Peroxynitrite preferentially oxidizes the dithiol redox motifs of protein disulfide isomerase (2018)
- Autores:
- Autor USP: AUGUSTO, OHARA - IQ
- Unidade: IQ
- DOI: 10.1074/jbc.M117.807016
- Assuntos: PERÓXIDO DE HIDROGÊNIO; CINÉTICA
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: Journal of Biological Chemistry
- ISSN: 0021-9258
- Volume/Número/Paginação/Ano: v. 293, n. 4, p. 1450-1465, 2018
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: hybrid
- Licença: cc-by
-
ABNT
PEIXOTO, Álbert Souza et al. Peroxynitrite preferentially oxidizes the dithiol redox motifs of protein disulfide isomerase. Journal of Biological Chemistry, v. 293, n. 4, p. 1450-1465, 2018Tradução . . Disponível em: http://www.jbc.org/content/early/2017/11/30/jbc.M117.807016. Acesso em: 19 set. 2024. -
APA
Peixoto, Á. S., Geyer, R. R., Iqbal, A., Truzzi, D. R., Moretti, A. I. S., Laurindo, F. R. M., & Augusto, O. (2018). Peroxynitrite preferentially oxidizes the dithiol redox motifs of protein disulfide isomerase. Journal of Biological Chemistry, 293( 4), 1450-1465. doi:10.1074/jbc.M117.807016 -
NLM
Peixoto ÁS, Geyer RR, Iqbal A, Truzzi DR, Moretti AIS, Laurindo FRM, Augusto O. Peroxynitrite preferentially oxidizes the dithiol redox motifs of protein disulfide isomerase [Internet]. Journal of Biological Chemistry. 2018 ; 293( 4): 1450-1465.[citado 2024 set. 19 ] Available from: http://www.jbc.org/content/early/2017/11/30/jbc.M117.807016 -
Vancouver
Peixoto ÁS, Geyer RR, Iqbal A, Truzzi DR, Moretti AIS, Laurindo FRM, Augusto O. Peroxynitrite preferentially oxidizes the dithiol redox motifs of protein disulfide isomerase [Internet]. Journal of Biological Chemistry. 2018 ; 293( 4): 1450-1465.[citado 2024 set. 19 ] Available from: http://www.jbc.org/content/early/2017/11/30/jbc.M117.807016 - Oxidation of the protein disulfide isomerase by peroxynitrite: kinetics, products and biological implications
- Marked increase in vascular superoxide generation early after vessel injury due to NAD(P)H oxidase (S)
- Nucleic acid alkylation by free radical metabolites of ethanol. Formation of 8-(1-hydroxyethyl) guanine and 8-(2-hydroxyethyl) guanine adducts
- Metabolism of acetaldehyde to methyl and acetyl radicals. In vitro and in vivo EPR spin-trapping studies
- Bicarbonate stimulates the production of thiyl, sulphinyl and disulphide radical anion from thiol oxidation by peroxynitrite
- In vivo formation of electron paramagnetic resonance-detectable nitric oxide and of nitrotyrosine is not impaired during murine leishmaniasis
- Especificidade de ataque do radical 2-feniletil foto-gerado a base guanina do dna
- Free radical intermediates from 5- hydroxyprimaquine
- Carbon - centered radicals: dna alkylation and biological sources
- Possible significance of carbon - centered radicals in the genotoricity of hydrazine derivatives
Informações sobre o DOI: 10.1074/jbc.M117.807016 (Fonte: oaDOI API)
Como citar
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
