Filtros : "Indexado no Chemical Abstracts" "CARDOSO, DANIEL RODRIGUES" Removidos: "PROTEÍNAS" "Livro de Resumos" Limpar

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  • Source: Journal of Physical Chemistry C. Unidades: IFSC, IQSC, IEA

    Assunto: RESSONÂNCIA PARAMAGNÉTICA ELETRÔNICA

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      ALI, Mian Abdul et al. Operando electron paramagnetic resonance for elucidating the electron transfer mechanism of coenzymes. Journal of Physical Chemistry C, v. 123, n. 26, p. 16058-16064, 2019Tradução . . Disponível em: https://doi.org/10.1021/acs.jpcc.9b01160. Acesso em: 28 set. 2024.
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      Ali, M. A., Hassan, A., Sedenho, G. C., Gonçalves, R. V., Cardoso, D. R., & Crespilho, F. N. (2019). Operando electron paramagnetic resonance for elucidating the electron transfer mechanism of coenzymes. Journal of Physical Chemistry C, 123( 26), 16058-16064. doi:10.1021/acs.jpcc.9b01160
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      Ali MA, Hassan A, Sedenho GC, Gonçalves RV, Cardoso DR, Crespilho FN. Operando electron paramagnetic resonance for elucidating the electron transfer mechanism of coenzymes [Internet]. Journal of Physical Chemistry C. 2019 ; 123( 26): 16058-16064.[citado 2024 set. 28 ] Available from: https://doi.org/10.1021/acs.jpcc.9b01160
    • Vancouver

      Ali MA, Hassan A, Sedenho GC, Gonçalves RV, Cardoso DR, Crespilho FN. Operando electron paramagnetic resonance for elucidating the electron transfer mechanism of coenzymes [Internet]. Journal of Physical Chemistry C. 2019 ; 123( 26): 16058-16064.[citado 2024 set. 28 ] Available from: https://doi.org/10.1021/acs.jpcc.9b01160
  • Source: RSC Advances. Unidade: IQSC

    Assunto: ÁCIDO ÚRICO

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      ZAWADZKI, Andressa de e CARDOSO, Daniel Rodrigues e SKIBSTED, Leif H. Proton-coupled electron transfer promotes the reduction of ferrylmyoglobin by uric acid under physiological conditions. RSC Advances, v. 7, p. 17824-17831, 2017Tradução . . Disponível em: https://doi.org/10.1039/c6ra28314d. Acesso em: 28 set. 2024.
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      Zawadzki, A. de, Cardoso, D. R., & Skibsted, L. H. (2017). Proton-coupled electron transfer promotes the reduction of ferrylmyoglobin by uric acid under physiological conditions. RSC Advances, 7, 17824-17831. doi:10.1039/c6ra28314d
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      Zawadzki A de, Cardoso DR, Skibsted LH. Proton-coupled electron transfer promotes the reduction of ferrylmyoglobin by uric acid under physiological conditions [Internet]. RSC Advances. 2017 ; 7 17824-17831.[citado 2024 set. 28 ] Available from: https://doi.org/10.1039/c6ra28314d
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      Zawadzki A de, Cardoso DR, Skibsted LH. Proton-coupled electron transfer promotes the reduction of ferrylmyoglobin by uric acid under physiological conditions [Internet]. RSC Advances. 2017 ; 7 17824-17831.[citado 2024 set. 28 ] Available from: https://doi.org/10.1039/c6ra28314d
  • Source: Food Research International. Unidades: IQSC, ESALQ

    Subjects: METABÓLITOS, ALIMENTAÇÃO ANIMAL

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      ZAWADZKI, Andressa de et al. Mate extract as fedd additive for improvement of beef quality. Food Research International, v. 99, p. 336-347, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.foodres.2017.05.033. Acesso em: 28 set. 2024.
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      Zawadzki, A. de, Arrivetti, L. de O. R., Vidal, M. P., Catai, J. R., Nassu, R. T., Tullio, R. R., et al. (2017). Mate extract as fedd additive for improvement of beef quality. Food Research International, 99, 336-347. doi:10.1016/j.foodres.2017.05.033
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      Zawadzki A de, Arrivetti L de OR, Vidal MP, Catai JR, Nassu RT, Tullio RR, Berndt A, Oliveira CR, Ferreira AG, Neves Junior LF, Colnago LA, Skibsted LH, Cardoso DR. Mate extract as fedd additive for improvement of beef quality [Internet]. Food Research International. 2017 ; 99 336-347.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.foodres.2017.05.033
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      Zawadzki A de, Arrivetti L de OR, Vidal MP, Catai JR, Nassu RT, Tullio RR, Berndt A, Oliveira CR, Ferreira AG, Neves Junior LF, Colnago LA, Skibsted LH, Cardoso DR. Mate extract as fedd additive for improvement of beef quality [Internet]. Food Research International. 2017 ; 99 336-347.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.foodres.2017.05.033
  • Source: Food Chemistry. Unidade: IQSC

    Subjects: PROCESSOS QUÍMICOS, ALIMENTOS

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      PAGANELLI, Marcella Oliva et al. Limited proteolysis of myoglobin opens channel in ferrochelatase-globin complex for iron to zinc transmetallation. Food Chemistry, v. 210, p. 491-499, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.foodchem.2016.04.109. Acesso em: 28 set. 2024.
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      Paganelli, M. O., Grossi, A. B., Dores-Silva, P. R. das, Borges, J. C., Cardoso, D. R., & Skibsted, L. H. (2016). Limited proteolysis of myoglobin opens channel in ferrochelatase-globin complex for iron to zinc transmetallation. Food Chemistry, 210, 491-499. doi:10.1016/j.foodchem.2016.04.109
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      Paganelli MO, Grossi AB, Dores-Silva PR das, Borges JC, Cardoso DR, Skibsted LH. Limited proteolysis of myoglobin opens channel in ferrochelatase-globin complex for iron to zinc transmetallation [Internet]. Food Chemistry. 2016 ; 210 491-499.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.foodchem.2016.04.109
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      Paganelli MO, Grossi AB, Dores-Silva PR das, Borges JC, Cardoso DR, Skibsted LH. Limited proteolysis of myoglobin opens channel in ferrochelatase-globin complex for iron to zinc transmetallation [Internet]. Food Chemistry. 2016 ; 210 491-499.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.foodchem.2016.04.109
  • Source: Photochemical & Photobiological Sciences. Unidade: IQSC

    Assunto: FOTOQUÍMICA

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      SANTOS, Willy G et al. New insight into the photophysics and reactivity of trigonal and tetrahedral arylboron compounds. Photochemical & Photobiological Sciences, 2016Tradução . . Disponível em: https://doi.org/10.1039/C6PP00139F. Acesso em: 28 set. 2024.
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      Santos, W. G., Pina, J., Burrows, D. H., Forbes, M. D. E., & Cardoso, D. R. (2016). New insight into the photophysics and reactivity of trigonal and tetrahedral arylboron compounds. Photochemical & Photobiological Sciences. doi:10.1039/C6PP00139F
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      Santos WG, Pina J, Burrows DH, Forbes MDE, Cardoso DR. New insight into the photophysics and reactivity of trigonal and tetrahedral arylboron compounds [Internet]. Photochemical & Photobiological Sciences. 2016 ;[citado 2024 set. 28 ] Available from: https://doi.org/10.1039/C6PP00139F
    • Vancouver

      Santos WG, Pina J, Burrows DH, Forbes MDE, Cardoso DR. New insight into the photophysics and reactivity of trigonal and tetrahedral arylboron compounds [Internet]. Photochemical & Photobiological Sciences. 2016 ;[citado 2024 set. 28 ] Available from: https://doi.org/10.1039/C6PP00139F
  • Source: Journal of Agricultural and Food Chemistry. Unidade: IQSC

    Subjects: VITAMINA D, FOTOQUÍMICA

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      SCURACHIO, Regina Spricigo et al. Isomerization of cholecalciferol through energy transfer as a protective mechanism against flavin-sensitized photooxidation. Journal of Agricultural and Food Chemistry, v. 63, n. 18, p. 4629-4637, 2015Tradução . . Disponível em: https://doi.org/10.1021/jf505958c. Acesso em: 28 set. 2024.
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      Scurachio, R. S., Santos, W. G. dos, Nascimento, E. S. P. do, Skibstede, L. H., & Cardoso, D. R. (2015). Isomerization of cholecalciferol through energy transfer as a protective mechanism against flavin-sensitized photooxidation. Journal of Agricultural and Food Chemistry, 63( 18), 4629-4637. doi:10.1021/jf505958c
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      Scurachio RS, Santos WG dos, Nascimento ESP do, Skibstede LH, Cardoso DR. Isomerization of cholecalciferol through energy transfer as a protective mechanism against flavin-sensitized photooxidation [Internet]. Journal of Agricultural and Food Chemistry. 2015 ; 63( 18):4629-4637.[citado 2024 set. 28 ] Available from: https://doi.org/10.1021/jf505958c
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      Scurachio RS, Santos WG dos, Nascimento ESP do, Skibstede LH, Cardoso DR. Isomerization of cholecalciferol through energy transfer as a protective mechanism against flavin-sensitized photooxidation [Internet]. Journal of Agricultural and Food Chemistry. 2015 ; 63( 18):4629-4637.[citado 2024 set. 28 ] Available from: https://doi.org/10.1021/jf505958c
  • Source: Journal of the Brazilian Chemical Society. Unidade: IQSC

    Assunto: QUÍMICA

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      SALE, Eric S. et al. Quinolines by three-component reaction: synthesis and photophysical studies. Journal of the Brazilian Chemical Society, v. 26, n. 3, p. 562-571, 2015Tradução . . Disponível em: https://doi.org/10.5935/0103-5053.20150011. Acesso em: 28 set. 2024.
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      Sale, E. S., Schneider, juliana M. F. M., Santos, J. L., Bortoluzzi, A. J., Cardoso, D. R., Santos, W. G. dos, & Merlo, A. A. (2015). Quinolines by three-component reaction: synthesis and photophysical studies. Journal of the Brazilian Chemical Society, 26( 3), 562-571. doi:10.5935/0103-5053.20150011
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      Sale ES, Schneider juliana MFM, Santos JL, Bortoluzzi AJ, Cardoso DR, Santos WG dos, Merlo AA. Quinolines by three-component reaction: synthesis and photophysical studies [Internet]. Journal of the Brazilian Chemical Society. 2015 ; 26( 3): 562-571.[citado 2024 set. 28 ] Available from: https://doi.org/10.5935/0103-5053.20150011
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      Sale ES, Schneider juliana MFM, Santos JL, Bortoluzzi AJ, Cardoso DR, Santos WG dos, Merlo AA. Quinolines by three-component reaction: synthesis and photophysical studies [Internet]. Journal of the Brazilian Chemical Society. 2015 ; 26( 3): 562-571.[citado 2024 set. 28 ] Available from: https://doi.org/10.5935/0103-5053.20150011
  • Source: Free Radical Research. Unidade: IQSC

    Assunto: SÍNTESE ORGÂNICA

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      PAPA, Thiago Bueno Ruiz et al. Astaxanthin diferulate as a bifunctional antioxidant. Free Radical Research, v. 49, n. 1, p. 102-111, 2015Tradução . . Disponível em: https://doi.org/10.3109/10715762.2014.982112. Acesso em: 28 set. 2024.
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      Papa, T. B. R., Pinho, V. D., Nascimento, E. S. P. do, Santos, W. G., Burtoloso, A. C. B., Skibstede, L. H., & Cardoso, D. R. (2015). Astaxanthin diferulate as a bifunctional antioxidant. Free Radical Research, 49( 1), 102-111. doi:10.3109/10715762.2014.982112
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      Papa TBR, Pinho VD, Nascimento ESP do, Santos WG, Burtoloso ACB, Skibstede LH, Cardoso DR. Astaxanthin diferulate as a bifunctional antioxidant [Internet]. Free Radical Research. 2015 ; 49( 1): 102-111.[citado 2024 set. 28 ] Available from: https://doi.org/10.3109/10715762.2014.982112
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      Papa TBR, Pinho VD, Nascimento ESP do, Santos WG, Burtoloso ACB, Skibstede LH, Cardoso DR. Astaxanthin diferulate as a bifunctional antioxidant [Internet]. Free Radical Research. 2015 ; 49( 1): 102-111.[citado 2024 set. 28 ] Available from: https://doi.org/10.3109/10715762.2014.982112
  • Source: Physiotherapy Theory and Practice. Unidades: IQSC, IFSC

    Assunto: QUÍMICA

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      FERRARESI, Cleber et al. Muscular pre-conditioning using light-emitting diode therapy (LEDT) for high-intensity exercise: a randomized double-blind placebo-controlled trial with a single elite runner. Physiotherapy Theory and Practice, v. 31, n. 5, p. 354-361, 2015Tradução . . Disponível em: https://doi.org/10.3109/09593985.2014.1003118. Acesso em: 28 set. 2024.
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      Ferraresi, C., Beltrame, T., Fabrizzi, F., Nascimento, E. S. do, Karsten, M., Francisco, C. de O., et al. (2015). Muscular pre-conditioning using light-emitting diode therapy (LEDT) for high-intensity exercise: a randomized double-blind placebo-controlled trial with a single elite runner. Physiotherapy Theory and Practice, 31( 5), 354-361. doi:10.3109/09593985.2014.1003118
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      Ferraresi C, Beltrame T, Fabrizzi F, Nascimento ES do, Karsten M, Francisco C de O, Borghi-Silva A, Catai AM, Cardoso DR, Ferreira AG, Hamblin MR, Bagnato VS, Parizotto NA. Muscular pre-conditioning using light-emitting diode therapy (LEDT) for high-intensity exercise: a randomized double-blind placebo-controlled trial with a single elite runner [Internet]. Physiotherapy Theory and Practice. 2015 ;31( 5): 354-361.[citado 2024 set. 28 ] Available from: https://doi.org/10.3109/09593985.2014.1003118
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      Ferraresi C, Beltrame T, Fabrizzi F, Nascimento ES do, Karsten M, Francisco C de O, Borghi-Silva A, Catai AM, Cardoso DR, Ferreira AG, Hamblin MR, Bagnato VS, Parizotto NA. Muscular pre-conditioning using light-emitting diode therapy (LEDT) for high-intensity exercise: a randomized double-blind placebo-controlled trial with a single elite runner [Internet]. Physiotherapy Theory and Practice. 2015 ;31( 5): 354-361.[citado 2024 set. 28 ] Available from: https://doi.org/10.3109/09593985.2014.1003118
  • Source: Journal of the Brazilian Chemical Society. Unidade: IQSC

    Assunto: CERVEJA

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      ALMEIDA, Natália Ellen Castilho de e AGUIAR, Inara de e CARDOSO, Daniel Rodrigues. Mechanism of Hop-derived terpenes oxidation in beer. Journal of the Brazilian Chemical Society, v. 26, n. 11, p. 2362-2368, 2015Tradução . . Disponível em: https://doi.org/10.5953/0103-5053.20150231. Acesso em: 28 set. 2024.
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      Almeida, N. E. C. de, Aguiar, I. de, & Cardoso, D. R. (2015). Mechanism of Hop-derived terpenes oxidation in beer. Journal of the Brazilian Chemical Society, 26( 11), 2362-2368. doi:10.5953/0103-5053.20150231
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      Almeida NEC de, Aguiar I de, Cardoso DR. Mechanism of Hop-derived terpenes oxidation in beer [Internet]. Journal of the Brazilian Chemical Society. 2015 ; 26( 11): 2362-2368.[citado 2024 set. 28 ] Available from: https://doi.org/10.5953/0103-5053.20150231
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      Almeida NEC de, Aguiar I de, Cardoso DR. Mechanism of Hop-derived terpenes oxidation in beer [Internet]. Journal of the Brazilian Chemical Society. 2015 ; 26( 11): 2362-2368.[citado 2024 set. 28 ] Available from: https://doi.org/10.5953/0103-5053.20150231
  • Source: Journal of Organometallic Chemistry. Unidade: IQSC

    Assunto: FOTOQUÍMICA

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      SANTOS, Willy Glen et al. DFT, spectroscopic, and photoproduct study of 2-aminoethyldiphenylborinate and tetraphenydiboroxane. Journal of Organometallic Chemistry, v. 755, p. 125-133, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2014.01.010. Acesso em: 28 set. 2024.
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      Santos, W. G., Cardoso, D. R., Arrivetti, L. de O. R., Cavalheiro, C. C. S., & Neumann, M. G. (2014). DFT, spectroscopic, and photoproduct study of 2-aminoethyldiphenylborinate and tetraphenydiboroxane. Journal of Organometallic Chemistry, 755, 125-133. doi:10.1016/j.jorganchem.2014.01.010
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      Santos WG, Cardoso DR, Arrivetti L de OR, Cavalheiro CCS, Neumann MG. DFT, spectroscopic, and photoproduct study of 2-aminoethyldiphenylborinate and tetraphenydiboroxane [Internet]. Journal of Organometallic Chemistry. 2014 ; 755 125-133.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.jorganchem.2014.01.010
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      Santos WG, Cardoso DR, Arrivetti L de OR, Cavalheiro CCS, Neumann MG. DFT, spectroscopic, and photoproduct study of 2-aminoethyldiphenylborinate and tetraphenydiboroxane [Internet]. Journal of Organometallic Chemistry. 2014 ; 755 125-133.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.jorganchem.2014.01.010
  • Source: RSC Advances: an international journal to further the chemical sciences. Unidade: IQSC

    Assunto: CINÉTICA

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      LIBARDI, Silvia Helena et al. Reduction of ferrylmyoglobin by cysteine as affected by pH. RSC Advances: an international journal to further the chemical sciences, v. 1, p. 1-10, 2014Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1039/C4RA10562A. Acesso em: 28 set. 2024.
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      Libardi, S. H., Pindstrup, H., Amigo, J. M., Cardoso, D. R., & Skibsted, L. H. (2014). Reduction of ferrylmyoglobin by cysteine as affected by pH. RSC Advances: an international journal to further the chemical sciences, 1, 1-10. doi:10.1039/C4RA10562A
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      Libardi SH, Pindstrup H, Amigo JM, Cardoso DR, Skibsted LH. Reduction of ferrylmyoglobin by cysteine as affected by pH [Internet]. RSC Advances: an international journal to further the chemical sciences. 2014 ; 1 1-10.[citado 2024 set. 28 ] Available from: http://pubs.acs.org/doi/pdf/10.1039/C4RA10562A
    • Vancouver

      Libardi SH, Pindstrup H, Amigo JM, Cardoso DR, Skibsted LH. Reduction of ferrylmyoglobin by cysteine as affected by pH [Internet]. RSC Advances: an international journal to further the chemical sciences. 2014 ; 1 1-10.[citado 2024 set. 28 ] Available from: http://pubs.acs.org/doi/pdf/10.1039/C4RA10562A
  • Source: Food Research International. Unidade: IQSC

    Subjects: ALIMENTOS, BIOTECNOLOGIA

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      GROSSI, Alberto B. et al. Proteolysis involvement in zinc–protoporphyrin IX formation during Parma ham maturation. Food Research International, v. 56, p. 252-259, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.foodres.2014.01.007. Acesso em: 28 set. 2024.
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      Grossi, A. B., Nascimento, E. S. P. do, Cardoso, D. R., & Skibstede, L. H. (2014). Proteolysis involvement in zinc–protoporphyrin IX formation during Parma ham maturation. Food Research International, 56, 252-259. doi:10.1016/j.foodres.2014.01.007
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      Grossi AB, Nascimento ESP do, Cardoso DR, Skibstede LH. Proteolysis involvement in zinc–protoporphyrin IX formation during Parma ham maturation [Internet]. Food Research International. 2014 ; 56 252-259.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.foodres.2014.01.007
    • Vancouver

      Grossi AB, Nascimento ESP do, Cardoso DR, Skibstede LH. Proteolysis involvement in zinc–protoporphyrin IX formation during Parma ham maturation [Internet]. Food Research International. 2014 ; 56 252-259.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.foodres.2014.01.007
  • Source: Analytical Methods. Unidade: IQSC

    Assunto: BEBIDAS DESTILADAS

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      SILVA, Alexandre Ataide da et al. Multivariate analyses of UV-Vis absorption spectral data from cachaça wood extracts: a model to classify aged Brazilian cachaças according to the wood species used. Analytical Methods, v. 4, n. 3, p. 642-646, 2012Tradução . . Disponível em: https://doi.org/10.1039/C2AY05670D. Acesso em: 28 set. 2024.
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      Silva, A. A. da, De Keukeleire, D., Cardoso, D. R., & Franco, D. W. (2012). Multivariate analyses of UV-Vis absorption spectral data from cachaça wood extracts: a model to classify aged Brazilian cachaças according to the wood species used. Analytical Methods, 4( 3), 642-646. doi:10.1039/C2AY05670D
    • NLM

      Silva AA da, De Keukeleire D, Cardoso DR, Franco DW. Multivariate analyses of UV-Vis absorption spectral data from cachaça wood extracts: a model to classify aged Brazilian cachaças according to the wood species used [Internet]. Analytical Methods. 2012 ; 4( 3): 642-646.[citado 2024 set. 28 ] Available from: https://doi.org/10.1039/C2AY05670D
    • Vancouver

      Silva AA da, De Keukeleire D, Cardoso DR, Franco DW. Multivariate analyses of UV-Vis absorption spectral data from cachaça wood extracts: a model to classify aged Brazilian cachaças according to the wood species used [Internet]. Analytical Methods. 2012 ; 4( 3): 642-646.[citado 2024 set. 28 ] Available from: https://doi.org/10.1039/C2AY05670D
  • Source: Journal of Agricultural and Food Chemistry. Unidade: IQSC

    Subjects: QUÍMICA INORGÂNICA, CERVEJA

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      ALMEIDA, Natália Ellen Castilho de et al. Reactivity of beer bitter acids toward the 1-hydroxyyethyl radical as probed by spin-trapping electro paramagnetic resonance (EPR) and electrospray ionization-tandem mass spectrometry (ESI-MS/MS). Journal of Agricultural and Food Chemistry, v. 59, n. 8, p. 4183-4191, 2011Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/jf104797d. Acesso em: 28 set. 2024.
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      Almeida, N. E. C. de, Homem de Mello, P., De Keukeleire, D., & Cardoso, D. R. (2011). Reactivity of beer bitter acids toward the 1-hydroxyyethyl radical as probed by spin-trapping electro paramagnetic resonance (EPR) and electrospray ionization-tandem mass spectrometry (ESI-MS/MS). Journal of Agricultural and Food Chemistry, 59( 8), 4183-4191. doi:10.1021/jf104797d
    • NLM

      Almeida NEC de, Homem de Mello P, De Keukeleire D, Cardoso DR. Reactivity of beer bitter acids toward the 1-hydroxyyethyl radical as probed by spin-trapping electro paramagnetic resonance (EPR) and electrospray ionization-tandem mass spectrometry (ESI-MS/MS) [Internet]. Journal of Agricultural and Food Chemistry. 2011 ; 59( 8): 4183-4191.[citado 2024 set. 28 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jf104797d
    • Vancouver

      Almeida NEC de, Homem de Mello P, De Keukeleire D, Cardoso DR. Reactivity of beer bitter acids toward the 1-hydroxyyethyl radical as probed by spin-trapping electro paramagnetic resonance (EPR) and electrospray ionization-tandem mass spectrometry (ESI-MS/MS) [Internet]. Journal of Agricultural and Food Chemistry. 2011 ; 59( 8): 4183-4191.[citado 2024 set. 28 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jf104797d
  • Source: Journal of Agricultural and Food Chemistry. Unidade: IQSC

    Subjects: QUÍMICA INORGÂNICA, ANTIOXIDANTES

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      LIBARDI, Silvia Helena et al. Deactivation of ferrylmyoglobin by vanillin as affected by vanillin binding to B-lactoglobulin. Journal of Agricultural and Food Chemistry, v. 59, n. 11, p. 6202-6208, 2011Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/jf1047173. Acesso em: 28 set. 2024.
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      Libardi, S. H., Borges, J. C., Skibsted, L. H., & Cardoso, D. R. (2011). Deactivation of ferrylmyoglobin by vanillin as affected by vanillin binding to B-lactoglobulin. Journal of Agricultural and Food Chemistry, 59( 11), 6202-6208. doi:10.1021/jf1047173
    • NLM

      Libardi SH, Borges JC, Skibsted LH, Cardoso DR. Deactivation of ferrylmyoglobin by vanillin as affected by vanillin binding to B-lactoglobulin [Internet]. Journal of Agricultural and Food Chemistry. 2011 ; 59( 11): 6202-6208.[citado 2024 set. 28 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jf1047173
    • Vancouver

      Libardi SH, Borges JC, Skibsted LH, Cardoso DR. Deactivation of ferrylmyoglobin by vanillin as affected by vanillin binding to B-lactoglobulin [Internet]. Journal of Agricultural and Food Chemistry. 2011 ; 59( 11): 6202-6208.[citado 2024 set. 28 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jf1047173
  • Source: Photochemistry and Photochemistry. Unidade: IQSC

    Assunto: QUÍMICA

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      SCURACHIO, Regina Spricigo et al. Photodegradation of folate sensitized by riboflavin. Photochemistry and Photochemistry, v. 87, n. 4, p. 840-845, 2011Tradução . . Disponível em: https://doi.org/10.1111/j.1751-1097.2011.00916.x. Acesso em: 28 set. 2024.
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      Scurachio, R. S., Skibsted, L. H., Metzker, G., & Cardoso, D. R. (2011). Photodegradation of folate sensitized by riboflavin. Photochemistry and Photochemistry, 87( 4), 840-845. doi:10.1111/j.1751-1097.2011.00916.x
    • NLM

      Scurachio RS, Skibsted LH, Metzker G, Cardoso DR. Photodegradation of folate sensitized by riboflavin [Internet]. Photochemistry and Photochemistry. 2011 ; 87( 4): 840-845.[citado 2024 set. 28 ] Available from: https://doi.org/10.1111/j.1751-1097.2011.00916.x
    • Vancouver

      Scurachio RS, Skibsted LH, Metzker G, Cardoso DR. Photodegradation of folate sensitized by riboflavin [Internet]. Photochemistry and Photochemistry. 2011 ; 87( 4): 840-845.[citado 2024 set. 28 ] Available from: https://doi.org/10.1111/j.1751-1097.2011.00916.x
  • Source: European Food Research and Technology. Unidade: IQSC

    Assunto: TECNOLOGIA DE ALIMENTOS

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      BECKER, Eleonora Miquel e CARDOSO, Daniel Rodrigues e SKIBSTED, Leif H. Quenching of excited states of red-pigment zinc protoporphyrin: IX by hemin and natural reductors in dry-cured hams. European Food Research and Technology, v. 232, n. 2, p. 343-349, 2011Tradução . . Disponível em: https://doi.org/10.1007/s00217-010-1392-6. Acesso em: 28 set. 2024.
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      Becker, E. M., Cardoso, D. R., & Skibsted, L. H. (2011). Quenching of excited states of red-pigment zinc protoporphyrin: IX by hemin and natural reductors in dry-cured hams. European Food Research and Technology, 232( 2), 343-349. doi:10.1007/s00217-010-1392-6
    • NLM

      Becker EM, Cardoso DR, Skibsted LH. Quenching of excited states of red-pigment zinc protoporphyrin: IX by hemin and natural reductors in dry-cured hams [Internet]. European Food Research and Technology. 2011 ; 232( 2): 343-349.[citado 2024 set. 28 ] Available from: https://doi.org/10.1007/s00217-010-1392-6
    • Vancouver

      Becker EM, Cardoso DR, Skibsted LH. Quenching of excited states of red-pigment zinc protoporphyrin: IX by hemin and natural reductors in dry-cured hams [Internet]. European Food Research and Technology. 2011 ; 232( 2): 343-349.[citado 2024 set. 28 ] Available from: https://doi.org/10.1007/s00217-010-1392-6
  • Source: Journal of the Brazilian Chemical Society. Unidade: IQSC

    Assunto: QUÍMICA

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      METZKER, Gustavo et al. Nitric oxide as an activation agent for nucleophilic attack in trans-[Ru(NO)'(NHIND.3)IND.4'{P'(OEt)IND.3}]'(PFIND.6)IND.3'. Journal of the Brazilian Chemical Society, v. 21, n. 7, p. 1266-1273, 2010Tradução . . Disponível em: http://www.scielo.br/scielo.php?script=sci_issues&pid=0103-5053&lng=pt&nrm=iso. Acesso em: 28 set. 2024.
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      Metzker, G., Toledo Junior, J. C., Lima, F. C. A., Magalhaes, A., Cardoso, D. R., & Franco, D. W. (2010). Nitric oxide as an activation agent for nucleophilic attack in trans-[Ru(NO)'(NHIND.3)IND.4'{P'(OEt)IND.3}]'(PFIND.6)IND.3'. Journal of the Brazilian Chemical Society, 21( 7), 1266-1273. Recuperado de http://www.scielo.br/scielo.php?script=sci_issues&pid=0103-5053&lng=pt&nrm=iso
    • NLM

      Metzker G, Toledo Junior JC, Lima FCA, Magalhaes A, Cardoso DR, Franco DW. Nitric oxide as an activation agent for nucleophilic attack in trans-[Ru(NO)'(NHIND.3)IND.4'{P'(OEt)IND.3}]'(PFIND.6)IND.3' [Internet]. Journal of the Brazilian Chemical Society. 2010 ; 21( 7): 1266-1273.[citado 2024 set. 28 ] Available from: http://www.scielo.br/scielo.php?script=sci_issues&pid=0103-5053&lng=pt&nrm=iso
    • Vancouver

      Metzker G, Toledo Junior JC, Lima FCA, Magalhaes A, Cardoso DR, Franco DW. Nitric oxide as an activation agent for nucleophilic attack in trans-[Ru(NO)'(NHIND.3)IND.4'{P'(OEt)IND.3}]'(PFIND.6)IND.3' [Internet]. Journal of the Brazilian Chemical Society. 2010 ; 21( 7): 1266-1273.[citado 2024 set. 28 ] Available from: http://www.scielo.br/scielo.php?script=sci_issues&pid=0103-5053&lng=pt&nrm=iso
  • Source: Química Nova. Unidade: IQSC

    Subjects: QUÍMICA, AGUARDENTE, DESTILAÇÃO

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      NASCIMENTO, Eduardo S. P. e CARDOSO, Daniel Rodrigues e FRANCO, Douglas Wagner. Comparação de técnicas de determinação de ésteres em cachaça. Química Nova, v. 32, n. 9, p. 2323-2327, 2009Tradução . . Disponível em: https://doi.org/10.1590/s0100-40422009000900016. Acesso em: 28 set. 2024.
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      Nascimento, E. S. P., Cardoso, D. R., & Franco, D. W. (2009). Comparação de técnicas de determinação de ésteres em cachaça. Química Nova, 32( 9), 2323-2327. doi:10.1590/s0100-40422009000900016
    • NLM

      Nascimento ESP, Cardoso DR, Franco DW. Comparação de técnicas de determinação de ésteres em cachaça [Internet]. Química Nova. 2009 ; 32( 9): 2323-2327.[citado 2024 set. 28 ] Available from: https://doi.org/10.1590/s0100-40422009000900016
    • Vancouver

      Nascimento ESP, Cardoso DR, Franco DW. Comparação de técnicas de determinação de ésteres em cachaça [Internet]. Química Nova. 2009 ; 32( 9): 2323-2327.[citado 2024 set. 28 ] Available from: https://doi.org/10.1590/s0100-40422009000900016

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