ReP USP - Resultado da busca

Artigo de periodico
Identiﬁcation of a non-competitive inhibitor of Plasmodium falciparum aspartate transcarbamoylase (2018)
Lunev, Sergey ; Bosch, Soraya S. ; Batista, Fernando A.; Wang, Chao; Li, Jingyao; Linzke, Marleen; Kruithof, Paul; Chamoun, George; Domling, Alexander S.S. ; Wrenger, Carsten ; Groves, Matthew R.
Source: Biochemical and Biophysical Research Communications. Unidade: ICB
Subjects: PARASITOLOGIA, PLASMODIUM FALCIPARUM, MALÁRIA
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ABNT
LUNEV, Sergey et al. Identiﬁcation of a non-competitive inhibitor of Plasmodium falciparum aspartate transcarbamoylase. Biochemical and Biophysical Research Communications, v. 497, n. 3, p. 835-842, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.bbrc.2018.02.112. Acesso em: 28 jun. 2024.
APA
Lunev, S., Bosch, S. S., Batista, F. A., Wang, C., Li, J., Linzke, M., et al. (2018). Identiﬁcation of a non-competitive inhibitor of Plasmodium falciparum aspartate transcarbamoylase. Biochemical and Biophysical Research Communications, 497(3), 835-842. doi:10.1016/j.bbrc.2018.02.112
NLM
Lunev S, Bosch SS, Batista FA, Wang C, Li J, Linzke M, Kruithof P, Chamoun G, Domling ASS, Wrenger C, Groves MR. Identiﬁcation of a non-competitive inhibitor of Plasmodium falciparum aspartate transcarbamoylase [Internet]. Biochemical and Biophysical Research Communications. 2018 ; 497(3): 835-842.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.bbrc.2018.02.112
Vancouver
Lunev S, Bosch SS, Batista FA, Wang C, Li J, Linzke M, Kruithof P, Chamoun G, Domling ASS, Wrenger C, Groves MR. Identiﬁcation of a non-competitive inhibitor of Plasmodium falciparum aspartate transcarbamoylase [Internet]. Biochemical and Biophysical Research Communications. 2018 ; 497(3): 835-842.[citado 2024 jun. 28 ] Available from: https://doi.org/10.1016/j.bbrc.2018.02.112
Artigo de periodico
Molecular modeling applied to nucleic acid-based molecule development (2018)
Krüger, Arne ; Zimbres, Flávia M. ; Kronenberger, Thales ; Wrenger, Carsten
Source: Biomolecules. Unidade: ICB
Subjects: 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: 28 jun. 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 jun. 28 ] 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 jun. 28 ] Available from: https://doi.org/10.3390/biom8030083
Artigo de periodico
Identification of approved drugs as potent inhibitors of pregnane X receptor activation with differential receptor interaction profiles (2018)
Burk, Oliver; Kuzikov, Maria; Kronenberger, Thales ; Jeske, Judith; Keminer, Oliver ; Thasler, Wolfgang E. ; Schwab, Matthias ; Wrenger, Carsten ; Windshügel, Bjorn
Source: Archives of Toxicology. Unidade: ICB
Subjects: 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: 28 jun. 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 jun. 28 ] 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 jun. 28 ] Available from: https://doi.org/10.1007/s00204-018-2165-4
Artigo de periodico
Oligomeric interfaces as a tool in drug discovery: Specific interference with activity of malate dehydrogenase of Plasmodium falciparum in vitro (2018)
Lunev, Sergey; Butzloff, Sabine; Romero, Atilio R.; Linzke, Marleen; Batista, Fernando A.; Meissner, Kamila A.; Müller, Ingrid B.; Adawy, Alaa; Wrenger, Carsten ; Groves, Matthew R.
Source: PLOS ONE. Unidade: ICB
Subjects: PARASITOLOGIA, PLASMODIUM FALCIPARUM, MALÁRIA
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ABNT
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: 28 jun. 2024.
APA
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 jun. 28 ] 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 jun. 28 ] Available from: https://doi.org/10.1371/journal.pone.0195011
Artigo de periodico
Targeting the Plasmodium falciparum Plasmepsin V by ligand-based virtual screening (2018)
Meissner, Kamila Anna ; Kronenberger, Thales ; Maltarollo, Vinícius Gonçalves ; Trossini, Gustavo Henrique Goulart ; Wrenger, Carsten
Source: Chemical Biology and Drug Design. Unidades: FCF, ICB
Subjects: 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: 28 jun. 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 jun. 28 ] 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 jun. 28 ] Available from: https://doi.org/10.1111/cbdd.13416
Artigo de periodico
Metabolite transporters in trypanosomatid parasites: promising therapeutic targets but... how to deal with them? (2014)
Pereira, C. A.; Mayé, M.; Wrenger, Carsten ; Miranda, M. R.
Source: Current Medicinal Chemistry. Unidade: ICB
Assunto: PARASITOLOGIA
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ABNT
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 jun. 2024.
APA
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 jun. 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 jun. 28 ]
Artigo de periodico-carta/editorial
Drug discovery for infectious agents causing neglected diseases (2014)
Silber, Ariel Mariano ; Pereira, Claudio A.; Wrenger, Carsten
Source: Current Medicinal Chemistry. Unidade: ICB
Assunto: PARASITOLOGIA
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ABNT
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 jun. 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 jun. 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 jun. 28 ]
Artigo de periodico
MRSA infections: from classical treatment to suicide drugs (2014)
Drebes, Julia; Künz, Madeleine; Pereira, Claudio A.; Betzel, Christian; Wrenger, Carsten
Source: Current Medicinal Chemistry. Unidade: ICB
Assunto: PARASITOLOGIA
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ABNT
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 jun. 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 jun. 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 jun. 28 ]
Artigo de periodico
Purification, crystallization and preliminary X-ray diffraction analysis of pyridoxal kinase from Plasmodium falciparum (PfPdxK) (2014)
Kronenberger, Thales; Lunev, Sergey; Wrenger, Carsten ; Groves, Matthew R.
Source: Acta Crystallographica Section F, Structural Biology Communications. Unidade: ICB
Subjects: 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: 28 jun. 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 jun. 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 jun. 28 ] Available from: https://doi.org/10.1107/S2053230X14019864
Artigo de periodico
Vitamin B6-dependent enzymes in the human malaria parasite Plasmodium falciparum: a druggable target? (2014)
Kronenberger, Thales; Lindner, Jasmin; Meissner, Kamila Anna; Zimbres, Flávia Menezes; Coronado, Monika A.; Sauer, Frank Martin; Schettert, Isolmar; Wrenger, Carsten
Source: 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: 28 jun. 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 jun. 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 jun. 28 ] Available from: https://doi.org/10.1155/2014/108516
Artigo de periodico
Exploring inhibition of Pdx1, a component of the PLP synthase complex of the human malaria parasite Plasmodium falciparum (2013)
Reeksting, Shaun B.; Müller, Ingrid B.; Burger, Pieter B.; Burgos, Emmanuel S.; Salmon, Laurent; Louw, Abraham I.; Birkholtz, Lyn-Marie; Wrenger, Carsten
Source: Biochemical Journal. Unidade: ICB
Subjects: PARASITOLOGIA, MALARIA, PLASMODIUM
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ABNT
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 jun. 2024.
APA
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 jun. 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 jun. 28 ] Available from: http://www.biochemj.org/bj/449/0175/bj4490175.htm
Artigo de periodico
Trafficked Proteins—Druggable in Plasmodium falciparum? (2013)
Lindner, Jasmin; Meissner, Kamila Anna; Schettert, Isolmar; Wrenger, Carsten
Source: International Journal of Cell Biology. Unidade: ICB
Assunto: PARASITOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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 jun. 2024.
APA
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 jun. 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 jun. 28 ] Available from: https://doi.org/10.1155/2013/435981
Artigo de periodico
Targeting the vitamin biosynthesis pathways for the treatment of malaria (2013)
Kronenberger, Thales; Schettert, Isolmar; Wrenger, Carsten
Source: Future Medicinal Chemistry. Unidade: ICB
Assunto: PARASITOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 28 jun. 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 jun. 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 jun. 28 ] Available from: https://doi.org/10.4155/FMC.13.43

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