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Artigo de periodico
Novel insights into the molecular mechanisms involved in the neuroprotective effects of C-Phycocyanin against brain ischemia in rats (2022)
Marín-Prida, Javier; Liberato, José Luiz ; Llópiz-Arzuaga, Alexey; Padovani, Karina Stringhetta; Pavón-Fuentes, Nancy; Leopoldino, Andréia Machado ; Cruz, Osmany Guirola; González, Ignacio Hernández; Pérez, Mariela León; Camins, Antoni; Santos, Wagner Ferreira dos; Uyemura, Sergio Akira ; Pardo-Andreu, Gilberto L.; Pentón-Rol, Giselle
Fonte: Current Pharmaceutical Design. Unidades: FCFRP, FFCLRP, FMRP
Assuntos: ACIDENTE VASCULAR CEREBRAL, ISQUEMIA CEREBRAL, FARMACOTERAPIA, MODELOS ANIMAIS DE DOENÇAS
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ABNT
MARÍN-PRIDA, Javier et al. Novel insights into the molecular mechanisms involved in the neuroprotective effects of C-Phycocyanin against brain ischemia in rats. Current Pharmaceutical Design, v. 28, n. 14, p. 1187-1197, 2022Tradução . . Disponível em: https://doi.org/10.2174/1381612828666220506145542. Acesso em: 29 ago. 2024.
APA
Marín-Prida, J., Liberato, J. L., Llópiz-Arzuaga, A., Padovani, K. S., Pavón-Fuentes, N., Leopoldino, A. M., et al. (2022). Novel insights into the molecular mechanisms involved in the neuroprotective effects of C-Phycocyanin against brain ischemia in rats. Current Pharmaceutical Design, 28( 14), 1187-1197. doi:10.2174/1381612828666220506145542
NLM
Marín-Prida J, Liberato JL, Llópiz-Arzuaga A, Padovani KS, Pavón-Fuentes N, Leopoldino AM, Cruz OG, González IH, Pérez ML, Camins A, Santos WF dos, Uyemura SA, Pardo-Andreu GL, Pentón-Rol G. Novel insights into the molecular mechanisms involved in the neuroprotective effects of C-Phycocyanin against brain ischemia in rats [Internet]. Current Pharmaceutical Design. 2022 ; 28( 14): 1187-1197.[citado 2024 ago. 29 ] Available from: https://doi.org/10.2174/1381612828666220506145542
Vancouver
Marín-Prida J, Liberato JL, Llópiz-Arzuaga A, Padovani KS, Pavón-Fuentes N, Leopoldino AM, Cruz OG, González IH, Pérez ML, Camins A, Santos WF dos, Uyemura SA, Pardo-Andreu GL, Pentón-Rol G. Novel insights into the molecular mechanisms involved in the neuroprotective effects of C-Phycocyanin against brain ischemia in rats [Internet]. Current Pharmaceutical Design. 2022 ; 28( 14): 1187-1197.[citado 2024 ago. 29 ] Available from: https://doi.org/10.2174/1381612828666220506145542
Artigo de periodico
Rapanone, a naturally occurring benzoquinone, inhibits mitochondrial respiration and induces HepG2 cell death (2020)
Andreu, Gilberto L. Pardo; Reis, Felipe Henrique Zuccolotto dos ; González-Durruthy, Michael; Hernández, René Delgado; D'Vries, Richard F.; Vanden Berghe, Wim; Alberici, Luciane Carla
Fonte: Toxicology in Vitro. Unidades: FCFRP, FMRP
Assuntos: ANTINEOPLÁSICOS, TOXICOLOGIA, NEOPLASIAS, MITOCÔNDRIAS, CARCINOMA HEPATOCELULAR
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ABNT
ANDREU, Gilberto L. Pardo et al. Rapanone, a naturally occurring benzoquinone, inhibits mitochondrial respiration and induces HepG2 cell death. Toxicology in Vitro, v. 63, p. 1-10, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.tiv.2019.104737. Acesso em: 29 ago. 2024.
APA
Andreu, G. L. P., Reis, F. H. Z. dos, González-Durruthy, M., Hernández, R. D., D'Vries, R. F., Vanden Berghe, W., & Alberici, L. C. (2020). Rapanone, a naturally occurring benzoquinone, inhibits mitochondrial respiration and induces HepG2 cell death. Toxicology in Vitro, 63, 1-10. doi:10.1016/j.tiv.2019.104737
NLM
Andreu GLP, Reis FHZ dos, González-Durruthy M, Hernández RD, D'Vries RF, Vanden Berghe W, Alberici LC. Rapanone, a naturally occurring benzoquinone, inhibits mitochondrial respiration and induces HepG2 cell death [Internet]. Toxicology in Vitro. 2020 ; 63 1-10.[citado 2024 ago. 29 ] Available from: https://doi.org/10.1016/j.tiv.2019.104737
Vancouver
Andreu GLP, Reis FHZ dos, González-Durruthy M, Hernández RD, D'Vries RF, Vanden Berghe W, Alberici LC. Rapanone, a naturally occurring benzoquinone, inhibits mitochondrial respiration and induces HepG2 cell death [Internet]. Toxicology in Vitro. 2020 ; 63 1-10.[citado 2024 ago. 29 ] Available from: https://doi.org/10.1016/j.tiv.2019.104737
Artigo de periodico
Synthesis and evaluation of [18F]FEtLos and [18F]AMBF3Los as novel 18F-Labelled Losartan derivatives for molecular imaging of Angiotensin II type 1 receptors (2020)
Ortega Pijeira, Martha Sahylí; Nunes, Paulo Sérgio Gonçalves ; Santos, Sofia Nascimento dos; Zhang, Zhengxing; Pérez Nario, Arian; Perini, Efrain Araujo; Turato, Walter Miguel; Rodríguez Riera, Zalua; Chammas, Roger ; Elsinga, Philip H.; Lin, Kuo-Shyan ; Carvalho, Ivone ; Bernardes, Emerson Soares
Fonte: Molecules. Unidades: FCF, FM, FCFRP
Assuntos: ANGIOTENSINA II, RECEPTORES DE ANGIOTENSINA, DOENÇAS CARDIOVASCULARES, INFLAMAÇÃO, NEOPLASIAS
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ABNT
ORTEGA PIJEIRA, Martha Sahylí et al. Synthesis and evaluation of [18F]FEtLos and [18F]AMBF3Los as novel 18F-Labelled Losartan derivatives for molecular imaging of Angiotensin II type 1 receptors. Molecules, v. 25, n. 8, p. 1-21, 2020Tradução . . Disponível em: https://doi.org/10.3390/molecules25081872. Acesso em: 29 ago. 2024.
APA
Ortega Pijeira, M. S., Nunes, P. S. G., Santos, S. N. dos, Zhang, Z., Pérez Nario, A., Perini, E. A., et al. (2020). Synthesis and evaluation of [18F]FEtLos and [18F]AMBF3Los as novel 18F-Labelled Losartan derivatives for molecular imaging of Angiotensin II type 1 receptors. Molecules, 25( 8), 1-21. doi:10.3390/molecules25081872
NLM
Ortega Pijeira MS, Nunes PSG, Santos SN dos, Zhang Z, Pérez Nario A, Perini EA, Turato WM, Rodríguez Riera Z, Chammas R, Elsinga PH, Lin K-S, Carvalho I, Bernardes ES. Synthesis and evaluation of [18F]FEtLos and [18F]AMBF3Los as novel 18F-Labelled Losartan derivatives for molecular imaging of Angiotensin II type 1 receptors [Internet]. Molecules. 2020 ; 25( 8): 1-21.[citado 2024 ago. 29 ] Available from: https://doi.org/10.3390/molecules25081872
Vancouver
Ortega Pijeira MS, Nunes PSG, Santos SN dos, Zhang Z, Pérez Nario A, Perini EA, Turato WM, Rodríguez Riera Z, Chammas R, Elsinga PH, Lin K-S, Carvalho I, Bernardes ES. Synthesis and evaluation of [18F]FEtLos and [18F]AMBF3Los as novel 18F-Labelled Losartan derivatives for molecular imaging of Angiotensin II type 1 receptors [Internet]. Molecules. 2020 ; 25( 8): 1-21.[citado 2024 ago. 29 ] Available from: https://doi.org/10.3390/molecules25081872
Artigo de periodico
Anti-cancer activity of a new dihydropyridine derivative, VdiE-2N, in head and neck squamous cell carcinoma (2018)
Goto, Renata Nishida; Sobral, Lays Martin ; Sousa, Lucas Oliveira ; Garcia, Cristiana Bernadelli; Lopes, Norberto Peporine ; Marín-Prida, Javier; Ochoa-Rodríguez, Estael; Verdecia-Reyes, Yamila; Pardo-Andreu, Gilberto Lázaro; Curti, Carlos ; Leopoldino, Andréia Machado
Fonte: European Journal of Pharmacology. Unidade: FCFRP
Assuntos: ANTINEOPLÁSICOS, APOPTOSE, NEOPLASIAS DE CABEÇA E PESCOÇO, MITOCÔNDRIAS, NEOVASCULARIZAÇÃO PATOLÓGICA
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ABNT
GOTO, Renata Nishida et al. Anti-cancer activity of a new dihydropyridine derivative, VdiE-2N, in head and neck squamous cell carcinoma. European Journal of Pharmacology, v. 819, p. 198-206, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.ejphar.2017.12.009. Acesso em: 29 ago. 2024.
APA
Goto, R. N., Sobral, L. M., Sousa, L. O., Garcia, C. B., Lopes, N. P., Marín-Prida, J., et al. (2018). Anti-cancer activity of a new dihydropyridine derivative, VdiE-2N, in head and neck squamous cell carcinoma. European Journal of Pharmacology, 819, 198-206. doi:10.1016/j.ejphar.2017.12.009
NLM
Goto RN, Sobral LM, Sousa LO, Garcia CB, Lopes NP, Marín-Prida J, Ochoa-Rodríguez E, Verdecia-Reyes Y, Pardo-Andreu GL, Curti C, Leopoldino AM. Anti-cancer activity of a new dihydropyridine derivative, VdiE-2N, in head and neck squamous cell carcinoma [Internet]. European Journal of Pharmacology. 2018 ; 819 198-206.[citado 2024 ago. 29 ] Available from: https://doi.org/10.1016/j.ejphar.2017.12.009
Vancouver
Goto RN, Sobral LM, Sousa LO, Garcia CB, Lopes NP, Marín-Prida J, Ochoa-Rodríguez E, Verdecia-Reyes Y, Pardo-Andreu GL, Curti C, Leopoldino AM. Anti-cancer activity of a new dihydropyridine derivative, VdiE-2N, in head and neck squamous cell carcinoma [Internet]. European Journal of Pharmacology. 2018 ; 819 198-206.[citado 2024 ago. 29 ] Available from: https://doi.org/10.1016/j.ejphar.2017.12.009
Artigo de periodico
The cytotoxic effects of VE-3N, a novel 1,4-dihydropyridine derivative, involve the mitochondrial bioenergetic disruption via uncoupling mechanisms (2017)
Prida, Javier Marín; Andreu, Gilberto L. Pardo; Rossignoli, Camila Pederiva; Durruthy, Michael González; Rodríguez, Estael Ochoa; Reyes, Yamila Verdecia; Acosta, Roberto Fernández; Uyemura, Sérgio Akira; Alberici, Luciane Carla
Fonte: Toxicology in Vitro. Unidade: FCFRP
Assuntos: NEOPLASIAS, CITOTOXICIDADE IMUNOLÓGICA, MITOCÔNDRIAS, FÁRMACOS
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ABNT
PRIDA, Javier Marín et al. The cytotoxic effects of VE-3N, a novel 1,4-dihydropyridine derivative, involve the mitochondrial bioenergetic disruption via uncoupling mechanisms. Toxicology in Vitro, v. 42, p. 21-30, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tiv.2017.03.011. Acesso em: 29 ago. 2024.
APA
Prida, J. M., Andreu, G. L. P., Rossignoli, C. P., Durruthy, M. G., Rodríguez, E. O., Reyes, Y. V., et al. (2017). The cytotoxic effects of VE-3N, a novel 1,4-dihydropyridine derivative, involve the mitochondrial bioenergetic disruption via uncoupling mechanisms. Toxicology in Vitro, 42, 21-30. doi:10.1016/j.tiv.2017.03.011
NLM
Prida JM, Andreu GLP, Rossignoli CP, Durruthy MG, Rodríguez EO, Reyes YV, Acosta RF, Uyemura SA, Alberici LC. The cytotoxic effects of VE-3N, a novel 1,4-dihydropyridine derivative, involve the mitochondrial bioenergetic disruption via uncoupling mechanisms [Internet]. Toxicology in Vitro. 2017 ; 42 21-30.[citado 2024 ago. 29 ] Available from: https://doi.org/10.1016/j.tiv.2017.03.011
Vancouver
Prida JM, Andreu GLP, Rossignoli CP, Durruthy MG, Rodríguez EO, Reyes YV, Acosta RF, Uyemura SA, Alberici LC. The cytotoxic effects of VE-3N, a novel 1,4-dihydropyridine derivative, involve the mitochondrial bioenergetic disruption via uncoupling mechanisms [Internet]. Toxicology in Vitro. 2017 ; 42 21-30.[citado 2024 ago. 29 ] Available from: https://doi.org/10.1016/j.tiv.2017.03.011
Artigo de periodico
The cytotoxic effects of brown Cuban propolis depend on the nemorosone content and may be mediated by mitochondrial uncoupling (2015)
Andreu, Gilberto L. Pardo; Reis, Felippe H. Z; Dalalio, Felipe M; Figueredo, Yanier Nuñez; Rubio, Osmany Cuesta; Uyemura, Sérgio Akira; Curti, Carlos; Alberici, Luciane Carla
Fonte: Chemico-Biological Interactions. Unidade: FCFRP
Assuntos: PRÓPOLIS, MITOCÔNDRIAS, TESTES DE TOXICIDADE, TOXICOLOGIA
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ABNT
ANDREU, Gilberto L. Pardo et al. The cytotoxic effects of brown Cuban propolis depend on the nemorosone content and may be mediated by mitochondrial uncoupling. Chemico-Biological Interactions, v. 228, p. 28-34, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.cbi.2015.01.010. Acesso em: 29 ago. 2024.
APA
Andreu, G. L. P., Reis, F. H. Z., Dalalio, F. M., Figueredo, Y. N., Rubio, O. C., Uyemura, S. A., et al. (2015). The cytotoxic effects of brown Cuban propolis depend on the nemorosone content and may be mediated by mitochondrial uncoupling. Chemico-Biological Interactions, 228, 28-34. doi:10.1016/j.cbi.2015.01.010
NLM
Andreu GLP, Reis FHZ, Dalalio FM, Figueredo YN, Rubio OC, Uyemura SA, Curti C, Alberici LC. The cytotoxic effects of brown Cuban propolis depend on the nemorosone content and may be mediated by mitochondrial uncoupling [Internet]. Chemico-Biological Interactions. 2015 ; 228 28-34.[citado 2024 ago. 29 ] Available from: https://doi.org/10.1016/j.cbi.2015.01.010
Vancouver
Andreu GLP, Reis FHZ, Dalalio FM, Figueredo YN, Rubio OC, Uyemura SA, Curti C, Alberici LC. The cytotoxic effects of brown Cuban propolis depend on the nemorosone content and may be mediated by mitochondrial uncoupling [Internet]. Chemico-Biological Interactions. 2015 ; 228 28-34.[citado 2024 ago. 29 ] Available from: https://doi.org/10.1016/j.cbi.2015.01.010

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