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LACERDA, Jessica Zani et al. Annexin A1(2-26) treatment improves skin heterologous transplantation by modulating inflammation and angiogenesis processes. Frontiers in Pharmacology, v. 9, p. 1-11 art. 1015, 2018Tradução . . Disponível em: https://doi.org/10.3389/fphar.2018.01015. Acesso em: 13 nov. 2024.
APA
Lacerda, J. Z., Drewes, C. C., Mimura, K. K. O., Zanon, C. de F., Ansari, T., Gil, C. D., et al. (2018). Annexin A1(2-26) treatment improves skin heterologous transplantation by modulating inflammation and angiogenesis processes. Frontiers in Pharmacology, 9, 1-11 art. 1015. doi:10.3389/fphar.2018.01015
NLM
Lacerda JZ, Drewes CC, Mimura KKO, Zanon C de F, Ansari T, Gil CD, Greco KV, Farsky SHP, Oliani SM. Annexin A1(2-26) treatment improves skin heterologous transplantation by modulating inflammation and angiogenesis processes [Internet]. Frontiers in Pharmacology. 2018 ; 9 1-11 art. 1015.[citado 2024 nov. 13 ] Available from: https://doi.org/10.3389/fphar.2018.01015
Vancouver
Lacerda JZ, Drewes CC, Mimura KKO, Zanon C de F, Ansari T, Gil CD, Greco KV, Farsky SHP, Oliani SM. Annexin A1(2-26) treatment improves skin heterologous transplantation by modulating inflammation and angiogenesis processes [Internet]. Frontiers in Pharmacology. 2018 ; 9 1-11 art. 1015.[citado 2024 nov. 13 ] Available from: https://doi.org/10.3389/fphar.2018.01015
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ALI, Bakat et al. Cytotoxic effects of a novel maleimide derivative on epithelial and tumor cells. Bioorganic Chemistry, v. 72, p. 199-207, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2017.04.013. Acesso em: 13 nov. 2024.
APA
Ali, B., Kupa, L. de V. K., Heluany, C. S., Drewes, C. C., Vasconcelos, S. N. S., Farsky, S. H. P., & Stefani, H. A. (2017). Cytotoxic effects of a novel maleimide derivative on epithelial and tumor cells. Bioorganic Chemistry, 72, 199-207. doi:10.1016/j.bioorg.2017.04.013
NLM
Ali B, Kupa L de VK, Heluany CS, Drewes CC, Vasconcelos SNS, Farsky SHP, Stefani HA. Cytotoxic effects of a novel maleimide derivative on epithelial and tumor cells [Internet]. Bioorganic Chemistry. 2017 ; 72 199-207.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.bioorg.2017.04.013
Vancouver
Ali B, Kupa L de VK, Heluany CS, Drewes CC, Vasconcelos SNS, Farsky SHP, Stefani HA. Cytotoxic effects of a novel maleimide derivative on epithelial and tumor cells [Internet]. Bioorganic Chemistry. 2017 ; 72 199-207.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.bioorg.2017.04.013
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KUPA, Léonard de Vinci Kanda et al. Role of Translocator 18 KDa ligands in the activation of leukotriene B4 activated G-protein coupled receptor and Toll Like Receptor-4 pathways in neutrophils. Frontiers in Pharmacology, v. 8, p. 1-14 art. 766, 2017Tradução . . Disponível em: https://doi.org/10.3389/fphar.2017.00766. Acesso em: 13 nov. 2024.
APA
Kupa, L. de V. K., Drewes, C. C., Barioni, E. D., Neves, C. L., Sampaio, S. C., & Farsky, S. H. P. (2017). Role of Translocator 18 KDa ligands in the activation of leukotriene B4 activated G-protein coupled receptor and Toll Like Receptor-4 pathways in neutrophils. Frontiers in Pharmacology, 8, 1-14 art. 766. doi:10.3389/fphar.2017.00766
NLM
Kupa L de VK, Drewes CC, Barioni ED, Neves CL, Sampaio SC, Farsky SHP. Role of Translocator 18 KDa ligands in the activation of leukotriene B4 activated G-protein coupled receptor and Toll Like Receptor-4 pathways in neutrophils [Internet]. Frontiers in Pharmacology. 2017 ; 8 1-14 art. 766.[citado 2024 nov. 13 ] Available from: https://doi.org/10.3389/fphar.2017.00766
Vancouver
Kupa L de VK, Drewes CC, Barioni ED, Neves CL, Sampaio SC, Farsky SHP. Role of Translocator 18 KDa ligands in the activation of leukotriene B4 activated G-protein coupled receptor and Toll Like Receptor-4 pathways in neutrophils [Internet]. Frontiers in Pharmacology. 2017 ; 8 1-14 art. 766.[citado 2024 nov. 13 ] Available from: https://doi.org/10.3389/fphar.2017.00766
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IBRAHIM, Beatriz Silva et al. Beneficial effects of vitamin C treatment on pregnant rats exposed to formaldehyde: Reversal of immunosuppression in the offspring. Toxicology and Applied Pharmacology, v. 300, p. 77-81, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.taap.2016.03.010. Acesso em: 13 nov. 2024.
APA
Ibrahim, B. S., Barioni, E. D., Heluany, C. S., Braga, T. T., Drewes, C. C., Costa, S. G., et al. (2016). Beneficial effects of vitamin C treatment on pregnant rats exposed to formaldehyde: Reversal of immunosuppression in the offspring. Toxicology and Applied Pharmacology, 300, 77-81. doi:10.1016/j.taap.2016.03.010
NLM
Ibrahim BS, Barioni ED, Heluany CS, Braga TT, Drewes CC, Costa SG, Câmara NOS, Farsky SHP, Franco AL dos S. Beneficial effects of vitamin C treatment on pregnant rats exposed to formaldehyde: Reversal of immunosuppression in the offspring [Internet]. Toxicology and Applied Pharmacology. 2016 ; 300 77-81.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.taap.2016.03.010
Vancouver
Ibrahim BS, Barioni ED, Heluany CS, Braga TT, Drewes CC, Costa SG, Câmara NOS, Farsky SHP, Franco AL dos S. Beneficial effects of vitamin C treatment on pregnant rats exposed to formaldehyde: Reversal of immunosuppression in the offspring [Internet]. Toxicology and Applied Pharmacology. 2016 ; 300 77-81.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.taap.2016.03.010
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LOIOLA, Rodrigo Azevedo et al. Long-term in vivo polychlorinated biphenyl 126 exposure induces oxidative stress and alters proteomic profile on islets of Langerhans. Scientific Reports, v. 6, p. 1-14 art. 27882, 2016Tradução . . Disponível em: https://doi.org/10.1038/srep27882. Acesso em: 13 nov. 2024.
APA
Loiola, R. A., Anjos, F. M. dos, Shimada, A. L., Cruz, W. S., Drewes, C. C., Rodrigues, S. F. de P., et al. (2016). Long-term in vivo polychlorinated biphenyl 126 exposure induces oxidative stress and alters proteomic profile on islets of Langerhans. Scientific Reports, 6, 1-14 art. 27882. doi:10.1038/srep27882
NLM
Loiola RA, Anjos FM dos, Shimada AL, Cruz WS, Drewes CC, Rodrigues SF de P, Cardozo KHM, Carvalho VM, Pinto E, Farsky SHP. Long-term in vivo polychlorinated biphenyl 126 exposure induces oxidative stress and alters proteomic profile on islets of Langerhans [Internet]. Scientific Reports. 2016 ; 6 1-14 art. 27882.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1038/srep27882
Vancouver
Loiola RA, Anjos FM dos, Shimada AL, Cruz WS, Drewes CC, Rodrigues SF de P, Cardozo KHM, Carvalho VM, Pinto E, Farsky SHP. Long-term in vivo polychlorinated biphenyl 126 exposure induces oxidative stress and alters proteomic profile on islets of Langerhans [Internet]. Scientific Reports. 2016 ; 6 1-14 art. 27882.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1038/srep27882
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IBRAHIM, Beatriz Silva et al. Formaldehyde inhalation during pregnancy abolishes the development of acute innate inflammation in offspring. Toxicology Letters, v. 235, n. 2, p. 147-154, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.toxlet.2015.04.001. Acesso em: 13 nov. 2024.
APA
Ibrahim, B. S., Silva, C. M. da, Barioni, É. D., Correa-Costa, M., Drewes, C. C., Câmara, N. O. S., et al. (2015). Formaldehyde inhalation during pregnancy abolishes the development of acute innate inflammation in offspring. Toxicology Letters, 235( 2), 147-154. doi:10.1016/j.toxlet.2015.04.001
NLM
Ibrahim BS, Silva CM da, Barioni ÉD, Correa-Costa M, Drewes CC, Câmara NOS, Lima WT de, Farsky SHP, Franco AL dos S. Formaldehyde inhalation during pregnancy abolishes the development of acute innate inflammation in offspring [Internet]. Toxicology Letters. 2015 ; 235( 2): 147-154.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.toxlet.2015.04.001
Vancouver
Ibrahim BS, Silva CM da, Barioni ÉD, Correa-Costa M, Drewes CC, Câmara NOS, Lima WT de, Farsky SHP, Franco AL dos S. Formaldehyde inhalation during pregnancy abolishes the development of acute innate inflammation in offspring [Internet]. Toxicology Letters. 2015 ; 235( 2): 147-154.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.toxlet.2015.04.001
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DREWES, Carine Cristiane et al. Post-transcriptional control of Amblyomin-X on secretion of vascular endothelial growth factor and expression of adhesion molecules in endothelial cells. Toxicon, v. 101, p. 1-10, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.toxicon.2015.04.002. Acesso em: 13 nov. 2024.
APA
Drewes, C. C., Dias, R. Y., Branco, V. G., Cavalcante, M. F., Souza, J. G., Abdalla, D. S. P., et al. (2015). Post-transcriptional control of Amblyomin-X on secretion of vascular endothelial growth factor and expression of adhesion molecules in endothelial cells. Toxicon, 101, 1-10. doi:10.1016/j.toxicon.2015.04.002
NLM
Drewes CC, Dias RY, Branco VG, Cavalcante MF, Souza JG, Abdalla DSP, Chudzinski-Tavassi AM, Farsky SHP. Post-transcriptional control of Amblyomin-X on secretion of vascular endothelial growth factor and expression of adhesion molecules in endothelial cells [Internet]. Toxicon. 2015 ; 101 1-10.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.toxicon.2015.04.002
Vancouver
Drewes CC, Dias RY, Branco VG, Cavalcante MF, Souza JG, Abdalla DSP, Chudzinski-Tavassi AM, Farsky SHP. Post-transcriptional control of Amblyomin-X on secretion of vascular endothelial growth factor and expression of adhesion molecules in endothelial cells [Internet]. Toxicon. 2015 ; 101 1-10.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.toxicon.2015.04.002
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SHIMADA, Ana Lucia Borges et al. Absorption of PCB126 by upper airways impairs G protein-coupled receptor-mediated immune response. Scientific Reports, v. 5, p. art. 14917 1-12, 2015Tradução . . Disponível em: https://doi.org/10.1038/srep14917. Acesso em: 13 nov. 2024.
APA
Shimada, A. L. B., Cruz, W. S., Loiola, R. A., Drewes, C. C., Doerr, F., Figueiredo, N. G. de, et al. (2015). Absorption of PCB126 by upper airways impairs G protein-coupled receptor-mediated immune response. Scientific Reports, 5, art. 14917 1-12. doi:10.1038/srep14917
NLM
Shimada ALB, Cruz WS, Loiola RA, Drewes CC, Doerr F, Figueiredo NG de, Pinto E, Farsky SHP. Absorption of PCB126 by upper airways impairs G protein-coupled receptor-mediated immune response [Internet]. Scientific Reports. 2015 ; 5 art. 14917 1-12.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1038/srep14917
Vancouver
Shimada ALB, Cruz WS, Loiola RA, Drewes CC, Doerr F, Figueiredo NG de, Pinto E, Farsky SHP. Absorption of PCB126 by upper airways impairs G protein-coupled receptor-mediated immune response [Internet]. Scientific Reports. 2015 ; 5 art. 14917 1-12.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1038/srep14917
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UCHIYAMA, Mayara Klimuk et al. In vivo and in vitro toxicity and anti-inflammatory properties of gold nanoparticle bioconjugates to the vascular system. Toxicological Sciences, v. 142, n. 2, p. 497-507, 2014Tradução . . Disponível em: https://doi.org/10.1093/toxsci/kfu202. Acesso em: 13 nov. 2024.
APA
Uchiyama, M. K., Deda, D. K., Rodrigues, S. F. de P., Drewes, C. C., Bolonheis, S. M., Kiyohara, P. K., et al. (2014). In vivo and in vitro toxicity and anti-inflammatory properties of gold nanoparticle bioconjugates to the vascular system. Toxicological Sciences, 142( 2), 497-507. doi:10.1093/toxsci/kfu202
NLM
Uchiyama MK, Deda DK, Rodrigues SF de P, Drewes CC, Bolonheis SM, Kiyohara PK, Toledo SP de, Colli W, Araki K, Farsky SHP. In vivo and in vitro toxicity and anti-inflammatory properties of gold nanoparticle bioconjugates to the vascular system [Internet]. Toxicological Sciences. 2014 ; 142( 2): 497-507.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1093/toxsci/kfu202
Vancouver
Uchiyama MK, Deda DK, Rodrigues SF de P, Drewes CC, Bolonheis SM, Kiyohara PK, Toledo SP de, Colli W, Araki K, Farsky SHP. In vivo and in vitro toxicity and anti-inflammatory properties of gold nanoparticle bioconjugates to the vascular system [Internet]. Toxicological Sciences. 2014 ; 142( 2): 497-507.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1093/toxsci/kfu202
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DREWES, Carine Cristiane et al. Mechanisms of acetyleugenol nanocapsules on melanoma development: in vitro and in vivo assays. Toxicological Sciences. Oxford: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 13 nov. 2024. , 2013
APA
Drewes, C. C., Bexiga, C. G., Fiel, L. A., Paula, V. F. de, Pohlmann, A. R., Guterres, S. S., et al. (2013). Mechanisms of acetyleugenol nanocapsules on melanoma development: in vitro and in vivo assays. Toxicological Sciences. Oxford: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Drewes CC, Bexiga CG, Fiel LA, Paula VF de, Pohlmann AR, Guterres SS, Farsky SHP, Barros SB de M. Mechanisms of acetyleugenol nanocapsules on melanoma development: in vitro and in vivo assays. Toxicological Sciences. 2013 ; 132( 1): 37 res. PS 179.[citado 2024 nov. 13 ]
Vancouver
Drewes CC, Bexiga CG, Fiel LA, Paula VF de, Pohlmann AR, Guterres SS, Farsky SHP, Barros SB de M. Mechanisms of acetyleugenol nanocapsules on melanoma development: in vitro and in vivo assays. Toxicological Sciences. 2013 ; 132( 1): 37 res. PS 179.[citado 2024 nov. 13 ]
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ABNT
DREWES, Carine Cristiane et al. Mechanisms of poly (epsilon-caprolactone) lipid-core nanocapsules in melanoma development. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 13 nov. 2024. , 2013
APA
Drewes, C. C., Bexiga, C. G., Fiel, L. A., Pohlmann, A., Guterres, S., & Farsky, S. H. P. (2013). Mechanisms of poly (epsilon-caprolactone) lipid-core nanocapsules in melanoma development. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Drewes CC, Bexiga CG, Fiel LA, Pohlmann A, Guterres S, Farsky SHP. Mechanisms of poly (epsilon-caprolactone) lipid-core nanocapsules in melanoma development. Brazilian Journal of Pharmaceutical Sciences. 2013 ; 49 69 res. FCF133.[citado 2024 nov. 13 ]
Vancouver
Drewes CC, Bexiga CG, Fiel LA, Pohlmann A, Guterres S, Farsky SHP. Mechanisms of poly (epsilon-caprolactone) lipid-core nanocapsules in melanoma development. Brazilian Journal of Pharmaceutical Sciences. 2013 ; 49 69 res. FCF133.[citado 2024 nov. 13 ]
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CARRAU, Gonzalo et al. Synthesis and preliminary biological evaluation of a compound library of triazolylcyclitols. Bioorganic & Medicinal Chemistry, v. 21, n. 14, p. 4225-4232, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2013.04.084. Acesso em: 13 nov. 2024.
APA
Carrau, G., Drewes, C. C., Shimada, A. L. B., Bertucci, A., Farsky, S. H. P., Stefani, H. A., & Gonzalez, D. (2013). Synthesis and preliminary biological evaluation of a compound library of triazolylcyclitols. Bioorganic & Medicinal Chemistry, 21( 14), 4225-4232. doi:10.1016/j.bmc.2013.04.084
NLM
Carrau G, Drewes CC, Shimada ALB, Bertucci A, Farsky SHP, Stefani HA, Gonzalez D. Synthesis and preliminary biological evaluation of a compound library of triazolylcyclitols [Internet]. Bioorganic & Medicinal Chemistry. 2013 ; 21( 14): 4225-4232.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.bmc.2013.04.084
Vancouver
Carrau G, Drewes CC, Shimada ALB, Bertucci A, Farsky SHP, Stefani HA, Gonzalez D. Synthesis and preliminary biological evaluation of a compound library of triazolylcyclitols [Internet]. Bioorganic & Medicinal Chemistry. 2013 ; 21( 14): 4225-4232.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.bmc.2013.04.084
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GIROL, Ana Paula et al. Anti-inflammatory mechanisms of the annexin A1 protein and its mimetic peptide Ac2-26 in models of ocular inflammation in vivo and in vitro. Journal of Immunology, v. 190, n. 11, p. 5689-5701, 2013Tradução . . Disponível em: https://doi.org/10.4049/jimmunol.1202030. Acesso em: 13 nov. 2024.
APA
Girol, A. P., Mimura, K. K. O., Drewes, C. C., Bolonheis, S. M. de, Solito, E., Farsky, S. H. P., et al. (2013). Anti-inflammatory mechanisms of the annexin A1 protein and its mimetic peptide Ac2-26 in models of ocular inflammation in vivo and in vitro. Journal of Immunology, 190( 11), 5689-5701. doi:10.4049/jimmunol.1202030
NLM
Girol AP, Mimura KKO, Drewes CC, Bolonheis SM de, Solito E, Farsky SHP, Gil CD, Oliani SM. Anti-inflammatory mechanisms of the annexin A1 protein and its mimetic peptide Ac2-26 in models of ocular inflammation in vivo and in vitro [Internet]. Journal of Immunology. 2013 ; 190( 11): 5689-5701.[citado 2024 nov. 13 ] Available from: https://doi.org/10.4049/jimmunol.1202030
Vancouver
Girol AP, Mimura KKO, Drewes CC, Bolonheis SM de, Solito E, Farsky SHP, Gil CD, Oliani SM. Anti-inflammatory mechanisms of the annexin A1 protein and its mimetic peptide Ac2-26 in models of ocular inflammation in vivo and in vitro [Internet]. Journal of Immunology. 2013 ; 190( 11): 5689-5701.[citado 2024 nov. 13 ] Available from: https://doi.org/10.4049/jimmunol.1202030
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DREWES, Carine Cristiane et al. Mechanisms of acetyleugenol poly(Epsilon-caprolactone) lipid-core nanocapsules on melanoma development. 2013, Anais.. São Paulo: Sociedade Brasileira de Toxicologia, 2013. Disponível em: http://www.cbtox2013.com.br/docs/trab-8620-364.pdf. Acesso em: 13 nov. 2024.
APA
Drewes, C. C., Fiel, L. A., Bexiga, C. G., Paula, V. Fde, Pohmann, A. R., Guterres, S. S., & Farsky, S. H. P. (2013). Mechanisms of acetyleugenol poly(Epsilon-caprolactone) lipid-core nanocapsules on melanoma development. In Resumos. São Paulo: Sociedade Brasileira de Toxicologia. Recuperado de http://www.cbtox2013.com.br/docs/trab-8620-364.pdf
NLM
Drewes CC, Fiel LA, Bexiga CG, Paula VFde, Pohmann AR, Guterres SS, Farsky SHP. Mechanisms of acetyleugenol poly(Epsilon-caprolactone) lipid-core nanocapsules on melanoma development [Internet]. Resumos. 2013 ;[citado 2024 nov. 13 ] Available from: http://www.cbtox2013.com.br/docs/trab-8620-364.pdf
Vancouver
Drewes CC, Fiel LA, Bexiga CG, Paula VFde, Pohmann AR, Guterres SS, Farsky SHP. Mechanisms of acetyleugenol poly(Epsilon-caprolactone) lipid-core nanocapsules on melanoma development [Internet]. Resumos. 2013 ;[citado 2024 nov. 13 ] Available from: http://www.cbtox2013.com.br/docs/trab-8620-364.pdf
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SANTIN, José Roberto et al. Role of a ppar-pan agonist and cyclooxygenase-2 inhibitor on neutrophil adhesion and migration induced by g protein-coupled receptor activation (GPCR). Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 13 nov. 2024. , 2013
APA
Santin, J. R., Machado, I. D., Drewes, C. C., Marcondes, R. S., Maia, D. C., Pitta, I. da R., & Farsky, S. H. P. (2013). Role of a ppar-pan agonist and cyclooxygenase-2 inhibitor on neutrophil adhesion and migration induced by g protein-coupled receptor activation (GPCR). Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Santin JR, Machado ID, Drewes CC, Marcondes RS, Maia DC, Pitta I da R, Farsky SHP. Role of a ppar-pan agonist and cyclooxygenase-2 inhibitor on neutrophil adhesion and migration induced by g protein-coupled receptor activation (GPCR). Brazilian Journal of Pharmaceutical Sciences. 2013 ; 49 40 res. FCF075.[citado 2024 nov. 13 ]
Vancouver
Santin JR, Machado ID, Drewes CC, Marcondes RS, Maia DC, Pitta I da R, Farsky SHP. Role of a ppar-pan agonist and cyclooxygenase-2 inhibitor on neutrophil adhesion and migration induced by g protein-coupled receptor activation (GPCR). Brazilian Journal of Pharmaceutical Sciences. 2013 ; 49 40 res. FCF075.[citado 2024 nov. 13 ]
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ABNT
DREWES, Carine Cristiane et al. Actions of the Kunitz-type serine protease inhibitor Amblyomin-X on VEGF-A-induced angiogenesis. Toxicon, v. 60, n. 3, p. 333-340, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.toxicon.2012.04.349. Acesso em: 13 nov. 2024.
APA
Drewes, C. C., Dias, R. Y. S., Hebeda, C. B., Simons, S. M., Barreto, S. A., Ferreira Junior, J. M., et al. (2012). Actions of the Kunitz-type serine protease inhibitor Amblyomin-X on VEGF-A-induced angiogenesis. Toxicon, 60( 3), 333-340. doi:10.1016/j.toxicon.2012.04.349
NLM
Drewes CC, Dias RYS, Hebeda CB, Simons SM, Barreto SA, Ferreira Junior JM, Chudzinski-Tavassi AM, Farsky SHP. Actions of the Kunitz-type serine protease inhibitor Amblyomin-X on VEGF-A-induced angiogenesis [Internet]. Toxicon. 2012 ; 60( 3): 333-340.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.toxicon.2012.04.349
Vancouver
Drewes CC, Dias RYS, Hebeda CB, Simons SM, Barreto SA, Ferreira Junior JM, Chudzinski-Tavassi AM, Farsky SHP. Actions of the Kunitz-type serine protease inhibitor Amblyomin-X on VEGF-A-induced angiogenesis [Internet]. Toxicon. 2012 ; 60( 3): 333-340.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.toxicon.2012.04.349
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ABNT
BEXIGA, Celina Goulart et al. Therapeutical effectiveness of acetyleugenol nanocapsules in in vivo melanoma model. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 13 nov. 2024. , 2012
APA
Bexiga, C. G., Drewes, C. C., Paula, V. F. de, Fiel, L. A., Pohlmann, A. R., Guterres, S., et al. (2012). Therapeutical effectiveness of acetyleugenol nanocapsules in in vivo melanoma model. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Bexiga CG, Drewes CC, Paula VF de, Fiel LA, Pohlmann AR, Guterres S, Fock RA, Farsky SHP. Therapeutical effectiveness of acetyleugenol nanocapsules in in vivo melanoma model. Brazilian Journal of Pharmaceutical Sciences. 2012 ; 48 89 res. FCF174.[citado 2024 nov. 13 ]
Vancouver
Bexiga CG, Drewes CC, Paula VF de, Fiel LA, Pohlmann AR, Guterres S, Fock RA, Farsky SHP. Therapeutical effectiveness of acetyleugenol nanocapsules in in vivo melanoma model. Brazilian Journal of Pharmaceutical Sciences. 2012 ; 48 89 res. FCF174.[citado 2024 nov. 13 ]
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ABNT
DREWES, Carine Cristiane et al. Toxic effects of acetyleugenol nanocapsules in melanoma cells. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 13 nov. 2024. , 2012
APA
Drewes, C. C., Fiel, L. A., Pohlmann, A. R., Guterres, S., & Farsky, S. H. P. (2012). Toxic effects of acetyleugenol nanocapsules in melanoma cells. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
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ABNT
FARSKY, Sandra Helena Poliselli et al. Amblyomin-X, a Kunitz-type serine protease inhibitor, impairs in vivo VEGF-induced angiogenesis. Inflammation Research. Basel: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 13 nov. 2024. , 2011
APA
Farsky, S. H. P., Drewes, C. C., Dias, R., Hebeda, C. B., Simons, S. M., & Chudzinski-Tavassi, A. M. (2011). Amblyomin-X, a Kunitz-type serine protease inhibitor, impairs in vivo VEGF-induced angiogenesis. Inflammation Research. Basel: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Farsky SHP, Drewes CC, Dias R, Hebeda CB, Simons SM, Chudzinski-Tavassi AM. Amblyomin-X, a Kunitz-type serine protease inhibitor, impairs in vivo VEGF-induced angiogenesis. Inflammation Research. 2011 ; 60 86.[citado 2024 nov. 13 ]
Vancouver
Farsky SHP, Drewes CC, Dias R, Hebeda CB, Simons SM, Chudzinski-Tavassi AM. Amblyomin-X, a Kunitz-type serine protease inhibitor, impairs in vivo VEGF-induced angiogenesis. Inflammation Research. 2011 ; 60 86.[citado 2024 nov. 13 ]
; Sandri, Silvana 
