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  • Fonte: Scientific Reports. Unidades: IQ, FCF

    Assuntos: PEPTÍDEOS, BIOQUÍMICA, BIOINFORMÁTICA, QUÍMICA DE SUPERFÍCIE

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      PARK, Peter et al. Vesicle protrusion induced by antimicrobial peptides suggests common carpet mechanism for short antimicrobial peptides. Scientific Reports, v. 14, p. 1-13 art. 9701, 2024Tradução . . Disponível em: https://dx.doi.org/10.1038/s41598-024-60601-w. Acesso em: 22 jul. 2024.
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      Park, P., Matsubara, D. K., Barzotto, D. R., Lima, F. S., Chaimovich Guralnik, H., Marrink, S. J., & Cuccovia, I. M. (2024). Vesicle protrusion induced by antimicrobial peptides suggests common carpet mechanism for short antimicrobial peptides. Scientific Reports, 14, 1-13 art. 9701. doi:10.1038/s41598-024-60601-w
    • NLM

      Park P, Matsubara DK, Barzotto DR, Lima FS, Chaimovich Guralnik H, Marrink SJ, Cuccovia IM. Vesicle protrusion induced by antimicrobial peptides suggests common carpet mechanism for short antimicrobial peptides [Internet]. Scientific Reports. 2024 ; 14 1-13 art. 9701.[citado 2024 jul. 22 ] Available from: https://dx.doi.org/10.1038/s41598-024-60601-w
    • Vancouver

      Park P, Matsubara DK, Barzotto DR, Lima FS, Chaimovich Guralnik H, Marrink SJ, Cuccovia IM. Vesicle protrusion induced by antimicrobial peptides suggests common carpet mechanism for short antimicrobial peptides [Internet]. Scientific Reports. 2024 ; 14 1-13 art. 9701.[citado 2024 jul. 22 ] Available from: https://dx.doi.org/10.1038/s41598-024-60601-w
  • Fonte: ACS Chemical Biology. Unidade: IQ

    Assuntos: CINÉTICA, PEPTÍDEOS, ESTRUTURA QUÍMICA, PROTEÍNAS

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      DÁVALOS, Angy Liseth et al. Uncovering the association mechanism between two intrinsically flexible proteins. ACS Chemical Biology, v. 19, p. 669−686, 2024Tradução . . Disponível em: https://dx.doi.org/10.1021/acschembio.3c00649. Acesso em: 22 jul. 2024.
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      Dávalos, A. L., Echeverri, J. D. R., Favaro, D. C., Oliveira, R. J., Carretero, G. P. B., Lacerda, C., et al. (2024). Uncovering the association mechanism between two intrinsically flexible proteins. ACS Chemical Biology, 19, 669−686. doi:10.1021/acschembio.3c00649
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      Dávalos AL, Echeverri JDR, Favaro DC, Oliveira RJ, Carretero GPB, Lacerda C, Cuccovia IM, Cardoso MVC, Farah CS, Salinas RK. Uncovering the association mechanism between two intrinsically flexible proteins [Internet]. ACS Chemical Biology. 2024 ; 19 669−686.[citado 2024 jul. 22 ] Available from: https://dx.doi.org/10.1021/acschembio.3c00649
    • Vancouver

      Dávalos AL, Echeverri JDR, Favaro DC, Oliveira RJ, Carretero GPB, Lacerda C, Cuccovia IM, Cardoso MVC, Farah CS, Salinas RK. Uncovering the association mechanism between two intrinsically flexible proteins [Internet]. ACS Chemical Biology. 2024 ; 19 669−686.[citado 2024 jul. 22 ] Available from: https://dx.doi.org/10.1021/acschembio.3c00649
  • Fonte: Journal of Inorganic Biochemistry. Unidade: IQ

    Assuntos: PEPTÍDEOS, ÍONS

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      WEGERMANN, Camila Anchau et al. Interaction studies of oxindole-derivatives with β-amyloid peptides inhibiting its aggregation induced by metal ions. Journal of Inorganic Biochemistry, v. 245, p. 1-16, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.jinorgbio.2023.112227. Acesso em: 22 jul. 2024.
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      Wegermann, C. A., Pirota, V., Monzani, E., Casella, L., Costa, L. A. S., Novato, W. T. G., et al. (2023). Interaction studies of oxindole-derivatives with β-amyloid peptides inhibiting its aggregation induced by metal ions. Journal of Inorganic Biochemistry, 245, 1-16. doi:10.1016/j.jinorgbio.2023.112227
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      Wegermann CA, Pirota V, Monzani E, Casella L, Costa LAS, Novato WTG, Machini MT, Ferreira AM da C. Interaction studies of oxindole-derivatives with β-amyloid peptides inhibiting its aggregation induced by metal ions [Internet]. Journal of Inorganic Biochemistry. 2023 ; 245 1-16.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1016/j.jinorgbio.2023.112227
    • Vancouver

      Wegermann CA, Pirota V, Monzani E, Casella L, Costa LAS, Novato WTG, Machini MT, Ferreira AM da C. Interaction studies of oxindole-derivatives with β-amyloid peptides inhibiting its aggregation induced by metal ions [Internet]. Journal of Inorganic Biochemistry. 2023 ; 245 1-16.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1016/j.jinorgbio.2023.112227
  • Fonte: Results in Chemistry. Unidades: IQ, FCF

    Assuntos: PEPTÍDEOS, DINÂMICA

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      LACERDA, C. D et al. Position matters in ester thiolysis by cysteine-containing peptides in micelles and vesicles. Results in Chemistry, v. 6, p. 1-10 art. 101028, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.rechem.2023.101028. Acesso em: 22 jul. 2024.
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      Lacerda, C. D., Juliano, M. A., Liria, C. W., Machini, M. T., Park, P., Matsubara, D. K., et al. (2023). Position matters in ester thiolysis by cysteine-containing peptides in micelles and vesicles. Results in Chemistry, 6, 1-10 art. 101028. doi:10.1016/j.rechem.2023.101028
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      Lacerda CD, Juliano MA, Liria CW, Machini MT, Park P, Matsubara DK, Barzotto DR, Lima FS, Chaimovich Guralnik H, Cuccovia IM. Position matters in ester thiolysis by cysteine-containing peptides in micelles and vesicles [Internet]. Results in Chemistry. 2023 ; 6 1-10 art. 101028.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1016/j.rechem.2023.101028
    • Vancouver

      Lacerda CD, Juliano MA, Liria CW, Machini MT, Park P, Matsubara DK, Barzotto DR, Lima FS, Chaimovich Guralnik H, Cuccovia IM. Position matters in ester thiolysis by cysteine-containing peptides in micelles and vesicles [Internet]. Results in Chemistry. 2023 ; 6 1-10 art. 101028.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1016/j.rechem.2023.101028
  • Fonte: Toxicon. Unidade: IQ

    Assuntos: METÁSTASE NEOPLÁSICA, NEUROBLASTOMA, ÓXIDO NÍTRICO, PEPTÍDEOS

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      COUTINHO, Fernanda et al. Bj-PRO-10c, as an allosteric regulator of argininosuccinate synthase, is a potential therapy for neuroblastoma metastasis. Toxicon, v. 233, p. 1-9 art. 107228, 2023Tradução . . Disponível em: https://dx.doi.org/10.1016/j.toxicon.2023.107228. Acesso em: 22 jul. 2024.
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      Coutinho, F., Guimarães, L. M. F., Seeger, R., Santos, A. P. J., Glaser, T., Yamamoto, D., et al. (2023). Bj-PRO-10c, as an allosteric regulator of argininosuccinate synthase, is a potential therapy for neuroblastoma metastasis. Toxicon, 233, 1-9 art. 107228. doi:10.1016/j.toxicon.2023.107228
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      Coutinho F, Guimarães LMF, Seeger R, Santos APJ, Glaser T, Yamamoto D, Lacerda L, Sampaio VFA, Rossini CVT, Rabelo I, Medeiros NM de, Truzzi DR, Juliano MA, Juliano L, Ulrich H, Lameu C. Bj-PRO-10c, as an allosteric regulator of argininosuccinate synthase, is a potential therapy for neuroblastoma metastasis [Internet]. Toxicon. 2023 ; 233 1-9 art. 107228.[citado 2024 jul. 22 ] Available from: https://dx.doi.org/10.1016/j.toxicon.2023.107228
    • Vancouver

      Coutinho F, Guimarães LMF, Seeger R, Santos APJ, Glaser T, Yamamoto D, Lacerda L, Sampaio VFA, Rossini CVT, Rabelo I, Medeiros NM de, Truzzi DR, Juliano MA, Juliano L, Ulrich H, Lameu C. Bj-PRO-10c, as an allosteric regulator of argininosuccinate synthase, is a potential therapy for neuroblastoma metastasis [Internet]. Toxicon. 2023 ; 233 1-9 art. 107228.[citado 2024 jul. 22 ] Available from: https://dx.doi.org/10.1016/j.toxicon.2023.107228
  • Fonte: Journal of Chemical Information and Modeling. Unidade: IQ

    Assuntos: PROTEÍNAS, PEPTÍDEOS

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      CURTOLO, Felipe e ARANTES, Guilherme Menegon. Dissecting reaction mechanisms and catalytic contributions in Flavoprotein fumarate Reductases. Journal of Chemical Information and Modeling, v. 63, p. 3510−3520, 2023Tradução . . Disponível em: https://doi.org/10.1021/acs.jcim.3c00292. Acesso em: 22 jul. 2024.
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      Curtolo, F., & Arantes, G. M. (2023). Dissecting reaction mechanisms and catalytic contributions in Flavoprotein fumarate Reductases. Journal of Chemical Information and Modeling, 63, 3510−3520. doi:10.1021/acs.jcim.3c00292
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      Curtolo F, Arantes GM. Dissecting reaction mechanisms and catalytic contributions in Flavoprotein fumarate Reductases [Internet]. Journal of Chemical Information and Modeling. 2023 ; 63 3510−3520.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1021/acs.jcim.3c00292
    • Vancouver

      Curtolo F, Arantes GM. Dissecting reaction mechanisms and catalytic contributions in Flavoprotein fumarate Reductases [Internet]. Journal of Chemical Information and Modeling. 2023 ; 63 3510−3520.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1021/acs.jcim.3c00292
  • Fonte: Pharmaceuticals. Unidades: IQ, FCF

    Assuntos: PEPTÍDEOS, FUNGOS, NANOPARTÍCULAS, BACTÉRIAS PATOGÊNICAS

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      ZAIA, Rachel et al. Transient coatings from nanoparticles achieving broad-spectrum and high antimicrobial performance. Pharmaceuticals, v. 16, p. 1-15 art. 816, 2023Tradução . . Disponível em: https://doi.org/10.3390/ph16060816. Acesso em: 22 jul. 2024.
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      Zaia, R., Quinto, G. M., Camargo, L. C. S., Ribeiro, R. T., & Carmona-Ribeiro, A. M. (2023). Transient coatings from nanoparticles achieving broad-spectrum and high antimicrobial performance. Pharmaceuticals, 16, 1-15 art. 816. doi:10.3390/ph16060816
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      Zaia R, Quinto GM, Camargo LCS, Ribeiro RT, Carmona-Ribeiro AM. Transient coatings from nanoparticles achieving broad-spectrum and high antimicrobial performance [Internet]. Pharmaceuticals. 2023 ; 16 1-15 art. 816.[citado 2024 jul. 22 ] Available from: https://doi.org/10.3390/ph16060816
    • Vancouver

      Zaia R, Quinto GM, Camargo LCS, Ribeiro RT, Carmona-Ribeiro AM. Transient coatings from nanoparticles achieving broad-spectrum and high antimicrobial performance [Internet]. Pharmaceuticals. 2023 ; 16 1-15 art. 816.[citado 2024 jul. 22 ] Available from: https://doi.org/10.3390/ph16060816
  • Fonte: Future Pharmacology. Unidade: IQ

    Assuntos: PEPTÍDEOS, RESISTÊNCIA MICROBIANA ÀS DROGAS

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      CARMONA-RIBEIRO, Ana Maria. Antimicrobial peptides and their assemblies. Future Pharmacology, v. 3, p. 763–788, 2023Tradução . . Disponível em: https://dx.doi.org/10.3390/futurepharmacol3040047. Acesso em: 22 jul. 2024.
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      Carmona-Ribeiro, A. M. (2023). Antimicrobial peptides and their assemblies. Future Pharmacology, 3, 763–788. doi:10.3390/futurepharmacol3040047
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      Carmona-Ribeiro AM. Antimicrobial peptides and their assemblies [Internet]. Future Pharmacology. 2023 ; 3 763–788.[citado 2024 jul. 22 ] Available from: https://dx.doi.org/10.3390/futurepharmacol3040047
    • Vancouver

      Carmona-Ribeiro AM. Antimicrobial peptides and their assemblies [Internet]. Future Pharmacology. 2023 ; 3 763–788.[citado 2024 jul. 22 ] Available from: https://dx.doi.org/10.3390/futurepharmacol3040047
  • Fonte: ACS Chemical Biology. Unidade: IQ

    Assuntos: AMINAS, GENÉTICA, OXIDAÇÃO, PEPTÍDEOS, PROTEÍNAS

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      GONÇALVES, Letícia C. P et al. Chemiexcited neurotransmitters and hormones create DNA photoproducts in the dark. ACS Chemical Biology, v. 18, p. 484-493, 2023Tradução . . Disponível em: https://doi.org/10.1021/acschembio.2c00787. Acesso em: 22 jul. 2024.
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      Gonçalves, L. C. P., Martínez, C. A., Premi, S., Palmatier, M. A., Prado, F. M., Di Mascio, P., et al. (2023). Chemiexcited neurotransmitters and hormones create DNA photoproducts in the dark. ACS Chemical Biology, 18, 484-493. doi:10.1021/acschembio.2c00787
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      Gonçalves LCP, Martínez CA, Premi S, Palmatier MA, Prado FM, Di Mascio P, Bastos EL, Brash DE. Chemiexcited neurotransmitters and hormones create DNA photoproducts in the dark [Internet]. ACS Chemical Biology. 2023 ; 18 484-493.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1021/acschembio.2c00787
    • Vancouver

      Gonçalves LCP, Martínez CA, Premi S, Palmatier MA, Prado FM, Di Mascio P, Bastos EL, Brash DE. Chemiexcited neurotransmitters and hormones create DNA photoproducts in the dark [Internet]. ACS Chemical Biology. 2023 ; 18 484-493.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1021/acschembio.2c00787
  • Fonte: Animals. Unidades: BIOTECNOLOGIA, IQ

    Assuntos: VENENOS, TOXINAS EM ANIMAL, COBRAS, IMUNIDADE, GENES, PEPTÍDEOS

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      OGUIURA, Nancy et al. Past, present, and future of naturally occurring antimicrobials related to snake venoms. Animals, v. 13, p. 1-35 art. 744, 2023Tradução . . Disponível em: https://doi.org/10.3390/ani13040744. Acesso em: 22 jul. 2024.
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      Oguiura, N., Sanches, L., Duarte , P. V., López, M. A. S., & Machini, M. T. (2023). Past, present, and future of naturally occurring antimicrobials related to snake venoms. Animals, 13, 1-35 art. 744. doi:10.3390/ani13040744
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      Oguiura N, Sanches L, Duarte PV, López MAS, Machini MT. Past, present, and future of naturally occurring antimicrobials related to snake venoms [Internet]. Animals. 2023 ; 13 1-35 art. 744.[citado 2024 jul. 22 ] Available from: https://doi.org/10.3390/ani13040744
    • Vancouver

      Oguiura N, Sanches L, Duarte PV, López MAS, Machini MT. Past, present, and future of naturally occurring antimicrobials related to snake venoms [Internet]. Animals. 2023 ; 13 1-35 art. 744.[citado 2024 jul. 22 ] Available from: https://doi.org/10.3390/ani13040744
  • Fonte: Gene. Unidades: FCF, IQ

    Assuntos: GENOMAS, PEPTÍDEOS, XANTHOMONAS

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      PATANÉ, José S. L et al. New insights into plant natriuretic peptide evolution: from the lysogenic conversion in Xanthomonas to the lateral transfer to the whitefly Bemisia tabaci. Gene, v. 821, p. 1-10 art. 146326, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.gene.2022.146326. Acesso em: 22 jul. 2024.
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      Patané, J. S. L., Moreira, L. M., Teixeira, M. de M., Martins Junior, J., Varani, A. de M., & Setubal, J. C. (2022). New insights into plant natriuretic peptide evolution: from the lysogenic conversion in Xanthomonas to the lateral transfer to the whitefly Bemisia tabaci. Gene, 821, 1-10 art. 146326. doi:10.1016/j.gene.2022.146326
    • NLM

      Patané JSL, Moreira LM, Teixeira M de M, Martins Junior J, Varani A de M, Setubal JC. New insights into plant natriuretic peptide evolution: from the lysogenic conversion in Xanthomonas to the lateral transfer to the whitefly Bemisia tabaci [Internet]. Gene. 2022 ; 821 1-10 art. 146326.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1016/j.gene.2022.146326
    • Vancouver

      Patané JSL, Moreira LM, Teixeira M de M, Martins Junior J, Varani A de M, Setubal JC. New insights into plant natriuretic peptide evolution: from the lysogenic conversion in Xanthomonas to the lateral transfer to the whitefly Bemisia tabaci [Internet]. Gene. 2022 ; 821 1-10 art. 146326.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1016/j.gene.2022.146326
  • Fonte: Photochemistry and Photobiology. Unidade: IQ

    Assuntos: OXIGÊNIO, AMINOÁCIDOS, PEPTÍDEOS

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      JAYME, Stella Boutris et al. Characterization and quantification of tryptophan- and tyrosine-derived hydroperoxides. Photochemistry and Photobiology, v. 98, p. 678–686, 2022Tradução . . Disponível em: https://doi.org/10.1111/php.13623. Acesso em: 22 jul. 2024.
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      Jayme, S. B., Prado, F. M., Massafera, M. P., Ronsein, G. E., & Di Mascio, P. (2022). Characterization and quantification of tryptophan- and tyrosine-derived hydroperoxides. Photochemistry and Photobiology, 98, 678–686. doi:10.1111/php.13623
    • NLM

      Jayme SB, Prado FM, Massafera MP, Ronsein GE, Di Mascio P. Characterization and quantification of tryptophan- and tyrosine-derived hydroperoxides [Internet]. Photochemistry and Photobiology. 2022 ; 98 678–686.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1111/php.13623
    • Vancouver

      Jayme SB, Prado FM, Massafera MP, Ronsein GE, Di Mascio P. Characterization and quantification of tryptophan- and tyrosine-derived hydroperoxides [Internet]. Photochemistry and Photobiology. 2022 ; 98 678–686.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1111/php.13623
  • Fonte: Pharmaceutics. Unidade: IQ

    Assuntos: NANOPARTÍCULAS, PEPTÍDEOS

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      PÉREZ-BETANCOURT, Yunys et al. Characterization and differential cytotoxicity of gramicidin nanoparticles combined with cationic polymer or lipid bilayer. Pharmaceutics, v. 14, p. 1-18 art. 2053, 2022Tradução . . Disponível em: https://doi.org/10.3390/pharmaceutics14102053. Acesso em: 22 jul. 2024.
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      Pérez-Betancourt, Y., Zaia, R., Evangelista, M. F., Ribeiro, R. T., Roncoleta, B. M., Mathiazzi, B. I., & Carmona-Ribeiro, A. M. (2022). Characterization and differential cytotoxicity of gramicidin nanoparticles combined with cationic polymer or lipid bilayer. Pharmaceutics, 14, 1-18 art. 2053. doi:10.3390/pharmaceutics14102053
    • NLM

      Pérez-Betancourt Y, Zaia R, Evangelista MF, Ribeiro RT, Roncoleta BM, Mathiazzi BI, Carmona-Ribeiro AM. Characterization and differential cytotoxicity of gramicidin nanoparticles combined with cationic polymer or lipid bilayer [Internet]. Pharmaceutics. 2022 ; 14 1-18 art. 2053.[citado 2024 jul. 22 ] Available from: https://doi.org/10.3390/pharmaceutics14102053
    • Vancouver

      Pérez-Betancourt Y, Zaia R, Evangelista MF, Ribeiro RT, Roncoleta BM, Mathiazzi BI, Carmona-Ribeiro AM. Characterization and differential cytotoxicity of gramicidin nanoparticles combined with cationic polymer or lipid bilayer [Internet]. Pharmaceutics. 2022 ; 14 1-18 art. 2053.[citado 2024 jul. 22 ] Available from: https://doi.org/10.3390/pharmaceutics14102053
  • Fonte: Journal of Drug Targeting. Unidades: IQ, FCF

    Assuntos: BACTÉRIAS, PEPTÍDEOS

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      SILVA, João Vitor da et al. Neglected tropical diseases and infectious illnesses: potential targeted peptides employed as hits compounds in drug design. Journal of Drug Targeting, v. 29, n. 3, p. 269–283, 2021Tradução . . Disponível em: https://doi.org/10.1080/1061186X.2020.1837843. Acesso em: 22 jul. 2024.
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      Silva, J. V. da, Santos, S. da S., Machini, M. T., & Giarolla, J. (2021). Neglected tropical diseases and infectious illnesses: potential targeted peptides employed as hits compounds in drug design. Journal of Drug Targeting, 29( 3), 269–283. doi:10.1080/1061186X.2020.1837843
    • NLM

      Silva JV da, Santos S da S, Machini MT, Giarolla J. Neglected tropical diseases and infectious illnesses: potential targeted peptides employed as hits compounds in drug design [Internet]. Journal of Drug Targeting. 2021 ; 29( 3): 269–283.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1080/1061186X.2020.1837843
    • Vancouver

      Silva JV da, Santos S da S, Machini MT, Giarolla J. Neglected tropical diseases and infectious illnesses: potential targeted peptides employed as hits compounds in drug design [Internet]. Journal of Drug Targeting. 2021 ; 29( 3): 269–283.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1080/1061186X.2020.1837843
  • Fonte: Journal of Chemical Information and Modeling. Unidade: IQ

    Assuntos: ELÉTRONS, PEPTÍDEOS, PROTEÍNAS

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      CAMILO, Sofia Rodrigues Guedes et al. Tunneling and nonadiabatic effects on a proton-coupled electron transfer model for the Qo site in cytochrome bc1. Journal of Chemical Information and Modeling, v. 61, p. 1840−1849, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.jcim.1c00008. Acesso em: 22 jul. 2024.
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      Camilo, S. R. G., Curtolo, F., Galassi, V. V., & Arantes, G. M. (2021). Tunneling and nonadiabatic effects on a proton-coupled electron transfer model for the Qo site in cytochrome bc1. Journal of Chemical Information and Modeling, 61, 1840−1849. doi:10.1021/acs.jcim.1c00008
    • NLM

      Camilo SRG, Curtolo F, Galassi VV, Arantes GM. Tunneling and nonadiabatic effects on a proton-coupled electron transfer model for the Qo site in cytochrome bc1 [Internet]. Journal of Chemical Information and Modeling. 2021 ; 61 1840−1849.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1021/acs.jcim.1c00008
    • Vancouver

      Camilo SRG, Curtolo F, Galassi VV, Arantes GM. Tunneling and nonadiabatic effects on a proton-coupled electron transfer model for the Qo site in cytochrome bc1 [Internet]. Journal of Chemical Information and Modeling. 2021 ; 61 1840−1849.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1021/acs.jcim.1c00008
  • Fonte: Biomolecules. Unidade: IQ

    Assuntos: PEPTÍDEOS, ESPECTROSCOPIA, CALORÍMETROS

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      CARRETERO, Gustavo Penteado Battesini et al. Naphthalimide-containing BP100 leads to higher model membranes interactions and antimicrobial activity. Biomolecules, v. 11, p. 1-20 art. 542, 2021Tradução . . Disponível em: https://doi.org/10.3390/biom11040542. Acesso em: 22 jul. 2024.
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      Carretero, G. P. B., Saraiva, G. K. V., Rodrigues, M. A., Kiyota, S., Bemquerer, M. P., Chaimovich Guralnik, H., & Cuccovia, I. M. (2021). Naphthalimide-containing BP100 leads to higher model membranes interactions and antimicrobial activity. Biomolecules, 11, 1-20 art. 542. doi:10.3390/biom11040542
    • NLM

      Carretero GPB, Saraiva GKV, Rodrigues MA, Kiyota S, Bemquerer MP, Chaimovich Guralnik H, Cuccovia IM. Naphthalimide-containing BP100 leads to higher model membranes interactions and antimicrobial activity [Internet]. Biomolecules. 2021 ; 11 1-20 art. 542.[citado 2024 jul. 22 ] Available from: https://doi.org/10.3390/biom11040542
    • Vancouver

      Carretero GPB, Saraiva GKV, Rodrigues MA, Kiyota S, Bemquerer MP, Chaimovich Guralnik H, Cuccovia IM. Naphthalimide-containing BP100 leads to higher model membranes interactions and antimicrobial activity [Internet]. Biomolecules. 2021 ; 11 1-20 art. 542.[citado 2024 jul. 22 ] Available from: https://doi.org/10.3390/biom11040542
  • Fonte: International Journal of Molecular Sciences. Unidade: IQ

    Assuntos: PEPTÍDEOS, BIOPOLÍMEROS, RESISTÊNCIA MICROBIANA ÀS DROGAS, BIOPOLÍMEROS

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      CARMONA-RIBEIRO, Ana Maria e ARAÚJO, Péricles Marques. Antimicrobial polymer−based assemblies: a review. International Journal of Molecular Sciences, v. 22, p. 1-27 art. 5424, 2021Tradução . . Disponível em: https://doi.org/10.3390/ijms22115424. Acesso em: 22 jul. 2024.
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      Carmona-Ribeiro, A. M., & Araújo, P. M. (2021). Antimicrobial polymer−based assemblies: a review. International Journal of Molecular Sciences, 22, 1-27 art. 5424. doi:10.3390/ijms22115424
    • NLM

      Carmona-Ribeiro AM, Araújo PM. Antimicrobial polymer−based assemblies: a review [Internet]. International Journal of Molecular Sciences. 2021 ; 22 1-27 art. 5424.[citado 2024 jul. 22 ] Available from: https://doi.org/10.3390/ijms22115424
    • Vancouver

      Carmona-Ribeiro AM, Araújo PM. Antimicrobial polymer−based assemblies: a review [Internet]. International Journal of Molecular Sciences. 2021 ; 22 1-27 art. 5424.[citado 2024 jul. 22 ] Available from: https://doi.org/10.3390/ijms22115424
  • Fonte: Journal of Chemical Information and Modeling. Unidades: IQ, IFSC

    Assuntos: CRISTALOGRAFIA, PEPTÍDEOS, PROTEÍNAS, LIGANTES

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      VELDMAN, Wayde et al. Differences in gluco and galacto substrate-binding interactions in a dual 6Pβ-Glucosidase/6Pβ-Galactosidase glycoside hydrolase 1 enzyme from Bacillus licheniformis. Journal of Chemical Information and Modeling, v. 61, n. 9, p. 4554-4570, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.jcim.1c00413. Acesso em: 22 jul. 2024.
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      Veldman, W., Liberato, M. V., Souza, V. P., Almeida, V. M., Marana, S. R., Bishop, O. T., & Polikarpov, I. (2021). Differences in gluco and galacto substrate-binding interactions in a dual 6Pβ-Glucosidase/6Pβ-Galactosidase glycoside hydrolase 1 enzyme from Bacillus licheniformis. Journal of Chemical Information and Modeling, 61( 9), 4554-4570. doi:10.1021/acs.jcim.1c00413
    • NLM

      Veldman W, Liberato MV, Souza VP, Almeida VM, Marana SR, Bishop OT, Polikarpov I. Differences in gluco and galacto substrate-binding interactions in a dual 6Pβ-Glucosidase/6Pβ-Galactosidase glycoside hydrolase 1 enzyme from Bacillus licheniformis [Internet]. Journal of Chemical Information and Modeling. 2021 ; 61( 9): 4554-4570.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1021/acs.jcim.1c00413
    • Vancouver

      Veldman W, Liberato MV, Souza VP, Almeida VM, Marana SR, Bishop OT, Polikarpov I. Differences in gluco and galacto substrate-binding interactions in a dual 6Pβ-Glucosidase/6Pβ-Galactosidase glycoside hydrolase 1 enzyme from Bacillus licheniformis [Internet]. Journal of Chemical Information and Modeling. 2021 ; 61( 9): 4554-4570.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1021/acs.jcim.1c00413
  • Fonte: Inorganic Chemistry. Unidade: IQ

    Assuntos: FERRO, PEPTÍDEOS, PROTEÍNAS

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      TRUZZI, Daniela Ramos et al. Dinitrosyl iron complexes (DNICs). From spontaneous assembly to biological roles. Inorganic Chemistry, v. 60, n. 21, p. 15835-15845, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.inorgchem.1c00823. Acesso em: 22 jul. 2024.
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      Truzzi, D. R., Medeiros, N. M. de, Augusto, O., & Ford, P. C. (2021). Dinitrosyl iron complexes (DNICs). From spontaneous assembly to biological roles. Inorganic Chemistry, 60( 21), 15835-15845. doi:10.1021/acs.inorgchem.1c00823
    • NLM

      Truzzi DR, Medeiros NM de, Augusto O, Ford PC. Dinitrosyl iron complexes (DNICs). From spontaneous assembly to biological roles [Internet]. Inorganic Chemistry. 2021 ; 60( 21): 15835-15845.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1021/acs.inorgchem.1c00823
    • Vancouver

      Truzzi DR, Medeiros NM de, Augusto O, Ford PC. Dinitrosyl iron complexes (DNICs). From spontaneous assembly to biological roles [Internet]. Inorganic Chemistry. 2021 ; 60( 21): 15835-15845.[citado 2024 jul. 22 ] Available from: https://doi.org/10.1021/acs.inorgchem.1c00823
  • Fonte: Frontiers in Neuroscience. Unidade: IQ

    Assuntos: HOMEOSTASE, SISTEMA NERVOSO CENTRAL, BRADICININA, BARREIRA HEMATO-ENCEFÁLICA, PEPTÍDEOS

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      RODRIGUEZ-MASSÓ, Sergio R et al. The bradykinin B2 receptor agonist (NG291) causes rapid onset of transient blood–brain barrier disruption without evidence of early brain injury. Frontiers in Neuroscience, v. 15, p. 1-17, 2021Tradução . . Disponível em: https://doi.org/10.3389/fnins.2021.791709. Acesso em: 22 jul. 2024.
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      Rodriguez-Massó, S. R., Erickson, M. A., Banks, W. A., Ulrich, H., & Martins, A. H. (2021). The bradykinin B2 receptor agonist (NG291) causes rapid onset of transient blood–brain barrier disruption without evidence of early brain injury. Frontiers in Neuroscience, 15, 1-17. doi:10.3389/fnins.2021.791709
    • NLM

      Rodriguez-Massó SR, Erickson MA, Banks WA, Ulrich H, Martins AH. The bradykinin B2 receptor agonist (NG291) causes rapid onset of transient blood–brain barrier disruption without evidence of early brain injury [Internet]. Frontiers in Neuroscience. 2021 ; 15 1-17.[citado 2024 jul. 22 ] Available from: https://doi.org/10.3389/fnins.2021.791709
    • Vancouver

      Rodriguez-Massó SR, Erickson MA, Banks WA, Ulrich H, Martins AH. The bradykinin B2 receptor agonist (NG291) causes rapid onset of transient blood–brain barrier disruption without evidence of early brain injury [Internet]. Frontiers in Neuroscience. 2021 ; 15 1-17.[citado 2024 jul. 22 ] Available from: https://doi.org/10.3389/fnins.2021.791709

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