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Artigo de periodico
Free radical formation evidence from Nimorazole electrochemical reduction in aqueous media (2022)
Brito, Charles de Lima; Lins, Renato Soares de Oliveira ; Bertotti, Mauro ; Ferreira, Elizabeth Igne ; Scalea, Mauro A. La
Fonte: Electrochimica Acta. Unidades: FCF, IQ
Assuntos: RADICAIS LIVRES, ELETROQUÍMICA, VOLTAMETRIA
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ABNT
BRITO, Charles de Lima et al. Free radical formation evidence from Nimorazole electrochemical reduction in aqueous media. Electrochimica Acta, v. 403, p. 1-8 art. 139709, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.electacta.2021.139709. Acesso em: 04 nov. 2024.
APA
Brito, C. de L., Lins, R. S. de O., Bertotti, M., Ferreira, E. I., & Scalea, M. A. L. (2022). Free radical formation evidence from Nimorazole electrochemical reduction in aqueous media. Electrochimica Acta, 403, 1-8 art. 139709. doi:10.1016/j.electacta.2021.139709
NLM
Brito C de L, Lins RS de O, Bertotti M, Ferreira EI, Scalea MAL. Free radical formation evidence from Nimorazole electrochemical reduction in aqueous media [Internet]. Electrochimica Acta. 2022 ; 403 1-8 art. 139709.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.electacta.2021.139709
Vancouver
Brito C de L, Lins RS de O, Bertotti M, Ferreira EI, Scalea MAL. Free radical formation evidence from Nimorazole electrochemical reduction in aqueous media [Internet]. Electrochimica Acta. 2022 ; 403 1-8 art. 139709.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.electacta.2021.139709
Artigo de periodico
Electrochemical characterization of para- and meta-nitro substituents in aqueous media of new antichagasic pharmaceutical leaders (2021)
Sanz, Caroline Gomes ; Dias, Kevin de Aquino ; Bacil, Raphael Prata ; Serafim, Ricardo Augusto Massarico; Andrade, Leandro Helgueira ; Ferreira, Elizabeth Igne ; Serrano, Silvia Helena Pires
Fonte: Electrochimica Acta. Unidades: IQ, FCF
Assuntos: DOENÇA DE CHAGAS, VOLTAMETRIA, ELETROQUÍMICA, DOENÇAS NEGLIGENCIADAS
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SANZ, Caroline Gomes et al. Electrochemical characterization of para- and meta-nitro substituents in aqueous media of new antichagasic pharmaceutical leaders. Electrochimica Acta, v. 368, p. 1-12 art. 137582, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.electacta.2020.137582. Acesso em: 04 nov. 2024.
APA
Sanz, C. G., Dias, K. de A., Bacil, R. P., Serafim, R. A. M., Andrade, L. H., Ferreira, E. I., & Serrano, S. H. P. (2021). Electrochemical characterization of para- and meta-nitro substituents in aqueous media of new antichagasic pharmaceutical leaders. Electrochimica Acta, 368, 1-12 art. 137582. doi:10.1016/j.electacta.2020.137582
NLM
Sanz CG, Dias K de A, Bacil RP, Serafim RAM, Andrade LH, Ferreira EI, Serrano SHP. Electrochemical characterization of para- and meta-nitro substituents in aqueous media of new antichagasic pharmaceutical leaders [Internet]. Electrochimica Acta. 2021 ; 368 1-12 art. 137582.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.electacta.2020.137582
Vancouver
Sanz CG, Dias K de A, Bacil RP, Serafim RAM, Andrade LH, Ferreira EI, Serrano SHP. Electrochemical characterization of para- and meta-nitro substituents in aqueous media of new antichagasic pharmaceutical leaders [Internet]. Electrochimica Acta. 2021 ; 368 1-12 art. 137582.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.electacta.2020.137582
Artigo de periodico
Structure-activity relationship and mechanistic studies for a series of cinnamyl hydroxamate histone deacetylase inhibitors (2021)
Tavares, Maurício Temotheo ; Almeida, Larissa Costa de ; Kronenberger, Thales ; Ferreira, Glaucio Monteiro ; Divitiis, Thainá Fujii de ; Toledo, Mônica Franco Zannini Junqueira ; Hassimotto, Neuza Mariko Aymoto ; Machado Neto, João Agostinho ; Costa-Lotufo, Letícia Veras ; Parise Filho, Roberto
Fonte: Bioorganic and Medicinal Chemistry. Unidades: FCF, ICB, PRÓ-G
Assuntos: CITOTOXICIDADE IMUNOLÓGICA, ENZIMAS, FARMACOLOGIA, CÉLULAS CULTIVADAS DE TUMOR, APOPTOSE, PROLIFERAÇÃO CELULAR
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TAVARES, Maurício Temotheo et al. Structure-activity relationship and mechanistic studies for a series of cinnamyl hydroxamate histone deacetylase inhibitors. Bioorganic and Medicinal Chemistry, v. 35, p. 1-42 art. 116085, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2021.116085. Acesso em: 04 nov. 2024.
APA
Tavares, M. T., Almeida, L. C. de, Kronenberger, T., Ferreira, G. M., Divitiis, T. F. de, Toledo, M. F. Z. J., et al. (2021). Structure-activity relationship and mechanistic studies for a series of cinnamyl hydroxamate histone deacetylase inhibitors. Bioorganic and Medicinal Chemistry, 35, 1-42 art. 116085. doi:10.1016/j.bmc.2021.116085
NLM
Tavares MT, Almeida LC de, Kronenberger T, Ferreira GM, Divitiis TF de, Toledo MFZJ, Hassimotto NMA, Machado Neto JA, Costa-Lotufo LV, Parise Filho R. Structure-activity relationship and mechanistic studies for a series of cinnamyl hydroxamate histone deacetylase inhibitors [Internet]. Bioorganic and Medicinal Chemistry. 2021 ; 35 1-42 art. 116085.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.bmc.2021.116085
Vancouver
Tavares MT, Almeida LC de, Kronenberger T, Ferreira GM, Divitiis TF de, Toledo MFZJ, Hassimotto NMA, Machado Neto JA, Costa-Lotufo LV, Parise Filho R. Structure-activity relationship and mechanistic studies for a series of cinnamyl hydroxamate histone deacetylase inhibitors [Internet]. Bioorganic and Medicinal Chemistry. 2021 ; 35 1-42 art. 116085.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.bmc.2021.116085
Artigo de periodico
Nanoencapsulation of anthocyanins from blackberry (Rubus spp.) through pectin and lysozyme self-assembling (2021)
Rosales, Thiecla Katiane Osvaldt ; Silva, Magner Pessoa da; Lourenço, Felipe Rebello ; Hassimotto, Neuza Mariko Aymoto ; Fabi, João Paulo
Fonte: Food Hydrocolloids. Unidade: FCF
Assuntos: AMORA, PECTINA, LISOZIMAS, RECEPTORES
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ABNT
ROSALES, Thiecla Katiane Osvaldt et al. Nanoencapsulation of anthocyanins from blackberry (Rubus spp.) through pectin and lysozyme self-assembling. Food Hydrocolloids, v. 114, p. 1-50 art. 106563, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.foodhyd.2020.106563. Acesso em: 04 nov. 2024.
APA
Rosales, T. K. O., Silva, M. P. da, Lourenço, F. R., Hassimotto, N. M. A., & Fabi, J. P. (2021). Nanoencapsulation of anthocyanins from blackberry (Rubus spp.) through pectin and lysozyme self-assembling. Food Hydrocolloids, 114, 1-50 art. 106563. doi:10.1016/j.foodhyd.2020.106563
NLM
Rosales TKO, Silva MP da, Lourenço FR, Hassimotto NMA, Fabi JP. Nanoencapsulation of anthocyanins from blackberry (Rubus spp.) through pectin and lysozyme self-assembling [Internet]. Food Hydrocolloids. 2021 ; 114 1-50 art. 106563.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.foodhyd.2020.106563
Vancouver
Rosales TKO, Silva MP da, Lourenço FR, Hassimotto NMA, Fabi JP. Nanoencapsulation of anthocyanins from blackberry (Rubus spp.) through pectin and lysozyme self-assembling [Internet]. Food Hydrocolloids. 2021 ; 114 1-50 art. 106563.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.foodhyd.2020.106563
Artigo de periodico
Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor (2020)
Paulino, Antonio Augusto Soares; Giroldo, Lilian; Pradie, Noriberto Araújo; Reis, Joel Savi dos; Back, Davi F; Braga, Ataualpa Albert Carmo ; Stefani, Hélio Alexandre ; Lodeiro, Carlos; Santos, Alcindo Aparecido dos
Fonte: Dyes and Pigments. Unidades: IQ, FCF
Assuntos: SELÊNIO, PALÁDIO, FLUORESCÊNCIA
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ABNT
PAULINO, Antonio Augusto Soares et al. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor. Dyes and Pigments, v. 179, p. 1-10 art. 108355, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2020.108355. Acesso em: 04 nov. 2024.
APA
Paulino, A. A. S., Giroldo, L., Pradie, N. A., Reis, J. S. dos, Back, D. F., Braga, A. A. C., et al. (2020). Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor. Dyes and Pigments, 179, 1-10 art. 108355. doi:10.1016/j.dyepig.2020.108355
NLM
Paulino AAS, Giroldo L, Pradie NA, Reis JS dos, Back DF, Braga AAC, Stefani HA, Lodeiro C, Santos AA dos. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor [Internet]. Dyes and Pigments. 2020 ; 179 1-10 art. 108355.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108355
Vancouver
Paulino AAS, Giroldo L, Pradie NA, Reis JS dos, Back DF, Braga AAC, Stefani HA, Lodeiro C, Santos AA dos. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor [Internet]. Dyes and Pigments. 2020 ; 179 1-10 art. 108355.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108355
Artigo de periodico
Is the Botryococcus braunii Dry biomass an adjuvant for Anti-UVB topical formulations? (2020)
Ariede, Maira Bueno; Jacome, Ana Lucia Morocho ; Cândido, Thalita Marcílio ; Lourenço, Felipe Rebello ; Kato, Edna Tomiko Myiake; Lima, Fabiana Vieira; Rosado, Catarina ; Velasco, Maria Valéria Robles ; Carvalho, João Carlos Monteiro de ; Baby, André Rolim
Fonte: Scientia Pharmaceutical. Unidade: FCF
Assuntos: RADIAÇÃO ULTRAVIOLETA, MICROALGAS
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ABNT
ARIEDE, Maira Bueno et al. Is the Botryococcus braunii Dry biomass an adjuvant for Anti-UVB topical formulations?. Scientia Pharmaceutical, v. 88, p. 1-9 art. 22, 2020Tradução . . Disponível em: https://doi.org/10.3390/scipharm88020022. Acesso em: 04 nov. 2024.
APA
Ariede, M. B., Jacome, A. L. M., Cândido, T. M., Lourenço, F. R., Kato, E. T. M., Lima, F. V., et al. (2020). Is the Botryococcus braunii Dry biomass an adjuvant for Anti-UVB topical formulations? Scientia Pharmaceutical, 88, 1-9 art. 22. doi:10.3390/scipharm88020022
NLM
Ariede MB, Jacome ALM, Cândido TM, Lourenço FR, Kato ETM, Lima FV, Rosado C, Velasco MVR, Carvalho JCM de, Baby AR. Is the Botryococcus braunii Dry biomass an adjuvant for Anti-UVB topical formulations? [Internet]. Scientia Pharmaceutical. 2020 ; 88 1-9 art. 22.[citado 2024 nov. 04 ] Available from: https://doi.org/10.3390/scipharm88020022
Vancouver
Ariede MB, Jacome ALM, Cândido TM, Lourenço FR, Kato ETM, Lima FV, Rosado C, Velasco MVR, Carvalho JCM de, Baby AR. Is the Botryococcus braunii Dry biomass an adjuvant for Anti-UVB topical formulations? [Internet]. Scientia Pharmaceutical. 2020 ; 88 1-9 art. 22.[citado 2024 nov. 04 ] Available from: https://doi.org/10.3390/scipharm88020022
Artigo de periodico
GQ-11: a new PPAR agonist improves obesity-induced metabolicalterations in 'LDLr −/− mice (2018)
Silva, Jacqueline Cavalcante; Oliveira, Edson Mendes de; Turato, Walter Miguel; Trossini, Gustavo Henrique Goulart ; Maltarollo, Vinícius Gonçalves; Pitta, Marina G. R; Pitta, Ivan da Rocha; Heras, Beatriz de Las; Boscá, Lisardo; Rudnicki, Martina; Abdalla, Dulcinéia Saes Parra
Fonte: International Journal of Obesity. Unidade: FCF
Assuntos: OBESIDADE, RATOS
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ABNT
SILVA, Jacqueline Cavalcante et al. GQ-11: a new PPAR agonist improves obesity-induced metabolicalterations in 'LDLr −/− mice. International Journal of Obesity, v. 42, p. 1062–1072 , 2018Tradução . . Disponível em: https://doi.org/10.1038/s41366-018-0011-7. Acesso em: 04 nov. 2024.
APA
Silva, J. C., Oliveira, E. M. de, Turato, W. M., Trossini, G. H. G., Maltarollo, V. G., Pitta, M. G. R., et al. (2018). GQ-11: a new PPAR agonist improves obesity-induced metabolicalterations in 'LDLr −/− mice. International Journal of Obesity, 42, 1062–1072 . doi:10.1038/s41366-018-0011-7
NLM
Silva JC, Oliveira EM de, Turato WM, Trossini GHG, Maltarollo VG, Pitta MGR, Pitta I da R, Heras B de L, Boscá L, Rudnicki M, Abdalla DSP. GQ-11: a new PPAR agonist improves obesity-induced metabolicalterations in 'LDLr −/− mice [Internet]. International Journal of Obesity. 2018 ; 42 1062–1072 .[citado 2024 nov. 04 ] Available from: https://doi.org/10.1038/s41366-018-0011-7
Vancouver
Silva JC, Oliveira EM de, Turato WM, Trossini GHG, Maltarollo VG, Pitta MGR, Pitta I da R, Heras B de L, Boscá L, Rudnicki M, Abdalla DSP. GQ-11: a new PPAR agonist improves obesity-induced metabolicalterations in 'LDLr −/− mice [Internet]. International Journal of Obesity. 2018 ; 42 1062–1072 .[citado 2024 nov. 04 ] Available from: https://doi.org/10.1038/s41366-018-0011-7
Artigo de periodico
Oxazoline as acceptor moiety for excited-state intramolecular proton transfer (2018)
Reis, Joel S; Fernandes, Arthur Bonfá; Dörr, Barbara Coelho de Freitas; Bastos, Erick Leite ; Stefani, Hélio Alexandre
Fonte: Tetrahedron. Unidades: IQ, FCF
Assuntos: FLUORESCÊNCIA, COMPOSTOS ORGÂNICOS
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ABNT
REIS, Joel S et al. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer. Tetrahedron, v. 74, p. 6866-6872, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2018.10.019. Acesso em: 04 nov. 2024.
APA
Reis, J. S., Fernandes, A. B., Dörr, B. C. de F., Bastos, E. L., & Stefani, H. A. (2018). Oxazoline as acceptor moiety for excited-state intramolecular proton transfer. Tetrahedron, 74, 6866-6872. doi:10.1016/j.tet.2018.10.019
NLM
Reis JS, Fernandes AB, Dörr BC de F, Bastos EL, Stefani HA. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer [Internet]. Tetrahedron. 2018 ; 74 6866-6872.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.tet.2018.10.019
Vancouver
Reis JS, Fernandes AB, Dörr BC de F, Bastos EL, Stefani HA. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer [Internet]. Tetrahedron. 2018 ; 74 6866-6872.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.tet.2018.10.019
Artigo de periodico
Convergent QSAR studies on a series of NK3 receptor antagonists for schizophrenia treatment (2016)
Primi, Marina Candido; Maltarollo, Vinícius Gonçalves; Magalhães, Juliana Gallottini de; Sá, Matheus Malta de; Rangel-Yagui, Carlota de Oliveira ; Trossini, Gustavo Henrique Goulart
Fonte: Journal of Enzyme Inhibition and Medicinal Chemistry. Unidade: FCF
Assuntos: RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, RECEPTORES, ESQUIZOFRENIA
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ABNT
PRIMI, Marina Candido et al. Convergent QSAR studies on a series of NK3 receptor antagonists for schizophrenia treatment. Journal of Enzyme Inhibition and Medicinal Chemistry, v. 31, n. 2, p. 283-294, 2016Tradução . . Disponível em: https://doi.org/10.3109/14756366.2015.1021250. Acesso em: 04 nov. 2024.
APA
Primi, M. C., Maltarollo, V. G., Magalhães, J. G. de, Sá, M. M. de, Rangel-Yagui, C. de O., & Trossini, G. H. G. (2016). Convergent QSAR studies on a series of NK3 receptor antagonists for schizophrenia treatment. Journal of Enzyme Inhibition and Medicinal Chemistry, 31( 2), 283-294. doi:10.3109/14756366.2015.1021250
NLM
Primi MC, Maltarollo VG, Magalhães JG de, Sá MM de, Rangel-Yagui C de O, Trossini GHG. Convergent QSAR studies on a series of NK3 receptor antagonists for schizophrenia treatment [Internet]. Journal of Enzyme Inhibition and Medicinal Chemistry. 2016 ; 31( 2): 283-294.[citado 2024 nov. 04 ] Available from: https://doi.org/10.3109/14756366.2015.1021250
Vancouver
Primi MC, Maltarollo VG, Magalhães JG de, Sá MM de, Rangel-Yagui C de O, Trossini GHG. Convergent QSAR studies on a series of NK3 receptor antagonists for schizophrenia treatment [Internet]. Journal of Enzyme Inhibition and Medicinal Chemistry. 2016 ; 31( 2): 283-294.[citado 2024 nov. 04 ] Available from: https://doi.org/10.3109/14756366.2015.1021250
Artigo de periodico
Caco-2 cells permeability evaluation of nifuroxazide derivatives with potential activity against methicillin-resistant Staphylococcus aureus (MRSA) (2015)
Fernandes, Mariane Ballerini; Gonçalves, José Eduardo; Tavares, Leoberto Costa ; Storpirtis, Silvia
Fonte: Drug Development and Industrial Pharmacy. Unidade: FCF
Assuntos: ANTI-INFECCIOSOS, BIOFARMÁCIA, RESISTÊNCIA MICROBIANA ÀS DROGAS, STAPHYLOCOCCUS
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ABNT
FERNANDES, Mariane Ballerini et al. Caco-2 cells permeability evaluation of nifuroxazide derivatives with potential activity against methicillin-resistant Staphylococcus aureus (MRSA). Drug Development and Industrial Pharmacy, v. 41, n. 7, p. 1066-1072, 2015Tradução . . Disponível em: https://doi.org/10.3109/03639045.2014.925919. Acesso em: 04 nov. 2024.
APA
Fernandes, M. B., Gonçalves, J. E., Tavares, L. C., & Storpirtis, S. (2015). Caco-2 cells permeability evaluation of nifuroxazide derivatives with potential activity against methicillin-resistant Staphylococcus aureus (MRSA). Drug Development and Industrial Pharmacy, 41( 7), 1066-1072. doi:10.3109/03639045.2014.925919
NLM
Fernandes MB, Gonçalves JE, Tavares LC, Storpirtis S. Caco-2 cells permeability evaluation of nifuroxazide derivatives with potential activity against methicillin-resistant Staphylococcus aureus (MRSA) [Internet]. Drug Development and Industrial Pharmacy. 2015 ; 41( 7): 1066-1072.[citado 2024 nov. 04 ] Available from: https://doi.org/10.3109/03639045.2014.925919
Vancouver
Fernandes MB, Gonçalves JE, Tavares LC, Storpirtis S. Caco-2 cells permeability evaluation of nifuroxazide derivatives with potential activity against methicillin-resistant Staphylococcus aureus (MRSA) [Internet]. Drug Development and Industrial Pharmacy. 2015 ; 41( 7): 1066-1072.[citado 2024 nov. 04 ] Available from: https://doi.org/10.3109/03639045.2014.925919
Artigo de periodico
Synthesis and preliminary biological evaluation of a compound library of triazolylcyclitols (2013)
Carrau, Gonzalo; Drewes, Carine Cristiane; Shimada, Ana Lucia Borges; Bertucci, Ana; Farsky, Sandra Helena Poliselli ; Stefani, Hélio Alexandre ; Gonzalez, David
Fonte: Bioorganic & Medicinal Chemistry. Unidade: FCF
Assuntos: ANTIFÚNGICOS, FÁRMACOS IMUNOSSUPRESSORES
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ABNT
CARRAU, Gonzalo et al. Synthesis and preliminary biological evaluation of a compound library of triazolylcyclitols. Bioorganic & Medicinal Chemistry, v. 21, n. 14, p. 4225-4232, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2013.04.084. Acesso em: 04 nov. 2024.
APA
Carrau, G., Drewes, C. C., Shimada, A. L. B., Bertucci, A., Farsky, S. H. P., Stefani, H. A., & Gonzalez, D. (2013). Synthesis and preliminary biological evaluation of a compound library of triazolylcyclitols. Bioorganic & Medicinal Chemistry, 21( 14), 4225-4232. doi:10.1016/j.bmc.2013.04.084
NLM
Carrau G, Drewes CC, Shimada ALB, Bertucci A, Farsky SHP, Stefani HA, Gonzalez D. Synthesis and preliminary biological evaluation of a compound library of triazolylcyclitols [Internet]. Bioorganic & Medicinal Chemistry. 2013 ; 21( 14): 4225-4232.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.bmc.2013.04.084
Vancouver
Carrau G, Drewes CC, Shimada ALB, Bertucci A, Farsky SHP, Stefani HA, Gonzalez D. Synthesis and preliminary biological evaluation of a compound library of triazolylcyclitols [Internet]. Bioorganic & Medicinal Chemistry. 2013 ; 21( 14): 4225-4232.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.bmc.2013.04.084
Artigo de periodico
Caco-2 cells cytotoxicity of nifuroxazide derivatives with potential activity against Methicillin-resistant Staphylococcus aureus (2012)
Fernandes, Mariane Ballerini; Gonçalves, José Eduardo; Scotti, Marcus Tullius; Oliveira, Alex Alfredo de; Tavares, Leoberto Costa ; Storpirtis, Silvia
Fonte: Toxicology in Vitro. Unidade: FCF
Assuntos: COMPOSTOS HETEROCÍCLICOS, STAPHYLOCOCCUS
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ABNT
FERNANDES, Mariane Ballerini et al. Caco-2 cells cytotoxicity of nifuroxazide derivatives with potential activity against Methicillin-resistant Staphylococcus aureus. Toxicology in Vitro, v. 28, n. 3, p. 535-540, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tiv.2012.01.018. Acesso em: 04 nov. 2024.
APA
Fernandes, M. B., Gonçalves, J. E., Scotti, M. T., Oliveira, A. A. de, Tavares, L. C., & Storpirtis, S. (2012). Caco-2 cells cytotoxicity of nifuroxazide derivatives with potential activity against Methicillin-resistant Staphylococcus aureus. Toxicology in Vitro, 28( 3), 535-540. doi:10.1016/j.tiv.2012.01.018
NLM
Fernandes MB, Gonçalves JE, Scotti MT, Oliveira AA de, Tavares LC, Storpirtis S. Caco-2 cells cytotoxicity of nifuroxazide derivatives with potential activity against Methicillin-resistant Staphylococcus aureus [Internet]. Toxicology in Vitro. 2012 ; 28( 3): 535-540.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.tiv.2012.01.018
Vancouver
Fernandes MB, Gonçalves JE, Scotti MT, Oliveira AA de, Tavares LC, Storpirtis S. Caco-2 cells cytotoxicity of nifuroxazide derivatives with potential activity against Methicillin-resistant Staphylococcus aureus [Internet]. Toxicology in Vitro. 2012 ; 28( 3): 535-540.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1016/j.tiv.2012.01.018
Artigo de periodico
Study of sunless tanning formulas using molted snake skin as an alternative membrane model (2011)
Balogh, Tatiana Santana; Pedriali, Carla Aparecida; Gama, R. M; Pinto, Claudinéia Aparecida Sales de Oliveira ; Bedin, Valcinir; Villa, Ricardo Tadeu; Kaneko, Telma Mary ; Consiglieri, Vladi Olga ; Velasco, Maria Valéria Robles ; Baby, André Rolim
Fonte: International Journal of Cosmetic Science. Unidade: FCF
Assuntos: EMULSÕES COSMÉTICAS, MELANINAS
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ABNT
BALOGH, Tatiana Santana et al. Study of sunless tanning formulas using molted snake skin as an alternative membrane model. International Journal of Cosmetic Science, v. 33, n. 4, p. 359-365, 2011Tradução . . Disponível em: https://doi.org/10.1111/j.1468-2494.2011.00638.x. Acesso em: 04 nov. 2024.
APA
Balogh, T. S., Pedriali, C. A., Gama, R. M., Pinto, C. A. S. de O., Bedin, V., Villa, R. T., et al. (2011). Study of sunless tanning formulas using molted snake skin as an alternative membrane model. International Journal of Cosmetic Science, 33( 4), 359-365. doi:10.1111/j.1468-2494.2011.00638.x
NLM
Balogh TS, Pedriali CA, Gama RM, Pinto CAS de O, Bedin V, Villa RT, Kaneko TM, Consiglieri VO, Velasco MVR, Baby AR. Study of sunless tanning formulas using molted snake skin as an alternative membrane model [Internet]. International Journal of Cosmetic Science. 2011 ; 33( 4): 359-365.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1111/j.1468-2494.2011.00638.x
Vancouver
Balogh TS, Pedriali CA, Gama RM, Pinto CAS de O, Bedin V, Villa RT, Kaneko TM, Consiglieri VO, Velasco MVR, Baby AR. Study of sunless tanning formulas using molted snake skin as an alternative membrane model [Internet]. International Journal of Cosmetic Science. 2011 ; 33( 4): 359-365.[citado 2024 nov. 04 ] Available from: https://doi.org/10.1111/j.1468-2494.2011.00638.x

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