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Artigo de periodico
Alpha 1-acid glycoprotein is upregulated in severe COVID-19 patients and decreases neutrophil NETs in SARS-CoV-2 infection (2024)
Mestriner, Fabíola Leslie Antunes Cardoso ; Francisco, Daniely Franco ; Campos, Lígia Cristina Borges ; Couto, Ariel Emiliano Souza do ; Fraga-Silva, Thais Fernanda de Campos ; Dugaich, Vinicius Flora ; D`Avila-Mesquita, Carolina ; Zukowski Kovacs, Henrique ; Vasconcelos, Jociany Lopes de ; Milani, Elizabete Rosa ; Sá, Keyla Santos Guedes de ; Martins, Ronaldo Bragança ; Jordani, Maria Cecília ; Corsi, Carlos Alexandre Curylofo ; Barbosa, Jéssyca Michelon; Vasconcelos, Tauana Fernandes ; Menegueti, Mayra Gonçalves ; Neto, Julio; Costa, Rafael Menezes da ; Evora, Paulo Roberto Barbosa ; Arruda, Eurico ; Tostes, Rita de Cássia Aleixo ; Polonis, Katarzyna ; Bonato, Vânia Luiza Deperon ; Auxiliadora-Martins, Maria ; Ribeiro, Maurício Serra ; Becari, Christiane
Source: Cytokine. Unidades: FMRP, FCFRP, EERP, FOB
Subjects: COVID-19, GLICOPROTEÍNAS, INFECÇÕES POR CORONAVIRUS
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MESTRINER, Fabíola Leslie Antunes Cardoso et al. Alpha 1-acid glycoprotein is upregulated in severe COVID-19 patients and decreases neutrophil NETs in SARS-CoV-2 infection. Cytokine, v. 176, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.cyto.2024.156503. Acesso em: 30 ago. 2024.
APA
Mestriner, F. L. A. C., Francisco, D. F., Campos, L. C. B., Couto, A. E. S. do, Fraga-Silva, T. F. de C., Dugaich, V. F., et al. (2024). Alpha 1-acid glycoprotein is upregulated in severe COVID-19 patients and decreases neutrophil NETs in SARS-CoV-2 infection. Cytokine, 176. doi:10.1016/j.cyto.2024.156503
NLM
Mestriner FLAC, Francisco DF, Campos LCB, Couto AES do, Fraga-Silva TF de C, Dugaich VF, D`Avila-Mesquita C, Zukowski Kovacs H, Vasconcelos JL de, Milani ER, Sá KSG de, Martins RB, Jordani MC, Corsi CAC, Barbosa JM, Vasconcelos TF, Menegueti MG, Neto J, Costa RM da, Evora PRB, Arruda E, Tostes R de CA, Polonis K, Bonato VLD, Auxiliadora-Martins M, Ribeiro MS, Becari C. Alpha 1-acid glycoprotein is upregulated in severe COVID-19 patients and decreases neutrophil NETs in SARS-CoV-2 infection [Internet]. Cytokine. 2024 ; 176[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.cyto.2024.156503
Vancouver
Mestriner FLAC, Francisco DF, Campos LCB, Couto AES do, Fraga-Silva TF de C, Dugaich VF, D`Avila-Mesquita C, Zukowski Kovacs H, Vasconcelos JL de, Milani ER, Sá KSG de, Martins RB, Jordani MC, Corsi CAC, Barbosa JM, Vasconcelos TF, Menegueti MG, Neto J, Costa RM da, Evora PRB, Arruda E, Tostes R de CA, Polonis K, Bonato VLD, Auxiliadora-Martins M, Ribeiro MS, Becari C. Alpha 1-acid glycoprotein is upregulated in severe COVID-19 patients and decreases neutrophil NETs in SARS-CoV-2 infection [Internet]. Cytokine. 2024 ; 176[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.cyto.2024.156503
Artigo de periodico
Different bacterial cargo in apoptotic cells drive distinct macrophage phenotypes (2024)
Salina, Ana Carolina Guerta ; Penteado, Letícia de Aquino; Dejani, Naiara Naiana; Silva-Pereira, Ludmilla; Raimundo, Breno Vilas Boas; Corrêa, Gabriel Ferranti; Oliveira, Karen Cristina; Ramalho, Leandra Naira Zambelli ; Boko, Mèdéton Mahoussi Michaël; Bonato, Vânia Luiza Deperon ; Serezani, C. Henrique; Medeiros, Alexandra Ivo
Source: Apoptosis. Unidade: FMRP
Subjects: MACRÓFAGOS, INFLAMAÇÃO, PULMÃO, APOPTOSE, FAGOCITOSE, FENÓTIPOS
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SALINA, Ana Carolina Guerta et al. Different bacterial cargo in apoptotic cells drive distinct macrophage phenotypes. Apoptosis, v. 29, n. 3-4, p. 321-330, 2024Tradução . . Disponível em: https://doi.org/10.1007/s10495-023-01899-1. Acesso em: 30 ago. 2024.
APA
Salina, A. C. G., Penteado, L. de A., Dejani, N. N., Silva-Pereira, L., Raimundo, B. V. B., Corrêa, G. F., et al. (2024). Different bacterial cargo in apoptotic cells drive distinct macrophage phenotypes. Apoptosis, 29( 3-4), 321-330. doi:10.1007/s10495-023-01899-1
NLM
Salina ACG, Penteado L de A, Dejani NN, Silva-Pereira L, Raimundo BVB, Corrêa GF, Oliveira KC, Ramalho LNZ, Boko MMM, Bonato VLD, Serezani CH, Medeiros AI. Different bacterial cargo in apoptotic cells drive distinct macrophage phenotypes [Internet]. Apoptosis. 2024 ; 29( 3-4): 321-330.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1007/s10495-023-01899-1
Vancouver
Salina ACG, Penteado L de A, Dejani NN, Silva-Pereira L, Raimundo BVB, Corrêa GF, Oliveira KC, Ramalho LNZ, Boko MMM, Bonato VLD, Serezani CH, Medeiros AI. Different bacterial cargo in apoptotic cells drive distinct macrophage phenotypes [Internet]. Apoptosis. 2024 ; 29( 3-4): 321-330.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1007/s10495-023-01899-1
Artigo de periodico
Extracellular vesicles from the mycoparasitic fungus Trichoderma harzianum (2024)
Silva, Gabrielle Rosa; Cavalcanti, Felipe de Pina; Melo, Reynaldo Magalhães ; Cintra, Emilio Ramos; Lima, Eliana Martins ; Hamann, Pedro Ricardo Vieira ; Vale, Luis Henrique Ferreira do ; Ulhoa, Cirano José ; Almeida, Fausto Bruno dos Reis ; Noronha, Eliane Ferreira
Source: Antonie van Leeuwenhoek. Unidades: FMRP, IFSC
Subjects: ENZIMAS, FUNGOS, TRICHODERMA
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SILVA, Gabrielle Rosa et al. Extracellular vesicles from the mycoparasitic fungus Trichoderma harzianum. Antonie van Leeuwenhoek, v. 117, p. 64-1-64-14 + supplementary information, 2024Tradução . . Disponível em: https://doi.org/10.1007/s10482-024-01958-w. Acesso em: 30 ago. 2024.
APA
Silva, G. R., Cavalcanti, F. de P., Melo, R. M., Cintra, E. R., Lima, E. M., Hamann, P. R. V., et al. (2024). Extracellular vesicles from the mycoparasitic fungus Trichoderma harzianum. Antonie van Leeuwenhoek, 117, 64-1-64-14 + supplementary information. doi:10.1007/s10482-024-01958-w
NLM
Silva GR, Cavalcanti F de P, Melo RM, Cintra ER, Lima EM, Hamann PRV, Vale LHF do, Ulhoa CJ, Almeida FB dos R, Noronha EF. Extracellular vesicles from the mycoparasitic fungus Trichoderma harzianum [Internet]. Antonie van Leeuwenhoek. 2024 ; 117 64-1-64-14 + supplementary information.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1007/s10482-024-01958-w
Vancouver
Silva GR, Cavalcanti F de P, Melo RM, Cintra ER, Lima EM, Hamann PRV, Vale LHF do, Ulhoa CJ, Almeida FB dos R, Noronha EF. Extracellular vesicles from the mycoparasitic fungus Trichoderma harzianum [Internet]. Antonie van Leeuwenhoek. 2024 ; 117 64-1-64-14 + supplementary information.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1007/s10482-024-01958-w
Artigo de periodico
Functional characterization of cullin-1-RING ubiquitin ligase (CRL1) complex in Leishmania infantum (2024)
Correia, Camila Rolemberg Santana Travaglini Berti de ; Torres, Caroline ; Gomes, Ellen; Rodriguez, Giovana Maffei ; Regatieri, Wesley Klaysson Pereira ; Takamiya, Nayore Tamie ; Rogerio, Luana Aparecida ; Malavazi, Iran ; Gomes, Marcelo Damário ; Damasceno, Jeziel Dener ; Silva, Vitor Luiz da ; Oliveira, Marcos Antonio Fernandes de ; Silva, Marcelo Santos da ; Nascimento, Alessandro Silva ; Coelho, Adriano Cappellazzo ; Maruyama, Sandra Regina Costa ; Teixeira, Felipe Roberti
Source: PLOS Pathogens. Unidades: FMRP, IQ, IFSC
Subjects: LEISHMANIA INFANTUM, ENZIMAS, ESPECTROSCOPIA
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CORREIA, Camila Rolemberg Santana Travaglini Berti de et al. Functional characterization of cullin-1-RING ubiquitin ligase (CRL1) complex in Leishmania infantum. PLOS Pathogens, v. 20, n. 7, p. e1012336-1-e1012336-34 + supporting information, 2024Tradução . . Disponível em: https://doi.org/10.1371/journal.ppat.1012336. Acesso em: 30 ago. 2024.
APA
Correia, C. R. S. T. B. de, Torres, C., Gomes, E., Rodriguez, G. M., Regatieri, W. K. P., Takamiya, N. T., et al. (2024). Functional characterization of cullin-1-RING ubiquitin ligase (CRL1) complex in Leishmania infantum. PLOS Pathogens, 20( 7), e1012336-1-e1012336-34 + supporting information. doi:10.1371/journal.ppat.1012336
NLM
Correia CRSTB de, Torres C, Gomes E, Rodriguez GM, Regatieri WKP, Takamiya NT, Rogerio LA, Malavazi I, Gomes MD, Damasceno JD, Silva VL da, Oliveira MAF de, Silva MS da, Nascimento AS, Coelho AC, Maruyama SRC, Teixeira FR. Functional characterization of cullin-1-RING ubiquitin ligase (CRL1) complex in Leishmania infantum [Internet]. PLOS Pathogens. 2024 ; 20( 7): e1012336-1-e1012336-34 + supporting information.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1371/journal.ppat.1012336
Vancouver
Correia CRSTB de, Torres C, Gomes E, Rodriguez GM, Regatieri WKP, Takamiya NT, Rogerio LA, Malavazi I, Gomes MD, Damasceno JD, Silva VL da, Oliveira MAF de, Silva MS da, Nascimento AS, Coelho AC, Maruyama SRC, Teixeira FR. Functional characterization of cullin-1-RING ubiquitin ligase (CRL1) complex in Leishmania infantum [Internet]. PLOS Pathogens. 2024 ; 20( 7): e1012336-1-e1012336-34 + supporting information.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1371/journal.ppat.1012336
Trabalho de evento-resumo
Nanotheranostic systems as a new strategy for the combined treatment of drug-resistant tuberculosis (2023)
Bernardi, Juliana Cancino; Galvani, Pietra de Barros; Corrêa, Giseli Furlan ; Cardoso, Valéria Maria de Oliveira; Ferreira, Natália Noronha ; Machado, Thales Rafael ; Bonato, Vânia Luiza Deperon ; Zucolotto, Valtencir
Source: Program. Conference titles: Brazil MRS Meeting. Unidades: FFCLRP, IFSC, FMRP
Subjects: NANOCIÊNCIA, NANOTECNOLOGIA, TUBERCULOSE, RESISTÊNCIA MICROBIANA ÀS DROGAS
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ABNT
BERNARDI, Juliana Cancino et al. Nanotheranostic systems as a new strategy for the combined treatment of drug-resistant tuberculosis. 2023, Anais.. Rio de Janeiro: Sociedade Brasileira de Pesquisa em Materiais - SBPMat, 2023. Disponível em: https://repositorio.usp.br/directbitstream/2a42962b-0605-44f0-81a4-be689d6100ca/3160747.pdf. Acesso em: 30 ago. 2024.
APA
Bernardi, J. C., Galvani, P. de B., Corrêa, G. F., Cardoso, V. M. de O., Ferreira, N. N., Machado, T. R., et al. (2023). Nanotheranostic systems as a new strategy for the combined treatment of drug-resistant tuberculosis. In Program. Rio de Janeiro: Sociedade Brasileira de Pesquisa em Materiais - SBPMat. Recuperado de https://repositorio.usp.br/directbitstream/2a42962b-0605-44f0-81a4-be689d6100ca/3160747.pdf
NLM
Bernardi JC, Galvani P de B, Corrêa GF, Cardoso VM de O, Ferreira NN, Machado TR, Bonato VLD, Zucolotto V. Nanotheranostic systems as a new strategy for the combined treatment of drug-resistant tuberculosis [Internet]. Program. 2023 ;[citado 2024 ago. 30 ] Available from: https://repositorio.usp.br/directbitstream/2a42962b-0605-44f0-81a4-be689d6100ca/3160747.pdf
Vancouver
Bernardi JC, Galvani P de B, Corrêa GF, Cardoso VM de O, Ferreira NN, Machado TR, Bonato VLD, Zucolotto V. Nanotheranostic systems as a new strategy for the combined treatment of drug-resistant tuberculosis [Internet]. Program. 2023 ;[citado 2024 ago. 30 ] Available from: https://repositorio.usp.br/directbitstream/2a42962b-0605-44f0-81a4-be689d6100ca/3160747.pdf
Artigo de periodico
Profiling the immune epigenome across global cattle breeds (2023)
Powell, Jessica; Talenti, Andrea; Fisch, Andressa ; Hemmink, Johanneke D.; Paxton, Edith; Toye, Philip; Santos, Isabel Kinney Ferreira de Miranda ; Ferreira, Beatriz Rossetti ; Connelley, Tim K.; Morrison, Liam J.; Prendergast, James G. D.
Source: Genome Biology. Unidades: FMRP, EERP
Subjects: BOVINOS, METILAÇÃO, DNA, CROMATINA, CÉLULAS, IMUNOLOGIA
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ABNT
POWELL, Jessica et al. Profiling the immune epigenome across global cattle breeds. Genome Biology, v. 24, n. 1, p. 1-31, 2023Tradução . . Disponível em: https://doi.org/10.1186/s13059-023-02964-3. Acesso em: 30 ago. 2024.
APA
Powell, J., Talenti, A., Fisch, A., Hemmink, J. D., Paxton, E., Toye, P., et al. (2023). Profiling the immune epigenome across global cattle breeds. Genome Biology, 24( 1), 1-31. doi:10.1186/s13059-023-02964-3
NLM
Powell J, Talenti A, Fisch A, Hemmink JD, Paxton E, Toye P, Santos IKF de M, Ferreira BR, Connelley TK, Morrison LJ, Prendergast JGD. Profiling the immune epigenome across global cattle breeds [Internet]. Genome Biology. 2023 ; 24( 1): 1-31.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1186/s13059-023-02964-3
Vancouver
Powell J, Talenti A, Fisch A, Hemmink JD, Paxton E, Toye P, Santos IKF de M, Ferreira BR, Connelley TK, Morrison LJ, Prendergast JGD. Profiling the immune epigenome across global cattle breeds [Internet]. Genome Biology. 2023 ; 24( 1): 1-31.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1186/s13059-023-02964-3
Artigo de periodico
Cell death induced by NLRP3–palmitate axis impairs pulmonary damage tolerance and aggravates immunopathology during obesity-tuberculosis comorbidity (2023)
Albornoz, Sandra Patrícia Palma ; Silva, Thais Fernanda de Campo Fraga da ; Carvalho, Renan Villanova Homem de ; Rodrigues, Tamara Silva; Gembre, Ana Flávia; Oliveira, Rômulo Silva de; Souza, Fernanda Mesquita de; Corrêa, Giseli Furlan ; Ramalho, Leandra Naira Zambelli ; Sartori, Daniela Carlos ; Câmara, Niels Olsen Saraiva ; Zamboni, Dario Simões ; Takahashi, Viviani Nardini ; Sorgi, Carlos Artério ; Faccioli, Lucia Helena ; Medeiros, Alexandra Ivo de ; Costa, Diego Luís ; Bonato, Vânia Luiza Deperon
Source: Journal of Pathology. Unidades: FMRP, ICB, FCFRP, FFCLRP, ESALQ
Assunto: IMUNOLOGIA
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ALBORNOZ, Sandra Patrícia Palma et al. Cell death induced by NLRP3–palmitate axis impairs pulmonary damage tolerance and aggravates immunopathology during obesity-tuberculosis comorbidity. Journal of Pathology, v. 259, p. 291-303, 2023Tradução . . Disponível em: https://doi.org/10.1002/path.6041. Acesso em: 30 ago. 2024.
APA
Albornoz, S. P. P., Silva, T. F. de C. F. da, Carvalho, R. V. H. de, Rodrigues, T. S., Gembre, A. F., Oliveira, R. S. de, et al. (2023). Cell death induced by NLRP3–palmitate axis impairs pulmonary damage tolerance and aggravates immunopathology during obesity-tuberculosis comorbidity. Journal of Pathology, 259, 291-303. doi:10.1002/path.6041
NLM
Albornoz SPP, Silva TF de CF da, Carvalho RVH de, Rodrigues TS, Gembre AF, Oliveira RS de, Souza FM de, Corrêa GF, Ramalho LNZ, Sartori DC, Câmara NOS, Zamboni DS, Takahashi VN, Sorgi CA, Faccioli LH, Medeiros AI de, Costa DL, Bonato VLD. Cell death induced by NLRP3–palmitate axis impairs pulmonary damage tolerance and aggravates immunopathology during obesity-tuberculosis comorbidity [Internet]. Journal of Pathology. 2023 ; 259 291-303.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1002/path.6041
Vancouver
Albornoz SPP, Silva TF de CF da, Carvalho RVH de, Rodrigues TS, Gembre AF, Oliveira RS de, Souza FM de, Corrêa GF, Ramalho LNZ, Sartori DC, Câmara NOS, Zamboni DS, Takahashi VN, Sorgi CA, Faccioli LH, Medeiros AI de, Costa DL, Bonato VLD. Cell death induced by NLRP3–palmitate axis impairs pulmonary damage tolerance and aggravates immunopathology during obesity-tuberculosis comorbidity [Internet]. Journal of Pathology. 2023 ; 259 291-303.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1002/path.6041
Artigo de periodico
Parasite detection in visceral leishmaniasis samples by dye-based qPCR using new gene targets of Leishmania infantum and crithidia (2023)
Takamiya, Nayore Tamie; Rogerio, Luana Aparecida; Torres, Caroline; Leonel, João Augusto Franco ; Vioti, Geovanna ; Oliveira, Trícia Maria Ferreira de Sousa ; Valeriano, Karoline Camila; Porcino, Gabriane Nascimento ; Santos, Isabel Kinney Ferreira de Miranda ; Costa, Carlos H. N. ; Costa, Dorcas L. ; Ferreira, Tauana Sousa; Gurgel-Gonçalves, Rodrigo ; Silva, João Santana da ; Teixeira, Felipe Roberti; Almeida, Roque Pacheco de ; Ribeiro, José M. ; Maruyama, Sandra Regina
Source: Tropical Medicine and Infectious Disease. Unidades: FZEA, FMRP, FMVZ
Subjects: LEISHMANIOSE VISCERAL, LEISHMANIA INFANTUM, CRITHIDIA, REAÇÃO EM CADEIA POR POLIMERASE
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TAKAMIYA, Nayore Tamie et al. Parasite detection in visceral leishmaniasis samples by dye-based qPCR using new gene targets of Leishmania infantum and crithidia. Tropical Medicine and Infectious Disease, v. 8, n. 9, p. 1-25, 2023Tradução . . Disponível em: https://doi.org/10.3390/tropicalmed8080405. Acesso em: 30 ago. 2024.
APA
Takamiya, N. T., Rogerio, L. A., Torres, C., Leonel, J. A. F., Vioti, G., Oliveira, T. M. F. de S., et al. (2023). Parasite detection in visceral leishmaniasis samples by dye-based qPCR using new gene targets of Leishmania infantum and crithidia. Tropical Medicine and Infectious Disease, 8( 9), 1-25. doi:10.3390/tropicalmed8080405
NLM
Takamiya NT, Rogerio LA, Torres C, Leonel JAF, Vioti G, Oliveira TMF de S, Valeriano KC, Porcino GN, Santos IKF de M, Costa CHN, Costa DL, Ferreira TS, Gurgel-Gonçalves R, Silva JS da, Teixeira FR, Almeida RP de, Ribeiro JM, Maruyama SR. Parasite detection in visceral leishmaniasis samples by dye-based qPCR using new gene targets of Leishmania infantum and crithidia [Internet]. Tropical Medicine and Infectious Disease. 2023 ; 8( 9): 1-25.[citado 2024 ago. 30 ] Available from: https://doi.org/10.3390/tropicalmed8080405
Vancouver
Takamiya NT, Rogerio LA, Torres C, Leonel JAF, Vioti G, Oliveira TMF de S, Valeriano KC, Porcino GN, Santos IKF de M, Costa CHN, Costa DL, Ferreira TS, Gurgel-Gonçalves R, Silva JS da, Teixeira FR, Almeida RP de, Ribeiro JM, Maruyama SR. Parasite detection in visceral leishmaniasis samples by dye-based qPCR using new gene targets of Leishmania infantum and crithidia [Internet]. Tropical Medicine and Infectious Disease. 2023 ; 8( 9): 1-25.[citado 2024 ago. 30 ] Available from: https://doi.org/10.3390/tropicalmed8080405
Artigo de periodico
The DEAD-box RNA helicase RhlB is required for efficient RNA processing at low temperature in Caulobacter (2023)
Araújo, Hugo Libonati de ; Piscinato, Beatriz A. ; Lorenzetti, Alan Péricles Rodrigues ; Muthunayake Nisansala S. ; Rathnayaka-Mudiyanselage, I. W. ; Santos, Naara Marcondes dos ; Schrader, Jared ; Koide, Tie ; Marques, Marilis do Valle
Source: Microbiology Spectrum. Unidades: FMRP, ICB, BIOINFORMÁTICA
Subjects: MICROBIOLOGIA, GENÉTICA BACTERIANA, REGULAÇÃO BACTERIANA DA EXPRESSÃO GÊNICA, RNA RIBOSSÔMICO, RIBOSSOMOS
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ABNT
ARAÚJO, Hugo Libonati de et al. The DEAD-box RNA helicase RhlB is required for efficient RNA processing at low temperature in Caulobacter. Microbiology Spectrum, v. 11, n. 6, p. 20 , 2023Tradução . . Disponível em: https://doi.org/10.1128/spectrum.01934-23. Acesso em: 30 ago. 2024.
APA
Araújo, H. L. de, Piscinato, B. A., Lorenzetti, A. P. R., Muthunayake Nisansala S.,, Rathnayaka-Mudiyanselage, I. W., Santos, N. M. dos, et al. (2023). The DEAD-box RNA helicase RhlB is required for efficient RNA processing at low temperature in Caulobacter. Microbiology Spectrum, 11( 6), 20 . doi:10.1128/spectrum.01934-23
NLM
Araújo HL de, Piscinato BA, Lorenzetti APR, Muthunayake Nisansala S., Rathnayaka-Mudiyanselage IW, Santos NM dos, Schrader J, Koide T, Marques M do V. The DEAD-box RNA helicase RhlB is required for efficient RNA processing at low temperature in Caulobacter [Internet]. Microbiology Spectrum. 2023 ; 11( 6): 20 .[citado 2024 ago. 30 ] Available from: https://doi.org/10.1128/spectrum.01934-23
Vancouver
Araújo HL de, Piscinato BA, Lorenzetti APR, Muthunayake Nisansala S., Rathnayaka-Mudiyanselage IW, Santos NM dos, Schrader J, Koide T, Marques M do V. The DEAD-box RNA helicase RhlB is required for efficient RNA processing at low temperature in Caulobacter [Internet]. Microbiology Spectrum. 2023 ; 11( 6): 20 .[citado 2024 ago. 30 ] Available from: https://doi.org/10.1128/spectrum.01934-23
Artigo de periodico
Divergent androgenic modulation of SARS-CoV-2 infection cooperates with dysregulated immune response to dictate worse COVID-19 outcomes in men (2023)
Duarte-Silva, Murillo ; Oliveira, Camilla Narjara Simão; Fuzo, Carlos Alessandro ; Silva Neto, Pedro Vieira da; Toro, Diana Mota; Pimentel, Vinícius Eduardo; Pérez, Malena Martínez; Fraga-Silva, Thais Fernanda de Campos ; Carvalho, Jonatan Constança Silva de; Santos Neto, Firmino Martins dos; Martins Júnior, Ronaldo Bragança; Arruda Neto, Eurico de; Vilar, Fernando Crivelenti; Degiovani, Augusto Marcussi; Ostini, Fátima M.; Feitosa, Marley Ribeiro; Parra, Rogério Serafim ; Gaspar, Gilberto Gambero ; Rocha, José Joaquim Ribeiro da; Féres, Omar; Fernandes, Ana Paula Morais ; Maruyama, Sandra Regina Costa; Russo, Elisa Maria de Sousa ; Bonato, Vânia Luiza Deperon ; Santos, Isabel Kinney Ferreira de Miranda ; Sorgi, Carlos Arterio ; Dias-Baruffi, Marcelo ; Faccioli, Lucia Helena ; Cardoso, Cristina Ribeiro de Barros
Source: Brain, Behavior, and Immunity. Unidades: FMRP, FCFRP, EERP, FFCLRP
Subjects: TESTOSTERONA, DIIDROTESTOSTERONA, RECEPTORES ADRENÉRGICOS
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DUARTE-SILVA, Murillo et al. Divergent androgenic modulation of SARS-CoV-2 infection cooperates with dysregulated immune response to dictate worse COVID-19 outcomes in men. Brain, Behavior, and Immunity, v. 114, p. 275-286, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.bbi.2023.08.026. Acesso em: 30 ago. 2024.
APA
Duarte-Silva, M., Oliveira, C. N. S., Fuzo, C. A., Silva Neto, P. V. da, Toro, D. M., Pimentel, V. E., et al. (2023). Divergent androgenic modulation of SARS-CoV-2 infection cooperates with dysregulated immune response to dictate worse COVID-19 outcomes in men. Brain, Behavior, and Immunity, 114, 275-286. doi:10.1016/j.bbi.2023.08.026
NLM
Duarte-Silva M, Oliveira CNS, Fuzo CA, Silva Neto PV da, Toro DM, Pimentel VE, Pérez MM, Fraga-Silva TF de C, Carvalho JCS de, Santos Neto FM dos, Martins Júnior RB, Arruda Neto E de, Vilar FC, Degiovani AM, Ostini FM, Feitosa MR, Parra RS, Gaspar GG, Rocha JJR da, Féres O, Fernandes APM, Maruyama SRC, Russo EM de S, Bonato VLD, Santos IKF de M, Sorgi CA, Dias-Baruffi M, Faccioli LH, Cardoso CR de B. Divergent androgenic modulation of SARS-CoV-2 infection cooperates with dysregulated immune response to dictate worse COVID-19 outcomes in men [Internet]. Brain, Behavior, and Immunity. 2023 ; 114 275-286.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.bbi.2023.08.026
Vancouver
Duarte-Silva M, Oliveira CNS, Fuzo CA, Silva Neto PV da, Toro DM, Pimentel VE, Pérez MM, Fraga-Silva TF de C, Carvalho JCS de, Santos Neto FM dos, Martins Júnior RB, Arruda Neto E de, Vilar FC, Degiovani AM, Ostini FM, Feitosa MR, Parra RS, Gaspar GG, Rocha JJR da, Féres O, Fernandes APM, Maruyama SRC, Russo EM de S, Bonato VLD, Santos IKF de M, Sorgi CA, Dias-Baruffi M, Faccioli LH, Cardoso CR de B. Divergent androgenic modulation of SARS-CoV-2 infection cooperates with dysregulated immune response to dictate worse COVID-19 outcomes in men [Internet]. Brain, Behavior, and Immunity. 2023 ; 114 275-286.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.bbi.2023.08.026
Artigo de periodico
FK506 impairs neutrophil migration that results in increased polymicrobial sepsis susceptibility (2023)
Borges, Vanessa de Fátima; Galant, Leticia Selinger; Kanashiro, Alexandre ; Castanheira, Fernanda Vargas e Silva; Monteiro, Valter Vinícius Silva; Duarte, Diego Ângelo; Rodrigues, Filipe Camargo; Silva, Camila Meirelles de Souza; Schneider, Ayda Henriques ; Cebinelli, Guilherme Cesar Martelossi ; Lima, Mikhael Haruo Fernandes de; Viola, João Paulo de Biaso; Cunha, Thiago Mattar ; Costa Neto, Claudio Miguel da ; Alves Filho, José Carlos Farias ; Pupo, André Sampaio; Cunha, Fernando de Queiroz
Source: Inflammation Research. Unidade: FMRP
Subjects: NEUTRÓFILOS, SEPSE, FÁRMACOS IMUNOSSUPRESSORES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BORGES, Vanessa de Fátima et al. FK506 impairs neutrophil migration that results in increased polymicrobial sepsis susceptibility. Inflammation Research, v. 72, n. 2, p. 203-215, 2023Tradução . . Disponível em: https://doi.org/10.1007/s00011-022-01669-w. Acesso em: 30 ago. 2024.
APA
Borges, V. de F., Galant, L. S., Kanashiro, A., Castanheira, F. V. e S., Monteiro, V. V. S., Duarte, D. Â., et al. (2023). FK506 impairs neutrophil migration that results in increased polymicrobial sepsis susceptibility. Inflammation Research, 72( 2), 203-215. doi:10.1007/s00011-022-01669-w
NLM
Borges V de F, Galant LS, Kanashiro A, Castanheira FV e S, Monteiro VVS, Duarte DÂ, Rodrigues FC, Silva CM de S, Schneider AH, Cebinelli GCM, Lima MHF de, Viola JP de B, Cunha TM, Costa Neto CM da, Alves Filho JCF, Pupo AS, Cunha F de Q. FK506 impairs neutrophil migration that results in increased polymicrobial sepsis susceptibility [Internet]. Inflammation Research. 2023 ; 72( 2): 203-215.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1007/s00011-022-01669-w
Vancouver
Borges V de F, Galant LS, Kanashiro A, Castanheira FV e S, Monteiro VVS, Duarte DÂ, Rodrigues FC, Silva CM de S, Schneider AH, Cebinelli GCM, Lima MHF de, Viola JP de B, Cunha TM, Costa Neto CM da, Alves Filho JCF, Pupo AS, Cunha F de Q. FK506 impairs neutrophil migration that results in increased polymicrobial sepsis susceptibility [Internet]. Inflammation Research. 2023 ; 72( 2): 203-215.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1007/s00011-022-01669-w
Artigo de periodico
Airway epithelial cells and macrophages trigger IL-6-CD95/CD95L axis and mediate initial immunopathology of COVID-19 (2023)
Fraga-Silva, Thais Fernanda de Campos ; Rosa, Ualter Guilherme Cipriano; Fumagalli, Marcílio Jorge ; Corrêa, Giseli Furlan ; Fuzo, Carlos Alessandro ; Santos, Douglas dos; Mestriner, Fabíola Leslie Antunes Cardoso ; Ribeiro, Christiane Becari ; Teixeira-Carvalho, Andrea; Coelho-dos-Reis, Jordana; Menegueti, Mayra Gonçalves ; Figueiredo, Luiz Tadeu Moraes ; Cunha, Larissa Dias da; Martins-Filho, Olindo A.; Baruffi, Marcelo Dias ; Martins, Maria Auxiliadora ; Passaglia, Rita de Cassia Aleixo Tostes ; Bonato, Vânia Luiza Deperon
Source: iScience. Unidades: FMRP, EERP, FCFRP
Subjects: SISTEMA IMUNE, VIROLOGIA, MACRÓFAGOS
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ABNT
FRAGA-SILVA, Thais Fernanda de Campos et al. Airway epithelial cells and macrophages trigger IL-6-CD95/CD95L axis and mediate initial immunopathology of COVID-19. iScience, v. 26, n. 12, p. 1-19, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.isci.2023.108366. Acesso em: 30 ago. 2024.
APA
Fraga-Silva, T. F. de C., Rosa, U. G. C., Fumagalli, M. J., Corrêa, G. F., Fuzo, C. A., Santos, D. dos, et al. (2023). Airway epithelial cells and macrophages trigger IL-6-CD95/CD95L axis and mediate initial immunopathology of COVID-19. iScience, 26( 12), 1-19. doi:10.1016/j.isci.2023.108366
NLM
Fraga-Silva TF de C, Rosa UGC, Fumagalli MJ, Corrêa GF, Fuzo CA, Santos D dos, Mestriner FLAC, Ribeiro CB, Teixeira-Carvalho A, Coelho-dos-Reis J, Menegueti MG, Figueiredo LTM, Cunha LD da, Martins-Filho OA, Baruffi MD, Martins MA, Passaglia R de CAT, Bonato VLD. Airway epithelial cells and macrophages trigger IL-6-CD95/CD95L axis and mediate initial immunopathology of COVID-19 [Internet]. iScience. 2023 ; 26( 12): 1-19.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.isci.2023.108366
Vancouver
Fraga-Silva TF de C, Rosa UGC, Fumagalli MJ, Corrêa GF, Fuzo CA, Santos D dos, Mestriner FLAC, Ribeiro CB, Teixeira-Carvalho A, Coelho-dos-Reis J, Menegueti MG, Figueiredo LTM, Cunha LD da, Martins-Filho OA, Baruffi MD, Martins MA, Passaglia R de CAT, Bonato VLD. Airway epithelial cells and macrophages trigger IL-6-CD95/CD95L axis and mediate initial immunopathology of COVID-19 [Internet]. iScience. 2023 ; 26( 12): 1-19.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.isci.2023.108366
Artigo de periodico
IL-22 is deleterious along with IL-17 in allergic asthma but is not detrimental in the comorbidity asthma and acute pneumonia (2023)
Goulart, Amanda; Boko, Mèdéton Mahoussi Michaël; Martins, Núbia Sabrina ; Gembre, Ana Flávia; Oliveira, Rômulo Silva de; Albornoz, Sandra Patrícia Palma ; Bertolini, Thaís Barboza ; Ribolla, Paulo Eduardo Martins; Ramalho, Leandra Naira Zambelli ; Silva, Thais Fernanda de Campos Fraga ; Bonato, Vânia Luiza Deperon
Source: International Journal of Molecular Sciences. Unidades: FMRP, FCFRP
Subjects: ALÉRGENOS, ASMA, COMORBIDADE, INTERLEUCINAS, PULMÃO, PNEUMONIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GOULART, Amanda et al. IL-22 is deleterious along with IL-17 in allergic asthma but is not detrimental in the comorbidity asthma and acute pneumonia. International Journal of Molecular Sciences, v. 24, n. 13, p. 1-16, 2023Tradução . . Disponível em: https://doi.org/10.3390/ijms241310418. Acesso em: 30 ago. 2024.
APA
Goulart, A., Boko, M. M. M., Martins, N. S., Gembre, A. F., Oliveira, R. S. de, Albornoz, S. P. P., et al. (2023). IL-22 is deleterious along with IL-17 in allergic asthma but is not detrimental in the comorbidity asthma and acute pneumonia. International Journal of Molecular Sciences, 24( 13), 1-16. doi:10.3390/ijms241310418
NLM
Goulart A, Boko MMM, Martins NS, Gembre AF, Oliveira RS de, Albornoz SPP, Bertolini TB, Ribolla PEM, Ramalho LNZ, Silva TF de CF, Bonato VLD. IL-22 is deleterious along with IL-17 in allergic asthma but is not detrimental in the comorbidity asthma and acute pneumonia [Internet]. International Journal of Molecular Sciences. 2023 ; 24( 13): 1-16.[citado 2024 ago. 30 ] Available from: https://doi.org/10.3390/ijms241310418
Vancouver
Goulart A, Boko MMM, Martins NS, Gembre AF, Oliveira RS de, Albornoz SPP, Bertolini TB, Ribolla PEM, Ramalho LNZ, Silva TF de CF, Bonato VLD. IL-22 is deleterious along with IL-17 in allergic asthma but is not detrimental in the comorbidity asthma and acute pneumonia [Internet]. International Journal of Molecular Sciences. 2023 ; 24( 13): 1-16.[citado 2024 ago. 30 ] Available from: https://doi.org/10.3390/ijms241310418
Artigo de periodico
The dose-dependent effect of curcumin supplementation on inflammatory response and gut microbiota profile in high-fat fed C57BL/6 mice (2023)
Silva, Caroline Bertoncini ; Fassini, Priscila Giacomo ; Sartori, Daniela Carlos ; Paula, Natália Aparecida de ; Ramalho, Leandra Naira Zambelli ; Giuliani, Marina Rodrigues; Pereira, Ítalo Sousa; Guimarães, Jhefferson Barbosa ; Suen, Vivian Marques Miguel
Source: Molecular Nutrition & Food Research. Unidade: FMRP
Subjects: POLIFENÓIS, ANTI-INFLAMATÓRIOS, GORDURAS NA DIETA, OBESIDADE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Caroline Bertoncini et al. The dose-dependent effect of curcumin supplementation on inflammatory response and gut microbiota profile in high-fat fed C57BL/6 mice. Molecular Nutrition & Food Research, v. 67, n. 23, p. 1-12, 2023Tradução . . Disponível em: https://doi.org/10.1002/mnfr.202300378. Acesso em: 30 ago. 2024.
APA
Silva, C. B., Fassini, P. G., Sartori, D. C., Paula, N. A. de, Ramalho, L. N. Z., Giuliani, M. R., et al. (2023). The dose-dependent effect of curcumin supplementation on inflammatory response and gut microbiota profile in high-fat fed C57BL/6 mice. Molecular Nutrition & Food Research, 67( 23), 1-12. doi:10.1002/mnfr.202300378
NLM
Silva CB, Fassini PG, Sartori DC, Paula NA de, Ramalho LNZ, Giuliani MR, Pereira ÍS, Guimarães JB, Suen VMM. The dose-dependent effect of curcumin supplementation on inflammatory response and gut microbiota profile in high-fat fed C57BL/6 mice [Internet]. Molecular Nutrition & Food Research. 2023 ; 67( 23): 1-12.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1002/mnfr.202300378
Vancouver
Silva CB, Fassini PG, Sartori DC, Paula NA de, Ramalho LNZ, Giuliani MR, Pereira ÍS, Guimarães JB, Suen VMM. The dose-dependent effect of curcumin supplementation on inflammatory response and gut microbiota profile in high-fat fed C57BL/6 mice [Internet]. Molecular Nutrition & Food Research. 2023 ; 67( 23): 1-12.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1002/mnfr.202300378
Artigo de periodico
AIM2 promotes TH17 cells differentiation by regulating RORgt transcription activity (2023)
Leite, Jefferson Antonio ; Menezes, Luísa ; Martins, Eloisa ; Rodrigues, Tamara Silva; Tavares, Lucas ; Ebering, Anna ; Schelmbauer, Carsten ; Cebinelli, Guilherme Cesar Martelossi ; Zinina, Valeriya ; Golden, Artemy ; Soshnikova, Natalia ; Zamboni, Dario S. ; Cunha, Fernando Q. ; Magdalena Huber ; Waisman, Ari ; Silva, João Santana da ; Carlos, Daniela ; Câmara, Niels Olsen Saraiva
Source: iScience. Unidades: FMRP, ICB
Subjects: IMUNOLOGIA, CAMUNDONGOS, PROTEÍNAS, DIFERENCIAÇÃO CELULAR, LINFÓCITOS T, CÉLULAS SANGUÍNEAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEITE, Jefferson Antonio et al. AIM2 promotes TH17 cells differentiation by regulating RORgt transcription activity. iScience, v. 26, n. 11, p. art. 108134. 19 , 2023Tradução . . Disponível em: https://doi.org/10.1016/j.isci.2023.108134. Acesso em: 30 ago. 2024.
APA
Leite, J. A., Menezes, L., Martins, E., Rodrigues, T. S., Tavares, L., Ebering, A., et al. (2023). AIM2 promotes TH17 cells differentiation by regulating RORgt transcription activity. iScience, 26( 11), art. 108134. 19 . doi:10.1016/j.isci.2023.108134
NLM
Leite JA, Menezes L, Martins E, Rodrigues TS, Tavares L, Ebering A, Schelmbauer C, Cebinelli GCM, Zinina V, Golden A, Soshnikova N, Zamboni DS, Cunha FQ, Magdalena Huber, Waisman A, Silva JS da, Carlos D, Câmara NOS. AIM2 promotes TH17 cells differentiation by regulating RORgt transcription activity [Internet]. iScience. 2023 ; 26( 11): art. 108134. 19 .[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.isci.2023.108134
Vancouver
Leite JA, Menezes L, Martins E, Rodrigues TS, Tavares L, Ebering A, Schelmbauer C, Cebinelli GCM, Zinina V, Golden A, Soshnikova N, Zamboni DS, Cunha FQ, Magdalena Huber, Waisman A, Silva JS da, Carlos D, Câmara NOS. AIM2 promotes TH17 cells differentiation by regulating RORgt transcription activity [Internet]. iScience. 2023 ; 26( 11): art. 108134. 19 .[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.isci.2023.108134
Artigo de periodico
Addressing microbial resistance worldwide: challenges over controlling life-threatening fungal infections (2023)
Santana, Leonardo Martins; Rezende, Caroline Patini; Rossi, Antônio ; Martinez-Rossi, Nilce Maria ; Almeida, Fausto Bruno dos Reis
Source: Pathogens. Unidade: FMRP
Subjects: CANDIDÍASE, CRIPTOCOCOSE, CORONAVIRUS, RESISTÊNCIA MICROBIANA ÀS DROGAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTANA, Leonardo Martins et al. Addressing microbial resistance worldwide: challenges over controlling life-threatening fungal infections. Pathogens, v. 12, n. 2, p. 1-15, 2023Tradução . . Disponível em: https://doi.org/10.3390/pathogens12020293. Acesso em: 30 ago. 2024.
APA
Santana, L. M., Rezende, C. P., Rossi, A., Martinez-Rossi, N. M., & Almeida, F. B. dos R. (2023). Addressing microbial resistance worldwide: challenges over controlling life-threatening fungal infections. Pathogens, 12( 2), 1-15. doi:10.3390/pathogens12020293
NLM
Santana LM, Rezende CP, Rossi A, Martinez-Rossi NM, Almeida FB dos R. Addressing microbial resistance worldwide: challenges over controlling life-threatening fungal infections [Internet]. Pathogens. 2023 ; 12( 2): 1-15.[citado 2024 ago. 30 ] Available from: https://doi.org/10.3390/pathogens12020293
Vancouver
Santana LM, Rezende CP, Rossi A, Martinez-Rossi NM, Almeida FB dos R. Addressing microbial resistance worldwide: challenges over controlling life-threatening fungal infections [Internet]. Pathogens. 2023 ; 12( 2): 1-15.[citado 2024 ago. 30 ] Available from: https://doi.org/10.3390/pathogens12020293
Artigo de periodico
Characterization of a new glucose-tolerant GH1 β-glycosidase from Aspergillus fumigatus with transglycosylation activity (2023)
Pereira, Lucas Matheus Soares; Bernardi, Aline Vianna ; Gerolamo, Luis Eduardo ; Pedersoli, Wellington Ramos; Carraro, Cláudia Batista; Silva, Roberto do Nascimento; Uyemura, Sergio Akira ; Dinamarco, Taisa Magnani
Source: International Journal of Molecular Sciences. Unidades: FMRP, FCFRP, FFCLRP
Subjects: GLICOSE, GLICOSÍDEOS, ASPERGILLUS, ENZIMAS HIDROLÍTICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PEREIRA, Lucas Matheus Soares et al. Characterization of a new glucose-tolerant GH1 β-glycosidase from Aspergillus fumigatus with transglycosylation activity. International Journal of Molecular Sciences, v. 24, n. 5, p. 1-23, 2023Tradução . . Disponível em: https://doi.org/10.3390/ijms24054489. Acesso em: 30 ago. 2024.
APA
Pereira, L. M. S., Bernardi, A. V., Gerolamo, L. E., Pedersoli, W. R., Carraro, C. B., Silva, R. do N., et al. (2023). Characterization of a new glucose-tolerant GH1 β-glycosidase from Aspergillus fumigatus with transglycosylation activity. International Journal of Molecular Sciences, 24( 5), 1-23. doi:10.3390/ijms24054489
NLM
Pereira LMS, Bernardi AV, Gerolamo LE, Pedersoli WR, Carraro CB, Silva R do N, Uyemura SA, Dinamarco TM. Characterization of a new glucose-tolerant GH1 β-glycosidase from Aspergillus fumigatus with transglycosylation activity [Internet]. International Journal of Molecular Sciences. 2023 ; 24( 5): 1-23.[citado 2024 ago. 30 ] Available from: https://doi.org/10.3390/ijms24054489
Vancouver
Pereira LMS, Bernardi AV, Gerolamo LE, Pedersoli WR, Carraro CB, Silva R do N, Uyemura SA, Dinamarco TM. Characterization of a new glucose-tolerant GH1 β-glycosidase from Aspergillus fumigatus with transglycosylation activity [Internet]. International Journal of Molecular Sciences. 2023 ; 24( 5): 1-23.[citado 2024 ago. 30 ] Available from: https://doi.org/10.3390/ijms24054489
Artigo de periodico
Cytokine storm in individuals with severe COVID-19 decreases endothelial cell antioxidant defense via downregulation of the Nrf2 transcriptional factor (2023)
Rodrigues, Daniel ; Machado, Mirele Resende ; Alves, Juliano Vilela ; Fraga-Silva, Thais Fernanda de Campos ; Martins, Ronaldo Bragança ; Campos, Lígia Cristina Borges ; Francisco, Daniely Franco ; Couto, Ariel Emiliano Souza do ; Bonato, Vânia Luiza Deperon ; Arruda, Eurico ; Becari, Christiane ; Auxiliadora-Martins, Maria ; Louzada Júnior, Paulo ; Costa, Rafael Menezes da ; Tostes, Rita de Cássia Aleixo
Source: American Journal of Physiology. Heart and Circulatory Physiology. Unidades: FCFRP, FMRP, FOB
Subjects: CÉLULAS ENDOTELIAIS, CITOCINAS, COVID-19, ANORMALIDADES CARDIOVASCULARES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RODRIGUES, Daniel et al. Cytokine storm in individuals with severe COVID-19 decreases endothelial cell antioxidant defense via downregulation of the Nrf2 transcriptional factor. American Journal of Physiology. Heart and Circulatory Physiology, v. 325, n. 2, p. H252–H263 Aug. 2023, 2023Tradução . . Disponível em: https://doi.org/10.1152/ajpheart.00096.2023. Acesso em: 30 ago. 2024.
APA
Rodrigues, D., Machado, M. R., Alves, J. V., Fraga-Silva, T. F. de C., Martins, R. B., Campos, L. C. B., et al. (2023). Cytokine storm in individuals with severe COVID-19 decreases endothelial cell antioxidant defense via downregulation of the Nrf2 transcriptional factor. American Journal of Physiology. Heart and Circulatory Physiology, 325( 2), H252–H263 Aug. 2023. doi:10.1152/ajpheart.00096.2023
NLM
Rodrigues D, Machado MR, Alves JV, Fraga-Silva TF de C, Martins RB, Campos LCB, Francisco DF, Couto AES do, Bonato VLD, Arruda E, Becari C, Auxiliadora-Martins M, Louzada Júnior P, Costa RM da, Tostes R de CA. Cytokine storm in individuals with severe COVID-19 decreases endothelial cell antioxidant defense via downregulation of the Nrf2 transcriptional factor [Internet]. American Journal of Physiology. Heart and Circulatory Physiology. 2023 ; 325( 2): H252–H263 Aug. 2023.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1152/ajpheart.00096.2023
Vancouver
Rodrigues D, Machado MR, Alves JV, Fraga-Silva TF de C, Martins RB, Campos LCB, Francisco DF, Couto AES do, Bonato VLD, Arruda E, Becari C, Auxiliadora-Martins M, Louzada Júnior P, Costa RM da, Tostes R de CA. Cytokine storm in individuals with severe COVID-19 decreases endothelial cell antioxidant defense via downregulation of the Nrf2 transcriptional factor [Internet]. American Journal of Physiology. Heart and Circulatory Physiology. 2023 ; 325( 2): H252–H263 Aug. 2023.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1152/ajpheart.00096.2023
Artigo de periodico
Trichoderma longibrachiatum and thermothelomyces thermophilus co-culture: improvement the saccharification profile of different sugarcane bagasse varieties (2023)
Contato, Alex Graça; Nogueira, Karoline Maria Vieira; Buckeridge, Marcos ; Silva, Roberto do Nascimento ; Polizeli, Maria De Lourdes Teixeira De Moraes
Source: Biotechnology Letters. Unidades: RUSP, FFCLRP, FMRP, EEL
Subjects: FUNGOS, TRICHODERMA, CANA-DE-AÇÚCAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CONTATO, Alex Graça et al. Trichoderma longibrachiatum and thermothelomyces thermophilus co-culture: improvement the saccharification profile of different sugarcane bagasse varieties. Biotechnology Letters, v. 45, p. 1093–1102, 2023Tradução . . Disponível em: https://doi.org/10.1007/s10529-023-03395-7. Acesso em: 30 ago. 2024.
APA
Contato, A. G., Nogueira, K. M. V., Buckeridge, M., Silva, R. do N., & Polizeli, M. D. L. T. D. M. (2023). Trichoderma longibrachiatum and thermothelomyces thermophilus co-culture: improvement the saccharification profile of different sugarcane bagasse varieties. Biotechnology Letters, 45, 1093–1102. doi:10.1007/s10529-023-03395-7
NLM
Contato AG, Nogueira KMV, Buckeridge M, Silva R do N, Polizeli MDLTDM. Trichoderma longibrachiatum and thermothelomyces thermophilus co-culture: improvement the saccharification profile of different sugarcane bagasse varieties [Internet]. Biotechnology Letters. 2023 ; 45 1093–1102.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1007/s10529-023-03395-7
Vancouver
Contato AG, Nogueira KMV, Buckeridge M, Silva R do N, Polizeli MDLTDM. Trichoderma longibrachiatum and thermothelomyces thermophilus co-culture: improvement the saccharification profile of different sugarcane bagasse varieties [Internet]. Biotechnology Letters. 2023 ; 45 1093–1102.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1007/s10529-023-03395-7
Artigo de periodico
SARS-CoV-2 uses CD4 to infect T helper lymphocytes (2023)
Brunetti, Natalia S.; Silva, João Victor Virgilio da ; Veras, Flávio Protásio ; Tavares, Lucas Alves ; Castro, Ícaro Maia Santos de ; Silvestrini, Virgínia Campos; Oliveira, Eduardo Brandt de; Faça, Vitor Marcel ; Sposito, Andrei Carvalho ; Velloso, Licio Augusto; Silva, Luis Lamberti Pinto da ; Cunha, Thiago Mattar ; Nakaya, Helder Takashi Imoto ; Skaf, Munir Salomão ; Vieira, Pedro Manoel Mendes de Moraes ; Farias, Alessandro dos Santos
Source: eLife. Unidades: FMRP, FM, IQ, FCF, FFCLRP, ICB, ESALQ, BIOINFORMÁTICA
Subjects: LINFÓCITOS T, COVID-19, PULMÃO, CORONAVIRUS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BRUNETTI, Natalia S. et al. SARS-CoV-2 uses CD4 to infect T helper lymphocytes. eLife, v. 12, p. 1-26, 2023Tradução . . Disponível em: https://doi.org/10.7554/eLife.84790. Acesso em: 30 ago. 2024.
APA
Brunetti, N. S., Silva, J. V. V. da, Veras, F. P., Tavares, L. A., Castro, Í. M. S. de, Silvestrini, V. C., et al. (2023). SARS-CoV-2 uses CD4 to infect T helper lymphocytes. eLife, 12, 1-26. doi:10.7554/eLife.84790
NLM
Brunetti NS, Silva JVV da, Veras FP, Tavares LA, Castro ÍMS de, Silvestrini VC, Oliveira EB de, Faça VM, Sposito AC, Velloso LA, Silva LLP da, Cunha TM, Nakaya HTI, Skaf MS, Vieira PMM de M, Farias A dos S. SARS-CoV-2 uses CD4 to infect T helper lymphocytes [Internet]. eLife. 2023 ; 12 1-26.[citado 2024 ago. 30 ] Available from: https://doi.org/10.7554/eLife.84790
Vancouver
Brunetti NS, Silva JVV da, Veras FP, Tavares LA, Castro ÍMS de, Silvestrini VC, Oliveira EB de, Faça VM, Sposito AC, Velloso LA, Silva LLP da, Cunha TM, Nakaya HTI, Skaf MS, Vieira PMM de M, Farias A dos S. SARS-CoV-2 uses CD4 to infect T helper lymphocytes [Internet]. eLife. 2023 ; 12 1-26.[citado 2024 ago. 30 ] Available from: https://doi.org/10.7554/eLife.84790

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