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  • Source: International journal of biological macromolecules. Unidade: EEL

    Subjects: BIOQUÍMICA, BIOTECNOLOGIA, BIOLOGIA MOLECULAR

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      CHAVES, Bruno Las Casas e ARANTES, Valdeir. Endoglucanase pretreatment aids in isolating tailored-cellulose nanofibrils combining energy saving and high-performance packaging. International journal of biological macromolecules, v. 242, n. art. 125057, p. 1-15, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.ijbiomac.2023.125057. Acesso em: 04 nov. 2024.
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      Chaves, B. L. C., & Arantes, V. (2023). Endoglucanase pretreatment aids in isolating tailored-cellulose nanofibrils combining energy saving and high-performance packaging. International journal of biological macromolecules, 242( art. 125057), 1-15. doi:10.1016/j.ijbiomac.2023.125057
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      Chaves BLC, Arantes V. Endoglucanase pretreatment aids in isolating tailored-cellulose nanofibrils combining energy saving and high-performance packaging [Internet]. International journal of biological macromolecules. 2023 ;242( art. 125057): 1-15.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.ijbiomac.2023.125057
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      Chaves BLC, Arantes V. Endoglucanase pretreatment aids in isolating tailored-cellulose nanofibrils combining energy saving and high-performance packaging [Internet]. International journal of biological macromolecules. 2023 ;242( art. 125057): 1-15.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.ijbiomac.2023.125057
  • Source: eLife. Unidade: FMRP

    Subjects: ATAXIA ANIMAL, DANO AO DNA, BIOQUÍMICA, BIOLOGIA DO DESENVOLVIMENTO, MEIOSE

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      SIMS, Jennie R et al. Phosphoproteomics of ATR signaling in mouse testes. eLife, v. 11, 2022Tradução . . Disponível em: https://doi.org/10.7554/eLife.68648. Acesso em: 04 nov. 2024.
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      Sims, J. R., Faça, V. M., Pereira, C., Ascenção, C., Comstock, W., Badar, J., et al. (2022). Phosphoproteomics of ATR signaling in mouse testes. eLife, 11. doi:10.7554/eLife.68648
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      Sims JR, Faça VM, Pereira C, Ascenção C, Comstock W, Badar J, Arroyo-Martinez GA, Freire R, Cohen PE, Weiss RS, Smolka MB. Phosphoproteomics of ATR signaling in mouse testes [Internet]. eLife. 2022 ; 11[citado 2024 nov. 04 ] Available from: https://doi.org/10.7554/eLife.68648
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      Sims JR, Faça VM, Pereira C, Ascenção C, Comstock W, Badar J, Arroyo-Martinez GA, Freire R, Cohen PE, Weiss RS, Smolka MB. Phosphoproteomics of ATR signaling in mouse testes [Internet]. eLife. 2022 ; 11[citado 2024 nov. 04 ] Available from: https://doi.org/10.7554/eLife.68648
  • Source: Pharmacological Reports. Unidade: FMVZ

    Subjects: ANÁLISE TOXICOLÓGICA, ANTIDEPRESSIVOS, BIOQUÍMICA, NEUROQUÍMICA

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      ZACCARELLI‐MAGALHÃES, Julia et al. Preclinical toxicological study of prolonged exposure to ketamine as an antidepressant. Pharmacological Reports, v. 72, p. 24-35, 2020Tradução . . Disponível em: https://doi.org/10.1007/s43440-019-00014-z. Acesso em: 04 nov. 2024.
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      Zaccarelli‐Magalhães, J., Fukushima, A. R., Moreira, N., Manes, M., Abreu, G. R. de, Ricci, E. L., et al. (2020). Preclinical toxicological study of prolonged exposure to ketamine as an antidepressant. Pharmacological Reports, 72, 24-35. doi:10.1007/s43440-019-00014-z
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      Zaccarelli‐Magalhães J, Fukushima AR, Moreira N, Manes M, Abreu GR de, Ricci EL, Waziry PAF, Spinosa H de S. Preclinical toxicological study of prolonged exposure to ketamine as an antidepressant [Internet]. Pharmacological Reports. 2020 ; 72 24-35.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s43440-019-00014-z
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      Zaccarelli‐Magalhães J, Fukushima AR, Moreira N, Manes M, Abreu GR de, Ricci EL, Waziry PAF, Spinosa H de S. Preclinical toxicological study of prolonged exposure to ketamine as an antidepressant [Internet]. Pharmacological Reports. 2020 ; 72 24-35.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s43440-019-00014-z
  • Source: International Journal of Molecular Sciences. Unidade: FFCLRP

    Subjects: BIOMINERALIZAÇÃO, PROTEÍNAS, OSSO E OSSOS, BIOQUÍMICA, LIPÍDEOS, GENES

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      VESCHI, Ekeveliny Amabile et al. Localization of annexin A6 in matrix vesicles during physiological mineralization. International Journal of Molecular Sciences, v. 21, n. 4, p. 1-16, 2020Tradução . . Disponível em: https://doi.org/10.3390/ijms21041367. Acesso em: 04 nov. 2024.
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      Veschi, E. A., Correia, M. B., Strzelecka-Kiliszek, A., Bandorowicz-Pikula, J., Pikula, S., Granjon, T., et al. (2020). Localization of annexin A6 in matrix vesicles during physiological mineralization. International Journal of Molecular Sciences, 21( 4), 1-16. doi:10.3390/ijms21041367
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      Veschi EA, Correia MB, Strzelecka-Kiliszek A, Bandorowicz-Pikula J, Pikula S, Granjon T, Mebarek S, Magne D, Ramos AP, Rosato N, Millán JL, Buchet R, Bottini M, Ciancaglini P. Localization of annexin A6 in matrix vesicles during physiological mineralization [Internet]. International Journal of Molecular Sciences. 2020 ; 21( 4): 1-16.[citado 2024 nov. 04 ] Available from: https://doi.org/10.3390/ijms21041367
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      Veschi EA, Correia MB, Strzelecka-Kiliszek A, Bandorowicz-Pikula J, Pikula S, Granjon T, Mebarek S, Magne D, Ramos AP, Rosato N, Millán JL, Buchet R, Bottini M, Ciancaglini P. Localization of annexin A6 in matrix vesicles during physiological mineralization [Internet]. International Journal of Molecular Sciences. 2020 ; 21( 4): 1-16.[citado 2024 nov. 04 ] Available from: https://doi.org/10.3390/ijms21041367
  • Source: International Journal of Biological Macromolecules. Unidade: IQSC

    Subjects: BIOQUÍMICA, BIOLOGIA MOLECULAR, PROTEÍNAS

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      KIRALY, Vanessa T. R et al. Thermal aggregates of human mortalin and Hsp70-1A behave as supramolecular assemblies. International Journal of Biological Macromolecules, v. 146, p. 320-331, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.ijbiomac.2019.12.236. Acesso em: 04 nov. 2024.
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      Kiraly, V. T. R., Dores-Silva, P. R., Serrão, V. H. B., Cauvi, D. M., De Maio, A., & Borges, J. C. (2020). Thermal aggregates of human mortalin and Hsp70-1A behave as supramolecular assemblies. International Journal of Biological Macromolecules, 146, 320-331. doi:10.1016/j.ijbiomac.2019.12.236
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      Kiraly VTR, Dores-Silva PR, Serrão VHB, Cauvi DM, De Maio A, Borges JC. Thermal aggregates of human mortalin and Hsp70-1A behave as supramolecular assemblies [Internet]. International Journal of Biological Macromolecules. 2020 ;146 320-331.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.ijbiomac.2019.12.236
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      Kiraly VTR, Dores-Silva PR, Serrão VHB, Cauvi DM, De Maio A, Borges JC. Thermal aggregates of human mortalin and Hsp70-1A behave as supramolecular assemblies [Internet]. International Journal of Biological Macromolecules. 2020 ;146 320-331.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.ijbiomac.2019.12.236
  • Source: Preparative Biochemistry and Biotechnology. Unidade: FCFRP

    Subjects: BIOTECNOLOGIA, ESPECTROMETRIA DE MASSAS, BIOQUÍMICA, CROMATOGRAFIA A GÁS, FUNGOS

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      COITINHO, Luciana Barbosa et al. Lapachol biotransformation by filamentous fungi yields bioactive quinone derivatives and lapachol-stimulated secondary metabolites. Preparative Biochemistry and Biotechnology, v. 49, n. 5, p. 459-463, 2019Tradução . . Disponível em: https://doi.org/10.1080/10826068.2019.1591991. Acesso em: 04 nov. 2024.
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      Coitinho, L. B., Fumagalli, F., Rosa-Garzon, N. G. da, Emery, F. da S., & Cabral, H. (2019). Lapachol biotransformation by filamentous fungi yields bioactive quinone derivatives and lapachol-stimulated secondary metabolites. Preparative Biochemistry and Biotechnology, 49( 5), 459-463. doi:10.1080/10826068.2019.1591991
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      Coitinho LB, Fumagalli F, Rosa-Garzon NG da, Emery F da S, Cabral H. Lapachol biotransformation by filamentous fungi yields bioactive quinone derivatives and lapachol-stimulated secondary metabolites [Internet]. Preparative Biochemistry and Biotechnology. 2019 ; 49( 5): 459-463.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1080/10826068.2019.1591991
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      Coitinho LB, Fumagalli F, Rosa-Garzon NG da, Emery F da S, Cabral H. Lapachol biotransformation by filamentous fungi yields bioactive quinone derivatives and lapachol-stimulated secondary metabolites [Internet]. Preparative Biochemistry and Biotechnology. 2019 ; 49( 5): 459-463.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1080/10826068.2019.1591991
  • Source: Journal of Neurochemistry. Unidade: EEFERP

    Subjects: CÉREBRO, BIOQUÍMICA, NEUROQUÍMICA

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      FRANCISCO, Annelise et al. Nicotinamide nucleotide transhydrogenase is required for brain mitochondrial redox balance under hampered energy substrate metabolism and high‐fat diet. Journal of Neurochemistry, v. 147, n. 5, p. 663-677, 2018Tradução . . Disponível em: https://doi.org/10.1111/jnc.14602. Acesso em: 04 nov. 2024.
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      Francisco, A., Ronchi, J. A., Navarro, C. D. C., Figueira, T. R., & Castilho, R. F. (2018). Nicotinamide nucleotide transhydrogenase is required for brain mitochondrial redox balance under hampered energy substrate metabolism and high‐fat diet. Journal of Neurochemistry, 147( 5), 663-677. doi:10.1111/jnc.14602
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      Francisco A, Ronchi JA, Navarro CDC, Figueira TR, Castilho RF. Nicotinamide nucleotide transhydrogenase is required for brain mitochondrial redox balance under hampered energy substrate metabolism and high‐fat diet [Internet]. Journal of Neurochemistry. 2018 ; 147( 5): 663-677.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1111/jnc.14602
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      Francisco A, Ronchi JA, Navarro CDC, Figueira TR, Castilho RF. Nicotinamide nucleotide transhydrogenase is required for brain mitochondrial redox balance under hampered energy substrate metabolism and high‐fat diet [Internet]. Journal of Neurochemistry. 2018 ; 147( 5): 663-677.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1111/jnc.14602
  • Source: Archives of Toxicology. Unidade: FCFRP

    Subjects: VENENOS DE ORIGEM ANIMAL (CARACTERÍSTICAS;FARMACOLOGIA), SERPENTES, BIOQUÍMICA, FOSFOLIPASES A

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      TEIXEIRA, Sabrina S. et al. Molecular characterization of an acidic phospholipase A(2) from Bothrops pirajai snake venom: synthetic C-terminal peptide identifies its antiplatelet region. Archives of Toxicology, v. 85, n. 10, p. 1219-1233, 2011Tradução . . Disponível em: https://doi.org/10.1007/s00204-011-0665-6. Acesso em: 04 nov. 2024.
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      Teixeira, S. S., Silveira, L. B., Silva, F. M. N. da, Marchi-Salvador, D. P., Silva Junior, F. P., Izidoro, L. F. M., et al. (2011). Molecular characterization of an acidic phospholipase A(2) from Bothrops pirajai snake venom: synthetic C-terminal peptide identifies its antiplatelet region. Archives of Toxicology, 85( 10), 1219-1233. doi:10.1007/s00204-011-0665-6
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      Teixeira SS, Silveira LB, Silva FMN da, Marchi-Salvador DP, Silva Junior FP, Izidoro LFM, Fuly AL, Juliano MA, Santos CR dos, Murakami MT, Sampaio SV, Silva SL da, Soares AM. Molecular characterization of an acidic phospholipase A(2) from Bothrops pirajai snake venom: synthetic C-terminal peptide identifies its antiplatelet region [Internet]. Archives of Toxicology. 2011 ; 85( 10): 1219-1233.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s00204-011-0665-6
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      Teixeira SS, Silveira LB, Silva FMN da, Marchi-Salvador DP, Silva Junior FP, Izidoro LFM, Fuly AL, Juliano MA, Santos CR dos, Murakami MT, Sampaio SV, Silva SL da, Soares AM. Molecular characterization of an acidic phospholipase A(2) from Bothrops pirajai snake venom: synthetic C-terminal peptide identifies its antiplatelet region [Internet]. Archives of Toxicology. 2011 ; 85( 10): 1219-1233.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1007/s00204-011-0665-6
  • Source: Microbial Ecology. Unidade: IQ

    Subjects: BIOQUÍMICA, ESPECTROMETRIA DE MASSAS

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      PUEYO, Manuel Troyano et al. Lipopeptides produced by a soil Bacillus megaterium strain. Microbial Ecology, v. 57, n. 2, p. 367-378, 2009Tradução . . Acesso em: 04 nov. 2024.
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      Pueyo, M. T., Bloch Junior, C., Carmona-Ribeiro, A. M., & Di Mascio, P. (2009). Lipopeptides produced by a soil Bacillus megaterium strain. Microbial Ecology, 57( 2), 367-378.
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      Pueyo MT, Bloch Junior C, Carmona-Ribeiro AM, Di Mascio P. Lipopeptides produced by a soil Bacillus megaterium strain. Microbial Ecology. 2009 ; 57( 2): 367-378.[citado 2024 nov. 04 ]
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      Pueyo MT, Bloch Junior C, Carmona-Ribeiro AM, Di Mascio P. Lipopeptides produced by a soil Bacillus megaterium strain. Microbial Ecology. 2009 ; 57( 2): 367-378.[citado 2024 nov. 04 ]
  • Source: Current Analytical Chemistry. Unidades: IQ, FCF

    Subjects: ALGAS, COMPOSTOS ORGÂNICOS, BIOQUÍMICA

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      GRESSLER, Vanessa e COLEPICOLO, Pio e PINTO, Ernani. Useful strategies for algal volatile analysis. Current Analytical Chemistry, v. 5, n. 3, p. 271-292, 2009Tradução . . Disponível em: https://www.researchgate.net/publication/233617145. Acesso em: 04 nov. 2024.
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      Gressler, V., Colepicolo, P., & Pinto, E. (2009). Useful strategies for algal volatile analysis. Current Analytical Chemistry, 5( 3), 271-292. Recuperado de https://www.researchgate.net/publication/233617145
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      Gressler V, Colepicolo P, Pinto E. Useful strategies for algal volatile analysis [Internet]. Current Analytical Chemistry. 2009 ; 5( 3): 271-292.[citado 2024 nov. 04 ] Available from: https://www.researchgate.net/publication/233617145
    • Vancouver

      Gressler V, Colepicolo P, Pinto E. Useful strategies for algal volatile analysis [Internet]. Current Analytical Chemistry. 2009 ; 5( 3): 271-292.[citado 2024 nov. 04 ] Available from: https://www.researchgate.net/publication/233617145
  • Source: Journal of Peptide Science. Unidade: IQ

    Subjects: PEPTÍDEOS, BIOQUÍMICA

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      LOFFREDO, Carina et al. Microwave-assisted solid-phase peptide synthesis at 60 'GRAUS CENTÍGRADOS': alternative conditions with low enantiomerization. Journal of Peptide Science, v. 15, n. 12, p. 808-817, 2009Tradução . . Disponível em: http://www3.interscience.wiley.com/cgi-bin/fulltext/122649327/PDFSTART. Acesso em: 04 nov. 2024.
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      Loffredo, C., Assunção, N. A., Gerhardt, J., & Miranda, M. T. M. de. (2009). Microwave-assisted solid-phase peptide synthesis at 60 'GRAUS CENTÍGRADOS': alternative conditions with low enantiomerization. Journal of Peptide Science, 15( 12), 808-817. Recuperado de http://www3.interscience.wiley.com/cgi-bin/fulltext/122649327/PDFSTART
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      Loffredo C, Assunção NA, Gerhardt J, Miranda MTM de. Microwave-assisted solid-phase peptide synthesis at 60 'GRAUS CENTÍGRADOS': alternative conditions with low enantiomerization [Internet]. Journal of Peptide Science. 2009 ; 15( 12): 808-817.[citado 2024 nov. 04 ] Available from: http://www3.interscience.wiley.com/cgi-bin/fulltext/122649327/PDFSTART
    • Vancouver

      Loffredo C, Assunção NA, Gerhardt J, Miranda MTM de. Microwave-assisted solid-phase peptide synthesis at 60 'GRAUS CENTÍGRADOS': alternative conditions with low enantiomerization [Internet]. Journal of Peptide Science. 2009 ; 15( 12): 808-817.[citado 2024 nov. 04 ] Available from: http://www3.interscience.wiley.com/cgi-bin/fulltext/122649327/PDFSTART
  • Unidade: IQ

    Subjects: DANO AO DNA, BIOQUÍMICA, DOENÇAS NEURODEGENERATIVAS

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      MUFTUOGLU, Meltem et al. Cockayne syndrome group B protein stimulates rapair of formamidopyrimidines by NEIL 1 DNA glycosylase. 2009Tradução . . Disponível em: http://www.jbc.org/cgi/reprint/284/14/9270. Acesso em: 04 nov. 2024.
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      Muftuoglu, M., Souza-Pinto, N. C. de, Dogan, A., Aamann, M., Stevnsner, T. V., Rybanska, I., et al. (2009). Cockayne syndrome group B protein stimulates rapair of formamidopyrimidines by NEIL 1 DNA glycosylase. Recuperado de http://www.jbc.org/cgi/reprint/284/14/9270
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      Muftuoglu M, Souza-Pinto NC de, Dogan A, Aamann M, Stevnsner TV, Rybanska I, Kirkali G, Dizdaroglu M, Bohr VA. Cockayne syndrome group B protein stimulates rapair of formamidopyrimidines by NEIL 1 DNA glycosylase [Internet]. 2009 ;[citado 2024 nov. 04 ] Available from: http://www.jbc.org/cgi/reprint/284/14/9270
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      Muftuoglu M, Souza-Pinto NC de, Dogan A, Aamann M, Stevnsner TV, Rybanska I, Kirkali G, Dizdaroglu M, Bohr VA. Cockayne syndrome group B protein stimulates rapair of formamidopyrimidines by NEIL 1 DNA glycosylase [Internet]. 2009 ;[citado 2024 nov. 04 ] Available from: http://www.jbc.org/cgi/reprint/284/14/9270
  • Source: Chemical Research in Toxicology. Unidade: IQ

    Subjects: PEROXIDASE, BIOQUÍMICA, SUPERÓXIDO DISMUTASE

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      MEDINAS, Danilo Bilches et al. Peroxymonocarbonate and carbonate radical displace the hydroxyl-like oxidant in the Sod1 peroxidase activity under physiological conditions. Chemical Research in Toxicology, v. 22, n. 4, p. 639-648, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/tx800287m. Acesso em: 04 nov. 2024.
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      Medinas, D. B., Toledo Junior, J. C., Cerchiaro, G., Amaral, A. T. do, Rezende, L. de, Malvezzi, A., & Augusto, O. (2009). Peroxymonocarbonate and carbonate radical displace the hydroxyl-like oxidant in the Sod1 peroxidase activity under physiological conditions. Chemical Research in Toxicology, 22( 4), 639-648. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/tx800287m
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      Medinas DB, Toledo Junior JC, Cerchiaro G, Amaral AT do, Rezende L de, Malvezzi A, Augusto O. Peroxymonocarbonate and carbonate radical displace the hydroxyl-like oxidant in the Sod1 peroxidase activity under physiological conditions [Internet]. Chemical Research in Toxicology. 2009 ; 22( 4): 639-648.[citado 2024 nov. 04 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800287m
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      Medinas DB, Toledo Junior JC, Cerchiaro G, Amaral AT do, Rezende L de, Malvezzi A, Augusto O. Peroxymonocarbonate and carbonate radical displace the hydroxyl-like oxidant in the Sod1 peroxidase activity under physiological conditions [Internet]. Chemical Research in Toxicology. 2009 ; 22( 4): 639-648.[citado 2024 nov. 04 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800287m
  • Source: Bioconjugate Chemistry. Unidades: IQ, FCF

    Subjects: PROTEÍNAS DE FLUORESCÊNCIA VERDE, BIOQUÍMICA

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      HERING, Vitor Renaux et al. Violet ZnSe/ZnS as an alternative to green CdSe/ZnS in nanocrystal-fluorescent protein FRET systems. Bioconjugate Chemistry, v. 20, n. 6, p. 1237-1241, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/bc9001085. Acesso em: 04 nov. 2024.
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      Hering, V. R., Faulin, T. do E. S., Triboni, E. R., Rodriguez, S. D., Bernik, D. L., Schumacher, R. I., et al. (2009). Violet ZnSe/ZnS as an alternative to green CdSe/ZnS in nanocrystal-fluorescent protein FRET systems. Bioconjugate Chemistry, 20( 6), 1237-1241. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/bc9001085
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      Hering VR, Faulin T do ES, Triboni ER, Rodriguez SD, Bernik DL, Schumacher RI, Mammana VP, Faljoni-Alário A, Abdalla DSP, Gibson G, Politi MJ. Violet ZnSe/ZnS as an alternative to green CdSe/ZnS in nanocrystal-fluorescent protein FRET systems [Internet]. Bioconjugate Chemistry. 2009 ; 20( 6): 1237-1241.[citado 2024 nov. 04 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/bc9001085
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      Hering VR, Faulin T do ES, Triboni ER, Rodriguez SD, Bernik DL, Schumacher RI, Mammana VP, Faljoni-Alário A, Abdalla DSP, Gibson G, Politi MJ. Violet ZnSe/ZnS as an alternative to green CdSe/ZnS in nanocrystal-fluorescent protein FRET systems [Internet]. Bioconjugate Chemistry. 2009 ; 20( 6): 1237-1241.[citado 2024 nov. 04 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/bc9001085
  • Source: Journal of Biological Chemistry. Unidade: IQ

    Subjects: BIOQUÍMICA, PEPTÍDEOS, HIPERTENSÃO (TERAPIA)

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      GUERREIRO, Juliano Rodrigo et al. Argininosuccinate synthetase is a functional target for a snake venom anti-hypertensive peptide: role in arginine and nitric oxide production. Journal of Biological Chemistry, v. 284, n. 30, p. 20022-20033, 2009Tradução . . Disponível em: http://www.jbc.org/cgi/reprint/284/30/20022. Acesso em: 04 nov. 2024.
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      Guerreiro, J. R., Lameu, C., Oliveira, E. F., Klitzke, C. F., Melo, R. L. de, Linares, E., et al. (2009). Argininosuccinate synthetase is a functional target for a snake venom anti-hypertensive peptide: role in arginine and nitric oxide production. Journal of Biological Chemistry, 284( 30), 20022-20033. Recuperado de http://www.jbc.org/cgi/reprint/284/30/20022
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      Guerreiro JR, Lameu C, Oliveira EF, Klitzke CF, Melo RL de, Linares E, Augusto O, Fox JW, Lebrun I, Serrano SM de T, Camargo ACM de. Argininosuccinate synthetase is a functional target for a snake venom anti-hypertensive peptide: role in arginine and nitric oxide production [Internet]. Journal of Biological Chemistry. 2009 ; 284( 30): 20022-20033.[citado 2024 nov. 04 ] Available from: http://www.jbc.org/cgi/reprint/284/30/20022
    • Vancouver

      Guerreiro JR, Lameu C, Oliveira EF, Klitzke CF, Melo RL de, Linares E, Augusto O, Fox JW, Lebrun I, Serrano SM de T, Camargo ACM de. Argininosuccinate synthetase is a functional target for a snake venom anti-hypertensive peptide: role in arginine and nitric oxide production [Internet]. Journal of Biological Chemistry. 2009 ; 284( 30): 20022-20033.[citado 2024 nov. 04 ] Available from: http://www.jbc.org/cgi/reprint/284/30/20022
  • Source: Journal of Neuroscience Research. Unidade: IQ

    Subjects: MITOCÔNDRIAS, BIOQUÍMICA, ISQUEMIA, CÁLCIO

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      FORNAZARI, Maynara et al. Redox properties of the adenoside triphosphate-sensitive 'K POT. +' channel in brain mitochondria. Journal of Neuroscience Research, v. 86, n. 7, p. 1548-1556, 2008Tradução . . Disponível em: https://doi.org/10.1002/jnr.21614. Acesso em: 04 nov. 2024.
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      Fornazari, M., Paula, J. G. de, Castilho, R. F., & Kowaltowski, A. J. (2008). Redox properties of the adenoside triphosphate-sensitive 'K POT. +' channel in brain mitochondria. Journal of Neuroscience Research, 86( 7), 1548-1556. doi:10.1002/jnr.21614
    • NLM

      Fornazari M, Paula JG de, Castilho RF, Kowaltowski AJ. Redox properties of the adenoside triphosphate-sensitive 'K POT. +' channel in brain mitochondria [Internet]. Journal of Neuroscience Research. 2008 ;86( 7): 1548-1556.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/jnr.21614
    • Vancouver

      Fornazari M, Paula JG de, Castilho RF, Kowaltowski AJ. Redox properties of the adenoside triphosphate-sensitive 'K POT. +' channel in brain mitochondria [Internet]. Journal of Neuroscience Research. 2008 ;86( 7): 1548-1556.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/jnr.21614
  • Source: Journal of Neuroscience Research. Unidade: IQ

    Assunto: BIOQUÍMICA

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      ULRICH, Henning et al. Mode of cembranoid action on embryonic muscle acetylcholine receptor. Journal of Neuroscience Research, v. 86, n. 1, p. 93-107, 2008Tradução . . Disponível em: https://doi.org/10.1002/jnr.21468. Acesso em: 04 nov. 2024.
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      Ulrich, H., Akk, G., Nery, A. A., Trujillo, C. A., Rodriguez, A. D., & Eterovic, V. A. (2008). Mode of cembranoid action on embryonic muscle acetylcholine receptor. Journal of Neuroscience Research, 86( 1), 93-107. doi:10.1002/jnr.21468
    • NLM

      Ulrich H, Akk G, Nery AA, Trujillo CA, Rodriguez AD, Eterovic VA. Mode of cembranoid action on embryonic muscle acetylcholine receptor [Internet]. Journal of Neuroscience Research. 2008 ;86( 1): 93-107.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/jnr.21468
    • Vancouver

      Ulrich H, Akk G, Nery AA, Trujillo CA, Rodriguez AD, Eterovic VA. Mode of cembranoid action on embryonic muscle acetylcholine receptor [Internet]. Journal of Neuroscience Research. 2008 ;86( 1): 93-107.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/jnr.21468
  • Source: Journal of Physical Chemistry B. Unidade: IQ

    Subjects: BIOQUÍMICA, DNA, BIOTECNOLOGIA

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      ROSA, Heloísa e PETRI, Denise Freitas Siqueira e CARMONA-RIBEIRO, Ana Maria. Interactions between bacteriophage DNA and cationic biomimetic particles. Journal of Physical Chemistry B, v. 112, n. 51, p. 16422-16430, 2008Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/jp806992f. Acesso em: 04 nov. 2024.
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      Rosa, H., Petri, D. F. S., & Carmona-Ribeiro, A. M. (2008). Interactions between bacteriophage DNA and cationic biomimetic particles. Journal of Physical Chemistry B, 112( 51), 16422-16430. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/jp806992f
    • NLM

      Rosa H, Petri DFS, Carmona-Ribeiro AM. Interactions between bacteriophage DNA and cationic biomimetic particles [Internet]. Journal of Physical Chemistry B. 2008 ; 112( 51): 16422-16430.[citado 2024 nov. 04 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jp806992f
    • Vancouver

      Rosa H, Petri DFS, Carmona-Ribeiro AM. Interactions between bacteriophage DNA and cationic biomimetic particles [Internet]. Journal of Physical Chemistry B. 2008 ; 112( 51): 16422-16430.[citado 2024 nov. 04 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/jp806992f
  • Source: Chemical Research in Toxicology. Unidades: EACH, IQ

    Subjects: ESTRESSE OXIDATIVO, DIABETES MELLITUS, BIOQUÍMICA

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      SARTORI, Adriano et al. Aminoacetone, a putative endogenous source of methylglyoxal, causes oxidative stress and death to insulin-producing RINm5f cells. Chemical Research in Toxicology, v. 21, n. 9, p. 1841-1850, 2008Tradução . . Disponível em: https://doi.org/10.1021/tx8001753. Acesso em: 04 nov. 2024.
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      Sartori, A., Garay-Malpartida, H. M., Forni, M. F., Schumacher, R. I., Dutra, F., Sogayar, M. C., & Bechara, E. J. H. (2008). Aminoacetone, a putative endogenous source of methylglyoxal, causes oxidative stress and death to insulin-producing RINm5f cells. Chemical Research in Toxicology, 21( 9), 1841-1850. doi:10.1021/tx8001753
    • NLM

      Sartori A, Garay-Malpartida HM, Forni MF, Schumacher RI, Dutra F, Sogayar MC, Bechara EJH. Aminoacetone, a putative endogenous source of methylglyoxal, causes oxidative stress and death to insulin-producing RINm5f cells [Internet]. Chemical Research in Toxicology. 2008 ; 21( 9): 1841-1850.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1021/tx8001753
    • Vancouver

      Sartori A, Garay-Malpartida HM, Forni MF, Schumacher RI, Dutra F, Sogayar MC, Bechara EJH. Aminoacetone, a putative endogenous source of methylglyoxal, causes oxidative stress and death to insulin-producing RINm5f cells [Internet]. Chemical Research in Toxicology. 2008 ; 21( 9): 1841-1850.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1021/tx8001753
  • Source: American Journal of Medical Genetics Part A. Unidade: IQ

    Subjects: POLIMORFISMO, BIOQUÍMICA

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      LETRA, Ariadne et al. Studies with MMP9 gene promoter polymorphism and nonsyndromic cleft lip and palate. American Journal of Medical Genetics Part A, v. 143A, n. 1, p. 89-91, 2007Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.31492. Acesso em: 04 nov. 2024.
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      Letra, A., Silva, R. A. da, Menezes, R., Souza, A. P. de, Almeida, A. L. P. F. de, Sogayar, M. C., & Granjeiro, J. M. (2007). Studies with MMP9 gene promoter polymorphism and nonsyndromic cleft lip and palate. American Journal of Medical Genetics Part A, 143A( 1), 89-91. doi:10.1002/ajmg.a.31492
    • NLM

      Letra A, Silva RA da, Menezes R, Souza AP de, Almeida ALPF de, Sogayar MC, Granjeiro JM. Studies with MMP9 gene promoter polymorphism and nonsyndromic cleft lip and palate [Internet]. American Journal of Medical Genetics Part A. 2007 ; 143A( 1): 89-91.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/ajmg.a.31492
    • Vancouver

      Letra A, Silva RA da, Menezes R, Souza AP de, Almeida ALPF de, Sogayar MC, Granjeiro JM. Studies with MMP9 gene promoter polymorphism and nonsyndromic cleft lip and palate [Internet]. American Journal of Medical Genetics Part A. 2007 ; 143A( 1): 89-91.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1002/ajmg.a.31492

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