Filtros : "CASARTELLI, CACILDA" "ARTIGO DE PERIODICO" Removido: "Costa, M I A" Limpar

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  • Source: Genetics and Molecular Research. Unidade: FMRP

    Subjects: POLIMORFISMO, NEOPLASIAS CRANIANAS, ASTRÓCITOS (COMPLICAÇÕES), CROMOSSOMOS (RECOMBINAÇÃO)

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    • ABNT

      CUSTÓDIO, A. C. et al. Variation in DNA repair gene XRCC3 affects susceptibility to astrocytomas and glioblastoma. Genetics and Molecular Research, v. 11, n. 1, p. 332-339, 2011Tradução . . Disponível em: https://doi.org/10.4238/2012.February.10.4. Acesso em: 18 ago. 2024.
    • APA

      Custódio, A. C., Almeida, L. O., Pinto, G. R., Santos, M. J., Almeida, J. R. W., Clara, C. A., et al. (2011). Variation in DNA repair gene XRCC3 affects susceptibility to astrocytomas and glioblastoma. Genetics and Molecular Research, 11( 1), 332-339. doi:10.4238/2012.February.10.4
    • NLM

      Custódio AC, Almeida LO, Pinto GR, Santos MJ, Almeida JRW, Clara CA, Rey JA, Casartelli C. Variation in DNA repair gene XRCC3 affects susceptibility to astrocytomas and glioblastoma [Internet]. Genetics and Molecular Research. 2011 ; 11( 1): 332-339.[citado 2024 ago. 18 ] Available from: https://doi.org/10.4238/2012.February.10.4
    • Vancouver

      Custódio AC, Almeida LO, Pinto GR, Santos MJ, Almeida JRW, Clara CA, Rey JA, Casartelli C. Variation in DNA repair gene XRCC3 affects susceptibility to astrocytomas and glioblastoma [Internet]. Genetics and Molecular Research. 2011 ; 11( 1): 332-339.[citado 2024 ago. 18 ] Available from: https://doi.org/10.4238/2012.February.10.4
  • Source: Genetics and Molecular Research. Unidade: FMRP

    Subjects: POLIMORFISMO, NEOPLASIAS

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      CUSTÓDIO, A. C. et al. Analysis of the polymorphisms XRCC1Arg194Trp and XRCC1Arg399Gln in gliomas. Genetics and Molecular Research, v. 10, n. 2, p. 1120-1129, 2011Tradução . . Disponível em: https://doi.org/10.4238/vol10-2gmr1125. Acesso em: 18 ago. 2024.
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      Custódio, A. C., Almeida, L. O., Pinto, G. R., Santos, M. J., Almeida, J. R. W., Clara, C. A., et al. (2011). Analysis of the polymorphisms XRCC1Arg194Trp and XRCC1Arg399Gln in gliomas. Genetics and Molecular Research, 10( 2), 1120-1129. doi:10.4238/vol10-2gmr1125
    • NLM

      Custódio AC, Almeida LO, Pinto GR, Santos MJ, Almeida JRW, Clara CA, Rey JA, Casartelli C. Analysis of the polymorphisms XRCC1Arg194Trp and XRCC1Arg399Gln in gliomas [Internet]. Genetics and Molecular Research. 2011 ; 10( 2): 1120-1129.[citado 2024 ago. 18 ] Available from: https://doi.org/10.4238/vol10-2gmr1125
    • Vancouver

      Custódio AC, Almeida LO, Pinto GR, Santos MJ, Almeida JRW, Clara CA, Rey JA, Casartelli C. Analysis of the polymorphisms XRCC1Arg194Trp and XRCC1Arg399Gln in gliomas [Internet]. Genetics and Molecular Research. 2011 ; 10( 2): 1120-1129.[citado 2024 ago. 18 ] Available from: https://doi.org/10.4238/vol10-2gmr1125
  • Source: Genetics and Molecular Research. Unidade: FMRP

    Subjects: POLIMORFISMO, GENÉTICA

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      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: 18 ago. 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 ago. 18 ]
    • 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 ago. 18 ]
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: POLIMORFISMO, NEOPLASIAS CEREBRAIS

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    • 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: 18 ago. 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 ago. 18 ] 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 ago. 18 ] 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: 18 ago. 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 ago. 18 ] 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 ago. 18 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.08.003
  • Source: International Journal of Oncology. Unidade: FMRP

    Subjects: EXPRESSÃO GÊNICA, MENINGIOMA

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      MARTINEZ-GLEZ, Victor et al. Meningiomas and schwannomas: molecular subgroup classification found by expression arrays. International Journal of Oncology, v. 34, n. 2, p. 493-504, 2009Tradução . . Disponível em: https://doi.org/10.3892/ijo_00000174. Acesso em: 18 ago. 2024.
    • APA

      Martinez-Glez, V., Franco-Hernandez, C., Alvarez, L., Campos, J. M. de, Isla, A., Vaquero, J., et al. (2009). Meningiomas and schwannomas: molecular subgroup classification found by expression arrays. International Journal of Oncology, 34( 2), 493-504. doi:10.3892/ijo_00000174
    • NLM

      Martinez-Glez V, Franco-Hernandez C, Alvarez L, Campos JM de, Isla A, Vaquero J, Lassaletta L, Casartelli C, Rey JA. Meningiomas and schwannomas: molecular subgroup classification found by expression arrays [Internet]. International Journal of Oncology. 2009 ; 34( 2): 493-504.[citado 2024 ago. 18 ] Available from: https://doi.org/10.3892/ijo_00000174
    • Vancouver

      Martinez-Glez V, Franco-Hernandez C, Alvarez L, Campos JM de, Isla A, Vaquero J, Lassaletta L, Casartelli C, Rey JA. Meningiomas and schwannomas: molecular subgroup classification found by expression arrays [Internet]. International Journal of Oncology. 2009 ; 34( 2): 493-504.[citado 2024 ago. 18 ] Available from: https://doi.org/10.3892/ijo_00000174
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: NEOPLASIAS, GENÉTICA

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    • 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: 18 ago. 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 ago. 18 ] 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 ago. 18 ] Available from: https://doi.org/10.1016/j.cancergencyto.2008.09.017
  • 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: 18 ago. 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 ago. 18 ] 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 ago. 18 ] 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: 18 ago. 2024.
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      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 ago. 18 ] 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 ago. 18 ] 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: 18 ago. 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 ago. 18 ] 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 ago. 18 ] Available from: https://doi.org/10.1016/s1130-1473(09)70178-2
  • Source: Journal of Neuro-Oncology. Unidade: FMRP

    Subjects: MUTAÇÃO GENÉTICA, PROGNÓSTICO, GENÉTICA MÉDICA

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      PINTO, Giovanny Rebouças et al. WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil. Journal of Neuro-Oncology, v. 90, n. 3, p. 253-258, 2008Tradução . . Disponível em: https://doi.org/10.1007/s11060-008-9664-8. Acesso em: 18 ago. 2024.
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      Pinto, G. R., Yoshioka, F. K. N., Clara, C. A., Santos, M. J. dos, Almeida, J. R. W. de, Burbano, R. R., et al. (2008). WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil. Journal of Neuro-Oncology, 90( 3), 253-258. doi:10.1007/s11060-008-9664-8
    • NLM

      Pinto GR, Yoshioka FKN, Clara CA, Santos MJ dos, Almeida JRW de, Burbano RR, Rey JA, Casartelli C. WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil [Internet]. Journal of Neuro-Oncology. 2008 ; 90( 3): 253-258.[citado 2024 ago. 18 ] Available from: https://doi.org/10.1007/s11060-008-9664-8
    • Vancouver

      Pinto GR, Yoshioka FKN, Clara CA, Santos MJ dos, Almeida JRW de, Burbano RR, Rey JA, Casartelli C. WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil [Internet]. Journal of Neuro-Oncology. 2008 ; 90( 3): 253-258.[citado 2024 ago. 18 ] Available from: https://doi.org/10.1007/s11060-008-9664-8
  • Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP

    Subjects: NEOPLASIAS GÁSTRICAS, DNA

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      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: 18 ago. 2024.
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      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 ago. 18 ] 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 ago. 18 ] Available from: https://doi.org/10.1590/s0100-879x2008000600017
  • Source: Genetics and Molecular Research. Unidade: FMRP

    Subjects: POLIMORFISMO, NEOPLASIAS

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    • ABNT

      PINTO, G. R. et al. Prognostic value of TP53 Pro47Ser and Arg72Pro single nucleotide polymosphisms and the susceptibility to gliomas in individuals from Southeast Brazil. Genetics and Molecular Research, v. 7, n. 1, p. 207-216, 2008Tradução . . Disponível em: https://doi.org/10.4238/vol7-1gmr415. Acesso em: 18 ago. 2024.
    • APA

      Pinto, G. R., Yoshioka, F. K. N., Silva, R. L. L., Clara, C. A., Santos, M. J., Almeida, J. R. W., et al. (2008). Prognostic value of TP53 Pro47Ser and Arg72Pro single nucleotide polymosphisms and the susceptibility to gliomas in individuals from Southeast Brazil. Genetics and Molecular Research, 7( 1), 207-216. doi:10.4238/vol7-1gmr415
    • NLM

      Pinto GR, Yoshioka FKN, Silva RLL, Clara CA, Santos MJ, Almeida JRW, Burbano RR, Rey JA, Casartelli C. Prognostic value of TP53 Pro47Ser and Arg72Pro single nucleotide polymosphisms and the susceptibility to gliomas in individuals from Southeast Brazil [Internet]. Genetics and Molecular Research. 2008 ; 7( 1): 207-216.[citado 2024 ago. 18 ] Available from: https://doi.org/10.4238/vol7-1gmr415
    • Vancouver

      Pinto GR, Yoshioka FKN, Silva RLL, Clara CA, Santos MJ, Almeida JRW, Burbano RR, Rey JA, Casartelli C. Prognostic value of TP53 Pro47Ser and Arg72Pro single nucleotide polymosphisms and the susceptibility to gliomas in individuals from Southeast Brazil [Internet]. Genetics and Molecular Research. 2008 ; 7( 1): 207-216.[citado 2024 ago. 18 ] Available from: https://doi.org/10.4238/vol7-1gmr415
  • 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: 18 ago. 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 ago. 18 ] 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 ago. 18 ] Available from: https://doi.org/10.4238/vol7-2gmr445
  • Source: Neoplasma. Unidade: FMRP

    Assunto: METÁSTASE NEOPLÁSICA

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    • ABNT

      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: 18 ago. 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 ago. 18 ]
    • 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 ago. 18 ]
  • Source: Genetics and Molecular Research. Unidade: FMRP

    Subjects: MUTAÇÃO, GENÉTICA MÉDICA

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    • ABNT

      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: 18 ago. 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 ago. 18 ]
    • 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 ago. 18 ]
  • Source: Oncology Reports. Unidade: FMRP

    Assunto: GLÂNDULA PITUITÁRIA

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      BELLO, M. Josefa et al. Promoter CpG methylation of multiple genes in pituitary adenomas: frequent involvement of Caspase-8. Oncology Reports, v. 15, n. 2, p. 443-448, 2006Tradução . . Disponível em: https://doi.org/10.3892/or.15.2.443. Acesso em: 18 ago. 2024.
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      Bello, M. J., Campos, J. M. de, Isla, A., Casartelli, C., & Rey, J. A. (2006). Promoter CpG methylation of multiple genes in pituitary adenomas: frequent involvement of Caspase-8. Oncology Reports, 15( 2), 443-448. doi:10.3892/or.15.2.443
    • NLM

      Bello MJ, Campos JM de, Isla A, Casartelli C, Rey JA. Promoter CpG methylation of multiple genes in pituitary adenomas: frequent involvement of Caspase-8 [Internet]. Oncology Reports. 2006 ; 15( 2): 443-448.[citado 2024 ago. 18 ] Available from: https://doi.org/10.3892/or.15.2.443
    • Vancouver

      Bello MJ, Campos JM de, Isla A, Casartelli C, Rey JA. Promoter CpG methylation of multiple genes in pituitary adenomas: frequent involvement of Caspase-8 [Internet]. Oncology Reports. 2006 ; 15( 2): 443-448.[citado 2024 ago. 18 ] Available from: https://doi.org/10.3892/or.15.2.443
  • Source: Clinical and Experimental Medicine. Unidade: FMRP

    Subjects: NEOPLASIAS, CROMOSSOMOS, CARCINOMA

    Acesso à fonteDOIHow to cite
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      LEITE, D. Soares et al. Investigation of chromosome 21 aneuploidies in breast fibroadenomas by fluorescence in situ hybridisation. Clinical and Experimental Medicine, v. 06, n. 04, p. 166-170, 2006Tradução . . Disponível em: https://doi.org/10.1007/s10238-006-0112-9. Acesso em: 18 ago. 2024.
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      Leite, D. S., Lima, P. D. L. de, Leal, M. F., Chen, E. S., Casartelli, C., Smith, M. de A. C., & Burdano, R. R. (2006). Investigation of chromosome 21 aneuploidies in breast fibroadenomas by fluorescence in situ hybridisation. Clinical and Experimental Medicine, 06( 04), 166-170. doi:10.1007/s10238-006-0112-9
    • NLM

      Leite DS, Lima PDL de, Leal MF, Chen ES, Casartelli C, Smith M de AC, Burdano RR. Investigation of chromosome 21 aneuploidies in breast fibroadenomas by fluorescence in situ hybridisation [Internet]. Clinical and Experimental Medicine. 2006 ; 06( 04): 166-170.[citado 2024 ago. 18 ] Available from: https://doi.org/10.1007/s10238-006-0112-9
    • Vancouver

      Leite DS, Lima PDL de, Leal MF, Chen ES, Casartelli C, Smith M de AC, Burdano RR. Investigation of chromosome 21 aneuploidies in breast fibroadenomas by fluorescence in situ hybridisation [Internet]. Clinical and Experimental Medicine. 2006 ; 06( 04): 166-170.[citado 2024 ago. 18 ] Available from: https://doi.org/10.1007/s10238-006-0112-9
  • Source: Genetics and Molecular Biology. Unidade: FMRP

    Subjects: NEOPLASIAS CEREBRAIS, GENÉTICA

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      ANSELMO, Nilson Praia et al. Epigenetic alterations in human brain tumors in a Brazilian population. Genetics and Molecular Biology, v. 29, n. 3, p. 413-422, 2006Tradução . . Disponível em: https://doi.org/10.1590/s1415-47572006000300001. Acesso em: 18 ago. 2024.
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      Anselmo, N. P., Bello, M. J., Gonzales-Gomez, P., Dias, L. A. A., Almeida, J. R. W. de, Santos, M. J. dos, et al. (2006). Epigenetic alterations in human brain tumors in a Brazilian population. Genetics and Molecular Biology, 29( 3), 413-422. doi:10.1590/s1415-47572006000300001
    • NLM

      Anselmo NP, Bello MJ, Gonzales-Gomez P, Dias LAA, Almeida JRW de, Santos MJ dos, Rey JA, Casartelli C. Epigenetic alterations in human brain tumors in a Brazilian population [Internet]. Genetics and Molecular Biology. 2006 ; 29( 3): 413-422.[citado 2024 ago. 18 ] Available from: https://doi.org/10.1590/s1415-47572006000300001
    • Vancouver

      Anselmo NP, Bello MJ, Gonzales-Gomez P, Dias LAA, Almeida JRW de, Santos MJ dos, Rey JA, Casartelli C. Epigenetic alterations in human brain tumors in a Brazilian population [Internet]. Genetics and Molecular Biology. 2006 ; 29( 3): 413-422.[citado 2024 ago. 18 ] Available from: https://doi.org/10.1590/s1415-47572006000300001
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: NEOPLASIAS MAMÁRIAS, MUTAÇÃO GENÉTICA

    Acesso à fonteDOIHow to cite
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    • ABNT

      LACERDA, Leandra Linhares et al. An intronic variant in the TP53 gene in a Brazilian woman with breast cancer. Cancer Genetics and Cytogenetics, v. 160, p. 160-163, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2004.11.014. Acesso em: 18 ago. 2024.
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      Lacerda, L. L., Serrano, S. V., Mathes, Â. do C. da S., Rey, J. A., Bello, M. J., & Casartelli, C. (2005). An intronic variant in the TP53 gene in a Brazilian woman with breast cancer. Cancer Genetics and Cytogenetics, 160, 160-163. doi:10.1016/j.cancergencyto.2004.11.014
    • NLM

      Lacerda LL, Serrano SV, Mathes  do C da S, Rey JA, Bello MJ, Casartelli C. An intronic variant in the TP53 gene in a Brazilian woman with breast cancer [Internet]. Cancer Genetics and Cytogenetics. 2005 ; 160 160-163.[citado 2024 ago. 18 ] Available from: https://doi.org/10.1016/j.cancergencyto.2004.11.014
    • Vancouver

      Lacerda LL, Serrano SV, Mathes  do C da S, Rey JA, Bello MJ, Casartelli C. An intronic variant in the TP53 gene in a Brazilian woman with breast cancer [Internet]. Cancer Genetics and Cytogenetics. 2005 ; 160 160-163.[citado 2024 ago. 18 ] Available from: https://doi.org/10.1016/j.cancergencyto.2004.11.014

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