Filtros : "Indexado no Scopus" "Passaglia, Rita de Cassia Aleixo Tostes" Limpar

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  • Source: Revista Brasileira de Farmacognosia. Unidade: FMRP

    Subjects: PEQUI, CALMODULINA, COMPOSTOS FENÓLICOS, ENDOTÉLIO

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    • ABNT

      OLIVEIRA, Lais Moraes de et al. Caryocar brasiliense induces vasorelaxation through endothelial Ca2+/calmodulin and PI3K/Akt/eNOS-dependent signaling pathways in rats. Revista Brasileira de Farmacognosia, v. 28, n. 6, p. 678-685, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.bjp.2018.07.007. Acesso em: 30 ago. 2024.
    • APA

      Oliveira, L. M. de, Oliveira, T. S. de, Costa, R. M. da, Martins, J. L. R., Freitas, C. S. de, Gil, E. de S., et al. (2018). Caryocar brasiliense induces vasorelaxation through endothelial Ca2+/calmodulin and PI3K/Akt/eNOS-dependent signaling pathways in rats. Revista Brasileira de Farmacognosia, 28( 6), 678-685. doi:10.1016/j.bjp.2018.07.007
    • NLM

      Oliveira LM de, Oliveira TS de, Costa RM da, Martins JLR, Freitas CS de, Gil E de S, Costa EA, Passaglia R de CAT, Vaz BG, Filgueira FP, Ghedini PC. Caryocar brasiliense induces vasorelaxation through endothelial Ca2+/calmodulin and PI3K/Akt/eNOS-dependent signaling pathways in rats [Internet]. Revista Brasileira de Farmacognosia. 2018 ; 28( 6): 678-685.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.bjp.2018.07.007
    • Vancouver

      Oliveira LM de, Oliveira TS de, Costa RM da, Martins JLR, Freitas CS de, Gil E de S, Costa EA, Passaglia R de CAT, Vaz BG, Filgueira FP, Ghedini PC. Caryocar brasiliense induces vasorelaxation through endothelial Ca2+/calmodulin and PI3K/Akt/eNOS-dependent signaling pathways in rats [Internet]. Revista Brasileira de Farmacognosia. 2018 ; 28( 6): 678-685.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.bjp.2018.07.007
  • Source: Journal of the American Society of Hypertension. Unidade: FMRP

    Subjects: HIPERTENSÃO, ALDEÍDOS

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    • ABNT

      CHOI, Hyehun e PASSAGLIA, Rita de Cassia Aleixo Tostes e WEBB, R. Clinton. Mitochondrial aldehyde dehydrogenase prevents ROS-induced vascular contraction in angiotensin-II hypertensive mice. Journal of the American Society of Hypertension, v. 5, n. 3, p. 154-160, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.jash.2011.02.005. Acesso em: 30 ago. 2024.
    • APA

      Choi, H., Passaglia, R. de C. A. T., & Webb, R. C. (2011). Mitochondrial aldehyde dehydrogenase prevents ROS-induced vascular contraction in angiotensin-II hypertensive mice. Journal of the American Society of Hypertension, 5( 3), 154-160. doi:10.1016/j.jash.2011.02.005
    • NLM

      Choi H, Passaglia R de CAT, Webb RC. Mitochondrial aldehyde dehydrogenase prevents ROS-induced vascular contraction in angiotensin-II hypertensive mice [Internet]. Journal of the American Society of Hypertension. 2011 ; 5( 3): 154-160.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.jash.2011.02.005
    • Vancouver

      Choi H, Passaglia R de CAT, Webb RC. Mitochondrial aldehyde dehydrogenase prevents ROS-induced vascular contraction in angiotensin-II hypertensive mice [Internet]. Journal of the American Society of Hypertension. 2011 ; 5( 3): 154-160.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1016/j.jash.2011.02.005
  • Source: Journal of Cardiovascular Pharmacology. Unidade: FMRP

    Subjects: SISTEMA CARDIOVASCULAR, PROTEÍNAS QUINASES

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    • ABNT

      CHOI, Hyehun e PASSAGLIA, Rita de Cassia Aleixo Tostes e WEBB, R. Clinton. S-nitrosylation inhibits protein kinase C-mediated contraction in mouse aorta. Journal of Cardiovascular Pharmacology, v. 57, n. 1, p. 65-71, 2011Tradução . . Acesso em: 30 ago. 2024.
    • APA

      Choi, H., Passaglia, R. de C. A. T., & Webb, R. C. (2011). S-nitrosylation inhibits protein kinase C-mediated contraction in mouse aorta. Journal of Cardiovascular Pharmacology, 57( 1), 65-71.
    • NLM

      Choi H, Passaglia R de CAT, Webb RC. S-nitrosylation inhibits protein kinase C-mediated contraction in mouse aorta. Journal of Cardiovascular Pharmacology. 2011 ; 57( 1): 65-71.[citado 2024 ago. 30 ]
    • Vancouver

      Choi H, Passaglia R de CAT, Webb RC. S-nitrosylation inhibits protein kinase C-mediated contraction in mouse aorta. Journal of Cardiovascular Pharmacology. 2011 ; 57( 1): 65-71.[citado 2024 ago. 30 ]
  • Source: American Journal of Physiology: Regulatory, Integrative and Comparative Physiology. Unidade: FMRP

    Subjects: SISTEMA CARDIOVASCULAR, ENDOTELINAS

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    • ABNT

      LIMA, Victor Vitorino et al. O-GlcNAcylation: a novel pathway contributing to the effects of endothelin in the vasculature. American Journal of Physiology: Regulatory, Integrative and Comparative Physiology, v. 300, n. 2, p. R236-R250, 2011Tradução . . Disponível em: https://doi.org/10.1152/ajpregu.00230.2010. Acesso em: 30 ago. 2024.
    • APA

      Lima, V. V., Giachini, F. R., Hardy, D. M., Webb, R. C., & Passaglia, R. de C. A. T. (2011). O-GlcNAcylation: a novel pathway contributing to the effects of endothelin in the vasculature. American Journal of Physiology: Regulatory, Integrative and Comparative Physiology, 300( 2), R236-R250. doi:10.1152/ajpregu.00230.2010
    • NLM

      Lima VV, Giachini FR, Hardy DM, Webb RC, Passaglia R de CAT. O-GlcNAcylation: a novel pathway contributing to the effects of endothelin in the vasculature [Internet]. American Journal of Physiology: Regulatory, Integrative and Comparative Physiology. 2011 ; 300( 2): R236-R250.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1152/ajpregu.00230.2010
    • Vancouver

      Lima VV, Giachini FR, Hardy DM, Webb RC, Passaglia R de CAT. O-GlcNAcylation: a novel pathway contributing to the effects of endothelin in the vasculature [Internet]. American Journal of Physiology: Regulatory, Integrative and Comparative Physiology. 2011 ; 300( 2): R236-R250.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1152/ajpregu.00230.2010
  • Source: Journal of Hypertension. Unidade: FMRP

    Subjects: RIM (DANOS), MAGNÉSIO, FÁRMACOS, INFLAMAÇÃO, PRESSÃO SANGUÍNEA

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    • ABNT

      YOGI, Álvaro et al. Dysregulation of renal transient receptor potential melastatin 6/7 but not paracellin-1 in aldosterone-induced hypertension and kidney damage in a model of hereditary hypomagnesemia. Journal of Hypertension, v. 29, n. 7, p. 1400-1410, 2011Tradução . . Disponível em: https://doi.org/10.1097/hjh.0b013e32834786d6. Acesso em: 30 ago. 2024.
    • APA

      Yogi, Á., Callera, G. E., O'Connor, S. E., He, Y., Corrêa, J. W., Passaglia, R. de C. A. T., et al. (2011). Dysregulation of renal transient receptor potential melastatin 6/7 but not paracellin-1 in aldosterone-induced hypertension and kidney damage in a model of hereditary hypomagnesemia. Journal of Hypertension, 29( 7), 1400-1410. doi:10.1097/hjh.0b013e32834786d6
    • NLM

      Yogi Á, Callera GE, O'Connor SE, He Y, Corrêa JW, Passaglia R de CAT, Mazur A, Touyz RM. Dysregulation of renal transient receptor potential melastatin 6/7 but not paracellin-1 in aldosterone-induced hypertension and kidney damage in a model of hereditary hypomagnesemia [Internet]. Journal of Hypertension. 2011 ; 29( 7): 1400-1410.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1097/hjh.0b013e32834786d6
    • Vancouver

      Yogi Á, Callera GE, O'Connor SE, He Y, Corrêa JW, Passaglia R de CAT, Mazur A, Touyz RM. Dysregulation of renal transient receptor potential melastatin 6/7 but not paracellin-1 in aldosterone-induced hypertension and kidney damage in a model of hereditary hypomagnesemia [Internet]. Journal of Hypertension. 2011 ; 29( 7): 1400-1410.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1097/hjh.0b013e32834786d6
  • Source: Circulation Journal. Unidade: FMRP

    Subjects: SISTEMA CARDIOVASCULAR, HIPERTENSÃO, MAGNÉSIO

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      YOGI, Álvaro et al. Transient receptor potential melastatin 7 (TRPM7) cation channels, magnesium and the vascular system in hypertension. Circulation Journal, v. 75, n. 2, p. 237-245, 2011Tradução . . Acesso em: 30 ago. 2024.
    • APA

      Yogi, Á., Callera, G. E., Antunes, T. T., Passaglia, R. de C. A. T., & Touyz, R. M. (2011). Transient receptor potential melastatin 7 (TRPM7) cation channels, magnesium and the vascular system in hypertension. Circulation Journal, 75( 2), 237-245.
    • NLM

      Yogi Á, Callera GE, Antunes TT, Passaglia R de CAT, Touyz RM. Transient receptor potential melastatin 7 (TRPM7) cation channels, magnesium and the vascular system in hypertension. Circulation Journal. 2011 ; 75( 2): 237-245.[citado 2024 ago. 30 ]
    • Vancouver

      Yogi Á, Callera GE, Antunes TT, Passaglia R de CAT, Touyz RM. Transient receptor potential melastatin 7 (TRPM7) cation channels, magnesium and the vascular system in hypertension. Circulation Journal. 2011 ; 75( 2): 237-245.[citado 2024 ago. 30 ]
  • Source: Cardiovascular Research. Unidade: FMRP

    Subjects: ALDOSTERONA, CÉLULAS MUSCULARES

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    • ABNT

      CALLERA, Gláucia Elena et al. Vascular proinflammatory responses by aldosterone are mediated via c-Src trafficking to cholesterol-rich microdomains: role of PDGFR. Cardiovascular Research, v. 91, n. 4, p. 720-731, 2011Tradução . . Disponível em: https://doi.org/10.1093/cvr/cvr131. Acesso em: 30 ago. 2024.
    • APA

      Callera, G. E., Yogi, Á., Briones, A. M., Montezano, A. C. I., He, Y., Passaglia, R. de C. A. T., et al. (2011). Vascular proinflammatory responses by aldosterone are mediated via c-Src trafficking to cholesterol-rich microdomains: role of PDGFR. Cardiovascular Research, 91( 4), 720-731. doi:10.1093/cvr/cvr131
    • NLM

      Callera GE, Yogi Á, Briones AM, Montezano ACI, He Y, Passaglia R de CAT, Schiffrin EL, Touyz RM. Vascular proinflammatory responses by aldosterone are mediated via c-Src trafficking to cholesterol-rich microdomains: role of PDGFR [Internet]. Cardiovascular Research. 2011 ; 91( 4): 720-731.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1093/cvr/cvr131
    • Vancouver

      Callera GE, Yogi Á, Briones AM, Montezano ACI, He Y, Passaglia R de CAT, Schiffrin EL, Touyz RM. Vascular proinflammatory responses by aldosterone are mediated via c-Src trafficking to cholesterol-rich microdomains: role of PDGFR [Internet]. Cardiovascular Research. 2011 ; 91( 4): 720-731.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1093/cvr/cvr131
  • Source: American Journal of Physiology: Heart and Circulatory Physiology. Unidade: FMRP

    Subjects: HIPERTENSÃO, ENDOTÉLIO, ANTAGONISTAS

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      MATSUMOTO, Takayuri e PASSAGLIA, Rita de Cassia Aleixo Tostes e WEBB, R. Clinton. Uridine adenosine tetraphosphate-induced contraction is increases in renal but not pulmonary arteries from DOCA-salt hypertensive rats. American Journal of Physiology: Heart and Circulatory Physiology, v. 301, n. 2, p. H409-H417, 2011Tradução . . Disponível em: https://doi.org/10.1152/ajpheart.00084.2011. Acesso em: 30 ago. 2024.
    • APA

      Matsumoto, T., Passaglia, R. de C. A. T., & Webb, R. C. (2011). Uridine adenosine tetraphosphate-induced contraction is increases in renal but not pulmonary arteries from DOCA-salt hypertensive rats. American Journal of Physiology: Heart and Circulatory Physiology, 301( 2), H409-H417. doi:10.1152/ajpheart.00084.2011
    • NLM

      Matsumoto T, Passaglia R de CAT, Webb RC. Uridine adenosine tetraphosphate-induced contraction is increases in renal but not pulmonary arteries from DOCA-salt hypertensive rats [Internet]. American Journal of Physiology: Heart and Circulatory Physiology. 2011 ; 301( 2): H409-H417.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1152/ajpheart.00084.2011
    • Vancouver

      Matsumoto T, Passaglia R de CAT, Webb RC. Uridine adenosine tetraphosphate-induced contraction is increases in renal but not pulmonary arteries from DOCA-salt hypertensive rats [Internet]. American Journal of Physiology: Heart and Circulatory Physiology. 2011 ; 301( 2): H409-H417.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1152/ajpheart.00084.2011
  • Source: Brazilaina Journal of Medical and Biological Research. Unidade: FMRP

    Assunto: CANAIS DE CÁLCIO

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      GIACHINI, Fernanda Regina Casagrande et al. STIM1/Orai1-mediated store-operated Ca2+ entry: the tip of the iceberg. Brazilaina Journal of Medical and Biological Research, v. 44, n. 11, p. 1080-1087, 2011Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2011007500133. Acesso em: 30 ago. 2024.
    • APA

      Giachini, F. R. C., Lima, V. V., Hannan, J., Carneiro, F. S., Webb, R. C., & Passaglia, R. de C. A. T. (2011). STIM1/Orai1-mediated store-operated Ca2+ entry: the tip of the iceberg. Brazilaina Journal of Medical and Biological Research, 44( 11), 1080-1087. doi:10.1590/s0100-879x2011007500133
    • NLM

      Giachini FRC, Lima VV, Hannan J, Carneiro FS, Webb RC, Passaglia R de CAT. STIM1/Orai1-mediated store-operated Ca2+ entry: the tip of the iceberg [Internet]. Brazilaina Journal of Medical and Biological Research. 2011 ; 44( 11): 1080-1087.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1590/s0100-879x2011007500133
    • Vancouver

      Giachini FRC, Lima VV, Hannan J, Carneiro FS, Webb RC, Passaglia R de CAT. STIM1/Orai1-mediated store-operated Ca2+ entry: the tip of the iceberg [Internet]. Brazilaina Journal of Medical and Biological Research. 2011 ; 44( 11): 1080-1087.[citado 2024 ago. 30 ] Available from: https://doi.org/10.1590/s0100-879x2011007500133

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