about
Ultrafast study of p-biphenylyldiazomethane and p-biphenylylcarbene.Ultrafast spectroscopic and matrix isolation studies of p-biphenylyl, o-biphenylyl, and 1-naphthylnitrenium cations.Direct detection of a transient oxenium ion in water generated by laser flash photolysis.A study of the photochemistry of Diazo Meldrum's acid by ultrafast time-resolved spectroscopies.2-Naphthyl(carbomethoxy)carbene revisited: combination of ultrafast UV-vis and infrared spectroscopic study.Characterization of reactive intermediates generated during photolysis of 4-acetoxy-4-aryl-2,5-cyclohexadienones: oxenium ions and aryloxy radicals.Quantitative real-time imaging of glutathioneThe complex role of multivalency in nanoparticles targeting the transferrin receptor for cancer therapies.Ultrafast study of 9-diazofluorene: direct observation of the first two singlet states of fluorenylidene.Rendering protein-based particles transiently insoluble for therapeutic applications.Theoretical and Experimental Investigation of Thermodynamics and Kinetics of Thiol-Michael Addition Reactions: A Case Study of Reversible Fluorescent Probes for Glutathione Imaging in Single Cells.RNA replicon delivery via lipid-complexed PRINT protein particles.Precisely tunable engineering of sub-30 nm monodisperse oligonucleotide nanoparticlesConcerted Wolff rearrangement in two simple acyclic diazocarbonyl compounds.Electrospray ionization tandem mass spectrometric characteristics and fragmentation mechanisms of distamycin analogues.Tunable thioesters as "reduction" responsive functionality for traceless reversible protein PEGylation.Loss of glutaredoxin 3 impedes mammary lobuloalveolar development during pregnancy and lactation.Direct observation of acyl azide excited states and their decay processes by ultrafast time resolved infrared spectroscopy.Ultrafast UV-vis and IR studies of p-biphenylyl acetyl and carbomethoxy carbenes.Ultrafast studies of some diarylcarbenes.Ultrafast carbene-carbene isomerization.Study of concerted and sequential photochemical Wolff Rearrangement by femtosecond UV-vis and IR spectroscopy.Time-resolved resonance Raman observation of the dimerization of didehydroazepines in solution.The dynamics of carbene solvation: an ultrafast study of p-biphenylyltrifluoromethylcarbene.Reversible Reaction-Based Fluorescent Probe for Real-Time Imaging of Glutathione Dynamics in Mitochondria.Metabolomics reveals the formation of aldehydes and iminium in gefitinib metabolism.Proteomic profiling identifies key coactivators utilized by mutant ERα proteins as potential new therapeutic targets.Reply to 'Pitfalls in the quantitative imaging of glutathione in living cells'.Heterozygous deletion of chromosome 17p renders prostate cancer vulnerable to inhibition of RNA polymerase IICharacterizing novel metabolic pathways of melatonin receptor agonist agomelatine using metabolomic approachesTime-Resolved Resonance Raman and Computational Investigation of the Influence of 4-Acetamido and 4-N-Methylacetamido Substituents on the Chemistry of PhenylnitrenePhotochemistry of 2-Naphthoyl Azide. An Ultrafast Time-Resolved UV–Vis and IR Spectroscopic and Computational StudyEarly Events in the Photochemistry of 2-Naphthyl Azide from Femtosecond UV/Vis Spectroscopy and Quantum Chemical Calculations: Direct Observation of a Very Short-Lived Singlet NitreneSolvent Effects on Intermolecular Proton Transfer: The Rates of Nitrene Protonation and Their Correlation with Swain AcityUltrafast Study ofp-Biphenylyldiazoethane. The Chemistry of the Diazo Excited State and the Relaxed CarbeneEarly Events in the Photochemistry of Aryl Azides from Femtosecond UV/Vis Spectroscopy and Quantum Chemical CalculationsUltrafast Spectroscopic Study of the Photochemistry and Photophysics of Arylhalodiazirines: Direct Observation of Carbene and Zwitterion FormationTranscriptional profiling and therapeutic targeting of oxidative stress in neuroinflammation
P50
Q33251955-1B6EDE95-8BC3-4255-9EFA-E6439A820CB3Q33287558-C6285914-3B00-495D-B028-3023E1FAB81DQ33305111-302B7BAB-0578-4C67-B76B-36E581382A0EQ33371748-9626B716-9095-4D41-BD87-724E48EE0C75Q33374857-45376EFF-3C9C-419A-85E7-233CF35BFCB0Q33381779-973A8C99-F4D5-490C-B2E0-E483B07DEC79Q33906402-4DC8B35A-E31D-485D-B566-BE3E33A05421Q34072375-3F794946-821E-489B-BB84-0748CBE73D24Q34700885-6FFFDC07-6522-4414-A489-BEFE4B109BD3Q36002525-D491D292-29C6-40C8-9DC9-C4063F0DFCC3Q36504946-885875A0-EDC6-43A9-BD8F-4B797761408AQ37628162-CE8BAC02-C519-4197-BDF1-156AF79E69B2Q41790614-212744D2-440C-4AEC-937D-4461D0F5848AQ42789975-FE21E5FE-8E23-4B53-911A-653782B6F0CFQ43981173-9FD85A00-BB75-42D7-BF5D-967A5846D937Q44001369-218E5248-B4C5-43F2-8CD8-E2AA4D330DDBQ45988712-097A9344-932E-4F41-931F-317643CE8D0BQ46076781-A01ACCA7-CD97-4F11-824F-3D8AFBE84476Q46461530-7152AFA1-6B59-423B-AE6A-AA5BBAA0F204Q46606119-8994C02D-5F97-4156-B9BC-F96D61F8858FQ46682736-E7750023-C5B4-46AD-A5DB-836C2FC85E45Q46724537-E84F6720-B758-409B-BFDD-758FF54DAB06Q46787678-9788286D-E663-4828-A76E-23C661B251C9Q46794855-A0E9A16D-CB84-490F-A694-5714E58E4265Q48237385-C6FEEF5B-D1B7-4577-819A-6BAA3219CBC4Q53407604-1AFC482D-5A64-459E-8348-9E5AB0BFBCBDQ53684285-3E8D5945-C6B1-4929-B7F1-998AC04891BFQ55334182-95990101-15A6-4E03-B44F-6D80FDDB93BAQ57804743-851BCFA8-E00F-4661-B0C0-D1D2D07649E7Q62066138-45F541EF-DB84-4E41-84C1-8570C12E5646Q62066141-99F77062-E54E-41AE-8235-3C195D88D29BQ62066143-2348810F-C691-4D11-90C4-960B872F8F51Q62066148-D8F345B0-3C2C-431D-9DE0-240C7272B520Q62066150-70794A00-1636-4C29-9734-6BC47DB00841Q62066151-A7841D33-C196-4F94-9A00-5279888FBC09Q62066152-A3CBC89B-83B3-4BDA-9054-45B61AA2B7DEQ62066154-135447DE-627B-4396-BB72-2A8124450B82Q91875027-903A717A-3CC9-41D5-A488-84FE63ED569B
P50
description
hulumtuese
@sq
researcher
@en
հետազոտող
@hy
name
Jin Wang
@ast
Jin Wang
@en
Jin Wang
@es
Jin Wang
@nl
Jin Wang
@sl
type
label
Jin Wang
@ast
Jin Wang
@en
Jin Wang
@es
Jin Wang
@nl
Jin Wang
@sl
prefLabel
Jin Wang
@ast
Jin Wang
@en
Jin Wang
@es
Jin Wang
@nl
Jin Wang
@sl
P1053
A-3245-2009
M-4036-2014
P106
P1153
55999032300
P21
P31
P3829
P496
0000-0003-3625-7919
P569
2000-01-01T00:00:00Z