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Artigo de periodico
AHR is a Zika virus host factor and a candidate target for antiviral therapy (2020)
Giovannoni, Federico ; Bosch, Irene ; Polonio, Carolina Manganeli ; Torti, María F.; Wheeler, Michael A.; Li, Zhaorong ; Romorini, Leonardo ; Varela, María S. Rodriguez; Rothhammer, Veit ; Barroso, Andreia ; Tjon, Emily C.; Sanmarco, Liliana M.; Takenaka, Maisa C.; Modaresi, Seyed Mohamad Sadegh ; Vázquez, Cristina Gutiérrez; Zanluqui, Nágela Ghabdan ; Santos, Nilton Barreto dos ; Munhoz, Carolina Demarchi ; Wang, Zhongyan; Damonte, Elsa B.; Sherr, David; Gehrke, Lee ; Peron, Jean Pierre Schatzmann ; Garcia, Cybele C. ; Quintana, Francisco J.
Fonte: Nature Neuroscience. Unidades: ICB, FM
Assuntos: IMUNOLOGIA, FARMACOLOGIA, ZIKA VÍRUS, VÍRUS, FLAVIVIRUS, MICROCEFALIA, TRANSCRIÇÃO GÊNICA, GENOMAS, HIDROCARBONETOS, INTERFERON TIPO I, ANTIVIRAIS, REPLICAÇÃO VIRAL, NANOPARTÍCULAS
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ABNT
GIOVANNONI, Federico et al. AHR is a Zika virus host factor and a candidate target for antiviral therapy. Nature Neuroscience, v. 23, p. 939–951, 2020Tradução . . Disponível em: https://doi.org/10.1038/s41593-020-0664-0. Acesso em: 25 set. 2024.
APA
Giovannoni, F., Bosch, I., Polonio, C. M., Torti, M. F., Wheeler, M. A., Li, Z., et al. (2020). AHR is a Zika virus host factor and a candidate target for antiviral therapy. Nature Neuroscience, 23, 939–951. doi:10.1038/s41593-020-0664-0
NLM
Giovannoni F, Bosch I, Polonio CM, Torti MF, Wheeler MA, Li Z, Romorini L, Varela MSR, Rothhammer V, Barroso A, Tjon EC, Sanmarco LM, Takenaka MC, Modaresi SMS, Vázquez CG, Zanluqui NG, Santos NB dos, Munhoz CD, Wang Z, Damonte EB, Sherr D, Gehrke L, Peron JPS, Garcia CC, Quintana FJ. AHR is a Zika virus host factor and a candidate target for antiviral therapy [Internet]. Nature Neuroscience. 2020 ; 23 939–951.[citado 2024 set. 25 ] Available from: https://doi.org/10.1038/s41593-020-0664-0
Vancouver
Giovannoni F, Bosch I, Polonio CM, Torti MF, Wheeler MA, Li Z, Romorini L, Varela MSR, Rothhammer V, Barroso A, Tjon EC, Sanmarco LM, Takenaka MC, Modaresi SMS, Vázquez CG, Zanluqui NG, Santos NB dos, Munhoz CD, Wang Z, Damonte EB, Sherr D, Gehrke L, Peron JPS, Garcia CC, Quintana FJ. AHR is a Zika virus host factor and a candidate target for antiviral therapy [Internet]. Nature Neuroscience. 2020 ; 23 939–951.[citado 2024 set. 25 ] Available from: https://doi.org/10.1038/s41593-020-0664-0
Artigo de periodico
Computational approaches for drug discovery against trypanosomatid-caused diseases (2020)
Pereira, Claudio A. ; Sayé, Melisa; Reigada, Chantal; Silber, Ariel Mariano ; Labadie, Guillermo R. ; Miranda, Mariana R. ; Vera, Edward Valera
Fonte: Parasitology. Unidade: ICB
Assuntos: PARASITOLOGIA, TRYPANOSOMATIDAE, MEDICAMENTO, INFECÇÕES POR PROTOZOÁRIOS, COMPUTAÇÃO APLICADA, DOENÇAS PARASITÁRIAS, FÁRMACOS
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ABNT
PEREIRA, Claudio A. et al. Computational approaches for drug discovery against trypanosomatid-caused diseases. Parasitology, 2020Tradução . . Disponível em: https://doi.org/10.1017/S0031182020000207. Acesso em: 25 set. 2024.
APA
Pereira, C. A., Sayé, M., Reigada, C., Silber, A. M., Labadie, G. R., Miranda, M. R., & Vera, E. V. (2020). Computational approaches for drug discovery against trypanosomatid-caused diseases. Parasitology. doi:10.1017/S0031182020000207
NLM
Pereira CA, Sayé M, Reigada C, Silber AM, Labadie GR, Miranda MR, Vera EV. Computational approaches for drug discovery against trypanosomatid-caused diseases [Internet]. Parasitology. 2020 ;[citado 2024 set. 25 ] Available from: https://doi.org/10.1017/S0031182020000207
Vancouver
Pereira CA, Sayé M, Reigada C, Silber AM, Labadie GR, Miranda MR, Vera EV. Computational approaches for drug discovery against trypanosomatid-caused diseases [Internet]. Parasitology. 2020 ;[citado 2024 set. 25 ] Available from: https://doi.org/10.1017/S0031182020000207
Artigo de periodico
Targeting L-Proline uptake as new strategy for anti-chagas drug development (2020)
Fargnoli, Lucía; Zénere, Esteban A. Panozzo; Pagura, Lucas ; Barisón, María Julia ; Cricco, Julia A. ; Silber, Ariel Mariano ; Labadie, Guillermo R.
Fonte: Frontiers in Chemistry. Unidade: ICB
Assuntos: PARASITOLOGIA, ANTIPARASITÁRIOS, MEDICAMENTO, AMINOÁCIDOS, DOENÇA DE CHAGAS, QUIMIOTERÁPICOS, TRYPANOSOMA CRUZI
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ABNT
FARGNOLI, Lucía et al. Targeting L-Proline uptake as new strategy for anti-chagas drug development. Frontiers in Chemistry, v. 8, p. 15 , 2020Tradução . . Disponível em: https://doi.org/10.3389/fchem.2020.00696. Acesso em: 25 set. 2024.
APA
Fargnoli, L., Zénere, E. A. P., Pagura, L., Barisón, M. J., Cricco, J. A., Silber, A. M., & Labadie, G. R. (2020). Targeting L-Proline uptake as new strategy for anti-chagas drug development. Frontiers in Chemistry, 8, 15 . doi:10.3389/fchem.2020.00696
NLM
Fargnoli L, Zénere EAP, Pagura L, Barisón MJ, Cricco JA, Silber AM, Labadie GR. Targeting L-Proline uptake as new strategy for anti-chagas drug development [Internet]. Frontiers in Chemistry. 2020 ; 8 15 .[citado 2024 set. 25 ] Available from: https://doi.org/10.3389/fchem.2020.00696
Vancouver
Fargnoli L, Zénere EAP, Pagura L, Barisón MJ, Cricco JA, Silber AM, Labadie GR. Targeting L-Proline uptake as new strategy for anti-chagas drug development [Internet]. Frontiers in Chemistry. 2020 ; 8 15 .[citado 2024 set. 25 ] Available from: https://doi.org/10.3389/fchem.2020.00696
Artigo de periodico
Growth hormone regulates neuroendocrine responses to weight loss via AgRP neurons (2019)
Furigo, Isadora Clivatti ; Teixeira, Pryscila Dryelle Sousa ; Souza, Gabriel Orefice de ; Couto, Gisele Cristina Lopes ; Romero, Guadalupe García ; Perelló, Mario ; Frazão, Renata ; Elias, Lucila Leico Kagohara ; Metzger, Martin Andreas ; List, Edward O. ; Kopchick, John J. ; Donato Junior, José
Fonte: Nature Communications. Unidades: ICB, FMRP
Assuntos: HORMÔNIO DO CRESCIMENTO, PERDA DE PESO, NEURÔNIOS, FISIOLOGIA
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ABNT
FURIGO, Isadora Clivatti et al. Growth hormone regulates neuroendocrine responses to weight loss via AgRP neurons. Nature Communications, v. 10, n. 1, 2019Tradução . . Disponível em: https://doi.org/10.1038/s41467-019-08607-1. Acesso em: 25 set. 2024.
APA
Furigo, I. C., Teixeira, P. D. S., Souza, G. O. de, Couto, G. C. L., Romero, G. G., Perelló, M., et al. (2019). Growth hormone regulates neuroendocrine responses to weight loss via AgRP neurons. Nature Communications, 10( 1). doi:10.1038/s41467-019-08607-1
NLM
Furigo IC, Teixeira PDS, Souza GO de, Couto GCL, Romero GG, Perelló M, Frazão R, Elias LLK, Metzger MA, List EO, Kopchick JJ, Donato Junior J. Growth hormone regulates neuroendocrine responses to weight loss via AgRP neurons [Internet]. Nature Communications. 2019 ; 10( 1):[citado 2024 set. 25 ] Available from: https://doi.org/10.1038/s41467-019-08607-1
Vancouver
Furigo IC, Teixeira PDS, Souza GO de, Couto GCL, Romero GG, Perelló M, Frazão R, Elias LLK, Metzger MA, List EO, Kopchick JJ, Donato Junior J. Growth hormone regulates neuroendocrine responses to weight loss via AgRP neurons [Internet]. Nature Communications. 2019 ; 10( 1):[citado 2024 set. 25 ] Available from: https://doi.org/10.1038/s41467-019-08607-1
Artigo de periodico
Influence of trans fatty acids on glucose metabolism in soleus muscle of rats fed diets enriched in or deprived of linoleic acid (2018)
Fariña, Ana Clara; Hirabara, Sandro Massao ; Sain, Juliana ; González, Marcela Aída; Curi, Rui ; Bernal, Claudio Adrián
Fonte: European Journal of Nutrition. Unidade: ICB
Assuntos: MEMBROS INFERIORES, ÁCIDOS GRAXOS, GLICOSE, INSULINA, RATOS WISTAR
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ABNT
FARIÑA, Ana Clara et al. Influence of trans fatty acids on glucose metabolism in soleus muscle of rats fed diets enriched in or deprived of linoleic acid. European Journal of Nutrition, v. 57, n. 4, p. 1343-1355, 2018Tradução . . Disponível em: https://doi.org/10.1007/s00394-017-1413-3. Acesso em: 25 set. 2024.
APA
Fariña, A. C., Hirabara, S. M., Sain, J., González, M. A., Curi, R., & Bernal, C. A. (2018). Influence of trans fatty acids on glucose metabolism in soleus muscle of rats fed diets enriched in or deprived of linoleic acid. European Journal of Nutrition, 57( 4), 1343-1355. doi:10.1007/s00394-017-1413-3
NLM
Fariña AC, Hirabara SM, Sain J, González MA, Curi R, Bernal CA. Influence of trans fatty acids on glucose metabolism in soleus muscle of rats fed diets enriched in or deprived of linoleic acid [Internet]. European Journal of Nutrition. 2018 ; 57( 4): 1343-1355.[citado 2024 set. 25 ] Available from: https://doi.org/10.1007/s00394-017-1413-3
Vancouver
Fariña AC, Hirabara SM, Sain J, González MA, Curi R, Bernal CA. Influence of trans fatty acids on glucose metabolism in soleus muscle of rats fed diets enriched in or deprived of linoleic acid [Internet]. European Journal of Nutrition. 2018 ; 57( 4): 1343-1355.[citado 2024 set. 25 ] Available from: https://doi.org/10.1007/s00394-017-1413-3
Artigo de periodico
Effect of tamoxifen on the sphingolipid biosynthetic pathway in the different intraerythrocytic stages of the apicomplexa Plasmodium falciparum (2018)
Piñero, Tamara A. ; Landoni, Malena; Duschak, Vilma G. ; Katzin, Alejandro Miguel ; Couto, Alicia S.
Fonte: Biochemical and Biophysical Research Communications. Unidade: ICB
Assuntos: PARASITOLOGIA, PLASMODIUM FALCIPARUM, ESPECTROMETRIA DE MASSAS, MALÁRIA
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ABNT
PIÑERO, Tamara A. et al. Effect of tamoxifen on the sphingolipid biosynthetic pathway in the different intraerythrocytic stages of the apicomplexa Plasmodium falciparum. Biochemical and Biophysical Research Communications, v. 497, n. 4, p. 1082-1088, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.bbrc.2018.02.183. Acesso em: 25 set. 2024.
APA
Piñero, T. A., Landoni, M., Duschak, V. G., Katzin, A. M., & Couto, A. S. (2018). Effect of tamoxifen on the sphingolipid biosynthetic pathway in the different intraerythrocytic stages of the apicomplexa Plasmodium falciparum. Biochemical and Biophysical Research Communications, 497( 4), 1082-1088. doi:10.1016/j.bbrc.2018.02.183
NLM
Piñero TA, Landoni M, Duschak VG, Katzin AM, Couto AS. Effect of tamoxifen on the sphingolipid biosynthetic pathway in the different intraerythrocytic stages of the apicomplexa Plasmodium falciparum [Internet]. Biochemical and Biophysical Research Communications. 2018 ; 497( 4): 1082-1088.[citado 2024 set. 25 ] Available from: https://doi.org/10.1016/j.bbrc.2018.02.183
Vancouver
Piñero TA, Landoni M, Duschak VG, Katzin AM, Couto AS. Effect of tamoxifen on the sphingolipid biosynthetic pathway in the different intraerythrocytic stages of the apicomplexa Plasmodium falciparum [Internet]. Biochemical and Biophysical Research Communications. 2018 ; 497( 4): 1082-1088.[citado 2024 set. 25 ] Available from: https://doi.org/10.1016/j.bbrc.2018.02.183
Artigo de periodico
Resveratrol inhibits Trypanosoma cruzi arginine kinase and exerts a trypanocidal activity (2016)
Vera, Edward A. Valera; Sayé, Melisa; Reigada, Chantal; Damasceno, Damasceno; Silber, Ariel Mariano ; Miranda, Mariana R.; Pereira, Claudio A.
Fonte: International Journal of Biological Macromolecules. Unidade: ICB
Assuntos: PARASITOLOGIA, DOENÇA DE CHAGAS, INIBIDORES QUÍMICOS, TRYPANOSOMA CRUZI
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VERA, Edward A. Valera et al. Resveratrol inhibits Trypanosoma cruzi arginine kinase and exerts a trypanocidal activity. International Journal of Biological Macromolecules, v. 87, p. 498-503, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.ijbiomac.2016.03.014. Acesso em: 25 set. 2024.
APA
Vera, E. A. V., Sayé, M., Reigada, C., Damasceno, D., Silber, A. M., Miranda, M. R., & Pereira, C. A. (2016). Resveratrol inhibits Trypanosoma cruzi arginine kinase and exerts a trypanocidal activity. International Journal of Biological Macromolecules, 87, 498-503. doi:10.1016/j.ijbiomac.2016.03.014
NLM
Vera EAV, Sayé M, Reigada C, Damasceno D, Silber AM, Miranda MR, Pereira CA. Resveratrol inhibits Trypanosoma cruzi arginine kinase and exerts a trypanocidal activity [Internet]. International Journal of Biological Macromolecules. 2016 ; 87 498-503.[citado 2024 set. 25 ] Available from: https://doi.org/10.1016/j.ijbiomac.2016.03.014
Vancouver
Vera EAV, Sayé M, Reigada C, Damasceno D, Silber AM, Miranda MR, Pereira CA. Resveratrol inhibits Trypanosoma cruzi arginine kinase and exerts a trypanocidal activity [Internet]. International Journal of Biological Macromolecules. 2016 ; 87 498-503.[citado 2024 set. 25 ] Available from: https://doi.org/10.1016/j.ijbiomac.2016.03.014

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