Radiation-induced (5′R)-and (5′S)-purine 5′,8-cyclo-2′-deoxyribonucleosides in human cells: a revisited analysis of HPLC-MS/MS measurements [Letter] (2019)
- Authors:
- Autor USP: MASCIO, PAOLO DI - IQ
- Unidade: IQ
- DOI: 10.1080/10715762.2019.1605169
- Subjects: NEOPLASIAS MAMÁRIAS; RADIAÇÃO IONIZANTE; PERÓXIDO DE HIDROGÊNIO
- Language: Inglês
- Imprenta:
- Source:
- Título: Free Radical Research
- ISSN: 1071-5762
- Volume/Número/Paginação/Ano: v. 53, n. 5, p. 574-577, 2019
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
CADET, Jean e DI MASCIO, Paolo e WAGNER, James Richard. Radiation-induced (5′R)-and (5′S)-purine 5′,8-cyclo-2′-deoxyribonucleosides in human cells: a revisited analysis of HPLC-MS/MS measurements [Letter]. Free Radical Research. Oxford: Instituto de Química, Universidade de São Paulo. Disponível em: https://doi.org/10.1080/10715762.2019.1605169. Acesso em: 14 fev. 2026. , 2019 -
APA
Cadet, J., Di Mascio, P., & Wagner, J. R. (2019). Radiation-induced (5′R)-and (5′S)-purine 5′,8-cyclo-2′-deoxyribonucleosides in human cells: a revisited analysis of HPLC-MS/MS measurements [Letter]. Free Radical Research. Oxford: Instituto de Química, Universidade de São Paulo. doi:10.1080/10715762.2019.1605169 -
NLM
Cadet J, Di Mascio P, Wagner JR. Radiation-induced (5′R)-and (5′S)-purine 5′,8-cyclo-2′-deoxyribonucleosides in human cells: a revisited analysis of HPLC-MS/MS measurements [Letter] [Internet]. Free Radical Research. 2019 ; 53( 5): 574-577.[citado 2026 fev. 14 ] Available from: https://doi.org/10.1080/10715762.2019.1605169 -
Vancouver
Cadet J, Di Mascio P, Wagner JR. Radiation-induced (5′R)-and (5′S)-purine 5′,8-cyclo-2′-deoxyribonucleosides in human cells: a revisited analysis of HPLC-MS/MS measurements [Letter] [Internet]. Free Radical Research. 2019 ; 53( 5): 574-577.[citado 2026 fev. 14 ] Available from: https://doi.org/10.1080/10715762.2019.1605169 - Cross-linking methionine and amine residues with reactive halogen species
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Informações sobre o DOI: 10.1080/10715762.2019.1605169 (Fonte: oaDOI API)
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