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Artigo de periodico
The toxicity of poly(acrylonitrile-styrene−butadiene) microplasticstoward Hyalella azteca Is associated with Biofragmentation and oxidative stress (2025)
Queiroz, Lucas Gonçalves ; Prado, Caio César Achiles do ; Oliveira, Paulo Filho Marques de ; Valezi, Daniel Farinha; Portes, Marcelo Cecconi ; Moraes, Beatriz Rocha de ; Ando, Rômulo Augusto ; Vicente, Eduardo; Paiva, Teresa Cristina Brazil de ; Pompêo, Marcelo ; Borges, Bárbara Rani
Fonte: Chemical Research in Toxicology. Unidades: IQ, EEL, IB, FO
Assuntos: ESTRESSE OXIDATIVO, FISIOLOGIA
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ABNT
QUEIROZ, Lucas Gonçalves et al. The toxicity of poly(acrylonitrile-styrene−butadiene) microplasticstoward Hyalella azteca Is associated with Biofragmentation and oxidative stress. Chemical Research in Toxicology, v. 38, n. 1, p. 91-101, 2025Tradução . . Disponível em: https://dx.doi.org/10.1021/acs.chemrestox.4c00300. Acesso em: 07 out. 2025.
APA
Queiroz, L. G., Prado, C. C. A. do, Oliveira, P. F. M. de, Valezi, D. F., Portes, M. C., Moraes, B. R. de, et al. (2025). The toxicity of poly(acrylonitrile-styrene−butadiene) microplasticstoward Hyalella azteca Is associated with Biofragmentation and oxidative stress. Chemical Research in Toxicology, 38( 1), 91-101. doi:10.1021/acs.chemrestox.4c00300
NLM
Queiroz LG, Prado CCA do, Oliveira PFM de, Valezi DF, Portes MC, Moraes BR de, Ando RA, Vicente E, Paiva TCB de, Pompêo M, Borges BR. The toxicity of poly(acrylonitrile-styrene−butadiene) microplasticstoward Hyalella azteca Is associated with Biofragmentation and oxidative stress [Internet]. Chemical Research in Toxicology. 2025 ; 38( 1): 91-101.[citado 2025 out. 07 ] Available from: https://dx.doi.org/10.1021/acs.chemrestox.4c00300
Vancouver
Queiroz LG, Prado CCA do, Oliveira PFM de, Valezi DF, Portes MC, Moraes BR de, Ando RA, Vicente E, Paiva TCB de, Pompêo M, Borges BR. The toxicity of poly(acrylonitrile-styrene−butadiene) microplasticstoward Hyalella azteca Is associated with Biofragmentation and oxidative stress [Internet]. Chemical Research in Toxicology. 2025 ; 38( 1): 91-101.[citado 2025 out. 07 ] Available from: https://dx.doi.org/10.1021/acs.chemrestox.4c00300
Artigo de periodico
Quantitative analysis of glutathione and carnosine Adducts with 4‑Hydroxy-2-nonenal in muscle in a hSOD1G93A ALS rat model (2024)
Reis, Pablo Victor Mendes dos; Vargas, Bianca Scigliano; Rebelo, Rafael Andrade; Massafera, Mariana Pereira ; Prado, Fernanda Manso ; Oreliana, Hector; Oliveira, Henrique V. de; Freitas, Florêncio Porto; Ronsein, Graziella Eliza ; Miyamoto, Sayuri ; Di Mascio, Paolo ; Medeiros, Marisa Helena Gennari de
Fonte: Chemical Research in Toxicology. Unidade: IQ
Assuntos: ESCLEROSE AMIOTRÓFICA LATERAL, DOENÇAS NEURODEGENERATIVAS
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REIS, Pablo Victor Mendes dos et al. Quantitative analysis of glutathione and carnosine Adducts with 4‑Hydroxy-2-nonenal in muscle in a hSOD1G93A ALS rat model. Chemical Research in Toxicology, v. 37, n. 8, p. 1306–1314, 2024Tradução . . Disponível em: https://dx.doi.org/10.1021/acs.chemrestox.4c00052. Acesso em: 07 out. 2025.
APA
Reis, P. V. M. dos, Vargas, B. S., Rebelo, R. A., Massafera, M. P., Prado, F. M., Oreliana, H., et al. (2024). Quantitative analysis of glutathione and carnosine Adducts with 4‑Hydroxy-2-nonenal in muscle in a hSOD1G93A ALS rat model. Chemical Research in Toxicology, 37( 8), 1306–1314. doi:10.1021/acs.chemrestox.4c00052
NLM
Reis PVM dos, Vargas BS, Rebelo RA, Massafera MP, Prado FM, Oreliana H, Oliveira HV de, Freitas FP, Ronsein GE, Miyamoto S, Di Mascio P, Medeiros MHG de. Quantitative analysis of glutathione and carnosine Adducts with 4‑Hydroxy-2-nonenal in muscle in a hSOD1G93A ALS rat model [Internet]. Chemical Research in Toxicology. 2024 ; 37( 8): 1306–1314.[citado 2025 out. 07 ] Available from: https://dx.doi.org/10.1021/acs.chemrestox.4c00052
Vancouver
Reis PVM dos, Vargas BS, Rebelo RA, Massafera MP, Prado FM, Oreliana H, Oliveira HV de, Freitas FP, Ronsein GE, Miyamoto S, Di Mascio P, Medeiros MHG de. Quantitative analysis of glutathione and carnosine Adducts with 4‑Hydroxy-2-nonenal in muscle in a hSOD1G93A ALS rat model [Internet]. Chemical Research in Toxicology. 2024 ; 37( 8): 1306–1314.[citado 2025 out. 07 ] Available from: https://dx.doi.org/10.1021/acs.chemrestox.4c00052
Artigo de periodico
Production of Peroxymonocarbonate by steady-state micromolar H2O2 and activated macrophages in the presence of CO2/HCO3– evidenced by boronate probes (2024)
Linares, Edlaine ; Severino, Divinomar ; Truzzi, Daniela Ramos ; Rios, Natalia ; Radi, Rafael ; Augusto, Ohara
Fonte: Chemical Research in Toxicology. Unidade: IQ
Assuntos: MACRÓFAGOS, CINÉTICA
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ABNT
LINARES, Edlaine et al. Production of Peroxymonocarbonate by steady-state micromolar H2O2 and activated macrophages in the presence of CO2/HCO3– evidenced by boronate probes. Chemical Research in Toxicology, v. 37, n. 7, p. 1129-1138, 2024Tradução . . Disponível em: https://dx.doi.org/10.1021/acs.chemrestox.4c00059. Acesso em: 07 out. 2025.
APA
Linares, E., Severino, D., Truzzi, D. R., Rios, N., Radi, R., & Augusto, O. (2024). Production of Peroxymonocarbonate by steady-state micromolar H2O2 and activated macrophages in the presence of CO2/HCO3– evidenced by boronate probes. Chemical Research in Toxicology, 37( 7), 1129-1138. doi:10.1021/acs.chemrestox.4c00059
NLM
Linares E, Severino D, Truzzi DR, Rios N, Radi R, Augusto O. Production of Peroxymonocarbonate by steady-state micromolar H2O2 and activated macrophages in the presence of CO2/HCO3– evidenced by boronate probes [Internet]. Chemical Research in Toxicology. 2024 ; 37( 7): 1129-1138.[citado 2025 out. 07 ] Available from: https://dx.doi.org/10.1021/acs.chemrestox.4c00059
Vancouver
Linares E, Severino D, Truzzi DR, Rios N, Radi R, Augusto O. Production of Peroxymonocarbonate by steady-state micromolar H2O2 and activated macrophages in the presence of CO2/HCO3– evidenced by boronate probes [Internet]. Chemical Research in Toxicology. 2024 ; 37( 7): 1129-1138.[citado 2025 out. 07 ] Available from: https://dx.doi.org/10.1021/acs.chemrestox.4c00059
Artigo de periodico
Nicotinamide riboside induced energy stress and metabolic reprogramming in BEAS-2B cells (2024)
Cordeiro, Everson Willan Fialho; Marzola, Elisabete Leide; Maekawa, Ricardo Soei ; Santos, Matheus Relvas dos; Assunção, Lucas Gade; Massafera, Mariana Pereira ; Oliveira, Joseana de; Batista, Thainá Gomes Cury; Sales, Maria Cármen Oliveira Pinho de; Maria-Engler, Silvya Stuchi ; Di Mascio, Paolo ; Medeiros, Marisa Helena Gennari de ; Ronsein, Graziella Eliza ; Loureiro, Ana Paula de Melo
Fonte: Chemical Research in Toxicology. Unidades: IQ, FCF
Assuntos: CÉLULAS, PEPTÍDEOS
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ABNT
CORDEIRO, Everson Willan Fialho et al. Nicotinamide riboside induced energy stress and metabolic reprogramming in BEAS-2B cells. Chemical Research in Toxicology, v. 37, p. 1246−1268, 2024Tradução . . Disponível em: https://dx.doi.org/10.1021/acs.chemrestox.3c00312. Acesso em: 07 out. 2025.
APA
Cordeiro, E. W. F., Marzola, E. L., Maekawa, R. S., Santos, M. R. dos, Assunção, L. G., Massafera, M. P., et al. (2024). Nicotinamide riboside induced energy stress and metabolic reprogramming in BEAS-2B cells. Chemical Research in Toxicology, 37, 1246−1268. doi:10.1021/acs.chemrestox.3c00312
NLM
Cordeiro EWF, Marzola EL, Maekawa RS, Santos MR dos, Assunção LG, Massafera MP, Oliveira J de, Batista TGC, Sales MCOP de, Maria-Engler SS, Di Mascio P, Medeiros MHG de, Ronsein GE, Loureiro AP de M. Nicotinamide riboside induced energy stress and metabolic reprogramming in BEAS-2B cells [Internet]. Chemical Research in Toxicology. 2024 ; 37 1246−1268.[citado 2025 out. 07 ] Available from: https://dx.doi.org/10.1021/acs.chemrestox.3c00312
Vancouver
Cordeiro EWF, Marzola EL, Maekawa RS, Santos MR dos, Assunção LG, Massafera MP, Oliveira J de, Batista TGC, Sales MCOP de, Maria-Engler SS, Di Mascio P, Medeiros MHG de, Ronsein GE, Loureiro AP de M. Nicotinamide riboside induced energy stress and metabolic reprogramming in BEAS-2B cells [Internet]. Chemical Research in Toxicology. 2024 ; 37 1246−1268.[citado 2025 out. 07 ] Available from: https://dx.doi.org/10.1021/acs.chemrestox.3c00312
Artigo de periodico
Adenanthin is an efficient inhibitor of peroxiredoxins from pathogens, inhibits bacterial growth, and potentiates antibiotic activities (2022)
Santos, Melina Cardoso dos ; Tairum, Carlos Abrunhosa ; Cabrera, Vitoria Isabela Montanhero ; Cauz, Ana Carolina Guimaraes; Ribeiro, Luiz Fernando ; Toledo Junior, José Carlos ; Toyama, Marcos Hikari; Lago, João Henrique Ghilardi ; Brocchi, Marcelo
Fonte: Chemical Research in Toxicology. Unidades: FFCLRP, IB, FCF
Assuntos: BACTÉRIAS PATOGÊNICAS, FÁRMACOS
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ABNT
SANTOS, Melina Cardoso dos et al. Adenanthin is an efficient inhibitor of peroxiredoxins from pathogens, inhibits bacterial growth, and potentiates antibiotic activities. Chemical Research in Toxicology, 2022Tradução . . Disponível em: https://doi.org/10.1021/acs.chemrestox.2c00049. Acesso em: 07 out. 2025.
APA
Santos, M. C. dos, Tairum, C. A., Cabrera, V. I. M., Cauz, A. C. G., Ribeiro, L. F., Toledo Junior, J. C., et al. (2022). Adenanthin is an efficient inhibitor of peroxiredoxins from pathogens, inhibits bacterial growth, and potentiates antibiotic activities. Chemical Research in Toxicology. doi:10.1021/acs.chemrestox.2c00049
NLM
Santos MC dos, Tairum CA, Cabrera VIM, Cauz ACG, Ribeiro LF, Toledo Junior JC, Toyama MH, Lago JHG, Brocchi M. Adenanthin is an efficient inhibitor of peroxiredoxins from pathogens, inhibits bacterial growth, and potentiates antibiotic activities [Internet]. Chemical Research in Toxicology. 2022 ;[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/acs.chemrestox.2c00049
Vancouver
Santos MC dos, Tairum CA, Cabrera VIM, Cauz ACG, Ribeiro LF, Toledo Junior JC, Toyama MH, Lago JHG, Brocchi M. Adenanthin is an efficient inhibitor of peroxiredoxins from pathogens, inhibits bacterial growth, and potentiates antibiotic activities [Internet]. Chemical Research in Toxicology. 2022 ;[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/acs.chemrestox.2c00049
Artigo de periodico
Nonclinical toxicological studies of Brazilian red propolis and its primary botanical source Dalbergia ecastaphyllum (2021)
Mejía, Jennyfer Andrea Aldana; Ccana-Ccapatinta, Gari Vidal ; Squarisi, Iara Silva; Nascimento, Samuel; Tanimoto, Matheus Hikaru ; Ribeiro, Victor Pena ; Arruda, Caroline; Nicolella, Heloiza; Esperandim, Tábata Rodrigues; Ribeiro, Arthur B.; Freitas, Karoline S. de; Silva, Lucas H. D. da; Ozelin, Saulo D.; Oliveira, Lucas T. S.; Melo, Alex L. A.; Tavares, Denise C.; Bastos, Jairo Kenupp
Fonte: Chemical Research in Toxicology. Unidade: FCFRP
Assuntos: CROMATOGRAFIA, TOXICOLOGIA, PRÓPOLIS, PRODUTOS NATURAIS
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ABNT
MEJÍA, Jennyfer Andrea Aldana et al. Nonclinical toxicological studies of Brazilian red propolis and its primary botanical source Dalbergia ecastaphyllum. Chemical Research in Toxicology, v. 34, n. 4, p. 1024-1033, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.chemrestox.0c00356. Acesso em: 07 out. 2025.
APA
Mejía, J. A. A., Ccana-Ccapatinta, G. V., Squarisi, I. S., Nascimento, S., Tanimoto, M. H., Ribeiro, V. P., et al. (2021). Nonclinical toxicological studies of Brazilian red propolis and its primary botanical source Dalbergia ecastaphyllum. Chemical Research in Toxicology, 34( 4), 1024-1033. doi:10.1021/acs.chemrestox.0c00356
NLM
Mejía JAA, Ccana-Ccapatinta GV, Squarisi IS, Nascimento S, Tanimoto MH, Ribeiro VP, Arruda C, Nicolella H, Esperandim TR, Ribeiro AB, Freitas KS de, Silva LHD da, Ozelin SD, Oliveira LTS, Melo ALA, Tavares DC, Bastos JK. Nonclinical toxicological studies of Brazilian red propolis and its primary botanical source Dalbergia ecastaphyllum [Internet]. Chemical Research in Toxicology. 2021 ; 34( 4): 1024-1033.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/acs.chemrestox.0c00356
Vancouver
Mejía JAA, Ccana-Ccapatinta GV, Squarisi IS, Nascimento S, Tanimoto MH, Ribeiro VP, Arruda C, Nicolella H, Esperandim TR, Ribeiro AB, Freitas KS de, Silva LHD da, Ozelin SD, Oliveira LTS, Melo ALA, Tavares DC, Bastos JK. Nonclinical toxicological studies of Brazilian red propolis and its primary botanical source Dalbergia ecastaphyllum [Internet]. Chemical Research in Toxicology. 2021 ; 34( 4): 1024-1033.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/acs.chemrestox.0c00356
Artigo de periodico
Mass spectrometry characterization of thiol conjugates linked to polyoxygenated polyunsaturated fatty acid species (2019)
Chaves Filho, Adriano de Britto ; Yoshinaga, Marcos Yukio ; Dantas, Lucas Souza; Diniz, Larissa Regina; Pinto, Isabella Fernanda Dantas; Miyamoto, Sayuri
Fonte: Chemical Research in Toxicology. Unidade: IQ
Assuntos: ESPECTROMETRIA DE MASSAS, ÁCIDOS GRAXOS
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ABNT
CHAVES FILHO, Adriano de Britto et al. Mass spectrometry characterization of thiol conjugates linked to polyoxygenated polyunsaturated fatty acid species. Chemical Research in Toxicology, v. 32, n. 10, p. 2028-2041, 2019Tradução . . Disponível em: https://doi.org/10.1021/acs.chemrestox.9b00199. Acesso em: 07 out. 2025.
APA
Chaves Filho, A. de B., Yoshinaga, M. Y., Dantas, L. S., Diniz, L. R., Pinto, I. F. D., & Miyamoto, S. (2019). Mass spectrometry characterization of thiol conjugates linked to polyoxygenated polyunsaturated fatty acid species. Chemical Research in Toxicology, 32( 10), 2028-2041. doi:10.1021/acs.chemrestox.9b00199
NLM
Chaves Filho A de B, Yoshinaga MY, Dantas LS, Diniz LR, Pinto IFD, Miyamoto S. Mass spectrometry characterization of thiol conjugates linked to polyoxygenated polyunsaturated fatty acid species [Internet]. Chemical Research in Toxicology. 2019 ; 32( 10): 2028-2041.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/acs.chemrestox.9b00199
Vancouver
Chaves Filho A de B, Yoshinaga MY, Dantas LS, Diniz LR, Pinto IFD, Miyamoto S. Mass spectrometry characterization of thiol conjugates linked to polyoxygenated polyunsaturated fatty acid species [Internet]. Chemical Research in Toxicology. 2019 ; 32( 10): 2028-2041.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/acs.chemrestox.9b00199
Artigo de periodico
Ferroptosis: the greasy side of cell death (2019)
Angeli, José Pedro Friedmann; Miyamoto, Sayuri ; Schulze, Almut
Fonte: Chemical Research in Toxicology. Unidade: IQ
Assunto: CÉLULAS
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ABNT
ANGELI, José Pedro Friedmann e MIYAMOTO, Sayuri e SCHULZE, Almut. Ferroptosis: the greasy side of cell death. Chemical Research in Toxicology, v. 32, p. 362-369, 2019Tradução . . Disponível em: https://doi.org/10.1021/acs.chemrestox.8b00349. Acesso em: 07 out. 2025.
APA
Angeli, J. P. F., Miyamoto, S., & Schulze, A. (2019). Ferroptosis: the greasy side of cell death. Chemical Research in Toxicology, 32, 362-369. doi:10.1021/acs.chemrestox.8b00349
NLM
Angeli JPF, Miyamoto S, Schulze A. Ferroptosis: the greasy side of cell death [Internet]. Chemical Research in Toxicology. 2019 ; 32 362-369.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/acs.chemrestox.8b00349
Vancouver
Angeli JPF, Miyamoto S, Schulze A. Ferroptosis: the greasy side of cell death [Internet]. Chemical Research in Toxicology. 2019 ; 32 362-369.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/acs.chemrestox.8b00349
Artigo de periodico
DNA adduct formation in the lungs and brain of rats exposed to low concentrations of [C-13(2)]-acetaldehyde (2018)
Sanchez, Angelica B; Garcia, Camila C. M; Freitas, Florêncio Porto; Batista, Guilherme Lopes; Lopes, Fernando Silva; Carvalho, Victor H; Ronsein, Graziella Eliza ; Gutz, Ivano Gebhardt Rolf ; Di Mascio, Paolo ; Medeiros, Marisa Helena Gennari de
Fonte: Chemical Research in Toxicology. Unidade: IQ
Assuntos: POLUIÇÃO ATMOSFÉRICA, ADUTOS DE DNA
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ABNT
SANCHEZ, Angelica B et al. DNA adduct formation in the lungs and brain of rats exposed to low concentrations of [C-13(2)]-acetaldehyde. Chemical Research in Toxicology, v. 31, n. 5, p. 332-339, 2018Tradução . . Disponível em: https://doi.org/10.1021/acs.chemrestox.8b00016. Acesso em: 07 out. 2025.
APA
Sanchez, A. B., Garcia, C. C. M., Freitas, F. P., Batista, G. L., Lopes, F. S., Carvalho, V. H., et al. (2018). DNA adduct formation in the lungs and brain of rats exposed to low concentrations of [C-13(2)]-acetaldehyde. Chemical Research in Toxicology, 31( 5), 332-339. doi:10.1021/acs.chemrestox.8b00016
NLM
Sanchez AB, Garcia CCM, Freitas FP, Batista GL, Lopes FS, Carvalho VH, Ronsein GE, Gutz IGR, Di Mascio P, Medeiros MHG de. DNA adduct formation in the lungs and brain of rats exposed to low concentrations of [C-13(2)]-acetaldehyde [Internet]. Chemical Research in Toxicology. 2018 ; 31( 5): 332-339.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/acs.chemrestox.8b00016
Vancouver
Sanchez AB, Garcia CCM, Freitas FP, Batista GL, Lopes FS, Carvalho VH, Ronsein GE, Gutz IGR, Di Mascio P, Medeiros MHG de. DNA adduct formation in the lungs and brain of rats exposed to low concentrations of [C-13(2)]-acetaldehyde [Internet]. Chemical Research in Toxicology. 2018 ; 31( 5): 332-339.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/acs.chemrestox.8b00016
Artigo de periodico
Chemical characterization of urate hydroperoxide, a pro-oxidant intermediate generated by urate oxidation in inflammatory and photoinduced processes (2015)
Patricio, Eliziane de Souza; Prado, Fernanda Manso ; Silva, Railmara Pereira da; Carvalho, Larissa Anastácio da Costa; Prates, Marcus Vinicius Camargo; Dadamos, Tony Rogério de Lima; Bertotti, Mauro ; Di Mascio, Paolo ; Kettle, Antony; Meotti, Flavia Carla
Fonte: Chemical Research in Toxicology. Unidade: IQ
Assuntos: OXIDAÇÃO, INFLAMAÇÃO
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ABNT
PATRICIO, Eliziane de Souza et al. Chemical characterization of urate hydroperoxide, a pro-oxidant intermediate generated by urate oxidation in inflammatory and photoinduced processes. Chemical Research in Toxicology, v. 28, n. 8, p. 1556-1566, 2015Tradução . . Disponível em: https://doi.org/10.1021/acs.chemrestox.5b00132. Acesso em: 07 out. 2025.
APA
Patricio, E. de S., Prado, F. M., Silva, R. P. da, Carvalho, L. A. da C., Prates, M. V. C., Dadamos, T. R. de L., et al. (2015). Chemical characterization of urate hydroperoxide, a pro-oxidant intermediate generated by urate oxidation in inflammatory and photoinduced processes. Chemical Research in Toxicology, 28( 8), 1556-1566. doi:10.1021/acs.chemrestox.5b00132
NLM
Patricio E de S, Prado FM, Silva RP da, Carvalho LA da C, Prates MVC, Dadamos TR de L, Bertotti M, Di Mascio P, Kettle A, Meotti FC. Chemical characterization of urate hydroperoxide, a pro-oxidant intermediate generated by urate oxidation in inflammatory and photoinduced processes [Internet]. Chemical Research in Toxicology. 2015 ; 28( 8): 1556-1566.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/acs.chemrestox.5b00132
Vancouver
Patricio E de S, Prado FM, Silva RP da, Carvalho LA da C, Prates MVC, Dadamos TR de L, Bertotti M, Di Mascio P, Kettle A, Meotti FC. Chemical characterization of urate hydroperoxide, a pro-oxidant intermediate generated by urate oxidation in inflammatory and photoinduced processes [Internet]. Chemical Research in Toxicology. 2015 ; 28( 8): 1556-1566.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/acs.chemrestox.5b00132
Artigo de periodico
Covalent binding and anchoring of cytochrome c to mitochondrial mimetic membranes promoted by cholesterol carboxyaldehyde (2013)
Genaro-Mattos, Thiago Cardoso; Appolinário, Patricia Postilione; Mugnol, Katia Cristina Ugolini; Junior, Carlos Bloch; Nantes, Iseli Lourenço; Di Mascio, Paolo ; Miyamoto, Sayuri
Fonte: Chemical Research in Toxicology. Unidade: IQ
Assunto: MITOCÔNDRIAS
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ABNT
GENARO-MATTOS, Thiago Cardoso et al. Covalent binding and anchoring of cytochrome c to mitochondrial mimetic membranes promoted by cholesterol carboxyaldehyde. Chemical Research in Toxicology, v. 26, n. 10, p. 1536-1544, 2013Tradução . . Disponível em: https://doi.org/10.1021/tx4002385. Acesso em: 07 out. 2025.
APA
Genaro-Mattos, T. C., Appolinário, P. P., Mugnol, K. C. U., Junior, C. B., Nantes, I. L., Di Mascio, P., & Miyamoto, S. (2013). Covalent binding and anchoring of cytochrome c to mitochondrial mimetic membranes promoted by cholesterol carboxyaldehyde. Chemical Research in Toxicology, 26( 10), 1536-1544. doi:10.1021/tx4002385
NLM
Genaro-Mattos TC, Appolinário PP, Mugnol KCU, Junior CB, Nantes IL, Di Mascio P, Miyamoto S. Covalent binding and anchoring of cytochrome c to mitochondrial mimetic membranes promoted by cholesterol carboxyaldehyde [Internet]. Chemical Research in Toxicology. 2013 ; 26( 10): 1536-1544.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/tx4002385
Vancouver
Genaro-Mattos TC, Appolinário PP, Mugnol KCU, Junior CB, Nantes IL, Di Mascio P, Miyamoto S. Covalent binding and anchoring of cytochrome c to mitochondrial mimetic membranes promoted by cholesterol carboxyaldehyde [Internet]. Chemical Research in Toxicology. 2013 ; 26( 10): 1536-1544.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/tx4002385
Artigo de periodico
Connecting the chemical and biological properties of nitric oxide (2012)
Toledo Junior, José Carlos; Augusto, Ohara
Fonte: Chemical Research in Toxicology. Unidades: FFCLRP, IQ
Assuntos: ÓXIDO NÍTRICO, BIOQUÍMICA
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ABNT
TOLEDO JUNIOR, José Carlos e AUGUSTO, Ohara. Connecting the chemical and biological properties of nitric oxide. Chemical Research in Toxicology, v. 25, n. 5, p. 975-989, 2012Tradução . . Disponível em: https://doi.org/10.1021/tx300042g. Acesso em: 07 out. 2025.
APA
Toledo Junior, J. C., & Augusto, O. (2012). Connecting the chemical and biological properties of nitric oxide. Chemical Research in Toxicology, 25( 5), 975-989. doi:10.1021/tx300042g
NLM
Toledo Junior JC, Augusto O. Connecting the chemical and biological properties of nitric oxide [Internet]. Chemical Research in Toxicology. 2012 ; 25( 5): 975-989.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/tx300042g
Vancouver
Toledo Junior JC, Augusto O. Connecting the chemical and biological properties of nitric oxide [Internet]. Chemical Research in Toxicology. 2012 ; 25( 5): 975-989.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/tx300042g
Artigo de periodico
Cholesterol hydroperoxides generate singlet molecular oxygen [O IND. 2'('ANTPOT. 1 delta IND. g')]': Near-IR emission, 'ANTPOT. 18 O'-labeled hydroperoxides, and mass spectrometry (2011)
Uemi, Miriam; Ronsein, Graziella Eliza ; Prado, Fernanda Manso ; Motta, Flávia Daniela; Miyamoto, Sayuri ; Medeiros, Marisa Helena Gennari de ; Di Mascio, Paolo
Fonte: Chemical Research in Toxicology. Unidade: IQ
Assuntos: ÁCIDO LINOLEICO, OZÔNIO, LIPÍDEOS
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ABNT
UEMI, Miriam et al. Cholesterol hydroperoxides generate singlet molecular oxygen [O IND. 2'('ANTPOT. 1 delta IND. g')]': Near-IR emission, 'ANTPOT. 18 O'-labeled hydroperoxides, and mass spectrometry. Chemical Research in Toxicology, v. 24, n. 6, p. 887-895, 2011Tradução . . Disponível em: https://doi.org/10.1021/tx200079d. Acesso em: 07 out. 2025.
APA
Uemi, M., Ronsein, G. E., Prado, F. M., Motta, F. D., Miyamoto, S., Medeiros, M. H. G. de, & Di Mascio, P. (2011). Cholesterol hydroperoxides generate singlet molecular oxygen [O IND. 2'('ANTPOT. 1 delta IND. g')]': Near-IR emission, 'ANTPOT. 18 O'-labeled hydroperoxides, and mass spectrometry. Chemical Research in Toxicology, 24( 6), 887-895. doi:10.1021/tx200079d
NLM
Uemi M, Ronsein GE, Prado FM, Motta FD, Miyamoto S, Medeiros MHG de, Di Mascio P. Cholesterol hydroperoxides generate singlet molecular oxygen [O IND. 2'('ANTPOT. 1 delta IND. g')]': Near-IR emission, 'ANTPOT. 18 O'-labeled hydroperoxides, and mass spectrometry [Internet]. Chemical Research in Toxicology. 2011 ; 24( 6): 887-895.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/tx200079d
Vancouver
Uemi M, Ronsein GE, Prado FM, Motta FD, Miyamoto S, Medeiros MHG de, Di Mascio P. Cholesterol hydroperoxides generate singlet molecular oxygen [O IND. 2'('ANTPOT. 1 delta IND. g')]': Near-IR emission, 'ANTPOT. 18 O'-labeled hydroperoxides, and mass spectrometry [Internet]. Chemical Research in Toxicology. 2011 ; 24( 6): 887-895.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/tx200079d
Artigo de periodico
Acetyl radical production by the methylglyoxal-peroxynitrite system: a possible route for L-lysine acetylation (2010)
Massari Filho, Júlio; Tokikawa, Rita; Zanolli Filho, Luiz Antonio; Tavares, Marina Franco Maggi ; Assunção, Nilson Antônio; Bechara, Etelvino José Henriques
Fonte: Chemical Research in Toxicology. Unidade: IQ
Assuntos: AMINOÁCIDOS, BIOQUÍMICA
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ABNT
MASSARI FILHO, Júlio et al. Acetyl radical production by the methylglyoxal-peroxynitrite system: a possible route for L-lysine acetylation. Chemical Research in Toxicology, v. 23, n. 11, p. 1762-1770, 2010Tradução . . Disponível em: https://doi.org/10.1021/tx1002244. Acesso em: 07 out. 2025.
APA
Massari Filho, J., Tokikawa, R., Zanolli Filho, L. A., Tavares, M. F. M., Assunção, N. A., & Bechara, E. J. H. (2010). Acetyl radical production by the methylglyoxal-peroxynitrite system: a possible route for L-lysine acetylation. Chemical Research in Toxicology, 23( 11), 1762-1770. doi:10.1021/tx1002244
NLM
Massari Filho J, Tokikawa R, Zanolli Filho LA, Tavares MFM, Assunção NA, Bechara EJH. Acetyl radical production by the methylglyoxal-peroxynitrite system: a possible route for L-lysine acetylation [Internet]. Chemical Research in Toxicology. 2010 ; 23( 11): 1762-1770.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/tx1002244
Vancouver
Massari Filho J, Tokikawa R, Zanolli Filho LA, Tavares MFM, Assunção NA, Bechara EJH. Acetyl radical production by the methylglyoxal-peroxynitrite system: a possible route for L-lysine acetylation [Internet]. Chemical Research in Toxicology. 2010 ; 23( 11): 1762-1770.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/tx1002244
Artigo de periodico
Ultrasensitive simultaneous quantification of 1,'N POT. 2'-Etheno-2′-deoxyguanosine and 1,'N POT. 2'-propano-2′-deoxyguanosine in DNA by an online liquid chromatography−electrospray tandem mass spectrometry assay (2010)
Garcia, Camila Carriao Machado; Freitas, Florêncio Porto; Di Mascio, Paolo ; Medeiros, Marisa Helena Gennari de
Fonte: Chemical Research in Toxicology. Unidade: IQ
Assuntos: DNA, POLUIÇÃO ATMOSFÉRICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GARCIA, Camila Carriao Machado et al. Ultrasensitive simultaneous quantification of 1,'N POT. 2'-Etheno-2′-deoxyguanosine and 1,'N POT. 2'-propano-2′-deoxyguanosine in DNA by an online liquid chromatography−electrospray tandem mass spectrometry assay. Chemical Research in Toxicology, v. 23, n. 7, p. 1245-1255, 2010Tradução . . Disponível em: https://doi.org/10.102/tx1001018. Acesso em: 07 out. 2025.
APA
Garcia, C. C. M., Freitas, F. P., Di Mascio, P., & Medeiros, M. H. G. de. (2010). Ultrasensitive simultaneous quantification of 1,'N POT. 2'-Etheno-2′-deoxyguanosine and 1,'N POT. 2'-propano-2′-deoxyguanosine in DNA by an online liquid chromatography−electrospray tandem mass spectrometry assay. Chemical Research in Toxicology, 23( 7), 1245-1255. doi:10.102/tx1001018
NLM
Garcia CCM, Freitas FP, Di Mascio P, Medeiros MHG de. Ultrasensitive simultaneous quantification of 1,'N POT. 2'-Etheno-2′-deoxyguanosine and 1,'N POT. 2'-propano-2′-deoxyguanosine in DNA by an online liquid chromatography−electrospray tandem mass spectrometry assay [Internet]. Chemical Research in Toxicology. 2010 ; 23( 7): 1245-1255.[citado 2025 out. 07 ] Available from: https://doi.org/10.102/tx1001018
Vancouver
Garcia CCM, Freitas FP, Di Mascio P, Medeiros MHG de. Ultrasensitive simultaneous quantification of 1,'N POT. 2'-Etheno-2′-deoxyguanosine and 1,'N POT. 2'-propano-2′-deoxyguanosine in DNA by an online liquid chromatography−electrospray tandem mass spectrometry assay [Internet]. Chemical Research in Toxicology. 2010 ; 23( 7): 1245-1255.[citado 2025 out. 07 ] Available from: https://doi.org/10.102/tx1001018
Artigo de periodico
Exocyclic DNA adducts as biomarkers of lipid oxidation and predictors of disease: challenges in developing sensitive and specific methods for clinical studies (2009)
Medeiros, Marisa Helena Gennari de
Fonte: Chemical Research in Toxicology. Unidade: IQ
Assuntos: BIOMARCADORES, ESTRESSE OXIDATIVO, DANO AO DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MEDEIROS, Marisa Helena Gennari de. Exocyclic DNA adducts as biomarkers of lipid oxidation and predictors of disease: challenges in developing sensitive and specific methods for clinical studies. Chemical Research in Toxicology, v. 22, n. 3, p. 419-425, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/tx800367d. Acesso em: 07 out. 2025.
APA
Medeiros, M. H. G. de. (2009). Exocyclic DNA adducts as biomarkers of lipid oxidation and predictors of disease: challenges in developing sensitive and specific methods for clinical studies. Chemical Research in Toxicology, 22( 3), 419-425. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/tx800367d
NLM
Medeiros MHG de. Exocyclic DNA adducts as biomarkers of lipid oxidation and predictors of disease: challenges in developing sensitive and specific methods for clinical studies [Internet]. Chemical Research in Toxicology. 2009 ; 22( 3): 419-425.[citado 2025 out. 07 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800367d
Vancouver
Medeiros MHG de. Exocyclic DNA adducts as biomarkers of lipid oxidation and predictors of disease: challenges in developing sensitive and specific methods for clinical studies [Internet]. Chemical Research in Toxicology. 2009 ; 22( 3): 419-425.[citado 2025 out. 07 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800367d
Artigo de periodico
Generation of cholesterol carboxyaldehyde by the reaction of singlet molecular oxygen ['O IND. 2' (ANTPOT. 1 delta IND. g)] as well as ozone with cholesterol (2009)
Uemi, Miriam; Ronsein, Graziella Eliza ; Miyamoto, Sayuri ; Medeiros, Marisa Helena Gennari de ; Di Mascio, Paolo
Fonte: Chemical Research in Toxicology. Unidade: IQ
Assuntos: DOENÇA DE ALZHEIMER, ÁCIDO LINOLEICO, DANO AO DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
UEMI, Miriam et al. Generation of cholesterol carboxyaldehyde by the reaction of singlet molecular oxygen ['O IND. 2' (ANTPOT. 1 delta IND. g)] as well as ozone with cholesterol. Chemical Research in Toxicology, v. 22, n. 5, p. 875-884, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/tx800447b. Acesso em: 07 out. 2025.
APA
Uemi, M., Ronsein, G. E., Miyamoto, S., Medeiros, M. H. G. de, & Di Mascio, P. (2009). Generation of cholesterol carboxyaldehyde by the reaction of singlet molecular oxygen ['O IND. 2' (ANTPOT. 1 delta IND. g)] as well as ozone with cholesterol. Chemical Research in Toxicology, 22( 5), 875-884. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/tx800447b
NLM
Uemi M, Ronsein GE, Miyamoto S, Medeiros MHG de, Di Mascio P. Generation of cholesterol carboxyaldehyde by the reaction of singlet molecular oxygen ['O IND. 2' (ANTPOT. 1 delta IND. g)] as well as ozone with cholesterol [Internet]. Chemical Research in Toxicology. 2009 ; 22( 5): 875-884.[citado 2025 out. 07 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800447b
Vancouver
Uemi M, Ronsein GE, Miyamoto S, Medeiros MHG de, Di Mascio P. Generation of cholesterol carboxyaldehyde by the reaction of singlet molecular oxygen ['O IND. 2' (ANTPOT. 1 delta IND. g)] as well as ozone with cholesterol [Internet]. Chemical Research in Toxicology. 2009 ; 22( 5): 875-884.[citado 2025 out. 07 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800447b
Artigo de periodico
Peroxymonocarbonate and carbonate radical displace the hydroxyl-like oxidant in the Sod1 peroxidase activity under physiological conditions (2009)
Medinas, Danilo Bilches ; Toledo Junior, José Carlos; Cerchiaro, Giselle; Amaral, Antonia Tavares do ; Rezende, Leandro de; Malvezzi, Alberto; Augusto, Ohara
Fonte: Chemical Research in Toxicology. Unidade: IQ
Assuntos: PEROXIDASE, BIOQUÍMICA, SUPERÓXIDO DISMUTASE
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ABNT
MEDINAS, Danilo Bilches et al. Peroxymonocarbonate and carbonate radical displace the hydroxyl-like oxidant in the Sod1 peroxidase activity under physiological conditions. Chemical Research in Toxicology, v. 22, n. 4, p. 639-648, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/tx800287m. Acesso em: 07 out. 2025.
APA
Medinas, D. B., Toledo Junior, J. C., Cerchiaro, G., Amaral, A. T. do, Rezende, L. de, Malvezzi, A., & Augusto, O. (2009). Peroxymonocarbonate and carbonate radical displace the hydroxyl-like oxidant in the Sod1 peroxidase activity under physiological conditions. Chemical Research in Toxicology, 22( 4), 639-648. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/tx800287m
NLM
Medinas DB, Toledo Junior JC, Cerchiaro G, Amaral AT do, Rezende L de, Malvezzi A, Augusto O. Peroxymonocarbonate and carbonate radical displace the hydroxyl-like oxidant in the Sod1 peroxidase activity under physiological conditions [Internet]. Chemical Research in Toxicology. 2009 ; 22( 4): 639-648.[citado 2025 out. 07 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800287m
Vancouver
Medinas DB, Toledo Junior JC, Cerchiaro G, Amaral AT do, Rezende L de, Malvezzi A, Augusto O. Peroxymonocarbonate and carbonate radical displace the hydroxyl-like oxidant in the Sod1 peroxidase activity under physiological conditions [Internet]. Chemical Research in Toxicology. 2009 ; 22( 4): 639-648.[citado 2025 out. 07 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/tx800287m
Artigo de periodico
Mass Spectrometric Analysis of a Cyclic 7,8-Butanoguanine Adduct of N-Nitrosopyrrolidine: Comparison to Other N-Nitrosopyrrolidine Adducts in Rat Hepatic DNA (2009)
Loureiro, Ana Paula de Melo ; Zhang, Wenbing; Kassie, Fekadu; Zhang, Siyi; Villalta, Peter W; Wang, Mingyao; Hecht, Stephen S
Fonte: Chemical Research in Toxicology. Unidade: FCF
Assuntos: ESPECTROMETRIA DE MASSAS (ANÁLISE), HEPATOPATIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOUREIRO, Ana Paula de Melo et al. Mass Spectrometric Analysis of a Cyclic 7,8-Butanoguanine Adduct of N-Nitrosopyrrolidine: Comparison to Other N-Nitrosopyrrolidine Adducts in Rat Hepatic DNA. Chemical Research in Toxicology, v. 22, n. 10, p. 1728-1735, 2009Tradução . . Disponível em: https://doi.org/10.1021/tx900238t. Acesso em: 07 out. 2025.
APA
Loureiro, A. P. de M., Zhang, W., Kassie, F., Zhang, S., Villalta, P. W., Wang, M., & Hecht, S. S. (2009). Mass Spectrometric Analysis of a Cyclic 7,8-Butanoguanine Adduct of N-Nitrosopyrrolidine: Comparison to Other N-Nitrosopyrrolidine Adducts in Rat Hepatic DNA. Chemical Research in Toxicology, 22( 10), 1728-1735. doi:10.1021/tx900238t
NLM
Loureiro AP de M, Zhang W, Kassie F, Zhang S, Villalta PW, Wang M, Hecht SS. Mass Spectrometric Analysis of a Cyclic 7,8-Butanoguanine Adduct of N-Nitrosopyrrolidine: Comparison to Other N-Nitrosopyrrolidine Adducts in Rat Hepatic DNA [Internet]. Chemical Research in Toxicology. 2009 ; 22( 10): 1728-1735.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/tx900238t
Vancouver
Loureiro AP de M, Zhang W, Kassie F, Zhang S, Villalta PW, Wang M, Hecht SS. Mass Spectrometric Analysis of a Cyclic 7,8-Butanoguanine Adduct of N-Nitrosopyrrolidine: Comparison to Other N-Nitrosopyrrolidine Adducts in Rat Hepatic DNA [Internet]. Chemical Research in Toxicology. 2009 ; 22( 10): 1728-1735.[citado 2025 out. 07 ] Available from: https://doi.org/10.1021/tx900238t
Artigo de periodico
Tryptophan oxidation by singlet molecular oxygen ['O IND. 2' ('ANTPOT. 1 Delta IND. g')]: Mechanistic studies using 'ANTPOT. 18 O'-labeled hydroperoxides, mass spectrometry, and light emission measurements (2008)
Ronsein, Graziella Eliza ; Oliveira, Mauricio César Bof de; Miyamoto, Sayuri ; Medeiros, Marisa Helena Gennari de ; Di Mascio, Paolo
Fonte: Chemical Research in Toxicology. Unidade: IQ
Assuntos: BIOQUÍMICA, ESPECTROMETRIA DE MASSAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RONSEIN, Graziella Eliza et al. Tryptophan oxidation by singlet molecular oxygen ['O IND. 2' ('ANTPOT. 1 Delta IND. g')]: Mechanistic studies using 'ANTPOT. 18 O'-labeled hydroperoxides, mass spectrometry, and light emission measurements. Chemical Research in Toxicology, v. 21, n. 6, p. 1271-1283, 2008Tradução . . Acesso em: 07 out. 2025.
APA
Ronsein, G. E., Oliveira, M. C. B. de, Miyamoto, S., Medeiros, M. H. G. de, & Di Mascio, P. (2008). Tryptophan oxidation by singlet molecular oxygen ['O IND. 2' ('ANTPOT. 1 Delta IND. g')]: Mechanistic studies using 'ANTPOT. 18 O'-labeled hydroperoxides, mass spectrometry, and light emission measurements. Chemical Research in Toxicology, 21( 6), 1271-1283.
NLM
Ronsein GE, Oliveira MCB de, Miyamoto S, Medeiros MHG de, Di Mascio P. Tryptophan oxidation by singlet molecular oxygen ['O IND. 2' ('ANTPOT. 1 Delta IND. g')]: Mechanistic studies using 'ANTPOT. 18 O'-labeled hydroperoxides, mass spectrometry, and light emission measurements. Chemical Research in Toxicology. 2008 ;21( 6): 1271-1283.[citado 2025 out. 07 ]
Vancouver
Ronsein GE, Oliveira MCB de, Miyamoto S, Medeiros MHG de, Di Mascio P. Tryptophan oxidation by singlet molecular oxygen ['O IND. 2' ('ANTPOT. 1 Delta IND. g')]: Mechanistic studies using 'ANTPOT. 18 O'-labeled hydroperoxides, mass spectrometry, and light emission measurements. Chemical Research in Toxicology. 2008 ;21( 6): 1271-1283.[citado 2025 out. 07 ]

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