about
Photoactivatable, biologically-relevant phenols with sensitivity toward 2-photon excitationBrominated 7-hydroxycoumarin-4-ylmethyls: photolabile protecting groups with biologically useful cross-sections for two photon photolysisLight-mediated inhibition of protein synthesis.Modulation of the inhibitor properties of dipeptidyl (acyloxy)methyl ketones toward the CaaX proteases.8-Hydroxyquinoline-based inhibitors of the Rce1 protease disrupt Ras membrane localization in human cells.Photochemical modulation of Ras-mediated signal transduction using caged farnesyltransferase inhibitors: activation by one- and two-photon excitationUnraveling the mechanism of the photodeprotection reaction of 8-bromo- and 8-chloro-7-hydroxyquinoline caged acetates.Light-activated serotonin for exploring its action in biological systems.Left-right patterning in Xenopus conjoined twin embryos requires serotonin signaling and gap junctions.Resonance Raman characterization of the different forms of ground-state 8-substituted 7-hydroxyquinoline caged acetate compounds in aqueous solutions.Imaging dynamic redox changes in mammalian cells with green fluorescent protein indicators.Sensitized two-photon photochemical deprotection.Resonance Raman characterization of different forms of ground-state 8-bromo-7-hydroxyquinoline caged acetate in aqueous solutions.Substituent effects on the sensitivity of a quinoline photoremovable protecting group to one- and two-photon excitation.Correlating enzyme activity and cellular behavior.Unravelling the early photochemical behavior of (8-substituted-7-hydroxyquinolinyl)methyl acetates through electronic structure theory and ultrafast transient absorption spectroscopy.Photochemical Activation of Tertiary Amines for Applications in Studying Cell Physiology.Targeting Type 2 Diabetes with C-Glucosyl Dihydrochalcones as Selective Sodium Glucose Co-Transporter 2 (SGLT2) Inhibitors: Synthesis and Biological Evaluation.Rce1: mechanism and inhibition.A spectroscopic study of the excited state proton transfer processes of (8-bromo-7-hydroxyquinolin-2-yl)methyl-protected phenol in aqueous solutions.Inhibition of kinesin motor proteins by adociasulfate-2.Bhc-diol as a photolabile protecting group for aldehydes and ketonesBrominated hydroxyquinoline as a photolabile protecting group with sensitivity to multiphoton excitation8-Bromo-7-hydroxyquinoline as a photoremovable protecting group for physiological use: mechanism and scopeComparison of the absorption, emission, and resonance Raman spectra of 7-hydroxyquinoline and 8-bromo-7-hydroxyquinoline caged acetateLight-Activated ChemotaxisPhotoactivatable Dopamine and Sulpiride to Explore the Function of Dopaminergic Neurons and CircuitsBypassing Glutamic Acid Decarboxylase 1 (Gad1) Induced Craniofacial Defects with a Photoactivatable Translation Blocker MorpholinoTwo-Photon Excitable Photoremovable Protecting Groups Based on the Quinoline Scaffold for Use in BiologyPhotorearrangement of Quinoline-Protected Dialkylanilines and the Photorelease of Aniline-Containing Biological EffectorsPractical Synthesis of Quinoline-Protected Morpholino Oligomers for Light-Triggered Regulation of Gene Function
P50
Q30683182-35BCA7AA-107D-4F16-BD36-B625545D27A4Q31904757-6D598322-57B7-40B9-894E-AE16EF37FFBFQ33217784-1BBA5D95-51B1-492E-AAA5-F1D770AE8219Q33653120-C354B660-8FFE-413D-A324-5C31D61A9F16Q35878817-B6278633-C3D3-4D0A-871C-D8EEE0B8635CQ36215605-8BD344DB-781F-447B-8F88-028B1AD3B459Q36492415-D3AD3311-2AF2-460F-950F-90DBBA63886BQ37540864-A1BF629F-010B-4D44-9F3D-E176DD08C4F3Q41036743-4457BF43-3B46-4A90-AAC7-BF5546F98C47Q43180608-C3A6DA38-1D65-4D1A-AB69-D5B944E91C46Q44777486-7F4B3F59-16D9-4B23-9612-4029B6EF8061Q45933130-AEBDF0EF-7B70-4A6A-9F41-3E956D3DEC59Q46083573-0547353C-30D4-438D-A881-2BACB562E5EBQ46165116-F72AB8FC-E33F-468E-BACC-9A303DE50753Q46893847-8F7218F2-D1A4-4FBE-B6B9-7379B9F13F91Q48165356-30056476-2363-4A40-B912-AC5B0A718616Q48243817-F18911E6-B667-4E1E-AD42-8050AC50EF7AQ48340648-4CE4EEA2-7926-48CF-8945-64C9ACF46E68Q50102683-58D5A000-A11D-4539-8E17-82A1362CCAC7Q50919969-1F5D49DF-7742-4334-A2F7-5E7082381CD0Q52010955-6025BD9E-CB25-4D77-98D9-C141FFC01697Q73488160-A8BFC27A-E355-4CC8-B7F0-D709021AA7EFQ77218984-A4ABD53D-3E92-4763-9C70-6FFE2994414DQ82992059-7000B456-7A25-47F2-8A8F-BAE46651DD50Q84924756-FBDB347A-7297-4652-8609-F8FAB4D4622CQ89246283-A26A9CBE-9805-489A-B694-16B2D240B712Q89798610-6B2B0971-9CBC-4EAC-BAE0-59B937C4CEAAQ91364163-27C92479-7C69-4433-9197-C786CE8F3C06Q91748211-6EC88B04-FAC3-4D41-AF5A-0A1E106E1C92Q92073217-7D1C818D-2485-49B6-9877-58468256E44BQ94514740-84423C54-D684-412F-B8B0-1DF8036D73BD
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Timothy M Dore
@es
Timothy M. Dore
@en
Timothy M. Dore
@nl
Timothy M. Dore
@sl
type
label
Timothy M Dore
@es
Timothy M. Dore
@en
Timothy M. Dore
@nl
Timothy M. Dore
@sl
prefLabel
Timothy M Dore
@es
Timothy M. Dore
@en
Timothy M. Dore
@nl
Timothy M. Dore
@sl
P106
P1153
6603830858
P21
P31
P496
0000-0002-3876-5012
P569
2000-01-01T00:00:00Z