ReP USP - Resultado da busca

Artigo de periodico
Characteristics and anatomic location of PD-1 + TCF1+ stem-like CD8 T cells in chronic viral infection and cancer (2023)
Im, Se Jin; Obeng, Rebecca C; Nasti, Tahseen H ; McManus, Daniel; Kamphorst, Alice O. ; Gunisetty, Sivaram ; Prokhnevska, Nataliya; Carlisle, Jennifer W; Yu, Ke; Sica, Gabriel L; Cardozo, Lucas E; Gonçalves, André N. A; Kissick, Haydn T; Nakaya, Helder Takashi Imoto ; Ramalingam, Suresh S ; Ahmed, Rafi
Source: Proceedings of the National Academy of Sciences (PNAS). Unidade: FCF
Subjects: SISTEMA IMUNE, NEOPLASIAS, IMUNOTERAPIA
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IM, Se Jin et al. Characteristics and anatomic location of PD-1 + TCF1+ stem-like CD8 T cells in chronic viral infection and cancer. Proceedings of the National Academy of Sciences (PNAS), v. 120, n. 41, p. 1-12 art. e2221985120, 2023Tradução . . Disponível em: https://doi.org/10.1073/pnas.2221985120. Acesso em: 14 nov. 2024.
APA
Im, S. J., Obeng, R. C., Nasti, T. H., McManus, D., Kamphorst, A. O., Gunisetty, S., et al. (2023). Characteristics and anatomic location of PD-1 + TCF1+ stem-like CD8 T cells in chronic viral infection and cancer. Proceedings of the National Academy of Sciences (PNAS), 120( 41), 1-12 art. e2221985120. doi:10.1073/pnas.2221985120
NLM
Im SJ, Obeng RC, Nasti TH, McManus D, Kamphorst AO, Gunisetty S, Prokhnevska N, Carlisle JW, Yu K, Sica GL, Cardozo LE, Gonçalves ANA, Kissick HT, Nakaya HTI, Ramalingam SS, Ahmed R. Characteristics and anatomic location of PD-1 + TCF1+ stem-like CD8 T cells in chronic viral infection and cancer [Internet]. Proceedings of the National Academy of Sciences (PNAS). 2023 ; 120( 41): 1-12 art. e2221985120.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1073/pnas.2221985120
Vancouver
Im SJ, Obeng RC, Nasti TH, McManus D, Kamphorst AO, Gunisetty S, Prokhnevska N, Carlisle JW, Yu K, Sica GL, Cardozo LE, Gonçalves ANA, Kissick HT, Nakaya HTI, Ramalingam SS, Ahmed R. Characteristics and anatomic location of PD-1 + TCF1+ stem-like CD8 T cells in chronic viral infection and cancer [Internet]. Proceedings of the National Academy of Sciences (PNAS). 2023 ; 120( 41): 1-12 art. e2221985120.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1073/pnas.2221985120
Artigo de periodico
Uptake of lipid core nanoparticles by fragments of tissues collected during cerebral tumor excision surgeries: hypotheses for use in drug targeting therapy (2022)
Pereira, Edmundo Luis Rodrigues; Feio, Danielle Cristinne Azevedo; Tavares, João Pojucan Lobo; Morikawa, Natalia Megumi; Deus, Debora Fernandes; Vital, Carolina Graziani ; Tavares, Elaine Rufo ; Maranhão, Raul Cavalcante
Source: Journal of Neuro-Oncology. Unidade: FCF
Subjects: GLIOMA, BARREIRA HEMATO-ENCEFÁLICA, RECEPTORES DE LDL, NEOPLASIAS, NANOPARTÍCULAS, LIPÍDEOS
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PEREIRA, Edmundo Luis Rodrigues et al. Uptake of lipid core nanoparticles by fragments of tissues collected during cerebral tumor excision surgeries: hypotheses for use in drug targeting therapy. Journal of Neuro-Oncology, v. 158, n. 3, p. 413-421, 2022Tradução . . Disponível em: https://doi.org/10.1007/s11060-022-04028-1. Acesso em: 14 nov. 2024.
APA
Pereira, E. L. R., Feio, D. C. A., Tavares, J. P. L., Morikawa, N. M., Deus, D. F., Vital, C. G., et al. (2022). Uptake of lipid core nanoparticles by fragments of tissues collected during cerebral tumor excision surgeries: hypotheses for use in drug targeting therapy. Journal of Neuro-Oncology, 158( 3), 413-421. doi:10.1007/s11060-022-04028-1
NLM
Pereira ELR, Feio DCA, Tavares JPL, Morikawa NM, Deus DF, Vital CG, Tavares ER, Maranhão RC. Uptake of lipid core nanoparticles by fragments of tissues collected during cerebral tumor excision surgeries: hypotheses for use in drug targeting therapy [Internet]. Journal of Neuro-Oncology. 2022 ; 158( 3): 413-421.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/s11060-022-04028-1
Vancouver
Pereira ELR, Feio DCA, Tavares JPL, Morikawa NM, Deus DF, Vital CG, Tavares ER, Maranhão RC. Uptake of lipid core nanoparticles by fragments of tissues collected during cerebral tumor excision surgeries: hypotheses for use in drug targeting therapy [Internet]. Journal of Neuro-Oncology. 2022 ; 158( 3): 413-421.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/s11060-022-04028-1
Trabalho de evento-resumo
Tumor heterogeneity and resistance to cancer therapies: peroxiredoxin 1 as a contributor in melanoma (2021)
Carvalho, Larissa Anastácio da Costa ; Maria-Engler, Silvya Stuchi ; Uehara, Adriana Hiromi; Siena, Ádamo Davi Diogenes; Mori, Matheus Prates; Souza-Pinto, Nadja Cristhina de ; Silva Junior, Wilson Araújo da ; Smalley, Keiran
Source: Anais. Conference titles: Congress of the Brazilian Society for Cell Biology. Unidades: FCF, IQ, FMRP
Subjects: HETEROGENEIDADE, NEOPLASIAS, MELANOMA, BIOMARCADORES
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CARVALHO, Larissa Anastácio da Costa et al. Tumor heterogeneity and resistance to cancer therapies: peroxiredoxin 1 as a contributor in melanoma. 2021, Anais.. São Paulo: SBBC, 2021. Disponível em: http://www.sbbc.org.br/wp-content/uploads/2014/08/SCIENTIFIC-PROGRAM-CONGRESS_2021.pdf. Acesso em: 14 nov. 2024.
APA
Carvalho, L. A. da C., Maria-Engler, S. S., Uehara, A. H., Siena, Á. D. D., Mori, M. P., Souza-Pinto, N. C. de, et al. (2021). Tumor heterogeneity and resistance to cancer therapies: peroxiredoxin 1 as a contributor in melanoma. In Anais. São Paulo: SBBC. Recuperado de http://www.sbbc.org.br/wp-content/uploads/2014/08/SCIENTIFIC-PROGRAM-CONGRESS_2021.pdf
NLM
Carvalho LA da C, Maria-Engler SS, Uehara AH, Siena ÁDD, Mori MP, Souza-Pinto NC de, Silva Junior WA da, Smalley K. Tumor heterogeneity and resistance to cancer therapies: peroxiredoxin 1 as a contributor in melanoma [Internet]. Anais. 2021 ;[citado 2024 nov. 14 ] Available from: http://www.sbbc.org.br/wp-content/uploads/2014/08/SCIENTIFIC-PROGRAM-CONGRESS_2021.pdf
Vancouver
Carvalho LA da C, Maria-Engler SS, Uehara AH, Siena ÁDD, Mori MP, Souza-Pinto NC de, Silva Junior WA da, Smalley K. Tumor heterogeneity and resistance to cancer therapies: peroxiredoxin 1 as a contributor in melanoma [Internet]. Anais. 2021 ;[citado 2024 nov. 14 ] Available from: http://www.sbbc.org.br/wp-content/uploads/2014/08/SCIENTIFIC-PROGRAM-CONGRESS_2021.pdf
Parte de monografia/livro
Organotypic models in drug development tumor models and cancer systems biology for the investigation of anticancer drugs and resistance development (2021)
Oliveira, Erica Aparecida de ; Goding, Colin R; Maria-Engler, Silvya Stuchi
Source: Organotypic Models in Drug Development. Unidade: FCF
Subjects: NEOPLASIAS, RESISTÊNCIA MICROBIANA ÀS DROGAS, GENÔMICA
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OLIVEIRA, Erica Aparecida de e GODING, Colin R e MARIA-ENGLER, Silvya Stuchi. Organotypic models in drug development tumor models and cancer systems biology for the investigation of anticancer drugs and resistance development. Organotypic Models in Drug Development. Tradução . Cham: Springer, 2021. . Disponível em: https://doi.org/10.1007/978-3-030-70063-8. Acesso em: 14 nov. 2024.
APA
Oliveira, E. A. de, Goding, C. R., & Maria-Engler, S. S. (2021). Organotypic models in drug development tumor models and cancer systems biology for the investigation of anticancer drugs and resistance development. In Organotypic Models in Drug Development. Cham: Springer. doi:10.1007/978-3-030-70063-8
NLM
Oliveira EA de, Goding CR, Maria-Engler SS. Organotypic models in drug development tumor models and cancer systems biology for the investigation of anticancer drugs and resistance development [Internet]. In: Organotypic Models in Drug Development. Cham: Springer; 2021. [citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/978-3-030-70063-8
Vancouver
Oliveira EA de, Goding CR, Maria-Engler SS. Organotypic models in drug development tumor models and cancer systems biology for the investigation of anticancer drugs and resistance development [Internet]. In: Organotypic Models in Drug Development. Cham: Springer; 2021. [citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/978-3-030-70063-8
Artigo de periodico
Human papillomavirus type 16 L1/L2 VLP experimental internalization by human peripheral blood leukocytes (2020)
Cianciarullo, Marques; Szulczewski, Vivian; Sasaki, Érica Akemi Kavati; Hosoda, Tania Matiko; Leao, Elizabeth; Borelli, Primavera ; Boccardo, Enrique ; Muller, Martin; Karanam, Balasubramanyam; Becak, Willy
Source: Journal of Cancer Biology and Clinical Oncology. Unidade: FCF
Subjects: LEUCÓCITOS, PAPILLOMAVIRUS, LEUCÓCITOS, LINFÓCITOS, NEOPLASIAS, FATORES DE RISCO
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CIANCIARULLO, Marques et al. Human papillomavirus type 16 L1/L2 VLP experimental internalization by human peripheral blood leukocytes. Journal of Cancer Biology and Clinical Oncology, v. 2, n. 2 p. 1-16, 2020Tradução . . Acesso em: 14 nov. 2024.
APA
Cianciarullo, M., Szulczewski, V., Sasaki, É. A. K., Hosoda, T. M., Leao, E., Borelli, P., et al. (2020). Human papillomavirus type 16 L1/L2 VLP experimental internalization by human peripheral blood leukocytes. Journal of Cancer Biology and Clinical Oncology, 2( 2 p. 1-16).
NLM
Cianciarullo M, Szulczewski V, Sasaki ÉAK, Hosoda TM, Leao E, Borelli P, Boccardo E, Muller M, Karanam B, Becak W. Human papillomavirus type 16 L1/L2 VLP experimental internalization by human peripheral blood leukocytes. Journal of Cancer Biology and Clinical Oncology. 2020 ; 2( 2 p. 1-16):[citado 2024 nov. 14 ]
Vancouver
Cianciarullo M, Szulczewski V, Sasaki ÉAK, Hosoda TM, Leao E, Borelli P, Boccardo E, Muller M, Karanam B, Becak W. Human papillomavirus type 16 L1/L2 VLP experimental internalization by human peripheral blood leukocytes. Journal of Cancer Biology and Clinical Oncology. 2020 ; 2( 2 p. 1-16):[citado 2024 nov. 14 ]
Artigo de periodico
Cisplatin treatment modulates Annexin A1 and inhibitor of differentiation to DNA 1 expression in cervical cancer cells (2020)
Prates, Janesly; Moreli, Jusciele B. ; Gimenes, Alexandre Dantas; Biselli, Joice Matos; D’Avila, Solange Correa Garcia Pires; Sandri, Silvana; Farsky, Sandra Helena Poliselli ; Lisoni, Flávia Cristina Rodrigues; Oliani, Sonia Maria
Source: Biomedicine & Pharmacotherapy. Unidade: FCF
Subjects: NEOPLASIAS, APOPTOSE, PEPTÍDEOS
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ABNT
PRATES, Janesly et al. Cisplatin treatment modulates Annexin A1 and inhibitor of differentiation to DNA 1 expression in cervical cancer cells. Biomedicine & Pharmacotherapy, v. 129, p. 1-9 art. 110331, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.biopha.2020.110331. Acesso em: 14 nov. 2024.
APA
Prates, J., Moreli, J. B., Gimenes, A. D., Biselli, J. M., D’Avila, S. C. G. P., Sandri, S., et al. (2020). Cisplatin treatment modulates Annexin A1 and inhibitor of differentiation to DNA 1 expression in cervical cancer cells. Biomedicine & Pharmacotherapy, 129, 1-9 art. 110331. doi:10.1016/j.biopha.2020.110331
NLM
Prates J, Moreli JB, Gimenes AD, Biselli JM, D’Avila SCGP, Sandri S, Farsky SHP, Lisoni FCR, Oliani SM. Cisplatin treatment modulates Annexin A1 and inhibitor of differentiation to DNA 1 expression in cervical cancer cells [Internet]. Biomedicine & Pharmacotherapy. 2020 ; 129 1-9 art. 110331.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.biopha.2020.110331
Vancouver
Prates J, Moreli JB, Gimenes AD, Biselli JM, D’Avila SCGP, Sandri S, Farsky SHP, Lisoni FCR, Oliani SM. Cisplatin treatment modulates Annexin A1 and inhibitor of differentiation to DNA 1 expression in cervical cancer cells [Internet]. Biomedicine & Pharmacotherapy. 2020 ; 129 1-9 art. 110331.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.biopha.2020.110331
Artigo de periodico
Effect of nanoemulsion modification with chitosan and sodium alginate on the topical delivery and efficacy of the cytotoxic agent piplartine in 2D and 3D skin cancer models (2020)
Giacone, Daniela Veronesi ; Dartora, Vanessa Franco Carvalho ; Matos, Jenyffer Kelly Rocha De ; Passos, Julia Sapienza ; Miranda, Daniel Augusto Gomes ; Oliveira, Erica Aparecida de ; Silveira, Edilberto R. ; Costa-Lotufo, Letícia Veras ; Maria-Engler, Silvya Stuchi ; Lopes, Luciana Biagini
Source: Journal of Biological Macromolecules. Unidades: ICB, FCF
Subjects: NEOPLASIAS, NEOPLASIAS EMBRIONÁRIAS DE CÉLULAS GERMINATIVAS, PELE, ALGINATOS, MELANOMA, QUITOSANA, POLISSACARÍDEOS, CITOTOXINAS, FARMACOLOGIA
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ABNT
GIACONE, Daniela Veronesi et al. Effect of nanoemulsion modification with chitosan and sodium alginate on the topical delivery and efficacy of the cytotoxic agent piplartine in 2D and 3D skin cancer models. Journal of Biological Macromolecules, v. 165, p. 1055-1065, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.ijbiomac.2020.09.167. Acesso em: 14 nov. 2024.
APA
Giacone, D. V., Dartora, V. F. C., Matos, J. K. R. D., Passos, J. S., Miranda, D. A. G., Oliveira, E. A. de, et al. (2020). Effect of nanoemulsion modification with chitosan and sodium alginate on the topical delivery and efficacy of the cytotoxic agent piplartine in 2D and 3D skin cancer models. Journal of Biological Macromolecules, 165, 1055-1065. doi:10.1016/j.ijbiomac.2020.09.167
NLM
Giacone DV, Dartora VFC, Matos JKRD, Passos JS, Miranda DAG, Oliveira EA de, Silveira ER, Costa-Lotufo LV, Maria-Engler SS, Lopes LB. Effect of nanoemulsion modification with chitosan and sodium alginate on the topical delivery and efficacy of the cytotoxic agent piplartine in 2D and 3D skin cancer models [Internet]. Journal of Biological Macromolecules. 2020 ; 165 1055-1065.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.ijbiomac.2020.09.167
Vancouver
Giacone DV, Dartora VFC, Matos JKRD, Passos JS, Miranda DAG, Oliveira EA de, Silveira ER, Costa-Lotufo LV, Maria-Engler SS, Lopes LB. Effect of nanoemulsion modification with chitosan and sodium alginate on the topical delivery and efficacy of the cytotoxic agent piplartine in 2D and 3D skin cancer models [Internet]. Journal of Biological Macromolecules. 2020 ; 165 1055-1065.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.ijbiomac.2020.09.167
Trabalho de evento-resumo
REPIN-1 as a tumoral marker in cervical cancer (2018)
Valentini, Vanessa Bottasso; Oliveira, Érica Aparecida de; Maria-Engler, Silvya Stuchi
Source: Resumos. Conference titles: International Symposium on Pathophysiology and Toxicology/ISPAT. Unidade: FCF
Subjects: ONCOGENES, HPV, NEOPLASIAS
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ABNT
VALENTINI, Vanessa Bottasso e OLIVEIRA, Érica Aparecida de e MARIA-ENGLER, Silvya Stuchi. REPIN-1 as a tumoral marker in cervical cancer. 2018, Anais.. São Paulo: FCF/USP, 2018. Disponível em: http://simpac.wixsite.com/simpac/symposium-publications. Acesso em: 14 nov. 2024.
APA
Valentini, V. B., Oliveira, É. A. de, & Maria-Engler, S. S. (2018). REPIN-1 as a tumoral marker in cervical cancer. In Resumos. São Paulo: FCF/USP. Recuperado de http://simpac.wixsite.com/simpac/symposium-publications
NLM
Valentini VB, Oliveira ÉA de, Maria-Engler SS. REPIN-1 as a tumoral marker in cervical cancer [Internet]. Resumos. 2018 ;[citado 2024 nov. 14 ] Available from: http://simpac.wixsite.com/simpac/symposium-publications
Vancouver
Valentini VB, Oliveira ÉA de, Maria-Engler SS. REPIN-1 as a tumoral marker in cervical cancer [Internet]. Resumos. 2018 ;[citado 2024 nov. 14 ] Available from: http://simpac.wixsite.com/simpac/symposium-publications
Artigo de periodico
Artepillin C induces selective oxidative stress and inhibits migration and invasion in a comprehensive panel of human cervical cancer cell lines (2018)
Souza, Raquel Pantarotto; Mendonca, Patricia de Souza Bonfim; Damke, Gabrielle Marconi Zago Ferreira; Carvalho, Analine Rosa Barquez De Assis; Ratti, Bianca Altrao; Dembogurski, Djaceli Sampaio de Oliveira; Silva, Vania Ramos Sela da; Silva, Sueli Oliveira; Silva, Denise Brentan da; Bruschi, Marcos Luciano; Maria-Engler, Silvya Stuchi ; Consolaro, Marcia Edilaine Lopes
Source: Anti Cancer Agents in Medicinal Chemistry. Unidade: FCF
Subjects: PRÓPOLIS, ESTRESSE OXIDATIVO, NEOPLASIAS
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SOUZA, Raquel Pantarotto et al. Artepillin C induces selective oxidative stress and inhibits migration and invasion in a comprehensive panel of human cervical cancer cell lines. Anti Cancer Agents in Medicinal Chemistry, v. 18, n. 12, p. 1750-1760, 2018Tradução . . Disponível em: https://doi.org/10.2174/1871520618666180604092930. Acesso em: 14 nov. 2024.
APA
Souza, R. P., Mendonca, P. de S. B., Damke, G. M. Z. F., Carvalho, A. R. B. D. A., Ratti, B. A., Dembogurski, D. S. de O., et al. (2018). Artepillin C induces selective oxidative stress and inhibits migration and invasion in a comprehensive panel of human cervical cancer cell lines. Anti Cancer Agents in Medicinal Chemistry, 18( 12), 1750-1760. doi:10.2174/1871520618666180604092930
NLM
Souza RP, Mendonca P de SB, Damke GMZF, Carvalho ARBDA, Ratti BA, Dembogurski DS de O, Silva VRS da, Silva SO, Silva DB da, Bruschi ML, Maria-Engler SS, Consolaro MEL. Artepillin C induces selective oxidative stress and inhibits migration and invasion in a comprehensive panel of human cervical cancer cell lines [Internet]. Anti Cancer Agents in Medicinal Chemistry. 2018 ; 18( 12): 1750-1760.[citado 2024 nov. 14 ] Available from: https://doi.org/10.2174/1871520618666180604092930
Vancouver
Souza RP, Mendonca P de SB, Damke GMZF, Carvalho ARBDA, Ratti BA, Dembogurski DS de O, Silva VRS da, Silva SO, Silva DB da, Bruschi ML, Maria-Engler SS, Consolaro MEL. Artepillin C induces selective oxidative stress and inhibits migration and invasion in a comprehensive panel of human cervical cancer cell lines [Internet]. Anti Cancer Agents in Medicinal Chemistry. 2018 ; 18( 12): 1750-1760.[citado 2024 nov. 14 ] Available from: https://doi.org/10.2174/1871520618666180604092930
Artigo de periodico
Clinical experience with drug delivery systems as tools to decrease the toxicity of anticancer chemotherapeutic agents (2017)
Maranhão, Raul Cavalcante ; Vital, Carolina Graziani; Tavani, Thauany Martins; Graziani, Silvia Regina
Source: Expert Opinion on Drug Delivery. Unidade: FCF
Subjects: QUIMIOTERAPIA, NEOPLASIAS, LIPOSSOMOS
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ABNT
MARANHÃO, Raul Cavalcante et al. Clinical experience with drug delivery systems as tools to decrease the toxicity of anticancer chemotherapeutic agents. Expert Opinion on Drug Delivery, v. 14, n. 10, p. 1217-1226, 2017Tradução . . Disponível em: https://doi.org/10.1080/17425247.2017.1276560. Acesso em: 14 nov. 2024.
APA
Maranhão, R. C., Vital, C. G., Tavani, T. M., & Graziani, S. R. (2017). Clinical experience with drug delivery systems as tools to decrease the toxicity of anticancer chemotherapeutic agents. Expert Opinion on Drug Delivery, 14( 10), 1217-1226. doi:10.1080/17425247.2017.1276560
NLM
Maranhão RC, Vital CG, Tavani TM, Graziani SR. Clinical experience with drug delivery systems as tools to decrease the toxicity of anticancer chemotherapeutic agents [Internet]. Expert Opinion on Drug Delivery. 2017 ; 14( 10): 1217-1226.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1080/17425247.2017.1276560
Vancouver
Maranhão RC, Vital CG, Tavani TM, Graziani SR. Clinical experience with drug delivery systems as tools to decrease the toxicity of anticancer chemotherapeutic agents [Internet]. Expert Opinion on Drug Delivery. 2017 ; 14( 10): 1217-1226.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1080/17425247.2017.1276560
Artigo de periodico
Tissue uptake mechanisms involved in the clearance of non-protein nanoparticles that mimic LDL composition: a study with knockout and transgenic mice (2017)
Daminelli, Elaine Nunes; Fotakis, Panagiotis; Mesquita, Carlos Henrique de; Maranhão, Raul Cavalcante ; Zannis, Vassilis I
Source: Lipids. Unidade: FCF
Subjects: NANOPARTÍCULAS, LIPÍDEOS, COLESTEROL, NEOPLASIAS
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ABNT
DAMINELLI, Elaine Nunes et al. Tissue uptake mechanisms involved in the clearance of non-protein nanoparticles that mimic LDL composition: a study with knockout and transgenic mice. Lipids, v. 52, n. 12, p. 991-998, 2017Tradução . . Disponível em: https://doi.org/10.1007/s11745-017-4306-6. Acesso em: 14 nov. 2024.
APA
Daminelli, E. N., Fotakis, P., Mesquita, C. H. de, Maranhão, R. C., & Zannis, V. I. (2017). Tissue uptake mechanisms involved in the clearance of non-protein nanoparticles that mimic LDL composition: a study with knockout and transgenic mice. Lipids, 52( 12), 991-998. doi:10.1007/s11745-017-4306-6
NLM
Daminelli EN, Fotakis P, Mesquita CH de, Maranhão RC, Zannis VI. Tissue uptake mechanisms involved in the clearance of non-protein nanoparticles that mimic LDL composition: a study with knockout and transgenic mice [Internet]. Lipids. 2017 ; 52( 12): 991-998.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/s11745-017-4306-6
Vancouver
Daminelli EN, Fotakis P, Mesquita CH de, Maranhão RC, Zannis VI. Tissue uptake mechanisms involved in the clearance of non-protein nanoparticles that mimic LDL composition: a study with knockout and transgenic mice [Internet]. Lipids. 2017 ; 52( 12): 991-998.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/s11745-017-4306-6
Artigo de jornal-dep/entr
Uso de partícula criada em laboratório auxilia o tratamento contra o câncer [Depoimento a Carina Brito] (2016)
Maranhão, Raul Cavalcante
Source: AUN - Agência Universitária de Notícias. Unidade: FCF
Subjects: NANOPARTÍCULAS, NEOPLASIAS
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ABNT
MARANHÃO, Raul Cavalcante. Uso de partícula criada em laboratório auxilia o tratamento contra o câncer [Depoimento a Carina Brito]. AUN - Agência Universitária de Notícias. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Disponível em: https://www.usp.br/aun/exibir?id=7964&ed=1412&f=30. Acesso em: 14 nov. 2024. , 2016
APA
Maranhão, R. C. (2016). Uso de partícula criada em laboratório auxilia o tratamento contra o câncer [Depoimento a Carina Brito]. AUN - Agência Universitária de Notícias. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Recuperado de https://www.usp.br/aun/exibir?id=7964&ed=1412&f=30
NLM
Maranhão RC. Uso de partícula criada em laboratório auxilia o tratamento contra o câncer [Depoimento a Carina Brito] [Internet]. AUN - Agência Universitária de Notícias. 2016 ; 49( 125): 1-3.[citado 2024 nov. 14 ] Available from: https://www.usp.br/aun/exibir?id=7964&ed=1412&f=30
Vancouver
Maranhão RC. Uso de partícula criada em laboratório auxilia o tratamento contra o câncer [Depoimento a Carina Brito] [Internet]. AUN - Agência Universitária de Notícias. 2016 ; 49( 125): 1-3.[citado 2024 nov. 14 ] Available from: https://www.usp.br/aun/exibir?id=7964&ed=1412&f=30
Trabalho de evento-resumo periodico
REPIN-1 as a tumoral marker in cervical cancer (2016)
Valentini, Vanessa; Oliveira, Erica Aparecida de; Maria-Engler, Silvya Stuchi
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Sciences and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo. Unidade: FCF
Assunto: NEOPLASIAS
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ABNT
VALENTINI, Vanessa e OLIVEIRA, Erica Aparecida de e MARIA-ENGLER, Silvya Stuchi. REPIN-1 as a tumoral marker in cervical cancer. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 14 nov. 2024. , 2016
APA
Valentini, V., Oliveira, E. A. de, & Maria-Engler, S. S. (2016). REPIN-1 as a tumoral marker in cervical cancer. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Valentini V, Oliveira EA de, Maria-Engler SS. REPIN-1 as a tumoral marker in cervical cancer. Brazilian Journal of Pharmaceutical Sciences. 2016 ; 52 42 res. FCF079.[citado 2024 nov. 14 ]
Vancouver
Valentini V, Oliveira EA de, Maria-Engler SS. REPIN-1 as a tumoral marker in cervical cancer. Brazilian Journal of Pharmaceutical Sciences. 2016 ; 52 42 res. FCF079.[citado 2024 nov. 14 ]
Artigo de jornal-dep/entr
Substância encontrada no ar pode gerar câncer [Depoimento a Carina Brito] (2016)
Loureiro, Ana Paula de Melo ; Oliveira, Tiago Franco de
Source: Agência Universitária de Notícias/AUN. Unidade: FCF
Subjects: SUBSTÂNCIAS TÓXICAS, NEOPLASIAS, POLUIÇÃO ATMOSFÉRICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOUREIRO, Ana Paula de Melo e OLIVEIRA, Tiago Franco de. Substância encontrada no ar pode gerar câncer [Depoimento a Carina Brito]. Agência Universitária de Notícias/AUN. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Disponível em: http://citrus.uspnet.usp.br/aun/exibir?id=7994. Acesso em: 14 nov. 2024. , 2016
APA
Loureiro, A. P. de M., & Oliveira, T. F. de. (2016). Substância encontrada no ar pode gerar câncer [Depoimento a Carina Brito]. Agência Universitária de Notícias/AUN. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Recuperado de http://citrus.uspnet.usp.br/aun/exibir?id=7994
NLM
Loureiro AP de M, Oliveira TF de. Substância encontrada no ar pode gerar câncer [Depoimento a Carina Brito] [Internet]. Agência Universitária de Notícias/AUN. 2016 ; 49( 131): 1-7.[citado 2024 nov. 14 ] Available from: http://citrus.uspnet.usp.br/aun/exibir?id=7994
Vancouver
Loureiro AP de M, Oliveira TF de. Substância encontrada no ar pode gerar câncer [Depoimento a Carina Brito] [Internet]. Agência Universitária de Notícias/AUN. 2016 ; 49( 131): 1-7.[citado 2024 nov. 14 ] Available from: http://citrus.uspnet.usp.br/aun/exibir?id=7994
Trabalho de evento-resumo periodico
Evaluation of invasive potential inhibition in vemurafenib-resistant melanoma cell lines after DM-1 treatment (2015)
Souza, Nayane de; Takashi, Gustavo; Flores, Fernanda Faião; Pennacchi, Paula Comune; Suárez, José Agustín Pablo Quincoces; Maria-Engler, Silvya Stuchi
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo. Unidade: FCF
Subjects: MELANOMA, NEOPLASIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOUZA, Nayane de et al. Evaluation of invasive potential inhibition in vemurafenib-resistant melanoma cell lines after DM-1 treatment. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 14 nov. 2024. , 2015
APA
Souza, N. de, Takashi, G., Flores, F. F., Pennacchi, P. C., Suárez, J. A. P. Q., & Maria-Engler, S. S. (2015). Evaluation of invasive potential inhibition in vemurafenib-resistant melanoma cell lines after DM-1 treatment. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Souza N de, Takashi G, Flores FF, Pennacchi PC, Suárez JAPQ, Maria-Engler SS. Evaluation of invasive potential inhibition in vemurafenib-resistant melanoma cell lines after DM-1 treatment. Brazilian Journal of Pharmaceutical Sciences. 2015 ; 51 4 res. FCF004.[citado 2024 nov. 14 ]
Vancouver
Souza N de, Takashi G, Flores FF, Pennacchi PC, Suárez JAPQ, Maria-Engler SS. Evaluation of invasive potential inhibition in vemurafenib-resistant melanoma cell lines after DM-1 treatment. Brazilian Journal of Pharmaceutical Sciences. 2015 ; 51 4 res. FCF004.[citado 2024 nov. 14 ]
Artigo de periodico
Can creatine supplementation form carcinogenic heterocyclic amines in humans (2015)
Pereira, Renato Tavares dos Santos; Dörr, Felipe Augusto; Pinto, Ernani ; Solis, Marina Yazigi; Artioli, G. G; Fernandes, Alan Lins; Murai, Igor Hisashi; Dantas, Wagner Silva; Seguro, Antonio Carlos; Santinho, Mirela Aparecida Rodrigues; Roschel, Hamilton; Carpentier, Alain; Poortmans, Jacques Remi; Gualano, Bruno
Source: The Journal of physiology (Physiological Society). Unidades: FCF, EEFE
Subjects: NUTRIÇÃO, AMINOÁCIDOS, SUPLEMENTAÇÃO ALIMENTAR, NEOPLASIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PEREIRA, Renato Tavares dos Santos et al. Can creatine supplementation form carcinogenic heterocyclic amines in humans. The Journal of physiology (Physiological Society), p. 13 , 2015Tradução . . Disponível em: https://doi.org/10.1113/JP270861. Acesso em: 14 nov. 2024.
APA
Pereira, R. T. dos S., Dörr, F. A., Pinto, E., Solis, M. Y., Artioli, G. G., Fernandes, A. L., et al. (2015). Can creatine supplementation form carcinogenic heterocyclic amines in humans. The Journal of physiology (Physiological Society), 13 . doi:10.1113/JP270861
NLM
Pereira RT dos S, Dörr FA, Pinto E, Solis MY, Artioli GG, Fernandes AL, Murai IH, Dantas WS, Seguro AC, Santinho MAR, Roschel H, Carpentier A, Poortmans JR, Gualano B. Can creatine supplementation form carcinogenic heterocyclic amines in humans [Internet]. The Journal of physiology (Physiological Society). 2015 ; 13 .[citado 2024 nov. 14 ] Available from: https://doi.org/10.1113/JP270861
Vancouver
Pereira RT dos S, Dörr FA, Pinto E, Solis MY, Artioli GG, Fernandes AL, Murai IH, Dantas WS, Seguro AC, Santinho MAR, Roschel H, Carpentier A, Poortmans JR, Gualano B. Can creatine supplementation form carcinogenic heterocyclic amines in humans [Internet]. The Journal of physiology (Physiological Society). 2015 ; 13 .[citado 2024 nov. 14 ] Available from: https://doi.org/10.1113/JP270861
Artigo de periodico-resenha
Resenha sem título próprio (2014)
Maria-Engler, Silvya Stuchi ; Massaro, Renato
Source: Brazilian Journal of Pharmaceutical Sciences. Unidade: FCF
Assunto: NEOPLASIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARIA-ENGLER, Silvya Stuchi e MASSARO, Renato. Resenha sem título próprio. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 14 nov. 2024. , 2014
APA
Maria-Engler, S. S., & Massaro, R. (2014). Resenha sem título próprio. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Maria-Engler SS, Massaro R. Resenha sem título próprio. Brazilian Journal of Pharmaceutical Sciences. 2014 ; 50( 4): 965-966.[citado 2024 nov. 14 ]
Vancouver
Maria-Engler SS, Massaro R. Resenha sem título próprio. Brazilian Journal of Pharmaceutical Sciences. 2014 ; 50( 4): 965-966.[citado 2024 nov. 14 ]
Artigo de periodico
Association of daunorubicin to a lipid nanoemulsion that binds to low-density lipoprotein receptors enhances the antitumour action and decreases the toxicity of the drug in melanoma-bearing mice (2014)
Contente, Thais Costa; Kretzer, Iara Fabricia; Monteiro, Fabiola Branco Filippin; Maria, Durvanei Augusto; Maranhão, Raul Cavalcante
Source: Journal of Pharmacy and Pharmacology. Unidade: FCF
Subjects: NANOPARTÍCULAS, LIPOPROTEÍNAS, NEOPLASIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CONTENTE, Thais Costa et al. Association of daunorubicin to a lipid nanoemulsion that binds to low-density lipoprotein receptors enhances the antitumour action and decreases the toxicity of the drug in melanoma-bearing mice. Journal of Pharmacy and Pharmacology, v. 66, n. 12, p. 1698-1709, 2014Tradução . . Disponível em: https://doi.org/10.1111/jphp.12296. Acesso em: 14 nov. 2024.
APA
Contente, T. C., Kretzer, I. F., Monteiro, F. B. F., Maria, D. A., & Maranhão, R. C. (2014). Association of daunorubicin to a lipid nanoemulsion that binds to low-density lipoprotein receptors enhances the antitumour action and decreases the toxicity of the drug in melanoma-bearing mice. Journal of Pharmacy and Pharmacology, 66( 12), 1698-1709. doi:10.1111/jphp.12296
NLM
Contente TC, Kretzer IF, Monteiro FBF, Maria DA, Maranhão RC. Association of daunorubicin to a lipid nanoemulsion that binds to low-density lipoprotein receptors enhances the antitumour action and decreases the toxicity of the drug in melanoma-bearing mice [Internet]. Journal of Pharmacy and Pharmacology. 2014 ; 66( 12): 1698-1709.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1111/jphp.12296
Vancouver
Contente TC, Kretzer IF, Monteiro FBF, Maria DA, Maranhão RC. Association of daunorubicin to a lipid nanoemulsion that binds to low-density lipoprotein receptors enhances the antitumour action and decreases the toxicity of the drug in melanoma-bearing mice [Internet]. Journal of Pharmacy and Pharmacology. 2014 ; 66( 12): 1698-1709.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1111/jphp.12296
Artigo de jornal
Uma esperança contra o câncer (2013)
Campa, Ana ; Pinto, Ernani ; Maria-Engler, Silvya Stuchi ; Moreno, Ana Carolina Ramos; Sandri, Silvana
Source: Jornal da USP. Unidade: FCF
Subjects: NEOPLASIAS, INIBIDORES DE ENZIMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAMPA, Ana et al. Uma esperança contra o câncer. Tradução . Jornal da USP, São Paulo, 2013. , p. 9. Acesso em: 14 nov. 2024.
APA
Campa, A., Pinto, E., Maria-Engler, S. S., Moreno, A. C. R., & Sandri, S. (2013). Uma esperança contra o câncer. Jornal da USP, p. 9. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Campa A, Pinto E, Maria-Engler SS, Moreno ACR, Sandri S. Uma esperança contra o câncer. Jornal da USP. 2013 ; 9.[citado 2024 nov. 14 ]
Vancouver
Campa A, Pinto E, Maria-Engler SS, Moreno ACR, Sandri S. Uma esperança contra o câncer. Jornal da USP. 2013 ; 9.[citado 2024 nov. 14 ]
Trabalho de evento-resumo periodico
Serum amyloid a(SAA1/SAA2 AND SAA4)genes: a possible e therapeutic target in glioblastomas multiformes (2013)
Knebel, Franciele Hinterholz; Bellé, Luziane Potrich; Haga, Raquel Brandão; Campa, Ana
Source: Brazilian Journal of Pharmaceutical Sciences. Conference titles: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences. Unidade: FCF
Subjects: BIOMARCADORES, NEOPLASIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KNEBEL, Franciele Hinterholz et al. Serum amyloid a(SAA1/SAA2 AND SAA4)genes: a possible e therapeutic target in glioblastomas multiformes. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 14 nov. 2024. , 2013
APA
Knebel, F. H., Bellé, L. P., Haga, R. B., & Campa, A. (2013). Serum amyloid a(SAA1/SAA2 AND SAA4)genes: a possible e therapeutic target in glioblastomas multiformes. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Knebel FH, Bellé LP, Haga RB, Campa A. Serum amyloid a(SAA1/SAA2 AND SAA4)genes: a possible e therapeutic target in glioblastomas multiformes. Brazilian Journal of Pharmaceutical Sciences. 2013 ; 49 65 res. FCF126.[citado 2024 nov. 14 ]
Vancouver
Knebel FH, Bellé LP, Haga RB, Campa A. Serum amyloid a(SAA1/SAA2 AND SAA4)genes: a possible e therapeutic target in glioblastomas multiformes. Brazilian Journal of Pharmaceutical Sciences. 2013 ; 49 65 res. FCF126.[citado 2024 nov. 14 ]

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