Filtros : "Indexado na Base de Dados Web of Science" "Kronenberger, Thales" Removidos: "Pinto, Ernani" "Current Drug Targets" Limpar

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  • Fonte: Biomolecules. Unidade: ICB

    Assuntos: PARASITOLOGIA, ÁCIDOS NUCLEICOS, MODELAGEM MOLECULAR, MOLÉCULA

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    • ABNT

      KRÜGER, Arne et al. Molecular modeling applied to nucleic acid-based molecule development. Biomolecules, v. 8, n. 3, p. 1-17, 2018Tradução . . Disponível em: https://doi.org/10.3390/biom8030083. Acesso em: 25 ago. 2024.
    • APA

      Krüger, A., Zimbres, F. M., Kronenberger, T., & Wrenger, C. (2018). Molecular modeling applied to nucleic acid-based molecule development. Biomolecules, 8( 3), 1-17. doi:10.3390/biom8030083
    • NLM

      Krüger A, Zimbres FM, Kronenberger T, Wrenger C. Molecular modeling applied to nucleic acid-based molecule development [Internet]. Biomolecules. 2018 ; 8( 3): 1-17.[citado 2024 ago. 25 ] Available from: https://doi.org/10.3390/biom8030083
    • Vancouver

      Krüger A, Zimbres FM, Kronenberger T, Wrenger C. Molecular modeling applied to nucleic acid-based molecule development [Internet]. Biomolecules. 2018 ; 8( 3): 1-17.[citado 2024 ago. 25 ] Available from: https://doi.org/10.3390/biom8030083
  • Fonte: Archives of Toxicology. Unidade: ICB

    Assuntos: PARASITOLOGIA, ANTAGONISMO DE DROGAS, CÉLULAS KUPFFER

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    • ABNT

      BURK, Oliver et al. Identification of approved drugs as potent inhibitors of pregnane X receptor activation with differential receptor interaction profiles. Archives of Toxicology, v. 92, p. 1435-1451, 2018Tradução . . Disponível em: https://doi.org/10.1007/s00204-018-2165-4. Acesso em: 25 ago. 2024.
    • APA

      Burk, O., Kuzikov, M., Kronenberger, T., Jeske, J., Keminer, O., Thasler, W.  E.  , et al. (2018). Identification of approved drugs as potent inhibitors of pregnane X receptor activation with differential receptor interaction profiles. Archives of Toxicology, 92, 1435-1451. doi:10.1007/s00204-018-2165-4
    • NLM

      Burk O, Kuzikov M, Kronenberger T, Jeske J, Keminer O, Thasler W E , Schwab M, Wrenger C, Windshügel B. Identification of approved drugs as potent inhibitors of pregnane X receptor activation with differential receptor interaction profiles [Internet]. Archives of Toxicology. 2018 ; 92 1435-1451.[citado 2024 ago. 25 ] Available from: https://doi.org/10.1007/s00204-018-2165-4
    • Vancouver

      Burk O, Kuzikov M, Kronenberger T, Jeske J, Keminer O, Thasler W E , Schwab M, Wrenger C, Windshügel B. Identification of approved drugs as potent inhibitors of pregnane X receptor activation with differential receptor interaction profiles [Internet]. Archives of Toxicology. 2018 ; 92 1435-1451.[citado 2024 ago. 25 ] Available from: https://doi.org/10.1007/s00204-018-2165-4
  • Fonte: Chemical Biology and Drug Design. Unidades: FCF, ICB

    Assuntos: PLASMODIUM FALCIPARUM, PARASITOLOGIA, MALÁRIA, QUIMIOTERAPIA, ENZIMAS PROTEOLITICAS, ATIVAÇÃO ENZIMÁTICA

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    • ABNT

      MEISSNER, Kamila Anna et al. Targeting the Plasmodium falciparum Plasmepsin V by ligand-based virtual screening. Chemical Biology and Drug Design, v. 2018 p. 1-13, 2018Tradução . . Disponível em: https://doi.org/10.1111/cbdd.13416. Acesso em: 25 ago. 2024.
    • APA

      Meissner, K. A., Kronenberger, T., Maltarollo, V. G., Trossini, G. H. G., & Wrenger, C. (2018). Targeting the Plasmodium falciparum Plasmepsin V by ligand-based virtual screening. Chemical Biology and Drug Design, 2018 p. 1-13. doi:10.1111/cbdd.13416
    • NLM

      Meissner KA, Kronenberger T, Maltarollo VG, Trossini GHG, Wrenger C. Targeting the Plasmodium falciparum Plasmepsin V by ligand-based virtual screening [Internet]. Chemical Biology and Drug Design. 2018 ; 2018 p. 1-13[citado 2024 ago. 25 ] Available from: https://doi.org/10.1111/cbdd.13416
    • Vancouver

      Meissner KA, Kronenberger T, Maltarollo VG, Trossini GHG, Wrenger C. Targeting the Plasmodium falciparum Plasmepsin V by ligand-based virtual screening [Internet]. Chemical Biology and Drug Design. 2018 ; 2018 p. 1-13[citado 2024 ago. 25 ] Available from: https://doi.org/10.1111/cbdd.13416
  • Fonte: Journal of Biomolecular Structure & Dynamics. Unidades: ICB, EACH

    Assuntos: PARASITOLOGIA, HOMEOSTASE, DOENÇAS METABÓLICAS

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    • ABNT

      KRONENBERGER, Thales et al. On the relationship of anthranilic derivatives structure and the FXR (Farnesoid X receptor) agonist activity. Journal of Biomolecular Structure & Dynamics, v. 36, n. 16, p. 4378–4391, 2018Tradução . . Disponível em: https://doi.org/10.1080/07391102.2017.1417161. Acesso em: 25 ago. 2024.
    • APA

      Kronenberger, T., Windshügel, B., Wrenger, C., Honório, K. M., & Maltarollo, V. G. (2018). On the relationship of anthranilic derivatives structure and the FXR (Farnesoid X receptor) agonist activity. Journal of Biomolecular Structure & Dynamics, 36( 16), 4378–4391. doi:10.1080/07391102.2017.1417161
    • NLM

      Kronenberger T, Windshügel B, Wrenger C, Honório KM, Maltarollo VG. On the relationship of anthranilic derivatives structure and the FXR (Farnesoid X receptor) agonist activity [Internet]. Journal of Biomolecular Structure & Dynamics. 2018 ; 36( 16): 4378–4391.[citado 2024 ago. 25 ] Available from: https://doi.org/10.1080/07391102.2017.1417161
    • Vancouver

      Kronenberger T, Windshügel B, Wrenger C, Honório KM, Maltarollo VG. On the relationship of anthranilic derivatives structure and the FXR (Farnesoid X receptor) agonist activity [Internet]. Journal of Biomolecular Structure & Dynamics. 2018 ; 36( 16): 4378–4391.[citado 2024 ago. 25 ] Available from: https://doi.org/10.1080/07391102.2017.1417161
  • Fonte: BioMed Research International. Unidade: ICB

    Assuntos: PARASITOLOGIA, ESTRESSE OXIDATIVO

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    • ABNT

      BOSCH, Soraya Soledad et al. Oxidative stress control by apicomplexan parasites. BioMed Research International, v. 2015, p. 1-10, 2015Tradução . . Disponível em: https://doi.org/10.1155/2015/351289. Acesso em: 25 ago. 2024.
    • APA

      Bosch, S. S., Kronenberger, T., Meissner, K. A., Zimbres, F. M., Stegehake, D., Izui, N. M., et al. (2015). Oxidative stress control by apicomplexan parasites. BioMed Research International, 2015, 1-10. doi:10.1155/2015/351289
    • NLM

      Bosch SS, Kronenberger T, Meissner KA, Zimbres FM, Stegehake D, Izui NM, Schettert I, Liebau E, Wrenger C. Oxidative stress control by apicomplexan parasites [Internet]. BioMed Research International. 2015 ; 2015 1-10.[citado 2024 ago. 25 ] Available from: https://doi.org/10.1155/2015/351289
    • Vancouver

      Bosch SS, Kronenberger T, Meissner KA, Zimbres FM, Stegehake D, Izui NM, Schettert I, Liebau E, Wrenger C. Oxidative stress control by apicomplexan parasites [Internet]. BioMed Research International. 2015 ; 2015 1-10.[citado 2024 ago. 25 ] Available from: https://doi.org/10.1155/2015/351289
  • Fonte: Acta Crystallographica Section F, Structural Biology Communications. Unidade: ICB

    Assuntos: PARASITOLOGIA, PLASMODIUM FALCIPARUM

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    • ABNT

      KRONENBERGER, Thales et al. Purification, crystallization and preliminary X-ray diffraction analysis of pyridoxal kinase from Plasmodium falciparum (PfPdxK). Acta Crystallographica Section F, Structural Biology Communications, v. 70, p. 1550-1555, 2014Tradução . . Disponível em: https://doi.org/10.1107/S2053230X14019864. Acesso em: 25 ago. 2024.
    • APA

      Kronenberger, T., Lunev, S., Wrenger, C., & Groves, M. R. (2014). Purification, crystallization and preliminary X-ray diffraction analysis of pyridoxal kinase from Plasmodium falciparum (PfPdxK). Acta Crystallographica Section F, Structural Biology Communications, 70, 1550-1555. doi:10.1107/S2053230X14019864
    • NLM

      Kronenberger T, Lunev S, Wrenger C, Groves MR. Purification, crystallization and preliminary X-ray diffraction analysis of pyridoxal kinase from Plasmodium falciparum (PfPdxK) [Internet]. Acta Crystallographica Section F, Structural Biology Communications. 2014 ; 70 1550-1555.[citado 2024 ago. 25 ] Available from: https://doi.org/10.1107/S2053230X14019864
    • Vancouver

      Kronenberger T, Lunev S, Wrenger C, Groves MR. Purification, crystallization and preliminary X-ray diffraction analysis of pyridoxal kinase from Plasmodium falciparum (PfPdxK) [Internet]. Acta Crystallographica Section F, Structural Biology Communications. 2014 ; 70 1550-1555.[citado 2024 ago. 25 ] Available from: https://doi.org/10.1107/S2053230X14019864
  • Fonte: Biomed Research International. Unidade: ICB

    Assunto: PARASITOLOGIA

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    • ABNT

      KRONENBERGER, Thales et al. Vitamin B6-dependent enzymes in the human malaria parasite Plasmodium falciparum: a druggable target?. Biomed Research International, v. 2014, p. 1-11, 2014Tradução . . Disponível em: https://doi.org/10.1155/2014/108516. Acesso em: 25 ago. 2024.
    • APA

      Kronenberger, T., Lindner, J., Meissner, K. A., Zimbres, F. M., Coronado, M. A., Sauer, F. M., et al. (2014). Vitamin B6-dependent enzymes in the human malaria parasite Plasmodium falciparum: a druggable target? Biomed Research International, 2014, 1-11. doi:10.1155/2014/108516
    • NLM

      Kronenberger T, Lindner J, Meissner KA, Zimbres FM, Coronado MA, Sauer FM, Schettert I, Wrenger C. Vitamin B6-dependent enzymes in the human malaria parasite Plasmodium falciparum: a druggable target? [Internet]. Biomed Research International. 2014 ; 2014 1-11.[citado 2024 ago. 25 ] Available from: https://doi.org/10.1155/2014/108516
    • Vancouver

      Kronenberger T, Lindner J, Meissner KA, Zimbres FM, Coronado MA, Sauer FM, Schettert I, Wrenger C. Vitamin B6-dependent enzymes in the human malaria parasite Plasmodium falciparum: a druggable target? [Internet]. Biomed Research International. 2014 ; 2014 1-11.[citado 2024 ago. 25 ] Available from: https://doi.org/10.1155/2014/108516

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