Filtros : "Indexado no Biological Abstracts" "MARTELLI, LUCIA REGINA" "FMRP" Removidos: "IQ004" "EP/FEA/IEE/IF" Limpar

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  • Source: Genetics and Molecular Biology. Unidade: FMRP

    Subjects: BOVINOS DE CORTE, MARCADOR MOLECULAR

    Versão PublicadaAcesso à fonteAcesso à fonteDOIHow to cite
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    • ABNT

      SOUZA, Fabio Ricardo Pablos de et al. Association between MUC1 gene polymorphism and expected progeny differences in Nelore cattle (Bos primigenius indicus). Genetics and Molecular Biology, v. 33, n. 1, p. 68-70, 2010Tradução . . Disponível em: https://doi.org/10.1590/s1415-47572009005000098. Acesso em: 03 out. 2024.
    • APA

      Souza, F. R. P. de, Vozzi, P. A., Vila, R. A., Boligon, A. A., Galerani, M. A. V., Lôbo, R. B., & Martelli, L. R. (2010). Association between MUC1 gene polymorphism and expected progeny differences in Nelore cattle (Bos primigenius indicus). Genetics and Molecular Biology, 33( 1), 68-70. doi:10.1590/s1415-47572009005000098
    • NLM

      Souza FRP de, Vozzi PA, Vila RA, Boligon AA, Galerani MAV, Lôbo RB, Martelli LR. Association between MUC1 gene polymorphism and expected progeny differences in Nelore cattle (Bos primigenius indicus) [Internet]. Genetics and Molecular Biology. 2010 ; 33( 1): 68-70.[citado 2024 out. 03 ] Available from: https://doi.org/10.1590/s1415-47572009005000098
    • Vancouver

      Souza FRP de, Vozzi PA, Vila RA, Boligon AA, Galerani MAV, Lôbo RB, Martelli LR. Association between MUC1 gene polymorphism and expected progeny differences in Nelore cattle (Bos primigenius indicus) [Internet]. Genetics and Molecular Biology. 2010 ; 33( 1): 68-70.[citado 2024 out. 03 ] Available from: https://doi.org/10.1590/s1415-47572009005000098
  • Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP

    Subjects: ENDOMETRIOSE, HIBRIDIZAÇÃO

    Versão PublicadaAcesso à fonteAcesso à fonteDOIHow to cite
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    • ABNT

      CASTELLI, Luciana Caricati Veiga et al. Genomic alterations detected by comparative genomic hybridization in ovarian endometriomas. Brazilian Journal of Medical and Biological Research, v. 43, n. 8, p. 799-805, 2010Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2010007500072. Acesso em: 03 out. 2024.
    • APA

      Castelli, L. C. V., Silva, J. C. R. e, Meola, J., Ferriani, R. A., Yoshimoto, M., Santos, S. A. dos, et al. (2010). Genomic alterations detected by comparative genomic hybridization in ovarian endometriomas. Brazilian Journal of Medical and Biological Research, 43( 8), 799-805. doi:10.1590/s0100-879x2010007500072
    • NLM

      Castelli LCV, Silva JCR e, Meola J, Ferriani RA, Yoshimoto M, Santos SA dos, Squire JA, Martelli LR. Genomic alterations detected by comparative genomic hybridization in ovarian endometriomas [Internet]. Brazilian Journal of Medical and Biological Research. 2010 ; 43( 8): 799-805.[citado 2024 out. 03 ] Available from: https://doi.org/10.1590/s0100-879x2010007500072
    • Vancouver

      Castelli LCV, Silva JCR e, Meola J, Ferriani RA, Yoshimoto M, Santos SA dos, Squire JA, Martelli LR. Genomic alterations detected by comparative genomic hybridization in ovarian endometriomas [Internet]. Brazilian Journal of Medical and Biological Research. 2010 ; 43( 8): 799-805.[citado 2024 out. 03 ] Available from: https://doi.org/10.1590/s0100-879x2010007500072
  • Source: Fertility and Sterility. Unidade: FMRP

    Subjects: ENDOMETRIOSE, ENDOMÉTRIO, EXPRESSÃO GÊNICA

    Acesso à fonteDOIHow to cite
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    • ABNT

      MEOLA, Juliana et al. Glycodelin expression in the endometrium of healthy women and in the eutopic and ectopic endometrium of women eith endometriosis. Fertility and Sterility, v. 91, n. 5, p. 1676-1680, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.fertnstert.2008.02.158. Acesso em: 03 out. 2024.
    • APA

      Meola, J., Dentillo, D. B., Rosa e Silva, J. C., Ferriani, R. A., Veiga, L. C. da S., Paz, C. C. P. de, et al. (2009). Glycodelin expression in the endometrium of healthy women and in the eutopic and ectopic endometrium of women eith endometriosis. Fertility and Sterility, 91( 5), 1676-1680. doi:10.1016/j.fertnstert.2008.02.158
    • NLM

      Meola J, Dentillo DB, Rosa e Silva JC, Ferriani RA, Veiga LC da S, Paz CCP de, Giuliatti S, Martelli LR. Glycodelin expression in the endometrium of healthy women and in the eutopic and ectopic endometrium of women eith endometriosis [Internet]. Fertility and Sterility. 2009 ; 91( 5): 1676-1680.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.fertnstert.2008.02.158
    • Vancouver

      Meola J, Dentillo DB, Rosa e Silva JC, Ferriani RA, Veiga LC da S, Paz CCP de, Giuliatti S, Martelli LR. Glycodelin expression in the endometrium of healthy women and in the eutopic and ectopic endometrium of women eith endometriosis [Internet]. Fertility and Sterility. 2009 ; 91( 5): 1676-1680.[citado 2024 out. 03 ] Available from: https://doi.org/10.1016/j.fertnstert.2008.02.158
  • Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP

    Subjects: POLIMORFISMO, REPRODUÇÃO

    Versão PublicadaAcesso à fonteDOIHow to cite
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    • ABNT

      DENTILLO, D. B. et al. No evidence of association of MUC-1 genetic polymorphism with embryo implantation failure. Brazilian Journal of Medical and Biological Research, v. 40, p. 793-797, 2007Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2007000600007. Acesso em: 03 out. 2024.
    • APA

      Dentillo, D. B., Souza, F. R. P., Meola, J., Vieira, G. S., Yazlle, M. E. H. D., Goulart, L. R., & Martelli, L. R. (2007). No evidence of association of MUC-1 genetic polymorphism with embryo implantation failure. Brazilian Journal of Medical and Biological Research, 40, 793-797. doi:10.1590/s0100-879x2007000600007
    • NLM

      Dentillo DB, Souza FRP, Meola J, Vieira GS, Yazlle MEHD, Goulart LR, Martelli LR. No evidence of association of MUC-1 genetic polymorphism with embryo implantation failure [Internet]. Brazilian Journal of Medical and Biological Research. 2007 ; 40 793-797.[citado 2024 out. 03 ] Available from: https://doi.org/10.1590/s0100-879x2007000600007
    • Vancouver

      Dentillo DB, Souza FRP, Meola J, Vieira GS, Yazlle MEHD, Goulart LR, Martelli LR. No evidence of association of MUC-1 genetic polymorphism with embryo implantation failure [Internet]. Brazilian Journal of Medical and Biological Research. 2007 ; 40 793-797.[citado 2024 out. 03 ] Available from: https://doi.org/10.1590/s0100-879x2007000600007
  • Source: Journal of Animal Breeding and Genetics. Unidade: FMRP

    Subjects: GADO NELORE, POLIMORFISMO

    Acesso à fonteDOIHow to cite
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    • ABNT

      SOUZA, F. R. P. et al. The polymorphism in MUC1 gene in nelore cattle. Journal of Animal Breeding and Genetics, v. 124, n. 1, p. 42-46, 2007Tradução . . Disponível em: https://doi.org/10.1111/j.1439-0388.2007.00628.x. Acesso em: 03 out. 2024.
    • APA

      Souza, F. R. P., Dentillo, D. B., Meola, J., Biase, F. H., Andréa, M. V., Vozzi, P. A., et al. (2007). The polymorphism in MUC1 gene in nelore cattle. Journal of Animal Breeding and Genetics, 124( 1), 42-46. doi:10.1111/j.1439-0388.2007.00628.x
    • NLM

      Souza FRP, Dentillo DB, Meola J, Biase FH, Andréa MV, Vozzi PA, Lôbo RB, Martelli LR. The polymorphism in MUC1 gene in nelore cattle [Internet]. Journal of Animal Breeding and Genetics. 2007 ; 124( 1): 42-46.[citado 2024 out. 03 ] Available from: https://doi.org/10.1111/j.1439-0388.2007.00628.x
    • Vancouver

      Souza FRP, Dentillo DB, Meola J, Biase FH, Andréa MV, Vozzi PA, Lôbo RB, Martelli LR. The polymorphism in MUC1 gene in nelore cattle [Internet]. Journal of Animal Breeding and Genetics. 2007 ; 124( 1): 42-46.[citado 2024 out. 03 ] Available from: https://doi.org/10.1111/j.1439-0388.2007.00628.x
  • Source: Genetics and Molecular Biology. Unidades: FMRP, IB

    Subjects: CROMOSSOMOS, GENÉTICA MOLECULAR

    Acesso à fonteDOIHow to cite
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    • ABNT

      MAZZEU, Juliana F. et al. Widening the clinical spectrum of Pitt-Rogers-Danks/Wolf-Hirschhorn syndromes. Genetics and Molecular Biology, v. 30, n. 2, p. 339-342, 2007Tradução . . Disponível em: https://doi.org/10.1590/s1415-47572007000300007. Acesso em: 03 out. 2024.
    • APA

      Mazzeu, J. F., Krepischi, A. C. V., Rosenberg, C., Lourenço, C. M., Lezirovitz, K., Szuhai, K., et al. (2007). Widening the clinical spectrum of Pitt-Rogers-Danks/Wolf-Hirschhorn syndromes. Genetics and Molecular Biology, 30( 2), 339-342. doi:10.1590/s1415-47572007000300007
    • NLM

      Mazzeu JF, Krepischi ACV, Rosenberg C, Lourenço CM, Lezirovitz K, Szuhai K, Martelli LR, Vianna-Morgante AM. Widening the clinical spectrum of Pitt-Rogers-Danks/Wolf-Hirschhorn syndromes [Internet]. Genetics and Molecular Biology. 2007 ; 30( 2): 339-342.[citado 2024 out. 03 ] Available from: https://doi.org/10.1590/s1415-47572007000300007
    • Vancouver

      Mazzeu JF, Krepischi ACV, Rosenberg C, Lourenço CM, Lezirovitz K, Szuhai K, Martelli LR, Vianna-Morgante AM. Widening the clinical spectrum of Pitt-Rogers-Danks/Wolf-Hirschhorn syndromes [Internet]. Genetics and Molecular Biology. 2007 ; 30( 2): 339-342.[citado 2024 out. 03 ] Available from: https://doi.org/10.1590/s1415-47572007000300007
  • Source: Clinical genetics. Unidades: FMRP, HRAC, FORP

    Subjects: GENÉTICA, DNA

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    • ABNT

      SANDRIN GARCIA, P et al. Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome. Clinical genetics, v. 61, n. 5, p. 380-383, 2002Tradução . . Disponível em: https://doi.org/10.1034/j.1399-0004.2002.610511.x. Acesso em: 03 out. 2024.
    • APA

      Sandrin Garcia, P., Macedo, C., Martelli, L. R., Ramos, E. S., Guion Almeida, M. L., Richieri Costa, A., & Passos, G. A. S. (2002). Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome. Clinical genetics, 61( 5), 380-383. doi:10.1034/j.1399-0004.2002.610511.x
    • NLM

      Sandrin Garcia P, Macedo C, Martelli LR, Ramos ES, Guion Almeida ML, Richieri Costa A, Passos GAS. Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome [Internet]. Clinical genetics. 2002 ; 61( 5): 380-383.[citado 2024 out. 03 ] Available from: https://doi.org/10.1034/j.1399-0004.2002.610511.x
    • Vancouver

      Sandrin Garcia P, Macedo C, Martelli LR, Ramos ES, Guion Almeida ML, Richieri Costa A, Passos GAS. Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome [Internet]. Clinical genetics. 2002 ; 61( 5): 380-383.[citado 2024 out. 03 ] Available from: https://doi.org/10.1034/j.1399-0004.2002.610511.x

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