Filtros : "IQ008" "Reino Unido" "2013" Limpar

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  • Source: Toxicology in Vitro. Unidade: IQ

    Subjects: APOPTOSE, NEUROBLASTOMA

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      MATIAS, Andreza C et al. Diethyldithiocarbamate induces apoptosis in neuroblastoma cells by raising the intracellular copper level, triggering cytochrome c release and caspase activation. Toxicology in Vitro, v. 27, n. 1, p. 349-357, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tiv.2012.08.017. Acesso em: 30 jul. 2024.
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      Matias, A. C., Manieri, T. M., Cipriano, S. S., Carioni, V. M. de O., Nomura, C. S., Machado, C. M. L., & Cerchiaro, G. (2013). Diethyldithiocarbamate induces apoptosis in neuroblastoma cells by raising the intracellular copper level, triggering cytochrome c release and caspase activation. Toxicology in Vitro, 27( 1), 349-357. doi:10.1016/j.tiv.2012.08.017
    • NLM

      Matias AC, Manieri TM, Cipriano SS, Carioni VM de O, Nomura CS, Machado CML, Cerchiaro G. Diethyldithiocarbamate induces apoptosis in neuroblastoma cells by raising the intracellular copper level, triggering cytochrome c release and caspase activation [Internet]. Toxicology in Vitro. 2013 ; 27( 1): 349-357.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1016/j.tiv.2012.08.017
    • Vancouver

      Matias AC, Manieri TM, Cipriano SS, Carioni VM de O, Nomura CS, Machado CML, Cerchiaro G. Diethyldithiocarbamate induces apoptosis in neuroblastoma cells by raising the intracellular copper level, triggering cytochrome c release and caspase activation [Internet]. Toxicology in Vitro. 2013 ; 27( 1): 349-357.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1016/j.tiv.2012.08.017
  • Source: Photochemistry and Photobiology. Unidade: IQ

    Assunto: FOTOQUÍMICA

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      AUGUSTO, Felipe Alberto et al. Efficiency of electron transfer initiated chemiluminescence. Photochemistry and Photobiology, v. 89, n. 6, p. 1299-1317, 2013Tradução . . Disponível em: https://doi.org/10.1111/php.12102. Acesso em: 30 jul. 2024.
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      Augusto, F. A., Souza, G. A. de, Souza Junior, S. P. de, khalid, M., & Baader, W. J. (2013). Efficiency of electron transfer initiated chemiluminescence. Photochemistry and Photobiology, 89( 6), 1299-1317. doi:10.1111/php.12102
    • NLM

      Augusto FA, Souza GA de, Souza Junior SP de, khalid M, Baader WJ. Efficiency of electron transfer initiated chemiluminescence [Internet]. Photochemistry and Photobiology. 2013 ; 89( 6): 1299-1317.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1111/php.12102
    • Vancouver

      Augusto FA, Souza GA de, Souza Junior SP de, khalid M, Baader WJ. Efficiency of electron transfer initiated chemiluminescence [Internet]. Photochemistry and Photobiology. 2013 ; 89( 6): 1299-1317.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1111/php.12102
  • Source: Carbohydrate Polymers. Unidade: IQ

    Subjects: CELULOSE, QUÍMICA ORGÂNICA

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      NAWAZ, Haq e PIRES, Paulo Augusto Rodrigues e EL SEOUD, Omar A. Kinetics and mechanism of imidazole-catalyzed acylation of cellulose in LiCl/N,N-dimethylacetamide. Carbohydrate Polymers, v. 92, n. 2, p. 997-1005, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.carbpol.2012.10.009. Acesso em: 30 jul. 2024.
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      Nawaz, H., Pires, P. A. R., & El Seoud, O. A. (2013). Kinetics and mechanism of imidazole-catalyzed acylation of cellulose in LiCl/N,N-dimethylacetamide. Carbohydrate Polymers, 92( 2), 997-1005. doi:10.1016/j.carbpol.2012.10.009
    • NLM

      Nawaz H, Pires PAR, El Seoud OA. Kinetics and mechanism of imidazole-catalyzed acylation of cellulose in LiCl/N,N-dimethylacetamide [Internet]. Carbohydrate Polymers. 2013 ; 92( 2): 997-1005.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1016/j.carbpol.2012.10.009
    • Vancouver

      Nawaz H, Pires PAR, El Seoud OA. Kinetics and mechanism of imidazole-catalyzed acylation of cellulose in LiCl/N,N-dimethylacetamide [Internet]. Carbohydrate Polymers. 2013 ; 92( 2): 997-1005.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1016/j.carbpol.2012.10.009
  • Source: Biophysical Journal. Conference titles: Annual Meeting of the Biophysical Society. Unidade: IQ

    Assunto: FOSFOLIPÍDEOS

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      DI VITTA, Cláudio e MARZORATI, Liliana e FUNARI, Sérgio S. Thionaphthoquinones destabilization of phospholipid bilayers. Biophysical Journal. Cambridge: Instituto de Química, Universidade de São Paulo. . Acesso em: 30 jul. 2024. , 2013
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      Di Vitta, C., Marzorati, L., & Funari, S. S. (2013). Thionaphthoquinones destabilization of phospholipid bilayers. Biophysical Journal. Cambridge: Instituto de Química, Universidade de São Paulo.
    • NLM

      Di Vitta C, Marzorati L, Funari SS. Thionaphthoquinones destabilization of phospholipid bilayers. Biophysical Journal. 2013 ; 104 429a.[citado 2024 jul. 30 ]
    • Vancouver

      Di Vitta C, Marzorati L, Funari SS. Thionaphthoquinones destabilization of phospholipid bilayers. Biophysical Journal. 2013 ; 104 429a.[citado 2024 jul. 30 ]
  • Source: Dyes and Pigments. Unidade: IQ

    Subjects: LÍQUIDOS IÔNICOS, SOLVENTE

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      LOFFREDO, Carina et al. β-carotene: a green, inexpensive, and convenient solvatochromic probe for the determination of solvent polarizability. Dyes and Pigments, v. 96, n. 1, p. 16-24, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2012.07.017. Acesso em: 30 jul. 2024.
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      Loffredo, C., Pires, P. A. R., Imran, M., & El Seoud, O. A. (2013). β-carotene: a green, inexpensive, and convenient solvatochromic probe for the determination of solvent polarizability. Dyes and Pigments, 96( 1), 16-24. doi:10.1016/j.dyepig.2012.07.017
    • NLM

      Loffredo C, Pires PAR, Imran M, El Seoud OA. β-carotene: a green, inexpensive, and convenient solvatochromic probe for the determination of solvent polarizability [Internet]. Dyes and Pigments. 2013 ; 96( 1): 16-24.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1016/j.dyepig.2012.07.017
    • Vancouver

      Loffredo C, Pires PAR, Imran M, El Seoud OA. β-carotene: a green, inexpensive, and convenient solvatochromic probe for the determination of solvent polarizability [Internet]. Dyes and Pigments. 2013 ; 96( 1): 16-24.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1016/j.dyepig.2012.07.017
  • Source: Carbohydrate Polymers. Unidade: IQ

    Subjects: CELULOSE, SOLVENTE

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      FIDALE, Ludmila de Carvalho e HEINZE, Thomas e EL SEOUD, Omar A. Perichromism: a powerful tool for probing the properties of cellulose and its derivatives. Carbohydrate Polymers, v. 93, n. 1, p. 129-134, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.carbpol.2012.06.061. Acesso em: 30 jul. 2024.
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      Fidale, L. de C., Heinze, T., & El Seoud, O. A. (2013). Perichromism: a powerful tool for probing the properties of cellulose and its derivatives. Carbohydrate Polymers, 93( 1), 129-134. doi:10.1016/j.carbpol.2012.06.061
    • NLM

      Fidale L de C, Heinze T, El Seoud OA. Perichromism: a powerful tool for probing the properties of cellulose and its derivatives [Internet]. Carbohydrate Polymers. 2013 ; 93( 1): 129-134.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1016/j.carbpol.2012.06.061
    • Vancouver

      Fidale L de C, Heinze T, El Seoud OA. Perichromism: a powerful tool for probing the properties of cellulose and its derivatives [Internet]. Carbohydrate Polymers. 2013 ; 93( 1): 129-134.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1016/j.carbpol.2012.06.061
  • Source: Journal of Sulfur Chemistry. Unidade: IQ

    Subjects: ESPECTROSCOPIA INFRAVERMELHA, RAIOS X

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      OLIVATO, Paulo Roberto et al. Conformational preferences for some 3,3-bis[(4′-substituted phenylsulfanyl)]1-methyl-2-piperidinones through spectroscopic and theoretical studies. Journal of Sulfur Chemistry, v. 34, n. 6, p. 617-626, 2013Tradução . . Disponível em: https://doi.org/10.1080/17415993.2013.771359. Acesso em: 30 jul. 2024.
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      Olivato, P. R., Junior, C. R. C., Contieri, B., Santos, J. M. M., & Zukerman Schpector, J. (2013). Conformational preferences for some 3,3-bis[(4′-substituted phenylsulfanyl)]1-methyl-2-piperidinones through spectroscopic and theoretical studies. Journal of Sulfur Chemistry, 34( 6), 617-626. doi:10.1080/17415993.2013.771359
    • NLM

      Olivato PR, Junior CRC, Contieri B, Santos JMM, Zukerman Schpector J. Conformational preferences for some 3,3-bis[(4′-substituted phenylsulfanyl)]1-methyl-2-piperidinones through spectroscopic and theoretical studies [Internet]. Journal of Sulfur Chemistry. 2013 ; 34( 6): 617-626.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1080/17415993.2013.771359
    • Vancouver

      Olivato PR, Junior CRC, Contieri B, Santos JMM, Zukerman Schpector J. Conformational preferences for some 3,3-bis[(4′-substituted phenylsulfanyl)]1-methyl-2-piperidinones through spectroscopic and theoretical studies [Internet]. Journal of Sulfur Chemistry. 2013 ; 34( 6): 617-626.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1080/17415993.2013.771359
  • Source: Dalton Transactions. Unidades: IF, IQ

    Subjects: ALBUMINAS, COBRE

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      SILVEIRA, Vivian Chagas da et al. Peculiar reactivity of a di-imine copper(II) complex regarding its binding to albumin protein. Dalton Transactions, v. 42, n. 18, p. 6386-6396, 2013Tradução . . Disponível em: https://doi.org/10.1039/c3dt00108c. Acesso em: 30 jul. 2024.
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      Silveira, V. C. da, Abbott, M. P., Cavicchioli, M., Gonçalves, M. B., Petrilli, H. M., Rezende, L. de, et al. (2013). Peculiar reactivity of a di-imine copper(II) complex regarding its binding to albumin protein. Dalton Transactions, 42( 18), 6386-6396. doi:10.1039/c3dt00108c
    • NLM

      Silveira VC da, Abbott MP, Cavicchioli M, Gonçalves MB, Petrilli HM, Rezende L de, Amaral AT do, Fonseca DEP, Caramori GF, Ferreira AM da C. Peculiar reactivity of a di-imine copper(II) complex regarding its binding to albumin protein [Internet]. Dalton Transactions. 2013 ; 42( 18): 6386-6396.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1039/c3dt00108c
    • Vancouver

      Silveira VC da, Abbott MP, Cavicchioli M, Gonçalves MB, Petrilli HM, Rezende L de, Amaral AT do, Fonseca DEP, Caramori GF, Ferreira AM da C. Peculiar reactivity of a di-imine copper(II) complex regarding its binding to albumin protein [Internet]. Dalton Transactions. 2013 ; 42( 18): 6386-6396.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1039/c3dt00108c
  • Source: Carbohydrate Polymers. Unidade: IQ

    Subjects: COMPORTAMENTO, ÁGUA

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      BUENO, Vânia Blasques et al. Synthesis and swelling behavior of xanthan-based hydrogels. Carbohydrate Polymers, v. 92, n. 2, p. 1091-1099, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.carbpol.2012.10.062. Acesso em: 30 jul. 2024.
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      Bueno, V. B., Bentini, R., Catalani, L. H., & Petri, D. F. S. (2013). Synthesis and swelling behavior of xanthan-based hydrogels. Carbohydrate Polymers, 92( 2), 1091-1099. doi:10.1016/j.carbpol.2012.10.062
    • NLM

      Bueno VB, Bentini R, Catalani LH, Petri DFS. Synthesis and swelling behavior of xanthan-based hydrogels [Internet]. Carbohydrate Polymers. 2013 ; 92( 2): 1091-1099.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1016/j.carbpol.2012.10.062
    • Vancouver

      Bueno VB, Bentini R, Catalani LH, Petri DFS. Synthesis and swelling behavior of xanthan-based hydrogels [Internet]. Carbohydrate Polymers. 2013 ; 92( 2): 1091-1099.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1016/j.carbpol.2012.10.062
  • Source: Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. Unidade: IQ

    Subjects: ESPECTROSCOPIA INFRAVERMELHA, DIFRAÇÃO POR RAIOS X

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      VINHATO, Elisângela et al. Conformational analysis of some N,N-diethyl-2-[(4′-substituted) phenylthio] acetamides. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, v. 115, p. 738-746, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.saa.2013.06.118. Acesso em: 30 jul. 2024.
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      Vinhato, E., Olivato, P. R., Zukerman-Schpector, J., & Dal Colle, M. (2013). Conformational analysis of some N,N-diethyl-2-[(4′-substituted) phenylthio] acetamides. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 115, 738-746. doi:10.1016/j.saa.2013.06.118
    • NLM

      Vinhato E, Olivato PR, Zukerman-Schpector J, Dal Colle M. Conformational analysis of some N,N-diethyl-2-[(4′-substituted) phenylthio] acetamides [Internet]. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2013 ; 115 738-746.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1016/j.saa.2013.06.118
    • Vancouver

      Vinhato E, Olivato PR, Zukerman-Schpector J, Dal Colle M. Conformational analysis of some N,N-diethyl-2-[(4′-substituted) phenylthio] acetamides [Internet]. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 2013 ; 115 738-746.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1016/j.saa.2013.06.118
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: OXIDAÇÃO, SÍNTESE ORGÂNICA

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      AHMAD, Anees et al. Oxidative rearrangement of alkenes using in situ generated hypervalent iodine(III). Tetrahedron Letters, v. 54, n. 43, p. 5818-5820, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2013.08.012. Acesso em: 30 jul. 2024.
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      Ahmad, A., Scarassati, P., Jalalian, N., Olofsson, B., & Silva Junior, L. F. da. (2013). Oxidative rearrangement of alkenes using in situ generated hypervalent iodine(III). Tetrahedron Letters, 54( 43), 5818-5820. doi:10.1016/j.tetlet.2013.08.012
    • NLM

      Ahmad A, Scarassati P, Jalalian N, Olofsson B, Silva Junior LF da. Oxidative rearrangement of alkenes using in situ generated hypervalent iodine(III) [Internet]. Tetrahedron Letters. 2013 ; 54( 43): 5818-5820.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.012
    • Vancouver

      Ahmad A, Scarassati P, Jalalian N, Olofsson B, Silva Junior LF da. Oxidative rearrangement of alkenes using in situ generated hypervalent iodine(III) [Internet]. Tetrahedron Letters. 2013 ; 54( 43): 5818-5820.[citado 2024 jul. 30 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.012

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