Considerations on the lactate consumption by CHO cells in the presence of galactose.
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In situ monitoring of intracellular glucose and glutamine in CHO cell cultureProliferation control strategies to improve productivity and survival during CHO based production culture : A summary of recent methods employed and the effects of proliferation control in product secreting CHO cell linesEngineering CHO cell metabolism for growth in galactoseLarge-scale production of red blood cells from stem cells: what are the technical challenges ahead?Use of a Plackett-Burman statistical design to determine the effect of selected amino acids on monoclonal antibody production in CHO cells.Towards dynamic metabolic flux analysis in CHO cell cultures.Metabolic flux rewiring in mammalian cell cultures.Optimizing eukaryotic cell hosts for protein production through systems biotechnology and genome-scale modeling.Over-expression of a Codon Optimized Yeast Cytosolic Pyruvate Carboxylase (PYC2) in CHO Cells for an Augmented Lactate Metabolism.Quantitative intracellular flux modeling and applications in biotherapeutic development and production using CHO cell cultures.Low glucose concentrations within typical industrial operating conditions have minimal effect on the transcriptome of recombinant CHO cells.Galactose supplementation enhance sialylation of recombinant Fc-fusion protein in CHO cell: an insight into the role of galactosylation in sialylation.Insights into pH-induced metabolic switch by flux balance analysis.Benchmarking of commercially available CHO cell culture media for antibody production.What can mathematical modelling say about CHO metabolism and protein glycosylation?Amino acid and glucose metabolism in fed-batch CHO cell culture affects antibody production and glycosylation.Effects of glutamine and asparagine on recombinant antibody production using CHO-GS cell lines.CHO cell line specific prediction and control of recombinant monoclonal antibody N-glycosylation.Determination of Chinese hamster ovary cell line stability and recombinant antibody expression during long-term culture.Effect of process parameters and product-host-interaction on hVEGFA-production by recombinant Chinese hamster ovary cells.Reduced glutamine concentration improves protein production in growth-arrested CHO-DG44 and HEK-293E cells.Combinatorial engineering of ldh-a and bcl-2 for reducing lactate production and improving cell growth in dihydrofolate reductase-deficient Chinese hamster ovary cells.Analysis of an artificially selected GS-NS0 variant with increased resistance to apoptosis.NMR-based metabolomics of mammalian cell and tissue cultures.Modulation of antibody galactosylation through feeding of uridine, manganese chloride, and galactose.Quantitative characterization of metabolism and metabolic shifts during growth of the new human cell line AGE1.HN using time resolved metabolic flux analysis.Influence of different ammonium, lactate and glutamine concentrations on CCO cell growth.Comparing BRIN-BD11 culture producing insulin using different type of microcarriers.Segmented linear modeling of CHO fed-batch culture and its application to large scale production.Analysis of Chinese hamster ovary cell metabolism through a combined computational and experimental approach.Feeding lactate for CHO cell culture processes: impact on culture metabolism and performance.Flux balance analysis of CHO cells before and after a metabolic switch from lactate production to consumption.Combining metabolic and process engineering strategies to improve recombinant glycoprotein production and quality.A Simple Method to Reduce both Lactic Acid and Ammonium Production in Industrial Animal Cell Culture.Lactate and glucose concomitant consumption as a self-regulated pH detoxification mechanism in HEK293 cell cultures.Advanced process monitoring and feedback control to enhance cell culture process production and robustness.Modulation of mAb quality attributes using microliter scale fed-batch cultures.Peak antibody production is associated with increased oxidative metabolism in an industrially relevant fed-batch CHO cell culture.Metabolic flux analysis of CHO cell metabolism in the late non-growth phase.Mild hypothermia upregulates myc and xbp1s expression and improves anti-TNFα production in CHO cells.
P2860
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P2860
Considerations on the lactate consumption by CHO cells in the presence of galactose.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Considerations on the lactate consumption by CHO cells in the presence of galactose.
@en
type
label
Considerations on the lactate consumption by CHO cells in the presence of galactose.
@en
prefLabel
Considerations on the lactate consumption by CHO cells in the presence of galactose.
@en
P2093
P1476
Considerations on the lactate consumption by CHO cells in the presence of galactose.
@en
P2093
Andres Illanes
Claudia Altamirano
Francesc Gòdia
Jordi Joan Cairó
P304
P356
10.1016/J.JBIOTEC.2006.03.023
P577
2006-07-05T00:00:00Z