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Artigo de periodico
Genome-wide promoter methylation profling in a cellular model of melanoma progression reveals markers of malignancy and metastasis that predict melanoma survival (2022)
Rius, Flávia Eichemberger ; Papaiz, Debora D'Angelo ; Azevedo, Hátylas ; Ayub, Ana Luísa P ; Pessoa, Diogo de Oliveira ; Oliveira, Tiago Franco de ; Loureiro, Ana Paula de Melo ; Andrade, Fernando; Fujita, André ; Reis, Eduardo Moraes ; Mason, Christopher E; Jasiulionis, Miriam Galvonas
Source: Clinical Epigenetics. Unidades: IME, FCF, IQ
Subjects: GENOMAS, MELANOMA, BIOINFORMÁTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIUS, Flávia Eichemberger et al. Genome-wide promoter methylation profling in a cellular model of melanoma progression reveals markers of malignancy and metastasis that predict melanoma survival. Clinical Epigenetics, v. 14, n. artigo 68, p. 1-20, 2022Tradução . . Disponível em: https://doi.org/10.1186/s13148-022-01291-x. Acesso em: 22 maio 2024.
APA
Rius, F. E., Papaiz, D. D. 'A., Azevedo, H., Ayub, A. L. P., Pessoa, D. de O., Oliveira, T. F. de, et al. (2022). Genome-wide promoter methylation profling in a cellular model of melanoma progression reveals markers of malignancy and metastasis that predict melanoma survival. Clinical Epigenetics, 14( artigo 68), 1-20. doi:10.1186/s13148-022-01291-x
NLM
Rius FE, Papaiz DD'A, Azevedo H, Ayub ALP, Pessoa D de O, Oliveira TF de, Loureiro AP de M, Andrade F, Fujita A, Reis EM, Mason CE, Jasiulionis MG. Genome-wide promoter methylation profling in a cellular model of melanoma progression reveals markers of malignancy and metastasis that predict melanoma survival [Internet]. Clinical Epigenetics. 2022 ; 14( artigo 68): 1-20.[citado 2024 maio 22 ] Available from: https://doi.org/10.1186/s13148-022-01291-x
Vancouver
Rius FE, Papaiz DD'A, Azevedo H, Ayub ALP, Pessoa D de O, Oliveira TF de, Loureiro AP de M, Andrade F, Fujita A, Reis EM, Mason CE, Jasiulionis MG. Genome-wide promoter methylation profling in a cellular model of melanoma progression reveals markers of malignancy and metastasis that predict melanoma survival [Internet]. Clinical Epigenetics. 2022 ; 14( artigo 68): 1-20.[citado 2024 maio 22 ] Available from: https://doi.org/10.1186/s13148-022-01291-x
Artigo de periodico
Expression of glypican-3 (GPC3) in malignant and non-malignant human breast tissues (2015)
Castillo, Lilian; Huvelle, María Amparo Lago; Fujita, André ; Lobba, Aline Ramos Maia; Tascón, Rocío; Garcia, Tatiene Romera; Armanasco, Eduardo; Bagnoli, Fabio; Oliveira, Vilmar Marques de; Galvão, Maria Antonieta Longo; Montor, Wagner Ricardo; Sogayar, Mari Cleide ; Joffé, Elisa Bal de Kier; Puricelli, Lydia; Labriola, Leticia ; Peters, María Giselle
Source: Open Cancer Journal. Unidades: IME, IQ
Subjects: BIOINFORMÁTICA, BIOMARCADORES, NEOPLASIAS MAMÁRIAS, METÁSTASE NEOPLÁSICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTILLO, Lilian et al. Expression of glypican-3 (GPC3) in malignant and non-malignant human breast tissues. Open Cancer Journal, v. 8, p. 12-23, 2015Tradução . . Disponível em: https://doi.org/10.2174/1874079001508010012. Acesso em: 22 maio 2024.
APA
Castillo, L., Huvelle, M. A. L., Fujita, A., Lobba, A. R. M., Tascón, R., Garcia, T. R., et al. (2015). Expression of glypican-3 (GPC3) in malignant and non-malignant human breast tissues. Open Cancer Journal, 8, 12-23. doi:10.2174/1874079001508010012
NLM
Castillo L, Huvelle MAL, Fujita A, Lobba ARM, Tascón R, Garcia TR, Armanasco E, Bagnoli F, Oliveira VM de, Galvão MAL, Montor WR, Sogayar MC, Joffé EB de K, Puricelli L, Labriola L, Peters MG. Expression of glypican-3 (GPC3) in malignant and non-malignant human breast tissues [Internet]. Open Cancer Journal. 2015 ; 8 12-23.[citado 2024 maio 22 ] Available from: https://doi.org/10.2174/1874079001508010012
Vancouver
Castillo L, Huvelle MAL, Fujita A, Lobba ARM, Tascón R, Garcia TR, Armanasco E, Bagnoli F, Oliveira VM de, Galvão MAL, Montor WR, Sogayar MC, Joffé EB de K, Puricelli L, Labriola L, Peters MG. Expression of glypican-3 (GPC3) in malignant and non-malignant human breast tissues [Internet]. Open Cancer Journal. 2015 ; 8 12-23.[citado 2024 maio 22 ] Available from: https://doi.org/10.2174/1874079001508010012
Trabalho de evento-resumo
Identification of MicroRNAs regulated by oncogenic KRAS in pancreatic cancer (2014)
Salviatto, Armando Padilha; Moura, A; Aoki, M. M; Carreira, Ana Claudia Oliveira; Fujita, André ; Sogayar, Mari Cleide ; Bassères, Daniela Sanchez
Source: Program and Index. Conference titles: Annual Meeting of the Brazilian Biochemistry and Molecular Biology Society (SBBq). Unidades: IME, IQ
Subjects: NEOPLASIAS PANCREÁTICAS, ONCOGENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SALVIATTO, Armando Padilha et al. Identification of MicroRNAs regulated by oncogenic KRAS in pancreatic cancer. 2014, Anais.. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular (SBBq), 2014. Disponível em: http://www.sigeventos.com.br/sbbq/cd/2014/resumos/R08438-1.pdf. Acesso em: 22 maio 2024.
APA
Salviatto, A. P., Moura, A., Aoki, M. M., Carreira, A. C. O., Fujita, A., Sogayar, M. C., & Bassères, D. S. (2014). Identification of MicroRNAs regulated by oncogenic KRAS in pancreatic cancer. In Program and Index. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular (SBBq). Recuperado de http://www.sigeventos.com.br/sbbq/cd/2014/resumos/R08438-1.pdf
NLM
Salviatto AP, Moura A, Aoki MM, Carreira ACO, Fujita A, Sogayar MC, Bassères DS. Identification of MicroRNAs regulated by oncogenic KRAS in pancreatic cancer [Internet]. Program and Index. 2014 ;[citado 2024 maio 22 ] Available from: http://www.sigeventos.com.br/sbbq/cd/2014/resumos/R08438-1.pdf
Vancouver
Salviatto AP, Moura A, Aoki MM, Carreira ACO, Fujita A, Sogayar MC, Bassères DS. Identification of MicroRNAs regulated by oncogenic KRAS in pancreatic cancer [Internet]. Program and Index. 2014 ;[citado 2024 maio 22 ] Available from: http://www.sigeventos.com.br/sbbq/cd/2014/resumos/R08438-1.pdf

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