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  • Fonte: Langmuir. Unidade: FCFRP

    Assuntos: LEITE, PROTEÍNAS, MACROMOLÉCULA, QUÍMICA DE ALIMENTOS, POLÍMEROS (QUÍMICA ORGÂNICA)

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      SRIVASTAVA, Deepti et al. Computationally Mapping pKa Shifts Due to the Presence of a Polyelectrolyte Chain around Whey Proteins. Langmuir, v. 33, n. 42, p. 11417-11428, 2017Tradução . . Disponível em: https://doi.org/10.1021/acs.langmuir.7b02271. Acesso em: 15 jul. 2024.
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      Srivastava, D., Santiso, E., Gubbins, K., & Silva, F. L. B. (2017). Computationally Mapping pKa Shifts Due to the Presence of a Polyelectrolyte Chain around Whey Proteins. Langmuir, 33( 42), 11417-11428. doi:10.1021/acs.langmuir.7b02271
    • NLM

      Srivastava D, Santiso E, Gubbins K, Silva FLB. Computationally Mapping pKa Shifts Due to the Presence of a Polyelectrolyte Chain around Whey Proteins [Internet]. Langmuir. 2017 ; 33( 42): 11417-11428.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1021/acs.langmuir.7b02271
    • Vancouver

      Srivastava D, Santiso E, Gubbins K, Silva FLB. Computationally Mapping pKa Shifts Due to the Presence of a Polyelectrolyte Chain around Whey Proteins [Internet]. Langmuir. 2017 ; 33( 42): 11417-11428.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1021/acs.langmuir.7b02271
  • Fonte: Chemical Research in Toxicology. Unidade: IQ

    Assuntos: BIOMARCADORES, ESTRESSE OXIDATIVO, DANO AO DNA

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      MEDEIROS, Marisa Helena Gennari de. Exocyclic DNA adducts as biomarkers of lipid oxidation and predictors of disease: challenges in developing sensitive and specific methods for clinical studies. Chemical Research in Toxicology, v. 22, n. 3, p. 419-425, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/tx800367d. Acesso em: 15 jul. 2024.
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      Medeiros, M. H. G. de. (2009). Exocyclic DNA adducts as biomarkers of lipid oxidation and predictors of disease: challenges in developing sensitive and specific methods for clinical studies. Chemical Research in Toxicology, 22( 3), 419-425. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/tx800367d
    • NLM

      Medeiros MHG de. Exocyclic DNA adducts as biomarkers of lipid oxidation and predictors of disease: challenges in developing sensitive and specific methods for clinical studies [Internet]. Chemical Research in Toxicology. 2009 ; 22( 3): 419-425.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800367d
    • Vancouver

      Medeiros MHG de. Exocyclic DNA adducts as biomarkers of lipid oxidation and predictors of disease: challenges in developing sensitive and specific methods for clinical studies [Internet]. Chemical Research in Toxicology. 2009 ; 22( 3): 419-425.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800367d
  • Fonte: Journal of Physical Chemistry A : Dynamics, Kinetics, Environmental Chemistry, Spectroscopy, Structure, Theory. Unidade: IQ

    Assuntos: COBRE, ESPECTROSCOPIA RAMAN, FÍSICO-QUÍMICA

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      ABREU, Heitor Avelino de et al. Solid-state experimental and theoretical investigation of the ammonium salt of croconate violet, a pseudo-oxocarbon ion. Journal of Physical Chemistry A : Dynamics, Kinetics, Environmental Chemistry, Spectroscopy, Structure, Theory, v. 113, n. 23, p. 6446-6452, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/jp901021c. Acesso em: 15 jul. 2024.
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      Abreu, H. A. de, Júnior, A. L. S., Leitão, A. A., De Sá, L. R. V., Ribeiro, M. C. C., Diniz, R., & Oliveira, L. F. C. de. (2009). Solid-state experimental and theoretical investigation of the ammonium salt of croconate violet, a pseudo-oxocarbon ion. Journal of Physical Chemistry A : Dynamics, Kinetics, Environmental Chemistry, Spectroscopy, Structure, Theory, 113( 23), 6446-6452. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/jp901021c
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      Abreu HA de, Júnior ALS, Leitão AA, De Sá LRV, Ribeiro MCC, Diniz R, Oliveira LFC de. Solid-state experimental and theoretical investigation of the ammonium salt of croconate violet, a pseudo-oxocarbon ion [Internet]. Journal of Physical Chemistry A : Dynamics, Kinetics, Environmental Chemistry, Spectroscopy, Structure, Theory. 2009 ; 113( 23): 6446-6452.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jp901021c
    • Vancouver

      Abreu HA de, Júnior ALS, Leitão AA, De Sá LRV, Ribeiro MCC, Diniz R, Oliveira LFC de. Solid-state experimental and theoretical investigation of the ammonium salt of croconate violet, a pseudo-oxocarbon ion [Internet]. Journal of Physical Chemistry A : Dynamics, Kinetics, Environmental Chemistry, Spectroscopy, Structure, Theory. 2009 ; 113( 23): 6446-6452.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jp901021c
  • Fonte: Journal of Agricultural and Food Chemistry. Unidade: FCF

    Assuntos: BIOQUÍMICA DE ALIMENTOS, SOJA, NUTRIÇÃO

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      BORRMANN, Daniela e ANDRADE, Juliana Castelhano de e LANFER MARQUEZ, Úrsula Maria. Chlorophyll degradation and formation of colorless chlorophyll derivatives during soybean (Glycine max L. merill) seed maturation. Journal of Agricultural and Food Chemistry, v. 57, n. 5, p. 2030-2034, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdfplus/10.1021/jf803191k. Acesso em: 15 jul. 2024.
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      Borrmann, D., Andrade, J. C. de, & Lanfer Marquez, Ú. M. (2009). Chlorophyll degradation and formation of colorless chlorophyll derivatives during soybean (Glycine max L. merill) seed maturation. Journal of Agricultural and Food Chemistry, 57( 5), 2030-2034. Recuperado de http://pubs.acs.org/doi/pdfplus/10.1021/jf803191k
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      Borrmann D, Andrade JC de, Lanfer Marquez ÚM. Chlorophyll degradation and formation of colorless chlorophyll derivatives during soybean (Glycine max L. merill) seed maturation [Internet]. Journal of Agricultural and Food Chemistry. 2009 ; 57( 5): 2030-2034.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdfplus/10.1021/jf803191k
    • Vancouver

      Borrmann D, Andrade JC de, Lanfer Marquez ÚM. Chlorophyll degradation and formation of colorless chlorophyll derivatives during soybean (Glycine max L. merill) seed maturation [Internet]. Journal of Agricultural and Food Chemistry. 2009 ; 57( 5): 2030-2034.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdfplus/10.1021/jf803191k
  • Fonte: Journal of Agricultural and Food Chemistry. Unidade: FCF

    Assuntos: MAMÃO, FRUTAS, BIOQUÍMICA DE ALIMENTOS

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      SHIGA, Tania Misuzu et al. Changes in cell wall composition associated to the softening of ripening papaya: evidence of extensive solubilization of large molecular mass galactouronides. Journal of Agricultural and Food Chemistry, v. 57, n. 15, p. 7064-7071, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdfplus/10.1021/jf901863w. Acesso em: 15 jul. 2024.
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      Shiga, T. M., Fabi, J. P., Nascimento, J. R. O. do, Petkowicz, C. L. de O., Vriesmann, L. C., Lajolo, F. M., & Cordenunsi-Lysenko, B. R. (2009). Changes in cell wall composition associated to the softening of ripening papaya: evidence of extensive solubilization of large molecular mass galactouronides. Journal of Agricultural and Food Chemistry, 57( 15), 7064-7071. Recuperado de http://pubs.acs.org/doi/pdfplus/10.1021/jf901863w
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      Shiga TM, Fabi JP, Nascimento JRO do, Petkowicz CL de O, Vriesmann LC, Lajolo FM, Cordenunsi-Lysenko BR. Changes in cell wall composition associated to the softening of ripening papaya: evidence of extensive solubilization of large molecular mass galactouronides [Internet]. Journal of Agricultural and Food Chemistry. 2009 ; 57( 15): 7064-7071.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdfplus/10.1021/jf901863w
    • Vancouver

      Shiga TM, Fabi JP, Nascimento JRO do, Petkowicz CL de O, Vriesmann LC, Lajolo FM, Cordenunsi-Lysenko BR. Changes in cell wall composition associated to the softening of ripening papaya: evidence of extensive solubilization of large molecular mass galactouronides [Internet]. Journal of Agricultural and Food Chemistry. 2009 ; 57( 15): 7064-7071.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdfplus/10.1021/jf901863w
  • Fonte: Organic Letters. Unidade: IQ

    Assuntos: LIPASE, REAÇÕES ORGÂNICAS

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      ANDRADE, Leandro Helgueira e BARCELLOS, Thiago. Lipase-catalyzed highly enantioselective kinetic resolution of boron-containing chiral alcohols. Organic Letters, v. 11, n. 14, p. 3052-3055, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/ol901091f. Acesso em: 15 jul. 2024.
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      Andrade, L. H., & Barcellos, T. (2009). Lipase-catalyzed highly enantioselective kinetic resolution of boron-containing chiral alcohols. Organic Letters, 11( 14), 3052-3055. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/ol901091f
    • NLM

      Andrade LH, Barcellos T. Lipase-catalyzed highly enantioselective kinetic resolution of boron-containing chiral alcohols [Internet]. Organic Letters. 2009 ; 11( 14): 3052-3055.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/ol901091f
    • Vancouver

      Andrade LH, Barcellos T. Lipase-catalyzed highly enantioselective kinetic resolution of boron-containing chiral alcohols [Internet]. Organic Letters. 2009 ; 11( 14): 3052-3055.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/ol901091f
  • Fonte: Journal of Organic Chemistry. Unidade: IQ

    Assuntos: SÍNTESE ORGÂNICA, PRODUTOS NATURAIS

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      BIANCO, Graziela Gallego et al. (+)- and (-)-Mutisianthol: first total synthesis, absolute configuration, and antitumor activity. Journal of Organic Chemistry, v. 74, n. 6, p. 2561-2566, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/jo9000405. Acesso em: 15 jul. 2024.
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      Bianco, G. G., Ferraz, H. M. C., Costa, A. M., Lotufo, L. V. C., Pessoa, C., Moraes, M. O. de, et al. (2009). (+)- and (-)-Mutisianthol: first total synthesis, absolute configuration, and antitumor activity. Journal of Organic Chemistry, 74( 6), 2561-2566. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/jo9000405
    • NLM

      Bianco GG, Ferraz HMC, Costa AM, Lotufo LVC, Pessoa C, Moraes MO de, Schrems MG, Pfaltz A, Silva Jr. LF da. (+)- and (-)-Mutisianthol: first total synthesis, absolute configuration, and antitumor activity [Internet]. Journal of Organic Chemistry. 2009 ; 74( 6): 2561-2566.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jo9000405
    • Vancouver

      Bianco GG, Ferraz HMC, Costa AM, Lotufo LVC, Pessoa C, Moraes MO de, Schrems MG, Pfaltz A, Silva Jr. LF da. (+)- and (-)-Mutisianthol: first total synthesis, absolute configuration, and antitumor activity [Internet]. Journal of Organic Chemistry. 2009 ; 74( 6): 2561-2566.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jo9000405
  • Fonte: Journal of Physical Chemistry A : Dynamics, Kinetics, Environmental Chemistry, Spectroscopy, Structure, Theory. Unidade: IQ

    Assuntos: QUÍMICA ATMOSFÉRICA, ESPECTROSCOPIA INFRAVERMELHA

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      DENIS, Pablo A. e ORNELLAS, Fernando Rei. Theoretical characterization of hydrogen polyoxides: HOOH, HOOOH, HOOOOH, and HOOO. Journal of Physical Chemistry A : Dynamics, Kinetics, Environmental Chemistry, Spectroscopy, Structure, Theory, v. 113, n. 2, p. 499-506, 2009Tradução . . Disponível em: https://doi.org/10.1021/jp808795e. Acesso em: 15 jul. 2024.
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      Denis, P. A., & Ornellas, F. R. (2009). Theoretical characterization of hydrogen polyoxides: HOOH, HOOOH, HOOOOH, and HOOO. Journal of Physical Chemistry A : Dynamics, Kinetics, Environmental Chemistry, Spectroscopy, Structure, Theory, 113( 2), 499-506. doi:10.1021/jp808795e
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      Denis PA, Ornellas FR. Theoretical characterization of hydrogen polyoxides: HOOH, HOOOH, HOOOOH, and HOOO [Internet]. Journal of Physical Chemistry A : Dynamics, Kinetics, Environmental Chemistry, Spectroscopy, Structure, Theory. 2009 ; 113( 2): 499-506.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1021/jp808795e
    • Vancouver

      Denis PA, Ornellas FR. Theoretical characterization of hydrogen polyoxides: HOOH, HOOOH, HOOOOH, and HOOO [Internet]. Journal of Physical Chemistry A : Dynamics, Kinetics, Environmental Chemistry, Spectroscopy, Structure, Theory. 2009 ; 113( 2): 499-506.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1021/jp808795e
  • Fonte: Journal of Physical Chemistry A : Dynamics, Kinetics, Environmental Chemistry, Spectroscopy, Structure, Theory. Unidade: IQ

    Assuntos: QUÍMICA ATMOSFÉRICA, ISÔMERO, COMPOSTOS DE ENXOFRE, BROMO

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      OLIVEIRA FILHO, Antonio Gustavo Sampaio de e AOTO, Yuri Alexandre e ORNELLAS, Fernando Rei. New molecular species of potential interest to atmospheric chemistry: isomers on the ['H', 'S IND. 2', 'BR'] potential energy surface. Journal of Physical Chemistry A : Dynamics, Kinetics, Environmental Chemistry, Spectroscopy, Structure, Theory, v. 113, n. 7, p. 1397-1402, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/jp8079793. Acesso em: 15 jul. 2024.
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      Oliveira Filho, A. G. S. de, Aoto, Y. A., & Ornellas, F. R. (2009). New molecular species of potential interest to atmospheric chemistry: isomers on the ['H', 'S IND. 2', 'BR'] potential energy surface. Journal of Physical Chemistry A : Dynamics, Kinetics, Environmental Chemistry, Spectroscopy, Structure, Theory, 113( 7), 1397-1402. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/jp8079793
    • NLM

      Oliveira Filho AGS de, Aoto YA, Ornellas FR. New molecular species of potential interest to atmospheric chemistry: isomers on the ['H', 'S IND. 2', 'BR'] potential energy surface [Internet]. Journal of Physical Chemistry A : Dynamics, Kinetics, Environmental Chemistry, Spectroscopy, Structure, Theory. 2009 ; 113( 7): 1397-1402.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jp8079793
    • Vancouver

      Oliveira Filho AGS de, Aoto YA, Ornellas FR. New molecular species of potential interest to atmospheric chemistry: isomers on the ['H', 'S IND. 2', 'BR'] potential energy surface [Internet]. Journal of Physical Chemistry A : Dynamics, Kinetics, Environmental Chemistry, Spectroscopy, Structure, Theory. 2009 ; 113( 7): 1397-1402.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jp8079793
  • Fonte: Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry. Unidade: IQ

    Assuntos: MOLÉCULA (SIMULAÇÃO), LÍQUIDOS IÔNICOS

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      SIQUEIRA, Leonardo José Amaral de e RIBEIRO, Mauro Carlos Costa. Alkoxy chain effect on the viscosity of a quaternary ammonium ionic liquid: molecular dynamics simulations. Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry, v. 113, n. 4, p. 1074-1079, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/jp807833a. Acesso em: 15 jul. 2024.
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      Siqueira, L. J. A. de, & Ribeiro, M. C. C. (2009). Alkoxy chain effect on the viscosity of a quaternary ammonium ionic liquid: molecular dynamics simulations. Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry, 113( 4), 1074-1079. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/jp807833a
    • NLM

      Siqueira LJA de, Ribeiro MCC. Alkoxy chain effect on the viscosity of a quaternary ammonium ionic liquid: molecular dynamics simulations [Internet]. Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry. 2009 ; 113( 4): 1074-1079.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jp807833a
    • Vancouver

      Siqueira LJA de, Ribeiro MCC. Alkoxy chain effect on the viscosity of a quaternary ammonium ionic liquid: molecular dynamics simulations [Internet]. Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry. 2009 ; 113( 4): 1074-1079.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jp807833a
  • Fonte: Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry. Unidade: IQ

    Assuntos: SOLVATAÇÃO, ESPECTROSCOPIA, SOLVENTE

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      SILVA, Priscilla Leandro et al. Solvatochromism in binary mixtures: first report on a solvation free energy relationship between solvent exchange equilibrium constants and the properties of the medium. Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry, v. 113, n. 28, p. 9512-9519, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/jp902272g. Acesso em: 15 jul. 2024.
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      Silva, P. L., Trassi, M. A. de S., Martins, C. T., & El Seoud, O. A. (2009). Solvatochromism in binary mixtures: first report on a solvation free energy relationship between solvent exchange equilibrium constants and the properties of the medium. Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry, 113( 28), 9512-9519. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/jp902272g
    • NLM

      Silva PL, Trassi MA de S, Martins CT, El Seoud OA. Solvatochromism in binary mixtures: first report on a solvation free energy relationship between solvent exchange equilibrium constants and the properties of the medium [Internet]. Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry. 2009 ; 113( 28): 9512-9519.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jp902272g
    • Vancouver

      Silva PL, Trassi MA de S, Martins CT, El Seoud OA. Solvatochromism in binary mixtures: first report on a solvation free energy relationship between solvent exchange equilibrium constants and the properties of the medium [Internet]. Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry. 2009 ; 113( 28): 9512-9519.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jp902272g
  • Fonte: Chemical Research in Toxicology. Unidade: IQ

    Assuntos: PEROXIDASE, BIOQUÍMICA, SUPERÓXIDO DISMUTASE

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      MEDINAS, Danilo Bilches et al. Peroxymonocarbonate and carbonate radical displace the hydroxyl-like oxidant in the Sod1 peroxidase activity under physiological conditions. Chemical Research in Toxicology, v. 22, n. 4, p. 639-648, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/tx800287m. Acesso em: 15 jul. 2024.
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      Medinas, D. B., Toledo Junior, J. C., Cerchiaro, G., Amaral, A. T. do, Rezende, L. de, Malvezzi, A., & Augusto, O. (2009). Peroxymonocarbonate and carbonate radical displace the hydroxyl-like oxidant in the Sod1 peroxidase activity under physiological conditions. Chemical Research in Toxicology, 22( 4), 639-648. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/tx800287m
    • NLM

      Medinas DB, Toledo Junior JC, Cerchiaro G, Amaral AT do, Rezende L de, Malvezzi A, Augusto O. Peroxymonocarbonate and carbonate radical displace the hydroxyl-like oxidant in the Sod1 peroxidase activity under physiological conditions [Internet]. Chemical Research in Toxicology. 2009 ; 22( 4): 639-648.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800287m
    • Vancouver

      Medinas DB, Toledo Junior JC, Cerchiaro G, Amaral AT do, Rezende L de, Malvezzi A, Augusto O. Peroxymonocarbonate and carbonate radical displace the hydroxyl-like oxidant in the Sod1 peroxidase activity under physiological conditions [Internet]. Chemical Research in Toxicology. 2009 ; 22( 4): 639-648.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800287m
  • Fonte: Chemical Research in Toxicology. Unidade: IQ

    Assuntos: DOENÇA DE ALZHEIMER, ÁCIDO LINOLEICO, DANO AO DNA

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      UEMI, Miriam et al. Generation of cholesterol carboxyaldehyde by the reaction of singlet molecular oxygen ['O IND. 2' (ANTPOT. 1 delta IND. g)] as well as ozone with cholesterol. Chemical Research in Toxicology, v. 22, n. 5, p. 875-884, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/tx800447b. Acesso em: 15 jul. 2024.
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      Uemi, M., Ronsein, G. E., Miyamoto, S., Medeiros, M. H. G. de, & Di Mascio, P. (2009). Generation of cholesterol carboxyaldehyde by the reaction of singlet molecular oxygen ['O IND. 2' (ANTPOT. 1 delta IND. g)] as well as ozone with cholesterol. Chemical Research in Toxicology, 22( 5), 875-884. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/tx800447b
    • NLM

      Uemi M, Ronsein GE, Miyamoto S, Medeiros MHG de, Di Mascio P. Generation of cholesterol carboxyaldehyde by the reaction of singlet molecular oxygen ['O IND. 2' (ANTPOT. 1 delta IND. g)] as well as ozone with cholesterol [Internet]. Chemical Research in Toxicology. 2009 ; 22( 5): 875-884.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800447b
    • Vancouver

      Uemi M, Ronsein GE, Miyamoto S, Medeiros MHG de, Di Mascio P. Generation of cholesterol carboxyaldehyde by the reaction of singlet molecular oxygen ['O IND. 2' (ANTPOT. 1 delta IND. g)] as well as ozone with cholesterol [Internet]. Chemical Research in Toxicology. 2009 ; 22( 5): 875-884.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800447b
  • Fonte: Bioconjugate Chemistry. Unidades: IQ, FCF

    Assuntos: PROTEÍNAS DE FLUORESCÊNCIA VERDE, BIOQUÍMICA

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      HERING, Vitor Renaux et al. Violet ZnSe/ZnS as an alternative to green CdSe/ZnS in nanocrystal-fluorescent protein FRET systems. Bioconjugate Chemistry, v. 20, n. 6, p. 1237-1241, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/bc9001085. Acesso em: 15 jul. 2024.
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      Hering, V. R., Faulin, T. do E. S., Triboni, E. R., Rodriguez, S. D., Bernik, D. L., Schumacher, R. I., et al. (2009). Violet ZnSe/ZnS as an alternative to green CdSe/ZnS in nanocrystal-fluorescent protein FRET systems. Bioconjugate Chemistry, 20( 6), 1237-1241. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/bc9001085
    • NLM

      Hering VR, Faulin T do ES, Triboni ER, Rodriguez SD, Bernik DL, Schumacher RI, Mammana VP, Faljoni-Alário A, Abdalla DSP, Gibson G, Politi MJ. Violet ZnSe/ZnS as an alternative to green CdSe/ZnS in nanocrystal-fluorescent protein FRET systems [Internet]. Bioconjugate Chemistry. 2009 ; 20( 6): 1237-1241.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/bc9001085
    • Vancouver

      Hering VR, Faulin T do ES, Triboni ER, Rodriguez SD, Bernik DL, Schumacher RI, Mammana VP, Faljoni-Alário A, Abdalla DSP, Gibson G, Politi MJ. Violet ZnSe/ZnS as an alternative to green CdSe/ZnS in nanocrystal-fluorescent protein FRET systems [Internet]. Bioconjugate Chemistry. 2009 ; 20( 6): 1237-1241.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/bc9001085
  • Fonte: Langmuir. Unidade: IQ

    Assuntos: CELULOSE, ENZIMAS

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      TÉBÉKA, Iris Raquel Maia e SILVA, Artur G. L. e PETRI, Denise Freitas Siqueira. Hydrolytic activity of free and immobilized cellulase. Langmuir, v. 25, n. 3, p. 1582-1587, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/la802882s. Acesso em: 15 jul. 2024.
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      Tébéka, I. R. M., Silva, A. G. L., & Petri, D. F. S. (2009). Hydrolytic activity of free and immobilized cellulase. Langmuir, 25( 3), 1582-1587. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/la802882s
    • NLM

      Tébéka IRM, Silva AGL, Petri DFS. Hydrolytic activity of free and immobilized cellulase [Internet]. Langmuir. 2009 ; 25( 3): 1582-1587.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/la802882s
    • Vancouver

      Tébéka IRM, Silva AGL, Petri DFS. Hydrolytic activity of free and immobilized cellulase [Internet]. Langmuir. 2009 ; 25( 3): 1582-1587.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/la802882s
  • Fonte: Journal of Chemical Information and Modeling. Unidade: FCF

    Assuntos: FARMACOLOGIA, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, MEDICAMENTO

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      ANDRADE, Carolina Horta et al. Rational design and 3D-pharmacophore mapping of 5 '-thiourea-substituted 'alpha'-thymidine analogues as mycobacterial TMPK inhibitors. Journal of Chemical Information and Modeling, v. 49, n. 4, p. 1070-1078, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/ci8004622. Acesso em: 15 jul. 2024.
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      Andrade, C. H., Pasqualoto, K. F. M., Ferreira, E. I., & Hopfinger, A. J. (2009). Rational design and 3D-pharmacophore mapping of 5 '-thiourea-substituted 'alpha'-thymidine analogues as mycobacterial TMPK inhibitors. Journal of Chemical Information and Modeling, 49( 4), 1070-1078. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/ci8004622
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      Andrade CH, Pasqualoto KFM, Ferreira EI, Hopfinger AJ. Rational design and 3D-pharmacophore mapping of 5 '-thiourea-substituted 'alpha'-thymidine analogues as mycobacterial TMPK inhibitors [Internet]. Journal of Chemical Information and Modeling. 2009 ; 49( 4): 1070-1078.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/ci8004622
    • Vancouver

      Andrade CH, Pasqualoto KFM, Ferreira EI, Hopfinger AJ. Rational design and 3D-pharmacophore mapping of 5 '-thiourea-substituted 'alpha'-thymidine analogues as mycobacterial TMPK inhibitors [Internet]. Journal of Chemical Information and Modeling. 2009 ; 49( 4): 1070-1078.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/ci8004622
  • Fonte: Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry. Unidade: IQ

    Assuntos: LÍQUIDOS IÔNICOS, FÍSICO-QUÍMICA

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      RIBEIRO, Mauro Carlos Costa e SCOPIGNO, Tullio e RUOCCO, Giancarlo. Prigogine-defay ratio for an ionic glass-former: molecular dynamics simulations. Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry, v. 113, n. 10, p. 3099-3104, 2009Tradução . . Acesso em: 15 jul. 2024.
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      Ribeiro, M. C. C., Scopigno, T., & Ruocco, G. (2009). Prigogine-defay ratio for an ionic glass-former: molecular dynamics simulations. Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry, 113( 10), 3099-3104.
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      Ribeiro MCC, Scopigno T, Ruocco G. Prigogine-defay ratio for an ionic glass-former: molecular dynamics simulations. Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry. 2009 ; 113( 10): 3099-3104.[citado 2024 jul. 15 ]
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      Ribeiro MCC, Scopigno T, Ruocco G. Prigogine-defay ratio for an ionic glass-former: molecular dynamics simulations. Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry. 2009 ; 113( 10): 3099-3104.[citado 2024 jul. 15 ]
  • Fonte: Inorganic Chemistry. Unidade: IQ

    Assuntos: NANOPARTÍCULAS, PALÁDIO, QUÍMICA INORGÂNICA

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      ROSSI, Liane Marcia e NANGOI, Inna M. e COSTA, Natália de Jesus da Silva. Ligand-assisted preparation of palladium supported nanoparticles: a step toward. Inorganic Chemistry, v. 48, n. 11, p. 4640-4642, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/ic900440p. Acesso em: 15 jul. 2024.
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      Rossi, L. M., Nangoi, I. M., & Costa, N. de J. da S. (2009). Ligand-assisted preparation of palladium supported nanoparticles: a step toward. Inorganic Chemistry, 48( 11), 4640-4642. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/ic900440p
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      Rossi LM, Nangoi IM, Costa N de J da S. Ligand-assisted preparation of palladium supported nanoparticles: a step toward [Internet]. Inorganic Chemistry. 2009 ; 48( 11): 4640-4642.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/ic900440p
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      Rossi LM, Nangoi IM, Costa N de J da S. Ligand-assisted preparation of palladium supported nanoparticles: a step toward [Internet]. Inorganic Chemistry. 2009 ; 48( 11): 4640-4642.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/ic900440p
  • Fonte: Journal of Agricultural and Food Chemistry. Unidade: FCF

    Assuntos: ANTIOXIDANTES, FEIJÃO

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      RANILLA, Lena Gálvez e GENOVESE, Maria Inês e LAJOLO, Franco Maria. Effect of different cooking conditions on phenolic compounds and antioxidant capacity of some selected Brazilian bean (Phaseolus vulgaris L.) cultivars. Journal of Agricultural and Food Chemistry, v. 57, n. 13, p. 5734-5742, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/jf900527v. Acesso em: 15 jul. 2024.
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      Ranilla, L. G., Genovese, M. I., & Lajolo, F. M. (2009). Effect of different cooking conditions on phenolic compounds and antioxidant capacity of some selected Brazilian bean (Phaseolus vulgaris L.) cultivars. Journal of Agricultural and Food Chemistry, 57( 13), 5734-5742. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/jf900527v
    • NLM

      Ranilla LG, Genovese MI, Lajolo FM. Effect of different cooking conditions on phenolic compounds and antioxidant capacity of some selected Brazilian bean (Phaseolus vulgaris L.) cultivars [Internet]. Journal of Agricultural and Food Chemistry. 2009 ; 57( 13): 5734-5742.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jf900527v
    • Vancouver

      Ranilla LG, Genovese MI, Lajolo FM. Effect of different cooking conditions on phenolic compounds and antioxidant capacity of some selected Brazilian bean (Phaseolus vulgaris L.) cultivars [Internet]. Journal of Agricultural and Food Chemistry. 2009 ; 57( 13): 5734-5742.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jf900527v
  • Fonte: Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry. Unidade: IQ

    Assuntos: MATERIAIS NANOESTRUTURADOS, ESPECTROSCOPIA RAMAN

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      DO NASCIMENTO, G. M. e KOBATA, Pedro Yuri Gerônimo e TEMPERINI, Márcia Laudelina Arruda. Structural and vibrational characterization of polyaniline nanofibers prepared from interfacial polymerization. Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry, v. 112, n. 37, p. 11551-11557, 2008Tradução . . Disponível em: http://pubs.acs.org/doi/pdfplus/10.1021/jp804154k. Acesso em: 15 jul. 2024.
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      Do Nascimento, G. M., Kobata, P. Y. G., & Temperini, M. L. A. (2008). Structural and vibrational characterization of polyaniline nanofibers prepared from interfacial polymerization. Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry, 112( 37), 11551-11557. Recuperado de http://pubs.acs.org/doi/pdfplus/10.1021/jp804154k
    • NLM

      Do Nascimento GM, Kobata PYG, Temperini MLA. Structural and vibrational characterization of polyaniline nanofibers prepared from interfacial polymerization [Internet]. Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry. 2008 ; 112( 37): 11551-11557.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdfplus/10.1021/jp804154k
    • Vancouver

      Do Nascimento GM, Kobata PYG, Temperini MLA. Structural and vibrational characterization of polyaniline nanofibers prepared from interfacial polymerization [Internet]. Journal of Physical Chemistry B : Soft Condensed Matter and Biophysical Chemistry. 2008 ; 112( 37): 11551-11557.[citado 2024 jul. 15 ] Available from: http://pubs.acs.org/doi/pdfplus/10.1021/jp804154k

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