Filtros : "Estados Unidos" "Ronsein, Graziella Eliza" Removido: "Colli, Walter" Limpar

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  • Source: Journal of Lipid Research. Unidade: IQ

    Subjects: NEFROPATIAS, DOENÇAS CARDIOVASCULARES, ESTUDO DE CASO, LIPOPROTEÍNAS HDL

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    • ABNT

      SHAO, Baohai et al. Low concentrations of medium-sized HDL particles predict incident CVD in chronic kidney disease patients. Journal of Lipid Research, v. 64, n. 6, p. 1-11 art. 100381, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.jlr.2023.100381. Acesso em: 01 nov. 2024.
    • APA

      Shao, B., Afshinnia, F., Mathew, A. V., Ronsein, G. E., Thornock, C., Irwin, A. D., et al. (2023). Low concentrations of medium-sized HDL particles predict incident CVD in chronic kidney disease patients. Journal of Lipid Research, 64( 6), 1-11 art. 100381. doi:10.1016/j.jlr.2023.100381
    • NLM

      Shao B, Afshinnia F, Mathew AV, Ronsein GE, Thornock C, Irwin AD, Kansal M, Rao PS, Dobre M, Al-Kindi S, Weir MR, Go A, He J, Chen J, Feldman H, Bornfeldt KE, Pennathur S. Low concentrations of medium-sized HDL particles predict incident CVD in chronic kidney disease patients [Internet]. Journal of Lipid Research. 2023 ; 64( 6): 1-11 art. 100381.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.jlr.2023.100381
    • Vancouver

      Shao B, Afshinnia F, Mathew AV, Ronsein GE, Thornock C, Irwin AD, Kansal M, Rao PS, Dobre M, Al-Kindi S, Weir MR, Go A, He J, Chen J, Feldman H, Bornfeldt KE, Pennathur S. Low concentrations of medium-sized HDL particles predict incident CVD in chronic kidney disease patients [Internet]. Journal of Lipid Research. 2023 ; 64( 6): 1-11 art. 100381.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.jlr.2023.100381
  • Source: Arteriosclerosis, Thrombosis, and Vascular Biology. Unidade: IQ

    Subjects: ESTATINAS, LIPOPROTEÍNAS HDL, PROTEÔMICA

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    • ABNT

      RONSEIN, Graziella Eliza et al. Niacin increases atherogenic proteins in high-density lipoprotein of statin-treated subjects. Arteriosclerosis, Thrombosis, and Vascular Biology, v. 41, p. 2330–2341, 2021Tradução . . Disponível em: https://doi.org/10.1161/ATVBAHA.121.316278. Acesso em: 01 nov. 2024.
    • APA

      Ronsein, G. E., Vaisar, T., Davidson, W. S., Bornfeldt, K. E., Probstfield, J. L., O’Brien, K. D., et al. (2021). Niacin increases atherogenic proteins in high-density lipoprotein of statin-treated subjects. Arteriosclerosis, Thrombosis, and Vascular Biology, 41, 2330–2341. doi:10.1161/ATVBAHA.121.316278
    • NLM

      Ronsein GE, Vaisar T, Davidson WS, Bornfeldt KE, Probstfield JL, O’Brien KD, Zhao X-Q, Heinecke JW. Niacin increases atherogenic proteins in high-density lipoprotein of statin-treated subjects [Internet]. Arteriosclerosis, Thrombosis, and Vascular Biology. 2021 ; 41 2330–2341.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1161/ATVBAHA.121.316278
    • Vancouver

      Ronsein GE, Vaisar T, Davidson WS, Bornfeldt KE, Probstfield JL, O’Brien KD, Zhao X-Q, Heinecke JW. Niacin increases atherogenic proteins in high-density lipoprotein of statin-treated subjects [Internet]. Arteriosclerosis, Thrombosis, and Vascular Biology. 2021 ; 41 2330–2341.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1161/ATVBAHA.121.316278
  • Source: Free Radical Biology and Medicine. Conference titles: SfRBM Annual Conference (Presented Virtually). Unidade: IQ

    Subjects: CATARATA, LENTES

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      SAMPAIO, Verônica Paviani et al. Human cataracts contain cross-links produced from crystallin-derived tryptophanyl and tyrosyl radicals. Free Radical Biology and Medicine. New York: Instituto de Química, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.freeradbiomed.2020.10.274. Acesso em: 01 nov. 2024. , 2020
    • APA

      Sampaio, V. P., Melo, P. J. de, Ronsein, G. E., Avakian, A., Di Mascio, P., & Augusto, O. (2020). Human cataracts contain cross-links produced from crystallin-derived tryptophanyl and tyrosyl radicals. Free Radical Biology and Medicine. New York: Instituto de Química, Universidade de São Paulo. doi:10.1016/j.freeradbiomed.2020.10.274
    • NLM

      Sampaio VP, Melo PJ de, Ronsein GE, Avakian A, Di Mascio P, Augusto O. Human cataracts contain cross-links produced from crystallin-derived tryptophanyl and tyrosyl radicals [Internet]. Free Radical Biology and Medicine. 2020 ; 159 S108 res. 219.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2020.10.274
    • Vancouver

      Sampaio VP, Melo PJ de, Ronsein GE, Avakian A, Di Mascio P, Augusto O. Human cataracts contain cross-links produced from crystallin-derived tryptophanyl and tyrosyl radicals [Internet]. Free Radical Biology and Medicine. 2020 ; 159 S108 res. 219.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2020.10.274
  • Source: Circulation Research. Unidade: IQ

    Subjects: DIABETES MELLITUS, COLESTEROL

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      HE, Yi et al. Diabetes impairs cellular cholesterol efflux from ABCA1 to small HDL particles. Circulation Research, v. 127, n. 9, p. 1198–1210, 2020Tradução . . Disponível em: https://doi.org/10.1161/CIRCRESAHA.120.317178. Acesso em: 01 nov. 2024.
    • APA

      He, Y., Ronsein, G. E., Tang, C., Jarvik, G. P., Davidson, W. S., Kothari, V., et al. (2020). Diabetes impairs cellular cholesterol efflux from ABCA1 to small HDL particles. Circulation Research, 127( 9), 1198–1210. doi:10.1161/CIRCRESAHA.120.317178
    • NLM

      He Y, Ronsein GE, Tang C, Jarvik GP, Davidson WS, Kothari V, Song HD, Segrest JP, Bornfeldt KE, Heinecke JW. Diabetes impairs cellular cholesterol efflux from ABCA1 to small HDL particles [Internet]. Circulation Research. 2020 ; 127( 9): 1198–1210.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1161/CIRCRESAHA.120.317178
    • Vancouver

      He Y, Ronsein GE, Tang C, Jarvik GP, Davidson WS, Kothari V, Song HD, Segrest JP, Bornfeldt KE, Heinecke JW. Diabetes impairs cellular cholesterol efflux from ABCA1 to small HDL particles [Internet]. Circulation Research. 2020 ; 127( 9): 1198–1210.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1161/CIRCRESAHA.120.317178
  • Source: Photochemical and Photobiological Sciences. Unidade: IQ

    Subjects: OXIGÊNIO, COMPOSTOS AROMÁTICOS

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      OLIVEIRA, Marilene Silva et al. Heck reaction synthesis of anthracene and naphthalene derivatives as traps and clean chemical sources of singlet molecular oxygen in biological systems. Photochemical and Photobiological Sciences, v. 19, p. 1590-1602, 2020Tradução . . Disponível em: https://doi.org/10.1039/d0pp00153h. Acesso em: 01 nov. 2024.
    • APA

      Oliveira, M. S., Chorociejus, G., Jose Pedro, F. A., Aquino, G. L. B., Ronsein, G. E., Oliveira, M. C. B. de, et al. (2020). Heck reaction synthesis of anthracene and naphthalene derivatives as traps and clean chemical sources of singlet molecular oxygen in biological systems. Photochemical and Photobiological Sciences, 19, 1590-1602. doi:10.1039/d0pp00153h
    • NLM

      Oliveira MS, Chorociejus G, Jose Pedro FA, Aquino GLB, Ronsein GE, Oliveira MCB de, Barbosa LF, Medeiros MHG de, Greer A, Di Mascio P. Heck reaction synthesis of anthracene and naphthalene derivatives as traps and clean chemical sources of singlet molecular oxygen in biological systems [Internet]. Photochemical and Photobiological Sciences. 2020 ; 19 1590-1602.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1039/d0pp00153h
    • Vancouver

      Oliveira MS, Chorociejus G, Jose Pedro FA, Aquino GLB, Ronsein GE, Oliveira MCB de, Barbosa LF, Medeiros MHG de, Greer A, Di Mascio P. Heck reaction synthesis of anthracene and naphthalene derivatives as traps and clean chemical sources of singlet molecular oxygen in biological systems [Internet]. Photochemical and Photobiological Sciences. 2020 ; 19 1590-1602.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1039/d0pp00153h
  • Source: Current Opinion in Lipidology. Unidade: IQ

    Subjects: COLESTEROL, DOENÇAS CARDIOVASCULARES

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      RONSEIN, Graziella Eliza e HEINECKE, Jay W. Time to ditch HOL-C as a measure of PINION HOL function?. Current Opinion in Lipidology, v. 28, n. 5, p. 414-418, 2017Tradução . . Disponível em: https://doi.org/10.1097/MOL.0000000000000446. Acesso em: 01 nov. 2024.
    • APA

      Ronsein, G. E., & Heinecke, J. W. (2017). Time to ditch HOL-C as a measure of PINION HOL function? Current Opinion in Lipidology, 28( 5), 414-418. doi:10.1097/MOL.0000000000000446
    • NLM

      Ronsein GE, Heinecke JW. Time to ditch HOL-C as a measure of PINION HOL function? [Internet]. Current Opinion in Lipidology. 2017 ; 28( 5): 414-418.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1097/MOL.0000000000000446
    • Vancouver

      Ronsein GE, Heinecke JW. Time to ditch HOL-C as a measure of PINION HOL function? [Internet]. Current Opinion in Lipidology. 2017 ; 28( 5): 414-418.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1097/MOL.0000000000000446
  • Source: Jcl insight. Unidade: IQ

    Subjects: COLESTEROL, MACRÓFAGOS, APOLIPOPROTEÍNAS

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      PAMIR, Nathalie et al. Plasminogen promotes cholesterol efflux by the ABCA1 pathway. Jcl insight, v. 2, n. 15, p. 1-15 art. 92176, 2017Tradução . . Disponível em: https://doi.org/10.1172/jci.insight.92176. Acesso em: 01 nov. 2024.
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      Pamir, N., Hutchins, P. M., Ronsein, G. E., Wei, H., Tang, C., Das, R., et al. (2017). Plasminogen promotes cholesterol efflux by the ABCA1 pathway. Jcl insight, 2( 15), 1-15 art. 92176. doi:10.1172/jci.insight.92176
    • NLM

      Pamir N, Hutchins PM, Ronsein GE, Wei H, Tang C, Das R, Vaisar T, Plow E, Schuster V, Reardon CA, Weinberg R, Dichek DA, Marcovina S, Getz GS, Heinecke JW. Plasminogen promotes cholesterol efflux by the ABCA1 pathway [Internet]. Jcl insight. 2017 ; 2( 15): 1-15 art. 92176.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1172/jci.insight.92176
    • Vancouver

      Pamir N, Hutchins PM, Ronsein GE, Wei H, Tang C, Das R, Vaisar T, Plow E, Schuster V, Reardon CA, Weinberg R, Dichek DA, Marcovina S, Getz GS, Heinecke JW. Plasminogen promotes cholesterol efflux by the ABCA1 pathway [Internet]. Jcl insight. 2017 ; 2( 15): 1-15 art. 92176.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1172/jci.insight.92176
  • Source: Circulation Research. Unidade: IQ

    Subjects: APOLIPOPROTEÍNAS, ARTERIOSCLEROSE, DOENÇAS CARDIOVASCULARES

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      MONETTE, Jeffrey S et al. Patients with coronary endothelial dysfunction have impaired cholesterol efflux capacity and reduced HDL particle concentration. Circulation Research, v. 119, n. 1, p. 83-90, 2016Tradução . . Disponível em: https://doi.org/10.1161/CIRCRESAHA.116.308357. Acesso em: 01 nov. 2024.
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      Monette, J. S., Hutchins, P. M., Ronsein, G. E., Wimberger, J., Irwin, A. D., Tang, C., et al. (2016). Patients with coronary endothelial dysfunction have impaired cholesterol efflux capacity and reduced HDL particle concentration. Circulation Research, 119( 1), 83-90. doi:10.1161/CIRCRESAHA.116.308357
    • NLM

      Monette JS, Hutchins PM, Ronsein GE, Wimberger J, Irwin AD, Tang C, Sara JD, Shao B, Vaisar T, Lerman A, Heinecke JW. Patients with coronary endothelial dysfunction have impaired cholesterol efflux capacity and reduced HDL particle concentration [Internet]. Circulation Research. 2016 ; 119( 1): 83-90.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1161/CIRCRESAHA.116.308357
    • Vancouver

      Monette JS, Hutchins PM, Ronsein GE, Wimberger J, Irwin AD, Tang C, Sara JD, Shao B, Vaisar T, Lerman A, Heinecke JW. Patients with coronary endothelial dysfunction have impaired cholesterol efflux capacity and reduced HDL particle concentration [Internet]. Circulation Research. 2016 ; 119( 1): 83-90.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1161/CIRCRESAHA.116.308357
  • Source: Molecular e Cellular Proteomics. Unidade: IQ

    Subjects: APOLIPOPROTEÍNAS, LIPOPROTEÍNAS HDL, DIABETES MELLITUS

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      RONSEIN, Graziella Eliza et al. Targeted proteomics identifies Paraoxonase/Arylesterase 1 (PON1) and apolipoprotein Cs as potential risk factors for hypoalphalipoproteinemia in diabetic subjects treated with fenofibrate and rosiglitazone. Molecular e Cellular Proteomics, v. 15, n. 3, p. 1083-1093, 2016Tradução . . Disponível em: https://doi.org/10.1074/mcp.M115.054528. Acesso em: 01 nov. 2024.
    • APA

      Ronsein, G. E., Reyes Soffer, G., He, Y., Oda, M., Ginsberg, H., & Heinecke, J. W. (2016). Targeted proteomics identifies Paraoxonase/Arylesterase 1 (PON1) and apolipoprotein Cs as potential risk factors for hypoalphalipoproteinemia in diabetic subjects treated with fenofibrate and rosiglitazone. Molecular e Cellular Proteomics, 15( 3), 1083-1093. doi:10.1074/mcp.M115.054528
    • NLM

      Ronsein GE, Reyes Soffer G, He Y, Oda M, Ginsberg H, Heinecke JW. Targeted proteomics identifies Paraoxonase/Arylesterase 1 (PON1) and apolipoprotein Cs as potential risk factors for hypoalphalipoproteinemia in diabetic subjects treated with fenofibrate and rosiglitazone [Internet]. Molecular e Cellular Proteomics. 2016 ; 15( 3): 1083-1093.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1074/mcp.M115.054528
    • Vancouver

      Ronsein GE, Reyes Soffer G, He Y, Oda M, Ginsberg H, Heinecke JW. Targeted proteomics identifies Paraoxonase/Arylesterase 1 (PON1) and apolipoprotein Cs as potential risk factors for hypoalphalipoproteinemia in diabetic subjects treated with fenofibrate and rosiglitazone [Internet]. Molecular e Cellular Proteomics. 2016 ; 15( 3): 1083-1093.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1074/mcp.M115.054528
  • Source: Arteriosclerosis Thrombosis and Vascular Biolology. Unidade: IQ

    Subjects: ARTERIOSCLEROSE, DOENÇAS CARDIOVASCULARES, MACRÓFAGOS

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      RONSEIN, Graziella Eliza et al. Niacin therapy increases high-density lipoprotein particles and total cholesterol efflux capacity but not ABCA1-specific cholesterol efflux in statin-treated subjects. Arteriosclerosis Thrombosis and Vascular Biolology, v. 36, n. 2, p. 404-411, 2016Tradução . . Disponível em: https://doi.org/10.1161/ATVBAHA.115.306268. Acesso em: 01 nov. 2024.
    • APA

      Ronsein, G. E., Hutchins, P. M., Isquith, D., Vaisar, T., Zhao, X. -Q., & Heinecke, J. W. (2016). Niacin therapy increases high-density lipoprotein particles and total cholesterol efflux capacity but not ABCA1-specific cholesterol efflux in statin-treated subjects. Arteriosclerosis Thrombosis and Vascular Biolology, 36( 2), 404-411. doi:10.1161/ATVBAHA.115.306268
    • NLM

      Ronsein GE, Hutchins PM, Isquith D, Vaisar T, Zhao X-Q, Heinecke JW. Niacin therapy increases high-density lipoprotein particles and total cholesterol efflux capacity but not ABCA1-specific cholesterol efflux in statin-treated subjects [Internet]. Arteriosclerosis Thrombosis and Vascular Biolology. 2016 ; 36( 2): 404-411.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1161/ATVBAHA.115.306268
    • Vancouver

      Ronsein GE, Hutchins PM, Isquith D, Vaisar T, Zhao X-Q, Heinecke JW. Niacin therapy increases high-density lipoprotein particles and total cholesterol efflux capacity but not ABCA1-specific cholesterol efflux in statin-treated subjects [Internet]. Arteriosclerosis Thrombosis and Vascular Biolology. 2016 ; 36( 2): 404-411.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1161/ATVBAHA.115.306268
  • Source: Journal of Lipid Research. Unidade: IQ

    Subjects: ARTERIOSCLEROSE, DOENÇAS CARDIOVASCULARES, APOLIPOPROTEÍNAS, LIPOPROTEÍNAS

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      PAMIR, Nathalie et al. Proteomic analysis of HDL from inbred mouse strains implicates APOE associated with HDL in reduced cholesterol efflux capacity via the ABCA1 pathway. Journal of Lipid Research, v. 57, n. 2, p. 246-257, 2016Tradução . . Disponível em: https://doi.org/10.1194/jlr.M063701. Acesso em: 01 nov. 2024.
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      Pamir, N., Hutchins, P., Ronsein, G. E., Vaisar, T., Reardon, C. A., Getz, G. S., et al. (2016). Proteomic analysis of HDL from inbred mouse strains implicates APOE associated with HDL in reduced cholesterol efflux capacity via the ABCA1 pathway. Journal of Lipid Research, 57( 2), 246-257. doi:10.1194/jlr.M063701
    • NLM

      Pamir N, Hutchins P, Ronsein GE, Vaisar T, Reardon CA, Getz GS, Lusis AJ, Heinecke JW. Proteomic analysis of HDL from inbred mouse strains implicates APOE associated with HDL in reduced cholesterol efflux capacity via the ABCA1 pathway [Internet]. Journal of Lipid Research. 2016 ; 57( 2): 246-257.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1194/jlr.M063701
    • Vancouver

      Pamir N, Hutchins P, Ronsein GE, Vaisar T, Reardon CA, Getz GS, Lusis AJ, Heinecke JW. Proteomic analysis of HDL from inbred mouse strains implicates APOE associated with HDL in reduced cholesterol efflux capacity via the ABCA1 pathway [Internet]. Journal of Lipid Research. 2016 ; 57( 2): 246-257.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1194/jlr.M063701
  • Source: Journal of Clinical Endocrinology & Metabolism. Unidade: IQ

    Subjects: DOENÇAS CARDIOVASCULARES, LIPOPROTEÍNAS HDL, COLESTEROL, MENOPAUSA

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      EL KHOUDARY, Samar R et al. Cholesterol efflux capacity and subclasses of HDL particles in healthy women transitioning through menopause. Journal of Clinical Endocrinology & Metabolism, v. 101, n. 9, p. 3419-3428, 2016Tradução . . Disponível em: https://doi.org/10.1210/jc.2016-2144. Acesso em: 01 nov. 2024.
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      el Khoudary, S. R., Hutchins, P. M., Matthews, K. A., Brooks, M. M., Orchard, T. J., Ronsein, G. E., & Heinecke, J. W. (2016). Cholesterol efflux capacity and subclasses of HDL particles in healthy women transitioning through menopause. Journal of Clinical Endocrinology & Metabolism, 101( 9), 3419-3428. doi:10.1210/jc.2016-2144
    • NLM

      el Khoudary SR, Hutchins PM, Matthews KA, Brooks MM, Orchard TJ, Ronsein GE, Heinecke JW. Cholesterol efflux capacity and subclasses of HDL particles in healthy women transitioning through menopause [Internet]. Journal of Clinical Endocrinology & Metabolism. 2016 ; 101( 9): 3419-3428.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1210/jc.2016-2144
    • Vancouver

      el Khoudary SR, Hutchins PM, Matthews KA, Brooks MM, Orchard TJ, Ronsein GE, Heinecke JW. Cholesterol efflux capacity and subclasses of HDL particles in healthy women transitioning through menopause [Internet]. Journal of Clinical Endocrinology & Metabolism. 2016 ; 101( 9): 3419-3428.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1210/jc.2016-2144

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