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Artigo de periodico
Assessing the impact of antineoplastic drugs in the aquatic environment: state of the art and future perspective for freshwater organisms (2023)
Damasceno, Évila Pinheiro ; Ribeiro, Fabianne ; Costa-Lotufo, Letícia Veras ; Soares, Amadeu M. V. M. ; Pavlaki, Maria D. ; Loureiro, Susana
Source: Environmental Toxicology and Pharmacology. Unidade: ICB
Subjects: FARMACOLOGIA, METABÓLITOS, ANTINEOPLÁSICOS, ANTICORPOS, ANTIBIÓTICOS, LINHAGEM CELULAR, ECOTOXICOLOGIA
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DAMASCENO, Évila Pinheiro et al. Assessing the impact of antineoplastic drugs in the aquatic environment: state of the art and future perspective for freshwater organisms. Environmental Toxicology and Pharmacology, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.etap.2023.104109. Acesso em: 02 nov. 2024.
APA
Damasceno, É. P., Ribeiro, F., Costa-Lotufo, L. V., Soares, A. M. V. M., Pavlaki, M. D., & Loureiro, S. (2023). Assessing the impact of antineoplastic drugs in the aquatic environment: state of the art and future perspective for freshwater organisms. Environmental Toxicology and Pharmacology. doi:10.1016/j.etap.2023.104109
NLM
Damasceno ÉP, Ribeiro F, Costa-Lotufo LV, Soares AMVM, Pavlaki MD, Loureiro S. Assessing the impact of antineoplastic drugs in the aquatic environment: state of the art and future perspective for freshwater organisms [Internet]. Environmental Toxicology and Pharmacology. 2023 ;[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.etap.2023.104109
Vancouver
Damasceno ÉP, Ribeiro F, Costa-Lotufo LV, Soares AMVM, Pavlaki MD, Loureiro S. Assessing the impact of antineoplastic drugs in the aquatic environment: state of the art and future perspective for freshwater organisms [Internet]. Environmental Toxicology and Pharmacology. 2023 ;[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.etap.2023.104109
Dissertação (Mestrado)
Estudo das atividades antitumorais de peptídeos presentes no veneno do escorpião amarelo Tityus serrulatus (2022)
Arcos, Stephanie Santos Suehiro ; Iwai, Leo Kei (Orientador)
Unidade: BIOTECNOLOGIA
Subjects: ANIMAIS PEÇONHENTOS, PEPTÍDEOS, LINHAGEM CELULAR, CÉLULAS CULTIVADAS DE TUMOR, ANTINEOPLÁSICOS, VENENOS DE ORIGEM ANIMAL, GLIOMA
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ARCOS, Stephanie Santos Suehiro. Estudo das atividades antitumorais de peptídeos presentes no veneno do escorpião amarelo Tityus serrulatus. 2022. Dissertação (Mestrado) – Universidade de São Paulo, São Paulo, 2022. Disponível em: https://www.teses.usp.br/teses/disponiveis/87/87131/tde-21122023-141247/. Acesso em: 02 nov. 2024.
APA
Arcos, S. S. S. (2022). Estudo das atividades antitumorais de peptídeos presentes no veneno do escorpião amarelo Tityus serrulatus (Dissertação (Mestrado). Universidade de São Paulo, São Paulo. Recuperado de https://www.teses.usp.br/teses/disponiveis/87/87131/tde-21122023-141247/
NLM
Arcos SSS. Estudo das atividades antitumorais de peptídeos presentes no veneno do escorpião amarelo Tityus serrulatus [Internet]. 2022 ;[citado 2024 nov. 02 ] Available from: https://www.teses.usp.br/teses/disponiveis/87/87131/tde-21122023-141247/
Vancouver
Arcos SSS. Estudo das atividades antitumorais de peptídeos presentes no veneno do escorpião amarelo Tityus serrulatus [Internet]. 2022 ;[citado 2024 nov. 02 ] Available from: https://www.teses.usp.br/teses/disponiveis/87/87131/tde-21122023-141247/
Artigo de periodico
PIMREG expression level predicts glioblastoma patient survival and affects temozolomide resistance and DNA damage response (2022)
Serafim, Rodolfo Bortolozo; Cardoso, Cibele; Arfelli, Vanessa Cristina; Valente, Valeria; Archangelo, Leticia Fröhlich
Source: Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. Unidade: FMRP
Subjects: ANTINEOPLÁSICOS, LINHAGEM CELULAR, DANO AO DNA, GLIOMA, FARMACOTERAPIA
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SERAFIM, Rodolfo Bortolozo et al. PIMREG expression level predicts glioblastoma patient survival and affects temozolomide resistance and DNA damage response. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, v. 1868, p. 166382, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.bbadis.2022.166382. Acesso em: 02 nov. 2024.
APA
Serafim, R. B., Cardoso, C., Arfelli, V. C., Valente, V., & Archangelo, L. F. (2022). PIMREG expression level predicts glioblastoma patient survival and affects temozolomide resistance and DNA damage response. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1868, 166382. doi:10.1016/j.bbadis.2022.166382
NLM
Serafim RB, Cardoso C, Arfelli VC, Valente V, Archangelo LF. PIMREG expression level predicts glioblastoma patient survival and affects temozolomide resistance and DNA damage response [Internet]. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 2022 ; 1868 166382.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.bbadis.2022.166382
Vancouver
Serafim RB, Cardoso C, Arfelli VC, Valente V, Archangelo LF. PIMREG expression level predicts glioblastoma patient survival and affects temozolomide resistance and DNA damage response [Internet]. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 2022 ; 1868 166382.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.bbadis.2022.166382
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: 02 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. 02 ] 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. 02 ] Available from: https://doi.org/10.1016/j.bioorg.2021.104982
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: 02 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. 02 ] 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. 02 ] Available from: https://doi.org/10.1016/j.ejps.2021.105834
Artigo de periodico
Attritional evaluation of lipophilic and hydrophilic metallated phthalocyanines for oncological photodynamic therapy (2021)
Dias, Lionel Mendes; Sharifi, Farangis; Keijzer, Mark J. de; Mesquita, Barbara; Desclos, Emilie; Kochan, Jakub A.; Klerk, Daniel J. de; Ernst, Daniël; Haan, Lianne R.; Tedesco, Antônio Cláudio
Source: Journal of Photochemistry and Photobiology B: Biology. Unidade: FFCLRP
Subjects: ANTINEOPLÁSICOS, APOPTOSE, LINHAGEM CELULAR, PERMEABILIDADE DA MEMBRANA CELULAR, TERAPIA FOTODINÂMICA
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DIAS, Lionel Mendes et al. Attritional evaluation of lipophilic and hydrophilic metallated phthalocyanines for oncological photodynamic therapy. Journal of Photochemistry and Photobiology B: Biology, v. 216, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.jphotobiol.2021.112146. Acesso em: 02 nov. 2024.
APA
Dias, L. M., Sharifi, F., Keijzer, M. J. de, Mesquita, B., Desclos, E., Kochan, J. A., et al. (2021). Attritional evaluation of lipophilic and hydrophilic metallated phthalocyanines for oncological photodynamic therapy. Journal of Photochemistry and Photobiology B: Biology, 216. doi:10.1016/j.jphotobiol.2021.112146
NLM
Dias LM, Sharifi F, Keijzer MJ de, Mesquita B, Desclos E, Kochan JA, Klerk DJ de, Ernst D, Haan LR, Tedesco AC. Attritional evaluation of lipophilic and hydrophilic metallated phthalocyanines for oncological photodynamic therapy [Internet]. Journal of Photochemistry and Photobiology B: Biology. 2021 ; 216[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.jphotobiol.2021.112146
Vancouver
Dias LM, Sharifi F, Keijzer MJ de, Mesquita B, Desclos E, Kochan JA, Klerk DJ de, Ernst D, Haan LR, Tedesco AC. Attritional evaluation of lipophilic and hydrophilic metallated phthalocyanines for oncological photodynamic therapy [Internet]. Journal of Photochemistry and Photobiology B: Biology. 2021 ; 216[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.jphotobiol.2021.112146
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: 02 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. 02 ] 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. 02 ] Available from: https://doi.org/10.2174/0929867327666201020155105
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
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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: 02 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. 02 ] 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. 02 ] Available from: https://doi.org/10.1038/s41598-020-61258-x
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
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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: 02 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. 02 ] 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. 02 ] 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
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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: 02 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. 02 ] 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. 02 ] Available from: https://doi.org/10.1016/j.ejphar.2020.173268
Artigo de periodico
SHOC2 scaffold protein modulates daunorubicin-induced cell death through p53 modulation in lymphoid leukemia cells (2020)
Silveira, Vanessa da Silva ; Borges, Kleiton Silva; Santos, Verena Silva; Ruckert, Mariana Tannús; Vieira, Gabriela Maciel; Vasconcelos, Elton José Rosas de; Nagano, Luis Fernando ; Tone, Luiz Gonzaga ; Scrideli, Carlos Alberto
Source: Scientific Reports. Unidade: FMRP
Subjects: ANTINEOPLÁSICOS, APOPTOSE, LINHAGEM CELULAR, DANO AO DNA, LEUCEMIA
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ABNT
SILVEIRA, Vanessa da Silva et al. SHOC2 scaffold protein modulates daunorubicin-induced cell death through p53 modulation in lymphoid leukemia cells. Scientific Reports, v. 10, n. 1, 2020Tradução . . Disponível em: https://doi.org/10.1038/s41598-020-72124-1. Acesso em: 02 nov. 2024.
APA
Silveira, V. da S., Borges, K. S., Santos, V. S., Ruckert, M. T., Vieira, G. M., Vasconcelos, E. J. R. de, et al. (2020). SHOC2 scaffold protein modulates daunorubicin-induced cell death through p53 modulation in lymphoid leukemia cells. Scientific Reports, 10( 1). doi:10.1038/s41598-020-72124-1
NLM
Silveira V da S, Borges KS, Santos VS, Ruckert MT, Vieira GM, Vasconcelos EJR de, Nagano LF, Tone LG, Scrideli CA. SHOC2 scaffold protein modulates daunorubicin-induced cell death through p53 modulation in lymphoid leukemia cells [Internet]. Scientific Reports. 2020 ; 10( 1):[citado 2024 nov. 02 ] Available from: https://doi.org/10.1038/s41598-020-72124-1
Vancouver
Silveira V da S, Borges KS, Santos VS, Ruckert MT, Vieira GM, Vasconcelos EJR de, Nagano LF, Tone LG, Scrideli CA. SHOC2 scaffold protein modulates daunorubicin-induced cell death through p53 modulation in lymphoid leukemia cells [Internet]. Scientific Reports. 2020 ; 10( 1):[citado 2024 nov. 02 ] Available from: https://doi.org/10.1038/s41598-020-72124-1
Dissertação (Mestrado)
Efeito do Vanilato de Metila e Divanilato de Metila em células de câncer de mama: regulação do complexo NADPH oxidase (2020)
Pessôa, Adriano de Souza; Oliveira, Rodrigo Cardoso de (Orientador); Ximenes, Valdecir Farias (Orientador)
Unidade: FOB
Subjects: NEOPLASIAS MAMÁRIAS, ANTINEOPLÁSICOS, LINHAGEM CELULAR, PROLIFERAÇÃO CELULAR
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PESSÔA, Adriano de Souza. Efeito do Vanilato de Metila e Divanilato de Metila em células de câncer de mama: regulação do complexo NADPH oxidase. 2020. Dissertação (Mestrado) – Universidade de São Paulo, Bauru, 2020. Disponível em: https://www.teses.usp.br/teses/disponiveis/25/25149/tde-22102021-132403/. Acesso em: 02 nov. 2024.
APA
Pessôa, A. de S. (2020). Efeito do Vanilato de Metila e Divanilato de Metila em células de câncer de mama: regulação do complexo NADPH oxidase (Dissertação (Mestrado). Universidade de São Paulo, Bauru. Recuperado de https://www.teses.usp.br/teses/disponiveis/25/25149/tde-22102021-132403/
NLM
Pessôa A de S. Efeito do Vanilato de Metila e Divanilato de Metila em células de câncer de mama: regulação do complexo NADPH oxidase [Internet]. 2020 ;[citado 2024 nov. 02 ] Available from: https://www.teses.usp.br/teses/disponiveis/25/25149/tde-22102021-132403/
Vancouver
Pessôa A de S. Efeito do Vanilato de Metila e Divanilato de Metila em células de câncer de mama: regulação do complexo NADPH oxidase [Internet]. 2020 ;[citado 2024 nov. 02 ] Available from: https://www.teses.usp.br/teses/disponiveis/25/25149/tde-22102021-132403/
Artigo de periodico
A tetraprenylated benzophenone 7-epiclusianone induces cell cycle arrest at G1/S transition by modulating critical regulators of cell cycle in breast cancer cell lines (2020)
Lamartine-Hanemann, Simone da Silva; Silva, Guilherme Álvaro Ferreira; Horvath, Renato de Oliveira ; Soncini, Roseli ; Caixeta, Ester Siqueira ; Rocha-Sales, Bianca; Niero, Evandro Luís ; Santos, Marcelo Henrique dos; Oliveira, Jaqueline Carvalho de; Miyazawwa, Marta; Ionta, Marisa ; Machado-Santelli, Glaucia Maria
Source: Toxicology in Vitro. Unidade: ICB
Subjects: BIOLOGIA CELULAR, NEOPLASIAS MAMÁRIAS, CÉLULAS CULTIVADAS DE TUMOR, CICLO CELULAR, PROLIFERAÇÃO CELULAR, LINHAGEM CELULAR, APOPTOSE, ANTINEOPLÁSICOS, CICLINA D1
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LAMARTINE-HANEMANN, Simone da Silva et al. A tetraprenylated benzophenone 7-epiclusianone induces cell cycle arrest at G1/S transition by modulating critical regulators of cell cycle in breast cancer cell lines. Toxicology in Vitro, v. 68, p. 14 , 2020Tradução . . Disponível em: https://doi.org/10.1016/j.tiv.2020.104927. Acesso em: 02 nov. 2024.
APA
Lamartine-Hanemann, S. da S., Silva, G. Á. F., Horvath, R. de O., Soncini, R., Caixeta, E. S., Rocha-Sales, B., et al. (2020). A tetraprenylated benzophenone 7-epiclusianone induces cell cycle arrest at G1/S transition by modulating critical regulators of cell cycle in breast cancer cell lines. Toxicology in Vitro, 68, 14 . doi:10.1016/j.tiv.2020.104927
NLM
Lamartine-Hanemann S da S, Silva GÁF, Horvath R de O, Soncini R, Caixeta ES, Rocha-Sales B, Niero EL, Santos MH dos, Oliveira JC de, Miyazawwa M, Ionta M, Machado-Santelli GM. A tetraprenylated benzophenone 7-epiclusianone induces cell cycle arrest at G1/S transition by modulating critical regulators of cell cycle in breast cancer cell lines [Internet]. Toxicology in Vitro. 2020 ; 68 14 .[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.tiv.2020.104927
Vancouver
Lamartine-Hanemann S da S, Silva GÁF, Horvath R de O, Soncini R, Caixeta ES, Rocha-Sales B, Niero EL, Santos MH dos, Oliveira JC de, Miyazawwa M, Ionta M, Machado-Santelli GM. A tetraprenylated benzophenone 7-epiclusianone induces cell cycle arrest at G1/S transition by modulating critical regulators of cell cycle in breast cancer cell lines [Internet]. Toxicology in Vitro. 2020 ; 68 14 .[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.tiv.2020.104927
Artigo de periodico
Novel lawsone-containing ruthenium(II) complexes: synthesis, characterization and anticancer activity on 2D and 3D spheroid models of prostate cancer cells (2019)
De Grandis, Rone Aparecido ; Santos, Patrick Wellington da Silva ; Oliveira, Katia Mara de ; Machado, Ana Rita Thomazela; Aissa, Alexandre Ferro ; Batista, Alzir Azevedo ; Antunes, Lusânia Maria Greggi ; Pavan, Fernando Rogério
Source: Bioorganic Chemistry. Unidades: FCFRP, FMRP
Subjects: NEOPLASIAS PROSTÁTICAS, CULTURA DE CÉLULAS, APOPTOSE, ANTINEOPLÁSICOS, LINHAGEM CELULAR, ESPÉCIES REATIVAS DE OXIGÊNIO, RUTÊNIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DE GRANDIS, Rone Aparecido et al. Novel lawsone-containing ruthenium(II) complexes: synthesis, characterization and anticancer activity on 2D and 3D spheroid models of prostate cancer cells. Bioorganic Chemistry, v. 85, p. 455-468, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2019.02.010. Acesso em: 02 nov. 2024.
APA
De Grandis, R. A., Santos, P. W. da S., Oliveira, K. M. de, Machado, A. R. T., Aissa, A. F., Batista, A. A., et al. (2019). Novel lawsone-containing ruthenium(II) complexes: synthesis, characterization and anticancer activity on 2D and 3D spheroid models of prostate cancer cells. Bioorganic Chemistry, 85, 455-468. doi:10.1016/j.bioorg.2019.02.010
NLM
De Grandis RA, Santos PW da S, Oliveira KM de, Machado ART, Aissa AF, Batista AA, Antunes LMG, Pavan FR. Novel lawsone-containing ruthenium(II) complexes: synthesis, characterization and anticancer activity on 2D and 3D spheroid models of prostate cancer cells [Internet]. Bioorganic Chemistry. 2019 ; 85 455-468.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.bioorg.2019.02.010
Vancouver
De Grandis RA, Santos PW da S, Oliveira KM de, Machado ART, Aissa AF, Batista AA, Antunes LMG, Pavan FR. Novel lawsone-containing ruthenium(II) complexes: synthesis, characterization and anticancer activity on 2D and 3D spheroid models of prostate cancer cells [Internet]. Bioorganic Chemistry. 2019 ; 85 455-468.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1016/j.bioorg.2019.02.010
Artigo de periodico
Assessing the cytotoxic potential of glycoalkaloidic extract in nanoparticles against bladder cancer cells (2019)
Miranda, Mariza Abreu ; Marcato, Priscyla Daniely ; Carvalho, Ivana Pereira Santos; Silva, Letícia Bueno ; Ribeiro, Diego Luis ; Amaral, Robson Luis Ferraz do ; Swiech, Kamilla ; Bastos, Jairo Kenupp ; Paschoal, Jonas Augusto Rizzato ; Reis, Rodolfo Borges dos ; Bentley, Maria Vitória Lopes Badra
Source: Journal of Pharmacy and Pharmacology. Unidades: FCFRP, FMRP
Subjects: NEOPLASIAS DA BEXIGA, ALCALOIDES, ANTINEOPLÁSICOS, APOPTOSE, LINHAGEM CELULAR, NANOTECNOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MIRANDA, Mariza Abreu et al. Assessing the cytotoxic potential of glycoalkaloidic extract in nanoparticles against bladder cancer cells. Journal of Pharmacy and Pharmacology, 2019Tradução . . Disponível em: https://doi.org/10.1111/jphp.13145. Acesso em: 02 nov. 2024.
APA
Miranda, M. A., Marcato, P. D., Carvalho, I. P. S., Silva, L. B., Ribeiro, D. L., Amaral, R. L. F. do, et al. (2019). Assessing the cytotoxic potential of glycoalkaloidic extract in nanoparticles against bladder cancer cells. Journal of Pharmacy and Pharmacology. doi:10.1111/jphp.13145
NLM
Miranda MA, Marcato PD, Carvalho IPS, Silva LB, Ribeiro DL, Amaral RLF do, Swiech K, Bastos JK, Paschoal JAR, Reis RB dos, Bentley MVLB. Assessing the cytotoxic potential of glycoalkaloidic extract in nanoparticles against bladder cancer cells [Internet]. Journal of Pharmacy and Pharmacology. 2019 ;[citado 2024 nov. 02 ] Available from: https://doi.org/10.1111/jphp.13145
Vancouver
Miranda MA, Marcato PD, Carvalho IPS, Silva LB, Ribeiro DL, Amaral RLF do, Swiech K, Bastos JK, Paschoal JAR, Reis RB dos, Bentley MVLB. Assessing the cytotoxic potential of glycoalkaloidic extract in nanoparticles against bladder cancer cells [Internet]. Journal of Pharmacy and Pharmacology. 2019 ;[citado 2024 nov. 02 ] Available from: https://doi.org/10.1111/jphp.13145
Artigo de periodico
Oxidative stress triggered by apigenin induces apoptosis in a comprehensive panel of human cervical cancer-derived cell lines (2017)
Souza, Raquel P; Mendonça, Patrícia de S. Bonfim; Gimenes, Fabrícia; Ratti, Bianca A; Kaplum, Vanessa; Bruschi, Marcos L; Nakamura, Celso Vataru; Silva, Sueli O; Maria-Engler, Silvya Stuchi ; Consolaro, Márcia E. L
Source: Oxidative Medicine and Cellular Longevity. Unidade: FCF
Subjects: ESTRESSE OXIDATIVO, APOPTOSE, LINHAGEM CELULAR, ANTINEOPLÁSICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOUZA, Raquel P et al. Oxidative stress triggered by apigenin induces apoptosis in a comprehensive panel of human cervical cancer-derived cell lines. Oxidative Medicine and Cellular Longevity, v. 2017, p. 1-18 Art. 1512745, 2017Tradução . . Disponível em: https://doi.org/10.1155/2017/1512745. Acesso em: 02 nov. 2024.
APA
Souza, R. P., Mendonça, P. de S. B., Gimenes, F., Ratti, B. A., Kaplum, V., Bruschi, M. L., et al. (2017). Oxidative stress triggered by apigenin induces apoptosis in a comprehensive panel of human cervical cancer-derived cell lines. Oxidative Medicine and Cellular Longevity, 2017, 1-18 Art. 1512745. doi:10.1155/2017/1512745
NLM
Souza RP, Mendonça P de SB, Gimenes F, Ratti BA, Kaplum V, Bruschi ML, Nakamura CV, Silva SO, Maria-Engler SS, Consolaro MEL. Oxidative stress triggered by apigenin induces apoptosis in a comprehensive panel of human cervical cancer-derived cell lines [Internet]. Oxidative Medicine and Cellular Longevity. 2017 ; 2017 1-18 Art. 1512745.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1155/2017/1512745
Vancouver
Souza RP, Mendonça P de SB, Gimenes F, Ratti BA, Kaplum V, Bruschi ML, Nakamura CV, Silva SO, Maria-Engler SS, Consolaro MEL. Oxidative stress triggered by apigenin induces apoptosis in a comprehensive panel of human cervical cancer-derived cell lines [Internet]. Oxidative Medicine and Cellular Longevity. 2017 ; 2017 1-18 Art. 1512745.[citado 2024 nov. 02 ] Available from: https://doi.org/10.1155/2017/1512745

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