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  • Source: Journal of Pharmacy and Pharmacology. Unidades: IQ, FCF

    Subjects: LIPOPROTEÍNAS, LEUCEMIA

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      TEIXEIRA, Raquel da Silva et al. Delivery of daunorubicin to cancer cells with decreased toxicity by association with a lipidic nanoemulsion that binds to LDL receptors. Journal of Pharmacy and Pharmacology, v. 60, n. 10, p. 1287-1295, 2008Tradução . . Disponível em: https://doi.org/10.1211/jpp/60.10.0004. Acesso em: 17 jun. 2024.
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      Teixeira, R. da S., Valduga, C. J., Benvenutti, L. A., Schreier, S., & Maranhão, R. C. (2008). Delivery of daunorubicin to cancer cells with decreased toxicity by association with a lipidic nanoemulsion that binds to LDL receptors. Journal of Pharmacy and Pharmacology, 60( 10), 1287-1295. doi:10.1211/jpp/60.10.0004
    • NLM

      Teixeira R da S, Valduga CJ, Benvenutti LA, Schreier S, Maranhão RC. Delivery of daunorubicin to cancer cells with decreased toxicity by association with a lipidic nanoemulsion that binds to LDL receptors [Internet]. Journal of Pharmacy and Pharmacology. 2008 ; 60( 10): 1287-1295.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1211/jpp/60.10.0004
    • Vancouver

      Teixeira R da S, Valduga CJ, Benvenutti LA, Schreier S, Maranhão RC. Delivery of daunorubicin to cancer cells with decreased toxicity by association with a lipidic nanoemulsion that binds to LDL receptors [Internet]. Journal of Pharmacy and Pharmacology. 2008 ; 60( 10): 1287-1295.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1211/jpp/60.10.0004
  • Source: International Journal of Peptide Research and Therapeutics. Unidade: IQ

    Subjects: PEPTÍDEOS, ANGIOTENSINA II

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      LOPES, Douglas Duarte et al. A proposed EPR approach to evaluating agonist binding site of a peptide receptor. International Journal of Peptide Research and Therapeutics, v. 14, n. 2, p. 121-126, 2008Tradução . . Acesso em: 17 jun. 2024.
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      Lopes, D. D., Poletti, E. F., Vieira, R. de F. F., Jubilut, G. N., Oliveira, L., Paiva, A. C. de M., et al. (2008). A proposed EPR approach to evaluating agonist binding site of a peptide receptor. International Journal of Peptide Research and Therapeutics, 14( 2), 121-126.
    • NLM

      Lopes DD, Poletti EF, Vieira R de FF, Jubilut GN, Oliveira L, Paiva AC de M, Schreier S, Nakaie CR. A proposed EPR approach to evaluating agonist binding site of a peptide receptor. International Journal of Peptide Research and Therapeutics. 2008 ;14( 2): 121-126.[citado 2024 jun. 17 ]
    • Vancouver

      Lopes DD, Poletti EF, Vieira R de FF, Jubilut GN, Oliveira L, Paiva AC de M, Schreier S, Nakaie CR. A proposed EPR approach to evaluating agonist binding site of a peptide receptor. International Journal of Peptide Research and Therapeutics. 2008 ;14( 2): 121-126.[citado 2024 jun. 17 ]
  • Source: Toxicon. Unidade: IQ

    Subjects: BIOQUÍMICA, TOXINAS

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      PAZOS, Fabiola et al. Structural and functional characterization of a recombinant sticholysin I (rSt I) from the sea anemone Stichodactyla helianthus. Toxicon, v. 48, n. 8, p. 1083-1094, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.toxicon.2006.09.004. Acesso em: 17 jun. 2024.
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      Pazos, F., Valle, A., Martínez, D., Ramírez, A., Calderon, L., Puppo, A., et al. (2007). Structural and functional characterization of a recombinant sticholysin I (rSt I) from the sea anemone Stichodactyla helianthus. Toxicon, 48( 8), 1083-1094. doi:10.1016/j.toxicon.2006.09.004
    • NLM

      Pazos F, Valle A, Martínez D, Ramírez A, Calderon L, Puppo A, Tejuca M, Morera V, Campos J, Fando R, Dyszy F, Schreier S, Horjales E, Alvarez C, Lanio ME, Lissi E. Structural and functional characterization of a recombinant sticholysin I (rSt I) from the sea anemone Stichodactyla helianthus [Internet]. Toxicon. 2007 ; 48( 8): 1083-1094.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/j.toxicon.2006.09.004
    • Vancouver

      Pazos F, Valle A, Martínez D, Ramírez A, Calderon L, Puppo A, Tejuca M, Morera V, Campos J, Fando R, Dyszy F, Schreier S, Horjales E, Alvarez C, Lanio ME, Lissi E. Structural and functional characterization of a recombinant sticholysin I (rSt I) from the sea anemone Stichodactyla helianthus [Internet]. Toxicon. 2007 ; 48( 8): 1083-1094.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/j.toxicon.2006.09.004
  • Source: Toxicon. Unidade: IQ

    Subjects: POLIPEPTÍDEOS, BIOQUÍMICA

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      CILLI, Eduardo Maffud et al. Correlations between differences in amino-terminal sequences and different hemolytic activity of sticholysins. Toxicon, v. 50, n. 8, p. 1201-1204, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.toxicon.2007.07.013. Acesso em: 17 jun. 2024.
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      Cilli, E. M., Pigossi, F. T., Crusca Junior, E., Ros, U., Martinez, D., Lanio, M. E., et al. (2007). Correlations between differences in amino-terminal sequences and different hemolytic activity of sticholysins. Toxicon, 50( 8), 1201-1204. doi:10.1016/j.toxicon.2007.07.013
    • NLM

      Cilli EM, Pigossi FT, Crusca Junior E, Ros U, Martinez D, Lanio ME, Alvarez C, Schreier S. Correlations between differences in amino-terminal sequences and different hemolytic activity of sticholysins [Internet]. Toxicon. 2007 ; 50( 8): 1201-1204.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/j.toxicon.2007.07.013
    • Vancouver

      Cilli EM, Pigossi FT, Crusca Junior E, Ros U, Martinez D, Lanio ME, Alvarez C, Schreier S. Correlations between differences in amino-terminal sequences and different hemolytic activity of sticholysins [Internet]. Toxicon. 2007 ; 50( 8): 1201-1204.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/j.toxicon.2007.07.013
  • Source: Toxicon. Unidade: IQ

    Subjects: FLUORESCÊNCIA, SURFACTANTES

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      LANIO, María E. et al. Sticholysins I and II interaction with cationic micelles promotes toxins' conformational changes and enhanced hemolytic activity. Toxicon, v. 50, n. 6, p. 731-739, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.toxicon.2007.06.007. Acesso em: 17 jun. 2024.
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      Lanio, M. E., Alvarez, C., Ochoa, C., Ros, U., Pazos, F., Martinez, D., et al. (2007). Sticholysins I and II interaction with cationic micelles promotes toxins' conformational changes and enhanced hemolytic activity. Toxicon, 50( 6), 731-739. doi:10.1016/j.toxicon.2007.06.007
    • NLM

      Lanio ME, Alvarez C, Ochoa C, Ros U, Pazos F, Martinez D, Tejuca M, Eugenio LM, Casallanovo F, Dyszy FH, Schreier S, Lissi E. Sticholysins I and II interaction with cationic micelles promotes toxins' conformational changes and enhanced hemolytic activity [Internet]. Toxicon. 2007 ; 50( 6): 731-739.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/j.toxicon.2007.06.007
    • Vancouver

      Lanio ME, Alvarez C, Ochoa C, Ros U, Pazos F, Martinez D, Tejuca M, Eugenio LM, Casallanovo F, Dyszy FH, Schreier S, Lissi E. Sticholysins I and II interaction with cationic micelles promotes toxins' conformational changes and enhanced hemolytic activity [Internet]. Toxicon. 2007 ; 50( 6): 731-739.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/j.toxicon.2007.06.007
  • Source: FEBS Letters. Unidade: IQ

    Subjects: ANGIOTENSINAS, PEPTÍDEOS, ENZIMAS

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      TEIXEIRA, Luis Gustavo de Deus et al. Analogues containing the paramagnetic amino acid TOAC as substrates for angiotensin I-converting enzyme. FEBS Letters, v. 581, n. 13, p. 2411-2415, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.febslet.2007.04.058. Acesso em: 17 jun. 2024.
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      Teixeira, L. G. de D., Bersanetti, P. A., Schreier, S., Carmona, A. K., & Nakaie, C. R. (2007). Analogues containing the paramagnetic amino acid TOAC as substrates for angiotensin I-converting enzyme. FEBS Letters, 581( 13), 2411-2415. doi:10.1016/j.febslet.2007.04.058
    • NLM

      Teixeira LG de D, Bersanetti PA, Schreier S, Carmona AK, Nakaie CR. Analogues containing the paramagnetic amino acid TOAC as substrates for angiotensin I-converting enzyme [Internet]. FEBS Letters. 2007 ; 581( 13): 2411-2415.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/j.febslet.2007.04.058
    • Vancouver

      Teixeira LG de D, Bersanetti PA, Schreier S, Carmona AK, Nakaie CR. Analogues containing the paramagnetic amino acid TOAC as substrates for angiotensin I-converting enzyme [Internet]. FEBS Letters. 2007 ; 581( 13): 2411-2415.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/j.febslet.2007.04.058
  • Source: Biophysical Chemistry. Unidade: IQ

    Subjects: LIPOSSOMOS, RESSONÂNCIA MAGNÉTICA NUCLEAR, ANESTESIA LOCAL

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      FRACETO, Leonardo Fernandes et al. Differential effects of uncharged aminoamide local anesthetics on phospholipid bilayers, as monitored by 'ANTPOT 1 H'-NMR measurements. Biophysical Chemistry, v. 115, n. 1, p. 11-18, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.bpc.2004.12.003. Acesso em: 17 jun. 2024.
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      Fraceto, L. F., Spisni, A., Schreier, S., & Paula, E. de. (2005). Differential effects of uncharged aminoamide local anesthetics on phospholipid bilayers, as monitored by 'ANTPOT 1 H'-NMR measurements. Biophysical Chemistry, 115( 1), 11-18. doi:10.1016/j.bpc.2004.12.003
    • NLM

      Fraceto LF, Spisni A, Schreier S, Paula E de. Differential effects of uncharged aminoamide local anesthetics on phospholipid bilayers, as monitored by 'ANTPOT 1 H'-NMR measurements [Internet]. Biophysical Chemistry. 2005 ; 115( 1): 11-18.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/j.bpc.2004.12.003
    • Vancouver

      Fraceto LF, Spisni A, Schreier S, Paula E de. Differential effects of uncharged aminoamide local anesthetics on phospholipid bilayers, as monitored by 'ANTPOT 1 H'-NMR measurements [Internet]. Biophysical Chemistry. 2005 ; 115( 1): 11-18.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/j.bpc.2004.12.003
  • Source: Biopolymers. Unidade: IQ

    Subjects: BIOQUÍMICA, ANGIOTENSINA II, RADICAIS LIVRES, SOLUÇÕES AQUOSAS

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      SCHREIER, Shirley et al. Conformational basis for the biological activity of TOAC-labeled angiotensin II and Bradykinin: Electron paramagnetic resonance, circular dichroism, and fluorescence studies. Biopolymers, v. 74, n. 5, p. 389-402, 2004Tradução . . Disponível em: https://doi.org/10.1002/bip.20092. Acesso em: 17 jun. 2024.
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      Schreier, S., Barbosa, S. R., Casallanovo, F., Vieira, R. de F. F., Cilli, E. M., Paiva, A. C. de M., & Nakaie, C. R. (2004). Conformational basis for the biological activity of TOAC-labeled angiotensin II and Bradykinin: Electron paramagnetic resonance, circular dichroism, and fluorescence studies. Biopolymers, 74( 5), 389-402. doi:10.1002/bip.20092
    • NLM

      Schreier S, Barbosa SR, Casallanovo F, Vieira R de FF, Cilli EM, Paiva AC de M, Nakaie CR. Conformational basis for the biological activity of TOAC-labeled angiotensin II and Bradykinin: Electron paramagnetic resonance, circular dichroism, and fluorescence studies [Internet]. Biopolymers. 2004 ; 74( 5): 389-402.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1002/bip.20092
    • Vancouver

      Schreier S, Barbosa SR, Casallanovo F, Vieira R de FF, Cilli EM, Paiva AC de M, Nakaie CR. Conformational basis for the biological activity of TOAC-labeled angiotensin II and Bradykinin: Electron paramagnetic resonance, circular dichroism, and fluorescence studies [Internet]. Biopolymers. 2004 ; 74( 5): 389-402.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1002/bip.20092
  • Source: Chemistry and Physics of Lipids. Unidade: IQ

    Subjects: BIOQUÍMICA, TOXINAS, RESSONÂNCIA PARAMAGNÉTICA

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      ALVAREZ, Carlos et al. Binding of sea anemone pore-forming toxins sticholysins I and II to interfaces - Modulation of conformation and activity, and lipid-protein interaction. Chemistry and Physics of Lipids, v. 122, n. 1-2, p. 97-105, 2003Tradução . . Disponível em: https://doi.org/10.1016/s0009-3084(02)00181-0. Acesso em: 17 jun. 2024.
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      Alvarez, C., Casallanovo, F., Shida, C. S., Nogueira, L. V., Martinez, D., Tejuca, M., et al. (2003). Binding of sea anemone pore-forming toxins sticholysins I and II to interfaces - Modulation of conformation and activity, and lipid-protein interaction. Chemistry and Physics of Lipids, 122( 1-2), 97-105. doi:10.1016/s0009-3084(02)00181-0
    • NLM

      Alvarez C, Casallanovo F, Shida CS, Nogueira LV, Martinez D, Tejuca M, Pazos IF, Lanio ME, Menestrina G, Lissi E, Schreier S. Binding of sea anemone pore-forming toxins sticholysins I and II to interfaces - Modulation of conformation and activity, and lipid-protein interaction [Internet]. Chemistry and Physics of Lipids. 2003 ; 122( 1-2): 97-105.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/s0009-3084(02)00181-0
    • Vancouver

      Alvarez C, Casallanovo F, Shida CS, Nogueira LV, Martinez D, Tejuca M, Pazos IF, Lanio ME, Menestrina G, Lissi E, Schreier S. Binding of sea anemone pore-forming toxins sticholysins I and II to interfaces - Modulation of conformation and activity, and lipid-protein interaction [Internet]. Chemistry and Physics of Lipids. 2003 ; 122( 1-2): 97-105.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/s0009-3084(02)00181-0
  • Source: Peptides. Unidade: IQ

    Subjects: BIOQUÍMICA, PEPTÍDEOS (SÍNTESE), RESSONÂNCIA PARAMAGNÉTICA DE SPIN, FARMACOLOGIA (PROPRIEDADES)

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      NAKAIE, C. R. et al. Synthesis and pharmacological properties of TOAC-labeled angiotensin and bradykinin analogs. Peptides, v. 23, n. 1, p. 65-70, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0196-9781(01)00580-0. Acesso em: 17 jun. 2024.
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      Nakaie, C. R., Silva, E. G., Cilli, E. M., Marchetto, R., Schreier, S., Paiva, T. B., & Paiva, A. C. M. (2002). Synthesis and pharmacological properties of TOAC-labeled angiotensin and bradykinin analogs. Peptides, 23( 1), 65-70. doi:10.1016/s0196-9781(01)00580-0
    • NLM

      Nakaie CR, Silva EG, Cilli EM, Marchetto R, Schreier S, Paiva TB, Paiva ACM. Synthesis and pharmacological properties of TOAC-labeled angiotensin and bradykinin analogs [Internet]. Peptides. 2002 ; 23( 1): 65-70.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/s0196-9781(01)00580-0
    • Vancouver

      Nakaie CR, Silva EG, Cilli EM, Marchetto R, Schreier S, Paiva TB, Paiva ACM. Synthesis and pharmacological properties of TOAC-labeled angiotensin and bradykinin analogs [Internet]. Peptides. 2002 ; 23( 1): 65-70.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/s0196-9781(01)00580-0
  • Source: Biophysical Chemistry. Unidade: IQ

    Subjects: BIOQUÍMICA, RESSONÂNCIA MAGNÉTICA NUCLEAR

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      FRACETO, Leonardo Fernandes et al. Spectroscopic evidence for a preferential location of lidocaine inside phospholipid bilayers. Biophysical Chemistry, v. 99, n. 3, p. 229-243, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0301-4622(02)00202-8. Acesso em: 17 jun. 2024.
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      Fraceto, L. F., Pinto, L. de M. A., Franzoni, L., Braga, A. A. C., Spisni, A., Schreier, S., & Paula, E. de. (2002). Spectroscopic evidence for a preferential location of lidocaine inside phospholipid bilayers. Biophysical Chemistry, 99( 3), 229-243. doi:10.1016/s0301-4622(02)00202-8
    • NLM

      Fraceto LF, Pinto L de MA, Franzoni L, Braga AAC, Spisni A, Schreier S, Paula E de. Spectroscopic evidence for a preferential location of lidocaine inside phospholipid bilayers [Internet]. Biophysical Chemistry. 2002 ; 99( 3): 229-243.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/s0301-4622(02)00202-8
    • Vancouver

      Fraceto LF, Pinto L de MA, Franzoni L, Braga AAC, Spisni A, Schreier S, Paula E de. Spectroscopic evidence for a preferential location of lidocaine inside phospholipid bilayers [Internet]. Biophysical Chemistry. 2002 ; 99( 3): 229-243.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/s0301-4622(02)00202-8
  • Source: Biopolymers. Unidade: IQ

    Subjects: BIOQUÍMICA, PEPTÍDEOS, ANGIOTENSINA II

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      SALINAS, Roberto Kopke et al. Trifluoroethanol and binding to model membranes stabilize a predicted turn in a peptide corresponding to the first extracellular loop of the angiotensin II 'AT AND. 1A' receptor. Biopolymers, v. 65, n. 1, p. 21-31, 2002Tradução . . Disponível em: https://doi.org/10.1002/bip.10209. Acesso em: 17 jun. 2024.
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      Salinas, R. K., Shida, C. S., Pertinhez, T. de A., Spisni, A., Nakaie, C. R., Paiva, A. C. M., & Schreier, S. (2002). Trifluoroethanol and binding to model membranes stabilize a predicted turn in a peptide corresponding to the first extracellular loop of the angiotensin II 'AT AND. 1A' receptor. Biopolymers, 65( 1), 21-31. doi:10.1002/bip.10209
    • NLM

      Salinas RK, Shida CS, Pertinhez T de A, Spisni A, Nakaie CR, Paiva ACM, Schreier S. Trifluoroethanol and binding to model membranes stabilize a predicted turn in a peptide corresponding to the first extracellular loop of the angiotensin II 'AT AND. 1A' receptor [Internet]. Biopolymers. 2002 ; 65( 1): 21-31.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1002/bip.10209
    • Vancouver

      Salinas RK, Shida CS, Pertinhez T de A, Spisni A, Nakaie CR, Paiva ACM, Schreier S. Trifluoroethanol and binding to model membranes stabilize a predicted turn in a peptide corresponding to the first extracellular loop of the angiotensin II 'AT AND. 1A' receptor [Internet]. Biopolymers. 2002 ; 65( 1): 21-31.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1002/bip.10209
  • Source: Toxicon. Unidade: IQ

    Subjects: POLIPEPTÍDEOS, AMINOÁCIDOS, MACROMOLÉCULAS NATURAIS, MEMBRANA CELULAR VEGETAL, TOXINAS, BIOQUÍMICA DE ALIMENTOS

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      MARTINEZ, D. et al. Properties of St I and St II, two isotoxins isolated from Stichodactyla helianthus: a comparison. Toxicon, v. 39, n. 10, p. 1547-1560, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0041-0101(01)00127-1. Acesso em: 17 jun. 2024.
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      Martinez, D., Campos, A. M., Pazos, F., Lanio, M. E., Casallanovo, F., Schreier, S., et al. (2001). Properties of St I and St II, two isotoxins isolated from Stichodactyla helianthus: a comparison. Toxicon, 39( 10), 1547-1560. doi:10.1016/s0041-0101(01)00127-1
    • NLM

      Martinez D, Campos AM, Pazos F, Lanio ME, Casallanovo F, Schreier S, Salinas RK, Vergara C, Lissi E. Properties of St I and St II, two isotoxins isolated from Stichodactyla helianthus: a comparison [Internet]. Toxicon. 2001 ; 39( 10): 1547-1560.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/s0041-0101(01)00127-1
    • Vancouver

      Martinez D, Campos AM, Pazos F, Lanio ME, Casallanovo F, Schreier S, Salinas RK, Vergara C, Lissi E. Properties of St I and St II, two isotoxins isolated from Stichodactyla helianthus: a comparison [Internet]. Toxicon. 2001 ; 39( 10): 1547-1560.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/s0041-0101(01)00127-1
  • Source: Biochimica et Biophysica Acta. Unidades: IF, IQ

    Assunto: BIOQUÍMICA

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      TEIXEIRA, Cilâine Verônica et al. Local anesthetic-induced microscopic and mesoscopic effects in micelles. A fluorescence, spin label and SAXS study. Biochimica et Biophysica Acta, v. 1510, n. 1-2, p. 93-105, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0005-2736(00)00338-2. Acesso em: 17 jun. 2024.
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      Teixeira, C. V., Itri, R., Casallanovo, F., & Schreier, S. (2001). Local anesthetic-induced microscopic and mesoscopic effects in micelles. A fluorescence, spin label and SAXS study. Biochimica et Biophysica Acta, 1510( 1-2), 93-105. doi:10.1016/s0005-2736(00)00338-2
    • NLM

      Teixeira CV, Itri R, Casallanovo F, Schreier S. Local anesthetic-induced microscopic and mesoscopic effects in micelles. A fluorescence, spin label and SAXS study [Internet]. Biochimica et Biophysica Acta. 2001 ; 1510( 1-2): 93-105.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/s0005-2736(00)00338-2
    • Vancouver

      Teixeira CV, Itri R, Casallanovo F, Schreier S. Local anesthetic-induced microscopic and mesoscopic effects in micelles. A fluorescence, spin label and SAXS study [Internet]. Biochimica et Biophysica Acta. 2001 ; 1510( 1-2): 93-105.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/s0005-2736(00)00338-2
  • Source: Biochimica et Biophysica Acta. Unidade: IQ

    Subjects: BIOQUÍMICA, INTERAÇÃO DE MEDICAMENTOS, RESSONÂNCIA MAGNÉTICA NUCLEAR, ANESTÉSICOS LOCAIS

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      SCHREIER, Shirley e MALHEIROS, Sônia V P e PAULA, Eneida de. Surface active drugs: self-association and interaction with membranes and surfactants. Physicochemical and biological aspects. Biochimica et Biophysica Acta, v. 1508, n. 1-2, p. 210-234, 2000Tradução . . Disponível em: https://doi.org/10.1016/s0304-4157(00)00012-5. Acesso em: 17 jun. 2024.
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      Schreier, S., Malheiros, S. V. P., & Paula, E. de. (2000). Surface active drugs: self-association and interaction with membranes and surfactants. Physicochemical and biological aspects. Biochimica et Biophysica Acta, 1508( 1-2), 210-234. doi:10.1016/s0304-4157(00)00012-5
    • NLM

      Schreier S, Malheiros SVP, Paula E de. Surface active drugs: self-association and interaction with membranes and surfactants. Physicochemical and biological aspects [Internet]. Biochimica et Biophysica Acta. 2000 ; 1508( 1-2): 210-234.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/s0304-4157(00)00012-5
    • Vancouver

      Schreier S, Malheiros SVP, Paula E de. Surface active drugs: self-association and interaction with membranes and surfactants. Physicochemical and biological aspects [Internet]. Biochimica et Biophysica Acta. 2000 ; 1508( 1-2): 210-234.[citado 2024 jun. 17 ] Available from: https://doi.org/10.1016/s0304-4157(00)00012-5

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