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Artigo de periodico
In vitro cellular division of Trypanosoma abeli reveals two pathways for organelle replication (2019)
Borges, Alyssa Rossi ; Toledo, Daniel Afonso de Mendonça; Fermino, Bruno Rafael ; Oliveira, José Carlos de; Silber, Ariel Mariano ; Elias, Maria Carolina ; D’Avila, Heloisa ; Scopel, Kézia Katiani Gorza
Fonte: Journal of Eukaryotic Microbiology. Unidade: ICB
Assuntos: PARASITOLOGIA, DIVISÃO CELULAR, TRYPANOSOMA CRUZI
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ABNT
BORGES, Alyssa Rossi et al. In vitro cellular division of Trypanosoma abeli reveals two pathways for organelle replication. Journal of Eukaryotic Microbiology, v. 66, n. 3, p. 385-392, 2019Tradução . . Disponível em: https://doi.org/10.1111/jeu.12678. Acesso em: 18 jun. 2024.
APA
Borges, A. R., Toledo, D. A. de M., Fermino, B. R., Oliveira, J. C. de, Silber, A. M., Elias, M. C., et al. (2019). In vitro cellular division of Trypanosoma abeli reveals two pathways for organelle replication. Journal of Eukaryotic Microbiology, 66( 3), 385-392. doi:10.1111/jeu.12678
NLM
Borges AR, Toledo DA de M, Fermino BR, Oliveira JC de, Silber AM, Elias MC, D’Avila H, Scopel KKG. In vitro cellular division of Trypanosoma abeli reveals two pathways for organelle replication [Internet]. Journal of Eukaryotic Microbiology. 2019 ; 66( 3): 385-392.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1111/jeu.12678
Vancouver
Borges AR, Toledo DA de M, Fermino BR, Oliveira JC de, Silber AM, Elias MC, D’Avila H, Scopel KKG. In vitro cellular division of Trypanosoma abeli reveals two pathways for organelle replication [Internet]. Journal of Eukaryotic Microbiology. 2019 ; 66( 3): 385-392.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1111/jeu.12678
Artigo de periodico
Topical tamoxifen in the therapy of cutaneous leishmaniasis (2018)
Trinconi, Cristina T. ; Reimão, Juliana Q.; Bonano, Vivian I.; Espada, Caroline Ricce ; Miguel, Danilo C. ; Yokoyama-Yasunaka, Jenicer Kasume Umada; Uliana, Silvia Reni Bortolin
Fonte: Parasitology. Unidade: ICB
Assuntos: PARASITOLOGIA, LEISHMANIOSE CUTÂNEA, PERMUTAÇÕES
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ABNT
TRINCONI, Cristina T. et al. Topical tamoxifen in the therapy of cutaneous leishmaniasis. Parasitology, v. 145, n. 4, p. 490-496, 2018Tradução . . Disponível em: https://doi.org/10.1017/S0031182017000130. Acesso em: 18 jun. 2024.
APA
Trinconi, C. T., Reimão, J. Q., Bonano, V. I., Espada, C. R., Miguel, D. C., Yokoyama-Yasunaka, J. K. U., & Uliana, S. R. B. (2018). Topical tamoxifen in the therapy of cutaneous leishmaniasis. Parasitology, 145( 4), 490-496. doi:10.1017/S0031182017000130
NLM
Trinconi CT, Reimão JQ, Bonano VI, Espada CR, Miguel DC, Yokoyama-Yasunaka JKU, Uliana SRB. Topical tamoxifen in the therapy of cutaneous leishmaniasis [Internet]. Parasitology. 2018 ; 145( 4): 490-496.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1017/S0031182017000130
Vancouver
Trinconi CT, Reimão JQ, Bonano VI, Espada CR, Miguel DC, Yokoyama-Yasunaka JKU, Uliana SRB. Topical tamoxifen in the therapy of cutaneous leishmaniasis [Internet]. Parasitology. 2018 ; 145( 4): 490-496.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1017/S0031182017000130
Artigo de periodico
Cytotoxic anti-circumsporozoite antibodies target malaria sporozoites in the host skin (2018)
Aliprandini, Eduardo ; Tavares, Joana; Panatieri, Raquel Hoffmann; Thiberge, Sabine ; Yamamoto, Marcio Massao ; Silvie, Olivier ; Ishino, Tomoko ; Dartevelle, Sylvie; Traincard, François; Boscardin, Silvia Beatriz ; Amino, Rogerio
Fonte: Nature Microbiology. Unidade: ICB
Assuntos: ANTICORPOS, PARASITOLOGIA, MALÁRIA, PLASMODIUM FALCIPARUM, MOSQUITOS
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ALIPRANDINI, Eduardo et al. Cytotoxic anti-circumsporozoite antibodies target malaria sporozoites in the host skin. Nature Microbiology, v. 3, p. 1224-1233, 2018Tradução . . Disponível em: https://doi.org/10.1038/s41564-018-0254-z. Acesso em: 18 jun. 2024.
APA
Aliprandini, E., Tavares, J., Panatieri, R. H., Thiberge, S., Yamamoto, M. M., Silvie, O., et al. (2018). Cytotoxic anti-circumsporozoite antibodies target malaria sporozoites in the host skin. Nature Microbiology, 3, 1224-1233. doi:10.1038/s41564-018-0254-z
NLM
Aliprandini E, Tavares J, Panatieri RH, Thiberge S, Yamamoto MM, Silvie O, Ishino T, Dartevelle S, Traincard F, Boscardin SB, Amino R. Cytotoxic anti-circumsporozoite antibodies target malaria sporozoites in the host skin [Internet]. Nature Microbiology. 2018 ; 3 1224-1233.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1038/s41564-018-0254-z
Vancouver
Aliprandini E, Tavares J, Panatieri RH, Thiberge S, Yamamoto MM, Silvie O, Ishino T, Dartevelle S, Traincard F, Boscardin SB, Amino R. Cytotoxic anti-circumsporozoite antibodies target malaria sporozoites in the host skin [Internet]. Nature Microbiology. 2018 ; 3 1224-1233.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1038/s41564-018-0254-z
Artigo de periodico
Identiﬁcation of Leishmania (Viannia) species and clinical isolates of Leishmania (Leishmania) amazonensis from Brazil using PCR-RFLP of the heat-shock protein 70 gene reveals some unexpected observations (2018)
Espada, Caroline Ricce ; Ortiz, Paola Andrea ; Shaw, Jeffrey Jon ; Barral, Aldina M.P. ; Costa, Jackson M.L.; Uliana, Silvia Reni Bortolin ; Coelho, Adriano C.
Fonte: Diagnostic Microbiology and Infectious Disease. Unidade: ICB
Assuntos: PARASITOLOGIA, LEISHMANIA, PROTEÍNAS, REAÇÃO EM CADEIA POR POLIMERASE
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ABNT
ESPADA, Caroline Ricce et al. Identiﬁcation of Leishmania (Viannia) species and clinical isolates of Leishmania (Leishmania) amazonensis from Brazil using PCR-RFLP of the heat-shock protein 70 gene reveals some unexpected observations. Diagnostic Microbiology and Infectious Disease, v. 91, p. 312-318, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.diagmicrobio.2018.03.004. Acesso em: 18 jun. 2024.
APA
Espada, C. R., Ortiz, P. A., Shaw, J. J., Barral, A. M. P., Costa, J. M. L., Uliana, S. R. B., & Coelho, A. C. (2018). Identiﬁcation of Leishmania (Viannia) species and clinical isolates of Leishmania (Leishmania) amazonensis from Brazil using PCR-RFLP of the heat-shock protein 70 gene reveals some unexpected observations. Diagnostic Microbiology and Infectious Disease, 91, 312-318. doi:10.1016/j.diagmicrobio.2018.03.004
NLM
Espada CR, Ortiz PA, Shaw JJ, Barral AMP, Costa JML, Uliana SRB, Coelho AC. Identiﬁcation of Leishmania (Viannia) species and clinical isolates of Leishmania (Leishmania) amazonensis from Brazil using PCR-RFLP of the heat-shock protein 70 gene reveals some unexpected observations [Internet]. Diagnostic Microbiology and Infectious Disease. 2018 ; 91 312-318.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1016/j.diagmicrobio.2018.03.004
Vancouver
Espada CR, Ortiz PA, Shaw JJ, Barral AMP, Costa JML, Uliana SRB, Coelho AC. Identiﬁcation of Leishmania (Viannia) species and clinical isolates of Leishmania (Leishmania) amazonensis from Brazil using PCR-RFLP of the heat-shock protein 70 gene reveals some unexpected observations [Internet]. Diagnostic Microbiology and Infectious Disease. 2018 ; 91 312-318.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1016/j.diagmicrobio.2018.03.004
Artigo de periodico
Identification of a gene encoding a flavoprotein involved in bile acid metabolism by the human gut bacterium Clostridium scindens ATCC 35704 (2018)
Harris, Spencer C. ; Devendran, Saravanan; Alves, João Marcelo Pereira ; Mythen, Sean M. ; Hylemon, Phillip B. ; Ridlon, Jason M.
Fonte: Biochimica and Biophysica Acta. Molecular and Cell Biology of Lipids. Unidade: ICB
Assuntos: PARASITOLOGIA, GENÉTICA BACTERIANA, CROMATOGRAFIA LÍQUIDA, ÁCIDOS, CLOSTRIDIUM, ESTEROIDES, ESPECTROMETRIA
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ABNT
HARRIS, Spencer C. et al. Identification of a gene encoding a flavoprotein involved in bile acid metabolism by the human gut bacterium Clostridium scindens ATCC 35704. Biochimica and Biophysica Acta. Molecular and Cell Biology of Lipids, v. 1863, n. 3, p. 276-283, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.bbalip.2017.12.001. Acesso em: 18 jun. 2024.
APA
Harris, S. C., Devendran, S., Alves, J. M. P., Mythen, S. M., Hylemon, P. B., & Ridlon, J. M. (2018). Identification of a gene encoding a flavoprotein involved in bile acid metabolism by the human gut bacterium Clostridium scindens ATCC 35704. Biochimica and Biophysica Acta. Molecular and Cell Biology of Lipids, 1863( 3), 276-283. doi:10.1016/j.bbalip.2017.12.001
NLM
Harris SC, Devendran S, Alves JMP, Mythen SM, Hylemon PB, Ridlon JM. Identification of a gene encoding a flavoprotein involved in bile acid metabolism by the human gut bacterium Clostridium scindens ATCC 35704 [Internet]. Biochimica and Biophysica Acta. Molecular and Cell Biology of Lipids. 2018 ; 1863( 3): 276-283.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1016/j.bbalip.2017.12.001
Vancouver
Harris SC, Devendran S, Alves JMP, Mythen SM, Hylemon PB, Ridlon JM. Identification of a gene encoding a flavoprotein involved in bile acid metabolism by the human gut bacterium Clostridium scindens ATCC 35704 [Internet]. Biochimica and Biophysica Acta. Molecular and Cell Biology of Lipids. 2018 ; 1863( 3): 276-283.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1016/j.bbalip.2017.12.001
Artigo de periodico
Plasmodium falciparum parasites overexpressing farnesyl diphosphate synthase/geranylgeranyl diphosphate synthase are more resistant to risedronate (2018)
Gabriel, Heloisa Berti ; Azevedo, Mauro F. ; Ichikawa, Emilia Akemi Shiraishi Kimura; Katzin, Alejandro Miguel
Fonte: Memorias do Instituto Oswaldo Cruz. Unidade: ICB
Assuntos: PARASITOLOGIA, PLASMODIUM FALCIPARUM, MALÁRIA, MALÁRIA
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ABNT
GABRIEL, Heloisa Berti et al. Plasmodium falciparum parasites overexpressing farnesyl diphosphate synthase/geranylgeranyl diphosphate synthase are more resistant to risedronate. Memorias do Instituto Oswaldo Cruz, v. 113, n. 10, p. e180174, 2018Tradução . . Disponível em: http://www.scielo.br/pdf/mioc/v113n10/1678-8060-mioc-113-10-e180174.pdf. Acesso em: 18 jun. 2024.
APA
Gabriel, H. B., Azevedo, M. F., Ichikawa, E. A. S. K., & Katzin, A. M. (2018). Plasmodium falciparum parasites overexpressing farnesyl diphosphate synthase/geranylgeranyl diphosphate synthase are more resistant to risedronate. Memorias do Instituto Oswaldo Cruz, 113( 10), e180174. doi:10.1590/0074-02760180174
NLM
Gabriel HB, Azevedo MF, Ichikawa EASK, Katzin AM. Plasmodium falciparum parasites overexpressing farnesyl diphosphate synthase/geranylgeranyl diphosphate synthase are more resistant to risedronate [Internet]. Memorias do Instituto Oswaldo Cruz. 2018 ; 113( 10): e180174.[citado 2024 jun. 18 ] Available from: http://www.scielo.br/pdf/mioc/v113n10/1678-8060-mioc-113-10-e180174.pdf
Vancouver
Gabriel HB, Azevedo MF, Ichikawa EASK, Katzin AM. Plasmodium falciparum parasites overexpressing farnesyl diphosphate synthase/geranylgeranyl diphosphate synthase are more resistant to risedronate [Internet]. Memorias do Instituto Oswaldo Cruz. 2018 ; 113( 10): e180174.[citado 2024 jun. 18 ] Available from: http://www.scielo.br/pdf/mioc/v113n10/1678-8060-mioc-113-10-e180174.pdf
Artigo de periodico
Identification and immunological characterization of the ligand domain of Plasmodium vivax reticulocyte binding protein 1a (2018)
Ntumngia, Francis B.; Thomson-Luque, Richard ; Galusic, Sandra ; Frato, Gabriel; Frischmann, Sarah; Peabody, David S.; Chackerian, Bryce ; Ferreira, Marcelo Urbano ; King, Christopher L.; Adams, John H.
Fonte: Journal of Infectious Diseases. Unidade: ICB
Assuntos: PARASITOLOGIA, PLASMODIUM, PROTEÍNAS, MALÁRIA, VACINAS
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ABNT
NTUMNGIA, Francis B. et al. Identification and immunological characterization of the ligand domain of Plasmodium vivax reticulocyte binding protein 1a. Journal of Infectious Diseases, v. 218, n. 7, p. 1110-1118, 2018Tradução . . Disponível em: https://doi.org/10.1093/infdis/jiy273. Acesso em: 18 jun. 2024.
APA
Ntumngia, F. B., Thomson-Luque, R., Galusic, S., Frato, G., Frischmann, S., Peabody, D. S., et al. (2018). Identification and immunological characterization of the ligand domain of Plasmodium vivax reticulocyte binding protein 1a. Journal of Infectious Diseases, 218( 7), 1110-1118. doi:10.1093/infdis/jiy273
NLM
Ntumngia FB, Thomson-Luque R, Galusic S, Frato G, Frischmann S, Peabody DS, Chackerian B, Ferreira MU, King CL, Adams JH. Identification and immunological characterization of the ligand domain of Plasmodium vivax reticulocyte binding protein 1a [Internet]. Journal of Infectious Diseases. 2018 ; 218( 7): 1110-1118.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1093/infdis/jiy273
Vancouver
Ntumngia FB, Thomson-Luque R, Galusic S, Frato G, Frischmann S, Peabody DS, Chackerian B, Ferreira MU, King CL, Adams JH. Identification and immunological characterization of the ligand domain of Plasmodium vivax reticulocyte binding protein 1a [Internet]. Journal of Infectious Diseases. 2018 ; 218( 7): 1110-1118.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1093/infdis/jiy273
Artigo de periodico
Mass spectrometry characterization of endophytic bacterium Curtobacterium sp. strain ER1/6 isolat ed from Citrus sinensis (2018)
Araújo, Francisca Diana da Silva; Santos, Daiene Souza; Pagotto, Carolina Clepf; Araújo, Welington Luiz de ; Eberlin, Marcos Nogueira
Fonte: Journal of Mass Spectrometry. Unidade: ICB
Assuntos: MICROBIOLOGIA, ESPECTROMETRIA DE MASSAS, METABÓLITOS, ÁCIDOS GRAXOS
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ABNT
ARAÚJO, Francisca Diana da Silva et al. Mass spectrometry characterization of endophytic bacterium Curtobacterium sp. strain ER1/6 isolat ed from Citrus sinensis. Journal of Mass Spectrometry, v. 53, n. 1, p. 91-97, 2018Tradução . . Disponível em: https://doi.org/10.1002/jms.4042. Acesso em: 18 jun. 2024.
APA
Araújo, F. D. da S., Santos, D. S., Pagotto, C. C., Araújo, W. L. de, & Eberlin, M. N. (2018). Mass spectrometry characterization of endophytic bacterium Curtobacterium sp. strain ER1/6 isolat ed from Citrus sinensis. Journal of Mass Spectrometry, 53( 1), 91-97. doi:10.1002/jms.4042
NLM
Araújo FD da S, Santos DS, Pagotto CC, Araújo WL de, Eberlin MN. Mass spectrometry characterization of endophytic bacterium Curtobacterium sp. strain ER1/6 isolat ed from Citrus sinensis [Internet]. Journal of Mass Spectrometry. 2018 ; 53( 1): 91-97.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1002/jms.4042
Vancouver
Araújo FD da S, Santos DS, Pagotto CC, Araújo WL de, Eberlin MN. Mass spectrometry characterization of endophytic bacterium Curtobacterium sp. strain ER1/6 isolat ed from Citrus sinensis [Internet]. Journal of Mass Spectrometry. 2018 ; 53( 1): 91-97.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1002/jms.4042
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.
Fonte: Biochemical and Biophysical Research Communications. Unidade: ICB
Assuntos: 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: 18 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. 18 ] 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. 18 ] Available from: https://doi.org/10.1016/j.bbrc.2018.02.112
Artigo de periodico
Does adaptation to vertebrate codon usage relate to flavivirus emergence potential? (2018)
Paola, Nicholas Di; Freire, Caio César de Melo; Zanotto, Paolo Marinho de Andrade
Fonte: PLOS ONE. Unidade: ICB
Assuntos: MICROBIOLOGIA, FLAVIVIRUS, NUCLEOTÍDEOS
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ABNT
PAOLA, Nicholas Di e FREIRE, Caio César de Melo e ZANOTTO, Paolo Marinho de Andrade. Does adaptation to vertebrate codon usage relate to flavivirus emergence potential?. PLOS ONE, v. 13, n. 1, p. 1-17, 2018Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0191652. Acesso em: 18 jun. 2024.
APA
Paola, N. D., Freire, C. C. de M., & Zanotto, P. M. de A. (2018). Does adaptation to vertebrate codon usage relate to flavivirus emergence potential? PLOS ONE, 13( 1), 1-17. doi:10.1371/journal.pone.0191652
NLM
Paola ND, Freire CC de M, Zanotto PM de A. Does adaptation to vertebrate codon usage relate to flavivirus emergence potential? [Internet]. PLOS ONE. 2018 ; 13( 1): 1-17.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1371/journal.pone.0191652
Vancouver
Paola ND, Freire CC de M, Zanotto PM de A. Does adaptation to vertebrate codon usage relate to flavivirus emergence potential? [Internet]. PLOS ONE. 2018 ; 13( 1): 1-17.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1371/journal.pone.0191652
Artigo de periodico
Molecular modeling applied to nucleic acid-based molecule development (2018)
Krüger, Arne ; Zimbres, Flávia M. ; Kronenberger, Thales ; Wrenger, Carsten
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: 18 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. 18 ] 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. 18 ] Available from: https://doi.org/10.3390/biom8030083
Artigo de periodico
Proanthocyanidin polymeric tannins from Stryphnodendron adstringens are effective against Candida spp. isolates and for vaginal candidiasis treatment (2018)
Freitas, Aline Luiza Duarte de; Kaplum, Vanessa; Rossi, Diego Conrado Pereira; Silva, Leandro Buffoni Roque da; Melhem, Márcia de Souza Carvalho; Taborda, Carlos Pelleschi ; Mello, João Carlos Palazzo de; Nakamura, Celso Vataru; Ishida, Kelly
Fonte: Journal of Ethnopharmacology. Unidade: ICB
Assuntos: MICROBIOLOGIA, PROANTOCIANIDINAS, CANDIDÍASE, CANDIDA, VAGINA
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ABNT
FREITAS, Aline Luiza Duarte de et al. Proanthocyanidin polymeric tannins from Stryphnodendron adstringens are effective against Candida spp. isolates and for vaginal candidiasis treatment. Journal of Ethnopharmacology, v. 216, p. 184-190, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.jep.2018.01.008. Acesso em: 18 jun. 2024.
APA
Freitas, A. L. D. de, Kaplum, V., Rossi, D. C. P., Silva, L. B. R. da, Melhem, M. de S. C., Taborda, C. P., et al. (2018). Proanthocyanidin polymeric tannins from Stryphnodendron adstringens are effective against Candida spp. isolates and for vaginal candidiasis treatment. Journal of Ethnopharmacology, 216, 184-190. doi:10.1016/j.jep.2018.01.008
NLM
Freitas ALD de, Kaplum V, Rossi DCP, Silva LBR da, Melhem M de SC, Taborda CP, Mello JCP de, Nakamura CV, Ishida K. Proanthocyanidin polymeric tannins from Stryphnodendron adstringens are effective against Candida spp. isolates and for vaginal candidiasis treatment [Internet]. Journal of Ethnopharmacology. 2018 ; 216 184-190.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1016/j.jep.2018.01.008
Vancouver
Freitas ALD de, Kaplum V, Rossi DCP, Silva LBR da, Melhem M de SC, Taborda CP, Mello JCP de, Nakamura CV, Ishida K. Proanthocyanidin polymeric tannins from Stryphnodendron adstringens are effective against Candida spp. isolates and for vaginal candidiasis treatment [Internet]. Journal of Ethnopharmacology. 2018 ; 216 184-190.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1016/j.jep.2018.01.008
Artigo de periodico
Effect of ultrasonic activation on the reduction of bacteria and endotoxins in root canals: a randomized clinical trial (2018)
Nakamura, Vitor Cesar; Pinheiro, E. T.; Prado, L. C.; Silveira, A. C.; Carvalho, A. P. L.; Mayer, Marcia Pinto Alves ; Gavini, G.
Fonte: International Endodontic Journal. Unidades: FO, ICB
Assuntos: MICROBIOLOGIA, ULTRASSOM, ENSAIO CLÍNICO, ENDOTOXINAS, PERIODONTITE PERIAPICAL
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ABNT
NAKAMURA, Vitor Cesar et al. Effect of ultrasonic activation on the reduction of bacteria and endotoxins in root canals: a randomized clinical trial. International Endodontic Journal, v. 51, p. e12-e22, 2018Tradução . . Disponível em: https://doi.org/10.1111/iej.12783. Acesso em: 18 jun. 2024.
APA
Nakamura, V. C., Pinheiro, E. T., Prado, L. C., Silveira, A. C., Carvalho, A. P. L., Mayer, M. P. A., & Gavini, G. (2018). Effect of ultrasonic activation on the reduction of bacteria and endotoxins in root canals: a randomized clinical trial. International Endodontic Journal, 51, e12-e22. doi:10.1111/iej.12783
NLM
Nakamura VC, Pinheiro ET, Prado LC, Silveira AC, Carvalho APL, Mayer MPA, Gavini G. Effect of ultrasonic activation on the reduction of bacteria and endotoxins in root canals: a randomized clinical trial [Internet]. International Endodontic Journal. 2018 ; 51 e12-e22.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1111/iej.12783
Vancouver
Nakamura VC, Pinheiro ET, Prado LC, Silveira AC, Carvalho APL, Mayer MPA, Gavini G. Effect of ultrasonic activation on the reduction of bacteria and endotoxins in root canals: a randomized clinical trial [Internet]. International Endodontic Journal. 2018 ; 51 e12-e22.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1111/iej.12783
Artigo de periodico
Tamoxifen and meglumine antimoniate combined therapy in cutaneous leishmaniasis patients: a randomised trial (2018)
Machado, Paulo R. L.; Ribeiro, Camila S.; França‐Costa, Jaqueline; Dourado, Mayra E. F.; Trinconi, Cristiana T.; Yokoyama‐Yasunaka, Jenicer Kazumi Umada; Malta‐Santos, Hayna; Borges, Valéria M.; Carvalho, Edgar M.; Uliana, Silvia Reni Bortolin
Fonte: Tropical Medicine & International Health. Unidade: ICB
Assuntos: PARASITOLOGIA, LEISHMANIOSE CUTÂNEA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MACHADO, Paulo R. L. et al. Tamoxifen and meglumine antimoniate combined therapy in cutaneous leishmaniasis patients: a randomised trial. Tropical Medicine & International Health, v. 23, n. 9, p. 936-942, 2018Tradução . . Disponível em: https://doi.org/10.1111/tmi.13119. Acesso em: 18 jun. 2024.
APA
Machado, P. R. L., Ribeiro, C. S., França‐Costa, J., Dourado, M. E. F., Trinconi, C. T., Yokoyama‐Yasunaka, J. K. U., et al. (2018). Tamoxifen and meglumine antimoniate combined therapy in cutaneous leishmaniasis patients: a randomised trial. Tropical Medicine & International Health, 23( 9), 936-942. doi:10.1111/tmi.13119
NLM
Machado PRL, Ribeiro CS, França‐Costa J, Dourado MEF, Trinconi CT, Yokoyama‐Yasunaka JKU, Malta‐Santos H, Borges VM, Carvalho EM, Uliana SRB. Tamoxifen and meglumine antimoniate combined therapy in cutaneous leishmaniasis patients: a randomised trial [Internet]. Tropical Medicine & International Health. 2018 ; 23( 9): 936-942.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1111/tmi.13119
Vancouver
Machado PRL, Ribeiro CS, França‐Costa J, Dourado MEF, Trinconi CT, Yokoyama‐Yasunaka JKU, Malta‐Santos H, Borges VM, Carvalho EM, Uliana SRB. Tamoxifen and meglumine antimoniate combined therapy in cutaneous leishmaniasis patients: a randomised trial [Internet]. Tropical Medicine & International Health. 2018 ; 23( 9): 936-942.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1111/tmi.13119
Artigo de periodico
Increased mutability to fosfomycin resistance in Proteus mirabilis clinical isolates (2018)
Fonseca, Marina R. B.; Sato, Juliana L.; Lima-Noronha, Marco A.; Fernández-Silva, Frank S.; Galhardo, Rodrigo da Silva
Fonte: Infection, Genetics and Evolution. Unidade: ICB
Assuntos: MICROBIOLOGIA, ANTIBIÓTICOS, MUTAGÊNESE, BACTÉRIAS GRAM-NEGATIVAS
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ABNT
FONSECA, Marina R. B. et al. Increased mutability to fosfomycin resistance in Proteus mirabilis clinical isolates. Infection, Genetics and Evolution, v. 58, p. 27-33, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.meegid.2017.12.012. Acesso em: 18 jun. 2024.
APA
Fonseca, M. R. B., Sato, J. L., Lima-Noronha, M. A., Fernández-Silva, F. S., & Galhardo, R. da S. (2018). Increased mutability to fosfomycin resistance in Proteus mirabilis clinical isolates. Infection, Genetics and Evolution, 58, 27-33. doi:10.1016/j.meegid.2017.12.012
NLM
Fonseca MRB, Sato JL, Lima-Noronha MA, Fernández-Silva FS, Galhardo R da S. Increased mutability to fosfomycin resistance in Proteus mirabilis clinical isolates [Internet]. Infection, Genetics and Evolution. 2018 ; 58 27-33.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1016/j.meegid.2017.12.012
Vancouver
Fonseca MRB, Sato JL, Lima-Noronha MA, Fernández-Silva FS, Galhardo R da S. Increased mutability to fosfomycin resistance in Proteus mirabilis clinical isolates [Internet]. Infection, Genetics and Evolution. 2018 ; 58 27-33.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1016/j.meegid.2017.12.012
Artigo de periodico
Promastigote parasites cultured from the lesions of patients with mucosal leishmaniasis are more resistant to oxidative stress than promastigotes from a cutaneous lesion (2018)
Ávila, Lucilla Ribeiro; Gomes, Clayson Moura ; Oliveira, Pollyana Guimarães ; Gomes, Rodrigo Saar ; Vinaud, Marina Clare ; Uliana, Silvia Reni Bortolin ; Ribeiro-Dias, Fátima ; Oliveira, Milton Adriano Pelli
Fonte: Free Radical Biology & Medicine. Unidade: ICB
Assuntos: PARASITOLOGIA, LEISHMANIOSE CUTÂNEA, LEISHMANIA BRASILIENSIS, ESTRESSE OXIDATIVO, ÓXIDO NÍTRICO, AMASTIGOTES
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ABNT
ÁVILA, Lucilla Ribeiro et al. Promastigote parasites cultured from the lesions of patients with mucosal leishmaniasis are more resistant to oxidative stress than promastigotes from a cutaneous lesion. Free Radical Biology & Medicine, v. 129, p. 35-45, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.freeradbiomed.2018.09.005. Acesso em: 18 jun. 2024.
APA
Ávila, L. R., Gomes, C. M., Oliveira, P. G., Gomes, R. S., Vinaud, M. C., Uliana, S. R. B., et al. (2018). Promastigote parasites cultured from the lesions of patients with mucosal leishmaniasis are more resistant to oxidative stress than promastigotes from a cutaneous lesion. Free Radical Biology & Medicine, 129, 35-45. doi:10.1016/j.freeradbiomed.2018.09.005
NLM
Ávila LR, Gomes CM, Oliveira PG, Gomes RS, Vinaud MC, Uliana SRB, Ribeiro-Dias F, Oliveira MAP. Promastigote parasites cultured from the lesions of patients with mucosal leishmaniasis are more resistant to oxidative stress than promastigotes from a cutaneous lesion [Internet]. Free Radical Biology & Medicine. 2018 ; 129 35-45.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2018.09.005
Vancouver
Ávila LR, Gomes CM, Oliveira PG, Gomes RS, Vinaud MC, Uliana SRB, Ribeiro-Dias F, Oliveira MAP. Promastigote parasites cultured from the lesions of patients with mucosal leishmaniasis are more resistant to oxidative stress than promastigotes from a cutaneous lesion [Internet]. Free Radical Biology & Medicine. 2018 ; 129 35-45.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2018.09.005
Artigo de periodico
Chemotherapy of Leishmaniasis: present challenges (2018)
Uliana, Silvia Reni Bortolin ; Trinconi, Cristiana T. ; Coelho, Adriano C.
Fonte: Parasitology. Unidade: ICB
Assuntos: PARASITOLOGIA, LEISHMANIOSE CUTÂNEA, QUIMIOTERAPIA, MEDICAMENTO
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ABNT
ULIANA, Silvia Reni Bortolin e TRINCONI, Cristiana T. e COELHO, Adriano C. Chemotherapy of Leishmaniasis: present challenges. Parasitology, v. 145, n. 4, p. 464-480, 2018Tradução . . Disponível em: https://doi.org/10.1017/S0031182016002523. Acesso em: 18 jun. 2024.
APA
Uliana, S. R. B., Trinconi, C. T., & Coelho, A. C. (2018). Chemotherapy of Leishmaniasis: present challenges. Parasitology, 145( 4), 464-480. doi:10.1017/S0031182016002523
NLM
Uliana SRB, Trinconi CT, Coelho AC. Chemotherapy of Leishmaniasis: present challenges [Internet]. Parasitology. 2018 ; 145( 4): 464-480.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1017/S0031182016002523
Vancouver
Uliana SRB, Trinconi CT, Coelho AC. Chemotherapy of Leishmaniasis: present challenges [Internet]. Parasitology. 2018 ; 145( 4): 464-480.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1017/S0031182016002523
Artigo de periodico
Diagnosis and genetic analysis of the worldwide distributed Rattus-borne Trypanosoma (Herpetosoma) lewisi and its allied species in blood and fleas of rodents (2018)
Ortiz, Paola Andrea ; Garcia, Herakles A. ; Lima, Luciana Vieira Rego; Silva, Flávia Maia da; Campaner,Marta; Pereira, Carlos Lopes; Jittapalapong, Sathaporn ; Neves, Luis C. B. G.; Desquesnes, Marc ; Camargo, Erney Felicio Plessmann ; Teixeira, Marta Maria Geraldes
Fonte: Infection, Genetics and Evolution. Unidade: ICB
Assuntos: PARASITOLOGIA, DIAGNÓSTICO, DIVERSIDADE GENÉTICA, PULGAS, TRYPANOSOMA, RODENTIA
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ABNT
ORTIZ, Paola Andrea et al. Diagnosis and genetic analysis of the worldwide distributed Rattus-borne Trypanosoma (Herpetosoma) lewisi and its allied species in blood and fleas of rodents. Infection, Genetics and Evolution, v. 63, p. 380-390, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.meegid.2017.09.001. Acesso em: 18 jun. 2024.
APA
Ortiz, P. A., Garcia, H. A., Lima, L. V. R., Silva, F. M. da, Campaner, M., Pereira, C. L., et al. (2018). Diagnosis and genetic analysis of the worldwide distributed Rattus-borne Trypanosoma (Herpetosoma) lewisi and its allied species in blood and fleas of rodents. Infection, Genetics and Evolution, 63, 380-390. doi:10.1016/j.meegid.2017.09.001
NLM
Ortiz PA, Garcia HA, Lima LVR, Silva FM da, Campaner M, Pereira CL, Jittapalapong S, Neves LCBG, Desquesnes M, Camargo EFP, Teixeira MMG. Diagnosis and genetic analysis of the worldwide distributed Rattus-borne Trypanosoma (Herpetosoma) lewisi and its allied species in blood and fleas of rodents [Internet]. Infection, Genetics and Evolution. 2018 ; 63 380-390.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1016/j.meegid.2017.09.001
Vancouver
Ortiz PA, Garcia HA, Lima LVR, Silva FM da, Campaner M, Pereira CL, Jittapalapong S, Neves LCBG, Desquesnes M, Camargo EFP, Teixeira MMG. Diagnosis and genetic analysis of the worldwide distributed Rattus-borne Trypanosoma (Herpetosoma) lewisi and its allied species in blood and fleas of rodents [Internet]. Infection, Genetics and Evolution. 2018 ; 63 380-390.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1016/j.meegid.2017.09.001
Artigo de periodico
Trypanosoma rangeli is phylogenetically closer to Old World trypanosomes than to Trypanosoma cruzi (2018)
Álvarez, Oneida Espinosa ; Ortiz, Paola Andrea ; Lima, Luciana; Costa-Martins, André G. ; Serrano, Myrna Garcia; Herder, Stephane ; Buck, Gregory A. ; Camargo, Erney Felicio Plessmann ; Hamilton, Patrick B. ; Stevens, Jamie R.; Teixeira, Marta Maria Geraldes
Fonte: International Journal for Parasitology. Unidade: ICB
Assuntos: PARASITOLOGIA, TRYPANOSOMA, FILOGENIA, MORCEGOS, TRYPANOSOMA CRUZI
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ÁLVAREZ, Oneida Espinosa et al. Trypanosoma rangeli is phylogenetically closer to Old World trypanosomes than to Trypanosoma cruzi. International Journal for Parasitology, v. 48, n. 7, p. 569-584, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.ijpara.2017.12.008. Acesso em: 18 jun. 2024.
APA
Álvarez, O. E., Ortiz, P. A., Lima, L., Costa-Martins, A. G., Serrano, M. G., Herder, S., et al. (2018). Trypanosoma rangeli is phylogenetically closer to Old World trypanosomes than to Trypanosoma cruzi. International Journal for Parasitology, 48( 7), 569-584. doi:10.1016/j.ijpara.2017.12.008
NLM
Álvarez OE, Ortiz PA, Lima L, Costa-Martins AG, Serrano MG, Herder S, Buck GA, Camargo EFP, Hamilton PB, Stevens JR, Teixeira MMG. Trypanosoma rangeli is phylogenetically closer to Old World trypanosomes than to Trypanosoma cruzi [Internet]. International Journal for Parasitology. 2018 ; 48( 7): 569-584.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1016/j.ijpara.2017.12.008
Vancouver
Álvarez OE, Ortiz PA, Lima L, Costa-Martins AG, Serrano MG, Herder S, Buck GA, Camargo EFP, Hamilton PB, Stevens JR, Teixeira MMG. Trypanosoma rangeli is phylogenetically closer to Old World trypanosomes than to Trypanosoma cruzi [Internet]. International Journal for Parasitology. 2018 ; 48( 7): 569-584.[citado 2024 jun. 18 ] Available from: https://doi.org/10.1016/j.ijpara.2017.12.008
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
Fonte: Archives of Toxicology. Unidade: ICB
Assuntos: PARASITOLOGIA, ANTAGONISMO DE DROGAS, CÉLULAS KUPFFER
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 18 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. 18 ] 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. 18 ] Available from: https://doi.org/10.1007/s00204-018-2165-4

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