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Artigo de periodico
A serum-based DNA methylation assay provides accurate detection of glioma (2021)
Sabedot, Thais S; Malta, Tathiane M; Snyder, James; Nelson, Kevin; Wells, Michael; Carvalho, Ana C. de; Mukherjee, Abir; Chitale, Dhananjay A; Mosella, Maritza S; Sokolov, Artem; Asmaro, Karam P; Robin, Adam; Rosenblum, Mark L; Mikkelsen, Tom; Rock, Jack; Poisson, Laila M; Lee, Ian; Walbert, Tobias; Kalkanis, Steven; Iavarone, Antonio; Castro, Ana Valeria; Noushmehr, Houtan
Source: Neuro-Oncology. Unidade: FMRP
Subjects: BIOMARCADORES, GLIOMA, NEOPLASIAS CEREBRAIS, METILAÇÃO DE DNA, EPIGÊNESE GENÉTICA, BIÓPSIA
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ABNT
SABEDOT, Thais S et al. A serum-based DNA methylation assay provides accurate detection of glioma. Neuro-Oncology, v. 23, n. 9, p. 1494-1508, 2021Tradução . . Disponível em: https://doi.org/10.1093/neuonc/noab023. Acesso em: 19 jun. 2024.
APA
Sabedot, T. S., Malta, T. M., Snyder, J., Nelson, K., Wells, M., Carvalho, A. C. de, et al. (2021). A serum-based DNA methylation assay provides accurate detection of glioma. Neuro-Oncology, 23( 9), 1494-1508. doi:10.1093/neuonc/noab023
NLM
Sabedot TS, Malta TM, Snyder J, Nelson K, Wells M, Carvalho AC de, Mukherjee A, Chitale DA, Mosella MS, Sokolov A, Asmaro KP, Robin A, Rosenblum ML, Mikkelsen T, Rock J, Poisson LM, Lee I, Walbert T, Kalkanis S, Iavarone A, Castro AV, Noushmehr H. A serum-based DNA methylation assay provides accurate detection of glioma [Internet]. Neuro-Oncology. 2021 ; 23( 9): 1494-1508.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1093/neuonc/noab023
Vancouver
Sabedot TS, Malta TM, Snyder J, Nelson K, Wells M, Carvalho AC de, Mukherjee A, Chitale DA, Mosella MS, Sokolov A, Asmaro KP, Robin A, Rosenblum ML, Mikkelsen T, Rock J, Poisson LM, Lee I, Walbert T, Kalkanis S, Iavarone A, Castro AV, Noushmehr H. A serum-based DNA methylation assay provides accurate detection of glioma [Internet]. Neuro-Oncology. 2021 ; 23( 9): 1494-1508.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1093/neuonc/noab023
Artigo de periodico
Adaptive thermogenesis in a mouse model lacking selenoprotein biosynthesis in brown adipocytes (2021)
Seale, Lucia A.; Ogawa-Wong, Ashley N.; Watanabe, Ligia Moriguchi ; Khadka, Vedbar S.; Menor, Mark; Torres, Daniel J.; Carlson, Bradley A.; Hatfield, Dolph L.; Berry, Marla J.
Source: International Journal of Molecular Sciences. Unidade: FMRP
Subjects: TECIDO ADIPOSO, PROTEÍNAS, AMINOÁCIDOS, SELÊNIO, TERMOGÊNESE, MODELOS ANIMAIS, NEOPLASIAS, FISIOPATOLOGIA, DELEÇÃO DE GENES
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SEALE, Lucia A. et al. Adaptive thermogenesis in a mouse model lacking selenoprotein biosynthesis in brown adipocytes. International Journal of Molecular Sciences, v. 22, n. 2, p. 1-20, 2021Tradução . . Disponível em: https://doi.org/10.3390/ijms22020611. Acesso em: 19 jun. 2024.
APA
Seale, L. A., Ogawa-Wong, A. N., Watanabe, L. M., Khadka, V. S., Menor, M., Torres, D. J., et al. (2021). Adaptive thermogenesis in a mouse model lacking selenoprotein biosynthesis in brown adipocytes. International Journal of Molecular Sciences, 22( 2), 1-20. doi:10.3390/ijms22020611
NLM
Seale LA, Ogawa-Wong AN, Watanabe LM, Khadka VS, Menor M, Torres DJ, Carlson BA, Hatfield DL, Berry MJ. Adaptive thermogenesis in a mouse model lacking selenoprotein biosynthesis in brown adipocytes [Internet]. International Journal of Molecular Sciences. 2021 ; 22( 2): 1-20.[citado 2024 jun. 19 ] Available from: https://doi.org/10.3390/ijms22020611
Vancouver
Seale LA, Ogawa-Wong AN, Watanabe LM, Khadka VS, Menor M, Torres DJ, Carlson BA, Hatfield DL, Berry MJ. Adaptive thermogenesis in a mouse model lacking selenoprotein biosynthesis in brown adipocytes [Internet]. International Journal of Molecular Sciences. 2021 ; 22( 2): 1-20.[citado 2024 jun. 19 ] Available from: https://doi.org/10.3390/ijms22020611
Artigo de periodico
Global burden of 87 risk factors in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019 (2020)
Murray, Christopher J. L.; Lotufo, Paulo Andrade; Palone, Marcos Roberto Tovani; Castaldelli-Maia, João Maurício ; Furtado, João Marcello Fortes; Bensenor, Isabela Judith Martins; Goulart, Alessandra Carvalho
Source: The Lancet. Unidades: FM, FMRP, HU
Subjects: SERVIÇOS DE SAÚDE, ASSISTÊNCIA À SAÚDE
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MURRAY, Christopher J. L. et al. Global burden of 87 risk factors in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019. The Lancet, v. 396, n. 10258, p. 1223–1249, 2020Tradução . . Disponível em: https://doi.org/10.1016/S0140-6736(20)30752-2. Acesso em: 19 jun. 2024.
APA
Murray, C. J. L., Lotufo, P. A., Palone, M. R. T., Castaldelli-Maia, J. M., Furtado, J. M. F., Bensenor, I. J. M., & Goulart, A. C. (2020). Global burden of 87 risk factors in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019. The Lancet, 396( 10258), 1223–1249. doi:10.1016/S0140-6736(20)30752-2
NLM
Murray CJL, Lotufo PA, Palone MRT, Castaldelli-Maia JM, Furtado JMF, Bensenor IJM, Goulart AC. Global burden of 87 risk factors in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019 [Internet]. The Lancet. 2020 ; 396( 10258): 1223–1249.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/S0140-6736(20)30752-2
Vancouver
Murray CJL, Lotufo PA, Palone MRT, Castaldelli-Maia JM, Furtado JMF, Bensenor IJM, Goulart AC. Global burden of 87 risk factors in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019 [Internet]. The Lancet. 2020 ; 396( 10258): 1223–1249.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/S0140-6736(20)30752-2
Artigo de periodico
Measuring universal health coverage based on an index of effective coverage of health services in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019 (2020)
Lozano, Rafael; Berman, A. E.; Furtado, João Marcello Fortes; Palone, Marcos Roberto Tovani; Lotufo, Paulo Andrade; Bensenor, Isabela Judith Martins; Castaldelli-Maia, João Maurício
Source: The Lancet. Unidades: FMRP, FM
Subjects: SERVIÇOS DE SAÚDE, GASTOS EM SAÚDE, COBERTURA DE SERVIÇOS DE SAÚDE
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ABNT
LOZANO, Rafael et al. Measuring universal health coverage based on an index of effective coverage of health services in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019. The Lancet, v. 396, n. 10258, p. 1250–1284, 2020Tradução . . Disponível em: https://doi.org/10.1016/S0140-6736(20)30750-9. Acesso em: 19 jun. 2024.
APA
Lozano, R., Berman, A. E., Furtado, J. M. F., Palone, M. R. T., Lotufo, P. A., Bensenor, I. J. M., & Castaldelli-Maia, J. M. (2020). Measuring universal health coverage based on an index of effective coverage of health services in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019. The Lancet, 396( 10258), 1250–1284. doi:10.1016/S0140-6736(20)30750-9
NLM
Lozano R, Berman AE, Furtado JMF, Palone MRT, Lotufo PA, Bensenor IJM, Castaldelli-Maia JM. Measuring universal health coverage based on an index of effective coverage of health services in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019 [Internet]. The Lancet. 2020 ; 396( 10258): 1250–1284.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/S0140-6736(20)30750-9
Vancouver
Lozano R, Berman AE, Furtado JMF, Palone MRT, Lotufo PA, Bensenor IJM, Castaldelli-Maia JM. Measuring universal health coverage based on an index of effective coverage of health services in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019 [Internet]. The Lancet. 2020 ; 396( 10258): 1250–1284.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/S0140-6736(20)30750-9
Artigo de periodico
Global burden of 369 diseases and injuries in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019 (2020)
Murray, Christopher J. L.; Lotufo, Paulo Andrade; Palone, Marcos Roberto Tovani; Castaldelli-Maia, João Maurício ; Furtado, João Marcello Fortes; Bensenor, Isabela Judith Martins; Goulart, Alessandra Carvalho
Source: The Lancet. Unidades: FM, FMRP, HU
Subjects: SERVIÇOS DE SAÚDE, ASSISTÊNCIA À SAÚDE
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ABNT
MURRAY, Christopher J. L. et al. Global burden of 369 diseases and injuries in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019. The Lancet, v. 396, n. 10258, p. 1204-1222, 2020Tradução . . Disponível em: https://doi.org/10.1016/S0140-6736(20)30925-9. Acesso em: 19 jun. 2024.
APA
Murray, C. J. L., Lotufo, P. A., Palone, M. R. T., Castaldelli-Maia, J. M., Furtado, J. M. F., Bensenor, I. J. M., & Goulart, A. C. (2020). Global burden of 369 diseases and injuries in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019. The Lancet, 396( 10258), 1204-1222. doi:10.1016/S0140-6736(20)30925-9
NLM
Murray CJL, Lotufo PA, Palone MRT, Castaldelli-Maia JM, Furtado JMF, Bensenor IJM, Goulart AC. Global burden of 369 diseases and injuries in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019 [Internet]. The Lancet. 2020 ; 396( 10258): 1204-1222.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/S0140-6736(20)30925-9
Vancouver
Murray CJL, Lotufo PA, Palone MRT, Castaldelli-Maia JM, Furtado JMF, Bensenor IJM, Goulart AC. Global burden of 369 diseases and injuries in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019 [Internet]. The Lancet. 2020 ; 396( 10258): 1204-1222.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/S0140-6736(20)30925-9
Artigo de periodico
Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanoma (2020)
Choi, Jiyeon; Zhang, Tongwu ; Vu, Andrew; Ablain, Julien; Makowski, Matthew M.; Colli, Leandro Machado ; Xu, Mai; Hennessey, Rebecca C.; Yin, Jinhu; Rothschild, Harriet; Gräwe, Cathrin; Kovacs, Michael A.; Funderburk, Karen M.; Brossard, Myriam; Taylor, John; Pasaniuc, Bogdan; Chari, Raj; Chanock, Stephen J.; Hoggart, Clive J.; Demenais, Florence; Barrett, Jennifer H.; Law, Matthew H.; Iles, Mark M.; Yu, Kai; Vermeulen, Michiel; Zon, Leonard I.; Brown, Kevin M.
Source: Nature Communications. Unidade: FMRP
Subjects: MELANOMA, EPIGÊNESE GENÉTICA, EXPRESSÃO GÊNICA, REGULAÇÃO GÊNICA
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CHOI, Jiyeon et al. Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanoma. Nature Communications, v. 11, 2020Tradução . . Disponível em: https://doi.org/10.1038/s41467-020-16590-1. Acesso em: 19 jun. 2024.
APA
Choi, J., Zhang, T., Vu, A., Ablain, J., Makowski, M. M., Colli, L. M., et al. (2020). Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanoma. Nature Communications, 11. doi:10.1038/s41467-020-16590-1
NLM
Choi J, Zhang T, Vu A, Ablain J, Makowski MM, Colli LM, Xu M, Hennessey RC, Yin J, Rothschild H, Gräwe C, Kovacs MA, Funderburk KM, Brossard M, Taylor J, Pasaniuc B, Chari R, Chanock SJ, Hoggart CJ, Demenais F, Barrett JH, Law MH, Iles MM, Yu K, Vermeulen M, Zon LI, Brown KM. Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanoma [Internet]. Nature Communications. 2020 ; 11[citado 2024 jun. 19 ] Available from: https://doi.org/10.1038/s41467-020-16590-1
Vancouver
Choi J, Zhang T, Vu A, Ablain J, Makowski MM, Colli LM, Xu M, Hennessey RC, Yin J, Rothschild H, Gräwe C, Kovacs MA, Funderburk KM, Brossard M, Taylor J, Pasaniuc B, Chari R, Chanock SJ, Hoggart CJ, Demenais F, Barrett JH, Law MH, Iles MM, Yu K, Vermeulen M, Zon LI, Brown KM. Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanoma [Internet]. Nature Communications. 2020 ; 11[citado 2024 jun. 19 ] Available from: https://doi.org/10.1038/s41467-020-16590-1
Artigo de periodico
Noninvasive neuromodulation of the prefrontal cortex in young women with obesity: a randomized clinical trial (2020)
Fassini, Priscila Giacomo; Das, Sai Krupa; Magerowski, Greta; Marchini, Julio Sergio ; Silva Junior, Wilson Araújo da ; Silva, Isabela Rozatte da; Salgueiro, Rafaella de Souza Ribeiro; Sousa, Cássia Dias Machado de; Suen, Vivian Marques Miguel; Alonso-Alonso, Miguel
Source: International Journal of Obesity. Unidade: FMRP
Subjects: CÓRTEX PRÉ-FRONTAL, MULHERES, OBESIDADE, ENSAIO CLÍNICO CONTROLADO RANDOMIZADO
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ABNT
FASSINI, Priscila Giacomo et al. Noninvasive neuromodulation of the prefrontal cortex in young women with obesity: a randomized clinical trial. International Journal of Obesity, v. 44, n. 6, p. 1279-1290, 2020Tradução . . Disponível em: https://doi.org/10.1038/s41366-020-0545-3. Acesso em: 19 jun. 2024.
APA
Fassini, P. G., Das, S. K., Magerowski, G., Marchini, J. S., Silva Junior, W. A. da, Silva, I. R. da, et al. (2020). Noninvasive neuromodulation of the prefrontal cortex in young women with obesity: a randomized clinical trial. International Journal of Obesity, 44( 6), 1279-1290. doi:10.1038/s41366-020-0545-3
NLM
Fassini PG, Das SK, Magerowski G, Marchini JS, Silva Junior WA da, Silva IR da, Salgueiro R de SR, Sousa CDM de, Suen VMM, Alonso-Alonso M. Noninvasive neuromodulation of the prefrontal cortex in young women with obesity: a randomized clinical trial [Internet]. International Journal of Obesity. 2020 ; 44( 6): 1279-1290.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1038/s41366-020-0545-3
Vancouver
Fassini PG, Das SK, Magerowski G, Marchini JS, Silva Junior WA da, Silva IR da, Salgueiro R de SR, Sousa CDM de, Suen VMM, Alonso-Alonso M. Noninvasive neuromodulation of the prefrontal cortex in young women with obesity: a randomized clinical trial [Internet]. International Journal of Obesity. 2020 ; 44( 6): 1279-1290.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1038/s41366-020-0545-3
Artigo de periodico
Global age-sex-specific fertility, mortality, healthy life expectancy (HALE), and population estimates in 204 countries and territories, 1950–2019: a comprehensive demographic analysis for the Global Burden of Disease Study 2019 (2020)
Wang, Haidong; Lotufo, Paulo Andrade; Palone, Marcos Roberto Tovani; Castaldelli-Maia, João Maurício ; Furtado, João Marcello Fortes; Bensenor, Isabela Judith Martins; Goulart, Alessandra Carvalho
Source: The Lancet. Unidades: FM, FMRP, HU
Subjects: SERVIÇOS DE SAÚDE, ASSISTÊNCIA À SAÚDE, DEMOGRAFIA EM SAÚDE PÚBLICA
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ABNT
WANG, Haidong et al. Global age-sex-specific fertility, mortality, healthy life expectancy (HALE), and population estimates in 204 countries and territories, 1950–2019: a comprehensive demographic analysis for the Global Burden of Disease Study 2019. The Lancet, v. 396, n. 10258, p. 1160-1203, 2020Tradução . . Disponível em: https://doi.org/10.1016/S0140-6736(20)30977-6. Acesso em: 19 jun. 2024.
APA
Wang, H., Lotufo, P. A., Palone, M. R. T., Castaldelli-Maia, J. M., Furtado, J. M. F., Bensenor, I. J. M., & Goulart, A. C. (2020). Global age-sex-specific fertility, mortality, healthy life expectancy (HALE), and population estimates in 204 countries and territories, 1950–2019: a comprehensive demographic analysis for the Global Burden of Disease Study 2019. The Lancet, 396( 10258), 1160-1203. doi:10.1016/S0140-6736(20)30977-6
NLM
Wang H, Lotufo PA, Palone MRT, Castaldelli-Maia JM, Furtado JMF, Bensenor IJM, Goulart AC. Global age-sex-specific fertility, mortality, healthy life expectancy (HALE), and population estimates in 204 countries and territories, 1950–2019: a comprehensive demographic analysis for the Global Burden of Disease Study 2019 [Internet]. The Lancet. 2020 ; 396( 10258): 1160-1203.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/S0140-6736(20)30977-6
Vancouver
Wang H, Lotufo PA, Palone MRT, Castaldelli-Maia JM, Furtado JMF, Bensenor IJM, Goulart AC. Global age-sex-specific fertility, mortality, healthy life expectancy (HALE), and population estimates in 204 countries and territories, 1950–2019: a comprehensive demographic analysis for the Global Burden of Disease Study 2019 [Internet]. The Lancet. 2020 ; 396( 10258): 1160-1203.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/S0140-6736(20)30977-6
Artigo de periodico
T cell-intrinsic role for Nod2 in protection against Th17-mediated uveitis (2020)
Napier, Ruth J.; Lee, Ellen J.; Davey, Michael P.; Vance, Emily E.; Furtado, João Marcello Fortes; Snow, Paige E.; Samson, Kimberly A.; Lashley, Sydney J.; Brown, Brieanna R.; Horai, Reiko; Mattapallil, Mary J.; Xu, Biying; Callegan, Michelle C.; Uebelhoer, Luke S.; Lancioni, Christina L.; Vehe, Richard K.; Binstadt, Bryce A.; Smith, Justine R.; Caspi, Rachel R.; Rosenzweig, Holly L.
Source: Nature Communications. Unidade: FMRP
Subjects: LINFÓCITOS T, UVEÍTE, MUTAÇÃO GENÉTICA
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ABNT
NAPIER, Ruth J. et al. T cell-intrinsic role for Nod2 in protection against Th17-mediated uveitis. Nature Communications, v. 11, n. 1, 2020Tradução . . Disponível em: https://doi.org/10.1038/s41467-020-18961-0. Acesso em: 19 jun. 2024.
APA
Napier, R. J., Lee, E. J., Davey, M. P., Vance, E. E., Furtado, J. M. F., Snow, P. E., et al. (2020). T cell-intrinsic role for Nod2 in protection against Th17-mediated uveitis. Nature Communications, 11( 1). doi:10.1038/s41467-020-18961-0
NLM
Napier RJ, Lee EJ, Davey MP, Vance EE, Furtado JMF, Snow PE, Samson KA, Lashley SJ, Brown BR, Horai R, Mattapallil MJ, Xu B, Callegan MC, Uebelhoer LS, Lancioni CL, Vehe RK, Binstadt BA, Smith JR, Caspi RR, Rosenzweig HL. T cell-intrinsic role for Nod2 in protection against Th17-mediated uveitis [Internet]. Nature Communications. 2020 ; 11( 1):[citado 2024 jun. 19 ] Available from: https://doi.org/10.1038/s41467-020-18961-0
Vancouver
Napier RJ, Lee EJ, Davey MP, Vance EE, Furtado JMF, Snow PE, Samson KA, Lashley SJ, Brown BR, Horai R, Mattapallil MJ, Xu B, Callegan MC, Uebelhoer LS, Lancioni CL, Vehe RK, Binstadt BA, Smith JR, Caspi RR, Rosenzweig HL. T cell-intrinsic role for Nod2 in protection against Th17-mediated uveitis [Internet]. Nature Communications. 2020 ; 11( 1):[citado 2024 jun. 19 ] Available from: https://doi.org/10.1038/s41467-020-18961-0
Artigo de periodico
Wnt/β-catenin activation cooperates with loss of p53 to cause adrenocortical carcinoma in mice (2020)
Borges, Kleiton Silva; Pignatti, Emanuele; Leng, Sining; Kariyawasam, Dulanjalee; Ruiz-Babot, Gerard; Ramalho, Fernando Silva ; Taketo, Makoto Mark; Carlone, Diana L.; Breault, David T.
Source: Oncogene. Unidade: FMRP
Subjects: NEOPLASIAS, CÓRTEX ADRENAL, CARCINOMA, PROLIFERAÇÃO CELULAR, REGULAÇÃO GÊNICA
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ABNT
BORGES, Kleiton Silva et al. Wnt/β-catenin activation cooperates with loss of p53 to cause adrenocortical carcinoma in mice. Oncogene, v. 39, p. 5282-5291, 2020Tradução . . Disponível em: https://doi.org/10.1038/s41388-020-1358-5. Acesso em: 19 jun. 2024.
APA
Borges, K. S., Pignatti, E., Leng, S., Kariyawasam, D., Ruiz-Babot, G., Ramalho, F. S., et al. (2020). Wnt/β-catenin activation cooperates with loss of p53 to cause adrenocortical carcinoma in mice. Oncogene, 39, 5282-5291. doi:10.1038/s41388-020-1358-5
NLM
Borges KS, Pignatti E, Leng S, Kariyawasam D, Ruiz-Babot G, Ramalho FS, Taketo MM, Carlone DL, Breault DT. Wnt/β-catenin activation cooperates with loss of p53 to cause adrenocortical carcinoma in mice [Internet]. Oncogene. 2020 ; 39 5282-5291.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1038/s41388-020-1358-5
Vancouver
Borges KS, Pignatti E, Leng S, Kariyawasam D, Ruiz-Babot G, Ramalho FS, Taketo MM, Carlone DL, Breault DT. Wnt/β-catenin activation cooperates with loss of p53 to cause adrenocortical carcinoma in mice [Internet]. Oncogene. 2020 ; 39 5282-5291.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1038/s41388-020-1358-5
Artigo de periodico
Does abdominal obesity accelerate muscle strength decline in older adults?: evidence from the english longitudinal study of ageing (2019)
Carvalho, Danilo Henrique Trevisan de; Scholes, Shaun; Santos, Jair Lício Ferreira; Oliveira, Cesar de; Alexandre, Tiago da Silva
Source: The Journals of Gerontology: Series A, Biological Sciences and Medical Sciences. Unidade: FMRP
Subjects: OBESIDADE, CIRCUNFERÊNCIA ABDOMINAL, IDOSOS, ENVELHECIMENTO
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ABNT
CARVALHO, Danilo Henrique Trevisan de et al. Does abdominal obesity accelerate muscle strength decline in older adults?: evidence from the english longitudinal study of ageing. The Journals of Gerontology: Series A, Biological Sciences and Medical Sciences, 2019Tradução . . Disponível em: https://doi.org/10.1093/gerona/gly178. Acesso em: 19 jun. 2024.
APA
Carvalho, D. H. T. de, Scholes, S., Santos, J. L. F., Oliveira, C. de, & Alexandre, T. da S. (2019). Does abdominal obesity accelerate muscle strength decline in older adults?: evidence from the english longitudinal study of ageing. The Journals of Gerontology: Series A, Biological Sciences and Medical Sciences. doi:10.1093/gerona/gly178
NLM
Carvalho DHT de, Scholes S, Santos JLF, Oliveira C de, Alexandre T da S. Does abdominal obesity accelerate muscle strength decline in older adults?: evidence from the english longitudinal study of ageing [Internet]. The Journals of Gerontology: Series A, Biological Sciences and Medical Sciences. 2019 ;[citado 2024 jun. 19 ] Available from: https://doi.org/10.1093/gerona/gly178
Vancouver
Carvalho DHT de, Scholes S, Santos JLF, Oliveira C de, Alexandre T da S. Does abdominal obesity accelerate muscle strength decline in older adults?: evidence from the english longitudinal study of ageing [Internet]. The Journals of Gerontology: Series A, Biological Sciences and Medical Sciences. 2019 ;[citado 2024 jun. 19 ] Available from: https://doi.org/10.1093/gerona/gly178
Artigo de periodico
Polymorphisms in TLR4 and TNFA and risk of mycobacterium tuberculosis mnfection and development of active disease in contacts of tuberculosis cases in Brazil: a prospective cohort study (2019)
Cubillos-Angulo, Juan Manuel; Arriaga, María B.; Silva, Elisângela C.; Müller, Beatriz L. A.; Ramalho, Daniela M. P.; Fukutani, Kiyoshi F.; Miranda, Pryscila F. C.; Moreira, Adriana S. R.; Ruffino Netto, Antônio; Silva, Jose R. Lapa e; Sterling, Timothy R.; Kritski, Afrânio L.; Oliveira, Martha M.; Andrade, Bruno B.
Source: Clinical Infectious Disease. Unidade: FMRP
Subjects: POLIMORFISMO, MYCOBACTERIUM TUBERCULOSIS, NECROSE, TUBERCULOSE
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ABNT
CUBILLOS-ANGULO, Juan Manuel et al. Polymorphisms in TLR4 and TNFA and risk of mycobacterium tuberculosis mnfection and development of active disease in contacts of tuberculosis cases in Brazil: a prospective cohort study. Clinical Infectious Disease, 2019Tradução . . Disponível em: https://doi.org/10.1093/cid/ciy1001/5204461. Acesso em: 19 jun. 2024.
APA
Cubillos-Angulo, J. M., Arriaga, M. B., Silva, E. C., Müller, B. L. A., Ramalho, D. M. P., Fukutani, K. F., et al. (2019). Polymorphisms in TLR4 and TNFA and risk of mycobacterium tuberculosis mnfection and development of active disease in contacts of tuberculosis cases in Brazil: a prospective cohort study. Clinical Infectious Disease. doi:10.1093/cid/ciy1001/5204461
NLM
Cubillos-Angulo JM, Arriaga MB, Silva EC, Müller BLA, Ramalho DMP, Fukutani KF, Miranda PFC, Moreira ASR, Ruffino Netto A, Silva JRL e, Sterling TR, Kritski AL, Oliveira MM, Andrade BB. Polymorphisms in TLR4 and TNFA and risk of mycobacterium tuberculosis mnfection and development of active disease in contacts of tuberculosis cases in Brazil: a prospective cohort study [Internet]. Clinical Infectious Disease. 2019 ;[citado 2024 jun. 19 ] Available from: https://doi.org/10.1093/cid/ciy1001/5204461
Vancouver
Cubillos-Angulo JM, Arriaga MB, Silva EC, Müller BLA, Ramalho DMP, Fukutani KF, Miranda PFC, Moreira ASR, Ruffino Netto A, Silva JRL e, Sterling TR, Kritski AL, Oliveira MM, Andrade BB. Polymorphisms in TLR4 and TNFA and risk of mycobacterium tuberculosis mnfection and development of active disease in contacts of tuberculosis cases in Brazil: a prospective cohort study [Internet]. Clinical Infectious Disease. 2019 ;[citado 2024 jun. 19 ] Available from: https://doi.org/10.1093/cid/ciy1001/5204461
Artigo de periodico
ELMER v.2: an R/Bioconductor package to reconstruct gene regulatory networks from DNA methylation and transcriptome profiles (2019)
Silva, Tiago Chedraoui ; Coetzee, Simon G.; Gull, Nicole; Yao, Lijing; Hazelett, Dennis J.; Noushmehr, Houtan ; Lin, De-Chen; Berman, Benjamin P.
Source: Bioinformatics. Unidade: FMRP
Subjects: DNA, METILAÇÃO, EXPRESSÃO GÊNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Tiago Chedraoui et al. ELMER v.2: an R/Bioconductor package to reconstruct gene regulatory networks from DNA methylation and transcriptome profiles. Bioinformatics, v. 35, n. 11, p. 1974-1977, 2019Tradução . . Disponível em: https://doi.org/10.1093/bioinformatics/bty902. Acesso em: 19 jun. 2024.
APA
Silva, T. C., Coetzee, S. G., Gull, N., Yao, L., Hazelett, D. J., Noushmehr, H., et al. (2019). ELMER v.2: an R/Bioconductor package to reconstruct gene regulatory networks from DNA methylation and transcriptome profiles. Bioinformatics, 35( 11), 1974-1977. doi:10.1093/bioinformatics/bty902
NLM
Silva TC, Coetzee SG, Gull N, Yao L, Hazelett DJ, Noushmehr H, Lin D-C, Berman BP. ELMER v.2: an R/Bioconductor package to reconstruct gene regulatory networks from DNA methylation and transcriptome profiles [Internet]. Bioinformatics. 2019 ; 35( 11): 1974-1977.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1093/bioinformatics/bty902
Vancouver
Silva TC, Coetzee SG, Gull N, Yao L, Hazelett DJ, Noushmehr H, Lin D-C, Berman BP. ELMER v.2: an R/Bioconductor package to reconstruct gene regulatory networks from DNA methylation and transcriptome profiles [Internet]. Bioinformatics. 2019 ; 35( 11): 1974-1977.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1093/bioinformatics/bty902
Artigo de periodico
Scalable open science approach for mutation calling of tumor exomes using multiple genomic pipelines (2018)
Ellrott, Kyle; Bailey, Matthew H.; Saksena, Gordon; Ding, Li; Noushmehr, Houtan; Carlotti Júnior, Carlos Gilberto; Santos, José Sebastião dos; Kemp, Rafael; Sankarankutty, Ajith Kumar; Tirapelli, Daniela Pretti da Cunha
Source: Cell Systems. Unidade: FMRP
Subjects: MUTAÇÃO GENÉTICA, GENÔMICA, NEOPLASIAS, COMPUTAÇÃO APLICADA, PROJETOS DE PESQUISA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ELLROTT, Kyle et al. Scalable open science approach for mutation calling of tumor exomes using multiple genomic pipelines. Cell Systems, v. 6, n. 3, p. 271-281.e7, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.cels.2018.03.002. Acesso em: 19 jun. 2024.
APA
Ellrott, K., Bailey, M. H., Saksena, G., Ding, L., Noushmehr, H., Carlotti Júnior, C. G., et al. (2018). Scalable open science approach for mutation calling of tumor exomes using multiple genomic pipelines. Cell Systems, 6( 3), 271-281.e7. doi:10.1016/j.cels.2018.03.002
NLM
Ellrott K, Bailey MH, Saksena G, Ding L, Noushmehr H, Carlotti Júnior CG, Santos JS dos, Kemp R, Sankarankutty AK, Tirapelli DP da C. Scalable open science approach for mutation calling of tumor exomes using multiple genomic pipelines [Internet]. Cell Systems. 2018 ; 6( 3): 271-281.e7.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/j.cels.2018.03.002
Vancouver
Ellrott K, Bailey MH, Saksena G, Ding L, Noushmehr H, Carlotti Júnior CG, Santos JS dos, Kemp R, Sankarankutty AK, Tirapelli DP da C. Scalable open science approach for mutation calling of tumor exomes using multiple genomic pipelines [Internet]. Cell Systems. 2018 ; 6( 3): 271-281.e7.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/j.cels.2018.03.002
Artigo de periodico
lncRNA epigenetic landscape analysis identifies EPIC1 as an oncogenic lncRNA that interacts with MYC and promotes cell-cycle progression in cancer (2018)
Wang, Zehua; Yang, Bob; Zhang, Min; Guo, Weiwei; Wu, Zhiyuan; Wang, Yue; Jia, Lin; Li, Song; Xie, Wen; Yang, Da; 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 MAMÁRIAS, EPIGÊNESE GENÉTICA, METILAÇÃO DE DNA, CICLO CELULAR, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WANG, Zehua et al. lncRNA epigenetic landscape analysis identifies EPIC1 as an oncogenic lncRNA that interacts with MYC and promotes cell-cycle progression in cancer. Cancer Cell, v. 33, n. 4, p. 706-720, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.ccell.2018.03.006. Acesso em: 19 jun. 2024.
APA
Wang, Z., Yang, B., Zhang, M., Guo, W., Wu, Z., Wang, Y., et al. (2018). lncRNA epigenetic landscape analysis identifies EPIC1 as an oncogenic lncRNA that interacts with MYC and promotes cell-cycle progression in cancer. Cancer Cell, 33( 4), 706-720. doi:10.1016/j.ccell.2018.03.006
NLM
Wang Z, Yang B, Zhang M, Guo W, Wu Z, Wang Y, Jia L, Li S, Xie W, Yang D, Carlotti Júnior CG, Santos JS dos, Kemp R, Sankarankuty AK, Tirapelli DP da C. lncRNA epigenetic landscape analysis identifies EPIC1 as an oncogenic lncRNA that interacts with MYC and promotes cell-cycle progression in cancer [Internet]. Cancer Cell. 2018 ; 33( 4): 706-720.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/j.ccell.2018.03.006
Vancouver
Wang Z, Yang B, Zhang M, Guo W, Wu Z, Wang Y, Jia L, Li S, Xie W, Yang D, Carlotti Júnior CG, Santos JS dos, Kemp R, Sankarankuty AK, Tirapelli DP da C. lncRNA epigenetic landscape analysis identifies EPIC1 as an oncogenic lncRNA that interacts with MYC and promotes cell-cycle progression in cancer [Internet]. Cancer Cell. 2018 ; 33( 4): 706-720.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/j.ccell.2018.03.006
Artigo de periodico
Heterogeneity within the PF-EPN-B ependymoma subgroup (2018)
Cavalli, Florence M. G.; Hübner, Jens-Martin; Sharma, Tanvi; Luu, Betty; Sill, Martin; Zapotocky, Michal; Mack, Stephen C.; Witt, Hendrik; Lin, Tong; Shih, David J. H.; Ho, Ben; Santi, Mariarita; Emery, Lyndsey; Hukin, Juliette; Dunham, Cristopher; McLendon, Roger E.; Lipp, Eric S.; Gururangan, Sridharan; Grossbach, Andrew; French, Pim; Kros, Johan M.; van Veelen, Marie-Lise C.; Rao, Amulya A. Nageswara; Giannini, Caterina; Leary, Sarah; Jung, Shin; Faria, Claudia C.; Mora, Jaume; Schüller, Ulrich; Alonso, Marta M.; Chan, Jennifer A.; Klekner, Almos; Chambless, Lola B.; Hwang, Eugene I.; Massimino, Maura; Eberhart, Charles G.; Karajannis, Matthias A.; Lu, Benjamin; Liau, Linda M.; Zollo, Massimo; Ferrucci, Veronica; Carlotti Júnior, Carlos Gilberto; Tirapelli, Daniela Pretti da Cunha; Tabori, Uri; Bouffet, Eric; Ryzhova, Marina; Ellison, David W.; Merchant, Thomas E.; Gilbert, Mark R.; Armstrong, Terri S.; Korshunov, Andrey; Pfister, Stefan M.; Taylor, Michael D.; Aldape, Kenneth; Pajtler, Kristian W.; Kool, Marcel; Ramaswamy, Vijay
Source: Acta Neuropathologica. Unidade: FMRP
Subjects: HETEROGENEIDADE, FOSSAS SÉPTICAS, CITOGENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAVALLI, Florence M. G. et al. Heterogeneity within the PF-EPN-B ependymoma subgroup. Acta Neuropathologica, v. 136, n. 2, p. 227-237, 2018Tradução . . Disponível em: https://doi.org/10.1007/s00401-018-1888-x. Acesso em: 19 jun. 2024.
APA
Cavalli, F. M. G., Hübner, J. -M., Sharma, T., Luu, B., Sill, M., Zapotocky, M., et al. (2018). Heterogeneity within the PF-EPN-B ependymoma subgroup. Acta Neuropathologica, 136( 2), 227-237. doi:10.1007/s00401-018-1888-x
NLM
Cavalli FMG, Hübner J-M, Sharma T, Luu B, Sill M, Zapotocky M, Mack SC, Witt H, Lin T, Shih DJH, Ho B, Santi M, Emery L, Hukin J, Dunham C, McLendon RE, Lipp ES, Gururangan S, Grossbach A, French P, Kros JM, van Veelen M-LC, Rao AAN, Giannini C, Leary S, Jung S, Faria CC, Mora J, Schüller U, Alonso MM, Chan JA, Klekner A, Chambless LB, Hwang EI, Massimino M, Eberhart CG, Karajannis MA, Lu B, Liau LM, Zollo M, Ferrucci V, Carlotti Júnior CG, Tirapelli DP da C, Tabori U, Bouffet E, Ryzhova M, Ellison DW, Merchant TE, Gilbert MR, Armstrong TS, Korshunov A, Pfister SM, Taylor MD, Aldape K, Pajtler KW, Kool M, Ramaswamy V. Heterogeneity within the PF-EPN-B ependymoma subgroup [Internet]. Acta Neuropathologica. 2018 ; 136( 2): 227-237.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1007/s00401-018-1888-x
Vancouver
Cavalli FMG, Hübner J-M, Sharma T, Luu B, Sill M, Zapotocky M, Mack SC, Witt H, Lin T, Shih DJH, Ho B, Santi M, Emery L, Hukin J, Dunham C, McLendon RE, Lipp ES, Gururangan S, Grossbach A, French P, Kros JM, van Veelen M-LC, Rao AAN, Giannini C, Leary S, Jung S, Faria CC, Mora J, Schüller U, Alonso MM, Chan JA, Klekner A, Chambless LB, Hwang EI, Massimino M, Eberhart CG, Karajannis MA, Lu B, Liau LM, Zollo M, Ferrucci V, Carlotti Júnior CG, Tirapelli DP da C, Tabori U, Bouffet E, Ryzhova M, Ellison DW, Merchant TE, Gilbert MR, Armstrong TS, Korshunov A, Pfister SM, Taylor MD, Aldape K, Pajtler KW, Kool M, Ramaswamy V. Heterogeneity within the PF-EPN-B ependymoma subgroup [Internet]. Acta Neuropathologica. 2018 ; 136( 2): 227-237.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1007/s00401-018-1888-x
Artigo de periodico
Pan-cancer alterations of the MYC oncogene and its proximal Network across the Cancer Genome Atlas (2018)
Schaub, Franz X.; Dhankani, Varsha; Berger, Ashton C.; Bernard, Brady; Grandori, Carla; Noushmehr, Houtan; Carlotti Júnior, Carlos Gilberto; Santos, José Sebastião dos; Kemp, Rafael; Sankarankutty, Ajith Kumar; Tirapelli, Daniela Pretti da Cunha
Source: Cell Systems. Unidade: FMRP
Subjects: GENÔMICA, GENES REGULADORES, ONCOGENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SCHAUB, Franz X. et al. Pan-cancer alterations of the MYC oncogene and its proximal Network across the Cancer Genome Atlas. Cell Systems, v. 6, n. 3, p. 282-300.e1-e2, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.cels.2018.03.003. Acesso em: 19 jun. 2024.
APA
Schaub, F. X., Dhankani, V., Berger, A. C., Bernard, B., Grandori, C., Noushmehr, H., et al. (2018). Pan-cancer alterations of the MYC oncogene and its proximal Network across the Cancer Genome Atlas. Cell Systems, 6( 3), 282-300.e1-e2. doi:10.1016/j.cels.2018.03.003
NLM
Schaub FX, Dhankani V, Berger AC, Bernard B, Grandori C, Noushmehr H, Carlotti Júnior CG, Santos JS dos, Kemp R, Sankarankutty AK, Tirapelli DP da C. Pan-cancer alterations of the MYC oncogene and its proximal Network across the Cancer Genome Atlas [Internet]. Cell Systems. 2018 ; 6( 3): 282-300.e1-e2.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/j.cels.2018.03.003
Vancouver
Schaub FX, Dhankani V, Berger AC, Bernard B, Grandori C, Noushmehr H, Carlotti Júnior CG, Santos JS dos, Kemp R, Sankarankutty AK, Tirapelli DP da C. Pan-cancer alterations of the MYC oncogene and its proximal Network across the Cancer Genome Atlas [Internet]. Cell Systems. 2018 ; 6( 3): 282-300.e1-e2.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/j.cels.2018.03.003
Artigo de periodico
Cell-of-origin patterns dominate the molecular classification of 10,000 tumors from 33 types of cancer (2018)
Hoadley, Katherine A.; Noushmehr, Houtan; Carlotti Júnior, Carlos Gilberto; Santos, José Sebastião dos; Kemp, Rafael; Sankarankutty, Ajith Kumar; Tirapelli, Daniela Pretti da Cunha
Source: Cell. Unidades: FMRP, HRAC
Subjects: NEOPLASIAS, GENOMAS, PROTEÔMICA, METILAÇÃO DE DNA, MUTAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HOADLEY, Katherine A. et al. Cell-of-origin patterns dominate the molecular classification of 10,000 tumors from 33 types of cancer. Cell, v. 173, n. 2, p. 291-304.e1-e6, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.cell.2018.03.022. Acesso em: 19 jun. 2024.
APA
Hoadley, K. A., Noushmehr, H., Carlotti Júnior, C. G., Santos, J. S. dos, Kemp, R., Sankarankutty, A. K., & Tirapelli, D. P. da C. (2018). Cell-of-origin patterns dominate the molecular classification of 10,000 tumors from 33 types of cancer. Cell, 173( 2), 291-304.e1-e6. doi:10.1016/j.cell.2018.03.022
NLM
Hoadley KA, Noushmehr H, Carlotti Júnior CG, Santos JS dos, Kemp R, Sankarankutty AK, Tirapelli DP da C. Cell-of-origin patterns dominate the molecular classification of 10,000 tumors from 33 types of cancer [Internet]. Cell. 2018 ; 173( 2): 291-304.e1-e6.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/j.cell.2018.03.022
Vancouver
Hoadley KA, Noushmehr H, Carlotti Júnior CG, Santos JS dos, Kemp R, Sankarankutty AK, Tirapelli DP da C. Cell-of-origin patterns dominate the molecular classification of 10,000 tumors from 33 types of cancer [Internet]. Cell. 2018 ; 173( 2): 291-304.e1-e6.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/j.cell.2018.03.022
Artigo de periodico
Perspective on oncogenic processes at the end of the beginning of cancer genomics (2018)
Ding, Li; Noushmehr, Houtan; Carlotti Júnior, Carlos Gilberto; Santos, José Sebastião dos; Kemp, Rafael; Sankarankutty, Ajith Kumar; Tirapelli, Daniela Pretti da Cunha
Source: Cell. Unidade: FMRP
Subjects: NEOPLASIAS, GENOMAS, CARCINOGÊNESE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DING, Li et al. Perspective on oncogenic processes at the end of the beginning of cancer genomics. Cell, v. 173, n. 2, p. 305-320.e1-e8, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.cell.2018.03.033. Acesso em: 19 jun. 2024.
APA
Ding, L., Noushmehr, H., Carlotti Júnior, C. G., Santos, J. S. dos, Kemp, R., Sankarankutty, A. K., & Tirapelli, D. P. da C. (2018). Perspective on oncogenic processes at the end of the beginning of cancer genomics. Cell, 173( 2), 305-320.e1-e8. doi:10.1016/j.cell.2018.03.033
NLM
Ding L, Noushmehr H, Carlotti Júnior CG, Santos JS dos, Kemp R, Sankarankutty AK, Tirapelli DP da C. Perspective on oncogenic processes at the end of the beginning of cancer genomics [Internet]. Cell. 2018 ; 173( 2): 305-320.e1-e8.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/j.cell.2018.03.033
Vancouver
Ding L, Noushmehr H, Carlotti Júnior CG, Santos JS dos, Kemp R, Sankarankutty AK, Tirapelli DP da C. Perspective on oncogenic processes at the end of the beginning of cancer genomics [Internet]. Cell. 2018 ; 173( 2): 305-320.e1-e8.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/j.cell.2018.03.033
Artigo de periodico
A pan-cancer analysis of enhancer expression in nearly 9000 patient samples (2018)
Chen, Han; Noushmehr, Houtan; Carlotti Júnior, Carlos Gilberto; Santos, José Sebastião dos; Kemp, Rafael; Sankarankutty, Ajith Kumar; Tirapelli, Daniela Pretti da Cunha
Source: Cell. Unidade: FMRP
Subjects: NEOPLASIAS, GENOMAS, TAXA DE SOBREVIVÊNCIA, IMUNOTERAPIA, CROMATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CHEN, Han et al. A pan-cancer analysis of enhancer expression in nearly 9000 patient samples. Cell, v. 173, n. 2, p. 386-399.e1-e5, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.cell.2018.03.027. Acesso em: 19 jun. 2024.
APA
Chen, H., Noushmehr, H., Carlotti Júnior, C. G., Santos, J. S. dos, Kemp, R., Sankarankutty, A. K., & Tirapelli, D. P. da C. (2018). A pan-cancer analysis of enhancer expression in nearly 9000 patient samples. Cell, 173( 2), 386-399.e1-e5. doi:10.1016/j.cell.2018.03.027
NLM
Chen H, Noushmehr H, Carlotti Júnior CG, Santos JS dos, Kemp R, Sankarankutty AK, Tirapelli DP da C. A pan-cancer analysis of enhancer expression in nearly 9000 patient samples [Internet]. Cell. 2018 ; 173( 2): 386-399.e1-e5.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/j.cell.2018.03.027
Vancouver
Chen H, Noushmehr H, Carlotti Júnior CG, Santos JS dos, Kemp R, Sankarankutty AK, Tirapelli DP da C. A pan-cancer analysis of enhancer expression in nearly 9000 patient samples [Internet]. Cell. 2018 ; 173( 2): 386-399.e1-e5.[citado 2024 jun. 19 ] Available from: https://doi.org/10.1016/j.cell.2018.03.027

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