Filtros : "Irmandade da Santa Casa de Misericórdia de São Paulo (ISCMSP)" "SCHREIER, SHIRLEY" "IQ" Removidos: "ABDALLA, DULCINEIA SAES PARRA" "Portugal" Limpar

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  • Source: Abstracts. Conference titles: Annual Meeting of the Brazilian Society for Biochemistry and Molecular Biology. Unidade: IQ

    Subjects: RESINAS, PEPTÍDEOS

    How to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      SOUZA, S. E. G et al. Efficiency of 4-tert-butyl-benzhydrylamine-resin (BUBHAR) for use in the Boc-chemistry peptide synthesis: an alternative solid support for the worldwide used MBHAR resin. 2017, Anais.. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular/SBBq, 2017. . Acesso em: 31 maio 2024.
    • APA

      Souza, S. E. G., Malavolta, L., Cilli, E. M., Schreier, S., Poletti, E. F., Jubilut, G. N., & Nakaie, C. R. (2017). Efficiency of 4-tert-butyl-benzhydrylamine-resin (BUBHAR) for use in the Boc-chemistry peptide synthesis: an alternative solid support for the worldwide used MBHAR resin. In Abstracts. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular/SBBq.
    • NLM

      Souza SEG, Malavolta L, Cilli EM, Schreier S, Poletti EF, Jubilut GN, Nakaie CR. Efficiency of 4-tert-butyl-benzhydrylamine-resin (BUBHAR) for use in the Boc-chemistry peptide synthesis: an alternative solid support for the worldwide used MBHAR resin. Abstracts. 2017 ;[citado 2024 maio 31 ]
    • Vancouver

      Souza SEG, Malavolta L, Cilli EM, Schreier S, Poletti EF, Jubilut GN, Nakaie CR. Efficiency of 4-tert-butyl-benzhydrylamine-resin (BUBHAR) for use in the Boc-chemistry peptide synthesis: an alternative solid support for the worldwide used MBHAR resin. Abstracts. 2017 ;[citado 2024 maio 31 ]
  • Source: Bioorganic Chemistry. Unidade: IQ

    Subjects: ANGIOTENSINAS, BRADICININA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      TEIXEIRA, Luis Gustavo de Deus et al. Paramagnetic bradykinin analogues as substrates for angiotensin I-converting enzyme: pharmacological and conformation studies. Bioorganic Chemistry, v. 69, p. 159-166, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2016.10.006. Acesso em: 31 maio 2024.
    • APA

      Teixeira, L. G. de D., Malavolta, L., Bersanetti, P. A., Schreier, S., Carmona, A. K., & Nakaie, C. R. (2016). Paramagnetic bradykinin analogues as substrates for angiotensin I-converting enzyme: pharmacological and conformation studies. Bioorganic Chemistry, 69, 159-166. doi:10.1016/j.bioorg.2016.10.006
    • NLM

      Teixeira LG de D, Malavolta L, Bersanetti PA, Schreier S, Carmona AK, Nakaie CR. Paramagnetic bradykinin analogues as substrates for angiotensin I-converting enzyme: pharmacological and conformation studies [Internet]. Bioorganic Chemistry. 2016 ; 69 159-166.[citado 2024 maio 31 ] Available from: https://doi.org/10.1016/j.bioorg.2016.10.006
    • Vancouver

      Teixeira LG de D, Malavolta L, Bersanetti PA, Schreier S, Carmona AK, Nakaie CR. Paramagnetic bradykinin analogues as substrates for angiotensin I-converting enzyme: pharmacological and conformation studies [Internet]. Bioorganic Chemistry. 2016 ; 69 159-166.[citado 2024 maio 31 ] Available from: https://doi.org/10.1016/j.bioorg.2016.10.006
  • Source: PLOS ONE. Unidade: IQ

    Subjects: ANGIOTENSINAS, PEPTÍDEOS

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      TEIXEIRA, Luis Gustavo de Deus et al. Conformational properties of seven toac-labeled angiotensin I analogues correlate with their muscle contraction activity and their ability to act as ACE substrates. PLOS ONE, v. 10, n. 8, p. 1-15 art. 0136608, 2015Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0136608. Acesso em: 31 maio 2024.
    • APA

      Teixeira, L. G. de D., Malavolta, L., Bersanetti, P. A., Schreier, S., Carmona, A. K., & Nakaie, C. R. (2015). Conformational properties of seven toac-labeled angiotensin I analogues correlate with their muscle contraction activity and their ability to act as ACE substrates. PLOS ONE, 10( 8), 1-15 art. 0136608. doi:10.1371/journal.pone.0136608
    • NLM

      Teixeira LG de D, Malavolta L, Bersanetti PA, Schreier S, Carmona AK, Nakaie CR. Conformational properties of seven toac-labeled angiotensin I analogues correlate with their muscle contraction activity and their ability to act as ACE substrates [Internet]. PLOS ONE. 2015 ; 10( 8): 1-15 art. 0136608.[citado 2024 maio 31 ] Available from: https://doi.org/10.1371/journal.pone.0136608
    • Vancouver

      Teixeira LG de D, Malavolta L, Bersanetti PA, Schreier S, Carmona AK, Nakaie CR. Conformational properties of seven toac-labeled angiotensin I analogues correlate with their muscle contraction activity and their ability to act as ACE substrates [Internet]. PLOS ONE. 2015 ; 10( 8): 1-15 art. 0136608.[citado 2024 maio 31 ] Available from: https://doi.org/10.1371/journal.pone.0136608
  • Source: Protein & Peptide Letters. Unidade: IQ

    Subjects: RESINAS, PEPTÍDEOS (SÍNTESE), BIOQUÍMICA

    Acesso à fonteDOIHow to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      SOUZA, Sinval E. G et al. Novel copoly(styrene-divinylbenzene)-resins with different phenylmethylamine groups for use in peptide synthesis method. Protein & Peptide Letters, v. 22, n. 5, p. 392-401, 2015Tradução . . Disponível em: https://doi.org/10.2174/0929866522666150206170329. Acesso em: 31 maio 2024.
    • APA

      Souza, S. E. G., Malavolta, L., Cilli, E. M., Schreier, S., Jubilut, G. N., & Nakaie, C. R. (2015). Novel copoly(styrene-divinylbenzene)-resins with different phenylmethylamine groups for use in peptide synthesis method. Protein & Peptide Letters, 22( 5), 392-401. doi:10.2174/0929866522666150206170329
    • NLM

      Souza SEG, Malavolta L, Cilli EM, Schreier S, Jubilut GN, Nakaie CR. Novel copoly(styrene-divinylbenzene)-resins with different phenylmethylamine groups for use in peptide synthesis method [Internet]. Protein & Peptide Letters. 2015 ; 22( 5): 392-401.[citado 2024 maio 31 ] Available from: https://doi.org/10.2174/0929866522666150206170329
    • Vancouver

      Souza SEG, Malavolta L, Cilli EM, Schreier S, Jubilut GN, Nakaie CR. Novel copoly(styrene-divinylbenzene)-resins with different phenylmethylamine groups for use in peptide synthesis method [Internet]. Protein & Peptide Letters. 2015 ; 22( 5): 392-401.[citado 2024 maio 31 ] Available from: https://doi.org/10.2174/0929866522666150206170329

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