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Filtros : "SCHREIER, SHIRLEY" "IQ" Removidos: "ABDALLA, DULCINEIA SAES PARRA" "MEDEIROS, MARISA HELENA GENNARI DE" "Portugal" Limpar

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  • Artigo de periodico

    Human diacylglycerol kinase ε N-terminal segment regulates the phosphatidylinositol cycle, controlling the rate but not the acyl chain composition of its lipid intermediates (2022)

    Bozelli Junior, José Carlos ; Yune, Jenny ; Aulakh, Sukhvershjit S ; Cao, Zihao ; Fernandes, Alexia; Seitova, Alma ; Tong, Yufeng ; Schreier, Shirley ; Epand, Richard M

    Source: ACS Chemical Biology. Unidade: IQ

    Subjects: LIPÍDEOS, PEPTÍDEOS, PROTEÍNAS

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    • ABNT

      BOZELLI JUNIOR, José Carlos et al. Human diacylglycerol kinase ε N-terminal segment regulates the phosphatidylinositol cycle, controlling the rate but not the acyl chain composition of its lipid intermediates. ACS Chemical Biology, v. 17, n. 9, p. 2495-2506, 2022Tradução . . Disponível em: https://doi.org/10.1021/acschembio.2c00387. Acesso em: 29 maio 2024.

    • APA

      Bozelli Junior, J. C., Yune, J., Aulakh, S. S., Cao, Z., Fernandes, A., Seitova, A., et al. (2022). Human diacylglycerol kinase ε N-terminal segment regulates the phosphatidylinositol cycle, controlling the rate but not the acyl chain composition of its lipid intermediates. ACS Chemical Biology, 17( 9), 2495-2506. doi:10.1021/acschembio.2c00387

    • NLM

      Bozelli Junior JC, Yune J, Aulakh SS, Cao Z, Fernandes A, Seitova A, Tong Y, Schreier S, Epand RM. Human diacylglycerol kinase ε N-terminal segment regulates the phosphatidylinositol cycle, controlling the rate but not the acyl chain composition of its lipid intermediates [Internet]. ACS Chemical Biology. 2022 ; 17( 9): 2495-2506.[citado 2024 maio 29 ] Available from: https://doi.org/10.1021/acschembio.2c00387

    • Vancouver

      Bozelli Junior JC, Yune J, Aulakh SS, Cao Z, Fernandes A, Seitova A, Tong Y, Schreier S, Epand RM. Human diacylglycerol kinase ε N-terminal segment regulates the phosphatidylinositol cycle, controlling the rate but not the acyl chain composition of its lipid intermediates [Internet]. ACS Chemical Biology. 2022 ; 17( 9): 2495-2506.[citado 2024 maio 29 ] Available from: https://doi.org/10.1021/acschembio.2c00387

  • Artigo de periodico

    Half a century deciphering membrane structure, dynamics and function: a short description of the life and research of Shirley Schreier (2021)

    Schreier, Shirley

    Source: Biophysical Reviews. Unidade: IQ

    Subjects: PEPTÍDEOS, BIOQUÍMICA

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    • ABNT

      SCHREIER, Shirley. Half a century deciphering membrane structure, dynamics and function: a short description of the life and research of Shirley Schreier. Biophysical Reviews, v. 13, p. 849–852, 2021Tradução . . Disponível em: https://doi.org/10.1007/s12551-021-00904-8. Acesso em: 29 maio 2024.

    • APA

      Schreier, S. (2021). Half a century deciphering membrane structure, dynamics and function: a short description of the life and research of Shirley Schreier. Biophysical Reviews, 13, 849–852. doi:10.1007/s12551-021-00904-8

    • NLM

      Schreier S. Half a century deciphering membrane structure, dynamics and function: a short description of the life and research of Shirley Schreier [Internet]. Biophysical Reviews. 2021 ; 13 849–852.[citado 2024 maio 29 ] Available from: https://doi.org/10.1007/s12551-021-00904-8

    • Vancouver

      Schreier S. Half a century deciphering membrane structure, dynamics and function: a short description of the life and research of Shirley Schreier [Internet]. Biophysical Reviews. 2021 ; 13 849–852.[citado 2024 maio 29 ] Available from: https://doi.org/10.1007/s12551-021-00904-8

  • Artigo de periodico

    Rondonin: antimicrobial properties and mechanism of action (2021)

    Riciluca, Katie Cristina Takeuti; Oliveira, Ursula Castro de ; Mendonça, Ronaldo Zucatelli ; Bozelli Junior, José Carlos ; Schreier, Shirley ; Silva Júnior, Pedro Ismael da

    Source: FEBS Open Bio. Unidades: BIOTECNOLOGIA, IQ

    Subjects: PEPTÍDEOS, ANTIFÚNGICOS, SISTEMA IMUNE, ARACNÍDEOS

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      RICILUCA, Katie Cristina Takeuti et al. Rondonin: antimicrobial properties and mechanism of action. FEBS Open Bio, v. 11, n. 9, p. 2541-2559, 2021Tradução . . Disponível em: https://doi.org/10.1002/2211-5463.13253. Acesso em: 29 maio 2024.

    • APA

      Riciluca, K. C. T., Oliveira, U. C. de, Mendonça, R. Z., Bozelli Junior, J. C., Schreier, S., & Silva Júnior, P. I. da. (2021). Rondonin: antimicrobial properties and mechanism of action. FEBS Open Bio, 11( 9), 2541-2559. doi:10.1002/2211-5463.13253

    • NLM

      Riciluca KCT, Oliveira UC de, Mendonça RZ, Bozelli Junior JC, Schreier S, Silva Júnior PI da. Rondonin: antimicrobial properties and mechanism of action [Internet]. FEBS Open Bio. 2021 ; 11( 9): 2541-2559.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/2211-5463.13253

    • Vancouver

      Riciluca KCT, Oliveira UC de, Mendonça RZ, Bozelli Junior JC, Schreier S, Silva Júnior PI da. Rondonin: antimicrobial properties and mechanism of action [Internet]. FEBS Open Bio. 2021 ; 11( 9): 2541-2559.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/2211-5463.13253

  • Artigo de periodico

    Lipid asymmetry of a model mitochondrial outer membrane affects Bax-dependent permeabilization (2020)

    Bozelli Junior, José Carlos ; Hou, Yu H; Schreier, Shirley ; Epand, Richard M

    Source: BBA - Biomembranes. Unidade: IQ

    Subjects: MITOCÔNDRIAS, APOPTOSE

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    • ABNT

      BOZELLI JUNIOR, José Carlos et al. Lipid asymmetry of a model mitochondrial outer membrane affects Bax-dependent permeabilization. BBA - Biomembranes, v. 1862, p. 1-12 art. 183241, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bbamem.2020.183241. Acesso em: 29 maio 2024.

    • APA

      Bozelli Junior, J. C., Hou, Y. H., Schreier, S., & Epand, R. M. (2020). Lipid asymmetry of a model mitochondrial outer membrane affects Bax-dependent permeabilization. BBA - Biomembranes, 1862, 1-12 art. 183241. doi:10.1016/j.bbamem.2020.183241

    • NLM

      Bozelli Junior JC, Hou YH, Schreier S, Epand RM. Lipid asymmetry of a model mitochondrial outer membrane affects Bax-dependent permeabilization [Internet]. BBA - Biomembranes. 2020 ; 1862 1-12 art. 183241.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.bbamem.2020.183241

    • Vancouver

      Bozelli Junior JC, Hou YH, Schreier S, Epand RM. Lipid asymmetry of a model mitochondrial outer membrane affects Bax-dependent permeabilization [Internet]. BBA - Biomembranes. 2020 ; 1862 1-12 art. 183241.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.bbamem.2020.183241

  • Artigo de periodico

    Characterization of phospholipid vesicles containing lauric acid: physicochemical basis for process and product development (2019)

    Farkuh, Laura; Hennies, Paulo T. ; Nunes, Cláudia; Reis, Salette; Barreiros, Luisa; Segundo, Marcela A.; Oseliero Filho, Pedro L.; Oliveira, Cristiano L.P. ; Cassago, Alexandre ; Portugal, Rodrigo V.; Carretero, Gustavo P.B. ; Schreier, Shirley ; Chaimovich Guralnik, Hernan ; Cuccovia, Iolanda Midea

    Source: Heliyon. Unidades: IF, IQ

    Subjects: BIOTECNOLOGIA, SOLUTO, BIOFÍSICA, FOSFOLIPÍDEOS, MICROSCOPIA ELETRÔNICA, SOLUBILIDADE, SURFACTANTES, BIOQUÍMICA, LIPOSSOMOS

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      FARKUH, Laura et al. Characterization of phospholipid vesicles containing lauric acid: physicochemical basis for process and product development. Heliyon, v. 5, n. 10, p. 1-10, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.heliyon.2019.e02648. Acesso em: 29 maio 2024.

    • APA

      Farkuh, L., Hennies, P. T., Nunes, C., Reis, S., Barreiros, L., Segundo, M. A., et al. (2019). Characterization of phospholipid vesicles containing lauric acid: physicochemical basis for process and product development. Heliyon, 5( 10), 1-10. doi:10.1016/j.heliyon.2019.e02648

    • NLM

      Farkuh L, Hennies PT, Nunes C, Reis S, Barreiros L, Segundo MA, Oseliero Filho PL, Oliveira CLP, Cassago A, Portugal RV, Carretero GPB, Schreier S, Chaimovich Guralnik H, Cuccovia IM. Characterization of phospholipid vesicles containing lauric acid: physicochemical basis for process and product development [Internet]. Heliyon. 2019 ; 5( 10): 1-10.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.heliyon.2019.e02648

    • Vancouver

      Farkuh L, Hennies PT, Nunes C, Reis S, Barreiros L, Segundo MA, Oseliero Filho PL, Oliveira CLP, Cassago A, Portugal RV, Carretero GPB, Schreier S, Chaimovich Guralnik H, Cuccovia IM. Characterization of phospholipid vesicles containing lauric acid: physicochemical basis for process and product development [Internet]. Heliyon. 2019 ; 5( 10): 1-10.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.heliyon.2019.e02648

  • Artigo de periodico

    Acemetacin-phosphatidylcholine interactions are determined by the drug ionization state (2018)

    Leite, Catarina Pereira; Nunes, Cláudia; Grahl, Débora; Bozelli Junior, José Carlos; Schreier, Shirley ; Lorger, Christina S. Kamma; Cuccovia, Iolanda Midea ; Reis, Salette

    Source: Physical Chemistry chemical Physics. Unidade: IQ

    Subjects: ANTI-INFLAMATÓRIOS NÃO ESTEROIDES, MUCOSA GÁSTRICA

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      LEITE, Catarina Pereira et al. Acemetacin-phosphatidylcholine interactions are determined by the drug ionization state. Physical Chemistry chemical Physics, v. 20, p. 14398-14409, 2018Tradução . . Disponível em: https://doi.org/10.1039/c8cp01698d. Acesso em: 29 maio 2024.

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      Leite, C. P., Nunes, C., Grahl, D., Bozelli Junior, J. C., Schreier, S., Lorger, C. S. K., et al. (2018). Acemetacin-phosphatidylcholine interactions are determined by the drug ionization state. Physical Chemistry chemical Physics, 20, 14398-14409. doi:10.1039/c8cp01698d

    • NLM

      Leite CP, Nunes C, Grahl D, Bozelli Junior JC, Schreier S, Lorger CSK, Cuccovia IM, Reis S. Acemetacin-phosphatidylcholine interactions are determined by the drug ionization state [Internet]. Physical Chemistry chemical Physics. 2018 ; 20 14398-14409.[citado 2024 maio 29 ] Available from: https://doi.org/10.1039/c8cp01698d

    • Vancouver

      Leite CP, Nunes C, Grahl D, Bozelli Junior JC, Schreier S, Lorger CSK, Cuccovia IM, Reis S. Acemetacin-phosphatidylcholine interactions are determined by the drug ionization state [Internet]. Physical Chemistry chemical Physics. 2018 ; 20 14398-14409.[citado 2024 maio 29 ] Available from: https://doi.org/10.1039/c8cp01698d

  • Artigo de periodico

    Can NO-indomethacin counteract the topical gastric toxicity induced by indomethacin interactions with phospholipid bilayers? (2018)

    Leite, Catarina Pereira; Nunes, Cláudia; Bozelli Junior, José Carlos; Schreier, Shirley ; Lorger, Christina S. Kamma; Cuccovia, Iolanda Midea ; Reis, Salette

    Source: Colloids and Surfaces B. Unidade: IQ

    Subjects: FOSFOLIPÍDEOS, ANTI-INFLAMATÓRIOS NÃO ESTEROIDES

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      LEITE, Catarina Pereira et al. Can NO-indomethacin counteract the topical gastric toxicity induced by indomethacin interactions with phospholipid bilayers?. Colloids and Surfaces B, v. 169, p. 375-383, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.colsurfb.2018.05.019. Acesso em: 29 maio 2024.

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      Leite, C. P., Nunes, C., Bozelli Junior, J. C., Schreier, S., Lorger, C. S. K., Cuccovia, I. M., & Reis, S. (2018). Can NO-indomethacin counteract the topical gastric toxicity induced by indomethacin interactions with phospholipid bilayers? Colloids and Surfaces B, 169, 375-383. doi:10.1016/j.colsurfb.2018.05.019

    • NLM

      Leite CP, Nunes C, Bozelli Junior JC, Schreier S, Lorger CSK, Cuccovia IM, Reis S. Can NO-indomethacin counteract the topical gastric toxicity induced by indomethacin interactions with phospholipid bilayers? [Internet]. Colloids and Surfaces B. 2018 ; 169 375-383.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.colsurfb.2018.05.019

    • Vancouver

      Leite CP, Nunes C, Bozelli Junior JC, Schreier S, Lorger CSK, Cuccovia IM, Reis S. Can NO-indomethacin counteract the topical gastric toxicity induced by indomethacin interactions with phospholipid bilayers? [Internet]. Colloids and Surfaces B. 2018 ; 169 375-383.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.colsurfb.2018.05.019

  • Artigo de periodico

    Dissecting the mechanism of action of actinoporins. Role of the N-terminal amphipathic alpha-helix in membrane binding and pore activity of sticholysins I and II (2018)

    Carretero, Gustavo Penteado Battesine; Vicente, Eduardo F; Cilli, Eduardo M; Alvarez, Carlos M; Jenssen, Havard; Schreier, Shirley

    Source: PLOS ONE. Unidade: IQ

    Subjects: PEPTÍDEOS, PROTEÍNAS

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      CARRETERO, Gustavo Penteado Battesine et al. Dissecting the mechanism of action of actinoporins. Role of the N-terminal amphipathic alpha-helix in membrane binding and pore activity of sticholysins I and II. PLOS ONE, v. 13, n. 8, p. 1-23 art. e0202981, 2018Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0202981. Acesso em: 29 maio 2024.

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      Carretero, G. P. B., Vicente, E. F., Cilli, E. M., Alvarez, C. M., Jenssen, H., & Schreier, S. (2018). Dissecting the mechanism of action of actinoporins. Role of the N-terminal amphipathic alpha-helix in membrane binding and pore activity of sticholysins I and II. PLOS ONE, 13( 8), 1-23 art. e0202981. doi:10.1371/journal.pone.0202981

    • NLM

      Carretero GPB, Vicente EF, Cilli EM, Alvarez CM, Jenssen H, Schreier S. Dissecting the mechanism of action of actinoporins. Role of the N-terminal amphipathic alpha-helix in membrane binding and pore activity of sticholysins I and II [Internet]. PLOS ONE. 2018 ; 13( 8): 1-23 art. e0202981.[citado 2024 maio 29 ] Available from: https://doi.org/10.1371/journal.pone.0202981

    • Vancouver

      Carretero GPB, Vicente EF, Cilli EM, Alvarez CM, Jenssen H, Schreier S. Dissecting the mechanism of action of actinoporins. Role of the N-terminal amphipathic alpha-helix in membrane binding and pore activity of sticholysins I and II [Internet]. PLOS ONE. 2018 ; 13( 8): 1-23 art. e0202981.[citado 2024 maio 29 ] Available from: https://doi.org/10.1371/journal.pone.0202981

  • Trabalho de evento-resumo

    Segments of the second transmembrane helix of three G-protein-coupled receptors (GPCR): comparative synthetic, structural and conformational studies (2018)

    Nakaie, Clovis Ryuichi; Lopes, Douglas Duarte; Cuvero, Jamile Haydée; Ferreira, Mariana Machado Leiva; Silva, Lauria Rogério; Souza, Sinval E. G; Malavolta, Luciana; Schreier, Shirley

    Source: Abstracts. Conference titles: Annual Meeting of the Brazilian Society for Biochemistry and Molecular Biology/SBBq. Unidade: IQ

    Subjects: BIOTECNOLOGIA, BIOQUÍMICA

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    • ABNT

      NAKAIE, Clovis Ryuichi et al. Segments of the second transmembrane helix of three G-protein-coupled receptors (GPCR): comparative synthetic, structural and conformational studies. 2018, Anais.. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular/SBBq, 2018. Disponível em: http://www.sbbq.org.br/reuniao/2018/livro_resumos_2018.pdf. Acesso em: 29 maio 2024.

    • APA

      Nakaie, C. R., Lopes, D. D., Cuvero, J. H., Ferreira, M. M. L., Silva, L. R., Souza, S. E. G., et al. (2018). Segments of the second transmembrane helix of three G-protein-coupled receptors (GPCR): comparative synthetic, structural and conformational studies. In Abstracts. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular/SBBq. Recuperado de http://www.sbbq.org.br/reuniao/2018/livro_resumos_2018.pdf

    • NLM

      Nakaie CR, Lopes DD, Cuvero JH, Ferreira MML, Silva LR, Souza SEG, Malavolta L, Schreier S. Segments of the second transmembrane helix of three G-protein-coupled receptors (GPCR): comparative synthetic, structural and conformational studies [Internet]. Abstracts. 2018 ;[citado 2024 maio 29 ] Available from: http://www.sbbq.org.br/reuniao/2018/livro_resumos_2018.pdf

    • Vancouver

      Nakaie CR, Lopes DD, Cuvero JH, Ferreira MML, Silva LR, Souza SEG, Malavolta L, Schreier S. Segments of the second transmembrane helix of three G-protein-coupled receptors (GPCR): comparative synthetic, structural and conformational studies [Internet]. Abstracts. 2018 ;[citado 2024 maio 29 ] Available from: http://www.sbbq.org.br/reuniao/2018/livro_resumos_2018.pdf

  • Artigo de periodico

    Synthesis, biophysical and functional studies of two BP100 analogues modified by a hydrophobic chain and a cyclic peptide (2018)

    Carretero, Gustavo Penteado Battesine; Saraiva, Greice Kelle Viegas; Cauz, Ana C. G; Rodrigues, Magali A; Kiyota, Sumika; Riske, Karin A; Santos, Alcindo Aparecido dos ; Botelho, Marcos Felipe Pinatto; Bemquerer, Marcelo P; Gueiros Filho, Frederico José ; Chaimovich Guralnik, Hernan ; Schreier, Shirley ; Cuccovia, Iolanda Midea

    Source: Biochimica et Biophysica Acta. Unidade: IQ

    Subjects: PEPTÍDEOS CÍCLICOS, ESPECTROSCOPIA

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      CARRETERO, Gustavo Penteado Battesine et al. Synthesis, biophysical and functional studies of two BP100 analogues modified by a hydrophobic chain and a cyclic peptide. Biochimica et Biophysica Acta, v. 1860, p. 1502-1516, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.bbamem.2018.05.003. Acesso em: 29 maio 2024.

    • APA

      Carretero, G. P. B., Saraiva, G. K. V., Cauz, A. C. G., Rodrigues, M. A., Kiyota, S., Riske, K. A., et al. (2018). Synthesis, biophysical and functional studies of two BP100 analogues modified by a hydrophobic chain and a cyclic peptide. Biochimica et Biophysica Acta, 1860, 1502-1516. doi:10.1016/j.bbamem.2018.05.003

    • NLM

      Carretero GPB, Saraiva GKV, Cauz ACG, Rodrigues MA, Kiyota S, Riske KA, Santos AA dos, Botelho MFP, Bemquerer MP, Gueiros Filho FJ, Chaimovich Guralnik H, Schreier S, Cuccovia IM. Synthesis, biophysical and functional studies of two BP100 analogues modified by a hydrophobic chain and a cyclic peptide [Internet]. Biochimica et Biophysica Acta. 2018 ; 1860 1502-1516.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.bbamem.2018.05.003

    • Vancouver

      Carretero GPB, Saraiva GKV, Cauz ACG, Rodrigues MA, Kiyota S, Riske KA, Santos AA dos, Botelho MFP, Bemquerer MP, Gueiros Filho FJ, Chaimovich Guralnik H, Schreier S, Cuccovia IM. Synthesis, biophysical and functional studies of two BP100 analogues modified by a hydrophobic chain and a cyclic peptide [Internet]. Biochimica et Biophysica Acta. 2018 ; 1860 1502-1516.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.bbamem.2018.05.003

  • Trabalho de evento-resumo

    Efficiency of 4-tert-butyl-benzhydrylamine-resin (BUBHAR) for use in the Boc-chemistry peptide synthesis: an alternative solid support for the worldwide used MBHAR resin (2017)

    Souza, S. E. G; Malavolta, L; Cilli, E. M; Schreier, Shirley ; Poletti, Erick Fernando; Jubilut, Guita Nicolaewsky; Nakaie, Clovis Ryuichi

    Source: Abstracts. Conference titles: Annual Meeting of the Brazilian Society for Biochemistry and Molecular Biology. Unidade: IQ

    Subjects: RESINAS, PEPTÍDEOS

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    • ABNT

      SOUZA, S. E. G et al. Efficiency of 4-tert-butyl-benzhydrylamine-resin (BUBHAR) for use in the Boc-chemistry peptide synthesis: an alternative solid support for the worldwide used MBHAR resin. 2017, Anais.. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular/SBBq, 2017. . Acesso em: 29 maio 2024.

    • APA

      Souza, S. E. G., Malavolta, L., Cilli, E. M., Schreier, S., Poletti, E. F., Jubilut, G. N., & Nakaie, C. R. (2017). Efficiency of 4-tert-butyl-benzhydrylamine-resin (BUBHAR) for use in the Boc-chemistry peptide synthesis: an alternative solid support for the worldwide used MBHAR resin. In Abstracts. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular/SBBq.

    • NLM

      Souza SEG, Malavolta L, Cilli EM, Schreier S, Poletti EF, Jubilut GN, Nakaie CR. Efficiency of 4-tert-butyl-benzhydrylamine-resin (BUBHAR) for use in the Boc-chemistry peptide synthesis: an alternative solid support for the worldwide used MBHAR resin. Abstracts. 2017 ;[citado 2024 maio 29 ]

    • Vancouver

      Souza SEG, Malavolta L, Cilli EM, Schreier S, Poletti EF, Jubilut GN, Nakaie CR. Efficiency of 4-tert-butyl-benzhydrylamine-resin (BUBHAR) for use in the Boc-chemistry peptide synthesis: an alternative solid support for the worldwide used MBHAR resin. Abstracts. 2017 ;[citado 2024 maio 29 ]

  • Artigo de periodico

    Paramagnetic bradykinin analogues as substrates for angiotensin I-converting enzyme: pharmacological and conformation studies (2016)

    Teixeira, Luis Gustavo de Deus; Malavolta, Luciana; Bersanetti, Patricia Alessandra; Schreier, Shirley ; Carmona, Adriana K; Nakaie, Clovis R

    Source: Bioorganic Chemistry. Unidade: IQ

    Subjects: ANGIOTENSINAS, BRADICININA

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      TEIXEIRA, Luis Gustavo de Deus et al. Paramagnetic bradykinin analogues as substrates for angiotensin I-converting enzyme: pharmacological and conformation studies. Bioorganic Chemistry, v. 69, p. 159-166, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2016.10.006. Acesso em: 29 maio 2024.

    • APA

      Teixeira, L. G. de D., Malavolta, L., Bersanetti, P. A., Schreier, S., Carmona, A. K., & Nakaie, C. R. (2016). Paramagnetic bradykinin analogues as substrates for angiotensin I-converting enzyme: pharmacological and conformation studies. Bioorganic Chemistry, 69, 159-166. doi:10.1016/j.bioorg.2016.10.006

    • NLM

      Teixeira LG de D, Malavolta L, Bersanetti PA, Schreier S, Carmona AK, Nakaie CR. Paramagnetic bradykinin analogues as substrates for angiotensin I-converting enzyme: pharmacological and conformation studies [Internet]. Bioorganic Chemistry. 2016 ; 69 159-166.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.bioorg.2016.10.006

    • Vancouver

      Teixeira LG de D, Malavolta L, Bersanetti PA, Schreier S, Carmona AK, Nakaie CR. Paramagnetic bradykinin analogues as substrates for angiotensin I-converting enzyme: pharmacological and conformation studies [Internet]. Bioorganic Chemistry. 2016 ; 69 159-166.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.bioorg.2016.10.006

  • Artigo de periodico

    Structural and dynamic insights of the interaction between tritrpticin and micelles: an NMR study (2016)

    Santos, Talita L; Moraes, Adolfo; Nakaie, Clovis R; Almeida, Fabio C. L; Schreier, Shirley ; Valente, Ana Paula

    Source: Biophysical Journal. Unidade: IQ

    Subjects: PEPTÍDEOS, BIOQUÍMICA

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      SANTOS, Talita L et al. Structural and dynamic insights of the interaction between tritrpticin and micelles: an NMR study. Biophysical Journal, v. 111, n. 12, p. 2676-2688, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.bpj.2016.10.034. Acesso em: 29 maio 2024.

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      Santos, T. L., Moraes, A., Nakaie, C. R., Almeida, F. C. L., Schreier, S., & Valente, A. P. (2016). Structural and dynamic insights of the interaction between tritrpticin and micelles: an NMR study. Biophysical Journal, 111( 12), 2676-2688. doi:10.1016/j.bpj.2016.10.034

    • NLM

      Santos TL, Moraes A, Nakaie CR, Almeida FCL, Schreier S, Valente AP. Structural and dynamic insights of the interaction between tritrpticin and micelles: an NMR study [Internet]. Biophysical Journal. 2016 ; 111( 12): 2676-2688.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.bpj.2016.10.034

    • Vancouver

      Santos TL, Moraes A, Nakaie CR, Almeida FCL, Schreier S, Valente AP. Structural and dynamic insights of the interaction between tritrpticin and micelles: an NMR study [Internet]. Biophysical Journal. 2016 ; 111( 12): 2676-2688.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.bpj.2016.10.034

  • Artigo de periodico

    Unfolding and folding pathway of lysozyme induced by sodium dodecyl sulfate (2015)

    Sun, Yang; Oseliero Filho, Pedro Leonidas; Bozelli Junior, José Carlos; Carvalho, Juliana; Schreier, Shirley ; Oliveira, Cristiano Luis Pinto de

    Source: Soft Matter. Unidades: IQ, IF

    Subjects: LISOZIMAS, SURFACTANTES

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      SUN, Yang et al. Unfolding and folding pathway of lysozyme induced by sodium dodecyl sulfate. Soft Matter, v. 11, n. 39, p. 7769-7777, 2015Tradução . . Disponível em: https://doi.org/10.1039/c5sm01231g. Acesso em: 29 maio 2024.

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      Sun, Y., Oseliero Filho, P. L., Bozelli Junior, J. C., Carvalho, J., Schreier, S., & Oliveira, C. L. P. de. (2015). Unfolding and folding pathway of lysozyme induced by sodium dodecyl sulfate. Soft Matter, 11( 39), 7769-7777. doi:10.1039/c5sm01231g

    • NLM

      Sun Y, Oseliero Filho PL, Bozelli Junior JC, Carvalho J, Schreier S, Oliveira CLP de. Unfolding and folding pathway of lysozyme induced by sodium dodecyl sulfate [Internet]. Soft Matter. 2015 ; 11( 39): 7769-7777.[citado 2024 maio 29 ] Available from: https://doi.org/10.1039/c5sm01231g

    • Vancouver

      Sun Y, Oseliero Filho PL, Bozelli Junior JC, Carvalho J, Schreier S, Oliveira CLP de. Unfolding and folding pathway of lysozyme induced by sodium dodecyl sulfate [Internet]. Soft Matter. 2015 ; 11( 39): 7769-7777.[citado 2024 maio 29 ] Available from: https://doi.org/10.1039/c5sm01231g

  • Artigo de periodico

    Conformational properties of seven toac-labeled angiotensin I analogues correlate with their muscle contraction activity and their ability to act as ACE substrates (2015)

    Teixeira, Luis Gustavo de Deus; Malavolta, Luciana; Bersanetti, Patricia Alessandra; Schreier, Shirley ; Carmona, Adriana Karaoglanovic; Nakaie, Clovis Ryuichi

    Source: PLOS ONE. Unidade: IQ

    Subjects: ANGIOTENSINAS, PEPTÍDEOS

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      TEIXEIRA, Luis Gustavo de Deus et al. Conformational properties of seven toac-labeled angiotensin I analogues correlate with their muscle contraction activity and their ability to act as ACE substrates. PLOS ONE, v. 10, n. 8, p. 1-15 art. 0136608, 2015Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0136608. Acesso em: 29 maio 2024.

    • APA

      Teixeira, L. G. de D., Malavolta, L., Bersanetti, P. A., Schreier, S., Carmona, A. K., & Nakaie, C. R. (2015). Conformational properties of seven toac-labeled angiotensin I analogues correlate with their muscle contraction activity and their ability to act as ACE substrates. PLOS ONE, 10( 8), 1-15 art. 0136608. doi:10.1371/journal.pone.0136608

    • NLM

      Teixeira LG de D, Malavolta L, Bersanetti PA, Schreier S, Carmona AK, Nakaie CR. Conformational properties of seven toac-labeled angiotensin I analogues correlate with their muscle contraction activity and their ability to act as ACE substrates [Internet]. PLOS ONE. 2015 ; 10( 8): 1-15 art. 0136608.[citado 2024 maio 29 ] Available from: https://doi.org/10.1371/journal.pone.0136608

    • Vancouver

      Teixeira LG de D, Malavolta L, Bersanetti PA, Schreier S, Carmona AK, Nakaie CR. Conformational properties of seven toac-labeled angiotensin I analogues correlate with their muscle contraction activity and their ability to act as ACE substrates [Internet]. PLOS ONE. 2015 ; 10( 8): 1-15 art. 0136608.[citado 2024 maio 29 ] Available from: https://doi.org/10.1371/journal.pone.0136608

  • Artigo de periodico

    Adsorption of the antimicrobial peptide tritrpticin onto solid and liquid surfaces: ion-specific effects (2015)

    Salay, Luiz C; Petri, Denise Freitas Siqueira ; Nakaie, Clovis Ryuichi; Schreier, Shirley

    Source: Biophysical Chemistry. Unidade: IQ

    Subjects: ADSORÇÃO, PEPTÍDEOS

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      SALAY, Luiz C et al. Adsorption of the antimicrobial peptide tritrpticin onto solid and liquid surfaces: ion-specific effects. Biophysical Chemistry, v. 207, p. 128-134 , 2015Tradução . . Disponível em: https://doi.org/10.1016/j.bpc.2015.10.004. Acesso em: 29 maio 2024.

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      Salay, L. C., Petri, D. F. S., Nakaie, C. R., & Schreier, S. (2015). Adsorption of the antimicrobial peptide tritrpticin onto solid and liquid surfaces: ion-specific effects. Biophysical Chemistry, 207, 128-134 . doi:10.1016/j.bpc.2015.10.004

    • NLM

      Salay LC, Petri DFS, Nakaie CR, Schreier S. Adsorption of the antimicrobial peptide tritrpticin onto solid and liquid surfaces: ion-specific effects [Internet]. Biophysical Chemistry. 2015 ; 207 128-134 .[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.bpc.2015.10.004

    • Vancouver

      Salay LC, Petri DFS, Nakaie CR, Schreier S. Adsorption of the antimicrobial peptide tritrpticin onto solid and liquid surfaces: ion-specific effects [Internet]. Biophysical Chemistry. 2015 ; 207 128-134 .[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.bpc.2015.10.004

  • Artigo de periodico

    Novel copoly(styrene-divinylbenzene)-resins with different phenylmethylamine groups for use in peptide synthesis method (2015)

    Souza, Sinval E. G; Malavolta, Luciana; Cilli, Eduardo Maffud; Schreier, Shirley ; Jubilut, Guita Nicolaewsky; Nakaie, Clovis Ryuichi

    Source: Protein & Peptide Letters. Unidade: IQ

    Subjects: RESINAS, PEPTÍDEOS (SÍNTESE), BIOQUÍMICA

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    • ABNT

      SOUZA, Sinval E. G et al. Novel copoly(styrene-divinylbenzene)-resins with different phenylmethylamine groups for use in peptide synthesis method. Protein & Peptide Letters, v. 22, n. 5, p. 392-401, 2015Tradução . . Disponível em: https://doi.org/10.2174/0929866522666150206170329. Acesso em: 29 maio 2024.

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      Souza, S. E. G., Malavolta, L., Cilli, E. M., Schreier, S., Jubilut, G. N., & Nakaie, C. R. (2015). Novel copoly(styrene-divinylbenzene)-resins with different phenylmethylamine groups for use in peptide synthesis method. Protein & Peptide Letters, 22( 5), 392-401. doi:10.2174/0929866522666150206170329

    • NLM

      Souza SEG, Malavolta L, Cilli EM, Schreier S, Jubilut GN, Nakaie CR. Novel copoly(styrene-divinylbenzene)-resins with different phenylmethylamine groups for use in peptide synthesis method [Internet]. Protein & Peptide Letters. 2015 ; 22( 5): 392-401.[citado 2024 maio 29 ] Available from: https://doi.org/10.2174/0929866522666150206170329

    • Vancouver

      Souza SEG, Malavolta L, Cilli EM, Schreier S, Jubilut GN, Nakaie CR. Novel copoly(styrene-divinylbenzene)-resins with different phenylmethylamine groups for use in peptide synthesis method [Internet]. Protein & Peptide Letters. 2015 ; 22( 5): 392-401.[citado 2024 maio 29 ] Available from: https://doi.org/10.2174/0929866522666150206170329

  • Artigo de periodico

    Peptide: lipid ratio and membrane surface charge determine the mechanism of action of the antimicrobial peptide BP100. Conformational and functional studies (2014)

    Manzini, Mariana Canale; Perez, Katia Regina; Riske, Karin do Amaral; Bozelli Junior, José Carlos; Santos, Talita Lopes dos; Silva, Marcia Aparecida da; Saraiva, Greice Kelle Viegas; Politi, Mário José ; Valente, Ana P; Almeida, Fábio C. L; Chaimovich Guralnik, Hernan ; Rodrigues, Magali Aparecida; Bemquerer, Marcelo Porto; Schreier, Shirley ; Cuccovia, Iolanda Midea

    Source: Biochimica et Biophysica Acta. Unidade: IQ

    Subjects: PEPTÍDEOS, RESSONÂNCIA MAGNÉTICA NUCLEAR

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      MANZINI, Mariana Canale et al. Peptide: lipid ratio and membrane surface charge determine the mechanism of action of the antimicrobial peptide BP100. Conformational and functional studies. Biochimica et Biophysica Acta, v. 1838, n. 7, p. 1985-1999, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.bbamem.2014.04.004. Acesso em: 29 maio 2024.

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      Manzini, M. C., Perez, K. R., Riske, K. do A., Bozelli Junior, J. C., Santos, T. L. dos, Silva, M. A. da, et al. (2014). Peptide: lipid ratio and membrane surface charge determine the mechanism of action of the antimicrobial peptide BP100. Conformational and functional studies. Biochimica et Biophysica Acta, 1838( 7), 1985-1999. doi:10.1016/j.bbamem.2014.04.004

    • NLM

      Manzini MC, Perez KR, Riske K do A, Bozelli Junior JC, Santos TL dos, Silva MA da, Saraiva GKV, Politi MJ, Valente AP, Almeida FCL, Chaimovich Guralnik H, Rodrigues MA, Bemquerer MP, Schreier S, Cuccovia IM. Peptide: lipid ratio and membrane surface charge determine the mechanism of action of the antimicrobial peptide BP100. Conformational and functional studies [Internet]. Biochimica et Biophysica Acta. 2014 ; 1838( 7): 1985-1999.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.bbamem.2014.04.004

    • Vancouver

      Manzini MC, Perez KR, Riske K do A, Bozelli Junior JC, Santos TL dos, Silva MA da, Saraiva GKV, Politi MJ, Valente AP, Almeida FCL, Chaimovich Guralnik H, Rodrigues MA, Bemquerer MP, Schreier S, Cuccovia IM. Peptide: lipid ratio and membrane surface charge determine the mechanism of action of the antimicrobial peptide BP100. Conformational and functional studies [Internet]. Biochimica et Biophysica Acta. 2014 ; 1838( 7): 1985-1999.[citado 2024 maio 29 ] Available from: https://doi.org/10.1016/j.bbamem.2014.04.004

  • Artigo de periodico

    Solution NMR analysis of the interaction between the actinoporin sticholysin i and DHPC micelles—correlation with backbone dynamics (2014)

    López-Castilla, Aracelys; Pazos, Fabiola; Schreier, Shirley ; Pires, José Ricardo

    Source: Proteins. Unidade: IQ

    Subjects: FOSFOLIPÍDEOS, TOXINAS

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      LÓPEZ-CASTILLA, Aracelys et al. Solution NMR analysis of the interaction between the actinoporin sticholysin i and DHPC micelles—correlation with backbone dynamics. Proteins, v. 82, n. 6, p. 1022-1034, 2014Tradução . . Disponível em: https://doi.org/10.1002/prot.24475. Acesso em: 29 maio 2024.

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      López-Castilla, A., Pazos, F., Schreier, S., & Pires, J. R. (2014). Solution NMR analysis of the interaction between the actinoporin sticholysin i and DHPC micelles—correlation with backbone dynamics. Proteins, 82( 6), 1022-1034. doi:10.1002/prot.24475

    • NLM

      López-Castilla A, Pazos F, Schreier S, Pires JR. Solution NMR analysis of the interaction between the actinoporin sticholysin i and DHPC micelles—correlation with backbone dynamics [Internet]. Proteins. 2014 ; 82( 6): 1022-1034.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/prot.24475

    • Vancouver

      López-Castilla A, Pazos F, Schreier S, Pires JR. Solution NMR analysis of the interaction between the actinoporin sticholysin i and DHPC micelles—correlation with backbone dynamics [Internet]. Proteins. 2014 ; 82( 6): 1022-1034.[citado 2024 maio 29 ] Available from: https://doi.org/10.1002/prot.24475

  • Trabalho de evento-resumo periodico

    Binding of peptides from the n-termini of sticholysins to lipid membranes (2014)

    Carretero, Gustavo Penteado Battesine; Paulino, Joana; Alvarez, C; Jenssen, Hans P; Schreier, Shirley

    Source: Journal Peptide Science. Conference titles: European Peptide Symposium. Unidade: IQ

    Subjects: PEPTÍDEOS, ESPECTROSCOPIA

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      CARRETERO, Gustavo Penteado Battesine et al. Binding of peptides from the n-termini of sticholysins to lipid membranes. Journal Peptide Science. Hoboken: Instituto de Química, Universidade de São Paulo. . Acesso em: 29 maio 2024. , 2014

    • APA

      Carretero, G. P. B., Paulino, J., Alvarez, C., Jenssen, H. P., & Schreier, S. (2014). Binding of peptides from the n-termini of sticholysins to lipid membranes. Journal Peptide Science. Hoboken: Instituto de Química, Universidade de São Paulo.

    • NLM

      Carretero GPB, Paulino J, Alvarez C, Jenssen HP, Schreier S. Binding of peptides from the n-termini of sticholysins to lipid membranes. Journal Peptide Science. 2014 ; 20 S87 res. YP11.[citado 2024 maio 29 ]

    • Vancouver

      Carretero GPB, Paulino J, Alvarez C, Jenssen HP, Schreier S. Binding of peptides from the n-termini of sticholysins to lipid membranes. Journal Peptide Science. 2014 ; 20 S87 res. YP11.[citado 2024 maio 29 ]

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