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Artigo de periodico
Targeting the Plasmodium falciparum Plasmepsin V by ligand-based virtual screening (2018)
Meissner, Kamila Anna ; Kronenberger, Thales ; Maltarollo, Vinícius Gonçalves ; Trossini, Gustavo Henrique Goulart ; Wrenger, Carsten
Fonte: Chemical Biology and Drug Design. Unidades: FCF, ICB
Assuntos: PLASMODIUM FALCIPARUM, PARASITOLOGIA, MALÁRIA, QUIMIOTERAPIA, ENZIMAS PROTEOLITICAS, ATIVAÇÃO ENZIMÁTICA
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MEISSNER, Kamila Anna et al. Targeting the Plasmodium falciparum Plasmepsin V by ligand-based virtual screening. Chemical Biology and Drug Design, v. 2018 p. 1-13, 2018Tradução . . Disponível em: https://doi.org/10.1111/cbdd.13416. Acesso em: 08 nov. 2024.
APA
Meissner, K. A., Kronenberger, T., Maltarollo, V. G., Trossini, G. H. G., & Wrenger, C. (2018). Targeting the Plasmodium falciparum Plasmepsin V by ligand-based virtual screening. Chemical Biology and Drug Design, 2018 p. 1-13. doi:10.1111/cbdd.13416
NLM
Meissner KA, Kronenberger T, Maltarollo VG, Trossini GHG, Wrenger C. Targeting the Plasmodium falciparum Plasmepsin V by ligand-based virtual screening [Internet]. Chemical Biology and Drug Design. 2018 ; 2018 p. 1-13[citado 2024 nov. 08 ] Available from: https://doi.org/10.1111/cbdd.13416
Vancouver
Meissner KA, Kronenberger T, Maltarollo VG, Trossini GHG, Wrenger C. Targeting the Plasmodium falciparum Plasmepsin V by ligand-based virtual screening [Internet]. Chemical Biology and Drug Design. 2018 ; 2018 p. 1-13[citado 2024 nov. 08 ] Available from: https://doi.org/10.1111/cbdd.13416
Artigo de periodico
Cagaita fruit (Eugenia dysenterica DC.) and obesity: role of polyphenols on already established obesity (2018)
Pestana, Carlos Mario Donado; Donado, Priscila Robertina dos Santos; Ramirez, Luis Daniel Daza; Oliveira, Thiago Belchior de; Festuccia, William Tadeu Lara ; Genovese, Maria Inês
Fonte: Food Research International. Unidades: ICB, FCF
Assuntos: CERRADO, OBESIDADE, FRUTAS, COMPOSTOS FENÓLICOS, DISLIPIDEMIAS
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PESTANA, Carlos Mario Donado et al. Cagaita fruit (Eugenia dysenterica DC.) and obesity: role of polyphenols on already established obesity. Food Research International, v. 103, p. 40-47, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.foodres.2017.10.011. Acesso em: 08 nov. 2024.
APA
Pestana, C. M. D., Donado, P. R. dos S., Ramirez, L. D. D., Oliveira, T. B. de, Festuccia, W. T. L., & Genovese, M. I. (2018). Cagaita fruit (Eugenia dysenterica DC.) and obesity: role of polyphenols on already established obesity. Food Research International, 103, 40-47. doi:10.1016/j.foodres.2017.10.011
NLM
Pestana CMD, Donado PR dos S, Ramirez LDD, Oliveira TB de, Festuccia WTL, Genovese MI. Cagaita fruit (Eugenia dysenterica DC.) and obesity: role of polyphenols on already established obesity [Internet]. Food Research International. 2018 ; 103 40-47.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1016/j.foodres.2017.10.011
Vancouver
Pestana CMD, Donado PR dos S, Ramirez LDD, Oliveira TB de, Festuccia WTL, Genovese MI. Cagaita fruit (Eugenia dysenterica DC.) and obesity: role of polyphenols on already established obesity [Internet]. Food Research International. 2018 ; 103 40-47.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1016/j.foodres.2017.10.011
Artigo de periodico
Alkaline pH promotes NADPH oxidase-independent neutrophil extracellular trap formation: a matter of mitochondrial reactive oxygen species generation and citrullination and cleavage of histone (2018)
Souza, Cristiane Naffah; Breda, Leandro Carvalho Dantas; Khan, Meraj A.; Sweezey, Neil; Palaniyar, Nades; Câmara, Niels Olsen Saraiva ; Almeida, Sandro Rogério de
Fonte: Frontiers in Immunology. Unidades: FCF, ICB
Assuntos: CÁLCIO, PROTEÍNAS, CROMATINA, MITOCÔNDRIAS, NEUTRÓFILOS, WESTERN BLOTTING, HIDROGÊNIO
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SOUZA, Cristiane Naffah et al. Alkaline pH promotes NADPH oxidase-independent neutrophil extracellular trap formation: a matter of mitochondrial reactive oxygen species generation and citrullination and cleavage of histone. Frontiers in Immunology, v. 8, p. 1-15, 2018Tradução . . Disponível em: https://doi.org/10.3389/fimmu.2017.01849. Acesso em: 08 nov. 2024.
APA
Souza, C. N., Breda, L. C. D., Khan, M. A., Sweezey, N., Palaniyar, N., Câmara, N. O. S., & Almeida, S. R. de. (2018). Alkaline pH promotes NADPH oxidase-independent neutrophil extracellular trap formation: a matter of mitochondrial reactive oxygen species generation and citrullination and cleavage of histone. Frontiers in Immunology, 8, 1-15. doi:10.3389/fimmu.2017.01849
NLM
Souza CN, Breda LCD, Khan MA, Sweezey N, Palaniyar N, Câmara NOS, Almeida SR de. Alkaline pH promotes NADPH oxidase-independent neutrophil extracellular trap formation: a matter of mitochondrial reactive oxygen species generation and citrullination and cleavage of histone [Internet]. Frontiers in Immunology. 2018 ; 8 1-15.[citado 2024 nov. 08 ] Available from: https://doi.org/10.3389/fimmu.2017.01849
Vancouver
Souza CN, Breda LCD, Khan MA, Sweezey N, Palaniyar N, Câmara NOS, Almeida SR de. Alkaline pH promotes NADPH oxidase-independent neutrophil extracellular trap formation: a matter of mitochondrial reactive oxygen species generation and citrullination and cleavage of histone [Internet]. Frontiers in Immunology. 2018 ; 8 1-15.[citado 2024 nov. 08 ] Available from: https://doi.org/10.3389/fimmu.2017.01849
Artigo de periodico
Down-regulation of 14q32-encoded miRNAs and tumor suppressorrole for miR-654-3p in papillary thyroid cancer (2017)
Geraldo, Murilo Vieira; Nakaya, Helder Takashi Imoto ; Kimura, Edna Teruko
Fonte: Oncotarget. Unidades: FCF, ICB
Assunto: HISTOLOGIA
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GERALDO, Murilo Vieira e NAKAYA, Helder Takashi Imoto e KIMURA, Edna Teruko. Down-regulation of 14q32-encoded miRNAs and tumor suppressorrole for miR-654-3p in papillary thyroid cancer. Oncotarget, v. 8, n. 6, p. 9597-9607, 2017Tradução . . Disponível em: https://doi.org/10.18632/oncotarget.14162. Acesso em: 08 nov. 2024.
APA
Geraldo, M. V., Nakaya, H. T. I., & Kimura, E. T. (2017). Down-regulation of 14q32-encoded miRNAs and tumor suppressorrole for miR-654-3p in papillary thyroid cancer. Oncotarget, 8( 6), 9597-9607. doi:10.18632/oncotarget.14162
NLM
Geraldo MV, Nakaya HTI, Kimura ET. Down-regulation of 14q32-encoded miRNAs and tumor suppressorrole for miR-654-3p in papillary thyroid cancer [Internet]. Oncotarget. 2017 ; 8( 6): 9597-9607.[citado 2024 nov. 08 ] Available from: https://doi.org/10.18632/oncotarget.14162
Vancouver
Geraldo MV, Nakaya HTI, Kimura ET. Down-regulation of 14q32-encoded miRNAs and tumor suppressorrole for miR-654-3p in papillary thyroid cancer [Internet]. Oncotarget. 2017 ; 8( 6): 9597-9607.[citado 2024 nov. 08 ] Available from: https://doi.org/10.18632/oncotarget.14162
Artigo de periodico
Changed epidemiology during intra and interhospital spread of high-risk clones of vanA-containing Enterococcus in Brazilian hospitals (2017)
Sacramento, Andrey G.; Zanella, Rosemeire C.; Esposito, Fernanda; Costa, Emanuela Avelar Silva; Almeida, Lara Mendes de; Pires, Carlos; Brito, Artemir Coelho de; Mamizuka, Elsa Masae; Cerdeira, Louise Teixeira; Lincopan, Nilton
Fonte: Diagnostic Microbiology and Infectious Disease. Unidades: ICB, FCF
Assuntos: MICROBIOLOGIA, ENTEROCOCCUS, CLONAGEM, HOSPITAIS, SURTOS DE DOENÇAS, INFECÇÕES BACTERIANAS GRAM-POSITIVAS, RESISTÊNCIA MICROBIANA ÀS DROGAS, ANTIBIÓTICOS
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SACRAMENTO, Andrey G. et al. Changed epidemiology during intra and interhospital spread of high-risk clones of vanA-containing Enterococcus in Brazilian hospitals. Diagnostic Microbiology and Infectious Disease, v. 88, n. 4, p. 348-351, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.diagmicrobio.2017.05.008. Acesso em: 08 nov. 2024.
APA
Sacramento, A. G., Zanella, R. C., Esposito, F., Costa, E. A. S., Almeida, L. M. de, Pires, C., et al. (2017). Changed epidemiology during intra and interhospital spread of high-risk clones of vanA-containing Enterococcus in Brazilian hospitals. Diagnostic Microbiology and Infectious Disease, 88( 4), 348-351. doi:10.1016/j.diagmicrobio.2017.05.008
NLM
Sacramento AG, Zanella RC, Esposito F, Costa EAS, Almeida LM de, Pires C, Brito AC de, Mamizuka EM, Cerdeira LT, Lincopan N. Changed epidemiology during intra and interhospital spread of high-risk clones of vanA-containing Enterococcus in Brazilian hospitals [Internet]. Diagnostic Microbiology and Infectious Disease. 2017 ; 88( 4): 348-351.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1016/j.diagmicrobio.2017.05.008
Vancouver
Sacramento AG, Zanella RC, Esposito F, Costa EAS, Almeida LM de, Pires C, Brito AC de, Mamizuka EM, Cerdeira LT, Lincopan N. Changed epidemiology during intra and interhospital spread of high-risk clones of vanA-containing Enterococcus in Brazilian hospitals [Internet]. Diagnostic Microbiology and Infectious Disease. 2017 ; 88( 4): 348-351.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1016/j.diagmicrobio.2017.05.008
Artigo de periodico
Co-encapsulation of paclitaxel and C6 ceramide in tributyrin-containing nanocarriers improve co-localization in the skin and potentiate cytotoxic effects in 2D and 3D models (2017)
Carvalho, Vanessa F. M; Migotto, Amanda; Giacone, Daniela V; Lemos, Débora P. de; Zanoni, Thalita B; Maria-Engler, Silvya Stuchi ; Costa-Lotufo, Letícia Veras ; Lopes, Luciana Biagini
Fonte: European Journal of Pharmaceutical Sciences. Unidades: FCF, ICB
Assuntos: PELE, MELANOMA
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CARVALHO, Vanessa F. M et al. Co-encapsulation of paclitaxel and C6 ceramide in tributyrin-containing nanocarriers improve co-localization in the skin and potentiate cytotoxic effects in 2D and 3D models. European Journal of Pharmaceutical Sciences, v. 109, p. 131-143, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.ejps.2017.07.023. Acesso em: 08 nov. 2024.
APA
Carvalho, V. F. M., Migotto, A., Giacone, D. V., Lemos, D. P. de, Zanoni, T. B., Maria-Engler, S. S., et al. (2017). Co-encapsulation of paclitaxel and C6 ceramide in tributyrin-containing nanocarriers improve co-localization in the skin and potentiate cytotoxic effects in 2D and 3D models. European Journal of Pharmaceutical Sciences, 109, 131-143. doi:10.1016/j.ejps.2017.07.023
NLM
Carvalho VFM, Migotto A, Giacone DV, Lemos DP de, Zanoni TB, Maria-Engler SS, Costa-Lotufo LV, Lopes LB. Co-encapsulation of paclitaxel and C6 ceramide in tributyrin-containing nanocarriers improve co-localization in the skin and potentiate cytotoxic effects in 2D and 3D models [Internet]. European Journal of Pharmaceutical Sciences. 2017 ; 109 131-143.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1016/j.ejps.2017.07.023
Vancouver
Carvalho VFM, Migotto A, Giacone DV, Lemos DP de, Zanoni TB, Maria-Engler SS, Costa-Lotufo LV, Lopes LB. Co-encapsulation of paclitaxel and C6 ceramide in tributyrin-containing nanocarriers improve co-localization in the skin and potentiate cytotoxic effects in 2D and 3D models [Internet]. European Journal of Pharmaceutical Sciences. 2017 ; 109 131-143.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1016/j.ejps.2017.07.023
Artigo de periodico
Recombinant BCG expressing LTAK63 adjuvant induces superior protection against Mycobacterium tuberculosis (2017)
Nascimento, Ivan Pereira; Rodriguez, Dúnia; Santos, Carina Carvalho dos; Amaral, Eduardo Pinheiro; Rofatto, Henrique Krambeck; Junqueira-Kipnis, Ana Paula; Gonçalves, Eduardo Dantas Casillo; Lima, Maria Regina D'Império ; Hirata, Mario Hiroyuki ; Silva, Célio Lopes; Winter, Nathalie; Gicquel, Brigitte; Mills, Kingston H G; Pizza, Mariagrazia; Rappuoli, Rino; Leite, Luciana C. C
Fonte: Scientific Reports. Unidades: ICB, FCF, FMRP
Assuntos: IMUNOLOGIA, TUBERCULOSE, MYCOBACTERIUM TUBERCULOSIS, ADJUVANTES IMUNOLÓGICOS, PROTEÍNAS RECOMBINANTES, VACINAS, CITOCININAS, CAMUNDONGOS
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NASCIMENTO, Ivan Pereira et al. Recombinant BCG expressing LTAK63 adjuvant induces superior protection against Mycobacterium tuberculosis. Scientific Reports, v. 7, n. 1, p. 1-11, 2017Tradução . . Disponível em: https://doi.org/10.1038/s41598-017-02003-9. Acesso em: 08 nov. 2024.
APA
Nascimento, I. P., Rodriguez, D., Santos, C. C. dos, Amaral, E. P., Rofatto, H. K., Junqueira-Kipnis, A. P., et al. (2017). Recombinant BCG expressing LTAK63 adjuvant induces superior protection against Mycobacterium tuberculosis. Scientific Reports, 7( 1), 1-11. doi:10.1038/s41598-017-02003-9
NLM
Nascimento IP, Rodriguez D, Santos CC dos, Amaral EP, Rofatto HK, Junqueira-Kipnis AP, Gonçalves EDC, Lima MRD'I, Hirata MH, Silva CL, Winter N, Gicquel B, Mills KHG, Pizza M, Rappuoli R, Leite LCC. Recombinant BCG expressing LTAK63 adjuvant induces superior protection against Mycobacterium tuberculosis [Internet]. Scientific Reports. 2017 ; 7( 1): 1-11.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1038/s41598-017-02003-9
Vancouver
Nascimento IP, Rodriguez D, Santos CC dos, Amaral EP, Rofatto HK, Junqueira-Kipnis AP, Gonçalves EDC, Lima MRD'I, Hirata MH, Silva CL, Winter N, Gicquel B, Mills KHG, Pizza M, Rappuoli R, Leite LCC. Recombinant BCG expressing LTAK63 adjuvant induces superior protection against Mycobacterium tuberculosis [Internet]. Scientific Reports. 2017 ; 7( 1): 1-11.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1038/s41598-017-02003-9
Artigo de periodico
4-Nerolidylcatechol induces autophagy in human glioblastoma cells (2017)
Massaro, Renato Ramos; Brohem, Carla Abdo; Almeida, Rebeca Leite de; Rivelli, Diogo Pineda; Miyake, Juliano Andreoli; Colquhoun, Alison ; Barros, Silvia Berlanga de Moraes ; Maria-Engler, Silvya Stuchi
Fonte: Brazilian Journal of Pharmaceutical Sciences. Unidades: ICB, FCF
Assunto: HISTOLOGIA
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ABNT
MASSARO, Renato Ramos et al. 4-Nerolidylcatechol induces autophagy in human glioblastoma cells. Brazilian Journal of Pharmaceutical Sciences, v. 53, n. 3, p. 1-10, 2017Tradução . . Disponível em: https://doi.org/10.1590/s2175-97902017000300169. Acesso em: 08 nov. 2024.
APA
Massaro, R. R., Brohem, C. A., Almeida, R. L. de, Rivelli, D. P., Miyake, J. A., Colquhoun, A., et al. (2017). 4-Nerolidylcatechol induces autophagy in human glioblastoma cells. Brazilian Journal of Pharmaceutical Sciences, 53( 3), 1-10. doi:10.1590/s2175-97902017000300169
NLM
Massaro RR, Brohem CA, Almeida RL de, Rivelli DP, Miyake JA, Colquhoun A, Barros SB de M, Maria-Engler SS. 4-Nerolidylcatechol induces autophagy in human glioblastoma cells [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2017 ; 53( 3): 1-10.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1590/s2175-97902017000300169
Vancouver
Massaro RR, Brohem CA, Almeida RL de, Rivelli DP, Miyake JA, Colquhoun A, Barros SB de M, Maria-Engler SS. 4-Nerolidylcatechol induces autophagy in human glioblastoma cells [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2017 ; 53( 3): 1-10.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1590/s2175-97902017000300169
Artigo de periodico
Influence of CYP3A4 and CYP3A5 polymorphisms on tacrolimus and sirolimus exposure in stable kidney transplant recipients (2017)
Tamashiro, Erika Yumi; Felipe, Claudia R; Genvigir, Fabiana Dalla Vecchia ; Rodrigues, Alice Cristina ; Campos, Antony B.; Hirata, Rosario Dominguez Crespo ; Silva Junior, Helio Tedesco; Pestana, José O. Medina
Fonte: Drug Metabolism Personalized Theraphy. Unidade: FCF
Assuntos: POLIMORFISMO, TRANSPLANTE DE RIM
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TAMASHIRO, Erika Yumi et al. Influence of CYP3A4 and CYP3A5 polymorphisms on tacrolimus and sirolimus exposure in stable kidney transplant recipients. Drug Metabolism Personalized Theraphy, v. 32, n. 2, p. 89-95, 2017Tradução . . Disponível em: https://doi.org/10.1515/dmpt-2016-0036. Acesso em: 08 nov. 2024.
APA
Tamashiro, E. Y., Felipe, C. R., Genvigir, F. D. V., Rodrigues, A. C., Campos, A. B., Hirata, R. D. C., et al. (2017). Influence of CYP3A4 and CYP3A5 polymorphisms on tacrolimus and sirolimus exposure in stable kidney transplant recipients. Drug Metabolism Personalized Theraphy, 32( 2), 89-95. doi:10.1515/dmpt-2016-0036
NLM
Tamashiro EY, Felipe CR, Genvigir FDV, Rodrigues AC, Campos AB, Hirata RDC, Silva Junior HT, Pestana JOM. Influence of CYP3A4 and CYP3A5 polymorphisms on tacrolimus and sirolimus exposure in stable kidney transplant recipients [Internet]. Drug Metabolism Personalized Theraphy. 2017 ; 32( 2): 89-95.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1515/dmpt-2016-0036
Vancouver
Tamashiro EY, Felipe CR, Genvigir FDV, Rodrigues AC, Campos AB, Hirata RDC, Silva Junior HT, Pestana JOM. Influence of CYP3A4 and CYP3A5 polymorphisms on tacrolimus and sirolimus exposure in stable kidney transplant recipients [Internet]. Drug Metabolism Personalized Theraphy. 2017 ; 32( 2): 89-95.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1515/dmpt-2016-0036
Artigo de periodico
The aggravation of arthritis by periodontitis is dependent of IL-17receptor A activation (2017)
Aquino, Sabrina G. de ; Talbot, Jhimmy; Sônego, Fabiane; Turato, Walter Miguel; Grespan, Renata; Campos, Mario Julio Avila; Cunha, Fernando de Queiroz; Cirelli, Joni Augusto
Fonte: Journal of Clinical Periodontology. Unidades: ICB, FCF, FMRP
Assuntos: MICROBIOLOGIA, PERIODONTITE AGRESSIVA, PORPHYROMONAS GINGIVALIS, ARTRITE REUMATOIDE, DOENÇAS PERIODONTAIS, RATOS, NEUTRÓFILOS
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AQUINO, Sabrina G. de et al. The aggravation of arthritis by periodontitis is dependent of IL-17receptor A activation. Journal of Clinical Periodontology, v. 44, n. 9, p. 881-891, 2017Tradução . . Disponível em: https://doi.org/10.1111/jcpe.1274. Acesso em: 08 nov. 2024.
APA
Aquino, S. G. de, Talbot, J., Sônego, F., Turato, W. M., Grespan, R., Campos, M. J. A., et al. (2017). The aggravation of arthritis by periodontitis is dependent of IL-17receptor A activation. Journal of Clinical Periodontology, 44( 9), 881-891. doi:10.1111/jcpe.1274
NLM
Aquino SG de, Talbot J, Sônego F, Turato WM, Grespan R, Campos MJA, Cunha F de Q, Cirelli JA. The aggravation of arthritis by periodontitis is dependent of IL-17receptor A activation [Internet]. Journal of Clinical Periodontology. 2017 ; 44( 9): 881-891.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1111/jcpe.1274
Vancouver
Aquino SG de, Talbot J, Sônego F, Turato WM, Grespan R, Campos MJA, Cunha F de Q, Cirelli JA. The aggravation of arthritis by periodontitis is dependent of IL-17receptor A activation [Internet]. Journal of Clinical Periodontology. 2017 ; 44( 9): 881-891.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1111/jcpe.1274
Artigo de periodico
TLR4-mediated placental pathology and pregnancy outcome in experimental malaria (2017)
Barboza, Renato ; Lima, Flávia Afonso ; Reis, Aramys Silva dos ; Murillo, Oscar Javier ; Peixoto, Erika Paula Machado ; Bandeira, Carla Letícia dos Santos ; Fotoran, Wesley Luzetti; Sardinha, Luiz Roberto ; Wunderlich, Gerhard ; Bevilacqua, Estela Maris Andrade Forell ; Lima, Maria Regina D'Império ; Alvarez, José Maria; Costa, Fabio Trindade Maranhão ; Gonçalves, Ligia Antunes ; Epiphanio, Sabrina ; Marinho, Claudio Romero Farias
Fonte: Scientific Reports. Unidades: ICB, FCF
Assuntos: GRAVIDEZ, MALÁRIA, PLACENTA
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ABNT
BARBOZA, Renato et al. TLR4-mediated placental pathology and pregnancy outcome in experimental malaria. Scientific Reports, v. 7, p. 1-12 art. 8623, 2017Tradução . . Disponível em: https://doi.org/10.1038/s41598-017-08299-x. Acesso em: 08 nov. 2024.
APA
Barboza, R., Lima, F. A., Reis, A. S. dos, Murillo, O. J., Peixoto, E. P. M., Bandeira, C. L. dos S., et al. (2017). TLR4-mediated placental pathology and pregnancy outcome in experimental malaria. Scientific Reports, 7, 1-12 art. 8623. doi:10.1038/s41598-017-08299-x
NLM
Barboza R, Lima FA, Reis AS dos, Murillo OJ, Peixoto EPM, Bandeira CL dos S, Fotoran WL, Sardinha LR, Wunderlich G, Bevilacqua EMAF, Lima MRD'I, Alvarez JM, Costa FTM, Gonçalves LA, Epiphanio S, Marinho CRF. TLR4-mediated placental pathology and pregnancy outcome in experimental malaria [Internet]. Scientific Reports. 2017 ; 7 1-12 art. 8623.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1038/s41598-017-08299-x
Vancouver
Barboza R, Lima FA, Reis AS dos, Murillo OJ, Peixoto EPM, Bandeira CL dos S, Fotoran WL, Sardinha LR, Wunderlich G, Bevilacqua EMAF, Lima MRD'I, Alvarez JM, Costa FTM, Gonçalves LA, Epiphanio S, Marinho CRF. TLR4-mediated placental pathology and pregnancy outcome in experimental malaria [Internet]. Scientific Reports. 2017 ; 7 1-12 art. 8623.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1038/s41598-017-08299-x
Artigo de periodico
Combination of a high-fat diet with sweetened condensed milk exacerbates inflammation and insulin resistance induced by each separately in mice (2017)
Masi, Laureane Nunes; Martins, Amanda Roque; Crisma, Amanda Rabello; Amaral, Cátia Lira do; Davanso, Mariana Rodrigues; Serdan, Tamires Duarte Afonso; Sá, Roberta Dourado Cavalcante da Cunha de; Cruz, Maysa Mariana; Alonso-Vale, Maria Isabel Cardoso; Torres, Rosângela Pavan; Mancini-Filho, Jorge ; Pereira, Joice Naiara Bertaglia; Righetti, Marta Maria da Silva; Liberti, Edson Aparecido; Hirabara, Sandro Massao; Curi, Rui
Fonte: Scientific Reports. Unidades: ICB, FCF
Assunto: ANATOMIA
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ABNT
MASI, Laureane Nunes et al. Combination of a high-fat diet with sweetened condensed milk exacerbates inflammation and insulin resistance induced by each separately in mice. Scientific Reports, v. 7, n. 1, p. 1-10, 2017Tradução . . Disponível em: https://doi.org/10.1038/s41598-017-04308-1. Acesso em: 08 nov. 2024.
APA
Masi, L. N., Martins, A. R., Crisma, A. R., Amaral, C. L. do, Davanso, M. R., Serdan, T. D. A., et al. (2017). Combination of a high-fat diet with sweetened condensed milk exacerbates inflammation and insulin resistance induced by each separately in mice. Scientific Reports, 7( 1), 1-10. doi:10.1038/s41598-017-04308-1
NLM
Masi LN, Martins AR, Crisma AR, Amaral CL do, Davanso MR, Serdan TDA, Sá RDC da C de, Cruz MM, Alonso-Vale MIC, Torres RP, Mancini-Filho J, Pereira JNB, Righetti MM da S, Liberti EA, Hirabara SM, Curi R. Combination of a high-fat diet with sweetened condensed milk exacerbates inflammation and insulin resistance induced by each separately in mice [Internet]. Scientific Reports. 2017 ; 7( 1): 1-10.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1038/s41598-017-04308-1
Vancouver
Masi LN, Martins AR, Crisma AR, Amaral CL do, Davanso MR, Serdan TDA, Sá RDC da C de, Cruz MM, Alonso-Vale MIC, Torres RP, Mancini-Filho J, Pereira JNB, Righetti MM da S, Liberti EA, Hirabara SM, Curi R. Combination of a high-fat diet with sweetened condensed milk exacerbates inflammation and insulin resistance induced by each separately in mice [Internet]. Scientific Reports. 2017 ; 7( 1): 1-10.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1038/s41598-017-04308-1
Artigo de periodico
The presence of T cell epitopes is important for induction of antibody responses against antigens directed to DEC205+ dendritic cells (2016)
Amorim, Kelly N. S.; Rampazo, Eline V.; Antonialli, Renan; Yamamoto, Marcio Massao; Rodrigues, Mauricio M.; Soares, Irene da Silva ; Boscardin, Silvia Beatriz
Fonte: Scientific Reports. Unidades: ICB, FCF
Assuntos: PARASITOLOGIA, CÉLULAS DENDRÍTICAS, PLASMODIUM, EPITOPOS, ANTICORPOS MONOCLONAIS
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ABNT
AMORIM, Kelly N. S. et al. The presence of T cell epitopes is important for induction of antibody responses against antigens directed to DEC205+ dendritic cells. Scientific Reports, v. 6, p. 1-15, 2016Tradução . . Disponível em: https://doi.org/10.1038/srep39250. Acesso em: 08 nov. 2024.
APA
Amorim, K. N. S., Rampazo, E. V., Antonialli, R., Yamamoto, M. M., Rodrigues, M. M., Soares, I. da S., & Boscardin, S. B. (2016). The presence of T cell epitopes is important for induction of antibody responses against antigens directed to DEC205+ dendritic cells. Scientific Reports, 6, 1-15. doi:10.1038/srep39250
NLM
Amorim KNS, Rampazo EV, Antonialli R, Yamamoto MM, Rodrigues MM, Soares I da S, Boscardin SB. The presence of T cell epitopes is important for induction of antibody responses against antigens directed to DEC205+ dendritic cells [Internet]. Scientific Reports. 2016 ; 6 1-15.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1038/srep39250
Vancouver
Amorim KNS, Rampazo EV, Antonialli R, Yamamoto MM, Rodrigues MM, Soares I da S, Boscardin SB. The presence of T cell epitopes is important for induction of antibody responses against antigens directed to DEC205+ dendritic cells [Internet]. Scientific Reports. 2016 ; 6 1-15.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1038/srep39250
Artigo de periodico
Beneficial effects of vitamin C treatment on pregnant rats exposed to formaldehyde: Reversal of immunosuppression in the offspring (2016)
Ibrahim, Beatriz Silva; Barioni, Eric Diego; Heluany, Cíntia Scucuglia; Braga, Tárcio Teodoro; Drewes, Carine Cristiane; Costa, Silvia Goes; Câmara, Niels Olsen Saraiva ; Farsky, Sandra Helena Poliselli ; Franco, Adriana Lino dos Santos
Fonte: Toxicology and Applied Pharmacology. Unidades: ICB, FCF
Assuntos: ESTRESSE OXIDATIVO, INFLAMAÇÃO, IMUNOSSUPRESSÃO, IMUNOLOGIA
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ABNT
IBRAHIM, Beatriz Silva et al. Beneficial effects of vitamin C treatment on pregnant rats exposed to formaldehyde: Reversal of immunosuppression in the offspring. Toxicology and Applied Pharmacology, v. 300, p. 77-81, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.taap.2016.03.010. Acesso em: 08 nov. 2024.
APA
Ibrahim, B. S., Barioni, E. D., Heluany, C. S., Braga, T. T., Drewes, C. C., Costa, S. G., et al. (2016). Beneficial effects of vitamin C treatment on pregnant rats exposed to formaldehyde: Reversal of immunosuppression in the offspring. Toxicology and Applied Pharmacology, 300, 77-81. doi:10.1016/j.taap.2016.03.010
NLM
Ibrahim BS, Barioni ED, Heluany CS, Braga TT, Drewes CC, Costa SG, Câmara NOS, Farsky SHP, Franco AL dos S. Beneficial effects of vitamin C treatment on pregnant rats exposed to formaldehyde: Reversal of immunosuppression in the offspring [Internet]. Toxicology and Applied Pharmacology. 2016 ; 300 77-81.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1016/j.taap.2016.03.010
Vancouver
Ibrahim BS, Barioni ED, Heluany CS, Braga TT, Drewes CC, Costa SG, Câmara NOS, Farsky SHP, Franco AL dos S. Beneficial effects of vitamin C treatment on pregnant rats exposed to formaldehyde: Reversal of immunosuppression in the offspring [Internet]. Toxicology and Applied Pharmacology. 2016 ; 300 77-81.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1016/j.taap.2016.03.010
Artigo de periodico
Oral administration of linoleic acid induces new vessel formation and improves skin wound healing in diabetic rats (2016)
Rodrigues, Hosana Gomes; Vinolo, Marco Aurélio Ramirez; Sato, Fabio Takeo; Magdalon, Juliana; Kuhl, Carolina Meneguetti Cintra; Yamagata, Ana Sayuri; Pessoa, Ana Flávia Marçal; Moraes, Gabriélla Malheiros; Santos, Marinilce Fagundes dos ; Lima, Camila; Farsky, Sandra Helena Poliselli ; Câmara, Niels Olsen Saraiva ; Williner, Maria Rosa; Bernal, Claudio Adrián; Calder,Philip C; Curi, Rui
Fonte: PLOS ONE. Unidades: ICB, FCF
Assuntos: ÁCIDO LINOLEICO, RATOS, CICATRIZAÇÃO
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ABNT
RODRIGUES, Hosana Gomes et al. Oral administration of linoleic acid induces new vessel formation and improves skin wound healing in diabetic rats. PLOS ONE, v. 11, n. 10, p. e0165115, 2016Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0165115. Acesso em: 08 nov. 2024.
APA
Rodrigues, H. G., Vinolo, M. A. R., Sato, F. T., Magdalon, J., Kuhl, C. M. C., Yamagata, A. S., et al. (2016). Oral administration of linoleic acid induces new vessel formation and improves skin wound healing in diabetic rats. PLOS ONE, 11( 10), e0165115. doi:10.1371/journal.pone.0165115
NLM
Rodrigues HG, Vinolo MAR, Sato FT, Magdalon J, Kuhl CMC, Yamagata AS, Pessoa AFM, Moraes GM, Santos MF dos, Lima C, Farsky SHP, Câmara NOS, Williner MR, Bernal CA, Calder PC, Curi R. Oral administration of linoleic acid induces new vessel formation and improves skin wound healing in diabetic rats [Internet]. PLOS ONE. 2016 ; 11( 10): e0165115.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1371/journal.pone.0165115
Vancouver
Rodrigues HG, Vinolo MAR, Sato FT, Magdalon J, Kuhl CMC, Yamagata AS, Pessoa AFM, Moraes GM, Santos MF dos, Lima C, Farsky SHP, Câmara NOS, Williner MR, Bernal CA, Calder PC, Curi R. Oral administration of linoleic acid induces new vessel formation and improves skin wound healing in diabetic rats [Internet]. PLOS ONE. 2016 ; 11( 10): e0165115.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1371/journal.pone.0165115
Artigo de periodico
BFD-22 a new potential inhibitor of BRAF inhibits the metastasis of B16F10 melanoma cells and simultaneously increased the tumor immunogenicity (2016)
Ferreira, Adilson Kleber; Pasqualoto, Kerly Fernanda Mesquita; Kruyt, Frank A. E; Berl, Fanny Palace; Azevedo, Ricardo Alexandre de; Turra, Kely Medeiros; Rodrigues, Cecília Pessoa; Ferreira, Ana Carolina Franco; Salomon, Maria Alejandra Clavijo; Sá Júnior, Paulo Luiz de; Farias, Camyla Fernandes; Figueiredo, Carlos Rogério; Tavares, Leoberto Costa ; Barbuto, José Alexandre Marzagão ; Jorge, Salomão Dória
Fonte: Toxicology and Applied Pharmacology. Unidades: FCF, ICB
Assuntos: MELANOMA, METÁSTASE NEOPLÁSICA, APOPTOSE
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ABNT
FERREIRA, Adilson Kleber et al. BFD-22 a new potential inhibitor of BRAF inhibits the metastasis of B16F10 melanoma cells and simultaneously increased the tumor immunogenicity. Toxicology and Applied Pharmacology, v. 295, p. 56-67, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.taap.2016.02.008. Acesso em: 08 nov. 2024.
APA
Ferreira, A. K., Pasqualoto, K. F. M., Kruyt, F. A. E., Berl, F. P., Azevedo, R. A. de, Turra, K. M., et al. (2016). BFD-22 a new potential inhibitor of BRAF inhibits the metastasis of B16F10 melanoma cells and simultaneously increased the tumor immunogenicity. Toxicology and Applied Pharmacology, 295, 56-67. doi:10.1016/j.taap.2016.02.008
NLM
Ferreira AK, Pasqualoto KFM, Kruyt FAE, Berl FP, Azevedo RA de, Turra KM, Rodrigues CP, Ferreira ACF, Salomon MAC, Sá Júnior PL de, Farias CF, Figueiredo CR, Tavares LC, Barbuto JAM, Jorge SD. BFD-22 a new potential inhibitor of BRAF inhibits the metastasis of B16F10 melanoma cells and simultaneously increased the tumor immunogenicity [Internet]. Toxicology and Applied Pharmacology. 2016 ; 295 56-67.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1016/j.taap.2016.02.008
Vancouver
Ferreira AK, Pasqualoto KFM, Kruyt FAE, Berl FP, Azevedo RA de, Turra KM, Rodrigues CP, Ferreira ACF, Salomon MAC, Sá Júnior PL de, Farias CF, Figueiredo CR, Tavares LC, Barbuto JAM, Jorge SD. BFD-22 a new potential inhibitor of BRAF inhibits the metastasis of B16F10 melanoma cells and simultaneously increased the tumor immunogenicity [Internet]. Toxicology and Applied Pharmacology. 2016 ; 295 56-67.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1016/j.taap.2016.02.008
Artigo de periodico
Molecular mechanisms of membrane impermeability in clinical isolates of Enterobacteriaceae exposed to imipenem selective pressure (2016)
Pavez, Mónica; Vieira, Camila; Araújo, Maria Rita de; Cerda, Alvaro; Almeida, Lara Mendes de; Lincopan, Nilton ; Mamizuka, Elsa Masae
Fonte: International Journal of Antimicrobial Agents. Unidades: FCF, ICB
Assuntos: ENTEROBACTERIACEAE, RESISTÊNCIA MICROBIANA ÀS DROGAS
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ABNT
PAVEZ, Mónica et al. Molecular mechanisms of membrane impermeability in clinical isolates of Enterobacteriaceae exposed to imipenem selective pressure. International Journal of Antimicrobial Agents, v. 48, n. 1, p. 78-85, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.ijantimicag.2016.04.016. Acesso em: 08 nov. 2024.
APA
Pavez, M., Vieira, C., Araújo, M. R. de, Cerda, A., Almeida, L. M. de, Lincopan, N., & Mamizuka, E. M. (2016). Molecular mechanisms of membrane impermeability in clinical isolates of Enterobacteriaceae exposed to imipenem selective pressure. International Journal of Antimicrobial Agents, 48( 1), 78-85. doi:10.1016/j.ijantimicag.2016.04.016
NLM
Pavez M, Vieira C, Araújo MR de, Cerda A, Almeida LM de, Lincopan N, Mamizuka EM. Molecular mechanisms of membrane impermeability in clinical isolates of Enterobacteriaceae exposed to imipenem selective pressure [Internet]. International Journal of Antimicrobial Agents. 2016 ; 48( 1): 78-85.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1016/j.ijantimicag.2016.04.016
Vancouver
Pavez M, Vieira C, Araújo MR de, Cerda A, Almeida LM de, Lincopan N, Mamizuka EM. Molecular mechanisms of membrane impermeability in clinical isolates of Enterobacteriaceae exposed to imipenem selective pressure [Internet]. International Journal of Antimicrobial Agents. 2016 ; 48( 1): 78-85.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1016/j.ijantimicag.2016.04.016
Artigo de periodico
First Report of the Globally Disseminated IncX4 Plasmid Carrying the mcr-1 Gene in a Colistin-Resistant Escherichia coli Sequence Type 101 Isolate from a Human Infection in Brazil (2016)
Fernandes, Miriam Rodriguez; McCulloch, John Anthony; Vianello, Marco Aurélio; Silva, Quézia Moura da; Chaparro, Paula Juliana Pérez; Esposito, Fernanda Ribeiro dos Santos; Sartori, Luciana; Dropa, Milena; Matté, Maria Helena; Lira, Débora P. A; Mamizuka, Elsa Masae; Lincopan, Nilton
Fonte: Antimicrobial Agents and Chemotherapy. Unidades: FSP, FCF, ICB
Assuntos: PLASMÍDEOS, ESCHERICHIA COLI, INFECÇÕES BACTERIANAS, GENÉTICA, SAÚDE PÚBLICA
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ABNT
FERNANDES, Miriam Rodriguez et al. First Report of the Globally Disseminated IncX4 Plasmid Carrying the mcr-1 Gene in a Colistin-Resistant Escherichia coli Sequence Type 101 Isolate from a Human Infection in Brazil. Antimicrobial Agents and Chemotherapy, v. 60, n. 10, p. 6415-6417, 2016Tradução . . Disponível em: https://doi.org/10.1128/AAC.01325-16. Acesso em: 08 nov. 2024.
APA
Fernandes, M. R., McCulloch, J. A., Vianello, M. A., Silva, Q. M. da, Chaparro, P. J. P., Esposito, F. R. dos S., et al. (2016). First Report of the Globally Disseminated IncX4 Plasmid Carrying the mcr-1 Gene in a Colistin-Resistant Escherichia coli Sequence Type 101 Isolate from a Human Infection in Brazil. Antimicrobial Agents and Chemotherapy, 60( 10), 6415-6417. doi:10.1128/AAC.01325-16
NLM
Fernandes MR, McCulloch JA, Vianello MA, Silva QM da, Chaparro PJP, Esposito FR dos S, Sartori L, Dropa M, Matté MH, Lira DPA, Mamizuka EM, Lincopan N. First Report of the Globally Disseminated IncX4 Plasmid Carrying the mcr-1 Gene in a Colistin-Resistant Escherichia coli Sequence Type 101 Isolate from a Human Infection in Brazil [Internet]. Antimicrobial Agents and Chemotherapy. 2016 ; 60( 10): 6415-6417.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1128/AAC.01325-16
Vancouver
Fernandes MR, McCulloch JA, Vianello MA, Silva QM da, Chaparro PJP, Esposito FR dos S, Sartori L, Dropa M, Matté MH, Lira DPA, Mamizuka EM, Lincopan N. First Report of the Globally Disseminated IncX4 Plasmid Carrying the mcr-1 Gene in a Colistin-Resistant Escherichia coli Sequence Type 101 Isolate from a Human Infection in Brazil [Internet]. Antimicrobial Agents and Chemotherapy. 2016 ; 60( 10): 6415-6417.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1128/AAC.01325-16
Artigo de periodico
Photobiomodulation therapy decreases oxidative stress in the lung tissue after formaldehyde exposure: role of oxidant/antioxidant enzymes (2016)
Macedo, Rodrigo Silva; Leal, Mayara Peres; Braga, Tárcio Teodoro; Barioni, Éric Diego; Duro, Stephanie de Oliveira ; Horliana, Anna Carolina Ratto Tempestini; Câmara, Niels Olsen Saraiva ; Marcourakis, Tania ; Farsky, Sandra Helena Poliselli ; Franco, Adriana Lino dos Santos
Fonte: Mediators of Inflammation. Unidades: FCF, ICB
Assuntos: ESTRESSE OXIDATIVO, ANTIOXIDANTES, ENZIMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MACEDO, Rodrigo Silva et al. Photobiomodulation therapy decreases oxidative stress in the lung tissue after formaldehyde exposure: role of oxidant/antioxidant enzymes. Mediators of Inflammation, v. 2016, p. 1-9 art. 9303126, 2016Tradução . . Disponível em: https://doi.org/10.1155/2016/9303126. Acesso em: 08 nov. 2024.
APA
Macedo, R. S., Leal, M. P., Braga, T. T., Barioni, É. D., Duro, S. de O., Horliana, A. C. R. T., et al. (2016). Photobiomodulation therapy decreases oxidative stress in the lung tissue after formaldehyde exposure: role of oxidant/antioxidant enzymes. Mediators of Inflammation, 2016, 1-9 art. 9303126. doi:10.1155/2016/9303126
NLM
Macedo RS, Leal MP, Braga TT, Barioni ÉD, Duro S de O, Horliana ACRT, Câmara NOS, Marcourakis T, Farsky SHP, Franco AL dos S. Photobiomodulation therapy decreases oxidative stress in the lung tissue after formaldehyde exposure: role of oxidant/antioxidant enzymes [Internet]. Mediators of Inflammation. 2016 ; 2016 1-9 art. 9303126.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1155/2016/9303126
Vancouver
Macedo RS, Leal MP, Braga TT, Barioni ÉD, Duro S de O, Horliana ACRT, Câmara NOS, Marcourakis T, Farsky SHP, Franco AL dos S. Photobiomodulation therapy decreases oxidative stress in the lung tissue after formaldehyde exposure: role of oxidant/antioxidant enzymes [Internet]. Mediators of Inflammation. 2016 ; 2016 1-9 art. 9303126.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1155/2016/9303126
Artigo de periodico
Toward chelerythrine optimization: Analogues designed by molecular simplification exhibit selective growth inhibition in non-small-cell lung cancer cells (2016)
Yang, Rosania; Tavares, Maurício T; Teixeira, Sarah Fernandes; Azevedo, Ricardo A; Pietro, Diego C; Fernandes, Thais Batista; Ferreira, Adilson K; Trossini, Gustavo Henrique Goulart ; Barbuto, José Alexandre Marzagão ; Parise Filho, Roberto
Fonte: Bioorganic & Medicinal Chemistry. Unidades: FCF, ICB
Assuntos: ANTINEOPLÁSICOS, NEOPLASIAS DO TRATO RESPIRATÓRIO, IMUNOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
YANG, Rosania et al. Toward chelerythrine optimization: Analogues designed by molecular simplification exhibit selective growth inhibition in non-small-cell lung cancer cells. Bioorganic & Medicinal Chemistry, v. 24, n. 19, p. 4600-4610, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2016.07.065. Acesso em: 08 nov. 2024.
APA
Yang, R., Tavares, M. T., Teixeira, S. F., Azevedo, R. A., Pietro, D. C., Fernandes, T. B., et al. (2016). Toward chelerythrine optimization: Analogues designed by molecular simplification exhibit selective growth inhibition in non-small-cell lung cancer cells. Bioorganic & Medicinal Chemistry, 24( 19), 4600-4610. doi:10.1016/j.bmc.2016.07.065
NLM
Yang R, Tavares MT, Teixeira SF, Azevedo RA, Pietro DC, Fernandes TB, Ferreira AK, Trossini GHG, Barbuto JAM, Parise Filho R. Toward chelerythrine optimization: Analogues designed by molecular simplification exhibit selective growth inhibition in non-small-cell lung cancer cells [Internet]. Bioorganic & Medicinal Chemistry. 2016 ; 24( 19): 4600-4610.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1016/j.bmc.2016.07.065
Vancouver
Yang R, Tavares MT, Teixeira SF, Azevedo RA, Pietro DC, Fernandes TB, Ferreira AK, Trossini GHG, Barbuto JAM, Parise Filho R. Toward chelerythrine optimization: Analogues designed by molecular simplification exhibit selective growth inhibition in non-small-cell lung cancer cells [Internet]. Bioorganic & Medicinal Chemistry. 2016 ; 24( 19): 4600-4610.[citado 2024 nov. 08 ] Available from: https://doi.org/10.1016/j.bmc.2016.07.065

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