Filtros : "Indexado no Chemical Abstracts" "TOXICOLOGIA" Removidos: "Imunologia" "SEM" "VPS" "MARANHAO, RAUL CAVALCANTE" Limpar

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  • Source: Dalton Transactions. Unidades: IQSC, FCFRP, FMRP

    Assunto: TOXICOLOGIA

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      MAIA, P. I. S et al. Organometallic gold(III) complexes with hybrid SNS-donating thiosemicarbazone ligands: cytotoxicity and anti-Trypanosoma cruzi activity. Dalton Transactions, v. 46, p. 2559-2571, 2017Tradução . . Disponível em: https://doi.org/10.1039/C6DT04307K. Acesso em: 24 dez. 2024.
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      Maia, P. I. S., Carneiro, Z. A., Lopes, C. D., Oliveira, C. G., Silva, J. S. da, Albuquerque, S. de, et al. (2017). Organometallic gold(III) complexes with hybrid SNS-donating thiosemicarbazone ligands: cytotoxicity and anti-Trypanosoma cruzi activity. Dalton Transactions, 46, 2559-2571. doi:10.1039/C6DT04307K
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      Maia PIS, Carneiro ZA, Lopes CD, Oliveira CG, Silva JS da, Albuquerque S de, Hagenbach A, Gust R, Deflon VM, Abram U. Organometallic gold(III) complexes with hybrid SNS-donating thiosemicarbazone ligands: cytotoxicity and anti-Trypanosoma cruzi activity [Internet]. Dalton Transactions. 2017 ; 46 2559-2571.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1039/C6DT04307K
    • Vancouver

      Maia PIS, Carneiro ZA, Lopes CD, Oliveira CG, Silva JS da, Albuquerque S de, Hagenbach A, Gust R, Deflon VM, Abram U. Organometallic gold(III) complexes with hybrid SNS-donating thiosemicarbazone ligands: cytotoxicity and anti-Trypanosoma cruzi activity [Internet]. Dalton Transactions. 2017 ; 46 2559-2571.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1039/C6DT04307K
  • Source: Biological and Pharmaceutical Bulletin. Unidade: FCFRP

    Subjects: ANTIOXIDANTES, PLANTAS MEDICINAIS, TOXICOLOGIA, GENÉTICA, SOLANACEAE

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      DAMASCENO, Jaqueline Lopes et al. Antigenotoxic and Antioxidant Properties of Solanum cernuum and Its Alkaloid, Cernumidine. Biological and Pharmaceutical Bulletin, v. 39, n. 6, p. 920-926, 2016Tradução . . Disponível em: https://doi.org/10.1248/bpb.b15-00638. Acesso em: 24 dez. 2024.
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      Damasceno, J. L., Oliveira, P. F. de, Miranda, M. A., Lima, M., Bastos, J. K., & Tavares, D. C. (2016). Antigenotoxic and Antioxidant Properties of Solanum cernuum and Its Alkaloid, Cernumidine. Biological and Pharmaceutical Bulletin, 39( 6), 920-926. doi:10.1248/bpb.b15-00638
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      Damasceno JL, Oliveira PF de, Miranda MA, Lima M, Bastos JK, Tavares DC. Antigenotoxic and Antioxidant Properties of Solanum cernuum and Its Alkaloid, Cernumidine [Internet]. Biological and Pharmaceutical Bulletin. 2016 ; 39( 6): 920-926.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1248/bpb.b15-00638
    • Vancouver

      Damasceno JL, Oliveira PF de, Miranda MA, Lima M, Bastos JK, Tavares DC. Antigenotoxic and Antioxidant Properties of Solanum cernuum and Its Alkaloid, Cernumidine [Internet]. Biological and Pharmaceutical Bulletin. 2016 ; 39( 6): 920-926.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1248/bpb.b15-00638
  • Source: Food and Chemical Toxicology. Unidade: FMVZ

    Subjects: TOXICOLOGIA, CETONA, DERMATOLOGIA, COSMÉTICOS

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      BELSITO, D et al. A toxicological and dermatological assessment of alkyl cyclic ketones when used as fragrance ingredients. Food and Chemical Toxicology, v. 62, p. S1-S44, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2013.09.033. Acesso em: 24 dez. 2024.
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      Belsito, D., Bickers, D., Bruze, M., Calow, P., Dagli, M. L. Z., Fryer, A. D., et al. (2013). A toxicological and dermatological assessment of alkyl cyclic ketones when used as fragrance ingredients. Food and Chemical Toxicology, 62, S1-S44. doi:10.1016/j.fct.2013.09.033
    • NLM

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of alkyl cyclic ketones when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2013 ; 62 S1-S44.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.fct.2013.09.033
    • Vancouver

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of alkyl cyclic ketones when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2013 ; 62 S1-S44.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.fct.2013.09.033
  • Source: Chemosphere. Unidades: EESC, IQSC

    Subjects: TOXICOLOGIA, INSETICIDAS

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      RIGOBELLO, Eliane Sloboda et al. Removal of diclofenac by conventional drinking water treatment processes and granular activated carbon filtration. Chemosphere, v. 92, p. 184-191, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.chemosphere.2013.03.010. Acesso em: 24 dez. 2024.
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      Rigobello, E. S., Dantas, A. D. B., Di Bernardo, L., & Vieira, E. M. (2013). Removal of diclofenac by conventional drinking water treatment processes and granular activated carbon filtration. Chemosphere, 92, 184-191. doi:10.1016/j.chemosphere.2013.03.010
    • NLM

      Rigobello ES, Dantas ADB, Di Bernardo L, Vieira EM. Removal of diclofenac by conventional drinking water treatment processes and granular activated carbon filtration [Internet]. Chemosphere. 2013 ; 92 184-191.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.chemosphere.2013.03.010
    • Vancouver

      Rigobello ES, Dantas ADB, Di Bernardo L, Vieira EM. Removal of diclofenac by conventional drinking water treatment processes and granular activated carbon filtration [Internet]. Chemosphere. 2013 ; 92 184-191.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.chemosphere.2013.03.010
  • Source: Toxicology. Unidades: FZEA, FMVZ

    Subjects: IMUNOTOXINAS, TOXICIDADE EM ANIMAL, TOXICOLOGIA

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      LATORRE, Andréia Oliveira et al. Ptaquiloside reduces NK cell activities by enhancing metallothionein expression, which is prevented by selenium. Toxicology, v. 304, p. 100-108, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tox.2012.12.010. Acesso em: 24 dez. 2024.
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      Latorre, A. O., Caniceiro, B. D., Fukumasu, H., Gardner, D. R., Lopes, F. M., Wysochi Jr, H. L., et al. (2013). Ptaquiloside reduces NK cell activities by enhancing metallothionein expression, which is prevented by selenium. Toxicology, 304, 100-108. doi:10.1016/j.tox.2012.12.010
    • NLM

      Latorre AO, Caniceiro BD, Fukumasu H, Gardner DR, Lopes FM, Wysochi Jr HL, Silva TC, Haraguchi M, Bressan FF, Górniak SL. Ptaquiloside reduces NK cell activities by enhancing metallothionein expression, which is prevented by selenium [Internet]. Toxicology. 2013 ; 304 100-108.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.tox.2012.12.010
    • Vancouver

      Latorre AO, Caniceiro BD, Fukumasu H, Gardner DR, Lopes FM, Wysochi Jr HL, Silva TC, Haraguchi M, Bressan FF, Górniak SL. Ptaquiloside reduces NK cell activities by enhancing metallothionein expression, which is prevented by selenium [Internet]. Toxicology. 2013 ; 304 100-108.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.tox.2012.12.010
  • Source: Toxicon. Unidade: FMVZ

    Subjects: TOXICOLOGIA, PLANTAS TÓXICAS, TOXICIDADE EM ANIMAL

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      CUNHA, Luciana Castro da et al. Isolation and characterization of sodium 2-fluoroacetate from Mascagnia rigida using chromatography and infrared spectroscopy. Toxicon, v. 60, n. 3, p. 329-332, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.toxicon.2012.04.346. Acesso em: 24 dez. 2024.
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      Cunha, L. C. da, Pípole, F., Carvalho, L. R. de, Lago, J. H. G., & Górniak, S. L. (2012). Isolation and characterization of sodium 2-fluoroacetate from Mascagnia rigida using chromatography and infrared spectroscopy. Toxicon, 60( 3), 329-332. doi:10.1016/j.toxicon.2012.04.346
    • NLM

      Cunha LC da, Pípole F, Carvalho LR de, Lago JHG, Górniak SL. Isolation and characterization of sodium 2-fluoroacetate from Mascagnia rigida using chromatography and infrared spectroscopy [Internet]. Toxicon. 2012 ; 60( 3): 329-332.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.toxicon.2012.04.346
    • Vancouver

      Cunha LC da, Pípole F, Carvalho LR de, Lago JHG, Górniak SL. Isolation and characterization of sodium 2-fluoroacetate from Mascagnia rigida using chromatography and infrared spectroscopy [Internet]. Toxicon. 2012 ; 60( 3): 329-332.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.toxicon.2012.04.346
  • Source: Chemosphere. Unidade: IQSC

    Subjects: TOXICOLOGIA, INSETICIDAS

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      ALVES, S. A. et al. A comparative study of the electrochemical oxidation of the herbicide tebuthiuron using boron-doped diamond electrode. Chemosphere, v. 88, n. 2, p. 155-160, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.chemosphere.2012.02.042. Acesso em: 24 dez. 2024.
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      Alves, S. A., Ferreira, T. C. R., Sabatini, N. S., Trientini, A. C. A., Migliorini, F. L., Baldan, M. R., et al. (2012). A comparative study of the electrochemical oxidation of the herbicide tebuthiuron using boron-doped diamond electrode. Chemosphere, 88( 2), 155-160. doi:10.1016/j.chemosphere.2012.02.042
    • NLM

      Alves SA, Ferreira TCR, Sabatini NS, Trientini ACA, Migliorini FL, Baldan MR, Ferreira NG, Lanza MR de V. A comparative study of the electrochemical oxidation of the herbicide tebuthiuron using boron-doped diamond electrode [Internet]. Chemosphere. 2012 ; 88( 2): 155-160.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.chemosphere.2012.02.042
    • Vancouver

      Alves SA, Ferreira TCR, Sabatini NS, Trientini ACA, Migliorini FL, Baldan MR, Ferreira NG, Lanza MR de V. A comparative study of the electrochemical oxidation of the herbicide tebuthiuron using boron-doped diamond electrode [Internet]. Chemosphere. 2012 ; 88( 2): 155-160.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.chemosphere.2012.02.042
  • Source: Food and Chemical Toxicology. Unidade: FMVZ

    Subjects: TOXICOLOGIA, AROMATIZANTES, DERMATOLOGIA

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      BELSITO, D et al. A toxicologic and dermatologic assessment of cyclopentanones and cyclopentenones when used as fragrance ingredients. Food and Chemical Toxicology, v. 50, p. S517-S556, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2012.04.019. Acesso em: 24 dez. 2024.
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      Belsito, D., Bickers, D., Bruze, M., Calow, P., Dagli, M. L. Z., Dekant, W., et al. (2012). A toxicologic and dermatologic assessment of cyclopentanones and cyclopentenones when used as fragrance ingredients. Food and Chemical Toxicology, 50, S517-S556. doi:10.1016/j.fct.2012.04.019
    • NLM

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Dekant W, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicologic and dermatologic assessment of cyclopentanones and cyclopentenones when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2012 ; 50 S517-S556.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.fct.2012.04.019
    • Vancouver

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Dekant W, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicologic and dermatologic assessment of cyclopentanones and cyclopentenones when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2012 ; 50 S517-S556.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.fct.2012.04.019
  • Source: Chemosphere. Unidades: IQSC, EESC

    Subjects: TOXICOLOGIA, INSETICIDAS

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      NOVELLI, Andrea et al. Lethal effects of abamectin on the aquatic organisms Daphnia similis, Chironomus xanthus and Danio rerio. Chemosphere, v. 86, n. 1, p. 36-40, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.chemosphere.2011.08.047. Acesso em: 24 dez. 2024.
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      Novelli, A., Vieira, B. H., Cordeiro, D., Cappelini, L. T. D., Vieira, E. M., & Espíndola, E. L. G. (2012). Lethal effects of abamectin on the aquatic organisms Daphnia similis, Chironomus xanthus and Danio rerio. Chemosphere, 86( 1), 36-40. doi:10.1016/j.chemosphere.2011.08.047
    • NLM

      Novelli A, Vieira BH, Cordeiro D, Cappelini LTD, Vieira EM, Espíndola ELG. Lethal effects of abamectin on the aquatic organisms Daphnia similis, Chironomus xanthus and Danio rerio [Internet]. Chemosphere. 2012 ; 86( 1): 36-40.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.chemosphere.2011.08.047
    • Vancouver

      Novelli A, Vieira BH, Cordeiro D, Cappelini LTD, Vieira EM, Espíndola ELG. Lethal effects of abamectin on the aquatic organisms Daphnia similis, Chironomus xanthus and Danio rerio [Internet]. Chemosphere. 2012 ; 86( 1): 36-40.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.chemosphere.2011.08.047
  • Source: Food and Chemical Toxicology. Unidade: FMVZ

    Assunto: TOXICOLOGIA

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      BELSITO, D et al. A toxicological and dermatological assessment of aryl alkyl alcohol simple acid ester derivatives when used as fragrance ingredients. Food and Chemical Toxicology, v. 50, p. S269-S313, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2012.02.091. Acesso em: 24 dez. 2024.
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      Belsito, D., Bickers, D., Bruze, M., Calow, P., Dagli, M. L. Z., Fryer, A. D., et al. (2012). A toxicological and dermatological assessment of aryl alkyl alcohol simple acid ester derivatives when used as fragrance ingredients. Food and Chemical Toxicology, 50, S269-S313. doi:10.1016/j.fct.2012.02.091
    • NLM

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of aryl alkyl alcohol simple acid ester derivatives when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2012 ; 50 S269-S313.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.fct.2012.02.091
    • Vancouver

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of aryl alkyl alcohol simple acid ester derivatives when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2012 ; 50 S269-S313.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.fct.2012.02.091
  • Source: Food and Chemical Toxicology. Unidade: FMVZ

    Subjects: QUÍMICA ORGÂNICA, DERMATOLOGIA, TOXICOLOGIA

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      BELSITO, D et al. A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients. Food and Chemical Toxicology, v. 50, p. S52-S99, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2011.10.042. Acesso em: 24 dez. 2024.
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      Belsito, D., Bickers, D., Bruze, M., Calow, P., Dagli, M. L. Z., Fryer, A. D., et al. (2012). A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients. Food and Chemical Toxicology, 50, S52-S99. doi:10.1016/j.fct.2011.10.042
    • NLM

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2012 ; 50 S52-S99.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.fct.2011.10.042
    • Vancouver

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2012 ; 50 S52-S99.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.fct.2011.10.042
  • Source: Mutation Research/Genetic Toxicology and Environmental Mutagenesis. Unidade: FCFRP

    Subjects: ANTIOXIDANTES, FLAVONÓIDES, TOXICOLOGIA, MERCÚRIO (ELEMENTO QUÍMICO), ESTRESSE OXIDATIVO

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      BARCELOS, Gustavo Rafael Mazzaron et al. Quercetin protects human-derived liver cells against mercury-induced DNA-damage and alterations of the redox status. Mutation Research/Genetic Toxicology and Environmental Mutagenesis, v. 726, n. 2, p. 109-115, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.mrgentox.2011.05.011. Acesso em: 24 dez. 2024.
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      Barcelos, G. R. M., Angeli, J. P. F., Serpeloni, J. M., Grotto, D., Rocha, B. A., Bastos, J. K., et al. (2011). Quercetin protects human-derived liver cells against mercury-induced DNA-damage and alterations of the redox status. Mutation Research/Genetic Toxicology and Environmental Mutagenesis, 726( 2), 109-115. doi:10.1016/j.mrgentox.2011.05.011
    • NLM

      Barcelos GRM, Angeli JPF, Serpeloni JM, Grotto D, Rocha BA, Bastos JK, Knasmuller S, Barbosa Júnior F. Quercetin protects human-derived liver cells against mercury-induced DNA-damage and alterations of the redox status [Internet]. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 2011 ; 726( 2): 109-115.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.mrgentox.2011.05.011
    • Vancouver

      Barcelos GRM, Angeli JPF, Serpeloni JM, Grotto D, Rocha BA, Bastos JK, Knasmuller S, Barbosa Júnior F. Quercetin protects human-derived liver cells against mercury-induced DNA-damage and alterations of the redox status [Internet]. Mutation Research/Genetic Toxicology and Environmental Mutagenesis. 2011 ; 726( 2): 109-115.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.mrgentox.2011.05.011
  • Source: Food and Chemical Toxicology. Unidade: FMVZ

    Subjects: AGENTE TÓXICO, TOXICOLOGIA, DERMATOLOGIA

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      BELSITO, D et al. A toxicological and dermatological assessment of macrocyclic ketones when used as fragrance ingredients. Food and Chemical Toxicology, v. 49, p. S126-S141, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2011.07.040. Acesso em: 24 dez. 2024.
    • APA

      Belsito, D., Bickers, D., Bruze, M., Calow, P., Dagli, M. L. Z., Fryer, A. D., et al. (2011). A toxicological and dermatological assessment of macrocyclic ketones when used as fragrance ingredients. Food and Chemical Toxicology, 49, S126-S141. doi:10.1016/j.fct.2011.07.040
    • NLM

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of macrocyclic ketones when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2011 ; 49 S126-S141.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.fct.2011.07.040
    • Vancouver

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of macrocyclic ketones when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2011 ; 49 S126-S141.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.fct.2011.07.040
  • Source: Food and Chemical Toxicology. Unidade: FMVZ

    Subjects: AGENTE TÓXICO, TOXICOLOGIA, DERMATOLOGIA

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      BELSITO, D et al. A toxicologic and dermatologic assessment of cinnamyl phenylpropyl materials when used as fragrance ingredients. Food and Chemical Toxicology, v. 49, p. S256-S267, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2011.07.053. Acesso em: 24 dez. 2024.
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      Belsito, D., Bickers, D., Bruze, M., Calow, P., Dagli, M. L. Z., Fryer, A. D., et al. (2011). A toxicologic and dermatologic assessment of cinnamyl phenylpropyl materials when used as fragrance ingredients. Food and Chemical Toxicology, 49, S256-S267. doi:10.1016/j.fct.2011.07.053
    • NLM

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicologic and dermatologic assessment of cinnamyl phenylpropyl materials when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2011 ; 49 S256-S267.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.fct.2011.07.053
    • Vancouver

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicologic and dermatologic assessment of cinnamyl phenylpropyl materials when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2011 ; 49 S256-S267.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.fct.2011.07.053
  • Source: Food and Chemical Toxicology. Unidade: FMVZ

    Subjects: AGENTE TÓXICO, TOXICOLOGIA, DERMATOLOGIA

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      BELSITO, D et al. A toxicological and dermatological assessment of macrocyclic lactone and lactide derivatives when used as fragrance ingredients. Food and Chemical Toxicology, v. 49, p. S219-S241, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2011.07.052. Acesso em: 24 dez. 2024.
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      Belsito, D., Bickers, D., Bruze, M., Calow, P., Dagli, M. L. Z., Fryer, A. D., et al. (2011). A toxicological and dermatological assessment of macrocyclic lactone and lactide derivatives when used as fragrance ingredients. Food and Chemical Toxicology, 49, S219-S241. doi:10.1016/j.fct.2011.07.052
    • NLM

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of macrocyclic lactone and lactide derivatives when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2011 ; 49 S219-S241.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.fct.2011.07.052
    • Vancouver

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of macrocyclic lactone and lactide derivatives when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2011 ; 49 S219-S241.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.fct.2011.07.052
  • Source: Toxicology in Vitro. Unidade: FCFRP

    Subjects: ESTRESSE OXIDATIVO, MITOCÔNDRIAS, TOXICOLOGIA

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      SANTOS, Neife Aparecida Guinaim et al. Involvement of oxidative stress in the hepatotoxicity induced by aromatic antiepileptic drugs. Toxicology in Vitro, v. 22, n. 8, p. 1820-1824, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.tiv.2008.08.004. Acesso em: 24 dez. 2024.
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      Santos, N. A. G., Medina, W. S. G., Martins, N. M., Carvalho Rodrigues, M. A., Curti, C., & Santos, A. C. dos. (2008). Involvement of oxidative stress in the hepatotoxicity induced by aromatic antiepileptic drugs. Toxicology in Vitro, 22( 8), 1820-1824. doi:10.1016/j.tiv.2008.08.004
    • NLM

      Santos NAG, Medina WSG, Martins NM, Carvalho Rodrigues MA, Curti C, Santos AC dos. Involvement of oxidative stress in the hepatotoxicity induced by aromatic antiepileptic drugs [Internet]. Toxicology in Vitro. 2008 ; 22( 8): 1820-1824.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.tiv.2008.08.004
    • Vancouver

      Santos NAG, Medina WSG, Martins NM, Carvalho Rodrigues MA, Curti C, Santos AC dos. Involvement of oxidative stress in the hepatotoxicity induced by aromatic antiepileptic drugs [Internet]. Toxicology in Vitro. 2008 ; 22( 8): 1820-1824.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.tiv.2008.08.004
  • Source: Rapid Communications in Mass Spectrometry. Unidades: FCFRP, FCF

    Subjects: TOXICOLOGIA, ESPECTROMETRIA DE MASSAS

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      DÖRR, Felipe Augusto et al. Comparative analysis of the gas-phase reactions of cylindrospermopsin and the difference in the alkali metal cation mobility. Rapid Communications in Mass Spectrometry, v. 22, p. 2015-2020, 2008Tradução . . Disponível em: https://doi.org/10.1002/rcm.3567. Acesso em: 24 dez. 2024.
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      Dörr, F. A., Tomaz, J. C., Lopes, N. P., & Pinto, E. (2008). Comparative analysis of the gas-phase reactions of cylindrospermopsin and the difference in the alkali metal cation mobility. Rapid Communications in Mass Spectrometry, 22, 2015-2020. doi:10.1002/rcm.3567
    • NLM

      Dörr FA, Tomaz JC, Lopes NP, Pinto E. Comparative analysis of the gas-phase reactions of cylindrospermopsin and the difference in the alkali metal cation mobility [Internet]. Rapid Communications in Mass Spectrometry. 2008 ; 22 2015-2020.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1002/rcm.3567
    • Vancouver

      Dörr FA, Tomaz JC, Lopes NP, Pinto E. Comparative analysis of the gas-phase reactions of cylindrospermopsin and the difference in the alkali metal cation mobility [Internet]. Rapid Communications in Mass Spectrometry. 2008 ; 22 2015-2020.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1002/rcm.3567
  • Source: Toxicon. Unidade: FMRP

    Subjects: TOXICOLOGIA, CITOTOXINAS, VENENOS

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      HAYASHI, Mirian A. F. et al. Cytotoxic effects of crotamine are mediated through lysosomal membrane permeabilization. Toxicon, v. 52, n. 3, p. 508-517, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.toxicon.2008.06.029. Acesso em: 24 dez. 2024.
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      Hayashi, M. A. F., Nascimento, F. D., Kerkis, A., Oliveira, V., Oliveira, E. B. de, Pereira, A., et al. (2008). Cytotoxic effects of crotamine are mediated through lysosomal membrane permeabilization. Toxicon, 52( 3), 508-517. doi:10.1016/j.toxicon.2008.06.029
    • NLM

      Hayashi MAF, Nascimento FD, Kerkis A, Oliveira V, Oliveira EB de, Pereira A, Rádis-Baptista G, Nader HB, Yamane T, Kerkis I, Tersariol ILS. Cytotoxic effects of crotamine are mediated through lysosomal membrane permeabilization [Internet]. Toxicon. 2008 ; 52( 3): 508-517.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.toxicon.2008.06.029
    • Vancouver

      Hayashi MAF, Nascimento FD, Kerkis A, Oliveira V, Oliveira EB de, Pereira A, Rádis-Baptista G, Nader HB, Yamane T, Kerkis I, Tersariol ILS. Cytotoxic effects of crotamine are mediated through lysosomal membrane permeabilization [Internet]. Toxicon. 2008 ; 52( 3): 508-517.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.toxicon.2008.06.029
  • Source: Journal of Hazardous Materials. Unidades: EESC, FFCLRP

    Subjects: ÁGUAS RESIDUÁRIAS, TOXICOLOGIA, ELETROQUÍMICA

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      COSTA, Carla Regina et al. Electrochemical treatment of tannery wastewater using DSA electrodes. Journal of Hazardous Materials, v. 153, n. 1-2, p. 616-627, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.jhazmat.2007.09.005. Acesso em: 24 dez. 2024.
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      Costa, C. R., Botta, C. M. R., Espíndola, E. L. G., & Olivi, P. (2008). Electrochemical treatment of tannery wastewater using DSA electrodes. Journal of Hazardous Materials, 153( 1-2), 616-627. doi:10.1016/j.jhazmat.2007.09.005
    • NLM

      Costa CR, Botta CMR, Espíndola ELG, Olivi P. Electrochemical treatment of tannery wastewater using DSA electrodes [Internet]. Journal of Hazardous Materials. 2008 ; 153( 1-2): 616-627.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.jhazmat.2007.09.005
    • Vancouver

      Costa CR, Botta CMR, Espíndola ELG, Olivi P. Electrochemical treatment of tannery wastewater using DSA electrodes [Internet]. Journal of Hazardous Materials. 2008 ; 153( 1-2): 616-627.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.jhazmat.2007.09.005
  • Source: Talanta. Unidade: FCFRP

    Subjects: PLASMA, ESPECTROMETRIA DE MASSAS, TOXICOLOGIA

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      BATISTA, Bruno L. et al. Simultaneous determination of Cd, Cu, Mn, Ni and Zn in nail samples by inductively coupled plasma mass spectrometry (ICP-MS) after tetramethylammonium hydroxide solubilization at room temperature: comparison with ETAAS. Talanta, v. 76, n. 3, p. 575-579, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.talanta.2008.03.046. Acesso em: 24 dez. 2024.
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      Batista, B. L., Rodrigues, J. L., Nunes, J. A., Tormen, L., Curtius, A. J., & Barbosa Júnior, F. (2008). Simultaneous determination of Cd, Cu, Mn, Ni and Zn in nail samples by inductively coupled plasma mass spectrometry (ICP-MS) after tetramethylammonium hydroxide solubilization at room temperature: comparison with ETAAS. Talanta, 76( 3), 575-579. doi:10.1016/j.talanta.2008.03.046
    • NLM

      Batista BL, Rodrigues JL, Nunes JA, Tormen L, Curtius AJ, Barbosa Júnior F. Simultaneous determination of Cd, Cu, Mn, Ni and Zn in nail samples by inductively coupled plasma mass spectrometry (ICP-MS) after tetramethylammonium hydroxide solubilization at room temperature: comparison with ETAAS [Internet]. Talanta. 2008 ; 76( 3): 575-579.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.talanta.2008.03.046
    • Vancouver

      Batista BL, Rodrigues JL, Nunes JA, Tormen L, Curtius AJ, Barbosa Júnior F. Simultaneous determination of Cd, Cu, Mn, Ni and Zn in nail samples by inductively coupled plasma mass spectrometry (ICP-MS) after tetramethylammonium hydroxide solubilization at room temperature: comparison with ETAAS [Internet]. Talanta. 2008 ; 76( 3): 575-579.[citado 2024 dez. 24 ] Available from: https://doi.org/10.1016/j.talanta.2008.03.046

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