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Artigo de periodico
UHMK1 is a novel splicing regulatory kinase (2023)
Arfelli, Vanessa Cristina; Chang, Yun-Chien; Bagnoli, Johannes W.; Kerbs, Paul; Ciamponi, Felipe E.; Paz, Laissa Mayara da Silva; Pankivskyi, Serhii; Salone, Jean de Matha; Maucuer, Alexandre; Massirer, Katlin B.; Enard, Wolfgang; Kuster, Bernhard; Greif, Philipp A.; Archangelo, Leticia Fröhlich
Source: Journal of Biological Chemistry. Unidade: FMRP
Subjects: PROTEÍNAS QUINASES, RNA, FATORES DE TRANSCRIÇÃO
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ARFELLI, Vanessa Cristina et al. UHMK1 is a novel splicing regulatory kinase. Journal of Biological Chemistry, v. 299, n. 4, p. 1-22, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.jbc.2023.103041. Acesso em: 18 nov. 2024.
APA
Arfelli, V. C., Chang, Y. -C., Bagnoli, J. W., Kerbs, P., Ciamponi, F. E., Paz, L. M. da S., et al. (2023). UHMK1 is a novel splicing regulatory kinase. Journal of Biological Chemistry, 299( 4), 1-22. doi:10.1016/j.jbc.2023.103041
NLM
Arfelli VC, Chang Y-C, Bagnoli JW, Kerbs P, Ciamponi FE, Paz LM da S, Pankivskyi S, Salone J de M, Maucuer A, Massirer KB, Enard W, Kuster B, Greif PA, Archangelo LF. UHMK1 is a novel splicing regulatory kinase [Internet]. Journal of Biological Chemistry. 2023 ; 299( 4): 1-22.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.jbc.2023.103041
Vancouver
Arfelli VC, Chang Y-C, Bagnoli JW, Kerbs P, Ciamponi FE, Paz LM da S, Pankivskyi S, Salone J de M, Maucuer A, Massirer KB, Enard W, Kuster B, Greif PA, Archangelo LF. UHMK1 is a novel splicing regulatory kinase [Internet]. Journal of Biological Chemistry. 2023 ; 299( 4): 1-22.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.jbc.2023.103041
Artigo de periodico
Sepsis expands a CD39 + plasmablast population that promotes immunosuppression via adenosine-mediated inhibition of macrophage antimicrobial activity (2021)
Nascimento, Daniele Carvalho ; Viacava, Paula Ramos; Ferreira, Raphael Gomes; Damaceno, Marina Alves; Piñeros, Annie Rocío Alvarez ; Melo, Paulo Henrique de; Donate, Paula Barbim ; Toller-Kawahisa, Juliana Escher; Zoppi, Daniel ; Veras, Flávio Protásio ; Peres, Raphael S. ; Silva, Luisa Menezes ; Caetité, Diego ; Oliveira, Antonio Edson Rocha; Castro, Icaro Maia Santos ; Kauffenstein, Gilles ; Nakaya, Helder Takashi Imoto ; Borges, Marcos de Carvalho ; Zamboni, Dario Simões ; Fonseca, Denise Morais da ; Paschoal, Jonas Augusto Rizzato ; Cunha, Thiago Mattar ; Quesniaux, Valerie ; Linden, Joel ; Cunha, Fernando Queiróz ; Ryffe, Bernhard; Alves-Filho, José Carlos
Source: Immunity. Unidades: FMRP, FCFRP, FCF, ICB, BIOINFORMÁTICA
Subjects: ADENOSINA, FÁRMACOS IMUNOSSUPRESSORES, SEPSE, CAMUNDONGOS, INTERLEUCINA 10, MACRÓFAGOS
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NASCIMENTO, Daniele Carvalho et al. Sepsis expands a CD39 + plasmablast population that promotes immunosuppression via adenosine-mediated inhibition of macrophage antimicrobial activity. Immunity, v. 54, n. 9, p. 2024-2041, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.immuni.2021.08.005. Acesso em: 18 nov. 2024.
APA
Nascimento, D. C., Viacava, P. R., Ferreira, R. G., Damaceno, M. A., Piñeros, A. R. A., Melo, P. H. de, et al. (2021). Sepsis expands a CD39 + plasmablast population that promotes immunosuppression via adenosine-mediated inhibition of macrophage antimicrobial activity. Immunity, 54( 9), 2024-2041. doi:10.1016/j.immuni.2021.08.005
NLM
Nascimento DC, Viacava PR, Ferreira RG, Damaceno MA, Piñeros ARA, Melo PH de, Donate PB, Toller-Kawahisa JE, Zoppi D, Veras FP, Peres RS, Silva LM, Caetité D, Oliveira AER, Castro IMS, Kauffenstein G, Nakaya HTI, Borges M de C, Zamboni DS, Fonseca DM da, Paschoal JAR, Cunha TM, Quesniaux V, Linden J, Cunha FQ, Ryffe B, Alves-Filho JC. Sepsis expands a CD39 + plasmablast population that promotes immunosuppression via adenosine-mediated inhibition of macrophage antimicrobial activity [Internet]. Immunity. 2021 ; 54( 9): 2024-2041.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.immuni.2021.08.005
Vancouver
Nascimento DC, Viacava PR, Ferreira RG, Damaceno MA, Piñeros ARA, Melo PH de, Donate PB, Toller-Kawahisa JE, Zoppi D, Veras FP, Peres RS, Silva LM, Caetité D, Oliveira AER, Castro IMS, Kauffenstein G, Nakaya HTI, Borges M de C, Zamboni DS, Fonseca DM da, Paschoal JAR, Cunha TM, Quesniaux V, Linden J, Cunha FQ, Ryffe B, Alves-Filho JC. Sepsis expands a CD39 + plasmablast population that promotes immunosuppression via adenosine-mediated inhibition of macrophage antimicrobial activity [Internet]. Immunity. 2021 ; 54( 9): 2024-2041.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.immuni.2021.08.005
Artigo de periodico
Apidologie 50 years (2021)
Courant, Christiane; Koeniger, Gudrun; Hartfelder, Klaus
Source: Apidologie. Unidade: FMRP
Subjects: ABELHAS, PESQUISA CIENTÍFICA, PERIÓDICOS CIENTÍFICOS
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ABNT
COURANT, Christiane e KOENIGER, Gudrun e HARTFELDER, Klaus. Apidologie 50 years. Apidologie, v. 52, n. 1, p. 35-44, 2021Tradução . . Disponível em: https://doi.org/10.1007/s13592-020-00797-8. Acesso em: 18 nov. 2024.
APA
Courant, C., Koeniger, G., & Hartfelder, K. (2021). Apidologie 50 years. Apidologie, 52( 1), 35-44. doi:10.1007/s13592-020-00797-8
NLM
Courant C, Koeniger G, Hartfelder K. Apidologie 50 years [Internet]. Apidologie. 2021 ; 52( 1): 35-44.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1007/s13592-020-00797-8
Vancouver
Courant C, Koeniger G, Hartfelder K. Apidologie 50 years [Internet]. Apidologie. 2021 ; 52( 1): 35-44.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1007/s13592-020-00797-8
Artigo de periodico
Molecular basis of carrageenan-induced cytokines production in macrophages (2020)
Lopes, Alexandre Hashimoto Pereira; Silva, Rangel Leal; Fonseca, Miriam das Dores Mendes; Gomes, Francisco Isaac Fernandes; Maganin, Alexandre Gomes de Macedo; Ribeiro, Lucas S.; Marques, Lucas Maciel Mauriz; Cunha, Fernando de Queiroz ; Alves Filho, José Carlos Farias ; Zamboni, Dario Simões; Lopes, Norberto Peporine ; Franklin, Bernardo S.; Gombault, Aurélie; Ramalho, Fernando Silva ; Quesniaux, Valérie F. J.; Couillin, Isabelle; Ryffel, Bernhard; Cunha, Thiago Mattar
Source: Cell Communication and Signaling. Unidades: FCFRP, FMRP
Subjects: CARRAGENINA, MACRÓFAGOS, POLISSACARÍDEOS, CITOCINAS, INFLAMAÇÃO
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LOPES, Alexandre Hashimoto Pereira et al. Molecular basis of carrageenan-induced cytokines production in macrophages. Cell Communication and Signaling, v. 18, n. 1, 2020Tradução . . Disponível em: https://doi.org/10.1186/s12964-020-00621-x. Acesso em: 18 nov. 2024.
APA
Lopes, A. H. P., Silva, R. L., Fonseca, M. das D. M., Gomes, F. I. F., Maganin, A. G. de M., Ribeiro, L. S., et al. (2020). Molecular basis of carrageenan-induced cytokines production in macrophages. Cell Communication and Signaling, 18( 1). doi:10.1186/s12964-020-00621-x
NLM
Lopes AHP, Silva RL, Fonseca M das DM, Gomes FIF, Maganin AG de M, Ribeiro LS, Marques LMM, Cunha F de Q, Alves Filho JCF, Zamboni DS, Lopes NP, Franklin BS, Gombault A, Ramalho FS, Quesniaux VFJ, Couillin I, Ryffel B, Cunha TM. Molecular basis of carrageenan-induced cytokines production in macrophages [Internet]. Cell Communication and Signaling. 2020 ; 18( 1):[citado 2024 nov. 18 ] Available from: https://doi.org/10.1186/s12964-020-00621-x
Vancouver
Lopes AHP, Silva RL, Fonseca M das DM, Gomes FIF, Maganin AG de M, Ribeiro LS, Marques LMM, Cunha F de Q, Alves Filho JCF, Zamboni DS, Lopes NP, Franklin BS, Gombault A, Ramalho FS, Quesniaux VFJ, Couillin I, Ryffel B, Cunha TM. Molecular basis of carrageenan-induced cytokines production in macrophages [Internet]. Cell Communication and Signaling. 2020 ; 18( 1):[citado 2024 nov. 18 ] Available from: https://doi.org/10.1186/s12964-020-00621-x
Artigo de periodico
Highlights of the São Paulo ISEV workshop on extracellular vesicles in cross-kingdom communication (2017)
Soares, Rodrigo Pedro; Xander, Patricia; Costa, Adriana Oliveira; Marcilla, Antonio; Menezes Neto, Armando; Del Portillo, Hernando; Witwer, Kenneth; Wauben, Marca; Nolte, Esther; Hoen, T; Olivier, Martin; Criado, Miriã Ferreira; Silva, Luis Lamberti Pinto da; Baqui, Munira Muhammad Abdel; Schenkman, Sergio; Colli, Walter ; Alves, Maria Júlia Manso ; Ferreira, Karen Spadari; Puccia, Rosana; Nejsum, Peter; Riesbeck, Kristian; Stensballe, Allan; Hansen, Eline Palm; Jaular, Lorena Martin; Ovstebo, Reidun; Canal, Laura de la; Bergese, Paolo; Pereira-Chioccola, Vera; Pfaffl, Michael W; Fritz, Joëlle; Gho, Yong Song; Torrecilhas, Ana Claudia
Source: Journal of Extracellular Vesicles. Unidades: FMRP, IQ
Subjects: DOENÇAS INFECCIOSAS, PATOLOGIA, INTERAÇÃO CELULAR
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SOARES, Rodrigo Pedro et al. Highlights of the São Paulo ISEV workshop on extracellular vesicles in cross-kingdom communication. Journal of Extracellular Vesicles, v. 6, n. 1, p. 1-10 art. 1407213, 2017Tradução . . Disponível em: https://doi.org/10.1080/20013078.2017.1407213. Acesso em: 18 nov. 2024.
APA
Soares, R. P., Xander, P., Costa, A. O., Marcilla, A., Menezes Neto, A., Del Portillo, H., et al. (2017). Highlights of the São Paulo ISEV workshop on extracellular vesicles in cross-kingdom communication. Journal of Extracellular Vesicles, 6( 1), 1-10 art. 1407213. doi:10.1080/20013078.2017.1407213
NLM
Soares RP, Xander P, Costa AO, Marcilla A, Menezes Neto A, Del Portillo H, Witwer K, Wauben M, Nolte E, Hoen T, Olivier M, Criado MF, Silva LLP da, Baqui MMA, Schenkman S, Colli W, Alves MJM, Ferreira KS, Puccia R, Nejsum P, Riesbeck K, Stensballe A, Hansen EP, Jaular LM, Ovstebo R, Canal L de la, Bergese P, Pereira-Chioccola V, Pfaffl MW, Fritz J, Gho YS, Torrecilhas AC. Highlights of the São Paulo ISEV workshop on extracellular vesicles in cross-kingdom communication [Internet]. Journal of Extracellular Vesicles. 2017 ; 6( 1): 1-10 art. 1407213.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1080/20013078.2017.1407213
Vancouver
Soares RP, Xander P, Costa AO, Marcilla A, Menezes Neto A, Del Portillo H, Witwer K, Wauben M, Nolte E, Hoen T, Olivier M, Criado MF, Silva LLP da, Baqui MMA, Schenkman S, Colli W, Alves MJM, Ferreira KS, Puccia R, Nejsum P, Riesbeck K, Stensballe A, Hansen EP, Jaular LM, Ovstebo R, Canal L de la, Bergese P, Pereira-Chioccola V, Pfaffl MW, Fritz J, Gho YS, Torrecilhas AC. Highlights of the São Paulo ISEV workshop on extracellular vesicles in cross-kingdom communication [Internet]. Journal of Extracellular Vesicles. 2017 ; 6( 1): 1-10 art. 1407213.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1080/20013078.2017.1407213
Artigo de periodico
Matriptase zymogen supports epithelial development, homeostasis and regeneration (2017)
Friis, Stine; Tadeo, Daniel; Le-Gall, Sylvain M.; Jürgensen, Henrik Jessen; Sales, Katiuchia Uzzun; Camerer, Eric; Bugge, Thomas H.
Source: BMC Biology. Unidade: FMRP
Subjects: HOMEOSTASE, CÉLULAS EPITELIAIS
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ABNT
FRIIS, Stine et al. Matriptase zymogen supports epithelial development, homeostasis and regeneration. BMC Biology, v. 15, 2017Tradução . . Disponível em: https://doi.org/10.1186/s12915-017-0384-4. Acesso em: 18 nov. 2024.
APA
Friis, S., Tadeo, D., Le-Gall, S. M., Jürgensen, H. J., Sales, K. U., Camerer, E., & Bugge, T. H. (2017). Matriptase zymogen supports epithelial development, homeostasis and regeneration. BMC Biology, 15. doi:10.1186/s12915-017-0384-4
NLM
Friis S, Tadeo D, Le-Gall SM, Jürgensen HJ, Sales KU, Camerer E, Bugge TH. Matriptase zymogen supports epithelial development, homeostasis and regeneration [Internet]. BMC Biology. 2017 ; 15[citado 2024 nov. 18 ] Available from: https://doi.org/10.1186/s12915-017-0384-4
Vancouver
Friis S, Tadeo D, Le-Gall SM, Jürgensen HJ, Sales KU, Camerer E, Bugge TH. Matriptase zymogen supports epithelial development, homeostasis and regeneration [Internet]. BMC Biology. 2017 ; 15[citado 2024 nov. 18 ] Available from: https://doi.org/10.1186/s12915-017-0384-4
Artigo de periodico
A soluble recombinant form of human leucocyte antigen-G 6 (srHLA-G6) (2017)
Pelá, Flávia Porto; Rustiguel, Joane Kathelen; Rodrigues, Lilian Cataldi; Mendonça, Jacqueline Nakau; Andrade, Camillo Del Cistia; Lopes, Norberto Peporine; Rosa, José Cesar; Nonato, Maria Cristina; Favier, Benoit; Donadi, Eduardo Antônio; Dias-Baruffi, Marcelo
Source: Biochemical and Biophysical Research Communications. Unidades: FCFRP, FMRP
Subjects: ANTÍGENOS, LEUCÓCITOS, PROTEÍNAS
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PELÁ, Flávia Porto et al. A soluble recombinant form of human leucocyte antigen-G 6 (srHLA-G6). Biochemical and Biophysical Research Communications, v. 487, n. 1, p. 28-33, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.bbrc.2017.03.149. Acesso em: 18 nov. 2024.
APA
Pelá, F. P., Rustiguel, J. K., Rodrigues, L. C., Mendonça, J. N., Andrade, C. D. C., Lopes, N. P., et al. (2017). A soluble recombinant form of human leucocyte antigen-G 6 (srHLA-G6). Biochemical and Biophysical Research Communications, 487( 1), 28-33. doi:10.1016/j.bbrc.2017.03.149
NLM
Pelá FP, Rustiguel JK, Rodrigues LC, Mendonça JN, Andrade CDC, Lopes NP, Rosa JC, Nonato MC, Favier B, Donadi EA, Dias-Baruffi M. A soluble recombinant form of human leucocyte antigen-G 6 (srHLA-G6) [Internet]. Biochemical and Biophysical Research Communications. 2017 ; 487( 1): 28-33.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.bbrc.2017.03.149
Vancouver
Pelá FP, Rustiguel JK, Rodrigues LC, Mendonça JN, Andrade CDC, Lopes NP, Rosa JC, Nonato MC, Favier B, Donadi EA, Dias-Baruffi M. A soluble recombinant form of human leucocyte antigen-G 6 (srHLA-G6) [Internet]. Biochemical and Biophysical Research Communications. 2017 ; 487( 1): 28-33.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.bbrc.2017.03.149
Artigo de periodico
Mitochondrial DNA activates the NLRP3 inflammasome and predisposes to type 1 diabetes in murine model (2017)
Carlos, Daniela ; Costa, Frederico Ribeiro Campos ; Pereira, Camila André; Rocha, Fernanda Agostini; Yaochite, Juliana Navarro Ueda; Oliveira, Gabriela G.; Carneiro, Fernando Silva ; Tostes, Rita de Cássia Aleixo ; Ramos, Simone Gusmão ; Zamboni, Dario Simões ; Câmara, Niels Olsen Saraiva ; Ryffel, Bernhard; Silva, João Santana da
Source: Frontiers in Immunology. Unidades: FMRP, ICB
Subjects: CITOCINAS, DIABETES MELLITUS, DNA MITOCONDRIAL
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ABNT
CARLOS, Daniela et al. Mitochondrial DNA activates the NLRP3 inflammasome and predisposes to type 1 diabetes in murine model. Frontiers in Immunology, v. 8, 2017Tradução . . Disponível em: https://doi.org/10.3389/fimmu.2017.00164. Acesso em: 18 nov. 2024.
APA
Carlos, D., Costa, F. R. C., Pereira, C. A., Rocha, F. A., Yaochite, J. N. U., Oliveira, G. G., et al. (2017). Mitochondrial DNA activates the NLRP3 inflammasome and predisposes to type 1 diabetes in murine model. Frontiers in Immunology, 8. doi:10.3389/fimmu.2017.00164
NLM
Carlos D, Costa FRC, Pereira CA, Rocha FA, Yaochite JNU, Oliveira GG, Carneiro FS, Tostes R de CA, Ramos SG, Zamboni DS, Câmara NOS, Ryffel B, Silva JS da. Mitochondrial DNA activates the NLRP3 inflammasome and predisposes to type 1 diabetes in murine model [Internet]. Frontiers in Immunology. 2017 ; 8[citado 2024 nov. 18 ] Available from: https://doi.org/10.3389/fimmu.2017.00164
Vancouver
Carlos D, Costa FRC, Pereira CA, Rocha FA, Yaochite JNU, Oliveira GG, Carneiro FS, Tostes R de CA, Ramos SG, Zamboni DS, Câmara NOS, Ryffel B, Silva JS da. Mitochondrial DNA activates the NLRP3 inflammasome and predisposes to type 1 diabetes in murine model [Internet]. Frontiers in Immunology. 2017 ; 8[citado 2024 nov. 18 ] Available from: https://doi.org/10.3389/fimmu.2017.00164
Artigo de periodico
Membrane-anchored serine protease matriptase is a trigger of pulmonary fibrogenesis (2016)
Bardou, Olivier; Menou, Awen; François, Charlène; Duitman, Jan Willem; Thüsen, Jan H. von der; Borie, Raphaël; Sales, Katiuchia Uzzun; Mutze, Kathrin; Castier, Yves; Sage, Edouard; Liu, Ligong; Bugge, Thomas H.; Fairlie, David P.; Königshoff, Mélanie; Crestani, Bruno; Borensztajn, Keren S.
Source: American Journal of Respiratory and Critical Care Medicine. Unidade: FMRP
Subjects: FIBROSE PULMONAR, FIBROBLASTOS, TERAPÊUTICA MÉDICA, ENZIMAS
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ABNT
BARDOU, Olivier et al. Membrane-anchored serine protease matriptase is a trigger of pulmonary fibrogenesis. American Journal of Respiratory and Critical Care Medicine, v. 193, n. 8, p. 847-860, 2016Tradução . . Disponível em: https://doi.org/10.1164/rccm.201502-0299OC. Acesso em: 18 nov. 2024.
APA
Bardou, O., Menou, A., François, C., Duitman, J. W., Thüsen, J. H. von der, Borie, R., et al. (2016). Membrane-anchored serine protease matriptase is a trigger of pulmonary fibrogenesis. American Journal of Respiratory and Critical Care Medicine, 193( 8), 847-860. doi:10.1164/rccm.201502-0299OC
NLM
Bardou O, Menou A, François C, Duitman JW, Thüsen JH von der, Borie R, Sales KU, Mutze K, Castier Y, Sage E, Liu L, Bugge TH, Fairlie DP, Königshoff M, Crestani B, Borensztajn KS. Membrane-anchored serine protease matriptase is a trigger of pulmonary fibrogenesis [Internet]. American Journal of Respiratory and Critical Care Medicine. 2016 ; 193( 8): 847-860.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1164/rccm.201502-0299OC
Vancouver
Bardou O, Menou A, François C, Duitman JW, Thüsen JH von der, Borie R, Sales KU, Mutze K, Castier Y, Sage E, Liu L, Bugge TH, Fairlie DP, Königshoff M, Crestani B, Borensztajn KS. Membrane-anchored serine protease matriptase is a trigger of pulmonary fibrogenesis [Internet]. American Journal of Respiratory and Critical Care Medicine. 2016 ; 193( 8): 847-860.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1164/rccm.201502-0299OC
Artigo de periodico
The large marseillevirus explores different entry pathways by forming giant infectious vesicles (2016)
Arantes, Thalita Souza; Rodrigues, Rodrigo Araújo Lima; Silva, Ludmila Karen dos Santos; Oliveira, Graziele Pereira; Souza, Helton Luís de; Khalil, Jacques Y. B.; Oliveira, Danilo Bretas de; Torres, Alice Abreu; Silva, Luis Lamberti da; Colson, Philippe; Kroon, Erna Geessien; Fonseca, Flávio Guimarães da; Bonjardim, Cláudio Antonio; La Scola, Bernard; Abrahão, Jônatas Santos
Source: Journal of Virology. Unidade: FMRP
Subjects: VÍRUS, FAGOCITOSE, AMOEBA, REPLICAÇÃO VIRAL
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ABNT
ARANTES, Thalita Souza et al. The large marseillevirus explores different entry pathways by forming giant infectious vesicles. Journal of Virology, v. 90, n. 11, p. 5246-5255, 2016Tradução . . Disponível em: https://doi.org/10.1128/JVI.00177-16. Acesso em: 18 nov. 2024.
APA
Arantes, T. S., Rodrigues, R. A. L., Silva, L. K. dos S., Oliveira, G. P., Souza, H. L. de, Khalil, J. Y. B., et al. (2016). The large marseillevirus explores different entry pathways by forming giant infectious vesicles. Journal of Virology, 90( 11), 5246-5255. doi:10.1128/JVI.00177-16
NLM
Arantes TS, Rodrigues RAL, Silva LK dos S, Oliveira GP, Souza HL de, Khalil JYB, Oliveira DB de, Torres AA, Silva LL da, Colson P, Kroon EG, Fonseca FG da, Bonjardim CA, La Scola B, Abrahão JS. The large marseillevirus explores different entry pathways by forming giant infectious vesicles [Internet]. Journal of Virology. 2016 ; 90( 11): 5246-5255.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1128/JVI.00177-16
Vancouver
Arantes TS, Rodrigues RAL, Silva LK dos S, Oliveira GP, Souza HL de, Khalil JYB, Oliveira DB de, Torres AA, Silva LL da, Colson P, Kroon EG, Fonseca FG da, Bonjardim CA, La Scola B, Abrahão JS. The large marseillevirus explores different entry pathways by forming giant infectious vesicles [Internet]. Journal of Virology. 2016 ; 90( 11): 5246-5255.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1128/JVI.00177-16
Trabalho de evento-resumo
Unraveling the pathogenesis of Legionella longbeachae infection: a role of type IV secretion system to induce mice lethality via pulmonary inflammation (2015)
Massis, Liliana Moura; Castanheira, Fernanda Vargas; Escoll, Pedro; Assis, Mariana Aprigio; Cunha, Fernando de Queiroz; Burcheiser, Carmen; Zamboni, Dario Simões
Source: Abstracts. Conference titles: INNATE IMMUNITY 2015. Unidade: FMRP
Subjects: LEGIONELLA, PNEUMONIA, TRANSPORTE BIOLÓGICO
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ABNT
MASSIS, Liliana Moura et al. Unraveling the pathogenesis of Legionella longbeachae infection: a role of type IV secretion system to induce mice lethality via pulmonary inflammation . 2015, Anais.. Guarujá: SBI, 2015. Disponível em: https://icongresso.itarget.com.br/useradm/anais/?clt=imu.3&lng=I. Acesso em: 18 nov. 2024.
APA
Massis, L. M., Castanheira, F. V., Escoll, P., Assis, M. A., Cunha, F. de Q., Burcheiser, C., & Zamboni, D. S. (2015). Unraveling the pathogenesis of Legionella longbeachae infection: a role of type IV secretion system to induce mice lethality via pulmonary inflammation . In Abstracts. Guarujá: SBI. Recuperado de https://icongresso.itarget.com.br/useradm/anais/?clt=imu.3&lng=I
NLM
Massis LM, Castanheira FV, Escoll P, Assis MA, Cunha F de Q, Burcheiser C, Zamboni DS. Unraveling the pathogenesis of Legionella longbeachae infection: a role of type IV secretion system to induce mice lethality via pulmonary inflammation [Internet]. Abstracts. 2015 ;[citado 2024 nov. 18 ] Available from: https://icongresso.itarget.com.br/useradm/anais/?clt=imu.3&lng=I
Vancouver
Massis LM, Castanheira FV, Escoll P, Assis MA, Cunha F de Q, Burcheiser C, Zamboni DS. Unraveling the pathogenesis of Legionella longbeachae infection: a role of type IV secretion system to induce mice lethality via pulmonary inflammation [Internet]. Abstracts. 2015 ;[citado 2024 nov. 18 ] Available from: https://icongresso.itarget.com.br/useradm/anais/?clt=imu.3&lng=I
Artigo de periodico
Peripheral NLCR4 inflammasome participates in the genesis of acute inflammatory pain (2015)
Lopes, Alexandre H.; Talbot, Jhimmy; Silva, Rangel L.; Lima, Jonilson B.; França, Rafael O.; Verri Júnior, Waldiceu Aparecido; Mascarenhas, Danielle Pini Alves; Ryffel, Bernhard; Cunha, Fernando de Queiroz; Zamboni, Dario Simões; Cunha, Thiago Mattar
Source: Pain. Unidade: FMRP
Subjects: APOPTOSE, PROTEÍNAS DE LIGAÇÃO DO CÁLCIO, INFLAMAÇÃO, MODELOS ANIMAIS DE DOENÇAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOPES, Alexandre H. et al. Peripheral NLCR4 inflammasome participates in the genesis of acute inflammatory pain. Pain, v. 156, n. 3, p. 451-459, 2015Tradução . . Disponível em: https://doi.org/10.1097/01.j.pain.0000460322.72396.53. Acesso em: 18 nov. 2024.
APA
Lopes, A. H., Talbot, J., Silva, R. L., Lima, J. B., França, R. O., Verri Júnior, W. A., et al. (2015). Peripheral NLCR4 inflammasome participates in the genesis of acute inflammatory pain. Pain, 156( 3), 451-459. doi:10.1097/01.j.pain.0000460322.72396.53
NLM
Lopes AH, Talbot J, Silva RL, Lima JB, França RO, Verri Júnior WA, Mascarenhas DPA, Ryffel B, Cunha F de Q, Zamboni DS, Cunha TM. Peripheral NLCR4 inflammasome participates in the genesis of acute inflammatory pain [Internet]. Pain. 2015 ; 156( 3): 451-459.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1097/01.j.pain.0000460322.72396.53
Vancouver
Lopes AH, Talbot J, Silva RL, Lima JB, França RO, Verri Júnior WA, Mascarenhas DPA, Ryffel B, Cunha F de Q, Zamboni DS, Cunha TM. Peripheral NLCR4 inflammasome participates in the genesis of acute inflammatory pain [Internet]. Pain. 2015 ; 156( 3): 451-459.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1097/01.j.pain.0000460322.72396.53
Artigo de periodico
Inflammasome activation is reactive oxygen species dependent and mediates irinotecan-induced mucositis through IL-1β and IL-18 in mice (2014)
Arifa, Raquel D. N.; Madeira, Mila F. M.; Paula, Talles P. de; Lima, Renata L.; Tavares, Livia D.; Menezes-Garcia, Zélia; Fagundes, Caio T.; Rachid, Milene A.; Ryffel, Bernhard; Zamboni, Dario Simões; Teixeira, Mauro M.; Souza, Danielle G.
Source: American Journal of Pathology. Unidade: FMRP
Subjects: INFLAMAÇÃO (PATOLOGIA), MUCOSA ESPECIALIZADA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ARIFA, Raquel D. N. et al. Inflammasome activation is reactive oxygen species dependent and mediates irinotecan-induced mucositis through IL-1β and IL-18 in mice. American Journal of Pathology, v. 184, n. 7, p. 2023-2034, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.ajpath.2014.03.012. Acesso em: 18 nov. 2024.
APA
Arifa, R. D. N., Madeira, M. F. M., Paula, T. P. de, Lima, R. L., Tavares, L. D., Menezes-Garcia, Z., et al. (2014). Inflammasome activation is reactive oxygen species dependent and mediates irinotecan-induced mucositis through IL-1β and IL-18 in mice. American Journal of Pathology, 184( 7), 2023-2034. doi:10.1016/j.ajpath.2014.03.012
NLM
Arifa RDN, Madeira MFM, Paula TP de, Lima RL, Tavares LD, Menezes-Garcia Z, Fagundes CT, Rachid MA, Ryffel B, Zamboni DS, Teixeira MM, Souza DG. Inflammasome activation is reactive oxygen species dependent and mediates irinotecan-induced mucositis through IL-1β and IL-18 in mice [Internet]. American Journal of Pathology. 2014 ; 184( 7): 2023-2034.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.ajpath.2014.03.012
Vancouver
Arifa RDN, Madeira MFM, Paula TP de, Lima RL, Tavares LD, Menezes-Garcia Z, Fagundes CT, Rachid MA, Ryffel B, Zamboni DS, Teixeira MM, Souza DG. Inflammasome activation is reactive oxygen species dependent and mediates irinotecan-induced mucositis through IL-1β and IL-18 in mice [Internet]. American Journal of Pathology. 2014 ; 184( 7): 2023-2034.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.ajpath.2014.03.012

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