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Trabalho de evento-resumo periodico
Formulação de extrato à base de romã (Punica granatum L.) para uso bucal: potencial antimicrobiano e atividade antioxidante (2020)
Lucas, Isabela Licursi Lambert; Gallas, Júlia Adornes; Corona, Silmara Aparecida Milori ; Salvador, Sérgio Luiz de Souza ; Souza-Gabriel, Aline Evangelista
Fonte: Brazilian Oral Research. Nome do evento: Reunião Anual da SBPqO / SBPqO Virtual Annual Meeting. Unidades: FORP, FCFRP
Assuntos: ODONTOLOGIA, PESQUISA CIENTÍFICA, EXTRATOS (FORMAS FARMACÊUTICAS), ROMÃ, ANTIOXIDANTES
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ABNT
LUCAS, Isabela Licursi Lambert et al. Formulação de extrato à base de romã (Punica granatum L.) para uso bucal: potencial antimicrobiano e atividade antioxidante. Brazilian Oral Research. São Paulo: Faculdade de Odontologia de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://sbpqo.org.br/hotsite2020/bor-v034-SBPqO-book_V2.pdf. Acesso em: 02 set. 2024. , 2020
APA
Lucas, I. L. L., Gallas, J. A., Corona, S. A. M., Salvador, S. L. de S., & Souza-Gabriel, A. E. (2020). Formulação de extrato à base de romã (Punica granatum L.) para uso bucal: potencial antimicrobiano e atividade antioxidante. Brazilian Oral Research. São Paulo: Faculdade de Odontologia de Ribeirão Preto, Universidade de São Paulo. Recuperado de https://sbpqo.org.br/hotsite2020/bor-v034-SBPqO-book_V2.pdf
NLM
Lucas ILL, Gallas JA, Corona SAM, Salvador SL de S, Souza-Gabriel AE. Formulação de extrato à base de romã (Punica granatum L.) para uso bucal: potencial antimicrobiano e atividade antioxidante [Internet]. Brazilian Oral Research. 2020 ; 34 185.[citado 2024 set. 02 ] Available from: https://sbpqo.org.br/hotsite2020/bor-v034-SBPqO-book_V2.pdf
Vancouver
Lucas ILL, Gallas JA, Corona SAM, Salvador SL de S, Souza-Gabriel AE. Formulação de extrato à base de romã (Punica granatum L.) para uso bucal: potencial antimicrobiano e atividade antioxidante [Internet]. Brazilian Oral Research. 2020 ; 34 185.[citado 2024 set. 02 ] Available from: https://sbpqo.org.br/hotsite2020/bor-v034-SBPqO-book_V2.pdf
Monografia/livro-ed/org
Chimeric antigen receptor T Cells: development and production (2020)
Swiech, Kamilla (Editor) ; Malmegrim, Kelen Cristina Ribeiro (Editor) ; Picanço-Castro, Virgínia (Editor)
Unidades: FCFRP, FMRP
Assuntos: IMUNOTERAPIA, ANTÍGENOS, BIOLOGIA MOLECULAR, NEOPLASIAS
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ABNT
Chimeric antigen receptor T Cells: development and production. . New York: Humana Press. Disponível em: https://doi.org/10.1007/978-1-0716-0146-4. Acesso em: 02 set. 2024. , 2020
APA
Chimeric antigen receptor T Cells: development and production. (2020). Chimeric antigen receptor T Cells: development and production. New York: Humana Press. doi:10.1007/978-1-0716-0146-4
NLM
Chimeric antigen receptor T Cells: development and production [Internet]. 2020 ;[citado 2024 set. 02 ] Available from: https://doi.org/10.1007/978-1-0716-0146-4
Vancouver
Chimeric antigen receptor T Cells: development and production [Internet]. 2020 ;[citado 2024 set. 02 ] Available from: https://doi.org/10.1007/978-1-0716-0146-4
Monografia/livro-ed/org
Chimeric antigen receptor T Cell: development and production (2020)
Swiech, Kamilla (Editor) ; Malmegrim, Kelen Cristina Ribeiro (Editor) ; Picanço-Castro, Virgínia (Editor)
Unidades: FCFRP, FMRP
Assuntos: IMUNOTERAPIA, RECEPTORES DE ANTÍGENOS, ANTÍGENOS, LINHAGEM CELULAR, NEOPLASIAS
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ABNT
Chimeric antigen receptor T Cell: development and production. . New York: Humana Press. Disponível em: https://doi.org/10.1007/978-1-0716-0146-4. Acesso em: 02 set. 2024. , 2020
APA
Chimeric antigen receptor T Cell: development and production. (2020). Chimeric antigen receptor T Cell: development and production. New York: Humana Press. doi:10.1007/978-1-0716-0146-4
NLM
Chimeric antigen receptor T Cell: development and production [Internet]. 2020 ;[citado 2024 set. 02 ] Available from: https://doi.org/10.1007/978-1-0716-0146-4
Vancouver
Chimeric antigen receptor T Cell: development and production [Internet]. 2020 ;[citado 2024 set. 02 ] Available from: https://doi.org/10.1007/978-1-0716-0146-4
Artigo de periodico
Gold-coated superparamagnetic iron oxide nanoparticles attenuate collagen-induced arthritis after magnetic targeting (2020)
Carneiro, Maria Fernanda Hornos ; Machado, Ana Rita Thomazela ; Antunes, Lusânia Maria Greggi ; Souza, Talita E.; Freitas, Victor A.; Oliveira, Luiz C. A.; Rodrigues, Jairo L.; Pereira, Marcio C.; Barbosa Junior, Fernando
Fonte: Biological Trace Element Research. Unidade: FCFRP
Assuntos: NANOPARTÍCULAS, OURO, INFLAMAÇÃO, MAGNETISMO, ARTRITE, COLÁGENO
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ABNT
CARNEIRO, Maria Fernanda Hornos et al. Gold-coated superparamagnetic iron oxide nanoparticles attenuate collagen-induced arthritis after magnetic targeting. Biological Trace Element Research, v. 194, n. 2, p. 502-513, 2020Tradução . . Disponível em: https://doi.org/10.1007/s12011-019-01799-z. Acesso em: 02 set. 2024.
APA
Carneiro, M. F. H., Machado, A. R. T., Antunes, L. M. G., Souza, T. E., Freitas, V. A., Oliveira, L. C. A., et al. (2020). Gold-coated superparamagnetic iron oxide nanoparticles attenuate collagen-induced arthritis after magnetic targeting. Biological Trace Element Research, 194( 2), 502-513. doi:10.1007/s12011-019-01799-z
NLM
Carneiro MFH, Machado ART, Antunes LMG, Souza TE, Freitas VA, Oliveira LCA, Rodrigues JL, Pereira MC, Barbosa Junior F. Gold-coated superparamagnetic iron oxide nanoparticles attenuate collagen-induced arthritis after magnetic targeting [Internet]. Biological Trace Element Research. 2020 ; 194( 2): 502-513.[citado 2024 set. 02 ] Available from: https://doi.org/10.1007/s12011-019-01799-z
Vancouver
Carneiro MFH, Machado ART, Antunes LMG, Souza TE, Freitas VA, Oliveira LCA, Rodrigues JL, Pereira MC, Barbosa Junior F. Gold-coated superparamagnetic iron oxide nanoparticles attenuate collagen-induced arthritis after magnetic targeting [Internet]. Biological Trace Element Research. 2020 ; 194( 2): 502-513.[citado 2024 set. 02 ] Available from: https://doi.org/10.1007/s12011-019-01799-z
Parte de monografia/livro-apres/pref/posf
Immunotherapy is a treatment that boosts the body’s natural defenses to fight cancer. [Prefácio] (2020)
Swiech, Kamilla ; Malmegrim, Kelen Cristina Ribeiro ; Picanço-Castro, Virgínia
Fonte: Chimeric antigen receptor T Cell: development and production. Unidades: FCFRP, FMRP
Assuntos: IMUNOTERAPIA, ANTÍGENOS, RECEPTORES DE ANTÍGENOS, NEOPLASIAS
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ABNT
SWIECH, Kamilla e MALMEGRIM, Kelen Cristina Ribeiro e PICANÇO-CASTRO, Virgínia. Immunotherapy is a treatment that boosts the body’s natural defenses to fight cancer. [Prefácio]. Chimeric antigen receptor T Cell: development and production. New York: Humana Press. Disponível em: https://doi.org/10.1007/978-1-0716-0146-4. Acesso em: 02 set. 2024. , 2020
APA
Swiech, K., Malmegrim, K. C. R., & Picanço-Castro, V. (2020). Immunotherapy is a treatment that boosts the body’s natural defenses to fight cancer. [Prefácio]. Chimeric antigen receptor T Cell: development and production. New York: Humana Press. doi:10.1007/978-1-0716-0146-4
NLM
Swiech K, Malmegrim KCR, Picanço-Castro V. Immunotherapy is a treatment that boosts the body’s natural defenses to fight cancer. [Prefácio] [Internet]. Chimeric antigen receptor T Cell: development and production. 2020 ;274 .[citado 2024 set. 02 ] Available from: https://doi.org/10.1007/978-1-0716-0146-4
Vancouver
Swiech K, Malmegrim KCR, Picanço-Castro V. Immunotherapy is a treatment that boosts the body’s natural defenses to fight cancer. [Prefácio] [Internet]. Chimeric antigen receptor T Cell: development and production. 2020 ;274 .[citado 2024 set. 02 ] Available from: https://doi.org/10.1007/978-1-0716-0146-4
Artigo de periodico
Niacin prevents mitochondrial oxidative stress caused by sub-chronic exposure to methylmercury (2020)
Pereira, Lílian Cristina ; Paula, Eloisa Silva de; Pazin, Murilo; Carneiro, Maria Fernanda Hornos; Grotto, Denise ; Barbosa Júnior, Fernando ; Dorta, Daniel Junqueira
Fonte: Drug and Chemical Toxicology. Unidades: FCFRP, FFCLRP
Assuntos: MITOCÔNDRIAS, VITAMINAS HIDROSSOLÚVEIS, MERCÚRIO (ELEMENTO QUÍMICO)
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ABNT
PEREIRA, Lílian Cristina et al. Niacin prevents mitochondrial oxidative stress caused by sub-chronic exposure to methylmercury. Drug and Chemical Toxicology, v. 43, n. 1, p. 64-70, 2020Tradução . . Disponível em: https://doi.org/10.1080/01480545.2018.1497045. Acesso em: 02 set. 2024.
APA
Pereira, L. C., Paula, E. S. de, Pazin, M., Carneiro, M. F. H., Grotto, D., Barbosa Júnior, F., & Dorta, D. J. (2020). Niacin prevents mitochondrial oxidative stress caused by sub-chronic exposure to methylmercury. Drug and Chemical Toxicology, 43( 1), 64-70. doi:10.1080/01480545.2018.1497045
NLM
Pereira LC, Paula ES de, Pazin M, Carneiro MFH, Grotto D, Barbosa Júnior F, Dorta DJ. Niacin prevents mitochondrial oxidative stress caused by sub-chronic exposure to methylmercury [Internet]. Drug and Chemical Toxicology. 2020 ; 43( 1): 64-70.[citado 2024 set. 02 ] Available from: https://doi.org/10.1080/01480545.2018.1497045
Vancouver
Pereira LC, Paula ES de, Pazin M, Carneiro MFH, Grotto D, Barbosa Júnior F, Dorta DJ. Niacin prevents mitochondrial oxidative stress caused by sub-chronic exposure to methylmercury [Internet]. Drug and Chemical Toxicology. 2020 ; 43( 1): 64-70.[citado 2024 set. 02 ] Available from: https://doi.org/10.1080/01480545.2018.1497045
Artigo de periodico
Publisher Correction: Leishmania RNA virus exacerbates Leishmaniasis by subverting innate immunity via TLR3-mediated NLRP3 inflammasome inhibition (2020)
Carvalho, Renan Villanova Homem de; Lima Júnior, Djalma Souza; Silva, Marcus Vinícius Gomes da; Dilucca, Marisa; Rodrigues, Tamara Silva; Horta, Catarina Veltrini; Silva, Alexandre Luiz Neves; Silva, Patrick Fernandes da; Frantz, Fabiani Gai ; Lorenzon, Lucas Bigolin; Souza, Marcos Michel de; Almeida, Fausto Bruno dos Reis ; Cantanhêde, Lilian Motta; Ferreira, Ricardo de Godoi Mattos; Cruz, Angela Kaysel ; Zamboni, Dario Simões
Fonte: Nature Communications. Unidades: FCFRP, FMRP
Assuntos: IMUNOLOGIA, VÍRUS DE RNA, LEISHMANIA, MACRÓFAGOS
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ABNT
CARVALHO, Renan Villanova Homem de et al. Publisher Correction: Leishmania RNA virus exacerbates Leishmaniasis by subverting innate immunity via TLR3-mediated NLRP3 inflammasome inhibition. Nature Communications, v. 11, 2020Tradução . . Disponível em: https://doi.org/10.1038/s41467-019-13356-2. Acesso em: 02 set. 2024.
APA
Carvalho, R. V. H. de, Lima Júnior, D. S., Silva, M. V. G. da, Dilucca, M., Rodrigues, T. S., Horta, C. V., et al. (2020). Publisher Correction: Leishmania RNA virus exacerbates Leishmaniasis by subverting innate immunity via TLR3-mediated NLRP3 inflammasome inhibition. Nature Communications, 11. doi:10.1038/s41467-019-13356-2
NLM
Carvalho RVH de, Lima Júnior DS, Silva MVG da, Dilucca M, Rodrigues TS, Horta CV, Silva ALN, Silva PF da, Frantz FG, Lorenzon LB, Souza MM de, Almeida FB dos R, Cantanhêde LM, Ferreira R de GM, Cruz AK, Zamboni DS. Publisher Correction: Leishmania RNA virus exacerbates Leishmaniasis by subverting innate immunity via TLR3-mediated NLRP3 inflammasome inhibition [Internet]. Nature Communications. 2020 ; 11[citado 2024 set. 02 ] Available from: https://doi.org/10.1038/s41467-019-13356-2
Vancouver
Carvalho RVH de, Lima Júnior DS, Silva MVG da, Dilucca M, Rodrigues TS, Horta CV, Silva ALN, Silva PF da, Frantz FG, Lorenzon LB, Souza MM de, Almeida FB dos R, Cantanhêde LM, Ferreira R de GM, Cruz AK, Zamboni DS. Publisher Correction: Leishmania RNA virus exacerbates Leishmaniasis by subverting innate immunity via TLR3-mediated NLRP3 inflammasome inhibition [Internet]. Nature Communications. 2020 ; 11[citado 2024 set. 02 ] Available from: https://doi.org/10.1038/s41467-019-13356-2
Artigo de periodico
Geological and taphonomic significance of electron spin resonance (ESR) ages of Middle-Late Pleistocene marine shells from barrier-lagoon systems of Southern Brazil (2020)
Lopes, Renato Pereira ; Pereira, Jamil Corrêa; Kinoshita, Angela; Mollemberg, Michelle; Barbosa Junior, Fernando ; Baffa, Oswaldo
Fonte: Journal of South American Earth Sciences. Unidades: FCFRP, FFCLRP
Assuntos: TAFONOMIA, ESPECTROSCOPIA, QUATERNÁRIO, GEOLOGIA, CRONOESTRATIGRAFIA, PLEISTOCENO, BIVALVIA
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ABNT
LOPES, Renato Pereira et al. Geological and taphonomic significance of electron spin resonance (ESR) ages of Middle-Late Pleistocene marine shells from barrier-lagoon systems of Southern Brazil. Journal of South American Earth Sciences, v. 101, p. 1-14, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.jsames.2020.102605. Acesso em: 02 set. 2024.
APA
Lopes, R. P., Pereira, J. C., Kinoshita, A., Mollemberg, M., Barbosa Junior, F., & Baffa, O. (2020). Geological and taphonomic significance of electron spin resonance (ESR) ages of Middle-Late Pleistocene marine shells from barrier-lagoon systems of Southern Brazil. Journal of South American Earth Sciences, 101, 1-14. doi:10.1016/j.jsames.2020.102605
NLM
Lopes RP, Pereira JC, Kinoshita A, Mollemberg M, Barbosa Junior F, Baffa O. Geological and taphonomic significance of electron spin resonance (ESR) ages of Middle-Late Pleistocene marine shells from barrier-lagoon systems of Southern Brazil [Internet]. Journal of South American Earth Sciences. 2020 ; 101 1-14.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.jsames.2020.102605
Vancouver
Lopes RP, Pereira JC, Kinoshita A, Mollemberg M, Barbosa Junior F, Baffa O. Geological and taphonomic significance of electron spin resonance (ESR) ages of Middle-Late Pleistocene marine shells from barrier-lagoon systems of Southern Brazil [Internet]. Journal of South American Earth Sciences. 2020 ; 101 1-14.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.jsames.2020.102605
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
Fonte: Neurotoxicity Research. Unidades: FCFRP, FMRP
Assuntos: VENENOS, COBRAS, PROTEÍNAS QUINASES, ANTAGONISTAS, TOXICIDADE EM ANIMAL, APOLIPOPROTEÍNAS, BIOMARCADORES, DIFERENCIAÇÃO CELULAR, GLICOSE, PLASTICIDADE NEURONAL
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ABNT
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 set. 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 set. 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 set. 02 ] Available from: https://doi.org/10.1007/s12640-019-00111-0
Artigo de periodico
Discovering selected antibodies from deep-sequenced phage-display antibody library using ATTILA (2020)
Maranhão, Andréa Queiroz; Silva, Heidi Muniz; Silva, Waldeyr Mendes Cordeiro da; França, Renato Kaylan Alves; Leo, Thais Canassa de ; Dias-Baruffi, Marcelo ; Burtet, Rafael Trindade; Brigido, Marcelo Macedo
Fonte: Bioinformatics and Biology Insights. Unidade: FCFRP
Assuntos: ANTICORPOS, BIOFARMÁCIA, SEQUENCIAMENTO GENÉTICO, IMUNOGLOBULINAS, ANTICORPOS MONOCLONAIS
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ABNT
MARANHÃO, Andréa Queiroz et al. Discovering selected antibodies from deep-sequenced phage-display antibody library using ATTILA. Bioinformatics and Biology Insights, v. 14, p. 1-8, 2020Tradução . . Disponível em: https://doi.org/10.1177/1177932220915240. Acesso em: 02 set. 2024.
APA
Maranhão, A. Q., Silva, H. M., Silva, W. M. C. da, França, R. K. A., Leo, T. C. de, Dias-Baruffi, M., et al. (2020). Discovering selected antibodies from deep-sequenced phage-display antibody library using ATTILA. Bioinformatics and Biology Insights, 14, 1-8. doi:10.1177/1177932220915240
NLM
Maranhão AQ, Silva HM, Silva WMC da, França RKA, Leo TC de, Dias-Baruffi M, Burtet RT, Brigido MM. Discovering selected antibodies from deep-sequenced phage-display antibody library using ATTILA [Internet]. Bioinformatics and Biology Insights. 2020 ; 14 1-8.[citado 2024 set. 02 ] Available from: https://doi.org/10.1177/1177932220915240
Vancouver
Maranhão AQ, Silva HM, Silva WMC da, França RKA, Leo TC de, Dias-Baruffi M, Burtet RT, Brigido MM. Discovering selected antibodies from deep-sequenced phage-display antibody library using ATTILA [Internet]. Bioinformatics and Biology Insights. 2020 ; 14 1-8.[citado 2024 set. 02 ] Available from: https://doi.org/10.1177/1177932220915240
Artigo de periodico
Epigenetic therapy induces transcription of inverted SINEs and ADAR1 dependency (2020)
Mehdipour, Parinaz; Marhon, Sajid A.; Ettayebi, Ilias; Chakravarthy, Ankur; Hosseini, Amir; Wang, Yadong; Castro, Fabíola Attié de ; Loo Yau, Helen; Ishak, Charles; Abelson, Sagi; O’Brien, Catherine A.; Carvalho, Daniel D. de
Fonte: Nature. Unidade: FCFRP
Assuntos: NEOPLASIAS, GENOMAS, RNA, IMUNOTERAPIA
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ABNT
MEHDIPOUR, Parinaz et al. Epigenetic therapy induces transcription of inverted SINEs and ADAR1 dependency. Nature, v. 588, n. 7836, p. 169-173, 2020Tradução . . Disponível em: https://doi.org/10.1038/s41586-020-2844-1. Acesso em: 02 set. 2024.
APA
Mehdipour, P., Marhon, S. A., Ettayebi, I., Chakravarthy, A., Hosseini, A., Wang, Y., et al. (2020). Epigenetic therapy induces transcription of inverted SINEs and ADAR1 dependency. Nature, 588( 7836), 169-173. doi:10.1038/s41586-020-2844-1
NLM
Mehdipour P, Marhon SA, Ettayebi I, Chakravarthy A, Hosseini A, Wang Y, Castro FA de, Loo Yau H, Ishak C, Abelson S, O’Brien CA, Carvalho DD de. Epigenetic therapy induces transcription of inverted SINEs and ADAR1 dependency [Internet]. Nature. 2020 ; 588( 7836): 169-173.[citado 2024 set. 02 ] Available from: https://doi.org/10.1038/s41586-020-2844-1
Vancouver
Mehdipour P, Marhon SA, Ettayebi I, Chakravarthy A, Hosseini A, Wang Y, Castro FA de, Loo Yau H, Ishak C, Abelson S, O’Brien CA, Carvalho DD de. Epigenetic therapy induces transcription of inverted SINEs and ADAR1 dependency [Internet]. Nature. 2020 ; 588( 7836): 169-173.[citado 2024 set. 02 ] Available from: https://doi.org/10.1038/s41586-020-2844-1
Artigo de periodico
Widespread high-risk clones of multidrug-resistant extended-spectrum β-lactamase-producing Escherichia coli B2-ST131 and F-ST648 in public aquatic environments (2020)
Furlan, João Pedro Rueda ; Savazzi, Eduardo Angelino; Stehling, Eliana Guedes
Fonte: International Journal of Antimicrobial Agents. Unidade: FCFRP
Assuntos: INFECÇÕES BACTERIANAS, BACTÉRIAS, ESCHERICHIA COLI, FARMACOLOGIA, QUIMIOTERAPIA, GENOMAS, PLASMÍDEOS, TESTES DE SENSIBILIDADE MICROBIANA
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ABNT
FURLAN, João Pedro Rueda e SAVAZZI, Eduardo Angelino e STEHLING, Eliana Guedes. Widespread high-risk clones of multidrug-resistant extended-spectrum β-lactamase-producing Escherichia coli B2-ST131 and F-ST648 in public aquatic environments. International Journal of Antimicrobial Agents, v. 56, n. 1, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.ijantimicag.2020.106040. Acesso em: 02 set. 2024.
APA
Furlan, J. P. R., Savazzi, E. A., & Stehling, E. G. (2020). Widespread high-risk clones of multidrug-resistant extended-spectrum β-lactamase-producing Escherichia coli B2-ST131 and F-ST648 in public aquatic environments. International Journal of Antimicrobial Agents, 56( 1). doi:10.1016/j.ijantimicag.2020.106040
NLM
Furlan JPR, Savazzi EA, Stehling EG. Widespread high-risk clones of multidrug-resistant extended-spectrum β-lactamase-producing Escherichia coli B2-ST131 and F-ST648 in public aquatic environments [Internet]. International Journal of Antimicrobial Agents. 2020 ; 56( 1):[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.ijantimicag.2020.106040
Vancouver
Furlan JPR, Savazzi EA, Stehling EG. Widespread high-risk clones of multidrug-resistant extended-spectrum β-lactamase-producing Escherichia coli B2-ST131 and F-ST648 in public aquatic environments [Internet]. International Journal of Antimicrobial Agents. 2020 ; 56( 1):[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.ijantimicag.2020.106040
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
Fonte: Brazilian Journal of Microbiology. Unidade: FCFRP
Assuntos: 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 set. 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 set. 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 set. 02 ] Available from: https://doi.org/10.1007/s42770-020-00392-0
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
Fonte: Glycoconjugate Journal. Unidade: FCFRP
Assuntos: 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 set. 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 set. 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 set. 02 ] Available from: https://doi.org/10.1007/s10719-019-09893-z
Artigo de periodico
Neutrophils and COVID-19:: what is going on? (2020)
Andrade, Micássio Fernandes de ; Marzocchi-Machado, Cleni Mara
Fonte: Critical Reviews in Immunology. Unidade: FCFRP
Assuntos: COVID-19, METABOLISMO, IMUNOLOGIA, NEUTRÓFILOS, FISIOLOGIA
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ABNT
ANDRADE, Micássio Fernandes de e MARZOCCHI-MACHADO, Cleni Mara. Neutrophils and COVID-19:: what is going on?. Critical Reviews in Immunology, v. 40, n. 6, p. 527-536, 2020Tradução . . Disponível em: https://doi.org/10.1615/CritRevImmunol.2020035900. Acesso em: 02 set. 2024.
APA
Andrade, M. F. de, & Marzocchi-Machado, C. M. (2020). Neutrophils and COVID-19:: what is going on? Critical Reviews in Immunology, 40( 6), 527-536. doi:10.1615/CritRevImmunol.2020035900
NLM
Andrade MF de, Marzocchi-Machado CM. Neutrophils and COVID-19:: what is going on? [Internet]. Critical Reviews in Immunology. 2020 ; 40( 6): 527-536.[citado 2024 set. 02 ] Available from: https://doi.org/10.1615/CritRevImmunol.2020035900
Vancouver
Andrade MF de, Marzocchi-Machado CM. Neutrophils and COVID-19:: what is going on? [Internet]. Critical Reviews in Immunology. 2020 ; 40( 6): 527-536.[citado 2024 set. 02 ] Available from: https://doi.org/10.1615/CritRevImmunol.2020035900
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
Fonte: Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. Unidades: FFCLRP, FCFRP, FMRP
Assuntos: TUBERCULOSE, LEUCOTRIENOS, PROSTAGLANDINAS, INFLAMAÇÃO, IMUNOPATOLOGIA
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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 set. 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 set. 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 set. 02 ] Available from: https://doi.org/10.1016/j.bbadis.2019.165574
Artigo de periodico
Effect of lercanidipine on the pharmacokinetics-pharmacodynamics of carvedilol enantiomers in patients with chronic kidney disease (2020)
Schaab, Estela Hanauer; Lanchote, Vera Lucia ; Nardotto, Glauco Henrique Balthazar ; Pereira, Maria Paula Marques ; Dantas, Márcio ; Paiva, Carlos Eduardo; Coelho, Eduardo Barbosa
Fonte: The Journal of Clinical Pharmacology. Unidades: FCFRP, FMRP
Assuntos: NEFROPATIAS, INTERAÇÃO ENTRE ALIMENTOS E MEDICAMENTOS, FARMACOCINÉTICA
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ABNT
SCHAAB, Estela Hanauer et al. Effect of lercanidipine on the pharmacokinetics-pharmacodynamics of carvedilol enantiomers in patients with chronic kidney disease. The Journal of Clinical Pharmacology, v. 60, n. 1, p. 75-85, 2020Tradução . . Disponível em: https://doi.org/10.1002/jcph.1485. Acesso em: 02 set. 2024.
APA
Schaab, E. H., Lanchote, V. L., Nardotto, G. H. B., Pereira, M. P. M., Dantas, M., Paiva, C. E., & Coelho, E. B. (2020). Effect of lercanidipine on the pharmacokinetics-pharmacodynamics of carvedilol enantiomers in patients with chronic kidney disease. The Journal of Clinical Pharmacology, 60( 1), 75-85. doi:10.1002/jcph.1485
NLM
Schaab EH, Lanchote VL, Nardotto GHB, Pereira MPM, Dantas M, Paiva CE, Coelho EB. Effect of lercanidipine on the pharmacokinetics-pharmacodynamics of carvedilol enantiomers in patients with chronic kidney disease [Internet]. The Journal of Clinical Pharmacology. 2020 ; 60( 1): 75-85.[citado 2024 set. 02 ] Available from: https://doi.org/10.1002/jcph.1485
Vancouver
Schaab EH, Lanchote VL, Nardotto GHB, Pereira MPM, Dantas M, Paiva CE, Coelho EB. Effect of lercanidipine on the pharmacokinetics-pharmacodynamics of carvedilol enantiomers in patients with chronic kidney disease [Internet]. The Journal of Clinical Pharmacology. 2020 ; 60( 1): 75-85.[citado 2024 set. 02 ] Available from: https://doi.org/10.1002/jcph.1485
Artigo de periodico
Association between creatine kinase activity, oxidative stress and selenoproteins mRNA expression changes after Brazil nut consumption of patients using statins (2020)
Watanabe, Ligia Moriguchi ; Lima, Lívia Fernandes de; Ferraz-Bannitz, Rafael ; Takaara, Daniela ; Romano, Beatriz Coimbra; Costa, Telma Maria Braga; Foss-Freitas, Maria Cristina ; Bueno, Ana Carolina ; Barbosa Junior, Fernando ; Navarro, Anderson Marliere
Fonte: Clinical Nutrition. Unidades: FMRP, FCFRP
Assuntos: ESTATINAS, SELÊNIO, CREATINA, ESTRESSE OXIDATIVO
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ABNT
WATANABE, Ligia Moriguchi et al. Association between creatine kinase activity, oxidative stress and selenoproteins mRNA expression changes after Brazil nut consumption of patients using statins. Clinical Nutrition, v. 39, n. 10, p. 3175-3181, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.clnu.2020.02.012. Acesso em: 02 set. 2024.
APA
Watanabe, L. M., Lima, L. F. de, Ferraz-Bannitz, R., Takaara, D., Romano, B. C., Costa, T. M. B., et al. (2020). Association between creatine kinase activity, oxidative stress and selenoproteins mRNA expression changes after Brazil nut consumption of patients using statins. Clinical Nutrition, 39( 10), 3175-3181. doi:10.1016/j.clnu.2020.02.012
NLM
Watanabe LM, Lima LF de, Ferraz-Bannitz R, Takaara D, Romano BC, Costa TMB, Foss-Freitas MC, Bueno AC, Barbosa Junior F, Navarro AM. Association between creatine kinase activity, oxidative stress and selenoproteins mRNA expression changes after Brazil nut consumption of patients using statins [Internet]. Clinical Nutrition. 2020 ; 39( 10): 3175-3181.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.clnu.2020.02.012
Vancouver
Watanabe LM, Lima LF de, Ferraz-Bannitz R, Takaara D, Romano BC, Costa TMB, Foss-Freitas MC, Bueno AC, Barbosa Junior F, Navarro AM. Association between creatine kinase activity, oxidative stress and selenoproteins mRNA expression changes after Brazil nut consumption of patients using statins [Internet]. Clinical Nutrition. 2020 ; 39( 10): 3175-3181.[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.clnu.2020.02.012
Artigo de periodico
Crotoxin-induced mice lung impairment: role of nicotinic acetylcholine receptors and COX-derived prostanoids (2020)
Sartim, Marco Aurélio; Souza, Camila Oliveira Silva; Diniz, Cassiano Ricardo Alves Faria; Fonseca, Vanessa Maciel Braulio da; Sousa, Lucas Oliveira ; Peti, Ana Paula Ferranti; Costa, Tássia Rafaella; Lourenço, Alan Grupioni ; Borges, Marcos de Carvalho ; Sorgi, Carlos Arterio ; Faccioli, Lucia Helena ; Sampaio, Suely Vilela
Fonte: Biomolecules. Unidades: FCFRP, FORP, FMRP, FFCLRP
Assuntos: CITOCINAS, PULMÃO, FISIOPATOLOGIA, INSUFICIÊNCIA RESPIRATÓRIA, VENENOS, COBRAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SARTIM, Marco Aurélio et al. Crotoxin-induced mice lung impairment: role of nicotinic acetylcholine receptors and COX-derived prostanoids. Biomolecules, v. 10, n. 5, 2020Tradução . . Disponível em: https://doi.org/10.3390/biom10050794. Acesso em: 02 set. 2024.
APA
Sartim, M. A., Souza, C. O. S., Diniz, C. R. A. F., Fonseca, V. M. B. da, Sousa, L. O., Peti, A. P. F., et al. (2020). Crotoxin-induced mice lung impairment: role of nicotinic acetylcholine receptors and COX-derived prostanoids. Biomolecules, 10( 5). doi:10.3390/biom10050794
NLM
Sartim MA, Souza COS, Diniz CRAF, Fonseca VMB da, Sousa LO, Peti APF, Costa TR, Lourenço AG, Borges M de C, Sorgi CA, Faccioli LH, Sampaio SV. Crotoxin-induced mice lung impairment: role of nicotinic acetylcholine receptors and COX-derived prostanoids [Internet]. Biomolecules. 2020 ; 10( 5):[citado 2024 set. 02 ] Available from: https://doi.org/10.3390/biom10050794
Vancouver
Sartim MA, Souza COS, Diniz CRAF, Fonseca VMB da, Sousa LO, Peti APF, Costa TR, Lourenço AG, Borges M de C, Sorgi CA, Faccioli LH, Sampaio SV. Crotoxin-induced mice lung impairment: role of nicotinic acetylcholine receptors and COX-derived prostanoids [Internet]. Biomolecules. 2020 ; 10( 5):[citado 2024 set. 02 ] Available from: https://doi.org/10.3390/biom10050794
Artigo de periodico
Bothrops moojeni venom and BmooLAAO-I downmodulate CXCL8/IL-8 and CCL2/MCP-1 production and oxidative burst response, and upregulate CD11b expression in human neutrophils (2020)
Crott, Luciana Simon Pereira; Casare-Ogasawara, Tânia Mara; Ambrosio, Luciana ; Chaim, Luiz Fernando Princi; Morais, Fabiana Rossetto de; Cintra, Adélia Cristina Oliveira; Canicoba, Nathália Cristina; Tucci, Luiz Fernando Fortunato; Torqueti, Maria Regina ; Sampaio, Suely Vilela ; Marzocchi-Machado, Cleni Mara ; Castro, Fabíola Attié de
Fonte: International Immunopharmacology. Unidade: FCFRP
Assuntos: VIPERIDAE, SERPENTES, ANTÍGENOS, SOBREVIVÊNCIA CELULAR, VENENOS, CITOCINAS, FARMACOLOGIA, AMINOÁCIDOS, NEUTRÓFILOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CROTT, Luciana Simon Pereira et al. Bothrops moojeni venom and BmooLAAO-I downmodulate CXCL8/IL-8 and CCL2/MCP-1 production and oxidative burst response, and upregulate CD11b expression in human neutrophils. International Immunopharmacology, v. 80, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.intimp.2019.106154. Acesso em: 02 set. 2024.
APA
Crott, L. S. P., Casare-Ogasawara, T. M., Ambrosio, L., Chaim, L. F. P., Morais, F. R. de, Cintra, A. C. O., et al. (2020). Bothrops moojeni venom and BmooLAAO-I downmodulate CXCL8/IL-8 and CCL2/MCP-1 production and oxidative burst response, and upregulate CD11b expression in human neutrophils. International Immunopharmacology, 80. doi:10.1016/j.intimp.2019.106154
NLM
Crott LSP, Casare-Ogasawara TM, Ambrosio L, Chaim LFP, Morais FR de, Cintra ACO, Canicoba NC, Tucci LFF, Torqueti MR, Sampaio SV, Marzocchi-Machado CM, Castro FA de. Bothrops moojeni venom and BmooLAAO-I downmodulate CXCL8/IL-8 and CCL2/MCP-1 production and oxidative burst response, and upregulate CD11b expression in human neutrophils [Internet]. International Immunopharmacology. 2020 ; 80[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.intimp.2019.106154
Vancouver
Crott LSP, Casare-Ogasawara TM, Ambrosio L, Chaim LFP, Morais FR de, Cintra ACO, Canicoba NC, Tucci LFF, Torqueti MR, Sampaio SV, Marzocchi-Machado CM, Castro FA de. Bothrops moojeni venom and BmooLAAO-I downmodulate CXCL8/IL-8 and CCL2/MCP-1 production and oxidative burst response, and upregulate CD11b expression in human neutrophils [Internet]. International Immunopharmacology. 2020 ; 80[citado 2024 set. 02 ] Available from: https://doi.org/10.1016/j.intimp.2019.106154

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