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Artigo de periodico
Autologous haematopoietic stem cell transplantation restores the suppressive capacity of regulatory B cells in systemic sclerosis patients (2021)
Lima-Júnior, João R.; Arruda, Lucas C. M.; Gonçalves, Maynara Santana; Dias, Juliana B. E.; Moraes, Daniela A.; Covas, Dimas Tadeu; Simões, Belinda Pinto; Oliveira, Maria Carolina; Malmegrim, Kelen Cristina Ribeiro
Source: Rheumatology. Unidades: FMRP, FCFRP
Subjects: DOENÇAS AUTOIMUNES, TRANSPLANTE AUTÓLOGO, CÉLULAS-TRONCO, TRANSPLANTE DE ÓRGÃOS, INTERLEUCINAS, SISTEMA IMUNE
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LIMA-JÚNIOR, João R. et al. Autologous haematopoietic stem cell transplantation restores the suppressive capacity of regulatory B cells in systemic sclerosis patients. Rheumatology, v. 60, n. 12, p. 5538–5548, 2021Tradução . . Disponível em: https://doi.org/10.1093/rheumatology/keab257. Acesso em: 02 jun. 2024.
APA
Lima-Júnior, J. R., Arruda, L. C. M., Gonçalves, M. S., Dias, J. B. E., Moraes, D. A., Covas, D. T., et al. (2021). Autologous haematopoietic stem cell transplantation restores the suppressive capacity of regulatory B cells in systemic sclerosis patients. Rheumatology, 60( 12), 5538–5548. doi:10.1093/rheumatology/keab257
NLM
Lima-Júnior JR, Arruda LCM, Gonçalves MS, Dias JBE, Moraes DA, Covas DT, Simões BP, Oliveira MC, Malmegrim KCR. Autologous haematopoietic stem cell transplantation restores the suppressive capacity of regulatory B cells in systemic sclerosis patients [Internet]. Rheumatology. 2021 ; 60( 12): 5538–5548.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1093/rheumatology/keab257
Vancouver
Lima-Júnior JR, Arruda LCM, Gonçalves MS, Dias JBE, Moraes DA, Covas DT, Simões BP, Oliveira MC, Malmegrim KCR. Autologous haematopoietic stem cell transplantation restores the suppressive capacity of regulatory B cells in systemic sclerosis patients [Internet]. Rheumatology. 2021 ; 60( 12): 5538–5548.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1093/rheumatology/keab257
Artigo de periodico
Generation of a three-dimensional in vitro ovarian cancer co-culture model for drug screening assays (2021)
Tofani, Larissa Bueno; Sousa, Lucas Oliveira ; Luiz, Marcela Tavares; Abriata, Juliana Palma; Marchetti, Juliana Maldonado; Leopoldino, Andréia Machado ; Swiech, Kamilla
Source: Journal of Pharmaceutical Sciences. Unidade: FCFRP
Subjects: LINHAGEM CELULAR, AVALIAÇÃO DE MEDICAMENTOS, NEOPLASIAS OVARIANAS, FARMACOTERAPIA, FIBROBLASTOS
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TOFANI, Larissa Bueno et al. Generation of a three-dimensional in vitro ovarian cancer co-culture model for drug screening assays. Journal of Pharmaceutical Sciences, v. 110, n. 7, p. 2629-2636, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.xphs.2021.04.003. Acesso em: 02 jun. 2024.
APA
Tofani, L. B., Sousa, L. O., Luiz, M. T., Abriata, J. P., Marchetti, J. M., Leopoldino, A. M., & Swiech, K. (2021). Generation of a three-dimensional in vitro ovarian cancer co-culture model for drug screening assays. Journal of Pharmaceutical Sciences, 110( 7), 2629-2636. doi:10.1016/j.xphs.2021.04.003
NLM
Tofani LB, Sousa LO, Luiz MT, Abriata JP, Marchetti JM, Leopoldino AM, Swiech K. Generation of a three-dimensional in vitro ovarian cancer co-culture model for drug screening assays [Internet]. Journal of Pharmaceutical Sciences. 2021 ; 110( 7): 2629-2636.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1016/j.xphs.2021.04.003
Vancouver
Tofani LB, Sousa LO, Luiz MT, Abriata JP, Marchetti JM, Leopoldino AM, Swiech K. Generation of a three-dimensional in vitro ovarian cancer co-culture model for drug screening assays [Internet]. Journal of Pharmaceutical Sciences. 2021 ; 110( 7): 2629-2636.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1016/j.xphs.2021.04.003
Artigo de periodico
Bone marrow soluble mediator signatures of patients with Philadelphia chromosome-negative myeloproliferative neoplasms (2021)
Cominal, Juçara Gastaldi; Cacemiro, Maira da Costa ; Berzoti-Coelho, Maria Gabriela ; Pereira, Illy Enne Gomes ; Frantz, Fabiani Gai ; Souto, Elizabeth Xisto; Covas, Dimas Tadeu; Figueiredo-Pontes, Lorena Lobo de; Oliveira, Maria Carolina; Malmegrim, Kelen Cristina Ribeiro ; Castro, Fabíola Attié de
Source: Frontiers in Oncology. Unidades: FCFRP, FMRP
Subjects: NEOVASCULARIZAÇÃO PATOLÓGICA, MEDULA ÓSSEA, CITOCINAS, INFLAMAÇÃO, NEOPLASIAS
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COMINAL, Juçara Gastaldi et al. Bone marrow soluble mediator signatures of patients with Philadelphia chromosome-negative myeloproliferative neoplasms. Frontiers in Oncology, v. 11, p. 1-12 , 2021Tradução . . Disponível em: https://doi.org/10.3389/fonc.2021.665037. Acesso em: 02 jun. 2024.
APA
Cominal, J. G., Cacemiro, M. da C., Berzoti-Coelho, M. G., Pereira, I. E. G., Frantz, F. G., Souto, E. X., et al. (2021). Bone marrow soluble mediator signatures of patients with Philadelphia chromosome-negative myeloproliferative neoplasms. Frontiers in Oncology, 11, 1-12 . doi:10.3389/fonc.2021.665037
NLM
Cominal JG, Cacemiro M da C, Berzoti-Coelho MG, Pereira IEG, Frantz FG, Souto EX, Covas DT, Figueiredo-Pontes LL de, Oliveira MC, Malmegrim KCR, Castro FA de. Bone marrow soluble mediator signatures of patients with Philadelphia chromosome-negative myeloproliferative neoplasms [Internet]. Frontiers in Oncology. 2021 ; 11 1-12 .[citado 2024 jun. 02 ] Available from: https://doi.org/10.3389/fonc.2021.665037
Vancouver
Cominal JG, Cacemiro M da C, Berzoti-Coelho MG, Pereira IEG, Frantz FG, Souto EX, Covas DT, Figueiredo-Pontes LL de, Oliveira MC, Malmegrim KCR, Castro FA de. Bone marrow soluble mediator signatures of patients with Philadelphia chromosome-negative myeloproliferative neoplasms [Internet]. Frontiers in Oncology. 2021 ; 11 1-12 .[citado 2024 jun. 02 ] Available from: https://doi.org/10.3389/fonc.2021.665037
Artigo de periodico
LPMO AfAA9_B and cellobiohydrolase AfCel6A from A. fumigatus boost enzymatic saccharification activity of cellulase cocktail (2021)
Bernardi, Aline Vianna ; Gerolamo, Luis Eduardo ; Gouvêa, Paula Fagundes de ; Yonamine, Deborah Kimie ; Pereira, Lucas Matheus Soares ; Oliveira, Arthur Henrique Cavalcante de ; Uyemura, Sérgio Akira ; Dinamarco, Taisa Magnani
Source: International Journal of Molecular Sciences. Unidades: FFCLRP, FCFRP
Subjects: HIDRÓLISE, BIOCOMBUSTÍVEIS, BIOMASSA, CELULOSE, FUNGOS, ASPERGILLUS, SACARIFICAÇÃO, BIOQUÍMICA
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BERNARDI, Aline Vianna et al. LPMO AfAA9_B and cellobiohydrolase AfCel6A from A. fumigatus boost enzymatic saccharification activity of cellulase cocktail. International Journal of Molecular Sciences, v. 22, n. 1, p. 1-23, 2021Tradução . . Disponível em: https://doi.org/10.3390/ijms22010276. Acesso em: 02 jun. 2024.
APA
Bernardi, A. V., Gerolamo, L. E., Gouvêa, P. F. de, Yonamine, D. K., Pereira, L. M. S., Oliveira, A. H. C. de, et al. (2021). LPMO AfAA9_B and cellobiohydrolase AfCel6A from A. fumigatus boost enzymatic saccharification activity of cellulase cocktail. International Journal of Molecular Sciences, 22( 1), 1-23. doi:10.3390/ijms22010276
NLM
Bernardi AV, Gerolamo LE, Gouvêa PF de, Yonamine DK, Pereira LMS, Oliveira AHC de, Uyemura SA, Dinamarco TM. LPMO AfAA9_B and cellobiohydrolase AfCel6A from A. fumigatus boost enzymatic saccharification activity of cellulase cocktail [Internet]. International Journal of Molecular Sciences. 2021 ; 22( 1): 1-23.[citado 2024 jun. 02 ] Available from: https://doi.org/10.3390/ijms22010276
Vancouver
Bernardi AV, Gerolamo LE, Gouvêa PF de, Yonamine DK, Pereira LMS, Oliveira AHC de, Uyemura SA, Dinamarco TM. LPMO AfAA9_B and cellobiohydrolase AfCel6A from A. fumigatus boost enzymatic saccharification activity of cellulase cocktail [Internet]. International Journal of Molecular Sciences. 2021 ; 22( 1): 1-23.[citado 2024 jun. 02 ] Available from: https://doi.org/10.3390/ijms22010276
Artigo de periodico
Glutathione reductase: a cytoplasmic antioxidant enzyme and a potential target for phenothiazinium dyes in Neospora caninum (2021)
Venancio-Brochi, Jade Cabestre; Pereira, Luiz Miguel; Calil, Felipe Antunes; Teixeira, Olívia; Baroni, Luciana; Abreu-Filho, Péricles Gama; Braga, Gilberto Ubida Leite; Nonato, Maria Cristina ; Yatsuda, Ana Patrícia
Source: International Journal of Biological Macromolecules. Unidade: FCFRP
Subjects: CITOPLASMA, INIBIDORES DE ENZIMAS, CINÉTICA, AZUL DE METILENO
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VENANCIO-BROCHI, Jade Cabestre et al. Glutathione reductase: a cytoplasmic antioxidant enzyme and a potential target for phenothiazinium dyes in Neospora caninum. International Journal of Biological Macromolecules, v. 187, p. 964-975, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.ijbiomac.2021.07.108. Acesso em: 02 jun. 2024.
APA
Venancio-Brochi, J. C., Pereira, L. M., Calil, F. A., Teixeira, O., Baroni, L., Abreu-Filho, P. G., et al. (2021). Glutathione reductase: a cytoplasmic antioxidant enzyme and a potential target for phenothiazinium dyes in Neospora caninum. International Journal of Biological Macromolecules, 187, 964-975. doi:10.1016/j.ijbiomac.2021.07.108
NLM
Venancio-Brochi JC, Pereira LM, Calil FA, Teixeira O, Baroni L, Abreu-Filho PG, Braga GUL, Nonato MC, Yatsuda AP. Glutathione reductase: a cytoplasmic antioxidant enzyme and a potential target for phenothiazinium dyes in Neospora caninum [Internet]. International Journal of Biological Macromolecules. 2021 ; 187 964-975.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1016/j.ijbiomac.2021.07.108
Vancouver
Venancio-Brochi JC, Pereira LM, Calil FA, Teixeira O, Baroni L, Abreu-Filho PG, Braga GUL, Nonato MC, Yatsuda AP. Glutathione reductase: a cytoplasmic antioxidant enzyme and a potential target for phenothiazinium dyes in Neospora caninum [Internet]. International Journal of Biological Macromolecules. 2021 ; 187 964-975.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1016/j.ijbiomac.2021.07.108
Artigo de periodico
Inflammasomes are activated in response to SARS-CoV-2 infection and are associated with COVID-19 severity in patients (2021)
Rodrigues, Tamara Silva ; Sá, Keyla Santos Guedes de ; Ishimoto, Adriene Yumi; Becerra, Amanda; Oliveira, Samuel; Almeida, Leticia; Gonçalves, Augusto V.; Perucello, Debora B.; Andrade, Warrison A. ; Castro, Ricardo; Veras, Flavio P.; Toller-Kawahisa, Juliana E.; Nascimento, Daniele C.; Lima, Mikhael H. F. de; Silva, Camila M. S.; Caetite, Diego B.; Martins, Ronaldo Bragança ; Castro, Italo A.; Pontelli, Marjorie C.; Barros, Fabio C. de; Amaral, Natália B. do; Giannini, Marcela C.; Bonjorno, Letícia P.; Lopes, Maria Isabel F.; Santana, Rodrigo de Carvalho ; Vilar, Fernando C.; Auxiliadora-Martins, Maria ; Luppino-Assad, Rodrigo; Almeida, Sergio C. L. de; Oliveira, Fabiola R. de; Batah, Sabrina Setembre ; Siyuan, Li; Benatti, Maira N.; Cunha, Thiago Mattar ; Alves Filho, José Carlos Farias ; Cunha, Fernando de Queiroz ; Cunha, Larissa D.; Frantz, Fabiani Gai ; Kohlsdorf, Tiana ; Fabro, Alexandre Todorovic ; Arruda, Eurico ; Oliveira, Renê D. R. de; Louzada Júnior, Paulo ; Zamboni, Dario Simões
Source: Journal of Experimental Medicine. Unidades: FMRP, FCFRP, FFCLRP
Subjects: COVID-19, INFLAMAÇÃO
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RODRIGUES, Tamara Silva et al. Inflammasomes are activated in response to SARS-CoV-2 infection and are associated with COVID-19 severity in patients. Journal of Experimental Medicine, v. 218, n. 3, 2021Tradução . . Disponível em: https://doi.org/10.1084/jem.20201707. Acesso em: 02 jun. 2024.
APA
Rodrigues, T. S., Sá, K. S. G. de, Ishimoto, A. Y., Becerra, A., Oliveira, S., Almeida, L., et al. (2021). Inflammasomes are activated in response to SARS-CoV-2 infection and are associated with COVID-19 severity in patients. Journal of Experimental Medicine, 218( 3). doi:10.1084/jem.20201707
NLM
Rodrigues TS, Sá KSG de, Ishimoto AY, Becerra A, Oliveira S, Almeida L, Gonçalves AV, Perucello DB, Andrade WA, Castro R, Veras FP, Toller-Kawahisa JE, Nascimento DC, Lima MHF de, Silva CMS, Caetite DB, Martins RB, Castro IA, Pontelli MC, Barros FC de, Amaral NB do, Giannini MC, Bonjorno LP, Lopes MIF, Santana R de C, Vilar FC, Auxiliadora-Martins M, Luppino-Assad R, Almeida SCL de, Oliveira FR de, Batah SS, Siyuan L, Benatti MN, Cunha TM, Alves Filho JCF, Cunha F de Q, Cunha LD, Frantz FG, Kohlsdorf T, Fabro AT, Arruda E, Oliveira RDR de, Louzada Júnior P, Zamboni DS. Inflammasomes are activated in response to SARS-CoV-2 infection and are associated with COVID-19 severity in patients [Internet]. Journal of Experimental Medicine. 2021 ; 218( 3):[citado 2024 jun. 02 ] Available from: https://doi.org/10.1084/jem.20201707
Vancouver
Rodrigues TS, Sá KSG de, Ishimoto AY, Becerra A, Oliveira S, Almeida L, Gonçalves AV, Perucello DB, Andrade WA, Castro R, Veras FP, Toller-Kawahisa JE, Nascimento DC, Lima MHF de, Silva CMS, Caetite DB, Martins RB, Castro IA, Pontelli MC, Barros FC de, Amaral NB do, Giannini MC, Bonjorno LP, Lopes MIF, Santana R de C, Vilar FC, Auxiliadora-Martins M, Luppino-Assad R, Almeida SCL de, Oliveira FR de, Batah SS, Siyuan L, Benatti MN, Cunha TM, Alves Filho JCF, Cunha F de Q, Cunha LD, Frantz FG, Kohlsdorf T, Fabro AT, Arruda E, Oliveira RDR de, Louzada Júnior P, Zamboni DS. Inflammasomes are activated in response to SARS-CoV-2 infection and are associated with COVID-19 severity in patients [Internet]. Journal of Experimental Medicine. 2021 ; 218( 3):[citado 2024 jun. 02 ] Available from: https://doi.org/10.1084/jem.20201707
Artigo de periodico
Hypoxia priming improves in vitro angiogenic properties of umbilical cord derived-mesenchymal stromal cells expanded in stirred-tank bioreactor (2021)
Noronha, Nadia de Cássia; Mizukami, Amanda; Orellana, Maristela Delgado; Oliveira, Maria Carolina de; Covas, Dimas Tadeu; Swiech, Kamilla; Malmegrim, Kelen Cristina Ribeiro
Source: Biochemical Engineering Journal. Unidades: FMRP, FCFRP
Subjects: CÉLULAS ESTROMAIS, ANÓXIA, REATORES BIOQUÍMICOS, ADJUVANTES IMUNOLÓGICOS
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NORONHA, Nadia de Cássia et al. Hypoxia priming improves in vitro angiogenic properties of umbilical cord derived-mesenchymal stromal cells expanded in stirred-tank bioreactor. Biochemical Engineering Journal, v. 168, p. 1-11, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bej.2021.107949. Acesso em: 02 jun. 2024.
APA
Noronha, N. de C., Mizukami, A., Orellana, M. D., Oliveira, M. C. de, Covas, D. T., Swiech, K., & Malmegrim, K. C. R. (2021). Hypoxia priming improves in vitro angiogenic properties of umbilical cord derived-mesenchymal stromal cells expanded in stirred-tank bioreactor. Biochemical Engineering Journal, 168, 1-11. doi:10.1016/j.bej.2021.107949
NLM
Noronha N de C, Mizukami A, Orellana MD, Oliveira MC de, Covas DT, Swiech K, Malmegrim KCR. Hypoxia priming improves in vitro angiogenic properties of umbilical cord derived-mesenchymal stromal cells expanded in stirred-tank bioreactor [Internet]. Biochemical Engineering Journal. 2021 ; 168 1-11.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1016/j.bej.2021.107949
Vancouver
Noronha N de C, Mizukami A, Orellana MD, Oliveira MC de, Covas DT, Swiech K, Malmegrim KCR. Hypoxia priming improves in vitro angiogenic properties of umbilical cord derived-mesenchymal stromal cells expanded in stirred-tank bioreactor [Internet]. Biochemical Engineering Journal. 2021 ; 168 1-11.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1016/j.bej.2021.107949
Artigo de periodico
Crosstalk between hnRNP K and SET in ATRA‐induced differentiation in acute promyelocytic leukemia (2021)
Padovani, Karina Stringhetta; Goto, Renata Nishida; Fugio, Lais Brigliadori; Garcia, Cristiana Bernadelli ; Alves, Vani Maria; Brassesco, Maria Sol ; Greene, Lewis Joel; Rego, Eduardo Magalhães; Leopoldino, Andréia Machado
Source: FEBS Open Bio. Unidades: FCFRP, FMRP, FFCLRP, FM
Subjects: LEUCEMIA, EXPRESSÃO GÊNICA, TRANSCRIÇÃO GÊNICA, CÉLULAS DA MEDULA ÓSSEA
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PADOVANI, Karina Stringhetta et al. Crosstalk between hnRNP K and SET in ATRA‐induced differentiation in acute promyelocytic leukemia. FEBS Open Bio, v. 11, n. 7, p. 2019-2032, 2021Tradução . . Disponível em: https://doi.org/10.1002/2211-5463.13210. Acesso em: 02 jun. 2024.
APA
Padovani, K. S., Goto, R. N., Fugio, L. B., Garcia, C. B., Alves, V. M., Brassesco, M. S., et al. (2021). Crosstalk between hnRNP K and SET in ATRA‐induced differentiation in acute promyelocytic leukemia. FEBS Open Bio, 11( 7), 2019-2032. doi:10.1002/2211-5463.13210
NLM
Padovani KS, Goto RN, Fugio LB, Garcia CB, Alves VM, Brassesco MS, Greene LJ, Rego EM, Leopoldino AM. Crosstalk between hnRNP K and SET in ATRA‐induced differentiation in acute promyelocytic leukemia [Internet]. FEBS Open Bio. 2021 ; 11( 7): 2019-2032.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1002/2211-5463.13210
Vancouver
Padovani KS, Goto RN, Fugio LB, Garcia CB, Alves VM, Brassesco MS, Greene LJ, Rego EM, Leopoldino AM. Crosstalk between hnRNP K and SET in ATRA‐induced differentiation in acute promyelocytic leukemia [Internet]. FEBS Open Bio. 2021 ; 11( 7): 2019-2032.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1002/2211-5463.13210
Artigo de periodico
Immortalized keratinocytes cells generates an effective model of Epidermal Human Equivalent for irritation and corrosion tests (2021)
Mini, Camila Alessandra ; Dreossi, Sonia Aparecida Carvalho; Abe, Flavia Renata ; Maria-Engler, Silvya Stuchi ; Oliveira, Danielle Palma de
Source: Toxicology in Vitro. Unidades: FCFRP, FCF
Subjects: TERCEIRA DIMENSÃO, PELE
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MINI, Camila Alessandra et al. Immortalized keratinocytes cells generates an effective model of Epidermal Human Equivalent for irritation and corrosion tests. Toxicology in Vitro, v. 71, p. 1-9, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.tiv.2020.105069. Acesso em: 02 jun. 2024.
APA
Mini, C. A., Dreossi, S. A. C., Abe, F. R., Maria-Engler, S. S., & Oliveira, D. P. de. (2021). Immortalized keratinocytes cells generates an effective model of Epidermal Human Equivalent for irritation and corrosion tests. Toxicology in Vitro, 71, 1-9. doi:10.1016/j.tiv.2020.105069
NLM
Mini CA, Dreossi SAC, Abe FR, Maria-Engler SS, Oliveira DP de. Immortalized keratinocytes cells generates an effective model of Epidermal Human Equivalent for irritation and corrosion tests [Internet]. Toxicology in Vitro. 2021 ; 71 1-9.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1016/j.tiv.2020.105069
Vancouver
Mini CA, Dreossi SAC, Abe FR, Maria-Engler SS, Oliveira DP de. Immortalized keratinocytes cells generates an effective model of Epidermal Human Equivalent for irritation and corrosion tests [Internet]. Toxicology in Vitro. 2021 ; 71 1-9.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1016/j.tiv.2020.105069
Artigo de periodico
A synthetic snake-venom-based tripeptide protects PC12 cells from the neurotoxicity of acrolein by improving axonal plasticity and bioenergetics (2020)
Bernardes, Carolina Petri ; Santos, Neife Aparecida Guinaim dos; Costa, Tassia R.; Sisti, Flávia Malvestio; Amaral, Lilian do ; Menaldo, Danilo Luccas ; Amstalden, Martin Krähenbühl; Ribeiro, Diego Luis ; Antunes, Lusânia Maria Greggi ; Sampaio, Suely Vilela ; Santos, Antônio Cardozo dos
Source: Neurotoxicity Research. Unidades: FCFRP, FMRP
Subjects: VENENOS, COBRAS, PROTEÍNAS QUINASES, ANTAGONISTAS, TOXICIDADE EM ANIMAL, APOLIPOPROTEÍNAS, BIOMARCADORES, DIFERENCIAÇÃO CELULAR, GLICOSE, PLASTICIDADE NEURONAL
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BERNARDES, Carolina Petri et al. A synthetic snake-venom-based tripeptide protects PC12 cells from the neurotoxicity of acrolein by improving axonal plasticity and bioenergetics. Neurotoxicity Research, v. 37, n. 1, p. 227-237, 2020Tradução . . Disponível em: https://doi.org/10.1007/s12640-019-00111-0. Acesso em: 02 jun. 2024.
APA
Bernardes, C. P., Santos, N. A. G. dos, Costa, T. R., Sisti, F. M., Amaral, L. do, Menaldo, D. L., et al. (2020). A synthetic snake-venom-based tripeptide protects PC12 cells from the neurotoxicity of acrolein by improving axonal plasticity and bioenergetics. Neurotoxicity Research, 37( 1), 227-237. doi:10.1007/s12640-019-00111-0
NLM
Bernardes CP, Santos NAG dos, Costa TR, Sisti FM, Amaral L do, Menaldo DL, Amstalden MK, Ribeiro DL, Antunes LMG, Sampaio SV, Santos AC dos. A synthetic snake-venom-based tripeptide protects PC12 cells from the neurotoxicity of acrolein by improving axonal plasticity and bioenergetics [Internet]. Neurotoxicity Research. 2020 ; 37( 1): 227-237.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1007/s12640-019-00111-0
Vancouver
Bernardes CP, Santos NAG dos, Costa TR, Sisti FM, Amaral L do, Menaldo DL, Amstalden MK, Ribeiro DL, Antunes LMG, Sampaio SV, Santos AC dos. A synthetic snake-venom-based tripeptide protects PC12 cells from the neurotoxicity of acrolein by improving axonal plasticity and bioenergetics [Internet]. Neurotoxicity Research. 2020 ; 37( 1): 227-237.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1007/s12640-019-00111-0
Artigo de periodico
Beyond hemostasis: a snake venom serine protease with potassium channel blocking and potential antitumor activities (2020)
Boldrini-França, Johara; Pinheiro-Júnior, Ernesto Lopes ; Peigneur, Steve; Pucca, Manuela Berto; Cerni, Felipe Augusto; Borges, Rafael Junqueira; Costa, Tássia Rafaella; Carone, Sante Emmanuel Imai; Fontes, Marcos Roberto de Mattos; Sampaio, Suely Vilela ; Arantes, Eliane Candiani ; Tytgat, Jan
Source: Scientific Reports. Unidade: FCFRP
Subjects: SEQUÊNCIA DE AMINOÁCIDOS, ANTINEOPLÁSICOS, FARMACOLOGIA, CATÁLISE, LINHAGEM CELULAR, CANAIS DE POTÁSSIO, ANTAGONISTAS, HEMOSTASIA, PROTEÍNAS RECOMBINANTES, VENENOS, PROTEÍNAS
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ABNT
BOLDRINI-FRANÇA, Johara et al. Beyond hemostasis: a snake venom serine protease with potassium channel blocking and potential antitumor activities. Scientific Reports, v. 10, n. 1, 2020Tradução . . Disponível em: https://doi.org/10.1038/s41598-020-61258-x. Acesso em: 02 jun. 2024.
APA
Boldrini-França, J., Pinheiro-Júnior, E. L., Peigneur, S., Pucca, M. B., Cerni, F. A., Borges, R. J., et al. (2020). Beyond hemostasis: a snake venom serine protease with potassium channel blocking and potential antitumor activities. Scientific Reports, 10( 1). doi:10.1038/s41598-020-61258-x
NLM
Boldrini-França J, Pinheiro-Júnior EL, Peigneur S, Pucca MB, Cerni FA, Borges RJ, Costa TR, Carone SEI, Fontes MR de M, Sampaio SV, Arantes EC, Tytgat J. Beyond hemostasis: a snake venom serine protease with potassium channel blocking and potential antitumor activities [Internet]. Scientific Reports. 2020 ; 10( 1):[citado 2024 jun. 02 ] Available from: https://doi.org/10.1038/s41598-020-61258-x
Vancouver
Boldrini-França J, Pinheiro-Júnior EL, Peigneur S, Pucca MB, Cerni FA, Borges RJ, Costa TR, Carone SEI, Fontes MR de M, Sampaio SV, Arantes EC, Tytgat J. Beyond hemostasis: a snake venom serine protease with potassium channel blocking and potential antitumor activities [Internet]. Scientific Reports. 2020 ; 10( 1):[citado 2024 jun. 02 ] Available from: https://doi.org/10.1038/s41598-020-61258-x
Artigo de periodico
Multifaceted antibodies development against synthetic α-dystroglycan mucin glycopeptide as promising tools for dystroglycanopathies diagnostic (2020)
Léo, Thais Canassa De ; Campo, Vanessa Leiria; Rodrigues, Lilian Cataldi ; Marchiori, Marcelo Fiori; Fuzo, Carlos Alessandro; Brigido, Marcelo Macedo; Sandomenico, Annamaria; Ruvo, Menotti; Maranhão, Andrea Queiroz; Dias-Baruffi, Marcelo
Source: Glycoconjugate Journal. Unidade: FCFRP
Subjects: ANTICORPOS MONOCLONAIS, IMUNOLOGIA, GLICOPROTEÍNAS, SÍNTESE QUÍMICA, DISTROFIA MUSCULAR
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ABNT
LÉO, Thais Canassa De et al. Multifaceted antibodies development against synthetic α-dystroglycan mucin glycopeptide as promising tools for dystroglycanopathies diagnostic. Glycoconjugate Journal, v. 37, n. 1, p. 77-93, 2020Tradução . . Disponível em: https://doi.org/10.1007/s10719-019-09893-z. Acesso em: 02 jun. 2024.
APA
Léo, T. C. D., Campo, V. L., Rodrigues, L. C., Marchiori, M. F., Fuzo, C. A., Brigido, M. M., et al. (2020). Multifaceted antibodies development against synthetic α-dystroglycan mucin glycopeptide as promising tools for dystroglycanopathies diagnostic. Glycoconjugate Journal, 37( 1), 77-93. doi:10.1007/s10719-019-09893-z
NLM
Léo TCD, Campo VL, Rodrigues LC, Marchiori MF, Fuzo CA, Brigido MM, Sandomenico A, Ruvo M, Maranhão AQ, Dias-Baruffi M. Multifaceted antibodies development against synthetic α-dystroglycan mucin glycopeptide as promising tools for dystroglycanopathies diagnostic [Internet]. Glycoconjugate Journal. 2020 ; 37( 1): 77-93.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1007/s10719-019-09893-z
Vancouver
Léo TCD, Campo VL, Rodrigues LC, Marchiori MF, Fuzo CA, Brigido MM, Sandomenico A, Ruvo M, Maranhão AQ, Dias-Baruffi M. Multifaceted antibodies development against synthetic α-dystroglycan mucin glycopeptide as promising tools for dystroglycanopathies diagnostic [Internet]. Glycoconjugate Journal. 2020 ; 37( 1): 77-93.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1007/s10719-019-09893-z
Artigo de periodico
Phenotypic analyses of Salmonella enterica serovar Enteritidis strains isolated in the pre- and post-epidemic period in Brazil (2020)
Campioni, Fábio; Gomes, Carolina Nogueira; Rodrigues, Dália dos Prazeres; Bergamini, Alzira Maria Morato; Falcão, Juliana Pfrimer
Source: Brazilian Journal of Microbiology. Unidade: FCFRP
Subjects: SURTOS DE DOENÇAS, MACRÓFAGOS, SOBREVIVÊNCIA CELULAR, SALMONELLA, ESTRESSE
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ABNT
CAMPIONI, Fábio et al. Phenotypic analyses of Salmonella enterica serovar Enteritidis strains isolated in the pre- and post-epidemic period in Brazil. Brazilian Journal of Microbiology, v. 52, n. 1, p. 173-183, 2020Tradução . . Disponível em: https://doi.org/10.1007/s42770-020-00392-0. Acesso em: 02 jun. 2024.
APA
Campioni, F., Gomes, C. N., Rodrigues, D. dos P., Bergamini, A. M. M., & Falcão, J. P. (2020). Phenotypic analyses of Salmonella enterica serovar Enteritidis strains isolated in the pre- and post-epidemic period in Brazil. Brazilian Journal of Microbiology, 52( 1), 173-183. doi:10.1007/s42770-020-00392-0
NLM
Campioni F, Gomes CN, Rodrigues D dos P, Bergamini AMM, Falcão JP. Phenotypic analyses of Salmonella enterica serovar Enteritidis strains isolated in the pre- and post-epidemic period in Brazil [Internet]. Brazilian Journal of Microbiology. 2020 ; 52( 1): 173-183.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1007/s42770-020-00392-0
Vancouver
Campioni F, Gomes CN, Rodrigues D dos P, Bergamini AMM, Falcão JP. Phenotypic analyses of Salmonella enterica serovar Enteritidis strains isolated in the pre- and post-epidemic period in Brazil [Internet]. Brazilian Journal of Microbiology. 2020 ; 52( 1): 173-183.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1007/s42770-020-00392-0
Artigo de periodico
Partial correlation between phenotypic and genotypic antimicrobial resistance of Salmonella enterica serovar enteritidis strains from Brazil (2020)
Campioni, Fábio; Gomes, Carolina Nogueira; Bergamini, Alzira M. M; Rodrigues, Dália P.; Falcão, Juliana Pfrimer
Source: Microbial Drug Resistance. Unidade: FCFRP
Subjects: SALMONELLA, GENÓTIPOS, FENÓTIPOS, SEQUENCIAMENTO GENÉTICO, RESISTÊNCIA MICROBIANA ÀS DROGAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAMPIONI, Fábio et al. Partial correlation between phenotypic and genotypic antimicrobial resistance of Salmonella enterica serovar enteritidis strains from Brazil. Microbial Drug Resistance, v. 26, n. 12, p. 1466-1471, 2020Tradução . . Disponível em: https://doi.org/10.1089/mdr.2019.0477. Acesso em: 02 jun. 2024.
APA
Campioni, F., Gomes, C. N., Bergamini, A. M. M., Rodrigues, D. P., & Falcão, J. P. (2020). Partial correlation between phenotypic and genotypic antimicrobial resistance of Salmonella enterica serovar enteritidis strains from Brazil. Microbial Drug Resistance, 26( 12), 1466-1471. doi:10.1089/mdr.2019.0477
NLM
Campioni F, Gomes CN, Bergamini AMM, Rodrigues DP, Falcão JP. Partial correlation between phenotypic and genotypic antimicrobial resistance of Salmonella enterica serovar enteritidis strains from Brazil [Internet]. Microbial Drug Resistance. 2020 ; 26( 12): 1466-1471.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1089/mdr.2019.0477
Vancouver
Campioni F, Gomes CN, Bergamini AMM, Rodrigues DP, Falcão JP. Partial correlation between phenotypic and genotypic antimicrobial resistance of Salmonella enterica serovar enteritidis strains from Brazil [Internet]. Microbial Drug Resistance. 2020 ; 26( 12): 1466-1471.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1089/mdr.2019.0477
Artigo de periodico
Polymorphisms in inflammatory genes modulate clinical complications in patients with sickle cell disease (2020)
Tozatto-Maio, Karina; Girot, Robert; Ly, Indou Deme ; Silva-Pinto, Ana Cristina; Rocha, Vanderson Geraldo ; Fernandes, Francisco José de Almeida; Diagne, Ibrahima; Benzerara, Yahia ; Dinardo, Carla Luana ; Soler, Júlia Maria Pavan ; Haddad, Simone Kashima ; Araujo, Itauá Leston ; Kenzey, Chantal ; Fonseca, Guilherme Henrique Hencklain; Sandoval, Evandra Strazza Rodrigues ; Volt, Fernanda; Jarduli, Luciana; Ruggeri, Annalisa ; Mariaselvam, Christina ; Gualandro, Sandra Fátima Menosi ; Rafii, Hanadi ; Cappelli, Barbara ; Nogueira, Felipe Melo; Scigliuolo, Graziana Maria; Cunha, Renato Luiz Guerino ; Farias, Kelen Cristina Ribeiro Malmegrim de ; Simões, Belinda Pinto ; Gluckman, Eliane ; Tamouza, Ryad
Source: Frontiers in Immunology. Unidades: FMRP, FM, FCFRP, IME
Subjects: ANEMIA FALCIFORME, REGRESSÃO LOGÍSTICA, R (SOFTWARE ESTATÍSTICO)
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ABNT
TOZATTO-MAIO, Karina et al. Polymorphisms in inflammatory genes modulate clinical complications in patients with sickle cell disease. Frontiers in Immunology, v. 11, 2020Tradução . . Disponível em: https://doi.org/10.3389/fimmu.2020.02041. Acesso em: 02 jun. 2024.
APA
Tozatto-Maio, K., Girot, R., Ly, I. D., Silva-Pinto, A. C., Rocha, V. G., Fernandes, F. J. de A., et al. (2020). Polymorphisms in inflammatory genes modulate clinical complications in patients with sickle cell disease. Frontiers in Immunology, 11. doi:10.3389/fimmu.2020.02041
NLM
Tozatto-Maio K, Girot R, Ly ID, Silva-Pinto AC, Rocha VG, Fernandes FJ de A, Diagne I, Benzerara Y, Dinardo CL, Soler JMP, Haddad SK, Araujo IL, Kenzey C, Fonseca GHH, Sandoval ESR, Volt F, Jarduli L, Ruggeri A, Mariaselvam C, Gualandro SFM, Rafii H, Cappelli B, Nogueira FM, Scigliuolo GM, Cunha RLG, Farias KCRM de, Simões BP, Gluckman E, Tamouza R. Polymorphisms in inflammatory genes modulate clinical complications in patients with sickle cell disease [Internet]. Frontiers in Immunology. 2020 ; 11[citado 2024 jun. 02 ] Available from: https://doi.org/10.3389/fimmu.2020.02041
Vancouver
Tozatto-Maio K, Girot R, Ly ID, Silva-Pinto AC, Rocha VG, Fernandes FJ de A, Diagne I, Benzerara Y, Dinardo CL, Soler JMP, Haddad SK, Araujo IL, Kenzey C, Fonseca GHH, Sandoval ESR, Volt F, Jarduli L, Ruggeri A, Mariaselvam C, Gualandro SFM, Rafii H, Cappelli B, Nogueira FM, Scigliuolo GM, Cunha RLG, Farias KCRM de, Simões BP, Gluckman E, Tamouza R. Polymorphisms in inflammatory genes modulate clinical complications in patients with sickle cell disease [Internet]. Frontiers in Immunology. 2020 ; 11[citado 2024 jun. 02 ] Available from: https://doi.org/10.3389/fimmu.2020.02041
Artigo de periodico
Photodynamic inactivation of Candida albicans and Candida tropicalis with aluminum phthalocyanine chloride nanoemulsion (2020)
Rodrigues, Gabriela Braga; Brancini, Guilherme Thomaz Pereira ; Pinto, Marcelo Rodrigues; Primo, Fernando Lucas ; Wainwright, Mark ; Tedesco, Antônio Cláudio ; Braga, Gilberto Ubida Leite
Source: Fungal Biology. Unidades: FCFRP, FFCLRP
Subjects: TERAPIA FOTODINÂMICA, CANDIDA ALBICANS, IMUNOSSUPRESSÃO
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ABNT
RODRIGUES, Gabriela Braga et al. Photodynamic inactivation of Candida albicans and Candida tropicalis with aluminum phthalocyanine chloride nanoemulsion. Fungal Biology, v. 124, n. 5, p. 297-303, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.funbio.2019.08.004. Acesso em: 02 jun. 2024.
APA
Rodrigues, G. B., Brancini, G. T. P., Pinto, M. R., Primo, F. L., Wainwright, M., Tedesco, A. C., & Braga, G. U. L. (2020). Photodynamic inactivation of Candida albicans and Candida tropicalis with aluminum phthalocyanine chloride nanoemulsion. Fungal Biology, 124( 5), 297-303. doi:10.1016/j.funbio.2019.08.004
NLM
Rodrigues GB, Brancini GTP, Pinto MR, Primo FL, Wainwright M, Tedesco AC, Braga GUL. Photodynamic inactivation of Candida albicans and Candida tropicalis with aluminum phthalocyanine chloride nanoemulsion [Internet]. Fungal Biology. 2020 ; 124( 5): 297-303.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1016/j.funbio.2019.08.004
Vancouver
Rodrigues GB, Brancini GTP, Pinto MR, Primo FL, Wainwright M, Tedesco AC, Braga GUL. Photodynamic inactivation of Candida albicans and Candida tropicalis with aluminum phthalocyanine chloride nanoemulsion [Internet]. Fungal Biology. 2020 ; 124( 5): 297-303.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1016/j.funbio.2019.08.004
Artigo de periodico
The Third International Symposium on Fungal Stress – ISFUS (2020)
Alder-Rangel, Alene; Idnurm, Alexander ; Brand, Alexandra C ; Brown, Alistair J. P. ; Gorbushina, Anna; Kelliher, Christina M; Campos, Claudia B; Levin, David E; Bell-Pedersen, Deborah ; Dadachova, Ekaterina ; Bauer, Florian Franz ; Gadd, Geoffrey M. ; Braus, Gerhard H. ; Braga, Gilberto Ubida Leite ; Brancini, Guilherme Thomaz Pereira ; Walker, Graeme Maxwell ; Druzhinina, Irina; Pócsi, István; Dijksterhuis, Jan; Aguirre, Jesús ; Hallsworth, John E. ; Schumacher, Julia; Wong, Koon Ho ; Selbmann, Laura; Corrochano, Luis M. ; Kupiec, Martin; Momany, Michelle ; Molin, Mikael ; Requena, Natalia; Yarden, Oded; Cordero, Radamés J. B ; Fischer, Reinhard; Pascon, Renata C ; Mancinelli, Rocco L; Emri, Tamas ; Basso, Thiago Olitta ; Rangel, Drauzio Eduardo Naretto
Source: Fungal Biology. Unidades: FCFRP, EP
Subjects: MICOLOGIA INDUSTRIAL, MICOLOGIA MÉDICA
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ABNT
ALDER-RANGEL, Alene et al. The Third International Symposium on Fungal Stress – ISFUS. Fungal Biology, v. 124, n. 5, p. 235-252, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.funbio.2020.02.007. Acesso em: 02 jun. 2024.
APA
Alder-Rangel, A., Idnurm, A., Brand, A. C., Brown, A. J. P., Gorbushina, A., Kelliher, C. M., et al. (2020). The Third International Symposium on Fungal Stress – ISFUS. Fungal Biology, 124( 5), 235-252. doi:10.1016/j.funbio.2020.02.007
NLM
Alder-Rangel A, Idnurm A, Brand AC, Brown AJP, Gorbushina A, Kelliher CM, Campos CB, Levin DE, Bell-Pedersen D, Dadachova E, Bauer FF, Gadd GM, Braus GH, Braga GUL, Brancini GTP, Walker GM, Druzhinina I, Pócsi I, Dijksterhuis J, Aguirre J, Hallsworth JE, Schumacher J, Wong KH, Selbmann L, Corrochano LM, Kupiec M, Momany M, Molin M, Requena N, Yarden O, Cordero RJB, Fischer R, Pascon RC, Mancinelli RL, Emri T, Basso TO, Rangel DEN. The Third International Symposium on Fungal Stress – ISFUS [Internet]. Fungal Biology. 2020 ; 124( 5): 235-252.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1016/j.funbio.2020.02.007
Vancouver
Alder-Rangel A, Idnurm A, Brand AC, Brown AJP, Gorbushina A, Kelliher CM, Campos CB, Levin DE, Bell-Pedersen D, Dadachova E, Bauer FF, Gadd GM, Braus GH, Braga GUL, Brancini GTP, Walker GM, Druzhinina I, Pócsi I, Dijksterhuis J, Aguirre J, Hallsworth JE, Schumacher J, Wong KH, Selbmann L, Corrochano LM, Kupiec M, Momany M, Molin M, Requena N, Yarden O, Cordero RJB, Fischer R, Pascon RC, Mancinelli RL, Emri T, Basso TO, Rangel DEN. The Third International Symposium on Fungal Stress – ISFUS [Internet]. Fungal Biology. 2020 ; 124( 5): 235-252.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1016/j.funbio.2020.02.007
Artigo de periodico
Global liver proteomic analysis of Wistar rats chronically exposed to low-levels of bisphenol A and S (2020)
Azevedo, Lara Ferreira ; Carneiro, Maria Fernanda Hornos ; Dechandt, Carlos Roberto Porto ; Cassoli, Juliana Silva ; Alberici, Luciane Carla ; Barbosa Junior, Fernando
Source: Environmental Research. Unidade: FCFRP
Subjects: HOMEOSTASE, FÍGADO, PROTEÔMICA, FENÓIS
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ABNT
AZEVEDO, Lara Ferreira et al. Global liver proteomic analysis of Wistar rats chronically exposed to low-levels of bisphenol A and S. Environmental Research, v. 182, p. 109080, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.envres.2019.109080. Acesso em: 02 jun. 2024.
APA
Azevedo, L. F., Carneiro, M. F. H., Dechandt, C. R. P., Cassoli, J. S., Alberici, L. C., & Barbosa Junior, F. (2020). Global liver proteomic analysis of Wistar rats chronically exposed to low-levels of bisphenol A and S. Environmental Research, 182, 109080. doi:10.1016/j.envres.2019.109080
NLM
Azevedo LF, Carneiro MFH, Dechandt CRP, Cassoli JS, Alberici LC, Barbosa Junior F. Global liver proteomic analysis of Wistar rats chronically exposed to low-levels of bisphenol A and S [Internet]. Environmental Research. 2020 ; 182 109080.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1016/j.envres.2019.109080
Vancouver
Azevedo LF, Carneiro MFH, Dechandt CRP, Cassoli JS, Alberici LC, Barbosa Junior F. Global liver proteomic analysis of Wistar rats chronically exposed to low-levels of bisphenol A and S [Internet]. Environmental Research. 2020 ; 182 109080.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1016/j.envres.2019.109080
Artigo de periodico
Eicosanoid pathway on host resistance and inflammation during Mycobacterium tuberculosis infection is comprised by LTB4 reduction but not PGE2 increment (2020)
Sorgi, Carlos Arterio ; Soares, Elyara Maria; Rosada, Rogério Silva; Bitencourt, Claudia Silva; Zoccal, Karina Furlani ; Pereira, Priscilla Aparecida Tártari; Fontanari, Caroline; Brandão, Izaira Tincani; Masson, Ana Paula ; Ramos, Simone Gusmão ; Silva, Célio Lopes ; Frantz, Fabiani Gai ; Faccioli, Lucia Helena
Source: Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. Unidades: FFCLRP, FCFRP, FMRP
Subjects: TUBERCULOSE, LEUCOTRIENOS, PROSTAGLANDINAS, INFLAMAÇÃO, IMUNOPATOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SORGI, Carlos Arterio et al. Eicosanoid pathway on host resistance and inflammation during Mycobacterium tuberculosis infection is comprised by LTB4 reduction but not PGE2 increment. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, v. 1866, n. 3, p. [10] , 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bbadis.2019.165574. Acesso em: 02 jun. 2024.
APA
Sorgi, C. A., Soares, E. M., Rosada, R. S., Bitencourt, C. S., Zoccal, K. F., Pereira, P. A. T., et al. (2020). Eicosanoid pathway on host resistance and inflammation during Mycobacterium tuberculosis infection is comprised by LTB4 reduction but not PGE2 increment. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1866( 3), [10] . doi:10.1016/j.bbadis.2019.165574
NLM
Sorgi CA, Soares EM, Rosada RS, Bitencourt CS, Zoccal KF, Pereira PAT, Fontanari C, Brandão IT, Masson AP, Ramos SG, Silva CL, Frantz FG, Faccioli LH. Eicosanoid pathway on host resistance and inflammation during Mycobacterium tuberculosis infection is comprised by LTB4 reduction but not PGE2 increment [Internet]. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 2020 ; 1866( 3): [10] .[citado 2024 jun. 02 ] Available from: https://doi.org/10.1016/j.bbadis.2019.165574
Vancouver
Sorgi CA, Soares EM, Rosada RS, Bitencourt CS, Zoccal KF, Pereira PAT, Fontanari C, Brandão IT, Masson AP, Ramos SG, Silva CL, Frantz FG, Faccioli LH. Eicosanoid pathway on host resistance and inflammation during Mycobacterium tuberculosis infection is comprised by LTB4 reduction but not PGE2 increment [Internet]. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 2020 ; 1866( 3): [10] .[citado 2024 jun. 02 ] Available from: https://doi.org/10.1016/j.bbadis.2019.165574
Artigo de periodico
Molecular epidemiology and resistance profile of Campylobacter jejuni and Campylobacter coli strains isolated from different sources in Brazil (2020)
Gomes, Carolina Nogueira; Frazão, Miliane Rodrigues; Passaglia, Jaqueline; Duque, Sheila S.; Medeiros, Marta Inês Cazentini; Falcão, Juliana Pfrimer
Source: Microbial Drug Resistance. Unidades: FFCLRP, FCFRP
Subjects: DIVERSIDADE GENÉTICA, BACTÉRIAS GRAM-NEGATIVAS, AVES, CAMPYLOBACTER
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOMES, Carolina Nogueira et al. Molecular epidemiology and resistance profile of Campylobacter jejuni and Campylobacter coli strains isolated from different sources in Brazil. Microbial Drug Resistance, v. 26, n. 12, p. 1516-1525, 2020Tradução . . Disponível em: https://doi.org/10.1089/mdr.2019.0266. Acesso em: 02 jun. 2024.
APA
Gomes, C. N., Frazão, M. R., Passaglia, J., Duque, S. S., Medeiros, M. I. C., & Falcão, J. P. (2020). Molecular epidemiology and resistance profile of Campylobacter jejuni and Campylobacter coli strains isolated from different sources in Brazil. Microbial Drug Resistance, 26( 12), 1516-1525. doi:10.1089/mdr.2019.0266
NLM
Gomes CN, Frazão MR, Passaglia J, Duque SS, Medeiros MIC, Falcão JP. Molecular epidemiology and resistance profile of Campylobacter jejuni and Campylobacter coli strains isolated from different sources in Brazil [Internet]. Microbial Drug Resistance. 2020 ; 26( 12): 1516-1525.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1089/mdr.2019.0266
Vancouver
Gomes CN, Frazão MR, Passaglia J, Duque SS, Medeiros MIC, Falcão JP. Molecular epidemiology and resistance profile of Campylobacter jejuni and Campylobacter coli strains isolated from different sources in Brazil [Internet]. Microbial Drug Resistance. 2020 ; 26( 12): 1516-1525.[citado 2024 jun. 02 ] Available from: https://doi.org/10.1089/mdr.2019.0266

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