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Artigo de periodico
Mass spectrometry-based characterization of protein aggregates in tissues and biofluid (2024)
Silva, Janaina Macedo da ; Fernandes, Livia Rosa ; Blanes, Claudia Angeli ; Palmisano, Giuseppe
Fonte: Advances in Experimental Medicine and Biology. Unidade: ICB
Assuntos: PARASITOLOGIA, COMPLEXOS MULTIENZIMÁTICOS, MICRORNAS, PROTEÍNAS SANGUÍNEAS, ESPECTROMETRIA DE MASSAS, MICROSCOPIA ELETRÔNICA ANIMAL, PLASMA, PLASMA DE ANIMAL, WESTERN BLOTTING, DOENÇAS NEURODEGENERATIVAS, CAMUNDONGOS
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SILVA, Janaina Macedo da et al. Mass spectrometry-based characterization of protein aggregates in tissues and biofluid. Advances in Experimental Medicine and Biology, v. 1443, p. 257-267, 2024Tradução . . Disponível em: https://doi.org/10.1007/978-3-031-50624-6_14. Acesso em: 15 jul. 2024.
APA
Silva, J. M. da, Fernandes, L. R., Blanes, C. A., & Palmisano, G. (2024). Mass spectrometry-based characterization of protein aggregates in tissues and biofluid. Advances in Experimental Medicine and Biology, 1443, 257-267. doi:10.1007/978-3-031-50624-6_14
NLM
Silva JM da, Fernandes LR, Blanes CA, Palmisano G. Mass spectrometry-based characterization of protein aggregates in tissues and biofluid [Internet]. Advances in Experimental Medicine and Biology. 2024 ; 1443 257-267.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1007/978-3-031-50624-6_14.
Vancouver
Silva JM da, Fernandes LR, Blanes CA, Palmisano G. Mass spectrometry-based characterization of protein aggregates in tissues and biofluid [Internet]. Advances in Experimental Medicine and Biology. 2024 ; 1443 257-267.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1007/978-3-031-50624-6_14.
Artigo de periodico
Glycosort: a computational solution to post-process quantitative large-scale intact glycopeptide analyses (2024)
Lazari, Lucas Cardoso ; Santiago, Veronica Feijoli ; Oliveira, Gilberto Santos de ; Mule, Simon Ngao ; Angeli, Claudia Blanes ; Fernandes, Livia Rosa ; Palmisano, Giuseppe
Fonte: Advances in Experimental Medicine and Biology. Unidade: ICB
Assuntos: PARASITOLOGIA, COMPLEXOS MULTIENZIMÁTICOS, ENZIMOLOGIA, ATIVAÇÃO ENZIMÁTICA, GLICOPEPTÍDEOS, GLICOPROTEÍNAS, GLICOSAMINOGLICANAS, ESPECTROMETRIA DE MASSAS
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LAZARI, Lucas Cardoso et al. Glycosort: a computational solution to post-process quantitative large-scale intact glycopeptide analyses. Advances in Experimental Medicine and Biology, v. 1443, p. 23-32, 2024Tradução . . Disponível em: https://doi.org/10.1007/978-3-031-50624-6_2. Acesso em: 15 jul. 2024.
APA
Lazari, L. C., Santiago, V. F., Oliveira, G. S. de, Mule, S. N., Angeli, C. B., Fernandes, L. R., & Palmisano, G. (2024). Glycosort: a computational solution to post-process quantitative large-scale intact glycopeptide analyses. Advances in Experimental Medicine and Biology, 1443, 23-32. doi:10.1007/978-3-031-50624-6_2
NLM
Lazari LC, Santiago VF, Oliveira GS de, Mule SN, Angeli CB, Fernandes LR, Palmisano G. Glycosort: a computational solution to post-process quantitative large-scale intact glycopeptide analyses [Internet]. Advances in Experimental Medicine and Biology. 2024 ; 1443 23-32.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1007/978-3-031-50624-6_2
Vancouver
Lazari LC, Santiago VF, Oliveira GS de, Mule SN, Angeli CB, Fernandes LR, Palmisano G. Glycosort: a computational solution to post-process quantitative large-scale intact glycopeptide analyses [Internet]. Advances in Experimental Medicine and Biology. 2024 ; 1443 23-32.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1007/978-3-031-50624-6_2
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
Fonte: PLoS Pathogens. Unidades: FCF, ICB
Assuntos: 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: 15 jul. 2024.
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 2024 jul. 15 ] 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 2024 jul. 15 ] Available from: https://doi.org/10.1371/journal.ppat.1011557
Artigo de periodico
A computational pipeline elucidating functions of conserved hypothetical Trypanosoma cruzi proteins based on public proteomic data (2024)
Macedo-da-Silva, Janaina ; Mule, Simon Ngao ; Rosa-Fernandes, Livia ; Palmisano, Giuseppe
Fonte: Advances in Protein Chemistry and Structural. Unidade: ICB
Assuntos: PARASITOLOGIA, DOENÇA DE CHAGAS, PROTEÔMICA, TRYPANOSOMA CRUZI, PROTEÍNAS, HARDWARE
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MACEDO-DA-SILVA, Janaina et al. A computational pipeline elucidating functions of conserved hypothetical Trypanosoma cruzi proteins based on public proteomic data. Advances in Protein Chemistry and Structural, p. 401-428, 2024Tradução . . Disponível em: https://doi.org/10.1016/bs.apcsb.2023.07.002. Acesso em: 15 jul. 2024.
APA
Macedo-da-Silva, J., Mule, S. N., Rosa-Fernandes, L., & Palmisano, G. (2024). A computational pipeline elucidating functions of conserved hypothetical Trypanosoma cruzi proteins based on public proteomic data. Advances in Protein Chemistry and Structural, 401-428. doi:10.1016/bs.apcsb.2023.07.002
NLM
Macedo-da-Silva J, Mule SN, Rosa-Fernandes L, Palmisano G. A computational pipeline elucidating functions of conserved hypothetical Trypanosoma cruzi proteins based on public proteomic data [Internet]. Advances in Protein Chemistry and Structural. 2024 ; 401-428.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/bs.apcsb.2023.07.002
Vancouver
Macedo-da-Silva J, Mule SN, Rosa-Fernandes L, Palmisano G. A computational pipeline elucidating functions of conserved hypothetical Trypanosoma cruzi proteins based on public proteomic data [Internet]. Advances in Protein Chemistry and Structural. 2024 ; 401-428.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/bs.apcsb.2023.07.002
Artigo de periodico
Molecular tools to regulate gene expression in Trypanosoma cruzi (2024)
Silva, Lays Adrianne Mendonça Trajano ; Mule, Simon Ngao ; Palmisano, Giuseppe
Fonte: Advances in Clinical Chemistry. Unidade: ICB
Assuntos: PARASITOLOGIA, GENÉTICA BACTERIANA, TRYPANOSOMA CRUZI, NUCLEOTÍDEOS, EXPRESSÃO GÊNICA, REGULAÇÃO GÊNICA, PROTOZOA, TRYPANOSOMATIDAE
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SILVA, Lays Adrianne Mendonça Trajano e MULE, Simon Ngao e PALMISANO, Giuseppe. Molecular tools to regulate gene expression in Trypanosoma cruzi. Advances in Clinical Chemistry, v. 120, p. 169-190, 2024Tradução . . Disponível em: https://doi.org/10.1016/bs.acc.2024.04.008. Acesso em: 15 jul. 2024.
APA
Silva, L. A. M. T., Mule, S. N., & Palmisano, G. (2024). Molecular tools to regulate gene expression in Trypanosoma cruzi. Advances in Clinical Chemistry, 120, 169-190. doi:10.1016/bs.acc.2024.04.008
NLM
Silva LAMT, Mule SN, Palmisano G. Molecular tools to regulate gene expression in Trypanosoma cruzi [Internet]. Advances in Clinical Chemistry. 2024 ; 120 169-190.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/bs.acc.2024.04.008
Vancouver
Silva LAMT, Mule SN, Palmisano G. Molecular tools to regulate gene expression in Trypanosoma cruzi [Internet]. Advances in Clinical Chemistry. 2024 ; 120 169-190.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/bs.acc.2024.04.008
Artigo de periodico
Changing clinical epidemiology of Plasmodium vivax Malaria as transmission decreases: population-based prospective panel survey in the Brazilian Amazon (2024)
Fontoura, Pablo Secato ; Macedo, Evelyn G. ; Corder, Rodrigo Malavazi ; Rodrigues, Priscila Thihara ; Tonini, Juliana ; Esquivel, Fabiana Dutra ; Ladeia, Winni Alves ; Fernandes, Anderson Rocha de Jesus; Johansen, Igor Cavallini ; Silva, Marcos Fernandes da; Fernandes, Amanda O. S.; Andrade, Simone Ladeia ; Castro, Marcia Caldas de ; Ferreira, Marcelo Urbano
Fonte: The Journal of Infectious Diseases. Unidade: ICB
Assuntos: PARASITOLOGIA, MALÁRIA, PLASMODIUM MALARIAE, PLASMODIUM FALCIPARUM, ESTUDOS PROSPECTIVOS
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FONTOURA, Pablo Secato et al. Changing clinical epidemiology of Plasmodium vivax Malaria as transmission decreases: population-based prospective panel survey in the Brazilian Amazon. The Journal of Infectious Diseases, v. 229, n. 4, p. 947-958, 2024Tradução . . Disponível em: https://doi.org/10.1093/infdis/jiad456. Acesso em: 15 jul. 2024.
APA
Fontoura, P. S., Macedo, E. G., Corder, R. M., Rodrigues, P. T., Tonini, J., Esquivel, F. D., et al. (2024). Changing clinical epidemiology of Plasmodium vivax Malaria as transmission decreases: population-based prospective panel survey in the Brazilian Amazon. The Journal of Infectious Diseases, 229( 4), 947-958. doi:10.1093/infdis/jiad456
NLM
Fontoura PS, Macedo EG, Corder RM, Rodrigues PT, Tonini J, Esquivel FD, Ladeia WA, Fernandes AR de J, Johansen IC, Silva MF da, Fernandes AOS, Andrade SL, Castro MC de, Ferreira MU. Changing clinical epidemiology of Plasmodium vivax Malaria as transmission decreases: population-based prospective panel survey in the Brazilian Amazon [Internet]. The Journal of Infectious Diseases. 2024 ; 229( 4): 947-958.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1093/infdis/jiad456
Vancouver
Fontoura PS, Macedo EG, Corder RM, Rodrigues PT, Tonini J, Esquivel FD, Ladeia WA, Fernandes AR de J, Johansen IC, Silva MF da, Fernandes AOS, Andrade SL, Castro MC de, Ferreira MU. Changing clinical epidemiology of Plasmodium vivax Malaria as transmission decreases: population-based prospective panel survey in the Brazilian Amazon [Internet]. The Journal of Infectious Diseases. 2024 ; 229( 4): 947-958.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1093/infdis/jiad456
Artigo de periodico
Isolation of extracellular vesicles using titanium dioxide microspheres (2024)
Santiago, Veronica Feijoli ; Fernandes, Livia Rosa ; Macedo-da-Silva, Janaina ; Angeli, Claudia Blanes ; Mule, Simon Ngao ; Torrecilhas, Ana Claudia Trocoli ; Marie, Suely Kazue Nagahashi ; Marinho, Claudio Romero Farias ; Palmisano, Giuseppe
Fonte: Advances in Experimental Medicine and Biology. Unidades: ICB, FM
Assuntos: PARASITOLOGIA, PROTEÔMICA, ESPECTROSCOPIA DE MASSA, PROTEÍNAS SANGUÍNEAS, PLASMA, NANOPARTÍCULAS
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SANTIAGO, Veronica Feijoli et al. Isolation of extracellular vesicles using titanium dioxide microspheres. Advances in Experimental Medicine and Biology, v. 1443, p. 1-22, 2024Tradução . . Disponível em: https://doi.org/10.1007/978-3-031-50624-6_1. Acesso em: 15 jul. 2024.
APA
Santiago, V. F., Fernandes, L. R., Macedo-da-Silva, J., Angeli, C. B., Mule, S. N., Torrecilhas, A. C. T., et al. (2024). Isolation of extracellular vesicles using titanium dioxide microspheres. Advances in Experimental Medicine and Biology, 1443, 1-22. doi:10.1007/978-3-031-50624-6_1
NLM
Santiago VF, Fernandes LR, Macedo-da-Silva J, Angeli CB, Mule SN, Torrecilhas ACT, Marie SKN, Marinho CRF, Palmisano G. Isolation of extracellular vesicles using titanium dioxide microspheres [Internet]. Advances in Experimental Medicine and Biology. 2024 ; 1443 1-22.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1007/978-3-031-50624-6_1
Vancouver
Santiago VF, Fernandes LR, Macedo-da-Silva J, Angeli CB, Mule SN, Torrecilhas ACT, Marie SKN, Marinho CRF, Palmisano G. Isolation of extracellular vesicles using titanium dioxide microspheres [Internet]. Advances in Experimental Medicine and Biology. 2024 ; 1443 1-22.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1007/978-3-031-50624-6_1
Artigo de periodico
Cysteine synthase: multiple structures of a key enzyme in cysteine synthesis and a potential drug target for Chagas disease and leishmaniasis (2023)
Sowerby, Kate ; Pohl, Stefanie Freitag ; Murillo, Ana Milena ; Silber, Ariel Mariano ; Pohl, Ehmke
Fonte: Acta Crystallographica. Section D: Structural Biology. Unidade: ICB
Assuntos: PARASITOLOGIA, DOENÇA DE CHAGAS, LEISHMANIA, TRYPANOSOMATIDAE, TRYPANOSOMA CRUZI, AMINOÁCIDOS, CRISTALOGRAFIA DE RAIOS X, ANTIPARASITÁRIOS, ATIVAÇÃO ENZIMÁTICA, INIBIDORES DE ENZIMAS
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SOWERBY, Kate et al. Cysteine synthase: multiple structures of a key enzyme in cysteine synthesis and a potential drug target for Chagas disease and leishmaniasis. Acta Crystallographica. Section D: Structural Biology, v. D79, p. 1-13, 2023Tradução . . Disponível em: https://doi.org/10.1107/S2059798323003613. Acesso em: 15 jul. 2024.
APA
Sowerby, K., Pohl, S. F., Murillo, A. M., Silber, A. M., & Pohl, E. (2023). Cysteine synthase: multiple structures of a key enzyme in cysteine synthesis and a potential drug target for Chagas disease and leishmaniasis. Acta Crystallographica. Section D: Structural Biology, D79, 1-13. doi:10.1107/S2059798323003613
NLM
Sowerby K, Pohl SF, Murillo AM, Silber AM, Pohl E. Cysteine synthase: multiple structures of a key enzyme in cysteine synthesis and a potential drug target for Chagas disease and leishmaniasis [Internet]. Acta Crystallographica. Section D: Structural Biology. 2023 ; D79 1-13.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1107/S2059798323003613
Vancouver
Sowerby K, Pohl SF, Murillo AM, Silber AM, Pohl E. Cysteine synthase: multiple structures of a key enzyme in cysteine synthesis and a potential drug target for Chagas disease and leishmaniasis [Internet]. Acta Crystallographica. Section D: Structural Biology. 2023 ; D79 1-13.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1107/S2059798323003613
Artigo de periodico
The branched chain amino acids (BCAAs) modulate the development of the intra-cellular stages of Trypanosoma cruzi (2023)
Rapado, Ludmila Nakamura; Nascimento, Janaina de Freitas ; Damasceno, Flavia Silva ; Achjian, Renan Weege ; Silber, Ariel Mariano
Fonte: Experimental Parasitology. Unidade: ICB
Assuntos: PARASITOLOGIA, TRYPANOSOMA CRUZI, ANIMAIS PARASITOS, AMINOÁCIDOS, ANTIPARASITÁRIOS
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RAPADO, Ludmila Nakamura et al. The branched chain amino acids (BCAAs) modulate the development of the intra-cellular stages of Trypanosoma cruzi. Experimental Parasitology, v. 255, p. 6 , 2023Tradução . . Disponível em: https://doi.org/10.1016/j.exppara.2023.108642. Acesso em: 15 jul. 2024.
APA
Rapado, L. N., Nascimento, J. de F., Damasceno, F. S., Achjian, R. W., & Silber, A. M. (2023). The branched chain amino acids (BCAAs) modulate the development of the intra-cellular stages of Trypanosoma cruzi. Experimental Parasitology, 255, 6 . doi:https://doi.org/10.1016/j.exppara.2023.108642
NLM
Rapado LN, Nascimento J de F, Damasceno FS, Achjian RW, Silber AM. The branched chain amino acids (BCAAs) modulate the development of the intra-cellular stages of Trypanosoma cruzi [Internet]. Experimental Parasitology. 2023 ; 255 6 .[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.exppara.2023.108642
Vancouver
Rapado LN, Nascimento J de F, Damasceno FS, Achjian RW, Silber AM. The branched chain amino acids (BCAAs) modulate the development of the intra-cellular stages of Trypanosoma cruzi [Internet]. Experimental Parasitology. 2023 ; 255 6 .[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.exppara.2023.108642
Artigo de periodico
The respiratory syncytial virus M2-2 protein is targeted for proteasome degradation and inhibits translation and stress granules assembly (2023)
Scudero, Orlando Bonito ; Santiago, Veronica Feijoli ; Palmisano, Giuseppe ; Simabuco, Fernando Moreira ; Ventura, Armando Morais
Fonte: PLOS ONE. Unidade: ICB
Assuntos: MICROBIOLOGIA, PARASITOLOGIA, DOENÇAS RESPIRATÓRIAS, PROTEÍNAS, REPLICAÇÃO VIRAL, GENOMAS, REAÇÃO EM CADEIA POR POLIMERASE, MICRORNAS, CITOPLASMA
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SCUDERO, Orlando Bonito et al. The respiratory syncytial virus M2-2 protein is targeted for proteasome degradation and inhibits translation and stress granules assembly. PLOS ONE, v. 18, n. 7, p. 26 , 2023Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0289100. Acesso em: 15 jul. 2024.
APA
Scudero, O. B., Santiago, V. F., Palmisano, G., Simabuco, F. M., & Ventura, A. M. (2023). The respiratory syncytial virus M2-2 protein is targeted for proteasome degradation and inhibits translation and stress granules assembly. PLOS ONE, 18( 7), 26 . doi:10.1371/journal.pone.0289100
NLM
Scudero OB, Santiago VF, Palmisano G, Simabuco FM, Ventura AM. The respiratory syncytial virus M2-2 protein is targeted for proteasome degradation and inhibits translation and stress granules assembly [Internet]. PLOS ONE. 2023 ; 18( 7): 26 .[citado 2024 jul. 15 ] Available from: https://doi.org/10.1371/journal.pone.0289100
Vancouver
Scudero OB, Santiago VF, Palmisano G, Simabuco FM, Ventura AM. The respiratory syncytial virus M2-2 protein is targeted for proteasome degradation and inhibits translation and stress granules assembly [Internet]. PLOS ONE. 2023 ; 18( 7): 26 .[citado 2024 jul. 15 ] Available from: https://doi.org/10.1371/journal.pone.0289100
Artigo de periodico
Conditional expression of NanoLuc luciferase through a multimodular system offers rapid detection of antimalarial drug activity (2023)
Lima, Caroline; Verdaguer, Ignasi Bofill ; Crabb, Brendan S. ; Gilson, Paul R.; Azevedo, Mauro F. de ; Wunderlich, Gerhard ; Katzin, Alejandro M.
Fonte: Experimental Parasitology. Unidade: ICB
Assuntos: PARASITOLOGIA, MALÁRIA, ANTIMALÁRICOS, EXPRESSÃO GÊNICA, PLASMODIUM FALCIPARUM, FENÓTIPOS, PLASMÍDEOS
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LIMA, Caroline et al. Conditional expression of NanoLuc luciferase through a multimodular system offers rapid detection of antimalarial drug activity. Experimental Parasitology, v. 254, p. 25 , 2023Tradução . . Disponível em: https://doi.org/10.1016/j.exppara.2023.108620. Acesso em: 15 jul. 2024.
APA
Lima, C., Verdaguer, I. B., Crabb, B. S., Gilson, P. R., Azevedo, M. F. de, Wunderlich, G., & Katzin, A. M. (2023). Conditional expression of NanoLuc luciferase through a multimodular system offers rapid detection of antimalarial drug activity. Experimental Parasitology, 254, 25 . doi:10.1016/j.exppara.2023.108620
NLM
Lima C, Verdaguer IB, Crabb BS, Gilson PR, Azevedo MF de, Wunderlich G, Katzin AM. Conditional expression of NanoLuc luciferase through a multimodular system offers rapid detection of antimalarial drug activity [Internet]. Experimental Parasitology. 2023 ; 254 25 .[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.exppara.2023.108620
Vancouver
Lima C, Verdaguer IB, Crabb BS, Gilson PR, Azevedo MF de, Wunderlich G, Katzin AM. Conditional expression of NanoLuc luciferase through a multimodular system offers rapid detection of antimalarial drug activity [Internet]. Experimental Parasitology. 2023 ; 254 25 .[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.exppara.2023.108620
Artigo de periodico
Comparison of sampling procedures for the molecular diagnosis of Leishmaniases (2023)
Zampieri, Ricardo Andrade ; Aoki, Juliana Ide ; Müller, Karl Erik ; Shaw, Jeffrey Jon ; Floeter-Winter, Lucile Maria
Fonte: American Journal of Tropical Medicine and Hygiene. Unidades: ICB, IB
Assuntos: PARASITOLOGIA, CAMUNDONGOS, LEISHMANIA BRASILIENSIS, LEISHMANIA INFANTUM, LEISHMANIA, PROTOZOA, DNA, REAÇÃO EM CADEIA POR POLIMERASE
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ZAMPIERI, Ricardo Andrade et al. Comparison of sampling procedures for the molecular diagnosis of Leishmaniases. American Journal of Tropical Medicine and Hygiene, v. 108, n. 3, p. 548-554, 2023Tradução . . Disponível em: https://doi.org/10.4269/ajtmh.21-1137. Acesso em: 15 jul. 2024.
APA
Zampieri, R. A., Aoki, J. I., Müller, K. E., Shaw, J. J., & Floeter-Winter, L. M. (2023). Comparison of sampling procedures for the molecular diagnosis of Leishmaniases. American Journal of Tropical Medicine and Hygiene, 108( 3), 548-554. doi:10.4269/ajtmh.21-1137
NLM
Zampieri RA, Aoki JI, Müller KE, Shaw JJ, Floeter-Winter LM. Comparison of sampling procedures for the molecular diagnosis of Leishmaniases [Internet]. American Journal of Tropical Medicine and Hygiene. 2023 ; 108( 3): 548-554.[citado 2024 jul. 15 ] Available from: https://doi.org/10.4269/ajtmh.21-1137
Vancouver
Zampieri RA, Aoki JI, Müller KE, Shaw JJ, Floeter-Winter LM. Comparison of sampling procedures for the molecular diagnosis of Leishmaniases [Internet]. American Journal of Tropical Medicine and Hygiene. 2023 ; 108( 3): 548-554.[citado 2024 jul. 15 ] Available from: https://doi.org/10.4269/ajtmh.21-1137
Artigo de periodico
Novel transmission-blocking antimalarials identified by high-throughput screening of plasmodium berghei Ookluc (2023)
Calit, Juliana ; Araújo, Jessica E.; Deng, Bingbing ; Miura, Kazutoyo ; Gaitán, Xiomara A. ; Araújo, Maisa da Silva ; Medeiros, Jansen F. ; Long, Carole A. ; Eastman, Richard T. ; Bargieri, Daniel Youssef
Fonte: Antimicrobial Agents and Chemotherapy. Unidade: ICB
Assuntos: PARASITOLOGIA, MALÁRIA, ANTIMALÁRICOS, PLASMODIUM, PLASMODIUM FALCIPARUM, QUIMIOTERÁPICOS
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CALIT, Juliana et al. Novel transmission-blocking antimalarials identified by high-throughput screening of plasmodium berghei Ookluc. Antimicrobial Agents and Chemotherapy, p. 1-11, 2023Tradução . . Disponível em: https://doi.org/10.1128/aac.01465-22. Acesso em: 15 jul. 2024.
APA
Calit, J., Araújo, J. E., Deng, B., Miura, K., Gaitán, X. A., Araújo, M. da S., et al. (2023). Novel transmission-blocking antimalarials identified by high-throughput screening of plasmodium berghei Ookluc. Antimicrobial Agents and Chemotherapy, 1-11. doi:10.1128/aac.01465-22
NLM
Calit J, Araújo JE, Deng B, Miura K, Gaitán XA, Araújo M da S, Medeiros JF, Long CA, Eastman RT, Bargieri DY. Novel transmission-blocking antimalarials identified by high-throughput screening of plasmodium berghei Ookluc [Internet]. Antimicrobial Agents and Chemotherapy. 2023 ; 1-11.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1128/aac.01465-22
Vancouver
Calit J, Araújo JE, Deng B, Miura K, Gaitán XA, Araújo M da S, Medeiros JF, Long CA, Eastman RT, Bargieri DY. Novel transmission-blocking antimalarials identified by high-throughput screening of plasmodium berghei Ookluc [Internet]. Antimicrobial Agents and Chemotherapy. 2023 ; 1-11.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1128/aac.01465-22
Artigo de periodico
Putrescine supplementation shifts macrophage L-arginine metabolism related-genes reducing Leishmania amazonensis infection (2023)
Zanatta, Jonathan Miguel ; Acuña, Stephanie Maia ; Angelo, Yan de Souza ; Bento, Camilla de Almeida; Muxel, Sandra Marcia ; Peron, Jean Pierre Schatzmann ; Stolf, Beatriz Simonsen
Fonte: PL o S One. Unidades: ICB, IB
Assuntos: IMUNOLOGA, PARASITOLOGIA, LEISHMANIOSE CUTÂNEA, LEISHMANIA, SUPLEMENTOS DIETÉTICOS, MACRÓFAGOS, ARGININA, ÓXIDO NÍTRICO, ANTIPROTOZOÁRIOS, ANIMAIS PARASITOS, EXPRESSÃO GÊNICA
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ABNT
ZANATTA, Jonathan Miguel et al. Putrescine supplementation shifts macrophage L-arginine metabolism related-genes reducing Leishmania amazonensis infection. PL o S One, v. 3, p. 1-25, 2023Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0283696. Acesso em: 15 jul. 2024.
APA
Zanatta, J. M., Acuña, S. M., Angelo, Y. de S., Bento, C. de A., Muxel, S. M., Peron, J. P. S., & Stolf, B. S. (2023). Putrescine supplementation shifts macrophage L-arginine metabolism related-genes reducing Leishmania amazonensis infection. PL o S One, 3, 1-25. doi:10.1371/journal.pone.0283696
NLM
Zanatta JM, Acuña SM, Angelo Y de S, Bento C de A, Muxel SM, Peron JPS, Stolf BS. Putrescine supplementation shifts macrophage L-arginine metabolism related-genes reducing Leishmania amazonensis infection [Internet]. PL o S One. 2023 ; 3 1-25.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1371/journal.pone.0283696
Vancouver
Zanatta JM, Acuña SM, Angelo Y de S, Bento C de A, Muxel SM, Peron JPS, Stolf BS. Putrescine supplementation shifts macrophage L-arginine metabolism related-genes reducing Leishmania amazonensis infection [Internet]. PL o S One. 2023 ; 3 1-25.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1371/journal.pone.0283696
Artigo de periodico
Branched chain amino acids catabolism as a source of new drug targets in pathogenic protists (2023)
Souza, H. F. Santos ; Marsiccobetre, S. ; Souza, R. O. O. ; Martínez, L. A. Luévano ; Silber, Ariel Mariano
Fonte: Experimental Parasitology. Unidade: ICB
Assuntos: PARASITOLOGIA, AMINOÁCIDOS, CÉLULAS EUCARIÓTICAS, CÉLULAS MUSCULARES, PROTEÍNAS
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SOUZA, H. F. Santos et al. Branched chain amino acids catabolism as a source of new drug targets in pathogenic protists. Experimental Parasitology, v. 249, p. 1-10, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.exppara.2023.108499. Acesso em: 15 jul. 2024.
APA
Souza, H. F. S., Marsiccobetre, S., Souza, R. O. O., Martínez, L. A. L., & Silber, A. M. (2023). Branched chain amino acids catabolism as a source of new drug targets in pathogenic protists. Experimental Parasitology, 249, 1-10. doi:10.1016/j.exppara.2023.108499
NLM
Souza HFS, Marsiccobetre S, Souza ROO, Martínez LAL, Silber AM. Branched chain amino acids catabolism as a source of new drug targets in pathogenic protists [Internet]. Experimental Parasitology. 2023 ; 249 1-10.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.exppara.2023.108499
Vancouver
Souza HFS, Marsiccobetre S, Souza ROO, Martínez LAL, Silber AM. Branched chain amino acids catabolism as a source of new drug targets in pathogenic protists [Internet]. Experimental Parasitology. 2023 ; 249 1-10.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.exppara.2023.108499
Artigo de periodico
High levels of infectiousness of asymptomatic Leishmania (Viannia) braziliensis infections in wild rodents highlights their importance in the epidemiology of American Tegumentary Leishmaniasis in Brazil (2023)
Marinho Júnior, José Ferreira; Monteiro, Juliana F. C. L. S.; Carvalho, Ana Waléria Sales de; Carvalho, Francisco Gomes de; Cavalcanti, Milena de Paiva ; Shaw, Jeffrey ; Courtenay, Orin ; Brandão Filho, Sinval Pinto
Fonte: PL o S Neglected Tropical Diseases. Unidade: ICB
Assuntos: PARASITOLOGIA, LEISHMANIA, LEISHMANIA BRASILIENSIS, LEISHMANIOSE CUTÂNEA ANIMAL, FLEBOTOMIA ANIMAL, ANIMAIS SILVESTRES, ROEDORES, REAÇÃO EM CADEIA POR POLIMERASE
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MARINHO JÚNIOR, José Ferreira et al. High levels of infectiousness of asymptomatic Leishmania (Viannia) braziliensis infections in wild rodents highlights their importance in the epidemiology of American Tegumentary Leishmaniasis in Brazil. PL o S Neglected Tropical Diseases, v. 17, n. 1, p. 1-23, 2023Tradução . . Disponível em: https://doi.org/10.1371/journal.pntd.0010996. Acesso em: 15 jul. 2024.
APA
Marinho Júnior, J. F., Monteiro, J. F. C. L. S., Carvalho, A. W. S. de, Carvalho, F. G. de, Cavalcanti, M. de P., Shaw, J., et al. (2023). High levels of infectiousness of asymptomatic Leishmania (Viannia) braziliensis infections in wild rodents highlights their importance in the epidemiology of American Tegumentary Leishmaniasis in Brazil. PL o S Neglected Tropical Diseases, 17( 1), 1-23. doi:10.1371/journal.pntd.0010996
NLM
Marinho Júnior JF, Monteiro JFCLS, Carvalho AWS de, Carvalho FG de, Cavalcanti M de P, Shaw J, Courtenay O, Brandão Filho SP. High levels of infectiousness of asymptomatic Leishmania (Viannia) braziliensis infections in wild rodents highlights their importance in the epidemiology of American Tegumentary Leishmaniasis in Brazil [Internet]. PL o S Neglected Tropical Diseases. 2023 ; 17( 1): 1-23.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1371/journal.pntd.0010996
Vancouver
Marinho Júnior JF, Monteiro JFCLS, Carvalho AWS de, Carvalho FG de, Cavalcanti M de P, Shaw J, Courtenay O, Brandão Filho SP. High levels of infectiousness of asymptomatic Leishmania (Viannia) braziliensis infections in wild rodents highlights their importance in the epidemiology of American Tegumentary Leishmaniasis in Brazil [Internet]. PL o S Neglected Tropical Diseases. 2023 ; 17( 1): 1-23.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1371/journal.pntd.0010996
Artigo de periodico
Navigating the boundaries between metabolism and epigenetics in trypanosomes (2023)
Menezes, Ana Paula de Jesus ; Giraldo, Ana Milena Murillo ; Castro, Camila Gachet de ; Bellini, Natália Karla ; Tosi, Luíz Ricardo Orsini ; Thiemann, Otávio Henrique ; Sabbaga, Maria Carolina Quartim Barbosa Elias ; Silber, Ariel Mariano ; Cunha, Julia Pinheiro Chagas da
Fonte: Trends in Parasitology. Unidades: FMRP, IFSC, ICB
Assuntos: EPIGÊNESE GENÉTICA, TRYPANOSOMA, METABOLISMO CELULAR, PARASITOLOGIA, METABOLITOS
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MENEZES, Ana Paula de Jesus et al. Navigating the boundaries between metabolism and epigenetics in trypanosomes. Trends in Parasitology, v. 39, n. 8, p. 682-695 + supplemental information, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.pt.2023.05.010. Acesso em: 15 jul. 2024.
APA
Menezes, A. P. de J., Giraldo, A. M. M., Castro, C. G. de, Bellini, N. K., Tosi, L. R. O., Thiemann, O. H., et al. (2023). Navigating the boundaries between metabolism and epigenetics in trypanosomes. Trends in Parasitology, 39( 8), 682-695 + supplemental information. doi:10.1016/j.pt.2023.05.010
NLM
Menezes AP de J, Giraldo AMM, Castro CG de, Bellini NK, Tosi LRO, Thiemann OH, Sabbaga MCQBE, Silber AM, Cunha JPC da. Navigating the boundaries between metabolism and epigenetics in trypanosomes [Internet]. Trends in Parasitology. 2023 ; 39( 8): 682-695 + supplemental information.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.pt.2023.05.010
Vancouver
Menezes AP de J, Giraldo AMM, Castro CG de, Bellini NK, Tosi LRO, Thiemann OH, Sabbaga MCQBE, Silber AM, Cunha JPC da. Navigating the boundaries between metabolism and epigenetics in trypanosomes [Internet]. Trends in Parasitology. 2023 ; 39( 8): 682-695 + supplemental information.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1016/j.pt.2023.05.010
Artigo de periodico
Complete genome sequence of the archetype bile acid 7α-dehydroxylating bacterium, Clostridium scindens VPI12708, isolated from human feces, circa 1980 (2023)
Caicedo, Kelly Yovani Olivos ; Fernández-Materán, Francelys V. ; Hernandez, Alvaro G. ; Daniel, Steven L. ; Ridlon, Jason M. ; Alves, João Marcelo Pereira
Fonte: Microbiology Resource Announcements. Unidade: ICB
Assuntos: PARASITOLOGIA, INFECÇÕES BACTERIANAS GRAM-POSITIVAS, GENOMAS, CLOSTRIDIUM, BACILOS GRAM-POSITIVOS, SEQUENCIAMENTO GENÉTICO, FEZES, GENÉTICA BACTERIANA
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ABNT
CAICEDO, Kelly Yovani Olivos et al. Complete genome sequence of the archetype bile acid 7α-dehydroxylating bacterium, Clostridium scindens VPI12708, isolated from human feces, circa 1980. Microbiology Resource Announcements, 2023Tradução . . Disponível em: https://doi.org/10.1128/MRA.00029-23. Acesso em: 15 jul. 2024.
APA
Caicedo, K. Y. O., Fernández-Materán, F. V., Hernandez, A. G., Daniel, S. L., Ridlon, J. M., & Alves, J. M. P. (2023). Complete genome sequence of the archetype bile acid 7α-dehydroxylating bacterium, Clostridium scindens VPI12708, isolated from human feces, circa 1980. Microbiology Resource Announcements. doi:10.1128/MRA.00029-23
NLM
Caicedo KYO, Fernández-Materán FV, Hernandez AG, Daniel SL, Ridlon JM, Alves JMP. Complete genome sequence of the archetype bile acid 7α-dehydroxylating bacterium, Clostridium scindens VPI12708, isolated from human feces, circa 1980 [Internet]. Microbiology Resource Announcements. 2023 ;[citado 2024 jul. 15 ] Available from: https://doi.org/10.1128/MRA.00029-23
Vancouver
Caicedo KYO, Fernández-Materán FV, Hernandez AG, Daniel SL, Ridlon JM, Alves JMP. Complete genome sequence of the archetype bile acid 7α-dehydroxylating bacterium, Clostridium scindens VPI12708, isolated from human feces, circa 1980 [Internet]. Microbiology Resource Announcements. 2023 ;[citado 2024 jul. 15 ] Available from: https://doi.org/10.1128/MRA.00029-23
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 F. ; 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
Fonte: PLoS Pathogens. Unidade: ICB
Assuntos: PARASITOLOGIA, TRYPANOSOMA, ANIMAIS PARASITOS, BIOMASSA, CICLO CELULAR, POLIMERIZAÇÃO, GLICOSE, GLICOPROTEÍNAS
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ABNT
NASCIMENTO, Janaina F. 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: 15 jul. 2024.
APA
Nascimento, J. 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 JF, 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 2024 jul. 15 ] Available from: https://doi.org/10.1371/journal.ppat.1011522
Vancouver
Nascimento JF, 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 2024 jul. 15 ] Available from: https://doi.org/10.1371/journal.ppat.1011522
Artigo de periodico
Transcriptomics-Guided in silico drug repurposing: identifying new candidates with dual-stage antiplasmodial activity (2023)
Borba, Joyce V. B. ; Azevedo, Beatriz Rosa de; Ferreira, Larissa A.; Rimoldi, Aline ; Alvares, Luis Carlos Salazar ; Calit, Juliana ; Costa, Fabio T. M. ; Bargieri, Daniel Y.
Fonte: ACS Omega. Unidade: ICB
Assuntos: PARASITOLOGIA, MALÁRIA, ANTIMALÁRICOS, ANIMAIS PARASITOS, MEDICAMENTO, PLASMODIUM FALCIPARUM, TRANSCRIÇÃO GÊNICA, GAMETOGÊNESE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BORBA, Joyce V. B. et al. Transcriptomics-Guided in silico drug repurposing: identifying new candidates with dual-stage antiplasmodial activity. ACS Omega, v. 8, n. 37, p. 34084-34090, 2023Tradução . . Disponível em: https://doi.org/10.1021/acsomega.3c05138. Acesso em: 15 jul. 2024.
APA
Borba, J. V. B., Azevedo, B. R. de, Ferreira, L. A., Rimoldi, A., Alvares, L. C. S., Calit, J., et al. (2023). Transcriptomics-Guided in silico drug repurposing: identifying new candidates with dual-stage antiplasmodial activity. ACS Omega, 8( 37), 34084-34090. doi:10.1021/acsomega.3c05138
NLM
Borba JVB, Azevedo BR de, Ferreira LA, Rimoldi A, Alvares LCS, Calit J, Costa FTM, Bargieri DY. Transcriptomics-Guided in silico drug repurposing: identifying new candidates with dual-stage antiplasmodial activity [Internet]. ACS Omega. 2023 ; 8( 37): 34084-34090.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1021/acsomega.3c05138
Vancouver
Borba JVB, Azevedo BR de, Ferreira LA, Rimoldi A, Alvares LCS, Calit J, Costa FTM, Bargieri DY. Transcriptomics-Guided in silico drug repurposing: identifying new candidates with dual-stage antiplasmodial activity [Internet]. ACS Omega. 2023 ; 8( 37): 34084-34090.[citado 2024 jul. 15 ] Available from: https://doi.org/10.1021/acsomega.3c05138

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