ReP USP - Resultado da busca

Artigo de periodico
Effects of treatment with a carbon monoxide donor and an activator of heme oxygenase 1 on the nociceptive, apoptotic and/or oxidative alterations induced by persistent inflammatory pain in the central nervous system of mice (2022)
Cazuza, Rafael A.; Batallé, Gerard; Bai, Xue; Leite-Panissi, Christie Ramos Andrade ; Pol, Olga
Fonte: Brain Research Bulletin. Unidade: FFCLRP
Assuntos: APOPTOSE, MONÓXIDO DE CARBONO, OXIGENASE, INFLAMAÇÃO, NOCICEPTIVIDADE, ESTRESSE OXIDATIVO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAZUZA, Rafael A. et al. Effects of treatment with a carbon monoxide donor and an activator of heme oxygenase 1 on the nociceptive, apoptotic and/or oxidative alterations induced by persistent inflammatory pain in the central nervous system of mice. Brain Research Bulletin, v. 188, n. 1, p. 169-178, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.brainresbull.2022.08.004. Acesso em: 05 nov. 2024.
APA
Cazuza, R. A., Batallé, G., Bai, X., Leite-Panissi, C. R. A., & Pol, O. (2022). Effects of treatment with a carbon monoxide donor and an activator of heme oxygenase 1 on the nociceptive, apoptotic and/or oxidative alterations induced by persistent inflammatory pain in the central nervous system of mice. Brain Research Bulletin, 188( 1), 169-178. doi:10.1016/j.brainresbull.2022.08.004
NLM
Cazuza RA, Batallé G, Bai X, Leite-Panissi CRA, Pol O. Effects of treatment with a carbon monoxide donor and an activator of heme oxygenase 1 on the nociceptive, apoptotic and/or oxidative alterations induced by persistent inflammatory pain in the central nervous system of mice [Internet]. Brain Research Bulletin. 2022 ; 188( 1): 169-178.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.brainresbull.2022.08.004
Vancouver
Cazuza RA, Batallé G, Bai X, Leite-Panissi CRA, Pol O. Effects of treatment with a carbon monoxide donor and an activator of heme oxygenase 1 on the nociceptive, apoptotic and/or oxidative alterations induced by persistent inflammatory pain in the central nervous system of mice [Internet]. Brain Research Bulletin. 2022 ; 188( 1): 169-178.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.brainresbull.2022.08.004
Artigo de periodico
Skeletal muscle heme oxygenase-1 activity regulates aerobic capacity (2021)
Souza, Rodrigo Wagner. Alves de ; Gallo, David; Lee, Ghee Rye; Katsuyama, Eri; Schaufler, Alexa; Weber, Janick; Csizmadia, Eva; Tsokos, George C; Koch, Lauren G; Britton, Steven L; Wisløff, Ulrik ; Brum, Patrícia Chakur ; Otterbein, Leo E
Fonte: Cell reports. Unidade: EEFE
Assuntos: OXIGENASE, MÚSCULO ESQUELÉTICO, CAPACIDADE AERÓBICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOUZA, Rodrigo Wagner. Alves de et al. Skeletal muscle heme oxygenase-1 activity regulates aerobic capacity. Cell reports, v. 35, n. 3, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.celrep.2021.109018. Acesso em: 05 nov. 2024.
APA
Souza, R. W. A. de, Gallo, D., Lee, G. R., Katsuyama, E., Schaufler, A., Weber, J., et al. (2021). Skeletal muscle heme oxygenase-1 activity regulates aerobic capacity. Cell reports, 35( 3). doi:10.1016/j.celrep.2021.109018
NLM
Souza RWA de, Gallo D, Lee GR, Katsuyama E, Schaufler A, Weber J, Csizmadia E, Tsokos GC, Koch LG, Britton SL, Wisløff U, Brum PC, Otterbein LE. Skeletal muscle heme oxygenase-1 activity regulates aerobic capacity [Internet]. Cell reports. 2021 ; 35( 3):[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.celrep.2021.109018
Vancouver
Souza RWA de, Gallo D, Lee GR, Katsuyama E, Schaufler A, Weber J, Csizmadia E, Tsokos GC, Koch LG, Britton SL, Wisløff U, Brum PC, Otterbein LE. Skeletal muscle heme oxygenase-1 activity regulates aerobic capacity [Internet]. Cell reports. 2021 ; 35( 3):[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.celrep.2021.109018
Artigo de periodico
HO-CO pathway activation may be associated with hippocampal μ and δ opioid receptors in inhibiting inflammatory pain aversiveness and nociception in WT but not NOS2-KO mice (2021)
Cazuza, Rafael A.; Arantes, Ana Luisa F.; Pol, Olga; Leite-Panissi, Christie Ramos Andrade
Fonte: Brain Research Bulletin. Unidade: FFCLRP
Assuntos: MONÓXIDO DE CARBONO, OXIGENASE, DOR, INFLAMAÇÃO, ÓXIDO NÍTRICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAZUZA, Rafael A. et al. HO-CO pathway activation may be associated with hippocampal μ and δ opioid receptors in inhibiting inflammatory pain aversiveness and nociception in WT but not NOS2-KO mice. Brain Research Bulletin, v. 169, p. 8-17, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.brainresbull.2021.01.002. Acesso em: 05 nov. 2024.
APA
Cazuza, R. A., Arantes, A. L. F., Pol, O., & Leite-Panissi, C. R. A. (2021). HO-CO pathway activation may be associated with hippocampal μ and δ opioid receptors in inhibiting inflammatory pain aversiveness and nociception in WT but not NOS2-KO mice. Brain Research Bulletin, 169, 8-17. doi:10.1016/j.brainresbull.2021.01.002
NLM
Cazuza RA, Arantes ALF, Pol O, Leite-Panissi CRA. HO-CO pathway activation may be associated with hippocampal μ and δ opioid receptors in inhibiting inflammatory pain aversiveness and nociception in WT but not NOS2-KO mice [Internet]. Brain Research Bulletin. 2021 ; 169 8-17.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.brainresbull.2021.01.002
Vancouver
Cazuza RA, Arantes ALF, Pol O, Leite-Panissi CRA. HO-CO pathway activation may be associated with hippocampal μ and δ opioid receptors in inhibiting inflammatory pain aversiveness and nociception in WT but not NOS2-KO mice [Internet]. Brain Research Bulletin. 2021 ; 169 8-17.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.brainresbull.2021.01.002
Artigo de periodico
Association of BDNF, HTR2A, TPH1, SLC6A4, and COMT polymorphisms with tDCS and escitalopram efficacy: ancillary analysis of a double-blind, placebo-controlled trial (2020)
Brunoni, Andre Russowsky ; Carracedo, Angel; Amigo, Olalla M; Pellicer, Ana L; Talib, Leda; Carvalho, Andre F; Lotufo, Paulo Andrade ; Benseñor, Isabela Judith Martins ; Gattaz, Wagner Farid ; Cappi, Carolina
Fonte: Brazilian journal of psychiatry. Unidade: FM
Assuntos: ANTIDEPRESSIVOS, DEPRESSÃO, MÉTODO DUPLO-CEGO, POLIMORFISMO, OXIGENASE, TERAPIA COMBINADA, TRANSFERASES, AMINAS (COMPOSTOS ORGÂNICOS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BRUNONI, Andre Russowsky et al. Association of BDNF, HTR2A, TPH1, SLC6A4, and COMT polymorphisms with tDCS and escitalopram efficacy: ancillary analysis of a double-blind, placebo-controlled trial. Brazilian journal of psychiatry, v. 42, n. 2, p. 128-135, 2020Tradução . . Disponível em: https://doi.org/10.1590/1516-4446-2019-0620. Acesso em: 05 nov. 2024.
APA
Brunoni, A. R., Carracedo, A., Amigo, O. M., Pellicer, A. L., Talib, L., Carvalho, A. F., et al. (2020). Association of BDNF, HTR2A, TPH1, SLC6A4, and COMT polymorphisms with tDCS and escitalopram efficacy: ancillary analysis of a double-blind, placebo-controlled trial. Brazilian journal of psychiatry, 42( 2), 128-135. doi:10.1590/1516-4446-2019-0620
NLM
Brunoni AR, Carracedo A, Amigo OM, Pellicer AL, Talib L, Carvalho AF, Lotufo PA, Benseñor IJM, Gattaz WF, Cappi C. Association of BDNF, HTR2A, TPH1, SLC6A4, and COMT polymorphisms with tDCS and escitalopram efficacy: ancillary analysis of a double-blind, placebo-controlled trial [Internet]. Brazilian journal of psychiatry. 2020 ; 42( 2): 128-135.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1590/1516-4446-2019-0620
Vancouver
Brunoni AR, Carracedo A, Amigo OM, Pellicer AL, Talib L, Carvalho AF, Lotufo PA, Benseñor IJM, Gattaz WF, Cappi C. Association of BDNF, HTR2A, TPH1, SLC6A4, and COMT polymorphisms with tDCS and escitalopram efficacy: ancillary analysis of a double-blind, placebo-controlled trial [Internet]. Brazilian journal of psychiatry. 2020 ; 42( 2): 128-135.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1590/1516-4446-2019-0620
Artigo de periodico
Modulation of inflammation and immune responses by heme oxygenase-1: implications for infection with intracellular pathogens (2020)
Costa, Diego Luís ; Amaral, Eduardo P.; Andrade, Bruno B.; Sher, Alan
Fonte: Antioxidants. Unidade: FMRP
Assuntos: OXIGENASE, INFLAMAÇÃO, SISTEMA IMUNE, DOENÇAS INFECCIOSAS, ENZIMAS, BIOMARCADORES, ANTIOXIDANTES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COSTA, Diego Luís et al. Modulation of inflammation and immune responses by heme oxygenase-1: implications for infection with intracellular pathogens. Antioxidants, v. 9, n. 12, p. 1-30, 2020Tradução . . Disponível em: https://doi.org/10.3390/antiox9121205. Acesso em: 05 nov. 2024.
APA
Costa, D. L., Amaral, E. P., Andrade, B. B., & Sher, A. (2020). Modulation of inflammation and immune responses by heme oxygenase-1: implications for infection with intracellular pathogens. Antioxidants, 9( 12), 1-30. doi:10.3390/antiox9121205
NLM
Costa DL, Amaral EP, Andrade BB, Sher A. Modulation of inflammation and immune responses by heme oxygenase-1: implications for infection with intracellular pathogens [Internet]. Antioxidants. 2020 ; 9( 12): 1-30.[citado 2024 nov. 05 ] Available from: https://doi.org/10.3390/antiox9121205
Vancouver
Costa DL, Amaral EP, Andrade BB, Sher A. Modulation of inflammation and immune responses by heme oxygenase-1: implications for infection with intracellular pathogens [Internet]. Antioxidants. 2020 ; 9( 12): 1-30.[citado 2024 nov. 05 ] Available from: https://doi.org/10.3390/antiox9121205
Artigo de periodico
Methyl farnesoate epoxidase (mfe) gene expression and juvenile hormone titers in the life cycle of a highly eusocial stingless bee, Melipona scutellaris (2017)
Cardoso Júnior, Carlos Antônio Mendes; Silva, Renato Pereira; Borges, Naiara Araújo; Carvalho, Washington João de; Walter, S. Leal; Simões, Zilá Luz Paulino; Bitondi, Márcia Maria Gentile; Vieira, Carlos Ueira; Bonetti, Ana Maria; Hartfelder, Klaus
Fonte: Journal of Insect Physiology. Unidades: FFCLRP, FMRP
Assuntos: OXIGENASE, ABELHAS, ANÁLISE DE SEQUÊNCIA DE DNA, PUPA, FILOGENIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARDOSO JÚNIOR, Carlos Antônio Mendes et al. Methyl farnesoate epoxidase (mfe) gene expression and juvenile hormone titers in the life cycle of a highly eusocial stingless bee, Melipona scutellaris. Journal of Insect Physiology, v. 101, p. 185-194, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.jinsphys.2017.08.001. Acesso em: 05 nov. 2024.
APA
Cardoso Júnior, C. A. M., Silva, R. P., Borges, N. A., Carvalho, W. J. de, Walter, S. L., Simões, Z. L. P., et al. (2017). Methyl farnesoate epoxidase (mfe) gene expression and juvenile hormone titers in the life cycle of a highly eusocial stingless bee, Melipona scutellaris. Journal of Insect Physiology, 101, 185-194. doi:10.1016/j.jinsphys.2017.08.001
NLM
Cardoso Júnior CAM, Silva RP, Borges NA, Carvalho WJ de, Walter SL, Simões ZLP, Bitondi MMG, Vieira CU, Bonetti AM, Hartfelder K. Methyl farnesoate epoxidase (mfe) gene expression and juvenile hormone titers in the life cycle of a highly eusocial stingless bee, Melipona scutellaris [Internet]. Journal of Insect Physiology. 2017 ; 101 185-194.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.jinsphys.2017.08.001
Vancouver
Cardoso Júnior CAM, Silva RP, Borges NA, Carvalho WJ de, Walter SL, Simões ZLP, Bitondi MMG, Vieira CU, Bonetti AM, Hartfelder K. Methyl farnesoate epoxidase (mfe) gene expression and juvenile hormone titers in the life cycle of a highly eusocial stingless bee, Melipona scutellaris [Internet]. Journal of Insect Physiology. 2017 ; 101 185-194.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.jinsphys.2017.08.001
Artigo de periodico
Nitric oxide donor [Ru(terpy)(bdq)NO]3+ induces uncoupling and phosphorylation of endothelial nitric oxide synthase promoting oxidant production (2017)
Potje, Simone R; Chend, Zhenlong; Oliveira, Suellen D’Arc S.; Bendhack, Lusiane Maria; Silva, Roberto Santana da; Bonini, Marcelo G.; Antoniali, Cristina; Minshall, Richard D
Fonte: Free Radical Biology and Medicine. Unidade: FCFRP
Assuntos: ÓXIDO NÍTRICO, ENDOTÉLIO, OXIGENASE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
POTJE, Simone R et al. Nitric oxide donor [Ru(terpy)(bdq)NO]3+ induces uncoupling and phosphorylation of endothelial nitric oxide synthase promoting oxidant production. Free Radical Biology and Medicine, v. 112, p. 587-596, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.freeradbiomed.2017.09.004. Acesso em: 05 nov. 2024.
APA
Potje, S. R., Chend, Z., Oliveira, S. D. ’A. S., Bendhack, L. M., Silva, R. S. da, Bonini, M. G., et al. (2017). Nitric oxide donor [Ru(terpy)(bdq)NO]3+ induces uncoupling and phosphorylation of endothelial nitric oxide synthase promoting oxidant production. Free Radical Biology and Medicine, 112, 587-596. doi:10.1016/j.freeradbiomed.2017.09.004
NLM
Potje SR, Chend Z, Oliveira SD’AS, Bendhack LM, Silva RS da, Bonini MG, Antoniali C, Minshall RD. Nitric oxide donor [Ru(terpy)(bdq)NO]3+ induces uncoupling and phosphorylation of endothelial nitric oxide synthase promoting oxidant production [Internet]. Free Radical Biology and Medicine. 2017 ; 112 587-596.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2017.09.004
Vancouver
Potje SR, Chend Z, Oliveira SD’AS, Bendhack LM, Silva RS da, Bonini MG, Antoniali C, Minshall RD. Nitric oxide donor [Ru(terpy)(bdq)NO]3+ induces uncoupling and phosphorylation of endothelial nitric oxide synthase promoting oxidant production [Internet]. Free Radical Biology and Medicine. 2017 ; 112 587-596.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2017.09.004
Artigo de periodico
Association of Heme Oxygenase 1 with Lung Protection in Malaria-Associated ALI/ARDS (2016)
Pereira, Marcelo Luís Monteiro; Ortolan, Luana dos Santos; Sercundes, Michelle Klein; Debone, Daniela; Murillo, Oscar; Lima, Flávia Afonso; Marinho, Claudio Romero Farias ; Epiphanio, Sabrina
Fonte: Mediators of Inflammation. Unidades: ICB, FCF
Assuntos: MALÁRIA, PARASITOLOGIA, OXIGENASE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PEREIRA, Marcelo Luís Monteiro et al. Association of Heme Oxygenase 1 with Lung Protection in Malaria-Associated ALI/ARDS. Mediators of Inflammation, p. 1-12 art. 4158698, 2016Tradução . . Disponível em: https://doi.org/10.1155/2016/4158698. Acesso em: 05 nov. 2024.
APA
Pereira, M. L. M., Ortolan, L. dos S., Sercundes, M. K., Debone, D., Murillo, O., Lima, F. A., et al. (2016). Association of Heme Oxygenase 1 with Lung Protection in Malaria-Associated ALI/ARDS. Mediators of Inflammation, 1-12 art. 4158698. doi:10.1155/2016/4158698
NLM
Pereira MLM, Ortolan L dos S, Sercundes MK, Debone D, Murillo O, Lima FA, Marinho CRF, Epiphanio S. Association of Heme Oxygenase 1 with Lung Protection in Malaria-Associated ALI/ARDS [Internet]. Mediators of Inflammation. 2016 ; 1-12 art. 4158698.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1155/2016/4158698
Vancouver
Pereira MLM, Ortolan L dos S, Sercundes MK, Debone D, Murillo O, Lima FA, Marinho CRF, Epiphanio S. Association of Heme Oxygenase 1 with Lung Protection in Malaria-Associated ALI/ARDS [Internet]. Mediators of Inflammation. 2016 ; 1-12 art. 4158698.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1155/2016/4158698
Artigo de periodico
Cyclo-oxygenase (COX) inhibitors for treating preterm labour (2015)
Reinebrant, Hanna E.; Pileggi-Castro, Cynthia; Romero, Carla L. T.; Santos, Rafaela A. N. dos; Kumar, Sailesh; Souza, João Paulo Dias de; Flenady, Vicki
Fonte: Cochrane Database of Systematic Reviews. Unidade: FMRP
Assuntos: GRAVIDEZ, TRABALHO DE PARTO PREMATURO, OXIGENASE, INIBIDORES QUÍMICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
REINEBRANT, Hanna E. et al. Cyclo-oxygenase (COX) inhibitors for treating preterm labour. Cochrane Database of Systematic Reviews, n. 6, 2015Tradução . . Disponível em: https://doi.org/10.1002/14651858.CD001992.pub3. Acesso em: 05 nov. 2024.
APA
Reinebrant, H. E., Pileggi-Castro, C., Romero, C. L. T., Santos, R. A. N. dos, Kumar, S., Souza, J. P. D. de, & Flenady, V. (2015). Cyclo-oxygenase (COX) inhibitors for treating preterm labour. Cochrane Database of Systematic Reviews, ( 6). doi:10.1002/14651858.CD001992.pub3
NLM
Reinebrant HE, Pileggi-Castro C, Romero CLT, Santos RAN dos, Kumar S, Souza JPD de, Flenady V. Cyclo-oxygenase (COX) inhibitors for treating preterm labour [Internet]. Cochrane Database of Systematic Reviews. 2015 ;( 6):[citado 2024 nov. 05 ] Available from: https://doi.org/10.1002/14651858.CD001992.pub3
Vancouver
Reinebrant HE, Pileggi-Castro C, Romero CLT, Santos RAN dos, Kumar S, Souza JPD de, Flenady V. Cyclo-oxygenase (COX) inhibitors for treating preterm labour [Internet]. Cochrane Database of Systematic Reviews. 2015 ;( 6):[citado 2024 nov. 05 ] Available from: https://doi.org/10.1002/14651858.CD001992.pub3
Artigo de periodico
Haeme oxygenase activity protects the host against excessive cardiac inflammation during experimental Trypanosoma cruzi infection (2014)
Gutierrez, Fredy R. S; Pavanelli, Wander R; Medina, Tiago S; Silva, Grace K; Mariano, Flávia S; Guedes, Paulo M. M.; Mineo, Tiago W. P.; Rossi, Marcos Antonio; Cunha, Fernando de Queiroz; Silva, João Santana da
Fonte: Microbes and Infection. Unidade: FMRP
Assuntos: TRYPANOSOMA CRUZI, OXIGENASE, LINFÓCITOS T
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GUTIERREZ, Fredy R. S et al. Haeme oxygenase activity protects the host against excessive cardiac inflammation during experimental Trypanosoma cruzi infection. Microbes and Infection, v. 16, n. 1, p. 28-39, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.micinf.2013.10.007. Acesso em: 05 nov. 2024.
APA
Gutierrez, F. R. S., Pavanelli, W. R., Medina, T. S., Silva, G. K., Mariano, F. S., Guedes, P. M. M., et al. (2014). Haeme oxygenase activity protects the host against excessive cardiac inflammation during experimental Trypanosoma cruzi infection. Microbes and Infection, 16( 1), 28-39. doi:10.1016/j.micinf.2013.10.007
NLM
Gutierrez FRS, Pavanelli WR, Medina TS, Silva GK, Mariano FS, Guedes PMM, Mineo TWP, Rossi MA, Cunha F de Q, Silva JS da. Haeme oxygenase activity protects the host against excessive cardiac inflammation during experimental Trypanosoma cruzi infection [Internet]. Microbes and Infection. 2014 ; 16( 1): 28-39.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.micinf.2013.10.007
Vancouver
Gutierrez FRS, Pavanelli WR, Medina TS, Silva GK, Mariano FS, Guedes PMM, Mineo TWP, Rossi MA, Cunha F de Q, Silva JS da. Haeme oxygenase activity protects the host against excessive cardiac inflammation during experimental Trypanosoma cruzi infection [Internet]. Microbes and Infection. 2014 ; 16( 1): 28-39.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.micinf.2013.10.007
Artigo de periodico
The flavonols quercetin, myricetin, kaempferol, and galangin inhibit the net oxygen consumption by immune complex stimulated human and rabbit neutrophils (2014)
Figueiredo-Rinhel, Andréa S. G.; Santos, Everton O. L.; Kabeya, Luciana M.; Azzolini, Ana Elisa Caleiro Seixas; Simões Ambrosio, Livia Maria Cordeiro; Lucisano-Valim, Yara Maria
Fonte: Zeitschrift fuer Naturforschung. Section C. Unidades: FCFRP, FMRP
Assuntos: OXIGENASE, NEUTRÓFILOS, FLAVONÓIDES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FIGUEIREDO-RINHEL, Andréa S. G. et al. The flavonols quercetin, myricetin, kaempferol, and galangin inhibit the net oxygen consumption by immune complex stimulated human and rabbit neutrophils. Zeitschrift fuer Naturforschung. Section C, v. 69c, n. 7-8, p. 346-356, 2014Tradução . . Disponível em: https://doi.org/10.5560/ZNC.2012-0122. Acesso em: 05 nov. 2024.
APA
Figueiredo-Rinhel, A. S. G., Santos, E. O. L., Kabeya, L. M., Azzolini, A. E. C. S., Simões Ambrosio, L. M. C., & Lucisano-Valim, Y. M. (2014). The flavonols quercetin, myricetin, kaempferol, and galangin inhibit the net oxygen consumption by immune complex stimulated human and rabbit neutrophils. Zeitschrift fuer Naturforschung. Section C, 69c( 7-8), 346-356. doi:10.5560/ZNC.2012-0122
NLM
Figueiredo-Rinhel ASG, Santos EOL, Kabeya LM, Azzolini AECS, Simões Ambrosio LMC, Lucisano-Valim YM. The flavonols quercetin, myricetin, kaempferol, and galangin inhibit the net oxygen consumption by immune complex stimulated human and rabbit neutrophils [Internet]. Zeitschrift fuer Naturforschung. Section C. 2014 ; 69c( 7-8): 346-356.[citado 2024 nov. 05 ] Available from: https://doi.org/10.5560/ZNC.2012-0122
Vancouver
Figueiredo-Rinhel ASG, Santos EOL, Kabeya LM, Azzolini AECS, Simões Ambrosio LMC, Lucisano-Valim YM. The flavonols quercetin, myricetin, kaempferol, and galangin inhibit the net oxygen consumption by immune complex stimulated human and rabbit neutrophils [Internet]. Zeitschrift fuer Naturforschung. Section C. 2014 ; 69c( 7-8): 346-356.[citado 2024 nov. 05 ] Available from: https://doi.org/10.5560/ZNC.2012-0122
Artigo de periodico
Heme oxygenase inhibition enhances neutrophil migration into the bronchoalveolar spaces and improves the outcome of murine pneumonia-induced sepsis (2013)
Czaikoski, Paula Giselle; Nascimento, Daniele Carvalho; Sônego, Fabiane; Freitas, Andressa de; Turato, Walter Miguel; Carvalho, Michel A. de; Santos, Raquel Souza; Oliveira, Gisele Pena de; Samary, Cynthia dos Santos; Tefe-Silva, Cristiane; Alves Filho, José Carlos Farias; Ferreira, Sérgio Henrique; Rossi, Marcos Antonio; Rocco, Patricia Rieken Macedo; Spiller, Fernando; Cunha, Fernando de Queiroz
Fonte: Shock. Unidades: FCF, FMRP
Assuntos: OXIGENASE, INIBIDORES DE ENZIMAS, NEUTRÓFILOS, SEPSE, PNEUMONIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CZAIKOSKI, Paula Giselle et al. Heme oxygenase inhibition enhances neutrophil migration into the bronchoalveolar spaces and improves the outcome of murine pneumonia-induced sepsis. Shock, v. 39, n. 4, p. 389-396, 2013Tradução . . Disponível em: https://doi.org/10.1097/SHK.0b013e31828bbcf9. Acesso em: 05 nov. 2024.
APA
Czaikoski, P. G., Nascimento, D. C., Sônego, F., Freitas, A. de, Turato, W. M., Carvalho, M. A. de, et al. (2013). Heme oxygenase inhibition enhances neutrophil migration into the bronchoalveolar spaces and improves the outcome of murine pneumonia-induced sepsis. Shock, 39( 4), 389-396. doi:10.1097/SHK.0b013e31828bbcf9
NLM
Czaikoski PG, Nascimento DC, Sônego F, Freitas A de, Turato WM, Carvalho MA de, Santos RS, Oliveira GP de, Samary C dos S, Tefe-Silva C, Alves Filho JCF, Ferreira SH, Rossi MA, Rocco PRM, Spiller F, Cunha F de Q. Heme oxygenase inhibition enhances neutrophil migration into the bronchoalveolar spaces and improves the outcome of murine pneumonia-induced sepsis [Internet]. Shock. 2013 ; 39( 4): 389-396.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1097/SHK.0b013e31828bbcf9
Vancouver
Czaikoski PG, Nascimento DC, Sônego F, Freitas A de, Turato WM, Carvalho MA de, Santos RS, Oliveira GP de, Samary C dos S, Tefe-Silva C, Alves Filho JCF, Ferreira SH, Rossi MA, Rocco PRM, Spiller F, Cunha F de Q. Heme oxygenase inhibition enhances neutrophil migration into the bronchoalveolar spaces and improves the outcome of murine pneumonia-induced sepsis [Internet]. Shock. 2013 ; 39( 4): 389-396.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1097/SHK.0b013e31828bbcf9
Artigo de periodico
P2X7 receptor activation contributes to an initial upstream mechanism of lipopolysaccharide-induced vascular dysfunction (2013)
Chiao, Chin-Wei; Santos, José Eduardo da Silva; Giachini, Fernanda R.; Tostes, Rita de Cássia Aleixo; Su, Ming‑Jai; Webb, R. Clinton
Fonte: Clinical Science. Unidade: FMRP
Assuntos: OXIGENASE, INTERLEUCINAS, LIPOPOLISSACARÍDEOS, ÓXIDO NÍTRICO, SEPSE, CITOCINAS, DOENÇAS VASCULARES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CHIAO, Chin-Wei et al. P2X7 receptor activation contributes to an initial upstream mechanism of lipopolysaccharide-induced vascular dysfunction. Clinical Science, v. 125, n. 3, p. 131-141, 2013Tradução . . Disponível em: https://doi.org/10.1042/CS20120479. Acesso em: 05 nov. 2024.
APA
Chiao, C. -W., Santos, J. E. da S., Giachini, F. R., Tostes, R. de C. A., Su, M. ‑J., & Webb, R. C. (2013). P2X7 receptor activation contributes to an initial upstream mechanism of lipopolysaccharide-induced vascular dysfunction. Clinical Science, 125( 3), 131-141. doi:10.1042/CS20120479
NLM
Chiao C-W, Santos JE da S, Giachini FR, Tostes R de CA, Su M‑J, Webb RC. P2X7 receptor activation contributes to an initial upstream mechanism of lipopolysaccharide-induced vascular dysfunction [Internet]. Clinical Science. 2013 ; 125( 3): 131-141.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1042/CS20120479
Vancouver
Chiao C-W, Santos JE da S, Giachini FR, Tostes R de CA, Su M‑J, Webb RC. P2X7 receptor activation contributes to an initial upstream mechanism of lipopolysaccharide-induced vascular dysfunction [Internet]. Clinical Science. 2013 ; 125( 3): 131-141.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1042/CS20120479
Artigo de periodico
3-Phenylcoumarin derivatives selectively modulate different steps of reactive oxygen species production by immune complex-stimulated human neutrophils (2013)
Andrade, Micássio F.; Kabeya, Luciana M.; Azzolini, Ana Elisa Caleiro Seixas; Santos, Everton O. L.; Figueiredo-Rinhel, Andréa Silva Garcia de; Paris, Márcio R. P.; Emery, Flavio da Silva; Pupo, Mônica Tallarico; Lucisano-Valim, Yara Maria
Fonte: International Immunopharmacology. Unidade: FCFRP
Assuntos: NEUTRÓFILOS, IMUNIDADE, OXIGÊNIO (ESPECIFICAÇÃO), OXIGENASE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ANDRADE, Micássio F. et al. 3-Phenylcoumarin derivatives selectively modulate different steps of reactive oxygen species production by immune complex-stimulated human neutrophils. International Immunopharmacology, v. 15, n. 2, p. 387-394, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.intimp.2013.01.001. Acesso em: 05 nov. 2024.
APA
Andrade, M. F., Kabeya, L. M., Azzolini, A. E. C. S., Santos, E. O. L., Figueiredo-Rinhel, A. S. G. de, Paris, M. R. P., et al. (2013). 3-Phenylcoumarin derivatives selectively modulate different steps of reactive oxygen species production by immune complex-stimulated human neutrophils. International Immunopharmacology, 15( 2), 387-394. doi:10.1016/j.intimp.2013.01.001
NLM
Andrade MF, Kabeya LM, Azzolini AECS, Santos EOL, Figueiredo-Rinhel ASG de, Paris MRP, Emery F da S, Pupo MT, Lucisano-Valim YM. 3-Phenylcoumarin derivatives selectively modulate different steps of reactive oxygen species production by immune complex-stimulated human neutrophils [Internet]. International Immunopharmacology. 2013 ; 15( 2): 387-394.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.intimp.2013.01.001
Vancouver
Andrade MF, Kabeya LM, Azzolini AECS, Santos EOL, Figueiredo-Rinhel ASG de, Paris MRP, Emery F da S, Pupo MT, Lucisano-Valim YM. 3-Phenylcoumarin derivatives selectively modulate different steps of reactive oxygen species production by immune complex-stimulated human neutrophils [Internet]. International Immunopharmacology. 2013 ; 15( 2): 387-394.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.intimp.2013.01.001
Artigo de periodico
Crystallization and preliminary X-ray diffraction analysis of recombinant chlorocatechol 1,2-dioxygenase from Pseudomonas putida (2011)
Rustiguel, Joane Kathelen; Pinheiro, Matheus Pinto; Araújo, Ana Paula Ulian de ; Nonato, Maria Cristina
Fonte: Acta Crystallographica F. Unidades: IFSC, FCFRP
Assuntos: MICROBIOLOGIA AMBIENTAL (ANÁLISE;TÉCNICAS), OXIGENASE, HIDROCARBONOS AROMÁTICOS, CRISTALOGRAFIA ESTRUTURAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RUSTIGUEL, Joane Kathelen et al. Crystallization and preliminary X-ray diffraction analysis of recombinant chlorocatechol 1,2-dioxygenase from Pseudomonas putida. Acta Crystallographica F, v. 67, p. 507-509, 2011Tradução . . Disponível em: https://doi.org/10.1107/S174430911100635X. Acesso em: 05 nov. 2024.
APA
Rustiguel, J. K., Pinheiro, M. P., Araújo, A. P. U. de, & Nonato, M. C. (2011). Crystallization and preliminary X-ray diffraction analysis of recombinant chlorocatechol 1,2-dioxygenase from Pseudomonas putida. Acta Crystallographica F, 67, 507-509. doi:10.1107/S174430911100635X
NLM
Rustiguel JK, Pinheiro MP, Araújo APU de, Nonato MC. Crystallization and preliminary X-ray diffraction analysis of recombinant chlorocatechol 1,2-dioxygenase from Pseudomonas putida [Internet]. Acta Crystallographica F. 2011 ; 67 507-509.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1107/S174430911100635X
Vancouver
Rustiguel JK, Pinheiro MP, Araújo APU de, Nonato MC. Crystallization and preliminary X-ray diffraction analysis of recombinant chlorocatechol 1,2-dioxygenase from Pseudomonas putida [Internet]. Acta Crystallographica F. 2011 ; 67 507-509.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1107/S174430911100635X
Trabalho de evento-resumo
Cloning, overexpression in Escherichia coli and purification of the Lacaase CotA from Bacillus subtilis (2008)
Ribeiro, L. F.; Furtado, G. P.; Ward, Richard John
Nome do evento: Annual Meeting of the Brazilian Society for Biochemistry and Molecular Biology (SBBQ). Unidade: FFCLRP
Assunto: OXIGENASE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIBEIRO, L. F. e FURTADO, G. P. e WARD, Richard John. Cloning, overexpression in Escherichia coli and purification of the Lacaase CotA from Bacillus subtilis. 2008, Anais.. São Paulo: SBBQ, 2008. . Acesso em: 05 nov. 2024.
APA
Ribeiro, L. F., Furtado, G. P., & Ward, R. J. (2008). Cloning, overexpression in Escherichia coli and purification of the Lacaase CotA from Bacillus subtilis. In . São Paulo: SBBQ.
NLM
Ribeiro LF, Furtado GP, Ward RJ. Cloning, overexpression in Escherichia coli and purification of the Lacaase CotA from Bacillus subtilis. 2008 ;[citado 2024 nov. 05 ]
Vancouver
Ribeiro LF, Furtado GP, Ward RJ. Cloning, overexpression in Escherichia coli and purification of the Lacaase CotA from Bacillus subtilis. 2008 ;[citado 2024 nov. 05 ]
Trabalho de evento-resumo
Heme oxygenase-carbon monoxide-cGMP antinociception: synergy between peripheral and spinal sites (2008)
Nascimento, C. G. O.; Branco, Luiz Guilherme de Siqueira
Fonte: New Challenges for the Physiologists. Nome do evento: Symposium Covian. Unidade: FORP
Assunto: OXIGENASE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NASCIMENTO, C. G. O. e BRANCO, Luiz Guilherme de Siqueira. Heme oxygenase-carbon monoxide-cGMP antinociception: synergy between peripheral and spinal sites. 2008, Anais.. Ribeirão Preto: FMRP-USP, 2008. . Acesso em: 05 nov. 2024.
APA
Nascimento, C. G. O., & Branco, L. G. de S. (2008). Heme oxygenase-carbon monoxide-cGMP antinociception: synergy between peripheral and spinal sites. In New Challenges for the Physiologists. Ribeirão Preto: FMRP-USP.
NLM
Nascimento CGO, Branco LG de S. Heme oxygenase-carbon monoxide-cGMP antinociception: synergy between peripheral and spinal sites. New Challenges for the Physiologists. 2008 ;[citado 2024 nov. 05 ]
Vancouver
Nascimento CGO, Branco LG de S. Heme oxygenase-carbon monoxide-cGMP antinociception: synergy between peripheral and spinal sites. New Challenges for the Physiologists. 2008 ;[citado 2024 nov. 05 ]

Unidades USP

ReP

Filtros

Unidades USP

Departamento

Autores

Autores USP

Ano de publicação

Assuntos

Título da fonte

País de publicação

Agência de fomento

Indexado em

Afiliação dos autores externos não normalizada

País das instituições de afiliação dos autores externos