Péter Nagy
Péter Nagy
National Institute of Oncology, Department of Molecular Immunology and Toxicology,
Verified email at oncol.hu
Cited by
Cited by
Chemical aspects of hydrogen sulfide measurements in physiological samples
P Nagy, Z Pálinkás, A Nagy, B Budai, I Tóth, A Vasas
Biochimica et Biophysica Acta (BBA)-General Subjects 1840 (2), 876-891, 2014
Isolation of exosomes from blood plasma: qualitative and quantitative comparison of ultracentrifugation and size exclusion chromatography methods
T Baranyai, K Herczeg, Z Onódi, I Voszka, K Módos, N Marton, G Nagy, ...
PloS one 10 (12), e0145686, 2015
Polysulfides link H2S to protein thiol oxidation
R Greiner, Z Pálinkás, K Bäsell, D Becher, H Antelmann, P Nagy, TP Dick
Antioxidants & redox signaling 19 (15), 1749-1765, 2013
Kinetics and mechanisms of thiol–disulfide exchange covering direct substitution and thiol oxidation-mediated pathways
P Nagy
Antioxidants & redox signaling 18 (13), 1623-1641, 2013
Redox chemistry and chemical biology of H2S, hydropersulfides, and derived species: implications of their possible biological activity and utility
K Ono, T Akaike, T Sawa, Y Kumagai, DA Wink, DJ Tantillo, AJ Hobbs, ...
Free Radical Biology and Medicine 77, 82-94, 2014
Cysteinyl-tRNA synthetase governs cysteine polysulfidation and mitochondrial bioenergetics
T Akaike, T Ida, FY Wei, M Nishida, Y Kumagai, MM Alam, H Ihara, ...
Nature communications 8 (1), 1-15, 2017
Key bioactive reaction products of the NO/H2S interaction are S/N-hybrid species, polysulfides, and nitroxyl
MM Cortese-Krott, GGC Kuhnle, A Dyson, BO Fernandez, M Grman, ...
Proceedings of the National Academy of Sciences 112 (34), E4651-E4660, 2015
A novel persulfide detection method reveals protein persulfide-and polysulfide-reducing functions of thioredoxin and glutathione systems
É Dóka, I Pader, A Bíró, K Johansson, Q Cheng, K Ballagó, JR Prigge, ...
Science advances 2 (1), e1500968, 2016
Rapid reaction of hydrogen sulfide with the neutrophil oxidant hypochlorous acid to generate polysulfides
P Nagy, CC Winterbourn
Chemical research in toxicology 23 (10), 1541-1543, 2010
The reactive species interactome: evolutionary emergence, biological significance, and opportunities for redox metabolomics and personalized medicine
MM Cortese-Krott, A Koning, GGC Kuhnle, P Nagy, CL Bianco, A Pasch, ...
Antioxidants & redox signaling 27 (10), 684-712, 2017
Reactive sulfur species: kinetics and mechanisms of the oxidation of cysteine by hypohalous acid to give cysteine sulfenic acid
P Nagy, MT Ashby
Journal of the American Chemical Society 129 (45), 14082-14091, 2007
A proton relay enhances H 2 O 2 sensitivity of GAPDH to facilitate metabolic adaptation
D Peralta, AK Bronowska, B Morgan, É Dóka, K Van Laer, P Nagy, ...
Nature chemical biology 11 (2), 156-163, 2015
Model for the exceptional reactivity of peroxiredoxins 2 and 3 with hydrogen peroxide: a kinetic and computational study
P Nagy, A Karton, A Betz, AV Peskin, P Pace, RJ O'Reilly, MB Hampton, ...
Journal of Biological Chemistry 286 (20), 18048-18055, 2011
Nitrosopersulfide (SSNO−) accounts for sustained NO bioactivity of S-nitrosothiols following reaction with sulfide
MM Cortese-Krott, BO Fernandez, JLT Santos, E Mergia, M Grman, ...
Redox biology 2, 234-244, 2014
Mechanistic chemical perspective of hydrogen sulfide signaling
P Nagy
Methods in enzymology 554, 3-29, 2015
Interactions of hydrogen sulfide with myeloperoxidase
Z Pálinkás, PG Furtmüller, A Nagy, C Jakopitsch, KF Pirker, ...
British journal of pharmacology 172 (6), 1516-1532, 2015
Kinetics and mechanisms of the reaction of hypothiocyanous acid with 5-thio-2-nitrobenzoic acid and reduced glutathione
P Nagy, GNL Jameson, CC Winterbourn
Chemical research in toxicology 22 (11), 1833-1840, 2009
Redox chemistry of biological thiols
P Nagy, CC Winterbourn
Advances in molecular toxicology 4, 183-222, 2010
Biological hydropersulfides and related polysulfides–a new concept and perspective in redox biology
JM Fukuto, LJ Ignarro, P Nagy, DA Wink, CG Kevil, M Feelisch, ...
FEBS letters 592 (12), 2140-2152, 2018
Thiocyanate is an efficient endogenous scavenger of the phagocytic killing agent hypobromous acid
P Nagy, JL Beal, MT Ashby
Chemical research in toxicology 19 (4), 587-593, 2006
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