ReP USP - Resultado da busca

Artigo de periodico
Chloroaluminium phthalocyanine polymeric nanoparticles as photosensitisers: photophysical and physicochemical characterisation, release and phototoxicity in vitro (2013)
Paula, Carina Silva de; Tedesco, Antonio Claudio; Primo, Fernando Lucas; Vilela, José Mário Carneiro; Andrade, Margareth Spangler; Mosqueira, Vanessa Carla Furtado
Source: European Journal of Pharmaceutical Sciences. Unidade: FFCLRP
Subjects: TERAPIA FOTODINÂMICA, NANOPARTÍCULAS, FLUORESCÊNCIA
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ABNT
PAULA, Carina Silva de et al. Chloroaluminium phthalocyanine polymeric nanoparticles as photosensitisers: photophysical and physicochemical characterisation, release and phototoxicity in vitro. European Journal of Pharmaceutical Sciences, v. 49, n. 3, p. 371-383, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.ejps.2013.03.011. Acesso em: 28 set. 2024.
APA
Paula, C. S. de, Tedesco, A. C., Primo, F. L., Vilela, J. M. C., Andrade, M. S., & Mosqueira, V. C. F. (2013). Chloroaluminium phthalocyanine polymeric nanoparticles as photosensitisers: photophysical and physicochemical characterisation, release and phototoxicity in vitro. European Journal of Pharmaceutical Sciences, 49( 3), 371-383. doi:10.1016/j.ejps.2013.03.011
NLM
Paula CS de, Tedesco AC, Primo FL, Vilela JMC, Andrade MS, Mosqueira VCF. Chloroaluminium phthalocyanine polymeric nanoparticles as photosensitisers: photophysical and physicochemical characterisation, release and phototoxicity in vitro [Internet]. European Journal of Pharmaceutical Sciences. 2013 ; 49( 3): 371-383.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.ejps.2013.03.011
Vancouver
Paula CS de, Tedesco AC, Primo FL, Vilela JMC, Andrade MS, Mosqueira VCF. Chloroaluminium phthalocyanine polymeric nanoparticles as photosensitisers: photophysical and physicochemical characterisation, release and phototoxicity in vitro [Internet]. European Journal of Pharmaceutical Sciences. 2013 ; 49( 3): 371-383.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.ejps.2013.03.011
Artigo de periodico
Computational studies of TGF-ßRI (ALK-5) inhibitors: analysis of the binding interactions between ligand–receptor using 2D and 3D techniques (2013)
Araujo, Sheila C; Maltarollo, Vinícius Gonçalves; Honório, Kathia Maria
Source: European Journal of Pharmaceutical Sciences. Unidade: EACH
Subjects: NEOPLASIAS, MODELAGEM MOLECULAR, RELAÇÕES ESTRUTURA-ATIVIDADE
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ABNT
ARAUJO, Sheila C e MALTAROLLO, Vinícius Gonçalves e HONÓRIO, Kathia Maria. Computational studies of TGF-ßRI (ALK-5) inhibitors: analysis of the binding interactions between ligand–receptor using 2D and 3D techniques. European Journal of Pharmaceutical Sciences, v. 49, n. 4, p. 542\2013549, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.ejps.2013.05.015. Acesso em: 28 set. 2024.
APA
Araujo, S. C., Maltarollo, V. G., & Honório, K. M. (2013). Computational studies of TGF-ßRI (ALK-5) inhibitors: analysis of the binding interactions between ligand–receptor using 2D and 3D techniques. European Journal of Pharmaceutical Sciences, 49( 4), 542\2013549. doi:10.1016/j.ejps.2013.05.015
NLM
Araujo SC, Maltarollo VG, Honório KM. Computational studies of TGF-ßRI (ALK-5) inhibitors: analysis of the binding interactions between ligand–receptor using 2D and 3D techniques [Internet]. European Journal of Pharmaceutical Sciences. 2013 ; 49( 4): 542\2013549.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.ejps.2013.05.015
Vancouver
Araujo SC, Maltarollo VG, Honório KM. Computational studies of TGF-ßRI (ALK-5) inhibitors: analysis of the binding interactions between ligand–receptor using 2D and 3D techniques [Internet]. European Journal of Pharmaceutical Sciences. 2013 ; 49( 4): 542\2013549.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.ejps.2013.05.015
Artigo de periodico
Chemical synthesis, docking studies and biological effects of a pan peroxisome proliferator-activated receptor agonist and cyclooxygenase inhibitor (2013)
Santin, José Roberto; Uchôa, Flávia de Toni; Lima, Maria do Carmo Alves; Rabello, Marcelo M; Machado, Isabel Daufenback; Hernandes, Marcelo Zaldini; Amato, Angelica A; Milton, Flora Aparecida; Webb, Paul; Neves, Francisco de Assis Rocha; Galdino, Suely Lins; Pitta, Ivan da Rocha; Farsky, Sandra Helena Poliselli
Source: European Journal of Pharmaceutical Sciences. Unidade: FCF
Subjects: INFLAMAÇÃO, NEUTRÓFILOS, INTERLEUCINA 1
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ABNT
SANTIN, José Roberto et al. Chemical synthesis, docking studies and biological effects of a pan peroxisome proliferator-activated receptor agonist and cyclooxygenase inhibitor. European Journal of Pharmaceutical Sciences, v. 48, n. 4-5, p. 689-697, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.ejps.2012.12.029. Acesso em: 28 set. 2024.
APA
Santin, J. R., Uchôa, F. de T., Lima, M. do C. A., Rabello, M. M., Machado, I. D., Hernandes, M. Z., et al. (2013). Chemical synthesis, docking studies and biological effects of a pan peroxisome proliferator-activated receptor agonist and cyclooxygenase inhibitor. European Journal of Pharmaceutical Sciences, 48( 4-5), 689-697. doi:10.1016/j.ejps.2012.12.029
NLM
Santin JR, Uchôa F de T, Lima M do CA, Rabello MM, Machado ID, Hernandes MZ, Amato AA, Milton FA, Webb P, Neves F de AR, Galdino SL, Pitta I da R, Farsky SHP. Chemical synthesis, docking studies and biological effects of a pan peroxisome proliferator-activated receptor agonist and cyclooxygenase inhibitor [Internet]. European Journal of Pharmaceutical Sciences. 2013 ; 48( 4-5): 689-697.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.ejps.2012.12.029
Vancouver
Santin JR, Uchôa F de T, Lima M do CA, Rabello MM, Machado ID, Hernandes MZ, Amato AA, Milton FA, Webb P, Neves F de AR, Galdino SL, Pitta I da R, Farsky SHP. Chemical synthesis, docking studies and biological effects of a pan peroxisome proliferator-activated receptor agonist and cyclooxygenase inhibitor [Internet]. European Journal of Pharmaceutical Sciences. 2013 ; 48( 4-5): 689-697.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.ejps.2012.12.029
Artigo de periodico
Liver, plasma and erythrocyte levels of thiamine and its phosphate esters in rats with acute ethanol intoxication: a comparison of thiamine and benfotiamine administration (2013)
Portari, Guilherme Vannucchi; Vannucchi, Hélio; Jordão Júnior, Alceu Afonso
Source: European Journal of Pharmaceutical Sciences. Unidade: FMRP
Subjects: BEBIDAS ALCOÓLICAS, INTOXICAÇÃO, VITAMINAS, SANGUE, FARMACOCINÉTICA
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ABNT
PORTARI, Guilherme Vannucchi e VANNUCCHI, Hélio e JORDÃO JÚNIOR, Alceu Afonso. Liver, plasma and erythrocyte levels of thiamine and its phosphate esters in rats with acute ethanol intoxication: a comparison of thiamine and benfotiamine administration. European Journal of Pharmaceutical Sciences, v. 48, n. 4-5, p. 799-802, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.ejps.2013.01.010. Acesso em: 28 set. 2024.
APA
Portari, G. V., Vannucchi, H., & Jordão Júnior, A. A. (2013). Liver, plasma and erythrocyte levels of thiamine and its phosphate esters in rats with acute ethanol intoxication: a comparison of thiamine and benfotiamine administration. European Journal of Pharmaceutical Sciences, 48( 4-5), 799-802. doi:10.1016/j.ejps.2013.01.010
NLM
Portari GV, Vannucchi H, Jordão Júnior AA. Liver, plasma and erythrocyte levels of thiamine and its phosphate esters in rats with acute ethanol intoxication: a comparison of thiamine and benfotiamine administration [Internet]. European Journal of Pharmaceutical Sciences. 2013 ; 48( 4-5): 799-802.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.ejps.2013.01.010
Vancouver
Portari GV, Vannucchi H, Jordão Júnior AA. Liver, plasma and erythrocyte levels of thiamine and its phosphate esters in rats with acute ethanol intoxication: a comparison of thiamine and benfotiamine administration [Internet]. European Journal of Pharmaceutical Sciences. 2013 ; 48( 4-5): 799-802.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.ejps.2013.01.010
Artigo de periodico
Nitric oxide generated by the compound RuBPY promotes the vascular smooth cell membrane hyperpolarization (2013)
Pereira, Amanda C.; Lunardi, Claure Nain; Paulo, Michele; Silva, Roberto Santana da; Bendhack, Lusiane Maria
Source: European Journal of Pharmaceutical Sciences. Unidade: FCFRP
Subjects: ÓXIDO NÍTRICO, MEMBRANAS CELULARES
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ABNT
PEREIRA, Amanda C. et al. Nitric oxide generated by the compound RuBPY promotes the vascular smooth cell membrane hyperpolarization. European Journal of Pharmaceutical Sciences, v. 48, n. 4-5, p. 604-610, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.ejps.2013.01.003. Acesso em: 28 set. 2024.
APA
Pereira, A. C., Lunardi, C. N., Paulo, M., Silva, R. S. da, & Bendhack, L. M. (2013). Nitric oxide generated by the compound RuBPY promotes the vascular smooth cell membrane hyperpolarization. European Journal of Pharmaceutical Sciences, 48( 4-5), 604-610. doi:10.1016/j.ejps.2013.01.003
NLM
Pereira AC, Lunardi CN, Paulo M, Silva RS da, Bendhack LM. Nitric oxide generated by the compound RuBPY promotes the vascular smooth cell membrane hyperpolarization [Internet]. European Journal of Pharmaceutical Sciences. 2013 ; 48( 4-5): 604-610.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.ejps.2013.01.003
Vancouver
Pereira AC, Lunardi CN, Paulo M, Silva RS da, Bendhack LM. Nitric oxide generated by the compound RuBPY promotes the vascular smooth cell membrane hyperpolarization [Internet]. European Journal of Pharmaceutical Sciences. 2013 ; 48( 4-5): 604-610.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.ejps.2013.01.003
Artigo de periodico
Lamivudine permeability study: a comparison between PAMPA, ex vivo and in situ Single-Pass Intestinal Perfusion (SPIP) in rat jejunum (2013)
Reis, J. M; Dezani, André Bersani; Pereira, Tacila Alves Muniz; Avdeef, Alex; Serra, Cristina Helena dos Reis
Source: European Journal of Pharmaceutical Sciences. Unidade: FCF
Subjects: GLICOPROTEÍNAS, MEDICAMENTO
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ABNT
REIS, J. M et al. Lamivudine permeability study: a comparison between PAMPA, ex vivo and in situ Single-Pass Intestinal Perfusion (SPIP) in rat jejunum. European Journal of Pharmaceutical Sciences, v. 48, n. 4-5, p. 781-789, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.ejps.2012.12.025. Acesso em: 28 set. 2024.
APA
Reis, J. M., Dezani, A. B., Pereira, T. A. M., Avdeef, A., & Serra, C. H. dos R. (2013). Lamivudine permeability study: a comparison between PAMPA, ex vivo and in situ Single-Pass Intestinal Perfusion (SPIP) in rat jejunum. European Journal of Pharmaceutical Sciences, 48( 4-5), 781-789. doi:10.1016/j.ejps.2012.12.025
NLM
Reis JM, Dezani AB, Pereira TAM, Avdeef A, Serra CH dos R. Lamivudine permeability study: a comparison between PAMPA, ex vivo and in situ Single-Pass Intestinal Perfusion (SPIP) in rat jejunum [Internet]. European Journal of Pharmaceutical Sciences. 2013 ; 48( 4-5): 781-789.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.ejps.2012.12.025
Vancouver
Reis JM, Dezani AB, Pereira TAM, Avdeef A, Serra CH dos R. Lamivudine permeability study: a comparison between PAMPA, ex vivo and in situ Single-Pass Intestinal Perfusion (SPIP) in rat jejunum [Internet]. European Journal of Pharmaceutical Sciences. 2013 ; 48( 4-5): 781-789.[citado 2024 set. 28 ] Available from: https://doi.org/10.1016/j.ejps.2012.12.025

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