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Artigo de periodico-carta/editorial
Cytogenetic heterogeneity in biphasic synovial sarcoma associated with telomere instability [Carta] (2010)
Brassesco, María Sol; Cortez, Maria Angélica; Valera, Elvis Terci; Engel, Edgard Eduard; Barbosa, Marcello Henrique Nogueira; Becker, Aline Nazareth de Paiva Paixão; Tone, Luiz Gonzaga
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: SARCOMA, CITOGENÉTICA
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ABNT
BRASSESCO, María Sol et al. Cytogenetic heterogeneity in biphasic synovial sarcoma associated with telomere instability [Carta]. Cancer Genetics and Cytogenetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 05 nov. 2024. , 2010
APA
Brassesco, M. S., Cortez, M. A., Valera, E. T., Engel, E. E., Barbosa, M. H. N., Becker, A. N. de P. P., & Tone, L. G. (2010). Cytogenetic heterogeneity in biphasic synovial sarcoma associated with telomere instability [Carta]. Cancer Genetics and Cytogenetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Brassesco MS, Cortez MA, Valera ET, Engel EE, Barbosa MHN, Becker AN de PP, Tone LG. Cytogenetic heterogeneity in biphasic synovial sarcoma associated with telomere instability [Carta]. Cancer Genetics and Cytogenetics. 2010 ; 197( 1): 86-90.[citado 2024 nov. 05 ]
Vancouver
Brassesco MS, Cortez MA, Valera ET, Engel EE, Barbosa MHN, Becker AN de PP, Tone LG. Cytogenetic heterogeneity in biphasic synovial sarcoma associated with telomere instability [Carta]. Cancer Genetics and Cytogenetics. 2010 ; 197( 1): 86-90.[citado 2024 nov. 05 ]
Artigo de periodico
The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival (2010)
Almeida, Luciana Oliveira de; Custódio, Aline Cadurin; Santos, Marcelo José dos; Almeida, José R. W.; Clara, Carlos Afonso; Pinto, Giovanny Rebouças; Rey, Juan A.; Casartelli, Cacilda
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: POLIMORFISMO, NEOPLASIAS CEREBRAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALMEIDA, Luciana Oliveira de et al. The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival. Cancer Genetics and Cytogenetics, v. 198, n. 1, p. 15-21, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2009.11.013. Acesso em: 05 nov. 2024.
APA
Almeida, L. O. de, Custódio, A. C., Santos, M. J. dos, Almeida, J. R. W., Clara, C. A., Pinto, G. R., et al. (2010). The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival. Cancer Genetics and Cytogenetics, 198( 1), 15-21. doi:10.1016/j.cancergencyto.2009.11.013
NLM
Almeida LO de, Custódio AC, Santos MJ dos, Almeida JRW, Clara CA, Pinto GR, Rey JA, Casartelli C. The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 198( 1): 15-21.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.11.013
Vancouver
Almeida LO de, Custódio AC, Santos MJ dos, Almeida JRW, Clara CA, Pinto GR, Rey JA, Casartelli C. The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 198( 1): 15-21.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.11.013
Artigo de periodico
Cryptic SYT/SXX1 fusion gene in high-grade biphasic synovial sarcoma with unique complex rearrangement and extensice BCL2 overexpression (2010)
Brassesco, María Sol; Cortez, Maria Angélica; Valera, Elvis Terci; Engel, Edgard Eduard; Barbosa, Marcello Henrique Nogueira; Becker, Aline Paixão; Scrideli, Carlos Alberto; Tone, Luiz Gonzaga
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: CITOGENÉTICA MOLECULAR, SARCOMA, MULHERES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BRASSESCO, María Sol et al. Cryptic SYT/SXX1 fusion gene in high-grade biphasic synovial sarcoma with unique complex rearrangement and extensice BCL2 overexpression. Cancer Genetics and Cytogenetics, v. 196, n. 2, p. 189-193, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2009.10.001. Acesso em: 05 nov. 2024.
APA
Brassesco, M. S., Cortez, M. A., Valera, E. T., Engel, E. E., Barbosa, M. H. N., Becker, A. P., et al. (2010). Cryptic SYT/SXX1 fusion gene in high-grade biphasic synovial sarcoma with unique complex rearrangement and extensice BCL2 overexpression. Cancer Genetics and Cytogenetics, 196( 2), 189-193. doi:10.1016/j.cancergencyto.2009.10.001
NLM
Brassesco MS, Cortez MA, Valera ET, Engel EE, Barbosa MHN, Becker AP, Scrideli CA, Tone LG. Cryptic SYT/SXX1 fusion gene in high-grade biphasic synovial sarcoma with unique complex rearrangement and extensice BCL2 overexpression [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 196( 2): 189-193.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.10.001
Vancouver
Brassesco MS, Cortez MA, Valera ET, Engel EE, Barbosa MHN, Becker AP, Scrideli CA, Tone LG. Cryptic SYT/SXX1 fusion gene in high-grade biphasic synovial sarcoma with unique complex rearrangement and extensice BCL2 overexpression [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 196( 2): 189-193.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.10.001
Artigo de periodico
Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas (2010)
Martínez-Glez, Victor; Alvarez, Luis; Franco-Hernández, Carmen; Torres-Martin, Miguel; Campos, Jose M. de; Isla, Alberto; Vaquero, Jesús; Lassaletta, Luis; Castresana, Javier S.; Casartelli, Cacilda; Rey, Juan A.
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: MENINGIOMA, EXPRESSÃO GÊNICA
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ABNT
MARTÍNEZ-GLEZ, Victor et al. Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas. Cancer Genetics and Cytogenetics, v. 196, n. 1, p. 1-6, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2009.08.003. Acesso em: 05 nov. 2024.
APA
Martínez-Glez, V., Alvarez, L., Franco-Hernández, C., Torres-Martin, M., Campos, J. M. de, Isla, A., et al. (2010). Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas. Cancer Genetics and Cytogenetics, 196( 1), 1-6. doi:10.1016/j.cancergencyto.2009.08.003
NLM
Martínez-Glez V, Alvarez L, Franco-Hernández C, Torres-Martin M, Campos JM de, Isla A, Vaquero J, Lassaletta L, Castresana JS, Casartelli C, Rey JA. Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 196( 1): 1-6.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.08.003
Vancouver
Martínez-Glez V, Alvarez L, Franco-Hernández C, Torres-Martin M, Campos JM de, Isla A, Vaquero J, Lassaletta L, Castresana JS, Casartelli C, Rey JA. Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 196( 1): 1-6.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.08.003
Artigo de periodico
Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity (2009)
Franco-Hernández, Carmen; Martínez-Glez, Victor; Campos, Jose M. de; Isla, Alberto; Vaquero, Jesús; Gutiérrez, Manuel; Casartelli, Cacilda; Rey, Juan A.
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: NEOPLASIAS, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FRANCO-HERNÁNDEZ, Carmen et al. Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity. Cancer Genetics and Cytogenetics, v. 190, n. 2, p. 93-96, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2008.09.017. Acesso em: 05 nov. 2024.
APA
Franco-Hernández, C., Martínez-Glez, V., Campos, J. M. de, Isla, A., Vaquero, J., Gutiérrez, M., et al. (2009). Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity. Cancer Genetics and Cytogenetics, 190( 2), 93-96. doi:10.1016/j.cancergencyto.2008.09.017
NLM
Franco-Hernández C, Martínez-Glez V, Campos JM de, Isla A, Vaquero J, Gutiérrez M, Casartelli C, Rey JA. Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity [Internet]. Cancer Genetics and Cytogenetics. 2009 ; 190( 2): 93-96.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.cancergencyto.2008.09.017
Vancouver
Franco-Hernández C, Martínez-Glez V, Campos JM de, Isla A, Vaquero J, Gutiérrez M, Casartelli C, Rey JA. Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity [Internet]. Cancer Genetics and Cytogenetics. 2009 ; 190( 2): 93-96.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.cancergencyto.2008.09.017

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