ReP USP - Resultado da busca

Trabalho de evento-resumo periodico
Polysaccharides from chayote fruit regulate nlrp3 inflammasome and lipid metabolism on macrophages (2017)
Auriemo, Ana Paula Franco; Ortega, Juliana Festa; Miranda, Mayara Lilian; Moreno, Fernando Salvador
Fonte: Brazilian Journal of Pharmaceutical Sciences. Nome do evento: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo. Unidade: FCF
Assuntos: CARCINOMA HEPATOCELULAR, PROTEÍNAS
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ABNT
AURIEMO, Ana Paula Franco et al. Polysaccharides from chayote fruit regulate nlrp3 inflammasome and lipid metabolism on macrophages. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 09 out. 2024. , 2017
APA
Auriemo, A. P. F., Ortega, J. F., Miranda, M. L., & Moreno, F. S. (2017). Polysaccharides from chayote fruit regulate nlrp3 inflammasome and lipid metabolism on macrophages. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Auriemo APF, Ortega JF, Miranda ML, Moreno FS. Polysaccharides from chayote fruit regulate nlrp3 inflammasome and lipid metabolism on macrophages. Brazilian Journal of Pharmaceutical Sciences. 2017 ; 53 25 res. FCF046.[citado 2024 out. 09 ]
Vancouver
Auriemo APF, Ortega JF, Miranda ML, Moreno FS. Polysaccharides from chayote fruit regulate nlrp3 inflammasome and lipid metabolism on macrophages. Brazilian Journal of Pharmaceutical Sciences. 2017 ; 53 25 res. FCF046.[citado 2024 out. 09 ]
Trabalho de evento-resumo periodico
In silico simulation of dissolution profiles applied to the development of extendedrelease doxazosin tablet formulation (2017)
Duque, Marcelo Dutra ; Issa, Michele Georges ; Silva, Daniela Amaral ; Barbosa, Eduardo José ; Löbenberg, Raimar ; Ferraz, Humberto Gomes
Fonte: Brazilian Journal of Pharmaceutical Sciences. Nome do evento: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo. Unidade: FCF
Assuntos: DESENVOLVIMENTO DE PRODUTOS, FÁRMACOS, TECNOLOGIA FARMACÊUTICA
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ABNT
DUQUE, Marcelo Dutra et al. In silico simulation of dissolution profiles applied to the development of extendedrelease doxazosin tablet formulation. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 09 out. 2024. , 2017
APA
Duque, M. D., Issa, M. G., Silva, D. A., Barbosa, E. J., Löbenberg, R., & Ferraz, H. G. (2017). In silico simulation of dissolution profiles applied to the development of extendedrelease doxazosin tablet formulation. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Duque MD, Issa MG, Silva DA, Barbosa EJ, Löbenberg R, Ferraz HG. In silico simulation of dissolution profiles applied to the development of extendedrelease doxazosin tablet formulation. Brazilian Journal of Pharmaceutical Sciences. 2017 ; 53 36 res. FCF067.[citado 2024 out. 09 ]
Vancouver
Duque MD, Issa MG, Silva DA, Barbosa EJ, Löbenberg R, Ferraz HG. In silico simulation of dissolution profiles applied to the development of extendedrelease doxazosin tablet formulation. Brazilian Journal of Pharmaceutical Sciences. 2017 ; 53 36 res. FCF067.[citado 2024 out. 09 ]
Trabalho de evento-resumo periodico
Synthesis of Pla optimized by contaminating bacteria (2017)
Uono, Magali Thiyomi; Bogsan, Cristina Stewart Bittencourt
Fonte: Brazilian Journal of Pharmaceutical Sciences. Nome do evento: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo. Unidade: FCF
Assuntos: ÁCIDO LÁCTICO, STAPHYLOCOCCUS
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ABNT
UONO, Magali Thiyomi e BOGSAN, Cristina Stewart Bittencourt. Synthesis of Pla optimized by contaminating bacteria. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 09 out. 2024. , 2017
APA
Uono, M. T., & Bogsan, C. S. B. (2017). Synthesis of Pla optimized by contaminating bacteria. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Uono MT, Bogsan CSB. Synthesis of Pla optimized by contaminating bacteria. Brazilian Journal of Pharmaceutical Sciences. 2017 ; 53 44 res. FCF083.[citado 2024 out. 09 ]
Vancouver
Uono MT, Bogsan CSB. Synthesis of Pla optimized by contaminating bacteria. Brazilian Journal of Pharmaceutical Sciences. 2017 ; 53 44 res. FCF083.[citado 2024 out. 09 ]
Trabalho de evento-resumo periodico
Targeting top1 gene in melanoma as a novel mechanism of resistance and combinational therapies (2017)
Oliveira, Erica Aparecida de; Fernandes, Débora Kristina Alves; Flores, Fernanda Faião; Lima, Diógenes Saulo de; Cardozo, Lucas Esteves; Nakaya, Helder Takashi Imoto ; Maria-Engler, Silvya Stuchi
Fonte: Brazilian Journal of Pharmaceutical Sciences. Nome do evento: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo. Unidade: FCF
Assuntos: MELANOMA, PELE
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ABNT
OLIVEIRA, Erica Aparecida de et al. Targeting top1 gene in melanoma as a novel mechanism of resistance and combinational therapies. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 09 out. 2024. , 2017
APA
Oliveira, E. A. de, Fernandes, D. K. A., Flores, F. F., Lima, D. S. de, Cardozo, L. E., Nakaya, H. T. I., & Maria-Engler, S. S. (2017). Targeting top1 gene in melanoma as a novel mechanism of resistance and combinational therapies. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Oliveira EA de, Fernandes DKA, Flores FF, Lima DS de, Cardozo LE, Nakaya HTI, Maria-Engler SS. Targeting top1 gene in melanoma as a novel mechanism of resistance and combinational therapies. Brazilian Journal of Pharmaceutical Sciences. 2017 ; 53 10 res. FCF016.[citado 2024 out. 09 ]
Vancouver
Oliveira EA de, Fernandes DKA, Flores FF, Lima DS de, Cardozo LE, Nakaya HTI, Maria-Engler SS. Targeting top1 gene in melanoma as a novel mechanism of resistance and combinational therapies. Brazilian Journal of Pharmaceutical Sciences. 2017 ; 53 10 res. FCF016.[citado 2024 out. 09 ]
Trabalho de evento-resumo periodico
Dendrimer prodrug derivative of acetylsalicylic acid and rosuvastatin: convergent synthesis of the respective dendron (2017)
Gonzaga, Rodrigo Vieira ; Ferreira, Elizabeth Igne
Fonte: Brazilian Journal of Pharmaceutical Sciences. Nome do evento: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo. Unidade: FCF
Assuntos: DOENÇAS CARDIOVASCULARES, FÁRMACOS (SISTEMA CARDIOVASCULAR)
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ABNT
GONZAGA, Rodrigo Vieira e FERREIRA, Elizabeth Igne. Dendrimer prodrug derivative of acetylsalicylic acid and rosuvastatin: convergent synthesis of the respective dendron. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 09 out. 2024. , 2017
APA
Gonzaga, R. V., & Ferreira, E. I. (2017). Dendrimer prodrug derivative of acetylsalicylic acid and rosuvastatin: convergent synthesis of the respective dendron. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Gonzaga RV, Ferreira EI. Dendrimer prodrug derivative of acetylsalicylic acid and rosuvastatin: convergent synthesis of the respective dendron. Brazilian Journal of Pharmaceutical Sciences. 2017 ; 53 29 res. FCF053.[citado 2024 out. 09 ]
Vancouver
Gonzaga RV, Ferreira EI. Dendrimer prodrug derivative of acetylsalicylic acid and rosuvastatin: convergent synthesis of the respective dendron. Brazilian Journal of Pharmaceutical Sciences. 2017 ; 53 29 res. FCF053.[citado 2024 out. 09 ]

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