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PRIST, Paula Ribeiro et al. Roads and forest edges facilitate yellow fever virus dispersion. Journal of Applied Ecology, v. 59, n. Ja 2022, p. 4-17, 2022Tradução . . Disponível em: https://doi.org/10.1111/1365-2664.14031. Acesso em: 14 out. 2024.
APA
Prist, P. R., Tambosi, L. R., Mucci, L. F., Pinter, A., Souza, R. P. de, Muylaert, R. de L., et al. (2022). Roads and forest edges facilitate yellow fever virus dispersion. Journal of Applied Ecology, 59( Ja 2022), 4-17. doi:10.1111/1365-2664.14031
NLM
Prist PR, Tambosi LR, Mucci LF, Pinter A, Souza RP de, Muylaert R de L, Rhodes JR, Comin CH, Costa L da F, D'Agostini TL, Deus JT de, Pavão M, Port-Carvalho M, Saad LDC, Sallum MAM, Spinola RMF, Metzger J-P. Roads and forest edges facilitate yellow fever virus dispersion [Internet]. Journal of Applied Ecology. 2022 ; 59( Ja 2022): 4-17.[citado 2024 out. 14 ] Available from: https://doi.org/10.1111/1365-2664.14031
Vancouver
Prist PR, Tambosi LR, Mucci LF, Pinter A, Souza RP de, Muylaert R de L, Rhodes JR, Comin CH, Costa L da F, D'Agostini TL, Deus JT de, Pavão M, Port-Carvalho M, Saad LDC, Sallum MAM, Spinola RMF, Metzger J-P. Roads and forest edges facilitate yellow fever virus dispersion [Internet]. Journal of Applied Ecology. 2022 ; 59( Ja 2022): 4-17.[citado 2024 out. 14 ] Available from: https://doi.org/10.1111/1365-2664.14031
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VIEIRA, Plinio S. et al. Xyloglucan processing machinery in Xanthomonas pathogens and its role in the transcriptional activation of virulence factors. Nature Communications, v. 12, p. 4049-1-4049-15, 2021Tradução . . Disponível em: https://doi.org/10.1038/s41467-021-24277-4. Acesso em: 14 out. 2024.
APA
Vieira, P. S., Bonfim, I. M., Araujo, E. A., Melo, R. R., Lima, A. R., Fessel, M. R., et al. (2021). Xyloglucan processing machinery in Xanthomonas pathogens and its role in the transcriptional activation of virulence factors. Nature Communications, 12, 4049-1-4049-15. doi:10.1038/s41467-021-24277-4
NLM
Vieira PS, Bonfim IM, Araujo EA, Melo RR, Lima AR, Fessel MR, Paixão DAA, Persinoti GF, Rocco SA, Lima TB, Pirolla RAS, Morais MAB, Correa JBL, Zanphorlin LM, Diogo JA, Lima EA, Grandis A, Buckeridge M, Gozzo FC, Benedetti CE, Polikarpov I, Giuseppe PO, Murakami MT. Xyloglucan processing machinery in Xanthomonas pathogens and its role in the transcriptional activation of virulence factors [Internet]. Nature Communications. 2021 ; 12 4049-1-4049-15.[citado 2024 out. 14 ] Available from: https://doi.org/10.1038/s41467-021-24277-4
Vancouver
Vieira PS, Bonfim IM, Araujo EA, Melo RR, Lima AR, Fessel MR, Paixão DAA, Persinoti GF, Rocco SA, Lima TB, Pirolla RAS, Morais MAB, Correa JBL, Zanphorlin LM, Diogo JA, Lima EA, Grandis A, Buckeridge M, Gozzo FC, Benedetti CE, Polikarpov I, Giuseppe PO, Murakami MT. Xyloglucan processing machinery in Xanthomonas pathogens and its role in the transcriptional activation of virulence factors [Internet]. Nature Communications. 2021 ; 12 4049-1-4049-15.[citado 2024 out. 14 ] Available from: https://doi.org/10.1038/s41467-021-24277-4
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TURANO, Helena Gabriela et al. Molecular structure and functional analysis of pyocin S8 from Pseudomonas aeruginosa reveals the essential requirement of a glutamate residue in the H-N-H motif for DNase activity. Journal of Bacteriology, v. No 2020, n. 21, p. 74-85, 2020Tradução . . Disponível em: https://doi.org/10.1128/JB.00346-20. Acesso em: 14 out. 2024.
APA
Turano, H. G., Gomes, F., Domingos, R. M., Degenhardt, M. F. de S., Oliveira, C. L. P. de, Garratt, R. C., et al. (2020). Molecular structure and functional analysis of pyocin S8 from Pseudomonas aeruginosa reveals the essential requirement of a glutamate residue in the H-N-H motif for DNase activity. Journal of Bacteriology, No 2020( 21), 74-85. doi:10.1128/JB.00346-20
NLM
Turano HG, Gomes F, Domingos RM, Degenhardt MF de S, Oliveira CLP de, Garratt RC, Netto LES, Lincopan N. Molecular structure and functional analysis of pyocin S8 from Pseudomonas aeruginosa reveals the essential requirement of a glutamate residue in the H-N-H motif for DNase activity [Internet]. Journal of Bacteriology. 2020 ; No 2020( 21): 74-85.[citado 2024 out. 14 ] Available from: https://doi.org/10.1128/JB.00346-20
Vancouver
Turano HG, Gomes F, Domingos RM, Degenhardt MF de S, Oliveira CLP de, Garratt RC, Netto LES, Lincopan N. Molecular structure and functional analysis of pyocin S8 from Pseudomonas aeruginosa reveals the essential requirement of a glutamate residue in the H-N-H motif for DNase activity [Internet]. Journal of Bacteriology. 2020 ; No 2020( 21): 74-85.[citado 2024 out. 14 ] Available from: https://doi.org/10.1128/JB.00346-20
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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: 14 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. 14 ] 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. 14 ] Available from: https://doi.org/10.1093/molehr/gaaa071
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MARTINS, Roberto de Andrade e SILVA, Cibelle Celestino e PRESTES, Maria Elice Brzezinski. Anna Carolina Krebs Pereira Regner (1947-2020). Isis, v. 111, n. 2, p. 362-364, 2020Tradução . . Disponível em: https://doi.org/10.1086/709410. Acesso em: 14 out. 2024.
APA
Martins, R. de A., Silva, C. C., & Prestes, M. E. B. (2020). Anna Carolina Krebs Pereira Regner (1947-2020). Isis, 111( 2), 362-364. doi:10.1086/709410
NLM
Martins R de A, Silva CC, Prestes MEB. Anna Carolina Krebs Pereira Regner (1947-2020) [Internet]. Isis. 2020 ; 111( 2): 362-364.[citado 2024 out. 14 ] Available from: https://doi.org/10.1086/709410
Vancouver
Martins R de A, Silva CC, Prestes MEB. Anna Carolina Krebs Pereira Regner (1947-2020) [Internet]. Isis. 2020 ; 111( 2): 362-364.[citado 2024 out. 14 ] Available from: https://doi.org/10.1086/709410
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AGUIAR, Anna Caroline Campos et al. New molecular targets and strategies for antimalarial discovery. Current Medicinal Chemistry, v. 26, n. 23, p. 4380-4402, 2019Tradução . . Disponível em: https://doi.org/10.2174/0929867324666170830103003. Acesso em: 14 out. 2024.
APA
Aguiar, A. C. C., Sousa, L. R. F., Garcia, C. R. da S., Oliva, G., & Guido, R. V. C. (2019). New molecular targets and strategies for antimalarial discovery. Current Medicinal Chemistry, 26( 23), 4380-4402. doi:10.2174/0929867324666170830103003
NLM
Aguiar ACC, Sousa LRF, Garcia CR da S, Oliva G, Guido RVC. New molecular targets and strategies for antimalarial discovery [Internet]. Current Medicinal Chemistry. 2019 ; 26( 23): 4380-4402.[citado 2024 out. 14 ] Available from: https://doi.org/10.2174/0929867324666170830103003
Vancouver
Aguiar ACC, Sousa LRF, Garcia CR da S, Oliva G, Guido RVC. New molecular targets and strategies for antimalarial discovery [Internet]. Current Medicinal Chemistry. 2019 ; 26( 23): 4380-4402.[citado 2024 out. 14 ] Available from: https://doi.org/10.2174/0929867324666170830103003
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ABNT
Brazilian Journal of Pharmaceutical Sciences. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Universidade de São Paulo - USP, Faculdade de Ciências Farmacêuticas - FCF. . Acesso em: 14 out. 2024. , 2019
APA
Brazilian Journal of Pharmaceutical Sciences. (2019). Brazilian Journal of Pharmaceutical Sciences. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Universidade de São Paulo - USP, Faculdade de Ciências Farmacêuticas - FCF.
NLM
Brazilian Journal of Pharmaceutical Sciences. Brazilian Journal of Pharmaceutical Sciences. 2019 ;[citado 2024 out. 14 ]
Vancouver
Brazilian Journal of Pharmaceutical Sciences. Brazilian Journal of Pharmaceutical Sciences. 2019 ;[citado 2024 out. 14 ]
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ABNT
Brazilian Journal of Pharmaceutical Sciences. . São Paulo: Universidade de São Paulo - USP, Faculdade de Ciências Farmacêuticas - FCF. . Acesso em: 14 out. 2024. , 2018
APA
Brazilian Journal of Pharmaceutical Sciences. (2018). Brazilian Journal of Pharmaceutical Sciences. São Paulo: Universidade de São Paulo - USP, Faculdade de Ciências Farmacêuticas - FCF.
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AGUIAR, Anna Caroline Campos et al. Discovery of marinoquinolines as potent and fast-acting plasmodium falciparum inhibitors with in Vivo activity. Journal of Medicinal Chemistry, v. 61, n. 13, p. 5547-5568, 2018Tradução . . Disponível em: https://doi.org/10.1021/acs.jmedchem.8b00143. Acesso em: 14 out. 2024.
APA
Aguiar, A. C. C., Panciera, M., Santos, E. F. S. dos, Singh, M. K., Garcia, M. L., Guido, R. V. C., et al. (2018). Discovery of marinoquinolines as potent and fast-acting plasmodium falciparum inhibitors with in Vivo activity. Journal of Medicinal Chemistry, 61( 13), 5547-5568. doi:10.1021/acs.jmedchem.8b00143
NLM
Aguiar ACC, Panciera M, Santos EFS dos, Singh MK, Garcia ML, Guido RVC, Souza GE de, Nakabashi M, Costa JL, Garcia CR da S, Oliva G, Correia CRD, Guido RVC. Discovery of marinoquinolines as potent and fast-acting plasmodium falciparum inhibitors with in Vivo activity [Internet]. Journal of Medicinal Chemistry. 2018 ; 61( 13): 5547-5568.[citado 2024 out. 14 ] Available from: https://doi.org/10.1021/acs.jmedchem.8b00143
Vancouver
Aguiar ACC, Panciera M, Santos EFS dos, Singh MK, Garcia ML, Guido RVC, Souza GE de, Nakabashi M, Costa JL, Garcia CR da S, Oliva G, Correia CRD, Guido RVC. Discovery of marinoquinolines as potent and fast-acting plasmodium falciparum inhibitors with in Vivo activity [Internet]. Journal of Medicinal Chemistry. 2018 ; 61( 13): 5547-5568.[citado 2024 out. 14 ] Available from: https://doi.org/10.1021/acs.jmedchem.8b00143
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
Brazilian Journal of Pharmaceutical Sciences. . São Paulo: Universidade de São Paulo - USP, Faculdade de Ciências Farmacêuticas - FCF. . Acesso em: 14 out. 2024. , 2017
APA
Brazilian Journal of Pharmaceutical Sciences. (2017). Brazilian Journal of Pharmaceutical Sciences. São Paulo: Universidade de São Paulo - USP, Faculdade de Ciências Farmacêuticas - FCF.
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ABNT
ALEGRIA, Thiago Gerônimo Pires et al. Ohr plays a central role in bacterial responses against fatty acid hydroperoxides and peroxynitrite. Proceedings of the National Academy of Sciences of the United States of America - PNAS, v. 114, n. Ja 2017, p. E132-E141 + supplementary materials: S1-S6, 2017Tradução . . Disponível em: https://doi.org/10.1073/pnas.1619659114. Acesso em: 14 out. 2024.
APA
Alegria, T. G. P., Meireles, D. A., Cussiol, J. R. R., Hugo, M., Trujillo, M., Oliveira, M. A. de, et al. (2017). Ohr plays a central role in bacterial responses against fatty acid hydroperoxides and peroxynitrite. Proceedings of the National Academy of Sciences of the United States of America - PNAS, 114( Ja 2017), E132-E141 + supplementary materials: S1-S6. doi:10.1073/pnas.1619659114
NLM
Alegria TGP, Meireles DA, Cussiol JRR, Hugo M, Trujillo M, Oliveira MA de, Miyamoto S, Queiroz RF, Valadares NF, Garratt RC, Radi R, Di Mascio P, Augusto O, Netto LES. Ohr plays a central role in bacterial responses against fatty acid hydroperoxides and peroxynitrite [Internet]. Proceedings of the National Academy of Sciences of the United States of America - PNAS. 2017 ; 114( Ja 2017): E132-E141 + supplementary materials: S1-S6.[citado 2024 out. 14 ] Available from: https://doi.org/10.1073/pnas.1619659114
Vancouver
Alegria TGP, Meireles DA, Cussiol JRR, Hugo M, Trujillo M, Oliveira MA de, Miyamoto S, Queiroz RF, Valadares NF, Garratt RC, Radi R, Di Mascio P, Augusto O, Netto LES. Ohr plays a central role in bacterial responses against fatty acid hydroperoxides and peroxynitrite [Internet]. Proceedings of the National Academy of Sciences of the United States of America - PNAS. 2017 ; 114( Ja 2017): E132-E141 + supplementary materials: S1-S6.[citado 2024 out. 14 ] Available from: https://doi.org/10.1073/pnas.1619659114
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FANGANIELLO, Roberto Dalto et al. Apert p.Ser252Trp mutation in FGFR2 alters osteogenic potential and gene expression of cranial periosteal cells. Molecular Medicine, v. 13, n. 7-8, p. 422-442, 2007Tradução . . Acesso em: 14 out. 2024.
APA
Fanganiello, R. D., Sertié, A. L., Reis, E. M., Yeh, E., Oliveira, N. A. de J., Bueno, D. F., et al. (2007). Apert p.Ser252Trp mutation in FGFR2 alters osteogenic potential and gene expression of cranial periosteal cells. Molecular Medicine, 13( 7-8), 422-442.
NLM
Fanganiello RD, Sertié AL, Reis EM, Yeh E, Oliveira NA de J, Bueno DF, Kerkis IE, Alonso N, Cavalheiro S, Matsushita H, Freitas R, Verjovski-Almeida S, Passos-Bueno MR. Apert p.Ser252Trp mutation in FGFR2 alters osteogenic potential and gene expression of cranial periosteal cells. Molecular Medicine. 2007 ; 13( 7-8): 422-442.[citado 2024 out. 14 ]
Vancouver
Fanganiello RD, Sertié AL, Reis EM, Yeh E, Oliveira NA de J, Bueno DF, Kerkis IE, Alonso N, Cavalheiro S, Matsushita H, Freitas R, Verjovski-Almeida S, Passos-Bueno MR. Apert p.Ser252Trp mutation in FGFR2 alters osteogenic potential and gene expression of cranial periosteal cells. Molecular Medicine. 2007 ; 13( 7-8): 422-442.[citado 2024 out. 14 ]