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  • 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: 28 mar. 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 mar. 28 ] 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 mar. 28 ] Available from: https://doi.org/10.1155/2015/351289
  • Source: Pesquisa FAPESP. Unidades: ICB, IFSC, IB

    Subjects: MALÁRIA (CONTROLE), RESISTÊNCIA (MEDICAMENTOS), PARASITOLOGIA, FÁRMACOS, EXTRATOS (FORMAS FARMACÊUTICAS), BIOQUÍMICA

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      LACERDA, Marcus Vinícius et al. Corrida contra a malária: médicos monitoram resistência do parasita aos medicamentos em uso, enquanto bioquímicos buscam alternativas. [Depoimento a Igor Zolnerkevic]. Pesquisa FAPESP. São Paulo: Instituto de Ciências Biomédicas, Universidade de São Paulo. Disponível em: http://revistapesquisa.fapesp.br/2015/11/17/corrida-contra-a-malaria/. Acesso em: 28 mar. 2024. , 2015
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      Lacerda, M. V., Ferreira, M. U., Magalhães, P. M., Guido, R. V. C., Garcia, C. R. da S., Wrenger, C., & Dias, L. C. (2015). Corrida contra a malária: médicos monitoram resistência do parasita aos medicamentos em uso, enquanto bioquímicos buscam alternativas. [Depoimento a Igor Zolnerkevic]. Pesquisa FAPESP. São Paulo: Instituto de Ciências Biomédicas, Universidade de São Paulo. Recuperado de http://revistapesquisa.fapesp.br/2015/11/17/corrida-contra-a-malaria/
    • NLM

      Lacerda MV, Ferreira MU, Magalhães PM, Guido RVC, Garcia CR da S, Wrenger C, Dias LC. Corrida contra a malária: médicos monitoram resistência do parasita aos medicamentos em uso, enquanto bioquímicos buscam alternativas. [Depoimento a Igor Zolnerkevic] [Internet]. Pesquisa FAPESP. 2015 ; no 2015( 237): 47-49.[citado 2024 mar. 28 ] Available from: http://revistapesquisa.fapesp.br/2015/11/17/corrida-contra-a-malaria/
    • Vancouver

      Lacerda MV, Ferreira MU, Magalhães PM, Guido RVC, Garcia CR da S, Wrenger C, Dias LC. Corrida contra a malária: médicos monitoram resistência do parasita aos medicamentos em uso, enquanto bioquímicos buscam alternativas. [Depoimento a Igor Zolnerkevic] [Internet]. Pesquisa FAPESP. 2015 ; no 2015( 237): 47-49.[citado 2024 mar. 28 ] Available from: http://revistapesquisa.fapesp.br/2015/11/17/corrida-contra-a-malaria/
  • 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: 28 mar. 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 mar. 28 ]
    • 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 mar. 28 ]
  • 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: 28 mar. 2024. , 2014
    • APA

      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 mar. 28 ]
    • Vancouver

      Silber AM, Pereira CA, Wrenger C. Drug discovery for infectious agents causing neglected diseases. Current Medicinal Chemistry. 2014 ; 21( 15): 1667.[citado 2024 mar. 28 ]
  • 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: 28 mar. 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 mar. 28 ] 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 mar. 28 ] 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: 28 mar. 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 mar. 28 ]
    • 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 mar. 28 ]
  • 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: 28 mar. 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 mar. 28 ] 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 mar. 28 ] 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: 28 mar. 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 mar. 28 ] 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 mar. 28 ] Available from: https://doi.org/10.1155/2014/108516
  • Source: 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: 28 mar. 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 mar. 28 ] 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 mar. 28 ] Available from: https://doi.org/10.3390/ijms14023395
  • 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: 28 mar. 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 mar. 28 ] 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 mar. 28 ] Available from: https://doi.org/10.1038/ncomms3060
  • Source: Drug discovery. Unidade: ICB

    Subjects: FARMÁCOS, PRODUTOS NATURAIS, DOENÇAS INFECIOSAS, ESTRESSE OXIDATIVO

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      WRENGER, Carsten e SCHETTER, Isolmar e LIEBAU, Eva. Oxidative stress in human infectious diseases - present and current - knowledge about its druggability. Drug discovery. Tradução . Rijeka, Croatia: In Tech, 2013. . Disponível em: http://www.intechopen.com/books/drug-discovery. Acesso em: 28 mar. 2024.
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      Wrenger, C., Schetter, I., & Liebau, E. (2013). Oxidative stress in human infectious diseases - present and current - knowledge about its druggability. In Drug discovery. Rijeka, Croatia: In Tech. Recuperado de http://www.intechopen.com/books/drug-discovery
    • NLM

      Wrenger C, Schetter I, Liebau E. Oxidative stress in human infectious diseases - present and current - knowledge about its druggability [Internet]. In: Drug discovery. Rijeka, Croatia: In Tech; 2013. [citado 2024 mar. 28 ] Available from: http://www.intechopen.com/books/drug-discovery
    • Vancouver

      Wrenger C, Schetter I, Liebau E. Oxidative stress in human infectious diseases - present and current - knowledge about its druggability [Internet]. In: Drug discovery. Rijeka, Croatia: In Tech; 2013. [citado 2024 mar. 28 ] Available from: http://www.intechopen.com/books/drug-discovery
  • 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: 28 mar. 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 mar. 28 ] 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 mar. 28 ] Available from: http://www.biochemj.org/bj/449/0175/bj4490175.htm
  • Source: 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: 28 mar. 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 mar. 28 ] 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 mar. 28 ] Available from: https://doi.org/10.1155/2013/435981
  • Source: Mehtods in Molecular Biology. Unidades: ICB, IQ

    Subjects: PARASITOLOGIA, OLIGONUCLEOTIDEOS, RECEPTORES DE ACETICOLINA, RNA

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      ULRICH, Henning e WRENGER, Carsten. Identification of aptamers as specific binders and modulators of cell-surface receptor activity. Mehtods in Molecular Biology, v. 986, p. 17-39, 2013Tradução . . Disponível em: https://doi.org/10.1007/978-1-62703-311-4_2 08/jul/14. Acesso em: 28 mar. 2024.
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      Ulrich, H., & Wrenger, C. (2013). Identification of aptamers as specific binders and modulators of cell-surface receptor activity. Mehtods in Molecular Biology, 986, 17-39. doi:10.1007/978-1-62703-311-4_2 08/jul/14
    • NLM

      Ulrich H, Wrenger C. Identification of aptamers as specific binders and modulators of cell-surface receptor activity [Internet]. Mehtods in Molecular Biology. 2013 ; 986 17-39.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1007/978-1-62703-311-4_2 08/jul/14
    • Vancouver

      Ulrich H, Wrenger C. Identification of aptamers as specific binders and modulators of cell-surface receptor activity [Internet]. Mehtods in Molecular Biology. 2013 ; 986 17-39.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1007/978-1-62703-311-4_2 08/jul/14
  • 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: 28 mar. 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
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      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 mar. 28 ] 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 mar. 28 ] Available from: https://doi.org/10.1107/S0907444913021550
  • Source: 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: 28 mar. 2024.
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      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 mar. 28 ] 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 mar. 28 ] Available from: https://doi.org/10.4155/FMC.13.43
  • Source: Parasitology Research. Unidade: ICB

    Assunto: PARASITOLOGIA

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      NDJONKA, Dieudonné et al. In vitro activity of extracts and isolated polyphenols from West African medicinal plants against Plasmodium falciparum. Parasitology Research, v. 111, n. 02, p. 827-834, 2012Tradução . . Disponível em: https://doi.org/10.1007/s00436-012-2905-y. Acesso em: 28 mar. 2024.
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      Ndjonka, D., Bergmann, B., Agyare, C., Zimbres, F. M., Lüersen, K., Hensel, A., et al. (2012). In vitro activity of extracts and isolated polyphenols from West African medicinal plants against Plasmodium falciparum. Parasitology Research, 111( 02), 827-834. doi:10.1007/s00436-012-2905-y
    • NLM

      Ndjonka D, Bergmann B, Agyare C, Zimbres FM, Lüersen K, Hensel A, Wrenger C, Liebau E. In vitro activity of extracts and isolated polyphenols from West African medicinal plants against Plasmodium falciparum [Internet]. Parasitology Research. 2012 ; 111( 02): 827-834.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1007/s00436-012-2905-y
    • Vancouver

      Ndjonka D, Bergmann B, Agyare C, Zimbres FM, Lüersen K, Hensel A, Wrenger C, Liebau E. In vitro activity of extracts and isolated polyphenols from West African medicinal plants against Plasmodium falciparum [Internet]. Parasitology Research. 2012 ; 111( 02): 827-834.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1007/s00436-012-2905-y
  • Source: Acta Crystallographica Section F. Structural Biology and Crystallization Communications. Unidade: ICB

    Assunto: PARASITOLOGIA

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      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: 28 mar. 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 mar. 28 ] 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 mar. 28 ] Available from: https://doi.org/10.1107/S1744309112014571
  • Source: Biochemical Journal. Unidade: ICB

    Assunto: PARASITOLOGIA

    Acesso à fonteDOIHow to cite
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    • ABNT

      KNÖCKEL, Julia et al. The antioxidative effect of de novo generated vitamin B6 in Plasmodium falciparum validated by protein interference. Biochemical Journal, v. 443, n. 2, p. 397-405, 2012Tradução . . Disponível em: https://doi.org/10.1042/BJ20111542. Acesso em: 28 mar. 2024.
    • APA

      Knöckel, J., Müller, I. B., Butzloff, S., Bergmann, B., Walter, R. D., & Wrenger, C. (2012). The antioxidative effect of de novo generated vitamin B6 in Plasmodium falciparum validated by protein interference. Biochemical Journal, 443( 2), 397-405. doi:10.1042/BJ20111542
    • NLM

      Knöckel J, Müller IB, Butzloff S, Bergmann B, Walter RD, Wrenger C. The antioxidative effect of de novo generated vitamin B6 in Plasmodium falciparum validated by protein interference [Internet]. Biochemical Journal. 2012 ; 443( 2): 397-405.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1042/BJ20111542
    • Vancouver

      Knöckel J, Müller IB, Butzloff S, Bergmann B, Walter RD, Wrenger C. The antioxidative effect of de novo generated vitamin B6 in Plasmodium falciparum validated by protein interference [Internet]. Biochemical Journal. 2012 ; 443( 2): 397-405.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1042/BJ20111542
  • 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: 28 mar. 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 mar. 28 ] 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 mar. 28 ] Available from: https://doi.org/10.1002/cyto.a.22081

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