Filtros : "Indexado na Base de Dados MEDLINE" "Wrenger, Carsten" Removido: "EEL" Limpar

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  • Source: Biomolecules. Unidade: ICB

    Subjects: PARASITOLOGIA, ÁCIDOS NUCLEICOS, MODELAGEM MOLECULAR, MOLÉCULA

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      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: 12 nov. 2024.
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      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 nov. 12 ] 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 nov. 12 ] Available from: https://doi.org/10.3390/biom8030083
  • Source: Archives of Toxicology. Unidade: ICB

    Subjects: PARASITOLOGIA, ANTAGONISMO DE DROGAS, CÉLULAS KUPFFER

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      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: 12 nov. 2024.
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      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 nov. 12 ] 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 nov. 12 ] Available from: https://doi.org/10.1007/s00204-018-2165-4
  • Source: PLOS ONE. Unidade: ICB

    Subjects: PARASITOLOGIA, PLASMODIUM FALCIPARUM, MALÁRIA

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      LUNEV, Sergey et al. Oligomeric interfaces as a tool in drug discovery: Specific interference with activity of malate dehydrogenase of Plasmodium falciparum in vitro. PLOS ONE, v. 13, n. 4, p. e0195011, 2018Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0195011. Acesso em: 12 nov. 2024.
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      Lunev, S., Butzloff, S., Romero, A. R., Linzke, M., Batista, F. A., Meissner, K. A., et al. (2018). Oligomeric interfaces as a tool in drug discovery: Specific interference with activity of malate dehydrogenase of Plasmodium falciparum in vitro. PLOS ONE, 13( 4), e0195011. doi:10.1371/journal.pone.0195011
    • NLM

      Lunev S, Butzloff S, Romero AR, Linzke M, Batista FA, Meissner KA, Müller IB, Adawy A, Wrenger C, Groves MR. Oligomeric interfaces as a tool in drug discovery: Specific interference with activity of malate dehydrogenase of Plasmodium falciparum in vitro [Internet]. PLOS ONE. 2018 ;13( 4): e0195011.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1371/journal.pone.0195011
    • Vancouver

      Lunev S, Butzloff S, Romero AR, Linzke M, Batista FA, Meissner KA, Müller IB, Adawy A, Wrenger C, Groves MR. Oligomeric interfaces as a tool in drug discovery: Specific interference with activity of malate dehydrogenase of Plasmodium falciparum in vitro [Internet]. PLOS ONE. 2018 ;13( 4): e0195011.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1371/journal.pone.0195011
  • Source: Chemical Biology and Drug Design. Unidades: FCF, ICB

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

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      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: 12 nov. 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 nov. 12 ] 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 nov. 12 ] Available from: https://doi.org/10.1111/cbdd.13416
  • Source: Journal of Pineal Research. Unidades: ICB, IB

    Subjects: PARASITOLOGIA, MELATONINA, PLASMODIUM FALCIPARUM, MALÁRIA

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      SCARPELLI, Pedro H. et al. Melatonin activates FIS1, DYN1, and DYN2 Plasmodium falciparum related‐genes for mitochondria fission: Mitoemerald‐GFP as a tool to visualize mitochondria structure. Journal of Pineal Research, p. 1-22, 2018Tradução . . Disponível em: https://doi.org/10.1111/jpi.12484. Acesso em: 12 nov. 2024.
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      Scarpelli, P. H., Tessarin‐Almeida, G., Viçoso, K. L., Lima, W. R., Borges‐Pereira, L., Meissner, K. A., et al. (2018). Melatonin activates FIS1, DYN1, and DYN2 Plasmodium falciparum related‐genes for mitochondria fission: Mitoemerald‐GFP as a tool to visualize mitochondria structure. Journal of Pineal Research, 1-22. doi:10.1111/jpi.12484
    • NLM

      Scarpelli PH, Tessarin‐Almeida G, Viçoso KL, Lima WR, Borges‐Pereira L, Meissner KA, Wrenger C, Rafaello A, Rizzuto R, Pozzan T, Garcia CR da S. Melatonin activates FIS1, DYN1, and DYN2 Plasmodium falciparum related‐genes for mitochondria fission: Mitoemerald‐GFP as a tool to visualize mitochondria structure [Internet]. Journal of Pineal Research. 2018 ; 1-22.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1111/jpi.12484
    • Vancouver

      Scarpelli PH, Tessarin‐Almeida G, Viçoso KL, Lima WR, Borges‐Pereira L, Meissner KA, Wrenger C, Rafaello A, Rizzuto R, Pozzan T, Garcia CR da S. Melatonin activates FIS1, DYN1, and DYN2 Plasmodium falciparum related‐genes for mitochondria fission: Mitoemerald‐GFP as a tool to visualize mitochondria structure [Internet]. Journal of Pineal Research. 2018 ; 1-22.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1111/jpi.12484
  • Source: Journal of Biomolecular Structure & Dynamics. Unidades: ICB, EACH

    Subjects: PARASITOLOGIA, HOMEOSTASE, DOENÇAS METABÓLICAS

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      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: 12 nov. 2024.
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      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 nov. 12 ] 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 nov. 12 ] Available from: https://doi.org/10.1080/07391102.2017.1417161
  • Source: Purinergic Signalling. Unidade: ICB

    Assunto: PARASITOLOGIA

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      BORGES-PEREIRA, Lucas et al. Plasmodium falciparum GFP-E-NTPDase expression at the intraerythrocytic stages and its inhibition blocks the development of the human malaria parasite. Purinergic Signalling, v. 13, n. 3, p. 267-277, 2017Tradução . . Disponível em: https://doi.org/10.1007/s11302-017-9557-4. Acesso em: 12 nov. 2024.
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      Borges-Pereira, L., Meissner, K. A., Wrenger, C., & Garcia, C. R. da S. (2017). Plasmodium falciparum GFP-E-NTPDase expression at the intraerythrocytic stages and its inhibition blocks the development of the human malaria parasite. Purinergic Signalling, 13( 3), 267-277. doi:10.1007/s11302-017-9557-4
    • NLM

      Borges-Pereira L, Meissner KA, Wrenger C, Garcia CR da S. Plasmodium falciparum GFP-E-NTPDase expression at the intraerythrocytic stages and its inhibition blocks the development of the human malaria parasite [Internet]. Purinergic Signalling. 2017 ; 13( 3): 267-277.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1007/s11302-017-9557-4
    • Vancouver

      Borges-Pereira L, Meissner KA, Wrenger C, Garcia CR da S. Plasmodium falciparum GFP-E-NTPDase expression at the intraerythrocytic stages and its inhibition blocks the development of the human malaria parasite [Internet]. Purinergic Signalling. 2017 ; 13( 3): 267-277.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1007/s11302-017-9557-4
  • Source: BioMed Research International. Unidade: ICB

    Subjects: PARASITOLOGIA, ESTRESSE OXIDATIVO

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      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: 12 nov. 2024.
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      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 nov. 12 ] 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 nov. 12 ] Available from: https://doi.org/10.1155/2015/351289
  • Source: Current Medicinal Chemistry. Unidade: ICB

    Assunto: PARASITOLOGIA

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      PEREIRA, C. A. et al. Metabolite transporters in trypanosomatid parasites: promising therapeutic targets but.. how to deal with them?. Current Medicinal Chemistry, v. 21, n. 15, p. 1707-1712, 2014Tradução . . Acesso em: 12 nov. 2024.
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      Pereira, C. A., Mayé, M., Wrenger, C., & Miranda, M. R. (2014). Metabolite transporters in trypanosomatid parasites: promising therapeutic targets but.. how to deal with them? Current Medicinal Chemistry, 21( 15), 1707-1712.
    • NLM

      Pereira CA, Mayé M, Wrenger C, Miranda MR. Metabolite transporters in trypanosomatid parasites: promising therapeutic targets but.. how to deal with them? Current Medicinal Chemistry. 2014 ; 21( 15): 1707-1712.[citado 2024 nov. 12 ]
    • Vancouver

      Pereira CA, Mayé M, Wrenger C, Miranda MR. Metabolite transporters in trypanosomatid parasites: promising therapeutic targets but.. how to deal with them? Current Medicinal Chemistry. 2014 ; 21( 15): 1707-1712.[citado 2024 nov. 12 ]
  • Source: Current Medicinal Chemistry. Unidade: ICB

    Assunto: PARASITOLOGIA

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      SILBER, Ariel Mariano e PEREIRA, Claudio A. e WRENGER, Carsten. Drug discovery for infectious agents causing neglected diseases. Current Medicinal Chemistry. Schiphol: Instituto de Ciências Biomédicas, Universidade de São Paulo. . Acesso em: 12 nov. 2024. , 2014
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      Silber, A. M., Pereira, C. A., & Wrenger, C. (2014). Drug discovery for infectious agents causing neglected diseases. Current Medicinal Chemistry. Schiphol: Instituto de Ciências Biomédicas, Universidade de São Paulo.
    • NLM

      Silber AM, Pereira CA, Wrenger C. Drug discovery for infectious agents causing neglected diseases. Current Medicinal Chemistry. 2014 ; 21( 15): 1667.[citado 2024 nov. 12 ]
    • Vancouver

      Silber AM, Pereira CA, Wrenger C. Drug discovery for infectious agents causing neglected diseases. Current Medicinal Chemistry. 2014 ; 21( 15): 1667.[citado 2024 nov. 12 ]
  • Source: BioMed Research International. Unidade: ICB

    Assunto: PARASITOLOGIA

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      DITGEN, Dana et al. Harnessing the helminth secretome for therapeutic immunomodulators. BioMed Research International, v. 2014, p. 1-14, 2014Tradução . . Disponível em: https://doi.org/10.1155/2014/964350. Acesso em: 12 nov. 2024.
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      Ditgen, D., Anandarajah, E. M., Meissner, K. A., Bratting, N., Wrenger, C., & Liebau, E. (2014). Harnessing the helminth secretome for therapeutic immunomodulators. BioMed Research International, 2014, 1-14. doi:10.1155/2014/964350
    • NLM

      Ditgen D, Anandarajah EM, Meissner KA, Bratting N, Wrenger C, Liebau E. Harnessing the helminth secretome for therapeutic immunomodulators [Internet]. BioMed Research International. 2014 ; 2014 1-14.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1155/2014/964350
    • Vancouver

      Ditgen D, Anandarajah EM, Meissner KA, Bratting N, Wrenger C, Liebau E. Harnessing the helminth secretome for therapeutic immunomodulators [Internet]. BioMed Research International. 2014 ; 2014 1-14.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1155/2014/964350
  • Source: Current Medicinal Chemistry. Unidade: ICB

    Assunto: PARASITOLOGIA

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      DREBES, Julia et al. MRSA infections: from classical treatment to suicide drugs. Current Medicinal Chemistry, v. 21, n. 15, p. 1809-1819, 2014Tradução . . Acesso em: 12 nov. 2024.
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      Drebes, J., Künz, M., Pereira, C. A., Betzel, C., & Wrenger, C. (2014). MRSA infections: from classical treatment to suicide drugs. Current Medicinal Chemistry, 21( 15), 1809-1819.
    • NLM

      Drebes J, Künz M, Pereira CA, Betzel C, Wrenger C. MRSA infections: from classical treatment to suicide drugs. Current Medicinal Chemistry. 2014 ; 21( 15): 1809-1819.[citado 2024 nov. 12 ]
    • Vancouver

      Drebes J, Künz M, Pereira CA, Betzel C, Wrenger C. MRSA infections: from classical treatment to suicide drugs. Current Medicinal Chemistry. 2014 ; 21( 15): 1809-1819.[citado 2024 nov. 12 ]
  • Source: Acta Crystallographica Section F, Structural Biology Communications. Unidade: ICB

    Subjects: PARASITOLOGIA, PLASMODIUM FALCIPARUM

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      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: 12 nov. 2024.
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      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 nov. 12 ] 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 nov. 12 ] Available from: https://doi.org/10.1107/S2053230X14019864
  • Source: Biomed Research International. Unidade: ICB

    Assunto: PARASITOLOGIA

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      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: 12 nov. 2024.
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      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 nov. 12 ] 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 nov. 12 ] Available from: https://doi.org/10.1155/2014/108516
  • Source: Nature Communications. Unidade: ICB

    Subjects: PARASITOLOGIA, ANTIMALÁRICOS, ANIMAIS PARASITOS, ERITRÓCITOS, PLASMODIUM FALCIPARUM, RNA MENSAGEIRO, CROMATOGRAFIA LÍQUIDA DE ALTA PRESSÃO, EXPRESSÃO GÊNICA, REGULAÇÃO GÊNICA, PROTEÍNAS RECOMBINANTES

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      CHAN, Xie Wah Audrey et al. Chemical and genetic validation of thiamine utilization as an antimalarial drug target. Nature Communications, v. 4, p. 1-11, 2013Tradução . . Disponível em: https://doi.org/10.1038/ncomms3060. Acesso em: 12 nov. 2024.
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      Chan, X. W. A., Wrenger, C., Stahl, K., Bärbel Bergmann,, Winterberg, M., Müller, I. B., & Saliba, K. J. (2013). Chemical and genetic validation of thiamine utilization as an antimalarial drug target. Nature Communications, 4, 1-11. doi:10.1038/ncomms3060
    • NLM

      Chan XWA, Wrenger C, Stahl K, Bärbel Bergmann, Winterberg M, Müller IB, Saliba KJ. Chemical and genetic validation of thiamine utilization as an antimalarial drug target [Internet]. Nature Communications. 2013 ; 4 1-11.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1038/ncomms3060
    • Vancouver

      Chan XWA, Wrenger C, Stahl K, Bärbel Bergmann, Winterberg M, Müller IB, Saliba KJ. Chemical and genetic validation of thiamine utilization as an antimalarial drug target [Internet]. Nature Communications. 2013 ; 4 1-11.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1038/ncomms3060
  • Source: Biochemical Journal. Unidade: ICB

    Subjects: PARASITOLOGIA, MALARIA, PLASMODIUM

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      REEKSTING, Shaun B. et al. Exploring inhibition of Pdx1, a component of the PLP synthase complex of the human malaria parasite Plasmodium falciparum. Biochemical Journal, v. 449, n. Ja 2013, p. 175-1871, 2013Tradução . . Disponível em: http://www.biochemj.org/bj/449/0175/bj4490175.htm. Acesso em: 12 nov. 2024.
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      Reeksting, S. B., Müller, I. B., Burger, P. B., Burgos, E. S., Salmon, L., Louw, A. I., et al. (2013). Exploring inhibition of Pdx1, a component of the PLP synthase complex of the human malaria parasite Plasmodium falciparum. Biochemical Journal, 449( Ja 2013), 175-1871. doi:10.1042/BJ20120925
    • NLM

      Reeksting SB, Müller IB, Burger PB, Burgos ES, Salmon L, Louw AI, Birkholtz L-M, Wrenger C. Exploring inhibition of Pdx1, a component of the PLP synthase complex of the human malaria parasite Plasmodium falciparum [Internet]. Biochemical Journal. 2013 ; 449( Ja 2013): 175-1871.[citado 2024 nov. 12 ] Available from: http://www.biochemj.org/bj/449/0175/bj4490175.htm
    • Vancouver

      Reeksting SB, Müller IB, Burger PB, Burgos ES, Salmon L, Louw AI, Birkholtz L-M, Wrenger C. Exploring inhibition of Pdx1, a component of the PLP synthase complex of the human malaria parasite Plasmodium falciparum [Internet]. Biochemical Journal. 2013 ; 449( Ja 2013): 175-1871.[citado 2024 nov. 12 ] Available from: http://www.biochemj.org/bj/449/0175/bj4490175.htm
  • Source: Acta Crystallographica Section D, Biological Crystallography. Unidade: ICB

    Assunto: PARASITOLOGIA

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      BEGUM, Afshan et al. Staphylococcus aureus thiaminase II: oligomerization warrants proteolytic protection against serine proteases. Acta Crystallographica Section D, Biological Crystallography, v. 69, p. 2320-2329, 2013Tradução . . Disponível em: https://doi.org/10.1107/S0907444913021550. Acesso em: 12 nov. 2024.
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      Begum, A., Drebes, J., Kikhney, A., Müller, I. B., Perbandt, M., Svergun, D., et al. (2013). Staphylococcus aureus thiaminase II: oligomerization warrants proteolytic protection against serine proteases. Acta Crystallographica Section D, Biological Crystallography, 69, 2320-2329. doi:10.1107/S0907444913021550
    • NLM

      Begum A, Drebes J, Kikhney A, Müller IB, Perbandt M, Svergun D, Wrenger C, Betzel C. Staphylococcus aureus thiaminase II: oligomerization warrants proteolytic protection against serine proteases [Internet]. Acta Crystallographica Section D, Biological Crystallography. 2013 ; 69 2320-2329.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1107/S0907444913021550
    • Vancouver

      Begum A, Drebes J, Kikhney A, Müller IB, Perbandt M, Svergun D, Wrenger C, Betzel C. Staphylococcus aureus thiaminase II: oligomerization warrants proteolytic protection against serine proteases [Internet]. Acta Crystallographica Section D, Biological Crystallography. 2013 ; 69 2320-2329.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1107/S0907444913021550
  • Source: Future Medicinal Chemistry. Unidade: ICB

    Assunto: PARASITOLOGIA

    Acesso à fonteDOIHow to cite
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    • ABNT

      KRONENBERGER, Thales e SCHETTERT, Isolmar e WRENGER, Carsten. Targeting the vitamin biosynthesis pathways for the treatment of malaria. Future Medicinal Chemistry, v. 5, n. 7, p. 769-779, 2013Tradução . . Disponível em: https://doi.org/10.4155/FMC.13.43. Acesso em: 12 nov. 2024.
    • APA

      Kronenberger, T., Schettert, I., & Wrenger, C. (2013). Targeting the vitamin biosynthesis pathways for the treatment of malaria. Future Medicinal Chemistry, 5( 7), 769-779. doi:10.4155/FMC.13.43
    • NLM

      Kronenberger T, Schettert I, Wrenger C. Targeting the vitamin biosynthesis pathways for the treatment of malaria [Internet]. Future Medicinal Chemistry. 2013 ; 5( 7): 769-779.[citado 2024 nov. 12 ] Available from: https://doi.org/10.4155/FMC.13.43
    • Vancouver

      Kronenberger T, Schettert I, Wrenger C. Targeting the vitamin biosynthesis pathways for the treatment of malaria [Internet]. Future Medicinal Chemistry. 2013 ; 5( 7): 769-779.[citado 2024 nov. 12 ] Available from: https://doi.org/10.4155/FMC.13.43
  • Source: Acta Crystallographica Section F. Structural Biology and Crystallization Communications. Unidade: ICB

    Assunto: PARASITOLOGIA

    Acesso à fonteDOIHow to cite
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    • ABNT

      WRENGER, Carsten et al. Crystallization and preliminary X-ray diffraction of malate dehydrogenase from Plasmodium falciparum. Acta Crystallographica Section F. Structural Biology and Crystallization Communications, v. 68, p. 659-662, 2012Tradução . . Disponível em: https://doi.org/10.1107/S1744309112014571. Acesso em: 12 nov. 2024.
    • APA

      Wrenger, C., Müller, I. B., Butzloff, S., Jordanova, R., Lunev, S., & Groves, M. R. (2012). Crystallization and preliminary X-ray diffraction of malate dehydrogenase from Plasmodium falciparum. Acta Crystallographica Section F. Structural Biology and Crystallization Communications, 68, 659-662. doi:10.1107/S1744309112014571
    • NLM

      Wrenger C, Müller IB, Butzloff S, Jordanova R, Lunev S, Groves MR. Crystallization and preliminary X-ray diffraction of malate dehydrogenase from Plasmodium falciparum [Internet]. Acta Crystallographica Section F. Structural Biology and Crystallization Communications. 2012 ; 68 659-662.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1107/S1744309112014571
    • Vancouver

      Wrenger C, Müller IB, Butzloff S, Jordanova R, Lunev S, Groves MR. Crystallization and preliminary X-ray diffraction of malate dehydrogenase from Plasmodium falciparum [Internet]. Acta Crystallographica Section F. Structural Biology and Crystallization Communications. 2012 ; 68 659-662.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1107/S1744309112014571
  • Source: Cytometry Part A. Unidade: ICB

    Assunto: PARASITOLOGIA

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    • ABNT

      BUTZLOFF, Sabine et al. Cytometric quantification of singlet oxygen in the human malaria parasite Plasmodium falciparum. Cytometry Part A, v. 81, n. 8, p. 698-703, 2012Tradução . . Disponível em: https://doi.org/10.1002/cyto.a.22081. Acesso em: 12 nov. 2024.
    • APA

      Butzloff, S., Groves, M. R., Wrenger, C., & Müller, I. B. (2012). Cytometric quantification of singlet oxygen in the human malaria parasite Plasmodium falciparum. Cytometry Part A, 81( 8), 698-703. doi:10.1002/cyto.a.22081
    • NLM

      Butzloff S, Groves MR, Wrenger C, Müller IB. Cytometric quantification of singlet oxygen in the human malaria parasite Plasmodium falciparum [Internet]. Cytometry Part A. 2012 ; 81( 8): 698-703.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1002/cyto.a.22081
    • Vancouver

      Butzloff S, Groves MR, Wrenger C, Müller IB. Cytometric quantification of singlet oxygen in the human malaria parasite Plasmodium falciparum [Internet]. Cytometry Part A. 2012 ; 81( 8): 698-703.[citado 2024 nov. 12 ] Available from: https://doi.org/10.1002/cyto.a.22081

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