Filtros : "Indexado no Excerpta Medica" "Casartelli, Cacilda" "FMRP" Removidos: "CAIRASCO, NORBERTO GARCIA" "DONADI, EDUARDO ANTONIO" "China" "Acta Cirurgica Brasileira" Limpar

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  • Source: Genetics and Molecular Research. Unidade: FMRP

    Subjects: POLIMORFISMO, GENÉTICA

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    • ABNT

      CUSTÓDIO, Aline Cadurin et al. GSTP1 Ile105Val polymorphism in astrocytomas and glioblastomas. Genetics and Molecular Research, v. 9, n. 4, p. 2328-2334, 2010Tradução . . Acesso em: 15 nov. 2024.
    • APA

      Custódio, A. C., Almeida, L. O. de, Pinto, G. R., Santos, M. J. dos, Almeida, J. R. W. de, Clara, C. A., et al. (2010). GSTP1 Ile105Val polymorphism in astrocytomas and glioblastomas. Genetics and Molecular Research, 9( 4), 2328-2334.
    • NLM

      Custódio AC, Almeida LO de, Pinto GR, Santos MJ dos, Almeida JRW de, Clara CA, Rey JA, Casartelli C. GSTP1 Ile105Val polymorphism in astrocytomas and glioblastomas. Genetics and Molecular Research. 2010 ; 9( 4): 2328-2334.[citado 2024 nov. 15 ]
    • Vancouver

      Custódio AC, Almeida LO de, Pinto GR, Santos MJ dos, Almeida JRW de, Clara CA, Rey JA, Casartelli C. GSTP1 Ile105Val polymorphism in astrocytomas and glioblastomas. Genetics and Molecular Research. 2010 ; 9( 4): 2328-2334.[citado 2024 nov. 15 ]
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: POLIMORFISMO, NEOPLASIAS CEREBRAIS

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      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: 15 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. 15 ] 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. 15 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.11.013
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: MENINGIOMA, EXPRESSÃO GÊNICA

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      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: 15 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. 15 ] 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. 15 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.08.003
  • Source: Genetics and Molecular Research. Unidade: FMRP

    Subjects: POLIMORFISMO, NEOPLASIAS CEREBRAIS, METÁSTASE NEOPLÁSICA

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    • ABNT

      ALMEIDA, L. O. et al. Polymorphisms and DNA methylation of gene TP53 associate with extra-axial brain tumors. Genetics and Molecular Research, v. 8, n. 1, p. 8-18, 2009Tradução . . Disponível em: https://doi.org/10.4238/vol8-1gmr518. Acesso em: 15 nov. 2024.
    • APA

      Almeida, L. O., Custódio, A. C., Pinto, G. R., Santos, M. J., Almeida, J. R. W., Clara, C. A., et al. (2009). Polymorphisms and DNA methylation of gene TP53 associate with extra-axial brain tumors. Genetics and Molecular Research, 8( 1), 8-18. doi:10.4238/vol8-1gmr518
    • NLM

      Almeida LO, Custódio AC, Pinto GR, Santos MJ, Almeida JRW, Clara CA, Rey JA, Casartelli C. Polymorphisms and DNA methylation of gene TP53 associate with extra-axial brain tumors [Internet]. Genetics and Molecular Research. 2009 ; 8( 1): 8-18.[citado 2024 nov. 15 ] Available from: https://doi.org/10.4238/vol8-1gmr518
    • Vancouver

      Almeida LO, Custódio AC, Pinto GR, Santos MJ, Almeida JRW, Clara CA, Rey JA, Casartelli C. Polymorphisms and DNA methylation of gene TP53 associate with extra-axial brain tumors [Internet]. Genetics and Molecular Research. 2009 ; 8( 1): 8-18.[citado 2024 nov. 15 ] Available from: https://doi.org/10.4238/vol8-1gmr518
  • Source: Genetics and Molecular Research. Unidade: FMRP

    Subjects: ASTRÓCITOS, GENÉTICA

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      ANSELMO, Nilson Praia et al. Concurrent sequence variation of TP53 and TP73 genes in anaplastic astrocytoma. Genetics and Molecular Research, v. 8, n. 4, p. 1257-1263, 2009Tradução . . Disponível em: https://doi.org/10.4238/vol8-4gmr631. Acesso em: 15 nov. 2024.
    • APA

      Anselmo, N. P., Rey, J. A., Almeida, L. O., Custódio, A. C., Almeida, J. R. W., Clara, C. A., et al. (2009). Concurrent sequence variation of TP53 and TP73 genes in anaplastic astrocytoma. Genetics and Molecular Research, 8( 4), 1257-1263. doi:10.4238/vol8-4gmr631
    • NLM

      Anselmo NP, Rey JA, Almeida LO, Custódio AC, Almeida JRW, Clara CA, Santos MJ, Casartelli C. Concurrent sequence variation of TP53 and TP73 genes in anaplastic astrocytoma [Internet]. Genetics and Molecular Research. 2009 ; 8( 4): 1257-1263.[citado 2024 nov. 15 ] Available from: https://doi.org/10.4238/vol8-4gmr631
    • Vancouver

      Anselmo NP, Rey JA, Almeida LO, Custódio AC, Almeida JRW, Clara CA, Santos MJ, Casartelli C. Concurrent sequence variation of TP53 and TP73 genes in anaplastic astrocytoma [Internet]. Genetics and Molecular Research. 2009 ; 8( 4): 1257-1263.[citado 2024 nov. 15 ] Available from: https://doi.org/10.4238/vol8-4gmr631
  • Source: Neurocirurgía. Unidade: FMRP

    Subjects: PROCEDIMENTOS NEUROCIRÚRGICOS, NEOPLASIAS

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      FRANCO-HERNANDEZ, Carmen et al. Identificación de alteraciones genéticas en oligodendrogliomas mediante amplificación dependiente de ligasa de múltiples sondas (MLPA) (multiple ligation-dependent probe amplification). Neurocirurgía, v. 20, n. 2, p. 117-123, 2009Tradução . . Disponível em: https://doi.org/10.1016/s1130-1473(09)70178-2. Acesso em: 15 nov. 2024.
    • APA

      Franco-Hernandez, C., Martínez-Glez, V., Torres-Martín, M., Campos, J. M. de, Isla, A., Vaquero, J., et al. (2009). Identificación de alteraciones genéticas en oligodendrogliomas mediante amplificación dependiente de ligasa de múltiples sondas (MLPA) (multiple ligation-dependent probe amplification). Neurocirurgía, 20( 2), 117-123. doi:10.1016/s1130-1473(09)70178-2
    • NLM

      Franco-Hernandez C, Martínez-Glez V, Torres-Martín M, Campos JM de, Isla A, Vaquero J, Casartelli C, Rey JA. Identificación de alteraciones genéticas en oligodendrogliomas mediante amplificación dependiente de ligasa de múltiples sondas (MLPA) (multiple ligation-dependent probe amplification) [Internet]. Neurocirurgía. 2009 ; 20( 2): 117-123.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/s1130-1473(09)70178-2
    • Vancouver

      Franco-Hernandez C, Martínez-Glez V, Torres-Martín M, Campos JM de, Isla A, Vaquero J, Casartelli C, Rey JA. Identificación de alteraciones genéticas en oligodendrogliomas mediante amplificación dependiente de ligasa de múltiples sondas (MLPA) (multiple ligation-dependent probe amplification) [Internet]. Neurocirurgía. 2009 ; 20( 2): 117-123.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/s1130-1473(09)70178-2
  • Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP

    Subjects: NEOPLASIAS GÁSTRICAS, DNA

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    • ABNT

      LIMA, E. M. et al. Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer. Brazilian Journal of Medical and Biological Research, v. 41, n. 6, p. 539-543, 2008Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2008000600017. Acesso em: 15 nov. 2024.
    • APA

      Lima, E. M., Leal, M. F., Burbano, R. R., Khayat, A. S., Assumpção, P. P., Bello, M. J., et al. (2008). Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer. Brazilian Journal of Medical and Biological Research, 41( 6), 539-543. doi:10.1590/s0100-879x2008000600017
    • NLM

      Lima EM, Leal MF, Burbano RR, Khayat AS, Assumpção PP, Bello MJ, Rey JA, Smith MAC, Casartelli C. Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer [Internet]. Brazilian Journal of Medical and Biological Research. 2008 ; 41( 6): 539-543.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1590/s0100-879x2008000600017
    • Vancouver

      Lima EM, Leal MF, Burbano RR, Khayat AS, Assumpção PP, Bello MJ, Rey JA, Smith MAC, Casartelli C. Methylation status of ANAPC1, CDKN2A and TP53 promoter genes in individuals with gastric cancer [Internet]. Brazilian Journal of Medical and Biological Research. 2008 ; 41( 6): 539-543.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1590/s0100-879x2008000600017
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: POLIMORFISMO, NEOPLASIAS

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    • ABNT

      TORRES-MARTÍN, et al. Mutation analysis of the CITED4 gene in glioblastomas. [Carta]. Cancer Genetics and Cytogenetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 15 nov. 2024. , 2008
    • APA

      Torres-Martín,, Franco-Hernandez, C., Matinez-Glez, V., Campos, J. M. de, Isla, A., Casartelli, C., & Rey, J. A. (2008). Mutation analysis of the CITED4 gene in glioblastomas. [Carta]. Cancer Genetics and Cytogenetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
    • NLM

      Torres-Martín, Franco-Hernandez C, Matinez-Glez V, Campos JM de, Isla A, Casartelli C, Rey JA. Mutation analysis of the CITED4 gene in glioblastomas. [Carta]. Cancer Genetics and Cytogenetics. 2008 ; 185( 2): 114-116.[citado 2024 nov. 15 ]
    • Vancouver

      Torres-Martín, Franco-Hernandez C, Matinez-Glez V, Campos JM de, Isla A, Casartelli C, Rey JA. Mutation analysis of the CITED4 gene in glioblastomas. [Carta]. Cancer Genetics and Cytogenetics. 2008 ; 185( 2): 114-116.[citado 2024 nov. 15 ]
  • Source: Genetics and Molecular Research. Unidade: FMRP

    Assunto: NEOPLASIAS DO SISTEMA NERVOSO

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      ALMEIDA, L. O. et al. Mutational analysis of genes p14ARF, p15INK4b, p16INK4a, and PTEN in human nervous system tumors. Genetics and Molecular Research, v. 7, n. 2, p. 451-459, 2008Tradução . . Disponível em: https://doi.org/10.4238/vol7-2gmr445. Acesso em: 15 nov. 2024.
    • APA

      Almeida, L. O., Custódio, A. C., Araújo, J. J., Rey, J. A., Almeida, J. R. W., Santos, M. J., et al. (2008). Mutational analysis of genes p14ARF, p15INK4b, p16INK4a, and PTEN in human nervous system tumors. Genetics and Molecular Research, 7( 2), 451-459. doi:10.4238/vol7-2gmr445
    • NLM

      Almeida LO, Custódio AC, Araújo JJ, Rey JA, Almeida JRW, Santos MJ, Clara CA, Casartelli C. Mutational analysis of genes p14ARF, p15INK4b, p16INK4a, and PTEN in human nervous system tumors [Internet]. Genetics and Molecular Research. 2008 ; 7( 2): 451-459.[citado 2024 nov. 15 ] Available from: https://doi.org/10.4238/vol7-2gmr445
    • Vancouver

      Almeida LO, Custódio AC, Araújo JJ, Rey JA, Almeida JRW, Santos MJ, Clara CA, Casartelli C. Mutational analysis of genes p14ARF, p15INK4b, p16INK4a, and PTEN in human nervous system tumors [Internet]. Genetics and Molecular Research. 2008 ; 7( 2): 451-459.[citado 2024 nov. 15 ] Available from: https://doi.org/10.4238/vol7-2gmr445
  • Source: Neoplasma. Unidade: FMRP

    Assunto: METÁSTASE NEOPLÁSICA

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      MARTINEZ-GLEZ, V. et al. DAPK1 promoter hypermethylaiton in brain metastases and peripheral blood. Neoplasma, v. 54, n. 2, p. 123-126, 2007Tradução . . Acesso em: 15 nov. 2024.
    • APA

      Martinez-Glez, V., Franco-Hernandez, C., Gonzalez-Gomez, P., Isla, A., Campos, J. M. de, Vaquero, J., et al. (2007). DAPK1 promoter hypermethylaiton in brain metastases and peripheral blood. Neoplasma, 54( 2), 123-126.
    • NLM

      Martinez-Glez V, Franco-Hernandez C, Gonzalez-Gomez P, Isla A, Campos JM de, Vaquero J, Gutierrez M, Casartelli C, Rey JA. DAPK1 promoter hypermethylaiton in brain metastases and peripheral blood. Neoplasma. 2007 ; 54( 2): 123-126.[citado 2024 nov. 15 ]
    • Vancouver

      Martinez-Glez V, Franco-Hernandez C, Gonzalez-Gomez P, Isla A, Campos JM de, Vaquero J, Gutierrez M, Casartelli C, Rey JA. DAPK1 promoter hypermethylaiton in brain metastases and peripheral blood. Neoplasma. 2007 ; 54( 2): 123-126.[citado 2024 nov. 15 ]
  • Source: Genetics and Molecular Research. Unidade: FMRP

    Subjects: MUTAÇÃO, GENÉTICA MÉDICA

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      PINTO, G. R. et al. Mutation analysis of gene PAX6 in human gliomas. Genetics and Molecular Research, v. 6, n. 4, p. 1019-1025, 2007Tradução . . Acesso em: 15 nov. 2024.
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      Pinto, G. R., Clara, C. A., Santos, M. J., Almeida, J. R. W., Burbano, R. R., Rey, J. A., & Casartelli, C. (2007). Mutation analysis of gene PAX6 in human gliomas. Genetics and Molecular Research, 6( 4), 1019-1025.
    • NLM

      Pinto GR, Clara CA, Santos MJ, Almeida JRW, Burbano RR, Rey JA, Casartelli C. Mutation analysis of gene PAX6 in human gliomas. Genetics and Molecular Research. 2007 ; 6( 4): 1019-1025.[citado 2024 nov. 15 ]
    • Vancouver

      Pinto GR, Clara CA, Santos MJ, Almeida JRW, Burbano RR, Rey JA, Casartelli C. Mutation analysis of gene PAX6 in human gliomas. Genetics and Molecular Research. 2007 ; 6( 4): 1019-1025.[citado 2024 nov. 15 ]
  • Source: Clinical and Experimental Medicine. Unidade: FMRP

    Subjects: NEOPLASIAS GÁSTRICAS, GENÉTICA MÉDICA

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      KHAYAT, A. S. et al. Polymorphisms of the TP53 codon 72 and WRN codon 1367 in individuals from Northern Brazil with gastric adenocarcinoma. Clinical and Experimental Medicine, v. 5, p. 161-168, 2005Tradução . . Disponível em: https://doi.org/10.1007/s10238-005-0081-4. Acesso em: 15 nov. 2024.
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      khayat, A. S., Gatti, L. L., Lima, E. M., Assumpção, P. P. de, Motta, F. J. N., Harada, M. L., et al. (2005). Polymorphisms of the TP53 codon 72 and WRN codon 1367 in individuals from Northern Brazil with gastric adenocarcinoma. Clinical and Experimental Medicine, 5, 161-168. doi:10.1007/s10238-005-0081-4
    • NLM

      khayat AS, Gatti LL, Lima EM, Assumpção PP de, Motta FJN, Harada ML, Casartelli C, Payão SLM, Smith MAC, Burbano RR. Polymorphisms of the TP53 codon 72 and WRN codon 1367 in individuals from Northern Brazil with gastric adenocarcinoma [Internet]. Clinical and Experimental Medicine. 2005 ; 5 161-168.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s10238-005-0081-4
    • Vancouver

      khayat AS, Gatti LL, Lima EM, Assumpção PP de, Motta FJN, Harada ML, Casartelli C, Payão SLM, Smith MAC, Burbano RR. Polymorphisms of the TP53 codon 72 and WRN codon 1367 in individuals from Northern Brazil with gastric adenocarcinoma [Internet]. Clinical and Experimental Medicine. 2005 ; 5 161-168.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s10238-005-0081-4
  • Source: Clinical and Experimental Medicine. Unidade: FMRP

    Subjects: NEOPLASIAS GÁSTRICAS, GENÉTICA MÉDICA

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      LIMA, E. M. et al. Molecular study of the tumour suppressor gene PTEN in gastric adenocarcinoma in Brazil. Clinical and Experimental Medicine, v. 5, p. 129-132, 2005Tradução . . Disponível em: https://doi.org/10.1007/s10238-005-0077-0. Acesso em: 15 nov. 2024.
    • APA

      Lima, E. M., Araújo, J. J., Harada, M. L., Assumpção, P. P., Burbano, R. R., & Casartelli, C. (2005). Molecular study of the tumour suppressor gene PTEN in gastric adenocarcinoma in Brazil. Clinical and Experimental Medicine, 5, 129-132. doi:10.1007/s10238-005-0077-0
    • NLM

      Lima EM, Araújo JJ, Harada ML, Assumpção PP, Burbano RR, Casartelli C. Molecular study of the tumour suppressor gene PTEN in gastric adenocarcinoma in Brazil [Internet]. Clinical and Experimental Medicine. 2005 ; 5 129-132.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s10238-005-0077-0
    • Vancouver

      Lima EM, Araújo JJ, Harada ML, Assumpção PP, Burbano RR, Casartelli C. Molecular study of the tumour suppressor gene PTEN in gastric adenocarcinoma in Brazil [Internet]. Clinical and Experimental Medicine. 2005 ; 5 129-132.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s10238-005-0077-0
  • Source: Mutation Research. Unidade: FMRP

    Subjects: GENÉTICA MÉDICA, PROCESSOS NEOPLÁSICOS

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      BELLO, M. Josefa et al. Hypermethylation of the DNA repair gene MGMT: association with TP53 G:C to A:T transitions in a series of 469 nervous system tumors. Mutation Research, v. 554, p. 23-32, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.mrfmmm.2004.02.011. Acesso em: 15 nov. 2024.
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      Bello, M. J., Alonso, M. E., Amiñoso, C., Anselmo, N. P., Arjona, D., Gonzalez-Gomez, P., et al. (2004). Hypermethylation of the DNA repair gene MGMT: association with TP53 G:C to A:T transitions in a series of 469 nervous system tumors. Mutation Research, 554, 23-32. doi:10.1016/j.mrfmmm.2004.02.011
    • NLM

      Bello MJ, Alonso ME, Amiñoso C, Anselmo NP, Arjona D, Gonzalez-Gomez P, Lopez-Marin I, Campos JM de, Gutierrez M, Isla A, Kusak ME, Lassaletta L, Sarasa JL, Vaquero J, Casartelli C. Hypermethylation of the DNA repair gene MGMT: association with TP53 G:C to A:T transitions in a series of 469 nervous system tumors [Internet]. Mutation Research. 2004 ; 554 23-32.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.mrfmmm.2004.02.011
    • Vancouver

      Bello MJ, Alonso ME, Amiñoso C, Anselmo NP, Arjona D, Gonzalez-Gomez P, Lopez-Marin I, Campos JM de, Gutierrez M, Isla A, Kusak ME, Lassaletta L, Sarasa JL, Vaquero J, Casartelli C. Hypermethylation of the DNA repair gene MGMT: association with TP53 G:C to A:T transitions in a series of 469 nervous system tumors [Internet]. Mutation Research. 2004 ; 554 23-32.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.mrfmmm.2004.02.011
  • Source: Genetics and Molecular Biology. Unidades: FMRP, FORP

    Subjects: GRANULOMA DE CÉLULAS GIGANTES, OSSO E OSSOS, CITOGENÉTICA

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      BARUFFI, Marcelo Razera et al. Distinct nonrandom patterns of chromosomal deletions in giant-cell lesions of bone. Genetics and Molecular Biology, v. 25, n. 3, p. 265-270, 2002Tradução . . Disponível em: https://doi.org/10.1590/s1415-47572002000300002. Acesso em: 15 nov. 2024.
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      Baruffi, M. R., Barbieri Neto, J., Pina Neto, J. M. de, Sverzut, C. E., & Casartelli, C. (2002). Distinct nonrandom patterns of chromosomal deletions in giant-cell lesions of bone. Genetics and Molecular Biology, 25( 3), 265-270. doi:10.1590/s1415-47572002000300002
    • NLM

      Baruffi MR, Barbieri Neto J, Pina Neto JM de, Sverzut CE, Casartelli C. Distinct nonrandom patterns of chromosomal deletions in giant-cell lesions of bone [Internet]. Genetics and Molecular Biology. 2002 ; 25( 3): 265-270.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1590/s1415-47572002000300002
    • Vancouver

      Baruffi MR, Barbieri Neto J, Pina Neto JM de, Sverzut CE, Casartelli C. Distinct nonrandom patterns of chromosomal deletions in giant-cell lesions of bone [Internet]. Genetics and Molecular Biology. 2002 ; 25( 3): 265-270.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1590/s1415-47572002000300002
  • Source: Brazilian Journal of Medical and Biological. Unidade: FMRP

    Subjects: NEOPLASIAS MAMÁRIAS, CITOGENÉTICA

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      BURBANO, R. R. et al. Cytogenetic description of breast fibroadenomas: alterations related solely to proliferation ?. Brazilian Journal of Medical and Biological, v. 34, p. 1003-1006, 2001Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2001000800005. Acesso em: 15 nov. 2024.
    • APA

      Burbano, R. R., Lima, E. M., Khayat, A. S., Barbieri Neto, J., Cabral, I. R., Bastos Júnior, L., et al. (2001). Cytogenetic description of breast fibroadenomas: alterations related solely to proliferation ? Brazilian Journal of Medical and Biological, 34, 1003-1006. doi:10.1590/s0100-879x2001000800005
    • NLM

      Burbano RR, Lima EM, Khayat AS, Barbieri Neto J, Cabral IR, Bastos Júnior L, Bahia M de O, Casartelli C. Cytogenetic description of breast fibroadenomas: alterations related solely to proliferation ? [Internet]. Brazilian Journal of Medical and Biological. 2001 ; 34 1003-1006.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1590/s0100-879x2001000800005
    • Vancouver

      Burbano RR, Lima EM, Khayat AS, Barbieri Neto J, Cabral IR, Bastos Júnior L, Bahia M de O, Casartelli C. Cytogenetic description of breast fibroadenomas: alterations related solely to proliferation ? [Internet]. Brazilian Journal of Medical and Biological. 2001 ; 34 1003-1006.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1590/s0100-879x2001000800005
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Assunto: MENINGIOMA

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      LOMAS, Jesus et al. Analysis of p73 gene in meningiomas with deletion at 1p. Cancer Genetics and Cytogenetics, v. 129, p. 88-91, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0165-4608(01)00430-7. Acesso em: 15 nov. 2024.
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      Lomas, J., Bello, J., Arjona, D., Gonzales-Gomez, P., Alonso, M. E., Campos, J. M. de, et al. (2001). Analysis of p73 gene in meningiomas with deletion at 1p. Cancer Genetics and Cytogenetics, 129, 88-91. doi:10.1016/s0165-4608(01)00430-7
    • NLM

      Lomas J, Bello J, Arjona D, Gonzales-Gomez P, Alonso ME, Campos JM de, Vaquero J, Ruiz-Barnes P, Sarasa JL, Casartelli C, Rey JA. Analysis of p73 gene in meningiomas with deletion at 1p [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 129 88-91.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/s0165-4608(01)00430-7
    • Vancouver

      Lomas J, Bello J, Arjona D, Gonzales-Gomez P, Alonso ME, Campos JM de, Vaquero J, Ruiz-Barnes P, Sarasa JL, Casartelli C, Rey JA. Analysis of p73 gene in meningiomas with deletion at 1p [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 129 88-91.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/s0165-4608(01)00430-7
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: LINFOMA, TESTÍCULO, GENÉTICA MÉDICA

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      ESPINOZA, Luis A. et al. Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma. Cancer Genetics and Cytogenetics, v. 131, p. 79-81, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0165-4608(01)00495-2. Acesso em: 15 nov. 2024.
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      Espinoza, L. A., Barbieri Neto, J., Popescu, N. C., & Casartelli, C. (2001). Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma. Cancer Genetics and Cytogenetics, 131, 79-81. doi:10.1016/s0165-4608(01)00495-2
    • NLM

      Espinoza LA, Barbieri Neto J, Popescu NC, Casartelli C. Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 131 79-81.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/s0165-4608(01)00495-2
    • Vancouver

      Espinoza LA, Barbieri Neto J, Popescu NC, Casartelli C. Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 131 79-81.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/s0165-4608(01)00495-2
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: CISTOS, OSSO E OSSOS, CITOGENÉTICA

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    • ABNT

      BARUFFI, Marcelo Razera et al. Aneurysmal bone cyst with chromosomal changes involving 7q and 16p. Cancer Genetics and Cytogenetics, v. 129, p. 177-180, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0165-4608(01)00453-8. Acesso em: 15 nov. 2024.
    • APA

      Baruffi, M. R., Barbieri Neto, J., Barbieri, C. H., & Casartelli, C. (2001). Aneurysmal bone cyst with chromosomal changes involving 7q and 16p. Cancer Genetics and Cytogenetics, 129, 177-180. doi:10.1016/s0165-4608(01)00453-8
    • NLM

      Baruffi MR, Barbieri Neto J, Barbieri CH, Casartelli C. Aneurysmal bone cyst with chromosomal changes involving 7q and 16p [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 129 177-180.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/s0165-4608(01)00453-8
    • Vancouver

      Baruffi MR, Barbieri Neto J, Barbieri CH, Casartelli C. Aneurysmal bone cyst with chromosomal changes involving 7q and 16p [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 129 177-180.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/s0165-4608(01)00453-8
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: ONCOLOGIA, OSSO E OSSOS (CIRURGIA), CITOGENÉTICA

    Acesso à fonteAcesso à fonteDOIHow to cite
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    • ABNT

      BARUFFI, Marcelo Razera et al. Osteoid osteomas with chromosome alterations involving 22q. Cancer Genetics and Cytogenetics, v. 124, p. 127-131, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0165-4608(00)00327-7. Acesso em: 15 nov. 2024.
    • APA

      Baruffi, M. R., Volpon, J. B., Barbieri Neto, J., & Casartelli, C. (2001). Osteoid osteomas with chromosome alterations involving 22q. Cancer Genetics and Cytogenetics, 124, 127-131. doi:10.1016/s0165-4608(00)00327-7
    • NLM

      Baruffi MR, Volpon JB, Barbieri Neto J, Casartelli C. Osteoid osteomas with chromosome alterations involving 22q [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 124 127-131.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/s0165-4608(00)00327-7
    • Vancouver

      Baruffi MR, Volpon JB, Barbieri Neto J, Casartelli C. Osteoid osteomas with chromosome alterations involving 22q [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 124 127-131.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/s0165-4608(00)00327-7

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