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

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1 - 6 (6 records)

  • Artigo de periodico

    Glycodelin expression in the endometrium of healthy women and in the eutopic and ectopic endometrium of women eith endometriosis (2009)

    Meola, Juliana; Dentillo, Daniel Blassioli; Rosa e Silva, Júlio César; Ferriani, Rui Alberto; Veiga, Luciana Caricati da Silva; Paz, Cláudia Cristina Paro de; Giuliatti, Silvana; Martelli, Lúcia Regina

    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: 05 nov. 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 nov. 05 ] 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 nov. 05 ] Available from: https://doi.org/10.1016/j.fertnstert.2008.02.158

  • Artigo de periodico

    No evidence of association of MUC-1 genetic polymorphism with embryo implantation failure (2007)

    Dentillo, D. B.; Souza, F. R. P.; Meola, J.; Vieira, G. S.; Yazlle, Marta Edna Holanda Diógenes; Goulart, L. R.; Martelli, Lúcia Regina

    Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP

    Subjects: POLIMORFISMO, REPRODUÇÃO

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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: 05 nov. 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 nov. 05 ] 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 nov. 05 ] Available from: https://doi.org/10.1590/s0100-879x2007000600007

  • Artigo de periodico

    Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2 (2007)

    Sandrin-Garcia, Paula; Abramides, Dagma Venturini Marques; Martelli, Lúcia Regina; Ramos, Ester Silveira; Richieri-Costa, Antonio; Passos, Geraldo Aleixo Silva

    Source: Molecular and Cellular Biochemistry. Unidades: FOB, FMRP, HRAC, FORP

    Subjects: ANORMALIDADES MÚLTIPLAS, ANORMALIDADES CRANIOFACIAIS, FENÓTIPOS

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    • ABNT

      SANDRIN-GARCIA, Paula et al. Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2. Molecular and Cellular Biochemistry, v. 303, n. 1/2, p. 9-17, 2007Tradução . . Disponível em: https://doi.org/10.1007/s11010-007-9450-5. Acesso em: 05 nov. 2024.

    • APA

      Sandrin-Garcia, P., Abramides, D. V. M., Martelli, L. R., Ramos, E. S., Richieri-Costa, A., & Passos, G. A. S. (2007). Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2. Molecular and Cellular Biochemistry, 303( 1/2), 9-17. doi:10.1007/s11010-007-9450-5

    • NLM

      Sandrin-Garcia P, Abramides DVM, Martelli LR, Ramos ES, Richieri-Costa A, Passos GAS. Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2 [Internet]. Molecular and Cellular Biochemistry. 2007 ; 303( 1/2): 9-17.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s11010-007-9450-5

    • Vancouver

      Sandrin-Garcia P, Abramides DVM, Martelli LR, Ramos ES, Richieri-Costa A, Passos GAS. Typical phenotypic spectrum of velocardiofacial syndrome occurs independently of deletion size in chromosome 22q11.2 [Internet]. Molecular and Cellular Biochemistry. 2007 ; 303( 1/2): 9-17.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s11010-007-9450-5

  • Artigo de periodico

    Down syndrome and precocious menopause (2005)

    Bartmann, Ana Karina; Araújo, Francielle M.; Iannetta, Odilon; Paneto, João C. C.; Martelli, Lúcia Regina; Ramos, Ester Silveira

    Source: Journal of Assisted Reproduction and Genetics. Unidade: FMRP

    Subjects: SÍNDROME DE DOWN, MENOPAUSA

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    • ABNT

      BARTMANN, Ana Karina et al. Down syndrome and precocious menopause. Journal of Assisted Reproduction and Genetics, v. 22, n. 3, p. 129-131, 2005Tradução . . Disponível em: https://doi.org/10.1007/s10815-005-4878-6. Acesso em: 05 nov. 2024.

    • APA

      Bartmann, A. K., Araújo, F. M., Iannetta, O., Paneto, J. C. C., Martelli, L. R., & Ramos, E. S. (2005). Down syndrome and precocious menopause. Journal of Assisted Reproduction and Genetics, 22( 3), 129-131. doi:10.1007/s10815-005-4878-6

    • NLM

      Bartmann AK, Araújo FM, Iannetta O, Paneto JCC, Martelli LR, Ramos ES. Down syndrome and precocious menopause [Internet]. Journal of Assisted Reproduction and Genetics. 2005 ; 22( 3): 129-131.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s10815-005-4878-6

    • Vancouver

      Bartmann AK, Araújo FM, Iannetta O, Paneto JCC, Martelli LR, Ramos ES. Down syndrome and precocious menopause [Internet]. Journal of Assisted Reproduction and Genetics. 2005 ; 22( 3): 129-131.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s10815-005-4878-6

  • Artigo de periodico

    Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients (2004)

    Bassi, C. L.; Martelli, Lúcia Regina; Cipolotti, R.; Scrideli, C. A.; Defavery, R.; Tone, Luiz Gonzaga

    Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP

    Subjects: ONCOLOGIA, PEDIATRIA, GENÉTICA

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    • ABNT

      BASSI, C. L. et al. Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients. Brazilian Journal of Medical and Biological Research, v. 37, n. 11, p. 1683-1687, 2004Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2004001100014. Acesso em: 05 nov. 2024.

    • APA

      Bassi, C. L., Martelli, L. R., Cipolotti, R., Scrideli, C. A., Defavery, R., & Tone, L. G. (2004). Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients. Brazilian Journal of Medical and Biological Research, 37( 11), 1683-1687. doi:10.1590/s0100-879x2004001100014

    • NLM

      Bassi CL, Martelli LR, Cipolotti R, Scrideli CA, Defavery R, Tone LG. Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients [Internet]. Brazilian Journal of Medical and Biological Research. 2004 ; 37( 11): 1683-1687.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1590/s0100-879x2004001100014

    • Vancouver

      Bassi CL, Martelli LR, Cipolotti R, Scrideli CA, Defavery R, Tone LG. Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients [Internet]. Brazilian Journal of Medical and Biological Research. 2004 ; 37( 11): 1683-1687.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1590/s0100-879x2004001100014

  • Artigo de periodico

    Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome (2002)

    Sandrin Garcia, P; Macedo, C; Martelli, Lúcia Regina; Ramos, Ester Silveira; Guion Almeida, Maria Leine; Richieri Costa, Antônio; Passos, Geraldo Aleixo Silva

    Source: Clinical genetics. Unidades: FMRP, HRAC, FORP

    Subjects: GENÉTICA, DNA

    Acesso à fonteDOIHow to cite
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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: 05 nov. 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 nov. 05 ] 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 nov. 05 ] Available from: https://doi.org/10.1034/j.1399-0004.2002.610511.x
  • 1

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