ReP USP - Resultado da busca

Artigo de periodico
Olive oil nanoemulsion preparation using high-pressure homogenization and D-phase emulsification - A design space approach (2019)
Yukuyama, Megumi Nishitani; Kato, Edna Tomiko Myiake; Araujo, Gabriel Lima Barros de ; Löbenberg, Raimar; Monteiro, Lis Marie; Lourenço, Felipe Rebello ; Bou-Chacra, Nadia Araci
Fonte: Journal of Drug Delivery Science and Technology. Unidade: FCF
Assuntos: AZEITE, ÁCIDOS GRAXOS, HOMOGENEIZAÇÃO
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ABNT
YUKUYAMA, Megumi Nishitani et al. Olive oil nanoemulsion preparation using high-pressure homogenization and D-phase emulsification - A design space approach. Journal of Drug Delivery Science and Technology, v. 49, p. 622-631, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.jddst.2018.12.029. Acesso em: 14 nov. 2024.
APA
Yukuyama, M. N., Kato, E. T. M., Araujo, G. L. B. de, Löbenberg, R., Monteiro, L. M., Lourenço, F. R., & Bou-Chacra, N. A. (2019). Olive oil nanoemulsion preparation using high-pressure homogenization and D-phase emulsification - A design space approach. Journal of Drug Delivery Science and Technology, 49, 622-631. doi:10.1016/j.jddst.2018.12.029
NLM
Yukuyama MN, Kato ETM, Araujo GLB de, Löbenberg R, Monteiro LM, Lourenço FR, Bou-Chacra NA. Olive oil nanoemulsion preparation using high-pressure homogenization and D-phase emulsification - A design space approach [Internet]. Journal of Drug Delivery Science and Technology. 2019 ; 49 622-631.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.jddst.2018.12.029
Vancouver
Yukuyama MN, Kato ETM, Araujo GLB de, Löbenberg R, Monteiro LM, Lourenço FR, Bou-Chacra NA. Olive oil nanoemulsion preparation using high-pressure homogenization and D-phase emulsification - A design space approach [Internet]. Journal of Drug Delivery Science and Technology. 2019 ; 49 622-631.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.jddst.2018.12.029
Artigo de periodico
β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders (2018)
Vaidergorn, Miguel M; Carneiro, Zumira A; Lopes, Carla D; Albuquerque, Sérgio de; Reis, Felipe C. C; Nikolaou, Sofia; Mello, Juliana F. R; Genesi, Giovani L; Trossini, Gustavo Henrique Goulart ; Ganesan, A; Emery, Flavio da Silva
Fonte: European Journal of Medicinal Chemistry. Unidades: FCFRP, FFCLRP, FCF
Assuntos: DNA, COMPOSTOS ORGÂNICOS
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ABNT
VAIDERGORN, Miguel M et al. β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders. European Journal of Medicinal Chemistry, v. 157, p. 657-664, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2018.07.055. Acesso em: 14 nov. 2024.
APA
Vaidergorn, M. M., Carneiro, Z. A., Lopes, C. D., Albuquerque, S. de, Reis, F. C. C., Nikolaou, S., et al. (2018). β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders. European Journal of Medicinal Chemistry, 157, 657-664. doi:10.1016/j.ejmech.2018.07.055
NLM
Vaidergorn MM, Carneiro ZA, Lopes CD, Albuquerque S de, Reis FCC, Nikolaou S, Mello JFR, Genesi GL, Trossini GHG, Ganesan A, Emery F da S. β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders [Internet]. European Journal of Medicinal Chemistry. 2018 ; 157 657-664.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.ejmech.2018.07.055
Vancouver
Vaidergorn MM, Carneiro ZA, Lopes CD, Albuquerque S de, Reis FCC, Nikolaou S, Mello JFR, Genesi GL, Trossini GHG, Ganesan A, Emery F da S. β-amino alcohols and their respective 2-phenyl-N-alkyl aziridines as potential DNA minor groove binders [Internet]. European Journal of Medicinal Chemistry. 2018 ; 157 657-664.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.ejmech.2018.07.055
Artigo de periodico
Multi-drug resistant Mycobacterium tuberculosis & oxidative stress complexity: emerging need for novel drug delivery approaches (2018)
Dua, Kamal; Krishna, Rapalli Vamshi; Shukla, Shakti Dhar; Singhvi, Gautam; Shastri, Madhur D; Chellappan, Dinesh Kumar; Satija, Saurabh; Mehta, Meenu; Gulati, Monica; Pinto, Terezinha de Jesus Andreoli ; Gupta, Gaurav; Hansbro, Philip M
Fonte: Biomedicine and Pharmacotherapy. Unidade: FCF
Assuntos: ESTRESSE OXIDATIVO, MYCOBACTERIUM TUBERCULOSIS, RESISTÊNCIA MICROBIANA ÀS DROGAS
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ABNT
DUA, Kamal et al. Multi-drug resistant Mycobacterium tuberculosis & oxidative stress complexity: emerging need for novel drug delivery approaches. Biomedicine and Pharmacotherapy, v. 107, p. 1218-1229, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.biopha.2018.08.101. Acesso em: 14 nov. 2024.
APA
Dua, K., Krishna, R. V., Shukla, S. D., Singhvi, G., Shastri, M. D., Chellappan, D. K., et al. (2018). Multi-drug resistant Mycobacterium tuberculosis & oxidative stress complexity: emerging need for novel drug delivery approaches. Biomedicine and Pharmacotherapy, 107, 1218-1229. doi:10.1016/j.biopha.2018.08.101
NLM
Dua K, Krishna RV, Shukla SD, Singhvi G, Shastri MD, Chellappan DK, Satija S, Mehta M, Gulati M, Pinto T de JA, Gupta G, Hansbro PM. Multi-drug resistant Mycobacterium tuberculosis & oxidative stress complexity: emerging need for novel drug delivery approaches [Internet]. Biomedicine and Pharmacotherapy. 2018 ; 107 1218-1229.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.biopha.2018.08.101
Vancouver
Dua K, Krishna RV, Shukla SD, Singhvi G, Shastri MD, Chellappan DK, Satija S, Mehta M, Gulati M, Pinto T de JA, Gupta G, Hansbro PM. Multi-drug resistant Mycobacterium tuberculosis & oxidative stress complexity: emerging need for novel drug delivery approaches [Internet]. Biomedicine and Pharmacotherapy. 2018 ; 107 1218-1229.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.biopha.2018.08.101
Artigo de periodico
Synthesis and trypanocidal activity of a library of 4-substituted 2-(1H-pyrrolo[3,2-c]pyridin-2-yl)propan-2-ols (2017)
Balfour, Michael N; Franco, Caio Haddad; Moraes, Carolina Borsoi; Freitas Junior, Lucio H; Stefani, Hélio Alexandre
Fonte: European Journal of Medicinal Chemistry. Unidade: FCF
Assuntos: DOENÇA DE CHAGAS, TRYPANOSOMA
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ABNT
BALFOUR, Michael N et al. Synthesis and trypanocidal activity of a library of 4-substituted 2-(1H-pyrrolo[3,2-c]pyridin-2-yl)propan-2-ols. European Journal of Medicinal Chemistry, v. 128, p. 202-212, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2017.01.040. Acesso em: 14 nov. 2024.
APA
Balfour, M. N., Franco, C. H., Moraes, C. B., Freitas Junior, L. H., & Stefani, H. A. (2017). Synthesis and trypanocidal activity of a library of 4-substituted 2-(1H-pyrrolo[3,2-c]pyridin-2-yl)propan-2-ols. European Journal of Medicinal Chemistry, 128, 202-212. doi:10.1016/j.ejmech.2017.01.040
NLM
Balfour MN, Franco CH, Moraes CB, Freitas Junior LH, Stefani HA. Synthesis and trypanocidal activity of a library of 4-substituted 2-(1H-pyrrolo[3,2-c]pyridin-2-yl)propan-2-ols [Internet]. European Journal of Medicinal Chemistry. 2017 ; 128 202-212.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.ejmech.2017.01.040
Vancouver
Balfour MN, Franco CH, Moraes CB, Freitas Junior LH, Stefani HA. Synthesis and trypanocidal activity of a library of 4-substituted 2-(1H-pyrrolo[3,2-c]pyridin-2-yl)propan-2-ols [Internet]. European Journal of Medicinal Chemistry. 2017 ; 128 202-212.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.ejmech.2017.01.040
Artigo de periodico
An integrated approach towards the discovery of novel non-nucleoside Leishmania major pteridine reductase 1 inhibitors (2017)
Leite, Franco Henrique Andrade; Froes, Thamires Quadros; Silva, Suellen Goncalves da; Souza, Evandro Italo Macedo de; Fujii, Drielli Gomes Vital; Trossini, Gustavo Henrique Goulart ; Pita, Samuel Silva da Rocha; Castilho, Marcelo Santos
Fonte: European Journal of Medicinal Chemistry. Unidade: FCF
Assuntos: PLANEJAMENTO DE FÁRMACOS, LEISHMANIA
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ABNT
LEITE, Franco Henrique Andrade et al. An integrated approach towards the discovery of novel non-nucleoside Leishmania major pteridine reductase 1 inhibitors. European Journal of Medicinal Chemistry, v. 132, p. 322-332, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2017.03.043. Acesso em: 14 nov. 2024.
APA
Leite, F. H. A., Froes, T. Q., Silva, S. G. da, Souza, E. I. M. de, Fujii, D. G. V., Trossini, G. H. G., et al. (2017). An integrated approach towards the discovery of novel non-nucleoside Leishmania major pteridine reductase 1 inhibitors. European Journal of Medicinal Chemistry, 132, 322-332. doi:10.1016/j.ejmech.2017.03.043
NLM
Leite FHA, Froes TQ, Silva SG da, Souza EIM de, Fujii DGV, Trossini GHG, Pita SS da R, Castilho MS. An integrated approach towards the discovery of novel non-nucleoside Leishmania major pteridine reductase 1 inhibitors [Internet]. European Journal of Medicinal Chemistry. 2017 ; 132 322-332.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.ejmech.2017.03.043
Vancouver
Leite FHA, Froes TQ, Silva SG da, Souza EIM de, Fujii DGV, Trossini GHG, Pita SS da R, Castilho MS. An integrated approach towards the discovery of novel non-nucleoside Leishmania major pteridine reductase 1 inhibitors [Internet]. European Journal of Medicinal Chemistry. 2017 ; 132 322-332.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.ejmech.2017.03.043
Artigo de periodico
Synthesis and application of the MCM-41 and SBA-15 as matrices for in vitro efavirenz release study (2016)
Jesus, R. A; Rabelo, Adriano Alves; Figueiredo, R. T; Silva, L. C. Cides da; Codentino, I. C; Fantini, Márcia Carvalho de Abreu ; Araujo, Gabriel Lima Barros de ; Araújo, A. A. S; Mesquita, M. E
Fonte: Journal of Drug Delivery Science and Technology. Unidades: IF, FCF
Assunto: FARMACOCINÉTICA
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ABNT
JESUS, R. A et al. Synthesis and application of the MCM-41 and SBA-15 as matrices for in vitro efavirenz release study. Journal of Drug Delivery Science and Technology, v. 31, p. 153-159, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.jddst.2015.11.008. Acesso em: 14 nov. 2024.
APA
Jesus, R. A., Rabelo, A. A., Figueiredo, R. T., Silva, L. C. C. da, Codentino, I. C., Fantini, M. C. de A., et al. (2016). Synthesis and application of the MCM-41 and SBA-15 as matrices for in vitro efavirenz release study. Journal of Drug Delivery Science and Technology, 31, 153-159. doi:10.1016/j.jddst.2015.11.008
NLM
Jesus RA, Rabelo AA, Figueiredo RT, Silva LCC da, Codentino IC, Fantini MC de A, Araujo GLB de, Araújo AAS, Mesquita ME. Synthesis and application of the MCM-41 and SBA-15 as matrices for in vitro efavirenz release study [Internet]. Journal of Drug Delivery Science and Technology. 2016 ; 31 153-159.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.jddst.2015.11.008
Vancouver
Jesus RA, Rabelo AA, Figueiredo RT, Silva LCC da, Codentino IC, Fantini MC de A, Araujo GLB de, Araújo AAS, Mesquita ME. Synthesis and application of the MCM-41 and SBA-15 as matrices for in vitro efavirenz release study [Internet]. Journal of Drug Delivery Science and Technology. 2016 ; 31 153-159.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.jddst.2015.11.008
Artigo de periodico
Design, synthesis and antitrypanosomal activity of some nitrofurazone 1,2,4-triazolic bioisosteric analogues (2016)
Silva, Fredson Torres; Franco, Caio Haddad; Favaro, Denize Cristina; Freitas Junior, Lucio H; Moraes, Carolina B; Ferreira, Elizabeth Igne
Fonte: European Journal of Medicinal Chemistry. Unidade: FCF
Assuntos: DOENÇA DE CHAGAS, HIBRIDIZAÇÃO, COMPOSTOS HETEROCÍCLICOS
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ABNT
SILVA, Fredson Torres et al. Design, synthesis and antitrypanosomal activity of some nitrofurazone 1,2,4-triazolic bioisosteric analogues. European Journal of Medicinal Chemistry, v. 121, p. 553-560, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2016.04.065. Acesso em: 14 nov. 2024.
APA
Silva, F. T., Franco, C. H., Favaro, D. C., Freitas Junior, L. H., Moraes, C. B., & Ferreira, E. I. (2016). Design, synthesis and antitrypanosomal activity of some nitrofurazone 1,2,4-triazolic bioisosteric analogues. European Journal of Medicinal Chemistry, 121, 553-560. doi:10.1016/j.ejmech.2016.04.065
NLM
Silva FT, Franco CH, Favaro DC, Freitas Junior LH, Moraes CB, Ferreira EI. Design, synthesis and antitrypanosomal activity of some nitrofurazone 1,2,4-triazolic bioisosteric analogues [Internet]. European Journal of Medicinal Chemistry. 2016 ; 121 553-560.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.ejmech.2016.04.065
Vancouver
Silva FT, Franco CH, Favaro DC, Freitas Junior LH, Moraes CB, Ferreira EI. Design, synthesis and antitrypanosomal activity of some nitrofurazone 1,2,4-triazolic bioisosteric analogues [Internet]. European Journal of Medicinal Chemistry. 2016 ; 121 553-560.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.ejmech.2016.04.065
Artigo de periodico
Cytotoxic effects of dillapiole on MDA-MB-231 cells involve the induction of apoptosis through the mitochondrial pathway by inducing an oxidative stress while altering the cytoskeleton network (2014)
Ferreira, Adilson Kleber; Sá Júnior, Paulo Luiz de; Pasqualoto, Kerly Fernanda Mesquita; Azevedo, Ricardo Alexandre de; Câmara, Diana Aparecida Dias; Costa, André Santos; Figueiredo, Carlos Rogério; Matsuo, Alisson Leonardo; Massaoka, Mariana Hiromi; Auada, Aline Vivian Vatti; Lebrun, Ivo; Damião, Mariana Celestina Frojuello Costa Bernstorff; Tavares, Maurício Temotheo; Magri, Fatima Maria Motter; Kerkis, Irina; Parise Filho, Roberto
Fonte: Biochimie. Unidade: FCF
Assuntos: CITOESQUELETO, ESTRESSE OXIDATIVO, APOPTOSE
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ABNT
FERREIRA, Adilson Kleber et al. Cytotoxic effects of dillapiole on MDA-MB-231 cells involve the induction of apoptosis through the mitochondrial pathway by inducing an oxidative stress while altering the cytoskeleton network. Biochimie, v. 99, p. 195-207, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.biochi.2013.12.008. Acesso em: 14 nov. 2024.
APA
Ferreira, A. K., Sá Júnior, P. L. de, Pasqualoto, K. F. M., Azevedo, R. A. de, Câmara, D. A. D., Costa, A. S., et al. (2014). Cytotoxic effects of dillapiole on MDA-MB-231 cells involve the induction of apoptosis through the mitochondrial pathway by inducing an oxidative stress while altering the cytoskeleton network. Biochimie, 99, 195-207. doi:10.1016/j.biochi.2013.12.008
NLM
Ferreira AK, Sá Júnior PL de, Pasqualoto KFM, Azevedo RA de, Câmara DAD, Costa AS, Figueiredo CR, Matsuo AL, Massaoka MH, Auada AVV, Lebrun I, Damião MCFCB, Tavares MT, Magri FMM, Kerkis I, Parise Filho R. Cytotoxic effects of dillapiole on MDA-MB-231 cells involve the induction of apoptosis through the mitochondrial pathway by inducing an oxidative stress while altering the cytoskeleton network [Internet]. Biochimie. 2014 ; 99 195-207.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.biochi.2013.12.008
Vancouver
Ferreira AK, Sá Júnior PL de, Pasqualoto KFM, Azevedo RA de, Câmara DAD, Costa AS, Figueiredo CR, Matsuo AL, Massaoka MH, Auada AVV, Lebrun I, Damião MCFCB, Tavares MT, Magri FMM, Kerkis I, Parise Filho R. Cytotoxic effects of dillapiole on MDA-MB-231 cells involve the induction of apoptosis through the mitochondrial pathway by inducing an oxidative stress while altering the cytoskeleton network [Internet]. Biochimie. 2014 ; 99 195-207.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.biochi.2013.12.008
Artigo de periodico
Synthesis, anti-inflammatory activity and molecular docking studies of 2,5-diarylfuran amino acid derivatives (2012)
Stefani, Hélio Alexandre ; Botteselle, Giancarlo Di Vaccari; Zukerman-Schpector, Júlio; Caracelli, Ignez; Corrêa, Denis da Silva; Farsky, Sandra Helena Poliselli ; Machado, Isabel Daufenback; Santin, José Roberto; Hebeda, Cristina Bichels
Fonte: European Journal of Medicinal Chemistry. Unidade: FCF
Assuntos: AMINOÁCIDOS, ANTI-INFLAMATÓRIOS
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ABNT
STEFANI, Hélio Alexandre et al. Synthesis, anti-inflammatory activity and molecular docking studies of 2,5-diarylfuran amino acid derivatives. European Journal of Medicinal Chemistry, v. 47, n. 1, p. 52-58 : + Supplementary materials ( S1-S6), 2012Tradução . . Disponível em: https://doi.org/10.1016/j.ejmech.2011.10.018. Acesso em: 14 nov. 2024.
APA
Stefani, H. A., Botteselle, G. D. V., Zukerman-Schpector, J., Caracelli, I., Corrêa, D. da S., Farsky, S. H. P., et al. (2012). Synthesis, anti-inflammatory activity and molecular docking studies of 2,5-diarylfuran amino acid derivatives. European Journal of Medicinal Chemistry, 47( 1), 52-58 : + Supplementary materials ( S1-S6). doi:10.1016/j.ejmech.2011.10.018
NLM
Stefani HA, Botteselle GDV, Zukerman-Schpector J, Caracelli I, Corrêa D da S, Farsky SHP, Machado ID, Santin JR, Hebeda CB. Synthesis, anti-inflammatory activity and molecular docking studies of 2,5-diarylfuran amino acid derivatives [Internet]. European Journal of Medicinal Chemistry. 2012 ; 47( 1): 52-58 : + Supplementary materials ( S1-S6).[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.ejmech.2011.10.018
Vancouver
Stefani HA, Botteselle GDV, Zukerman-Schpector J, Caracelli I, Corrêa D da S, Farsky SHP, Machado ID, Santin JR, Hebeda CB. Synthesis, anti-inflammatory activity and molecular docking studies of 2,5-diarylfuran amino acid derivatives [Internet]. European Journal of Medicinal Chemistry. 2012 ; 47( 1): 52-58 : + Supplementary materials ( S1-S6).[citado 2024 nov. 14 ] Available from: https://doi.org/10.1016/j.ejmech.2011.10.018
Trabalho de evento-resumo periodico
Smoking cessation pharmacotherapy improves patients adherence and increases the ability to achieve abstinence from cigarette smoking in a brazilian teaching hospital (2012)
Sousa, Altamir Benedito de; Lotufo, João Paulo Becker; Fukuoka, M H; Sakai, Maria Cristina; França, Gustavo Galvão de; Ribeiro, Eliane ; Wasicovichi, N N; Fuchida, C L; Takahashi, Patricia Sayuri Katayose; Souza, Edinalva Tanajura Cruz
Fonte: European Journal of Hospital Pharmacy. Nome do evento: Congress of European Association of Hospital Pharmacists. Unidade: HU
Assunto: TABAGISMO
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ABNT
SOUSA, Altamir Benedito de et al. Smoking cessation pharmacotherapy improves patients adherence and increases the ability to achieve abstinence from cigarette smoking in a brazilian teaching hospital. European Journal of Hospital Pharmacy. Paris: Hospital Universitário, Universidade de São Paulo. . Acesso em: 14 nov. 2024. , 2012
APA
Sousa, A. B. de, Lotufo, J. P. B., Fukuoka, M. H., Sakai, M. C., França, G. G. de, Ribeiro, E., et al. (2012). Smoking cessation pharmacotherapy improves patients adherence and increases the ability to achieve abstinence from cigarette smoking in a brazilian teaching hospital. European Journal of Hospital Pharmacy. Paris: Hospital Universitário, Universidade de São Paulo.
NLM
Sousa AB de, Lotufo JPB, Fukuoka MH, Sakai MC, França GG de, Ribeiro E, Wasicovichi NN, Fuchida CL, Takahashi PSK, Souza ETC. Smoking cessation pharmacotherapy improves patients adherence and increases the ability to achieve abstinence from cigarette smoking in a brazilian teaching hospital. European Journal of Hospital Pharmacy. 2012 ; 19( 2): 220-221 res. CPC005.[citado 2024 nov. 14 ]
Vancouver
Sousa AB de, Lotufo JPB, Fukuoka MH, Sakai MC, França GG de, Ribeiro E, Wasicovichi NN, Fuchida CL, Takahashi PSK, Souza ETC. Smoking cessation pharmacotherapy improves patients adherence and increases the ability to achieve abstinence from cigarette smoking in a brazilian teaching hospital. European Journal of Hospital Pharmacy. 2012 ; 19( 2): 220-221 res. CPC005.[citado 2024 nov. 14 ]
Artigo de periodico
Heat shock proteins (HSP): dermatological implications and perspectives (2012)
Magalhães, Wagner Vidal; Gouveia, Marcelo Fábio; Kaneko, Telma Mary
Fonte: European Journal of Dermatology. Unidade: FCF
Assuntos: FIBROBLASTOS, ESTRESSE OXIDATIVO, EXPRESSÃO GÊNICA
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ABNT
MAGALHÃES, Wagner Vidal e GOUVEIA, Marcelo Fábio e KANEKO, Telma Mary. Heat shock proteins (HSP): dermatological implications and perspectives. European Journal of Dermatology, v. 22, n. 1, p. 8-13, 2012Tradução . . Disponível em: https://doi.org/10.1684/ejd.2011.1530. Acesso em: 14 nov. 2024.
APA
Magalhães, W. V., Gouveia, M. F., & Kaneko, T. M. (2012). Heat shock proteins (HSP): dermatological implications and perspectives. European Journal of Dermatology, 22( 1), 8-13. doi:10.1684/ejd.2011.1530
NLM
Magalhães WV, Gouveia MF, Kaneko TM. Heat shock proteins (HSP): dermatological implications and perspectives [Internet]. European Journal of Dermatology. 2012 ; 22( 1): 8-13.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1684/ejd.2011.1530
Vancouver
Magalhães WV, Gouveia MF, Kaneko TM. Heat shock proteins (HSP): dermatological implications and perspectives [Internet]. European Journal of Dermatology. 2012 ; 22( 1): 8-13.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1684/ejd.2011.1530

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