Source: Program and Index. Conference titles: Annual Meeting of the Brazilian Biochemistry and Molecular Biology Society (SBBq). Unidades: EACH, IME, IQ
Assunto: COMPUTAÇÃO APLICADA
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ABNT
REIS, Marcelo da Silva et al. Modeling the kinetics of Ras/MAPK and PI3K/AKT signaling pathways in the K-Ras-driven mouse Y1 adrenocortical tumor cells: novel insights into the mechanisms of FGF2-driven cell cycle arrest. 2014, Anais.. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular (SBBq), 2014. Disponível em: https://f1000research.com/posters/1095752. Acesso em: 01 maio 2024.APA
Reis, M. da S., Dias, M. H. S., Nakano, F., Nöel, V., Barrera, J., & Armelin, H. A. (2014). Modeling the kinetics of Ras/MAPK and PI3K/AKT signaling pathways in the K-Ras-driven mouse Y1 adrenocortical tumor cells: novel insights into the mechanisms of FGF2-driven cell cycle arrest. In Program and Index. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular (SBBq). Recuperado de https://f1000research.com/posters/1095752NLM
Reis M da S, Dias MHS, Nakano F, Nöel V, Barrera J, Armelin HA. Modeling the kinetics of Ras/MAPK and PI3K/AKT signaling pathways in the K-Ras-driven mouse Y1 adrenocortical tumor cells: novel insights into the mechanisms of FGF2-driven cell cycle arrest [Internet]. Program and Index. 2014 ;[citado 2024 maio 01 ] Available from: https://f1000research.com/posters/1095752Vancouver
Reis M da S, Dias MHS, Nakano F, Nöel V, Barrera J, Armelin HA. Modeling the kinetics of Ras/MAPK and PI3K/AKT signaling pathways in the K-Ras-driven mouse Y1 adrenocortical tumor cells: novel insights into the mechanisms of FGF2-driven cell cycle arrest [Internet]. Program and Index. 2014 ;[citado 2024 maio 01 ] Available from: https://f1000research.com/posters/1095752