361D865D3Q67435814-3CCB0D95-2E9C-43C4-B35D-2A0D885F65DBQ67468334-94688D9F-6FB7-4064-82DF-97463F8E32FFQ67560884-9ED661BB-01EA-4D0D-8631-BBD397AA8315Q67922846-ECB9B234-59F7-4595-BD7B-CE03843CB2EFQ68042410-6A86FCF4-DC09-4F42-83E8-C4CD7AC0E7CBQ68346844-BCFDAE74-0CB7-4465-93CD-160C88A70BB7Q69816217-E6E8A2B4-A132-47C5-AA97-02147148C26AQ70048720-CEBFF206-DC19-4995-AEC9-095998E40C30Q70382534-A602951E-605D-492C-B0B6-7C3671B32DB9
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Chi K Chang
@ast
Chi K Chang
@en
Chi K Chang
@es
Chi K Chang
@nl
Chi K Chang
@sl
type
label
Chi K Chang
@ast
Chi K Chang
@en
Chi K Chang
@es
Chi K Chang
@nl
Chi K Chang
@sl
prefLabel
Chi K Chang
@ast
Chi K Chang
@en
Chi K Chang
@es
Chi K Chang
@nl
Chi K Chang
@sl
P1053
B-1675-2010
P106
P31
P3829
P496
0000-0002-4113-1950