Filtros : "Pinto, G. R." Removido: "Português" Limpar

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  • Source: Genetics and Molecular Research. Unidade: FMRP

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

    Acesso à fonteDOIHow to cite
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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: 03 nov. 2025.
    • 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 2025 nov. 03 ] 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 2025 nov. 03 ] Available from: https://doi.org/10.4238/2012.February.10.4
  • Source: Genetics and Molecular Research. Unidade: FMRP

    Subjects: POLIMORFISMO, NEOPLASIAS CEREBRAIS, METÁSTASE NEOPLÁSICA

    Acesso à fonteDOIHow to cite
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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: 03 nov. 2025.
    • 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 2025 nov. 03 ] 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 2025 nov. 03 ] Available from: https://doi.org/10.4238/vol8-1gmr518
  • Source: Clinical Chemistry and Laboratory Medicine. Conference titles: IFCC - WorldLab. Unidade: FMRP

    Subjects: POLIMORFISMO, NEOPLASIAS

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    • ABNT

      PINTO, G. R. et al. No association of werner syndrome gene Cys1367 Arg polymorphism with risk of gliomas and prognosis in Brazil. Clinical Chemistry and Laboratory Medicine. Berlin: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 03 nov. 2025. , 2008
    • APA

      Pinto, G. R., Yoshioka, F. K. N., Clara, C. A., Santos, M. J., Almeida, J. R. W., Oliveira, V. M., et al. (2008). No association of werner syndrome gene Cys1367 Arg polymorphism with risk of gliomas and prognosis in Brazil. Clinical Chemistry and Laboratory Medicine. Berlin: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
    • NLM

      Pinto GR, Yoshioka FKN, Clara CA, Santos MJ, Almeida JRW, Oliveira VM, Penha MR, Casartelli C. No association of werner syndrome gene Cys1367 Arg polymorphism with risk of gliomas and prognosis in Brazil. Clinical Chemistry and Laboratory Medicine. 2008 ; 46 S237.[citado 2025 nov. 03 ]
    • Vancouver

      Pinto GR, Yoshioka FKN, Clara CA, Santos MJ, Almeida JRW, Oliveira VM, Penha MR, Casartelli C. No association of werner syndrome gene Cys1367 Arg polymorphism with risk of gliomas and prognosis in Brazil. Clinical Chemistry and Laboratory Medicine. 2008 ; 46 S237.[citado 2025 nov. 03 ]
  • Source: Genetics and Molecular Research. Unidade: FMRP

    Subjects: POLIMORFISMO, NEOPLASIAS

    Acesso à fonteDOIHow to cite
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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: 03 nov. 2025.
    • 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 2025 nov. 03 ] 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 2025 nov. 03 ] Available from: https://doi.org/10.4238/vol7-1gmr415
  • 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: 03 nov. 2025.
    • APA

      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 2025 nov. 03 ]
    • 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 2025 nov. 03 ]
  • Source: Revista Brasileira de Hematologia e Hemoterapia. Conference titles: Congresso Brasileiro de Hematologia e Hemoterapia. Unidade: FMRP

    Subjects: HEMATOLOGIA, GENÉTICA MÉDICA

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    • ABNT

      PINTO, G. R. et al. Diagnosis algorithm proposed for the initial evaluation of patients with possible myelodysplastic syndrome, according to World Health Organization (WHO) recommendations. Revista Brasileira de Hematologia e Hemoterapia. São José do Rio Preto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 03 nov. 2025. , 2004
    • APA

      Pinto, G. R., Overal, D. J., Moraes, L. S., Moreira, C. F. A., Leal, M. F., Calcagno, D. Q., et al. (2004). Diagnosis algorithm proposed for the initial evaluation of patients with possible myelodysplastic syndrome, according to World Health Organization (WHO) recommendations. Revista Brasileira de Hematologia e Hemoterapia. São José do Rio Preto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
    • NLM

      Pinto GR, Overal DJ, Moraes LS, Moreira CFA, Leal MF, Calcagno DQ, Casartelli C, Burbano RR. Diagnosis algorithm proposed for the initial evaluation of patients with possible myelodysplastic syndrome, according to World Health Organization (WHO) recommendations. Revista Brasileira de Hematologia e Hemoterapia. 2004 ; 26 135.[citado 2025 nov. 03 ]
    • Vancouver

      Pinto GR, Overal DJ, Moraes LS, Moreira CFA, Leal MF, Calcagno DQ, Casartelli C, Burbano RR. Diagnosis algorithm proposed for the initial evaluation of patients with possible myelodysplastic syndrome, according to World Health Organization (WHO) recommendations. Revista Brasileira de Hematologia e Hemoterapia. 2004 ; 26 135.[citado 2025 nov. 03 ]

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