Filtros : "Hayashi, M. A. F" Limpar

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  • Source: Toxicon. Unidade: FMRP

    Subjects: PEPTÍDEOS, VENENOS, ERITRÓCITOS, PLASMODIUM FALCIPARUM

    Acesso à fonteDOIHow to cite
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    • ABNT

      EL CHAMY MALUF, S. et al. South American rattlesnake cationic polypeptide crotamine trafficking dynamic in Plasmodium falciparum-infected erythrocytes: pharmacological inhibitors, parasite cycle and incubation time influences in uptake. Toxicon, v. 208, p. 47-52, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.toxicon.2022.01.006. Acesso em: 21 maio 2024.
    • APA

      El Chamy Maluf, S., Hayashi, M. A. F., Campeiro, J. D., Oliveira, E. B. de, Gazarini, M. L., & Carmona, A. K. (2022). South American rattlesnake cationic polypeptide crotamine trafficking dynamic in Plasmodium falciparum-infected erythrocytes: pharmacological inhibitors, parasite cycle and incubation time influences in uptake. Toxicon, 208, 47-52. doi:10.1016/j.toxicon.2022.01.006
    • NLM

      El Chamy Maluf S, Hayashi MAF, Campeiro JD, Oliveira EB de, Gazarini ML, Carmona AK. South American rattlesnake cationic polypeptide crotamine trafficking dynamic in Plasmodium falciparum-infected erythrocytes: pharmacological inhibitors, parasite cycle and incubation time influences in uptake [Internet]. Toxicon. 2022 ; 208 47-52.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.toxicon.2022.01.006
    • Vancouver

      El Chamy Maluf S, Hayashi MAF, Campeiro JD, Oliveira EB de, Gazarini ML, Carmona AK. South American rattlesnake cationic polypeptide crotamine trafficking dynamic in Plasmodium falciparum-infected erythrocytes: pharmacological inhibitors, parasite cycle and incubation time influences in uptake [Internet]. Toxicon. 2022 ; 208 47-52.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.toxicon.2022.01.006
  • Source: Biochemical Pharmacology. Unidades: ICB, IQ

    Subjects: ANGIOTENSINAS, RECEPTORES DE ACETILCOLINA, ÓXIDO NÍTRICO

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    • ABNT

      MORAIS, K. L. P et al. Bj-PRO-5a, a natural angiotensin-converting enzyme inhibitor, promotes vasodilatation mediated by both bradykinin 'B IND. 2' and M1 muscarinic acetylcholine receptors. Biochemical Pharmacology, v. 81, n. 6, p. 736-742, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.bcp.2010.12.016. Acesso em: 21 maio 2024.
    • APA

      Morais, K. L. P., Hayashi, M. A. F., Bruni, F. M., Lopes-Ferreira, M., Camargo, A. C. M., Ulrich, H., & Lameu, C. (2011). Bj-PRO-5a, a natural angiotensin-converting enzyme inhibitor, promotes vasodilatation mediated by both bradykinin 'B IND. 2' and M1 muscarinic acetylcholine receptors. Biochemical Pharmacology, 81( 6), 736-742. doi:10.1016/j.bcp.2010.12.016
    • NLM

      Morais KLP, Hayashi MAF, Bruni FM, Lopes-Ferreira M, Camargo ACM, Ulrich H, Lameu C. Bj-PRO-5a, a natural angiotensin-converting enzyme inhibitor, promotes vasodilatation mediated by both bradykinin 'B IND. 2' and M1 muscarinic acetylcholine receptors [Internet]. Biochemical Pharmacology. 2011 ; 81( 6): 736-742.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.bcp.2010.12.016
    • Vancouver

      Morais KLP, Hayashi MAF, Bruni FM, Lopes-Ferreira M, Camargo ACM, Ulrich H, Lameu C. Bj-PRO-5a, a natural angiotensin-converting enzyme inhibitor, promotes vasodilatation mediated by both bradykinin 'B IND. 2' and M1 muscarinic acetylcholine receptors [Internet]. Biochemical Pharmacology. 2011 ; 81( 6): 736-742.[citado 2024 maio 21 ] Available from: https://doi.org/10.1016/j.bcp.2010.12.016

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