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Artigo de periodico
Engineering NK-CAR.19 cells with the IL-15/IL-15Rα complex improved proliferation and anti-tumor effect in vivo (2023)
Silvestre, Renata Nacasaki ; Eitler, Jiri; Azevedo, Júlia Teixeira Cottas de ; Tirapelle, Mariane Cariati; Fantacini, Daianne Maciely Carvalho ; Souza, Lucas Eduardo Botelho de ; Swiech, Kamilla ; Covas, Dimas Tadeu ; Calado, Rodrigo Tocantins ; Montero, Paola Ortiz; Malmegrim, Kelen Cristina Ribeiro ; Figueiredo, Marxa L.; Tonn, Torsten; Picanço-Castro, Virgínia
Source: Frontiers in Immunology. Unidades: FMRP, FCFRP
Subjects: ANTÍGENOS, LINHAGEM CELULAR, PROLIFERAÇÃO CELULAR, INTERLEUCINAS
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SILVESTRE, Renata Nacasaki et al. Engineering NK-CAR.19 cells with the IL-15/IL-15Rα complex improved proliferation and anti-tumor effect in vivo. Frontiers in Immunology, v. 14, p. 1-15, 2023Tradução . . Disponível em: https://doi.org/10.3389/fimmu.2023.1226518. Acesso em: 19 nov. 2024.
APA
Silvestre, R. N., Eitler, J., Azevedo, J. T. C. de, Tirapelle, M. C., Fantacini, D. M. C., Souza, L. E. B. de, et al. (2023). Engineering NK-CAR.19 cells with the IL-15/IL-15Rα complex improved proliferation and anti-tumor effect in vivo. Frontiers in Immunology, 14, 1-15. doi:10.3389/fimmu.2023.1226518
NLM
Silvestre RN, Eitler J, Azevedo JTC de, Tirapelle MC, Fantacini DMC, Souza LEB de, Swiech K, Covas DT, Calado RT, Montero PO, Malmegrim KCR, Figueiredo ML, Tonn T, Picanço-Castro V. Engineering NK-CAR.19 cells with the IL-15/IL-15Rα complex improved proliferation and anti-tumor effect in vivo [Internet]. Frontiers in Immunology. 2023 ; 14 1-15.[citado 2024 nov. 19 ] Available from: https://doi.org/10.3389/fimmu.2023.1226518
Vancouver
Silvestre RN, Eitler J, Azevedo JTC de, Tirapelle MC, Fantacini DMC, Souza LEB de, Swiech K, Covas DT, Calado RT, Montero PO, Malmegrim KCR, Figueiredo ML, Tonn T, Picanço-Castro V. Engineering NK-CAR.19 cells with the IL-15/IL-15Rα complex improved proliferation and anti-tumor effect in vivo [Internet]. Frontiers in Immunology. 2023 ; 14 1-15.[citado 2024 nov. 19 ] Available from: https://doi.org/10.3389/fimmu.2023.1226518
Artigo de periodico
Glucosinolate-enriched fractions from maca (Lepidium meyenii) exert myrosinase-dependent cytotoxic effects against HepG2/C3A and HT29 tumor cell lines (2022)
Lenzi, Raquely M.; Campestrini, Luciano H.; Semprebon, Simone C.; Paschoal, Jonas Augusto Rizzato ; Silva, Monique A. G.; Zawadzki-Baggio, Selma F.; Mantovani, Mário S.; Petkowicz, Carmen L. O.; Maurer, Juliana B. B.
Source: Nutrition and Cancer. Unidade: FCFRP
Subjects: ADENOCARCINOMA, LINHAGEM CELULAR, NEOPLASIAS COLORRETAIS, FARMACOTERAPIA, ENZIMAS HIDROLÍTICAS, EXTRATOS (FORMAS FARMACÊUTICAS)
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LENZI, Raquely M. et al. Glucosinolate-enriched fractions from maca (Lepidium meyenii) exert myrosinase-dependent cytotoxic effects against HepG2/C3A and HT29 tumor cell lines. Nutrition and Cancer, v. 74, n. 4, p. 1322-1337, 2022Tradução . . Disponível em: https://doi.org/10.1080/01635581.2021.1952444. Acesso em: 19 nov. 2024.
APA
Lenzi, R. M., Campestrini, L. H., Semprebon, S. C., Paschoal, J. A. R., Silva, M. A. G., Zawadzki-Baggio, S. F., et al. (2022). Glucosinolate-enriched fractions from maca (Lepidium meyenii) exert myrosinase-dependent cytotoxic effects against HepG2/C3A and HT29 tumor cell lines. Nutrition and Cancer, 74( 4), 1322-1337. doi:10.1080/01635581.2021.1952444
NLM
Lenzi RM, Campestrini LH, Semprebon SC, Paschoal JAR, Silva MAG, Zawadzki-Baggio SF, Mantovani MS, Petkowicz CLO, Maurer JBB. Glucosinolate-enriched fractions from maca (Lepidium meyenii) exert myrosinase-dependent cytotoxic effects against HepG2/C3A and HT29 tumor cell lines [Internet]. Nutrition and Cancer. 2022 ; 74( 4): 1322-1337.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1080/01635581.2021.1952444
Vancouver
Lenzi RM, Campestrini LH, Semprebon SC, Paschoal JAR, Silva MAG, Zawadzki-Baggio SF, Mantovani MS, Petkowicz CLO, Maurer JBB. Glucosinolate-enriched fractions from maca (Lepidium meyenii) exert myrosinase-dependent cytotoxic effects against HepG2/C3A and HT29 tumor cell lines [Internet]. Nutrition and Cancer. 2022 ; 74( 4): 1322-1337.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1080/01635581.2021.1952444
Artigo de periodico
Pharmacological inhibition of HDAC6 overcomes cisplatin chemoresistance by targeting cancer stem cells in oral squamous cell carcinoma (2022)
Tavares, Marcela de Oliveira ; Milan, Thais Moré; Bighetti-Trevisan, Rayana Longo ; Leopoldino, Andréia Machado ; Almeida, Luciana Oliveira de
Source: Journal of Oral Pathology & Medicine. Unidades: FCFRP, FORP
Subjects: CARCINOMA DE CÉLULAS ESCAMOSAS, FARMACOTERAPIA, LINHAGEM CELULAR, NEOPLASIAS, NEOPLASIAS DE CABEÇA E PESCOÇO, NEOPLASIAS BUCAIS, ESPÉCIES REATIVAS DE OXIGÊNIO
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TAVARES, Marcela de Oliveira et al. Pharmacological inhibition of HDAC6 overcomes cisplatin chemoresistance by targeting cancer stem cells in oral squamous cell carcinoma. Journal of Oral Pathology & Medicine, v. 51, n. 6, p. 529-537, 2022Tradução . . Disponível em: https://doi.org/10.1111/jop.13326. Acesso em: 19 nov. 2024.
APA
Tavares, M. de O., Milan, T. M., Bighetti-Trevisan, R. L., Leopoldino, A. M., & Almeida, L. O. de. (2022). Pharmacological inhibition of HDAC6 overcomes cisplatin chemoresistance by targeting cancer stem cells in oral squamous cell carcinoma. Journal of Oral Pathology & Medicine, 51( 6), 529-537. doi:10.1111/jop.13326
NLM
Tavares M de O, Milan TM, Bighetti-Trevisan RL, Leopoldino AM, Almeida LO de. Pharmacological inhibition of HDAC6 overcomes cisplatin chemoresistance by targeting cancer stem cells in oral squamous cell carcinoma [Internet]. Journal of Oral Pathology & Medicine. 2022 ; 51( 6): 529-537.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1111/jop.13326
Vancouver
Tavares M de O, Milan TM, Bighetti-Trevisan RL, Leopoldino AM, Almeida LO de. Pharmacological inhibition of HDAC6 overcomes cisplatin chemoresistance by targeting cancer stem cells in oral squamous cell carcinoma [Internet]. Journal of Oral Pathology & Medicine. 2022 ; 51( 6): 529-537.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1111/jop.13326
Artigo de periodico
Synthesis, biological evaluation and molecular docking studies of novel 1,2,3-triazole-quinazolines as antiproliferative agents displaying ERK inhibitory activity (2021)
Nunes, Paulo Sergio Gonçalves; Silva, Gabriel da ; Nascimento, Sofia; Mantoani, Susimaire Pedersoli; Andrade, Peterson de; Bernardes, Emerson Soares; Kawano, Daniel Fábio; Leopoldino, Andréia Machado ; Carvalho, Ivone
Source: Bioorganic Chemistry. Unidades: IPEN, FCFRP
Subjects: ANTINEOPLÁSICOS, LINHAGEM CELULAR, PROLIFERAÇÃO CELULAR, PROTEÍNAS QUINASES, ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA)
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NUNES, Paulo Sergio Gonçalves et al. Synthesis, biological evaluation and molecular docking studies of novel 1,2,3-triazole-quinazolines as antiproliferative agents displaying ERK inhibitory activity. Bioorganic Chemistry, v. 113, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2021.104982. Acesso em: 19 nov. 2024.
APA
Nunes, P. S. G., Silva, G. da, Nascimento, S., Mantoani, S. P., Andrade, P. de, Bernardes, E. S., et al. (2021). Synthesis, biological evaluation and molecular docking studies of novel 1,2,3-triazole-quinazolines as antiproliferative agents displaying ERK inhibitory activity. Bioorganic Chemistry, 113. doi:10.1016/j.bioorg.2021.104982
NLM
Nunes PSG, Silva G da, Nascimento S, Mantoani SP, Andrade P de, Bernardes ES, Kawano DF, Leopoldino AM, Carvalho I. Synthesis, biological evaluation and molecular docking studies of novel 1,2,3-triazole-quinazolines as antiproliferative agents displaying ERK inhibitory activity [Internet]. Bioorganic Chemistry. 2021 ; 113[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.bioorg.2021.104982
Vancouver
Nunes PSG, Silva G da, Nascimento S, Mantoani SP, Andrade P de, Bernardes ES, Kawano DF, Leopoldino AM, Carvalho I. Synthesis, biological evaluation and molecular docking studies of novel 1,2,3-triazole-quinazolines as antiproliferative agents displaying ERK inhibitory activity [Internet]. Bioorganic Chemistry. 2021 ; 113[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.bioorg.2021.104982
Artigo de periodico
Chikungunya virus entry is strongly inhibited by phospholipase A2 isolated from the venom of Crotalus durissus terrifcus (2021)
Santos, Igor Andrade; Shimizu, Jacqueline Farinha; Oliveira, Débora Moraes de; Martins, Daniel Oliveira Silva; Cardoso‑Sousa, Léia; Cintra, Adélia Cristina Oliveira; Quintana, Victor Hugo Aquino; Sampaio, Suely Vilela ; Nicolau‑Junior, Nilson; Sabino‑Silva, Robinson
Source: Scientific Reports. Unidade: FCFRP
Subjects: LINHAGEM CELULAR, VÍRUS CHIKUNGUNYA, VENENOS, CROTALIDAE, GLICOPROTEÍNAS, FOSFOLIPASES A, REPLICAÇÃO VIRAL
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SANTOS, Igor Andrade et al. Chikungunya virus entry is strongly inhibited by phospholipase A2 isolated from the venom of Crotalus durissus terrifcus. Scientific Reports, v. 11, n. 1, p. 1-12, 2021Tradução . . Disponível em: https://doi.org/10.1038/s41598-021-88039-4. Acesso em: 19 nov. 2024.
APA
Santos, I. A., Shimizu, J. F., Oliveira, D. M. de, Martins, D. O. S., Cardoso‑Sousa, L., Cintra, A. C. O., et al. (2021). Chikungunya virus entry is strongly inhibited by phospholipase A2 isolated from the venom of Crotalus durissus terrifcus. Scientific Reports, 11( 1), 1-12. doi:10.1038/s41598-021-88039-4
NLM
Santos IA, Shimizu JF, Oliveira DM de, Martins DOS, Cardoso‑Sousa L, Cintra ACO, Quintana VHA, Sampaio SV, Nicolau‑Junior N, Sabino‑Silva R. Chikungunya virus entry is strongly inhibited by phospholipase A2 isolated from the venom of Crotalus durissus terrifcus [Internet]. Scientific Reports. 2021 ; 11( 1): 1-12.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/s41598-021-88039-4
Vancouver
Santos IA, Shimizu JF, Oliveira DM de, Martins DOS, Cardoso‑Sousa L, Cintra ACO, Quintana VHA, Sampaio SV, Nicolau‑Junior N, Sabino‑Silva R. Chikungunya virus entry is strongly inhibited by phospholipase A2 isolated from the venom of Crotalus durissus terrifcus [Internet]. Scientific Reports. 2021 ; 11( 1): 1-12.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/s41598-021-88039-4
Artigo de periodico
Generation of a three-dimensional in vitro ovarian cancer co-culture model for drug screening assays (2021)
Tofani, Larissa Bueno; Sousa, Lucas Oliveira ; Luiz, Marcela Tavares; Abriata, Juliana Palma; Marchetti, Juliana Maldonado; Leopoldino, Andréia Machado ; Swiech, Kamilla
Source: Journal of Pharmaceutical Sciences. Unidade: FCFRP
Subjects: LINHAGEM CELULAR, AVALIAÇÃO DE MEDICAMENTOS, NEOPLASIAS OVARIANAS, FARMACOTERAPIA, FIBROBLASTOS
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TOFANI, Larissa Bueno et al. Generation of a three-dimensional in vitro ovarian cancer co-culture model for drug screening assays. Journal of Pharmaceutical Sciences, v. 110, n. 7, p. 2629-2636, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.xphs.2021.04.003. Acesso em: 19 nov. 2024.
APA
Tofani, L. B., Sousa, L. O., Luiz, M. T., Abriata, J. P., Marchetti, J. M., Leopoldino, A. M., & Swiech, K. (2021). Generation of a three-dimensional in vitro ovarian cancer co-culture model for drug screening assays. Journal of Pharmaceutical Sciences, 110( 7), 2629-2636. doi:10.1016/j.xphs.2021.04.003
NLM
Tofani LB, Sousa LO, Luiz MT, Abriata JP, Marchetti JM, Leopoldino AM, Swiech K. Generation of a three-dimensional in vitro ovarian cancer co-culture model for drug screening assays [Internet]. Journal of Pharmaceutical Sciences. 2021 ; 110( 7): 2629-2636.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.xphs.2021.04.003
Vancouver
Tofani LB, Sousa LO, Luiz MT, Abriata JP, Marchetti JM, Leopoldino AM, Swiech K. Generation of a three-dimensional in vitro ovarian cancer co-culture model for drug screening assays [Internet]. Journal of Pharmaceutical Sciences. 2021 ; 110( 7): 2629-2636.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.xphs.2021.04.003
Artigo de periodico
Gold(III) complexes with thiosemicarbazonate ligands as potential anticancer agents: cytotoxicity and interactions with biomolecular targets (2021)
Possato, Bruna; Dalmolin, Luciana Facco; Pereira, Luiz Miguel; Alves, Jacqueline Querino; Silva, Raphael Tristão Cruvinel; Gelamo, Rogerio Valentim; Yatsuda, Ana Patrícia ; Lopez, Renata Fonseca Vianna ; Albuquerque, Sérgio de ; Leite, Natália Bueno; Maia, Pedro Ivo da Silva
Source: European Journal of Pharmaceutical Sciences. Unidades: FCFRP, PUSP-RP
Subjects: ANTINEOPLÁSICOS, APOPTOSE, LINHAGEM CELULAR, LIGANTES, NEOPLASIAS OVARIANAS
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POSSATO, Bruna et al. Gold(III) complexes with thiosemicarbazonate ligands as potential anticancer agents: cytotoxicity and interactions with biomolecular targets. European Journal of Pharmaceutical Sciences, v. 162, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.ejps.2021.105834. Acesso em: 19 nov. 2024.
APA
Possato, B., Dalmolin, L. F., Pereira, L. M., Alves, J. Q., Silva, R. T. C., Gelamo, R. V., et al. (2021). Gold(III) complexes with thiosemicarbazonate ligands as potential anticancer agents: cytotoxicity and interactions with biomolecular targets. European Journal of Pharmaceutical Sciences, 162. doi:10.1016/j.ejps.2021.105834
NLM
Possato B, Dalmolin LF, Pereira LM, Alves JQ, Silva RTC, Gelamo RV, Yatsuda AP, Lopez RFV, Albuquerque S de, Leite NB, Maia PI da S. Gold(III) complexes with thiosemicarbazonate ligands as potential anticancer agents: cytotoxicity and interactions with biomolecular targets [Internet]. European Journal of Pharmaceutical Sciences. 2021 ; 162[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.ejps.2021.105834
Vancouver
Possato B, Dalmolin LF, Pereira LM, Alves JQ, Silva RTC, Gelamo RV, Yatsuda AP, Lopez RFV, Albuquerque S de, Leite NB, Maia PI da S. Gold(III) complexes with thiosemicarbazonate ligands as potential anticancer agents: cytotoxicity and interactions with biomolecular targets [Internet]. European Journal of Pharmaceutical Sciences. 2021 ; 162[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.ejps.2021.105834
Trabalho de evento-resumo periodico
Desregulação da via de WNT/B-catenina e metilação de histonas participam do processo de quimiorresistência e acúmulo de Células-Tronco Tumorais (CTT) em carcinoma de cabeça e pescoço (2021)
Milan, Thais Moré; Trevisan, Rayana Longo Bighetti ; Almeida, Luciana Oliveira de
Source: Anais da Faculdade de Odontologia de Ribeirão Preto da Universidade de São Paulo. Conference titles: Jornada Odontológica de Ribeirão Preto - JORP. Unidades: FCFRP, FORP
Subjects: CARCINOMA, CABEÇA, PESCOÇO, EPIGÊNESE GENÉTICA, QUIMIOTERÁPICOS, LINHAGEM CELULAR
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MILAN, Thais Moré e TREVISAN, Rayana Longo Bighetti e ALMEIDA, Luciana Oliveira de. Desregulação da via de WNT/B-catenina e metilação de histonas participam do processo de quimiorresistência e acúmulo de Células-Tronco Tumorais (CTT) em carcinoma de cabeça e pescoço. Anais da Faculdade de Odontologia de Ribeirão Preto da Universidade de São Paulo. Ribeirão Preto: FORP-USP. Disponível em: https://www.forp.usp.br/wp-content/uploads/2022/01/Volume-37-43a-JORP-2021-reduzido.pdf. Acesso em: 19 nov. 2024. , 2021
APA
Milan, T. M., Trevisan, R. L. B., & Almeida, L. O. de. (2021). Desregulação da via de WNT/B-catenina e metilação de histonas participam do processo de quimiorresistência e acúmulo de Células-Tronco Tumorais (CTT) em carcinoma de cabeça e pescoço. Anais da Faculdade de Odontologia de Ribeirão Preto da Universidade de São Paulo. Ribeirão Preto: FORP-USP. Recuperado de https://www.forp.usp.br/wp-content/uploads/2022/01/Volume-37-43a-JORP-2021-reduzido.pdf
NLM
Milan TM, Trevisan RLB, Almeida LO de. Desregulação da via de WNT/B-catenina e metilação de histonas participam do processo de quimiorresistência e acúmulo de Células-Tronco Tumorais (CTT) em carcinoma de cabeça e pescoço [Internet]. Anais da Faculdade de Odontologia de Ribeirão Preto da Universidade de São Paulo. 2021 ; 37 [21].[citado 2024 nov. 19 ] Available from: https://www.forp.usp.br/wp-content/uploads/2022/01/Volume-37-43a-JORP-2021-reduzido.pdf
Vancouver
Milan TM, Trevisan RLB, Almeida LO de. Desregulação da via de WNT/B-catenina e metilação de histonas participam do processo de quimiorresistência e acúmulo de Células-Tronco Tumorais (CTT) em carcinoma de cabeça e pescoço [Internet]. Anais da Faculdade de Odontologia de Ribeirão Preto da Universidade de São Paulo. 2021 ; 37 [21].[citado 2024 nov. 19 ] Available from: https://www.forp.usp.br/wp-content/uploads/2022/01/Volume-37-43a-JORP-2021-reduzido.pdf
Artigo de periodico
Generation of hyperfunctional recombinant human factor IX variants expressed in human cell line SK-Hep-1 (2021)
Bomfim, Aline de Sousa; Freitas, Marcela Cristina Corrêa de; Castro, Virgínia Picanço e; Soares Neto, Mario Abreu; Pádua, Ricardo; Covas, Dimas Tadeu ; Russo, Elisa Maria de Sousa
Source: Biotechnology Letters. Unidades: FMRP, FCFRP
Subjects: FATORES DE COAGULAÇÃO SANGUÍNEA, HEMOFILIA, LINHAGEM CELULAR
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BOMFIM, Aline de Sousa et al. Generation of hyperfunctional recombinant human factor IX variants expressed in human cell line SK-Hep-1. Biotechnology Letters, v. 43, n. 1, p. 143-152, 2021Tradução . . Disponível em: https://doi.org/10.1007/s10529-020-03040-7. Acesso em: 19 nov. 2024.
APA
Bomfim, A. de S., Freitas, M. C. C. de, Castro, V. P. e, Soares Neto, M. A., Pádua, R., Covas, D. T., & Russo, E. M. de S. (2021). Generation of hyperfunctional recombinant human factor IX variants expressed in human cell line SK-Hep-1. Biotechnology Letters, 43( 1), 143-152. doi:10.1007/s10529-020-03040-7
NLM
Bomfim A de S, Freitas MCC de, Castro VP e, Soares Neto MA, Pádua R, Covas DT, Russo EM de S. Generation of hyperfunctional recombinant human factor IX variants expressed in human cell line SK-Hep-1 [Internet]. Biotechnology Letters. 2021 ; 43( 1): 143-152.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1007/s10529-020-03040-7
Vancouver
Bomfim A de S, Freitas MCC de, Castro VP e, Soares Neto MA, Pádua R, Covas DT, Russo EM de S. Generation of hyperfunctional recombinant human factor IX variants expressed in human cell line SK-Hep-1 [Internet]. Biotechnology Letters. 2021 ; 43( 1): 143-152.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1007/s10529-020-03040-7
Trabalho de evento-resumo
Interaction of genetically encoded photosensitizers with scintillating nanoparticles for X-PDT (2021)
Micheletto, Mariana Chaves ; Guidelli, Eder José ; Faccin, João Paulo de Mauro; Costa Filho, Antonio José da
Source: Resumos. Conference titles: International Congress of the International Union for Pure Applied Biophysics (IUPAB). Unidades: FFCLRP, FCFRP
Subjects: NANOPARTÍCULAS, LINHAGEM CELULAR, PROTEÍNAS LUMINESCENTES, NEOPLASIAS, TERAPIA FOTODINÂMICA
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MICHELETTO, Mariana Chaves et al. Interaction of genetically encoded photosensitizers with scintillating nanoparticles for X-PDT. 2021, Anais.. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular (SBBq), 2021. Disponível em: https://easyapp.ekmf.com.br/sg/uploads/eventos/evento8/documentos/abstract_book.pdf. Acesso em: 19 nov. 2024.
APA
Micheletto, M. C., Guidelli, E. J., Faccin, J. P. de M., & Costa Filho, A. J. da. (2021). Interaction of genetically encoded photosensitizers with scintillating nanoparticles for X-PDT. In Resumos. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular (SBBq). Recuperado de https://easyapp.ekmf.com.br/sg/uploads/eventos/evento8/documentos/abstract_book.pdf
NLM
Micheletto MC, Guidelli EJ, Faccin JP de M, Costa Filho AJ da. Interaction of genetically encoded photosensitizers with scintillating nanoparticles for X-PDT [Internet]. Resumos. 2021 ;[citado 2024 nov. 19 ] Available from: https://easyapp.ekmf.com.br/sg/uploads/eventos/evento8/documentos/abstract_book.pdf
Vancouver
Micheletto MC, Guidelli EJ, Faccin JP de M, Costa Filho AJ da. Interaction of genetically encoded photosensitizers with scintillating nanoparticles for X-PDT [Internet]. Resumos. 2021 ;[citado 2024 nov. 19 ] Available from: https://easyapp.ekmf.com.br/sg/uploads/eventos/evento8/documentos/abstract_book.pdf
Trabalho de evento-resumo periodico
Interaction of genetically encoded photosensitizers with scintillating nanoparticles for X-PDT (2021)
Micheletto, Mariana Chaves ; Guidelli, Eder José ; Faccin, João Paulo de Mauro; Costa Filho, Antonio José da
Source: Biophysical Reviews. Conference titles: IUPAB International Congress. Unidades: FFCLRP, FCFRP
Subjects: NANOPARTÍCULAS, LINHAGEM CELULAR, PROTEÍNAS LUMINESCENTES, NEOPLASIAS, TERAPIA FOTODINÂMICA
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MICHELETTO, Mariana Chaves et al. Interaction of genetically encoded photosensitizers with scintillating nanoparticles for X-PDT. Biophysical Reviews. Heidelberg: Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://link.springer.com/article/10.1007/s12551-021-00844-3. Acesso em: 19 nov. 2024. , 2021
APA
Micheletto, M. C., Guidelli, E. J., Faccin, J. P. de M., & Costa Filho, A. J. da. (2021). Interaction of genetically encoded photosensitizers with scintillating nanoparticles for X-PDT. Biophysical Reviews. Heidelberg: Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo. Recuperado de https://link.springer.com/article/10.1007/s12551-021-00844-3
NLM
Micheletto MC, Guidelli EJ, Faccin JP de M, Costa Filho AJ da. Interaction of genetically encoded photosensitizers with scintillating nanoparticles for X-PDT [Internet]. Biophysical Reviews. 2021 ; 13( 6): 1484-1485.[citado 2024 nov. 19 ] Available from: https://link.springer.com/article/10.1007/s12551-021-00844-3
Vancouver
Micheletto MC, Guidelli EJ, Faccin JP de M, Costa Filho AJ da. Interaction of genetically encoded photosensitizers with scintillating nanoparticles for X-PDT [Internet]. Biophysical Reviews. 2021 ; 13( 6): 1484-1485.[citado 2024 nov. 19 ] Available from: https://link.springer.com/article/10.1007/s12551-021-00844-3
Artigo de periodico
Improving cytotoxicity against breast cancer cells by using mixed-ligand ruthenium(II) complexes of 2,2 -bipyridine, amino acid, and nitric oxide derivatives as potential anticancer agents (2021)
Gaspari, Ana Paula Segantin ; Silva, Roberto Santana da; Carneiro, Zumira Aparecida; Carvalho, Marcelo Rodrigues de; Carvalho, Ivone ; Pernomian, Laena ; Ferreira, Lucimara P.; Ramos, Loyanne Carla Barbosa; Souza, Gabriel Aguiar de; Formiga, André Luiz Barboza
Source: Anti-Cancer Agents in Medicinal Chemistry. Unidades: FCFRP, FMRP
Subjects: AMINOÁCIDOS, ANTINEOPLÁSICOS, NEOPLASIAS MAMÁRIAS, LINHAGEM CELULAR, PROLIFERAÇÃO CELULAR, ÓXIDO NÍTRICO
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ABNT
GASPARI, Ana Paula Segantin et al. Improving cytotoxicity against breast cancer cells by using mixed-ligand ruthenium(II) complexes of 2,2 -bipyridine, amino acid, and nitric oxide derivatives as potential anticancer agents. Anti-Cancer Agents in Medicinal Chemistry, v. 21, n. 12, p. 1602-1611, 2021Tradução . . Disponível em: https://doi.org/10.2174/0929867327666201020155105. Acesso em: 19 nov. 2024.
APA
Gaspari, A. P. S., Silva, R. S. da, Carneiro, Z. A., Carvalho, M. R. de, Carvalho, I., Pernomian, L., et al. (2021). Improving cytotoxicity against breast cancer cells by using mixed-ligand ruthenium(II) complexes of 2,2 -bipyridine, amino acid, and nitric oxide derivatives as potential anticancer agents. Anti-Cancer Agents in Medicinal Chemistry, 21( 12), 1602-1611. doi:10.2174/0929867327666201020155105
NLM
Gaspari APS, Silva RS da, Carneiro ZA, Carvalho MR de, Carvalho I, Pernomian L, Ferreira LP, Ramos LCB, Souza GA de, Formiga ALB. Improving cytotoxicity against breast cancer cells by using mixed-ligand ruthenium(II) complexes of 2,2 -bipyridine, amino acid, and nitric oxide derivatives as potential anticancer agents [Internet]. Anti-Cancer Agents in Medicinal Chemistry. 2021 ; 21( 12): 1602-1611.[citado 2024 nov. 19 ] Available from: https://doi.org/10.2174/0929867327666201020155105
Vancouver
Gaspari APS, Silva RS da, Carneiro ZA, Carvalho MR de, Carvalho I, Pernomian L, Ferreira LP, Ramos LCB, Souza GA de, Formiga ALB. Improving cytotoxicity against breast cancer cells by using mixed-ligand ruthenium(II) complexes of 2,2 -bipyridine, amino acid, and nitric oxide derivatives as potential anticancer agents [Internet]. Anti-Cancer Agents in Medicinal Chemistry. 2021 ; 21( 12): 1602-1611.[citado 2024 nov. 19 ] Available from: https://doi.org/10.2174/0929867327666201020155105
Artigo de periodico
A novel substitution in NS5A enhances the resistance of hepatitis C virus genotype 3 to daclatasvir (2021)
Campos, Guilherme Rodrigues Fernandes; Ward, Joseph; Chen, Shucheng; Bittar, Cíntia; Rodrigues, João Paulo Vilela; Martinelli, Ana de Lourdes Candolo; Souza, Fernanda Fernandes; Pereira, Leonardo Régis Leira ; Rahal, Paula; Harris, Mark
Source: Journal of General Virology. Unidades: FCFRP, FMRP
Subjects: ANTIVIRAIS, LINHAGEM CELULAR, ESTUDOS DE COORTES, FARMACOTERAPIA, HEPATITE C, MUTAÇÃO, REPLICAÇÃO VIRAL
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ABNT
CAMPOS, Guilherme Rodrigues Fernandes et al. A novel substitution in NS5A enhances the resistance of hepatitis C virus genotype 3 to daclatasvir. Journal of General Virology, v. 102, n. 1, p. 11-7, 2021Tradução . . Disponível em: https://doi.org/10.1099/jgv.0.001496. Acesso em: 19 nov. 2024.
APA
Campos, G. R. F., Ward, J., Chen, S., Bittar, C., Rodrigues, J. P. V., Martinelli, A. de L. C., et al. (2021). A novel substitution in NS5A enhances the resistance of hepatitis C virus genotype 3 to daclatasvir. Journal of General Virology, 102( 1), 11-7. doi:10.1099/jgv.0.001496
NLM
Campos GRF, Ward J, Chen S, Bittar C, Rodrigues JPV, Martinelli A de LC, Souza FF, Pereira LRL, Rahal P, Harris M. A novel substitution in NS5A enhances the resistance of hepatitis C virus genotype 3 to daclatasvir [Internet]. Journal of General Virology. 2021 ; 102( 1): 11-7.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1099/jgv.0.001496
Vancouver
Campos GRF, Ward J, Chen S, Bittar C, Rodrigues JPV, Martinelli A de LC, Souza FF, Pereira LRL, Rahal P, Harris M. A novel substitution in NS5A enhances the resistance of hepatitis C virus genotype 3 to daclatasvir [Internet]. Journal of General Virology. 2021 ; 102( 1): 11-7.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1099/jgv.0.001496
Artigo de periodico
Bellis perennis extract mitigates UVA-induced keratinocyte damage: photoprotective and immunomodulatory effects (2021)
Carvalho, Vivian Maria Souza de; Covre, Joyce Luciana; Correia-Silva, Rebeca D.; Lice, Izabella; Corrêa, Mab P.; Leopoldino, Andréia Machado ; Gil, Cristiane Damas
Source: Journal of Photochemistry and Photobiology B: Biology. Unidade: FCFRP
Subjects: COMPOSITAE, LINHAGEM CELULAR, SOBREVIVÊNCIA CELULAR, ADJUVANTES IMUNOLÓGICOS, ESPÉCIES REATIVAS DE OXIGÊNIO
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ABNT
CARVALHO, Vivian Maria Souza de et al. Bellis perennis extract mitigates UVA-induced keratinocyte damage: photoprotective and immunomodulatory effects. Journal of Photochemistry and Photobiology B: Biology, v. 221, p. 1-8, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.jphotobiol.2021.112247. Acesso em: 19 nov. 2024.
APA
Carvalho, V. M. S. de, Covre, J. L., Correia-Silva, R. D., Lice, I., Corrêa, M. P., Leopoldino, A. M., & Gil, C. D. (2021). Bellis perennis extract mitigates UVA-induced keratinocyte damage: photoprotective and immunomodulatory effects. Journal of Photochemistry and Photobiology B: Biology, 221, 1-8. doi:10.1016/j.jphotobiol.2021.112247
NLM
Carvalho VMS de, Covre JL, Correia-Silva RD, Lice I, Corrêa MP, Leopoldino AM, Gil CD. Bellis perennis extract mitigates UVA-induced keratinocyte damage: photoprotective and immunomodulatory effects [Internet]. Journal of Photochemistry and Photobiology B: Biology. 2021 ; 221 1-8.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.jphotobiol.2021.112247
Vancouver
Carvalho VMS de, Covre JL, Correia-Silva RD, Lice I, Corrêa MP, Leopoldino AM, Gil CD. Bellis perennis extract mitigates UVA-induced keratinocyte damage: photoprotective and immunomodulatory effects [Internet]. Journal of Photochemistry and Photobiology B: Biology. 2021 ; 221 1-8.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.jphotobiol.2021.112247
Artigo de periodico
Mutagenic and genotoxic activities of Phospholipase A2 Bothropstoxin-I from Bothrops jararacussu in Drosophila melanogaster and human cell lines (2021)
Naves, Maria Paula Carvalho; Morais, Cássio Resende de; Freitas, Vitor de; Ribeiro, Diego Luis ; Lopes, Daiana Silva; Antunes, Lusânia Maria Greggi ; Rodrigues, Veridiana de Melo; Rezende, Alexandre Azenha Alvesde; Spanó, Mário Antônio
Source: International Journal of Biological Macromolecules. Unidade: FCFRP
Subjects: SERPENTES, VIPERIDAE, VENENOS DE ORIGEM ANIMAL, CROTALIDAE, LINHAGEM CELULAR, SOBREVIVÊNCIA CELULAR, CÉLULAS ENDOTELIAIS, MUTAÇÃO GENÉTICA, FOSFOLIPASES A
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ABNT
NAVES, Maria Paula Carvalho et al. Mutagenic and genotoxic activities of Phospholipase A2 Bothropstoxin-I from Bothrops jararacussu in Drosophila melanogaster and human cell lines. International Journal of Biological Macromolecules, v. 182, p. 1602-1610, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.ijbiomac.2021.05.114. Acesso em: 19 nov. 2024.
APA
Naves, M. P. C., Morais, C. R. de, Freitas, V. de, Ribeiro, D. L., Lopes, D. S., Antunes, L. M. G., et al. (2021). Mutagenic and genotoxic activities of Phospholipase A2 Bothropstoxin-I from Bothrops jararacussu in Drosophila melanogaster and human cell lines. International Journal of Biological Macromolecules, 182, 1602-1610. doi:10.1016/j.ijbiomac.2021.05.114
NLM
Naves MPC, Morais CR de, Freitas V de, Ribeiro DL, Lopes DS, Antunes LMG, Rodrigues V de M, Rezende AAA, Spanó MA. Mutagenic and genotoxic activities of Phospholipase A2 Bothropstoxin-I from Bothrops jararacussu in Drosophila melanogaster and human cell lines [Internet]. International Journal of Biological Macromolecules. 2021 ; 182 1602-1610.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.ijbiomac.2021.05.114
Vancouver
Naves MPC, Morais CR de, Freitas V de, Ribeiro DL, Lopes DS, Antunes LMG, Rodrigues V de M, Rezende AAA, Spanó MA. Mutagenic and genotoxic activities of Phospholipase A2 Bothropstoxin-I from Bothrops jararacussu in Drosophila melanogaster and human cell lines [Internet]. International Journal of Biological Macromolecules. 2021 ; 182 1602-1610.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.ijbiomac.2021.05.114
Monografia/livro-ed/org
Chimeric antigen receptor T Cell: development and production (2020)
Swiech, Kamilla (Editor) ; Malmegrim, Kelen Cristina Ribeiro (Editor) ; Picanço-Castro, Virgínia (Editor)
Unidades: FCFRP, FMRP
Subjects: IMUNOTERAPIA, RECEPTORES DE ANTÍGENOS, ANTÍGENOS, LINHAGEM CELULAR, NEOPLASIAS
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ABNT
Chimeric antigen receptor T Cell: development and production. . New York: Humana Press. Disponível em: https://doi.org/10.1007/978-1-0716-0146-4. Acesso em: 19 nov. 2024. , 2020
APA
Chimeric antigen receptor T Cell: development and production. (2020). Chimeric antigen receptor T Cell: development and production. New York: Humana Press. doi:10.1007/978-1-0716-0146-4
NLM
Chimeric antigen receptor T Cell: development and production [Internet]. 2020 ;[citado 2024 nov. 19 ] Available from: https://doi.org/10.1007/978-1-0716-0146-4
Vancouver
Chimeric antigen receptor T Cell: development and production [Internet]. 2020 ;[citado 2024 nov. 19 ] Available from: https://doi.org/10.1007/978-1-0716-0146-4
Artigo de periodico
Beyond hemostasis: a snake venom serine protease with potassium channel blocking and potential antitumor activities (2020)
Boldrini-França, Johara; Pinheiro-Júnior, Ernesto Lopes ; Peigneur, Steve; Pucca, Manuela Berto; Cerni, Felipe Augusto; Borges, Rafael Junqueira; Costa, Tássia Rafaella; Carone, Sante Emmanuel Imai; Fontes, Marcos Roberto de Mattos; Sampaio, Suely Vilela ; Arantes, Eliane Candiani ; Tytgat, Jan
Source: Scientific Reports. Unidade: FCFRP
Subjects: SEQUÊNCIA DE AMINOÁCIDOS, ANTINEOPLÁSICOS, FARMACOLOGIA, CATÁLISE, LINHAGEM CELULAR, CANAIS DE POTÁSSIO, ANTAGONISTAS, HEMOSTASIA, PROTEÍNAS RECOMBINANTES, VENENOS, PROTEÍNAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BOLDRINI-FRANÇA, Johara et al. Beyond hemostasis: a snake venom serine protease with potassium channel blocking and potential antitumor activities. Scientific Reports, v. 10, n. 1, 2020Tradução . . Disponível em: https://doi.org/10.1038/s41598-020-61258-x. Acesso em: 19 nov. 2024.
APA
Boldrini-França, J., Pinheiro-Júnior, E. L., Peigneur, S., Pucca, M. B., Cerni, F. A., Borges, R. J., et al. (2020). Beyond hemostasis: a snake venom serine protease with potassium channel blocking and potential antitumor activities. Scientific Reports, 10( 1). doi:10.1038/s41598-020-61258-x
NLM
Boldrini-França J, Pinheiro-Júnior EL, Peigneur S, Pucca MB, Cerni FA, Borges RJ, Costa TR, Carone SEI, Fontes MR de M, Sampaio SV, Arantes EC, Tytgat J. Beyond hemostasis: a snake venom serine protease with potassium channel blocking and potential antitumor activities [Internet]. Scientific Reports. 2020 ; 10( 1):[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/s41598-020-61258-x
Vancouver
Boldrini-França J, Pinheiro-Júnior EL, Peigneur S, Pucca MB, Cerni FA, Borges RJ, Costa TR, Carone SEI, Fontes MR de M, Sampaio SV, Arantes EC, Tytgat J. Beyond hemostasis: a snake venom serine protease with potassium channel blocking and potential antitumor activities [Internet]. Scientific Reports. 2020 ; 10( 1):[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/s41598-020-61258-x
Artigo de periodico
Evaluation of cytoprotective effects of compounds isolated from Copaifera langsdorffii Desf. against induced cytotoxicity by exposure to methylmercury and lead (2020)
Aldana, Jennyfer Andrea; De Grandis, Rone Aparecido ; Nicolella, Heloiza D.; Guissoni, Ana Paula Prado; Squarisi, Iara Silva; Arruda, Caroline ; Ribeiro, Victor Pena ; Tavares, Denise Crispim ; Barcelos, Gustavo Rafael Mazzaron ; Antunes, Lusânia Maria Greggi ; Bastos, Jairo Kenupp
Source: Natural Product Research. Unidades: FFCLRP, FCFRP
Subjects: CAESALPINIACEAE, FLAVONOIDES, METAIS PESADOS, PROANTOCIANIDINAS, ANTIOXIDANTES, LINHAGEM CELULAR, FABACEAE
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ABNT
ALDANA, Jennyfer Andrea et al. Evaluation of cytoprotective effects of compounds isolated from Copaifera langsdorffii Desf. against induced cytotoxicity by exposure to methylmercury and lead. Natural Product Research, v. 34, n. 17, p. 2528-2532, 2020Tradução . . Disponível em: https://doi.org/10.1080/14786419.2018.1543673. Acesso em: 19 nov. 2024.
APA
Aldana, J. A., De Grandis, R. A., Nicolella, H. D., Guissoni, A. P. P., Squarisi, I. S., Arruda, C., et al. (2020). Evaluation of cytoprotective effects of compounds isolated from Copaifera langsdorffii Desf. against induced cytotoxicity by exposure to methylmercury and lead. Natural Product Research, 34( 17), 2528-2532. doi:10.1080/14786419.2018.1543673
NLM
Aldana JA, De Grandis RA, Nicolella HD, Guissoni APP, Squarisi IS, Arruda C, Ribeiro VP, Tavares DC, Barcelos GRM, Antunes LMG, Bastos JK. Evaluation of cytoprotective effects of compounds isolated from Copaifera langsdorffii Desf. against induced cytotoxicity by exposure to methylmercury and lead [Internet]. Natural Product Research. 2020 ; 34( 17): 2528-2532.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1080/14786419.2018.1543673
Vancouver
Aldana JA, De Grandis RA, Nicolella HD, Guissoni APP, Squarisi IS, Arruda C, Ribeiro VP, Tavares DC, Barcelos GRM, Antunes LMG, Bastos JK. Evaluation of cytoprotective effects of compounds isolated from Copaifera langsdorffii Desf. against induced cytotoxicity by exposure to methylmercury and lead [Internet]. Natural Product Research. 2020 ; 34( 17): 2528-2532.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1080/14786419.2018.1543673
Artigo de periodico
Ruthenium (II) complex cis-[RuII(ŋ2-O2CC7H7O2)(dppm)2]PF6-hmxbato induces ROS-mediated apoptosis in lung tumor cells producing selective cytotoxicity (2020)
Costa, Mônica Soares; Gonçalves, Yasmim Garcia; Borges, Bruna Cristina; Silva, Marcelo José Barbosa; Amstalden, Martin Krähenbühl; Costa, Tássia Rafaella; Antunes, Lusânia Maria Greggi ; Rodrigues, Renata Santos; Rodrigues, Veridiana de Melo; Franca, Eduardo de Faria; Zóia, Mariana Alves Pereira; Araújo, Thaise Gonçalves de; Goulart, Luiz Ricardo; Von Poelhsitz, Gustavo; Yoneyama, Kelly Aparecida Geraldo
Source: Scientific Reports. Unidade: FCFRP
Subjects: ANTINEOPLÁSICOS, FARMACOLOGIA, APOPTOSE, LINHAGEM CELULAR, PROLIFERAÇÃO CELULAR, DANO AO DNA, LEISHMANIA, METABOLISMO, NEOPLASIAS PULMONARES, QUIMIOTERAPIA, ESPÉCIES REATIVAS DE OXIGÊNIO, RUTÊNIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COSTA, Mônica Soares et al. Ruthenium (II) complex cis-[RuII(ŋ2-O2CC7H7O2)(dppm)2]PF6-hmxbato induces ROS-mediated apoptosis in lung tumor cells producing selective cytotoxicity. Scientific Reports, v. 10, 2020Tradução . . Disponível em: https://doi.org/10.1038/s41598-020-72420-w. Acesso em: 19 nov. 2024.
APA
Costa, M. S., Gonçalves, Y. G., Borges, B. C., Silva, M. J. B., Amstalden, M. K., Costa, T. R., et al. (2020). Ruthenium (II) complex cis-[RuII(ŋ2-O2CC7H7O2)(dppm)2]PF6-hmxbato induces ROS-mediated apoptosis in lung tumor cells producing selective cytotoxicity. Scientific Reports, 10. doi:10.1038/s41598-020-72420-w
NLM
Costa MS, Gonçalves YG, Borges BC, Silva MJB, Amstalden MK, Costa TR, Antunes LMG, Rodrigues RS, Rodrigues V de M, Franca E de F, Zóia MAP, Araújo TG de, Goulart LR, Von Poelhsitz G, Yoneyama KAG. Ruthenium (II) complex cis-[RuII(ŋ2-O2CC7H7O2)(dppm)2]PF6-hmxbato induces ROS-mediated apoptosis in lung tumor cells producing selective cytotoxicity [Internet]. Scientific Reports. 2020 ; 10[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/s41598-020-72420-w
Vancouver
Costa MS, Gonçalves YG, Borges BC, Silva MJB, Amstalden MK, Costa TR, Antunes LMG, Rodrigues RS, Rodrigues V de M, Franca E de F, Zóia MAP, Araújo TG de, Goulart LR, Von Poelhsitz G, Yoneyama KAG. Ruthenium (II) complex cis-[RuII(ŋ2-O2CC7H7O2)(dppm)2]PF6-hmxbato induces ROS-mediated apoptosis in lung tumor cells producing selective cytotoxicity [Internet]. Scientific Reports. 2020 ; 10[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/s41598-020-72420-w
Artigo de periodico
Synergic effect of OP449 and FTY720 on oral squamous cell carcinoma (2020)
Goto, Renata Nishida; Sobral, Lays Martin; Padovani, Karina Stringhetta; Garcia, Cristiana Bernadelli ; Silva, Gabriel da; Vitek, Michael P.; Leopoldino, Andréia Machado
Source: European Journal of Pharmacology. Unidade: FCFRP
Subjects: ANTINEOPLÁSICOS, FARMACOLOGIA, CARCINOMA DE CÉLULAS ESCAMOSAS, QUIMIOTERAPIA, METABOLISMO, LINHAGEM CELULAR, PROLIFERAÇÃO CELULAR, SOBREVIVÊNCIA CELULAR, SINERGISMO DE DROGAS, NEOPLASIAS BUCAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOTO, Renata Nishida et al. Synergic effect of OP449 and FTY720 on oral squamous cell carcinoma. European Journal of Pharmacology, v. 882, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.ejphar.2020.173268. Acesso em: 19 nov. 2024.
APA
Goto, R. N., Sobral, L. M., Padovani, K. S., Garcia, C. B., Silva, G. da, Vitek, M. P., & Leopoldino, A. M. (2020). Synergic effect of OP449 and FTY720 on oral squamous cell carcinoma. European Journal of Pharmacology, 882. doi:10.1016/j.ejphar.2020.173268
NLM
Goto RN, Sobral LM, Padovani KS, Garcia CB, Silva G da, Vitek MP, Leopoldino AM. Synergic effect of OP449 and FTY720 on oral squamous cell carcinoma [Internet]. European Journal of Pharmacology. 2020 ; 882[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.ejphar.2020.173268
Vancouver
Goto RN, Sobral LM, Padovani KS, Garcia CB, Silva G da, Vitek MP, Leopoldino AM. Synergic effect of OP449 and FTY720 on oral squamous cell carcinoma [Internet]. European Journal of Pharmacology. 2020 ; 882[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.ejphar.2020.173268

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