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Ansorge, S., Lanthier, S., Transfiguracion, J., Henry, O., & Kamen, A. A. (2011). Monitoring lentiviral vector production kinetics using online permittivity measurements. Biochemical Engineering Journal, 54(1), 16-25. Lien externe
Ansorge, S., Henry, O., Aucoin, M., Voyer, R., Carvell, J. P., & Kamen, A. (juin 2007). Monitoring the Cell Size Distribution of Mammalian Cell Cultures Using On-Line Capacitance Measurements [Communication écrite]. 20th ESACT Meeting, Dresen, Germany. Lien externe
Ansorge, S., Henry, O., & Kamen, A. A. (2010). Recent progress in lentiviral vector mass production. Biochemical Engineering Journal, 48(3), 362-377. Lien externe
Ansorge, S., Lanthier, S., Transfiguracion, J., Durocher, Y., Henry, O., & Kamen, A. (2009). Development of a Scalable Process for High-Yield Lentiviral Vector Production by Transient Transfection of Hek293 Suspension Cultures. Journal of Gene Medicine, 11(10), 868-876. Lien externe
Cambay, F., Forest-Nault, C., Dumoulin, L., Seguin, A., Henry, O., Durocher, Y., & De Crescenzo, G. (2020). Glycosylation of Fcγ receptors influences their interaction with various IgG1 glycoforms. Molecular Immunology, 121, 144-158. Lien externe
Cambay, F., Raymond, C., Brochu, D., Gilbert, M., Tu, T. M., Cantin, C., Lenferink, A., Grail, M., Henry, O., De Crescenzo, G., & Durocher, Y. (2020). Impact of IgG1 N-glycosylation on their interaction with Fc gamma receptors. Current Research in Immunology, 1, 23-37. Lien externe
Cambay, F., Henry, O., Durocher, Y., & De Crescenzo, G. (2019). Impact of N-glycosylation on Fcγ receptor / IgG interactions: unravelling differences with an enhanced surface plasmon resonance biosensor assay based on coiled-coil interactions. mAbs, 11(3), 435-452. Lien externe
Dégardin, M., Liberelle, B., Oliverio, R., Baniahmad, S. F., Darviot, C., Largillière, I., Henry, O., Durocher, Y., Banquy, X., Meunier, M., & De Crescenzo, G. (2023). Coiled-Coil-Based Biofunctionalization of 100 nm Gold Nanoparticles with the Trastuzumab Antibody for the Detection of HER2-Positive Cancer Cells. Langmuir, 39(34), 12235-12247. Lien externe
Durocher, Y., Toussaint, C., & Henry, O. (mai 2018). Regulation of recombinant protein expression during CHO pool selection enhances high producer frequency [Communication écrite]. Cell Culture Engineering XVI, Tampa, FL. Non disponible
Forest-Nault, C., Koyuturk, I., Gaudreault, J., Pelletier, A., L’Abbé, D., Cass, B., Bisson, L., Burlacu, A., Delafosse, L., Stuible, M., Henry, O., De Crescenzo, G., & Durocher, Y. (2024). A Biosensor Assay Based on Coiled-Coil-Mediated Human ACE2 Receptor Capture for the Analysis of Its Interactions with the SARS-CoV-2 Receptor Binding Domain. Dans Bradfute, S. B. (édit.), Recombinant Glycoproteins: Methods and Protocols (89-105). Lien externe
Forest-Nault, C., Koyuturk, I., Gaudreault, J., Pelletier, A., L'Abbe, D., Cass, B., Bisson, L., Burlacu, A., Delafosse, L., Stuible, M., Henry, O., De Crescenzo, G., & Durocher, Y. (2022). Impact of the temperature on the interactions between common variants of the SARS-CoV-2 receptor binding domain and the human ACE2. Scientific Reports, 12(1), 11520 (11 pages). Lien externe
Forest-Nault, C., Gaudreault, J., Henry, O., Durocher, Y., & De Crescenzo, G. (2021). On the use of surface plasmon resonance biosensing to understand IgG-FcγR interactions. International Journal of Molecular Sciences, 22(12), 6616 (27 pages). Disponible
Gaudreault, J., Forest‐Nault, C., Gilbert, M., Durocher, Y., Henry, O., & De Crescenzo, G. (2024). A low‐temperature SPR‐based assay for monoclonal antibody galactosylation and fucosylation assessment using FcγRIIA/B. Biotechnology and Bioengineering, 15 pages. Disponible
Gaudreault, J., Durocher, Y., Henry, O., & De Crescenzo, G. (2022). Multi-temperature experiments to ease analysis of heterogeneous binder solutions by surface plasmon resonance biosensing. Scientific Reports, 12(1), 14401 (25 pages). Lien externe
Gaudreault, J., Liberelle, B., Durocher, Y., Henry, O., & De Crescenzo, G. (2021). Determination of the composition of heterogeneous binder solutions by surface plasmon resonance biosensing. Scientific Reports, 11(1), 3685 (16 pages). Disponible
Gaudreault, J., Forest-Nault, C., De Crescenzo, G., Durocher, Y., & Henry, O. (2021). On the Use of Surface Plasmon Resonance-Based Biosensors for Advanced Bioprocess Monitoring. Processes, 9(11), 1996 (28 pages). Lien externe
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
Ghorbaniaghdam, A., Henry, O., & Jolicoeur, M. (2014). An in-silico study of the regulation of CHO cells glycolysis. Journal of Theoretical Biology, 357, 112-122. Lien externe
Ghorbaniaghdam, A., Henry, O., & Jolicoeur, M. (2013). A kinetic-metabolic model based on cell energetic state: study of CHO cells behaviour under Na-butyrate stimulation. Bioprocess and Biosystems Engineering, 36(4), 469-487. Lien externe
Ghorbaniaghdam, A., Henry, O., & Jolicoeur, M. (juillet 2010). A kinetic modelling approach to study the role of energy regulatory pathways in CHO cells [Communication écrite]. 11th IFAC Symposium on Computer Applications in Biotechnology, Leuven, Belgium. Publié dans IFAC Proceedings Volumes, 43(6). Lien externe
Henry, O., Karengera, E., Cambay, F., & De Crescenzo, G. (2020). Surface Plasmon Resonance-Based Method for Rapid Product Sialylation Assessment in Cell Culture. Dans Pörtner, R. (édit.), Animal Cell Biotechnology: Methods and Protocols (Vol. 2095, 285-293). Lien externe
Henry, O., & Durocher, Y. (2011). Enhanced glycoprotein production in HEK-293 cells expressing pyruvate carboxylase. Metabolic Engineering, 13(5), 499-507. Lien externe
Henry, O., Jolicoeur, M., & Kamen, A. A. (2011). Unraveling the metabolism of HEK-293 cells using lactate isotopomer analysis. Bioprocess and Biosystems Engineering, 34(3), 263-73. Lien externe
Henry, O., & Durocher, Y. (juillet 2010). Engineering of the Human Cell Line HEK-293 to Enhance Recombinant Protein Production [Communication écrite]. 11th IFAC Symposium on Computer Applications in Bioitechnology (CAB 2020), Leuven, Belgium. Publié dans IFAC Proceedings Volumes, 43(6). Lien externe
Henry, O., Kwok, E., & Piret, J. M. (2008). Simpler Noninstrumented Batch and Semicontinuous Cultures Provide Mammalian Cell Kinetic Data Comparable to Continuous and Perfusion Cultures. Biotechnology Progress, 24(4), 921-931. Lien externe
Henry, O., Kamen, A., & Perrier, M. (avril 2006). Monitoring the Physiological State of Mammalian Cell Perfusion Processes by on-Line Estimation of Intracellular Fluxes [Communication écrite]. ADCHEM 2006 Symposium, Gramado, Brazil. Publié dans Journal of Process Control, 17(3). Lien externe
Henry, O., Ansorge, S., Aucoin, M., Voyer, R., & Kamen, A. (juin 2007). On-line monitoring of cell size distribution in mammalian cell culture processes [Communication écrite]. 10th IFAC Symposium on Computer Applications in Biotechnology, Cancun, Mexico. Publié dans IFAC Proceedings Volumes, 40(4). Lien externe
Henry, O., Perrier, M., & Kamen, A. (avril 2006). Monitoring the physiological state of mammalian cell perfusion processes by on-line estimation of intracellular fluxes [Communication écrite]. International Symposium on Advanced Control of Chemical Processes, Gramado, Brazil. Lien externe
Henry, O., Perrier, M., & Kamen, A. (2005). Metabolic Flux Analysis of Hek-293 Cells in Perfusion Cultures for the Production of Adenoviral Vectors. Metabolic Engineering, 7(5-6), 467-476. Lien externe
Henry, O. (2004). Caractérisation et modélisation de la production de vecteurs adénoviraux dans un bioréacteur opérant en mode perfusion [Thèse de doctorat, École Polytechnique de Montréal]. Disponible
Henry, O., Dormond, E., Perrier, M., & Kamen, A. (2004). Insights into adenoviral vector production kinetics in acoustic filter-based perfusion cultures. Biotechnology and Bioengineering, 86(7), 765-774. Lien externe
Henry, O., Perrier, M., & Kamen, A. (mars 2004). On-line monitoring of adenovirus production in perfusion cultures [Communication écrite]. 9th International Symposium on Computer Applications in Biotechnology (CAB9), Nancy, France. Lien externe
Henry, O., Perrier, M., & Kamen, A. (septembre 2003). Optimization of adenovirus production in perfusion cultures using an ultrasonic retention device [Communication écrite]. 6th Conference on Protein Expression in Animal Cells, Mont-Tremblant. Non disponible
Karengera, E., Robotham, A., Kelly, J., Durocher, Y., De Crescenzo, G., & Henry, O. (2018). Concomitant reduction of lactate and ammonia accumulation in fed-batch cultures: Impact on glycoprotein production and quality. Biotechnology Progress, 34(2), 494-504. Lien externe
Karengera, E., Robotham, A., Kelly, J., Durocher, Y., De Crescenzo, G., & Henry, O. (2017). Altering the central carbon metabolism of HEK293 cells: Impact on recombinant glycoprotein quality. Journal of Biotechnology, 242, 73-82. Lien externe
Karengera, E., Durocher, Y., De Crescenzo, G., & Henry, O. (2017). Combining metabolic and process engineering strategies to improve recombinant glycoprotein production and quality. Applied Microbiology and Biotechnology, 101(21), 7837-7851. Lien externe
Karengera, E., De Crescenzo, G., Durocher, Y., & Henry, O. (mai 2016). Improving the metabolic efficiency of mammalian cells and its impact on glycoproteins quality [Affiche]. Cell Culture Engineering XV, Palm Spring (CA). Non disponible
Kamen, A., & Henry, O. (2004). Development and optimization of an adenovirus production process. Journal of Gene Medicine, 6(S1), S184-S192. Lien externe
Kamen, A., Henry, O., Jacob, D., & Bernier, A. (mai 2003). Successful development of a robust adenovirus production process primarily relies on a better understanding of packaging cell line physiology and vector replication kinetics [Communication écrite]. 18th ESACT Meeting, Granada, Spain. Lien externe
Lemire, L., Pham, P. L., Durocher, Y., & Henry, O. (2021). Practical Considerations for the Scale-Up of Chinese Hamster Ovary (CHO) Cell Cultures. Dans Cell Culture Engineering and Technology: In appreciation to Professor Mohamed Al-Rubeai (Vol. 10, 367-400). Lien externe
Le Ru, A., Jacob, D., Transfiguracion, J., Ansorge, S., Henry, O., & Kamen, A. A. (2010). Scalable Production of Influenza Virus in Hek-293 Cells for Efficient Vaccine Manufacturing. Vaccine, 28(21), 3661-3671. Lien externe
Mellahi, K., Brochu, D., Gilbert, M., Perrier, M., Ansorge, S., Durocher, Y., & Henry, O. (2019). Assessment of fed-batch cultivation strategies for an inducible CHO cell line. Journal of Biotechnology, 298, 45-56. Lien externe
Mellahi, K., Cambay, F., Brochu, D., Gilbert, M., Perrier, M., Ansorge, S., Durocher, Y., & Henry, O. (2019). Process development for an inducible rituximab-expressing Chinese hamster ovary cell line. Biotechnology Progress, 35(1), e2742. Lien externe
Mellahi, K., Brochu, D., Gilbert, M., Perrier, M., Ansorge, S., Durocher, Y., & Henry, O. (2019). Process intensification for the production of rituximab by an inducible CHO cell line. Bioprocess and Biosystems Engineering, 42(5), 711-725. Lien externe
Nadeau, I., Henry, O., Jacob, D., Perrier, M., & Kamen, A. (juin 2001). Effect of Medium Composition on the 293SF Central Metabolic Fluxes during Growth and Infection with Adenovirus [Communication écrite]. 8th International Symposium on Computer Applications in Biotechnology (CAB8), Québec City, Qc. Non disponible
Reyes, S. J., Durocher, Y., Pham, P. L., & Henry, O. (2022). Modern Sensor Tools and Techniques for Monitoring, Controlling, and Improving Cell Culture Processes. Processes, 10(2), 189 (36 pages). Lien externe
Riahi, N., Murschel, F., Lerouge, S., Durocher, Y., Henry, O., & De Crescenzo, G. (2017). Bioavailability of immobilized epidermal growth factor: Covalent versus noncovalent grafting. Biointerphases, 12(1), 010501 (8 pages). Lien externe
Riahi, N., Liberelle, B., Henry, O., & De Crescenzo, G. (2017). Impact of RGD amount in dextran-based hydrogels for cell delivery. Carbohydrate Polymers, 161, 219-227. Lien externe
Riahi, N., Cappadocia, L., Henry, O., Omichinski, J., & De Crescenzo, G. (2016). Soluble expression, purification and functional characterization of a coil peptide composed of a positively charged and hydrophobic motif. Amino Acids, 48(2), 567-577. Lien externe
Silva, C. A. T., Kamen, A. A., & Henry, O. Intensified Influenza Virus Production in Suspension HEK293SF Cell Cultures Operated in Fed-Batch or Perfusion with Continuous Harvest [Communication écrite]. Non spécifié (19 pages). Lien externe
Silva, C. A. T., Kamen, A. A., & Henry, O. (juin 2022). Intensification of influenza virus production in fed-batch and perfusion cultures of HEK293SF cells [Communication écrite]. Vaccine Technology VIII, Stiges, Spain. Lien externe
Silva, C. A. T., Kamen, A. A., & Henry, O. (2021). Recent advances and current challenges in process intensification of cell culture-based influenza virus vaccine manufacturing. Canadian Journal of Chemical Engineering, 99(11), 2525-2535. Lien externe
Sheikholeslami, Z., Jolicoeur, M., & Henry, O. (2014). Elucidating the effects of postinduction glutamine feeding on the growth and productivity of CHO cells. Biotechnology Progress, 30(3), 535-546. Lien externe
Sheikholeslami, Z., Jolicoeur, M., & Henry, O. (2013). The impact of the timing of induction on the metabolism and productivity of CHO cells in culture. Biochemical Engineering Journal, 79, 162-171. Lien externe
Sheikholeslami, Z., Jolicoeur, M., & Henry, O. (2013). Probing the metabolism of an inducible mammalian expression system using extracellular isotopomer analysis. Journal of Biotechnology, 164(4), 469-478. Lien externe
Toussaint, C., Henry, O., & Durocher, Y. (2016). Metabolic engineering of CHO cells to alter lactate metabolism during fed-batch cultures. Journal of Biotechnology, 217(C), 122-131. Disponible
Thompson, C. M., Petiot, E., Mullick, A., Aucoin, M. G., Henry, O., & Kamen, A. A. (2015). Critical assessment of influenza VLP production in Sf9 and HEK293 expression systems. BMC Biotechnology, 15(1). Disponible
Thompson, C. M., Petiot, E., Aucoin, M. G., Henry, O., & Kamen, A. A. (juin 2013). Developing a production process for influenza VLPs: a comparison between HEK 293SF and Sf9 production platforms [Affiche]. 23rd European Society for Animal Cell Technology Meeting (ESACT 2013), Lille, France (2 pages). Publié dans BMC Proceedings, 7(S6). Disponible
Thompson, C. M., Petiot, E., Lennaertz, A., Henry, O., & Kamen, A. A. (2013). Analytical technologies for influenza virus-like particle candidate vaccines: challenges and emerging approaches. Virology Journal, 10(1). Disponible
Venereo-Sanchez, A., Fulton, K., Koczka, K., Twine, S., Chahal, P., Ansorge, S., Gilbert, R., Henry, O., & Kamen, A. (2019). Characterization of influenza H1N1 Gag virus-like particles and extracellular vesicles co-produced in HEK-293SF. Vaccine, 37(47), 7100-7107. Lien externe
Venereo-Sanchez, A., Simoneau, M., Lanthier, S., Chahal, P., Bourget, L., Ansorge, S., Gilbert, R., Henry, O., & Kamen, A. (2017). Process intensification for high yield production of influenza H1N1 Gag virus-like particles using an inducible HEK-293 stable cell line. Vaccine, 35(33), 4220-4228. Lien externe
Venereo-Sanchez, A., Gilbert, R., Simoneau, M., Caron, A., Chahal, P., Chen, W., Ansorge, S., Li, X., Henry, O., & Kamen, A. (2016). Hemagglutinin and neuraminidase containing virus-like particles produced in HEK-293 suspension culture: An effective influenza vaccine candidate. Vaccine, 34(29), 3371-3380. Lien externe
Vallee, C., Durocher, Y., & Henry, O. (2014). Exploiting the metabolism of PYC expressing HEK293 cells in fed-batch cultures. Journal of Biotechnology, 169(1), 63-70. Lien externe
Yang, Z., Xu, X., Silva, C. A. T., Farnos, O., Venereo-Sanchez, A., Toussaint, C., Dash, S., Gonzalez-Dominguez, I., Bernier, A., Henry, O., & Kamen, A. (2022). Membrane chromatography-based downstream processing for cell-culture produced influenza vaccines. Vaccines, 10(8), 1310 (13 pages). Lien externe
