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  • Source: The Journal of Biological Chemistry. Unidade: ICB

    Assunto: MICROBIOLOGIA

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      BARROS, Mário Henrique de et al. Characterization of Gtf1p, the connector subunit of yeast mitochondrial tRNA-dependent amidotransferase. The Journal of Biological Chemistry, v. 286, n. 38, p. 32937-32947, 2011Tradução . . Disponível em: https://doi.org/10.1074/jbc.M111.265371. Acesso em: 23 out. 2025.
    • APA

      Barros, M. H. de, Rak, M., Paulela, J. A., & Tzagoloff, A. (2011). Characterization of Gtf1p, the connector subunit of yeast mitochondrial tRNA-dependent amidotransferase. The Journal of Biological Chemistry, 286( 38), 32937-32947. doi:10.1074/jbc.M111.265371
    • NLM

      Barros MH de, Rak M, Paulela JA, Tzagoloff A. Characterization of Gtf1p, the connector subunit of yeast mitochondrial tRNA-dependent amidotransferase [Internet]. The Journal of Biological Chemistry. 2011 ; 286( 38): 32937-32947.[citado 2025 out. 23 ] Available from: https://doi.org/10.1074/jbc.M111.265371
    • Vancouver

      Barros MH de, Rak M, Paulela JA, Tzagoloff A. Characterization of Gtf1p, the connector subunit of yeast mitochondrial tRNA-dependent amidotransferase [Internet]. The Journal of Biological Chemistry. 2011 ; 286( 38): 32937-32947.[citado 2025 out. 23 ] Available from: https://doi.org/10.1074/jbc.M111.265371
  • Source: The Journal of Biological Chemistry. Unidade: ICB

    Assunto: HISTOLOGIA

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      BERTI, Denise Aparecida et al. Analysis of intracellular substrates and products of thimet oligopeptidase in human embryonic kidney 293 cells. The Journal of Biological Chemistry, v. 284, n. 21, p. 14105-14116, 2009Tradução . . Acesso em: 23 out. 2025.
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      Berti, D. A., Morano, C., Russo, L. C., Castro, L. M., Cunha, F. M., Zhang, X., et al. (2009). Analysis of intracellular substrates and products of thimet oligopeptidase in human embryonic kidney 293 cells. The Journal of Biological Chemistry, 284( 21), 14105-14116.
    • NLM

      Berti DA, Morano C, Russo LC, Castro LM, Cunha FM, Zhang X, Sironi J, Klitzke CF, Ferro ES, Fricker LD. Analysis of intracellular substrates and products of thimet oligopeptidase in human embryonic kidney 293 cells. The Journal of Biological Chemistry. 2009 ; 284( 21): 14105-14116.[citado 2025 out. 23 ]
    • Vancouver

      Berti DA, Morano C, Russo LC, Castro LM, Cunha FM, Zhang X, Sironi J, Klitzke CF, Ferro ES, Fricker LD. Analysis of intracellular substrates and products of thimet oligopeptidase in human embryonic kidney 293 cells. The Journal of Biological Chemistry. 2009 ; 284( 21): 14105-14116.[citado 2025 out. 23 ]
  • Source: The Journal of Biological Chemistry. Unidade: ICB

    Assunto: MICROBIOLOGIA

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      MA, Li et al. Evidence of ball-and-chain transport of ferric enterobactin through FepA. The Journal of Biological Chemistry, v. 282, n. 1, p. 397-406, 2007Tradução . . Acesso em: 23 out. 2025.
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      Ma, L., Kaserer, W., Annamali, R., Scott, D. C., Jin, B., Jiang, X., et al. (2007). Evidence of ball-and-chain transport of ferric enterobactin through FepA. The Journal of Biological Chemistry, 282( 1), 397-406.
    • NLM

      Ma L, Kaserer W, Annamali R, Scott DC, Jin B, Jiang X, Xiao Q, Maymani H, Massis LM, Ferreira LC de S, Newton SM, Klebba PE. Evidence of ball-and-chain transport of ferric enterobactin through FepA. The Journal of Biological Chemistry. 2007 ; 282( 1): 397-406.[citado 2025 out. 23 ]
    • Vancouver

      Ma L, Kaserer W, Annamali R, Scott DC, Jin B, Jiang X, Xiao Q, Maymani H, Massis LM, Ferreira LC de S, Newton SM, Klebba PE. Evidence of ball-and-chain transport of ferric enterobactin through FepA. The Journal of Biological Chemistry. 2007 ; 282( 1): 397-406.[citado 2025 out. 23 ]
  • Source: The Journal of Biological Chemistry. Unidade: ICB

    Assunto: MICROBIOLOGIA

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      BARROS, Mário Henrique de et al. COX24 codes for a mitochondrial protein required for processing of the COX1 transcript. The Journal of Biological Chemistry, v. 281, n. 6, p. 3743-3751, 2006Tradução . . Acesso em: 23 out. 2025.
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      Barros, M. H. de, Myers, A. M., Driesche, S. V., & Tzagoloff, A. (2006). COX24 codes for a mitochondrial protein required for processing of the COX1 transcript. The Journal of Biological Chemistry, 281( 6), 3743-3751.
    • NLM

      Barros MH de, Myers AM, Driesche SV, Tzagoloff A. COX24 codes for a mitochondrial protein required for processing of the COX1 transcript. The Journal of Biological Chemistry. 2006 ; 281( 6): 3743-3751.[citado 2025 out. 23 ]
    • Vancouver

      Barros MH de, Myers AM, Driesche SV, Tzagoloff A. COX24 codes for a mitochondrial protein required for processing of the COX1 transcript. The Journal of Biological Chemistry. 2006 ; 281( 6): 3743-3751.[citado 2025 out. 23 ]
  • Source: The Journal of Biological Chemistry. Unidade: ICB

    Assunto: FARMACOLOGIA

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      JANISZEWSKI, Mariano et al. Regulation of NAD(P)H oxidase by associated protein disulfide isomerase in vascular smooth muscle cells. The Journal of Biological Chemistry, v. 280, n. 49, p. 40813-40819, 2005Tradução . . Acesso em: 23 out. 2025.
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      Janiszewski, M., Lopes, L. R., Carmo, A. O., Pedro, M. A., Brandes, R. P., Santos, C. X. C., & Laurindo, F. R. M. (2005). Regulation of NAD(P)H oxidase by associated protein disulfide isomerase in vascular smooth muscle cells. The Journal of Biological Chemistry, 280( 49), 40813-40819.
    • NLM

      Janiszewski M, Lopes LR, Carmo AO, Pedro MA, Brandes RP, Santos CXC, Laurindo FRM. Regulation of NAD(P)H oxidase by associated protein disulfide isomerase in vascular smooth muscle cells. The Journal of Biological Chemistry. 2005 ; 280( 49): 40813-40819.[citado 2025 out. 23 ]
    • Vancouver

      Janiszewski M, Lopes LR, Carmo AO, Pedro MA, Brandes RP, Santos CXC, Laurindo FRM. Regulation of NAD(P)H oxidase by associated protein disulfide isomerase in vascular smooth muscle cells. The Journal of Biological Chemistry. 2005 ; 280( 49): 40813-40819.[citado 2025 out. 23 ]
  • Source: The Journal of Biological Chemistry. Unidades: IQSC, IF

    Subjects: BIOQUÍMICA, BIOLOGIA MOLECULAR

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      GELAMO, Emerson Luiz e ITRI, Rosangela e TABAK, Marcel. Small angle X-ray Scattering (SAXS) study of the extracellular hemoglobin of Glossoscolex paulistus: effect of pH, iron oxidation state, and interaction with anionic SDS surfactant. The Journal of Biological Chemistry, v. 279, n. 32, p. 33298-33305, 2004Tradução . . Acesso em: 23 out. 2025.
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      Gelamo, E. L., Itri, R., & Tabak, M. (2004). Small angle X-ray Scattering (SAXS) study of the extracellular hemoglobin of Glossoscolex paulistus: effect of pH, iron oxidation state, and interaction with anionic SDS surfactant. The Journal of Biological Chemistry, 279( 32), 33298-33305.
    • NLM

      Gelamo EL, Itri R, Tabak M. Small angle X-ray Scattering (SAXS) study of the extracellular hemoglobin of Glossoscolex paulistus: effect of pH, iron oxidation state, and interaction with anionic SDS surfactant. The Journal of Biological Chemistry. 2004 ; 279( 32): 33298-33305.[citado 2025 out. 23 ]
    • Vancouver

      Gelamo EL, Itri R, Tabak M. Small angle X-ray Scattering (SAXS) study of the extracellular hemoglobin of Glossoscolex paulistus: effect of pH, iron oxidation state, and interaction with anionic SDS surfactant. The Journal of Biological Chemistry. 2004 ; 279( 32): 33298-33305.[citado 2025 out. 23 ]
  • Source: The Journal of Biological Chemistry. Unidade: FCFRP

    Assunto: BIOQUÍMICA

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      LUO, Shuhong et al. Trypanosoma brucei Plasma membrane-type 'Ca POT. 2+'-ATPase 1 (TbPMC1) and 2 (TbPMC2) genes encode functional 'Ca POT. 2+'-ATPases localized to the acidocalcisomes and plasma membrane, and essential for 'Ca POT. 2+' homeostasis and growth. The Journal of Biological Chemistry, v. 279, n. 14, p. 14427-14439, 2004Tradução . . Acesso em: 23 out. 2025.
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      Luo, S., Rohloff, P., Cox, J., Uyemura, S. A., & Docampo, R. (2004). Trypanosoma brucei Plasma membrane-type 'Ca POT. 2+'-ATPase 1 (TbPMC1) and 2 (TbPMC2) genes encode functional 'Ca POT. 2+'-ATPases localized to the acidocalcisomes and plasma membrane, and essential for 'Ca POT. 2+' homeostasis and growth. The Journal of Biological Chemistry, 279( 14), 14427-14439.
    • NLM

      Luo S, Rohloff P, Cox J, Uyemura SA, Docampo R. Trypanosoma brucei Plasma membrane-type 'Ca POT. 2+'-ATPase 1 (TbPMC1) and 2 (TbPMC2) genes encode functional 'Ca POT. 2+'-ATPases localized to the acidocalcisomes and plasma membrane, and essential for 'Ca POT. 2+' homeostasis and growth. The Journal of Biological Chemistry. 2004 ; 279( 14): 14427-14439.[citado 2025 out. 23 ]
    • Vancouver

      Luo S, Rohloff P, Cox J, Uyemura SA, Docampo R. Trypanosoma brucei Plasma membrane-type 'Ca POT. 2+'-ATPase 1 (TbPMC1) and 2 (TbPMC2) genes encode functional 'Ca POT. 2+'-ATPases localized to the acidocalcisomes and plasma membrane, and essential for 'Ca POT. 2+' homeostasis and growth. The Journal of Biological Chemistry. 2004 ; 279( 14): 14427-14439.[citado 2025 out. 23 ]
  • Source: The Journal of Biological Chemistry. Unidade: FCFRP

    Assunto: BIOQUÍMICA

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      UYEMURA, Sérgio Akira et al. Oxidative phosphorylation and rotenone-insensitive malate- and NADH-quinone oxidoreductases in Plasmodium yoelii yoelii mitocondria in situ. The Journal of Biological Chemistry, v. 279, n. 1, p. 385-393, 2004Tradução . . Acesso em: 23 out. 2025.
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      Uyemura, S. A., Luo, S., Vieira, M., Moreno, S. N. J., & Docampo, R. (2004). Oxidative phosphorylation and rotenone-insensitive malate- and NADH-quinone oxidoreductases in Plasmodium yoelii yoelii mitocondria in situ. The Journal of Biological Chemistry, 279( 1), 385-393.
    • NLM

      Uyemura SA, Luo S, Vieira M, Moreno SNJ, Docampo R. Oxidative phosphorylation and rotenone-insensitive malate- and NADH-quinone oxidoreductases in Plasmodium yoelii yoelii mitocondria in situ. The Journal of Biological Chemistry. 2004 ; 279( 1): 385-393.[citado 2025 out. 23 ]
    • Vancouver

      Uyemura SA, Luo S, Vieira M, Moreno SNJ, Docampo R. Oxidative phosphorylation and rotenone-insensitive malate- and NADH-quinone oxidoreductases in Plasmodium yoelii yoelii mitocondria in situ. The Journal of Biological Chemistry. 2004 ; 279( 1): 385-393.[citado 2025 out. 23 ]
  • Source: The Journal of Biological Chemistry. Unidade: IF

    Subjects: BIOLOGIA MOLECULAR, BIOLOGIA CELULAR, BIOQUÍMICA

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      BORGES, Julio Cesar et al. Free human mitochondrial GrpE is a symmetric dimer in solution. The Journal of Biological Chemistry, v. 278, n. 37, p. 35337-35344, 2003Tradução . . Disponível em: http://intl.jbc.org/cgi/reprint/278/37/35337.pdf. Acesso em: 23 out. 2025.
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      Borges, J. C., Fischer, H., Craievich, A. F., Hansen, L. D., & Ramos, C. H. I. (2003). Free human mitochondrial GrpE is a symmetric dimer in solution. The Journal of Biological Chemistry, 278( 37), 35337-35344. Recuperado de http://intl.jbc.org/cgi/reprint/278/37/35337.pdf
    • NLM

      Borges JC, Fischer H, Craievich AF, Hansen LD, Ramos CHI. Free human mitochondrial GrpE is a symmetric dimer in solution [Internet]. The Journal of Biological Chemistry. 2003 ; 278( 37): 35337-35344.[citado 2025 out. 23 ] Available from: http://intl.jbc.org/cgi/reprint/278/37/35337.pdf
    • Vancouver

      Borges JC, Fischer H, Craievich AF, Hansen LD, Ramos CHI. Free human mitochondrial GrpE is a symmetric dimer in solution [Internet]. The Journal of Biological Chemistry. 2003 ; 278( 37): 35337-35344.[citado 2025 out. 23 ] Available from: http://intl.jbc.org/cgi/reprint/278/37/35337.pdf
  • Source: The Journal of Biological Chemistry. Unidade: ICB

    Assunto: FISIOLOGIA

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      XIMENES, Helena Maria et al. Opposite effects of glucose on plasma membrane Ca2+ - ATPase and Na/Ca exchanger transcription, expression, and activity in rat pancreatic beta-cell. The Journal of Biological Chemistry, v. 278, n. 25, p. 22956-22963, 2003Tradução . . Acesso em: 23 out. 2025.
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      Ximenes, H. M., Kamagate, A., Eylen, F. V., Herchuelz, A., & Carpinelli, A. R. (2003). Opposite effects of glucose on plasma membrane Ca2+ - ATPase and Na/Ca exchanger transcription, expression, and activity in rat pancreatic beta-cell. The Journal of Biological Chemistry, 278( 25), 22956-22963.
    • NLM

      Ximenes HM, Kamagate A, Eylen FV, Herchuelz A, Carpinelli AR. Opposite effects of glucose on plasma membrane Ca2+ - ATPase and Na/Ca exchanger transcription, expression, and activity in rat pancreatic beta-cell. The Journal of Biological Chemistry. 2003 ; 278( 25): 22956-22963.[citado 2025 out. 23 ]
    • Vancouver

      Ximenes HM, Kamagate A, Eylen FV, Herchuelz A, Carpinelli AR. Opposite effects of glucose on plasma membrane Ca2+ - ATPase and Na/Ca exchanger transcription, expression, and activity in rat pancreatic beta-cell. The Journal of Biological Chemistry. 2003 ; 278( 25): 22956-22963.[citado 2025 out. 23 ]
  • Source: The Journal of Biological Chemistry. Unidade: FM

    Assunto: BIOQUÍMICA

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      MAGALHÃES, Ana C. et al. Endocytic intermediates involved with the intracellular trafficking of a fluorescent cellular prion protein. The Journal of Biological Chemistry, v. 277, n. 36, p. 33311-33318, 2002Tradução . . Acesso em: 23 out. 2025.
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      Magalhães, A. C., Silva, J. A., Lee, K. S., Martins, V. R., Prado, V. F., Ferguson, S. S. G., et al. (2002). Endocytic intermediates involved with the intracellular trafficking of a fluorescent cellular prion protein. The Journal of Biological Chemistry, 277( 36), 33311-33318.
    • NLM

      Magalhães AC, Silva JA, Lee KS, Martins VR, Prado VF, Ferguson SSG, Gomez MV, Brentani RR, Prado MAM. Endocytic intermediates involved with the intracellular trafficking of a fluorescent cellular prion protein. The Journal of Biological Chemistry. 2002 ; 277( 36): 33311-33318.[citado 2025 out. 23 ]
    • Vancouver

      Magalhães AC, Silva JA, Lee KS, Martins VR, Prado VF, Ferguson SSG, Gomez MV, Brentani RR, Prado MAM. Endocytic intermediates involved with the intracellular trafficking of a fluorescent cellular prion protein. The Journal of Biological Chemistry. 2002 ; 277( 36): 33311-33318.[citado 2025 out. 23 ]
  • Source: The Journal of Biological Chemistry. Unidade: FM

    Subjects: BIOQUÍMICA, DNA

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      CORDEIRO, Yraima et al. DNA converts cellular prion protein into the beta-sheet conformation and inhibits prion peptide aggregation. The Journal of Biological Chemistry, v. 276, n. 52, p. 49400-49409, 2002Tradução . . Acesso em: 23 out. 2025.
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      Cordeiro, Y., Machado, F., Juliano, L., Juliano, M. A., Foguel, D., Silva, J. L., & Brentani, R. R. (2002). DNA converts cellular prion protein into the beta-sheet conformation and inhibits prion peptide aggregation. The Journal of Biological Chemistry, 276( 52), 49400-49409.
    • NLM

      Cordeiro Y, Machado F, Juliano L, Juliano MA, Foguel D, Silva JL, Brentani RR. DNA converts cellular prion protein into the beta-sheet conformation and inhibits prion peptide aggregation. The Journal of Biological Chemistry. 2002 ; 276( 52): 49400-49409.[citado 2025 out. 23 ]
    • Vancouver

      Cordeiro Y, Machado F, Juliano L, Juliano MA, Foguel D, Silva JL, Brentani RR. DNA converts cellular prion protein into the beta-sheet conformation and inhibits prion peptide aggregation. The Journal of Biological Chemistry. 2002 ; 276( 52): 49400-49409.[citado 2025 out. 23 ]
  • Source: The Journal of Biological Chemistry. Unidades: FCFRP, FMRP

    Assunto: BIOLOGIA CELULAR

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      BRANDT, Guillermo et al. Dermaseptins from Phyllomedusa oreads and Phyllomedusa distincta. The Journal of Biological Chemistry, v. 277, n. 51, p. 49332-49340, 2002Tradução . . Acesso em: 23 out. 2025.
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      Brandt, G., Leite, J. R. S. A., Silva, L. P., Albuquerque, S. de, Prates, M. V., Azevedo, R. A. A., et al. (2002). Dermaseptins from Phyllomedusa oreads and Phyllomedusa distincta. The Journal of Biological Chemistry, 277( 51), 49332-49340.
    • NLM

      Brandt G, Leite JRSA, Silva LP, Albuquerque S de, Prates MV, Azevedo RAA, Carregaro V, Silva JS da, Sá VCL, Brandão R, Bloch Junior C. Dermaseptins from Phyllomedusa oreads and Phyllomedusa distincta. The Journal of Biological Chemistry. 2002 ; 277( 51): 49332-49340.[citado 2025 out. 23 ]
    • Vancouver

      Brandt G, Leite JRSA, Silva LP, Albuquerque S de, Prates MV, Azevedo RAA, Carregaro V, Silva JS da, Sá VCL, Brandão R, Bloch Junior C. Dermaseptins from Phyllomedusa oreads and Phyllomedusa distincta. The Journal of Biological Chemistry. 2002 ; 277( 51): 49332-49340.[citado 2025 out. 23 ]
  • Source: The Journal of Biological Chemistry. Unidade: FM

    Assunto: BIOLOGIA MOLECULAR

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      KAWAGUCHI, Mio e ONUCHIC, Luiz Fernando e HUANG, Shau-Ku. Activation of extracellular signal-regulated kinase (ERK) 1/2, but not p38 and c-jun N-terminal kinase, is involved in signaling of a novel cytokine, ML-1. The Journal of Biological Chemistry, v. 277, n. 18, p. 15229-15232, 2002Tradução . . Acesso em: 23 out. 2025.
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      Kawaguchi, M., Onuchic, L. F., & Huang, S. -K. (2002). Activation of extracellular signal-regulated kinase (ERK) 1/2, but not p38 and c-jun N-terminal kinase, is involved in signaling of a novel cytokine, ML-1. The Journal of Biological Chemistry, 277( 18), 15229-15232.
    • NLM

      Kawaguchi M, Onuchic LF, Huang S-K. Activation of extracellular signal-regulated kinase (ERK) 1/2, but not p38 and c-jun N-terminal kinase, is involved in signaling of a novel cytokine, ML-1. The Journal of Biological Chemistry. 2002 ; 277( 18): 15229-15232.[citado 2025 out. 23 ]
    • Vancouver

      Kawaguchi M, Onuchic LF, Huang S-K. Activation of extracellular signal-regulated kinase (ERK) 1/2, but not p38 and c-jun N-terminal kinase, is involved in signaling of a novel cytokine, ML-1. The Journal of Biological Chemistry. 2002 ; 277( 18): 15229-15232.[citado 2025 out. 23 ]
  • Source: The Journal of Biological Chemistry. Unidade: ICB

    Assunto: FISIOLOGIA

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      AMINO, Rogerio et al. Trialysin a novel pore-forming protein from saliva of hematophagous insects activated by limited proteolysis. The Journal of Biological Chemistry, v. 277, p. 6207-6213, 2002Tradução . . Acesso em: 23 out. 2025.
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      Amino, R., Martins, R. M., Procópio, J., Hirata, I. Y., Juliano, M. A., & Schenkman, S. (2002). Trialysin a novel pore-forming protein from saliva of hematophagous insects activated by limited proteolysis. The Journal of Biological Chemistry, 277, 6207-6213.
    • NLM

      Amino R, Martins RM, Procópio J, Hirata IY, Juliano MA, Schenkman S. Trialysin a novel pore-forming protein from saliva of hematophagous insects activated by limited proteolysis. The Journal of Biological Chemistry. 2002 ;277 6207-6213.[citado 2025 out. 23 ]
    • Vancouver

      Amino R, Martins RM, Procópio J, Hirata IY, Juliano MA, Schenkman S. Trialysin a novel pore-forming protein from saliva of hematophagous insects activated by limited proteolysis. The Journal of Biological Chemistry. 2002 ;277 6207-6213.[citado 2025 out. 23 ]
  • Source: The Journal of Biological Chemistry. Unidade: FMRP

    Subjects: MIOSINA, BIOLOGIA CELULAR

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      TAUHATA, Sinji Borges Ferreira et al. High affinity binding of brain myosin-Va to F-action induced by calcium in the presençe of ATP. The Journal of Biological Chemistry, v. 276, n. 43, p. 39812-39818, 2001Tradução . . Acesso em: 23 out. 2025.
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      Tauhata, S. B. F., Santos, D. V. dos, Taylor, E. W., Mooseker, M. S., & Larson, R. E. (2001). High affinity binding of brain myosin-Va to F-action induced by calcium in the presençe of ATP. The Journal of Biological Chemistry, 276( 43), 39812-39818.
    • NLM

      Tauhata SBF, Santos DV dos, Taylor EW, Mooseker MS, Larson RE. High affinity binding of brain myosin-Va to F-action induced by calcium in the presençe of ATP. The Journal of Biological Chemistry. 2001 ; 276( 43): 39812-39818.[citado 2025 out. 23 ]
    • Vancouver

      Tauhata SBF, Santos DV dos, Taylor EW, Mooseker MS, Larson RE. High affinity binding of brain myosin-Va to F-action induced by calcium in the presençe of ATP. The Journal of Biological Chemistry. 2001 ; 276( 43): 39812-39818.[citado 2025 out. 23 ]
  • Source: The Journal of Biological Chemistry. Unidade: FM

    Assunto: MEDICINA

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      VEIGA, Sílvio S et al. Post-translational modifications of alfa5beta1 integrin by glycosaminoglycan chain: the alfa5beta1 integrin is a facultative proteoglycan. The Journal of Biological Chemistry, v. 272, n. 19, p. 12529-12535, 1997Tradução . . Acesso em: 23 out. 2025.
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      Veiga, S. S., Elias, M. C. Q. B., Gremski, W., Porcionatto, M. A., Silva, R. da, Nader, H. B., & Brentani, R. R. (1997). Post-translational modifications of alfa5beta1 integrin by glycosaminoglycan chain: the alfa5beta1 integrin is a facultative proteoglycan. The Journal of Biological Chemistry, 272( 19), 12529-12535.
    • NLM

      Veiga SS, Elias MCQB, Gremski W, Porcionatto MA, Silva R da, Nader HB, Brentani RR. Post-translational modifications of alfa5beta1 integrin by glycosaminoglycan chain: the alfa5beta1 integrin is a facultative proteoglycan. The Journal of Biological Chemistry. 1997 ; 272( 19): 12529-12535.[citado 2025 out. 23 ]
    • Vancouver

      Veiga SS, Elias MCQB, Gremski W, Porcionatto MA, Silva R da, Nader HB, Brentani RR. Post-translational modifications of alfa5beta1 integrin by glycosaminoglycan chain: the alfa5beta1 integrin is a facultative proteoglycan. The Journal of Biological Chemistry. 1997 ; 272( 19): 12529-12535.[citado 2025 out. 23 ]

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