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  • Source: International Journal of Molecular Sciences. Unidades: IQ, Interunidades em Biotecnologia

    Subjects: ARANHAS, DIGESTÃO, INIBIDORES DE ENZIMAS

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      SILVA, Jefferson Oliveira et al. Exploring spiders without venom as new sources of peptidase inhibitors. International Journal of Molecular Sciences, v. 27, p. 1-18 art. 186, 2026Tradução . . Disponível em: https://dx.doi.org/10.3390/ijms27010186. Acesso em: 26 abr. 2026.
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      Silva, J. O., Silva, A. C. O., Valladão, R., Bento Neto, O., Souza, V. C. de, Ferreira, C., et al. (2026). Exploring spiders without venom as new sources of peptidase inhibitors. International Journal of Molecular Sciences, 27, 1-18 art. 186. doi:10.3390/ijms27010186
    • NLM

      Silva JO, Silva ACO, Valladão R, Bento Neto O, Souza VC de, Ferreira C, Terra WR, Lopes AR. Exploring spiders without venom as new sources of peptidase inhibitors [Internet]. International Journal of Molecular Sciences. 2026 ; 27 1-18 art. 186.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.3390/ijms27010186
    • Vancouver

      Silva JO, Silva ACO, Valladão R, Bento Neto O, Souza VC de, Ferreira C, Terra WR, Lopes AR. Exploring spiders without venom as new sources of peptidase inhibitors [Internet]. International Journal of Molecular Sciences. 2026 ; 27 1-18 art. 186.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.3390/ijms27010186
  • Source: Immunology Letters. Unidade: IQ

    Subjects: COVID-19, BRADICININA, ÓXIDO NÍTRICO, INFLAMAÇÃO

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      LARA, Jéssica Dotto de et al. Compartment-specific activation of kinin B1 and B2 receptors drives the production of vasoactive and inflammatory mediators during SARS-CoV-2 infection. Immunology Letters, v. 279, p. 1-9 art. 107125, 2026Tradução . . Disponível em: https://dx.doi.org/10.1016/j.imlet.2025.107125. Acesso em: 26 abr. 2026.
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      Lara, J. D. de, Vidal, T., Souza, J. B. de, Kodavara, E., Decker, E. R., Grotto, F. S., et al. (2026). Compartment-specific activation of kinin B1 and B2 receptors drives the production of vasoactive and inflammatory mediators during SARS-CoV-2 infection. Immunology Letters, 279, 1-9 art. 107125. doi:10.1016/j.imlet.2025.107125
    • NLM

      Lara JD de, Vidal T, Souza JB de, Kodavara E, Decker ER, Grotto FS, Bortoluzzi LD, Santos APS dos, Brusco I, Oliveira SM de, Viero FT, Glaser T, Wilot LC, Bernasconi T de LG, Weber A de AP, Librelotto DRN, Silveira MD, Sperotto ND de M, Ulrich H, Basso LA, Bizarro CV. Compartment-specific activation of kinin B1 and B2 receptors drives the production of vasoactive and inflammatory mediators during SARS-CoV-2 infection [Internet]. Immunology Letters. 2026 ; 279 1-9 art. 107125.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1016/j.imlet.2025.107125
    • Vancouver

      Lara JD de, Vidal T, Souza JB de, Kodavara E, Decker ER, Grotto FS, Bortoluzzi LD, Santos APS dos, Brusco I, Oliveira SM de, Viero FT, Glaser T, Wilot LC, Bernasconi T de LG, Weber A de AP, Librelotto DRN, Silveira MD, Sperotto ND de M, Ulrich H, Basso LA, Bizarro CV. Compartment-specific activation of kinin B1 and B2 receptors drives the production of vasoactive and inflammatory mediators during SARS-CoV-2 infection [Internet]. Immunology Letters. 2026 ; 279 1-9 art. 107125.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1016/j.imlet.2025.107125
  • Source: Handbook of Antimicrobial Photoinactivation. Unidade: IQ

    Subjects: TERAPIA FOTODINÂMICA, ESPÉCIES REATIVAS DE OXIGÊNIO

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      FRANCO, Márcia Silvana Freire e YAYA-CANDELA, A. P e BAPTISTA, Maurício da Silva. Photophysical, photochemical, and biochemical mechanisms. Handbook of Antimicrobial Photoinactivation. Tradução . Cham: Springer, 2026. . Disponível em: https://dx.doi.org/10.1007/978-3-031-55858-0_5-1. Acesso em: 26 abr. 2026.
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      Franco, M. S. F., Yaya-Candela, A. P., & Baptista, M. da S. (2026). Photophysical, photochemical, and biochemical mechanisms. In Handbook of Antimicrobial Photoinactivation. Cham: Springer. doi:10.1007/978-3-031-55858-0_5-1
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      Franco MSF, Yaya-Candela AP, Baptista M da S. Photophysical, photochemical, and biochemical mechanisms [Internet]. In: Handbook of Antimicrobial Photoinactivation. Cham: Springer; 2026. [citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1007/978-3-031-55858-0_5-1
    • Vancouver

      Franco MSF, Yaya-Candela AP, Baptista M da S. Photophysical, photochemical, and biochemical mechanisms [Internet]. In: Handbook of Antimicrobial Photoinactivation. Cham: Springer; 2026. [citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1007/978-3-031-55858-0_5-1
  • Source: nature communications. Unidade: IQ

    Subjects: MICROSCOPIA ELETRÔNICA, PROTEÍNAS

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      CHUNG, Injae et al. Post catalysis structures of mitochondrial complex l with ubiquinol-10 bound in the active site. nature communications, 2026Tradução . . Disponível em: https://dx.doi.org/10.1038/s41467-026-70030-0. Acesso em: 26 abr. 2026.
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      Chung, I., Pereira, C. S., Wright, J. J., Arantes, G. M., & Hirst, J. (2026). Post catalysis structures of mitochondrial complex l with ubiquinol-10 bound in the active site. nature communications. doi:10.1038/s41467-026-70030-0
    • NLM

      Chung I, Pereira CS, Wright JJ, Arantes GM, Hirst J. Post catalysis structures of mitochondrial complex l with ubiquinol-10 bound in the active site [Internet]. nature communications. 2026 ;[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1038/s41467-026-70030-0
    • Vancouver

      Chung I, Pereira CS, Wright JJ, Arantes GM, Hirst J. Post catalysis structures of mitochondrial complex l with ubiquinol-10 bound in the active site [Internet]. nature communications. 2026 ;[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1038/s41467-026-70030-0
  • Source: Journal of Biomolecular Structure and Dynamics. Unidade: IQ

    Subjects: HOMEOSTASE, NEUROTRANSMISSORES

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      NASCIMENTO, Lucas Rodrigues Couto et al. In silico analysis of the multitarget potential of GlyT1 inhibitors in SLC6 transporters. Journal of Biomolecular Structure and Dynamics, 2026Tradução . . Disponível em: https://dx.doi.org/10.1080/07391102.2026.2618607. Acesso em: 26 abr. 2026.
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      Nascimento, L. R. C., Tambwea, P. M., Carvalho, G. A. de, Zanchi, F. B., Neves, B. J., Ulrich, H., & Pinto, M. C. X. (2026). In silico analysis of the multitarget potential of GlyT1 inhibitors in SLC6 transporters. Journal of Biomolecular Structure and Dynamics. doi:10.1080/07391102.2026.2618607
    • NLM

      Nascimento LRC, Tambwea PM, Carvalho GA de, Zanchi FB, Neves BJ, Ulrich H, Pinto MCX. In silico analysis of the multitarget potential of GlyT1 inhibitors in SLC6 transporters [Internet]. Journal of Biomolecular Structure and Dynamics. 2026 ;[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1080/07391102.2026.2618607
    • Vancouver

      Nascimento LRC, Tambwea PM, Carvalho GA de, Zanchi FB, Neves BJ, Ulrich H, Pinto MCX. In silico analysis of the multitarget potential of GlyT1 inhibitors in SLC6 transporters [Internet]. Journal of Biomolecular Structure and Dynamics. 2026 ;[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1080/07391102.2026.2618607
  • Source: Atherosclerosis. Unidade: IQ

    Subjects: LIPOPROTEÍNAS, DIABETES MELLITUS

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      BONILHA, Isabella et al. LDL subspecies and lipidome change by evolocumab add-on therapy to empagliflozin in patients with type 2 diabetes: a prespecified secondary analysis of a randomized clinical trial. Atherosclerosis, v. 415, p. 1-10 art. 120686, 2026Tradução . . Disponível em: https://dx.doi.org/10.1016/j.atherosclerosis.2026.120686. Acesso em: 26 abr. 2026.
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      Bonilha, I., Yoshinaga, M. Y., Chaves Filho, A. de B., Gomes, É. I. L., Santos, R. S., Breder, I., et al. (2026). LDL subspecies and lipidome change by evolocumab add-on therapy to empagliflozin in patients with type 2 diabetes: a prespecified secondary analysis of a randomized clinical trial. Atherosclerosis, 415, 1-10 art. 120686. doi:10.1016/j.atherosclerosis.2026.120686
    • NLM

      Bonilha I, Yoshinaga MY, Chaves Filho A de B, Gomes ÉIL, Santos RS, Breder I, Breder J, Miyamoto S, Nadruz W, Kontush A, Sposito AC. LDL subspecies and lipidome change by evolocumab add-on therapy to empagliflozin in patients with type 2 diabetes: a prespecified secondary analysis of a randomized clinical trial [Internet]. Atherosclerosis. 2026 ; 415 1-10 art. 120686.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1016/j.atherosclerosis.2026.120686
    • Vancouver

      Bonilha I, Yoshinaga MY, Chaves Filho A de B, Gomes ÉIL, Santos RS, Breder I, Breder J, Miyamoto S, Nadruz W, Kontush A, Sposito AC. LDL subspecies and lipidome change by evolocumab add-on therapy to empagliflozin in patients with type 2 diabetes: a prespecified secondary analysis of a randomized clinical trial [Internet]. Atherosclerosis. 2026 ; 415 1-10 art. 120686.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1016/j.atherosclerosis.2026.120686
  • Source: Purinergic Signalling. Unidade: IQ

    Assunto: CIENTISTAS

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      FALZONI, Simonetta et al. In tribute to Francesco Di Virgilio, a great scientist and a wonderful friend. Purinergic Signalling, v. 22, n. 20, p. 1-9, 2026Tradução . . Disponível em: https://dx.doi.org/10.1007/s11302-026-10135-9. Acesso em: 26 abr. 2026.
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      Falzoni, S., Giuliani, A. L., Adinolfi, E., Silva, R. C., Illes, P., Robson, S. C., et al. (2026). In tribute to Francesco Di Virgilio, a great scientist and a wonderful friend. Purinergic Signalling, 22( 20), 1-9. doi:10.1007/s11302-026-10135-9
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      Falzoni S, Giuliani AL, Adinolfi E, Silva RC, Illes P, Robson SC, Tang Y, Ulrich H, Kennedy C. In tribute to Francesco Di Virgilio, a great scientist and a wonderful friend [Internet]. Purinergic Signalling. 2026 ; 22( 20): 1-9.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1007/s11302-026-10135-9
    • Vancouver

      Falzoni S, Giuliani AL, Adinolfi E, Silva RC, Illes P, Robson SC, Tang Y, Ulrich H, Kennedy C. In tribute to Francesco Di Virgilio, a great scientist and a wonderful friend [Internet]. Purinergic Signalling. 2026 ; 22( 20): 1-9.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1007/s11302-026-10135-9
  • Source: Archives of Insect Biochemistry and Physiology. Unidade: IQ

    Subjects: OVO, MITOCÔNDRIAS

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      SANTOS, Marcelo Francisco dos et al. Gené's organ of Amblyomma sculptum (Acari: Ixodidae): morphological aspects on the first day of oviposition and participation in the lipid composition of the Egg wax. Archives of Insect Biochemistry and Physiology, v. 121, p. 1-12 art. e70133, 2026Tradução . . Disponível em: https://dx.doi.org/10.1002/arch.70133. Acesso em: 26 abr. 2026.
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      Santos, M. F. dos, Angelo, I. da C., Faria, H. O. F., Miyamoto, S., Morena, D. D. S., & Lallo, M. A. (2026). Gené's organ of Amblyomma sculptum (Acari: Ixodidae): morphological aspects on the first day of oviposition and participation in the lipid composition of the Egg wax. Archives of Insect Biochemistry and Physiology, 121, 1-12 art. e70133. doi:10.1002/arch.70133
    • NLM

      Santos MF dos, Angelo I da C, Faria HOF, Miyamoto S, Morena DDS, Lallo MA. Gené's organ of Amblyomma sculptum (Acari: Ixodidae): morphological aspects on the first day of oviposition and participation in the lipid composition of the Egg wax [Internet]. Archives of Insect Biochemistry and Physiology. 2026 ; 121 1-12 art. e70133.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1002/arch.70133
    • Vancouver

      Santos MF dos, Angelo I da C, Faria HOF, Miyamoto S, Morena DDS, Lallo MA. Gené's organ of Amblyomma sculptum (Acari: Ixodidae): morphological aspects on the first day of oviposition and participation in the lipid composition of the Egg wax [Internet]. Archives of Insect Biochemistry and Physiology. 2026 ; 121 1-12 art. e70133.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1002/arch.70133
  • Source: Diabetes. Unidade: IQ

    Subjects: ANOREXÍGENOS, INSULINA

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      VOGT, Éverton Lopes e KOWALTOWSKI, Alicia Juliana. GLP-1, Pancreatic β-Cells, and Insulin Secretion: what we know and where we need to go. Diabetes, v. 75, p. 403–413, 2026Tradução . . Disponível em: https://dx.doi.org/10.2337/db25-0695. Acesso em: 26 abr. 2026.
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      Vogt, É. L., & Kowaltowski, A. J. (2026). GLP-1, Pancreatic β-Cells, and Insulin Secretion: what we know and where we need to go. Diabetes, 75, 403–413. doi:10.2337/db25-0695
    • NLM

      Vogt ÉL, Kowaltowski AJ. GLP-1, Pancreatic β-Cells, and Insulin Secretion: what we know and where we need to go [Internet]. Diabetes. 2026 ; 75 403–413.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.2337/db25-0695
    • Vancouver

      Vogt ÉL, Kowaltowski AJ. GLP-1, Pancreatic β-Cells, and Insulin Secretion: what we know and where we need to go [Internet]. Diabetes. 2026 ; 75 403–413.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.2337/db25-0695
  • Source: bioRxiv. Unidade: IQ

    Subjects: BACTÉRIAS, PLASMÍDEOS

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      YUAN, Ling et al. A distinct class of conjugative megaplasmids includes potential vehicles for prophage dissemination. bioRxiv, 2026Tradução . . Disponível em: https://dx.doi.org/10.64898/2026.02.21.707213. Acesso em: 26 abr. 2026.
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      Yuan, L., Qin, Y., Roberts, J. W., Anantharaman, K., Wang, H., Zou, Y., et al. (2026). A distinct class of conjugative megaplasmids includes potential vehicles for prophage dissemination. bioRxiv. doi:10.64898/2026.02.21.707213
    • NLM

      Yuan L, Qin Y, Roberts JW, Anantharaman K, Wang H, Zou Y, Duan Y, Camargo AP, Koonin EV, Chen LX. A distinct class of conjugative megaplasmids includes potential vehicles for prophage dissemination [Internet]. bioRxiv. 2026 ;[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.64898/2026.02.21.707213
    • Vancouver

      Yuan L, Qin Y, Roberts JW, Anantharaman K, Wang H, Zou Y, Duan Y, Camargo AP, Koonin EV, Chen LX. A distinct class of conjugative megaplasmids includes potential vehicles for prophage dissemination [Internet]. bioRxiv. 2026 ;[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.64898/2026.02.21.707213
  • Source: Frontiers in Genetics. Unidade: IQ

    Subjects: CÉLULAS-TRONCO, RNA

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      REIS, Eduardo Moraes e BASSÈRES, Daniela Sanchez. Long noncoding RNAs in tumor stemness: emerging mechanisms and therapeutic opportunities. Frontiers in Genetics, v. 17, p. 1-9 art. 1772938, 2026Tradução . . Disponível em: https://dx.doi.org/10.3389/fgene.2026.1772938. Acesso em: 26 abr. 2026.
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      Reis, E. M., & Bassères, D. S. (2026). Long noncoding RNAs in tumor stemness: emerging mechanisms and therapeutic opportunities. Frontiers in Genetics, 17, 1-9 art. 1772938. doi:10.3389/fgene.2026.1772938
    • NLM

      Reis EM, Bassères DS. Long noncoding RNAs in tumor stemness: emerging mechanisms and therapeutic opportunities [Internet]. Frontiers in Genetics. 2026 ; 17 1-9 art. 1772938.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.3389/fgene.2026.1772938
    • Vancouver

      Reis EM, Bassères DS. Long noncoding RNAs in tumor stemness: emerging mechanisms and therapeutic opportunities [Internet]. Frontiers in Genetics. 2026 ; 17 1-9 art. 1772938.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.3389/fgene.2026.1772938
  • Source: Journal of Lipid Research. Unidade: IQ

    Subjects: LIPOPROTEÍNAS, PROTEÔMICA

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      GOMES, Francielle Aguiar et al. Proteomic analysis of HDL isolates reveals method-driven variability: an interlaboratory approach. Journal of Lipid Research, v. 67, n. 1, p. 1-14 art. 100957, 2026Tradução . . Disponível em: https://dx.doi.org/10.1016/j.jlr.2025.100957. Acesso em: 26 abr. 2026.
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      Gomes, F. A., Souza Junior, D. R. de, Holzer, M., & Ronsein, G. E. (2026). Proteomic analysis of HDL isolates reveals method-driven variability: an interlaboratory approach. Journal of Lipid Research, 67( 1), 1-14 art. 100957. doi:10.1016/j.jlr.2025.100957
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      Gomes FA, Souza Junior DR de, Holzer M, Ronsein GE. Proteomic analysis of HDL isolates reveals method-driven variability: an interlaboratory approach [Internet]. Journal of Lipid Research. 2026 ; 67( 1): 1-14 art. 100957.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1016/j.jlr.2025.100957
    • Vancouver

      Gomes FA, Souza Junior DR de, Holzer M, Ronsein GE. Proteomic analysis of HDL isolates reveals method-driven variability: an interlaboratory approach [Internet]. Journal of Lipid Research. 2026 ; 67( 1): 1-14 art. 100957.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1016/j.jlr.2025.100957
  • Source: bioRxiv. Unidades: IQ, FCFRP, FMRP

    Subjects: XANTHOMONAS, BACTERIÓFAGOS

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      FARAH, Chuck Shaker et al. Cryo-EM structure analysis of phage ΦXacm4-11 that infects the phytopathogen Xanthomonas citri. bioRxiv, 2026Tradução . . Disponível em: https://dx.doi.org/10.64898/2026.02.16.706137. Acesso em: 26 abr. 2026.
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      Farah, C. S., Silva, G. O., Llontop, E. E., Cassago, A., Dunger, G., Jones, J. B., et al. (2026). Cryo-EM structure analysis of phage ΦXacm4-11 that infects the phytopathogen Xanthomonas citri. bioRxiv. doi:10.64898/2026.02.16.706137
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      Farah CS, Silva GO, Llontop EE, Cassago A, Dunger G, Jones JB, Setubal JC, Da Silva AM, Portugal R, Sgro GG. Cryo-EM structure analysis of phage ΦXacm4-11 that infects the phytopathogen Xanthomonas citri [Internet]. bioRxiv. 2026 ;[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.64898/2026.02.16.706137
    • Vancouver

      Farah CS, Silva GO, Llontop EE, Cassago A, Dunger G, Jones JB, Setubal JC, Da Silva AM, Portugal R, Sgro GG. Cryo-EM structure analysis of phage ΦXacm4-11 that infects the phytopathogen Xanthomonas citri [Internet]. bioRxiv. 2026 ;[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.64898/2026.02.16.706137
  • Source: Toxicology and Applied Pharmacology. Unidade: IQ

    Subjects: ESTRESSE OXIDATIVO, QUIMIOTERÁPICOS

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      SCHIESS, Mariana Caprio et al. Paclitaxel impairs mitochondrial dynamics in human sensory-like neuron cells. Toxicology and Applied Pharmacology, v. 508, p. 1-35 art. 117715, 2026Tradução . . Disponível em: https://dx.doi.org/10.1016/j.taap.2026.117715. Acesso em: 26 abr. 2026.
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      Schiess, M. C., Silva, G. S. de A., Hösch, N. G., Troitiño, V. C., Souza, M. M. de, Pereira, C. D. O., et al. (2026). Paclitaxel impairs mitochondrial dynamics in human sensory-like neuron cells. Toxicology and Applied Pharmacology, 508, 1-35 art. 117715. doi:10.1016/j.taap.2026.117715
    • NLM

      Schiess MC, Silva GS de A, Hösch NG, Troitiño VC, Souza MM de, Pereira CDO, Glaser T, Ulrich H, Tavassi AMC, Bufalo MC, Zambelli VO. Paclitaxel impairs mitochondrial dynamics in human sensory-like neuron cells [Internet]. Toxicology and Applied Pharmacology. 2026 ; 508 1-35 art. 117715.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1016/j.taap.2026.117715
    • Vancouver

      Schiess MC, Silva GS de A, Hösch NG, Troitiño VC, Souza MM de, Pereira CDO, Glaser T, Ulrich H, Tavassi AMC, Bufalo MC, Zambelli VO. Paclitaxel impairs mitochondrial dynamics in human sensory-like neuron cells [Internet]. Toxicology and Applied Pharmacology. 2026 ; 508 1-35 art. 117715.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1016/j.taap.2026.117715
  • Source: Redox Biochemistry and Chemistry. Unidades: IQ, ICB

    Subjects: ÁCIDO ÚRICO, ALBUMINAS

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      SILVA, Railmara Pereira da et al. Uratylated albumin activates endothelial cells to induce monocyte adhesion and the release of pro-inflammatory cytokines. Redox Biochemistry and Chemistry, v. 15, p. 1-10 art. 100071, 2026Tradução . . Disponível em: https://dx.doi.org/10.1016/j.rbc.2026.100071. Acesso em: 26 abr. 2026.
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      Silva, R. P. da, Silva, B. P. da, Pratti, A. P. S., Dempsey, B., Lacerda, C. D., Carretero, G. P. B., et al. (2026). Uratylated albumin activates endothelial cells to induce monocyte adhesion and the release of pro-inflammatory cytokines. Redox Biochemistry and Chemistry, 15, 1-10 art. 100071. doi:/10.1016/j.rbc.2026.100071
    • NLM

      Silva RP da, Silva BP da, Pratti APS, Dempsey B, Lacerda CD, Carretero GPB, Peixoto AS, Cruz LC da, Adan C, Cuccovia IM, Meotti FC. Uratylated albumin activates endothelial cells to induce monocyte adhesion and the release of pro-inflammatory cytokines [Internet]. Redox Biochemistry and Chemistry. 2026 ; 15 1-10 art. 100071.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1016/j.rbc.2026.100071
    • Vancouver

      Silva RP da, Silva BP da, Pratti APS, Dempsey B, Lacerda CD, Carretero GPB, Peixoto AS, Cruz LC da, Adan C, Cuccovia IM, Meotti FC. Uratylated albumin activates endothelial cells to induce monocyte adhesion and the release of pro-inflammatory cytokines [Internet]. Redox Biochemistry and Chemistry. 2026 ; 15 1-10 art. 100071.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1016/j.rbc.2026.100071
  • Source: ACS Applied Nano Materials. Unidade: IQ

    Subjects: PEPTÍDEOS, ANTINEOPLÁSICOS

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      ZULUAGA, Norma Lucía Buriticá et al. Theranostic nanoscaffold for targeted delivery of cisplatin. ACS Applied Nano Materials, v. 9, n. 5, p. 2204–2217, 2026Tradução . . Disponível em: https://dx.doi.org/10.1021/acsanm.5c04519. Acesso em: 26 abr. 2026.
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      Zuluaga, N. L. B., Carretero, G. P. B., Torres, Y. Y. S., Toma, S. H., Meotti, F. C., Cugnasca, B. dos S., et al. (2026). Theranostic nanoscaffold for targeted delivery of cisplatin. ACS Applied Nano Materials, 9( 5), 2204–2217. doi:10.1021/acsanm.5c04519
    • NLM

      Zuluaga NLB, Carretero GPB, Torres YYS, Toma SH, Meotti FC, Cugnasca B dos S, Araki K, Santos AA dos, Ulrich H, Chaimovich Guralnik H, Cuccovia IM. Theranostic nanoscaffold for targeted delivery of cisplatin [Internet]. ACS Applied Nano Materials. 2026 ; 9( 5): 2204–2217.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1021/acsanm.5c04519
    • Vancouver

      Zuluaga NLB, Carretero GPB, Torres YYS, Toma SH, Meotti FC, Cugnasca B dos S, Araki K, Santos AA dos, Ulrich H, Chaimovich Guralnik H, Cuccovia IM. Theranostic nanoscaffold for targeted delivery of cisplatin [Internet]. ACS Applied Nano Materials. 2026 ; 9( 5): 2204–2217.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1021/acsanm.5c04519
  • Source: International Journal of Biological Macromolecules. Unidades: IQ, PRÓ-G

    Assunto: PROTEÍNAS TIROSINA FOSFATASES

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      PACHECO, Diana Reis Della Corte Guimarães e FORTI, Sofia Figueiredo e FORTI, Fabio Luis. Intrinsically disordered regions in atypical dual-specificity phosphatases: a review. International Journal of Biological Macromolecules, v. 323, p. 1-14 art. 147230, 2025Tradução . . Disponível em: https://dx.doi.org/10.1016/j.ijbiomac.2025.147230. Acesso em: 26 abr. 2026.
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      Pacheco, D. R. D. C. G., Forti, S. F., & Forti, F. L. (2025). Intrinsically disordered regions in atypical dual-specificity phosphatases: a review. International Journal of Biological Macromolecules, 323, 1-14 art. 147230. doi:10.1016/j.ijbiomac.2025.147230
    • NLM

      Pacheco DRDCG, Forti SF, Forti FL. Intrinsically disordered regions in atypical dual-specificity phosphatases: a review [Internet]. International Journal of Biological Macromolecules. 2025 ; 323 1-14 art. 147230.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1016/j.ijbiomac.2025.147230
    • Vancouver

      Pacheco DRDCG, Forti SF, Forti FL. Intrinsically disordered regions in atypical dual-specificity phosphatases: a review [Internet]. International Journal of Biological Macromolecules. 2025 ; 323 1-14 art. 147230.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1016/j.ijbiomac.2025.147230
  • Source: New Phytologist. Unidade: IQ

    Subjects: HERBICIDAS, RITMO CIRCADIANO, CRONOBIOLOGIA

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      OGASAWARA, Gustavo Akio e HOTTA, Carlos Takeshi e DODD, Antony N. Using plant circadian programs to optimize agrochemical use. New Phytologist, 2025Tradução . . Disponível em: https://dx.doi.org/10.1111/nph.70346. Acesso em: 26 abr. 2026.
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      Ogasawara, G. A., Hotta, C. T., & Dodd, A. N. (2025). Using plant circadian programs to optimize agrochemical use. New Phytologist. doi:10.1111/nph.70346
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      Ogasawara GA, Hotta CT, Dodd AN. Using plant circadian programs to optimize agrochemical use [Internet]. New Phytologist. 2025 ;[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1111/nph.70346
    • Vancouver

      Ogasawara GA, Hotta CT, Dodd AN. Using plant circadian programs to optimize agrochemical use [Internet]. New Phytologist. 2025 ;[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1111/nph.70346
  • Source: Expert Review of Proteomics. Unidade: IQ

    Subjects: PROTEÔMICA, LIPOPROTEÍNAS

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      VAISAR, Tomas e RONSEIN, Graziella Eliza. HDL proteome: from its characterization to quantitative measurements in particle subspecies and functional associations. Expert Review of Proteomics, v. 22, n. 7, p. 273-286, 2025Tradução . . Disponível em: https://dx.doi.org/10.1080/14789450.2025.2534397. Acesso em: 26 abr. 2026.
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      Vaisar, T., & Ronsein, G. E. (2025). HDL proteome: from its characterization to quantitative measurements in particle subspecies and functional associations. Expert Review of Proteomics, 22( 7), 273-286. doi:10.1080/14789450.2025.2534397
    • NLM

      Vaisar T, Ronsein GE. HDL proteome: from its characterization to quantitative measurements in particle subspecies and functional associations [Internet]. Expert Review of Proteomics. 2025 ; 22( 7): 273-286.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1080/14789450.2025.2534397
    • Vancouver

      Vaisar T, Ronsein GE. HDL proteome: from its characterization to quantitative measurements in particle subspecies and functional associations [Internet]. Expert Review of Proteomics. 2025 ; 22( 7): 273-286.[citado 2026 abr. 26 ] Available from: https://dx.doi.org/10.1080/14789450.2025.2534397
  • Source: Abstracts. Conference titles: Annual Meeting of the Brazilian Society for Biochemistry and Molecular Biology/SBBQ. Unidade: IQ

    Assunto: PROTEÍNAS

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      ROLDÃO, Allan Pradelli e HYVÖNEN, Marko e SCHECHTMAN, Deborah. Establishment of PLCg as a target for covalent fragment‐based drug discovery. 2025, Anais.. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Celular, 2025. Disponível em: https://www2.sbbq.org.br/reuniao/2025/images/resumos.pdf. Acesso em: 26 abr. 2026.
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      Roldão, A. P., Hyvönen, M., & Schechtman, D. (2025). Establishment of PLCg as a target for covalent fragment‐based drug discovery. In Abstracts. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Celular. Recuperado de https://www2.sbbq.org.br/reuniao/2025/images/resumos.pdf
    • NLM

      Roldão AP, Hyvönen M, Schechtman D. Establishment of PLCg as a target for covalent fragment‐based drug discovery [Internet]. Abstracts. 2025 ;[citado 2026 abr. 26 ] Available from: https://www2.sbbq.org.br/reuniao/2025/images/resumos.pdf
    • Vancouver

      Roldão AP, Hyvönen M, Schechtman D. Establishment of PLCg as a target for covalent fragment‐based drug discovery [Internet]. Abstracts. 2025 ;[citado 2026 abr. 26 ] Available from: https://www2.sbbq.org.br/reuniao/2025/images/resumos.pdf

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