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  • Source: Biochemistry and Cell Biology. Unidades: EACH, ICB

    Subjects: BIOLOGIA MOLECULAR, BIOLOGIA CELULAR, AMINOÁCIDOS, APOPTOSE

    Acesso à fonteDOIHow to cite
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    • ABNT

      ALVES, Juliano et al. Modulation of procaspase-7 self-activation by pest amino acid residues of the n-terminal prodomain and intersubunit linker. Biochemistry and Cell Biology, v. 95, n. 6, p. 634-643, 2017Tradução . . Disponível em: https://doi.org/10.1139/bcb-2016-0220. Acesso em: 10 nov. 2024.
    • APA

      Alves, J., Garay-Malpartida, H. M., Occhiucci, J. M., & Belizario, J. E. (2017). Modulation of procaspase-7 self-activation by pest amino acid residues of the n-terminal prodomain and intersubunit linker. Biochemistry and Cell Biology, 95( 6), 634-643. doi:10.1139/bcb-2016-0220
    • NLM

      Alves J, Garay-Malpartida HM, Occhiucci JM, Belizario JE. Modulation of procaspase-7 self-activation by pest amino acid residues of the n-terminal prodomain and intersubunit linker [Internet]. Biochemistry and Cell Biology. 2017 ; 95( 6): 634-643.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1139/bcb-2016-0220
    • Vancouver

      Alves J, Garay-Malpartida HM, Occhiucci JM, Belizario JE. Modulation of procaspase-7 self-activation by pest amino acid residues of the n-terminal prodomain and intersubunit linker [Internet]. Biochemistry and Cell Biology. 2017 ; 95( 6): 634-643.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1139/bcb-2016-0220
  • Source: Genome Announcements. Unidades: FCF, ICB

    Subjects: STAPHYLOCOCCUS, GENOMAS

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    • ABNT

      ALMEIDA, Lara Mendes de et al. Complete genome sequence of linezolid-susceptible Staphylococcus haemolyticus Sh29/312/L2, a clonal derivative of a linezolid-resistant clinical strain. Genome Announcements. Ottawa: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Disponível em: https://doi.org/10.1128/genomeA.00494-15. Acesso em: 10 nov. 2024. , 2015
    • APA

      Almeida, L. M. de, Pires, C., Cerdeira, L. T., Oliveira, T. G. M. de, Mcculloch, J. A., Pérez Chaparro, P. J., et al. (2015). Complete genome sequence of linezolid-susceptible Staphylococcus haemolyticus Sh29/312/L2, a clonal derivative of a linezolid-resistant clinical strain. Genome Announcements. Ottawa: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. doi:10.1128/genomeA.00494-15
    • NLM

      Almeida LM de, Pires C, Cerdeira LT, Oliveira TGM de, Mcculloch JA, Pérez Chaparro PJ, Sacramento AG, Brito AC de, Silva JL da, Araújo MRE de, Lincopan N, Martin MJ, Gilmore MS, Mamizuka EM. Complete genome sequence of linezolid-susceptible Staphylococcus haemolyticus Sh29/312/L2, a clonal derivative of a linezolid-resistant clinical strain [Internet]. Genome Announcements. 2015 ; 3( 3): 1 art. E00494-15.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1128/genomeA.00494-15
    • Vancouver

      Almeida LM de, Pires C, Cerdeira LT, Oliveira TGM de, Mcculloch JA, Pérez Chaparro PJ, Sacramento AG, Brito AC de, Silva JL da, Araújo MRE de, Lincopan N, Martin MJ, Gilmore MS, Mamizuka EM. Complete genome sequence of linezolid-susceptible Staphylococcus haemolyticus Sh29/312/L2, a clonal derivative of a linezolid-resistant clinical strain [Internet]. Genome Announcements. 2015 ; 3( 3): 1 art. E00494-15.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1128/genomeA.00494-15
  • Source: Clinical and Experimental Obstetrics and Gynecology. Unidade: ICB

    Assunto: FARMACOLOGIA

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    • ABNT

      KULAY JR, L et al. Administration of lopinavir/ritonavir association during rat pregnancy: maternal and fetal effects. Clinical and Experimental Obstetrics and Gynecology, v. 40, n. 1, p. 151-1545, 2013Tradução . . Acesso em: 10 nov. 2024.
    • APA

      Kulay Jr, L., Hagemann, C. C., Nakamura, M. U., Simões, R. S., Carvalho, A. M., Oliveira-Filho, R. M. de, & Espiridião, S. (2013). Administration of lopinavir/ritonavir association during rat pregnancy: maternal and fetal effects. Clinical and Experimental Obstetrics and Gynecology, 40( 1), 151-1545.
    • NLM

      Kulay Jr L, Hagemann CC, Nakamura MU, Simões RS, Carvalho AM, Oliveira-Filho RM de, Espiridião S. Administration of lopinavir/ritonavir association during rat pregnancy: maternal and fetal effects. Clinical and Experimental Obstetrics and Gynecology. 2013 ; 40( 1): 151-1545.[citado 2024 nov. 10 ]
    • Vancouver

      Kulay Jr L, Hagemann CC, Nakamura MU, Simões RS, Carvalho AM, Oliveira-Filho RM de, Espiridião S. Administration of lopinavir/ritonavir association during rat pregnancy: maternal and fetal effects. Clinical and Experimental Obstetrics and Gynecology. 2013 ; 40( 1): 151-1545.[citado 2024 nov. 10 ]
  • Source: Clinical and Experimental Obstetrics and Gynecology. Unidades: ICB, HU

    Assunto: FARMACOLOGIA

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    • ABNT

      CARVALHO, L. P. Fogarolli de et al. Effects of combined zidovudine/lopinavir/ritonavir therapy during rat pregnancy: morphological aspects. Clinical and Experimental Obstetrics and Gynecology, v. 40, n. 3, p. 345-349, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.ejogrb.2006.08.004. Acesso em: 10 nov. 2024.
    • APA

      Carvalho, L. P. F. de, Simões, R. dos S., Wagner, A., Tavella Jr, J. S., Oliveira-Filho, R. M. de, Kulay Jr, L., & Nakamura, M. U. (2013). Effects of combined zidovudine/lopinavir/ritonavir therapy during rat pregnancy: morphological aspects. Clinical and Experimental Obstetrics and Gynecology, 40( 3), 345-349. doi:10.1016/j.ejogrb.2006.08.004
    • NLM

      Carvalho LPF de, Simões R dos S, Wagner A, Tavella Jr JS, Oliveira-Filho RM de, Kulay Jr L, Nakamura MU. Effects of combined zidovudine/lopinavir/ritonavir therapy during rat pregnancy: morphological aspects [Internet]. Clinical and Experimental Obstetrics and Gynecology. 2013 ; 40( 3): 345-349.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejogrb.2006.08.004
    • Vancouver

      Carvalho LPF de, Simões R dos S, Wagner A, Tavella Jr JS, Oliveira-Filho RM de, Kulay Jr L, Nakamura MU. Effects of combined zidovudine/lopinavir/ritonavir therapy during rat pregnancy: morphological aspects [Internet]. Clinical and Experimental Obstetrics and Gynecology. 2013 ; 40( 3): 345-349.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.ejogrb.2006.08.004
  • Source: Canadian Journal of Physiology and Pharmacology. Unidade: ICB

    Assunto: FISIOLOGIA

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    • ABNT

      CAMPELLO, Raquel Saldanha et al. Carbohydrate- and lipid-enriched meals acutely disrupt glycemic homeostasis by inducing transient insulin resistance in rats. Canadian Journal of Physiology and Pharmacology, v. 90, n. 5, p. 537-545, 2012Tradução . . Disponível em: https://doi.org/10.1139/Y2012-056. Acesso em: 10 nov. 2024.
    • APA

      Campello, R. S., Alves-Wagner, A. B. T., Abdulkader, F. R. de M., Mori, R. C. T., & Machado, U. F. (2012). Carbohydrate- and lipid-enriched meals acutely disrupt glycemic homeostasis by inducing transient insulin resistance in rats. Canadian Journal of Physiology and Pharmacology, 90( 5), 537-545. doi:10.1139/Y2012-056
    • NLM

      Campello RS, Alves-Wagner ABT, Abdulkader FR de M, Mori RCT, Machado UF. Carbohydrate- and lipid-enriched meals acutely disrupt glycemic homeostasis by inducing transient insulin resistance in rats [Internet]. Canadian Journal of Physiology and Pharmacology. 2012 ; 90( 5): 537-545.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1139/Y2012-056
    • Vancouver

      Campello RS, Alves-Wagner ABT, Abdulkader FR de M, Mori RCT, Machado UF. Carbohydrate- and lipid-enriched meals acutely disrupt glycemic homeostasis by inducing transient insulin resistance in rats [Internet]. Canadian Journal of Physiology and Pharmacology. 2012 ; 90( 5): 537-545.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1139/Y2012-056

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