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Artigo de periodico
NTAL is associated with treatment outcome, cell proliferation and differentiation in acute promyelocytic leukemia (2020)
Thomé, Carolina Hassibe ; Ferreira, Germano Aguiar ; Martins, Diego Antonio Pereira ; Santos, Guilherme Augusto dos; Ortiz, César Alexander; Souza, Lucas Eduardo Botelho de ; Sobral, Lays Martins; Silva, Cleide Lúcia Araújo; Scheucher, Priscila Santos ; Gil, Cristiane Damas; Leopoldino, Andréia Machado ; Silveira, Douglas Rafaele Almeida ; Silva, Juan Luiz Coelho da ; Traina, Fabiola ; Koury, Luisa C.; Melo, Raul A. M.; Bittencourt, Rosane; Pagnano, Katia; Pasquini, Ricardo; Nunes, Elenaide C.; Fagundes, Evandro M.; Gloria, Ana Beatriz F.; kerbauy, Fábio Rodrigues; Chauffaille, Maria de Lourdes; Keating, Armand; Tallman, Martin S.; Ribeiro, Raul C.; Dillon, Richard; Ganser, Arnold; Löwenberg, Bob; Valk, Peter; Lo-Coco, Francesco; Sanz, Miguel A.; Berliner, Nancy; Faça, Vitor Marcel ; Rego, Eduardo Magalhaes
Source: Scientific Reports. Unidades: FMRP, FCFRP, FM
Subjects: PROTEÍNAS, TRANSDUÇÃO DE SINAL CELULAR, QUIMIOTERAPIA, ANTINEOPLÁSICOS, MEDULA ÓSSEA, DIFERENCIAÇÃO CELULAR, SOBREVIVÊNCIA CELULAR, LEUCEMIA, FARMACOTERAPIA, ANÁLISE DE SOBREVIVÊNCIA, ESTUDOS RETROSPECTIVOS
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THOMÉ, Carolina Hassibe et al. NTAL is associated with treatment outcome, cell proliferation and differentiation in acute promyelocytic leukemia. Scientific Reports, v. 10, n. 1, 2020Tradução . . Disponível em: https://doi.org/10.1038/s41598-020-66223-2. Acesso em: 24 jun. 2024.
APA
Thomé, C. H., Ferreira, G. A., Martins, D. A. P., Santos, G. A. dos, Ortiz, C. A., Souza, L. E. B. de, et al. (2020). NTAL is associated with treatment outcome, cell proliferation and differentiation in acute promyelocytic leukemia. Scientific Reports, 10( 1). doi:10.1038/s41598-020-66223-2
NLM
Thomé CH, Ferreira GA, Martins DAP, Santos GA dos, Ortiz CA, Souza LEB de, Sobral LM, Silva CLA, Scheucher PS, Gil CD, Leopoldino AM, Silveira DRA, Silva JLC da, Traina F, Koury LC, Melo RAM, Bittencourt R, Pagnano K, Pasquini R, Nunes EC, Fagundes EM, Gloria ABF, kerbauy FR, Chauffaille M de L, Keating A, Tallman MS, Ribeiro RC, Dillon R, Ganser A, Löwenberg B, Valk P, Lo-Coco F, Sanz MA, Berliner N, Faça VM, Rego EM. NTAL is associated with treatment outcome, cell proliferation and differentiation in acute promyelocytic leukemia [Internet]. Scientific Reports. 2020 ; 10( 1):[citado 2024 jun. 24 ] Available from: https://doi.org/10.1038/s41598-020-66223-2
Vancouver
Thomé CH, Ferreira GA, Martins DAP, Santos GA dos, Ortiz CA, Souza LEB de, Sobral LM, Silva CLA, Scheucher PS, Gil CD, Leopoldino AM, Silveira DRA, Silva JLC da, Traina F, Koury LC, Melo RAM, Bittencourt R, Pagnano K, Pasquini R, Nunes EC, Fagundes EM, Gloria ABF, kerbauy FR, Chauffaille M de L, Keating A, Tallman MS, Ribeiro RC, Dillon R, Ganser A, Löwenberg B, Valk P, Lo-Coco F, Sanz MA, Berliner N, Faça VM, Rego EM. NTAL is associated with treatment outcome, cell proliferation and differentiation in acute promyelocytic leukemia [Internet]. Scientific Reports. 2020 ; 10( 1):[citado 2024 jun. 24 ] Available from: https://doi.org/10.1038/s41598-020-66223-2
Artigo de periodico
The Aspergillus fumigatus transcription factor RglT is important for gliotoxin biosynthesis and self-protection, and virulence (2020)
Ries, Laure Nicolas Annick ; Pardeshi, Lakhansing; Dong, Zhiqiang; Tan, Kaeling; Steenwyk, Jacob L.; Colabardini, Ana Cristina ; Ferreira Filho, Jaire Alves ; Silva, Patrícia Alves de Castro ; Silva, Lilian Pereira; Preite, Nycolas W.; Almeida, Fausto Bruno dos Reis ; Assis, Leandro José de ; Santos, Renato A. C. dos; Bowyer, Paul; Bromley, Michael; Owens, Rebecca A.; Doyle, Sean; Demasi, Marilene; Rodríguez-Hernández, Diego Carlos ; Netto, Luis Eduardo Soares ; Pupo, Monica Tallarico ; Rokas, Antonis; Loures, Flavio V.; Wong, Koon H.; Goldman, Gustavo Henrique
Source: PLOS Pathogens. Unidades: FMRP, IQ, IB, FCFRP
Subjects: ASPERGILLUS, ESTRESSE OXIDATIVO, EXPRESSÃO GÊNICA, REGULAÇÃO GÊNICA, MACRÓFAGOS, FATORES DE TRANSCRIÇÃO, VIRULÊNCIA, MICOTOXINAS
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RIES, Laure Nicolas Annick et al. The Aspergillus fumigatus transcription factor RglT is important for gliotoxin biosynthesis and self-protection, and virulence. PLOS Pathogens, v. 16, n. 7, p. 1-29, 2020Tradução . . Disponível em: https://doi.org/10.1371/journal.ppat.1008645. Acesso em: 24 jun. 2024.
APA
Ries, L. N. A., Pardeshi, L., Dong, Z., Tan, K., Steenwyk, J. L., Colabardini, A. C., et al. (2020). The Aspergillus fumigatus transcription factor RglT is important for gliotoxin biosynthesis and self-protection, and virulence. PLOS Pathogens, 16( 7), 1-29. doi:10.1371/journal.ppat.1008645
NLM
Ries LNA, Pardeshi L, Dong Z, Tan K, Steenwyk JL, Colabardini AC, Ferreira Filho JA, Silva PA de C, Silva LP, Preite NW, Almeida FB dos R, Assis LJ de, Santos RAC dos, Bowyer P, Bromley M, Owens RA, Doyle S, Demasi M, Rodríguez-Hernández DC, Netto LES, Pupo MT, Rokas A, Loures FV, Wong KH, Goldman GH. The Aspergillus fumigatus transcription factor RglT is important for gliotoxin biosynthesis and self-protection, and virulence [Internet]. PLOS Pathogens. 2020 ; 16( 7): 1-29.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1371/journal.ppat.1008645
Vancouver
Ries LNA, Pardeshi L, Dong Z, Tan K, Steenwyk JL, Colabardini AC, Ferreira Filho JA, Silva PA de C, Silva LP, Preite NW, Almeida FB dos R, Assis LJ de, Santos RAC dos, Bowyer P, Bromley M, Owens RA, Doyle S, Demasi M, Rodríguez-Hernández DC, Netto LES, Pupo MT, Rokas A, Loures FV, Wong KH, Goldman GH. The Aspergillus fumigatus transcription factor RglT is important for gliotoxin biosynthesis and self-protection, and virulence [Internet]. PLOS Pathogens. 2020 ; 16( 7): 1-29.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1371/journal.ppat.1008645
Artigo de periodico
Activation of the kinin B1 receptor by its agonist reduces melanoma metastasis by playing a dual effect on tumor cells and host immune response (2019)
Maria, Andrea Gutierrez; Dillemburg-Pilla, Patrícia; Durand, Marina de Toledo ; Floriano, Elaine Medeiros; Manfiolli, Adriana Oliveira ; Ramos, Simone Gusmão ; Pesquero, João Bosco ; Nahmias, Clara ; Costa Neto, Claudio Miguel da
Source: Frontiers in Pharmacology. Unidades: FMRP, ICB
Subjects: MELANOMA, SISTEMA IMUNE, INFLAMAÇÃO, METÁSTASE NEOPLÁSICA
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MARIA, Andrea Gutierrez et al. Activation of the kinin B1 receptor by its agonist reduces melanoma metastasis by playing a dual effect on tumor cells and host immune response. Frontiers in Pharmacology, v. 10, n. 11, p. [13] , 2019Tradução . . Disponível em: https://doi.org/10.3389/fphar.2019.01106. Acesso em: 24 jun. 2024.
APA
Maria, A. G., Dillemburg-Pilla, P., Durand, M. de T., Floriano, E. M., Manfiolli, A. O., Ramos, S. G., et al. (2019). Activation of the kinin B1 receptor by its agonist reduces melanoma metastasis by playing a dual effect on tumor cells and host immune response. Frontiers in Pharmacology, 10( 11), [13] . doi:10.3389/fphar.2019.01106
NLM
Maria AG, Dillemburg-Pilla P, Durand M de T, Floriano EM, Manfiolli AO, Ramos SG, Pesquero JB, Nahmias C, Costa Neto CM da. Activation of the kinin B1 receptor by its agonist reduces melanoma metastasis by playing a dual effect on tumor cells and host immune response [Internet]. Frontiers in Pharmacology. 2019 ; 10( 11): [13] .[citado 2024 jun. 24 ] Available from: https://doi.org/10.3389/fphar.2019.01106
Vancouver
Maria AG, Dillemburg-Pilla P, Durand M de T, Floriano EM, Manfiolli AO, Ramos SG, Pesquero JB, Nahmias C, Costa Neto CM da. Activation of the kinin B1 receptor by its agonist reduces melanoma metastasis by playing a dual effect on tumor cells and host immune response [Internet]. Frontiers in Pharmacology. 2019 ; 10( 11): [13] .[citado 2024 jun. 24 ] Available from: https://doi.org/10.3389/fphar.2019.01106
Artigo de periodico
Host kinin B1 receptor plays a protective role against melanoma progression (2016)
Maria, Andrea G.; Dillenburg-Pilla, Patricia; Reis, Rosana I.; Floriano, Elaine M.; Tefé-Silva, Cristiane; Ramos, Simone Gusmão; Pesquero, João Bosco; Nahmias, Clara; Costa Neto, Cláudio Miguel
Source: Scientific Reports. Unidade: FMRP
Subjects: MELANOMA, CININAS, CALICREINA, PROGNÓSTICO
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MARIA, Andrea G. et al. Host kinin B1 receptor plays a protective role against melanoma progression. Scientific Reports, v. 6, 2016Tradução . . Disponível em: https://doi.org/10.1038/srep22078. Acesso em: 24 jun. 2024.
APA
Maria, A. G., Dillenburg-Pilla, P., Reis, R. I., Floriano, E. M., Tefé-Silva, C., Ramos, S. G., et al. (2016). Host kinin B1 receptor plays a protective role against melanoma progression. Scientific Reports, 6. doi:10.1038/srep22078
NLM
Maria AG, Dillenburg-Pilla P, Reis RI, Floriano EM, Tefé-Silva C, Ramos SG, Pesquero JB, Nahmias C, Costa Neto CM. Host kinin B1 receptor plays a protective role against melanoma progression [Internet]. Scientific Reports. 2016 ; 6[citado 2024 jun. 24 ] Available from: https://doi.org/10.1038/srep22078
Vancouver
Maria AG, Dillenburg-Pilla P, Reis RI, Floriano EM, Tefé-Silva C, Ramos SG, Pesquero JB, Nahmias C, Costa Neto CM. Host kinin B1 receptor plays a protective role against melanoma progression [Internet]. Scientific Reports. 2016 ; 6[citado 2024 jun. 24 ] Available from: https://doi.org/10.1038/srep22078
Artigo de periodico
Synthesis and biological evaluation of novel antihypertensive compounds (2016)
Ronchi, Fernanda A.; Fernandes, Adriana B.; Reis, Rosana I.; Mendes, Lys A. F.; Robello, Luis G.; Huber, Paula C.; Baraldi, Patricia T.; Marques, Ricardo V.; Costa Neto, Cláudio Miguel; Casarini, Dulce E.
Source: Open Chemistry Journal. Unidade: FMRP
Subjects: PRESSÃO SANGUÍNEA, HIPERTENSÃO, SISTEMA RENINA-ANGIOTENSINA, RECEPTORES
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RONCHI, Fernanda A. et al. Synthesis and biological evaluation of novel antihypertensive compounds. Open Chemistry Journal, v. 3, p. 56-68, 2016Tradução . . Disponível em: https://doi.org/10.2174/1874842201603010056. Acesso em: 24 jun. 2024.
APA
Ronchi, F. A., Fernandes, A. B., Reis, R. I., Mendes, L. A. F., Robello, L. G., Huber, P. C., et al. (2016). Synthesis and biological evaluation of novel antihypertensive compounds. Open Chemistry Journal, 3, 56-68. doi:10.2174/1874842201603010056
NLM
Ronchi FA, Fernandes AB, Reis RI, Mendes LAF, Robello LG, Huber PC, Baraldi PT, Marques RV, Costa Neto CM, Casarini DE. Synthesis and biological evaluation of novel antihypertensive compounds [Internet]. Open Chemistry Journal. 2016 ; 3 56-68.[citado 2024 jun. 24 ] Available from: https://doi.org/10.2174/1874842201603010056
Vancouver
Ronchi FA, Fernandes AB, Reis RI, Mendes LAF, Robello LG, Huber PC, Baraldi PT, Marques RV, Costa Neto CM, Casarini DE. Synthesis and biological evaluation of novel antihypertensive compounds [Internet]. Open Chemistry Journal. 2016 ; 3 56-68.[citado 2024 jun. 24 ] Available from: https://doi.org/10.2174/1874842201603010056
Artigo de periodico-carta/editorial
Highlight [Editorial]: Kinin 2015 at São Paulo, Brazil (2016)
Buck, Hudson Sousa; Calixto, João Batista; Pesquero, João Bosco; Campos, Maria Martha; Viel, Tânia Araújo; Costa Neto, Cláudio Miguel
Source: Biological Chemistry. Unidades: EACH, FMRP
Subjects: CININAS, RECEPTORES
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ABNT
BUCK, Hudson Sousa et al. Highlight [Editorial]: Kinin 2015 at São Paulo, Brazil. Biological Chemistry. Berlin: Escola de Artes, Ciências e Humanidades, Universidade de São Paulo. Disponível em: https://doi.org/10.1515/hsz-2016-0115. Acesso em: 24 jun. 2024. , 2016
APA
Buck, H. S., Calixto, J. B., Pesquero, J. B., Campos, M. M., Viel, T. A., & Costa Neto, C. M. (2016). Highlight [Editorial]: Kinin 2015 at São Paulo, Brazil. Biological Chemistry. Berlin: Escola de Artes, Ciências e Humanidades, Universidade de São Paulo. doi:10.1515/hsz-2016-0115
NLM
Buck HS, Calixto JB, Pesquero JB, Campos MM, Viel TA, Costa Neto CM. Highlight [Editorial]: Kinin 2015 at São Paulo, Brazil [Internet]. Biological Chemistry. 2016 ; 397( 4): 281–282.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1515/hsz-2016-0115
Vancouver
Buck HS, Calixto JB, Pesquero JB, Campos MM, Viel TA, Costa Neto CM. Highlight [Editorial]: Kinin 2015 at São Paulo, Brazil [Internet]. Biological Chemistry. 2016 ; 397( 4): 281–282.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1515/hsz-2016-0115
Artigo de periodico
Anthelmintic effects of a cationic toxin from a South American rattlesnake venom (2016)
Dal Mas, Caroline; Moreira, J. T.; Pinto, S.; Monte, G. G.; Nering, M. B.; Oliveira, Eduardo Brandt de; Gazarini, Marcos L.; Mori, M. A.; Hayashi, M. A. F.
Source: Toxicon. Unidade: FMRP
Subjects: CANDIDA ALBICANS, VENENOS DE ORIGEM ANIMAL, SERPENTES
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DAL MAS, Caroline et al. Anthelmintic effects of a cationic toxin from a South American rattlesnake venom. Toxicon, v. 116, p. 49-55, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.toxicon.2015.11.021. Acesso em: 24 jun. 2024.
APA
Dal Mas, C., Moreira, J. T., Pinto, S., Monte, G. G., Nering, M. B., Oliveira, E. B. de, et al. (2016). Anthelmintic effects of a cationic toxin from a South American rattlesnake venom. Toxicon, 116, 49-55. doi:10.1016/j.toxicon.2015.11.021
NLM
Dal Mas C, Moreira JT, Pinto S, Monte GG, Nering MB, Oliveira EB de, Gazarini ML, Mori MA, Hayashi MAF. Anthelmintic effects of a cationic toxin from a South American rattlesnake venom [Internet]. Toxicon. 2016 ; 116 49-55.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1016/j.toxicon.2015.11.021
Vancouver
Dal Mas C, Moreira JT, Pinto S, Monte GG, Nering MB, Oliveira EB de, Gazarini ML, Mori MA, Hayashi MAF. Anthelmintic effects of a cationic toxin from a South American rattlesnake venom [Internet]. Toxicon. 2016 ; 116 49-55.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1016/j.toxicon.2015.11.021
Artigo de periodico
Inhibition of malaria parasite Plasmodium falciparum development by crotamine, a cell penetrating peptide from the snake venom (2016)
El Chamy Maluf, S.; Dal Mas, Caroline; Oliveira, Eduardo Brandt de; Melo, P. M.; Carmona, Adriana Karaoglanovic; Gazarini, Marcos L.; Hayashi, M. A. F.
Source: Peptides. Unidade: FMRP
Subjects: PLASMODIUM FALCIPARUM, ANTIMALÁRICOS, CROMATINA, PEPTÍDEOS, VENENOS DE ORIGEM ANIMAL, SERPENTES
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ABNT
EL CHAMY MALUF, S. et al. Inhibition of malaria parasite Plasmodium falciparum development by crotamine, a cell penetrating peptide from the snake venom. Peptides, v. 78, p. 11-16, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.peptides.2016.01.013. Acesso em: 24 jun. 2024.
APA
El Chamy Maluf, S., Dal Mas, C., Oliveira, E. B. de, Melo, P. M., Carmona, A. K., Gazarini, M. L., & Hayashi, M. A. F. (2016). Inhibition of malaria parasite Plasmodium falciparum development by crotamine, a cell penetrating peptide from the snake venom. Peptides, 78, 11-16. doi:10.1016/j.peptides.2016.01.013
NLM
El Chamy Maluf S, Dal Mas C, Oliveira EB de, Melo PM, Carmona AK, Gazarini ML, Hayashi MAF. Inhibition of malaria parasite Plasmodium falciparum development by crotamine, a cell penetrating peptide from the snake venom [Internet]. Peptides. 2016 ; 78 11-16.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1016/j.peptides.2016.01.013
Vancouver
El Chamy Maluf S, Dal Mas C, Oliveira EB de, Melo PM, Carmona AK, Gazarini ML, Hayashi MAF. Inhibition of malaria parasite Plasmodium falciparum development by crotamine, a cell penetrating peptide from the snake venom [Internet]. Peptides. 2016 ; 78 11-16.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1016/j.peptides.2016.01.013
Artigo de periodico
Leucine supplementation does not affect protein turnover and impairs the beneficial effects of endurance training on glucose homeostasis in healthy mice (2015)
Costa-Júnior, José M.; Rosa, Morgana R.; Protzek, André O. P.; Paula, Flávia M.; Ferreira, Sandra M.; Rezende, Luiz Fernando; Vanzela, Emerielle C.; Zoppi, Claudio Cesar; Silveira, Leonardo dos Reis; Kettelhut, Isis do Carmo; Boschero, Antonio C.; Oliveira, Camila A. M.; Carneiro, Everardo M.
Source: Amino Acids. Unidades: EEFERP, FMRP
Subjects: HOMEOSTASE, TREINAMENTO FÍSICO, PROTEÍNAS, GLICOSE, MÚSCULO ESQUELÉTICO
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ABNT
COSTA-JÚNIOR, José M. et al. Leucine supplementation does not affect protein turnover and impairs the beneficial effects of endurance training on glucose homeostasis in healthy mice. Amino Acids, v. 47, n. 4, p. 745-755, 2015Tradução . . Disponível em: https://doi.org/10.1007/s00726-014-1903-z. Acesso em: 24 jun. 2024.
APA
Costa-Júnior, J. M., Rosa, M. R., Protzek, A. O. P., Paula, F. M., Ferreira, S. M., Rezende, L. F., et al. (2015). Leucine supplementation does not affect protein turnover and impairs the beneficial effects of endurance training on glucose homeostasis in healthy mice. Amino Acids, 47( 4), 745-755. doi:10.1007/s00726-014-1903-z
NLM
Costa-Júnior JM, Rosa MR, Protzek AOP, Paula FM, Ferreira SM, Rezende LF, Vanzela EC, Zoppi CC, Silveira L dos R, Kettelhut I do C, Boschero AC, Oliveira CAM, Carneiro EM. Leucine supplementation does not affect protein turnover and impairs the beneficial effects of endurance training on glucose homeostasis in healthy mice [Internet]. Amino Acids. 2015 ; 47( 4): 745-755.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1007/s00726-014-1903-z
Vancouver
Costa-Júnior JM, Rosa MR, Protzek AOP, Paula FM, Ferreira SM, Rezende LF, Vanzela EC, Zoppi CC, Silveira L dos R, Kettelhut I do C, Boschero AC, Oliveira CAM, Carneiro EM. Leucine supplementation does not affect protein turnover and impairs the beneficial effects of endurance training on glucose homeostasis in healthy mice [Internet]. Amino Acids. 2015 ; 47( 4): 745-755.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1007/s00726-014-1903-z
Artigo de periodico
Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion (2015)
Campo, Vanessa Leiria; Ivanova, Irina M.; Carvalho, Ivone; Lopes, Carla Duque; Carneiro, Zumira, A.; Saalbach, Gerhard; Schenkman, Sérgio; Silva, João Santana da; Nepogodiev, Sergey A.; Field, Robert A.
Source: Tetrahedron. Unidades: FCFRP, FMRP
Subjects: TRIPANOSSOMICIDAS, TRYPANOSOMA CRUZI, MACRÓFAGOS
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ABNT
CAMPO, Vanessa Leiria et al. Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion. Tetrahedron, v. 71, n. 39, p. 7344–7353, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2015.04.085. Acesso em: 24 jun. 2024.
APA
Campo, V. L., Ivanova, I. M., Carvalho, I., Lopes, C. D., Carneiro, Z., Saalbach, G., et al. (2015). Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion. Tetrahedron, 71( 39), 7344–7353. doi:10.1016/j.tet.2015.04.085
NLM
Campo VL, Ivanova IM, Carvalho I, Lopes CD, Carneiro Z, Saalbach G, Schenkman S, Silva JS da, Nepogodiev SA, Field RA. Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion [Internet]. Tetrahedron. 2015 ; 71( 39): 7344–7353.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1016/j.tet.2015.04.085
Vancouver
Campo VL, Ivanova IM, Carvalho I, Lopes CD, Carneiro Z, Saalbach G, Schenkman S, Silva JS da, Nepogodiev SA, Field RA. Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion [Internet]. Tetrahedron. 2015 ; 71( 39): 7344–7353.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1016/j.tet.2015.04.085
Artigo de periodico
Molecular characterization of trypanosoma cruzi Tc8.2 gene indicates two differential locations for the encoded protein in epimastigote and trypomastigote forms (2015)
Kian, Danielle; Lancheros, César Armando Contreras; Damiani, Igor Alexandre Campos; Fernandes, Tamiris Zanforlin Olmos; Pinge-Filho, Phileno; Santos, Márcia Regina Machado dos; Silveira, José Franco da; Nakamura, Celso Vataru; Silva, João Santana da; Yamada-Ogatta, Sueli Fumie; Yamauchi, Lucy Megumi
Source: Korean Journal of Parasitology. Unidade: FMRP
Subjects: TRYPANOSOMA CRUZI, DOENÇAS DE CHAGAS, EXPRESSÃO GÊNICA, GENÉTICA
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ABNT
KIAN, Danielle et al. Molecular characterization of trypanosoma cruzi Tc8.2 gene indicates two differential locations for the encoded protein in epimastigote and trypomastigote forms. Korean Journal of Parasitology, v. 53, n. 4, p. 483-488, 2015Tradução . . Disponível em: https://doi.org/10.3347/kjp.2015.53.4.483. Acesso em: 24 jun. 2024.
APA
Kian, D., Lancheros, C. A. C., Damiani, I. A. C., Fernandes, T. Z. O., Pinge-Filho, P., Santos, M. R. M. dos, et al. (2015). Molecular characterization of trypanosoma cruzi Tc8.2 gene indicates two differential locations for the encoded protein in epimastigote and trypomastigote forms. Korean Journal of Parasitology, 53( 4), 483-488. doi:10.3347/kjp.2015.53.4.483
NLM
Kian D, Lancheros CAC, Damiani IAC, Fernandes TZO, Pinge-Filho P, Santos MRM dos, Silveira JF da, Nakamura CV, Silva JS da, Yamada-Ogatta SF, Yamauchi LM. Molecular characterization of trypanosoma cruzi Tc8.2 gene indicates two differential locations for the encoded protein in epimastigote and trypomastigote forms [Internet]. Korean Journal of Parasitology. 2015 ; 53( 4): 483-488.[citado 2024 jun. 24 ] Available from: https://doi.org/10.3347/kjp.2015.53.4.483
Vancouver
Kian D, Lancheros CAC, Damiani IAC, Fernandes TZO, Pinge-Filho P, Santos MRM dos, Silveira JF da, Nakamura CV, Silva JS da, Yamada-Ogatta SF, Yamauchi LM. Molecular characterization of trypanosoma cruzi Tc8.2 gene indicates two differential locations for the encoded protein in epimastigote and trypomastigote forms [Internet]. Korean Journal of Parasitology. 2015 ; 53( 4): 483-488.[citado 2024 jun. 24 ] Available from: https://doi.org/10.3347/kjp.2015.53.4.483
Artigo de periodico
Interaction of the rattlesnake toxin crotamine with model membranes (2014)
Costa, Bruno A.; Dal Mas, Caroline; Hayashi, Mirian A. F.; Sanches, Leonardo; Oguiura, Nancy; Bizerra, Fernando; Oliveira, Eduardo B.; Perez, Katia Regina; Gomide, Andreza Barbosa; Itri, Rosangela
Source: JOURNAL OF PHYSICAL CHEMISTRY B. Unidades: IF, FMRP
Subjects: MEMBRANAS (BIOLOGIA), VENENOS DE ORIGEM ANIMAL
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ABNT
COSTA, Bruno A. et al. Interaction of the rattlesnake toxin crotamine with model membranes. JOURNAL OF PHYSICAL CHEMISTRY B, v. 118, n. 20, p. 5471-5479, 2014Tradução . . Disponível em: https://doi.org/10.1021/jp411886u. Acesso em: 24 jun. 2024.
APA
Costa, B. A., Dal Mas, C., Hayashi, M. A. F., Sanches, L., Oguiura, N., Bizerra, F., et al. (2014). Interaction of the rattlesnake toxin crotamine with model membranes. JOURNAL OF PHYSICAL CHEMISTRY B, 118( 20), 5471-5479. doi:10.1021/jp411886u
NLM
Costa BA, Dal Mas C, Hayashi MAF, Sanches L, Oguiura N, Bizerra F, Oliveira EB, Perez KR, Gomide AB, Itri R. Interaction of the rattlesnake toxin crotamine with model membranes [Internet]. JOURNAL OF PHYSICAL CHEMISTRY B. 2014 ; 118( 20): 5471-5479.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1021/jp411886u
Vancouver
Costa BA, Dal Mas C, Hayashi MAF, Sanches L, Oguiura N, Bizerra F, Oliveira EB, Perez KR, Gomide AB, Itri R. Interaction of the rattlesnake toxin crotamine with model membranes [Internet]. JOURNAL OF PHYSICAL CHEMISTRY B. 2014 ; 118( 20): 5471-5479.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1021/jp411886u
Artigo de periodico
The kinin B1 receptor regulates muscle-specific E3 ligases expression and is involved in skeletal muscle mass control (2014)
Parreiras‑e‑Silva, Lucas T; Reis, Rosana I; Santos, Geisa A; Pires‑Oliveira, Marcelo; Pesquero, João B; Gomes, Marcelo D; Godinho, Rosely O; Costa Neto, Cláudio Miguel
Source: Clinical Science. Unidade: FMRP
Subjects: CININAS (METABOLISMO), FIBRAS MUSCULARES (ENZIMOLOGIA), PROTEÍNAS MUSCULARES, ATROFIA MUSCULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PARREIRAS‑E‑SILVA, Lucas T et al. The kinin B1 receptor regulates muscle-specific E3 ligases expression and is involved in skeletal muscle mass control. Clinical Science, v. 127, n. 3, p. 185-194, 2014Tradução . . Disponível em: https://doi.org/10.1042/CS20130358. Acesso em: 24 jun. 2024.
APA
Parreiras‑e‑Silva, L. T., Reis, R. I., Santos, G. A., Pires‑Oliveira, M., Pesquero, J. B., Gomes, M. D., et al. (2014). The kinin B1 receptor regulates muscle-specific E3 ligases expression and is involved in skeletal muscle mass control. Clinical Science, 127( 3), 185-194. doi:10.1042/CS20130358
NLM
Parreiras‑e‑Silva LT, Reis RI, Santos GA, Pires‑Oliveira M, Pesquero JB, Gomes MD, Godinho RO, Costa Neto CM. The kinin B1 receptor regulates muscle-specific E3 ligases expression and is involved in skeletal muscle mass control [Internet]. Clinical Science. 2014 ; 127( 3): 185-194.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1042/CS20130358
Vancouver
Parreiras‑e‑Silva LT, Reis RI, Santos GA, Pires‑Oliveira M, Pesquero JB, Gomes MD, Godinho RO, Costa Neto CM. The kinin B1 receptor regulates muscle-specific E3 ligases expression and is involved in skeletal muscle mass control [Internet]. Clinical Science. 2014 ; 127( 3): 185-194.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1042/CS20130358
Artigo de periodico
Macrophage trafficking as key mediator of adenine-induced kidney injury (2014)
Correa-Costa, Matheus; Braga, Tárcio Teodoro; Felizardo, Raphael José Ferreira; Andrade-Oliveira, Vinicius; Perez, Katia Regina; Cuccovia, Iolanda Midea ; Hiyane, Meire Ioshie; Silva, João Santana da; Câmara, Niels Olsen Saraiva
Source: Mediators of Inflammation. Unidades: IQ, ICB, FMRP
Subjects: MACRÓFAGOS, BIOQUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CORREA-COSTA, Matheus et al. Macrophage trafficking as key mediator of adenine-induced kidney injury. Mediators of Inflammation, p. 1-12 art. 291024, 2014Tradução . . Disponível em: https://doi.org/10.1155/2014/291024. Acesso em: 24 jun. 2024.
APA
Correa-Costa, M., Braga, T. T., Felizardo, R. J. F., Andrade-Oliveira, V., Perez, K. R., Cuccovia, I. M., et al. (2014). Macrophage trafficking as key mediator of adenine-induced kidney injury. Mediators of Inflammation, 1-12 art. 291024. doi:10.1155/2014/291024
NLM
Correa-Costa M, Braga TT, Felizardo RJF, Andrade-Oliveira V, Perez KR, Cuccovia IM, Hiyane MI, Silva JS da, Câmara NOS. Macrophage trafficking as key mediator of adenine-induced kidney injury [Internet]. Mediators of Inflammation. 2014 ; 1-12 art. 291024.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1155/2014/291024
Vancouver
Correa-Costa M, Braga TT, Felizardo RJF, Andrade-Oliveira V, Perez KR, Cuccovia IM, Hiyane MI, Silva JS da, Câmara NOS. Macrophage trafficking as key mediator of adenine-induced kidney injury [Internet]. Mediators of Inflammation. 2014 ; 1-12 art. 291024.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1155/2014/291024
Artigo de periodico
Mycobacterium tuberculosis expressing phospholipase C subverts PGE2 synthesis and induces necrosis in alveolar macrophages (2014)
Assis, Patrícia A; Espíndola, Milena S; Paula-Silva, Francisco Wanderley Garcia de; Rios, Wendy Martin; Pereira, Priscilla A. T; Leão, Sylvia C; Silva, Célio Lopes; Faccioli, Lucia Helena
Source: BMC Microbiology. Unidades: FORP, FMRP, FCFRP
Subjects: MYCOBACTERIUM TUBERCULOSIS, FOSFOLIPASES, PROSTAGLANDINAS, NECROSE, MACRÓFAGOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ASSIS, Patrícia A et al. Mycobacterium tuberculosis expressing phospholipase C subverts PGE2 synthesis and induces necrosis in alveolar macrophages. BMC Microbiology, v. 14, 2014Tradução . . Disponível em: http://www.biomedcentral.com/1471-2180/14/128. Acesso em: 24 jun. 2024.
APA
Assis, P. A., Espíndola, M. S., Paula-Silva, F. W. G. de, Rios, W. M., Pereira, P. A. T., Leão, S. C., et al. (2014). Mycobacterium tuberculosis expressing phospholipase C subverts PGE2 synthesis and induces necrosis in alveolar macrophages. BMC Microbiology, 14. doi:10.1186/1471-2180-14-128
NLM
Assis PA, Espíndola MS, Paula-Silva FWG de, Rios WM, Pereira PAT, Leão SC, Silva CL, Faccioli LH. Mycobacterium tuberculosis expressing phospholipase C subverts PGE2 synthesis and induces necrosis in alveolar macrophages [Internet]. BMC Microbiology. 2014 ; 14[citado 2024 jun. 24 ] Available from: http://www.biomedcentral.com/1471-2180/14/128
Vancouver
Assis PA, Espíndola MS, Paula-Silva FWG de, Rios WM, Pereira PAT, Leão SC, Silva CL, Faccioli LH. Mycobacterium tuberculosis expressing phospholipase C subverts PGE2 synthesis and induces necrosis in alveolar macrophages [Internet]. BMC Microbiology. 2014 ; 14[citado 2024 jun. 24 ] Available from: http://www.biomedcentral.com/1471-2180/14/128
Artigo de periodico
Activating cAMP/PKA signaling in skeletal muscle suppresses the ubiquitin-proteasome-dependent proteolysis: implications for sympathetic regulation (2014)
Silveira, W. A.; Gonçalves, D. A.; Graça, F. A.; Andrade-Lopes, A. L.; Bergantin, L. B.; Zanon, Neusa Maria; Godinho, R. O.; Kettelhut, Isis do Carmo; Navegantes, Luiz Carlos Carvalho
Source: Journal of Applied Physiology. Unidade: FMRP
Subjects: PROTEÍNAS MUSCULARES, MÚSCULO ESQUELÉTICO (METABOLISMO), PROTEÍNAS PROTO-ONCOGÊNICAS, SISTEMA NERVOSO SIMPÁTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVEIRA, W. A. et al. Activating cAMP/PKA signaling in skeletal muscle suppresses the ubiquitin-proteasome-dependent proteolysis: implications for sympathetic regulation. Journal of Applied Physiology, v. 117, n. 1, p. 11-19, 2014Tradução . . Disponível em: https://doi.org/10.1152/japplphysiol.01055.2013. Acesso em: 24 jun. 2024.
APA
Silveira, W. A., Gonçalves, D. A., Graça, F. A., Andrade-Lopes, A. L., Bergantin, L. B., Zanon, N. M., et al. (2014). Activating cAMP/PKA signaling in skeletal muscle suppresses the ubiquitin-proteasome-dependent proteolysis: implications for sympathetic regulation. Journal of Applied Physiology, 117( 1), 11-19. doi:10.1152/japplphysiol.01055.2013
NLM
Silveira WA, Gonçalves DA, Graça FA, Andrade-Lopes AL, Bergantin LB, Zanon NM, Godinho RO, Kettelhut I do C, Navegantes LCC. Activating cAMP/PKA signaling in skeletal muscle suppresses the ubiquitin-proteasome-dependent proteolysis: implications for sympathetic regulation [Internet]. Journal of Applied Physiology. 2014 ; 117( 1): 11-19.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1152/japplphysiol.01055.2013
Vancouver
Silveira WA, Gonçalves DA, Graça FA, Andrade-Lopes AL, Bergantin LB, Zanon NM, Godinho RO, Kettelhut I do C, Navegantes LCC. Activating cAMP/PKA signaling in skeletal muscle suppresses the ubiquitin-proteasome-dependent proteolysis: implications for sympathetic regulation [Internet]. Journal of Applied Physiology. 2014 ; 117( 1): 11-19.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1152/japplphysiol.01055.2013
Artigo de periodico
Inflammasome-derived IL-1'beta' production induces nitric oxide-mediated resistance to Leishmania (2013)
Lima Júnior, Djalma S.; Costa, Diego L.; Carregaro, Vanessa; Cunha, Larissa D.; Silva, Alexandre L. N.; Mineo, Tiago Wilson Patriarca; Gutierrez, Fredy R. S.; Bellio, Maria; Bortoluci, Karina R.; Flavell, Richard A.; Bozza, Marcelo T.; Silva, João Santana da; Zamboni, Dario Simões
Source: Nature Medicine. Unidade: FMRP
Subjects: PROTEÍNAS DE TRANSPORTE, LEISHMANIA, ÓXIDO NÍTRICO (IMUNOLOGIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIMA JÚNIOR, Djalma S. et al. Inflammasome-derived IL-1'beta' production induces nitric oxide-mediated resistance to Leishmania. Nature Medicine, v. 19, n. 7, p. 909-915, 2013Tradução . . Disponível em: https://doi.org/10.1038/nm.3221. Acesso em: 24 jun. 2024.
APA
Lima Júnior, D. S., Costa, D. L., Carregaro, V., Cunha, L. D., Silva, A. L. N., Mineo, T. W. P., et al. (2013). Inflammasome-derived IL-1'beta' production induces nitric oxide-mediated resistance to Leishmania. Nature Medicine, 19( 7), 909-915. doi:10.1038/nm.3221
NLM
Lima Júnior DS, Costa DL, Carregaro V, Cunha LD, Silva ALN, Mineo TWP, Gutierrez FRS, Bellio M, Bortoluci KR, Flavell RA, Bozza MT, Silva JS da, Zamboni DS. Inflammasome-derived IL-1'beta' production induces nitric oxide-mediated resistance to Leishmania [Internet]. Nature Medicine. 2013 ; 19( 7): 909-915.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1038/nm.3221
Vancouver
Lima Júnior DS, Costa DL, Carregaro V, Cunha LD, Silva ALN, Mineo TWP, Gutierrez FRS, Bellio M, Bortoluci KR, Flavell RA, Bozza MT, Silva JS da, Zamboni DS. Inflammasome-derived IL-1'beta' production induces nitric oxide-mediated resistance to Leishmania [Internet]. Nature Medicine. 2013 ; 19( 7): 909-915.[citado 2024 jun. 24 ] Available from: https://doi.org/10.1038/nm.3221
Trabalho de evento-resumo
Resistance to Leishmania spp. is mediated by the inflammasome induced duo: IL- 1β and nitric oxide (2013)
Lima Júnior, Djalma de Souza; Costa, Diego Luís; Carregaro, Vanessa; Cunha, Larissa Dias da; Mineo, Tiago Wilson Patriarca; Gutierrez, Fredy Roberto Salazar; Bellio, Maria; Bortoluci, Karina; Flavell, Richard A.; Bozza, Marcelo T.; Silva, João Santana da; Zamboni, Dario Simões
Source: Abstracts. Conference titles: Keystone Symposia Global Health Series : The Innate Immune Response in the Pathogenesis of Infectious Disease. Unidade: FMRP
Subjects: LEISHMANIA, ÓXIDO NÍTRICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIMA JÚNIOR, Djalma de Souza et al. Resistance to Leishmania spp. is mediated by the inflammasome induced duo: IL- 1β and nitric oxide. 2013, Anais.. Ouro Preto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 2013. . Acesso em: 24 jun. 2024.
APA
Lima Júnior, D. de S., Costa, D. L., Carregaro, V., Cunha, L. D. da, Mineo, T. W. P., Gutierrez, F. R. S., et al. (2013). Resistance to Leishmania spp. is mediated by the inflammasome induced duo: IL- 1β and nitric oxide. In Abstracts. Ouro Preto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Lima Júnior D de S, Costa DL, Carregaro V, Cunha LD da, Mineo TWP, Gutierrez FRS, Bellio M, Bortoluci K, Flavell RA, Bozza MT, Silva JS da, Zamboni DS. Resistance to Leishmania spp. is mediated by the inflammasome induced duo: IL- 1β and nitric oxide. Abstracts. 2013 ;[citado 2024 jun. 24 ]
Vancouver
Lima Júnior D de S, Costa DL, Carregaro V, Cunha LD da, Mineo TWP, Gutierrez FRS, Bellio M, Bortoluci K, Flavell RA, Bozza MT, Silva JS da, Zamboni DS. Resistance to Leishmania spp. is mediated by the inflammasome induced duo: IL- 1β and nitric oxide. Abstracts. 2013 ;[citado 2024 jun. 24 ]
Artigo de periodico
Non-peptidic cruzain inhibitors with trypanocidal activity discovered by virtual screening and in vitro assay (2013)
Wiggers, Helton José; Rocha, Josmar Rodrigues da; Fernandes, Willian B.; Sesti-Costa, Renata; Carneiro, Zumira, A; Cheleski, Juliana; Silva, Alberico Borges Ferreira da ; Juliano, Luiz; Cezari, Maria Helena Sedenho; Silva, João Santana da; McKerrow, James H.; Montanari, Carlos Alberto
Source: PloS Neglected Tropical Diseases. Unidades: IQSC, FMRP
Subjects: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WIGGERS, Helton José et al. Non-peptidic cruzain inhibitors with trypanocidal activity discovered by virtual screening and in vitro assay. PloS Neglected Tropical Diseases, v. 7, n. 7, p. (online), 2013Tradução . . Disponível em: https://doi.org/10.1371/journal.pntd.0002370. Acesso em: 24 jun. 2024.
APA
Wiggers, H. J., Rocha, J. R. da, Fernandes, W. B., Sesti-Costa, R., Carneiro, Z., Cheleski, J., et al. (2013). Non-peptidic cruzain inhibitors with trypanocidal activity discovered by virtual screening and in vitro assay. PloS Neglected Tropical Diseases, 7( 7), (online). doi:10.1371/journal.pntd.0002370
NLM
Wiggers HJ, Rocha JR da, Fernandes WB, Sesti-Costa R, Carneiro Z, Cheleski J, Silva ABF da, Juliano L, Cezari MHS, Silva JS da, McKerrow JH, Montanari CA. Non-peptidic cruzain inhibitors with trypanocidal activity discovered by virtual screening and in vitro assay [Internet]. PloS Neglected Tropical Diseases. 2013 ; 7( 7): (online).[citado 2024 jun. 24 ] Available from: https://doi.org/10.1371/journal.pntd.0002370
Vancouver
Wiggers HJ, Rocha JR da, Fernandes WB, Sesti-Costa R, Carneiro Z, Cheleski J, Silva ABF da, Juliano L, Cezari MHS, Silva JS da, McKerrow JH, Montanari CA. Non-peptidic cruzain inhibitors with trypanocidal activity discovered by virtual screening and in vitro assay [Internet]. PloS Neglected Tropical Diseases. 2013 ; 7( 7): (online).[citado 2024 jun. 24 ] Available from: https://doi.org/10.1371/journal.pntd.0002370
Artigo de periodico
Regulatory T cells migrate to airways via CCR4 and attenuate the severity of airway allergic inflammation (2013)
Faustino, Lucas da Silva; Fonseca, Denise Morais da ; Takenaka, Maisa Carla; Mirotti, Luciana; Florsheim, Esther Borges; Guereschi, Marcia Grando; Silva, João Santana; Basso, Alexandre Salgado; Russo, Momtchilo
Source: Journal of Immunology. Unidades: ICB, FMRP
Assunto: IMUNOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FAUSTINO, Lucas da Silva et al. Regulatory T cells migrate to airways via CCR4 and attenuate the severity of airway allergic inflammation. Journal of Immunology, v. 190, n. 6, p. 2614-2621, 2013Tradução . . Disponível em: https://doi.org/10.4049/jimmunol.1202354. Acesso em: 24 jun. 2024.
APA
Faustino, L. da S., Fonseca, D. M. da, Takenaka, M. C., Mirotti, L., Florsheim, E. B., Guereschi, M. G., et al. (2013). Regulatory T cells migrate to airways via CCR4 and attenuate the severity of airway allergic inflammation. Journal of Immunology, 190( 6), 2614-2621. doi:10.4049/jimmunol.1202354
NLM
Faustino L da S, Fonseca DM da, Takenaka MC, Mirotti L, Florsheim EB, Guereschi MG, Silva JS, Basso AS, Russo M. Regulatory T cells migrate to airways via CCR4 and attenuate the severity of airway allergic inflammation [Internet]. Journal of Immunology. 2013 ; 190( 6): 2614-2621.[citado 2024 jun. 24 ] Available from: https://doi.org/10.4049/jimmunol.1202354
Vancouver
Faustino L da S, Fonseca DM da, Takenaka MC, Mirotti L, Florsheim EB, Guereschi MG, Silva JS, Basso AS, Russo M. Regulatory T cells migrate to airways via CCR4 and attenuate the severity of airway allergic inflammation [Internet]. Journal of Immunology. 2013 ; 190( 6): 2614-2621.[citado 2024 jun. 24 ] Available from: https://doi.org/10.4049/jimmunol.1202354

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