Filtros : "Indexado no SCISEARCH" "Instituto Butantan (IB)" "IQ" Removido: "1984" Limpar

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  • Fonte: Journal of Molecular Biology. Unidade: IQ

    Assuntos: LEPTOSPIROSE, DOENÇAS INFECCIOSAS, ANTÍGENOS

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      HAUK, Pricila et al. Structure and calcium-binding activity of LipL32, the major surface antigen of pathogenic Leptospira sp. Journal of Molecular Biology, v. 390, n. 4, p. 722-736, 2009Tradução . . Acesso em: 17 nov. 2024.
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      Hauk, P., Carvalho, C. R. G., Ramos, H. R., Ho, P. L., & Farah, C. S. (2009). Structure and calcium-binding activity of LipL32, the major surface antigen of pathogenic Leptospira sp. Journal of Molecular Biology, 390( 4), 722-736.
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      Hauk P, Carvalho CRG, Ramos HR, Ho PL, Farah CS. Structure and calcium-binding activity of LipL32, the major surface antigen of pathogenic Leptospira sp. Journal of Molecular Biology. 2009 ; 390( 4): 722-736.[citado 2024 nov. 17 ]
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      Hauk P, Carvalho CRG, Ramos HR, Ho PL, Farah CS. Structure and calcium-binding activity of LipL32, the major surface antigen of pathogenic Leptospira sp. Journal of Molecular Biology. 2009 ; 390( 4): 722-736.[citado 2024 nov. 17 ]
  • Fonte: Molecular Immunology. Unidades: IQ, ICB

    Assuntos: MENINGITE, IMUNOLOGIA

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      AGUILAR-RAMIREZ, Priscilia et al. Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability. Molecular Immunology, v. 46, n. 10, p. 2116-2123, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.molimm.2008.10.035. Acesso em: 17 nov. 2024.
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      Aguilar-Ramirez, P., Reis, E. da S., Florido, M. P. C., Barbosa, A. S., Farah, C. S., Costa-Carvalho, B. T., & Isaac, L. (2009). Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability. Molecular Immunology, 46( 10), 2116-2123. doi:10.1016/j.molimm.2008.10.035
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      Aguilar-Ramirez P, Reis E da S, Florido MPC, Barbosa AS, Farah CS, Costa-Carvalho BT, Isaac L. Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability [Internet]. Molecular Immunology. 2009 ; 46( 10): 2116-2123.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.molimm.2008.10.035
    • Vancouver

      Aguilar-Ramirez P, Reis E da S, Florido MPC, Barbosa AS, Farah CS, Costa-Carvalho BT, Isaac L. Skipping of exon 30 in C5 gene results in complete human C5 deficiency and demonstrates the importance of C5d and CUB domains for stability [Internet]. Molecular Immunology. 2009 ; 46( 10): 2116-2123.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.molimm.2008.10.035
  • Fonte: Peptides. Unidade: IQ

    Assuntos: ANGIOTENSINAS, COCAÍNA

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      NERY, Arthur Andrade et al. A novel physiological property of snake bradykinin-potentiating peptides: reversion of MK-801 inhibition of nicotinic acetylcholine receptors. Peptides, v. 29, n. 10, p. 1708-1715, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.peptides.2008.06.002. Acesso em: 17 nov. 2024.
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      Nery, A. A., Trujillo, C. A., Lameu, C., Konno, K., Oliveira, V., Camargo, A. C. M. de, et al. (2008). A novel physiological property of snake bradykinin-potentiating peptides: reversion of MK-801 inhibition of nicotinic acetylcholine receptors. Peptides, 29( 10), 1708-1715. doi:10.1016/j.peptides.2008.06.002
    • NLM

      Nery AA, Trujillo CA, Lameu C, Konno K, Oliveira V, Camargo ACM de, Ulrich H, Hayashi MAF. A novel physiological property of snake bradykinin-potentiating peptides: reversion of MK-801 inhibition of nicotinic acetylcholine receptors [Internet]. Peptides. 2008 ; 29( 10): 1708-1715.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.peptides.2008.06.002
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      Nery AA, Trujillo CA, Lameu C, Konno K, Oliveira V, Camargo ACM de, Ulrich H, Hayashi MAF. A novel physiological property of snake bradykinin-potentiating peptides: reversion of MK-801 inhibition of nicotinic acetylcholine receptors [Internet]. Peptides. 2008 ; 29( 10): 1708-1715.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.peptides.2008.06.002
  • Fonte: Journal of Steroid Biochemistry & Molecular Biology. Unidade: IQ

    Assuntos: LEUCEMIA, EXPRESSÃO GÊNICA, BIOQUÍMICA

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      DEMASI, Marcos Angelo Almeida et al. Differential proteomic analysis of the anti-proliferative effect of glucocorticoid hormones in ST1 rat glioma cells. Journal of Steroid Biochemistry & Molecular Biology, v. 103, n. 2, p. 137-148, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.jsbmb.2006.08.004. Acesso em: 17 nov. 2024.
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      Demasi, M. A. A., Montor, W. R., Ferreira, G. B., Pimenta, D. C., Labriola, L., & Sogayar, M. C. (2007). Differential proteomic analysis of the anti-proliferative effect of glucocorticoid hormones in ST1 rat glioma cells. Journal of Steroid Biochemistry & Molecular Biology, 103( 2), 137-148. doi:10.1016/j.jsbmb.2006.08.004
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      Demasi MAA, Montor WR, Ferreira GB, Pimenta DC, Labriola L, Sogayar MC. Differential proteomic analysis of the anti-proliferative effect of glucocorticoid hormones in ST1 rat glioma cells [Internet]. Journal of Steroid Biochemistry & Molecular Biology. 2007 ; 103( 2): 137-148.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.jsbmb.2006.08.004
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      Demasi MAA, Montor WR, Ferreira GB, Pimenta DC, Labriola L, Sogayar MC. Differential proteomic analysis of the anti-proliferative effect of glucocorticoid hormones in ST1 rat glioma cells [Internet]. Journal of Steroid Biochemistry & Molecular Biology. 2007 ; 103( 2): 137-148.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.jsbmb.2006.08.004
  • Fonte: Biochemical and Biophysical Research Communications. Unidades: IQ, ICB, FFCLRP

    Assuntos: ARACHNIDA, SISTEMA IMUNE, CATALASE

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      PEREIRA, Lourivaldo dos Santos et al. Structural and biological characterization of one antibacterial acylpolyamine isolated from the hemocytes of the spider Acanthocurria gomesiana. Biochemical and Biophysical Research Communications, v. 352, n. 4, p. 953-959, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.bbrc.2006.11.128. Acesso em: 17 nov. 2024.
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      Pereira, L. dos S., Silva Jr., P. I. da, Miranda, M. T. M. de, Almeida, I. C. de, Naoki, H., Konno, K., & Daffre, S. (2007). Structural and biological characterization of one antibacterial acylpolyamine isolated from the hemocytes of the spider Acanthocurria gomesiana. Biochemical and Biophysical Research Communications, 352( 4), 953-959. doi:10.1016/j.bbrc.2006.11.128
    • NLM

      Pereira L dos S, Silva Jr. PI da, Miranda MTM de, Almeida IC de, Naoki H, Konno K, Daffre S. Structural and biological characterization of one antibacterial acylpolyamine isolated from the hemocytes of the spider Acanthocurria gomesiana [Internet]. Biochemical and Biophysical Research Communications. 2007 ; 352( 4): 953-959.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.bbrc.2006.11.128
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      Pereira L dos S, Silva Jr. PI da, Miranda MTM de, Almeida IC de, Naoki H, Konno K, Daffre S. Structural and biological characterization of one antibacterial acylpolyamine isolated from the hemocytes of the spider Acanthocurria gomesiana [Internet]. Biochemical and Biophysical Research Communications. 2007 ; 352( 4): 953-959.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.bbrc.2006.11.128
  • Fonte: Biochemical and Biophysical Research Communications. Unidade: IQ

    Assuntos: NEOPLASIAS DOS GENITAIS MASCULINOS, BIOQUÍMICA, GENOMAS

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      LOURO, Rodrigo et al. RASL11A, member of a novel small monomeric GTPase gene family, is down-regulated in prostate tumors. Biochemical and Biophysical Research Communications, v. 316, n. 2, p. 618-627, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.bbrc.2004.02.091. Acesso em: 17 nov. 2024.
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      Louro, R., Nakaya, H. T. I., Paquola, A. C. M., Martins, E. A. L., Da Silva, A. M., Verjovski-Almeida, S., & Reis, E. M. (2004). RASL11A, member of a novel small monomeric GTPase gene family, is down-regulated in prostate tumors. Biochemical and Biophysical Research Communications, 316( 2), 618-627. doi:10.1016/j.bbrc.2004.02.091
    • NLM

      Louro R, Nakaya HTI, Paquola ACM, Martins EAL, Da Silva AM, Verjovski-Almeida S, Reis EM. RASL11A, member of a novel small monomeric GTPase gene family, is down-regulated in prostate tumors [Internet]. Biochemical and Biophysical Research Communications. 2004 ; 316( 2): 618-627.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.bbrc.2004.02.091
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      Louro R, Nakaya HTI, Paquola ACM, Martins EAL, Da Silva AM, Verjovski-Almeida S, Reis EM. RASL11A, member of a novel small monomeric GTPase gene family, is down-regulated in prostate tumors [Internet]. Biochemical and Biophysical Research Communications. 2004 ; 316( 2): 618-627.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.bbrc.2004.02.091

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