Filtros : "Estados Unidos" "FMRP-RGE" "Rey, Juan A." Limpar

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  • 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: 03 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. 03 ] 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. 03 ] 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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    • 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: 03 ago. 2024.
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      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. 03 ] 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. 03 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.08.003
  • 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: 03 ago. 2024.
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      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. 03 ] 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. 03 ] Available from: https://doi.org/10.1016/j.cancergencyto.2008.09.017
  • 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: 03 ago. 2024.
    • APA

      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. 03 ] 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. 03 ] Available from: https://doi.org/10.1007/s11060-008-9664-8
  • 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: 03 ago. 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 ago. 03 ]
    • 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 ago. 03 ]
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: NEOPLASIAS MAMÁRIAS, MUTAÇÃO GENÉTICA

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      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: 03 ago. 2024.
    • APA

      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. 03 ] 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. 03 ] Available from: https://doi.org/10.1016/j.cancergencyto.2004.11.014
  • Source: Câncer Therapy. Unidade: FMRP

    Assunto: GASTROENTEROPATIAS (GENÉTICA)

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      BELLO, M. Josefa et al. Methylation analysis of cell cycle control genes RB1, 'p14 IND ARF' and 'p16 IND INK4a' in human gliomas. Câncer Therapy, v. 2, p. 187-194, 2004Tradução . . Acesso em: 03 ago. 2024.
    • APA

      Bello, M. J., Gonzales-Gomez, P., Alonso, M. E., Anselmo, N. P., Arjona, D., Amiñoso, C., et al. (2004). Methylation analysis of cell cycle control genes RB1, 'p14 IND ARF' and 'p16 IND INK4a' in human gliomas. Câncer Therapy, 2, 187-194.
    • NLM

      Bello MJ, Gonzales-Gomez P, Alonso ME, Anselmo NP, Arjona D, Amiñoso C, Lopez-Marin I, Campos JM, Isla A, Vaquero J, Casartelli C, Rey JA. Methylation analysis of cell cycle control genes RB1, 'p14 IND ARF' and 'p16 IND INK4a' in human gliomas. Câncer Therapy. 2004 ; 2 187-194.[citado 2024 ago. 03 ]
    • Vancouver

      Bello MJ, Gonzales-Gomez P, Alonso ME, Anselmo NP, Arjona D, Amiñoso C, Lopez-Marin I, Campos JM, Isla A, Vaquero J, Casartelli C, Rey JA. Methylation analysis of cell cycle control genes RB1, 'p14 IND ARF' and 'p16 IND INK4a' in human gliomas. Câncer Therapy. 2004 ; 2 187-194.[citado 2024 ago. 03 ]
  • 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: 03 ago. 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 ago. 03 ] 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 ago. 03 ] Available from: https://doi.org/10.1016/s0165-4608(01)00430-7

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