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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
Source: Journal of Eukaryotic Microbiology. Unidade: ICB
Subjects: 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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] 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
Source: Parasitology. Unidade: ICB
Subjects: 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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] 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
Source: Nature Microbiology. Unidade: ICB
Subjects: 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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] 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.
Source: Diagnostic Microbiology and Infectious Disease. Unidade: ICB
Subjects: 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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] 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.
Source: Biochimica and Biophysica Acta. Molecular and Cell Biology of Lipids. Unidade: ICB
Subjects: PARASITOLOGIA, GENÉTICA BACTERIANA, CROMATOGRAFIA LÍQUIDA, ÁCIDOS, CLOSTRIDIUM, ESTEROIDES, ESPECTROMETRIA
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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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] 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
Source: Memorias do Instituto Oswaldo Cruz. Unidade: ICB
Subjects: 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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] 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.
Source: Journal of Infectious Diseases. Unidade: ICB
Subjects: 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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] Available from: https://doi.org/10.1093/infdis/jiy273
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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] Available from: https://doi.org/10.1016/j.bbrc.2018.02.112
Artigo de periodico
Independent regulation of Plasmodium falciparum rif gene promoters (2018)
Araujo, Rosana Beatriz Duque; Silva, Tatiane Macedo; Kaiser, Charlotte Sophie; Leite, Gabriela Fernandes; Ribolla, Paulo Eduardo Martins; Wunderlich, Gerhard
Source: Scientific Reports. Unidade: ICB
Subjects: PARASITOLOGIA, PLASMODIUM FALCIPARUM, ANTÍGENOS, EXPRESSÃO GÊNICA, FÁRMACOS
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ARAUJO, Rosana Beatriz Duque et al. Independent regulation of Plasmodium falciparum rif gene promoters. Scientific Reports, v. 8, p. 1-10, 2018Tradução . . Disponível em: https://doi.org/10.1038/s41598-018-27646-0. Acesso em: 10 nov. 2024.
APA
Araujo, R. B. D., Silva, T. M., Kaiser, C. S., Leite, G. F., Ribolla, P. E. M., & Wunderlich, G. (2018). Independent regulation of Plasmodium falciparum rif gene promoters. Scientific Reports, 8, 1-10. doi:10.1038/s41598-018-27646-0
NLM
Araujo RBD, Silva TM, Kaiser CS, Leite GF, Ribolla PEM, Wunderlich G. Independent regulation of Plasmodium falciparum rif gene promoters [Internet]. Scientific Reports. 2018 ; 8 1-10.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1038/s41598-018-27646-0
Vancouver
Araujo RBD, Silva TM, Kaiser CS, Leite GF, Ribolla PEM, Wunderlich G. Independent regulation of Plasmodium falciparum rif gene promoters [Internet]. Scientific Reports. 2018 ; 8 1-10.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1038/s41598-018-27646-0
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: 10 nov. 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 nov. 10 ] Available from: https://doi.org/10.3390/biom8030083
Vancouver
Krüger A, Zimbres FM, Kronenberger T, Wrenger C. Molecular modeling applied to nucleic acid-based molecule development [Internet]. Biomolecules. 2018 ; 8( 3): 1-17.[citado 2024 nov. 10 ] Available from: https://doi.org/10.3390/biom8030083
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
Source: Tropical Medicine & International Health. Unidade: ICB
Subjects: PARASITOLOGIA, LEISHMANIOSE CUTÂNEA
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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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] Available from: https://doi.org/10.1111/tmi.13119
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
Source: Free Radical Biology & Medicine. Unidade: ICB
Subjects: 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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] 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.
Source: Parasitology. Unidade: ICB
Subjects: 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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] 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
Source: Infection, Genetics and Evolution. Unidade: ICB
Subjects: 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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] 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
Source: International Journal for Parasitology. Unidade: ICB
Subjects: PARASITOLOGIA, TRYPANOSOMA, FILOGENIA, MORCEGOS, TRYPANOSOMA CRUZI
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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: 10 nov. 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 nov. 10 ] 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 nov. 10 ] 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
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: 10 nov. 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 nov. 10 ] Available from: https://doi.org/10.1007/s00204-018-2165-4
Vancouver
Burk O, Kuzikov M, Kronenberger T, Jeske J, Keminer O, Thasler W E , Schwab M, Wrenger C, Windshügel B. Identification of approved drugs as potent inhibitors of pregnane X receptor activation with differential receptor interaction profiles [Internet]. Archives of Toxicology. 2018 ; 92 1435-1451.[citado 2024 nov. 10 ] 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: 10 nov. 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 nov. 10 ] Available from: https://doi.org/10.1371/journal.pone.0195011
Vancouver
Lunev S, Butzloff S, Romero AR, Linzke M, Batista FA, Meissner KA, Müller IB, Adawy A, Wrenger C, Groves MR. Oligomeric interfaces as a tool in drug discovery: Specific interference with activity of malate dehydrogenase of Plasmodium falciparum in vitro [Internet]. PLOS ONE. 2018 ;13( 4): e0195011.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1371/journal.pone.0195011
Artigo de periodico
Ethanolic extract of the fungus Trichoderma stromaticum decreases inflammation and ameliorates experimental cerebral malaria in C57BL/6 mice (2018)
Cariaco, Yusmaris; Lima, Wânia Rezende; Sousa, Romulo; Nascimento, Layane Alencar Costa; Briceño, Marisol Pallete; Fotoran, Wesley Luzetti; Wunderlich, Gerhard ; Santos, Jane Lima dos; Silva, Neide Maria
Source: Scientific Reports. Unidade: ICB
Subjects: PARASITOLOGIA, FUNGOS, MALÁRIA, PLASMODIUM FALCIPARUM
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ABNT
CARIACO, Yusmaris et al. Ethanolic extract of the fungus Trichoderma stromaticum decreases inflammation and ameliorates experimental cerebral malaria in C57BL/6 mice. Scientific Reports, v. 8, p. 1-15, 2018Tradução . . Disponível em: https://doi.org/10.1038/s41598-018-19840-x. Acesso em: 10 nov. 2024.
APA
Cariaco, Y., Lima, W. R., Sousa, R., Nascimento, L. A. C., Briceño, M. P., Fotoran, W. L., et al. (2018). Ethanolic extract of the fungus Trichoderma stromaticum decreases inflammation and ameliorates experimental cerebral malaria in C57BL/6 mice. Scientific Reports, 8, 1-15. doi:10.1038/s41598-018-19840-x
NLM
Cariaco Y, Lima WR, Sousa R, Nascimento LAC, Briceño MP, Fotoran WL, Wunderlich G, Santos JL dos, Silva NM. Ethanolic extract of the fungus Trichoderma stromaticum decreases inflammation and ameliorates experimental cerebral malaria in C57BL/6 mice [Internet]. Scientific Reports. 2018 ; 8 1-15.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1038/s41598-018-19840-x
Vancouver
Cariaco Y, Lima WR, Sousa R, Nascimento LAC, Briceño MP, Fotoran WL, Wunderlich G, Santos JL dos, Silva NM. Ethanolic extract of the fungus Trichoderma stromaticum decreases inflammation and ameliorates experimental cerebral malaria in C57BL/6 mice [Internet]. Scientific Reports. 2018 ; 8 1-15.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1038/s41598-018-19840-x
Artigo de periodico
Chemokine (C- C motif) ligand 25 expressed by trophoblast cells and leukocytes bearing its receptor Ccr9: an alliance during embryo implantation? (2018)
Weingrill, Rodrigo Barbano ; Hoshida, Mara Sandra ; Martinhago, Ciro Dresch; Silva, Simone Corrêa da; Cardoso, Elaine Cristina; Jorge, Patrícia Palmeira Daenekas; Marinho, Claudio Romero Farias ; Bevilacqua, Estela Maris Andrade Forell
Source: American Journal of Reproductive Immunology. Unidade: ICB
Subjects: BLASTOCISTO, QUIMIOTAXIA DE LEUCÓCITO, PROTEÍNAS RECOMBINANTES, TROFOBLASTO, CAMUNDONGOS, ENDOMÉTRIO, COMPORTAMENTO MATERNO ANIMAL
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ABNT
WEINGRILL, Rodrigo Barbano et al. Chemokine (C- C motif) ligand 25 expressed by trophoblast cells and leukocytes bearing its receptor Ccr9: an alliance during embryo implantation?. American Journal of Reproductive Immunology, v. 79, n. 1, 2018Tradução . . Disponível em: https://doi.org/10.1111/aji.12783. Acesso em: 10 nov. 2024.
APA
Weingrill, R. B., Hoshida, M. S., Martinhago, C. D., Silva, S. C. da, Cardoso, E. C., Jorge, P. P. D., et al. (2018). Chemokine (C- C motif) ligand 25 expressed by trophoblast cells and leukocytes bearing its receptor Ccr9: an alliance during embryo implantation? American Journal of Reproductive Immunology, 79( 1). doi:10.1111/aji.12783
NLM
Weingrill RB, Hoshida MS, Martinhago CD, Silva SC da, Cardoso EC, Jorge PPD, Marinho CRF, Bevilacqua EMAF. Chemokine (C- C motif) ligand 25 expressed by trophoblast cells and leukocytes bearing its receptor Ccr9: an alliance during embryo implantation? [Internet]. American Journal of Reproductive Immunology. 2018 ; 79( 1):[citado 2024 nov. 10 ] Available from: https://doi.org/10.1111/aji.12783
Vancouver
Weingrill RB, Hoshida MS, Martinhago CD, Silva SC da, Cardoso EC, Jorge PPD, Marinho CRF, Bevilacqua EMAF. Chemokine (C- C motif) ligand 25 expressed by trophoblast cells and leukocytes bearing its receptor Ccr9: an alliance during embryo implantation? [Internet]. American Journal of Reproductive Immunology. 2018 ; 79( 1):[citado 2024 nov. 10 ] Available from: https://doi.org/10.1111/aji.12783
Artigo de periodico
Technical challenges of working with extracellular vesicles (2018)
Ramirez, Marcel I.; Amorim, Maria G.; Gadelha, Catarina ; Milic, Ivana ; Welsh, Joshua A. ; Freitas, Vanessa Morais ; Nawaz, Muhammad ; Akbar, Naveed ; Couch, Yvonne ; Makin, Laura ; Cooke, Fiona ; Vettore, André Luiz ; Batista, Patricia X. ; Freezor, Roberta; Pezuk, Julia Alejandra ; Rosa-Fernandes, Lívia ; Carreira, Ana Claudia O. ; Devitt, Andrew ; Jacobs, Laura; Silva, Israel T. ; Coakley, Gillian ; Nunes, Diana N. ; Carter, Dave; Palmisano, Giuseppe ; Dias-Neto, Emmanuel
Source: Nanoscale. Unidade: ICB
Subjects: ÁCIDOS NUCLEICOS, BIÓPSIA, NANOPARTÍCULAS, LIPÍDEOS
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ABNT
RAMIREZ, Marcel I. et al. Technical challenges of working with extracellular vesicles. Nanoscale, v. 10, n. 3, p. 881-906, 2018Tradução . . Disponível em: https://doi.org/10.1039/c7nr08360b. Acesso em: 10 nov. 2024.
APA
Ramirez, M. I., Amorim, M. G., Gadelha, C., Milic, I., Welsh, J. A., Freitas, V. M., et al. (2018). Technical challenges of working with extracellular vesicles. Nanoscale, 10( 3), 881-906. doi:10.1039/c7nr08360b
NLM
Ramirez MI, Amorim MG, Gadelha C, Milic I, Welsh JA, Freitas VM, Nawaz M, Akbar N, Couch Y, Makin L, Cooke F, Vettore AL, Batista PX, Freezor R, Pezuk JA, Rosa-Fernandes L, Carreira ACO, Devitt A, Jacobs L, Silva IT, Coakley G, Nunes DN, Carter D, Palmisano G, Dias-Neto E. Technical challenges of working with extracellular vesicles [Internet]. Nanoscale. 2018 ; 10( 3): 881-906.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1039/c7nr08360b
Vancouver
Ramirez MI, Amorim MG, Gadelha C, Milic I, Welsh JA, Freitas VM, Nawaz M, Akbar N, Couch Y, Makin L, Cooke F, Vettore AL, Batista PX, Freezor R, Pezuk JA, Rosa-Fernandes L, Carreira ACO, Devitt A, Jacobs L, Silva IT, Coakley G, Nunes DN, Carter D, Palmisano G, Dias-Neto E. Technical challenges of working with extracellular vesicles [Internet]. Nanoscale. 2018 ; 10( 3): 881-906.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1039/c7nr08360b

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