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  • Source: Phytochemistry. Unidade: IQ

    Subjects: FLAVONÓIDES, BIOQUÍMICA, RADIAÇÃO ULTRAVIOLETA

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    • ABNT

      YAMAGUCHI, Lydia Fumiko e KATO, Massuo Jorge e DI MASCIO, Paolo. Biflavonoids from Araucaria angustifolia protect against DNA UV-induced damage. Phytochemistry, v. 70, n. 5, p. 615-620, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.phytochem.2009.03.003. Acesso em: 13 nov. 2024.
    • APA

      Yamaguchi, L. F., Kato, M. J., & Di Mascio, P. (2009). Biflavonoids from Araucaria angustifolia protect against DNA UV-induced damage. Phytochemistry, 70( 5), 615-620. doi:10.1016/j.phytochem.2009.03.003
    • NLM

      Yamaguchi LF, Kato MJ, Di Mascio P. Biflavonoids from Araucaria angustifolia protect against DNA UV-induced damage [Internet]. Phytochemistry. 2009 ; 70( 5): 615-620.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.phytochem.2009.03.003
    • Vancouver

      Yamaguchi LF, Kato MJ, Di Mascio P. Biflavonoids from Araucaria angustifolia protect against DNA UV-induced damage [Internet]. Phytochemistry. 2009 ; 70( 5): 615-620.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.phytochem.2009.03.003
  • Source: Dalton Transactions. Unidade: IQ

    Subjects: SUPERÓXIDO DISMUTASE, DOENÇAS NEURODEGENERATIVAS

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    • ABNT

      BARBOSA, Lívea Fujita et al. DNA oxidation, strand-breaks and etheno-adducts formation promoted by 'CU', 'ZN'-superoxide dismutase-'H IND. 2''O IND. 2' in the presence and absence of bicarbonate. Dalton Transactions, n. 8, p. 1450-1459, 2009Tradução . . Disponível em: http://www.rsc.org/ej/DT/2009/b813235f.pdf. Acesso em: 13 nov. 2024.
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      Barbosa, L. F., Garcia, C. C. M., Di Mascio, P., & Medeiros, M. H. G. de. (2009). DNA oxidation, strand-breaks and etheno-adducts formation promoted by 'CU', 'ZN'-superoxide dismutase-'H IND. 2''O IND. 2' in the presence and absence of bicarbonate. Dalton Transactions, ( 8), 1450-1459. Recuperado de http://www.rsc.org/ej/DT/2009/b813235f.pdf
    • NLM

      Barbosa LF, Garcia CCM, Di Mascio P, Medeiros MHG de. DNA oxidation, strand-breaks and etheno-adducts formation promoted by 'CU', 'ZN'-superoxide dismutase-'H IND. 2''O IND. 2' in the presence and absence of bicarbonate [Internet]. Dalton Transactions. 2009 ;( 8): 1450-1459.[citado 2024 nov. 13 ] Available from: http://www.rsc.org/ej/DT/2009/b813235f.pdf
    • Vancouver

      Barbosa LF, Garcia CCM, Di Mascio P, Medeiros MHG de. DNA oxidation, strand-breaks and etheno-adducts formation promoted by 'CU', 'ZN'-superoxide dismutase-'H IND. 2''O IND. 2' in the presence and absence of bicarbonate [Internet]. Dalton Transactions. 2009 ;( 8): 1450-1459.[citado 2024 nov. 13 ] Available from: http://www.rsc.org/ej/DT/2009/b813235f.pdf
  • Source: Archives of Biochemistry and Biophysics. Unidade: IQ

    Subjects: ZINCO, COBRE, SUPERÓXIDO DISMUTASE, ÓXIDO NÍTRICO, PROTEÍNAS

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    • ABNT

      VAZ, Sandra Muntz et al. Oxidation and nitration of ribonuclease and lysozyme by peroxynitrite and myeloperoxidase. Archives of Biochemistry and Biophysics, v. 484, n. 2, p. 127-133, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.abb.2008.12.017. Acesso em: 13 nov. 2024.
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      Vaz, S. M., Prado, F. M., Di Mascio, P., & Augusto, O. (2009). Oxidation and nitration of ribonuclease and lysozyme by peroxynitrite and myeloperoxidase. Archives of Biochemistry and Biophysics, 484( 2), 127-133. doi:10.1016/j.abb.2008.12.017
    • NLM

      Vaz SM, Prado FM, Di Mascio P, Augusto O. Oxidation and nitration of ribonuclease and lysozyme by peroxynitrite and myeloperoxidase [Internet]. Archives of Biochemistry and Biophysics. 2009 ; 484( 2): 127-133.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.abb.2008.12.017
    • Vancouver

      Vaz SM, Prado FM, Di Mascio P, Augusto O. Oxidation and nitration of ribonuclease and lysozyme by peroxynitrite and myeloperoxidase [Internet]. Archives of Biochemistry and Biophysics. 2009 ; 484( 2): 127-133.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.abb.2008.12.017
  • Source: Biochemistry. Unidade: IQ

    Subjects: RESSONÂNCIA MAGNÉTICA NUCLEAR, ESPECTROSCOPIA, BIOQUÍMICA

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    • ABNT

      KAWAI, Cintia et al. pH-sensitive binding of cytochrome C to the inner mitochondrial membrane: implications for the participation of the protein in cell respiration and apoptosis. Biochemistry, v. 48, n. 35, p. 8335-8342, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdfplus/10.1021/bi9006463. Acesso em: 13 nov. 2024.
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      Kawai, C., Pessoto, F. S., Rodrigues, T., Mugnol, K. C. U., Tórtora, V., Castro, L., et al. (2009). pH-sensitive binding of cytochrome C to the inner mitochondrial membrane: implications for the participation of the protein in cell respiration and apoptosis. Biochemistry, 48( 35), 8335-8342. Recuperado de http://pubs.acs.org/doi/pdfplus/10.1021/bi9006463
    • NLM

      Kawai C, Pessoto FS, Rodrigues T, Mugnol KCU, Tórtora V, Castro L, Milicchio VA, Tersariol IL dos S, Di Mascio P, Radi R, Carmona-Ribeiro AM, Nantes IL. pH-sensitive binding of cytochrome C to the inner mitochondrial membrane: implications for the participation of the protein in cell respiration and apoptosis [Internet]. Biochemistry. 2009 ; 48( 35): 8335-8342.[citado 2024 nov. 13 ] Available from: http://pubs.acs.org/doi/pdfplus/10.1021/bi9006463
    • Vancouver

      Kawai C, Pessoto FS, Rodrigues T, Mugnol KCU, Tórtora V, Castro L, Milicchio VA, Tersariol IL dos S, Di Mascio P, Radi R, Carmona-Ribeiro AM, Nantes IL. pH-sensitive binding of cytochrome C to the inner mitochondrial membrane: implications for the participation of the protein in cell respiration and apoptosis [Internet]. Biochemistry. 2009 ; 48( 35): 8335-8342.[citado 2024 nov. 13 ] Available from: http://pubs.acs.org/doi/pdfplus/10.1021/bi9006463
  • Source: Free Radical Biology & Medicine. Unidade: IQ

    Subjects: DANO AO DNA, RADICAIS LIVRES, CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA

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    • ABNT

      PRADO, Fernanda Manso et al. Thymine hydroperoxide as a potential source of singlet molecular oxygen in DNA. Free Radical Biology & Medicine, v. 47, n. 4, p. 401-409, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.freeradbiomed.2009.05.001. Acesso em: 13 nov. 2024.
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      Prado, F. M., Oliveira, M. C. B. de, Miyamoto, S., Martinez, G. R., Medeiros, M. H. G. de, Ronsein, G. E., & Di Mascio, P. (2009). Thymine hydroperoxide as a potential source of singlet molecular oxygen in DNA. Free Radical Biology & Medicine, 47( 4), 401-409. doi:10.1016/j.freeradbiomed.2009.05.001
    • NLM

      Prado FM, Oliveira MCB de, Miyamoto S, Martinez GR, Medeiros MHG de, Ronsein GE, Di Mascio P. Thymine hydroperoxide as a potential source of singlet molecular oxygen in DNA [Internet]. Free Radical Biology & Medicine. 2009 ; 47( 4): 401-409.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2009.05.001
    • Vancouver

      Prado FM, Oliveira MCB de, Miyamoto S, Martinez GR, Medeiros MHG de, Ronsein GE, Di Mascio P. Thymine hydroperoxide as a potential source of singlet molecular oxygen in DNA [Internet]. Free Radical Biology & Medicine. 2009 ; 47( 4): 401-409.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2009.05.001
  • Source: Tetrahedron. Unidade: IQ

    Subjects: BIOQUÍMICA, CROMATOGRAFIA LÍQUIDA DE ALTA EFICIÊNCIA (MÉTODOS)

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      MARTINEZ, Glaucia Regina et al. Synthesis of a hydrophilic and non-ionic anthracene derivative, the N,N '-di-(2,3-dihydroxypropyl)-9,10-anthracenedipropanamide as a chemical trap for singlet molecular oxygen detection in biological systems. Tetrahedron, v. 62, n. 46, p. 10762-10770, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2006.08.094. Acesso em: 13 nov. 2024.
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      Martinez, G. R., Garcia, F., Catalani, L. H., Cadet, J., Oliveira, M. C. B. de, Ronsein, G. E., et al. (2006). Synthesis of a hydrophilic and non-ionic anthracene derivative, the N,N '-di-(2,3-dihydroxypropyl)-9,10-anthracenedipropanamide as a chemical trap for singlet molecular oxygen detection in biological systems. Tetrahedron, 62( 46), 10762-10770. doi:10.1016/j.tet.2006.08.094
    • NLM

      Martinez GR, Garcia F, Catalani LH, Cadet J, Oliveira MCB de, Ronsein GE, Miyamoto S, Medeiros MHG de, Di Mascio P. Synthesis of a hydrophilic and non-ionic anthracene derivative, the N,N '-di-(2,3-dihydroxypropyl)-9,10-anthracenedipropanamide as a chemical trap for singlet molecular oxygen detection in biological systems [Internet]. Tetrahedron. 2006 ; 62( 46): 10762-10770.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.tet.2006.08.094
    • Vancouver

      Martinez GR, Garcia F, Catalani LH, Cadet J, Oliveira MCB de, Ronsein GE, Miyamoto S, Medeiros MHG de, Di Mascio P. Synthesis of a hydrophilic and non-ionic anthracene derivative, the N,N '-di-(2,3-dihydroxypropyl)-9,10-anthracenedipropanamide as a chemical trap for singlet molecular oxygen detection in biological systems [Internet]. Tetrahedron. 2006 ; 62( 46): 10762-10770.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.tet.2006.08.094
  • Source: Tetrahedron. Unidade: IQ

    Subjects: OXIDAÇÃO, BIOQUÍMICA

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      RAVANAT, Jean-Luc et al. Singlet oxygen oxidation of 2 '-deoxyguanosine. Formation and mechanistic insights. Tetrahedron, v. 62, n. 46, p. 10709-10715, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2006.08.097. Acesso em: 13 nov. 2024.
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      Ravanat, J. -L., Martinez, G. R., Medeiros, M. H. G. de, Di Mascio, P., & Cadet, J. (2006). Singlet oxygen oxidation of 2 '-deoxyguanosine. Formation and mechanistic insights. Tetrahedron, 62( 46), 10709-10715. doi:10.1016/j.tet.2006.08.097
    • NLM

      Ravanat J-L, Martinez GR, Medeiros MHG de, Di Mascio P, Cadet J. Singlet oxygen oxidation of 2 '-deoxyguanosine. Formation and mechanistic insights [Internet]. Tetrahedron. 2006 ; 62( 46): 10709-10715.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.tet.2006.08.097
    • Vancouver

      Ravanat J-L, Martinez GR, Medeiros MHG de, Di Mascio P, Cadet J. Singlet oxygen oxidation of 2 '-deoxyguanosine. Formation and mechanistic insights [Internet]. Tetrahedron. 2006 ; 62( 46): 10709-10715.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.tet.2006.08.097
  • Source: Phytochemistry. Unidade: IQ

    Subjects: ANTIOXIDANTES (ATIVIDADE), PRODUTOS NATURAIS

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      YAMAGUCHI, Lydia Fumiko et al. Antioxidant activity of prenylated hydroquinone and benzoic acid derivatives from Piper crassinervium Kunth. Phytochemistry, v. 67, n. 16, p. 1838-1843, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.phytochem.2006.03.001. Acesso em: 13 nov. 2024.
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      Yamaguchi, L. F., Lago, J. H. G., Tanizaki, T. M., Di Mascio, P., & Kato, M. J. (2006). Antioxidant activity of prenylated hydroquinone and benzoic acid derivatives from Piper crassinervium Kunth. Phytochemistry, 67( 16), 1838-1843. doi:10.1016/j.phytochem.2006.03.001
    • NLM

      Yamaguchi LF, Lago JHG, Tanizaki TM, Di Mascio P, Kato MJ. Antioxidant activity of prenylated hydroquinone and benzoic acid derivatives from Piper crassinervium Kunth [Internet]. Phytochemistry. 2006 ; 67( 16): 1838-1843.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.phytochem.2006.03.001
    • Vancouver

      Yamaguchi LF, Lago JHG, Tanizaki TM, Di Mascio P, Kato MJ. Antioxidant activity of prenylated hydroquinone and benzoic acid derivatives from Piper crassinervium Kunth [Internet]. Phytochemistry. 2006 ; 67( 16): 1838-1843.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.phytochem.2006.03.001
  • Source: Phytochemistry. Unidade: IQ

    Subjects: RADIAÇÃO ULTRAVIOLETA, PRODUTOS NATURAIS

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      YAMAGUCHI, Lydia Fumiko et al. Biflavonoids from Brazilian pine Araucaria angustifolia as potentials protective agents against DNA damage and lipoperoxidation. Phytochemistry, v. 66, n. 18, p. 2238-2247, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.phytochem.2004.11.014. Acesso em: 13 nov. 2024.
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      Yamaguchi, L. F., Vassão, D. G., Kato, M. J., & Di Mascio, P. (2005). Biflavonoids from Brazilian pine Araucaria angustifolia as potentials protective agents against DNA damage and lipoperoxidation. Phytochemistry, 66( 18), 2238-2247. doi:10.1016/j.phytochem.2004.11.014
    • NLM

      Yamaguchi LF, Vassão DG, Kato MJ, Di Mascio P. Biflavonoids from Brazilian pine Araucaria angustifolia as potentials protective agents against DNA damage and lipoperoxidation [Internet]. Phytochemistry. 2005 ; 66( 18): 2238-2247.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.phytochem.2004.11.014
    • Vancouver

      Yamaguchi LF, Vassão DG, Kato MJ, Di Mascio P. Biflavonoids from Brazilian pine Araucaria angustifolia as potentials protective agents against DNA damage and lipoperoxidation [Internet]. Phytochemistry. 2005 ; 66( 18): 2238-2247.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.phytochem.2004.11.014
  • Source: Free Radical Biology and Medicine. Unidade: IQ

    Subjects: DANO AO DNA, ESPECTROMETRIA DE MASSAS, RADICAIS LIVRES

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      MARTINEZ, Glaucia Regina et al. Identification of the main oxidation products of 8-methoxy-2'-deoxyguanosine by singlet molecular oxygen. Free Radical Biology and Medicine, v. 38, n. 11, p. 1491-1500, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.freeradbiomed.2005.02.008. Acesso em: 13 nov. 2024.
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      Martinez, G. R., Gasparutto, D., Ravanat, J. -L., Cadet, J., Medeiros, M. H. G. de, & Di Mascio, P. (2005). Identification of the main oxidation products of 8-methoxy-2'-deoxyguanosine by singlet molecular oxygen. Free Radical Biology and Medicine, 38( 11), 1491-1500. doi:10.1016/j.freeradbiomed.2005.02.008
    • NLM

      Martinez GR, Gasparutto D, Ravanat J-L, Cadet J, Medeiros MHG de, Di Mascio P. Identification of the main oxidation products of 8-methoxy-2'-deoxyguanosine by singlet molecular oxygen [Internet]. Free Radical Biology and Medicine. 2005 ; 38( 11): 1491-1500.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2005.02.008
    • Vancouver

      Martinez GR, Gasparutto D, Ravanat J-L, Cadet J, Medeiros MHG de, Di Mascio P. Identification of the main oxidation products of 8-methoxy-2'-deoxyguanosine by singlet molecular oxygen [Internet]. Free Radical Biology and Medicine. 2005 ; 38( 11): 1491-1500.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2005.02.008

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