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  • Source: Journal of Biological Chemistry. Unidade: IQ

    Subjects: METABOLISMO, MITOCÔNDRIAS

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      VILAS-BOAS, Eloisa Aparecida et al. Goldilocks calcium concentrations and the regulation of oxidative phosphorylation: too much, too little, or just right. Journal of Biological Chemistry, v. 299, p. 1-17 art. 102904, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.jbc.2023.102904. Acesso em: 08 out. 2024.
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      Vilas-Boas, E. A., Costa, J. V. C., Ramos, V. de M., Silva, C. C. C. da, & Kowaltowski, A. J. (2023). Goldilocks calcium concentrations and the regulation of oxidative phosphorylation: too much, too little, or just right. Journal of Biological Chemistry, 299, 1-17 art. 102904. doi:10.1016/j.jbc.2023.102904
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      Vilas-Boas EA, Costa JVC, Ramos V de M, Silva CCC da, Kowaltowski AJ. Goldilocks calcium concentrations and the regulation of oxidative phosphorylation: too much, too little, or just right [Internet]. Journal of Biological Chemistry. 2023 ; 299 1-17 art. 102904.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.jbc.2023.102904
    • Vancouver

      Vilas-Boas EA, Costa JVC, Ramos V de M, Silva CCC da, Kowaltowski AJ. Goldilocks calcium concentrations and the regulation of oxidative phosphorylation: too much, too little, or just right [Internet]. Journal of Biological Chemistry. 2023 ; 299 1-17 art. 102904.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.jbc.2023.102904
  • Source: Journal of Biological Chemistry. Unidade: IQ

    Subjects: AUTOIMUNIDADE, NEOPLASIAS

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      TUN, May Thwe et al. Macromolecular crowding amplifies allosteric regulation of T-cell protein tyrosine phosphatase. Journal of Biological Chemistry, v. 298 , n. 12, p. 1-11, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.jbc.2022.102655. Acesso em: 08 out. 2024.
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      Tun, M. T., Yang, S., Forti, F. L., Santelli, E., & Bottini, N. (2022). Macromolecular crowding amplifies allosteric regulation of T-cell protein tyrosine phosphatase. Journal of Biological Chemistry, 298 ( 12), 1-11. doi:10.1016/j.jbc.2022.102655
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      Tun MT, Yang S, Forti FL, Santelli E, Bottini N. Macromolecular crowding amplifies allosteric regulation of T-cell protein tyrosine phosphatase [Internet]. Journal of Biological Chemistry. 2022 ; 298 ( 12): 1-11.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.jbc.2022.102655
    • Vancouver

      Tun MT, Yang S, Forti FL, Santelli E, Bottini N. Macromolecular crowding amplifies allosteric regulation of T-cell protein tyrosine phosphatase [Internet]. Journal of Biological Chemistry. 2022 ; 298 ( 12): 1-11.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.jbc.2022.102655
  • Source: Journal of Biological Chemistry. Unidades: FM, ICB, IQ

    Subjects: MÚSCULO ESQUELÉTICO, SÓDIO, RESISTÊNCIA À INSULINA, LIPÍDEOS, CAMUNDONGOS, FISIOLOGIA

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      PINTO, Paula Ramos et al. Dietary sodium restriction alters muscle lipidomics that relates to insulin resistance in mice. Journal of Biological Chemistry, v. 296, p. 1-12 art. 100344, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.jbc.2021.100344. Acesso em: 08 out. 2024.
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      Pinto, P. R., Yoshinaga, M. Y., Bianco, V. D., Bochi, A. P. G., Ferreira, G. S., Pinto, I. F. D., et al. (2021). Dietary sodium restriction alters muscle lipidomics that relates to insulin resistance in mice. Journal of Biological Chemistry, 296, 1-12 art. 100344. doi:10.1016/j.jbc.2021.100344
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      Pinto PR, Yoshinaga MY, Bianco VD, Bochi APG, Ferreira GS, Pinto IFD, Rodrigues LG, Nakandakare ER, Okamoto MM, Machado UF, Miyamoto S, Catanozi S, Passarelli M. Dietary sodium restriction alters muscle lipidomics that relates to insulin resistance in mice [Internet]. Journal of Biological Chemistry. 2021 ; 296 1-12 art. 100344.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.jbc.2021.100344
    • Vancouver

      Pinto PR, Yoshinaga MY, Bianco VD, Bochi APG, Ferreira GS, Pinto IFD, Rodrigues LG, Nakandakare ER, Okamoto MM, Machado UF, Miyamoto S, Catanozi S, Passarelli M. Dietary sodium restriction alters muscle lipidomics that relates to insulin resistance in mice [Internet]. Journal of Biological Chemistry. 2021 ; 296 1-12 art. 100344.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.jbc.2021.100344
  • Source: Journal of Biological Chemistry. Unidade: IQ

    Subjects: CORONAVIRUS, COVID-19, ANTIVIRAIS

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      RUSSO, Lilian Cristina et al. The SARS-CoV-2 Nsp3 macrodomain reverses PARP9/DTX3L-dependent ADP-ribosylation induced by interferon signalling. Journal of Biological Chemistry, v. 297, n. 3, p. 1-14 art. 101041, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.jbc.2021.101041. Acesso em: 08 out. 2024.
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      Russo, L. C., Tomasin, R., Matos, I. de A., Manucci, A. C., Sowa, S. T., Dale, K., et al. (2021). The SARS-CoV-2 Nsp3 macrodomain reverses PARP9/DTX3L-dependent ADP-ribosylation induced by interferon signalling. Journal of Biological Chemistry, 297( 3), 1-14 art. 101041. doi:10.1016/j.jbc.2021.101041
    • NLM

      Russo LC, Tomasin R, Matos I de A, Manucci AC, Sowa ST, Dale K, Caldecott KW, Lehtiö L, Schechtman D, Meotti FC, Bruni-Cardoso A, Hoch NC. The SARS-CoV-2 Nsp3 macrodomain reverses PARP9/DTX3L-dependent ADP-ribosylation induced by interferon signalling [Internet]. Journal of Biological Chemistry. 2021 ; 297( 3): 1-14 art. 101041.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.jbc.2021.101041
    • Vancouver

      Russo LC, Tomasin R, Matos I de A, Manucci AC, Sowa ST, Dale K, Caldecott KW, Lehtiö L, Schechtman D, Meotti FC, Bruni-Cardoso A, Hoch NC. The SARS-CoV-2 Nsp3 macrodomain reverses PARP9/DTX3L-dependent ADP-ribosylation induced by interferon signalling [Internet]. Journal of Biological Chemistry. 2021 ; 297( 3): 1-14 art. 101041.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.jbc.2021.101041
  • Source: Journal of Biological Chemistry. Unidade: IQ

    Subjects: PERÓXIDO DE HIDROGÊNIO, CINÉTICA, PEROXIDASE

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      PESKIN, Alexander V et al. Modifying the resolving cysteine affects the structure and hydrogen peroxide reactivity of peroxiredoxin 2. Journal of Biological Chemistry, v. 296, p. 1-15, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.jbc.2021.100494. Acesso em: 08 out. 2024.
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      Peskin, A. V., Meotti, F. C., Kean, K. M., Göbl, C., Peixoto, A. S., Pace, P. E., et al. (2021). Modifying the resolving cysteine affects the structure and hydrogen peroxide reactivity of peroxiredoxin 2. Journal of Biological Chemistry, 296, 1-15. doi:10.1016/j.jbc.2021.100494
    • NLM

      Peskin AV, Meotti FC, Kean KM, Göbl C, Peixoto AS, Pace PE, Horne CR, Heath SG, Crowther JM, Dobson RCJ, Karplus PA, Winterbourn CC. Modifying the resolving cysteine affects the structure and hydrogen peroxide reactivity of peroxiredoxin 2 [Internet]. Journal of Biological Chemistry. 2021 ; 296 1-15.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.jbc.2021.100494
    • Vancouver

      Peskin AV, Meotti FC, Kean KM, Göbl C, Peixoto AS, Pace PE, Horne CR, Heath SG, Crowther JM, Dobson RCJ, Karplus PA, Winterbourn CC. Modifying the resolving cysteine affects the structure and hydrogen peroxide reactivity of peroxiredoxin 2 [Internet]. Journal of Biological Chemistry. 2021 ; 296 1-15.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.jbc.2021.100494
  • Source: Journal of Biological Chemistry. Unidades: IFSC, IQ, FFCLRP

    Subjects: BACTÉRIAS GRAM-POSITIVAS, LIPÍDEOS

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      SASTRE, Diego Emiliano et al. The phosphatidic acid pathway enzyme PlsX plays both catalytic and channeling roles in bacterial phospholipid synthesis. Journal of Biological Chemistry, v. 295, n. 7, p. 2148-2159 + Supplementary materials Figs. S1-S5 and Tables S1 and S2, 2020Tradução . . Disponível em: https://doi.org/10.1074/jbc.RA119.011147. Acesso em: 08 out. 2024.
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      Sastre, D. E., Pulschen, A. A., Basso, L. G. M., Pariente, J. S. B., Marques Netto, C. G. C., Machinandiarena, F., et al. (2020). The phosphatidic acid pathway enzyme PlsX plays both catalytic and channeling roles in bacterial phospholipid synthesis. Journal of Biological Chemistry, 295( 7), 2148-2159 + Supplementary materials Figs. S1-S5 and Tables S1 and S2. doi:10.1074/jbc.RA119.011147
    • NLM

      Sastre DE, Pulschen AA, Basso LGM, Pariente JSB, Marques Netto CGC, Machinandiarena F, Albanesi D, Navarro MV de AS, Mendoza D de, Gueiros Filho FJ. The phosphatidic acid pathway enzyme PlsX plays both catalytic and channeling roles in bacterial phospholipid synthesis [Internet]. Journal of Biological Chemistry. 2020 ; 295( 7): 2148-2159 + Supplementary materials Figs. S1-S5 and Tables S1 and S2.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.RA119.011147
    • Vancouver

      Sastre DE, Pulschen AA, Basso LGM, Pariente JSB, Marques Netto CGC, Machinandiarena F, Albanesi D, Navarro MV de AS, Mendoza D de, Gueiros Filho FJ. The phosphatidic acid pathway enzyme PlsX plays both catalytic and channeling roles in bacterial phospholipid synthesis [Internet]. Journal of Biological Chemistry. 2020 ; 295( 7): 2148-2159 + Supplementary materials Figs. S1-S5 and Tables S1 and S2.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.RA119.011147
  • Source: Journal of Biological Chemistry. Unidade: IQ

    Subjects: RNA, PROTEÍNAS NUCLEARES

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      OKUDA, Ellen Kazumi et al. Nucleolar localization of the yeast RNA exosome subunit Rrp44 hints at early pre-rRNA processing as its main function. Journal of Biological Chemistry, v. 295, n. 32, p. 11195-11213, 2020Tradução . . Disponível em: https://doi.org/10.1074/jbc.RA120.013589. Acesso em: 08 out. 2024.
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      Okuda, E. K., Zubiate, F. A. G., Gadal, O., & Oliveira, C. C. de. (2020). Nucleolar localization of the yeast RNA exosome subunit Rrp44 hints at early pre-rRNA processing as its main function. Journal of Biological Chemistry, 295( 32), 11195-11213. doi:10.1074/jbc.RA120.013589
    • NLM

      Okuda EK, Zubiate FAG, Gadal O, Oliveira CC de. Nucleolar localization of the yeast RNA exosome subunit Rrp44 hints at early pre-rRNA processing as its main function [Internet]. Journal of Biological Chemistry. 2020 ; 295( 32): 11195-11213.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.RA120.013589
    • Vancouver

      Okuda EK, Zubiate FAG, Gadal O, Oliveira CC de. Nucleolar localization of the yeast RNA exosome subunit Rrp44 hints at early pre-rRNA processing as its main function [Internet]. Journal of Biological Chemistry. 2020 ; 295( 32): 11195-11213.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.RA120.013589
  • Source: Journal of Biological Chemistry. Unidades: IQ, IFSC, FFCLRP

    Subjects: FOSFOLIPÍDEOS, LIPÍDEOS

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      SASTRE, Diego Emiliano et al. Membrane fluidity adjusts the insertion of the transacylase PlsX to regulate phospholipid biosynthesis in Gram-positive bacteria. Journal of Biological Chemistry, v. 295, n. 7, p. 2136-2147 + Supplementary materials Figs. S1-S9, 2020Tradução . . Disponível em: https://doi.org/10.1074/jbc.RA119.011122. Acesso em: 08 out. 2024.
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      Sastre, D. E., Basso, L. G. M., Trastoy, B., Cifuente, J. O., Contreras, X., Gueiros Filho, F. J., et al. (2020). Membrane fluidity adjusts the insertion of the transacylase PlsX to regulate phospholipid biosynthesis in Gram-positive bacteria. Journal of Biological Chemistry, 295( 7), 2136-2147 + Supplementary materials Figs. S1-S9. doi:10.1074/jbc.RA119.011122
    • NLM

      Sastre DE, Basso LGM, Trastoy B, Cifuente JO, Contreras X, Gueiros Filho FJ, Mendoza D de, Navarro MV de AS, Guerin ME. Membrane fluidity adjusts the insertion of the transacylase PlsX to regulate phospholipid biosynthesis in Gram-positive bacteria [Internet]. Journal of Biological Chemistry. 2020 ; 295( 7): 2136-2147 + Supplementary materials Figs. S1-S9.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.RA119.011122
    • Vancouver

      Sastre DE, Basso LGM, Trastoy B, Cifuente JO, Contreras X, Gueiros Filho FJ, Mendoza D de, Navarro MV de AS, Guerin ME. Membrane fluidity adjusts the insertion of the transacylase PlsX to regulate phospholipid biosynthesis in Gram-positive bacteria [Internet]. Journal of Biological Chemistry. 2020 ; 295( 7): 2136-2147 + Supplementary materials Figs. S1-S9.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.RA119.011122
  • Source: Journal of Biological Chemistry. Unidades: IQ, IB

    Subjects: DIÓXIDO DE CARBONO, PEROXIDASE

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      TRUZZI, Daniela Ramos et al. The bicarbonate/carbon dioxide pair increases hydrogen peroxide−mediated hyperoxidation of human peroxiredoxin 1. Journal of Biological Chemistry, v. 294, n. 38, p. 14055-14067 :+Supplementary materials (S1-19), 2019Tradução . . Disponível em: https://doi.org/10.1074/jbc.RA119.008825. Acesso em: 08 out. 2024.
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      Truzzi, D. R., Coelho, F. R., Paviani, V., Alves, S. V., Netto, L. E. S., & Augusto, O. (2019). The bicarbonate/carbon dioxide pair increases hydrogen peroxide−mediated hyperoxidation of human peroxiredoxin 1. Journal of Biological Chemistry, 294( 38), 14055-14067 :+Supplementary materials (S1-19). doi:10.1074/jbc.RA119.008825
    • NLM

      Truzzi DR, Coelho FR, Paviani V, Alves SV, Netto LES, Augusto O. The bicarbonate/carbon dioxide pair increases hydrogen peroxide−mediated hyperoxidation of human peroxiredoxin 1 [Internet]. Journal of Biological Chemistry. 2019 ; 294( 38): 14055-14067 :+Supplementary materials (S1-19).[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.RA119.008825
    • Vancouver

      Truzzi DR, Coelho FR, Paviani V, Alves SV, Netto LES, Augusto O. The bicarbonate/carbon dioxide pair increases hydrogen peroxide−mediated hyperoxidation of human peroxiredoxin 1 [Internet]. Journal of Biological Chemistry. 2019 ; 294( 38): 14055-14067 :+Supplementary materials (S1-19).[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.RA119.008825
  • Source: Journal of Biological Chemistry. Unidade: IQ

    Subjects: CÁLCIO, PROTEINASES, PROLIFERAÇÃO CELULAR

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      MIRANDA, Marcelo Coutinho et al. Epidermal growth factor (EGF) triggers nuclear calcium signaling through the intranuclear phospholipase C delta-4 (PLCδ4). Journal of Biological Chemistry, v. 294, n. 45, p. 16650-16662, 2019Tradução . . Disponível em: https://doi.org/10.1074/jbc.RA118.006961. Acesso em: 08 out. 2024.
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      Miranda, M. C., Rodrigues, M. A., Campos, A. C. de A., Faria, J. A. Q. A., Lima, M. K., Mignery, G. A., et al. (2019). Epidermal growth factor (EGF) triggers nuclear calcium signaling through the intranuclear phospholipase C delta-4 (PLCδ4). Journal of Biological Chemistry, 294( 45), 16650-16662. doi:10.1074/jbc.RA118.006961
    • NLM

      Miranda MC, Rodrigues MA, Campos AC de A, Faria JAQA, Lima MK, Mignery GA, Schechtman D, Goes AM, Nathanson MH, Gomes DA. Epidermal growth factor (EGF) triggers nuclear calcium signaling through the intranuclear phospholipase C delta-4 (PLCδ4) [Internet]. Journal of Biological Chemistry. 2019 ; 294( 45): 16650-16662.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.RA118.006961
    • Vancouver

      Miranda MC, Rodrigues MA, Campos AC de A, Faria JAQA, Lima MK, Mignery GA, Schechtman D, Goes AM, Nathanson MH, Gomes DA. Epidermal growth factor (EGF) triggers nuclear calcium signaling through the intranuclear phospholipase C delta-4 (PLCδ4) [Internet]. Journal of Biological Chemistry. 2019 ; 294( 45): 16650-16662.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.RA118.006961
  • Source: Journal of Biological Chemistry. Unidades: IQ, FFCLRP

    Subjects: ÓXIDO NÍTRICO, ESTRESSE OXIDATIVO

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      DAMASCENO, Fernando Cruvinel et al. The labile iron pool attenuates peroxynitrite-dependent damage and can no longer be considered solely a pro-oxidative cellular iron source. Journal of Biological Chemistry, v. 293, p. 8530-8542 : + Supplementary materials ( S1-S13), 2018Tradução . . Disponível em: https://doi.org/10.1074/jbc.RA117.000883. Acesso em: 08 out. 2024.
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      Damasceno, F. C., Condeles, A. L., Lopes, A. K. B., Facci, R. R., Linares, E., Truzzi, D. R., et al. (2018). The labile iron pool attenuates peroxynitrite-dependent damage and can no longer be considered solely a pro-oxidative cellular iron source. Journal of Biological Chemistry, 293, 8530-8542 : + Supplementary materials ( S1-S13). doi:10.1074/jbc.RA117.000883
    • NLM

      Damasceno FC, Condeles AL, Lopes AKB, Facci RR, Linares E, Truzzi DR, Augusto O, Toledo Junior JC. The labile iron pool attenuates peroxynitrite-dependent damage and can no longer be considered solely a pro-oxidative cellular iron source [Internet]. Journal of Biological Chemistry. 2018 ; 293 8530-8542 : + Supplementary materials ( S1-S13).[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.RA117.000883
    • Vancouver

      Damasceno FC, Condeles AL, Lopes AKB, Facci RR, Linares E, Truzzi DR, Augusto O, Toledo Junior JC. The labile iron pool attenuates peroxynitrite-dependent damage and can no longer be considered solely a pro-oxidative cellular iron source [Internet]. Journal of Biological Chemistry. 2018 ; 293 8530-8542 : + Supplementary materials ( S1-S13).[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.RA117.000883
  • Source: Journal of Biological Chemistry. Unidades: ICB, IQ

    Subjects: XANTHOMONAS, FITOPATÓGENOS, TRANSDUÇÃO DE SINAL CELULAR

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      TEIXEIRA, Raphael Dias et al. A bipartite periplasmic receptor–diguanylate cyclase pair (XAC2383–XAC2382) in the bacterium Xanthomonas citri. Journal of Biological Chemistry, v. 293, n. 2, p. 10767–10781, 2018Tradução . . Disponível em: https://doi.org/10.1074/jbc.RA118.003475. Acesso em: 08 out. 2024.
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      Teixeira, R. D., Carvalho, C. R. G., Arévalo, S. J., Andrade, M. O., Abrahão, J., Souza, R. F. de, & Farah, C. S. (2018). A bipartite periplasmic receptor–diguanylate cyclase pair (XAC2383–XAC2382) in the bacterium Xanthomonas citri. Journal of Biological Chemistry, 293( 2), 10767–10781. doi:10.1074/jbc.RA118.003475
    • NLM

      Teixeira RD, Carvalho CRG, Arévalo SJ, Andrade MO, Abrahão J, Souza RF de, Farah CS. A bipartite periplasmic receptor–diguanylate cyclase pair (XAC2383–XAC2382) in the bacterium Xanthomonas citri [Internet]. Journal of Biological Chemistry. 2018 ; 293( 2): 10767–10781.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.RA118.003475
    • Vancouver

      Teixeira RD, Carvalho CRG, Arévalo SJ, Andrade MO, Abrahão J, Souza RF de, Farah CS. A bipartite periplasmic receptor–diguanylate cyclase pair (XAC2383–XAC2382) in the bacterium Xanthomonas citri [Internet]. Journal of Biological Chemistry. 2018 ; 293( 2): 10767–10781.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.RA118.003475
  • Source: Journal of Biological Chemistry. Unidade: IQ

    Subjects: PERÓXIDO DE HIDROGÊNIO, CINÉTICA

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      PEIXOTO, Álbert Souza et al. Peroxynitrite preferentially oxidizes the dithiol redox motifs of protein disulfide isomerase. Journal of Biological Chemistry, v. 293, n. 4, p. 1450-1465, 2018Tradução . . Disponível em: http://www.jbc.org/content/early/2017/11/30/jbc.M117.807016. Acesso em: 08 out. 2024.
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      Peixoto, Á. S., Geyer, R. R., Iqbal, A., Truzzi, D. R., Moretti, A. I. S., Laurindo, F. R. M., & Augusto, O. (2018). Peroxynitrite preferentially oxidizes the dithiol redox motifs of protein disulfide isomerase. Journal of Biological Chemistry, 293( 4), 1450-1465. doi:10.1074/jbc.M117.807016
    • NLM

      Peixoto ÁS, Geyer RR, Iqbal A, Truzzi DR, Moretti AIS, Laurindo FRM, Augusto O. Peroxynitrite preferentially oxidizes the dithiol redox motifs of protein disulfide isomerase [Internet]. Journal of Biological Chemistry. 2018 ; 293( 4): 1450-1465.[citado 2024 out. 08 ] Available from: http://www.jbc.org/content/early/2017/11/30/jbc.M117.807016
    • Vancouver

      Peixoto ÁS, Geyer RR, Iqbal A, Truzzi DR, Moretti AIS, Laurindo FRM, Augusto O. Peroxynitrite preferentially oxidizes the dithiol redox motifs of protein disulfide isomerase [Internet]. Journal of Biological Chemistry. 2018 ; 293( 4): 1450-1465.[citado 2024 out. 08 ] Available from: http://www.jbc.org/content/early/2017/11/30/jbc.M117.807016
  • Source: Journal of Biological Chemistry. Unidade: IQ

    Subjects: CICLO CELULAR, ESPECTROMETRIA DE MASSAS, RNA RIBOSSÔMICO

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      ZUBIATE, Fernando Alexis Gonzales et al. Identification of karyopherins involved in the nuclear import of RNA exosome subunit Rrp6 in Saccharomyces cerevisiae. Journal of Biological Chemistry, v. 292, n. 29, p. 12267-12384, 2017Tradução . . Disponível em: https://doi.org/10.1074/jbc.M116.772376. Acesso em: 08 out. 2024.
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      Zubiate, F. A. G., Okuda, E. K., Cunha, J. P. C. da, & Oliveira, C. C. de. (2017). Identification of karyopherins involved in the nuclear import of RNA exosome subunit Rrp6 in Saccharomyces cerevisiae. Journal of Biological Chemistry, 292( 29), 12267-12384. doi:10.1074/jbc.M116.772376
    • NLM

      Zubiate FAG, Okuda EK, Cunha JPC da, Oliveira CC de. Identification of karyopherins involved in the nuclear import of RNA exosome subunit Rrp6 in Saccharomyces cerevisiae [Internet]. Journal of Biological Chemistry. 2017 ; 292( 29): 12267-12384.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.M116.772376
    • Vancouver

      Zubiate FAG, Okuda EK, Cunha JPC da, Oliveira CC de. Identification of karyopherins involved in the nuclear import of RNA exosome subunit Rrp6 in Saccharomyces cerevisiae [Internet]. Journal of Biological Chemistry. 2017 ; 292( 29): 12267-12384.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.M116.772376
  • Source: Journal of Biological Chemistry. Unidades: IB, FFCLRP, IQ

    Subjects: PERÓXIDO DE HIDROGÊNIO, INFLAMAÇÃO, ÁCIDO ÚRICO, OXIDAÇÃO

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    • ABNT

      CARVALHO, Larissa Anastácio da Costa et al. Urate hydroperoxide oxidizes human peroxiredoxin 1 and peroxiredoxin 2. Journal of Biological Chemistry, v. 292, n. 21, p. 8705-8715, 2017Tradução . . Disponível em: https://doi.org/10.1074/jbc.M116.767657. Acesso em: 08 out. 2024.
    • APA

      Carvalho, L. A. da C., Truzzi, D. R., Fallani, T. S., Alves, S. V., Toledo Junior, J. C., Augusto, O., et al. (2017). Urate hydroperoxide oxidizes human peroxiredoxin 1 and peroxiredoxin 2. Journal of Biological Chemistry, 292( 21), 8705-8715. doi:10.1074/jbc.M116.767657
    • NLM

      Carvalho LA da C, Truzzi DR, Fallani TS, Alves SV, Toledo Junior JC, Augusto O, Netto LES, Meotti FC. Urate hydroperoxide oxidizes human peroxiredoxin 1 and peroxiredoxin 2 [Internet]. Journal of Biological Chemistry. 2017 ; 292( 21): 8705-8715.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.M116.767657
    • Vancouver

      Carvalho LA da C, Truzzi DR, Fallani TS, Alves SV, Toledo Junior JC, Augusto O, Netto LES, Meotti FC. Urate hydroperoxide oxidizes human peroxiredoxin 1 and peroxiredoxin 2 [Internet]. Journal of Biological Chemistry. 2017 ; 292( 21): 8705-8715.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.M116.767657
  • Source: Journal of Biological Chemistry. Unidades: ICB, IQ

    Subjects: FENÓTIPOS, OLIGOPEPTÍDEOS

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    • ABNT

      CAVALCANTI, Diogo Manuel Lopes de Paiva et al. Neurolysin knockout mice generation and initial phenotype characterization. Journal of Biological Chemistry, v. 289, n. 22, p. 15426-15440, 2014Tradução . . Disponível em: https://doi.org/10.1074/jbc.M113.539148. Acesso em: 08 out. 2024.
    • APA

      Cavalcanti, D. M. L. de P., Castro, L. M. de, Rosa Neto, J. C., Seelaender, M. C. L., Neves, R. X. das, Oliveira, V., et al. (2014). Neurolysin knockout mice generation and initial phenotype characterization. Journal of Biological Chemistry, 289( 22), 15426-15440. doi:10.1074/jbc.M113.539148
    • NLM

      Cavalcanti DML de P, Castro LM de, Rosa Neto JC, Seelaender MCL, Neves RX das, Oliveira V, Forti FL, Iwai LK, Gozzo FC, Todiras M, Schadock I, Barros CC, Bader M, Ferro ES. Neurolysin knockout mice generation and initial phenotype characterization [Internet]. Journal of Biological Chemistry. 2014 ; 289( 22): 15426-15440.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.M113.539148
    • Vancouver

      Cavalcanti DML de P, Castro LM de, Rosa Neto JC, Seelaender MCL, Neves RX das, Oliveira V, Forti FL, Iwai LK, Gozzo FC, Todiras M, Schadock I, Barros CC, Bader M, Ferro ES. Neurolysin knockout mice generation and initial phenotype characterization [Internet]. Journal of Biological Chemistry. 2014 ; 289( 22): 15426-15440.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.M113.539148
  • Source: Journal of Biological Chemistry. Unidade: IQ

    Subjects: PROTEÍNAS QUINASES, GENES SUPRESSORES

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    • ABNT

      DAN, Han C et al. Akt-dependent activation of mTORC1 complex involves phosphorylation of mTOR (Mammalian target of rapamycin) by IκB Kinase α (IKK α). Journal of Biological Chemistry, v. 289, n. 36, p. 25227-25240, 2014Tradução . . Disponível em: https://doi.org/10.1074/jbc.M114.554881. Acesso em: 08 out. 2024.
    • APA

      Dan, H. C., Ebbs, A., Pasparakis, M., Dyke, T. V., Bassères, D. S., & Baldwin, A. S. (2014). Akt-dependent activation of mTORC1 complex involves phosphorylation of mTOR (Mammalian target of rapamycin) by IκB Kinase α (IKK α). Journal of Biological Chemistry, 289( 36), 25227-25240. doi:10.1074/jbc.M114.554881
    • NLM

      Dan HC, Ebbs A, Pasparakis M, Dyke TV, Bassères DS, Baldwin AS. Akt-dependent activation of mTORC1 complex involves phosphorylation of mTOR (Mammalian target of rapamycin) by IκB Kinase α (IKK α) [Internet]. Journal of Biological Chemistry. 2014 ; 289( 36): 25227-25240.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.M114.554881
    • Vancouver

      Dan HC, Ebbs A, Pasparakis M, Dyke TV, Bassères DS, Baldwin AS. Akt-dependent activation of mTORC1 complex involves phosphorylation of mTOR (Mammalian target of rapamycin) by IκB Kinase α (IKK α) [Internet]. Journal of Biological Chemistry. 2014 ; 289( 36): 25227-25240.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.M114.554881
  • Source: Journal of Biological Chemistry. Unidades: ICB, IQ

    Subjects: PEPTÍDEOS, METABOLISMO DE PROTEÍNA

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    • ABNT

      ARAUJO, Christiane Bezerra de et al. A novel intracellular peptide derived from `G IND. 1´/S cyclin D2 induces cell death. Journal of Biological Chemistry, v. 289, n. 24, p. 16711-16726, 2014Tradução . . Disponível em: https://doi.org/10.1074/jbc.M113.537118. Acesso em: 08 out. 2024.
    • APA

      Araujo, C. B. de, Russo, L. C., Castro, L. M. de, Forti, F. L., Monte, E. R. do, Rioli, V., et al. (2014). A novel intracellular peptide derived from `G IND. 1´/S cyclin D2 induces cell death. Journal of Biological Chemistry, 289( 24), 16711-16726. doi:10.1074/jbc.M113.537118
    • NLM

      Araujo CB de, Russo LC, Castro LM de, Forti FL, Monte ER do, Rioli V, Gozzo FC, Colquhoun A, Ferro ES. A novel intracellular peptide derived from `G IND. 1´/S cyclin D2 induces cell death [Internet]. Journal of Biological Chemistry. 2014 ; 289( 24): 16711-16726.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.M113.537118
    • Vancouver

      Araujo CB de, Russo LC, Castro LM de, Forti FL, Monte ER do, Rioli V, Gozzo FC, Colquhoun A, Ferro ES. A novel intracellular peptide derived from `G IND. 1´/S cyclin D2 induces cell death [Internet]. Journal of Biological Chemistry. 2014 ; 289( 24): 16711-16726.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.M113.537118
  • Source: Journal of Biological Chemistry. Unidade: IQ

    Subjects: FIBRONECTINAS, LEPTOSPIROSE

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    • ABNT

      HAUK, Pricila et al. Calcium binding to Leptospira outer membrane antigen LipL32 is not necessary for its interaction with plasma fibronectin, collagen type IV, and plasminogen. Journal of Biological Chemistry, v. 287, n. 7, p. 4826-4834 : + Supplementary materials ( S1-S7), 2012Tradução . . Disponível em: https://doi.org/10.1074/jbc.M111.277210. Acesso em: 08 out. 2024.
    • APA

      Hauk, P., Barbosa, A. S., Ho, P. L., & Farah, C. S. (2012). Calcium binding to Leptospira outer membrane antigen LipL32 is not necessary for its interaction with plasma fibronectin, collagen type IV, and plasminogen. Journal of Biological Chemistry, 287( 7), 4826-4834 : + Supplementary materials ( S1-S7). doi:10.1074/jbc.M111.277210
    • NLM

      Hauk P, Barbosa AS, Ho PL, Farah CS. Calcium binding to Leptospira outer membrane antigen LipL32 is not necessary for its interaction with plasma fibronectin, collagen type IV, and plasminogen [Internet]. Journal of Biological Chemistry. 2012 ; 287( 7): 4826-4834 : + Supplementary materials ( S1-S7).[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.M111.277210
    • Vancouver

      Hauk P, Barbosa AS, Ho PL, Farah CS. Calcium binding to Leptospira outer membrane antigen LipL32 is not necessary for its interaction with plasma fibronectin, collagen type IV, and plasminogen [Internet]. Journal of Biological Chemistry. 2012 ; 287( 7): 4826-4834 : + Supplementary materials ( S1-S7).[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.M111.277210
  • Source: Journal of Biological Chemistry. Unidades: ICB, IQ

    Assunto: HISTOLOGIA

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    • ABNT

      TRUJILLO, Cleber A. et al. Kinin-B2 receptor activity determines the differentiation fate of neural stem cells. Journal of Biological Chemistry, v. 287, n. 53, p. 44046-44061, 2012Tradução . . Disponível em: https://doi.org/10.1074/jbc.M112.407197. Acesso em: 08 out. 2024.
    • APA

      Trujillo, C. A., Negraes, P. D., Schwindit, T. T., Lameu, C., Carromeu, C., Muotri, A. R., et al. (2012). Kinin-B2 receptor activity determines the differentiation fate of neural stem cells. Journal of Biological Chemistry, 287( 53), 44046-44061. doi:10.1074/jbc.M112.407197
    • NLM

      Trujillo CA, Negraes PD, Schwindit TT, Lameu C, Carromeu C, Muotri AR, Pesquero JB, Cerqueira DM, Pillat MM, Souza HDN, Turaça LT, Abreu JG, Ulrich H. Kinin-B2 receptor activity determines the differentiation fate of neural stem cells [Internet]. Journal of Biological Chemistry. 2012 ; 287( 53): 44046-44061.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.M112.407197
    • Vancouver

      Trujillo CA, Negraes PD, Schwindit TT, Lameu C, Carromeu C, Muotri AR, Pesquero JB, Cerqueira DM, Pillat MM, Souza HDN, Turaça LT, Abreu JG, Ulrich H. Kinin-B2 receptor activity determines the differentiation fate of neural stem cells [Internet]. Journal of Biological Chemistry. 2012 ; 287( 53): 44046-44061.[citado 2024 out. 08 ] Available from: https://doi.org/10.1074/jbc.M112.407197

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