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| Registros recuperados : 83 | |
| 3. |  | MURAD, A. M.; MOLINARI, H. B. C.; TAKAHASHI, F.; FRANCO, O. L.; QUIRINO, B. F. Análises proteômicas e fisiológicas em Saccharum spp. submetidas a estresse salino. In: SIMPÓSIO BRASILEIRO DE RECURSOS GENÉTICOS, 2., 2008, Brasília, DF. Anais... Brasília, DF: Embrapa Recursos Genéticos e Biotecnologia, 2008. p. 105.| Biblioteca(s): Embrapa Agroenergia. |
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| 4. | | MURAD, A. M.; NORONHA, E. F.; MEHTA, A.; LAUMANN, R. A.; FRANCO, O. L. Beauveria bassiana proteomics: understanding fungi-host mechanisms for development of novel strategies on Callosobruchus maculatus biocontrol. In: REUNIÃO ANUAL DA SOCIEDADE BRASILEIRA DE BIOQUÍMICA E BIOLOGIA MOLECULAR, 35., 2006, Águas de Lindóia, SP. Programas e resumos... São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular, 2006. Não paginado.| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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| 10. | | LACORTE, C. C.; MURAD, A. M.; MADEIRA, L.; CUNHA, N. B.; RECH FILHO, E. L. Subcellular targeting of recombinant Cyanovirin-N, An-HIV microbiocide, in soybean and Nicotiana bethamiana plants. In: SIMPÓSIO BRASILEIRO DE GENÉTICA MOLECULAR DE PLANTAS, 2., 2009, Búzios. Programa e resumos. [s.l.]: Sociedade Brasileira de Genética, 2009. p. 252.| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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| 11. | | CUNHA, N. B. da; MURAD, A. M.; VIANNA, G. R.; RECH FILHO, E. L. Recombinant biosynthesis of functional human growth hormone and coagulation factor IX in transgenic soybean seeds. BMC Proceedings, v.8, suppl, P.112, 2014. (Open access) Edição do Congress of the Brazilian Biotechnology Society, Florianópolis, 2013.| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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| 12. | | LACORTE, C. C.; FERREIRA, A. L.; MURAD, A. M.; CUNHA, N. B. da; PINHEIRO, P. V. Seed-based production of recombinant proteins. In: KOLE, C.; CHAURASIA, A.; HEFFERON, K. L.; PANIGRAHI, J. (ed.). Tools & techniques of plant molecular farming. [S.l.]: Springer Singapore, 2023. Cap. 6. Cap. 6, p. 185-208.| Biblioteca(s): Embrapa Arroz e Feijão; Embrapa Recursos Genéticos e Biotecnologia. |
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| 15. | | MURAD, A. M.; CARNEIRO, R. M. D. G.; BRILHANTE, O.; GROSSI DE SÁ, M. F.; ROCHA, T. L. Bioprospecção de extratos de plantas do bioma Cerrado (família Meliaceae e Solanacea) ativos sobre Meloidogyne incognita. Nematologia Brasileira, Brasília, v. 31, n. 2, p. 113, 2007. Edição dos resumos do XXVII Congresso Brasileiro de Nematologia, Goiânia, GO, maio 2007.| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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| 16. | | MURAD, A. M.; CUNHA, N.; LACORTE, C. C.; COELHO, M. C. F.; VIANNA, G. R.; RECH FILHO, E. L. Expression, purification and analysis of the anti-HIV Cyanovirin-N produced in transgenic soybeans seeds. BMC Proceedings, v.8, suppl, P.105, 2014. (Open access) Edição do Congress of the Brazilian Biotechnology Society, Florianópolis, 2013.| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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| 17. | | SANTOS, H. L. dos; BAHIA FILHO, A. F. C.; BAHIA, F.; MAGNAVACA, R.; SILVA, J.; MURAD, A. M.; PACHECO, E. Ensaio de adubação com nitrogênio, fósforo e potássio na cultura do milho em Minas Gerais. II. Avaliação da nutrição do milho pela análise foliar. Pesquisa Agropecuária Brasileira, Brasília, v. 10, p. 47-51, 1975.| Biblioteca(s): Embrapa Milho e Sorgo. |
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| 18. | | SANTOS, C.; MAXIMIANO, M. R.; RIBEIRO, D. G.; OLIVEIRA-NETO, O. B.; MURAD, A. M.; FRANCO, O. L.; MEHTA, A. Differential accumulation of Xanthomonas campestris pv. campestris proteins during the interaction with the host plant: contributions of an in vivo system. Proteomics, v. 17, n, 12, 2017. 1700086.| Biblioteca(s): Embrapa Recursos Genéticos e Biotecnologia. |
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| Registros recuperados : 83 | |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Recursos Genéticos e Biotecnologia. Para informações adicionais entre em contato com cenargen.biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Recursos Genéticos e Biotecnologia. |
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Data corrente: |
07/12/2015 |
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Data da última atualização: |
20/03/2023 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
A - 1 |
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Autoria: |
PETRIZ, B. A.; ALMEIDA, J. A.; GOMES, C. P. C.; PEREIRA, R. W.; MURAD, A. M.; FRANCO, O. L. |
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Afiliação: |
Bernardo A. Petriz, UCB; Jeeser A. Almeida, UCB; Clarissa P. C. Gomes, UCB; Rinaldo W. Pereira, UCB; ANDRE MELRO MURAD, CENARGEN; Octavio l. Franco, UCB. |
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Título: |
NanoUPLC/MSE proteomic analysis reveals modulation on left ventricle proteome from hypertensive rats after exercise training. |
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Ano de publicação: |
2015 |
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Fonte/Imprenta: |
Journal of Proteomics, v. 113, p. 351-365, 2015. |
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Idioma: |
Inglês |
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Conteúdo: |
NanoUPLC/MSE was used to verify the effects of 8 weeks of low (SHR-LIT = 4) and high (SHR-HIT = 4) intensity training over the left ventricle proteome of hypertensive rats (SHR-C = 4). Training enhanced the aerobic capacity and reduced the systolic blood pressure in all exercised rats.NanoUPLC/MSE identified 250 proteins, with 233 in common to all groups and 16 exclusive to SHR-C, 2 to SHR-LIT, and 2 to the SHR-HIT. Cardiac hypertrophy related proteins appeared only in SHR-C. The SHR-LIT enhanced the abundance of 30 proteins and diminished 6, while SHR-HIT enhanced the abundance of 39 proteins and reduced other 7. The levels of metabolic (? and ?-enolase, adenine phosphoribosultransferase, and cytochrome b-c1), myofibril (myosin light chain 4, tropomyosin ? and ?-chain), and transporter proteins (hemoglobin, serum albumin, and hemopexin)were increased by both intensities. Transcription regulator and histone variants were enhanced by SHR-LIT and SHR-HIT respectively. SHR-LIT reduced the concentration of myosin binding protein C, while desmin and membrane voltage dependent anion selective channel protein-3 were reduced only by SHR-HIT. In addition, polyubiquitin B and C, and transcription regulators decreased in both intensities. Exercise also increased the concentration of anti-oxidant proteins, peroxiredozin-6 and glutathione peroxidase-1. Biological significance Pathologic left ventricle hypertrophy if one of the major outcomes of hypertension being a strong predictor of heart failure. Among the various risk factors for cardiovascular disorders, arterial hypertension is responsible for the highest rates of mortality worldwide. In this way,this present study contribute to the understanding of the molecular mechanisms involved in the attenuation of hypertension and the regression of pathological cardiac hypertrophy induced by exercise training. MenosNanoUPLC/MSE was used to verify the effects of 8 weeks of low (SHR-LIT = 4) and high (SHR-HIT = 4) intensity training over the left ventricle proteome of hypertensive rats (SHR-C = 4). Training enhanced the aerobic capacity and reduced the systolic blood pressure in all exercised rats.NanoUPLC/MSE identified 250 proteins, with 233 in common to all groups and 16 exclusive to SHR-C, 2 to SHR-LIT, and 2 to the SHR-HIT. Cardiac hypertrophy related proteins appeared only in SHR-C. The SHR-LIT enhanced the abundance of 30 proteins and diminished 6, while SHR-HIT enhanced the abundance of 39 proteins and reduced other 7. The levels of metabolic (? and ?-enolase, adenine phosphoribosultransferase, and cytochrome b-c1), myofibril (myosin light chain 4, tropomyosin ? and ?-chain), and transporter proteins (hemoglobin, serum albumin, and hemopexin)were increased by both intensities. Transcription regulator and histone variants were enhanced by SHR-LIT and SHR-HIT respectively. SHR-LIT reduced the concentration of myosin binding protein C, while desmin and membrane voltage dependent anion selective channel protein-3 were reduced only by SHR-HIT. In addition, polyubiquitin B and C, and transcription regulators decreased in both intensities. Exercise also increased the concentration of anti-oxidant proteins, peroxiredozin-6 and glutathione peroxidase-1. Biological significance Pathologic left ventricle hypertrophy if one of the major outcomes of hypertension being a strong predictor of he... Mostrar Tudo |
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Palavras-Chave: |
Análise proteômica; Hipertensão. |
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Categoria do assunto: |
-- |
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Marc: |
LEADER 02514naa a2200205 a 4500
001 2030868
005 2023-03-20
008 2015 bl uuuu u00u1 u #d
100 1 $aPETRIZ, B. A.
245 $aNanoUPLC/MSE proteomic analysis reveals modulation on left ventricle proteome from hypertensive rats after exercise training.$h[electronic resource]
260 $c2015
520 $aNanoUPLC/MSE was used to verify the effects of 8 weeks of low (SHR-LIT = 4) and high (SHR-HIT = 4) intensity training over the left ventricle proteome of hypertensive rats (SHR-C = 4). Training enhanced the aerobic capacity and reduced the systolic blood pressure in all exercised rats.NanoUPLC/MSE identified 250 proteins, with 233 in common to all groups and 16 exclusive to SHR-C, 2 to SHR-LIT, and 2 to the SHR-HIT. Cardiac hypertrophy related proteins appeared only in SHR-C. The SHR-LIT enhanced the abundance of 30 proteins and diminished 6, while SHR-HIT enhanced the abundance of 39 proteins and reduced other 7. The levels of metabolic (? and ?-enolase, adenine phosphoribosultransferase, and cytochrome b-c1), myofibril (myosin light chain 4, tropomyosin ? and ?-chain), and transporter proteins (hemoglobin, serum albumin, and hemopexin)were increased by both intensities. Transcription regulator and histone variants were enhanced by SHR-LIT and SHR-HIT respectively. SHR-LIT reduced the concentration of myosin binding protein C, while desmin and membrane voltage dependent anion selective channel protein-3 were reduced only by SHR-HIT. In addition, polyubiquitin B and C, and transcription regulators decreased in both intensities. Exercise also increased the concentration of anti-oxidant proteins, peroxiredozin-6 and glutathione peroxidase-1. Biological significance Pathologic left ventricle hypertrophy if one of the major outcomes of hypertension being a strong predictor of heart failure. Among the various risk factors for cardiovascular disorders, arterial hypertension is responsible for the highest rates of mortality worldwide. In this way,this present study contribute to the understanding of the molecular mechanisms involved in the attenuation of hypertension and the regression of pathological cardiac hypertrophy induced by exercise training.
653 $aAnálise proteômica
653 $aHipertensão
700 1 $aALMEIDA, J. A.
700 1 $aGOMES, C. P. C.
700 1 $aPEREIRA, R. W.
700 1 $aMURAD, A. M.
700 1 $aFRANCO, O. L.
773 $tJournal of Proteomics$gv. 113, p. 351-365, 2015.
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