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Filtros : "Pharmacological Research" Limpar

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  • Artigo de periodico

    DF2755A, a novel non-competitive allosteric inhibitor of CXCR1/2, reduces inflammatory and post-operative pain (2016)

    Lopes, Alexandre H.; Brandolini, Laura; Aramini, Andrea; Bianchini, Gianluca; Silva, Rangel L.; Zaperlon, Ana C.; Verri Júnior, Waldiceu Aparecido; Alves Filho, José Carlos Farias; Cunha, Fernando de Queiroz; Teixeira, Mauro M.; Allegretti, Marcello; Cunha, Thiago Mattar

    Source: Pharmacological Research. Unidade: FMRP

    Subjects: DOR, COMPLICAÇÕES PÓS-OPERATÓRIAS, QUIMIOCINAS, NEUTRÓFILOS, QUIMIOTAXIA

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    • ABNT

      LOPES, Alexandre H. et al. DF2755A, a novel non-competitive allosteric inhibitor of CXCR1/2, reduces inflammatory and post-operative pain. Pharmacological Research, v. 103, p. 69-79, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.phrs.2015.11.005. Acesso em: 19 abr. 2024.

    • APA

      Lopes, A. H., Brandolini, L., Aramini, A., Bianchini, G., Silva, R. L., Zaperlon, A. C., et al. (2016). DF2755A, a novel non-competitive allosteric inhibitor of CXCR1/2, reduces inflammatory and post-operative pain. Pharmacological Research, 103, 69-79. doi:10.1016/j.phrs.2015.11.005

    • NLM

      Lopes AH, Brandolini L, Aramini A, Bianchini G, Silva RL, Zaperlon AC, Verri Júnior WA, Alves Filho JCF, Cunha F de Q, Teixeira MM, Allegretti M, Cunha TM. DF2755A, a novel non-competitive allosteric inhibitor of CXCR1/2, reduces inflammatory and post-operative pain [Internet]. Pharmacological Research. 2016 ; 103 69-79.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2015.11.005

    • Vancouver

      Lopes AH, Brandolini L, Aramini A, Bianchini G, Silva RL, Zaperlon AC, Verri Júnior WA, Alves Filho JCF, Cunha F de Q, Teixeira MM, Allegretti M, Cunha TM. DF2755A, a novel non-competitive allosteric inhibitor of CXCR1/2, reduces inflammatory and post-operative pain [Internet]. Pharmacological Research. 2016 ; 103 69-79.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2015.11.005

  • Artigo de periodico

    Pharmacological opportunities to control inflammatory diseases through inhibition of the leukocyte recruitment (2016)

    Peres, Raphael S.; Menezes, Gustavo B.; Teixeira, Mauro Martins; Cunha, Fernando de Queiroz

    Source: Pharmacological Research. Unidade: FMRP

    Subjects: ANTI-INFLAMATÓRIOS, LEUCÓCITOS, INFLAMAÇÃO, QUIMIOCINAS, TRANSDUÇÃO DE SINAL CELULAR

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    • ABNT

      PERES, Raphael S. et al. Pharmacological opportunities to control inflammatory diseases through inhibition of the leukocyte recruitment. Pharmacological Research, v. 112, p. 37-48, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.phrs.2016.01.015. Acesso em: 19 abr. 2024.

    • APA

      Peres, R. S., Menezes, G. B., Teixeira, M. M., & Cunha, F. de Q. (2016). Pharmacological opportunities to control inflammatory diseases through inhibition of the leukocyte recruitment. Pharmacological Research, 112, 37-48. doi:10.1016/j.phrs.2016.01.015

    • NLM

      Peres RS, Menezes GB, Teixeira MM, Cunha F de Q. Pharmacological opportunities to control inflammatory diseases through inhibition of the leukocyte recruitment [Internet]. Pharmacological Research. 2016 ; 112 37-48.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2016.01.015

    • Vancouver

      Peres RS, Menezes GB, Teixeira MM, Cunha F de Q. Pharmacological opportunities to control inflammatory diseases through inhibition of the leukocyte recruitment [Internet]. Pharmacological Research. 2016 ; 112 37-48.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2016.01.015

  • Artigo de periodico

    Cannabidiol, neuroprotection and neuropsychiatric disorders (2016)

    Campos, Alline Cristina de; Fogaça, Manoela V; Sonego, Andreza B.; Guimarães, Francisco Silveira

    Source: Pharmacological Research. Unidade: FMRP

    Subjects: DOENÇAS CEREBRAIS, TRANSTORNOS MENTAIS, FARMACOTERAPIA, CANABINOIDES

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    • ABNT

      CAMPOS, Alline Cristina de et al. Cannabidiol, neuroprotection and neuropsychiatric disorders. Pharmacological Research, v. 112, p. 119-127, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.phrs.2016.01.033. Acesso em: 19 abr. 2024.

    • APA

      Campos, A. C. de, Fogaça, M. V., Sonego, A. B., & Guimarães, F. S. (2016). Cannabidiol, neuroprotection and neuropsychiatric disorders. Pharmacological Research, 112, 119-127. doi:10.1016/j.phrs.2016.01.033

    • NLM

      Campos AC de, Fogaça MV, Sonego AB, Guimarães FS. Cannabidiol, neuroprotection and neuropsychiatric disorders [Internet]. Pharmacological Research. 2016 ; 112 119-127.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2016.01.033

    • Vancouver

      Campos AC de, Fogaça MV, Sonego AB, Guimarães FS. Cannabidiol, neuroprotection and neuropsychiatric disorders [Internet]. Pharmacological Research. 2016 ; 112 119-127.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2016.01.033

  • Artigo de periodico

    C5a and pain development: an old molecule, a new target (2016)

    Quadros, Andreza U.; Cunha, Thiago Mattar

    Source: Pharmacological Research. Unidade: FMRP

    Subjects: ANALGÉSICOS, INFLAMAÇÃO, TRANSDUÇÃO DE SINAL CELULAR, DOR CRÔNICA

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    • ABNT

      QUADROS, Andreza U. e CUNHA, Thiago Mattar. C5a and pain development: an old molecule, a new target. Pharmacological Research, v. 112, p. 58-67, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.phrs.2016.02.004. Acesso em: 19 abr. 2024.

    • APA

      Quadros, A. U., & Cunha, T. M. (2016). C5a and pain development: an old molecule, a new target. Pharmacological Research, 112, 58-67. doi:10.1016/j.phrs.2016.02.004

    • NLM

      Quadros AU, Cunha TM. C5a and pain development: an old molecule, a new target [Internet]. Pharmacological Research. 2016 ; 112 58-67.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2016.02.004

    • Vancouver

      Quadros AU, Cunha TM. C5a and pain development: an old molecule, a new target [Internet]. Pharmacological Research. 2016 ; 112 58-67.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2016.02.004

  • Artigo de periodico

    Vemurafenib resistance increases melanoma invasiveness and modulates the tumor microenvironment by MMP-2 upregulation (2016)

    Sandri, Silvana; Flores, Fernanda Faião; Tiago, Manoela; Pennacchi, Paula Comune; Massaro, Renato Ramos; Fernandes, Débora Kristina Alves; Berardinelli, Gustavo Nóriz; Evangelista, Adriane Feijó; Vazquez, Vinicius de Lima; Reis, Rui Manuel; Maria-Engler, Silvya Stuchi

    Source: Pharmacological Research. Unidade: FCF

    Subjects: METALOPROTEINASES, MELANOMA

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    • ABNT

      SANDRI, Silvana et al. Vemurafenib resistance increases melanoma invasiveness and modulates the tumor microenvironment by MMP-2 upregulation. Pharmacological Research, v. 111, p. 523-533, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.phrs.2016.07.017. Acesso em: 19 abr. 2024.

    • APA

      Sandri, S., Flores, F. F., Tiago, M., Pennacchi, P. C., Massaro, R. R., Fernandes, D. K. A., et al. (2016). Vemurafenib resistance increases melanoma invasiveness and modulates the tumor microenvironment by MMP-2 upregulation. Pharmacological Research, 111, 523-533. doi:10.1016/j.phrs.2016.07.017

    • NLM

      Sandri S, Flores FF, Tiago M, Pennacchi PC, Massaro RR, Fernandes DKA, Berardinelli GN, Evangelista AF, Vazquez V de L, Reis RM, Maria-Engler SS. Vemurafenib resistance increases melanoma invasiveness and modulates the tumor microenvironment by MMP-2 upregulation [Internet]. Pharmacological Research. 2016 ; 111 523-533.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2016.07.017

    • Vancouver

      Sandri S, Flores FF, Tiago M, Pennacchi PC, Massaro RR, Fernandes DKA, Berardinelli GN, Evangelista AF, Vazquez V de L, Reis RM, Maria-Engler SS. Vemurafenib resistance increases melanoma invasiveness and modulates the tumor microenvironment by MMP-2 upregulation [Internet]. Pharmacological Research. 2016 ; 111 523-533.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2016.07.017

  • Artigo de periodico

    Microenvironment and autophagy cross-talk: implications in cancer therapy (2016)

    Gomes, Luciana R.; Vessoni, Alexandre T.; Menck, Carlos Frederico Martins

    Source: Pharmacological Research. Unidade: ICB

    Assunto: MICROBIOLOGIA

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    • ABNT

      GOMES, Luciana R. e VESSONI, Alexandre T. e MENCK, Carlos Frederico Martins. Microenvironment and autophagy cross-talk: implications in cancer therapy. Pharmacological Research, v. 107, p. 300-307, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.phrs.2016.03.031. Acesso em: 19 abr. 2024.

    • APA

      Gomes, L. R., Vessoni, A. T., & Menck, C. F. M. (2016). Microenvironment and autophagy cross-talk: implications in cancer therapy. Pharmacological Research, 107, 300-307. doi:10.1016/j.phrs.2016.03.031

    • NLM

      Gomes LR, Vessoni AT, Menck CFM. Microenvironment and autophagy cross-talk: implications in cancer therapy [Internet]. Pharmacological Research. 2016 ; 107 300-307.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2016.03.031

    • Vancouver

      Gomes LR, Vessoni AT, Menck CFM. Microenvironment and autophagy cross-talk: implications in cancer therapy [Internet]. Pharmacological Research. 2016 ; 107 300-307.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2016.03.031

  • Artigo de periodico

    Hydrogen sulfide donors alleviate itch secondary to the activation of type-2 protease activated receptors (PAR-2) in mice (2016)

    Coavoy-Sanchez, S. A.; Rodrigues, L.; Teixeira, S. A.; Soares, A. G.; Torregrossa, R.; Wood, M. E.; Whiteman, M.; Costa, Soraia Katia Pereira ; Muscará, Marcelo Nicolás

    Source: Pharmacological Research. Unidade: ICB

    Assunto: FARMACOLOGIA

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    • ABNT

      COAVOY-SANCHEZ, S. A. et al. Hydrogen sulfide donors alleviate itch secondary to the activation of type-2 protease activated receptors (PAR-2) in mice. Pharmacological Research, v. 113, p. 686-694, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.phrs.2016.09.030. Acesso em: 19 abr. 2024.

    • APA

      Coavoy-Sanchez, S. A., Rodrigues, L., Teixeira, S. A., Soares, A. G., Torregrossa, R., Wood, M. E., et al. (2016). Hydrogen sulfide donors alleviate itch secondary to the activation of type-2 protease activated receptors (PAR-2) in mice. Pharmacological Research, 113, 686-694. doi:10.1016/j.phrs.2016.09.030

    • NLM

      Coavoy-Sanchez SA, Rodrigues L, Teixeira SA, Soares AG, Torregrossa R, Wood ME, Whiteman M, Costa SKP, Muscará MN. Hydrogen sulfide donors alleviate itch secondary to the activation of type-2 protease activated receptors (PAR-2) in mice [Internet]. Pharmacological Research. 2016 ; 113 686-694.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2016.09.030

    • Vancouver

      Coavoy-Sanchez SA, Rodrigues L, Teixeira SA, Soares AG, Torregrossa R, Wood ME, Whiteman M, Costa SKP, Muscará MN. Hydrogen sulfide donors alleviate itch secondary to the activation of type-2 protease activated receptors (PAR-2) in mice [Internet]. Pharmacological Research. 2016 ; 113 686-694.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2016.09.030

  • Artigo de periodico

    Aorta from angiotensin II hypertensive mice exhibit preserved nitroxyl anion mediated relaxation responses (2012)

    Wynne, Brandi M.; Labazi, Hicham; Tostes, Rita de Cassia Aleixo; Webb, R. Clinton

    Source: Pharmacological Research. Unidade: FMRP

    Subjects: AORTA, ANGIOTENSINA II, HIPERTENSÃO, ÓXIDO NÍTRICO

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    • ABNT

      WYNNE, Brandi M. et al. Aorta from angiotensin II hypertensive mice exhibit preserved nitroxyl anion mediated relaxation responses. Pharmacological Research, v. 65, n. 1, p. 41-47, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.phrs.2011.07.002. Acesso em: 19 abr. 2024.

    • APA

      Wynne, B. M., Labazi, H., Tostes, R. de C. A., & Webb, R. C. (2012). Aorta from angiotensin II hypertensive mice exhibit preserved nitroxyl anion mediated relaxation responses. Pharmacological Research, 65( 1), 41-47. doi:10.1016/j.phrs.2011.07.002

    • NLM

      Wynne BM, Labazi H, Tostes R de CA, Webb RC. Aorta from angiotensin II hypertensive mice exhibit preserved nitroxyl anion mediated relaxation responses [Internet]. Pharmacological Research. 2012 ; 65( 1): 41-47.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2011.07.002

    • Vancouver

      Wynne BM, Labazi H, Tostes R de CA, Webb RC. Aorta from angiotensin II hypertensive mice exhibit preserved nitroxyl anion mediated relaxation responses [Internet]. Pharmacological Research. 2012 ; 65( 1): 41-47.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2011.07.002

  • Artigo de periodico

    Alterations in vaso constrictor responses to the endothelium-derived contracting factor uridine adenosine tetraphosphate are region specific in DOCA-salt hypertensive rats (2012)

    Matsumoto, Takayuki; Tostes, Rita de Cassia Aleixo; Webb, R. Clinton

    Source: Pharmacological Research. Unidade: FMRP

    Subjects: HIPERTENSÃO, NUCLEOTÍDEOS, FÁRMACOS (SISTEMA CARDIOVASCULAR)

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    • ABNT

      MATSUMOTO, Takayuki e TOSTES, Rita de Cassia Aleixo e WEBB, R. Clinton. Alterations in vaso constrictor responses to the endothelium-derived contracting factor uridine adenosine tetraphosphate are region specific in DOCA-salt hypertensive rats. Pharmacological Research, v. 65, n. 1, p. 81-90, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.phrs.2011.09.005. Acesso em: 19 abr. 2024.

    • APA

      Matsumoto, T., Tostes, R. de C. A., & Webb, R. C. (2012). Alterations in vaso constrictor responses to the endothelium-derived contracting factor uridine adenosine tetraphosphate are region specific in DOCA-salt hypertensive rats. Pharmacological Research, 65( 1), 81-90. doi:10.1016/j.phrs.2011.09.005

    • NLM

      Matsumoto T, Tostes R de CA, Webb RC. Alterations in vaso constrictor responses to the endothelium-derived contracting factor uridine adenosine tetraphosphate are region specific in DOCA-salt hypertensive rats [Internet]. Pharmacological Research. 2012 ; 65( 1): 81-90.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2011.09.005

    • Vancouver

      Matsumoto T, Tostes R de CA, Webb RC. Alterations in vaso constrictor responses to the endothelium-derived contracting factor uridine adenosine tetraphosphate are region specific in DOCA-salt hypertensive rats [Internet]. Pharmacological Research. 2012 ; 65( 1): 81-90.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2011.09.005

  • Artigo de periodico

    Impaired β-adrenoceptor-induced relaxation in small mesenteric arteries from DOCA-salt hypertensive rats is due to reduced Kca channel activity (2012)

    Matsumoto, Takayuki; Szasz, Theodora; Tostes, Rita de Cassia Aleixo; Webb, R. Clinton

    Source: Pharmacological Research. Unidade: FMRP

    Subjects: VASODILATAÇÃO, ADRENORECEPTORES, ARTÉRIAS, HIPERTENSÃO

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    • ABNT

      MATSUMOTO, Takayuki et al. Impaired β-adrenoceptor-induced relaxation in small mesenteric arteries from DOCA-salt hypertensive rats is due to reduced Kca channel activity. Pharmacological Research, v. 65, n. 5, p. 537-545, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.phrs.2012.02.004. Acesso em: 19 abr. 2024.

    • APA

      Matsumoto, T., Szasz, T., Tostes, R. de C. A., & Webb, R. C. (2012). Impaired β-adrenoceptor-induced relaxation in small mesenteric arteries from DOCA-salt hypertensive rats is due to reduced Kca channel activity. Pharmacological Research, 65( 5), 537-545. doi:10.1016/j.phrs.2012.02.004

    • NLM

      Matsumoto T, Szasz T, Tostes R de CA, Webb RC. Impaired β-adrenoceptor-induced relaxation in small mesenteric arteries from DOCA-salt hypertensive rats is due to reduced Kca channel activity [Internet]. Pharmacological Research. 2012 ; 65( 5): 537-545.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2012.02.004

    • Vancouver

      Matsumoto T, Szasz T, Tostes R de CA, Webb RC. Impaired β-adrenoceptor-induced relaxation in small mesenteric arteries from DOCA-salt hypertensive rats is due to reduced Kca channel activity [Internet]. Pharmacological Research. 2012 ; 65( 5): 537-545.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2012.02.004

  • Artigo de periodico

    Matrix metalloproteinases: targets for doxycycline to prevent the vascular alterations of hypertension (2011)

    Castro, Michele M.; Tanus-Santos, José Eduardo; Gerlach, Raquel Fernanda

    Source: Pharmacological Research. Unidades: FMRP, FORP

    Subjects: HIPERTENSÃO, METALOPROTEINASES

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    • ABNT

      CASTRO, Michele M. e TANUS-SANTOS, José Eduardo e GERLACH, Raquel Fernanda. Matrix metalloproteinases: targets for doxycycline to prevent the vascular alterations of hypertension. Pharmacological Research, v. 64, n. 6, p. 567-572, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.phrs.2011.04.002. Acesso em: 19 abr. 2024.

    • APA

      Castro, M. M., Tanus-Santos, J. E., & Gerlach, R. F. (2011). Matrix metalloproteinases: targets for doxycycline to prevent the vascular alterations of hypertension. Pharmacological Research, 64( 6), 567-572. doi:10.1016/j.phrs.2011.04.002

    • NLM

      Castro MM, Tanus-Santos JE, Gerlach RF. Matrix metalloproteinases: targets for doxycycline to prevent the vascular alterations of hypertension [Internet]. Pharmacological Research. 2011 ; 64( 6): 567-572.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2011.04.002

    • Vancouver

      Castro MM, Tanus-Santos JE, Gerlach RF. Matrix metalloproteinases: targets for doxycycline to prevent the vascular alterations of hypertension [Internet]. Pharmacological Research. 2011 ; 64( 6): 567-572.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2011.04.002

  • Artigo de periodico

    The activity of medicinal plants and secondary metabolites on eosinophilic (2010)

    Rogerio, Alexandre de Paula; Nunes, Anderson de Sá ; Faccioli, Lucia Helena

    Source: Pharmacological Research. Unidades: ICB, FCFRP

    Subjects: PLANTAS MEDICINAIS (ESTUDO;PROPRIEDADES), ALERGIA E IMUNOLOGIA, LEUCÓCITOS

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    • ABNT

      ROGERIO, Alexandre de Paula e NUNES, Anderson de Sá e FACCIOLI, Lucia Helena. The activity of medicinal plants and secondary metabolites on eosinophilic. Pharmacological Research, v. 62, n. 4, p. 298-307, 2010Tradução . . Acesso em: 19 abr. 2024.

    • APA

      Rogerio, A. de P., Nunes, A. de S., & Faccioli, L. H. (2010). The activity of medicinal plants and secondary metabolites on eosinophilic. Pharmacological Research, 62( 4), 298-307.

    • NLM

      Rogerio A de P, Nunes A de S, Faccioli LH. The activity of medicinal plants and secondary metabolites on eosinophilic. Pharmacological Research. 2010 ; 62( 4): 298-307.[citado 2024 abr. 19 ]

    • Vancouver

      Rogerio A de P, Nunes A de S, Faccioli LH. The activity of medicinal plants and secondary metabolites on eosinophilic. Pharmacological Research. 2010 ; 62( 4): 298-307.[citado 2024 abr. 19 ]

  • Artigo de periodico

    Cannabidiol injected into the bed nucleus of the stria terminalis modulates baroreflex activity through 5-HT1A receptors (2010)

    Alves, Fernando H. F.; Crestani, Carlos C.; Gomes, Felipe V.; Guimarães, Francisco Silveira; Corrêa, Fernando Morgan de Aguiar; Resstel, Leonardo Barbosa Moraes

    Source: Pharmacological Research. Unidade: FMRP

    Subjects: CANNABIS, NEUROTRANSMISSORES, SEROTONINA

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    • ABNT

      ALVES, Fernando H. F. et al. Cannabidiol injected into the bed nucleus of the stria terminalis modulates baroreflex activity through 5-HT1A receptors. Pharmacological Research, v. 62, n. 3, p. 228-236, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.phrs.2010.05.003. Acesso em: 19 abr. 2024.

    • APA

      Alves, F. H. F., Crestani, C. C., Gomes, F. V., Guimarães, F. S., Corrêa, F. M. de A., & Resstel, L. B. M. (2010). Cannabidiol injected into the bed nucleus of the stria terminalis modulates baroreflex activity through 5-HT1A receptors. Pharmacological Research, 62( 3), 228-236. doi:10.1016/j.phrs.2010.05.003

    • NLM

      Alves FHF, Crestani CC, Gomes FV, Guimarães FS, Corrêa FM de A, Resstel LBM. Cannabidiol injected into the bed nucleus of the stria terminalis modulates baroreflex activity through 5-HT1A receptors [Internet]. Pharmacological Research. 2010 ; 62( 3): 228-236.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2010.05.003

    • Vancouver

      Alves FHF, Crestani CC, Gomes FV, Guimarães FS, Corrêa FM de A, Resstel LBM. Cannabidiol injected into the bed nucleus of the stria terminalis modulates baroreflex activity through 5-HT1A receptors [Internet]. Pharmacological Research. 2010 ; 62( 3): 228-236.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2010.05.003

  • Artigo de periodico

    Total stenosis triggers compensatory responsiveness of carotid and basilar arteries to endothelin-1 and phenylephrine (2008)

    Andrade, Claudia Roberta de; Tirapelli, Carlos Renato; Corrêa, Fernando Morgan de Aguiar; Ramalho, Leandra Naíra Zambelli; Oliveira, Ana Maria de

    Source: Pharmacological Research. Unidades: FMRP, EERP, FCFRP

    Subjects: ANTIOXIDANTES, EXTRATOS (FORMAS FARMACÊUTICAS), PLANTAS

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    • ABNT

      ANDRADE, Claudia Roberta de et al. Total stenosis triggers compensatory responsiveness of carotid and basilar arteries to endothelin-1 and phenylephrine. Pharmacological Research, v. 57, n. 1, p. 32-42, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.phrs.2007.10.009. Acesso em: 19 abr. 2024.

    • APA

      Andrade, C. R. de, Tirapelli, C. R., Corrêa, F. M. de A., Ramalho, L. N. Z., & Oliveira, A. M. de. (2008). Total stenosis triggers compensatory responsiveness of carotid and basilar arteries to endothelin-1 and phenylephrine. Pharmacological Research, 57( 1), 32-42. doi:10.1016/j.phrs.2007.10.009

    • NLM

      Andrade CR de, Tirapelli CR, Corrêa FM de A, Ramalho LNZ, Oliveira AM de. Total stenosis triggers compensatory responsiveness of carotid and basilar arteries to endothelin-1 and phenylephrine [Internet]. Pharmacological Research. 2008 ; 57( 1): 32-42.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2007.10.009

    • Vancouver

      Andrade CR de, Tirapelli CR, Corrêa FM de A, Ramalho LNZ, Oliveira AM de. Total stenosis triggers compensatory responsiveness of carotid and basilar arteries to endothelin-1 and phenylephrine [Internet]. Pharmacological Research. 2008 ; 57( 1): 32-42.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2007.10.009

  • Artigo de periodico

    Interaction of Vimang (Mangifera indica L. extract) with Fe(III) improves its antioxidant and cytoprotecting activity (2006)

    Pardo-Andreu, Gilberto L.; Sánchez-Baldoquín, Carlos; Ávila González, Rizette; Yamamoto, Edgar T. Suzuki; Revilla, Andrés; Uyemura, Sérgio Akira; Naal, Zeki; Delgado, René; Curti, Carlos

    Source: Pharmacological Research. Unidade: FCFRP

    Subjects: EXTRATOS (FORMAS FARMACÊUTICAS), PLANTAS, ANTIOXIDANTES, FERRO

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    • ABNT

      PARDO-ANDREU, Gilberto L. et al. Interaction of Vimang (Mangifera indica L. extract) with Fe(III) improves its antioxidant and cytoprotecting activity. Pharmacological Research, n. 5, p. 389-395, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.phrs.2006.08.001. Acesso em: 19 abr. 2024.

    • APA

      Pardo-Andreu, G. L., Sánchez-Baldoquín, C., Ávila González, R., Yamamoto, E. T. S., Revilla, A., Uyemura, S. A., et al. (2006). Interaction of Vimang (Mangifera indica L. extract) with Fe(III) improves its antioxidant and cytoprotecting activity. Pharmacological Research, ( 5), 389-395. doi:10.1016/j.phrs.2006.08.001

    • NLM

      Pardo-Andreu GL, Sánchez-Baldoquín C, Ávila González R, Yamamoto ETS, Revilla A, Uyemura SA, Naal Z, Delgado R, Curti C. Interaction of Vimang (Mangifera indica L. extract) with Fe(III) improves its antioxidant and cytoprotecting activity [Internet]. Pharmacological Research. 2006 ;( 5): 389-395.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2006.08.001

    • Vancouver

      Pardo-Andreu GL, Sánchez-Baldoquín C, Ávila González R, Yamamoto ETS, Revilla A, Uyemura SA, Naal Z, Delgado R, Curti C. Interaction of Vimang (Mangifera indica L. extract) with Fe(III) improves its antioxidant and cytoprotecting activity [Internet]. Pharmacological Research. 2006 ;( 5): 389-395.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2006.08.001

  • Artigo de periodico

    Mangifera indica L. extract (Vimang) inhibits 'Fe POT 2+'-citrate-induced lipoperoxidation in isolated rat liver mitochondria (2005)

    Andreu, Gilberto Pardo; Delgado, René; Velho, Jorge; Inada, Natalia M.; Curti, Carlos; Vercesi, Anibal Eugenio

    Source: Pharmacological Research. Unidade: FCFRP

    Subjects: METABOLISMO, BIOENERGÉTICA

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    • ABNT

      ANDREU, Gilberto Pardo et al. Mangifera indica L. extract (Vimang) inhibits 'Fe POT 2+'-citrate-induced lipoperoxidation in isolated rat liver mitochondria. Pharmacological Research, v. 51, p. 427-435, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.phrs.2004.11.002. Acesso em: 19 abr. 2024.

    • APA

      Andreu, G. P., Delgado, R., Velho, J., Inada, N. M., Curti, C., & Vercesi, A. E. (2005). Mangifera indica L. extract (Vimang) inhibits 'Fe POT 2+'-citrate-induced lipoperoxidation in isolated rat liver mitochondria. Pharmacological Research, 51, 427-435. doi:10.1016/j.phrs.2004.11.002

    • NLM

      Andreu GP, Delgado R, Velho J, Inada NM, Curti C, Vercesi AE. Mangifera indica L. extract (Vimang) inhibits 'Fe POT 2+'-citrate-induced lipoperoxidation in isolated rat liver mitochondria [Internet]. Pharmacological Research. 2005 ;51 427-435.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2004.11.002

    • Vancouver

      Andreu GP, Delgado R, Velho J, Inada NM, Curti C, Vercesi AE. Mangifera indica L. extract (Vimang) inhibits 'Fe POT 2+'-citrate-induced lipoperoxidation in isolated rat liver mitochondria [Internet]. Pharmacological Research. 2005 ;51 427-435.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2004.11.002

  • Artigo de periodico

    Effects of sibutramine on anxiety-related behaviours in rats (2004)

    Jorge, Salim Demétrio; Pobbe, Roger Luís Henschel; Soares, Vanessa de Paula; Oliveira, Ana Maria de; Zangrossi Júnior, Hélio

    Source: Pharmacological Research. Unidades: FCFRP, FMRP

    Subjects: TRANSTORNO DO PÂNICO, FARMACOLOGIA

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    • ABNT

      JORGE, Salim Demétrio et al. Effects of sibutramine on anxiety-related behaviours in rats. Pharmacological Research, v. 50, p. 517-522, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.phrs.2004.05.003. Acesso em: 19 abr. 2024.

    • APA

      Jorge, S. D., Pobbe, R. L. H., Soares, V. de P., Oliveira, A. M. de, & Zangrossi Júnior, H. (2004). Effects of sibutramine on anxiety-related behaviours in rats. Pharmacological Research, 50, 517-522. doi:10.1016/j.phrs.2004.05.003

    • NLM

      Jorge SD, Pobbe RLH, Soares V de P, Oliveira AM de, Zangrossi Júnior H. Effects of sibutramine on anxiety-related behaviours in rats [Internet]. Pharmacological Research. 2004 ; 50 517-522.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2004.05.003

    • Vancouver

      Jorge SD, Pobbe RLH, Soares V de P, Oliveira AM de, Zangrossi Júnior H. Effects of sibutramine on anxiety-related behaviours in rats [Internet]. Pharmacological Research. 2004 ; 50 517-522.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/j.phrs.2004.05.003

  • Artigo de jornal

    Comparison of the cytotoxicity of two nitroheterociclic drugs (NHCD) towards transformed and non-transformed cells (2003)

    Rossa, Marcelo M.; Rocha-e-Sillva, Thomaz A. A.; Terruggi, Cristina H. B.; Tedesco, Antônio Cláudio; Selistre-de- Araújo, Heloisa S.; Borissevich, Iouri E.; Degterev, Igor A.

    Source: Pharmacological Research. Unidade: FFCLRP

    Assunto: FARMACOLOGIA

    How to cite
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    • ABNT

      ROSSA, Marcelo M. et al. Comparison of the cytotoxicity of two nitroheterociclic drugs (NHCD) towards transformed and non-transformed cells. Tradução . Pharmacological Research, London, 2003. , v. 48, p. 369-375. Acesso em: 19 abr. 2024.

    • APA

      Rossa, M. M., Rocha-e-Sillva, T. A. A., Terruggi, C. H. B., Tedesco, A. C., Selistre-de- Araújo, H. S., Borissevich, I. E., & Degterev, I. A. (2003). Comparison of the cytotoxicity of two nitroheterociclic drugs (NHCD) towards transformed and non-transformed cells. Pharmacological Research, p. 369-375. London: Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo.

    • NLM

      Rossa MM, Rocha-e-Sillva TAA, Terruggi CHB, Tedesco AC, Selistre-de- Araújo HS, Borissevich IE, Degterev IA. Comparison of the cytotoxicity of two nitroheterociclic drugs (NHCD) towards transformed and non-transformed cells. Pharmacological Research. 2003 ; 48 369-375.[citado 2024 abr. 19 ]

    • Vancouver

      Rossa MM, Rocha-e-Sillva TAA, Terruggi CHB, Tedesco AC, Selistre-de- Araújo HS, Borissevich IE, Degterev IA. Comparison of the cytotoxicity of two nitroheterociclic drugs (NHCD) towards transformed and non-transformed cells. Pharmacological Research. 2003 ; 48 369-375.[citado 2024 abr. 19 ]

  • Artigo de periodico

    The effects of oral glutamine on cisplatin-induced nephrotoxicity in rats (2003)

    Mora, Luciana de Oliveira; Antunes, Lusânia Maria Greggi; Francescato, Heloísa Della Coletta; Bianchi, Maria de Lourdes Pires

    Source: Pharmacological Research. Unidade: FCFRP

    Assunto: MICROBIOLOGIA

    Acesso à fonteDOIHow to cite
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    • ABNT

      MORA, Luciana de Oliveira et al. The effects of oral glutamine on cisplatin-induced nephrotoxicity in rats. Pharmacological Research, v. 47, p. 517-522, 2003Tradução . . Disponível em: https://doi.org/10.1016/s1043-6618(03)00040-9. Acesso em: 19 abr. 2024.

    • APA

      Mora, L. de O., Antunes, L. M. G., Francescato, H. D. C., & Bianchi, M. de L. P. (2003). The effects of oral glutamine on cisplatin-induced nephrotoxicity in rats. Pharmacological Research, 47, 517-522. doi:10.1016/s1043-6618(03)00040-9

    • NLM

      Mora L de O, Antunes LMG, Francescato HDC, Bianchi M de LP. The effects of oral glutamine on cisplatin-induced nephrotoxicity in rats [Internet]. Pharmacological Research. 2003 ; 47 517-522.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/s1043-6618(03)00040-9

    • Vancouver

      Mora L de O, Antunes LMG, Francescato HDC, Bianchi M de LP. The effects of oral glutamine on cisplatin-induced nephrotoxicity in rats [Internet]. Pharmacological Research. 2003 ; 47 517-522.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/s1043-6618(03)00040-9

  • Artigo de periodico

    Determination of paroxetine in geriatric depression by high-performance liquid chromatography (2003)

    Zainaghi, Isis Amaral; Lanchote, Vera Lúcia; Queiroz, Regina Helena Costa

    Source: Pharmacological Research. Unidades: FM, FCFRP

    Assunto: QUÍMICA ANALÍTICA

    Acesso à fonteDOIHow to cite
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    • ABNT

      ZAINAGHI, Isis Amaral e LANCHOTE, Vera Lúcia e QUEIROZ, Regina Helena Costa. Determination of paroxetine in geriatric depression by high-performance liquid chromatography. Pharmacological Research, v. 48, p. 217-221, 2003Tradução . . Disponível em: https://doi.org/10.1016/s1043-6618(03)00098-7. Acesso em: 19 abr. 2024.

    • APA

      Zainaghi, I. A., Lanchote, V. L., & Queiroz, R. H. C. (2003). Determination of paroxetine in geriatric depression by high-performance liquid chromatography. Pharmacological Research, 48, 217-221. doi:10.1016/s1043-6618(03)00098-7

    • NLM

      Zainaghi IA, Lanchote VL, Queiroz RHC. Determination of paroxetine in geriatric depression by high-performance liquid chromatography [Internet]. Pharmacological Research. 2003 ; 48 217-221.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/s1043-6618(03)00098-7

    • Vancouver

      Zainaghi IA, Lanchote VL, Queiroz RHC. Determination of paroxetine in geriatric depression by high-performance liquid chromatography [Internet]. Pharmacological Research. 2003 ; 48 217-221.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1016/s1043-6618(03)00098-7

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