about
A specific fluorescent probe reveals compromised activity of methionine sulfoxide reductases in Parkinson's disease.Activation of Nrf2-driven antioxidant enzymes by cardamonin confers neuroprotection of PC12 cells against oxidative damage.Redox-Dependent Copper Carrier Promotes Cellular Copper Uptake and Oxidative Stress-Mediated Apoptosis of Cancer CellsSelective Activation of a Prodrug by Thioredoxin Reductase Providing a Strategy to Target Cancer CellsSmall molecule inhibitors of mammalian thioredoxin reductase as potential anticancer agents: An updateXanthatin Promotes Apoptosis via Inhibiting Thioredoxin Reductase and Eliciting Oxidative StressHonokiol Alleviates Oxidative Stress-Induced Neurotoxicity via Activation of Nrf2A β-allyl carbamate fluorescent probe for vicinal dithiol proteinsDecrease of Protein Vicinal Dithiols in Parkinsonism Disclosed by a Monoarsenical Fluorescent ProbeA water-soluble dual-site fluorescent probe for the rapid detection of cysteine with high sensitivity and specificityIsolation, Identification, and Activity Evaluation of Chemical Constituents from Soil Fungus Fusarium avenaceum SF-1502 and Endophytic Fungus Fusarium proliferatum AF-04Small Molecules to Target the Selenoprotein Thioredoxin Reductase(±)-Alternamgin, a Pair of Enantiomeric Polyketides, from the Endophytic Fungi Alternaria sp. MG1Lipoamide Ameliorates Oxidative Stress via Induction of Nrf2/ARE Signaling Pathway in PC12 CellsXanthohumol Analogues as Potent Nrf2 Activators against Oxidative Stress Mediated Damages of PC12 CellsFluorophore-Dependent Cleavage of Disulfide Bond Leading to a Highly Selective Fluorescent Probe of ThioredoxinA fast and specific fluorescent probe for thioredoxin reductase that works via disulphide bond cleavageSynthesis of Dithiolethiones and Identification of Potential Neuroprotective Agents via Activation of Nrf2-Driven Antioxidant EnzymesAn Azo Coupling Strategy for Protein 3-Nitrotyrosine Derivatization
P50
Q30401465-7F5AD6F3-F45C-42A4-971D-10579A6E7ED2Q46407584-661E9380-4DF4-46DD-A462-6DE6F518068FQ57032824-65178899-67EC-442D-BF50-B5A3778BB58BQ88185864-6F0BBC1A-CC52-48C2-BABB-B8F511929881Q88569294-35BE5B0B-F734-46D8-82CD-5D29BC6173AAQ89233042-D4930A87-D972-4F5F-9C01-F12F0E37636AQ89495993-D2DA3A9F-1B60-407F-A71E-22DF1D302350Q89591314-5E513085-4B8D-4F5E-A026-D503F13F3F8FQ89846579-AE5E4EE4-B906-4BB6-87A1-2B85B5958F15Q90074793-0962185E-FB89-4E03-B87A-866872079427Q91247274-A138A8DA-9B14-4B7E-8193-798B3995902EQ91382310-16845F54-1548-4E6A-87EB-ECFADE7B2C42Q91793394-0C4FCEAC-CBD6-4F11-956D-629BB75A10A0Q91829540-57939D62-F472-4C91-81EC-D889C1C2079AQ92217403-4CEDE9EA-5633-4D98-BD10-A23DBFC666ACQ92611808-D4AB172D-1A1C-49D0-8176-9A57E401AFDEQ92948104-A411A38D-3979-42F1-9771-1E9DBE4ED6E8Q92966312-B8F1EA3E-8EDA-4E37-9E90-9F083387AD35Q93042977-05500441-ED78-46CD-9F1B-723DD3B215D0
P50
description
researcher
@en
wetenschapper
@nl
name
Jianguo Fang
@en
Jianguo Fang
@nl
type
label
Jianguo Fang
@en
Jianguo Fang
@nl
prefLabel
Jianguo Fang
@en
Jianguo Fang
@nl
P31
P496
0000-0002-2884-3363