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Brazilian Symposium on Medicinal Chemistry - BrazMedChem, 11. . Salvador: Universidade Federal da Bahia - UFBA. . Acesso em: 26 set. 2024. , 2023
APA
Brazilian Symposium on Medicinal Chemistry - BrazMedChem, 11. (2023). Brazilian Symposium on Medicinal Chemistry - BrazMedChem, 11. Salvador: Universidade Federal da Bahia - UFBA.
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ABNT
CAMPOS, Patrícia Mazureki et al. Liquid crystalline nanodispersion functionalized with cell-penetrating peptides improves skin penetration and anti-inflammatory effect of lipoic acid after in vivo skin exposure to UVB radiation. Drug Delivery and Translational Research, v. 10, n. 6, p. 1810-1828, 2020Tradução . . Disponível em: https://doi.org/10.1007/s13346-020-00840-2. Acesso em: 26 set. 2024.
APA
Campos, P. M., Praça, F. G., Mussi, S. V., Figueiredo, S. A., Fantini, M., Fonseca, M. J. V., et al. (2020). Liquid crystalline nanodispersion functionalized with cell-penetrating peptides improves skin penetration and anti-inflammatory effect of lipoic acid after in vivo skin exposure to UVB radiation. Drug Delivery and Translational Research, 10( 6), 1810-1828. doi:10.1007/s13346-020-00840-2
NLM
Campos PM, Praça FG, Mussi SV, Figueiredo SA, Fantini M, Fonseca MJV, Torchilin VP, Bentley MVLB. Liquid crystalline nanodispersion functionalized with cell-penetrating peptides improves skin penetration and anti-inflammatory effect of lipoic acid after in vivo skin exposure to UVB radiation [Internet]. Drug Delivery and Translational Research. 2020 ; 10( 6): 1810-1828.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/s13346-020-00840-2
Vancouver
Campos PM, Praça FG, Mussi SV, Figueiredo SA, Fantini M, Fonseca MJV, Torchilin VP, Bentley MVLB. Liquid crystalline nanodispersion functionalized with cell-penetrating peptides improves skin penetration and anti-inflammatory effect of lipoic acid after in vivo skin exposure to UVB radiation [Internet]. Drug Delivery and Translational Research. 2020 ; 10( 6): 1810-1828.[citado 2024 set. 26 ] Available from: https://doi.org/10.1007/s13346-020-00840-2
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BONALUMI, Joane Kathelen Rustiguel et al. Crystal structure of Pseudomonas putida Chlorocatechol 1,2-dioxygenase: structural basis for substrate uptake and specificity. 2012, Anais.. Boston: American Crystallographic Association (ACA), 2012. . Acesso em: 26 set. 2024.
APA
Bonalumi, J. K. R., Bernardi, D. S., Lopez, R. F. V., & Nonato, M. C. (2012). Crystal structure of Pseudomonas putida Chlorocatechol 1,2-dioxygenase: structural basis for substrate uptake and specificity. In Abstracts. Boston: American Crystallographic Association (ACA).
NLM
Bonalumi JKR, Bernardi DS, Lopez RFV, Nonato MC. Crystal structure of Pseudomonas putida Chlorocatechol 1,2-dioxygenase: structural basis for substrate uptake and specificity. Abstracts. 2012 ;[citado 2024 set. 26 ]
Vancouver
Bonalumi JKR, Bernardi DS, Lopez RFV, Nonato MC. Crystal structure of Pseudomonas putida Chlorocatechol 1,2-dioxygenase: structural basis for substrate uptake and specificity. Abstracts. 2012 ;[citado 2024 set. 26 ]
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MARCHI, Anderson Aparecido de et al. New 3-piperonylcoumarins as inhibitors of glycosomal glyceraldehyde-3-phosphate dehydrogenase (gGAPDH) from Trypanosoma cruzi. Bioorganic & Medicinal Chemistry, v. 12, n. 18, p. Se 2004, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2004.07.018. Acesso em: 26 set. 2024.
APA
Marchi, A. A. de, Castilho, M. S., Nascimento, P. G. B., Archanjo, F. C., Del Ponte, G., Oliva, G., & Pupo, M. T. (2004). New 3-piperonylcoumarins as inhibitors of glycosomal glyceraldehyde-3-phosphate dehydrogenase (gGAPDH) from Trypanosoma cruzi. Bioorganic & Medicinal Chemistry, 12( 18), Se 2004. doi:10.1016/j.bmc.2004.07.018
NLM
Marchi AA de, Castilho MS, Nascimento PGB, Archanjo FC, Del Ponte G, Oliva G, Pupo MT. New 3-piperonylcoumarins as inhibitors of glycosomal glyceraldehyde-3-phosphate dehydrogenase (gGAPDH) from Trypanosoma cruzi [Internet]. Bioorganic & Medicinal Chemistry. 2004 ; 12( 18): Se 2004.[citado 2024 set. 26 ] Available from: https://doi.org/10.1016/j.bmc.2004.07.018
Vancouver
Marchi AA de, Castilho MS, Nascimento PGB, Archanjo FC, Del Ponte G, Oliva G, Pupo MT. New 3-piperonylcoumarins as inhibitors of glycosomal glyceraldehyde-3-phosphate dehydrogenase (gGAPDH) from Trypanosoma cruzi [Internet]. Bioorganic & Medicinal Chemistry. 2004 ; 12( 18): Se 2004.[citado 2024 set. 26 ] Available from: https://doi.org/10.1016/j.bmc.2004.07.018
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ABNT
LEITÃO, Andrei et al. Structure-activity relationships of novel inhibitors of glyceraldehyde-3-phosphate dehydrogenase. Bioorganic & Medicinal Chemistry Letters, v. 14, n. 9, p. 2199-2204, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2004.02.025. Acesso em: 26 set. 2024.
APA
Leitão, A., Andricopulo, A. D., Oliva, G., Pupo, M. T., Marchi, A. A. de, Vieira, P. C., et al. (2004). Structure-activity relationships of novel inhibitors of glyceraldehyde-3-phosphate dehydrogenase. Bioorganic & Medicinal Chemistry Letters, 14( 9), 2199-2204. doi:10.1016/j.bmcl.2004.02.025
NLM
Leitão A, Andricopulo AD, Oliva G, Pupo MT, Marchi AA de, Vieira PC, Silva MFGF da, Ferreira VF, Souza MCBV de, Sá MM, Moraes VRS, Montanari CA. Structure-activity relationships of novel inhibitors of glyceraldehyde-3-phosphate dehydrogenase [Internet]. Bioorganic & Medicinal Chemistry Letters. 2004 ; 14( 9): 2199-2204.[citado 2024 set. 26 ] Available from: https://doi.org/10.1016/j.bmcl.2004.02.025
Vancouver
Leitão A, Andricopulo AD, Oliva G, Pupo MT, Marchi AA de, Vieira PC, Silva MFGF da, Ferreira VF, Souza MCBV de, Sá MM, Moraes VRS, Montanari CA. Structure-activity relationships of novel inhibitors of glyceraldehyde-3-phosphate dehydrogenase [Internet]. Bioorganic & Medicinal Chemistry Letters. 2004 ; 14( 9): 2199-2204.[citado 2024 set. 26 ] Available from: https://doi.org/10.1016/j.bmcl.2004.02.025
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PAVÃO, Fernando et al. Structure of Trypanosoma cruzi glycosomal glyceraldehyde-3-phosphate dehydrogenase complexed with chalepin, a natural product inhibitor, at 1.95 'ANGSTRON' resolution. Febs Letters, v. 520, n. 1-3, p. 13-17, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0014-5793(02)02700-x. Acesso em: 26 set. 2024.
APA
Pavão, F., Castilho, M. S., Pupo, M. T., Dias, R. L. A., Correa, A. G., Fernandes, J. B., et al. (2002). Structure of Trypanosoma cruzi glycosomal glyceraldehyde-3-phosphate dehydrogenase complexed with chalepin, a natural product inhibitor, at 1.95 'ANGSTRON' resolution. Febs Letters, 520( 1-3), 13-17. doi:10.1016/s0014-5793(02)02700-x
NLM
Pavão F, Castilho MS, Pupo MT, Dias RLA, Correa AG, Fernandes JB, Silva MFGF da, Mafezoli J, Vieira PC, Oliva G. Structure of Trypanosoma cruzi glycosomal glyceraldehyde-3-phosphate dehydrogenase complexed with chalepin, a natural product inhibitor, at 1.95 'ANGSTRON' resolution [Internet]. Febs Letters. 2002 ; 520( 1-3): 13-17.[citado 2024 set. 26 ] Available from: https://doi.org/10.1016/s0014-5793(02)02700-x
Vancouver
Pavão F, Castilho MS, Pupo MT, Dias RLA, Correa AG, Fernandes JB, Silva MFGF da, Mafezoli J, Vieira PC, Oliva G. Structure of Trypanosoma cruzi glycosomal glyceraldehyde-3-phosphate dehydrogenase complexed with chalepin, a natural product inhibitor, at 1.95 'ANGSTRON' resolution [Internet]. Febs Letters. 2002 ; 520( 1-3): 13-17.[citado 2024 set. 26 ] Available from: https://doi.org/10.1016/s0014-5793(02)02700-x