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ZÚÑIGA, Gerardo Andrés Libreros et al. Integration of biophysical and biological approaches to validate fragment-like compounds targeting l,d-transpeptidases from Mycobacterium tuberculosis. Bioorganic Chemistry, v. 142, n. Ja 2024, p. 106960-1-106960-11, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2023.106960. Acesso em: 03 out. 2024.
APA
Zúñiga, G. A. L., Pavão, D. P. e, Barroso, V. de M., Mesquita, N. C. de M. R., Braga, S. F. P., Oliva, G., et al. (2024). Integration of biophysical and biological approaches to validate fragment-like compounds targeting l,d-transpeptidases from Mycobacterium tuberculosis. Bioorganic Chemistry, 142( Ja 2024), 106960-1-106960-11. doi:10.1016/j.bioorg.2023.106960
NLM
Zúñiga GAL, Pavão DP e, Barroso V de M, Mesquita NC de MR, Braga SFP, Oliva G, Ferreira RS, Ishida K, Dias MVB. Integration of biophysical and biological approaches to validate fragment-like compounds targeting l,d-transpeptidases from Mycobacterium tuberculosis [Internet]. Bioorganic Chemistry. 2024 ; 142( Ja 2024): 106960-1-106960-11.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.bioorg.2023.106960
Vancouver
Zúñiga GAL, Pavão DP e, Barroso V de M, Mesquita NC de MR, Braga SFP, Oliva G, Ferreira RS, Ishida K, Dias MVB. Integration of biophysical and biological approaches to validate fragment-like compounds targeting l,d-transpeptidases from Mycobacterium tuberculosis [Internet]. Bioorganic Chemistry. 2024 ; 142( Ja 2024): 106960-1-106960-11.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.bioorg.2023.106960
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MENEZES, Ana Paula de Jesus et al. Navigating the boundaries between metabolism and epigenetics in trypanosomes. Trends in Parasitology, v. 39, n. 8, p. 682-695 + supplemental information, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.pt.2023.05.010. Acesso em: 03 out. 2024.
APA
Menezes, A. P. de J., Giraldo, A. M. M., Castro, C. G. de, Bellini, N. K., Tosi, L. R. O., Thiemann, O. H., et al. (2023). Navigating the boundaries between metabolism and epigenetics in trypanosomes. Trends in Parasitology, 39( 8), 682-695 + supplemental information. doi:10.1016/j.pt.2023.05.010
NLM
Menezes AP de J, Giraldo AMM, Castro CG de, Bellini NK, Tosi LRO, Thiemann OH, Sabbaga MCQBE, Silber AM, Cunha JPC da. Navigating the boundaries between metabolism and epigenetics in trypanosomes [Internet]. Trends in Parasitology. 2023 ; 39( 8): 682-695 + supplemental information.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.pt.2023.05.010
Vancouver
Menezes AP de J, Giraldo AMM, Castro CG de, Bellini NK, Tosi LRO, Thiemann OH, Sabbaga MCQBE, Silber AM, Cunha JPC da. Navigating the boundaries between metabolism and epigenetics in trypanosomes [Internet]. Trends in Parasitology. 2023 ; 39( 8): 682-695 + supplemental information.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.pt.2023.05.010
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MOLLO, María Cruz et al. Antitrypanosomal Benzoxazinone series: hit-to-lead campaign and multiparametric optimization. 2022, Anais.. Campinas: Galoá, 2022. Disponível em: https://proceedings.science/brazmedchem-2022/papers/antitrypanosomal-benzoxazinone-series--hit-to-lead-campaign-and-multiparametric-optimization-. Acesso em: 03 out. 2024.
APA
Mollo, M. C., Cruz, L., Dessoy, M. A., Lee, E., Oliveira, R. G. de, Dutra, F., et al. (2022). Antitrypanosomal Benzoxazinone series: hit-to-lead campaign and multiparametric optimization. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/brazmedchem-2022/papers/antitrypanosomal-benzoxazinone-series--hit-to-lead-campaign-and-multiparametric-optimization-.
NLM
Mollo MC, Cruz L, Dessoy MA, Lee E, Oliveira RG de, Dutra F, Duarte SM, Andricopulo RK, Ferreira LLG, Chelucci RC, Feltrin C, Moraes CB, Andricopulo AD, Kratz J, Sjö P, Mowbray C, Dias LC. Antitrypanosomal Benzoxazinone series: hit-to-lead campaign and multiparametric optimization [Internet]. Anais eletrônicos. 2022 ;[citado 2024 out. 03 ] Available from: https://proceedings.science/brazmedchem-2022/papers/antitrypanosomal-benzoxazinone-series--hit-to-lead-campaign-and-multiparametric-optimization-.
Vancouver
Mollo MC, Cruz L, Dessoy MA, Lee E, Oliveira RG de, Dutra F, Duarte SM, Andricopulo RK, Ferreira LLG, Chelucci RC, Feltrin C, Moraes CB, Andricopulo AD, Kratz J, Sjö P, Mowbray C, Dias LC. Antitrypanosomal Benzoxazinone series: hit-to-lead campaign and multiparametric optimization [Internet]. Anais eletrônicos. 2022 ;[citado 2024 out. 03 ] Available from: https://proceedings.science/brazmedchem-2022/papers/antitrypanosomal-benzoxazinone-series--hit-to-lead-campaign-and-multiparametric-optimization-.
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SADRAEIAN, Mohammad et al. Study of viral photoinactivation by UV-C light and photosensitizer using a pseudotyped model. Pharmaceutics, v. 14, n. 3, p. 683-1-683-15, 2022Tradução . . Disponível em: https://doi.org/10.3390/pharmaceutics14030683. Acesso em: 03 out. 2024.
APA
Sadraeian, M., Pinto-Júnior, F. F., Miranda, M., Galinskas, J., Fernandes, R. S., Cruz, E. F. da, et al. (2022). Study of viral photoinactivation by UV-C light and photosensitizer using a pseudotyped model. Pharmaceutics, 14( 3), 683-1-683-15. doi:10.3390/pharmaceutics14030683
NLM
Sadraeian M, Pinto-Júnior FF, Miranda M, Galinskas J, Fernandes RS, Cruz EF da, Fu L, Zhang L, Diaz RS, Miranda GC de, Guimarães FEG. Study of viral photoinactivation by UV-C light and photosensitizer using a pseudotyped model [Internet]. Pharmaceutics. 2022 ; 14( 3): 683-1-683-15.[citado 2024 out. 03 ] Available from: https://doi.org/10.3390/pharmaceutics14030683
Vancouver
Sadraeian M, Pinto-Júnior FF, Miranda M, Galinskas J, Fernandes RS, Cruz EF da, Fu L, Zhang L, Diaz RS, Miranda GC de, Guimarães FEG. Study of viral photoinactivation by UV-C light and photosensitizer using a pseudotyped model [Internet]. Pharmaceutics. 2022 ; 14( 3): 683-1-683-15.[citado 2024 out. 03 ] Available from: https://doi.org/10.3390/pharmaceutics14030683
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OLIVEIRA, Valeria Maia de et al. Microorganisms: the secret agents of the biosphere, and their key roles in biotechnology. Biota Neotropica, v. 22 Nesp, p. 1-10, 2022Tradução . . Disponível em: https://doi.org/10.1590/1676-0611-BN-2022-1343. Acesso em: 03 out. 2024.
APA
Oliveira, V. M. de, Andreote, F. D., Cortelo, P. C., Castro-Gamboa, I., Costa-Lotufo, L. V., Polizeli, M. de L. T. D. M., et al. (2022). Microorganisms: the secret agents of the biosphere, and their key roles in biotechnology. Biota Neotropica, 22 Nesp, 1-10. doi:10.1590/1676-0611-BN-2022-1343
NLM
Oliveira VM de, Andreote FD, Cortelo PC, Castro-Gamboa I, Costa-Lotufo LV, Polizeli M de LTDM, Thiemann OH, Setubal JC. Microorganisms: the secret agents of the biosphere, and their key roles in biotechnology [Internet]. Biota Neotropica. 2022 ; 22 Nesp 1-10.[citado 2024 out. 03 ] Available from: https://doi.org/10.1590/1676-0611-BN-2022-1343
Vancouver
Oliveira VM de, Andreote FD, Cortelo PC, Castro-Gamboa I, Costa-Lotufo LV, Polizeli M de LTDM, Thiemann OH, Setubal JC. Microorganisms: the secret agents of the biosphere, and their key roles in biotechnology [Internet]. Biota Neotropica. 2022 ; 22 Nesp 1-10.[citado 2024 out. 03 ] Available from: https://doi.org/10.1590/1676-0611-BN-2022-1343
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PINTO-JÚNIOR, Fabio Francisco et al. Study of the mechanism of viral entry inhibitors and SARS-CoV-2 pseudovirus neutralization assay in the BSL2 laboratory. 2022, Anais.. São Carlos: Instituto de Física de São Carlos - IFSC, 2022. Disponível em: https://repositorio.usp.br/directbitstream/0b11cba7-9ae0-40de-9e49-d8e52a0431ea/3117161.pdf. Acesso em: 03 out. 2024.
APA
Pinto-Júnior, F. F., Sadraeian, M., Miranda, M., Guimarães, F. E. G., Diaz, R. S., & Miranda, G. C. de. (2022). Study of the mechanism of viral entry inhibitors and SARS-CoV-2 pseudovirus neutralization assay in the BSL2 laboratory. In Livro de Resumos. São Carlos: Instituto de Física de São Carlos - IFSC. Recuperado de https://repositorio.usp.br/directbitstream/0b11cba7-9ae0-40de-9e49-d8e52a0431ea/3117161.pdf
NLM
Pinto-Júnior FF, Sadraeian M, Miranda M, Guimarães FEG, Diaz RS, Miranda GC de. Study of the mechanism of viral entry inhibitors and SARS-CoV-2 pseudovirus neutralization assay in the BSL2 laboratory [Internet]. Livro de Resumos. 2022 ;[citado 2024 out. 03 ] Available from: https://repositorio.usp.br/directbitstream/0b11cba7-9ae0-40de-9e49-d8e52a0431ea/3117161.pdf
Vancouver
Pinto-Júnior FF, Sadraeian M, Miranda M, Guimarães FEG, Diaz RS, Miranda GC de. Study of the mechanism of viral entry inhibitors and SARS-CoV-2 pseudovirus neutralization assay in the BSL2 laboratory [Internet]. Livro de Resumos. 2022 ;[citado 2024 out. 03 ] Available from: https://repositorio.usp.br/directbitstream/0b11cba7-9ae0-40de-9e49-d8e52a0431ea/3117161.pdf
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SRINIVASAN, Vasundara et al. Antiviral activity of natural phenolic compounds in complex at an allosteric site of SARS-CoV-2 papain-like protease. Communications Biology, v. 5, p. 1-12, 2022Tradução . . Disponível em: https://doi.org/10.1038/s42003-022-03737-7. Acesso em: 03 out. 2024.
APA
Srinivasan, V., Brognaro, H., Prabhu, P. R., Souza, E. E. de, Günther, S., Reinke, P. Y. A., et al. (2022). Antiviral activity of natural phenolic compounds in complex at an allosteric site of SARS-CoV-2 papain-like protease. Communications Biology, 5, 1-12. doi:10.1038/s42003-022-03737-7
NLM
Srinivasan V, Brognaro H, Prabhu PR, Souza EE de, Günther S, Reinke PYA, Barra ALC, Machado RRG, Durigon EL, Wrenger C. Antiviral activity of natural phenolic compounds in complex at an allosteric site of SARS-CoV-2 papain-like protease [Internet]. Communications Biology. 2022 ; 5 1-12.[citado 2024 out. 03 ] Available from: https://doi.org/10.1038/s42003-022-03737-7
Vancouver
Srinivasan V, Brognaro H, Prabhu PR, Souza EE de, Günther S, Reinke PYA, Barra ALC, Machado RRG, Durigon EL, Wrenger C. Antiviral activity of natural phenolic compounds in complex at an allosteric site of SARS-CoV-2 papain-like protease [Internet]. Communications Biology. 2022 ; 5 1-12.[citado 2024 out. 03 ] Available from: https://doi.org/10.1038/s42003-022-03737-7
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VICARI, Hugo Passos et al. Synthetic cyclopenta[b]indoles exhibit antineoplastic activity by targeting microtubule dynamics in acute myeloid leukemia cells. European Journal of Pharmacology, v. 894, p. 173853-1-173853-10, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.ejphar.2021.173853. Acesso em: 03 out. 2024.
APA
Vicari, H. P., Lima, K., Gomes, R. da C., Fernandes, D. C., Silva, J. C. L. da, Rodrigues Junior, M. T., et al. (2021). Synthetic cyclopenta[b]indoles exhibit antineoplastic activity by targeting microtubule dynamics in acute myeloid leukemia cells. European Journal of Pharmacology, 894, 173853-1-173853-10. doi:10.1016/j.ejphar.2021.173853
NLM
Vicari HP, Lima K, Gomes R da C, Fernandes DC, Silva JCL da, Rodrigues Junior MT, Oliveira ASB de, Santos RN dos, Andricopulo AD, Coelho F, Costa-Lotufo LV, Machado Neto JA. Synthetic cyclopenta[b]indoles exhibit antineoplastic activity by targeting microtubule dynamics in acute myeloid leukemia cells [Internet]. European Journal of Pharmacology. 2021 ; 894 173853-1-173853-10.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.ejphar.2021.173853
Vancouver
Vicari HP, Lima K, Gomes R da C, Fernandes DC, Silva JCL da, Rodrigues Junior MT, Oliveira ASB de, Santos RN dos, Andricopulo AD, Coelho F, Costa-Lotufo LV, Machado Neto JA. Synthetic cyclopenta[b]indoles exhibit antineoplastic activity by targeting microtubule dynamics in acute myeloid leukemia cells [Internet]. European Journal of Pharmacology. 2021 ; 894 173853-1-173853-10.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.ejphar.2021.173853
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FREIRE, Marjorie Caroline Liberato Cavalcanti et al. Non-Toxic dimeric peptides derived from the bothropstoxin-I are potent SARS-CoV-2 and papain-like protease inhibitors. Molecules, v. 26, n. 16, p. 4896-1-4896-17, 2021Tradução . . Disponível em: https://doi.org/10.3390/molecules26164896. Acesso em: 03 out. 2024.
APA
Freire, M. C. L. C., Noske, G. D., Bitencourt, N. V., Sanches, P. R. S., Santos-Filho, N. A., Oliveira, V. G. F., et al. (2021). Non-Toxic dimeric peptides derived from the bothropstoxin-I are potent SARS-CoV-2 and papain-like protease inhibitors. Molecules, 26( 16), 4896-1-4896-17. doi:10.3390/molecules26164896
NLM
Freire MCLC, Noske GD, Bitencourt NV, Sanches PRS, Santos-Filho NA, Oliveira VGF, Souza EP de, Nogueira VHR, Godoy MO de, Nakamura AM, Fernandes RS, Godoy AS de, Juliano MA, Peres B de M, Barbosa CG, Moraes CB, Freitas Junior LHG de, Cilli EM, Guido RVC, Oliva G. Non-Toxic dimeric peptides derived from the bothropstoxin-I are potent SARS-CoV-2 and papain-like protease inhibitors [Internet]. Molecules. 2021 ; 26( 16): 4896-1-4896-17.[citado 2024 out. 03 ] Available from: https://doi.org/10.3390/molecules26164896
Vancouver
Freire MCLC, Noske GD, Bitencourt NV, Sanches PRS, Santos-Filho NA, Oliveira VGF, Souza EP de, Nogueira VHR, Godoy MO de, Nakamura AM, Fernandes RS, Godoy AS de, Juliano MA, Peres B de M, Barbosa CG, Moraes CB, Freitas Junior LHG de, Cilli EM, Guido RVC, Oliva G. Non-Toxic dimeric peptides derived from the bothropstoxin-I are potent SARS-CoV-2 and papain-like protease inhibitors [Internet]. Molecules. 2021 ; 26( 16): 4896-1-4896-17.[citado 2024 out. 03 ] Available from: https://doi.org/10.3390/molecules26164896
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FEU, Amanda Eiriz et al. Glycosylated narciclasine alkaloid in Hippeastrum puniceum (Lam.) Kuntze. South African Journal of Botany, v. 136, n. Ja 2021, p. 30-34, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.sajb.2020.09.006. Acesso em: 03 out. 2024.
APA
Feu, A. E., Andrade, J. P. de, Ayala, A. P., Almeida, L. C. de, Costa-Lotufo, L. V., Bastida, J., et al. (2021). Glycosylated narciclasine alkaloid in Hippeastrum puniceum (Lam.) Kuntze. South African Journal of Botany, 136( Ja 2021), 30-34. doi:10.1016/j.sajb.2020.09.006
NLM
Feu AE, Andrade JP de, Ayala AP, Almeida LC de, Costa-Lotufo LV, Bastida J, Ellena J, Borges W de S. Glycosylated narciclasine alkaloid in Hippeastrum puniceum (Lam.) Kuntze [Internet]. South African Journal of Botany. 2021 ; 136( Ja 2021): 30-34.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.sajb.2020.09.006
Vancouver
Feu AE, Andrade JP de, Ayala AP, Almeida LC de, Costa-Lotufo LV, Bastida J, Ellena J, Borges W de S. Glycosylated narciclasine alkaloid in Hippeastrum puniceum (Lam.) Kuntze [Internet]. South African Journal of Botany. 2021 ; 136( Ja 2021): 30-34.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.sajb.2020.09.006
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CARRASCO, Letícia Dias de Melo et al. Polymyxin resistance among XDR ST1 carbapenem-resistant Acinetobacter baumannii clone expanding in a teaching hospital. Frontiers in Microbiology, v. 12, p. 622704-1-622704-11 + supplementary material, 2021Tradução . . Disponível em: https://doi.org/10.3389/fmicb.2021.622704. Acesso em: 03 out. 2024.
APA
Carrasco, L. D. de M., Dabul, A. N. G., Boralli, C. M. dos S., Righetto, G. M., Carvalho, I. S. e, Dornelas, J. V., et al. (2021). Polymyxin resistance among XDR ST1 carbapenem-resistant Acinetobacter baumannii clone expanding in a teaching hospital. Frontiers in Microbiology, 12, 622704-1-622704-11 + supplementary material. doi:10.3389/fmicb.2021.622704
NLM
Carrasco LD de M, Dabul ANG, Boralli CM dos S, Righetto GM, Carvalho IS e, Dornelas JV, Mata CPSM da, Araújo CA de, Leite EMM, Lincopan N, Camargo ILB da C. Polymyxin resistance among XDR ST1 carbapenem-resistant Acinetobacter baumannii clone expanding in a teaching hospital [Internet]. Frontiers in Microbiology. 2021 ; 12 622704-1-622704-11 + supplementary material.[citado 2024 out. 03 ] Available from: https://doi.org/10.3389/fmicb.2021.622704
Vancouver
Carrasco LD de M, Dabul ANG, Boralli CM dos S, Righetto GM, Carvalho IS e, Dornelas JV, Mata CPSM da, Araújo CA de, Leite EMM, Lincopan N, Camargo ILB da C. Polymyxin resistance among XDR ST1 carbapenem-resistant Acinetobacter baumannii clone expanding in a teaching hospital [Internet]. Frontiers in Microbiology. 2021 ; 12 622704-1-622704-11 + supplementary material.[citado 2024 out. 03 ] Available from: https://doi.org/10.3389/fmicb.2021.622704
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FERREIRA, Rafael Augusto Alves et al. 2-aminobenzimidazoles for leishmaniasis: from initial hit discovery to in vivo profiling. PLOS Neglected Tropical Diseases, v. 15, n. 2, p. e0009196-1-e0009196-20, 2021Tradução . . Disponível em: https://doi.org/10.1371/journal.pntd.0009196. Acesso em: 03 out. 2024.
APA
Ferreira, R. A. A., Rezende Junior, C. de, Martinez, P. D. G., Koovits, P. J., Soares, B. M., Ferreira, L. L. G., et al. (2021). 2-aminobenzimidazoles for leishmaniasis: from initial hit discovery to in vivo profiling. PLOS Neglected Tropical Diseases, 15( 2), e0009196-1-e0009196-20. doi:10.1371/journal.pntd.0009196
NLM
Ferreira RAA, Rezende Junior C de, Martinez PDG, Koovits PJ, Soares BM, Ferreira LLG, Duarte SM, Chelucci RC, Andricopulo AD, Galuppo MK, Uliana SRB, Matheeussen A, Caljon G, Maes L, Campbell S, Kratz JM, Mowbray CE, Dias LC. 2-aminobenzimidazoles for leishmaniasis: from initial hit discovery to in vivo profiling [Internet]. PLOS Neglected Tropical Diseases. 2021 ; 15( 2): e0009196-1-e0009196-20.[citado 2024 out. 03 ] Available from: https://doi.org/10.1371/journal.pntd.0009196
Vancouver
Ferreira RAA, Rezende Junior C de, Martinez PDG, Koovits PJ, Soares BM, Ferreira LLG, Duarte SM, Chelucci RC, Andricopulo AD, Galuppo MK, Uliana SRB, Matheeussen A, Caljon G, Maes L, Campbell S, Kratz JM, Mowbray CE, Dias LC. 2-aminobenzimidazoles for leishmaniasis: from initial hit discovery to in vivo profiling [Internet]. PLOS Neglected Tropical Diseases. 2021 ; 15( 2): e0009196-1-e0009196-20.[citado 2024 out. 03 ] Available from: https://doi.org/10.1371/journal.pntd.0009196
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SAHM, Bianca Del'Bianco et al. Com falta de investimento nacional, farmacêuticas estrangeiras lucram com remédios que saem da biodiversidade brasileira. [Depoimento a Marcelo Canellas]. Fantástico. Rio de Janeiro: Instituto de Ciências Biomédicas, Universidade de São Paulo. Disponível em: https://globoplay.globo.com/v/9956824/. Acesso em: 03 out. 2024. , 2021
APA
Sahm, B. D. 'B., Costa-Lotufo, L. V., Queiroz, E., Andersen, P., Espíndola, L., Pupo, M. T., et al. (2021). Com falta de investimento nacional, farmacêuticas estrangeiras lucram com remédios que saem da biodiversidade brasileira. [Depoimento a Marcelo Canellas]. Fantástico. Rio de Janeiro: Instituto de Ciências Biomédicas, Universidade de São Paulo. Recuperado de https://globoplay.globo.com/v/9956824/
NLM
Sahm BD'B, Costa-Lotufo LV, Queiroz E, Andersen P, Espíndola L, Pupo MT, Vieira PC, Andricopulo AD. Com falta de investimento nacional, farmacêuticas estrangeiras lucram com remédios que saem da biodiversidade brasileira. [Depoimento a Marcelo Canellas] [Internet]. Fantástico. 2021 ;[citado 2024 out. 03 ] Available from: https://globoplay.globo.com/v/9956824/
Vancouver
Sahm BD'B, Costa-Lotufo LV, Queiroz E, Andersen P, Espíndola L, Pupo MT, Vieira PC, Andricopulo AD. Com falta de investimento nacional, farmacêuticas estrangeiras lucram com remédios que saem da biodiversidade brasileira. [Depoimento a Marcelo Canellas] [Internet]. Fantástico. 2021 ;[citado 2024 out. 03 ] Available from: https://globoplay.globo.com/v/9956824/
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SOUZA, Juliana Oliveira de et al. Parasitological profiling shows 4(1H)-quinolone derivatives as new lead candidates for malaria. European Journal of Medicinal Chemistry Reports, v. 3, p. 100012-1-100012-16 + supplementary data, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.ejmcr.2021.100012. Acesso em: 03 out. 2024.
APA
Souza, J. O. de, Almeida, S. M., Souza, G. E. de, Zanini, C. L., Silva, E. M. da, Paim, J. C., et al. (2021). Parasitological profiling shows 4(1H)-quinolone derivatives as new lead candidates for malaria. European Journal of Medicinal Chemistry Reports, 3, 100012-1-100012-16 + supplementary data. doi:10.1016/j.ejmcr.2021.100012
NLM
Souza JO de, Almeida SM, Souza GE de, Zanini CL, Silva EM da, Paim JC, Bargieri DY, Amporndanai K, Antonyuk SV, Hasnain SS, Cruz FC, Pereira DB, Oliva G, Corrêa AG, Aguiar ACC, Guido RVC. Parasitological profiling shows 4(1H)-quinolone derivatives as new lead candidates for malaria [Internet]. European Journal of Medicinal Chemistry Reports. 2021 ; 3 100012-1-100012-16 + supplementary data.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.ejmcr.2021.100012
Vancouver
Souza JO de, Almeida SM, Souza GE de, Zanini CL, Silva EM da, Paim JC, Bargieri DY, Amporndanai K, Antonyuk SV, Hasnain SS, Cruz FC, Pereira DB, Oliva G, Corrêa AG, Aguiar ACC, Guido RVC. Parasitological profiling shows 4(1H)-quinolone derivatives as new lead candidates for malaria [Internet]. European Journal of Medicinal Chemistry Reports. 2021 ; 3 100012-1-100012-16 + supplementary data.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.ejmcr.2021.100012
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SILVA, Marco Túlio Alves da et al. Trypanosomatid selenophosphate synthetase structure, function and interaction with selenocysteine lyase. PLOS Neglected Tropical Diseases, v. 14, n. 10, p. e0008091-1-e0008091-31, 2020Tradução . . Disponível em: https://doi.org/10.1371/journal.pntd.0008091. Acesso em: 03 out. 2024.
APA
Silva, M. T. A. da, Silva, I. R. e, Faim, L. M., Bellini, N. K., Pereira, M. L., Lima, A. L., et al. (2020). Trypanosomatid selenophosphate synthetase structure, function and interaction with selenocysteine lyase. PLOS Neglected Tropical Diseases, 14( 10), e0008091-1-e0008091-31. doi:10.1371/journal.pntd.0008091
NLM
Silva MTA da, Silva IR e, Faim LM, Bellini NK, Pereira ML, Lima AL, Jesus TCL de, Costa FC, Watanabe TF, Pereira H d'M, Valentini SR, Zanelli CF, Borges JC, Dias MVB, Cunha JPC da, Mittra B, Andrews NW, Thiemann OH. Trypanosomatid selenophosphate synthetase structure, function and interaction with selenocysteine lyase [Internet]. PLOS Neglected Tropical Diseases. 2020 ; 14( 10): e0008091-1-e0008091-31.[citado 2024 out. 03 ] Available from: https://doi.org/10.1371/journal.pntd.0008091
Vancouver
Silva MTA da, Silva IR e, Faim LM, Bellini NK, Pereira ML, Lima AL, Jesus TCL de, Costa FC, Watanabe TF, Pereira H d'M, Valentini SR, Zanelli CF, Borges JC, Dias MVB, Cunha JPC da, Mittra B, Andrews NW, Thiemann OH. Trypanosomatid selenophosphate synthetase structure, function and interaction with selenocysteine lyase [Internet]. PLOS Neglected Tropical Diseases. 2020 ; 14( 10): e0008091-1-e0008091-31.[citado 2024 out. 03 ] Available from: https://doi.org/10.1371/journal.pntd.0008091
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVA, Glaucius et al. Em busca de diagnósticos e tratamentos. [Entrevista a Fabrício Marques]. Pesquisa FAPESP. São Paulo: Fundação de Amparo à Pesquisa do Estado de São Paulo - FAPESP. Disponível em: https://revistapesquisa.fapesp.br/em-busca-de-diagnosticos-e-tratamentos. Acesso em: 03 out. 2024. , 2020
APA
Oliva, G., Ribeiro, A. F., Lotufo, P. A., & Charlie-Silva, I. (2020). Em busca de diagnósticos e tratamentos. [Entrevista a Fabrício Marques]. Pesquisa FAPESP. São Paulo: Fundação de Amparo à Pesquisa do Estado de São Paulo - FAPESP. Recuperado de https://revistapesquisa.fapesp.br/em-busca-de-diagnosticos-e-tratamentos
NLM
Oliva G, Ribeiro AF, Lotufo PA, Charlie-Silva I. Em busca de diagnósticos e tratamentos. [Entrevista a Fabrício Marques] [Internet]. Pesquisa FAPESP. 2020 ;(6 ju 2020):[citado 2024 out. 03 ] Available from: https://revistapesquisa.fapesp.br/em-busca-de-diagnosticos-e-tratamentos
Vancouver
Oliva G, Ribeiro AF, Lotufo PA, Charlie-Silva I. Em busca de diagnósticos e tratamentos. [Entrevista a Fabrício Marques] [Internet]. Pesquisa FAPESP. 2020 ;(6 ju 2020):[citado 2024 out. 03 ] Available from: https://revistapesquisa.fapesp.br/em-busca-de-diagnosticos-e-tratamentos
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GARCIA, Bruna M. et al. Mice born to females with oocytespecific deletion of mitofusin 2 have increased weight gain and impaired glucose homeostasis. Molecular Human Reproduction, v. 26, n. 12, p. 938-952 + supplementary data, 2020Tradução . . Disponível em: https://doi.org/10.1093/molehr/gaaa071. Acesso em: 03 out. 2024.
APA
Garcia, B. M., Machado, T. S., Carvalho, K. F., Nolasco, P., Nociti, R. P., Del Collado, M. B., et al. (2020). Mice born to females with oocytespecific deletion of mitofusin 2 have increased weight gain and impaired glucose homeostasis. Molecular Human Reproduction, 26( 12), 938-952 + supplementary data. doi:10.1093/molehr/gaaa071
NLM
Garcia BM, Machado TS, Carvalho KF, Nolasco P, Nociti RP, Del Collado MB, Bianco MJDC, Grejo MP, Augustro Neto JDA, Sugiyama FHC, Tostes K, Pandey AK, Gonçalves LM, Perecin F, Meirelles FV, Ferraz JBS, Vanzela EC, Boschero AC, Guimarães FEG, Abdulkader FR de M, Laurindo FRM, Kowaltowski AJ, Chiaratti MR. Mice born to females with oocytespecific deletion of mitofusin 2 have increased weight gain and impaired glucose homeostasis [Internet]. Molecular Human Reproduction. 2020 ; 26( 12): 938-952 + supplementary data.[citado 2024 out. 03 ] Available from: https://doi.org/10.1093/molehr/gaaa071
Vancouver
Garcia BM, Machado TS, Carvalho KF, Nolasco P, Nociti RP, Del Collado MB, Bianco MJDC, Grejo MP, Augustro Neto JDA, Sugiyama FHC, Tostes K, Pandey AK, Gonçalves LM, Perecin F, Meirelles FV, Ferraz JBS, Vanzela EC, Boschero AC, Guimarães FEG, Abdulkader FR de M, Laurindo FRM, Kowaltowski AJ, Chiaratti MR. Mice born to females with oocytespecific deletion of mitofusin 2 have increased weight gain and impaired glucose homeostasis [Internet]. Molecular Human Reproduction. 2020 ; 26( 12): 938-952 + supplementary data.[citado 2024 out. 03 ] Available from: https://doi.org/10.1093/molehr/gaaa071