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Artigo de periodico
Beyond the MEP pathway: A novel kinase required for prenol utilization by malaria parasites (2024)
Crispim, Marcell ; Verdaguer, Ignasi Bofill ; Hernández, Agustín ; Kronenberger, Thales ; Fenollar, Àngel ; Yamaguchi, Lydia Fumiko ; Alberione, María Pía ; Ramirez, Miriam; Oliveira, Sandra Souza de; Izquierdo, Luis ; Katzin, Alejandro Miguel
Source: PLoS Pathogens. Unidades: FCF, ICB
Subjects: PARASITOLOGIA, MALÁRIA, ANTIMALÁRICOS, METABÓLITOS, PROTEÍNAS QUINASES, ANIMAIS PARASITOS, PLASMODIUM FALCIPARUM, ESPECTROMETRIA DE MASSAS
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CRISPIM, Marcell et al. Beyond the MEP pathway: A novel kinase required for prenol utilization by malaria parasites. PLoS Pathogens, v. 20, n. 1, p. 29 , 2024Tradução . . Disponível em: https://doi.org/10.1371/journal.ppat.1011557. Acesso em: 07 out. 2025.
APA
Crispim, M., Verdaguer, I. B., Hernández, A., Kronenberger, T., Fenollar, À., Yamaguchi, L. F., et al. (2024). Beyond the MEP pathway: A novel kinase required for prenol utilization by malaria parasites. PLoS Pathogens, 20( 1), 29 . doi:10.1371/journal.ppat.1011557
NLM
Crispim M, Verdaguer IB, Hernández A, Kronenberger T, Fenollar À, Yamaguchi LF, Alberione MP, Ramirez M, Oliveira SS de, Izquierdo L, Katzin AM. Beyond the MEP pathway: A novel kinase required for prenol utilization by malaria parasites [Internet]. PLoS Pathogens. 2024 ; 20( 1): 29 .[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1011557
Vancouver
Crispim M, Verdaguer IB, Hernández A, Kronenberger T, Fenollar À, Yamaguchi LF, Alberione MP, Ramirez M, Oliveira SS de, Izquierdo L, Katzin AM. Beyond the MEP pathway: A novel kinase required for prenol utilization by malaria parasites [Internet]. PLoS Pathogens. 2024 ; 20( 1): 29 .[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1011557
Artigo de periodico
A novel 4-aminoquinoline chemotype with multistage antimalarial activity and lack of cross-resistance with PfCRT and PfMDR1 mutants (2024)
Ferreira, Letícia Tiburcio ; Cassiano, Gustavo Capatti ; Alvarez, Luis Carlos Salazar ; Okombo, John ; Calit, Juliana ; Fontinha, Diana ; Gil-Iturbe, Eva ; Coyle, Rachael ; Andrade, Carolina Horta ; Prudencio, Miguel ; Quick, Matthias ; Cravo, Pedro Vitor Lemos ; Lee, Marcus C. S.; Fidock, David A. ; Costa, Fabio Trindade Maranhão ; Bargieri, Daniel Youssef
Source: PLoS Pathogens. Unidade: ICB
Subjects: PARASITOLOGIA, ANTIMALÁRICOS, ÓLEOS ESSENCIAIS, MALÁRIA, PLASMODIUM FALCIPARUM, PROTOZOA, PROTEÍNAS DA MEMBRANA, MUTAÇÃO GENÉTICA
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FERREIRA, Letícia Tiburcio et al. A novel 4-aminoquinoline chemotype with multistage antimalarial activity and lack of cross-resistance with PfCRT and PfMDR1 mutants. PLoS Pathogens, v. 20, n. 10, p. 25 , 2024Tradução . . Disponível em: https://doi.org/10.1371/journal.ppat.1012627. Acesso em: 07 out. 2025.
APA
Ferreira, L. T., Cassiano, G. C., Alvarez, L. C. S., Okombo, J., Calit, J., Fontinha, D., et al. (2024). A novel 4-aminoquinoline chemotype with multistage antimalarial activity and lack of cross-resistance with PfCRT and PfMDR1 mutants. PLoS Pathogens, 20( 10), 25 . doi:10.1371/journal.ppat.1012627
NLM
Ferreira LT, Cassiano GC, Alvarez LCS, Okombo J, Calit J, Fontinha D, Gil-Iturbe E, Coyle R, Andrade CH, Prudencio M, Quick M, Cravo PVL, Lee MCS, Fidock DA, Costa FTM, Bargieri DY. A novel 4-aminoquinoline chemotype with multistage antimalarial activity and lack of cross-resistance with PfCRT and PfMDR1 mutants [Internet]. PLoS Pathogens. 2024 ; 20( 10): 25 .[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1012627
Vancouver
Ferreira LT, Cassiano GC, Alvarez LCS, Okombo J, Calit J, Fontinha D, Gil-Iturbe E, Coyle R, Andrade CH, Prudencio M, Quick M, Cravo PVL, Lee MCS, Fidock DA, Costa FTM, Bargieri DY. A novel 4-aminoquinoline chemotype with multistage antimalarial activity and lack of cross-resistance with PfCRT and PfMDR1 mutants [Internet]. PLoS Pathogens. 2024 ; 20( 10): 25 .[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1012627
Artigo de periodico
How much (ATP) does it cost to build a trypanosome? A theoretical study on the quantity of ATP needed to maintain and duplicate a bloodstream-form Trypanosoma brucei cell (2023)
Nascimento, Janaina de Freitas ; Souza, Rodolpho Ornitz Oliveira ; Alencar, Mayke B. ; Marsiccobetre, S. ; Murillo, Ana M. ; Damasceno, Flávia ; Girard, Richard M. B. M. ; Marchese, Letícia ; Luévano-Martinez, Luis A. ; Achjian, Renan W. ; Haanstra, Jurgen R. ; Michels, Paul A. M. ; Silber, Ariel Mariano
Source: PLoS Pathogens. Unidade: ICB
Subjects: PARASITOLOGIA, TRYPANOSOMA, ANIMAIS PARASITOS, BIOMASSA, CICLO CELULAR, POLIMERIZAÇÃO, GLICOSE, GLICOPROTEÍNAS
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NASCIMENTO, Janaina de Freitas et al. How much (ATP) does it cost to build a trypanosome? A theoretical study on the quantity of ATP needed to maintain and duplicate a bloodstream-form Trypanosoma brucei cell. PLoS Pathogens, v. 19, n. 7, p. 35, 2023Tradução . . Disponível em: https://doi.org/10.1371/journal.ppat.1011522. Acesso em: 07 out. 2025.
APA
Nascimento, J. de F., Souza, R. O. O., Alencar, M. B., Marsiccobetre, S., Murillo, A. M., Damasceno, F., et al. (2023). How much (ATP) does it cost to build a trypanosome? A theoretical study on the quantity of ATP needed to maintain and duplicate a bloodstream-form Trypanosoma brucei cell. PLoS Pathogens, 19( 7), 35. doi:10.1371/journal.ppat.1011522
NLM
Nascimento J de F, Souza ROO, Alencar MB, Marsiccobetre S, Murillo AM, Damasceno F, Girard RMBM, Marchese L, Luévano-Martinez LA, Achjian RW, Haanstra JR, Michels PAM, Silber AM. How much (ATP) does it cost to build a trypanosome? A theoretical study on the quantity of ATP needed to maintain and duplicate a bloodstream-form Trypanosoma brucei cell [Internet]. PLoS Pathogens. 2023 ; 19( 7): 35.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1011522
Vancouver
Nascimento J de F, Souza ROO, Alencar MB, Marsiccobetre S, Murillo AM, Damasceno F, Girard RMBM, Marchese L, Luévano-Martinez LA, Achjian RW, Haanstra JR, Michels PAM, Silber AM. How much (ATP) does it cost to build a trypanosome? A theoretical study on the quantity of ATP needed to maintain and duplicate a bloodstream-form Trypanosoma brucei cell [Internet]. PLoS Pathogens. 2023 ; 19( 7): 35.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1011522
Artigo de periodico
Gasdermin-D and Caspase-7 are the key Caspase-1/8 substrates downstream of the NAIP5/NLRC4 inflammasome required for restriction of Legionella pneumophila (2019)
Gonçalves, Augusto Velozo ; Margolis, Shally R.; Quirino, Gustavo Fernando da Silva ; Mascarenhas, Danielle P. A; Rauch, Isabella; Nichols, Randilea D.; Ansaldo, Eduard; Fontana, Mary F.; Vance, Russell E.; Zamboni, Dario Simões
Source: PLoS Pathogens. Unidade: FMRP
Subjects: LEGIONELLA PNEUMOPHILA, BACTÉRIAS ANAERÓBICAS GRAM-NEGATIVAS, PROTEÍNAS
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GONÇALVES, Augusto Velozo et al. Gasdermin-D and Caspase-7 are the key Caspase-1/8 substrates downstream of the NAIP5/NLRC4 inflammasome required for restriction of Legionella pneumophila. PLoS Pathogens, v. 15, n. 6, p. e1007886, 2019Tradução . . Disponível em: https://doi.org/10.1371/journal.ppat.1007886. Acesso em: 07 out. 2025.
APA
Gonçalves, A. V., Margolis, S. R., Quirino, G. F. da S., Mascarenhas, D. P. A., Rauch, I., Nichols, R. D., et al. (2019). Gasdermin-D and Caspase-7 are the key Caspase-1/8 substrates downstream of the NAIP5/NLRC4 inflammasome required for restriction of Legionella pneumophila. PLoS Pathogens, 15( 6), e1007886. doi:10.1371/journal.ppat.1007886
NLM
Gonçalves AV, Margolis SR, Quirino GF da S, Mascarenhas DPA, Rauch I, Nichols RD, Ansaldo E, Fontana MF, Vance RE, Zamboni DS. Gasdermin-D and Caspase-7 are the key Caspase-1/8 substrates downstream of the NAIP5/NLRC4 inflammasome required for restriction of Legionella pneumophila [Internet]. PLoS Pathogens. 2019 ; 15( 6): e1007886.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1007886
Vancouver
Gonçalves AV, Margolis SR, Quirino GF da S, Mascarenhas DPA, Rauch I, Nichols RD, Ansaldo E, Fontana MF, Vance RE, Zamboni DS. Gasdermin-D and Caspase-7 are the key Caspase-1/8 substrates downstream of the NAIP5/NLRC4 inflammasome required for restriction of Legionella pneumophila [Internet]. PLoS Pathogens. 2019 ; 15( 6): e1007886.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1007886
Artigo de periodico
Caspase-11-dependent IL-1α release boosts Th17 immunity against Paracoccidioides brasiliensis (2019)
Ketelut-Carneiro, Natália ; Souza, Camila de Oliveira Silva e ; Benevides, Luciana ; Gardinassi, Luiz Gustavo Araujo ; Silva, Maria Claúdia; Tavares, Lucas Alves ; Zamboni, Dario Simões ; Silva, João Santana da
Source: PLoS Pathogens. Unidades: FMRP, FCFRP
Subjects: IMUNIDADE, INTERLEUCINA 1, MACRÓFAGOS, PARACOCCIDIOIDOMICOSE
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KETELUT-CARNEIRO, Natália et al. Caspase-11-dependent IL-1α release boosts Th17 immunity against Paracoccidioides brasiliensis. PLoS Pathogens, v. 15, n. 8, p. e1007990, 2019Tradução . . Disponível em: https://doi.org/10.1371/journal.ppat.1007990. Acesso em: 07 out. 2025.
APA
Ketelut-Carneiro, N., Souza, C. de O. S. e, Benevides, L., Gardinassi, L. G. A., Silva, M. C., Tavares, L. A., et al. (2019). Caspase-11-dependent IL-1α release boosts Th17 immunity against Paracoccidioides brasiliensis. PLoS Pathogens, 15( 8), e1007990. doi:10.1371/journal.ppat.1007990
NLM
Ketelut-Carneiro N, Souza C de OS e, Benevides L, Gardinassi LGA, Silva MC, Tavares LA, Zamboni DS, Silva JS da. Caspase-11-dependent IL-1α release boosts Th17 immunity against Paracoccidioides brasiliensis [Internet]. PLoS Pathogens. 2019 ; 15( 8): e1007990.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1007990
Vancouver
Ketelut-Carneiro N, Souza C de OS e, Benevides L, Gardinassi LGA, Silva MC, Tavares LA, Zamboni DS, Silva JS da. Caspase-11-dependent IL-1α release boosts Th17 immunity against Paracoccidioides brasiliensis [Internet]. PLoS Pathogens. 2019 ; 15( 8): e1007990.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1007990
Artigo de periodico
The NLRP3 inflammasome is involved with the pathogenesis of Mayaro virus (2019)
Castro-Jorge, Luiza Antunes de ; Carvalho, Renan Villanova Homem de ; Klein, Taline M. ; Hiroki, Carlos Hiroji ; Lopes, Alexandre Hashimoto Pereira ; Guimarães, Rafaela Mano ; Fumagalli, Marcilio Jorge ; Floriano, Vitor Gonçalves ; Agostinho, Mayara Rovariz ; Slhessrenko, Renata Dezengrini; Ramalho, Fernando Silva ; Cunha, Thiago Mattar ; Cunha, Fernando de Queiroz ; Fonseca, Benedito Antonio Lopes da ; Zamboni, Dario Simões
Source: PLoS Pathogens. Unidade: FMRP
Subjects: INFECÇÕES POR ARBOVIRUS, DOENÇAS INFECCIOSAS, ARTRALGIA
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CASTRO-JORGE, Luiza Antunes de et al. The NLRP3 inflammasome is involved with the pathogenesis of Mayaro virus. PLoS Pathogens, v. 15, n. 9, p. e1007934, 2019Tradução . . Disponível em: https://doi.org/10.1371/journal.ppat.1007934. Acesso em: 07 out. 2025.
APA
Castro-Jorge, L. A. de, Carvalho, R. V. H. de, Klein, T. M., Hiroki, C. H., Lopes, A. H. P., Guimarães, R. M., et al. (2019). The NLRP3 inflammasome is involved with the pathogenesis of Mayaro virus. PLoS Pathogens, 15( 9), e1007934. doi:10.1371/journal.ppat.1007934
NLM
Castro-Jorge LA de, Carvalho RVH de, Klein TM, Hiroki CH, Lopes AHP, Guimarães RM, Fumagalli MJ, Floriano VG, Agostinho MR, Slhessrenko RD, Ramalho FS, Cunha TM, Cunha F de Q, Fonseca BAL da, Zamboni DS. The NLRP3 inflammasome is involved with the pathogenesis of Mayaro virus [Internet]. PLoS Pathogens. 2019 ; 15( 9): e1007934.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1007934
Vancouver
Castro-Jorge LA de, Carvalho RVH de, Klein TM, Hiroki CH, Lopes AHP, Guimarães RM, Fumagalli MJ, Floriano VG, Agostinho MR, Slhessrenko RD, Ramalho FS, Cunha TM, Cunha F de Q, Fonseca BAL da, Zamboni DS. The NLRP3 inflammasome is involved with the pathogenesis of Mayaro virus [Internet]. PLoS Pathogens. 2019 ; 15( 9): e1007934.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1007934
Artigo de periodico
P2X7 receptor drives Th1 cell differentiation and controls the follicular helper T cell population to protect against Plasmodium chabaudi malaria (2017)
Salles, Érika Machado de; Menezes, Maria Nogueira de; Siqueira, Renan; Silva, Henrique Borges da; Amaral, Eduardo Pinheiro; Castillo-Méndez, Sheyla Inés; Cunha, Isabella; Cassado, Alexandra dos Anjos; Vieira, Flávia Sarmento; Olivieri, David Nicholas; Tadokoro, Carlos Eduardo; Alvarez, José Maria ; Coutinho-Silva, Robson; Lima, Maria Regina D'Império
Source: PLoS Pathogens. Unidade: ICB
Subjects: IMUNOLOGIA, PLASMODIUM, ERITRÓCITOS, ADENOSINA TRIFOSFATO, MALÁRIA
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SALLES, Érika Machado de et al. P2X7 receptor drives Th1 cell differentiation and controls the follicular helper T cell population to protect against Plasmodium chabaudi malaria. PLoS Pathogens, v. 13, n. 8, p. 1-29, 2017Tradução . . Disponível em: https://doi.org/10.1371/journal.ppat.1006595. Acesso em: 07 out. 2025.
APA
Salles, É. M. de, Menezes, M. N. de, Siqueira, R., Silva, H. B. da, Amaral, E. P., Castillo-Méndez, S. I., et al. (2017). P2X7 receptor drives Th1 cell differentiation and controls the follicular helper T cell population to protect against Plasmodium chabaudi malaria. PLoS Pathogens, 13( 8), 1-29. doi:10.1371/journal.ppat.1006595
NLM
Salles ÉM de, Menezes MN de, Siqueira R, Silva HB da, Amaral EP, Castillo-Méndez SI, Cunha I, Cassado A dos A, Vieira FS, Olivieri DN, Tadokoro CE, Alvarez JM, Coutinho-Silva R, Lima MRD'I. P2X7 receptor drives Th1 cell differentiation and controls the follicular helper T cell population to protect against Plasmodium chabaudi malaria [Internet]. PLoS Pathogens. 2017 ; 13( 8): 1-29.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1006595
Vancouver
Salles ÉM de, Menezes MN de, Siqueira R, Silva HB da, Amaral EP, Castillo-Méndez SI, Cunha I, Cassado A dos A, Vieira FS, Olivieri DN, Tadokoro CE, Alvarez JM, Coutinho-Silva R, Lima MRD'I. P2X7 receptor drives Th1 cell differentiation and controls the follicular helper T cell population to protect against Plasmodium chabaudi malaria [Internet]. PLoS Pathogens. 2017 ; 13( 8): 1-29.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1006595
Artigo de periodico
Proline metabolism is essential for Trypanosoma brucei brucei survival in the tsetse vector (2017)
Mantilla, Brian S.; Marchese, Letícia; Casas-Sánchez, Aitor; Dyer, Naomi A.; Ejeh, Nicholas; Biran, Marc; Bringaud, Frédéric; Lehane, Michael J.; Acosta-Serrano, Alvaro; Silber, Ariel Mariano
Source: PLoS Pathogens. Unidade: ICB
Assunto: PARASITOLOGIA
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MANTILLA, Brian S. et al. Proline metabolism is essential for Trypanosoma brucei brucei survival in the tsetse vector. PLoS Pathogens, v. 13, n. 1, p. 1-29, 2017Tradução . . Disponível em: https://doi.org/10.1371/journal.ppat.1006158. Acesso em: 07 out. 2025.
APA
Mantilla, B. S., Marchese, L., Casas-Sánchez, A., Dyer, N. A., Ejeh, N., Biran, M., et al. (2017). Proline metabolism is essential for Trypanosoma brucei brucei survival in the tsetse vector. PLoS Pathogens, 13( 1), 1-29. doi:10.1371/journal.ppat.1006158
NLM
Mantilla BS, Marchese L, Casas-Sánchez A, Dyer NA, Ejeh N, Biran M, Bringaud F, Lehane MJ, Acosta-Serrano A, Silber AM. Proline metabolism is essential for Trypanosoma brucei brucei survival in the tsetse vector [Internet]. PLoS Pathogens. 2017 ; 13( 1): 1-29.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1006158
Vancouver
Mantilla BS, Marchese L, Casas-Sánchez A, Dyer NA, Ejeh N, Biran M, Bringaud F, Lehane MJ, Acosta-Serrano A, Silber AM. Proline metabolism is essential for Trypanosoma brucei brucei survival in the tsetse vector [Internet]. PLoS Pathogens. 2017 ; 13( 1): 1-29.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1006158
Artigo de periodico
A human Trypanosome suppresses CD8+ T cell priming by dendritic cells through the induction of immune regulatory CD4+ Foxp3+ T cells (2016)
Ersching, Jonatan; Basso, Alexandre Salgado; Kalich, Vera Lucia Garcia; Bortoluci, Karina Ramalho; Rodrigues, Maurício M.
Source: PLoS Pathogens. Unidade: ICB
Assunto: IMUNOLOGIA
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ERSCHING, Jonatan et al. A human Trypanosome suppresses CD8+ T cell priming by dendritic cells through the induction of immune regulatory CD4+ Foxp3+ T cells. PLoS Pathogens, v. 12, n. 6, p. 1-23, 2016Tradução . . Disponível em: https://doi.org/10.1371/journal.ppat.1005698. Acesso em: 07 out. 2025.
APA
Ersching, J., Basso, A. S., Kalich, V. L. G., Bortoluci, K. R., & Rodrigues, M. M. (2016). A human Trypanosome suppresses CD8+ T cell priming by dendritic cells through the induction of immune regulatory CD4+ Foxp3+ T cells. PLoS Pathogens, 12( 6), 1-23. doi:10.1371/journal.ppat.1005698
NLM
Ersching J, Basso AS, Kalich VLG, Bortoluci KR, Rodrigues MM. A human Trypanosome suppresses CD8+ T cell priming by dendritic cells through the induction of immune regulatory CD4+ Foxp3+ T cells [Internet]. PLoS Pathogens. 2016 ; 12( 6): 1-23.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1005698
Vancouver
Ersching J, Basso AS, Kalich VLG, Bortoluci KR, Rodrigues MM. A human Trypanosome suppresses CD8+ T cell priming by dendritic cells through the induction of immune regulatory CD4+ Foxp3+ T cells [Internet]. PLoS Pathogens. 2016 ; 12( 6): 1-23.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1005698
Artigo de periodico
Correction: a human Trypanosome suppresses CD8+ T cell priming by dendritic cells through the induction of immune regulatory CD4+ Foxp3+ T cells (2016)
Ersching, Jonatan; Basso, Alexandre Salgado; Calich, Vera Lucia Garcia; Bortoluci, Karina Ramalho; Rodrigues, Maurício M.
Source: PLoS Pathogens. Unidade: ICB
Assunto: IMUNOLOGIA
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ERSCHING, Jonatan et al. Correction: a human Trypanosome suppresses CD8+ T cell priming by dendritic cells through the induction of immune regulatory CD4+ Foxp3+ T cells. PLoS Pathogens, v. 12, n. 7, p. 1, 2016Tradução . . Disponível em: https://doi.org/10.1371/journal.ppat.1005771. Acesso em: 07 out. 2025.
APA
Ersching, J., Basso, A. S., Calich, V. L. G., Bortoluci, K. R., & Rodrigues, M. M. (2016). Correction: a human Trypanosome suppresses CD8+ T cell priming by dendritic cells through the induction of immune regulatory CD4+ Foxp3+ T cells. PLoS Pathogens, 12( 7), 1. doi:10.1371/journal.ppat.1005771
NLM
Ersching J, Basso AS, Calich VLG, Bortoluci KR, Rodrigues MM. Correction: a human Trypanosome suppresses CD8+ T cell priming by dendritic cells through the induction of immune regulatory CD4+ Foxp3+ T cells [Internet]. PLoS Pathogens. 2016 ; 12( 7): 1.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1005771
Vancouver
Ersching J, Basso AS, Calich VLG, Bortoluci KR, Rodrigues MM. Correction: a human Trypanosome suppresses CD8+ T cell priming by dendritic cells through the induction of immune regulatory CD4+ Foxp3+ T cells [Internet]. PLoS Pathogens. 2016 ; 12( 7): 1.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1005771
Artigo de periodico
Tolerogenic plasmacytoid dendritic cells control Paracoccidioides brasiliensis infection by inducting regulatory T cells in an IDO-dependent manner (2016)
Araújo, Eliseu Frank de; Medeiros, Daniella Helena; Galdino, Nayane Alves de Lima; Condino-Neto, Antônio; Calich, Vera Lúcia Garcia; Loures, Flávio Vieira
Source: PLoS Pathogens. Unidade: ICB
Assunto: IMUNOLOGIA
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ARAÚJO, Eliseu Frank de et al. Tolerogenic plasmacytoid dendritic cells control Paracoccidioides brasiliensis infection by inducting regulatory T cells in an IDO-dependent manner. PLoS Pathogens, v. 12, n. 12, p. 1-29, 2016Tradução . . Disponível em: https://doi.org/10.1371/journal.ppat.1006115. Acesso em: 07 out. 2025.
APA
Araújo, E. F. de, Medeiros, D. H., Galdino, N. A. de L., Condino-Neto, A., Calich, V. L. G., & Loures, F. V. (2016). Tolerogenic plasmacytoid dendritic cells control Paracoccidioides brasiliensis infection by inducting regulatory T cells in an IDO-dependent manner. PLoS Pathogens, 12( 12), 1-29. doi:10.1371/journal.ppat.1006115
NLM
Araújo EF de, Medeiros DH, Galdino NA de L, Condino-Neto A, Calich VLG, Loures FV. Tolerogenic plasmacytoid dendritic cells control Paracoccidioides brasiliensis infection by inducting regulatory T cells in an IDO-dependent manner [Internet]. PLoS Pathogens. 2016 ; 12( 12): 1-29.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1006115
Vancouver
Araújo EF de, Medeiros DH, Galdino NA de L, Condino-Neto A, Calich VLG, Loures FV. Tolerogenic plasmacytoid dendritic cells control Paracoccidioides brasiliensis infection by inducting regulatory T cells in an IDO-dependent manner [Internet]. PLoS Pathogens. 2016 ; 12( 12): 1-29.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1006115
Artigo de periodico
Recognition of Aspergillus fumigatus hyphae by human plasmacytoid dendritic cells is mediated by dectin-2 and results in formation of extracellular traps (2015)
Loures, Flávio Vieira; Röhm, Marc; Lee, Chrono K.; Santos, Evelyn; Wang, Jennifer P.; Specht, Charles A.; Calich, Vera Lucia Garcia; Urban, Constantin F.; Levitz, Stuart M.
Source: PLoS Pathogens. Unidade: ICB
Subjects: IMUNOLOGIA, ASPERGILLUS, CÉLULAS DENDRÍTICAS, ANTIFÚNGICOS
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LOURES, Flávio Vieira et al. Recognition of Aspergillus fumigatus hyphae by human plasmacytoid dendritic cells is mediated by dectin-2 and results in formation of extracellular traps. PLoS Pathogens, v. 11, n. 2, p. 1-23, 2015Tradução . . Disponível em: https://doi.org/10.1371/journal.ppat.1004643. Acesso em: 07 out. 2025.
APA
Loures, F. V., Röhm, M., Lee, C. K., Santos, E., Wang, J. P., Specht, C. A., et al. (2015). Recognition of Aspergillus fumigatus hyphae by human plasmacytoid dendritic cells is mediated by dectin-2 and results in formation of extracellular traps. PLoS Pathogens, 11( 2), 1-23. doi:10.1371/journal.ppat.1004643
NLM
Loures FV, Röhm M, Lee CK, Santos E, Wang JP, Specht CA, Calich VLG, Urban CF, Levitz SM. Recognition of Aspergillus fumigatus hyphae by human plasmacytoid dendritic cells is mediated by dectin-2 and results in formation of extracellular traps [Internet]. PLoS Pathogens. 2015 ; 11( 2): 1-23.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1004643
Vancouver
Loures FV, Röhm M, Lee CK, Santos E, Wang JP, Specht CA, Calich VLG, Urban CF, Levitz SM. Recognition of Aspergillus fumigatus hyphae by human plasmacytoid dendritic cells is mediated by dectin-2 and results in formation of extracellular traps [Internet]. PLoS Pathogens. 2015 ; 11( 2): 1-23.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1004643
Artigo de periodico
Involvement of a 1-Cys Peroxiredoxin in Bacterial Virulence (2014)
Kaihami, Gilberto Hideo; Almeida, José Roberto Fogaça de; Santos, Suelen Silvana dos; Netto, Luis Eduardo Soares ; Almeida, Sandro Rogério de ; Baldini, Regina Lúcia
Source: PLoS Pathogens. Unidades: IB, FCF, IQ
Subjects: PEROXIDASE, ENZIMAS OXIRREDUTORAS, BIOQUÍMICA, ANTIOXIDANTES, MECANISMOS DE DEFESA, VIRULÊNCIA, MACRÓFAGOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KAIHAMI, Gilberto Hideo et al. Involvement of a 1-Cys Peroxiredoxin in Bacterial Virulence. PLoS Pathogens, v. 10, n. 10, p. e1004442, 2014Tradução . . Disponível em: https://doi.org/10.1371/journal.ppat.1004442. Acesso em: 07 out. 2025.
APA
Kaihami, G. H., Almeida, J. R. F. de, Santos, S. S. dos, Netto, L. E. S., Almeida, S. R. de, & Baldini, R. L. (2014). Involvement of a 1-Cys Peroxiredoxin in Bacterial Virulence. PLoS Pathogens, 10( 10), e1004442. doi:10.1371/journal.ppat.1004442
NLM
Kaihami GH, Almeida JRF de, Santos SS dos, Netto LES, Almeida SR de, Baldini RL. Involvement of a 1-Cys Peroxiredoxin in Bacterial Virulence [Internet]. PLoS Pathogens. 2014 ; 10( 10): e1004442.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1004442
Vancouver
Kaihami GH, Almeida JRF de, Santos SS dos, Netto LES, Almeida SR de, Baldini RL. Involvement of a 1-Cys Peroxiredoxin in Bacterial Virulence [Internet]. PLoS Pathogens. 2014 ; 10( 10): e1004442.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1004442
Artigo de periodico
Transcriptome analyses of inhibitor-treated schistosome females provide evidence for cooperating Src-kinase and TGFβ receptor pathways controlling mitosis and eggshell formation (2013)
Buro, Christin; Oliveira, Kátia Cristina de; Lu, Zhigang; Leutner, Silke; Beckmann, Svenja; Dissous, Colette; Cailliau, Kátia; Verjovski-Almeida, Sergio ; Grevelding, Christoph G
Source: PLoS Pathogens. Unidade: IQ
Subjects: SCHISTOSOMA MANSONI, EXPRESSÃO GÊNICA, IMUNOHISTOQUÍMICA
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ABNT
BURO, Christin et al. Transcriptome analyses of inhibitor-treated schistosome females provide evidence for cooperating Src-kinase and TGFβ receptor pathways controlling mitosis and eggshell formation. PLoS Pathogens, v. 9, n. 6, p. 1-20 art. e1003448, 2013Tradução . . Disponível em: https://doi.org/10.1371/journal.ppat.1003448. Acesso em: 07 out. 2025.
APA
Buro, C., Oliveira, K. C. de, Lu, Z., Leutner, S., Beckmann, S., Dissous, C., et al. (2013). Transcriptome analyses of inhibitor-treated schistosome females provide evidence for cooperating Src-kinase and TGFβ receptor pathways controlling mitosis and eggshell formation. PLoS Pathogens, 9( 6), 1-20 art. e1003448. doi:10.1371/journal.ppat.1003448
NLM
Buro C, Oliveira KC de, Lu Z, Leutner S, Beckmann S, Dissous C, Cailliau K, Verjovski-Almeida S, Grevelding CG. Transcriptome analyses of inhibitor-treated schistosome females provide evidence for cooperating Src-kinase and TGFβ receptor pathways controlling mitosis and eggshell formation [Internet]. PLoS Pathogens. 2013 ; 9( 6): 1-20 art. e1003448.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1003448
Vancouver
Buro C, Oliveira KC de, Lu Z, Leutner S, Beckmann S, Dissous C, Cailliau K, Verjovski-Almeida S, Grevelding CG. Transcriptome analyses of inhibitor-treated schistosome females provide evidence for cooperating Src-kinase and TGFβ receptor pathways controlling mitosis and eggshell formation [Internet]. PLoS Pathogens. 2013 ; 9( 6): 1-20 art. e1003448.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1003448
Artigo de periodico
A component of the xanthomonadaceae type IV secretion system combines a VirB7 motif with a NO domain found in outer membrane transport proteins (2011)
Souza, Diorge Paulo de; Andrade, Maxuel de Oliveira; Alvarez-Martinez, Cristina Elisa; Arantes, Guilherme Menegon ; Farah, Chuck Shaker ; Salinas, Roberto Kopke
Source: PLoS Pathogens. Unidades: IQ, IB
Subjects: XANTHOMONAS, BIOQUÍMICA
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ABNT
SOUZA, Diorge Paulo de et al. A component of the xanthomonadaceae type IV secretion system combines a VirB7 motif with a NO domain found in outer membrane transport proteins. PLoS Pathogens, v. 7, n. 5, p. 1-18 art. e1002031, 2011Tradução . . Disponível em: https://doi.org/10.1371/journal.ppat.1002031. Acesso em: 07 out. 2025.
APA
Souza, D. P. de, Andrade, M. de O., Alvarez-Martinez, C. E., Arantes, G. M., Farah, C. S., & Salinas, R. K. (2011). A component of the xanthomonadaceae type IV secretion system combines a VirB7 motif with a NO domain found in outer membrane transport proteins. PLoS Pathogens, 7( 5), 1-18 art. e1002031. doi:10.1371/journal.ppat.1002031
NLM
Souza DP de, Andrade M de O, Alvarez-Martinez CE, Arantes GM, Farah CS, Salinas RK. A component of the xanthomonadaceae type IV secretion system combines a VirB7 motif with a NO domain found in outer membrane transport proteins [Internet]. PLoS Pathogens. 2011 ; 7( 5): 1-18 art. e1002031.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1002031
Vancouver
Souza DP de, Andrade M de O, Alvarez-Martinez CE, Arantes GM, Farah CS, Salinas RK. A component of the xanthomonadaceae type IV secretion system combines a VirB7 motif with a NO domain found in outer membrane transport proteins [Internet]. PLoS Pathogens. 2011 ; 7( 5): 1-18 art. e1002031.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1002031
Artigo de periodico
The plant pathogen pseudomonas syringae pv. tomato Is genetically monomorphic and under strong selection to evade tomato immunity (2011)
Cai, Rongman; Lewis, James; Yan, Shuangchun; Liu, Haijie; Clarke, Christopher R; Campanile, Francesco; Almeida, Nalvo F; Studholme, David J; Lindeberg, Magdalen; Schneider, David; Zaccardelli, Massimo; Setubal, João Carlos ; Morales Lizcano, Nadia P; Bernal, Adriana; Coaker, Gitta; Baker, Christy; Bender, Carol L; Leman, Scotland; Vinatzer, Boris A
Source: PLoS Pathogens. Unidade: IQ
Subjects: BACTÉRIAS FITOPATOGÊNICAS, GENOMAS, MANCHA BACTERIANA, PSEUDOMONAS, TOMATE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAI, Rongman et al. The plant pathogen pseudomonas syringae pv. tomato Is genetically monomorphic and under strong selection to evade tomato immunity. PLoS Pathogens, v. 7, n. 8, p. 1-15 art. e1002130, 2011Tradução . . Disponível em: https://doi.org/10.1371/journal.ppat.1002130. Acesso em: 07 out. 2025.
APA
Cai, R., Lewis, J., Yan, S., Liu, H., Clarke, C. R., Campanile, F., et al. (2011). The plant pathogen pseudomonas syringae pv. tomato Is genetically monomorphic and under strong selection to evade tomato immunity. PLoS Pathogens, 7( 8), 1-15 art. e1002130. doi:10.1371/journal.ppat.1002130
NLM
Cai R, Lewis J, Yan S, Liu H, Clarke CR, Campanile F, Almeida NF, Studholme DJ, Lindeberg M, Schneider D, Zaccardelli M, Setubal JC, Morales Lizcano NP, Bernal A, Coaker G, Baker C, Bender CL, Leman S, Vinatzer BA. The plant pathogen pseudomonas syringae pv. tomato Is genetically monomorphic and under strong selection to evade tomato immunity [Internet]. PLoS Pathogens. 2011 ; 7( 8): 1-15 art. e1002130.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1002130
Vancouver
Cai R, Lewis J, Yan S, Liu H, Clarke CR, Campanile F, Almeida NF, Studholme DJ, Lindeberg M, Schneider D, Zaccardelli M, Setubal JC, Morales Lizcano NP, Bernal A, Coaker G, Baker C, Bender CL, Leman S, Vinatzer BA. The plant pathogen pseudomonas syringae pv. tomato Is genetically monomorphic and under strong selection to evade tomato immunity [Internet]. PLoS Pathogens. 2011 ; 7( 8): 1-15 art. e1002130.[citado 2025 out. 07 ] Available from: https://doi.org/10.1371/journal.ppat.1002130
Artigo de periodico
Schistosoma mansoni TGF-beta receptor II: role in host ligand-induced regulation of a schistosome target gene (2006)
Osman, Ahmed; Niles, Edward G.; Verjovski-Almeida, Sergio ; LoVerde, Philip T.
Source: PLoS Pathogens. Unidade: IQ
Subjects: SCHISTOSOMA MANSONI, BIOQUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OSMAN, Ahmed et al. Schistosoma mansoni TGF-beta receptor II: role in host ligand-induced regulation of a schistosome target gene. PLoS Pathogens, v. 2, n. 6, p. 536-550, 2006Tradução . . Acesso em: 07 out. 2025.
APA
Osman, A., Niles, E. G., Verjovski-Almeida, S., & LoVerde, P. T. (2006). Schistosoma mansoni TGF-beta receptor II: role in host ligand-induced regulation of a schistosome target gene. PLoS Pathogens, 2( 6), 536-550.
NLM
Osman A, Niles EG, Verjovski-Almeida S, LoVerde PT. Schistosoma mansoni TGF-beta receptor II: role in host ligand-induced regulation of a schistosome target gene. PLoS Pathogens. 2006 ; 2( 6): 536-550.[citado 2025 out. 07 ]
Vancouver
Osman A, Niles EG, Verjovski-Almeida S, LoVerde PT. Schistosoma mansoni TGF-beta receptor II: role in host ligand-induced regulation of a schistosome target gene. PLoS Pathogens. 2006 ; 2( 6): 536-550.[citado 2025 out. 07 ]
Artigo de periodico
Flagellin-deficient Legionella mutants evade caspase-1- and Naip5-mediated macrophage immunity (2006)
Ren, Tao; Zamboni, Dario Simões; Roy, Craig R.; Dietrich, William F.; Vance, Russell E.
Source: PLoS Pathogens. Unidade: FMRP
Assunto: MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
REN, Tao et al. Flagellin-deficient Legionella mutants evade caspase-1- and Naip5-mediated macrophage immunity. PLoS Pathogens, v. 02, n. 03, p. 01-09, 2006Tradução . . Acesso em: 07 out. 2025.
APA
Ren, T., Zamboni, D. S., Roy, C. R., Dietrich, W. F., & Vance, R. E. (2006). Flagellin-deficient Legionella mutants evade caspase-1- and Naip5-mediated macrophage immunity. PLoS Pathogens, 02( 03), 01-09.
NLM
Ren T, Zamboni DS, Roy CR, Dietrich WF, Vance RE. Flagellin-deficient Legionella mutants evade caspase-1- and Naip5-mediated macrophage immunity. PLoS Pathogens. 2006 ; 02( 03): 01-09.[citado 2025 out. 07 ]
Vancouver
Ren T, Zamboni DS, Roy CR, Dietrich WF, Vance RE. Flagellin-deficient Legionella mutants evade caspase-1- and Naip5-mediated macrophage immunity. PLoS Pathogens. 2006 ; 02( 03): 01-09.[citado 2025 out. 07 ]

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