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Artigo de periodico
Shotgun proteomic analysis of the caterpillar Lonomia obliqua (Lepitoptera, Saturniidae) hemolymph and effects in rat hippocampal neurons culture (2023)
Maggi, Silviane; Pinto, Antônio Frederico Michel; Udo, Mariana Sayuri Berto ; Silva, Mariana Aguilera Alencar da; Garcia, Raphael Caio Tamborelli ; Minetto, Luciane; Tasso, Leandro; Machado, Pablo; Santos, Diógenes Santiago; Barcellos, Thiago; Silva Junior, Pedro Ismael da ; Mendonça, Ronaldo Zucatelli ; Marcourakis, Tania ; Moura, Sidnei
Source: bioRxiv. Unidade: FCF
Subjects: NEURÔNIOS, APOPTOSE
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ABNT
MAGGI, Silviane et al. Shotgun proteomic analysis of the caterpillar Lonomia obliqua (Lepitoptera, Saturniidae) hemolymph and effects in rat hippocampal neurons culture. bioRxiv, 2023Tradução . . Disponível em: https://doi.org/10.1101/2023.03.20.533482. Acesso em: 03 nov. 2024.
APA
Maggi, S., Pinto, A. F. M., Udo, M. S. B., Silva, M. A. A. da, Garcia, R. C. T., Minetto, L., et al. (2023). Shotgun proteomic analysis of the caterpillar Lonomia obliqua (Lepitoptera, Saturniidae) hemolymph and effects in rat hippocampal neurons culture. bioRxiv. doi:10.1101/2023.03.20.533482
NLM
Maggi S, Pinto AFM, Udo MSB, Silva MAA da, Garcia RCT, Minetto L, Tasso L, Machado P, Santos DS, Barcellos T, Silva Junior PI da, Mendonça RZ, Marcourakis T, Moura S. Shotgun proteomic analysis of the caterpillar Lonomia obliqua (Lepitoptera, Saturniidae) hemolymph and effects in rat hippocampal neurons culture [Internet]. bioRxiv. 2023 ;[citado 2024 nov. 03 ] Available from: https://doi.org/10.1101/2023.03.20.533482
Vancouver
Maggi S, Pinto AFM, Udo MSB, Silva MAA da, Garcia RCT, Minetto L, Tasso L, Machado P, Santos DS, Barcellos T, Silva Junior PI da, Mendonça RZ, Marcourakis T, Moura S. Shotgun proteomic analysis of the caterpillar Lonomia obliqua (Lepitoptera, Saturniidae) hemolymph and effects in rat hippocampal neurons culture [Internet]. bioRxiv. 2023 ;[citado 2024 nov. 03 ] Available from: https://doi.org/10.1101/2023.03.20.533482
Artigo de periodico
Development of recombinant human granulocyte colony-stimulating factor (nartograstim) production process in Escherichia coli compatible with industrial scale and with no antibiotics in the culture medium (2021)
Eguia, Fara A. P; Mascarelli, Daniele Enriquetto ; Carvalho, Enéas de ; Rodríguez, Gretel Rodríguez ; Makiyama, Edson Naoto ; Borelli, Primavera ; Lieberman, Celia; Ho, Paulo Lee ; Barazzone, Giovana Cappio ; Gonçalves, Viviane Maimoni
Source: Applied Microbiology and Biotechnology. Unidades: FCF, BIOTECNOLOGIA, IQ
Subjects: GRANULÓCITOS, ESCHERICHIA COLI
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EGUIA, Fara A. P et al. Development of recombinant human granulocyte colony-stimulating factor (nartograstim) production process in Escherichia coli compatible with industrial scale and with no antibiotics in the culture medium. Applied Microbiology and Biotechnology, v. 105, p. 169–183, 2021Tradução . . Disponível em: https://doi.org/10.1007/s00253-020-11014-y. Acesso em: 03 nov. 2024.
APA
Eguia, F. A. P., Mascarelli, D. E., Carvalho, E. de, Rodríguez, G. R., Makiyama, E. N., Borelli, P., et al. (2021). Development of recombinant human granulocyte colony-stimulating factor (nartograstim) production process in Escherichia coli compatible with industrial scale and with no antibiotics in the culture medium. Applied Microbiology and Biotechnology, 105, 169–183. doi:10.1007/s00253-020-11014-y
NLM
Eguia FAP, Mascarelli DE, Carvalho E de, Rodríguez GR, Makiyama EN, Borelli P, Lieberman C, Ho PL, Barazzone GC, Gonçalves VM. Development of recombinant human granulocyte colony-stimulating factor (nartograstim) production process in Escherichia coli compatible with industrial scale and with no antibiotics in the culture medium [Internet]. Applied Microbiology and Biotechnology. 2021 ; 105 169–183.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1007/s00253-020-11014-y
Vancouver
Eguia FAP, Mascarelli DE, Carvalho E de, Rodríguez GR, Makiyama EN, Borelli P, Lieberman C, Ho PL, Barazzone GC, Gonçalves VM. Development of recombinant human granulocyte colony-stimulating factor (nartograstim) production process in Escherichia coli compatible with industrial scale and with no antibiotics in the culture medium [Internet]. Applied Microbiology and Biotechnology. 2021 ; 105 169–183.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1007/s00253-020-11014-y
Artigo de periodico
Anhydroecgonine methyl ester (AEME), a cocaine pyrolysis product, impairs glutathione-related enzymes response and increases lipid peroxidation in the hippocampal cell culture (2019)
Garcia, Raphael Caio Tamborelli; Torres, Larissa Lobo; Dati, Lívia Mendonça Munhoz; Loureiro, Ana Paula de Melo ; Afeche, Solange Castro ; Sandoval, Maria Regina Lopes ; Marcourakis, Tania
Source: Toxicology Reports. Unidades: FCF, IP
Subjects: CULTURA DE CÉLULAS, COCAÍNA, ESTRESSE OXIDATIVO
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ABNT
GARCIA, Raphael Caio Tamborelli et al. Anhydroecgonine methyl ester (AEME), a cocaine pyrolysis product, impairs glutathione-related enzymes response and increases lipid peroxidation in the hippocampal cell culture. Toxicology Reports, v. 6, p. 1223-1229, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.toxrep.2019.11.001. Acesso em: 03 nov. 2024.
APA
Garcia, R. C. T., Torres, L. L., Dati, L. M. M., Loureiro, A. P. de M., Afeche, S. C., Sandoval, M. R. L., & Marcourakis, T. (2019). Anhydroecgonine methyl ester (AEME), a cocaine pyrolysis product, impairs glutathione-related enzymes response and increases lipid peroxidation in the hippocampal cell culture. Toxicology Reports, 6, 1223-1229. doi:10.1016/j.toxrep.2019.11.001
NLM
Garcia RCT, Torres LL, Dati LMM, Loureiro AP de M, Afeche SC, Sandoval MRL, Marcourakis T. Anhydroecgonine methyl ester (AEME), a cocaine pyrolysis product, impairs glutathione-related enzymes response and increases lipid peroxidation in the hippocampal cell culture [Internet]. Toxicology Reports. 2019 ; 6 1223-1229.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.toxrep.2019.11.001
Vancouver
Garcia RCT, Torres LL, Dati LMM, Loureiro AP de M, Afeche SC, Sandoval MRL, Marcourakis T. Anhydroecgonine methyl ester (AEME), a cocaine pyrolysis product, impairs glutathione-related enzymes response and increases lipid peroxidation in the hippocampal cell culture [Internet]. Toxicology Reports. 2019 ; 6 1223-1229.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.toxrep.2019.11.001
Artigo de periodico
Transport of cowpea bean derived peptides and their modulator effects on mRNA expression of cholesterol-related genes in Caco-2 and HepG2 cells (2018)
Marques, Marcelo Rodrigues; Cerda, Alvaro; Fontanari, Gustavo Guadagnucci; Pimenta, Daniel Carvalho; Freitas, Rosana Manólio Soares; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo ; Areas, José Alfredo Gomes
Source: Food Research International. Unidades: FCF, FSP
Subjects: PEPTÍDEOS, HOMEOSTASE, COLESTEROL
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ABNT
MARQUES, Marcelo Rodrigues et al. Transport of cowpea bean derived peptides and their modulator effects on mRNA expression of cholesterol-related genes in Caco-2 and HepG2 cells. Food Research International, v. 107, p. 165–171, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.foodres.2018.01.031. Acesso em: 03 nov. 2024.
APA
Marques, M. R., Cerda, A., Fontanari, G. G., Pimenta, D. C., Freitas, R. M. S., Hirata, M. H., et al. (2018). Transport of cowpea bean derived peptides and their modulator effects on mRNA expression of cholesterol-related genes in Caco-2 and HepG2 cells. Food Research International, 107, 165–171. doi:10.1016/j.foodres.2018.01.031
NLM
Marques MR, Cerda A, Fontanari GG, Pimenta DC, Freitas RMS, Hirata MH, Hirata RDC, Areas JAG. Transport of cowpea bean derived peptides and their modulator effects on mRNA expression of cholesterol-related genes in Caco-2 and HepG2 cells [Internet]. Food Research International. 2018 ; 107 165–171.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.foodres.2018.01.031
Vancouver
Marques MR, Cerda A, Fontanari GG, Pimenta DC, Freitas RMS, Hirata MH, Hirata RDC, Areas JAG. Transport of cowpea bean derived peptides and their modulator effects on mRNA expression of cholesterol-related genes in Caco-2 and HepG2 cells [Internet]. Food Research International. 2018 ; 107 165–171.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.foodres.2018.01.031
Artigo de periodico
Chick embryo model: homing and host interactions of Tissue Engineering aimed human Dental Stem Cells (2018)
Santos, Jennifer Adriane dos; Duailibi, Mônica Talarico; Maria, Durvanei Augusto; Will, Sonia Elisabete Alves de Lima; Silva, Paulo Cesar Simoes; Gomes, Lígia Ferreira ; Duailibi, Silvio Eduardo
Source: Tissue Engineering A. Unidade: FCF
Subjects: CÉLULAS-TRONCO, EMBRIÃO
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ABNT
SANTOS, Jennifer Adriane dos et al. Chick embryo model: homing and host interactions of Tissue Engineering aimed human Dental Stem Cells. Tissue Engineering A, v. 24, n. 11-12, p. 882-888, 2018Tradução . . Acesso em: 03 nov. 2024.
APA
Santos, J. A. dos, Duailibi, M. T., Maria, D. A., Will, S. E. A. de L., Silva, P. C. S., Gomes, L. F., & Duailibi, S. E. (2018). Chick embryo model: homing and host interactions of Tissue Engineering aimed human Dental Stem Cells. Tissue Engineering A, 24( 11-12), 882-888.
NLM
Santos JA dos, Duailibi MT, Maria DA, Will SEA de L, Silva PCS, Gomes LF, Duailibi SE. Chick embryo model: homing and host interactions of Tissue Engineering aimed human Dental Stem Cells. Tissue Engineering A. 2018 ; 24( 11-12): 882-888.[citado 2024 nov. 03 ]
Vancouver
Santos JA dos, Duailibi MT, Maria DA, Will SEA de L, Silva PCS, Gomes LF, Duailibi SE. Chick embryo model: homing and host interactions of Tissue Engineering aimed human Dental Stem Cells. Tissue Engineering A. 2018 ; 24( 11-12): 882-888.[citado 2024 nov. 03 ]
Artigo de periodico
New insights into the mechanistic action of methyldehydrodieugenol B towards Leishmania (L.) infantum via a multiplatform based untargeted metabolomics approach (2017)
Canuto, Gisele André Baptista; Dörr, Fabiane ; Lago, João Henrique Ghilardi; Tempone, André Gustavo; Pinto, Ernani ; Pimenta, Daniel Carvalho; Farah, João Pedro Simon ; Alves, Maria Júlia Manso ; Tavares, Marina Franco Maggi
Source: Metabolomics. Unidades: FCF, IQ
Subjects: DOENÇAS NEGLIGENCIADAS, PRODUTOS NATURAIS, LEISHMANIA
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ABNT
CANUTO, Gisele André Baptista et al. New insights into the mechanistic action of methyldehydrodieugenol B towards Leishmania (L.) infantum via a multiplatform based untargeted metabolomics approach. Metabolomics, v. 13, n. 5, p. 1-14 : + supplementary materials (pS1-S60), 2017Tradução . . Disponível em: https://doi.org/10.1007/s11306-017-1193-z. Acesso em: 03 nov. 2024.
APA
Canuto, G. A. B., Dörr, F., Lago, J. H. G., Tempone, A. G., Pinto, E., Pimenta, D. C., et al. (2017). New insights into the mechanistic action of methyldehydrodieugenol B towards Leishmania (L.) infantum via a multiplatform based untargeted metabolomics approach. Metabolomics, 13( 5), 1-14 : + supplementary materials (pS1-S60). doi:10.1007/s11306-017-1193-z
NLM
Canuto GAB, Dörr F, Lago JHG, Tempone AG, Pinto E, Pimenta DC, Farah JPS, Alves MJM, Tavares MFM. New insights into the mechanistic action of methyldehydrodieugenol B towards Leishmania (L.) infantum via a multiplatform based untargeted metabolomics approach [Internet]. Metabolomics. 2017 ; 13( 5): 1-14 : + supplementary materials (pS1-S60).[citado 2024 nov. 03 ] Available from: https://doi.org/10.1007/s11306-017-1193-z
Vancouver
Canuto GAB, Dörr F, Lago JHG, Tempone AG, Pinto E, Pimenta DC, Farah JPS, Alves MJM, Tavares MFM. New insights into the mechanistic action of methyldehydrodieugenol B towards Leishmania (L.) infantum via a multiplatform based untargeted metabolomics approach [Internet]. Metabolomics. 2017 ; 13( 5): 1-14 : + supplementary materials (pS1-S60).[citado 2024 nov. 03 ] Available from: https://doi.org/10.1007/s11306-017-1193-z
Parte de monografia/livro
A simple, fast, inexpensive and efficient method for leukocytes separation with preservation of morphology and cell viability for use in education and research (2017)
Kavati, Érica Akemi; Hosada, T. M; Szulczewski, Vivian; Leao, Elizabeth; Borelli, Primavera ; Cianciarullo, Aurora Marques
Source: Microscopy and imaging science: practical approaches to applied research and education. Unidade: FCF
Subjects: LEUCÓCITOS, EDUCAÇÃO, PESQUISA, MICROSCOPIA, CÉLULAS SANGUÍNEAS
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ABNT
KAVATI, Érica Akemi et al. A simple, fast, inexpensive and efficient method for leukocytes separation with preservation of morphology and cell viability for use in education and research. Microscopy and imaging science: practical approaches to applied research and education. Tradução . Badajoz: Formatex Research Center, 2017. . . Acesso em: 03 nov. 2024.
APA
Kavati, É. A., Hosada, T. M., Szulczewski, V., Leao, E., Borelli, P., & Cianciarullo, A. M. (2017). A simple, fast, inexpensive and efficient method for leukocytes separation with preservation of morphology and cell viability for use in education and research. In Microscopy and imaging science: practical approaches to applied research and education. Badajoz: Formatex Research Center.
NLM
Kavati ÉA, Hosada TM, Szulczewski V, Leao E, Borelli P, Cianciarullo AM. A simple, fast, inexpensive and efficient method for leukocytes separation with preservation of morphology and cell viability for use in education and research. In: Microscopy and imaging science: practical approaches to applied research and education. Badajoz: Formatex Research Center; 2017. [citado 2024 nov. 03 ]
Vancouver
Kavati ÉA, Hosada TM, Szulczewski V, Leao E, Borelli P, Cianciarullo AM. A simple, fast, inexpensive and efficient method for leukocytes separation with preservation of morphology and cell viability for use in education and research. In: Microscopy and imaging science: practical approaches to applied research and education. Badajoz: Formatex Research Center; 2017. [citado 2024 nov. 03 ]
Artigo de periodico
Role of Translocator 18 KDa ligands in the activation of leukotriene B4 activated G-protein coupled receptor and Toll Like Receptor-4 pathways in neutrophils (2017)
Kupa, Léonard de Vinci Kanda; Drewes, Carine Cristiane; Barioni, Eric Diego; Neves, Camila Lima; Sampaio, Sandra Coccuzzo; Farsky, Sandra Helena Poliselli
Source: Frontiers in Pharmacology. Unidade: FCF
Subjects: NEUTRÓFILOS, CITOCINAS
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ABNT
KUPA, Léonard de Vinci Kanda et al. Role of Translocator 18 KDa ligands in the activation of leukotriene B4 activated G-protein coupled receptor and Toll Like Receptor-4 pathways in neutrophils. Frontiers in Pharmacology, v. 8, p. 1-14 art. 766, 2017Tradução . . Disponível em: https://doi.org/10.3389/fphar.2017.00766. Acesso em: 03 nov. 2024.
APA
Kupa, L. de V. K., Drewes, C. C., Barioni, E. D., Neves, C. L., Sampaio, S. C., & Farsky, S. H. P. (2017). Role of Translocator 18 KDa ligands in the activation of leukotriene B4 activated G-protein coupled receptor and Toll Like Receptor-4 pathways in neutrophils. Frontiers in Pharmacology, 8, 1-14 art. 766. doi:10.3389/fphar.2017.00766
NLM
Kupa L de VK, Drewes CC, Barioni ED, Neves CL, Sampaio SC, Farsky SHP. Role of Translocator 18 KDa ligands in the activation of leukotriene B4 activated G-protein coupled receptor and Toll Like Receptor-4 pathways in neutrophils [Internet]. Frontiers in Pharmacology. 2017 ; 8 1-14 art. 766.[citado 2024 nov. 03 ] Available from: https://doi.org/10.3389/fphar.2017.00766
Vancouver
Kupa L de VK, Drewes CC, Barioni ED, Neves CL, Sampaio SC, Farsky SHP. Role of Translocator 18 KDa ligands in the activation of leukotriene B4 activated G-protein coupled receptor and Toll Like Receptor-4 pathways in neutrophils [Internet]. Frontiers in Pharmacology. 2017 ; 8 1-14 art. 766.[citado 2024 nov. 03 ] Available from: https://doi.org/10.3389/fphar.2017.00766
Artigo de periodico
Anhydroecgonine methyl ester, a cocaine pyrolysis product, may contribute to cocaine behavioral sensitization (2017)
Garcia, Raphael Caio Tamborelli; Torres, Larissa Helena Lobo; Balestrin, Natália Trigo; Andrioli, Tatiana Costa; Florio, Jorge Camilo; Oliveira, Carolina Dizioli Rodrigues de; Costa, José Luiz da; Yonamine, Maurício ; Sandoval, Maria Regina Lopes; Camarini, Rosana ; Marcourakis, Tania
Source: Toxicology. Unidades: FMVZ, FCF, ICB
Subjects: DROGAS DE ABUSO, COCAÍNA, DROGA (VÍCIO)
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ABNT
GARCIA, Raphael Caio Tamborelli et al. Anhydroecgonine methyl ester, a cocaine pyrolysis product, may contribute to cocaine behavioral sensitization. Toxicology, v. 376, p. 44-50, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tox.2016.04.009. Acesso em: 03 nov. 2024.
APA
Garcia, R. C. T., Torres, L. H. L., Balestrin, N. T., Andrioli, T. C., Florio, J. C., Oliveira, C. D. R. de, et al. (2017). Anhydroecgonine methyl ester, a cocaine pyrolysis product, may contribute to cocaine behavioral sensitization. Toxicology, 376, 44-50. doi:10.1016/j.tox.2016.04.009
NLM
Garcia RCT, Torres LHL, Balestrin NT, Andrioli TC, Florio JC, Oliveira CDR de, Costa JL da, Yonamine M, Sandoval MRL, Camarini R, Marcourakis T. Anhydroecgonine methyl ester, a cocaine pyrolysis product, may contribute to cocaine behavioral sensitization [Internet]. Toxicology. 2017 ; 376 44-50.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tox.2016.04.009
Vancouver
Garcia RCT, Torres LHL, Balestrin NT, Andrioli TC, Florio JC, Oliveira CDR de, Costa JL da, Yonamine M, Sandoval MRL, Camarini R, Marcourakis T. Anhydroecgonine methyl ester, a cocaine pyrolysis product, may contribute to cocaine behavioral sensitization [Internet]. Toxicology. 2017 ; 376 44-50.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tox.2016.04.009
Artigo de periodico
The muscarinic effect of anhydroecgonine methyl ester, a crack cocaine pyrolysis product, impairs melatonin synthesis in the rat pineal gland (2017)
Mesquita, Lívia Silva Medeiros de; Garcia, Raphael Caio Tamborelli; Amaral, Fernanda Gaspar do; Peres, Rafael; Wood, Simone Miller; Lucena, Rodrigo Vicenzo de Luca; Frare, Eduardo Osório; Abrahão, Mariana Vieira; Marcourakis, Tania ; Cipolla-Neto, José; Afeche, Solange Castro
Source: Toxicology Research. Unidades: FCF, ICB
Subjects: DROGAS DE ABUSO, MELATONINA, PIRÓLISE
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ABNT
MESQUITA, Lívia Silva Medeiros de et al. The muscarinic effect of anhydroecgonine methyl ester, a crack cocaine pyrolysis product, impairs melatonin synthesis in the rat pineal gland. Toxicology Research, v. 6, n. 4, p. 420-431, 2017Tradução . . Disponível em: https://doi.org/10.1039/c7tx00009j. Acesso em: 03 nov. 2024.
APA
Mesquita, L. S. M. de, Garcia, R. C. T., Amaral, F. G. do, Peres, R., Wood, S. M., Lucena, R. V. de L., et al. (2017). The muscarinic effect of anhydroecgonine methyl ester, a crack cocaine pyrolysis product, impairs melatonin synthesis in the rat pineal gland. Toxicology Research, 6( 4), 420-431. doi:10.1039/c7tx00009j
NLM
Mesquita LSM de, Garcia RCT, Amaral FG do, Peres R, Wood SM, Lucena RV de L, Frare EO, Abrahão MV, Marcourakis T, Cipolla-Neto J, Afeche SC. The muscarinic effect of anhydroecgonine methyl ester, a crack cocaine pyrolysis product, impairs melatonin synthesis in the rat pineal gland [Internet]. Toxicology Research. 2017 ; 6( 4): 420-431.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1039/c7tx00009j
Vancouver
Mesquita LSM de, Garcia RCT, Amaral FG do, Peres R, Wood SM, Lucena RV de L, Frare EO, Abrahão MV, Marcourakis T, Cipolla-Neto J, Afeche SC. The muscarinic effect of anhydroecgonine methyl ester, a crack cocaine pyrolysis product, impairs melatonin synthesis in the rat pineal gland [Internet]. Toxicology Research. 2017 ; 6( 4): 420-431.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1039/c7tx00009j
Artigo de periodico
Analysis of LexA binding sites and transcriptomics in response to genotoxic stress in Leptospira interrogans (2016)
Schons-Fonseca, Luciane; Silva, Josefa B. da; Milanez, Juliana S; Domingos, Renan H; Smith, Janet L; Nakaya, Helder Takashi Imoto ; Grossman, Alan D; Ho, Paulo Lee; Costa, Renata Maria Augusto da
Source: Nucleic Acids Research. Unidade: FCF
Subjects: DANO AO DNA, EXPRESSÃO GÊNICA
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ABNT
SCHONS-FONSECA, Luciane et al. Analysis of LexA binding sites and transcriptomics in response to genotoxic stress in Leptospira interrogans. Nucleic Acids Research, v. 44, n. 3, p. 1179-1191, 2016Tradução . . Disponível em: https://doi.org/10.1093/nar/gkv1536. Acesso em: 03 nov. 2024.
APA
Schons-Fonseca, L., Silva, J. B. da, Milanez, J. S., Domingos, R. H., Smith, J. L., Nakaya, H. T. I., et al. (2016). Analysis of LexA binding sites and transcriptomics in response to genotoxic stress in Leptospira interrogans. Nucleic Acids Research, 44( 3), 1179-1191. doi:10.1093/nar/gkv1536
NLM
Schons-Fonseca L, Silva JB da, Milanez JS, Domingos RH, Smith JL, Nakaya HTI, Grossman AD, Ho PL, Costa RMA da. Analysis of LexA binding sites and transcriptomics in response to genotoxic stress in Leptospira interrogans [Internet]. Nucleic Acids Research. 2016 ; 44( 3): 1179-1191.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1093/nar/gkv1536
Vancouver
Schons-Fonseca L, Silva JB da, Milanez JS, Domingos RH, Smith JL, Nakaya HTI, Grossman AD, Ho PL, Costa RMA da. Analysis of LexA binding sites and transcriptomics in response to genotoxic stress in Leptospira interrogans [Internet]. Nucleic Acids Research. 2016 ; 44( 3): 1179-1191.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1093/nar/gkv1536
Artigo de periodico
Microcirculation abnormalities provoked by Loxosceles spiders' envenomation (2016)
Oliveira Lima, Kátia Cristina; Farsky, Sandra Helena Poliselli ; Lopes, Priscila Hess; Andrade, Rute Maria Gonçalves de; Van Den Berg, Carmen W; Tambourgi, Denise Vilarinho
Source: Toxicon. Unidade: FCF
Subjects: MICROCIRCULAÇÃO, LOXOCEMIDAE, VENENOS DE ORIGEM ANIMAL
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ABNT
OLIVEIRA LIMA, Kátia Cristina et al. Microcirculation abnormalities provoked by Loxosceles spiders' envenomation. Toxicon, v. 116, p. 35-42, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.toxicon.2015.08.005. Acesso em: 03 nov. 2024.
APA
Oliveira Lima, K. C., Farsky, S. H. P., Lopes, P. H., Andrade, R. M. G. de, Van Den Berg, C. W., & Tambourgi, D. V. (2016). Microcirculation abnormalities provoked by Loxosceles spiders' envenomation. Toxicon, 116, 35-42. doi:10.1016/j.toxicon.2015.08.005
NLM
Oliveira Lima KC, Farsky SHP, Lopes PH, Andrade RMG de, Van Den Berg CW, Tambourgi DV. Microcirculation abnormalities provoked by Loxosceles spiders' envenomation [Internet]. Toxicon. 2016 ; 116 35-42.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.toxicon.2015.08.005
Vancouver
Oliveira Lima KC, Farsky SHP, Lopes PH, Andrade RMG de, Van Den Berg CW, Tambourgi DV. Microcirculation abnormalities provoked by Loxosceles spiders' envenomation [Internet]. Toxicon. 2016 ; 116 35-42.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.toxicon.2015.08.005
Artigo de periodico
7,12-Dimethylbenz(a)anthracene-induced genotoxicity on bone marrow cells from mice phenotypically selected for low acute inflammatory response (2016)
Katz, Iana Suly Santos; Albuquerque, Layra Lucy; Suppa, Alessandra Paes; Silva, Graziela Batista da; Jensen, José Ricardo; Borrego, Andrea; Massa, Solange; Starobinas, Nancy; Cabrera, Wafa Hanna Koury; Franco, Marcelo de; Borelli, Primavera ; Ibañez, Olga Martinez; Ribeiro, Orlando Garcia
Source: DNA Repair. Unidade: FCF
Subjects: HIDROCARBONETOS POLICÍCLICOS, MEDULA ÓSSEA
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ABNT
KATZ, Iana Suly Santos et al. 7,12-Dimethylbenz(a)anthracene-induced genotoxicity on bone marrow cells from mice phenotypically selected for low acute inflammatory response. DNA Repair, v. 47, p. 37-42, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.dnarep.2015.11.006. Acesso em: 03 nov. 2024.
APA
Katz, I. S. S., Albuquerque, L. L., Suppa, A. P., Silva, G. B. da, Jensen, J. R., Borrego, A., et al. (2016). 7,12-Dimethylbenz(a)anthracene-induced genotoxicity on bone marrow cells from mice phenotypically selected for low acute inflammatory response. DNA Repair, 47, 37-42. doi:10.1016/j.dnarep.2015.11.006
NLM
Katz ISS, Albuquerque LL, Suppa AP, Silva GB da, Jensen JR, Borrego A, Massa S, Starobinas N, Cabrera WHK, Franco M de, Borelli P, Ibañez OM, Ribeiro OG. 7,12-Dimethylbenz(a)anthracene-induced genotoxicity on bone marrow cells from mice phenotypically selected for low acute inflammatory response [Internet]. DNA Repair. 2016 ; 47 37-42.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.dnarep.2015.11.006
Vancouver
Katz ISS, Albuquerque LL, Suppa AP, Silva GB da, Jensen JR, Borrego A, Massa S, Starobinas N, Cabrera WHK, Franco M de, Borelli P, Ibañez OM, Ribeiro OG. 7,12-Dimethylbenz(a)anthracene-induced genotoxicity on bone marrow cells from mice phenotypically selected for low acute inflammatory response [Internet]. DNA Repair. 2016 ; 47 37-42.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.dnarep.2015.11.006
Artigo de periodico
Simvastatin increases the antineoplastic actions of paclitaxel carried in lipid nanoemulsions in melanoma-bearing mice (2016)
Kretzer, Iara Fabricia; Maria, Durvanei Augusto; Guido, Maria Carolina; Contente, Thais Costa; Maranhão, Raul Cavalcante
Source: International Journal of Nanomedicine. Unidades: FM, FCF
Subjects: LIPOPROTEÍNAS LDL, MELANOMA, NEOPLASIAS OVARIANAS
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ABNT
KRETZER, Iara Fabricia et al. Simvastatin increases the antineoplastic actions of paclitaxel carried in lipid nanoemulsions in melanoma-bearing mice. International Journal of Nanomedicine, v. 11, p. 885-904, 2016Tradução . . Disponível em: https://doi.org/10.2147/IJN.S88546. Acesso em: 03 nov. 2024.
APA
Kretzer, I. F., Maria, D. A., Guido, M. C., Contente, T. C., & Maranhão, R. C. (2016). Simvastatin increases the antineoplastic actions of paclitaxel carried in lipid nanoemulsions in melanoma-bearing mice. International Journal of Nanomedicine, 11, 885-904. doi:10.2147/IJN.S88546
NLM
Kretzer IF, Maria DA, Guido MC, Contente TC, Maranhão RC. Simvastatin increases the antineoplastic actions of paclitaxel carried in lipid nanoemulsions in melanoma-bearing mice [Internet]. International Journal of Nanomedicine. 2016 ; 11 885-904.[citado 2024 nov. 03 ] Available from: https://doi.org/10.2147/IJN.S88546
Vancouver
Kretzer IF, Maria DA, Guido MC, Contente TC, Maranhão RC. Simvastatin increases the antineoplastic actions of paclitaxel carried in lipid nanoemulsions in melanoma-bearing mice [Internet]. International Journal of Nanomedicine. 2016 ; 11 885-904.[citado 2024 nov. 03 ] Available from: https://doi.org/10.2147/IJN.S88546
Artigo de periodico
'M IND. 1' and 'M IND. 3' muscarinic receptors may play a role in the neurotoxicity of anhydroecgonine methyl ester, a cocaine pyrolysis product (2015)
Garcia, Raphael Caio Tamborelli; Dati, Lívia Mendonça Munhoz ; Torres, Larissa Helena; Silva, Mariana Aguilera Alencar da; Udo, Mariana Sayuri Berto ; Abdalla, Fernando Maurício Francis; Costa, José Luiz da; Gorjão, Renata; Afeche, Solange Castro; Yonamine, Maurício ; Niswender, Colleen M; Conn, P. Jeffrey; Camarini, Rosana ; Sandoval, Maria Regina Lopes; Marcourakis, Tania
Source: Scientific Reports. Unidades: ICB, FCF
Subjects: PIRÓLISE, COCAÍNA
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ABNT
GARCIA, Raphael Caio Tamborelli et al. 'M IND. 1' and 'M IND. 3' muscarinic receptors may play a role in the neurotoxicity of anhydroecgonine methyl ester, a cocaine pyrolysis product. Scientific Reports, v. 5, p. 1-12, 2015Tradução . . Disponível em: https://doi.org/10.1038/srep17555. Acesso em: 03 nov. 2024.
APA
Garcia, R. C. T., Dati, L. M. M., Torres, L. H., Silva, M. A. A. da, Udo, M. S. B., Abdalla, F. M. F., et al. (2015). 'M IND. 1' and 'M IND. 3' muscarinic receptors may play a role in the neurotoxicity of anhydroecgonine methyl ester, a cocaine pyrolysis product. Scientific Reports, 5, 1-12. doi:10.1038/srep17555
NLM
Garcia RCT, Dati LMM, Torres LH, Silva MAA da, Udo MSB, Abdalla FMF, Costa JL da, Gorjão R, Afeche SC, Yonamine M, Niswender CM, Conn PJ, Camarini R, Sandoval MRL, Marcourakis T. 'M IND. 1' and 'M IND. 3' muscarinic receptors may play a role in the neurotoxicity of anhydroecgonine methyl ester, a cocaine pyrolysis product [Internet]. Scientific Reports. 2015 ; 5 1-12.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1038/srep17555
Vancouver
Garcia RCT, Dati LMM, Torres LH, Silva MAA da, Udo MSB, Abdalla FMF, Costa JL da, Gorjão R, Afeche SC, Yonamine M, Niswender CM, Conn PJ, Camarini R, Sandoval MRL, Marcourakis T. 'M IND. 1' and 'M IND. 3' muscarinic receptors may play a role in the neurotoxicity of anhydroecgonine methyl ester, a cocaine pyrolysis product [Internet]. Scientific Reports. 2015 ; 5 1-12.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1038/srep17555
Artigo de periodico
Curcumin analog DM-1 in monotherapy or combinatory treatment with dacarbazine as a strategy to inhibit in vivo melanoma progression (2015)
Flores, Fernanda Faião; Suárez, José Agustin Quincoces; Fruet, Andrea Costa; Maria-Engler, Silvya Stuchi ; Pardi, Paulo Celso; Maria, Durvanei Augusto
Source: PLOS ONE. Unidade: FCF
Subjects: FARMACOTERAPIA, AÇAFRÃO (COMPONENTES)
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ABNT
FLORES, Fernanda Faião et al. Curcumin analog DM-1 in monotherapy or combinatory treatment with dacarbazine as a strategy to inhibit in vivo melanoma progression. PLOS ONE, v. 10, n. 3, p. 1-16 art e0118702, 2015Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0118702. Acesso em: 03 nov. 2024.
APA
Flores, F. F., Suárez, J. A. Q., Fruet, A. C., Maria-Engler, S. S., Pardi, P. C., & Maria, D. A. (2015). Curcumin analog DM-1 in monotherapy or combinatory treatment with dacarbazine as a strategy to inhibit in vivo melanoma progression. PLOS ONE, 10( 3), 1-16 art e0118702. doi:10.1371/journal.pone.0118702
NLM
Flores FF, Suárez JAQ, Fruet AC, Maria-Engler SS, Pardi PC, Maria DA. Curcumin analog DM-1 in monotherapy or combinatory treatment with dacarbazine as a strategy to inhibit in vivo melanoma progression [Internet]. PLOS ONE. 2015 ; 10( 3): 1-16 art e0118702.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1371/journal.pone.0118702
Vancouver
Flores FF, Suárez JAQ, Fruet AC, Maria-Engler SS, Pardi PC, Maria DA. Curcumin analog DM-1 in monotherapy or combinatory treatment with dacarbazine as a strategy to inhibit in vivo melanoma progression [Internet]. PLOS ONE. 2015 ; 10( 3): 1-16 art e0118702.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1371/journal.pone.0118702
Artigo de periodico
Post-transcriptional control of Amblyomin-X on secretion of vascular endothelial growth factor and expression of adhesion molecules in endothelial cells (2015)
Drewes, Carine Cristiane; Dias, R. Y; Branco, V. G; Cavalcante, Marcela Frota; Souza, J. G; Abdalla, Dulcinéia Saes Parra ; Chudzinski-Tavassi, Ana Marisa; Farsky, Sandra Helena Poliselli
Source: Toxicon. Unidade: FCF
Subjects: AMBLYOMMA CAJENNENSE, INTEGRINAS
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ABNT
DREWES, Carine Cristiane et al. Post-transcriptional control of Amblyomin-X on secretion of vascular endothelial growth factor and expression of adhesion molecules in endothelial cells. Toxicon, v. 101, p. 1-10, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.toxicon.2015.04.002. Acesso em: 03 nov. 2024.
APA
Drewes, C. C., Dias, R. Y., Branco, V. G., Cavalcante, M. F., Souza, J. G., Abdalla, D. S. P., et al. (2015). Post-transcriptional control of Amblyomin-X on secretion of vascular endothelial growth factor and expression of adhesion molecules in endothelial cells. Toxicon, 101, 1-10. doi:10.1016/j.toxicon.2015.04.002
NLM
Drewes CC, Dias RY, Branco VG, Cavalcante MF, Souza JG, Abdalla DSP, Chudzinski-Tavassi AM, Farsky SHP. Post-transcriptional control of Amblyomin-X on secretion of vascular endothelial growth factor and expression of adhesion molecules in endothelial cells [Internet]. Toxicon. 2015 ; 101 1-10.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.toxicon.2015.04.002
Vancouver
Drewes CC, Dias RY, Branco VG, Cavalcante MF, Souza JG, Abdalla DSP, Chudzinski-Tavassi AM, Farsky SHP. Post-transcriptional control of Amblyomin-X on secretion of vascular endothelial growth factor and expression of adhesion molecules in endothelial cells [Internet]. Toxicon. 2015 ; 101 1-10.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.toxicon.2015.04.002
Trabalho de evento-resumo periodico
Hydroquinone exposure aggravates collagen induced arthritis (CIA) development in rats (2015)
Heluany, Cíntia Scucuglia; Kupa, Leonard de Vinci Kanda; Viana, Mariana N; Fernandes, Cristina Maria; Farsky, Sandra Helena Poliselli
Source: Inflammation Research. Conference titles: World Congress on Inflammation. Unidade: FCF
Assunto: ARTRITE REUMATOIDE
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ABNT
HELUANY, Cíntia Scucuglia et al. Hydroquinone exposure aggravates collagen induced arthritis (CIA) development in rats. Inflammation Research. Basel: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 03 nov. 2024. , 2015
APA
Heluany, C. S., Kupa, L. de V. K., Viana, M. N., Fernandes, C. M., & Farsky, S. H. P. (2015). Hydroquinone exposure aggravates collagen induced arthritis (CIA) development in rats. Inflammation Research. Basel: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo.
NLM
Heluany CS, Kupa L de VK, Viana MN, Fernandes CM, Farsky SHP. Hydroquinone exposure aggravates collagen induced arthritis (CIA) development in rats. Inflammation Research. 2015 ; 64 S110 res. B021 .[citado 2024 nov. 03 ]
Vancouver
Heluany CS, Kupa L de VK, Viana MN, Fernandes CM, Farsky SHP. Hydroquinone exposure aggravates collagen induced arthritis (CIA) development in rats. Inflammation Research. 2015 ; 64 S110 res. B021 .[citado 2024 nov. 03 ]
Artigo de periodico
Synergy of omeprazole and praziquantel In Vitro treatment against Schistosoma mansoni adult worms (2015)
Almeida, Giulliana Tessarin e; Lage, Regina Coeli Gonçalves; Anderson, Letícia; Venancio, Thiago Motta; Nakaya, Helder Takashi Imoto ; Miyasato, Patricia Aoki; Rofatto, Henrique Krambeck; Zerlotini, Adhemar; Nakano, Eliana; Oliveira, Guilherme; Verjovski-Almeida, Sergio
Source: Plos Neglected Tropical Diseases. Unidades: FCF, IQ
Subjects: SCHISTOSOMA MANSONI, ANTIPARASITÁRIOS
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ABNT
ALMEIDA, Giulliana Tessarin e et al. Synergy of omeprazole and praziquantel In Vitro treatment against Schistosoma mansoni adult worms. Plos Neglected Tropical Diseases, v. 9, n. 9, p. 1-23 art. e0004086, 2015Tradução . . Disponível em: https://doi.org/10.1371/journal.pntd.0004086. Acesso em: 03 nov. 2024.
APA
Almeida, G. T. e, Lage, R. C. G., Anderson, L., Venancio, T. M., Nakaya, H. T. I., Miyasato, P. A., et al. (2015). Synergy of omeprazole and praziquantel In Vitro treatment against Schistosoma mansoni adult worms. Plos Neglected Tropical Diseases, 9( 9), 1-23 art. e0004086. doi:10.1371/journal.pntd.0004086
NLM
Almeida GT e, Lage RCG, Anderson L, Venancio TM, Nakaya HTI, Miyasato PA, Rofatto HK, Zerlotini A, Nakano E, Oliveira G, Verjovski-Almeida S. Synergy of omeprazole and praziquantel In Vitro treatment against Schistosoma mansoni adult worms [Internet]. Plos Neglected Tropical Diseases. 2015 ; 9( 9): 1-23 art. e0004086.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1371/journal.pntd.0004086
Vancouver
Almeida GT e, Lage RCG, Anderson L, Venancio TM, Nakaya HTI, Miyasato PA, Rofatto HK, Zerlotini A, Nakano E, Oliveira G, Verjovski-Almeida S. Synergy of omeprazole and praziquantel In Vitro treatment against Schistosoma mansoni adult worms [Internet]. Plos Neglected Tropical Diseases. 2015 ; 9( 9): 1-23 art. e0004086.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1371/journal.pntd.0004086
Artigo de periodico
7,12-Dimethylbenz(a)anthracene-induced myelotoxicity differs in mice selected for high or low acute inflammatory response: relationship with aryl hydrocarbon receptor polymorphism (2014)
Katz, Iana Suly Santos; Albuquerque, Layra Lucy; Suppa, Alessandra Paes; Siqueira, Débora Mathias de; Rossato, Cristiano; Silva, Graziela Batista da; Jensen, José Ricardo; Starobinas, Nancy; Cabrera, Wafa Hanna Koury; Franco, Marcelo de; Borelli, Primavera ; Ibañez, Olga Célia Martinez; Ribeiro, Orlando Garcia
Source: International Journal of Toxicology. Unidade: FCF
Subjects: INFLAMAÇÃO, POLIMORFISMO, HIDROCARBONOS AROMÁTICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KATZ, Iana Suly Santos et al. 7,12-Dimethylbenz(a)anthracene-induced myelotoxicity differs in mice selected for high or low acute inflammatory response: relationship with aryl hydrocarbon receptor polymorphism. International Journal of Toxicology, v. 33, n. 2, p. 130-142, 2014Tradução . . Disponível em: https://doi.org/10.1177/1091581814522837. Acesso em: 03 nov. 2024.
APA
Katz, I. S. S., Albuquerque, L. L., Suppa, A. P., Siqueira, D. M. de, Rossato, C., Silva, G. B. da, et al. (2014). 7,12-Dimethylbenz(a)anthracene-induced myelotoxicity differs in mice selected for high or low acute inflammatory response: relationship with aryl hydrocarbon receptor polymorphism. International Journal of Toxicology, 33( 2), 130-142. doi:10.1177/1091581814522837
NLM
Katz ISS, Albuquerque LL, Suppa AP, Siqueira DM de, Rossato C, Silva GB da, Jensen JR, Starobinas N, Cabrera WHK, Franco M de, Borelli P, Ibañez OCM, Ribeiro OG. 7,12-Dimethylbenz(a)anthracene-induced myelotoxicity differs in mice selected for high or low acute inflammatory response: relationship with aryl hydrocarbon receptor polymorphism [Internet]. International Journal of Toxicology. 2014 ; 33( 2): 130-142.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1177/1091581814522837
Vancouver
Katz ISS, Albuquerque LL, Suppa AP, Siqueira DM de, Rossato C, Silva GB da, Jensen JR, Starobinas N, Cabrera WHK, Franco M de, Borelli P, Ibañez OCM, Ribeiro OG. 7,12-Dimethylbenz(a)anthracene-induced myelotoxicity differs in mice selected for high or low acute inflammatory response: relationship with aryl hydrocarbon receptor polymorphism [Internet]. International Journal of Toxicology. 2014 ; 33( 2): 130-142.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1177/1091581814522837

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