Studies involving sample source:Cells
Study ID | Study Title | Species | Institute |
---|---|---|---|
ST000043 | MDA-MB-231 cells and p38 gamma knockdown | Human | University of Michigan |
ST000170 | 13C mass isotopomer analysis (LCMS flux studies) MLL-AF9 (part III) | Mouse | University of Michigan |
ST000199 | IDH1 and Glioma knockdown idh1 (part II) | Human | University of Michigan |
ST000211 | T cell metabolism during graft-versus-host disease (CAB 307)-PART II | Mouse | University of Michigan |
ST000246 | Lipid Extraction Efficiency Comparison | Human | University of Florida |
ST000249 | Measurement of free amino acid (AA) in response to MYC | Human | University of Florida |
ST000251 | Amino Acid levels in preB cells under starvation | Mouse | University of Florida |
ST000258 | Metabolic contribution of pSymA and pSymB megaplasmid/chromid for multipartite Sinorhizobium meliloti cultured in minimal M9 medium | Sinorhizobium | McMaster University |
ST000259 | Metabolic contribution of pSymA and pSymB megaplasmid/chromid for multipartite Sinorhizobium meliloti cultured in rich LBmc medium | Sinorhizobium | McMaster University |
ST000271 | C13 Pyruvate Flux in 3t3 L1 | Mouse | University of Michigan |
ST000274 | HIF 1 alpha type 2 cells metabolomics | Mouse | University of Michigan |
ST000282 | Pilot Study 13C flux effects when RhoC or RhoA perturbed (13C BCs) | Human | University of Michigan |
ST000307 | Targeting CRBN to alter CD8 T cell metabolism | Mouse | University of Florida |
ST000308 | 13C mass isotopomer analysis (LCMS flux studies) MLL-AF9 (part I) | Mouse | University of Michigan |
ST000312 | IDH1R132H activity in glioma cell lines and tumnor tissue (2HG) | Mouse | University of Michigan |
ST000339 | Metabolites in peritoneal macrophages and bone marrow derived macrophages | Mouse | University of California, Davis |
ST000399 | E.coli effects on growth and substrate uptake of green algae (part I - HILIC) | E. coli | University of California, Davis |
ST000400 | E.coli effects on growth and substrate uptake of green algae (part II - Reverse Phase) | E. coli | University of California, Davis |
ST000402 | Impact of glucose on the central metabolome of C. minutissima | Chlorella | University of California, Davis |
ST000403 | Metabolomics-based elucidation of active metabolic pathways in erythrocytes and HSC-derived reticulocytes | Human | Monash Institute of Pharmaceutical Sciences |
ST000404 | Role of HVCN1 in B cell malignancies | Human | University of California, Davis |
ST000414 | Metabolomics-based screening of the Malaria Box reveals both novel and established mechanisms of action | Plasmodium falciparum | Monash Institute of Pharmaceutical Sciences |
ST000423 | Differences in mycoplasma growth due to different mediums | Mouse | University of California, Davis |
ST000442 | Metabolomics Analysis of Triple Negative Breast Cancer (BCa) Cell Lines | Human | University of North Carolina |
ST000528 | Regulation of Metabolism by LSR | Human | University of North Carolina |
ST000529 | Regulation of Metabolism by LSR (part II) | Human | University of North Carolina |
ST000539 | Metabolomics-based elucidation of active metabolic pathways in erythrocytes and HSC-derived reticulocytes (part II) | Human | Monash University |
ST000546 | Multi-omics based identification of specific biochemical changes associated with PfKelch13-mutant artemisinin resistant Plasmodium | Plasmodium falciparum | Monash University |
ST000548 | Replication study: The common feature of leukemia-associated IDH1 and IDH2 mutations is a neomorphic enzyme activity converting alpha-ketoglutarate to 2-hydroxyglutarate | Human | University of California, Davis |
ST000817 | Dynamics of metabolism, proliferation and differentiation in Toxoplasma gondii mutants deficient in glycolysis and gluconeogenesis | Toxoplasma gondii | CSIR-National Chemical Laboratory |
ST000884 | Evidence that COG0325 proteins are involved in PLP homeostasis | E. coli | University of California, Davis |
ST000898 | TAp73 is a marker of glutamine addiction in medulloblastoma | Human | Queen Mary University of London |
ST000900 | Evidence that the metabolite repair enzyme NAD(P)HX epimerase has a moonlighting function | E. coli | University of California, Davis |
ST000914 | Metabolomic adaptation of a deep sea Microbacterium sediminis to prolonged low temperature under high pressure | Microbacterium sediminis | Third Institute of Oceanography, State Oceanic Administration |
ST000921 | Karenia brevis allelopathy compromises the lipidome, membrane integrity, and photosynthetic efficiency of competitors | Karenia brevis | Georgia Institute of Technology |
ST000921 | Karenia brevis allelopathy compromises the lipidome, membrane integrity, and photosynthetic efficiency of competitors | Thalassiosira pseudonana | Georgia Institute of Technology |
ST000926 | Probing the metabolic phenotype of breast cancer cells by multiple tracer stable isotope resolved metabolomics (part I) | Human | University of Kentucky |
ST000927 | Probing the metabolic phenotype of breast cancer cells by multiple tracer stable isotope resolved metabolomics (part II) | Human | University of Kentucky |
ST000928 | Probing the metabolic phenotype of breast cancer cells by multiple tracer stable isotope resolved metabolomics (part III) | Human | University of Kentucky |
ST002321 | 13C NMR metabolomics: integrating J-resolved STOCSY and INADEQUATE | Thalassiosira pseudonana | University of Georgia |
ST002397 | System-level analysis of flux regulation of yeast show that glycolytic flux is controlled by allosteric regulation and enzyme phosphorylation | Yeast | Shanghai Center for Systems Biomedicine, Shanghai Jiaotong University |