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  • Source: Chemical Biology & Drug Design. Unidade: IQSC

    Subjects: BIOQUÍMICA, BIOLOGIA

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      Chemical Biology & Drug Design. Chemical Biology & Drug Design. Hoboken: Instituto de Química de São Carlos, Universidade de São Paulo. Disponível em: https://onlinelibrary.wiley.com/page/journal/17470285/homepage/editorialboard.html. Acesso em: 06 nov. 2024. , 2024
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      Chemical Biology & Drug Design. (2024). Chemical Biology & Drug Design. Chemical Biology & Drug Design. Hoboken: Instituto de Química de São Carlos, Universidade de São Paulo. Recuperado de https://onlinelibrary.wiley.com/page/journal/17470285/homepage/editorialboard.html
    • NLM

      Chemical Biology & Drug Design [Internet]. Chemical Biology & Drug Design. 2024 ;[citado 2024 nov. 06 ] Available from: https://onlinelibrary.wiley.com/page/journal/17470285/homepage/editorialboard.html
    • Vancouver

      Chemical Biology & Drug Design [Internet]. Chemical Biology & Drug Design. 2024 ;[citado 2024 nov. 06 ] Available from: https://onlinelibrary.wiley.com/page/journal/17470285/homepage/editorialboard.html
  • Source: International journal of biological macromolecules. Unidade: EEL

    Subjects: BIOQUÍMICA, BIOTECNOLOGIA

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      CHAVES, Bruno Las Casas et al. The emergence of hybrid cellulose nanomaterials as promising biomaterials. International journal of biological macromolecules, v. 250, p. 1-27, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.ijbiomac.2023.126007. Acesso em: 06 nov. 2024.
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      Chaves, B. L. C., Dias, I. K. R., Mendoza, S. L. Y., Pereira, B., Costa, G. R., Rojas, O. J., & Arantes, V. (2023). The emergence of hybrid cellulose nanomaterials as promising biomaterials. International journal of biological macromolecules, 250, 1-27. doi:10.1016/j.ijbiomac.2023.126007
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      Chaves BLC, Dias IKR, Mendoza SLY, Pereira B, Costa GR, Rojas OJ, Arantes V. The emergence of hybrid cellulose nanomaterials as promising biomaterials [Internet]. International journal of biological macromolecules. 2023 ;250 1-27.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.ijbiomac.2023.126007
    • Vancouver

      Chaves BLC, Dias IKR, Mendoza SLY, Pereira B, Costa GR, Rojas OJ, Arantes V. The emergence of hybrid cellulose nanomaterials as promising biomaterials [Internet]. International journal of biological macromolecules. 2023 ;250 1-27.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.ijbiomac.2023.126007
  • Source: International journal of biological macromolecules. Unidade: EEL

    Subjects: BIOTECNOLOGIA, BIOQUÍMICA, BIOLOGIA MOLECULAR

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      BERTO, Gabriela Leila et al. Endoglucanase effects on energy consumption in the mechanical fibrillation of cellulose fibers into nanocelluloses. International journal of biological macromolecules, v. 243, p. 1-9, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.ijbiomac.2023.125002. Acesso em: 06 nov. 2024.
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      Berto, G. L., Mattos, B. D., Velasco, J., Segato, F., Rojas, O. J., Arantes, V., & Zhao, B. (2023). Endoglucanase effects on energy consumption in the mechanical fibrillation of cellulose fibers into nanocelluloses. International journal of biological macromolecules, 243, 1-9. doi:10.1016/j.ijbiomac.2023.125002
    • NLM

      Berto GL, Mattos BD, Velasco J, Segato F, Rojas OJ, Arantes V, Zhao B. Endoglucanase effects on energy consumption in the mechanical fibrillation of cellulose fibers into nanocelluloses [Internet]. International journal of biological macromolecules. 2023 ;243 1-9.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.ijbiomac.2023.125002
    • Vancouver

      Berto GL, Mattos BD, Velasco J, Segato F, Rojas OJ, Arantes V, Zhao B. Endoglucanase effects on energy consumption in the mechanical fibrillation of cellulose fibers into nanocelluloses [Internet]. International journal of biological macromolecules. 2023 ;243 1-9.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.ijbiomac.2023.125002
  • Source: International journal of biological macromolecules. Unidade: EEL

    Subjects: BIOQUÍMICA, BIOTECNOLOGIA, BIOLOGIA MOLECULAR, ENZIMAS CELULOLÍTICAS

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      DIAS, Isabella Karoline Ribeiro e COSTA, Bruna Karoline Lacerda e ARANTES, Valdeir. High-yield production of rod-like and spherical nanocellulose by controlled enzymatic hydrolysis of mechanically pretreated cellulose. International journal of biological macromolecules, v. 242, n. art. 125053, p. 1-15, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.ijbiomac.2023.125053. Acesso em: 06 nov. 2024.
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      Dias, I. K. R., Costa, B. K. L., & Arantes, V. (2023). High-yield production of rod-like and spherical nanocellulose by controlled enzymatic hydrolysis of mechanically pretreated cellulose. International journal of biological macromolecules, 242( art. 125053), 1-15. doi:10.1016/j.ijbiomac.2023.125053
    • NLM

      Dias IKR, Costa BKL, Arantes V. High-yield production of rod-like and spherical nanocellulose by controlled enzymatic hydrolysis of mechanically pretreated cellulose [Internet]. International journal of biological macromolecules. 2023 ;242( art. 125053): 1-15.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.ijbiomac.2023.125053
    • Vancouver

      Dias IKR, Costa BKL, Arantes V. High-yield production of rod-like and spherical nanocellulose by controlled enzymatic hydrolysis of mechanically pretreated cellulose [Internet]. International journal of biological macromolecules. 2023 ;242( art. 125053): 1-15.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.ijbiomac.2023.125053
  • Source: Chemical Biology and Drug Design. Unidade: IQSC

    Subjects: BIOQUÍMICA, BIOLOGIA

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      MELANDER, Roberta e MONTANARI, Carlos Alberto. Chemical Biology and Drug Design. Chemical Biology and Drug Design. Hoboken: Instituto de Química de São Carlos, Universidade de São Paulo. Disponível em: https://onlinelibrary-wiley.ez67.periodicos.capes.gov.br/page/journal/17470285/homepage/editorialboard.html. Acesso em: 06 nov. 2024. , 2023
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      Melander, R., & Montanari, C. A. (2023). Chemical Biology and Drug Design. Chemical Biology and Drug Design. Hoboken: Instituto de Química de São Carlos, Universidade de São Paulo. Recuperado de https://onlinelibrary-wiley.ez67.periodicos.capes.gov.br/page/journal/17470285/homepage/editorialboard.html
    • NLM

      Melander R, Montanari CA. Chemical Biology and Drug Design [Internet]. Chemical Biology and Drug Design. 2023 ;[citado 2024 nov. 06 ] Available from: https://onlinelibrary-wiley.ez67.periodicos.capes.gov.br/page/journal/17470285/homepage/editorialboard.html
    • Vancouver

      Melander R, Montanari CA. Chemical Biology and Drug Design [Internet]. Chemical Biology and Drug Design. 2023 ;[citado 2024 nov. 06 ] Available from: https://onlinelibrary-wiley.ez67.periodicos.capes.gov.br/page/journal/17470285/homepage/editorialboard.html
  • Source: International journal of biological macromolecules. Unidade: EEL

    Subjects: BIOQUÍMICA, BIOTECNOLOGIA, BIOLOGIA MOLECULAR

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      CHAVES, Bruno Las Casas e ARANTES, Valdeir. Endoglucanase pretreatment aids in isolating tailored-cellulose nanofibrils combining energy saving and high-performance packaging. International journal of biological macromolecules, v. 242, n. art. 125057, p. 1-15, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.ijbiomac.2023.125057. Acesso em: 06 nov. 2024.
    • APA

      Chaves, B. L. C., & Arantes, V. (2023). Endoglucanase pretreatment aids in isolating tailored-cellulose nanofibrils combining energy saving and high-performance packaging. International journal of biological macromolecules, 242( art. 125057), 1-15. doi:10.1016/j.ijbiomac.2023.125057
    • NLM

      Chaves BLC, Arantes V. Endoglucanase pretreatment aids in isolating tailored-cellulose nanofibrils combining energy saving and high-performance packaging [Internet]. International journal of biological macromolecules. 2023 ;242( art. 125057): 1-15.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.ijbiomac.2023.125057
    • Vancouver

      Chaves BLC, Arantes V. Endoglucanase pretreatment aids in isolating tailored-cellulose nanofibrils combining energy saving and high-performance packaging [Internet]. International journal of biological macromolecules. 2023 ;242( art. 125057): 1-15.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.ijbiomac.2023.125057
  • Source: Structure. Unidades: IQSC, IF

    Subjects: BIOQUÍMICA, BIOFÍSICA, MACROMOLÉCULA, PROTEÍNAS

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      SERAPHIM, Thiago V et al. Assembly principles of the human R2TP chaperone complex reveal the presence of R2T and R2P complexes. Structure, v. 30, p. 156–171, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.str.2021.08.002. Acesso em: 06 nov. 2024.
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      Seraphim, T. V., Nano, N., Cheung, Y. W. S., Aluksanasuwan, S., Colleti, C., Mao, Y. -Q., et al. (2022). Assembly principles of the human R2TP chaperone complex reveal the presence of R2T and R2P complexes. Structure, 30, 156–171. doi:10.1016/j.str.2021.08.002
    • NLM

      Seraphim TV, Nano N, Cheung YWS, Aluksanasuwan S, Colleti C, Mao Y-Q, Bhandari V, Young G, Holl L, Phanse S, Gordiyenko Y, Southworth DR, Robinson CV, Thongboonkerd V, Gava LM, Borges JC, Babu M, Barbosa LRS, Ramos CHI, Kukura P, Houry WA. Assembly principles of the human R2TP chaperone complex reveal the presence of R2T and R2P complexes [Internet]. Structure. 2022 ; 30 156–171.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.str.2021.08.002
    • Vancouver

      Seraphim TV, Nano N, Cheung YWS, Aluksanasuwan S, Colleti C, Mao Y-Q, Bhandari V, Young G, Holl L, Phanse S, Gordiyenko Y, Southworth DR, Robinson CV, Thongboonkerd V, Gava LM, Borges JC, Babu M, Barbosa LRS, Ramos CHI, Kukura P, Houry WA. Assembly principles of the human R2TP chaperone complex reveal the presence of R2T and R2P complexes [Internet]. Structure. 2022 ; 30 156–171.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.str.2021.08.002
  • Source: Chemical Biology and Drug Design. Unidade: IQSC

    Subjects: BIOQUÍMICA, BIOLOGIA

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      Chemical Biology and Drug Design. Chemical Biology and Drug Design. Hoboken: Instituto de Química de São Carlos, Universidade de São Paulo. Disponível em: https://onlinelibrary-wiley.ez67.periodicos.capes.gov.br/page/journal/17470285/homepage/editorialboard.html. Acesso em: 06 nov. 2024. , 2022
    • APA

      Chemical Biology and Drug Design. (2022). Chemical Biology and Drug Design. Chemical Biology and Drug Design. Hoboken: Instituto de Química de São Carlos, Universidade de São Paulo. Recuperado de https://onlinelibrary-wiley.ez67.periodicos.capes.gov.br/page/journal/17470285/homepage/editorialboard.html
    • NLM

      Chemical Biology and Drug Design [Internet]. Chemical Biology and Drug Design. 2022 ;[citado 2024 nov. 06 ] Available from: https://onlinelibrary-wiley.ez67.periodicos.capes.gov.br/page/journal/17470285/homepage/editorialboard.html
    • Vancouver

      Chemical Biology and Drug Design [Internet]. Chemical Biology and Drug Design. 2022 ;[citado 2024 nov. 06 ] Available from: https://onlinelibrary-wiley.ez67.periodicos.capes.gov.br/page/journal/17470285/homepage/editorialboard.html
  • Source: Antimicrobial Agents and Chemotherapy. Unidades: FMRP, FOB, IQSC

    Subjects: BIOQUÍMICA, MICROBIOLOGIA, LEISHMANIOSE CUTÂNEA, MITOCÔNDRIAS

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      VELÁSQUEZ, Angela M. A et al. New insights into the mechanism of action of the Cyclopalladated Complex (CP2) in Leishmania:: calcium dysregulation, mitochondrial dysfunction, and cell death. Antimicrobial Agents and Chemotherapy, v. 66, n. 1, 2022Tradução . . Disponível em: https://doi.org/10.1128/AAC.00767-21. Acesso em: 06 nov. 2024.
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      Velásquez, A. M. A., Bartlett, P. J., Linares, I. A. P., Passalacqua, T. G., Teodoro, D. D. L., Imamura, K. B., et al. (2022). New insights into the mechanism of action of the Cyclopalladated Complex (CP2) in Leishmania:: calcium dysregulation, mitochondrial dysfunction, and cell death. Antimicrobial Agents and Chemotherapy, 66( 1). doi:10.1128/AAC.00767-21
    • NLM

      Velásquez AMA, Bartlett PJ, Linares IAP, Passalacqua TG, Teodoro DDL, Imamura KB, Virgilio S, Tosi LRO, Leite A de L, Buzalaf MAR, Velasques JM, Netto AVG, Thomas AP, Graminha MAS. New insights into the mechanism of action of the Cyclopalladated Complex (CP2) in Leishmania:: calcium dysregulation, mitochondrial dysfunction, and cell death [Internet]. Antimicrobial Agents and Chemotherapy. 2022 ; 66( 1):[citado 2024 nov. 06 ] Available from: https://doi.org/10.1128/AAC.00767-21
    • Vancouver

      Velásquez AMA, Bartlett PJ, Linares IAP, Passalacqua TG, Teodoro DDL, Imamura KB, Virgilio S, Tosi LRO, Leite A de L, Buzalaf MAR, Velasques JM, Netto AVG, Thomas AP, Graminha MAS. New insights into the mechanism of action of the Cyclopalladated Complex (CP2) in Leishmania:: calcium dysregulation, mitochondrial dysfunction, and cell death [Internet]. Antimicrobial Agents and Chemotherapy. 2022 ; 66( 1):[citado 2024 nov. 06 ] Available from: https://doi.org/10.1128/AAC.00767-21
  • Source: Journal of Medicinal Chemistry. Unidade: IFSC

    Subjects: ANTIMALÁRICOS, PLASMODIUM FALCIPARUM, PLANEJAMENTO DE FÁRMACOS, ANTIPARASITÁRIOS, MALÁRIA, BIOQUÍMICA, QUÍMICA MÉDICA

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      TAFT, Benjamin R. e AGUIAR, Anna Caroline Campos. Discovery and preclinical pharmacology of INE963, a potent and fast-acting blood-stage antimalarial with a high barrier to resistance and potential for single-dose cures in uncomplicated malaria. Journal of Medicinal Chemistry, v. 65, n. 5, p. 3798-3813, 2022Tradução . . Disponível em: https://doi.org/10.1021/acs.jmedchem.1c01995. Acesso em: 06 nov. 2024.
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      Taft, B. R., & Aguiar, A. C. C. (2022). Discovery and preclinical pharmacology of INE963, a potent and fast-acting blood-stage antimalarial with a high barrier to resistance and potential for single-dose cures in uncomplicated malaria. Journal of Medicinal Chemistry, 65( 5), 3798-3813. doi:10.1021/acs.jmedchem.1c01995
    • NLM

      Taft BR, Aguiar ACC. Discovery and preclinical pharmacology of INE963, a potent and fast-acting blood-stage antimalarial with a high barrier to resistance and potential for single-dose cures in uncomplicated malaria [Internet]. Journal of Medicinal Chemistry. 2022 ; 65( 5): 3798-3813.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.jmedchem.1c01995
    • Vancouver

      Taft BR, Aguiar ACC. Discovery and preclinical pharmacology of INE963, a potent and fast-acting blood-stage antimalarial with a high barrier to resistance and potential for single-dose cures in uncomplicated malaria [Internet]. Journal of Medicinal Chemistry. 2022 ; 65( 5): 3798-3813.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.jmedchem.1c01995
  • Source: Journal of Medicinal Chemistry. Unidade: IFSC

    Subjects: ANTIMALÁRICOS, PLASMODIUM FALCIPARUM, PLANEJAMENTO DE FÁRMACOS, ANTIPARASITÁRIOS, MALÁRIA, BIOQUÍMICA, QUÍMICA MÉDICA

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      PALMER, Michael J. e AGUIAR, Anna Caroline Campos e GUIDO, Rafael Victorio Carvalho. Potent antimalarials with development potential identified by structure-guided computational optimization of a pyrrole-based dihydroorotate dehydrogenase inhibitor series. Journal of Medicinal Chemistry, v. 64, n. 9, p. 6085-6136, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.jmedchem.1c00173. Acesso em: 06 nov. 2024.
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      Palmer, M. J., Aguiar, A. C. C., & Guido, R. V. C. (2021). Potent antimalarials with development potential identified by structure-guided computational optimization of a pyrrole-based dihydroorotate dehydrogenase inhibitor series. Journal of Medicinal Chemistry, 64( 9), 6085-6136. doi:10.1021/acs.jmedchem.1c00173
    • NLM

      Palmer MJ, Aguiar ACC, Guido RVC. Potent antimalarials with development potential identified by structure-guided computational optimization of a pyrrole-based dihydroorotate dehydrogenase inhibitor series [Internet]. Journal of Medicinal Chemistry. 2021 ; 64( 9): 6085-6136.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.jmedchem.1c00173
    • Vancouver

      Palmer MJ, Aguiar ACC, Guido RVC. Potent antimalarials with development potential identified by structure-guided computational optimization of a pyrrole-based dihydroorotate dehydrogenase inhibitor series [Internet]. Journal of Medicinal Chemistry. 2021 ; 64( 9): 6085-6136.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.jmedchem.1c00173
  • Source: Journal of Agricultural and Food Chemistry. Unidade: IFSC

    Subjects: BIOTECNOLOGIA, BACTÉRIAS, BIOQUÍMICA

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      LIMA, Mariana Zuliani Theodoro de et al. Crystal structure of a sucrose-6-phosphate hydrolase from lactobacillus gasseri with potential applications in fructan production and the food industry. Journal of Agricultural and Food Chemistry, v. 69, n. 35, p. 10223-10234, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.jafc.1c03901. Acesso em: 06 nov. 2024.
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      Lima, M. Z. T. de, Almeida, L. R. de, Mera, A. E. M., Bernardes, A., Garcia, W., & Muniz, J. R. C. (2021). Crystal structure of a sucrose-6-phosphate hydrolase from lactobacillus gasseri with potential applications in fructan production and the food industry. Journal of Agricultural and Food Chemistry, 69( 35), 10223-10234. doi:10.1021/acs.jafc.1c03901
    • NLM

      Lima MZT de, Almeida LR de, Mera AEM, Bernardes A, Garcia W, Muniz JRC. Crystal structure of a sucrose-6-phosphate hydrolase from lactobacillus gasseri with potential applications in fructan production and the food industry [Internet]. Journal of Agricultural and Food Chemistry. 2021 ; 69( 35): 10223-10234.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.jafc.1c03901
    • Vancouver

      Lima MZT de, Almeida LR de, Mera AEM, Bernardes A, Garcia W, Muniz JRC. Crystal structure of a sucrose-6-phosphate hydrolase from lactobacillus gasseri with potential applications in fructan production and the food industry [Internet]. Journal of Agricultural and Food Chemistry. 2021 ; 69( 35): 10223-10234.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1021/acs.jafc.1c03901
  • Source: Chemical biology and drug design. Unidade: IQSC

    Subjects: BIOQUÍMICA, BIOLOGIA

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      Chemical biology and drug design. Chemical biology and drug design. Hoboken: Wiley-Blackwell Publishing, Inc. Disponível em: https://repositorio.usp.br/directbitstream/4fe96630-45ee-4a8c-8a14-46a20aa75f89/P19198.pdf. Acesso em: 06 nov. 2024. , 2021
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      Chemical biology and drug design. (2021). Chemical biology and drug design. Chemical biology and drug design. Hoboken: Wiley-Blackwell Publishing, Inc. Recuperado de https://repositorio.usp.br/directbitstream/4fe96630-45ee-4a8c-8a14-46a20aa75f89/P19198.pdf
    • NLM

      Chemical biology and drug design [Internet]. Chemical biology and drug design. 2021 ;[citado 2024 nov. 06 ] Available from: https://repositorio.usp.br/directbitstream/4fe96630-45ee-4a8c-8a14-46a20aa75f89/P19198.pdf
    • Vancouver

      Chemical biology and drug design [Internet]. Chemical biology and drug design. 2021 ;[citado 2024 nov. 06 ] Available from: https://repositorio.usp.br/directbitstream/4fe96630-45ee-4a8c-8a14-46a20aa75f89/P19198.pdf
  • Source: Journal of Inorganic Biochemistry. Unidade: IQSC

    Subjects: BIOQUÍMICA, NEOVASCULARIZAÇÃO FISIOLÓGICA, NEOPLASIAS MAMÁRIAS

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      CARVALHO, Edinilton Muniz et al. A divergent mode of activation of a nitrosyl iron complex with unusual antiangiogenic activity. Journal of Inorganic Biochemistry, v. 210, p. 111133 June 2020, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.jinorgbio.2020.111133. Acesso em: 06 nov. 2024.
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      Carvalho, E. M., Ridnour, L. A., Gouveia Júnior, F. S., Cabral, P. H. B., Nascimento, N. R. F. do, Wink, D. A., et al. (2020). A divergent mode of activation of a nitrosyl iron complex with unusual antiangiogenic activity. Journal of Inorganic Biochemistry, 210, 111133 June 2020. doi:10.1016/j.jinorgbio.2020.111133
    • NLM

      Carvalho EM, Ridnour LA, Gouveia Júnior FS, Cabral PHB, Nascimento NRF do, Wink DA, Franco DW, Medeiros MJC de, Pontes D de LI, Longhinotti E, Paulo T de F, Bernardes-Génisson V, Chauvin R, Sousa EHS, Lopes LG de F. A divergent mode of activation of a nitrosyl iron complex with unusual antiangiogenic activity [Internet]. Journal of Inorganic Biochemistry. 2020 ; 210 111133 June 2020.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.jinorgbio.2020.111133
    • Vancouver

      Carvalho EM, Ridnour LA, Gouveia Júnior FS, Cabral PHB, Nascimento NRF do, Wink DA, Franco DW, Medeiros MJC de, Pontes D de LI, Longhinotti E, Paulo T de F, Bernardes-Génisson V, Chauvin R, Sousa EHS, Lopes LG de F. A divergent mode of activation of a nitrosyl iron complex with unusual antiangiogenic activity [Internet]. Journal of Inorganic Biochemistry. 2020 ; 210 111133 June 2020.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.jinorgbio.2020.111133
  • Source: Nitric Oxide: Biology and Chemistry. Unidades: FCFRP, IQSC

    Subjects: BIOQUÍMICA, NEOPLASIAS, PULMÃO, ÓXIDO NÍTRICO

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      RODRIGUES, Fernando Postalli et al. Real-time redox monitoring of a nitrosyl ruthenium complex acting as NO-donor agent in a single A549 cancer cell with multiplex Fourier-transform infrared microscopy. Nitric Oxide: Biology and Chemistry, v. 96, p. 29-34, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.niox.2020.01.005. Acesso em: 06 nov. 2024.
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      Rodrigues, F. P., Macedo, L. J. A. de, Máximo, L. N. C., Sales, F. C. P. F., Silva, R. S. da, & Crespilho, F. N. (2020). Real-time redox monitoring of a nitrosyl ruthenium complex acting as NO-donor agent in a single A549 cancer cell with multiplex Fourier-transform infrared microscopy. Nitric Oxide: Biology and Chemistry, 96, 29-34. doi:10.1016/j.niox.2020.01.005
    • NLM

      Rodrigues FP, Macedo LJA de, Máximo LNC, Sales FCPF, Silva RS da, Crespilho FN. Real-time redox monitoring of a nitrosyl ruthenium complex acting as NO-donor agent in a single A549 cancer cell with multiplex Fourier-transform infrared microscopy [Internet]. Nitric Oxide: Biology and Chemistry. 2020 ; 96 29-34.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.niox.2020.01.005
    • Vancouver

      Rodrigues FP, Macedo LJA de, Máximo LNC, Sales FCPF, Silva RS da, Crespilho FN. Real-time redox monitoring of a nitrosyl ruthenium complex acting as NO-donor agent in a single A549 cancer cell with multiplex Fourier-transform infrared microscopy [Internet]. Nitric Oxide: Biology and Chemistry. 2020 ; 96 29-34.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.niox.2020.01.005
  • Source: Archives of Biochemistry and Biophysics. Unidades: IQ, ICB

    Subjects: ÓLEOS VEGETAIS, BIOQUÍMICA, BIOFÍSICA, BIOLOGIA CELULAR, CITOMETRIA DE FLUXO, MICROSCOPIA CONFOCAL, MICROSCOPIA DE FLUORESCÊNCIA, MICROTÚBULOS, ESTRESSE OXIDATIVO

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      TAKAYASU, Bianca Sayuri et al. Biological effects of an oxyphytosterol generated by β-Sitosterol ozonization. Archives of Biochemistry and Biophysics, v. 695, p. 1-10 art. 108654, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.abb.2020.108654. Acesso em: 06 nov. 2024.
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      Takayasu, B. S., Martins, I. R., Garnique, A. D. M. B., Miyamoto, S., Santelli, G. M. M., Uemi, M., & Onuki, J. (2020). Biological effects of an oxyphytosterol generated by β-Sitosterol ozonization. Archives of Biochemistry and Biophysics, 695, 1-10 art. 108654. doi:10.1016/j.abb.2020.108654
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      Takayasu BS, Martins IR, Garnique ADMB, Miyamoto S, Santelli GMM, Uemi M, Onuki J. Biological effects of an oxyphytosterol generated by β-Sitosterol ozonization [Internet]. Archives of Biochemistry and Biophysics. 2020 ; 695 1-10 art. 108654.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.abb.2020.108654
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      Takayasu BS, Martins IR, Garnique ADMB, Miyamoto S, Santelli GMM, Uemi M, Onuki J. Biological effects of an oxyphytosterol generated by β-Sitosterol ozonization [Internet]. Archives of Biochemistry and Biophysics. 2020 ; 695 1-10 art. 108654.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.abb.2020.108654
  • Source: Cell Biochemistry and Biophysics. Unidade: FMRP

    Subjects: ESTRESSE OXIDATIVO, COGUMELOS COMESTÍVEIS, BIOQUÍMICA, ANTIOXIDANTES

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      CONTATO, Alex Graça et al. Biochemical properties and effects on mitochondrial respiration of aqueous extracts of Basidiomycete mushrooms. Cell Biochemistry and Biophysics, v. 78, n. 1, p. 111-119, 2020Tradução . . Disponível em: https://doi.org/10.1007/s12013-020-00901-w. Acesso em: 06 nov. 2024.
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      Contato, A. G., Brugnari, T., Sibin, A. P. A., Buzzo, A. J. dos R., Sá-Nakanishi, A. B. de, Bracht, L., et al. (2020). Biochemical properties and effects on mitochondrial respiration of aqueous extracts of Basidiomycete mushrooms. Cell Biochemistry and Biophysics, 78( 1), 111-119. doi:10.1007/s12013-020-00901-w
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      Contato AG, Brugnari T, Sibin APA, Buzzo AJ dos R, Sá-Nakanishi AB de, Bracht L, Bersani-Amado CA, Peralta RM, Souza CGM de. Biochemical properties and effects on mitochondrial respiration of aqueous extracts of Basidiomycete mushrooms [Internet]. Cell Biochemistry and Biophysics. 2020 ; 78( 1): 111-119.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1007/s12013-020-00901-w
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      Contato AG, Brugnari T, Sibin APA, Buzzo AJ dos R, Sá-Nakanishi AB de, Bracht L, Bersani-Amado CA, Peralta RM, Souza CGM de. Biochemical properties and effects on mitochondrial respiration of aqueous extracts of Basidiomycete mushrooms [Internet]. Cell Biochemistry and Biophysics. 2020 ; 78( 1): 111-119.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1007/s12013-020-00901-w
  • Source: Chemical biology and drug design. Unidade: IQSC

    Subjects: BIOQUÍMICA, BIOLOGIA

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      Chemical biology and drug design. Chemical biology and drug design. Hoboken: Wiley-Blackwell Publishing, Inc. Disponível em: https://repositorio.usp.br/directbitstream/318f4e8b-f71c-40be-94c5-054d0dd048d1/P18696.pdf. Acesso em: 06 nov. 2024. , 2020
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      Chemical biology and drug design. (2020). Chemical biology and drug design. Chemical biology and drug design. Hoboken: Wiley-Blackwell Publishing, Inc. Recuperado de https://repositorio.usp.br/directbitstream/318f4e8b-f71c-40be-94c5-054d0dd048d1/P18696.pdf
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      Chemical biology and drug design [Internet]. Chemical biology and drug design. 2020 ;[citado 2024 nov. 06 ] Available from: https://repositorio.usp.br/directbitstream/318f4e8b-f71c-40be-94c5-054d0dd048d1/P18696.pdf
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      Chemical biology and drug design [Internet]. Chemical biology and drug design. 2020 ;[citado 2024 nov. 06 ] Available from: https://repositorio.usp.br/directbitstream/318f4e8b-f71c-40be-94c5-054d0dd048d1/P18696.pdf
  • Source: American Phytopathological Society/APS. Unidade: IQ

    Subjects: BACTERIOLOGIA, BIOQUÍMICA, BIOLOGIA CELULAR

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      FEITOSA JUNIOR, Oséias Rodrigues et al. Proteomic and metabolomic analyses of Xylella fastidiosa OMV-enriched fractions reveal association with virulence factors and signaling molecules of the DSF family. American Phytopathological Society/APS, v. 109, n. 8, p. 1344-1353, 2019Tradução . . Disponível em: https://doi.org/10.1094/PHYTO-03-19-0083-R. Acesso em: 06 nov. 2024.
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      Feitosa Junior, O. R., Stefanello, E., Zaini, P. A., Zaini, R. N. P., Pierry, P. M., Dandekar, A. M., et al. (2019). Proteomic and metabolomic analyses of Xylella fastidiosa OMV-enriched fractions reveal association with virulence factors and signaling molecules of the DSF family. American Phytopathological Society/APS, 109( 8), 1344-1353. doi:10.1094/PHYTO-03-19-0083-R
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      Feitosa Junior OR, Stefanello E, Zaini PA, Zaini RNP, Pierry PM, Dandekar AM, Lindow SE, Da Silva AM. Proteomic and metabolomic analyses of Xylella fastidiosa OMV-enriched fractions reveal association with virulence factors and signaling molecules of the DSF family [Internet]. American Phytopathological Society/APS. 2019 ; 109( 8): 1344-1353.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1094/PHYTO-03-19-0083-R
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      Feitosa Junior OR, Stefanello E, Zaini PA, Zaini RNP, Pierry PM, Dandekar AM, Lindow SE, Da Silva AM. Proteomic and metabolomic analyses of Xylella fastidiosa OMV-enriched fractions reveal association with virulence factors and signaling molecules of the DSF family [Internet]. American Phytopathological Society/APS. 2019 ; 109( 8): 1344-1353.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1094/PHYTO-03-19-0083-R
  • Source: Preparative Biochemistry and Biotechnology. Unidade: FCFRP

    Subjects: BIOTECNOLOGIA, ESPECTROMETRIA DE MASSAS, BIOQUÍMICA, CROMATOGRAFIA A GÁS, FUNGOS

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      COITINHO, Luciana Barbosa et al. Lapachol biotransformation by filamentous fungi yields bioactive quinone derivatives and lapachol-stimulated secondary metabolites. Preparative Biochemistry and Biotechnology, v. 49, n. 5, p. 459-463, 2019Tradução . . Disponível em: https://doi.org/10.1080/10826068.2019.1591991. Acesso em: 06 nov. 2024.
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      Coitinho, L. B., Fumagalli, F., Rosa-Garzon, N. G. da, Emery, F. da S., & Cabral, H. (2019). Lapachol biotransformation by filamentous fungi yields bioactive quinone derivatives and lapachol-stimulated secondary metabolites. Preparative Biochemistry and Biotechnology, 49( 5), 459-463. doi:10.1080/10826068.2019.1591991
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      Coitinho LB, Fumagalli F, Rosa-Garzon NG da, Emery F da S, Cabral H. Lapachol biotransformation by filamentous fungi yields bioactive quinone derivatives and lapachol-stimulated secondary metabolites [Internet]. Preparative Biochemistry and Biotechnology. 2019 ; 49( 5): 459-463.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1080/10826068.2019.1591991
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      Coitinho LB, Fumagalli F, Rosa-Garzon NG da, Emery F da S, Cabral H. Lapachol biotransformation by filamentous fungi yields bioactive quinone derivatives and lapachol-stimulated secondary metabolites [Internet]. Preparative Biochemistry and Biotechnology. 2019 ; 49( 5): 459-463.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1080/10826068.2019.1591991

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