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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
Fonte: Clinical Epigenetics. Unidades: IME, FCF, IQ
Assuntos: GENOMAS, MELANOMA, BIOINFORMÁTICA
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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: 09 set. 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 set. 09 ] 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 set. 09 ] Available from: https://doi.org/10.1186/s13148-022-01291-x
Artigo de periodico
Transcriptional signatures underlying dynamic phenotypic switching and novel disease biomarkers in a linear cellular model of melanoma progression (2021)
Pessoa, Diogo de Oliveira ; Rius, Flávia Eichemberger ; Papaiz, Debora D'Angelo ; Ayub, Ana Luísa Pedroso ; Morais, Alice Santana ; Souza, Camila Ferreira de; Paixão, Vinicius Ferreira da ; Setubal, João Carlos ; Bishop, Julia Newton ; Nsengimana, Jérémie ; Azevedo, Hátylas ; Reis, Eduardo Moraes ; Jasiulionis, Miriam Galvonas
Fonte: Neoplasia. Unidade: IQ
Assuntos: MELANOMA, METÁSTASE NEOPLÁSICA, FENÓTIPOS, PROGNÓSTICO
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PESSOA, Diogo de Oliveira et al. Transcriptional signatures underlying dynamic phenotypic switching and novel disease biomarkers in a linear cellular model of melanoma progression. Neoplasia, v. 23, n. 4, p. 439-455 , 2021Tradução . . Disponível em: https://doi.org/10.1016/j.neo.2021.03.007. Acesso em: 09 set. 2024.
APA
Pessoa, D. de O., Rius, F. E., Papaiz, D. D. 'A., Ayub, A. L. P., Morais, A. S., Souza, C. F. de, et al. (2021). Transcriptional signatures underlying dynamic phenotypic switching and novel disease biomarkers in a linear cellular model of melanoma progression. Neoplasia, 23( 4), 439-455 . doi:10.1016/j.neo.2021.03.007
NLM
Pessoa D de O, Rius FE, Papaiz DD'A, Ayub ALP, Morais AS, Souza CF de, Paixão VF da, Setubal JC, Bishop JN, Nsengimana J, Azevedo H, Reis EM, Jasiulionis MG. Transcriptional signatures underlying dynamic phenotypic switching and novel disease biomarkers in a linear cellular model of melanoma progression [Internet]. Neoplasia. 2021 ; 23( 4): 439-455 .[citado 2024 set. 09 ] Available from: https://doi.org/10.1016/j.neo.2021.03.007
Vancouver
Pessoa D de O, Rius FE, Papaiz DD'A, Ayub ALP, Morais AS, Souza CF de, Paixão VF da, Setubal JC, Bishop JN, Nsengimana J, Azevedo H, Reis EM, Jasiulionis MG. Transcriptional signatures underlying dynamic phenotypic switching and novel disease biomarkers in a linear cellular model of melanoma progression [Internet]. Neoplasia. 2021 ; 23( 4): 439-455 .[citado 2024 set. 09 ] Available from: https://doi.org/10.1016/j.neo.2021.03.007
Artigo de periodico
Gene co-expression and histone modification signatures are associated with melanoma progression, epithelial-tomesenchymal transition, and metastasis (2020)
Azevedo, Hátylas; Pessoa, Guilherme Cavalcante; Vitorino, Francisca Nathalia de Luna; Nsengimana, Jérémie; Bishop, Julia Newton; Reis, Eduardo Moraes ; Cunha, Julia Pinheiro Chagas da ; Jasiulionis, Miriam Galvonas
Fonte: Clinical Epigenetics. Unidades: IQ, BIOTECNOLOGIA
Assunto: MELANOMA
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AZEVEDO, Hátylas et al. Gene co-expression and histone modification signatures are associated with melanoma progression, epithelial-tomesenchymal transition, and metastasis. Clinical Epigenetics, v. 12, p. 1-24 art. 127, 2020Tradução . . Disponível em: https://doi.org/10.1186/s13148-020-00910-9. Acesso em: 09 set. 2024.
APA
Azevedo, H., Pessoa, G. C., Vitorino, F. N. de L., Nsengimana, J., Bishop, J. N., Reis, E. M., et al. (2020). Gene co-expression and histone modification signatures are associated with melanoma progression, epithelial-tomesenchymal transition, and metastasis. Clinical Epigenetics, 12, 1-24 art. 127. doi:10.1186/s13148-020-00910-9
NLM
Azevedo H, Pessoa GC, Vitorino FN de L, Nsengimana J, Bishop JN, Reis EM, Cunha JPC da, Jasiulionis MG. Gene co-expression and histone modification signatures are associated with melanoma progression, epithelial-tomesenchymal transition, and metastasis [Internet]. Clinical Epigenetics. 2020 ; 12 1-24 art. 127.[citado 2024 set. 09 ] Available from: https://doi.org/10.1186/s13148-020-00910-9
Vancouver
Azevedo H, Pessoa GC, Vitorino FN de L, Nsengimana J, Bishop JN, Reis EM, Cunha JPC da, Jasiulionis MG. Gene co-expression and histone modification signatures are associated with melanoma progression, epithelial-tomesenchymal transition, and metastasis [Internet]. Clinical Epigenetics. 2020 ; 12 1-24 art. 127.[citado 2024 set. 09 ] Available from: https://doi.org/10.1186/s13148-020-00910-9
Artigo de periodico
A regulatory miRNA-mRNA network is associated with tissue repair induced by mesenchymal stromal cells in acute kidney injury (2017)
Almeida, Danilo Candido de; Bassi, Ênio José; Azevedo, Hátylas; Anderson, Letícia; Origassa, Clarice Silvia Taemi; Cenedeze, Marcos Antonio; Oliveira, Vinicius de Andrade; Felizardo, Raphael Jose Ferreira; Silva, Reinaldo Correia da; Hiyane, Meire Ioshie; Semedo, Patricia; Reis, Marlene Antonia dos; Moreira-Filho, Carlos Alberto; Verjovski-Almeida, Sergio ; Silva, Alvaro Pacheco; Câmara, Niels Olsen Saraiva
Fonte: Frontiers in Immunology. Unidades: FM, IQ, ICB
Assuntos: EXPRESSÃO GÊNICA, REPROGRAMAÇÃO NUCLEAR, INSUFICIÊNCIA RENAL AGUDA
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ABNT
ALMEIDA, Danilo Candido de et al. A regulatory miRNA-mRNA network is associated with tissue repair induced by mesenchymal stromal cells in acute kidney injury. Frontiers in Immunology, v. 7, p. 1-18 art. 645, 2017Tradução . . Disponível em: https://doi.org/10.3389/fimmu.2016.00645. Acesso em: 09 set. 2024.
APA
Almeida, D. C. de, Bassi, Ê. J., Azevedo, H., Anderson, L., Origassa, C. S. T., Cenedeze, M. A., et al. (2017). A regulatory miRNA-mRNA network is associated with tissue repair induced by mesenchymal stromal cells in acute kidney injury. Frontiers in Immunology, 7, 1-18 art. 645. doi:10.3389/fimmu.2016.00645
NLM
Almeida DC de, Bassi ÊJ, Azevedo H, Anderson L, Origassa CST, Cenedeze MA, Oliveira V de A, Felizardo RJF, Silva RC da, Hiyane MI, Semedo P, Reis MA dos, Moreira-Filho CA, Verjovski-Almeida S, Silva AP, Câmara NOS. A regulatory miRNA-mRNA network is associated with tissue repair induced by mesenchymal stromal cells in acute kidney injury [Internet]. Frontiers in Immunology. 2017 ; 7 1-18 art. 645.[citado 2024 set. 09 ] Available from: https://doi.org/10.3389/fimmu.2016.00645
Vancouver
Almeida DC de, Bassi ÊJ, Azevedo H, Anderson L, Origassa CST, Cenedeze MA, Oliveira V de A, Felizardo RJF, Silva RC da, Hiyane MI, Semedo P, Reis MA dos, Moreira-Filho CA, Verjovski-Almeida S, Silva AP, Câmara NOS. A regulatory miRNA-mRNA network is associated with tissue repair induced by mesenchymal stromal cells in acute kidney injury [Internet]. Frontiers in Immunology. 2017 ; 7 1-18 art. 645.[citado 2024 set. 09 ] Available from: https://doi.org/10.3389/fimmu.2016.00645
Artigo de periodico
Early infiltration of p40IL12(+)CCR7(+)CD11b(+) cells is critical for fibrosis development (2016)
Braga, Tárcio Teodoro; Costa, Matheus Correa; Azevedo, Hátylas; Silva, Reinaldo Correia; Cruz, Mário Costa; Almeida, Maíra Estanislau Soares de; Hiyane, Meire Ioshie; Moreira-Filho, Carlos Alberto; Santos, Marinilce Fagundes dos ; Perez, Katia Regina; Cuccovia, Iolanda Midea ; Câmara, Niels Olsen Saraiva
Fonte: Immunity, Inflammation and Disease. Unidades: ICB, FM, IQ
Assuntos: COLÁGENO, MACRÓFAGOS
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ABNT
BRAGA, Tárcio Teodoro et al. Early infiltration of p40IL12(+)CCR7(+)CD11b(+) cells is critical for fibrosis development. Immunity, Inflammation and Disease, v. 4, n. 3, p. 300–314, 2016Tradução . . Disponível em: https://doi.org/10.1002/iid3.114. Acesso em: 09 set. 2024.
APA
Braga, T. T., Costa, M. C., Azevedo, H., Silva, R. C., Cruz, M. C., Almeida, M. E. S. de, et al. (2016). Early infiltration of p40IL12(+)CCR7(+)CD11b(+) cells is critical for fibrosis development. Immunity, Inflammation and Disease, 4( 3), 300–314. doi:10.1002/iid3.114
NLM
Braga TT, Costa MC, Azevedo H, Silva RC, Cruz MC, Almeida MES de, Hiyane MI, Moreira-Filho CA, Santos MF dos, Perez KR, Cuccovia IM, Câmara NOS. Early infiltration of p40IL12(+)CCR7(+)CD11b(+) cells is critical for fibrosis development [Internet]. Immunity, Inflammation and Disease. 2016 ; 4( 3): 300–314.[citado 2024 set. 09 ] Available from: https://doi.org/10.1002/iid3.114
Vancouver
Braga TT, Costa MC, Azevedo H, Silva RC, Cruz MC, Almeida MES de, Hiyane MI, Moreira-Filho CA, Santos MF dos, Perez KR, Cuccovia IM, Câmara NOS. Early infiltration of p40IL12(+)CCR7(+)CD11b(+) cells is critical for fibrosis development [Internet]. Immunity, Inflammation and Disease. 2016 ; 4( 3): 300–314.[citado 2024 set. 09 ] Available from: https://doi.org/10.1002/iid3.114
Artigo de periodico
Topological robustness analysis of protein interaction networks reveals key targets for overcoming chemotherapy resistance in glioma (2015)
Azevedo, Hátylas; Moreira-Filho, Carlos Alberto
Fonte: Scientific Reports. Unidade: FM
Assuntos: REDE DE COMUNICAÇÃO, NEOPLASIAS DE CABEÇA E PESCOÇO, GLIOMA (FISIOPATOLOGIA), QUIMIOTERAPIA (TENDÊNCIAS)
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AZEVEDO, Hátylas e MOREIRA-FILHO, Carlos Alberto. Topological robustness analysis of protein interaction networks reveals key targets for overcoming chemotherapy resistance in glioma. Scientific Reports, v. 5, n. 16830, p. 13 , 2015Tradução . . Disponível em: https://doi.org/10.1038/srep16830. Acesso em: 09 set. 2024.
APA
Azevedo, H., & Moreira-Filho, C. A. (2015). Topological robustness analysis of protein interaction networks reveals key targets for overcoming chemotherapy resistance in glioma. Scientific Reports, 5( 16830), 13 . doi:10.1038/srep16830
NLM
Azevedo H, Moreira-Filho CA. Topological robustness analysis of protein interaction networks reveals key targets for overcoming chemotherapy resistance in glioma [Internet]. Scientific Reports. 2015 ; 5( 16830): 13 .[citado 2024 set. 09 ] Available from: https://doi.org/10.1038/srep16830
Vancouver
Azevedo H, Moreira-Filho CA. Topological robustness analysis of protein interaction networks reveals key targets for overcoming chemotherapy resistance in glioma [Internet]. Scientific Reports. 2015 ; 5( 16830): 13 .[citado 2024 set. 09 ] Available from: https://doi.org/10.1038/srep16830
Artigo de periodico
Transcriptional network analysis reveals that AT1 and AT2 angiotensin II receptors are both involved in the regulation of genes essential for glioma progression (2014)
Azevedo, Hátylas ; Fujita, André ; Bando, Sílvia Yumi ; Iamashita, Priscila ; Moreira-Filho, Carlos Alberto
Fonte: PLOS ONE. Unidades: FM, IME
Assuntos: REGULAÇÃO GÊNICA, ANGIOTENSINA II, GLIOMA, ESTATÍSTICA COMPUTACIONAL
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ABNT
AZEVEDO, Hátylas et al. Transcriptional network analysis reveals that AT1 and AT2 angiotensin II receptors are both involved in the regulation of genes essential for glioma progression. PLOS ONE, v. 9, n. 11, p. 1-17, 2014Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0110934. Acesso em: 09 set. 2024.
APA
Azevedo, H., Fujita, A., Bando, S. Y., Iamashita, P., & Moreira-Filho, C. A. (2014). Transcriptional network analysis reveals that AT1 and AT2 angiotensin II receptors are both involved in the regulation of genes essential for glioma progression. PLOS ONE, 9( 11), 1-17. doi:10.1371/journal.pone.0110934
NLM
Azevedo H, Fujita A, Bando SY, Iamashita P, Moreira-Filho CA. Transcriptional network analysis reveals that AT1 and AT2 angiotensin II receptors are both involved in the regulation of genes essential for glioma progression [Internet]. PLOS ONE. 2014 ; 9( 11): 1-17.[citado 2024 set. 09 ] Available from: https://doi.org/10.1371/journal.pone.0110934
Vancouver
Azevedo H, Fujita A, Bando SY, Iamashita P, Moreira-Filho CA. Transcriptional network analysis reveals that AT1 and AT2 angiotensin II receptors are both involved in the regulation of genes essential for glioma progression [Internet]. PLOS ONE. 2014 ; 9( 11): 1-17.[citado 2024 set. 09 ] Available from: https://doi.org/10.1371/journal.pone.0110934
Artigo de periodico
Transcriptome analysis of renal ischemia/reperfusion injury and its modulation by ischemic pre-conditioning or hemin treatment (2012)
Correa-Costa, Matheus; Azevedo, Hátylas; Amano, Mariane Tami; Gonçalves, Giselle Martins; Hyane, Meire Ioshie; Cenedeze, Marcos Antonio; Renesto, Paulo Guilherme; Pacheco-Silva, Alvaro; Moreira-Filho, Carlos Alberto; Câmara, Niels Olsen Saraiva
Fonte: PLOS ONE. Unidades: FM, ICB
Assunto: IMUNOLOGIA
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ABNT
CORREA-COSTA, Matheus et al. Transcriptome analysis of renal ischemia/reperfusion injury and its modulation by ischemic pre-conditioning or hemin treatment. PLOS ONE, v. 7, n. 11, p. 1-19, 2012Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0049569. Acesso em: 09 set. 2024.
APA
Correa-Costa, M., Azevedo, H., Amano, M. T., Gonçalves, G. M., Hyane, M. I., Cenedeze, M. A., et al. (2012). Transcriptome analysis of renal ischemia/reperfusion injury and its modulation by ischemic pre-conditioning or hemin treatment. PLOS ONE, 7( 11), 1-19. doi:10.1371/journal.pone.0049569
NLM
Correa-Costa M, Azevedo H, Amano MT, Gonçalves GM, Hyane MI, Cenedeze MA, Renesto PG, Pacheco-Silva A, Moreira-Filho CA, Câmara NOS. Transcriptome analysis of renal ischemia/reperfusion injury and its modulation by ischemic pre-conditioning or hemin treatment [Internet]. PLOS ONE. 2012 ; 7( 11): 1-19.[citado 2024 set. 09 ] Available from: https://doi.org/10.1371/journal.pone.0049569
Vancouver
Correa-Costa M, Azevedo H, Amano MT, Gonçalves GM, Hyane MI, Cenedeze MA, Renesto PG, Pacheco-Silva A, Moreira-Filho CA, Câmara NOS. Transcriptome analysis of renal ischemia/reperfusion injury and its modulation by ischemic pre-conditioning or hemin treatment [Internet]. PLOS ONE. 2012 ; 7( 11): 1-19.[citado 2024 set. 09 ] Available from: https://doi.org/10.1371/journal.pone.0049569

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