Effect of the Antioxidant Lipoic Acid in Aortic Phenotype in a Marfan Syndrome Mouse Model (2018)
- Authors:
- Autor USP: DEBBAS, VICTOR - FM
- Unidade: FM
- DOI: 10.1155/2018/3967213
- Subjects: ANEURISMA AÓRTICO; ANTIOXIDANTES; RATOS
- Agências de fomento:
- Financiado pela Fundação Zerbini
- Instituto Nacional de Ciencia e Tecnologia de Processos Redox em Biomedicina (INCT Redoxoma, CNPq)
- Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
- Centro de Pesquisa, Inovacao e Difusao FAPESP (CEPID ""Processos Redox em Biomedicina"") [13/07937-8]
- Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
Processo FAPESP: 2009/54764-6
- Language: Inglês
- Imprenta:
- Source:
- Título: Oxidative medicine and cellular longevity
- ISSN: 1942-0900
- Volume/Número/Paginação/Ano: article ID 3967213, 16p, 2018
- Status:
- Artigo aberto em periódico híbrido (Hybrid Open Access)
- Versão do Documento:
- Versão publicada (Published version)
- Acessar versão aberta:
-
ABNT
GUIDO, Maria C. e DEBBAS, Victor. Effect of the Antioxidant Lipoic Acid in Aortic Phenotype in a Marfan Syndrome Mouse Model. Oxidative medicine and cellular longevity, 2018Tradução . . Disponível em: https://doi.org/10.1155/2018/3967213. Acesso em: 01 abr. 2026. -
APA
Guido, M. C., & Debbas, V. (2018). Effect of the Antioxidant Lipoic Acid in Aortic Phenotype in a Marfan Syndrome Mouse Model. Oxidative medicine and cellular longevity. doi:10.1155/2018/3967213 -
NLM
Guido MC, Debbas V. Effect of the Antioxidant Lipoic Acid in Aortic Phenotype in a Marfan Syndrome Mouse Model [Internet]. Oxidative medicine and cellular longevity. 2018 ;[citado 2026 abr. 01 ] Available from: https://doi.org/10.1155/2018/3967213 -
Vancouver
Guido MC, Debbas V. Effect of the Antioxidant Lipoic Acid in Aortic Phenotype in a Marfan Syndrome Mouse Model [Internet]. Oxidative medicine and cellular longevity. 2018 ;[citado 2026 abr. 01 ] Available from: https://doi.org/10.1155/2018/3967213 - Protein disulfide isomerase plasma levels in healthy humans reveal proteomic signatures involved in contrasting endothelial phenotypes
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