Filtros : "Foguel, Debora" Limpar

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  • Source: Journal of Neurochemistry. Unidade: IQ

    Subjects: NEURÔNIOS, SISTEMA NERVOSO CENTRAL

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    • ABNT

      SANTOS, Raphael de Siqueira et al. Cerebral dopamine neurotrophic factor (CDNF) acts as a trophic factor promoting Neuritogenesis in the dorsal root ganglia (DRG) neurons through activation of the PI3K signaling pathway. Journal of Neurochemistry, v. 169, p. 1-18 art. e70194, 2025Tradução . . Disponível em: https://dx.doi.org/10.1111/jnc.70194. Acesso em: 03 maio 2026.
    • APA

      Santos, R. de S., Borba, F. N., Oliveira, D. F. de, Santiago, M. F., Nascimento, A. M. do, Schechtman, D., & Foguel, D. (2025). Cerebral dopamine neurotrophic factor (CDNF) acts as a trophic factor promoting Neuritogenesis in the dorsal root ganglia (DRG) neurons through activation of the PI3K signaling pathway. Journal of Neurochemistry, 169, 1-18 art. e70194. doi:10.1111/jnc.70194
    • NLM

      Santos R de S, Borba FN, Oliveira DF de, Santiago MF, Nascimento AM do, Schechtman D, Foguel D. Cerebral dopamine neurotrophic factor (CDNF) acts as a trophic factor promoting Neuritogenesis in the dorsal root ganglia (DRG) neurons through activation of the PI3K signaling pathway [Internet]. Journal of Neurochemistry. 2025 ; 169 1-18 art. e70194.[citado 2026 maio 03 ] Available from: https://dx.doi.org/10.1111/jnc.70194
    • Vancouver

      Santos R de S, Borba FN, Oliveira DF de, Santiago MF, Nascimento AM do, Schechtman D, Foguel D. Cerebral dopamine neurotrophic factor (CDNF) acts as a trophic factor promoting Neuritogenesis in the dorsal root ganglia (DRG) neurons through activation of the PI3K signaling pathway [Internet]. Journal of Neurochemistry. 2025 ; 169 1-18 art. e70194.[citado 2026 maio 03 ] Available from: https://dx.doi.org/10.1111/jnc.70194
  • Source: Proceedings of the Prion 2025. Conference titles: Prion 2025 - Advancing the understanding and treatment of prion diseases. Unidade: IQSC

    Subjects: DOENÇA DE PARKINSON, PROTEÍNAS

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      SILVA, Antônio et al. Targeting α-synuclein aggregation via hHEP1-mediated phase separation: Mechanistic insights into the cochaperone–α-synuclein interaction. 2025, Anais.. Rio de Janeiro: Universidade Federal do Rio de Janeiro, UFRJ, Rio de Janeiro, RJ, 2025. Disponível em: https://proceedings.science/prion-2025/papers/targeting-a-synuclein-aggregation-via-hhep1-mediated-phase-separation-mechanisti?lang=en. Acesso em: 03 maio 2026.
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      Silva, A., Ladeira, B., Silva, N. S. M. da, Tavares, M. O., Borges, J. C., & Foguel, D. (2025). Targeting α-synuclein aggregation via hHEP1-mediated phase separation: Mechanistic insights into the cochaperone–α-synuclein interaction. In Proceedings of the Prion 2025. Rio de Janeiro: Universidade Federal do Rio de Janeiro, UFRJ, Rio de Janeiro, RJ. Recuperado de https://proceedings.science/prion-2025/papers/targeting-a-synuclein-aggregation-via-hhep1-mediated-phase-separation-mechanisti?lang=en
    • NLM

      Silva A, Ladeira B, Silva NSM da, Tavares MO, Borges JC, Foguel D. Targeting α-synuclein aggregation via hHEP1-mediated phase separation: Mechanistic insights into the cochaperone–α-synuclein interaction [Internet]. Proceedings of the Prion 2025. 2025 ;[citado 2026 maio 03 ] Available from: https://proceedings.science/prion-2025/papers/targeting-a-synuclein-aggregation-via-hhep1-mediated-phase-separation-mechanisti?lang=en
    • Vancouver

      Silva A, Ladeira B, Silva NSM da, Tavares MO, Borges JC, Foguel D. Targeting α-synuclein aggregation via hHEP1-mediated phase separation: Mechanistic insights into the cochaperone–α-synuclein interaction [Internet]. Proceedings of the Prion 2025. 2025 ;[citado 2026 maio 03 ] Available from: https://proceedings.science/prion-2025/papers/targeting-a-synuclein-aggregation-via-hhep1-mediated-phase-separation-mechanisti?lang=en
    ODS 03. Saúde e bem-estar
  • Source: Abstract book. Conference titles: Annual Meeting of the Brazilian Society for Biochemistry and Molecular Biology - SBBq. Unidade: IFSC

    Subjects: MIOCARDIOPATIAS, AMILOIDOSE, PROTEÍNAS

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      MARTINS, Lucas do Amaral et al. Characterization of a novel dimeric variant of the amyloidogenic protein transthyretin involved in familial amyloidotic cardiomyopathy. 2022, Anais.. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular - SBBq, 2022. Disponível em: https://repositorio.usp.br/directbitstream/e156b1ee-7526-4d5e-8bc8-e90c2b185157/3100577.pdf. Acesso em: 03 maio 2026.
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      Martins, L. do A., Ferreira, P., Lima, C., Vasques, J., Jager, M., Monteiro, C., et al. (2022). Characterization of a novel dimeric variant of the amyloidogenic protein transthyretin involved in familial amyloidotic cardiomyopathy. In Abstract book. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular - SBBq. Recuperado de https://repositorio.usp.br/directbitstream/e156b1ee-7526-4d5e-8bc8-e90c2b185157/3100577.pdf
    • NLM

      Martins L do A, Ferreira P, Lima C, Vasques J, Jager M, Monteiro C, Pereira H d'M, Palhano F, Kelly J, Waddington-Cruz M, Foguel D. Characterization of a novel dimeric variant of the amyloidogenic protein transthyretin involved in familial amyloidotic cardiomyopathy [Internet]. Abstract book. 2022 ;[citado 2026 maio 03 ] Available from: https://repositorio.usp.br/directbitstream/e156b1ee-7526-4d5e-8bc8-e90c2b185157/3100577.pdf
    • Vancouver

      Martins L do A, Ferreira P, Lima C, Vasques J, Jager M, Monteiro C, Pereira H d'M, Palhano F, Kelly J, Waddington-Cruz M, Foguel D. Characterization of a novel dimeric variant of the amyloidogenic protein transthyretin involved in familial amyloidotic cardiomyopathy [Internet]. Abstract book. 2022 ;[citado 2026 maio 03 ] Available from: https://repositorio.usp.br/directbitstream/e156b1ee-7526-4d5e-8bc8-e90c2b185157/3100577.pdf
  • Source: Biochemistry. Unidade: IQSC

    Assunto: BIOLOGIA MOLECULAR

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      ARAUJO, Thaís L. S. et al. Conformational changes in human Hsp70 induced by high hydrostatic pressure produce oligomers with ATPase activity but without chaperone activity. Biochemistry, v. 53, n. 18, p. 2884-2889, 2014Tradução . . Disponível em: https://doi.org/10.1021/bi500004q. Acesso em: 03 maio 2026.
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      Araujo, T. L. S., Borges, J. C., Ramos, C. H. I., Meyer-Fernandes, J. R., Oliveira Júnior, R. S., Pascutti, P. G., et al. (2014). Conformational changes in human Hsp70 induced by high hydrostatic pressure produce oligomers with ATPase activity but without chaperone activity. Biochemistry, 53( 18), 2884-2889. doi:10.1021/bi500004q
    • NLM

      Araujo TLS, Borges JC, Ramos CHI, Meyer-Fernandes JR, Oliveira Júnior RS, Pascutti PG, Foguel D, Palhano FL. Conformational changes in human Hsp70 induced by high hydrostatic pressure produce oligomers with ATPase activity but without chaperone activity [Internet]. Biochemistry. 2014 ; 53( 18): 2884-2889.[citado 2026 maio 03 ] Available from: https://doi.org/10.1021/bi500004q
    • Vancouver

      Araujo TLS, Borges JC, Ramos CHI, Meyer-Fernandes JR, Oliveira Júnior RS, Pascutti PG, Foguel D, Palhano FL. Conformational changes in human Hsp70 induced by high hydrostatic pressure produce oligomers with ATPase activity but without chaperone activity [Internet]. Biochemistry. 2014 ; 53( 18): 2884-2889.[citado 2026 maio 03 ] Available from: https://doi.org/10.1021/bi500004q
  • Source: International Journal of Molecular Sciences. Unidade: IFSC

    Subjects: ANTI-INFLAMATÓRIOS NÃO ESTEROIDES, PROTEÍNAS, CRISTALOGRAFIA

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      SANT'ANNA, Ricardo O. et al. Inhibition of human transthyretin aggregation by non-steroidal anti-inflammatory compounds: a structural and thermodynamic analysis. International Journal of Molecular Sciences, v. 14, n. 3, p. 5284-5311, 2013Tradução . . Disponível em: https://doi.org/10.3390/ijms14035284. Acesso em: 03 maio 2026.
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      Sant'Anna, R. O., Braga, C. A., Polikarpov, I., Ventura, S., Lima, L. M. T. R., & Foguel, D. (2013). Inhibition of human transthyretin aggregation by non-steroidal anti-inflammatory compounds: a structural and thermodynamic analysis. International Journal of Molecular Sciences, 14( 3), 5284-5311. doi:10.3390/ijms14035284
    • NLM

      Sant'Anna RO, Braga CA, Polikarpov I, Ventura S, Lima LMTR, Foguel D. Inhibition of human transthyretin aggregation by non-steroidal anti-inflammatory compounds: a structural and thermodynamic analysis [Internet]. International Journal of Molecular Sciences. 2013 ; 14( 3): 5284-5311.[citado 2026 maio 03 ] Available from: https://doi.org/10.3390/ijms14035284
    • Vancouver

      Sant'Anna RO, Braga CA, Polikarpov I, Ventura S, Lima LMTR, Foguel D. Inhibition of human transthyretin aggregation by non-steroidal anti-inflammatory compounds: a structural and thermodynamic analysis [Internet]. International Journal of Molecular Sciences. 2013 ; 14( 3): 5284-5311.[citado 2026 maio 03 ] Available from: https://doi.org/10.3390/ijms14035284
  • Source: Journal of Structural Biology. Unidade: IFSC

    Subjects: CRISTALOGRAFIA, HORMÔNIOS TIREOIDIANOS, RECEPTORES

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      TRIVELLA, Daniela B. B. et al. The binding of synthetic triiodo L-thyronine analogs to human transthyretin: Molecular basis of cooperative and non-cooperative ligand recognition. Journal of Structural Biology, v. 173, n. 2, p. 323-332, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.jsb.2010.10.003. Acesso em: 03 maio 2026.
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      Trivella, D. B. B., Sairre, M. I., Foguel, D., Lima, L. M. T. R., & Polikarpov, I. (2011). The binding of synthetic triiodo L-thyronine analogs to human transthyretin: Molecular basis of cooperative and non-cooperative ligand recognition. Journal of Structural Biology, 173( 2), 323-332. doi:10.1016/j.jsb.2010.10.003
    • NLM

      Trivella DBB, Sairre MI, Foguel D, Lima LMTR, Polikarpov I. The binding of synthetic triiodo L-thyronine analogs to human transthyretin: Molecular basis of cooperative and non-cooperative ligand recognition [Internet]. Journal of Structural Biology. 2011 ; 173( 2): 323-332.[citado 2026 maio 03 ] Available from: https://doi.org/10.1016/j.jsb.2010.10.003
    • Vancouver

      Trivella DBB, Sairre MI, Foguel D, Lima LMTR, Polikarpov I. The binding of synthetic triiodo L-thyronine analogs to human transthyretin: Molecular basis of cooperative and non-cooperative ligand recognition [Internet]. Journal of Structural Biology. 2011 ; 173( 2): 323-332.[citado 2026 maio 03 ] Available from: https://doi.org/10.1016/j.jsb.2010.10.003
  • Source: Biochemistry. Unidade: IFSC

    Subjects: PROTEÍNAS (ESTUDO), CRISTALOGRAFIA ESTRUTURAL, MODELOS (ESTRUTURA)

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      AZEVEDO, Estefania P. C. et al. Dissecting the structure, thermodynamic stability, and aggregation properties of the A25T transthyretin (A25T-TTR) variant involved in leptomeningeal amyloidosis: identifying protein partners that co-aggregate during A25T-TTR fibrillogenesis in cerebrospinal fluid. Biochemistry, v. 50, n. 51, p. 11070-11083, 2011Tradução . . Disponível em: https://doi.org/10.1021/bi201365r. Acesso em: 03 maio 2026.
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      Azevedo, E. P. C., Pereira, H. D. 'M., Garratt, R. C., Kelly, J. W., Foguel, D., & Palhano, F. L. (2011). Dissecting the structure, thermodynamic stability, and aggregation properties of the A25T transthyretin (A25T-TTR) variant involved in leptomeningeal amyloidosis: identifying protein partners that co-aggregate during A25T-TTR fibrillogenesis in cerebrospinal fluid. Biochemistry, 50( 51), 11070-11083. doi:10.1021/bi201365r
    • NLM

      Azevedo EPC, Pereira HD'M, Garratt RC, Kelly JW, Foguel D, Palhano FL. Dissecting the structure, thermodynamic stability, and aggregation properties of the A25T transthyretin (A25T-TTR) variant involved in leptomeningeal amyloidosis: identifying protein partners that co-aggregate during A25T-TTR fibrillogenesis in cerebrospinal fluid [Internet]. Biochemistry. 2011 ; 50( 51): 11070-11083.[citado 2026 maio 03 ] Available from: https://doi.org/10.1021/bi201365r
    • Vancouver

      Azevedo EPC, Pereira HD'M, Garratt RC, Kelly JW, Foguel D, Palhano FL. Dissecting the structure, thermodynamic stability, and aggregation properties of the A25T transthyretin (A25T-TTR) variant involved in leptomeningeal amyloidosis: identifying protein partners that co-aggregate during A25T-TTR fibrillogenesis in cerebrospinal fluid [Internet]. Biochemistry. 2011 ; 50( 51): 11070-11083.[citado 2026 maio 03 ] Available from: https://doi.org/10.1021/bi201365r

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