Reductive ligation mediated one-step disulfide formation of S-nitrosothiols.
about
Mass spectrometry in studies of protein thiol chemistry and signaling: opportunities and caveatsMechanism-based triarylphosphine-ester probes for capture of endogenous RSNOsMethodologies for the characterization, identification and quantification of S-nitrosylated proteins.Effects of ionizing radiation on biological molecules--mechanisms of damage and emerging methods of detectionCysteine-mediated redox signaling: chemistry, biology, and tools for discoveryConversion of S-phenylsulfonylcysteine residues to mixed disulfides at pH 4.0: utility in protein thiol blocking and in protein-S-nitrosothiol detection.Strategies and tools to explore protein S-nitrosylation.The Expanding Landscape of the Thiol Redox Proteome.Chemical methods for the direct detection and labeling of S-nitrosothiols.Solid-phase capture for the detection and relative quantification of S-nitrosoproteins by mass spectrometry.Design, Synthesis, and Cardioprotective Effects of N-Mercapto-Based Hydrogen Sulfide Donors.Oxidative stress and the HIV-infected brain proteome.Selective trapping of SNO-BSA and GSNO by benzenesulfinic acid sodium salt: mechanistic study of thiosulphonate formation and feasibility as a protein S-nitrosothiol detection strategyChemical methods to detect S-nitrosation.Proteomics insights into deregulated protein S-nitrosylation and disease.Nitric oxide-cold stress signalling cross-talk, evolution of a novel regulatory mechanism.Direct methods for detection of protein S-nitrosylation.Proteomic approaches to evaluate protein S-nitrosylation in disease.Gel-free proteomic methodologies to study reversible cysteine oxidation and irreversible protein carbonyl formation.Proline-based phosphoramidite reagents for the reductive ligation of S-nitrosothiols.Facile amide formation via S-nitrosothioacids.Identification of protein nitrosothiols using phosphine-mediated selective reduction.Cysteine-activated hydrogen sulfide (H2S) donors.One-pot thioether formation from S-nitrosothiols.S-Nitrosothiols: chemistry and reactions.Chemical methods for mapping cysteine oxidation.Rethinking Cysteine Protective Groups: S-Alkylsulfonyl-l-Cysteines for Chemoselective Disulfide Formation.
P2860
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P2860
Reductive ligation mediated one-step disulfide formation of S-nitrosothiols.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Reductive ligation mediated one-step disulfide formation of S-nitrosothiols.
@en
Reductive ligation mediated one-step disulfide formation of S-nitrosothiols.
@nl
type
label
Reductive ligation mediated one-step disulfide formation of S-nitrosothiols.
@en
Reductive ligation mediated one-step disulfide formation of S-nitrosothiols.
@nl
prefLabel
Reductive ligation mediated one-step disulfide formation of S-nitrosothiols.
@en
Reductive ligation mediated one-step disulfide formation of S-nitrosothiols.
@nl
P2093
P2860
P356
P1433
P1476
Reductive ligation mediated one-step disulfide formation of S-nitrosothiols.
@en
P2093
A Richard Whorton
Dehui Zhang
Jiming Zhang
P2860
P304
P356
10.1021/OL101863S
P407
P577
2010-09-01T00:00:00Z