Filtros : "GARCIA, CELIA REGINA DA SILVA" "Suiça" Limpar

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  • Source: International Journal o f Molecular Sciences. Unidade: FCF

    Subjects: PLASMODIUM, TOXOPLASMA GONDII

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      SANTOS, Benedito Matheus dos e PRZYBORSKI, Jude Marek e GARCIA, Célia Regina da Silva. Changes in K+ concentration as a signaling mechanism in the apicomplexa parasites plasmodium and toxoplasma. International Journal o f Molecular Sciences, v. 24, n. 8, p. 1-11, 2023Tradução . . Disponível em: https://doi.org/10.3390/ijms24087276. Acesso em: 16 out. 2024.
    • APA

      Santos, B. M. dos, Przyborski, J. M., & Garcia, C. R. da S. (2023). Changes in K+ concentration as a signaling mechanism in the apicomplexa parasites plasmodium and toxoplasma. International Journal o f Molecular Sciences, 24( 8), 1-11. doi:10.3390/ijms24087276
    • NLM

      Santos BM dos, Przyborski JM, Garcia CR da S. Changes in K+ concentration as a signaling mechanism in the apicomplexa parasites plasmodium and toxoplasma [Internet]. International Journal o f Molecular Sciences. 2023 ; 24( 8): 1-11.[citado 2024 out. 16 ] Available from: https://doi.org/10.3390/ijms24087276
    • Vancouver

      Santos BM dos, Przyborski JM, Garcia CR da S. Changes in K+ concentration as a signaling mechanism in the apicomplexa parasites plasmodium and toxoplasma [Internet]. International Journal o f Molecular Sciences. 2023 ; 24( 8): 1-11.[citado 2024 out. 16 ] Available from: https://doi.org/10.3390/ijms24087276
  • Source: Biomolecules. Unidades: FCF, IQ, ICB

    Subjects: PLASMODIUM FALCIPARUM, ANTIMALÁRICOS, MELATONINA

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      MALLAUPOMA, Lenna Rosanie Cordero et al. Decoding the role of melatonin structure on Plasmodium falciparum human malaria parasites synchronization using 2-sulfenylindoles derivatives. Biomolecules, v. 12, p. 1-15, 2022Tradução . . Disponível em: https://doi.org/10.3390/biom12050638. Acesso em: 16 out. 2024.
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      Mallaupoma, L. R. C., Dias, B. K. de M., Singh, M. K., Honorio, R. I., Nakabashi, M., Kisukuri, C. de M., et al. (2022). Decoding the role of melatonin structure on Plasmodium falciparum human malaria parasites synchronization using 2-sulfenylindoles derivatives. Biomolecules, 12, 1-15. doi:10.3390/biom12050638
    • NLM

      Mallaupoma LRC, Dias BK de M, Singh MK, Honorio RI, Nakabashi M, Kisukuri C de M, Paixão MW, Garcia CR da S. Decoding the role of melatonin structure on Plasmodium falciparum human malaria parasites synchronization using 2-sulfenylindoles derivatives [Internet]. Biomolecules. 2022 ; 12 1-15.[citado 2024 out. 16 ] Available from: https://doi.org/10.3390/biom12050638
    • Vancouver

      Mallaupoma LRC, Dias BK de M, Singh MK, Honorio RI, Nakabashi M, Kisukuri C de M, Paixão MW, Garcia CR da S. Decoding the role of melatonin structure on Plasmodium falciparum human malaria parasites synchronization using 2-sulfenylindoles derivatives [Internet]. Biomolecules. 2022 ; 12 1-15.[citado 2024 out. 16 ] Available from: https://doi.org/10.3390/biom12050638
  • Source: International Journal of Molecular Sciences. Unidade: FCF

    Subjects: PLASMODIUM FALCIPARUM, CÁLCIO, PROTEÍNAS G, ANTIMALÁRICOS

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      PEREIRA, Pedro Henrique Scarpelli e GARCIA, Célia Regina da Silva. Evidence of G-protein-coupled receptors (GPCR) in the parasitic protozoa Plasmodium falciparum—sensing the host environment and coupling within its molecular signaling toolkit. International Journal of Molecular Sciences, v. 22, p. 1-12 art. 12381, 2021Tradução . . Disponível em: https://doi.org/10.3390/ijms222212381. Acesso em: 16 out. 2024.
    • APA

      Pereira, P. H. S., & Garcia, C. R. da S. (2021). Evidence of G-protein-coupled receptors (GPCR) in the parasitic protozoa Plasmodium falciparum—sensing the host environment and coupling within its molecular signaling toolkit. International Journal of Molecular Sciences, 22, 1-12 art. 12381. doi:10.3390/ijms222212381
    • NLM

      Pereira PHS, Garcia CR da S. Evidence of G-protein-coupled receptors (GPCR) in the parasitic protozoa Plasmodium falciparum—sensing the host environment and coupling within its molecular signaling toolkit [Internet]. International Journal of Molecular Sciences. 2021 ; 22 1-12 art. 12381.[citado 2024 out. 16 ] Available from: https://doi.org/10.3390/ijms222212381
    • Vancouver

      Pereira PHS, Garcia CR da S. Evidence of G-protein-coupled receptors (GPCR) in the parasitic protozoa Plasmodium falciparum—sensing the host environment and coupling within its molecular signaling toolkit [Internet]. International Journal of Molecular Sciences. 2021 ; 22 1-12 art. 12381.[citado 2024 out. 16 ] Available from: https://doi.org/10.3390/ijms222212381
  • Source: Frontiers in Microbiology. Unidades: FCF, ICB

    Subjects: ANTIMALÁRICOS, PLASMODIUM FALCIPARUM, POTÁSSIO

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      SANTOS, Benedito Matheus dos et al. The knockout for G protein-coupled receptor-like PfSR25 increases the susceptibility of malaria parasites to the antimalarials lumefantrine and piperaquine but not to medicine for malaria venture compounds. Frontiers in Microbiology, v. 12, p. 1-12 art. 638869, 2021Tradução . . Disponível em: https://doi.org/10.3389/fmicb.2021.638869. Acesso em: 16 out. 2024.
    • APA

      Santos, B. M. dos, Dias, B. K. de M., Nakabashi, M., & Garcia, C. R. da S. (2021). The knockout for G protein-coupled receptor-like PfSR25 increases the susceptibility of malaria parasites to the antimalarials lumefantrine and piperaquine but not to medicine for malaria venture compounds. Frontiers in Microbiology, 12, 1-12 art. 638869. doi:10.3389/fmicb.2021.638869
    • NLM

      Santos BM dos, Dias BK de M, Nakabashi M, Garcia CR da S. The knockout for G protein-coupled receptor-like PfSR25 increases the susceptibility of malaria parasites to the antimalarials lumefantrine and piperaquine but not to medicine for malaria venture compounds [Internet]. Frontiers in Microbiology. 2021 ; 12 1-12 art. 638869.[citado 2024 out. 16 ] Available from: https://doi.org/10.3389/fmicb.2021.638869
    • Vancouver

      Santos BM dos, Dias BK de M, Nakabashi M, Garcia CR da S. The knockout for G protein-coupled receptor-like PfSR25 increases the susceptibility of malaria parasites to the antimalarials lumefantrine and piperaquine but not to medicine for malaria venture compounds [Internet]. Frontiers in Microbiology. 2021 ; 12 1-12 art. 638869.[citado 2024 out. 16 ] Available from: https://doi.org/10.3389/fmicb.2021.638869
  • Source: International Journal of Molecular Sciences. Unidade: FCF

    Subjects: PROTOZOA, MITOCÔNDRIAS

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      SCARPELLI, Pedro H e PECENIN, Mateus Fila e GARCIA, Célia Regina da Silva. Intracellular Ca2+ signaling in protozoan parasites: an overview with a focus on mitochondria. International Journal of Molecular Sciences, v. 22, p. 1-12 art. 469, 2021Tradução . . Disponível em: https://doi.org/10.3390/ijms22010469. Acesso em: 16 out. 2024.
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      Scarpelli, P. H., Pecenin, M. F., & Garcia, C. R. da S. (2021). Intracellular Ca2+ signaling in protozoan parasites: an overview with a focus on mitochondria. International Journal of Molecular Sciences, 22, 1-12 art. 469. doi:10.3390/ijms22010469
    • NLM

      Scarpelli PH, Pecenin MF, Garcia CR da S. Intracellular Ca2+ signaling in protozoan parasites: an overview with a focus on mitochondria [Internet]. International Journal of Molecular Sciences. 2021 ; 22 1-12 art. 469.[citado 2024 out. 16 ] Available from: https://doi.org/10.3390/ijms22010469
    • Vancouver

      Scarpelli PH, Pecenin MF, Garcia CR da S. Intracellular Ca2+ signaling in protozoan parasites: an overview with a focus on mitochondria [Internet]. International Journal of Molecular Sciences. 2021 ; 22 1-12 art. 469.[citado 2024 out. 16 ] Available from: https://doi.org/10.3390/ijms22010469
  • Source: Molecules. Unidades: IQ, FCF

    Subjects: ANTIPARASITÁRIOS, PORFIRINAS

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      DEDA, Daiana K et al. Porphyrin derivative nanoformulations for therapy and antiparasitic agents. Molecules, v. 25, n. 9, p. 1-31 art. 2080, 2020Tradução . . Disponível em: https://doi.org/10.3390/molecules25092080. Acesso em: 16 out. 2024.
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      Deda, D. K., Iglesias, B. A., Alves, E., Araki, K., & Garcia, C. R. da S. (2020). Porphyrin derivative nanoformulations for therapy and antiparasitic agents. Molecules, 25( 9), 1-31 art. 2080. doi:10.3390/molecules25092080
    • NLM

      Deda DK, Iglesias BA, Alves E, Araki K, Garcia CR da S. Porphyrin derivative nanoformulations for therapy and antiparasitic agents [Internet]. Molecules. 2020 ; 25( 9): 1-31 art. 2080.[citado 2024 out. 16 ] Available from: https://doi.org/10.3390/molecules25092080
    • Vancouver

      Deda DK, Iglesias BA, Alves E, Araki K, Garcia CR da S. Porphyrin derivative nanoformulations for therapy and antiparasitic agents [Internet]. Molecules. 2020 ; 25( 9): 1-31 art. 2080.[citado 2024 out. 16 ] Available from: https://doi.org/10.3390/molecules25092080
  • Source: Biomolecules. Unidade: FCF

    Subjects: PLASMODIUM FALCIPARUM, MALÁRIA

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      SANTOS, Benedito M. dos et al. Plasmodium falciparum knockout for the GPCR-Like PfSR25 receptor displays greater susceptibility to 1,2,3-triazole compounds that block malaria parasite development. Biomolecules, v. 10, p. 1-14 art. 1197, 2020Tradução . . Disponível em: https://doi.org/10.3390/biom10081197. Acesso em: 16 out. 2024.
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      Santos, B. M. dos, Gonzaga, D. T. G., Silva, F. C. da, Ferreira, V. F., & Garcia, C. R. da S. (2020). Plasmodium falciparum knockout for the GPCR-Like PfSR25 receptor displays greater susceptibility to 1,2,3-triazole compounds that block malaria parasite development. Biomolecules, 10, 1-14 art. 1197. doi:10.3390/biom10081197
    • NLM

      Santos BM dos, Gonzaga DTG, Silva FC da, Ferreira VF, Garcia CR da S. Plasmodium falciparum knockout for the GPCR-Like PfSR25 receptor displays greater susceptibility to 1,2,3-triazole compounds that block malaria parasite development [Internet]. Biomolecules. 2020 ; 10 1-14 art. 1197.[citado 2024 out. 16 ] Available from: https://doi.org/10.3390/biom10081197
    • Vancouver

      Santos BM dos, Gonzaga DTG, Silva FC da, Ferreira VF, Garcia CR da S. Plasmodium falciparum knockout for the GPCR-Like PfSR25 receptor displays greater susceptibility to 1,2,3-triazole compounds that block malaria parasite development [Internet]. Biomolecules. 2020 ; 10 1-14 art. 1197.[citado 2024 out. 16 ] Available from: https://doi.org/10.3390/biom10081197
  • Source: Biomolecules. Unidades: FCF, ICB

    Subjects: PLASMODIUM FALCIPARUM, MELATONINA

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      SINGH, Maneesh Kumar e DIAS, Bárbara Karina de Menezes e GARCIA, Célia Regina da Silva. Role of melatonin in the synchronization of asexual forms in the parasite Plasmodium falciparum. Biomolecules, v. 10, p. 1-16 art. 1243, 2020Tradução . . Disponível em: https://doi.org/10.3390/biom10091243. Acesso em: 16 out. 2024.
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      Singh, M. K., Dias, B. K. de M., & Garcia, C. R. da S. (2020). Role of melatonin in the synchronization of asexual forms in the parasite Plasmodium falciparum. Biomolecules, 10, 1-16 art. 1243. doi:10.3390/biom10091243
    • NLM

      Singh MK, Dias BK de M, Garcia CR da S. Role of melatonin in the synchronization of asexual forms in the parasite Plasmodium falciparum [Internet]. Biomolecules. 2020 ; 10 1-16 art. 1243.[citado 2024 out. 16 ] Available from: https://doi.org/10.3390/biom10091243
    • Vancouver

      Singh MK, Dias BK de M, Garcia CR da S. Role of melatonin in the synchronization of asexual forms in the parasite Plasmodium falciparum [Internet]. Biomolecules. 2020 ; 10 1-16 art. 1243.[citado 2024 out. 16 ] Available from: https://doi.org/10.3390/biom10091243
  • Source: International Journal of Molecular Sciences. Unidade: IB

    Subjects: MALÁRIA, PLASMODIUM, MELATONINA, RITMO CIRCADIANO, EXPRESSÃO GÊNICA, PARASITISMO

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      KOYAMA, Fernanda C et al. Melatonin-induced temporal Up-regulation of gene expression related to Ubiquitin/Proteasome System (UPS) in the human malaria parasite Plasmodium falciparum. International Journal of Molecular Sciences, v. 15, n. 12, p. 22320-22330, 2014Tradução . . Disponível em: https://doi.org/10.3390/ijms151222320. Acesso em: 16 out. 2024.
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      Koyama, F. C., Azevedo, M. F., Budu, A., Chakrabarti, D., & Garcia, C. R. da S. (2014). Melatonin-induced temporal Up-regulation of gene expression related to Ubiquitin/Proteasome System (UPS) in the human malaria parasite Plasmodium falciparum. International Journal of Molecular Sciences, 15( 12), 22320-22330. doi:10.3390/ijms151222320
    • NLM

      Koyama FC, Azevedo MF, Budu A, Chakrabarti D, Garcia CR da S. Melatonin-induced temporal Up-regulation of gene expression related to Ubiquitin/Proteasome System (UPS) in the human malaria parasite Plasmodium falciparum [Internet]. International Journal of Molecular Sciences. 2014 ; 15( 12): 22320-22330.[citado 2024 out. 16 ] Available from: https://doi.org/10.3390/ijms151222320
    • Vancouver

      Koyama FC, Azevedo MF, Budu A, Chakrabarti D, Garcia CR da S. Melatonin-induced temporal Up-regulation of gene expression related to Ubiquitin/Proteasome System (UPS) in the human malaria parasite Plasmodium falciparum [Internet]. International Journal of Molecular Sciences. 2014 ; 15( 12): 22320-22330.[citado 2024 out. 16 ] Available from: https://doi.org/10.3390/ijms151222320
  • Source: Pharmacology. Unidade: IB

    Subjects: ENZIMAS, FISIOLOGIA ANIMAL

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      FERREIRA, Zulma S et al. P2Y, receptor activation enhances the rate of rat pinealocyte-induced extracellular acidification via a calcium-dependent mechanism. Pharmacology, v. 69, n. 1, p. 33-37, 2003Tradução . . Acesso em: 16 out. 2024.
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      Ferreira, Z. S., Garcia, C. R. da S., Spray, D. C., & Markus, R. P. (2003). P2Y, receptor activation enhances the rate of rat pinealocyte-induced extracellular acidification via a calcium-dependent mechanism. Pharmacology, 69( 1), 33-37.
    • NLM

      Ferreira ZS, Garcia CR da S, Spray DC, Markus RP. P2Y, receptor activation enhances the rate of rat pinealocyte-induced extracellular acidification via a calcium-dependent mechanism. Pharmacology. 2003 ; 69( 1): 33-37.[citado 2024 out. 16 ]
    • Vancouver

      Ferreira ZS, Garcia CR da S, Spray DC, Markus RP. P2Y, receptor activation enhances the rate of rat pinealocyte-induced extracellular acidification via a calcium-dependent mechanism. Pharmacology. 2003 ; 69( 1): 33-37.[citado 2024 out. 16 ]
  • Source: Experientia. Unidade: IB

    Subjects: INFECÇÕES POR PROTOZOÁRIOS, PLASMODIUM

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      DLUZEWSKI, A R e GARCIA, Célia Regina da Silva. Inhibition of invasion and intraerythrocytic development of plasmodium falciparum by kinase inhibitors. Experientia, v. 52, p. 621-3, 1996Tradução . . Disponível em: https://doi.org/10.1007/bf01969742. Acesso em: 16 out. 2024.
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      Dluzewski, A. R., & Garcia, C. R. da S. (1996). Inhibition of invasion and intraerythrocytic development of plasmodium falciparum by kinase inhibitors. Experientia, 52, 621-3. doi:10.1007/bf01969742
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      Dluzewski AR, Garcia CR da S. Inhibition of invasion and intraerythrocytic development of plasmodium falciparum by kinase inhibitors [Internet]. Experientia. 1996 ;52 621-3.[citado 2024 out. 16 ] Available from: https://doi.org/10.1007/bf01969742
    • Vancouver

      Dluzewski AR, Garcia CR da S. Inhibition of invasion and intraerythrocytic development of plasmodium falciparum by kinase inhibitors [Internet]. Experientia. 1996 ;52 621-3.[citado 2024 out. 16 ] Available from: https://doi.org/10.1007/bf01969742

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