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Artigo de periodico
Characterization of Gtf1p, the connector subunit of yeast mitochondrial tRNA-dependent amidotransferase (2011)
Barros, Mário Henrique de ; Rak, Malgorzata; Paulela, Janaina A.; Tzagoloff, Alexander
Source: The Journal of Biological Chemistry. Unidade: ICB
Assunto: MICROBIOLOGIA
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ABNT
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: 24 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. 24 ] 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. 24 ] Available from: https://doi.org/10.1074/jbc.M111.265371
Artigo de periodico
Analysis of intracellular substrates and products of thimet oligopeptidase in human embryonic kidney 293 cells (2009)
Berti, Denise Aparecida; Morano, Cain; Russo, Lilian Cristina; Castro, Leandro M.; Cunha, Fernanda M.; Zhang, Xin; Sironi, Juan; Klitzke, Clécio F.; Ferro, Emer Suavinho ; Fricker, Lloyd D.
Source: The Journal of Biological Chemistry. Unidade: ICB
Assunto: HISTOLOGIA
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ABNT
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: 24 out. 2025.
APA
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. 24 ]
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. 24 ]
Artigo de periodico
COX24 codes for a mitochondrial protein required for processing of the COX1 transcript (2006)
Barros, Mário Henrique de ; Myers, Alan M.; Driesche, Sarah Van; Tzagoloff, Alexander
Source: The Journal of Biological Chemistry. Unidade: ICB
Assunto: MICROBIOLOGIA
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ABNT
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: 24 out. 2025.
APA
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. 24 ]
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. 24 ]
Artigo de periodico
A solanesyl-diphosphate synthase localizes in glycosomes of Trypanosoma cruzi (2006)
Ferella, Marcela; Montalvetti, Andrea; Rohloff, Peter; Miranda, Kildare; Fang, Jianmin; Reina, Silvia; Kawamukai, Makoto; Búa, Jacqueline; Nilsson, Daniel; Pravia, Carlos; Katzin, Alejandro Miguel ; Cassera, Maria B.; Åslund, Lena; Andersson, Björn; Docampo, Roberto; Bontempi, Esteban J.
Source: The Journal of Biological Chemistry. Unidade: ICB
Assunto: PARASITOLOGIA
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ABNT
FERELLA, Marcela et al. A solanesyl-diphosphate synthase localizes in glycosomes of Trypanosoma cruzi. The Journal of Biological Chemistry, v. 281, n. 51, p. 39339-39348, 2006Tradução . . Acesso em: 24 out. 2025.
APA
Ferella, M., Montalvetti, A., Rohloff, P., Miranda, K., Fang, J., Reina, S., et al. (2006). A solanesyl-diphosphate synthase localizes in glycosomes of Trypanosoma cruzi. The Journal of Biological Chemistry, 281( 51), 39339-39348.
NLM
Ferella M, Montalvetti A, Rohloff P, Miranda K, Fang J, Reina S, Kawamukai M, Búa J, Nilsson D, Pravia C, Katzin AM, Cassera MB, Åslund L, Andersson B, Docampo R, Bontempi EJ. A solanesyl-diphosphate synthase localizes in glycosomes of Trypanosoma cruzi. The Journal of Biological Chemistry. 2006 ; 281( 51): 39339-39348.[citado 2025 out. 24 ]
Vancouver
Ferella M, Montalvetti A, Rohloff P, Miranda K, Fang J, Reina S, Kawamukai M, Búa J, Nilsson D, Pravia C, Katzin AM, Cassera MB, Åslund L, Andersson B, Docampo R, Bontempi EJ. A solanesyl-diphosphate synthase localizes in glycosomes of Trypanosoma cruzi. The Journal of Biological Chemistry. 2006 ; 281( 51): 39339-39348.[citado 2025 out. 24 ]
Artigo de periodico
Regulation of NAD(P)H oxidase by associated protein disulfide isomerase in vascular smooth muscle cells (2005)
Janiszewski, Mariano; Lopes, Lucia Rossetti ; Carmo, Alípio O.; Pedro, Marcelo A.; Brandes, Ralf P.; Santos, Célio X. C.; Laurindo, Francisco R. M.
Source: The Journal of Biological Chemistry. Unidade: ICB
Assunto: FARMACOLOGIA
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ABNT
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: 24 out. 2025.
APA
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. 24 ]
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. 24 ]
Artigo de periodico
The surface coat of the mammal-dwelling infective trypomastigote stage of Trypanosoma cruzi isformed by highly diverse immunogenic mucins (2004)
Buscaglia, Carlos A.; Campo, Vanina A.; Noia, Javier M. di; Torrecilhas, Ana C. T.; Marchi, Cláudia R. de; Ferguson, Michael A. J.; Frasch, Alberto C. C.; Almeida, Igor Correia de
Source: The Journal of Biological Chemistry. Unidade: ICB
Assunto: PARASITOLOGIA
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ABNT
BUSCAGLIA, Carlos A. et al. The surface coat of the mammal-dwelling infective trypomastigote stage of Trypanosoma cruzi isformed by highly diverse immunogenic mucins. The Journal of Biological Chemistry, v. 279, n. 16, p. 15860-15869, 2004Tradução . . Acesso em: 24 out. 2025.
APA
Buscaglia, C. A., Campo, V. A., Noia, J. M. di, Torrecilhas, A. C. T., Marchi, C. R. de, Ferguson, M. A. J., et al. (2004). The surface coat of the mammal-dwelling infective trypomastigote stage of Trypanosoma cruzi isformed by highly diverse immunogenic mucins. The Journal of Biological Chemistry, 279( 16), 15860-15869.
NLM
Buscaglia CA, Campo VA, Noia JM di, Torrecilhas ACT, Marchi CR de, Ferguson MAJ, Frasch ACC, Almeida IC de. The surface coat of the mammal-dwelling infective trypomastigote stage of Trypanosoma cruzi isformed by highly diverse immunogenic mucins. The Journal of Biological Chemistry. 2004 ; 279( 16): 15860-15869.[citado 2025 out. 24 ]
Vancouver
Buscaglia CA, Campo VA, Noia JM di, Torrecilhas ACT, Marchi CR de, Ferguson MAJ, Frasch ACC, Almeida IC de. The surface coat of the mammal-dwelling infective trypomastigote stage of Trypanosoma cruzi isformed by highly diverse immunogenic mucins. The Journal of Biological Chemistry. 2004 ; 279( 16): 15860-15869.[citado 2025 out. 24 ]
Artigo de periodico
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 (2004)
Gelamo, Emerson Luiz; Itri, Rosangela ; Tabak, Marcel
Source: The Journal of Biological Chemistry. Unidades: IQSC, IF
Subjects: BIOQUÍMICA, BIOLOGIA MOLECULAR
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ABNT
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: 24 out. 2025.
APA
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. 24 ]
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. 24 ]
Artigo de periodico
The surface coat of the mammal-dwelling infective trypomastigote stage of Trypanosoma cruzi is formed by highly diverse immunogenic mucins (2004)
Buscaglia, Carlos A.; Campo, Vanina A.; DI NOIA, JAVIER M.; Torrecilhas, Ana C. T.; Marchi, Claúdia R. De; Ferguson, Michael A. J.; Frasch, Alberto C. C.; Almeida, Igor C.
Source: The Journal of Biological Chemistry. Unidade: ICB
Assunto: PARASITOLOGIA
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ABNT
BUSCAGLIA, Carlos A. et al. The surface coat of the mammal-dwelling infective trypomastigote stage of Trypanosoma cruzi is formed by highly diverse immunogenic mucins. The Journal of Biological Chemistry, v. 279, p. 15860-15869, 2004Tradução . . Acesso em: 24 out. 2025.
APA
Buscaglia, C. A., Campo, V. A., DI NOIA, J. A. V. I. E. R. M., Torrecilhas, A. C. T., Marchi, C. R. D., Ferguson, M. A. J., et al. (2004). The surface coat of the mammal-dwelling infective trypomastigote stage of Trypanosoma cruzi is formed by highly diverse immunogenic mucins. The Journal of Biological Chemistry, 279, 15860-15869.
NLM
Buscaglia CA, Campo VA, DI NOIA JAVIERM, Torrecilhas ACT, Marchi CRD, Ferguson MAJ, Frasch ACC, Almeida IC. The surface coat of the mammal-dwelling infective trypomastigote stage of Trypanosoma cruzi is formed by highly diverse immunogenic mucins. The Journal of Biological Chemistry. 2004 ; 279 15860-15869.[citado 2025 out. 24 ]
Vancouver
Buscaglia CA, Campo VA, DI NOIA JAVIERM, Torrecilhas ACT, Marchi CRD, Ferguson MAJ, Frasch ACC, Almeida IC. The surface coat of the mammal-dwelling infective trypomastigote stage of Trypanosoma cruzi is formed by highly diverse immunogenic mucins. The Journal of Biological Chemistry. 2004 ; 279 15860-15869.[citado 2025 out. 24 ]
Artigo de periodico
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 (2004)
Luo, Shuhong; Rohloff, Peter; Cox, Joanna; Uyemura, Sérgio Akira; Docampo, Roberto
Source: The Journal of Biological Chemistry. Unidade: FCFRP
Assunto: BIOQUÍMICA
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ABNT
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: 24 out. 2025.
APA
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. 24 ]
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. 24 ]
Artigo de periodico
Oxidative phosphorylation and rotenone-insensitive malate- and NADH-quinone oxidoreductases in Plasmodium yoelii yoelii mitocondria in situ (2004)
Uyemura, Sérgio Akira; Luo, Shuhong; Vieira, Maurício; Moreno, Silvia N. J.; Docampo, Roberto
Source: The Journal of Biological Chemistry. Unidade: FCFRP
Assunto: BIOQUÍMICA
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ABNT
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: 24 out. 2025.
APA
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. 24 ]
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. 24 ]
Artigo de periodico
The methylerythritol phosphate pathway is functionally active in all intraerythrocytic stages of Plasmodium falciparum (2004)
Cassera, María B.; Gozzo, Fabio C.; D'Alexandri, Fabio L.; Merino, Emilio F.; del Portillo, Hernando Antonio; Peres, Valnice J.; Almeida, Igor Correia de; Eberlin, Marcos N.; Wunderlich, Gerhard ; Wiesner, Jochen; Jomaa, Hassan; Kimura, Emilia A.; Katzin, Alejandro Miguel
Source: The Journal of Biological Chemistry. Unidade: ICB
Assunto: PARASITOLOGIA
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ABNT
CASSERA, María B. et al. The methylerythritol phosphate pathway is functionally active in all intraerythrocytic stages of Plasmodium falciparum. The Journal of Biological Chemistry, v. 279, n. 50, p. 51749-51759, 2004Tradução . . Acesso em: 24 out. 2025.
APA
Cassera, M. B., Gozzo, F. C., D'Alexandri, F. L., Merino, E. F., del Portillo, H. A., Peres, V. J., et al. (2004). The methylerythritol phosphate pathway is functionally active in all intraerythrocytic stages of Plasmodium falciparum. The Journal of Biological Chemistry, 279( 50), 51749-51759.
NLM
Cassera MB, Gozzo FC, D'Alexandri FL, Merino EF, del Portillo HA, Peres VJ, Almeida IC de, Eberlin MN, Wunderlich G, Wiesner J, Jomaa H, Kimura EA, Katzin AM. The methylerythritol phosphate pathway is functionally active in all intraerythrocytic stages of Plasmodium falciparum. The Journal of Biological Chemistry. 2004 ; 279( 50): 51749-51759.[citado 2025 out. 24 ]
Vancouver
Cassera MB, Gozzo FC, D'Alexandri FL, Merino EF, del Portillo HA, Peres VJ, Almeida IC de, Eberlin MN, Wunderlich G, Wiesner J, Jomaa H, Kimura EA, Katzin AM. The methylerythritol phosphate pathway is functionally active in all intraerythrocytic stages of Plasmodium falciparum. The Journal of Biological Chemistry. 2004 ; 279( 50): 51749-51759.[citado 2025 out. 24 ]
Artigo de periodico
Free human mitochondrial GrpE is a symmetric dimer in solution (2003)
Borges, Julio Cesar ; Fischer, Hannes; Craievich, Aldo Felix; Hansen, Lee D.; Ramos, Carlos H. I.
Source: The Journal of Biological Chemistry. Unidade: IF
Subjects: BIOLOGIA MOLECULAR, BIOLOGIA CELULAR, BIOQUÍMICA
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ABNT
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: 24 out. 2025.
APA
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. 24 ] 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. 24 ] Available from: http://intl.jbc.org/cgi/reprint/278/37/35337.pdf
Artigo de periodico
Opposite effects of glucose on plasma membrane Ca2+ - ATPase and Na/Ca exchanger transcription, expression, and activity in rat pancreatic beta-cell (2003)
Ximenes, Helena Maria; Kamagate, Adama; Eylen, Françoise Van; Herchuelz, André; Carpinelli, Angelo Rafael
Source: The Journal of Biological Chemistry. Unidade: ICB
Assunto: FISIOLOGIA
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ABNT
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: 24 out. 2025.
APA
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. 24 ]
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. 24 ]
Artigo de periodico
Endocytic intermediates involved with the intracellular trafficking of a fluorescent cellular prion protein (2002)
Magalhães, Ana C.; Silva, Juliana A.; Lee, Kil S.; Martins, Vilma Regina; Prado, Vania F.; Ferguson, Stephen S. G.; Gomez, Marcus V.; Brentani, Ricardo R.; Prado, Marco A. M.
Source: The Journal of Biological Chemistry. Unidade: FM
Assunto: BIOQUÍMICA
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ABNT
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: 24 out. 2025.
APA
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. 24 ]
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. 24 ]
Artigo de periodico
DNA converts cellular prion protein into the beta-sheet conformation and inhibits prion peptide aggregation (2002)
Cordeiro, Yraima; Machado, Filipe; Juliano, Luiz; Juliano, Maria Aparecida; Foguel, Débora; Silva, Jerson L.; Brentani, Ricardo R.
Source: The Journal of Biological Chemistry. Unidade: FM
Subjects: BIOQUÍMICA, DNA
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ABNT
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: 24 out. 2025.
APA
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. 24 ]
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. 24 ]
Artigo de periodico
Dermaseptins from Phyllomedusa oreads and Phyllomedusa distincta (2002)
Brandt, Guillermo; Leite, J. R. S. A.; Silva, Luciano P.; Albuquerque, Sérgio de; Prates, Maura V.; Azevedo, Ricardo A. Azevedo; Carregaro, Vanessa; Silva, João Santana da; Sá, Vanuza C. L.; Brandão, Ruber; Bloch Junior, Carlos
Source: The Journal of Biological Chemistry. Unidades: FCFRP, FMRP
Assunto: BIOLOGIA CELULAR
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ABNT
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: 24 out. 2025.
APA
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. 24 ]
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. 24 ]
Artigo de periodico
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 (2002)
Kawaguchi, Mio; Onuchic, Luiz Fernando; Huang, Shau-Ku
Source: The Journal of Biological Chemistry. Unidade: FM
Assunto: BIOLOGIA MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 24 out. 2025.
APA
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. 24 ]
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. 24 ]
Artigo de periodico
Trialysin a novel pore-forming protein from saliva of hematophagous insects activated by limited proteolysis (2002)
Amino, Rogerio; Martins, Rafael Miyazawa; Procópio, Joaquim; Hirata, Izaura Yoshico; Juliano, Maria Aparecida; Schenkman, Sergio
Source: The Journal of Biological Chemistry. Unidade: ICB
Assunto: FISIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 24 out. 2025.
APA
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. 24 ]
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. 24 ]
Artigo de periodico
High affinity binding of brain myosin-Va to F-action induced by calcium in the presençe of ATP (2001)
Tauhata, Sinji Borges Ferreira; Santos, Daniela Vital dos; Taylor, Edwin Windle; Mooseker, Mark S.; Larson, Roy Edward
Source: The Journal of Biological Chemistry. Unidade: FMRP
Subjects: MIOSINA, BIOLOGIA CELULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 24 out. 2025.
APA
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. 24 ]
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. 24 ]
Artigo de periodico
Post-translational modifications of alfa5beta1 integrin by glycosaminoglycan chain: the alfa5beta1 integrin is a facultative proteoglycan (1997)
Veiga, Sílvio S; Elias, Maria Carolina Q B; Gremski, Waldemiro; Porcionatto, Marimélia A; Silva, Roseli da; Nader, Helena B; Brentani, Ricardo Renzo
Source: The Journal of Biological Chemistry. Unidade: FM
Assunto: MEDICINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 24 out. 2025.
APA
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. 24 ]
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. 24 ]

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