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Artigo de periodico
Carcinogenicity of perfluorooctanoic acid and perfluorooctanesulfonic acid (2024)
Zahm, Shelia ; Bonde, Jens Peter ; Chiu, Weihsueh A ; Hoppin, Jane ; Kanno, Jun ; Abdallah, Mohamed; Blystone, Chad R ; Calkins, Miriam M ; Dong, Guang Hui ; Dorman, David C; Fry, Rebecca; Guo, Huan; Haug, Line Småstuen ; Hofmann, Jonathan N. ; Iwasaki, Motoki; Machala, Miroslav ; Mancini, Francesca Romana ; Maria-Engler, Silvya Stuchi ; Møller, Peter Rsak ; Ng, Jack Chakmeng; Pallardy, Marc ; Post, Gloria B ; Salihovic, Samira ; Schlezinger, Jennifer ; Soshilov, Anatoly; Steenland, Kyle ; Steffensen, Inger Lise ; Tryndyak, Volodymyr ; White, Alexandra; Woskie, Susan
Source: The Lancet Oncology. Unidade: FCF
Subjects: CARCINOGÊNESE, PRODUTOS QUÍMICOS
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ABNT
ZAHM, Shelia et al. Carcinogenicity of perfluorooctanoic acid and perfluorooctanesulfonic acid. The Lancet Oncology, v. 25, n. 1, p. 16-17, 2024Tradução . . Disponível em: https://dx.doi.org/10.1016/S1470-2045(23)00622-8. Acesso em: 16 nov. 2024.
APA
Zahm, S., Bonde, J. P., Chiu, W. A., Hoppin, J., Kanno, J., Abdallah, M., et al. (2024). Carcinogenicity of perfluorooctanoic acid and perfluorooctanesulfonic acid. The Lancet Oncology, 25( 1), 16-17. doi:10.1016/S1470-2045(23)00622-8
NLM
Zahm S, Bonde JP, Chiu WA, Hoppin J, Kanno J, Abdallah M, Blystone CR, Calkins MM, Dong GH, Dorman DC, Fry R, Guo H, Haug LS, Hofmann JN, Iwasaki M, Machala M, Mancini FR, Maria-Engler SS, Møller PR, Ng JC, Pallardy M, Post GB, Salihovic S, Schlezinger J, Soshilov A, Steenland K, Steffensen IL, Tryndyak V, White A, Woskie S. Carcinogenicity of perfluorooctanoic acid and perfluorooctanesulfonic acid [Internet]. The Lancet Oncology. 2024 ; 25( 1): 16-17.[citado 2024 nov. 16 ] Available from: https://dx.doi.org/10.1016/S1470-2045(23)00622-8
Vancouver
Zahm S, Bonde JP, Chiu WA, Hoppin J, Kanno J, Abdallah M, Blystone CR, Calkins MM, Dong GH, Dorman DC, Fry R, Guo H, Haug LS, Hofmann JN, Iwasaki M, Machala M, Mancini FR, Maria-Engler SS, Møller PR, Ng JC, Pallardy M, Post GB, Salihovic S, Schlezinger J, Soshilov A, Steenland K, Steffensen IL, Tryndyak V, White A, Woskie S. Carcinogenicity of perfluorooctanoic acid and perfluorooctanesulfonic acid [Internet]. The Lancet Oncology. 2024 ; 25( 1): 16-17.[citado 2024 nov. 16 ] Available from: https://dx.doi.org/10.1016/S1470-2045(23)00622-8
Artigo de periodico
Mutually exclusive genetic interactions and gene essentiality shape the genomic landscape of primary melanoma (2023)
Birkeälv, Sofia; Harland, Mark; Matsuyama, Larissa Satiko Alcântara Sekimoto ; Rashid, Mamun; Mehta, Ishan; Laye, Jonathan P; Haase, Kerstin; Mell, Tracey; Iyer, Vivek; Espinoza, Carla Daniela Robles; Possik, Patricia Abrão ; Maria-Engler, Silvya Stuchi
Source: Journal of Pathology. Unidade: FCF
Subjects: MELANOMA, GENÔMICA
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BIRKEÄLV, Sofia et al. Mutually exclusive genetic interactions and gene essentiality shape the genomic landscape of primary melanoma. Journal of Pathology, v. 259, p. 56–68, 2023Tradução . . Disponível em: https://doi.org/10.1002/path.6019. Acesso em: 16 nov. 2024.
APA
Birkeälv, S., Harland, M., Matsuyama, L. S. A. S., Rashid, M., Mehta, I., Laye, J. P., et al. (2023). Mutually exclusive genetic interactions and gene essentiality shape the genomic landscape of primary melanoma. Journal of Pathology, 259, 56–68. doi:10.1002/path.6019
NLM
Birkeälv S, Harland M, Matsuyama LSAS, Rashid M, Mehta I, Laye JP, Haase K, Mell T, Iyer V, Espinoza CDR, Possik PA, Maria-Engler SS. Mutually exclusive genetic interactions and gene essentiality shape the genomic landscape of primary melanoma [Internet]. Journal of Pathology. 2023 ; 259 56–68.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/path.6019
Vancouver
Birkeälv S, Harland M, Matsuyama LSAS, Rashid M, Mehta I, Laye JP, Haase K, Mell T, Iyer V, Espinoza CDR, Possik PA, Maria-Engler SS. Mutually exclusive genetic interactions and gene essentiality shape the genomic landscape of primary melanoma [Internet]. Journal of Pathology. 2023 ; 259 56–68.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1002/path.6019
Artigo de periodico
Kynurenine inhibits melanogenesis in human melanocyte-keratinocyte co-cultures and in a reconstructed 3D skin model (2022)
Branquinho, Maryana Stephany Ferreira ; Silva, Maysa Braga Barros ; Castilho, Gabriela Ansanelo; Cavalcante, Jacqueline; Barros, Silvia Berlanga de Moraes ; Clara, Renan Orsati; Maria-Engler, Silvya Stuchi ; Campa, Ana
Source: Experimental Dermatology. Unidade: FCF
Subjects: METABÓLITOS, PELE, TERCEIRA DIMENSÃO, MELANINAS
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BRANQUINHO, Maryana Stephany Ferreira et al. Kynurenine inhibits melanogenesis in human melanocyte-keratinocyte co-cultures and in a reconstructed 3D skin model. Experimental Dermatology, v. 31, n. 3, p. 427-432, 2022Tradução . . Disponível em: https://doi.org/10.1111/exd.14486. Acesso em: 16 nov. 2024.
APA
Branquinho, M. S. F., Silva, M. B. B., Castilho, G. A., Cavalcante, J., Barros, S. B. de M., Clara, R. O., et al. (2022). Kynurenine inhibits melanogenesis in human melanocyte-keratinocyte co-cultures and in a reconstructed 3D skin model. Experimental Dermatology, 31( 3), 427-432. doi:10.1111/exd.14486
NLM
Branquinho MSF, Silva MBB, Castilho GA, Cavalcante J, Barros SB de M, Clara RO, Maria-Engler SS, Campa A. Kynurenine inhibits melanogenesis in human melanocyte-keratinocyte co-cultures and in a reconstructed 3D skin model [Internet]. Experimental Dermatology. 2022 ; 31( 3): 427-432.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/exd.14486
Vancouver
Branquinho MSF, Silva MBB, Castilho GA, Cavalcante J, Barros SB de M, Clara RO, Maria-Engler SS, Campa A. Kynurenine inhibits melanogenesis in human melanocyte-keratinocyte co-cultures and in a reconstructed 3D skin model [Internet]. Experimental Dermatology. 2022 ; 31( 3): 427-432.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/exd.14486
Artigo de periodico
Upregulation of the novel lncRNA U731166 is associated with migration, invasion and vemurafenib resistance in melanoma (2022)
Siena, Ádamo Davi Diógenes ; Barros, Isabela Ichihara de ; Storti, Camila Baldin ; Biagi Junior, Carlos Alberto Oliveira de ; Carvalho, Larissa Anastácio da Costa ; Maria-Engler, Silvya Stuchi ; Sousa, Josane de Freitas ; Silva Junior, Wilson Araújo da
Source: Journal of Cellular and Molecular Medicine. Unidades: FCF, FMRP
Subjects: MELANOMA, GENES, BIOMARCADORES
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ABNT
SIENA, Ádamo Davi Diógenes et al. Upregulation of the novel lncRNA U731166 is associated with migration, invasion and vemurafenib resistance in melanoma. Journal of Cellular and Molecular Medicine, v. 26, n. 3, p. 671-683, 2022Tradução . . Disponível em: https://doi.org/10.1111/jcmm.16987. Acesso em: 16 nov. 2024.
APA
Siena, Á. D. D., Barros, I. I. de, Storti, C. B., Biagi Junior, C. A. O. de, Carvalho, L. A. da C., Maria-Engler, S. S., et al. (2022). Upregulation of the novel lncRNA U731166 is associated with migration, invasion and vemurafenib resistance in melanoma. Journal of Cellular and Molecular Medicine, 26( 3), 671-683. doi:10.1111/jcmm.16987
NLM
Siena ÁDD, Barros II de, Storti CB, Biagi Junior CAO de, Carvalho LA da C, Maria-Engler SS, Sousa J de F, Silva Junior WA da. Upregulation of the novel lncRNA U731166 is associated with migration, invasion and vemurafenib resistance in melanoma [Internet]. Journal of Cellular and Molecular Medicine. 2022 ; 26( 3): 671-683.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/jcmm.16987
Vancouver
Siena ÁDD, Barros II de, Storti CB, Biagi Junior CAO de, Carvalho LA da C, Maria-Engler SS, Sousa J de F, Silva Junior WA da. Upregulation of the novel lncRNA U731166 is associated with migration, invasion and vemurafenib resistance in melanoma [Internet]. Journal of Cellular and Molecular Medicine. 2022 ; 26( 3): 671-683.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/jcmm.16987
Artigo de periodico
Melatonin inhibits human melanoma cells proliferation and invasion via cell cycle arrest and cytoskeleton remodeling (2020)
Moreno, Ana Carolina Ramos ; Saito, Renata de Freitas; Tiago, Manoela; Massaro, Renato Ramos; Pagni, Roberta Liberato ; Pegoraro, Rafael; Souza, Patricia da Cruz; Reiter, Russel J. ; Campa, Ana ; Soengas, Maria S; Maria-Engler, Silvya Stuchi
Source: Melatonin Research. Unidades: FCF, ICB
Subjects: MELATONINA, CITOESQUELETO, CICLO CELULAR
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ABNT
MORENO, Ana Carolina Ramos et al. Melatonin inhibits human melanoma cells proliferation and invasion via cell cycle arrest and cytoskeleton remodeling. Melatonin Research, v. 3, n. 2, p. 194-209, 2020Tradução . . Disponível em: https://doi.org/10.32794/mr11250057. Acesso em: 16 nov. 2024.
APA
Moreno, A. C. R., Saito, R. de F., Tiago, M., Massaro, R. R., Pagni, R. L., Pegoraro, R., et al. (2020). Melatonin inhibits human melanoma cells proliferation and invasion via cell cycle arrest and cytoskeleton remodeling. Melatonin Research, 3( 2), 194-209. doi:10.32794/mr11250057
NLM
Moreno ACR, Saito R de F, Tiago M, Massaro RR, Pagni RL, Pegoraro R, Souza P da C, Reiter RJ, Campa A, Soengas MS, Maria-Engler SS. Melatonin inhibits human melanoma cells proliferation and invasion via cell cycle arrest and cytoskeleton remodeling [Internet]. Melatonin Research. 2020 ; 3( 2): 194-209.[citado 2024 nov. 16 ] Available from: https://doi.org/10.32794/mr11250057
Vancouver
Moreno ACR, Saito R de F, Tiago M, Massaro RR, Pagni RL, Pegoraro R, Souza P da C, Reiter RJ, Campa A, Soengas MS, Maria-Engler SS. Melatonin inhibits human melanoma cells proliferation and invasion via cell cycle arrest and cytoskeleton remodeling [Internet]. Melatonin Research. 2020 ; 3( 2): 194-209.[citado 2024 nov. 16 ] Available from: https://doi.org/10.32794/mr11250057
Artigo de periodico
Air particulate matter induces skin barrier dysfunction and water transport alteration on a reconstructed human epidermis model (2020)
Hieda, Daniele Seo ; Carvalho, Larissa Anastácio da Costa ; Mello, Barbara Vaz de ; Oliveira, Erica Aparecida de ; Assis, Sílvia Romano de ; Wu, Joanna ; Du-Thumm, Laurence ; Silva, Claudia Larissa Viana da ; Roubicek, Deborah Arnsdorff ; Maria-Engler, Silvya Stuchi ; Barros, Silvia Berlanga de Moraes
Source: Journal of Investigative Dermatology. Unidade: FCF
Subjects: PELE, POLUIÇÃO ATMOSFÉRICA
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ABNT
HIEDA, Daniele Seo et al. Air particulate matter induces skin barrier dysfunction and water transport alteration on a reconstructed human epidermis model. Journal of Investigative Dermatology, v. 140, n. 12, p. 2343-2352, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.jid.2020.03.971. Acesso em: 16 nov. 2024.
APA
Hieda, D. S., Carvalho, L. A. da C., Mello, B. V. de, Oliveira, E. A. de, Assis, S. R. de, Wu, J., et al. (2020). Air particulate matter induces skin barrier dysfunction and water transport alteration on a reconstructed human epidermis model. Journal of Investigative Dermatology, 140( 12), 2343-2352. doi:10.1016/j.jid.2020.03.971
NLM
Hieda DS, Carvalho LA da C, Mello BV de, Oliveira EA de, Assis SR de, Wu J, Du-Thumm L, Silva CLV da, Roubicek DA, Maria-Engler SS, Barros SB de M. Air particulate matter induces skin barrier dysfunction and water transport alteration on a reconstructed human epidermis model [Internet]. Journal of Investigative Dermatology. 2020 ; 140( 12): 2343-2352.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.jid.2020.03.971
Vancouver
Hieda DS, Carvalho LA da C, Mello BV de, Oliveira EA de, Assis SR de, Wu J, Du-Thumm L, Silva CLV da, Roubicek DA, Maria-Engler SS, Barros SB de M. Air particulate matter induces skin barrier dysfunction and water transport alteration on a reconstructed human epidermis model [Internet]. Journal of Investigative Dermatology. 2020 ; 140( 12): 2343-2352.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.jid.2020.03.971
Artigo de periodico
A 2D and 3D melanogenesis model with human primary cells induced by tyrosine (2020)
Branquinho, Maryana Stephany Ferreira; Silva, Maysa Braga Barros ; Silva, Jacqueline C; Sales, Maria C; Barros, Silvia B; Maria-Engler, Silvya Stuchi ; Campa, Ana
Source: Journal of Biological Methods. Unidade: FCF
Subjects: MELANINAS, CÉLULAS
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ABNT
BRANQUINHO, Maryana Stephany Ferreira et al. A 2D and 3D melanogenesis model with human primary cells induced by tyrosine. Journal of Biological Methods, v. 7 , n. 3, p. 1-7, 2020Tradução . . Disponível em: https://doi.org/10.14440/jbm.2020.327. Acesso em: 16 nov. 2024.
APA
Branquinho, M. S. F., Silva, M. B. B., Silva, J. C., Sales, M. C., Barros, S. B., Maria-Engler, S. S., & Campa, A. (2020). A 2D and 3D melanogenesis model with human primary cells induced by tyrosine. Journal of Biological Methods, 7 ( 3), 1-7. doi:10.14440/jbm.2020.327
NLM
Branquinho MSF, Silva MBB, Silva JC, Sales MC, Barros SB, Maria-Engler SS, Campa A. A 2D and 3D melanogenesis model with human primary cells induced by tyrosine [Internet]. Journal of Biological Methods. 2020 ; 7 ( 3): 1-7.[citado 2024 nov. 16 ] Available from: https://doi.org/10.14440/jbm.2020.327
Vancouver
Branquinho MSF, Silva MBB, Silva JC, Sales MC, Barros SB, Maria-Engler SS, Campa A. A 2D and 3D melanogenesis model with human primary cells induced by tyrosine [Internet]. Journal of Biological Methods. 2020 ; 7 ( 3): 1-7.[citado 2024 nov. 16 ] Available from: https://doi.org/10.14440/jbm.2020.327
Trabalho de evento-resumo periodico
Adaptation of uveal melanoma cells to MEK inhibition can be overcome through HDAC inhibition (2018)
Faião-Flores, Fernanda; Maria-Engler, Silvya Stuchi ; Eroglu, Zeynep; Smalley, Keiran S
Source: Cancer Research. Conference titles: Annual Meeting of the American Association for Cancer Research. Unidade: FCF
Subjects: MELANOMA, METÁSTASE NEOPLÁSICA
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ABNT
FAIÃO-FLORES, Fernanda et al. Adaptation of uveal melanoma cells to MEK inhibition can be overcome through HDAC inhibition. Cancer Research. Philadelphia: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 16 nov. 2024. , 2018
APA
Faião-Flores, F., Maria-Engler, S. S., Eroglu, Z., & Smalley, K. S. (2018). Adaptation of uveal melanoma cells to MEK inhibition can be overcome through HDAC inhibition. Cancer Research. Philadelphia: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Faião-Flores F, Maria-Engler SS, Eroglu Z, Smalley KS. Adaptation of uveal melanoma cells to MEK inhibition can be overcome through HDAC inhibition. Cancer Research. 2018 ; 78( 13): 1232 res. 4814.[citado 2024 nov. 16 ]
Vancouver
Faião-Flores F, Maria-Engler SS, Eroglu Z, Smalley KS. Adaptation of uveal melanoma cells to MEK inhibition can be overcome through HDAC inhibition. Cancer Research. 2018 ; 78( 13): 1232 res. 4814.[citado 2024 nov. 16 ]
Trabalho de evento-resumo periodico
Upregulation of IDO in bacterial vaginosis: role in HPV coinfection (2018)
Venancio, Paloma Almeida; Maria-Engler, Silvya Stuchi ; Consolaro, Marcia Edilaine Lopes; Villa, Luisa Lina; Derchain, Sophie Françoise Mauricette; Campa, Ana ; Discacciati, Michelle Garcia
Source: Clinical Cancer Research. Conference titles: AACR International Conference on Translational Cancer Medicine. Unidades: FM, FCF
Subjects: HPV, BACTÉRIAS
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ABNT
VENANCIO, Paloma Almeida et al. Upregulation of IDO in bacterial vaginosis: role in HPV coinfection. Clinical Cancer Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://clincancerres.aacrjournals.org/content/24/1_Supplement/A46. Acesso em: 16 nov. 2024. , 2018
APA
Venancio, P. A., Maria-Engler, S. S., Consolaro, M. E. L., Villa, L. L., Derchain, S. F. M., Campa, A., & Discacciati, M. G. (2018). Upregulation of IDO in bacterial vaginosis: role in HPV coinfection. Clinical Cancer Research. Philadelphia: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://clincancerres.aacrjournals.org/content/24/1_Supplement/A46
NLM
Venancio PA, Maria-Engler SS, Consolaro MEL, Villa LL, Derchain SFM, Campa A, Discacciati MG. Upregulation of IDO in bacterial vaginosis: role in HPV coinfection [Internet]. Clinical Cancer Research. 2018 ; 24( 5):[citado 2024 nov. 16 ] Available from: http://clincancerres.aacrjournals.org/content/24/1_Supplement/A46
Vancouver
Venancio PA, Maria-Engler SS, Consolaro MEL, Villa LL, Derchain SFM, Campa A, Discacciati MG. Upregulation of IDO in bacterial vaginosis: role in HPV coinfection [Internet]. Clinical Cancer Research. 2018 ; 24( 5):[citado 2024 nov. 16 ] Available from: http://clincancerres.aacrjournals.org/content/24/1_Supplement/A46
Trabalho de evento-resumo periodico
Pyrimidobenzimidazoles as a potential new drug to treat human melanoma (2018)
Azevedo, Jéssica Gonçalves; Schultz, Iago Carvalho; Santos, Jacqueline Fraga de Souza; Maria-Engler, Silvya Stuchi ; Lenz, Guido; Wink, Márcia Rosângela
Source: Clinical Cancer Research. Conference titles: AACR International Conference on Translational Cancer Medicine. Unidade: FCF
Subjects: MELANOMA, MEDICAMENTO
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ABNT
AZEVEDO, Jéssica Gonçalves et al. Pyrimidobenzimidazoles as a potential new drug to treat human melanoma. Clinical Cancer Research. Philadelphia: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Disponível em: http://clincancerres.aacrjournals.org/content/24/1_Supplement/B34. Acesso em: 16 nov. 2024. , 2018
APA
Azevedo, J. G., Schultz, I. C., Santos, J. F. de S., Maria-Engler, S. S., Lenz, G., & Wink, M. R. (2018). Pyrimidobenzimidazoles as a potential new drug to treat human melanoma. Clinical Cancer Research. Philadelphia: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Recuperado de http://clincancerres.aacrjournals.org/content/24/1_Supplement/B34
NLM
Azevedo JG, Schultz IC, Santos JF de S, Maria-Engler SS, Lenz G, Wink MR. Pyrimidobenzimidazoles as a potential new drug to treat human melanoma [Internet]. Clinical Cancer Research. 2018 ; 24( 5):[citado 2024 nov. 16 ] Available from: http://clincancerres.aacrjournals.org/content/24/1_Supplement/B34
Vancouver
Azevedo JG, Schultz IC, Santos JF de S, Maria-Engler SS, Lenz G, Wink MR. Pyrimidobenzimidazoles as a potential new drug to treat human melanoma [Internet]. Clinical Cancer Research. 2018 ; 24( 5):[citado 2024 nov. 16 ] Available from: http://clincancerres.aacrjournals.org/content/24/1_Supplement/B34
Trabalho de evento-resumo periodico
The influence of UVA protection on skin during sun exposure (2018)
Lago, Juliana Carvalhães; Oliveira, E. Aparecida; Maria-Engler, Silvya Stuchi
Source: Journal of Investigative Dermatology. Conference titles: International Investigative Dermatology Meeting/IID. Unidade: FCF
Subjects: FILTRO SOLAR, RADIAÇÃO ULTRAVIOLETA
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ABNT
LAGO, Juliana Carvalhães e OLIVEIRA, E. Aparecida e MARIA-ENGLER, Silvya Stuchi. The influence of UVA protection on skin during sun exposure. Journal of Investigative Dermatology. New York: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.jid.2018.03.1152. Acesso em: 16 nov. 2024. , 2018
APA
Lago, J. C., Oliveira, E. A., & Maria-Engler, S. S. (2018). The influence of UVA protection on skin during sun exposure. Journal of Investigative Dermatology. New York: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. doi:10.1016/j.jid.2018.03.1152
NLM
Lago JC, Oliveira EA, Maria-Engler SS. The influence of UVA protection on skin during sun exposure [Internet]. Journal of Investigative Dermatology. 2018 ; 138( 5): S193 res. 1138.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.jid.2018.03.1152
Vancouver
Lago JC, Oliveira EA, Maria-Engler SS. The influence of UVA protection on skin during sun exposure [Internet]. Journal of Investigative Dermatology. 2018 ; 138( 5): S193 res. 1138.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.jid.2018.03.1152
Trabalho de evento-resumo periodico
Targeting protein disulfide isomerase to overcome resistance to BRAF inhibitors in melanoma (2018)
Beyerstedt, Stephany; Franco, Marcela; Oliveira, Tamires; Mendonça, Gabriella; Fernandes, Débora Alves; Maria-Engler, Silvya Stuchi ; Machado Neto, João Agostinho ; Lopes, Lucia Rossetti
Source: Free Radical Biology and Medicine. Conference titles: Annual Meeting Society for Redox Biology and Medicine's/SfRBM. Unidade: FCF
Subjects: MELANOMA, PROTEÍNAS, INIBIDORES DE ENZIMAS
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ABNT
BEYERSTEDT, Stephany et al. Targeting protein disulfide isomerase to overcome resistance to BRAF inhibitors in melanoma. Free Radical Biology and Medicine. New York: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.freeradbiomed.2018.10.125. Acesso em: 16 nov. 2024. , 2018
APA
Beyerstedt, S., Franco, M., Oliveira, T., Mendonça, G., Fernandes, D. A., Maria-Engler, S. S., et al. (2018). Targeting protein disulfide isomerase to overcome resistance to BRAF inhibitors in melanoma. Free Radical Biology and Medicine. New York: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. doi:10.1016/j.freeradbiomed.2018.10.125
NLM
Beyerstedt S, Franco M, Oliveira T, Mendonça G, Fernandes DA, Maria-Engler SS, Machado Neto JA, Lopes LR. Targeting protein disulfide isomerase to overcome resistance to BRAF inhibitors in melanoma [Internet]. Free Radical Biology and Medicine. 2018 ; 128 S62 res. 121.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2018.10.125
Vancouver
Beyerstedt S, Franco M, Oliveira T, Mendonça G, Fernandes DA, Maria-Engler SS, Machado Neto JA, Lopes LR. Targeting protein disulfide isomerase to overcome resistance to BRAF inhibitors in melanoma [Internet]. Free Radical Biology and Medicine. 2018 ; 128 S62 res. 121.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2018.10.125
Artigo de periodico-divulgacao
Assessing the effects of advanced glycation end products in the skin (2017)
Maria-Engler, Silvya Stuchi
Source: British Journal of Dermatology. Unidade: FCF
Subjects: PELE, ENVELHECIMENTO
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ABNT
MARIA-ENGLER, Silvya Stuchi. Assessing the effects of advanced glycation end products in the skin. British Journal of Dermatology. Hoboken: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Disponível em: https://doi.org/10.1111/bjd.15166. Acesso em: 16 nov. 2024. , 2017
APA
Maria-Engler, S. S. (2017). Assessing the effects of advanced glycation end products in the skin. British Journal of Dermatology. Hoboken: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. doi:10.1111/bjd.15166
NLM
Maria-Engler SS. Assessing the effects of advanced glycation end products in the skin [Internet]. British Journal of Dermatology. 2017 ; 176( 1): 12-13.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/bjd.15166
Vancouver
Maria-Engler SS. Assessing the effects of advanced glycation end products in the skin [Internet]. British Journal of Dermatology. 2017 ; 176( 1): 12-13.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/bjd.15166
Trabalho de evento-resumo periodico
HPV16 E6 oncoprotein modulates the DPPIV/CD26 in primary keratinocytes (2017)
Beckenkamp, Aline; Prati, Bruna; Maria-Engler, Silvya Stuchi ; Lenz, Guido; Pilger, Diogo André; Boccardo, Enrique ; Buffon, Andréia
Source: Cancer Research. Conference titles: American Association for Cancer Research/AACR Annual Meeting. Unidades: FCF, ICB
Subjects: ONCOPROTEÍNAS, HPV
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BECKENKAMP, Aline et al. HPV16 E6 oncoprotein modulates the DPPIV/CD26 in primary keratinocytes. Cancer Research. Philadelphia: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 16 nov. 2024. , 2017
APA
Beckenkamp, A., Prati, B., Maria-Engler, S. S., Lenz, G., Pilger, D. A., Boccardo, E., & Buffon, A. (2017). HPV16 E6 oncoprotein modulates the DPPIV/CD26 in primary keratinocytes. Cancer Research. Philadelphia: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Beckenkamp A, Prati B, Maria-Engler SS, Lenz G, Pilger DA, Boccardo E, Buffon A. HPV16 E6 oncoprotein modulates the DPPIV/CD26 in primary keratinocytes. Cancer Research. 2017 ; 77( 13):[citado 2024 nov. 16 ]
Vancouver
Beckenkamp A, Prati B, Maria-Engler SS, Lenz G, Pilger DA, Boccardo E, Buffon A. HPV16 E6 oncoprotein modulates the DPPIV/CD26 in primary keratinocytes. Cancer Research. 2017 ; 77( 13):[citado 2024 nov. 16 ]
Artigo de periodico
Methyl-beta-cyclodextrin treatment combined to incubation with interleukin-4 reproduces major features of atopic dermatitis in a 3D-culture model (2017)
Pedrosa, Tatiana do Nascimento; De Vuyst, Evelyne; Mound, Abdallah; Rouvroit, Catherine Lambert de; Maria-Engler, Silvya Stuchi ; Poumay, Yves
Source: Archives of Dermatological Research. Unidade: FCF
Subjects: DERMATITE, INTERLEUCINA 4
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PEDROSA, Tatiana do Nascimento et al. Methyl-beta-cyclodextrin treatment combined to incubation with interleukin-4 reproduces major features of atopic dermatitis in a 3D-culture model. Archives of Dermatological Research, v. 309, n. 1, p. 63-69, 2017Tradução . . Disponível em: https://doi.org/10.1007/s00403-016-1699-7. Acesso em: 16 nov. 2024.
APA
Pedrosa, T. do N., De Vuyst, E., Mound, A., Rouvroit, C. L. de, Maria-Engler, S. S., & Poumay, Y. (2017). Methyl-beta-cyclodextrin treatment combined to incubation with interleukin-4 reproduces major features of atopic dermatitis in a 3D-culture model. Archives of Dermatological Research, 309( 1), 63-69. doi:10.1007/s00403-016-1699-7
NLM
Pedrosa T do N, De Vuyst E, Mound A, Rouvroit CL de, Maria-Engler SS, Poumay Y. Methyl-beta-cyclodextrin treatment combined to incubation with interleukin-4 reproduces major features of atopic dermatitis in a 3D-culture model [Internet]. Archives of Dermatological Research. 2017 ; 309( 1): 63-69.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1007/s00403-016-1699-7
Vancouver
Pedrosa T do N, De Vuyst E, Mound A, Rouvroit CL de, Maria-Engler SS, Poumay Y. Methyl-beta-cyclodextrin treatment combined to incubation with interleukin-4 reproduces major features of atopic dermatitis in a 3D-culture model [Internet]. Archives of Dermatological Research. 2017 ; 309( 1): 63-69.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1007/s00403-016-1699-7
Trabalho de evento-resumo periodico
Evaluation of native and non-native bio-inks for 3D printing of human tissues (2017)
Catarino, Carolina Motter; Baltazar, T; Dai, Guangping; Maria-Engler, Silvya Stuchi ; Karande, P
Source: Journal of Investigative Dermatology. Conference titles: Annual Meeting of the Society for Investigative Dermatology. Unidade: FCF
Subjects: MEDICINA REGENERATIVA, TERCEIRA DIMENSÃO, FIBROBLASTOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CATARINO, Carolina Motter et al. Evaluation of native and non-native bio-inks for 3D printing of human tissues. Journal of Investigative Dermatology. New York: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 16 nov. 2024. , 2017
APA
Catarino, C. M., Baltazar, T., Dai, G., Maria-Engler, S. S., & Karande, P. (2017). Evaluation of native and non-native bio-inks for 3D printing of human tissues. Journal of Investigative Dermatology. New York: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Catarino CM, Baltazar T, Dai G, Maria-Engler SS, Karande P. Evaluation of native and non-native bio-inks for 3D printing of human tissues. Journal of Investigative Dermatology. 2017 ; 137( 5): S94 res. 542.[citado 2024 nov. 16 ]
Vancouver
Catarino CM, Baltazar T, Dai G, Maria-Engler SS, Karande P. Evaluation of native and non-native bio-inks for 3D printing of human tissues. Journal of Investigative Dermatology. 2017 ; 137( 5): S94 res. 542.[citado 2024 nov. 16 ]
Trabalho de evento-resumo periodico
Evaluation of native and non-native bio-inks for 3D printing of human tissues (2017)
Catarino, Carolina Motter; Baltazar, T; Maria-Engler, Silvya Stuchi ; Karande, P
Source: Tissue Engineering Part A. Conference titles: TERMIS - Americas Conference & Exhibition. Unidade: FCF
Subjects: TERCEIRA DIMENSÃO, IMPRESSÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CATARINO, Carolina Motter et al. Evaluation of native and non-native bio-inks for 3D printing of human tissues. Tissue Engineering Part A. New Rochelle: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Disponível em: https://doi.org/10.1089/ten.tea.2017.29003.abstracts. Acesso em: 16 nov. 2024. , 2017
APA
Catarino, C. M., Baltazar, T., Maria-Engler, S. S., & Karande, P. (2017). Evaluation of native and non-native bio-inks for 3D printing of human tissues. Tissue Engineering Part A. New Rochelle: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. doi:10.1089/ten.tea.2017.29003.abstracts
NLM
Catarino CM, Baltazar T, Maria-Engler SS, Karande P. Evaluation of native and non-native bio-inks for 3D printing of human tissues [Internet]. Tissue Engineering Part A. 2017 ; 23 S-99 res. 396.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1089/ten.tea.2017.29003.abstracts
Vancouver
Catarino CM, Baltazar T, Maria-Engler SS, Karande P. Evaluation of native and non-native bio-inks for 3D printing of human tissues [Internet]. Tissue Engineering Part A. 2017 ; 23 S-99 res. 396.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1089/ten.tea.2017.29003.abstracts
Artigo de periodico
Oxidative stress triggered by apigenin induces apoptosis in a comprehensive panel of human cervical cancer-derived cell lines (2017)
Souza, Raquel P; Mendonça, Patrícia de S. Bonfim; Gimenes, Fabrícia; Ratti, Bianca A; Kaplum, Vanessa; Bruschi, Marcos L; Nakamura, Celso Vataru; Silva, Sueli O; Maria-Engler, Silvya Stuchi ; Consolaro, Márcia E. L
Source: Oxidative Medicine and Cellular Longevity. Unidade: FCF
Subjects: ESTRESSE OXIDATIVO, APOPTOSE, LINHAGEM CELULAR, ANTINEOPLÁSICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOUZA, Raquel P et al. Oxidative stress triggered by apigenin induces apoptosis in a comprehensive panel of human cervical cancer-derived cell lines. Oxidative Medicine and Cellular Longevity, v. 2017, p. 1-18 Art. 1512745, 2017Tradução . . Disponível em: https://doi.org/10.1155/2017/1512745. Acesso em: 16 nov. 2024.
APA
Souza, R. P., Mendonça, P. de S. B., Gimenes, F., Ratti, B. A., Kaplum, V., Bruschi, M. L., et al. (2017). Oxidative stress triggered by apigenin induces apoptosis in a comprehensive panel of human cervical cancer-derived cell lines. Oxidative Medicine and Cellular Longevity, 2017, 1-18 Art. 1512745. doi:10.1155/2017/1512745
NLM
Souza RP, Mendonça P de SB, Gimenes F, Ratti BA, Kaplum V, Bruschi ML, Nakamura CV, Silva SO, Maria-Engler SS, Consolaro MEL. Oxidative stress triggered by apigenin induces apoptosis in a comprehensive panel of human cervical cancer-derived cell lines [Internet]. Oxidative Medicine and Cellular Longevity. 2017 ; 2017 1-18 Art. 1512745.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1155/2017/1512745
Vancouver
Souza RP, Mendonça P de SB, Gimenes F, Ratti BA, Kaplum V, Bruschi ML, Nakamura CV, Silva SO, Maria-Engler SS, Consolaro MEL. Oxidative stress triggered by apigenin induces apoptosis in a comprehensive panel of human cervical cancer-derived cell lines [Internet]. Oxidative Medicine and Cellular Longevity. 2017 ; 2017 1-18 Art. 1512745.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1155/2017/1512745
Artigo de periodico
Ozone gas as a benign sterilization treatment for PLGA Nanofiber Scaffolds (2016)
Rediguieri, Carolina Fracalossi; Pinto, Terezinha de Jesus Andreoli ; Bou-Chacra, Nadia Araci ; Galante, Raquel; Araujo, Gabriel Lima Barros de ; Pedrosa, Tatiana do Nascimento; Maria-Engler, Silvya Stuchi ; Bank, Paul A. de
Source: Tissue Engineering Part C: Methods. Unidade: FCF
Subjects: OZÔNIO, MATERIAIS NANOESTRUTURADOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
REDIGUIERI, Carolina Fracalossi et al. Ozone gas as a benign sterilization treatment for PLGA Nanofiber Scaffolds. Tissue Engineering Part C: Methods, v. 22, n. 4, p. 338-347, 2016Tradução . . Disponível em: https://doi.org/10.1089/ten.tec.2015.0298. Acesso em: 16 nov. 2024.
APA
Rediguieri, C. F., Pinto, T. de J. A., Bou-Chacra, N. A., Galante, R., Araujo, G. L. B. de, Pedrosa, T. do N., et al. (2016). Ozone gas as a benign sterilization treatment for PLGA Nanofiber Scaffolds. Tissue Engineering Part C: Methods, 22( 4), 338-347. doi:10.1089/ten.tec.2015.0298
NLM
Rediguieri CF, Pinto T de JA, Bou-Chacra NA, Galante R, Araujo GLB de, Pedrosa T do N, Maria-Engler SS, Bank PA de. Ozone gas as a benign sterilization treatment for PLGA Nanofiber Scaffolds [Internet]. Tissue Engineering Part C: Methods. 2016 ; 22( 4): 338-347.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1089/ten.tec.2015.0298
Vancouver
Rediguieri CF, Pinto T de JA, Bou-Chacra NA, Galante R, Araujo GLB de, Pedrosa T do N, Maria-Engler SS, Bank PA de. Ozone gas as a benign sterilization treatment for PLGA Nanofiber Scaffolds [Internet]. Tissue Engineering Part C: Methods. 2016 ; 22( 4): 338-347.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1089/ten.tec.2015.0298
Trabalho de evento-resumo periodico
Targeting hedgehog transcription factors GLl1 and GLl2 restores sensitivity to vemurafenib resistant human melanoma cells (2016)
Faião-Flores, Fernanda; Fernandes, Débora Kristina Magalhães Alves; Pennacchi, Paula Comune; Sandri, Silvana; Vicente, Anna Luiza Silva Almeida; Scapulatempo Neto, Cristovam; Vasquez, Vinicius de Lima; Reis, Rui Manuel Vieira; Smalley, Keiran S; Maria-Engler, Silvya Stuchi
Source: Cancer Research. Conference titles: Annual Meeting of the American Association for Cancer Research (AACR). Unidade: FCF
Assunto: MELANOMA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FAIÃO-FLORES, Fernanda et al. Targeting hedgehog transcription factors GLl1 and GLl2 restores sensitivity to vemurafenib resistant human melanoma cells. Cancer Research. Philadelphia: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Disponível em: http://cancerres.aacrjournals.org/content/76/14_supplement/4669.short. Acesso em: 16 nov. 2024. , 2016
APA
Faião-Flores, F., Fernandes, D. K. M. A., Pennacchi, P. C., Sandri, S., Vicente, A. L. S. A., Scapulatempo Neto, C., et al. (2016). Targeting hedgehog transcription factors GLl1 and GLl2 restores sensitivity to vemurafenib resistant human melanoma cells. Cancer Research. Philadelphia: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. Recuperado de http://cancerres.aacrjournals.org/content/76/14_supplement/4669.short
NLM
Faião-Flores F, Fernandes DKMA, Pennacchi PC, Sandri S, Vicente ALSA, Scapulatempo Neto C, Vasquez V de L, Reis RMV, Smalley KS, Maria-Engler SS. Targeting hedgehog transcription factors GLl1 and GLl2 restores sensitivity to vemurafenib resistant human melanoma cells [Internet]. Cancer Research. 2016 ; 76( 14):[citado 2024 nov. 16 ] Available from: http://cancerres.aacrjournals.org/content/76/14_supplement/4669.short
Vancouver
Faião-Flores F, Fernandes DKMA, Pennacchi PC, Sandri S, Vicente ALSA, Scapulatempo Neto C, Vasquez V de L, Reis RMV, Smalley KS, Maria-Engler SS. Targeting hedgehog transcription factors GLl1 and GLl2 restores sensitivity to vemurafenib resistant human melanoma cells [Internet]. Cancer Research. 2016 ; 76( 14):[citado 2024 nov. 16 ] Available from: http://cancerres.aacrjournals.org/content/76/14_supplement/4669.short

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