about
Protein-mediated dethreading of a biotin-functionalised pseudorotaxane.Bioavailability of [2-(14)C]quercetin-4'-glucoside in rats.A prototypical small-molecule modulator uncouples mitochondria in response to endogenous hydrogen peroxide production.Selective uncoupling of individual mitochondria within a cell using a mitochondria-targeted photoactivated protonophore.Highly stable tetrathiafulvalene radical dimers in [3]catenanes.Synthesis of an azido-tagged low affinity ratiometric calcium sensor.Dendron-anchored organocatalysts: the asymmetric reduction of imines with trichlorosilane, catalysed by an amino acid-derived formamide appended to a dendron.Determination of flavonol metabolites in plasma and tissues of rats by HPLC-radiocounting and tandem mass spectrometry following oral ingestion of [2-(14)C]quercetin-4'-glucoside.Potential therapeutic antioxidants that combine the radical scavenging ability of myricetin and the lipophilic chain of vitamin E to effectively inhibit microsomal lipid peroxidation.Organocatalysts immobilised onto gold nanoparticles: application in the asymmetric reduction of imines with trichlorosilane.Disposition and metabolism of [2-14C]quercetin-4'-glucoside in rats.Excited state charge redistribution and dynamics in the donor-π-acceptor flavin derivative ABFL.Tuneable pseudorotaxane formation between a biotin-avidin bioconjugate and CBPQT4+.Absorption, disposition, metabolism, and excretion of [3-(14)C]caffeic acid in rats.Methionine Sulfoxide Reductase B3 Requires Resolving Cysteine Residues for full Activity and can act as a Stereospecific Methionine Oxidase.MitoNeoD: A Mitochondria-Targeted Superoxide Probe.A dual sensor spin trap for use with EPR spectroscopy.Controlled self-assembly of organic nanowires and platelets using dipolar and hydrogen-bonding interactions.Mitochondrial oxidative stress causes insulin resistance without disrupting oxidative phosphorylation.Itaconate is an anti-inflammatory metabolite that activates Nrf2 via alkylation of KEAP1.Model systems for flavoenzyme activity: intramolecular self-assembly of a flavin derivative via hydrogen bonding and aromatic interactions.Naphthoxanthenyl, a New Stable Phenalenyl Type Radical Stabilized by Electronic EffectsModel systems for flavoenzyme activity: an investigation of the role functionality attached to the C(7) position of the flavin unit has on redox and molecular recognition propertiesMolecular recognition at the liquid–liquid interface of colloidal microcapsules‘Lock and key’ control of optical properties in a push–pull systemA flavin-based [2]catenaneDendron-based model systems for flavoenzyme activity: towards a new class of synthetic flavoenzymeProbing the solvent-induced tautomerism of a redox-active ureidopyrimidinoneSelective Disruption of Mitochondrial Thiol Redox State in Cells and In Vivo
P50
Q30702445-AB7F74B1-200D-4A63-8B62-2DD2F768676CQ34601298-E2ACA1C1-6296-4A17-B728-52A773F8CBE5Q37094601-25213EB1-7B7F-41BA-B353-492E58BD096BQ40485681-ECAA494C-BE51-4EAD-A654-5059B4CF1138Q42878956-BF2E61F2-FD92-4D35-8A18-C0F3E4F6868DQ43155350-DDEC0CCD-9CA4-4F6A-AE59-E068F77129B0Q43213874-F3AD2B7F-E0C2-48AC-B3D6-2F1A07655C74Q44197798-E071D5BD-9C51-4C1B-9764-12A77B00BEC6Q44841480-610B4AF4-0F07-4816-9485-54BF15E5CC2AQ45933216-F63AD21B-999D-4FD3-B01B-45C975E6E56BQ46440377-094ED26C-5FDE-460E-B177-504DEE68F63AQ46535473-882D901E-4783-4ABD-9D53-BAFBC24994B4Q46554916-2223E4C0-6334-445B-81D1-0EC1C575438AQ48582013-6C108718-9DE2-4CE1-9A5B-FD982E95303CQ50115762-2F19CE2D-DFEE-4C54-B3B6-49DF21F356BDQ50175598-F35FF526-D0E5-45C3-A564-0D76F2DAC54CQ50799309-091D8610-ADD3-4EBB-BA5A-E82F1B8D2BCAQ52589700-D65C9313-7BA4-4772-AE3E-87FF5EEB07C2Q52620904-74C43FD5-4324-49F9-AD9A-F2ADBED9B14CQ52723589-0476C0FD-E0F2-417B-8759-13CBD4EADA33Q54379713-20F4BFEF-46CE-4018-A032-AD40E3D9A0B9Q57383035-7F868D3F-8372-4B76-95D1-6DD13564CC55Q63971400-B79D8397-95BD-498D-A6AC-3BDF2A59EF8BQ63971401-788A714E-D673-4704-A01D-DA444724234BQ63971404-08DBD3D3-E583-4883-8946-4169F10E8D96Q63971407-B47A02E3-18C4-40ED-A95A-5AC5FB4219E0Q63971411-16DB92BB-2A55-43AA-ACFF-22BA6754F1F0Q63972218-B48DEF4E-09AF-439D-86F7-5BA192472675Q64064592-6E9BF661-2C0D-4F80-BABC-D775A24DE6CA
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Stuart T Caldwell
@ast
Stuart T Caldwell
@en
Stuart T Caldwell
@es
Stuart T Caldwell
@nl
Stuart T Caldwell
@sl
type
label
Stuart T Caldwell
@ast
Stuart T Caldwell
@en
Stuart T Caldwell
@es
Stuart T Caldwell
@nl
Stuart T Caldwell
@sl
prefLabel
Stuart T Caldwell
@ast
Stuart T Caldwell
@en
Stuart T Caldwell
@es
Stuart T Caldwell
@nl
Stuart T Caldwell
@sl
P1053
J-8863-2014
P106
P31
P3829
P496
0000-0003-1604-3462