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Documents dont l'auteur est "Chen, Jingkui"

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Nombre de documents: 16

Abusarah, J., Khodayarian, F., El-Hachem, N., Salame, N., Olivier, M., Balood, M., Roversi, K., Talbot, S., Bikorimana, J.-P., Chen, J., Jolicoeur, M., Trudeau, L.-É., Kamyabiazar, S., Annabi, B., Robert, F., Pelletier, J., El-Kadiry, A. E.-H., Shammaa, R., & Rafei, M. (2021). Engineering immunoproteasome-expressing mesenchymal stromal cells: A potent cellular vaccine for lymphoma and melanoma in mice. Cell Reports Medicine, 2(12), 100455 (27 pages). Lien externe

Bardyn, M., Chen, J., Dussiot, M., Crettaz, D., Schmid, L., Längst, E., Amireault, P., Tissot, J.-D., Jolicoeur, M., & Prudent, M. (2020). Restoration of physiological levels of uric acid and ascorbic acid reroutes the metabolism of stored red blood cells. Metabolites, 10(6), 226 (18 pages). Disponible

Laflaquière, B., Leclercq, G., Choey, C., Chen, J., Peres, S., Ito, C., & Jolicoeur, M. (2018). Identifying biomarkers of Wharton's Jelly mesenchymal stromal cells using a dynamic metabolic model: the cell passage effect. Metabolites, 8(1), 18. Disponible

Zhao, X., Kasbi, M., Chen, J., Peres, S., & Jolicoeur, M. (2017). A dynamic metabolic flux analysis of ABE (acetone-butanol-ethanol) fermentation by Clostridium acetobutylicum ATCC 824, with riboflavin as a by-product. Biotechnology and Bioengineering, 114(12), 2907-2919. Lien externe

Zhao, X., Condruz, S., Chen, J., & Jolicoeur, M. (2016). A quantitative metabolomics study of high sodium response in Clostridium acetobutylicum ATCC 824 acetone-butanol-ethanol (ABE) fermentation. Scientific Reports, 6(1), 1-13. Disponible

Ren, X., Chen, J., Deschênes, J.-S., Tremblay, R., & Jolicoeur, M. (2016). Glucose feeding recalibrates carbon flux distribution and favours lipid accumulation in Chlorella protothecoides through cell energetic management. Algal Research-Biomass Biofuels and Bioproducts, 14, 83-91. Lien externe

Arnold, E., Hammami, I., Chen, J., Gupte, S., Durocher, Y., & Jolicoeur, M. (2016). Overexpression of G6PDH does not affect the behavior of HEK-293 clones stably expressing interferon-α2b. AIMS Bioengineering, 3(3), 319-336. Disponible

Robitaille, J., Chen, J., & Jolicoeur, M. (2015). A Single Dynamic Metabolic Model Can Describe mAb Producing CHO Cell Batch and Fed-Batch Cultures on Different Culture Media. PLOS One, 10(9). Disponible

Ghorbaniaghdam, A., Chen, J., Henry, O., & Jolicoeur, M. (2014). Analyzing Clonal Variation of Monoclonal Antibody-Producing CHO Cell Lines Using an In Silico Metabolomic Platform. PLOS One, 9(3). Disponible

Claeyssen, É., Dorion, S., Clendenning, A., He, J. Z., Wally, O., Chen, J., Auslender, E. L., Moisan, M.-C., Jolicoeur, M., & Rivoal, J. (2013). The futile cycling of hexose phosphates could account for the fact that hexokinase exerts a high control on glucose phosphorylation but not on glycolytic rate in transgenic potato (solanum tuberosum) roots. PLOS One, 8(1), e53898. Disponible

Poliquin, P. O., Chen, J., Cloutier, M., Trudeau, L.-É., & Jolicoeur, M. (2013). Metabolomics and in-silico analysis reveal critical energy deregulations in animal models of Parkinson's disease. PLOS One, 8(7). Disponible

Hammami, I., Chen, J., Murschel, F., Bronte, V., De Crescenzo, G., & Jolicoeur, M. (2012). Immunosuppressive activity enhances central carbon metabolism and bioenergetics in myeloid-derived suppressor cells in vitro models. BMC Cell Biology, 13(1). Disponible

Hammami, I., Bertrand, M., Chen, J., Bronte, V., De Crescenzo, G., & Jolicoeur, M. (2012). Nitric Oxide Affects Immune Cells Bioenergetics: Long-Term Effects of Nitric-Oxide Derivatives on Leukaemic Jurkat Cell Metabolism. Immunobiology, 217(8), 808-815. Lien externe

Hammami, I., Chen, J., Bronte, V., De Crescenzo, G., & Jolicoeur, M. (2011). Myeloid-derived suppressor cells exhibit two bioenergetic steady-states in vitro. Journal of Biotechnology, 152(1-2), 43-48. Lien externe

Aucoin, M. G., McMurray-Beaulieu, V., Poulin, F., Boivin, E. B., Chen, J., Ardelean, F. M., Cloutier, M., Choi, Y. J., Miguez, C. B., & Jolicoeur, M. (2006). Identifying conditions for inducible protein production in E. coli: combining a fed-batch and multiple induction approach. Microbial Cell Factories, 5(1). Disponible

Chen, J. (2004). In vivo ³¹P-NMR study of phosphate metabolism for Eschscholtzia californica using a small-scale perfused bioreactor [Mémoire de maîtrise, École Polytechnique de Montréal]. Disponible

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