Filtros : "MEDEIROS, MARISA HELENA GENNARI DE" "Indexado no Current Contents" Removidos: "Indexado na Base de Dados PubMed" "CETEPE" "IP" Limpar

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  • Source: Journal of The American Society for Mass Spectrometry. Unidade: IQ

    Subjects: BIOQUÍMICA, ESPECTROMETRIA DE MASSAS

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    • ABNT

      RONSEIN, Graziella Eliza et al. Characterization of 'O IND.2' ('ANTPOT. 1 delta IND. g')-derived oxidation products of tryptophan: a combination of tandem mass spectrometry analyses and isotopic labeling studies. Journal of The American Society for Mass Spectrometry, v. 20, n. 2, p. 188-197, 2009Tradução . . Acesso em: 14 ago. 2024.
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      Ronsein, G. E., Oliveira, M. C. B. de, Medeiros, M. H. G. de, & Di Mascio, P. (2009). Characterization of 'O IND.2' ('ANTPOT. 1 delta IND. g')-derived oxidation products of tryptophan: a combination of tandem mass spectrometry analyses and isotopic labeling studies. Journal of The American Society for Mass Spectrometry, 20( 2), 188-197.
    • NLM

      Ronsein GE, Oliveira MCB de, Medeiros MHG de, Di Mascio P. Characterization of 'O IND.2' ('ANTPOT. 1 delta IND. g')-derived oxidation products of tryptophan: a combination of tandem mass spectrometry analyses and isotopic labeling studies. Journal of The American Society for Mass Spectrometry. 2009 ; 20( 2): 188-197.[citado 2024 ago. 14 ]
    • Vancouver

      Ronsein GE, Oliveira MCB de, Medeiros MHG de, Di Mascio P. Characterization of 'O IND.2' ('ANTPOT. 1 delta IND. g')-derived oxidation products of tryptophan: a combination of tandem mass spectrometry analyses and isotopic labeling studies. Journal of The American Society for Mass Spectrometry. 2009 ; 20( 2): 188-197.[citado 2024 ago. 14 ]
  • Source: Dalton Transactions. Unidade: IQ

    Subjects: SUPERÓXIDO DISMUTASE, DOENÇAS NEURODEGENERATIVAS

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      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: 14 ago. 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
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      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 ago. 14 ] 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 ago. 14 ] Available from: http://www.rsc.org/ej/DT/2009/b813235f.pdf
  • Source: Free Radical Biology & Medicine. Unidade: IQ

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

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      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: 14 ago. 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 ago. 14 ] 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 ago. 14 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2009.05.001
  • Source: Dalton Transactions. Unidade: IQ

    Subjects: DANO AO DNA, COBALTO

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      ALIPÁZAGA, María Vespertina et al. DNA damage by sulfite autoxidation catalyzed by cobalt complexes. Dalton Transactions, n. 41, p. 5636-5644, 2008Tradução . . Disponível em: https://doi.org/10.1039/b805222k. Acesso em: 14 ago. 2024.
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      Alipázaga, M. V., Moreno, R. G. M., Linares, E., Medeiros, M. H. G. de, & Coichev, N. (2008). DNA damage by sulfite autoxidation catalyzed by cobalt complexes. Dalton Transactions, ( 41), 5636-5644. doi:10.1039/b805222k
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      Alipázaga MV, Moreno RGM, Linares E, Medeiros MHG de, Coichev N. DNA damage by sulfite autoxidation catalyzed by cobalt complexes [Internet]. Dalton Transactions. 2008 ;( 41): 5636-5644.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1039/b805222k
    • Vancouver

      Alipázaga MV, Moreno RGM, Linares E, Medeiros MHG de, Coichev N. DNA damage by sulfite autoxidation catalyzed by cobalt complexes [Internet]. Dalton Transactions. 2008 ;( 41): 5636-5644.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1039/b805222k
  • Source: Proceedings of the National Academy of Sciences of the United States of America - PNAS. Unidade: IQ

    Subjects: ESPECTROMETRIA DE MASSAS, SOLUÇÕES AQUOSAS

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      MIYAMOTO, Sayuri et al. Linoleic acid hydroperoxide reacts with hypochlorous acid, generating peroxyl radical intermediates and singlet molecular oxygen. Proceedings of the National Academy of Sciences of the United States of America - PNAS, v. 103, n. 2, p. 293-298, 2006Tradução . . Disponível em: https://doi.org/10.1073/pnas.0508170103. Acesso em: 14 ago. 2024.
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      Miyamoto, S., Martinez, G. R., Rettori, D., Augusto, O., Medeiros, M. H. G. de, & Di Mascio, P. (2006). Linoleic acid hydroperoxide reacts with hypochlorous acid, generating peroxyl radical intermediates and singlet molecular oxygen. Proceedings of the National Academy of Sciences of the United States of America - PNAS, 103( 2), 293-298. doi:10.1073/pnas.0508170103
    • NLM

      Miyamoto S, Martinez GR, Rettori D, Augusto O, Medeiros MHG de, Di Mascio P. Linoleic acid hydroperoxide reacts with hypochlorous acid, generating peroxyl radical intermediates and singlet molecular oxygen [Internet]. Proceedings of the National Academy of Sciences of the United States of America - PNAS. 2006 ; 103( 2): 293-298.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1073/pnas.0508170103
    • Vancouver

      Miyamoto S, Martinez GR, Rettori D, Augusto O, Medeiros MHG de, Di Mascio P. Linoleic acid hydroperoxide reacts with hypochlorous acid, generating peroxyl radical intermediates and singlet molecular oxygen [Internet]. Proceedings of the National Academy of Sciences of the United States of America - PNAS. 2006 ; 103( 2): 293-298.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1073/pnas.0508170103
  • 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: 14 ago. 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 ago. 14 ] 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 ago. 14 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2005.02.008
  • Source: Bioorganic and Medicinal Chemistry. Unidade: IQ

    Subjects: BIOQUÍMICA, DNA, OLIGONUCLEOTÍDEOS

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      CARVALHO, Valdemir M. et al. Site-specific incorporation of the 1-hexanol-1,'N POT. 6'-etheno-2'-deoxyadenosine adduct into oligodeoxyribonucleotides. Bioorganic and Medicinal Chemistry, v. 11, n. 11, p. 2445-2452, 2003Tradução . . Acesso em: 14 ago. 2024.
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      Carvalho, V. M., Gasparutto, D., Di Mascio, P., Medeiros, M. H. G. de, & Cadet, J. (2003). Site-specific incorporation of the 1-hexanol-1,'N POT. 6'-etheno-2'-deoxyadenosine adduct into oligodeoxyribonucleotides. Bioorganic and Medicinal Chemistry, 11( 11), 2445-2452.
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      Carvalho VM, Gasparutto D, Di Mascio P, Medeiros MHG de, Cadet J. Site-specific incorporation of the 1-hexanol-1,'N POT. 6'-etheno-2'-deoxyadenosine adduct into oligodeoxyribonucleotides. Bioorganic and Medicinal Chemistry. 2003 ; 11( 11): 2445-2452.[citado 2024 ago. 14 ]
    • Vancouver

      Carvalho VM, Gasparutto D, Di Mascio P, Medeiros MHG de, Cadet J. Site-specific incorporation of the 1-hexanol-1,'N POT. 6'-etheno-2'-deoxyadenosine adduct into oligodeoxyribonucleotides. Bioorganic and Medicinal Chemistry. 2003 ; 11( 11): 2445-2452.[citado 2024 ago. 14 ]
  • Source: Journal of Inorganic Biochemistry. Unidade: IQ

    Subjects: QUÍMICA INORGÂNICA, BIOQUÍMICA, DNA

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      ARAKI, Koiti et al. Zinc tetraruthenated porphyrin binding and photoinduced oxidation of calf-thymus DNA. Journal of Inorganic Biochemistry, v. 78, n. 4, p. 269-273, 2000Tradução . . Disponível em: https://doi.org/10.1016/s0162-0134(00)00053-2. Acesso em: 14 ago. 2024.
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      Araki, K., Silva, C. A., Toma, H. E., Catalani, L. H., Medeiros, M. H. G. de, & Di Mascio, P. (2000). Zinc tetraruthenated porphyrin binding and photoinduced oxidation of calf-thymus DNA. Journal of Inorganic Biochemistry, 78( 4), 269-273. doi:10.1016/s0162-0134(00)00053-2
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      Araki K, Silva CA, Toma HE, Catalani LH, Medeiros MHG de, Di Mascio P. Zinc tetraruthenated porphyrin binding and photoinduced oxidation of calf-thymus DNA [Internet]. Journal of Inorganic Biochemistry. 2000 ; 78( 4): 269-273.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/s0162-0134(00)00053-2
    • Vancouver

      Araki K, Silva CA, Toma HE, Catalani LH, Medeiros MHG de, Di Mascio P. Zinc tetraruthenated porphyrin binding and photoinduced oxidation of calf-thymus DNA [Internet]. Journal of Inorganic Biochemistry. 2000 ; 78( 4): 269-273.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/s0162-0134(00)00053-2
  • Source: Journal of Chromatography B: Biomedical Sciences and Applications. Unidade: IQ

    Assunto: BIOQUÍMICA

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      UMMUS, Rafael E. et al. Measurement of 4,5-dioxovaleric acid by high-peformance liquid chromatography and fluorescence detection. Journal of Chromatography B: Biomedical Sciences and Applications, v. 729, n. 1/2, p. 237-243, 1999Tradução . . Disponível em: https://doi.org/10.1016/s0378-4347(99)00153-x. Acesso em: 14 ago. 2024.
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      Ummus, R. E., Onuki, J., Dörnemann, D., Medeiros, M. H. G. de, & Di Mascio, P. (1999). Measurement of 4,5-dioxovaleric acid by high-peformance liquid chromatography and fluorescence detection. Journal of Chromatography B: Biomedical Sciences and Applications, 729( 1/2), 237-243. doi:10.1016/s0378-4347(99)00153-x
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      Ummus RE, Onuki J, Dörnemann D, Medeiros MHG de, Di Mascio P. Measurement of 4,5-dioxovaleric acid by high-peformance liquid chromatography and fluorescence detection [Internet]. Journal of Chromatography B: Biomedical Sciences and Applications. 1999 ; 729( 1/2): 237-243.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/s0378-4347(99)00153-x
    • Vancouver

      Ummus RE, Onuki J, Dörnemann D, Medeiros MHG de, Di Mascio P. Measurement of 4,5-dioxovaleric acid by high-peformance liquid chromatography and fluorescence detection [Internet]. Journal of Chromatography B: Biomedical Sciences and Applications. 1999 ; 729( 1/2): 237-243.[citado 2024 ago. 14 ] Available from: https://doi.org/10.1016/s0378-4347(99)00153-x

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