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  • Source: Phage Engineering and Analysis. Unidade: IQ

    Subjects: PEPTÍDEOS, MUTAGÊNESE

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      GIORDANO, Ricardo José e OLIVEIRA, Lilian Cristina Costa Alecrim de. Protocols for building and producing high diversity peptide phage display libraries. Phage Engineering and Analysis. Tradução . New York: Humana Press, 2024. . Disponível em: https://doi.org/10.1007/978-1-0716-3798-2. Acesso em: 30 set. 2024.
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      Giordano, R. J., & Oliveira, L. C. C. A. de. (2024). Protocols for building and producing high diversity peptide phage display libraries. In Phage Engineering and Analysis. New York: Humana Press. doi:10.1007/978-1-0716-3798-2
    • NLM

      Giordano RJ, Oliveira LCCA de. Protocols for building and producing high diversity peptide phage display libraries [Internet]. In: Phage Engineering and Analysis. New York: Humana Press; 2024. [citado 2024 set. 30 ] Available from: https://doi.org/10.1007/978-1-0716-3798-2
    • Vancouver

      Giordano RJ, Oliveira LCCA de. Protocols for building and producing high diversity peptide phage display libraries [Internet]. In: Phage Engineering and Analysis. New York: Humana Press; 2024. [citado 2024 set. 30 ] Available from: https://doi.org/10.1007/978-1-0716-3798-2
  • Source: ACS Chemical Biology. Unidade: IQ

    Subjects: 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: 30 set. 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
    • NLM

      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 set. 30 ] 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 set. 30 ] Available from: https://dx.doi.org/10.1021/acschembio.3c00649
  • Source: Journal of Medicinal Chemistry. Unidades: IQ, ICB

    Subjects: BIOQUÍMICA INORGÂNICA, PEPTÍDEOS, PROTEÍNAS, PEROXIDASE

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      MATOS, Isaac de Araújo et al. Targeting myeloperoxidase ameliorates gouty arthritis: a virtual screening success Story. Journal of Medicinal Chemistry, v. 67, n. 14, p. 12012–12032, 2024Tradução . . Disponível em: https://dx.doi.org/10.1021/acs.jmedchem.4c00721. Acesso em: 30 set. 2024.
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      Matos, I. de A., Dallazen, J. L., Reis, L. R., Souza, L. F., Bevevino, R. C., Moura, R. D. de, et al. (2024). Targeting myeloperoxidase ameliorates gouty arthritis: a virtual screening success Story. Journal of Medicinal Chemistry, 67( 14), 12012–12032. doi:10.1021/acs.jmedchem.4c00721
    • NLM

      Matos I de A, Dallazen JL, Reis LR, Souza LF, Bevevino RC, Moura RD de, Costa Júnior NB da, Ronsein GE, Hoch NC, Costa SKP, Meotti FC. Targeting myeloperoxidase ameliorates gouty arthritis: a virtual screening success Story [Internet]. Journal of Medicinal Chemistry. 2024 ; 67( 14): 12012–12032.[citado 2024 set. 30 ] Available from: https://dx.doi.org/10.1021/acs.jmedchem.4c00721
    • Vancouver

      Matos I de A, Dallazen JL, Reis LR, Souza LF, Bevevino RC, Moura RD de, Costa Júnior NB da, Ronsein GE, Hoch NC, Costa SKP, Meotti FC. Targeting myeloperoxidase ameliorates gouty arthritis: a virtual screening success Story [Internet]. Journal of Medicinal Chemistry. 2024 ; 67( 14): 12012–12032.[citado 2024 set. 30 ] Available from: https://dx.doi.org/10.1021/acs.jmedchem.4c00721
  • Source: Journal of Inorganic Biochemistry. Unidade: IQ

    Subjects: 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: 30 set. 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 set. 30 ] 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 set. 30 ] Available from: https://doi.org/10.1016/j.jinorgbio.2023.112227
  • Source: ACS Applied Bio Materials. Unidade: IQ

    Subjects: BACTÉRIAS, PEPTÍDEOS

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      PHAKATKAR, Abhijit H et al. Enhanced bacterial growth by polyelemental glycerolate particles. ACS Applied Bio Materials, v. 6, n. 4, p. 1515-1524, 2023Tradução . . Disponível em: https://doi.org/10.1021/acsabm.2c01052. Acesso em: 30 set. 2024.
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      Phakatkar, A. H., Gonçalves, J. M., Zhou, J., Ritter, T. G., Saray, M. T., Sorokina, L. V., et al. (2023). Enhanced bacterial growth by polyelemental glycerolate particles. ACS Applied Bio Materials, 6( 4), 1515-1524. doi:10.1021/acsabm.2c01052
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      Phakatkar AH, Gonçalves JM, Zhou J, Ritter TG, Saray MT, Sorokina LV, Amiri A, Angnes L, Shokuhfar T, Yassar RS. Enhanced bacterial growth by polyelemental glycerolate particles [Internet]. ACS Applied Bio Materials. 2023 ;6( 4): 1515-1524.[citado 2024 set. 30 ] Available from: https://doi.org/10.1021/acsabm.2c01052
    • Vancouver

      Phakatkar AH, Gonçalves JM, Zhou J, Ritter TG, Saray MT, Sorokina LV, Amiri A, Angnes L, Shokuhfar T, Yassar RS. Enhanced bacterial growth by polyelemental glycerolate particles [Internet]. ACS Applied Bio Materials. 2023 ;6( 4): 1515-1524.[citado 2024 set. 30 ] Available from: https://doi.org/10.1021/acsabm.2c01052
  • Source: Journal of Chemical Information and Modeling. Unidade: IQ

    Subjects: 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: 30 set. 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 set. 30 ] 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 set. 30 ] Available from: https://doi.org/10.1021/acs.jcim.3c00292
  • Source: ACS Chemical Biology. Unidade: IQ

    Subjects: 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: 30 set. 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
    • NLM

      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 set. 30 ] 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 set. 30 ] Available from: https://doi.org/10.1021/acschembio.2c00787
  • Source: Photochemistry and Photobiology. Unidade: IQ

    Subjects: 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: 30 set. 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 set. 30 ] 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 set. 30 ] Available from: https://doi.org/10.1111/php.13623
  • Source: ACS Chemical Biology. Unidade: IQ

    Subjects: LIPÍDEOS, PEPTÍDEOS, PROTEÍNAS

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      BOZELLI JUNIOR, José Carlos et al. Human diacylglycerol kinase ε N-terminal segment regulates the phosphatidylinositol cycle, controlling the rate but not the acyl chain composition of its lipid intermediates. ACS Chemical Biology, v. 17, n. 9, p. 2495-2506, 2022Tradução . . Disponível em: https://doi.org/10.1021/acschembio.2c00387. Acesso em: 30 set. 2024.
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      Bozelli Junior, J. C., Yune, J., Aulakh, S. S., Cao, Z., Fernandes, A., Seitova, A., et al. (2022). Human diacylglycerol kinase ε N-terminal segment regulates the phosphatidylinositol cycle, controlling the rate but not the acyl chain composition of its lipid intermediates. ACS Chemical Biology, 17( 9), 2495-2506. doi:10.1021/acschembio.2c00387
    • NLM

      Bozelli Junior JC, Yune J, Aulakh SS, Cao Z, Fernandes A, Seitova A, Tong Y, Schreier S, Epand RM. Human diacylglycerol kinase ε N-terminal segment regulates the phosphatidylinositol cycle, controlling the rate but not the acyl chain composition of its lipid intermediates [Internet]. ACS Chemical Biology. 2022 ; 17( 9): 2495-2506.[citado 2024 set. 30 ] Available from: https://doi.org/10.1021/acschembio.2c00387
    • Vancouver

      Bozelli Junior JC, Yune J, Aulakh SS, Cao Z, Fernandes A, Seitova A, Tong Y, Schreier S, Epand RM. Human diacylglycerol kinase ε N-terminal segment regulates the phosphatidylinositol cycle, controlling the rate but not the acyl chain composition of its lipid intermediates [Internet]. ACS Chemical Biology. 2022 ; 17( 9): 2495-2506.[citado 2024 set. 30 ] Available from: https://doi.org/10.1021/acschembio.2c00387
  • Source: Bioconjugate Chemistry. Unidade: IQ

    Subjects: NANOPARTÍCULAS, PEPTÍDEOS, PROTEÍNAS

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      SILVA, Rafael Trivella Pacheco da et al. Stimuli-responsive regulation of Biocatalysis through metallic nanoparticle interaction. Bioconjugate Chemistry, v. 33, n. 1, p. 53–66, 2022Tradução . . Disponível em: https://doi.org/10.1021/acs.bioconjchem.1c00515. Acesso em: 30 set. 2024.
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      Silva, R. T. P. da, Barros, H. R. de, Sandrini, D. M. F., & Torresi, S. I. C. de. (2022). Stimuli-responsive regulation of Biocatalysis through metallic nanoparticle interaction. Bioconjugate Chemistry, 33( 1), 53–66. doi:10.1021/acs.bioconjchem.1c00515
    • NLM

      Silva RTP da, Barros HR de, Sandrini DMF, Torresi SIC de. Stimuli-responsive regulation of Biocatalysis through metallic nanoparticle interaction [Internet]. Bioconjugate Chemistry. 2022 ; 33( 1): 53–66.[citado 2024 set. 30 ] Available from: https://doi.org/10.1021/acs.bioconjchem.1c00515
    • Vancouver

      Silva RTP da, Barros HR de, Sandrini DMF, Torresi SIC de. Stimuli-responsive regulation of Biocatalysis through metallic nanoparticle interaction [Internet]. Bioconjugate Chemistry. 2022 ; 33( 1): 53–66.[citado 2024 set. 30 ] Available from: https://doi.org/10.1021/acs.bioconjchem.1c00515
  • Source: ACS Omega. Unidade: IQ

    Subjects: PEPTÍDEOS, ESPECTROSCOPIA

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      CONCEPCION, Odette et al. Facile synthesis of diversely functionalized Peptoids, spectroscopic characterization, and DFT-Based nonlinear optical exploration. ACS Omega, v. 6, n. 40, p. 26016−26025, 2021Tradução . . Disponível em: https://doi.org/10.1021/acsomega.1c02962. Acesso em: 30 set. 2024.
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      Concepcion, O., Ali, A., Khalid, M., Torre, A. F. de la, Khan, M. U., Raza, A. R., et al. (2021). Facile synthesis of diversely functionalized Peptoids, spectroscopic characterization, and DFT-Based nonlinear optical exploration. ACS Omega, 6( 40), 26016−26025. doi:10.1021/acsomega.1c02962
    • NLM

      Concepcion O, Ali A, Khalid M, Torre AF de la, Khan MU, Raza AR, Kamal GM, Rehman MF ur, Alam MM, Imran M, Braga AAC, Pertino MW. Facile synthesis of diversely functionalized Peptoids, spectroscopic characterization, and DFT-Based nonlinear optical exploration [Internet]. ACS Omega. 2021 ; 6( 40): 26016−26025.[citado 2024 set. 30 ] Available from: https://doi.org/10.1021/acsomega.1c02962
    • Vancouver

      Concepcion O, Ali A, Khalid M, Torre AF de la, Khan MU, Raza AR, Kamal GM, Rehman MF ur, Alam MM, Imran M, Braga AAC, Pertino MW. Facile synthesis of diversely functionalized Peptoids, spectroscopic characterization, and DFT-Based nonlinear optical exploration [Internet]. ACS Omega. 2021 ; 6( 40): 26016−26025.[citado 2024 set. 30 ] Available from: https://doi.org/10.1021/acsomega.1c02962
  • Source: Journal of Drug Targeting. Unidades: IQ, FCF

    Subjects: 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: 30 set. 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 set. 30 ] 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 set. 30 ] Available from: https://doi.org/10.1080/1061186X.2020.1837843
  • Source: ACS Food Science and Technology. Unidade: IQ

    Subjects: AÇAÍ, POLPA, PEPTÍDEOS, PROTEÍNAS, ELEMENTOS DE TRANSIÇÃO

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      SANTOS, Giselaine Alves dos et al. Bioaccessibility of essential elements in açaí (Euterpe oleracea Mart.) pulp. ACS Food Science and Technology, v. 1, p. 874−883, 2021Tradução . . Disponível em: https://doi.org/10.1021/acsfoodscitech.1c00070. Acesso em: 30 set. 2024.
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      Santos, G. A. dos, Carvalho, A. A. C., Oliveira, A. P., Naozuka, J., Matta, F. V., Felipe-Sotelo, M., et al. (2021). Bioaccessibility of essential elements in açaí (Euterpe oleracea Mart.) pulp. ACS Food Science and Technology, 1, 874−883. doi:10.1021/acsfoodscitech.1c00070
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      Santos GA dos, Carvalho AAC, Oliveira AP, Naozuka J, Matta FV, Felipe-Sotelo M, Ward NI, Correa NCF, Nomura CS. Bioaccessibility of essential elements in açaí (Euterpe oleracea Mart.) pulp [Internet]. ACS Food Science and Technology. 2021 ; 1 874−883.[citado 2024 set. 30 ] Available from: https://doi.org/10.1021/acsfoodscitech.1c00070
    • Vancouver

      Santos GA dos, Carvalho AAC, Oliveira AP, Naozuka J, Matta FV, Felipe-Sotelo M, Ward NI, Correa NCF, Nomura CS. Bioaccessibility of essential elements in açaí (Euterpe oleracea Mart.) pulp [Internet]. ACS Food Science and Technology. 2021 ; 1 874−883.[citado 2024 set. 30 ] Available from: https://doi.org/10.1021/acsfoodscitech.1c00070
  • Source: Journal of Chemical Information and Modeling. Unidade: IQ

    Subjects: 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: 30 set. 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
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      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 set. 30 ] 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 set. 30 ] Available from: https://doi.org/10.1021/acs.jcim.1c00008
  • Source: Journal of Chemical Information and Modeling. Unidades: IQ, IFSC

    Subjects: 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: 30 set. 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 set. 30 ] Available from: https://doi.org/10.1021/acs.jcim.1c00413
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      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 set. 30 ] Available from: https://doi.org/10.1021/acs.jcim.1c00413
  • Source: Inorganic Chemistry. Unidade: IQ

    Subjects: 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: 30 set. 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
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      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 set. 30 ] 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 set. 30 ] Available from: https://doi.org/10.1021/acs.inorgchem.1c00823
  • Source: FEBS Open Bio. Unidades: BIOTECNOLOGIA, IQ

    Subjects: PEPTÍDEOS, ANTIFÚNGICOS, SISTEMA IMUNE, ARACNÍDEOS

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      RICILUCA, Katie Cristina Takeuti et al. Rondonin: antimicrobial properties and mechanism of action. FEBS Open Bio, v. 11, n. 9, p. 2541-2559, 2021Tradução . . Disponível em: https://doi.org/10.1002/2211-5463.13253. Acesso em: 30 set. 2024.
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      Riciluca, K. C. T., Oliveira, U. C. de, Mendonça, R. Z., Bozelli Junior, J. C., Schreier, S., & Silva Júnior, P. I. da. (2021). Rondonin: antimicrobial properties and mechanism of action. FEBS Open Bio, 11( 9), 2541-2559. doi:10.1002/2211-5463.13253
    • NLM

      Riciluca KCT, Oliveira UC de, Mendonça RZ, Bozelli Junior JC, Schreier S, Silva Júnior PI da. Rondonin: antimicrobial properties and mechanism of action [Internet]. FEBS Open Bio. 2021 ; 11( 9): 2541-2559.[citado 2024 set. 30 ] Available from: https://doi.org/10.1002/2211-5463.13253
    • Vancouver

      Riciluca KCT, Oliveira UC de, Mendonça RZ, Bozelli Junior JC, Schreier S, Silva Júnior PI da. Rondonin: antimicrobial properties and mechanism of action [Internet]. FEBS Open Bio. 2021 ; 11( 9): 2541-2559.[citado 2024 set. 30 ] Available from: https://doi.org/10.1002/2211-5463.13253
  • Source: Journal of Chemical Information and Modeling. Unidade: IQ

    Subjects: PEPTÍDEOS, PROTEÍNAS, BIOINFORMÁTICA, INIBIDORES DE ENZIMAS

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      MATOS, Isaac de Araújo e COSTA JÚNIOR, Nivan Bezerra da e MEOTTI, Flavia Carla. Integration of an inhibitor-like rule and structure-based virtual screening for the discovery of novel myeloperoxidase inhibitors. Journal of Chemical Information and Modeling, v. 60, p. 6408−6418, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.jcim.0c00813. Acesso em: 30 set. 2024.
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      Matos, I. de A., Costa Júnior, N. B. da, & Meotti, F. C. (2020). Integration of an inhibitor-like rule and structure-based virtual screening for the discovery of novel myeloperoxidase inhibitors. Journal of Chemical Information and Modeling, 60, 6408−6418. doi:10.1021/acs.jcim.0c00813
    • NLM

      Matos I de A, Costa Júnior NB da, Meotti FC. Integration of an inhibitor-like rule and structure-based virtual screening for the discovery of novel myeloperoxidase inhibitors [Internet]. Journal of Chemical Information and Modeling. 2020 ; 60 6408−6418.[citado 2024 set. 30 ] Available from: https://doi.org/10.1021/acs.jcim.0c00813
    • Vancouver

      Matos I de A, Costa Júnior NB da, Meotti FC. Integration of an inhibitor-like rule and structure-based virtual screening for the discovery of novel myeloperoxidase inhibitors [Internet]. Journal of Chemical Information and Modeling. 2020 ; 60 6408−6418.[citado 2024 set. 30 ] Available from: https://doi.org/10.1021/acs.jcim.0c00813
  • Source: Stem Cell Reviews and Reports. Unidades: FM, IQ

    Subjects: PEPTÍDEOS, MIOBLASTOS, MÚSCULO ESQUELÉTICO

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      ALVES, Janaina Maria et al. Kinin-B2 receptor activity in skeletal muscle regeneration and myoblast differentiation. Stem Cell Reviews and Reports, v. 15, n. 1, p. 48-58, 2019Tradução . . Disponível em: https://doi.org/10.1007/s12015-018-9850-9. Acesso em: 30 set. 2024.
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      Alves, J. M., Martins, A. H., Lameu, C., Glaser, T., Boukli, N. M., Bassaneze, V., et al. (2019). Kinin-B2 receptor activity in skeletal muscle regeneration and myoblast differentiation. Stem Cell Reviews and Reports, 15( 1), 48-58. doi:10.1007/s12015-018-9850-9
    • NLM

      Alves JM, Martins AH, Lameu C, Glaser T, Boukli NM, Bassaneze V, Dariolli R, Nascimento IC, Martins PCM, Souza HDN de, Krieger JE, Casarini DE, Sales VM, Pesquero JB, Ulrich H. Kinin-B2 receptor activity in skeletal muscle regeneration and myoblast differentiation [Internet]. Stem Cell Reviews and Reports. 2019 ; 15( 1): 48-58.[citado 2024 set. 30 ] Available from: https://doi.org/10.1007/s12015-018-9850-9
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      Alves JM, Martins AH, Lameu C, Glaser T, Boukli NM, Bassaneze V, Dariolli R, Nascimento IC, Martins PCM, Souza HDN de, Krieger JE, Casarini DE, Sales VM, Pesquero JB, Ulrich H. Kinin-B2 receptor activity in skeletal muscle regeneration and myoblast differentiation [Internet]. Stem Cell Reviews and Reports. 2019 ; 15( 1): 48-58.[citado 2024 set. 30 ] Available from: https://doi.org/10.1007/s12015-018-9850-9
  • Source: PLOS ONE. Unidade: IQ

    Subjects: PEPTÍDEOS, PROTEÍNAS

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      CARRETERO, Gustavo Penteado Battesine et al. Dissecting the mechanism of action of actinoporins. Role of the N-terminal amphipathic alpha-helix in membrane binding and pore activity of sticholysins I and II. PLOS ONE, v. 13, n. 8, p. 1-23 art. e0202981, 2018Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0202981. Acesso em: 30 set. 2024.
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      Carretero, G. P. B., Vicente, E. F., Cilli, E. M., Alvarez, C. M., Jenssen, H., & Schreier, S. (2018). Dissecting the mechanism of action of actinoporins. Role of the N-terminal amphipathic alpha-helix in membrane binding and pore activity of sticholysins I and II. PLOS ONE, 13( 8), 1-23 art. e0202981. doi:10.1371/journal.pone.0202981
    • NLM

      Carretero GPB, Vicente EF, Cilli EM, Alvarez CM, Jenssen H, Schreier S. Dissecting the mechanism of action of actinoporins. Role of the N-terminal amphipathic alpha-helix in membrane binding and pore activity of sticholysins I and II [Internet]. PLOS ONE. 2018 ; 13( 8): 1-23 art. e0202981.[citado 2024 set. 30 ] Available from: https://doi.org/10.1371/journal.pone.0202981
    • Vancouver

      Carretero GPB, Vicente EF, Cilli EM, Alvarez CM, Jenssen H, Schreier S. Dissecting the mechanism of action of actinoporins. Role of the N-terminal amphipathic alpha-helix in membrane binding and pore activity of sticholysins I and II [Internet]. PLOS ONE. 2018 ; 13( 8): 1-23 art. e0202981.[citado 2024 set. 30 ] Available from: https://doi.org/10.1371/journal.pone.0202981

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