human | Q5 |
P735 | given name | Emma | Q541194 |
Emma | Q541194 | ||
P106 | occupation | researcher | Q1650915 |
P21 | sex or gender | female | Q6581072 |
Q28543615 | Air-adapted Methanosarcina acetivorans shows high methane production and develops resistance against oxygen stress |
Q40614249 | Albendazole induces oxidative stress and DNA damage in the parasitic protozoan Giardia duodenalis |
Q39477031 | Assessment of the low inhibitory specificity of oxamate, aminooxyacetate and dichloroacetate on cancer energy metabolism. |
Q38827395 | Biochemistry and Physiology of Heavy Metal Resistance and Accumulation in Euglena. |
Q47414193 | Buthionine sulfoximine is a multitarget inhibitor of trypanothione synthesis in Trypanosoma cruzi |
Q46770225 | Cadmium removal by Euglena gracilis is enhanced under anaerobic growth conditions. |
Q57044354 | Complement is a rat natural resistance factor to amoebic liver infection |
Q96603262 | Computational Drug Repositioning for Chagas Disease Using Protein-Ligand Interaction Profiling |
Q44800795 | Conserved cysteine 126 in triosephosphate isomerase is required not for enzymatic activity but for proper folding and stability. |
Q91649232 | Control and regulation of the pyrophosphate-dependent glucose metabolism in Entamoeba histolytica |
Q90573112 | Control of the NADPH supply and GSH recycling for oxidative stress management in hepatoma and liver mitochondria |
Q38663844 | Control of the NADPH supply for oxidative stress handling in cancer cells |
Q46809023 | Dehydroepiandrosterone decreases while cortisol increases in vitro growth and viability of Entamoeba histolytica |
Q91477065 | Drug Target Selection for Trypanosoma cruzi Metabolism by Metabolic Control Analysis and Kinetic Modeling |
Q48051536 | Drug target validation of the trypanothione pathway enzymes through metabolic modelling |
Q51587575 | Dual regulation of energy metabolism by p53 in human cervix and breast cancer cells. |
Q27308873 | Endoplasmic reticulum stress-sensing mechanism is activated in Entamoeba histolytica upon treatment with nitric oxide |
Q28288377 | Energy metabolism in tumor cells |
Q45018318 | Entamoeba histolytica: apoptosis induced in vitro by nitric oxide species |
Q44795167 | Entamoeba histolytica: kinetic and molecular evidence of a previously unidentified pyruvate kinase. |
Q46203112 | Entamoeba histolytica: oxygen resistance and virulence |
Q46569238 | Experimental validation of metabolic pathway modeling |
Q89706101 | Functional characterization and subcellular distribution of two recombinant cytosolic HSP70 isoforms from Entamoeba histolytica under normal and stress conditions |
Q92774155 | Gamma-glutamylcysteine synthetase and tryparedoxin 1 exert high control on the antioxidant system in Trypanosoma cruzi contributing to drug resistance and infectivity |
Q45128885 | Gene cloning and biochemical characterization of an alcohol dehydrogenase from Euglena gracilis |
Q46407795 | Glycolysis in Entamoeba histolytica. Biochemical characterization of recombinant glycolytic enzymes and flux control analysis. |
Q46357748 | Glycolysis in Ustilago maydis. |
Q92545210 | Heart myxoma develops oncogenic and metastatic phenotype |
Q98303095 | Identification of flux checkpoints in a metabolic pathway through white-box, grey-box and black-box modeling approaches |
Q85886030 | In vivo identification of the steps that control energy metabolism and survival of Entamoeba histolytica |
Q37277390 | Inhibition of Non-flux-Controlling Enzymes Deters Cancer Glycolysis by Accumulation of Regulatory Metabolites of Controlling Steps |
Q81157393 | Kinetic modeling can describe in vivo glycolysis in Entamoeba histolytica |
Q97874964 | Kinetic modeling of glucose central metabolism in hepatocytes and hepatoma cells |
Q41544290 | Maintenance of intracellular hypoxia and adequate heat shock response are essential requirements for pathogenicity and virulence of Entamoeba histolytica |
Q65000166 | Mechanisms of natural resistance of Balb/c mice to experimental liver amoebiasis. |
Q90717484 | Metabolic Control Analysis for Drug Target Prioritization in Trypanosomatids |
Q104904931 | Metabolic Control Theory |
Q37769788 | Metabolic control analysis indicates a change of strategy in the treatment of cancer |
Q58842743 | Metabolic control analysis of the Trypanosoma cruzi peroxide detoxification pathway identifies tryparedoxin as a suitable drug target |
Q37217309 | Metabolic control analysis: a tool for designing strategies to manipulate metabolic pathways. |
Q82624228 | Modeling cancer glycolysis |
Q51080469 | Modeling cancer glycolysis under hypoglycemia, and the role played by the differential expression of glycolytic isoforms. |
Q46085372 | Molecular basis of the unusual catalytic preference for GDP/GTP in Entamoeba histolytica 3-phosphoglycerate kinase. |
Q57114649 | Mutant p53 downregulates oxidative phosphorylation and upregulates glycolysis under normoxia and hypoxia in human cervix cancer cells |
Q42960308 | Oxidative phosphorylation is impaired by prolonged hypoxia in breast and possibly in cervix carcinoma |
Q39418406 | Phosphofructokinase type 1 kinetics, isoform expression, and gene polymorphisms in cancer cells |
Q93200202 | Physiological Role of Glutamate Dehydrogenase in Cancer Cells |
Q34328874 | Plant-like traits associated with metabolism of Trypanosoma parasites |
Q44299299 | Pyruvate:ferredoxin oxidoreductase (PFO) is a surface-associated cell-binding protein in Trichomonas vaginalis and is involved in trichomonal adherence to host cells |
Q42970732 | Pyruvate:ferredoxin oxidoreductase and bifunctional aldehyde-alcohol dehydrogenase are essential for energy metabolism under oxidative stress in Entamoeba histolytica. |
Q98949548 | Rabeprazole inhibits several functions of Entamoeba histolytica related with its virulence |
Q40774764 | Roles of acetyl-CoA synthetase (ADP-forming) and acetate kinase (PPi-forming) in ATP and PPi supply in Entamoeba histolytica |
Q51780524 | Sulfate uptake in photosynthetic Euglena gracilis. Mechanisms of regulation and contribution to cysteine homeostasis. |
Q38699107 | Synthesis and biological evaluation of 2-methyl-1H-benzimidazole-5-carbohydrazides derivatives as modifiers of redox homeostasis of Trypanosoma cruzi. |
Q37782110 | Targeting Trypanothione Metabolism in Trypanosomatid Human Parasites |
Q45054094 | The 2-oxoglutarate supply exerts significant control on the lysine synthesis flux in Saccharomyces cerevisiae. |
Q84898954 | The Lys20 homocitrate synthase isoform exerts most of the flux control over the lysine synthesis pathway in Saccharomyces cerevisiae |
Q85585048 | The bifunctional aldehyde-alcohol dehydrogenase controls ethanol and acetate production in Entamoeba histolytica under aerobic conditions |
Q37486411 | The bioenergetics of cancer: is glycolysis the main ATP supplier in all tumor cells? |
Q37703526 | The causes of cancer revisited: "mitochondrial malignancy" and ROS-induced oncogenic transformation - why mitochondria are targets for cancer therapy |
Q40959108 | The contribution of two isozymes to the pyruvate kinase activity of Vibrio cholerae: One K+-dependent constitutively active and another K+-independent with essential allosteric activation |
Q39900820 | The nutritional status of Methanosarcina acetivorans regulates glycogen metabolism and gluconeogenesis and glycolysis fluxes. |
Q38641195 | The oxygen reduction pathway and heat shock stress response are both required for Entamoeba histolytica pathogenicity |
Q90633242 | Transcriptional Regulation of Energy Metabolism in Cancer Cells |
Q38595074 | Understanding the cancer cell phenotype beyond the limitations of current omics analyses |
Q38186917 | Who controls the ATP supply in cancer cells? Biochemistry lessons to understand cancer energy metabolism |
Q87165668 | Zn-bis-glutathionate is the best co-substrate of the monomeric phytochelatin synthase from the photosynthetic heavy metal-hyperaccumulator Euglena gracilis |
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