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Artigo de periodico
Prognostic significance of genome-wide DNA methylation profiles within the randomized, phase 3, EORTC CATNON trial on non-1p/19q deleted anaplastic glioma (2021)
Tesileanu, C. Mircea S.; Van den Bent, Martin; Sanson, Marc; Wick, Wolfgang; Brandes, Alba; Clement, Paul M.; Erridge, Sara C.; Vogelbaum, Michael A.; Nowak, Anna; Baurain, Jean; Mason, Warren P.; Wheeler, Helen; Chinot, Olivier L.; Gill, Sanjeev; Griffin, Matthew; Rogers, Leland; Taal, Walter; Rudà, Roberta; Weller, Michael; McBain, Catherine; Linde, Myra E. van; Sabedot, Thais S.; Hoogstrate, Youri; Deimling, Andreas von; Heer, Iris de; IJcken, Wilfred F. J. van; Brouwer, Rutger W. W.; Aldape, Kenneth; Jenkins, Robert B.; Dubbink, Hendrikus; Kros, Johan M.; Wesseling, Pieter; Cheung, Kin Jip; Golfinopoulos, Vassilis; Baumert, Brigitta; Gorlia, Thierry; Noushmehr, Houtan; French, Pim
Source: Neuro-Oncology. Unidade: FMRP
Subjects: NEOPLASIAS CEREBRAIS, METILAÇÃO DE DNA, GLIOMA, MUTAÇÃO, ESTUDOS PROSPECTIVOS
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ABNT
TESILEANU, C. Mircea S. et al. Prognostic significance of genome-wide DNA methylation profiles within the randomized, phase 3, EORTC CATNON trial on non-1p/19q deleted anaplastic glioma. Neuro-Oncology, v. 23, n. 9, p. 1547-1559, 2021Tradução . . Disponível em: https://doi.org/10.1093/neuonc/noab088. Acesso em: 16 nov. 2024.
APA
Tesileanu, C. M. S., Van den Bent, M., Sanson, M., Wick, W., Brandes, A., Clement, P. M., et al. (2021). Prognostic significance of genome-wide DNA methylation profiles within the randomized, phase 3, EORTC CATNON trial on non-1p/19q deleted anaplastic glioma. Neuro-Oncology, 23( 9), 1547-1559. doi:10.1093/neuonc/noab088
NLM
Tesileanu CMS, Van den Bent M, Sanson M, Wick W, Brandes A, Clement PM, Erridge SC, Vogelbaum MA, Nowak A, Baurain J, Mason WP, Wheeler H, Chinot OL, Gill S, Griffin M, Rogers L, Taal W, Rudà R, Weller M, McBain C, Linde ME van, Sabedot TS, Hoogstrate Y, Deimling A von, Heer I de, IJcken WFJ van, Brouwer RWW, Aldape K, Jenkins RB, Dubbink H, Kros JM, Wesseling P, Cheung KJ, Golfinopoulos V, Baumert B, Gorlia T, Noushmehr H, French P. Prognostic significance of genome-wide DNA methylation profiles within the randomized, phase 3, EORTC CATNON trial on non-1p/19q deleted anaplastic glioma [Internet]. Neuro-Oncology. 2021 ; 23( 9): 1547-1559.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1093/neuonc/noab088
Vancouver
Tesileanu CMS, Van den Bent M, Sanson M, Wick W, Brandes A, Clement PM, Erridge SC, Vogelbaum MA, Nowak A, Baurain J, Mason WP, Wheeler H, Chinot OL, Gill S, Griffin M, Rogers L, Taal W, Rudà R, Weller M, McBain C, Linde ME van, Sabedot TS, Hoogstrate Y, Deimling A von, Heer I de, IJcken WFJ van, Brouwer RWW, Aldape K, Jenkins RB, Dubbink H, Kros JM, Wesseling P, Cheung KJ, Golfinopoulos V, Baumert B, Gorlia T, Noushmehr H, French P. Prognostic significance of genome-wide DNA methylation profiles within the randomized, phase 3, EORTC CATNON trial on non-1p/19q deleted anaplastic glioma [Internet]. Neuro-Oncology. 2021 ; 23( 9): 1547-1559.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1093/neuonc/noab088
Artigo de periodico
Contribution of genetic ancestry and polygenic risk score in meeting vitamin B12 needs in healthy Brazilian children and adolescents (2021)
Fuzo, Carlos Alessandro; Ued, Fábio da Veiga ; Moco, Sofia; Cominetti, Ornella; Métairon, Sylviane; Pruvost, Solenn; Charpagne, Aline; Carayol, Jerome; Torrieri, Raul; Silva Junior, Wilson Araújo da ; Descombes, Patrick; Kaput, Jim; Monteiro, Jacqueline Pontes
Source: Scientific Reports. Unidades: FMRP, FCFRP
Subjects: GENEALOGIA, VITAMINA B12, POLIMORFISMO, ESTUDOS TRANSVERSAIS
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FUZO, Carlos Alessandro et al. Contribution of genetic ancestry and polygenic risk score in meeting vitamin B12 needs in healthy Brazilian children and adolescents. Scientific Reports, v. 11, n. 1, 2021Tradução . . Disponível em: https://doi.org/10.1038/s41598-021-91530-7. Acesso em: 16 nov. 2024.
APA
Fuzo, C. A., Ued, F. da V., Moco, S., Cominetti, O., Métairon, S., Pruvost, S., et al. (2021). Contribution of genetic ancestry and polygenic risk score in meeting vitamin B12 needs in healthy Brazilian children and adolescents. Scientific Reports, 11( 1). doi:10.1038/s41598-021-91530-7
NLM
Fuzo CA, Ued F da V, Moco S, Cominetti O, Métairon S, Pruvost S, Charpagne A, Carayol J, Torrieri R, Silva Junior WA da, Descombes P, Kaput J, Monteiro JP. Contribution of genetic ancestry and polygenic risk score in meeting vitamin B12 needs in healthy Brazilian children and adolescents [Internet]. Scientific Reports. 2021 ; 11( 1):[citado 2024 nov. 16 ] Available from: https://doi.org/10.1038/s41598-021-91530-7
Vancouver
Fuzo CA, Ued F da V, Moco S, Cominetti O, Métairon S, Pruvost S, Charpagne A, Carayol J, Torrieri R, Silva Junior WA da, Descombes P, Kaput J, Monteiro JP. Contribution of genetic ancestry and polygenic risk score in meeting vitamin B12 needs in healthy Brazilian children and adolescents [Internet]. Scientific Reports. 2021 ; 11( 1):[citado 2024 nov. 16 ] Available from: https://doi.org/10.1038/s41598-021-91530-7
Trabalho de evento-resumo periodico
Prognostic significance of epigenetic subtypes and CPGS associated with progression to G-CIMP low in the eortc randomized phase III intergroup catnon (2020)
Tesileanu, C. Mircea S.; Van den Bent, Martin; Sabedot, Thais; Sanson, Marc; Brandes, Alba; Wick, Wolfgang; Clement, Paul; Erridge, Sarah; Vogelbaum, Michael; Nowak, Anna; Baurain, Jean; Mason, Warren; Wheeler, Helen; Weller, Michael; Heer, Iris de; Dubbink, Hendrikus; Kros, Johan M; Aldape, Kenneth; Wesseling, Pieter; Golfinopoulos, Vassilis; Gorlia, Thierry; Baumert, Brigitta; Noushmehr, Houtan ; French, Pim
Source: Neuro-Oncology. Conference titles: Annual Scientific Meeting and Education Day of the Society for Neuro-Oncology. Unidade: FMRP
Subjects: EPIGÊNESE GENÉTICA, GLIOMA, NEOPLASIAS CEREBRAIS, METILAÇÃO DE DNA, RADIOTERAPIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TESILEANU, C. Mircea S. et al. Prognostic significance of epigenetic subtypes and CPGS associated with progression to G-CIMP low in the eortc randomized phase III intergroup catnon. Neuro-Oncology. Cary: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1093/neuonc/noaa215.693. Acesso em: 16 nov. 2024. , 2020
APA
Tesileanu, C. M. S., Van den Bent, M., Sabedot, T., Sanson, M., Brandes, A., Wick, W., et al. (2020). Prognostic significance of epigenetic subtypes and CPGS associated with progression to G-CIMP low in the eortc randomized phase III intergroup catnon. Neuro-Oncology. Cary: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1093/neuonc/noaa215.693
NLM
Tesileanu CMS, Van den Bent M, Sabedot T, Sanson M, Brandes A, Wick W, Clement P, Erridge S, Vogelbaum M, Nowak A, Baurain J, Mason W, Wheeler H, Weller M, Heer I de, Dubbink H, Kros JM, Aldape K, Wesseling P, Golfinopoulos V, Gorlia T, Baumert B, Noushmehr H, French P. Prognostic significance of epigenetic subtypes and CPGS associated with progression to G-CIMP low in the eortc randomized phase III intergroup catnon [Internet]. Neuro-Oncology. 2020 ; 22( suppl. 2): ii166.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1093/neuonc/noaa215.693
Vancouver
Tesileanu CMS, Van den Bent M, Sabedot T, Sanson M, Brandes A, Wick W, Clement P, Erridge S, Vogelbaum M, Nowak A, Baurain J, Mason W, Wheeler H, Weller M, Heer I de, Dubbink H, Kros JM, Aldape K, Wesseling P, Golfinopoulos V, Gorlia T, Baumert B, Noushmehr H, French P. Prognostic significance of epigenetic subtypes and CPGS associated with progression to G-CIMP low in the eortc randomized phase III intergroup catnon [Internet]. Neuro-Oncology. 2020 ; 22( suppl. 2): ii166.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1093/neuonc/noaa215.693
Artigo de periodico-carta/editorial
Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta] (2019)
Maia, Luana Sella Motta ; Moreno, Adriana Santos ; Ferriani, Mariana Paes Leme; Nunes, Fernanda Leonel; Ferraro, Maria Fernanda; Dias, Marina Mendonça; Roxo-Junior, Pérsio ; Dias, Fabrício Moura; Valle, Solange Oliveira Rodrigues; Levy, Soloni ; Alonso, Maria Luiza Oliva; França, Alfeu Tavares; Serpa, Faradiba Sarquis; Motta, Antônio Abílio; Maia, Felipe Gonçalves Motta ; Aragon, Davi Casale ; Sarti, Willy; Silva Junior, Wilson Araújo da ; Bork, Konrad ; Cichon, Sven; Arruda, Luisa Karla de Paula
Source: Allergy. Unidades: FMRP, FM, ICB
Subjects: BRADICININA, ANGIOEDEMA, DOENÇAS HEREDITÁRIAS
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ABNT
MAIA, Luana Sella Motta et al. Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta]. Allergy. West Sussex: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1111/all.13699. Acesso em: 16 nov. 2024. , 2019
APA
Maia, L. S. M., Moreno, A. S., Ferriani, M. P. L., Nunes, F. L., Ferraro, M. F., Dias, M. M., et al. (2019). Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta]. Allergy. West Sussex: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1111/all.13699
NLM
Maia LSM, Moreno AS, Ferriani MPL, Nunes FL, Ferraro MF, Dias MM, Roxo-Junior P, Dias FM, Valle SOR, Levy S , Alonso MLO, França AT, Serpa FS, Motta AA, Maia FGM, Aragon DC, Sarti W, Silva Junior WA da, Bork K , Cichon S, Arruda LK de P. Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta] [Internet]. Allergy. 2019 ; 74( 5): 1013-1016.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/all.13699
Vancouver
Maia LSM, Moreno AS, Ferriani MPL, Nunes FL, Ferraro MF, Dias MM, Roxo-Junior P, Dias FM, Valle SOR, Levy S , Alonso MLO, França AT, Serpa FS, Motta AA, Maia FGM, Aragon DC, Sarti W, Silva Junior WA da, Bork K , Cichon S, Arruda LK de P. Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta] [Internet]. Allergy. 2019 ; 74( 5): 1013-1016.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1111/all.13699
Artigo de periodico
Comprehensive analysis of alternative splicing across tumors from 8,705 patients (2018)
Kahles, André; Lehmann, Kjong-Van; Toussaint, Nora C.; Huser, Matthias; Stark, Stefan G.; Sachsenberg, Timo; Stegle, Oliver; Kohlbacher, Oliver; Sander, Chris; Ratsch, Gunnar; Noushmehr, Houtan; Carlotti Júnior, Carlos Gilberto; Santos, José Sebastião dos; Kemp, Rafael; Sankarankuty, Ajith Kumar; Tirapelli, Daniela Pretti da Cunha
Source: Cancer Cell. Unidade: FMRP
Subjects: NEOPLASIAS, IMUNOTERAPIA, ANTÍGENOS, PROTEÔMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KAHLES, André et al. Comprehensive analysis of alternative splicing across tumors from 8,705 patients. Cancer Cell, v. 34, n. 2, p. 211–224, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.ccell.2018.07.001. Acesso em: 16 nov. 2024.
APA
Kahles, A., Lehmann, K. -V., Toussaint, N. C., Huser, M., Stark, S. G., Sachsenberg, T., et al. (2018). Comprehensive analysis of alternative splicing across tumors from 8,705 patients. Cancer Cell, 34( 2), 211–224. doi:10.1016/j.ccell.2018.07.001
NLM
Kahles A, Lehmann K-V, Toussaint NC, Huser M, Stark SG, Sachsenberg T, Stegle O, Kohlbacher O, Sander C, Ratsch G, Noushmehr H, Carlotti Júnior CG, Santos JS dos, Kemp R, Sankarankuty AK, Tirapelli DP da C. Comprehensive analysis of alternative splicing across tumors from 8,705 patients [Internet]. Cancer Cell. 2018 ; 34( 2): 211–224.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.ccell.2018.07.001
Vancouver
Kahles A, Lehmann K-V, Toussaint NC, Huser M, Stark SG, Sachsenberg T, Stegle O, Kohlbacher O, Sander C, Ratsch G, Noushmehr H, Carlotti Júnior CG, Santos JS dos, Kemp R, Sankarankuty AK, Tirapelli DP da C. Comprehensive analysis of alternative splicing across tumors from 8,705 patients [Internet]. Cancer Cell. 2018 ; 34( 2): 211–224.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.ccell.2018.07.001
Trabalho de evento-resumo periodico
Comprehensive analysis of cancer stemness (2018)
Malta, Tathiane M.; Sokolov, Artem; Gentles, Andrew J.; Burzykowski, Tomasz; Poisson, Laila; Weinstein, John; Kaminska, Bozena; Huelsken, Joerg; Omberg, Larsson; Gevaert, Olivier; Noushmehr, Houtan
Source: Cancer Research. Conference titles: Annual Meeting of the American Association for Cancer Research (AACR). Unidade: FMRP
Subjects: NEOPLASIAS, EXPRESSÃO GÊNICA
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ABNT
MALTA, Tathiane M. et al. Comprehensive analysis of cancer stemness. Cancer Research. Baltimore: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1158/1538-7445.AM2018-LB-373. Acesso em: 16 nov. 2024. , 2018
APA
Malta, T. M., Sokolov, A., Gentles, A. J., Burzykowski, T., Poisson, L., Weinstein, J., et al. (2018). Comprehensive analysis of cancer stemness. Cancer Research. Baltimore: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1158/1538-7445.AM2018-LB-373
NLM
Malta TM, Sokolov A, Gentles AJ, Burzykowski T, Poisson L, Weinstein J, Kaminska B, Huelsken J, Omberg L, Gevaert O, Noushmehr H. Comprehensive analysis of cancer stemness [Internet]. Cancer Research. 2018 ; 78( 13):[citado 2024 nov. 16 ] Available from: https://doi.org/10.1158/1538-7445.AM2018-LB-373
Vancouver
Malta TM, Sokolov A, Gentles AJ, Burzykowski T, Poisson L, Weinstein J, Kaminska B, Huelsken J, Omberg L, Gevaert O, Noushmehr H. Comprehensive analysis of cancer stemness [Internet]. Cancer Research. 2018 ; 78( 13):[citado 2024 nov. 16 ] Available from: https://doi.org/10.1158/1538-7445.AM2018-LB-373

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