Filtros : "Indexado na Base de Dados PubMed" "WRENGER, CARSTEN" Removido: "Müller, Ingrid B." Limpar

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  • Fonte: Purinergic Signalling. Unidade: ICB

    Assunto: PARASITOLOGIA

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    • ABNT

      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: 09 ago. 2024.
    • APA

      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 ago. 09 ] 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 ago. 09 ] Available from: https://doi.org/10.1007/s11302-017-9557-4
  • Fonte: BioMed Research International. Unidade: ICB

    Assuntos: 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: 09 ago. 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 ago. 09 ] 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. 09 ] Available from: https://doi.org/10.1155/2015/351289
  • Fonte: 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: 09 ago. 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 ago. 09 ]
    • 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 ago. 09 ]
  • Fonte: 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: 09 ago. 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 ago. 09 ]
    • Vancouver

      Silber AM, Pereira CA, Wrenger C. Drug discovery for infectious agents causing neglected diseases. Current Medicinal Chemistry. 2014 ; 21( 15): 1667.[citado 2024 ago. 09 ]
  • Fonte: 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: 09 ago. 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 ago. 09 ] 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 ago. 09 ] Available from: https://doi.org/10.1155/2014/964350
  • Fonte: 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: 09 ago. 2024.
    • APA

      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 ago. 09 ]
    • 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 ago. 09 ]
  • Fonte: Acta Crystallographica Section F, Structural Biology Communications. Unidade: ICB

    Assuntos: 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: 09 ago. 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 ago. 09 ] 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. 09 ] Available from: https://doi.org/10.1107/S2053230X14019864
  • Fonte: 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: 09 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. 09 ] 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. 09 ] Available from: https://doi.org/10.1155/2014/108516
  • Fonte: International Journal of Molecular Sciences. Unidade: ICB

    Assunto: PARASITOLOGIA

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      NDJONKA, Dieudonné et al. Natural products as a source for treating neglected parasitic diseases. International Journal of Molecular Sciences, v. 14, n. 2, p. 3395-3439, 2013Tradução . . Disponível em: https://doi.org/10.3390/ijms14023395. Acesso em: 09 ago. 2024.
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      Ndjonka, D., Rapado, L. N., Silber, A. M., Liebau, E., & Wrenger, C. (2013). Natural products as a source for treating neglected parasitic diseases. International Journal of Molecular Sciences, 14( 2), 3395-3439. doi:10.3390/ijms14023395
    • NLM

      Ndjonka D, Rapado LN, Silber AM, Liebau E, Wrenger C. Natural products as a source for treating neglected parasitic diseases [Internet]. International Journal of Molecular Sciences. 2013 ; 14( 2): 3395-3439.[citado 2024 ago. 09 ] Available from: https://doi.org/10.3390/ijms14023395
    • Vancouver

      Ndjonka D, Rapado LN, Silber AM, Liebau E, Wrenger C. Natural products as a source for treating neglected parasitic diseases [Internet]. International Journal of Molecular Sciences. 2013 ; 14( 2): 3395-3439.[citado 2024 ago. 09 ] Available from: https://doi.org/10.3390/ijms14023395
  • Fonte: International Journal of Cell Biology. Unidade: ICB

    Assunto: PARASITOLOGIA

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      LINDNER, Jasmin et al. Trafficked Proteins—Druggable in Plasmodium falciparum?. International Journal of Cell Biology, v. 2013, p. 1-13, 2013Tradução . . Disponível em: https://doi.org/10.1155/2013/435981. Acesso em: 09 ago. 2024.
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      Lindner, J., Meissner, K. A., Schettert, I., & Wrenger, C. (2013). Trafficked Proteins—Druggable in Plasmodium falciparum? International Journal of Cell Biology, 2013, 1-13. doi:10.1155/2013/435981
    • NLM

      Lindner J, Meissner KA, Schettert I, Wrenger C. Trafficked Proteins—Druggable in Plasmodium falciparum? [Internet]. International Journal of Cell Biology. 2013 ; 2013 1-13.[citado 2024 ago. 09 ] Available from: https://doi.org/10.1155/2013/435981
    • Vancouver

      Lindner J, Meissner KA, Schettert I, Wrenger C. Trafficked Proteins—Druggable in Plasmodium falciparum? [Internet]. International Journal of Cell Biology. 2013 ; 2013 1-13.[citado 2024 ago. 09 ] Available from: https://doi.org/10.1155/2013/435981
  • Fonte: Future Medicinal Chemistry. Unidade: ICB

    Assunto: PARASITOLOGIA

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      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: 09 ago. 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 ago. 09 ] 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 ago. 09 ] Available from: https://doi.org/10.4155/FMC.13.43

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