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Filtros : "Inglês" "OXIDAÇÃO" " GRU999" Limpar

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  • Artigo de periodico

    Aerobic co-oxidation of hemoglobin and aminoacetone, a putative source of methylglyoxal (2021)

    Ramos, Luiz Duarte ; Mantovani, Mariana C ; Sartori, Adriano; Dutra, Fernando; Stevani, Cassius Vinicius ; Bechara, Etelvino José Henriques

    Source: Free Radical Biology and Medicine. Unidade: IQ

    Subjects: HEMOGLOBINAS, ELÉTRONS, OXIDAÇÃO

    PrivadoAcesso à fonteDOIHow to cite
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    • ABNT

      RAMOS, Luiz Duarte et al. Aerobic co-oxidation of hemoglobin and aminoacetone, a putative source of methylglyoxal. Free Radical Biology and Medicine, v. 166, p. 178–186, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.freeradbiomed.2021.02.023. Acesso em: 18 nov. 2024.

    • APA

      Ramos, L. D., Mantovani, M. C., Sartori, A., Dutra, F., Stevani, C. V., & Bechara, E. J. H. (2021). Aerobic co-oxidation of hemoglobin and aminoacetone, a putative source of methylglyoxal. Free Radical Biology and Medicine, 166, 178–186. doi:10.1016/j.freeradbiomed.2021.02.023

    • NLM

      Ramos LD, Mantovani MC, Sartori A, Dutra F, Stevani CV, Bechara EJH. Aerobic co-oxidation of hemoglobin and aminoacetone, a putative source of methylglyoxal [Internet]. Free Radical Biology and Medicine. 2021 ; 166 178–186.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2021.02.023

    • Vancouver

      Ramos LD, Mantovani MC, Sartori A, Dutra F, Stevani CV, Bechara EJH. Aerobic co-oxidation of hemoglobin and aminoacetone, a putative source of methylglyoxal [Internet]. Free Radical Biology and Medicine. 2021 ; 166 178–186.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2021.02.023

  • Artigo de periodico

    Development of analytical method by free solution capillary electrophoresis for furosemide under stress degradation (2019)

    Souza, Aline de ; Kedor-Hackmann, Erika Rosa Maria; Santoro, Maria Inês Rocha Miritello; Aurora-Prado, Maria Segunda

    Source: Separation Science Plus. Unidade: FCF

    Subjects: ELETROFORESE (MÉTODO DE SEPARAÇÃO), OXIDAÇÃO

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas

    • ABNT

      SOUZA, Aline de et al. Development of analytical method by free solution capillary electrophoresis for furosemide under stress degradation. Separation Science Plus, v. 20, n. 7, p. 253-261, 2019Tradução . . Disponível em: https://doi.org/10.1002/sscp.201900008. Acesso em: 18 nov. 2024.

    • APA

      Souza, A. de, Kedor-Hackmann, E. R. M., Santoro, M. I. R. M., & Aurora-Prado, M. S. (2019). Development of analytical method by free solution capillary electrophoresis for furosemide under stress degradation. Separation Science Plus, 20( 7), 253-261. doi:10.1002/sscp.201900008

    • NLM

      Souza A de, Kedor-Hackmann ERM, Santoro MIRM, Aurora-Prado MS. Development of analytical method by free solution capillary electrophoresis for furosemide under stress degradation [Internet]. Separation Science Plus. 2019 ; 20( 7): 253-261.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1002/sscp.201900008

    • Vancouver

      Souza A de, Kedor-Hackmann ERM, Santoro MIRM, Aurora-Prado MS. Development of analytical method by free solution capillary electrophoresis for furosemide under stress degradation [Internet]. Separation Science Plus. 2019 ; 20( 7): 253-261.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1002/sscp.201900008

  • Artigo de periodico

    1,4-Diamino-2-butanone, a wide-spectrum microbicide, yields reactive species by metal-catalyzed oxidation (2011)

    Soares, Chrislaine Oliveira; Alves, Maria Júlia Manso ; Bechara, Etelvino José Henriques

    Source: Free Radical Biology & Medicine. Unidade: IQ

    Subjects: RADICAIS LIVRES, OXIDAÇÃO

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas

    • ABNT

      SOARES, Chrislaine Oliveira e ALVES, Maria Júlia Manso e BECHARA, Etelvino José Henriques. 1,4-Diamino-2-butanone, a wide-spectrum microbicide, yields reactive species by metal-catalyzed oxidation. Free Radical Biology & Medicine, v. 50, n. 12, p. 1760-1770, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.freeradbiomed.2011.03.033. Acesso em: 18 nov. 2024.

    • APA

      Soares, C. O., Alves, M. J. M., & Bechara, E. J. H. (2011). 1,4-Diamino-2-butanone, a wide-spectrum microbicide, yields reactive species by metal-catalyzed oxidation. Free Radical Biology & Medicine, 50( 12), 1760-1770. doi:10.1016/j.freeradbiomed.2011.03.033

    • NLM

      Soares CO, Alves MJM, Bechara EJH. 1,4-Diamino-2-butanone, a wide-spectrum microbicide, yields reactive species by metal-catalyzed oxidation [Internet]. Free Radical Biology & Medicine. 2011 ; 50( 12): 1760-1770.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2011.03.033

    • Vancouver

      Soares CO, Alves MJM, Bechara EJH. 1,4-Diamino-2-butanone, a wide-spectrum microbicide, yields reactive species by metal-catalyzed oxidation [Internet]. Free Radical Biology & Medicine. 2011 ; 50( 12): 1760-1770.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2011.03.033
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