ReP USP - Resultado da busca

Artigo de periodico
Identification of HDAC4 as a potential therapeutic target and prognostic biomarker for ZFTA-fused ependymomas (2023)
Sousa, Graziella Ribeiro de ; Salomão, Karina B.; Nagano, Luís Fernando Peinado ; Riemondy, Kent A.; Chagas, Pablo Shimaoka ; Veronez, Luciana Chain ; Saggioro, Fabiano Pinto ; Marie, Suely Kazue Nagahashi ; Yunes, José A.; Cardinalli, Izilda Aparecida; Brandalise, Silvia Regina ; Queiroz, Rosane Gomes de Paula; Scrideli, Carlos Alberto ; Donson, Andrew M.; Foreman, Nicholas K.; Tone, Luiz Gonzaga ; Valera, Elvis Terci
Source: Cancer Gene Therapy. Unidades: FMRP, FM, FCFRP
Subjects: NEOPLASIAS CEREBRAIS, PERFILAÇÃO DA EXPRESSÃO GÊNICA, PROGNÓSTICO, FATORES DE TRANSCRIÇÃO, BIOMARCADORES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOUSA, Graziella Ribeiro de et al. Identification of HDAC4 as a potential therapeutic target and prognostic biomarker for ZFTA-fused ependymomas. Cancer Gene Therapy, v. 30, p. 1105-1113, 2023Tradução . . Disponível em: https://doi.org/10.1038/s41417-023-00616-z. Acesso em: 19 nov. 2024.
APA
Sousa, G. R. de, Salomão, K. B., Nagano, L. F. P., Riemondy, K. A., Chagas, P. S., Veronez, L. C., et al. (2023). Identification of HDAC4 as a potential therapeutic target and prognostic biomarker for ZFTA-fused ependymomas. Cancer Gene Therapy, 30, 1105-1113. doi:10.1038/s41417-023-00616-z
NLM
Sousa GR de, Salomão KB, Nagano LFP, Riemondy KA, Chagas PS, Veronez LC, Saggioro FP, Marie SKN, Yunes JA, Cardinalli IA, Brandalise SR, Queiroz RG de P, Scrideli CA, Donson AM, Foreman NK, Tone LG, Valera ET. Identification of HDAC4 as a potential therapeutic target and prognostic biomarker for ZFTA-fused ependymomas [Internet]. Cancer Gene Therapy. 2023 ; 30 1105-1113.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/s41417-023-00616-z
Vancouver
Sousa GR de, Salomão KB, Nagano LFP, Riemondy KA, Chagas PS, Veronez LC, Saggioro FP, Marie SKN, Yunes JA, Cardinalli IA, Brandalise SR, Queiroz RG de P, Scrideli CA, Donson AM, Foreman NK, Tone LG, Valera ET. Identification of HDAC4 as a potential therapeutic target and prognostic biomarker for ZFTA-fused ependymomas [Internet]. Cancer Gene Therapy. 2023 ; 30 1105-1113.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/s41417-023-00616-z
Artigo de periodico
Evaluating H3F3A K27M and G34R/V somatic mutations in a cohort of pediatric brain tumors of different and rare histologies (2020)
Oliveira, Vinicius Fernandes; Sousa, Graziella Ribeiro de ; Santos, Antonio Carlos dos ; Saggioro, Fabiano Pinto ; Machado, Hélio Rubens ; Oliveira, Ricardo Santos de ; Tone, Luiz Gonzaga ; Valera, Elvis Terci
Source: Child's Nervous System. Unidades: FMRP, SVOI
Subjects: NEOPLASIAS CEREBRAIS, EPIGÊNESE GENÉTICA, GLIOMA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Vinicius Fernandes et al. Evaluating H3F3A K27M and G34R/V somatic mutations in a cohort of pediatric brain tumors of different and rare histologies. Child's Nervous System, v. 37, n. 2, p. 375-382, 2020Tradução . . Disponível em: https://doi.org/10.1007/s00381-020-04852-8. Acesso em: 19 nov. 2024.
APA
Oliveira, V. F., Sousa, G. R. de, Santos, A. C. dos, Saggioro, F. P., Machado, H. R., Oliveira, R. S. de, et al. (2020). Evaluating H3F3A K27M and G34R/V somatic mutations in a cohort of pediatric brain tumors of different and rare histologies. Child's Nervous System, 37( 2), 375-382. doi:10.1007/s00381-020-04852-8
NLM
Oliveira VF, Sousa GR de, Santos AC dos, Saggioro FP, Machado HR, Oliveira RS de, Tone LG, Valera ET. Evaluating H3F3A K27M and G34R/V somatic mutations in a cohort of pediatric brain tumors of different and rare histologies [Internet]. Child's Nervous System. 2020 ; 37( 2): 375-382.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1007/s00381-020-04852-8
Vancouver
Oliveira VF, Sousa GR de, Santos AC dos, Saggioro FP, Machado HR, Oliveira RS de, Tone LG, Valera ET. Evaluating H3F3A K27M and G34R/V somatic mutations in a cohort of pediatric brain tumors of different and rare histologies [Internet]. Child's Nervous System. 2020 ; 37( 2): 375-382.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1007/s00381-020-04852-8
Artigo de periodico-carta/editorial
Perinatal complex low- and high-grade glial tumor harboring a novel GIGYF2-ALK fusion [Carta] (2020)
Valera, Elvis Terci ; Neder, Luciano ; Queiroz, Rosane Gomes de Paula; Santos, Antonio Carlos dos ; Sousa, Graziella Ribeiro de ; Oliveira, Ricardo Santos de ; Santos, Marcelo Volpon ; Machado, Hélio Rubens ; Tone, Luiz Gonzaga
Source: Pediatric Blood & Cancer. Unidade: FMRP
Subjects: NEOPLASIAS CEREBRAIS, FETO, NEONATOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VALERA, Elvis Terci et al. Perinatal complex low- and high-grade glial tumor harboring a novel GIGYF2-ALK fusion [Carta]. Pediatric Blood & Cancer. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1002/pbc.28015. Acesso em: 19 nov. 2024. , 2020
APA
Valera, E. T., Neder, L., Queiroz, R. G. de P., Santos, A. C. dos, Sousa, G. R. de, Oliveira, R. S. de, et al. (2020). Perinatal complex low- and high-grade glial tumor harboring a novel GIGYF2-ALK fusion [Carta]. Pediatric Blood & Cancer. Hoboken: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1002/pbc.28015
NLM
Valera ET, Neder L, Queiroz RG de P, Santos AC dos, Sousa GR de, Oliveira RS de, Santos MV, Machado HR, Tone LG. Perinatal complex low- and high-grade glial tumor harboring a novel GIGYF2-ALK fusion [Carta] [Internet]. Pediatric Blood & Cancer. 2020 ; 67( 1): 101-103.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1002/pbc.28015
Vancouver
Valera ET, Neder L, Queiroz RG de P, Santos AC dos, Sousa GR de, Oliveira RS de, Santos MV, Machado HR, Tone LG. Perinatal complex low- and high-grade glial tumor harboring a novel GIGYF2-ALK fusion [Carta] [Internet]. Pediatric Blood & Cancer. 2020 ; 67( 1): 101-103.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1002/pbc.28015
Artigo de periodico
The TP53 p.R337H mutation is uncommon in a Brazilian cohort of pediatric patients diagnosed with ependymoma (2020)
Magalhães, Taciani de Almeida ; Borges, Kleiton Silva ; Sousa, Graziella Ribeiro de ; Brandalise, Silvia Regina; Seidinger, Ana Luiza; Scrideli, Carlos Alberto ; Shinjo, Sueli Mieko Oba ; Yunes, Jose Andres ; Tone, Luiz Gonzaga
Source: Neurological Sciences. Unidades: FMRP, FM
Subjects: DOENÇAS CEREBRAIS, PROTEÍNAS DO TECIDO NERVOSO, NEOPLASIAS CEREBRAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MAGALHÃES, Taciani de Almeida et al. The TP53 p.R337H mutation is uncommon in a Brazilian cohort of pediatric patients diagnosed with ependymoma. Neurological Sciences, v. 41, n. 3, p. 691-694, 2020Tradução . . Disponível em: https://doi.org/10.1007/s10072-019-04112-x. Acesso em: 19 nov. 2024.
APA
Magalhães, T. de A., Borges, K. S., Sousa, G. R. de, Brandalise, S. R., Seidinger, A. L., Scrideli, C. A., et al. (2020). The TP53 p.R337H mutation is uncommon in a Brazilian cohort of pediatric patients diagnosed with ependymoma. Neurological Sciences, 41( 3), 691-694. doi:10.1007/s10072-019-04112-x
NLM
Magalhães T de A, Borges KS, Sousa GR de, Brandalise SR, Seidinger AL, Scrideli CA, Shinjo SMO, Yunes JA, Tone LG. The TP53 p.R337H mutation is uncommon in a Brazilian cohort of pediatric patients diagnosed with ependymoma [Internet]. Neurological Sciences. 2020 ; 41( 3): 691-694.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1007/s10072-019-04112-x
Vancouver
Magalhães T de A, Borges KS, Sousa GR de, Brandalise SR, Seidinger AL, Scrideli CA, Shinjo SMO, Yunes JA, Tone LG. The TP53 p.R337H mutation is uncommon in a Brazilian cohort of pediatric patients diagnosed with ependymoma [Internet]. Neurological Sciences. 2020 ; 41( 3): 691-694.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1007/s10072-019-04112-x

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