Quantitative proteomics analysis of heat shock proteins involved in unfoldeld protein response in glioblastoma cell lines induced by different drugs (2017)
- Authors:
- USP affiliated authors: ROSA, JOSE CESAR - FMRP ; MARIE, SUELY KAZUE NAGAHASHI - FM ; SHINJO, SUELI MIEKO OBA - FM ; IZUMI, CLARICE - FMRP
- Unidades: FMRP; FM
- Assunto: ESPECTROMETRIA
- Language: Inglês
- Imprenta:
- Source:
- Título: Journal of the American Society for Mass Spectrometry
- ISSN: 1044-0305
- Volume/Número/Paginação/Ano: v. 28, suppl. 1, res. WP690, 2017
- Conference titles: Conference on Mass Spectrometry and Allied Topics
-
ABNT
ROSA, José César et al. Quantitative proteomics analysis of heat shock proteins involved in unfoldeld protein response in glioblastoma cell lines induced by different drugs. Journal of the American Society for Mass Spectrometry. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 02 out. 2024. , 2017 -
APA
Rosa, J. C., Laure, H. J., Thomé, C. H., Ferreira, G. A., Marie, S. K. N., Shinjo, S. M. O., & Izumi, C. (2017). Quantitative proteomics analysis of heat shock proteins involved in unfoldeld protein response in glioblastoma cell lines induced by different drugs. Journal of the American Society for Mass Spectrometry. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Rosa JC, Laure HJ, Thomé CH, Ferreira GA, Marie SKN, Shinjo SMO, Izumi C. Quantitative proteomics analysis of heat shock proteins involved in unfoldeld protein response in glioblastoma cell lines induced by different drugs. Journal of the American Society for Mass Spectrometry. 2017 ; 28[citado 2024 out. 02 ] -
Vancouver
Rosa JC, Laure HJ, Thomé CH, Ferreira GA, Marie SKN, Shinjo SMO, Izumi C. Quantitative proteomics analysis of heat shock proteins involved in unfoldeld protein response in glioblastoma cell lines induced by different drugs. Journal of the American Society for Mass Spectrometry. 2017 ; 28[citado 2024 out. 02 ] - Evaluation of proliferation and migration of T98G and U87MG cells under EGF stimulus
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