Aluminum-phthalocyanine chloride-based photodynamic therapy inhibits PI3K/AKT/Mtor pathway in oral squamous cell carcinoma cells in vitro (2012)
- Authors:
- Autor USP: TEDESCO, ANTONIO CLAUDIO - FFCLRP
- Unidade: FFCLRP
- DOI: 10.4172/2167-7700.1000107
- Subjects: RADIOTERAPIA; NEOPLASIAS; CARCINOMA
- Language: Inglês
- Imprenta:
- Publisher place: Los Angeles
- Date published: 2012
- Source:
- Título: Chemoterapy : Open Access
- ISSN: 2167-7700
- Volume/Número/Paginação/Ano: v. 1, n. 5, on-line, 2012
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
VELLOSO, Nathália Vieira et al. Aluminum-phthalocyanine chloride-based photodynamic therapy inhibits PI3K/AKT/Mtor pathway in oral squamous cell carcinoma cells in vitro. Chemoterapy : Open Access, v. 1, n. 5, 2012Tradução . . Disponível em: https://doi.org/10.4172/2167-7700.1000107. Acesso em: 24 jan. 2026. -
APA
Velloso, N. V., Muehlmann, L. A., Longo, J. P. F., Silva, J. R. da, Zancanela, D. C., Tedesco, A. C., & Azevedo, R. B. de. (2012). Aluminum-phthalocyanine chloride-based photodynamic therapy inhibits PI3K/AKT/Mtor pathway in oral squamous cell carcinoma cells in vitro. Chemoterapy : Open Access, 1( 5). doi:10.4172/2167-7700.1000107 -
NLM
Velloso NV, Muehlmann LA, Longo JPF, Silva JR da, Zancanela DC, Tedesco AC, Azevedo RB de. Aluminum-phthalocyanine chloride-based photodynamic therapy inhibits PI3K/AKT/Mtor pathway in oral squamous cell carcinoma cells in vitro [Internet]. Chemoterapy : Open Access. 2012 ; 1( 5):[citado 2026 jan. 24 ] Available from: https://doi.org/10.4172/2167-7700.1000107 -
Vancouver
Velloso NV, Muehlmann LA, Longo JPF, Silva JR da, Zancanela DC, Tedesco AC, Azevedo RB de. Aluminum-phthalocyanine chloride-based photodynamic therapy inhibits PI3K/AKT/Mtor pathway in oral squamous cell carcinoma cells in vitro [Internet]. Chemoterapy : Open Access. 2012 ; 1( 5):[citado 2026 jan. 24 ] Available from: https://doi.org/10.4172/2167-7700.1000107 - Evaluation of dark toxicity of 'chlorine IND E6' in cell line J774-A
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Informações sobre o DOI: 10.4172/2167-7700.1000107 (Fonte: oaDOI API)
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