Documents dont l'auteur est "Chen, Jingkui"

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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

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

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

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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

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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

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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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

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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

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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

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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

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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

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

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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