List of Studies ( Metabolite:S-Adenosylmethionine)
Study_id | Analysis_id | Study_title | Source | Species | Disease | Institute | Units(range) |
---|---|---|---|---|---|---|---|
ST001413 | AN002363 | Metabolomic and Transcriptomic Signatures of Prenatal Excessive Methionine in Mice | Brain | Mouse | University of California, Irvine | - | |
ST002497 | AN004101 | Postnatal hyperglycemia alters amino acid profile in retinas | Retina | Mouse | Eye disease | Boston Childrens Hospital | Absolute Intensity |
ST000923 | AN001513 | Longitudinal Metabolomics of the Human Microbiome in Inflammatory Bowel Disease | Feces | Human | Inflammatory bowel disease | The Broad Institute | Abundance |
ST001037 | AN001698 | High Resolution GC-MS and FID Metabolomics of Human Serum | Blood | Human | Wake Forest Baptist Medical Center | Abundance | |
ST001192 | AN001984 | A library of human gut bacterial isolates paired with longitudinal multiomics data enables mechanistic microbiome research | Feces | Human | The Broad Institute | Abundance | |
ST001680 | AN002738 | Metabolome of NAFLD in high fat diet mouse model | Liver | Mouse | Fatty liver disease | Weill Cornell Medicine | Abundance |
ST002471 | AN004033 | Linking bacterial metabolites to disease-associated microbes to uncover mechanisms of host-microbial interactions in intestinal inflammation. Human stool profiling | Feces | Human | Ulcerative colitis | Broad Institute of MIT and Harvard | Abundance |
ST002864 | AN004696 | Metabolic profiling, glucose tracing and glutamine tracing in naive and Enzalutamide-treated 16D prostate cancer cells expressing RFP or MYC | Prostate cancer cells | Human | Cancer | University of California, Los Angeles | Abundance |
ST002865 | AN004697 | Metabolic profiling, glucose tracing and glutamine tracing in 16D prostate cancer cells treated with vehicle, AR inhibitor Enzalutamide, AR inhibitor Apalutamide, or AR degrader/PROTAC ARCC-4 | Prostate cancer cells | Human | Cancer | University of California, Los Angeles | Abundance |
ST002830 | AN004623 | L-isoleucine in P10 STZ | Retina | Mouse | Retinopathy of prematurity | Boston Childrens Hospital | abundance/intensity |
ST002247 | AN003670 | Microbiota and Health Study (Dhaka, Bangladesh) | Feces | Human | Broad Institute of MIT and Harvard | Abundances | |
ST003438 | AN005649 | Unbiased genetic screening and metabolomics identifies glial adenosine metabolism as a therapeutic target in Parkinson’s disease | Fly Head | Fly | Parkinson's Disease | Broad Institute of MIT and Harvard | Abundances |
ST001822 | AN002958 | The RNA-binding protein RBP42 regulates cellular energy metabolism in mammalian-infective Trypanosoma brucei | Cultured cells | Trypanosoma brucei | Rutgers University | arbitrary | |
ST001986 | AN003237 | Fbxo7 promotes Cdk6 activity to inhibit PFKP and glycolysis in T cells | T-cells | Mouse | University of Cambridge | arbitrary unit | |
ST003076 | AN005034 | Data-dependent and -independent acquisition lipidomics analysis reveals the tissue-dependent effect of metformin on lipid metabolism | Adipose tissue | Mouse | North Carolina State University | arbitrary unit | |
ST003076 | AN005034 | Data-dependent and -independent acquisition lipidomics analysis reveals the tissue-dependent effect of metformin on lipid metabolism | Blood | Mouse | North Carolina State University | arbitrary unit | |
ST003076 | AN005034 | Data-dependent and -independent acquisition lipidomics analysis reveals the tissue-dependent effect of metformin on lipid metabolism | Heart | Mouse | North Carolina State University | arbitrary unit | |
ST003076 | AN005034 | Data-dependent and -independent acquisition lipidomics analysis reveals the tissue-dependent effect of metformin on lipid metabolism | Intestine | Mouse | North Carolina State University | arbitrary unit | |
ST003076 | AN005034 | Data-dependent and -independent acquisition lipidomics analysis reveals the tissue-dependent effect of metformin on lipid metabolism | Kidney | Mouse | North Carolina State University | arbitrary unit | |
ST003076 | AN005034 | Data-dependent and -independent acquisition lipidomics analysis reveals the tissue-dependent effect of metformin on lipid metabolism | Liver | Mouse | North Carolina State University | arbitrary unit | |
ST003076 | AN005034 | Data-dependent and -independent acquisition lipidomics analysis reveals the tissue-dependent effect of metformin on lipid metabolism | Muscle | Mouse | North Carolina State University | arbitrary unit | |
ST000509 | AN000780 | Metabolic changes to maternal rat liver tissue during and post-pregnancy | Liver | Rat | University of Colorado, Denver | Arbitrary units | |
ST000510 | AN000782 | Assessing metabolic changes to maternal rat liver tissue during and post-pregnancy (part II) | Liver | Mouse | University of Colorado, Denver | Arbitrary units | |
ST001062 | AN001736 | Arabidopsis Nit1 knockout metabolomics | Plant | Arabidopsis thaliana | University of California, Davis | Arbitrary units | |
ST003102 | AN005076 | Cellular adaptation to cancer therapy occurs by progressive state transitions along a resistance continuum | Ovarian cancer cells | Human | Cancer | NYU Langone Health | Arbitrary units |
ST002831 | AN004624 | Folate depletion upregulates heme synthesis | Cultured cells | Human | Anemia | Boston Children's Hospital, Harvard Medical School | Arbitrary Units |
ST003018 | AN004952 | Polar metabolite levels in K562 cells following PKC inhibition in 2,000 nM or 100 nM FA conditions | Cultured cells | Human | Anemia | Boston Children's Hospital, Harvard Medical School | Arbitrary Units |
ST003020 | AN004954 | Polar metabolite levels in MEL cells following PKC inhibition in 2,000 nM or 100 nM FA conditions | Cultured cells | Mouse | Anemia | Boston Children's Hospital, Harvard Medical School | Arbitrary Units |
ST003254 | AN005333 | The impact of grass- and grain-finishing on metabolomic profiles of North American Black Angus Beef cattle. | Bovine meat | Cow | Duke University | Arbitrary Units | |
ST002316 | AN003783 | Differential requirements for mitochondrial electron transport chain components in the adult murine liver - Untargeted Metabolomics (qTOF) | Liver | Mouse | Metabolic syndrome | The University of Texas Southwestern Medical Center at Dallas | area |
ST003108 | AN005087 | Complete absence of GLUT1 does not impair human terminal erythroid differentiation | Cultured cells | Human | GLUT1 Deficiency Syndrome | University of Colorado | area |
ST003046 | AN004997 | Multi-Omics Plasma Signatures of Severe Injury with Influence of REBOA Intervention in a Swine Model. | Blood | Pig | Trauma | University of Colorado Anschutz Medical Campus | area under curve |
ST003327 | AN005451 | Control Of Major Bleeding After Trauma (COMBAT) Clinical Research Trial Metabolomics | Blood | Human | Trauma | University of Colorado Anschutz Medical Campus | area under curve |
ST000903 | AN001470 | Pharmacometabolomic analysis of rat hippocampus and plasma in response to chronic stress and albiflorin treament | Blood | Rat | Stress | Beijing Woner Biotech Co. Ltd | Area under curve |
ST001143 | AN001883 | Microbial depletion and ozone exposure - Lung tissue (part I) | Lung | Mouse | Asthma | Harvard School of Public Health | Area under curve |
ST002840 | AN004648 | Collaborative role of YqgC and superoxide dismutase (MnSOD) in manganese intoxication: Replicate Experiment 1 | Bacterial cells | Bacillus subtilis | Cornell University | Area under the curve | |
ST002841 | AN004650 | Collaborative role of YqgC and superoxide dismutase (MnSOD) in manganese intoxication: Replicate Experiment 2 | Bacterial cells | Bacillus subtilis | Cornell University | Area under the curve | |
ST002708 | AN004390 | Levels of central carbon metabolites in choroid plexus as part of natural diurnal variation | Brain | Mouse | Circadian Rhythm Disorder | Boston Childrens Hospital | a.u. |
ST003072 | AN005030 | Investigation of polar metabolites by targeted LC-MS analysis from mouse adult or embryonic CSF and from adult serum. | Cerebrospinal fluid | Mouse | Boston Childrens Hospital | a.u. | |
ST003081 | AN005039 | Metabolome changes in embryonic CSF (Part 3) | CSF | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST003082 | AN005040 | Metabolome changes in embryonic CSF (Part 4) | CSF | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST003083 | AN005041 | Metabolome changes in embryonic CSF (Part 5) | CSF | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST003084 | AN005042 | Metabolic changes in embryonic CSF (Part 6) | CSF | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST003085 | AN005044 | Metabolome changes in embryonic CSF (Part 7) | CSF | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST003086 | AN005046 | Metabolome changes in embryonic CSF (Part 8) | CSF | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST003087 | AN005048 | Metabolome changes in embryonic CSF (Part 9) | CSF | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST003088 | AN005050 | Metabolome changes in embryonic CSF (Part 10) | Blood | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST003088 | AN005050 | Metabolome changes in embryonic CSF (Part 10) | CSF | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST003088 | AN005050 | Metabolome changes in embryonic CSF (Part 10) | Liver | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST003089 | AN005052 | Metabolome changes in embryonic CSF (Part 11) | CSF | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST003199 | AN005249 | Metabolite profiling in the liver from fasted eIF4ES209A (S209A) mice compared to fasted wild type (WT) mice | Liver | Mouse | Cancer | University of Chicago | A.U. |
ST002058 | AN003350 | Muscle/Lung/Tumor metabolomics | Lung | Mouse | Cancer | University of Colorado Anschutz Medical Campus | AU |
ST002058 | AN003350 | Muscle/Lung/Tumor metabolomics | Muscle | Mouse | Cancer | University of Colorado Anschutz Medical Campus | AU |
ST002059 | AN003352 | 4T1 and SkM cells | Cultured cells | Human | Cancer | University of Colorado Anschutz Medical Campus | AU |
ST002123 | AN003476 | GCN2 regulates mitochondrial OXPHOS in HSPCs under proliferation conditions. | Bone marrow | Mouse | Sun Yat-sen University | AU | |
ST001856 | AN003008 | The metabolomic resetting effect of FG4592 in AKI to CKD transition-day 21 (Part 2) | Kidney | Mouse | Kidney disease | Children's Hospital of Nanjing Medical University | AUC |
ST002374 | AN003869 | Metabolomics analysis of WT vs. GOT1 knockout CD8+ T cells | Cultured cells | Mouse | Johns Hopkins University | AUC | |
ST002375 | AN003870 | Metabolomics analysis of WT or GOT1 knockout CD8+ T cells cultured in serine-replete or serine-free media | Cultured cells | Mouse | Johns Hopkins University | AUC | |
ST001875 | AN003037 | Metabolomics analysis of multiple samples on AB 5600-Part 2 | Feces | Mouse | Dalian Institute Of Chemical Physics | blank-substracted abundances | |
ST001875 | AN003037 | Metabolomics analysis of multiple samples on AB 5600-Part 2 | Liver | Mouse | Dalian Institute Of Chemical Physics | blank-substracted abundances | |
ST002457 | AN004009 | Mouse kidney metabolomics (Whole kidney) | Kidney | Mouse | Chronic kidney disease | Hadassah Medical Center | concentration |
ST002458 | AN004010 | Mouse kidney metabolomics (Proximal tubular cells) | Proximal tubular cells | Mouse | Chronic kidney disease | Hadassah Medical Center | concentration |
ST003028 | AN004965 | Chronic stress dampens Lactobacillus johnsonii-mediated tumor suppression to enhance colorectal cancer progression | Colon | Mouse | Cancer | China Pharmaceutical University | count per second (cps) |
ST002178 | AN003566 | Age-independent Cardiac Protection by Pharmacological Activation of Beclin-1 During Endotoxemia and Its Association with Energy Metabolic Reprograming in Myocardium — A Targeted Metabolomics Study | Heart | Mouse | Endotoxemia | Loyola University Chicago Stritch School of Medicine | count per second (CPS) |
ST001922 | AN003123 | Sublytic membrane attack complex drives glycolysis and mitochondrial dysfunction with inflammatory consequences in human monocyte-derived macrophages | Macrophages | Human | MST-MedDesign, Discovery Analytical, GSK, Upper Providence, US | counts | |
ST001922 | AN003124 | Sublytic membrane attack complex drives glycolysis and mitochondrial dysfunction with inflammatory consequences in human monocyte-derived macrophages | Macrophages | Human | MST-MedDesign, Discovery Analytical, GSK, Upper Providence, US | counts | |
ST000041 | AN000063 | High PUFA diet in humans | Blood | Human | University of Michigan | Counts | |
ST000043 | AN000070 | MDA-MB-231 cells and p38 gamma knockdown | Cells | Human | University of Michigan | Counts | |
ST000044 | AN000068 | Pilot experiment looking for the existence of certain molecules in pancreatic cancer cells | Pancreas | Human | Cancer | University of Michigan | Counts |
ST000090 | AN000143 | Caloric Restriction vs drugs | Blood | Mouse | University of Michigan | Counts | |
ST000105 | AN000173 | SCOR Metabolomics | Blood | Human | University of Chicago | Counts | |
ST000106 | AN000175 | IWMS Study 1:Weight comparison of obese and lean patients | Blood | Human | Obesity | University of Michigan | Counts |
ST003362 | AN005504 | Metabolomics analysis of Glioblastoma (GBM) cell line U251 labeled by 13C-glutamine after treatment with pimozide | Cultured cells | Human | Cancer | The Ohio State University | Counts |
ST003362 | AN005506 | Metabolomics analysis of Glioblastoma (GBM) cell line U251 labeled by 13C-glutamine after treatment with pimozide | Cultured cells | Human | Cancer | The Ohio State University | Counts |
ST002747 | AN004454 | Evolutionary genomics identifies host-directed therapeutics to treat intracellular bacterial infections | Cultured cells | Human | CZ Biohub | counts, height | |
ST002747 | AN004454 | Evolutionary genomics identifies host-directed therapeutics to treat intracellular bacterial infections | Cultured cells | Rickettsia parkeri | CZ Biohub | counts, height | |
ST001402 | AN002344 | Ontogeny related changes in the pediatric liver metabolome | Liver | Human | Moffitt Cancer Center | estimated abundances | |
ST001403 | AN002345 | Ontogeny related changes in the pediatric liver metabolome (part-II) | Liver | Human | Moffitt Cancer Center | estimated abundances | |
ST002539 | AN004183 | Microbial metabolomic responses to changes in temperature and salinity along the western Antarctic Peninsula. | Suspended Marine Particulate Matter | Marine microbes | Abiotic stress | University of Washington, School of Oceanography | Estimated metabolite carbon concentration (nmol C per L) |
ST002323 | AN003791 | SETD1A regulates transcriptional pause release of heme biosynthesis genes in leukemia | Cultured cells | Human | Cancer | Chiba University | fmol/cell |
ST001179 | AN001956 | Metabolomic analysis of skeletal muscle in young and aged mice | Muscle | Mouse | Sarcopenia | Kyoto Prefectural University | fold |
ST002555 | AN004207 | Ethnicity-Specific Differences in Ovarian Cancer Metabolic Signatures | Cultured cells | Human | Cancer | University of Oklahoma Health Sciences Center | Fold change over standard |
ST002379 | AN003877 | Glucose flux analysis of NLRP3 inflammasome activated macrophages | Macrophages | Mouse | Wake Forest School of Medicine | Fractional enrichment | |
ST002327 | AN003796 | Effect of PARK7 gene KO on midbrain organoids | Cultured cells | Human | Icahn School of Medicine at Mount Sinai | intensity | |
ST001788 | AN002899 | β-Adrenergic regulation of metabolism in macrophages (part-IV) | Macrophages | Human | Monash University | Intensity | |
ST003291 | AN005390 | Atopic dermatitis and STAT3 double null mutant skin biopsies during healing. | Skin | Human | Eczema | National Institutes of Health | Intensity |
ST002069 | AN003378 | Systemic impact of the expression of the mitochondrial alternative oxidase on Drosophila development | Larvae | Fruit fly | Tampere University | intensity (area under the curve) | |
ST003323 | AN005439 | Global Metabolomics and U-13C6-Glucose Tracing in Bone Marrow Derived Macrophages (BMDM) | Bone marrow | Mouse | Immune system disorders | University of Colorado Anschutz Medical Campus | Intensity Counts |
ST002459 | AN004013 | Comparison of metabolite profiles from matched whole blood microsamplers, whole blood dried blood spots, and plasma. | Blood | Human | Icahn School of Medicine at Mount Sinai | Ion abundance | |
ST002744 | AN004449 | Biomolecular condensates create phospholipid-enriched microenvironments (Part 4) | Liver | Mouse | Cornell University | Ion abundance | |
ST001860 | AN003016 | Spontaneous hydrolysis and spurious metabolic properties of α-ketoglutarate esters | Cultured cells | Human | University of British Columbia | ion counts | |
ST002119 | AN003467 | Metabolomics analysis of zebrafish response to CID661578 treatment | Larvae | Zebrafish | Diabetes | North Carolina State University | ion counts |
ST002152 | AN003523 | Metabolomics analysis of mouse liver with or without SIRT5 deficiency | Liver | Mouse | North Carolina State University | ion counts | |
ST002847 | AN004665 | Targeting Pancreatic Cancer Metabolic Dependencies through Glutamine Antagonism. | Cultured cells | Mouse | Cancer | New York University | ion counts |
ST002349 | AN004095 | Biomolecular condensates create phospholipid-enriched microenvironments (Part 1) | Liver | Mouse | Cornell University | Ion counts | |
ST002352 | AN004097 | Biomolecular condensates create phospholipid-enriched microenvironments (Part 2) | Liver | Mouse | Cornell University | Ion counts | |
ST002824 | AN004606 | Leukemia inhibitory factor suppresses hepatic de novo lipogenesis and induces cachexia | Blood | Mouse | Cancer | Rutgers University | Ion counts |
ST003549 | AN005833 | Metabolomics analysis of kidney, brain, liver, and plasma from Aldh7a1-/- and Aldh7a1+/+ mice. | Blood, Tissue | Mouse | Metabolic Disorders | University of British Columbia | Ion counts |
ST003549 | AN005834 | Metabolomics analysis of kidney, brain, liver, and plasma from Aldh7a1-/- and Aldh7a1+/+ mice. | Blood, Tissue | Mouse | Metabolic Disorders | University of British Columbia | Ion counts |
ST003551 | AN005837 | Metabolomics analysis of N-methyl-arginine-treated HEK293 control (sgTomato) and ALDH7A1-deficient (sgALDH7A1) cells. | Cultured cells | Human | University of British Columbia | Ion counts | |
ST003551 | AN005838 | Metabolomics analysis of N-methyl-arginine-treated HEK293 control (sgTomato) and ALDH7A1-deficient (sgALDH7A1) cells. | Cultured cells | Human | University of British Columbia | Ion counts | |
ST003454 | AN005675 | Branched chain alpha-ketoacids impact pulmonary artery smooth muscle cell metabolism | Cultured cells | Human | Hypertension | Peking University | ion intensity |
ST003455 | AN005676 | Metabolic alterations in pulmonary artery smooth muscle cells of idiopathic pulmonary arterial hypertension (IPAH) patients. | Cultured cells | Human | Hypertension | Peking University | ion intensity |
ST003501 | AN005748 | TREM2 expression level is critical for microglial state, metabolic capacity and efficacy of TREM2 agonism | Microglia | Mouse | Alzheimers disease | Denali Therapeutics | log2(area) |
ST003405 | AN005588 | Specific activation of the integrated stress response uncovers regulation of central carbon metabolism and lipid droplet biogenesis | Cultured cells | Human | Cancer | Calico Life Sciences | log2 peak area top |
ST002822 | AN004599 | Effect of ERR Agonist in Mouse Heart Post Pressure Overload | Heart | Mouse | Baylor College of Medicine | log transformed data | |
ST001480 | AN002456 | Large diversity in nitrogen- and sulfur-containing compatible solute profiles in polar and temperate diatoms | Cultured cells | Algae | University of Washington | mM (intracellular concentration) | |
ST001480 | AN002456 | Large diversity in nitrogen- and sulfur-containing compatible solute profiles in polar and temperate diatoms | Cultured cells | Fragilariopsis cylindrus | University of Washington | mM (intracellular concentration) | |
ST001480 | AN002456 | Large diversity in nitrogen- and sulfur-containing compatible solute profiles in polar and temperate diatoms | Cultured cells | Navicula cf. perminuta | University of Washington | mM (intracellular concentration) | |
ST001480 | AN002456 | Large diversity in nitrogen- and sulfur-containing compatible solute profiles in polar and temperate diatoms | Cultured cells | Nitzschia lecointei | University of Washington | mM (intracellular concentration) | |
ST001320 | AN002196 | Examination of labeled glucose utilization in central carbon metabolism in HeLa cells post WNT stimulation | Cultured cells | Human | Cancer | University of California, Los Angeles | MS1 AUC integration |
ST002477 | AN004046 | Neutrophil metabolomics in COVID-19 | Neutrophils | Human | COVID-19 | UT Southwestern Medical Center | MS reading |
ST001324 | AN002202 | Metabolomics Adaptation of Juvenile Pacific Abalone Haliotis discus hannai to Heat Stress | Pacific Abalone | Institute of Oceanology, Chinese Academy of Sciences | mV*min | ||
ST003027 | AN004962 | NMR- and MS-based omics reveal characteristic metabolome atlas and optimize biofluid earlydiagnostic biomarkers for esophageal squamous cell carcinoma (part-Ⅳ) | Tissue | Human | Cancer | Radiology Department, Second Affiliated Hospital, Shantou University Medical College, Shantou | m/z |
ST000966 | AN001580 | Metabolite and gene expression profiles suggest a putative mechanism through which high dietary carbohydrates reduce the content of hepatic betaine in Megalobrama amblycephala | Blood | Fish | College of Fisheries Huazhong Agricultural University | ng/ml or umol/L | |
ST002174 | AN003562 | Identifying a tryptophan derivative in hydrogen peroxide-treated cell culture medium | Media | Abiotic | NYU Langone Health | N/L | |
ST002377 | AN003873 | Hepatic Phosphatidylcholine Catabolism Driven by PNPLA7 and PNPLA8 Supplies Endogenous Choline to Replenish the Methionine Cycle with Methyl Groups (Pnpla7-knockout) | Liver | Mouse | Tokyo Metropolitan Institute of Medical Science | nmol | |
ST000570 | AN000878 | Metabolome analysis of the cecal contents of GF mice and GF mice colonized with dominant gut microbes present in the ceca of neonatal and adult mice | Feces | Mouse | Keio University | nmol/g | |
ST001250 | AN002075 | Luminal metabolome profiles of mice developed dextran sulfate sodium (DSS) colitis | Feces | Mouse | Colitis | University of Michigan | nmol/g |
ST001300 | AN002164 | Luminal metabolome profiles ofUC-HMA mice transplanted with a healthy human-derived fecal microbiota (FMT). | Feces | Mouse | Bacterial infection | University of Michigan | nmol/g |
ST001301 | AN002166 | Luminal metabolome profiles of human microbiota-associated (HMA) mice treated with anti-IL-22 antibody or control antibody | Feces | Mouse | Bacterial infection | University of Michigan | nmol/g |
ST001961 | AN003197 | Metabolomics of brown adipose tissue in murine heart failure model | Adipose tissue | Mouse | Juntendo University | nmol/g | |
ST002170 | AN003555 | Cecal metabolome of specific-pathogen-free mice fed with five distinct rodent diets with varying fiber content and source. | Cecum | Mouse | Luxembourg Institute of Health | nmol/g | |
ST002172 | AN003559 | Cecal metabolome of gnotobiotic (containing a 14-member synthetic human gut microbiota), and germ-free mice fed with two distinct rodent diets with varying fiber content. | Cecum | Mouse | Luxembourg Institute of Health | nmol/g | |
ST002476 | AN004077 | High body temperature increases gut microbiota-dependent host resistance to influenza A virus and SARS-CoV-2 infection (Mouse) | Intestine | Mouse | COVID-19 | Keio University | nmol/g |
ST002476 | AN004077 | High body temperature increases gut microbiota-dependent host resistance to influenza A virus and SARS-CoV-2 infection (Mouse) | Intestine | Mouse | Influenza | Keio University | nmol/g |
ST002479 | AN004079 | High body temperature increases gut microbiota-dependent host resistance to influenza A virus and SARS-CoV-2 infection (Hamster) | Intestine | Mouse | COVID-19 | Keio University | nmol/g |
ST002479 | AN004079 | High body temperature increases gut microbiota-dependent host resistance to influenza A virus and SARS-CoV-2 infection (Hamster) | Intestine | Mouse | Influenza | Keio University | nmol/g |
ST001136 | AN001863 | Metabolme analysis of OPC-163493 on the Liver of ZDF rats (part-II) | Liver | Rat | Diabetes | Otsuka Pharmaceuticals | nmol/g tissue |
ST003143 | AN005157 | Mitochondrial complex I promotes kidney cancer metastasis | Kidney | Human | Cancer | University of Texas Southwestern Medical Center at Dallas | Normalized Abundance |
ST003143 | AN005157 | Mitochondrial complex I promotes kidney cancer metastasis | Tumor cells | Human | Cancer | University of Texas Southwestern Medical Center at Dallas | Normalized Abundance |
ST003143 | AN005158 | Mitochondrial complex I promotes kidney cancer metastasis | Kidney | Human | Cancer | University of Texas Southwestern Medical Center at Dallas | Normalized Abundance |
ST003143 | AN005158 | Mitochondrial complex I promotes kidney cancer metastasis | Tumor cells | Human | Cancer | University of Texas Southwestern Medical Center at Dallas | Normalized Abundance |
ST002969 | AN004878 | Polar metabolites in cecal tissue of mice treated with or without ampicillin and tributyrin | Cecum | Mouse | Bacterial infection | The Rockefeller University | Normalized Area |
ST002322 | AN003789 | Metabolomics study comparing SCAP KO and WT B cells | Cultured cells | Mouse | Indiana University School of Medicine | Normalized AUC | |
ST003193 | AN005241 | Metabolomics study on frozen tissue derived from the tumor and adjacent non-malignant liver tissue (NML) of patient afflicted with fibrolamellar carinoma (FLC) | Liver | Human | Cancer | Cornell University | normalized-BatchCorrected-Imputed-log2transformed Intensity |
ST003193 | AN005241 | Metabolomics study on frozen tissue derived from the tumor and adjacent non-malignant liver tissue (NML) of patient afflicted with fibrolamellar carinoma (FLC) | Lung | Human | Cancer | Cornell University | normalized-BatchCorrected-Imputed-log2transformed Intensity |
ST003193 | AN005241 | Metabolomics study on frozen tissue derived from the tumor and adjacent non-malignant liver tissue (NML) of patient afflicted with fibrolamellar carinoma (FLC) | Lymph node | Human | Cancer | Cornell University | normalized-BatchCorrected-Imputed-log2transformed Intensity |
ST003193 | AN005241 | Metabolomics study on frozen tissue derived from the tumor and adjacent non-malignant liver tissue (NML) of patient afflicted with fibrolamellar carinoma (FLC) | Peritoneal fluid | Human | Cancer | Cornell University | normalized-BatchCorrected-Imputed-log2transformed Intensity |
ST003193 | AN005241 | Metabolomics study on frozen tissue derived from the tumor and adjacent non-malignant liver tissue (NML) of patient afflicted with fibrolamellar carinoma (FLC) | Spinal cord | Human | Cancer | Cornell University | normalized-BatchCorrected-Imputed-log2transformed Intensity |
ST002775 | AN004517 | Zebrafish Retina Regeneration Metabolomics - 3 Days Post Crush | Eye tissue | Zebrafish | Eye disease | University of Miami | Normalized Concentrations |
ST002160 | AN003539 | Global metabolomics analysis of neutrophils isolated from tumor | Tumor cells | Mouse | Cancer | The Wistar Institute | Normalized MS Peak Area |
ST002383 | AN003882 | Metabolomics of B-cell Acute Lymphoblastic Leukemia in Response to Adipocyte Conditioned Media | Cultured cells | Human | Cancer | Emory University | normalized peak area |
ST002266 | AN003701 | Kīlauea lava fuels phytoplankton bloom in the North Pacific Ocean - study of particulate metabolites | Water | Plankton | University of Washington | Normalized peak area | |
ST002467 | AN004023 | Nano-hijacked myeloid cells potentiate antitumor immunity and radiotherapy for glioblastoma | Brain | Mouse | Cancer | Northwestern University, Feinberg School of Medicine | Normalized peak area |
ST002216 | AN003625 | Non-targeted metabolomics screen comparing metabolite profiles of serum from PDAC-bearing mice that received metronidazole using high-resolution, high-performance LC-MS/MS analysis. | Blood | Mouse | Cancer | The Wistar Institute | Normalized Peak Area |
ST002217 | AN003626 | Non-targeted metabolomics screen comparing metabolite profiles of serum from PDAC-bearing mice that received 1% choline supplementation or control diet using high-resolution, high-performance LC-MS/MS analysis. | Blood | Mouse | Cancer | The Wistar Institute | Normalized Peak Area |
ST001356 | AN002255 | Diel Metabolites in the North Pacific Subtropical Gyre (KM1513) | Suspended Marine Particulate Matter | Ilyonectria estremocensis | University of Washington | Normalized Peak Area per L of SW filtered | |
ST001356 | AN002255 | Diel Metabolites in the North Pacific Subtropical Gyre (KM1513) | Suspended Marine Particulate Matter | Ilyonectria mors-panacis | University of Washington | Normalized Peak Area per L of SW filtered | |
ST001356 | AN002255 | Diel Metabolites in the North Pacific Subtropical Gyre (KM1513) | Suspended Marine Particulate Matter | Ilyonectria robusta | University of Washington | Normalized Peak Area per L of SW filtered | |
ST001356 | AN002255 | Diel Metabolites in the North Pacific Subtropical Gyre (KM1513) | Suspended Marine Particulate Matter | Ilyonectria rufa | University of Washington | Normalized Peak Area per L of SW filtered | |
ST001356 | AN002255 | Diel Metabolites in the North Pacific Subtropical Gyre (KM1513) | Suspended Marine Particulate Matter | Ilyonectria torresensis | University of Washington | Normalized Peak Area per L of SW filtered | |
ST001356 | AN002255 | Diel Metabolites in the North Pacific Subtropical Gyre (KM1513) | Suspended Marine Particulate Matter | Neonectria obtusispora | University of Washington | Normalized Peak Area per L of SW filtered | |
ST001393 | AN002324 | Sea-ice diatom compatible solute shifts | Diatom cells | Nitzschia lecointei | University of Washington | Normalized Peak Area Per L Seawater | |
ST001393 | AN002323 | Sea-ice diatom compatible solute shifts | Diatom cells | Nitzschia lecointei | University of Washington | Normalized Peak Area Per RFU | |
ST002444 | AN003981 | Zebrafish Optic Nerve Regeneration Metabolomics - 3 Days Post Crush | Eye tissue | Zebrafish | Eye disease | University of Miami | normalized peak areas |
ST001841 | AN002984 | Metabolomics of lung microdissections reveals region- and sex-specific metabolic effects of acute naphthalene exposure in mice (part II) | Liver | Mouse | Oxidative stress | University of California, Davis | normalized peak height |
ST001844 | AN002987 | Identification of unique metabolite networks between Latino and Caucasian patients with nonalcoholic fatty liver disease (NAFLD) (part III) | Blood | Human | Fatty liver disease | University of California, Davis | normalized peak height |
ST001844 | AN002987 | Identification of unique metabolite networks between Latino and Caucasian patients with nonalcoholic fatty liver disease (NAFLD) (part III) | Liver | Human | Fatty liver disease | University of California, Davis | normalized peak height |
ST002028 | AN003298 | Metabolomics Analysis of Blood Plasma and Stool from Six Week Flaxseed Dietary Intervention in Postmenopausal Women (Stool/HILIC) | Feces | Human | UC Davis | normalized peak height | |
ST002254 | AN003682 | Maternal obesity alters offspring liver and skeletal muscle metabolism in early post-puberty despite maintaining a normal post-weaning dietary lifestyle | Blood | Baboon | Obesity | Wake Forest School of Medicine | Normalized Peak Intensities |
ST002254 | AN003682 | Maternal obesity alters offspring liver and skeletal muscle metabolism in early post-puberty despite maintaining a normal post-weaning dietary lifestyle | Liver | Baboon | Obesity | Wake Forest School of Medicine | Normalized Peak Intensities |
ST002254 | AN003682 | Maternal obesity alters offspring liver and skeletal muscle metabolism in early post-puberty despite maintaining a normal post-weaning dietary lifestyle | Muscle | Baboon | Obesity | Wake Forest School of Medicine | Normalized Peak Intensities |
ST002809 | AN004566 | Role of cilia in mitochondrial function | Cultured cells | Dog | Kidney disease | Medical University of South Carolina | Normalized/scaled raw area counts |
ST002809 | AN004566 | Role of cilia in mitochondrial function | Cultured cells | Mouse | Kidney disease | Medical University of South Carolina | Normalized/scaled raw area counts |
ST002020 | AN003290 | TIPs Metabolomics (urine) | Urine | Human | Vanderbilt University Medical Center | osmolality normalized scaled imputed | |
ST001747 | AN002844 | Lung metabolomics after ischemic acute kidney injury reveals increased oxidative stress, altered energy production, and ATP depletion | Lung | Mouse | Acute kidney injury | University of Colorado Anschutz Medical Campus | peak area |
ST001873 | AN003035 | Metabolomics analysis of multiple samples on AB 5600-Part 1 | Blood | Human | Dalian Institute Of Chemical Physics | peak area | |
ST001873 | AN003035 | Metabolomics analysis of multiple samples on AB 5600-Part 1 | Hep G2 cells | Human | Dalian Institute Of Chemical Physics | peak area | |
ST001873 | AN003035 | Metabolomics analysis of multiple samples on AB 5600-Part 1 | Urine | Human | Dalian Institute Of Chemical Physics | peak area | |
ST001996 | AN003255 | Polyamine import and accumulation causes immunomodulation in macrophages engulfing apoptotic cells (Part 1) | Macrophages | Mouse | University of Colorado Denver | peak area | |
ST001998 | AN003259 | Polyamine import and accumulation causes immunomodulation in macrophages engulfing apoptotic cells (Part 3) | Macrophages | Mouse | University of Colorado Denver | peak area | |
ST001999 | AN003261 | Polyamine import and accumulation causes immunomodulation in macrophages engulfing apoptotic cells (Part 4) | Macrophages | Mouse | University of Colorado Denver | peak area | |
ST002011 | AN003278 | The anticancer human mTOR inhibitor MLN0128/Sapanisertib with potent multistage in vitro antiplasmodium activity and in vivo antimalarial efficacy in a humanised mouse model is an inhibitor of multiple Plasmodium falciparum kinases. | Blood | Plasmodium falciparum | Malaria | Pennsylvania State University | peak area |
ST002153 | AN003526 | Data from plasma metabolome analysis of APP-KI and Wild type mice treated with B. breve MCC1274 | Blood | Mouse | Morinaga milk industry CO., LTD. | peak area | |
ST002163 | AN003545 | Remote solid cancers rewire hepatic nitrogen metabolism via host nicotinamide-N-methyltransferase | Liver | Mouse | Cancer | Tohoku University | peak area |
ST002167 | AN003551 | Remote solid cancers rewire hepatic nitrogen metabolism via host nicotinamide-N-methyltransferase (AML cells) | AML cells | Mouse | Cancer | Tohoku University | peak area |
ST002184 | AN003577 | Metabolic effect of the loss of mitochondrial-specific aspartyl-tRNA synthetase Das2 on mouse intestinal epithelial cells | Intestine | Mouse | CECAD Research Center | peak area | |
ST002199 | AN003599 | FOXA2 controls the anti-oxidant response in FH-deficient cells independent of NRF2 | Cultured cells | Mouse | Cancer | CECAD Research Center | peak area |
ST002205 | AN003608 | Effect of Hira loss in the metabolic landscape of Fh1-deficient cells | Cultured cells | Mouse | Cancer | CECAD Research Center, University Hospital Cologne | peak area |
ST002218 | AN003627 | Effect of Hira loss in the metabolic landscape of Fh1-deficient cells Part 2 | Cultured cells | Mouse | Cancer | CECAD Research Center | peak area |
ST002220 | AN003629 | Cataboslim of branched-chain amino acids (BCAAs) in renal cells HK2 and 786-O | Cultured cells | Human | Cancer | CECAD Research Center | peak area |
ST002221 | AN003630 | Glutaminolysis contribution to the carbon backbone of aspartate through ATP Citrate Lyase (ACLY) in ccRCC | Cultured cells | Human | Cancer | CECAD Research Center | peak area |
ST002222 | AN003631 | Glutaminolysis contribution to the carbon backbone of aspartate and glutamate in ccRCC | Cultured cells | Human | Cancer | CECAD Research Center | peak area |
ST002223 | AN003632 | Metabolic profiling of mouse tissues and tissue interstitial fluids | Heart | Mouse | Cancer | CECAD Research Center | peak area |
ST002223 | AN003632 | Metabolic profiling of mouse tissues and tissue interstitial fluids | Kidney | Mouse | Cancer | CECAD Research Center | peak area |
ST002223 | AN003632 | Metabolic profiling of mouse tissues and tissue interstitial fluids | Liver | Mouse | Cancer | CECAD Research Center | peak area |
ST002223 | AN003632 | Metabolic profiling of mouse tissues and tissue interstitial fluids | Lung | Mouse | Cancer | CECAD Research Center | peak area |
ST002224 | AN003633 | Intracellular metabolic profile of renal cells cultured in Plasmax | Cultured cells | Human | Cancer | CECAD Research Center | peak area |
ST002225 | AN003634 | Time sensitive contribution of the BCAA catabolism to the TCA cycle carbons in HK2, 786-O, OS-RC-2 and RFX-631 | Cultured cells | Human | Cancer | CECAD Research Center | peak area |
ST002242 | AN003660 | Hypoxia promotes osteogenesis via regulating the acetyl-CoA-mediated mito-nuclear communication. | Cultured cells | Mouse | CECAD Research Center | peak area | |
ST002306 | AN003768 | Metabolomics profiling of full extracts of bacterial culture supernatants. | Bacterial cells | Bacillus megaterium | Myalgic encephalomyelitis/chronic fatigue syndrome | University of Connecticut | peak area |
ST002306 | AN003768 | Metabolomics profiling of full extracts of bacterial culture supernatants. | Bacterial cells | Enterococcus faecium | Myalgic encephalomyelitis/chronic fatigue syndrome | University of Connecticut | peak area |
ST002361 | AN003855 | UCP2-dependent redox-sensing in POMC neurons regulates feeding | Cultured cells | Mouse | Columbia University | peak area | |
ST002431 | AN003957 | MS profiling of the Long Term Evolution Experiment | Bacterial cells | E. coli | Rutgers University | peak area | |
ST002634 | AN004306 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Hippocampus Powder - Untargeted HILIC-Positive | Hippocampus | Rat | Broad Institute | peak area | |
ST002640 | AN004312 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Cortex Powder - Untargeted HILIC-Positive | Cortex | Rat | Broad Institute | peak area | |
ST002641 | AN004313 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Hypothalamus Powder - Untargeted HILIC-Positive | Hypothalamus | Rat | Broad Institute | peak area | |
ST002642 | AN004314 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Gastrocnemius Powder - Untargeted HILIC-Positive | Gastrocnemius | Rat | Broad Institute | peak area | |
ST002648 | AN004320 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Vastus Lateralis Powder - Untargeted HILIC-Positive | Vastus lateralis | Rat | Broad Institute | peak area | |
ST002649 | AN004321 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Heart Powder - Untargeted HILIC-Positive | Heart | Rat | Broad Institute | peak area | |
ST002654 | AN004326 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Kidney Powder - Untargeted HILIC-Positive | Kidney | Rat | Broad Institute | peak area | |
ST002659 | AN004331 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Adrenal Powder - Untargeted HILIC-Positive | Adrenal gland | Rat | Broad Institute | peak area | |
ST002664 | AN004336 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Colon Powder - Untargeted HILIC-Positive | Colon | Rat | Broad Institute | peak area | |
ST002665 | AN004337 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Spleen Powder - Untargeted HILIC-Positive | Spleen | Rat | Broad Institute | peak area | |
ST002666 | AN004338 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Testes Powder - Untargeted HILIC-Positive | Testes | Rat | Broad Institute | peak area | |
ST002667 | AN004339 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Ovaries Powder - Untargeted HILIC-Positive | Ovaries | Rat | Broad Institute | peak area | |
ST002668 | AN004340 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Lung Powder - Untargeted HILIC-Positive | Lung | Rat | Broad Institute | peak area | |
ST002674 | AN004346 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Small Intestine Powder - Untargeted HILIC-Positive | Small intestine | Rat | Broad Institute | peak area | |
ST002675 | AN004347 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Liver Powder - Untargeted HILIC-Positive | Liver | Rat | Broad Institute | peak area | |
ST002682 | AN004355 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Brown Adipose Powder - Untargeted HILIC-Positive | Brown adipose | Rat | Broad Institute | peak area | |
ST002688 | AN004361 | MoTrPAC: Endurance exercise training study in young adult rats, Rat White Adipose Powder - Untargeted HILIC-Positive | White adipose | Rat | Broad Institute | peak area | |
ST002695 | AN004368 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Vena Cava Powder - Untargeted HILIC-Positive | Vena cava | Rat | Broad Institute | peak area | |
ST002712 | AN004396 | Ranolazine induced metabolic rewiring improves melanoma responses to targeted therapy and immunotherapy - metabolomics | Cultured cells | Human | Cancer | University of Colorado Denver | peak area |
ST002714 | AN004400 | Loss of microglial MCT4 leads to defective synaptic pruning and anxiety-like behavior in mice | Brain | Mouse | University of Colorado Denver | peak area | |
ST002736 | AN004438 | Assessing mitochondrial bioenergetics in coronary artery disease: A translational multiomic tissue study in humans (The AMBITION study). | Heart | Human | Cardiovascular disease | Imperial College London | peak area |
ST002897 | AN004756 | Polar metabolite levels in K562 cells following folate depletion, SHIN1 or AICAR treatment | Cultured cells | Human | Anemia | Boston Children's Hospital, Harvard Medical School | peak area |
ST002898 | AN004757 | Polar metabolite levels in MEL cells following folate depletion, SHIN1 or AICAR treatment | Cultured cells | Mouse | Anemia | Boston Children's Hospital, Harvard Medical School | peak area |
ST002906 | AN004769 | Polar metabolite levels in K562 cells following short-term folate depletion | Cultured cells | Human | Anemia | Boston Children's Hospital, Harvard Medical School | peak area |
ST002912 | AN004782 | Polar metabolite levels in MEL cells following folate depletion | Cultured cells | Mouse | Anemia | Boston Children's Hospital, Harvard Medical School | peak area |
ST002913 | AN004783 | Polar metabolite levels in K562 cells following folate depletion | Cultured cells | Human | Anemia | Boston Children's Hospital, Harvard Medical School | peak area |
ST003162 | AN005188 | Loss of dihydroceramide desaturase drives neurodegeneration by disrupting endoplasmic reticulum and lipid droplet homeostasis in glial cells | CNS | Drosophila melanogaster | Brain disease | Washington University in St. Louis | peak area |
ST003162 | AN005188 | Loss of dihydroceramide desaturase drives neurodegeneration by disrupting endoplasmic reticulum and lipid droplet homeostasis in glial cells | Larvae | Drosophila melanogaster | Brain disease | Washington University in St. Louis | peak area |
ST003172 | AN005206 | Untargeted Metabolomic Profile Of Chili Pepper (Capsicum Chinensed) Developmental Cycle | Capsicum Chinense | Plant | University of Alberta | peak area | |
ST003331 | AN005457 | Increased Cholesterol Synthesis Drives Neurotoxicity in Patient Stem Cell-Derived Model of Multiple Sclerosis - cellular metabolomics | Stem cells | Human | Multiple sclerosis | University of Colorado Denver | peak area |
ST003347 | AN005482 | ADSL deficiency drives mitochondrial dysfunction and ERK2 dysregulation in a linear genotype to phenotype correlation | Skin | Human | Neuropathy | Catholic University of the Sacred Heart | peak area |
ST003499 | AN005743 | Metabolic analysis of ADSL deficiency patients' EBV-LCLs. | Blood | Human | Mitochondrial Dysfunction | Catholic University of the Sacred Heart | peak area |
ST003499 | AN005744 | Metabolic analysis of ADSL deficiency patients' EBV-LCLs. | Blood | Human | Mitochondrial Dysfunction | Catholic University of the Sacred Heart | peak area |
ST000009 | AN000023 | Mixed meal tolerance | Human | University of Michigan | Peak area | ||
ST000010 | AN000025 | Lung Cancer Cells 4 | Lung | Human | Cancer | University of Michigan | Peak area |
ST000011 | AN000027 | African Metabolomics | Human | University of Michigan | Peak area | ||
ST000016 | AN000033 | NPM-ALK metabolic regulation | Lymphoma cells | Human | University of Michigan | Peak area | |
ST000017 | AN000034 | Rat HCR/LCR Stamina Study | Blood | Rat | University of Michigan | Peak area | |
ST000116 | AN000197 | Comparative metabolomics analysis of the key metabolic nodes in propionic acid synthesis in Propionibacterium acidipropionici | Bacterial cells | Propionibacterium | Jiangnan University | Peak area | |
ST000230 | AN000344 | Comprehensive analysis of transcriptome and metabolome in Intrahepatic Cholangiocarcinoma and Hepatocellular Carcinoma | Liver | Human | Cancer | Osaka City University | Peak area |
ST000231 | AN000346 | Comprehensive analysis of transcriptome and metabolome in Intrahepatic Cholangiocarcinoma and Hepatocellular Carcinoma (part II) | Liver | Human | Cancer | Osaka City University | Peak area |
ST000289 | AN000460 | PPDK RNAi effects in endosperm metabolite pools | Maize starchy endosperm | Maize | University of Florida | Peak area | |
ST000290 | AN000462 | 2014 Biotron Experiment Metabolites | Maize kernel | Maize | University of Florida | Peak area | |
ST000689 | AN001064 | Influence of Noxa knockdown on cell metabolism | Cultured cells | Human | University of Michigan | Peak area | |
ST000692 | AN001070 | Metabolites produced by strains associated with inflammation | Bacterial cells | Treponema | Inflammation | University of Michigan | Peak area |
ST000693 | AN001072 | Lanthanide-mineral induced alteration of bile acid metabolism in a murine model of steatohepatitis (part II) | Mouse | Fatty liver disease | University of Michigan | Peak area | |
ST000694 | AN001074 | Differences in bile acids composition between ASCL5 knockout and floxed mice. | Intestine | Mouse | University of Michigan | Peak area | |
ST000696 | AN001080 | Brain-Immune system-Gut Interaction in Chronic Mild Stress (CMS +/- Lacto) | Mouse | Stress | University of Michigan | Peak area | |
ST000697 | AN001082 | Cytokines correlation with metabolomic profiling of psoriatic and normal skin | Keratinocytes | Human | University of Michigan | Peak area | |
ST000741 | AN001156 | Metabolite-phenotype link in X-linked Adrenoleukodystrophy (fibroblast cell culture) | Cultured cells | Human | Adrenoleukodystrophy | University of Michigan | Peak area |
ST000748 | AN001173 | Placental cells (BeWo) phthalate exposure metabolomics | Cultured cells | Human | University of Michigan | Peak area | |
ST000751 | AN001179 | Mouse placentas-DEHP exposure (part II) | Placenta | Mouse | University of Michigan | Peak area | |
ST000768 | AN001215 | Metabolites of human neurons and stem cells (siNeuron metabolomics) | Stem cells | Human | University of Michigan | Peak area | |
ST000880 | AN001433 | Diet, genetics and gut microbiome drive dynamic changes in plasma metabolites [cecal] | Mouse | The Broad Institute | Peak area | ||
ST001222 | AN002035 | Effects of selenate and cadmium exposure on the honey bee metabolome (part-II) | Insect tissue | Honey Bee | Environmental exposure | University of California, Riverside | Peak area |
ST001232 | AN002050 | Combining stage - specificity and metabolomic profiling to advance drug discovery for malaria | Cultured cells | Plasmodium falciparum | Malaria | Pennsylvania State University | Peak area |
ST001256 | AN002085 | Metabolic landscape remodeling in dystrophic muscle through glucocorticoid steroid regimens | Muscle | Mouse | Muscular dystrophy | Northwestern University | Peak area |
ST001329 | AN002215 | SS-31 and NMN: Two Paths to Improve Metabolism and Function in Aged Hearts | Heart | Mouse | University of Washington | Peak area | |
ST001441 | AN002407 | Metabolomics of patient-derived fibroblasts | Fibroblast cells | Human | Mitochondrial disease | North Carolina State University | Peak area |
ST001507 | AN002498 | Hepatic [U-13C]Lactate tracing and metabolomics in young and old WT and SIRT6 overexpressing mice | Liver | Mouse | Bar Ilan University | Peak area | |
ST001611 | AN002645 | Mouse model of sarcoma (STS) to characterize tumor vulnerabilities and identify novel targets for anti-cancer treatment | Muscle | Mouse | Cancer | North Carolina State University | Peak area |
ST001611 | AN002645 | Mouse model of sarcoma (STS) to characterize tumor vulnerabilities and identify novel targets for anti-cancer treatment | Sarcoma | Mouse | Cancer | North Carolina State University | Peak area |
ST001709 | AN002783 | SARS-CoV-2 infection rewires host cell metabolism and is potentially susceptible to mTORC1 inhibition | Cultured cells | Human | COVID-19 | University of California, Los Angeles | Peak area |
ST002237 | AN003650 | Metabolomic analysis of brain cortex from neuronal specific Depdc5 knockout in fed and fasting state | Brain | Mouse | Northwestern University Feinberg School of Medicine | Peak area | |
ST002376 | AN003871 | Hepatic Phosphatidylcholine Catabolism Driven by PNPLA7 and PNPLA8 Supplies Endogenous Choline to Replenish the Methionine Cycle with Methyl Groups(Pnpla8-knockout) | Liver | Mouse | Tokyo Metropolitan Institute of Medical Science | Peak area | |
ST002492 | AN004081 | Composition of raw plant-based food items | Plant | Plants | Northeastern University | Peak area | |
ST002505 | AN004126 | A Mammalian Conserved Circular RNA CircLARP2 Regulates Hepatocellular Carcinoma Metastasis and Lipid Metabolism (Part 1) | Cultured cells | Human | Cancer | University of Science and Technology of China | Peak area |
ST002506 | AN004128 | Natural abundance of isotopic metabolite detection in mouse eye orgnaoids. | Retina | Mouse | Northwestern University | Peak area | |
ST002507 | AN004129 | Time-course analysis of C13 labeling in mouse eye organoids. | Retina | Mouse | Northwestern University | Peak area | |
ST002508 | AN004130 | 13C-isotopic labeling of mouse eye organoids under three conditions. | Retina | Mouse | Northwestern University | Peak area | |
ST002846 | AN004664 | Apolipoprotein E suppresses hyperlipidemia-driven hematopoiesis & inflammation by controlling mitochondrial metabolism | Macrophages | Mouse | Hyperlipidemia | Northwestern University | Peak area |
ST002876 | AN004713 | High Level Expression of NSD2 Creates a Metabolic Dependency in Multiple Myeloma | B-cells | Human | Cancer | University of Florida | Peak area |
ST003177 | AN005215 | A Longitudinal Study in Rheumatoid Arthritis Unveils Metabolomic Biomarkers Preceding Clinical Onset, Assessing Disease Severity, and Anticipating Treatment Response to csDMARDs | Blood | Human | Rheumatoid arthritis | West China Hospital of Sichuan University | Peak area |
ST003249 | AN005322 | Mitochondrial respiration impairment in microglia dampens response to demyelinating injury but is not sufficient to induce an aging phenotype | Microglia | Mouse | Alzheimers disease | Northwestern University | Peak area |
ST003262 | AN005346 | A Covalent Creatine Kinase Inhibitor Ablates Glioblastoma Migration and Sensitizes Tumors to Oxidative Stress. | Brain | Human | Cancer | Northwestern University, Feinberg School of Medicine | Peak area |
ST003264 | AN005348 | SLC25A48 controls mitochondrial choline import and metabolism | Blood | Mouse | Harvard Medical School | Peak area | |
ST003504 | AN005752 | Methionine-SAM metabolism-dependent ubiquinone synthesis is crucial for ROS accumulation in ferroptosis induction | Cultured cells | Human | Cancer; Cardiomyopathy | Northeast Normal University | Peak area |
ST003537 | AN005809 | Metabolomic analysis of fluorescent hairy roots overexpressing the Gretchen Hagen 3_3 genes enhancing soybean resistance to cyst nematodes | Plant Root | Soyabean | Shenyang Agricultural University | Peak area | |
ST003538 | AN005810 | Metabolomic analysis of fluorescent hairy roots overexpressing the Gretchen Hagen 3_2 genes enhancing soybean resistance to cyst nematodes | Plant Root | Soyabean | Shenyang Agricultural University | Peak area | |
ST003539 | AN005811 | Metabolomic analysis of fluorescent hairy roots overexpressing the Gretchen Hagen 3_1 genes enhancing soybean resistance to cyst nematodes | Plant Root | Soyabean | Shenyang Agricultural University | Peak area | |
ST003540 | AN005812 | Metabolomic analysis of fluorescent hairy roots overexpressing the Gretchen Hagen 3_61 genes enhancing soybean resistance to cyst nematodes | Plant Root | Soyabean | Shenyang Agricultural University | Peak area | |
ST001954 | AN003179 | A pathogenic role for histone H3 copper reductase activity in a yeast model of Friedreich’s Ataxia | Yeast cells | Yeast | Friedreichs Ataxia | University of California, Los Angeles | Peak Area |
ST002292 | AN003744 | Quantification of Dissolved Metabolites in Environmental Samples through Cation-Exchange Solid Phase Extraction (CX-SPE) paired with Liquid Chromatography-Mass Spectrometry | Water | Other | University of Washington | Peak Area | |
ST002292 | AN003746 | Quantification of Dissolved Metabolites in Environmental Samples through Cation-Exchange Solid Phase Extraction (CX-SPE) paired with Liquid Chromatography-Mass Spectrometry | Water | Other | University of Washington | Peak Area | |
ST002709 | AN004391 | FH variant pathogenicity promotes purine salvage pathway dependence in kidney cancer | Cultured cells | Other | Cancer | University of California, Los Angeles | Peak Area |
ST002776 | AN004519 | Zebrafish Optic Nerve Regeneration, Tectum Metabolomics - 3 Days Post Crush | Eye tissue | Zebrafish | Eye disease | University of Miami | Peak Area |
ST002814 | AN004705 | Atlas of fetal metabolism during mid-to-late gestation and diabetic pregnancy | Embryonic cells | Mouse | Diabetes | University of California, Los Angeles | Peak Area |
ST002814 | AN004705 | Atlas of fetal metabolism during mid-to-late gestation and diabetic pregnancy | Embryonic cells | Mouse | Hypoglycemia | University of California, Los Angeles | Peak Area |
ST002814 | AN004705 | Atlas of fetal metabolism during mid-to-late gestation and diabetic pregnancy | Embryonic cells | Mouse | Hypoglycemia; Diabetes | University of California, Los Angeles | Peak Area |
ST002852 | AN004672 | MYC is a regulator of androgen receptor inhibition-induced metabolic requirements in prostate cancer | Prostate | Mouse | Cancer | University of California, Los Angeles | Peak Area |
ST002878 | AN004715 | Atlas of fetal metabolism during mid-to-late gestation and diabetic pregnancy. Dynamic Labelling experiment. | Embryonic cells | Mouse | Diabetes | University of California, Los Angeles | Peak Area |
ST002935 | AN004814 | Title: Myeloid cell-derived creatine in the hypoxic niche promotes glioblastoma growth | Brain | Human | Cancer | Northwestern University, Feinberg School of Medicine | Peak Area |
ST003111 | AN005094 | Inhibition of Asparagine Synthetase Effectively Retards Polycystic Kidney Disease Progression, investigated with targeted metabolomics in Tam-Cre;Pkd1ΔC/flox mouse model kidneys. | Kidney | Mouse | Kidney disease | San Raffaele University | Peak Area |
ST003166 | AN005195 | Metabolomics of Murine WT or MCJ KO CD19-BBz CD8 CAR-T cells | T-cells | Mouse | Cancer | University of Colorado School of Medicine | Peak Area |
ST002572 | AN004237 | Steady State and Cysteine Flux Metabolomics Study in PTEN WT and PTEN KO MEFs | Fibroblast cells | Mouse | Cancer | Mount Sinai | peak area intensity |
ST002984 | AN004904 | Amino acid catabolite markers for early prognostication of pneumonia in patients with COVID-19 | Blood | Human | COVID-19 | Graduate School of Medicine, Kyoto University | Peak area/Internal Standard |
ST000698 | AN001084 | Metabolomics analysis of Sirt5 knockdown (KD) melanoma | Human | University of Michigan | Peak area normalized | ||
ST002031 | AN003301 | Irradiation causes alterations of polyamine, purine and sulfur metabolism in red blood cells and multiple organs (Whole blood) | Blood | Mouse | University of Colorado Anschutz Medical Campus | peak area top | |
ST002033 | AN003306 | Irradiation causes alterations of polyamine, purine and sulfur metabolism in red blood cells and multiple organs (Feces-part1) | Feces | Mouse | University of Colorado Anschutz School of Medicine | peak area top | |
ST002034 | AN003308 | Irradiation causes alterations of polyamine, purine and sulfur metabolism in red blood cells and multiple organs (Feces-part2) | Feces | Mouse | University of Colorado Anschutz Medical Campus | peak area top | |
ST002035 | AN003309 | Irradiation causes alterations of polyamine, purine and sulfur metabolism in red blood cells and multiple organs (Heart) | Heart | Mouse | University of Colorado Anschutz Medical Campus | peak area top | |
ST002036 | AN003311 | Irradiation causes alterations of polyamine, purine and sulfur metabolism in red blood cells and multiple organs (Kidney) | Kidney | Mouse | University of Colorado Anschutz Medical Campus | peak area top | |
ST002037 | AN003313 | Irradiation causes alterations of polyamine, purine and sulfur metabolism in red blood cells and multiple organs (Liver) | Liver | Mouse | University of Colorado Anschutz Medical Campus | peak area top | |
ST002038 | AN003315 | Irradiation causes alterations of polyamine, purine and sulfur metabolism in red blood cells and multiple organs (Duodenum) | Duodenum | Mouse | University of Colorado Anschutz Medical Campus | peak area top | |
ST002039 | AN003317 | Irradiation causes alterations of polyamine, purine and sulfur metabolism in red blood cells and multiple organs (Brain) | Brain | Mouse | University of Colorado Anschutz Medical Campus | peak area top | |
ST002040 | AN003319 | Irradiation causes alterations of polyamine, purine and sulfur metabolism in red blood cells and multiple organs (Colon) | Colon | Mouse | University of Colorado Anschutz School of Medicine | peak area top | |
ST002066 | AN003366 | Glutaminase inhibition impairs CD8 T cell activation in STK11/Lkb1 deficient lung cancer | Lung | Mouse | Cancer | The Walter and Eliza Hall Institute of Medical Research | peak height |
ST002075 | AN003382 | Profiling of the human intestinal microbiome and bile acids under physiologic conditions using an ingestible sampling device (Part 2) | Intestine | Human | UC Davis | peak height | |
ST002926 | AN004798 | Multi-“omics” analysis reveals the orphan P. falciparum protein kinase PfPK8 regulates multi-gene family expression | Blood | Plasmodium falciparum | Malaria | Monash University | peak height |
ST003053 | AN005006 | Providing insight into the mechanism of action of Cationic Lipidated Oligomers (CLOs) using metabolomics | Bacterial cells | Staphylococcus aureus | Bacterial infection | Monash University | peak height |
ST003521 | AN005782 | Metabolic Profiling Unveils Enhanced Antibacterial Synergy of Polymyxin B and Teixobactin against Multi-Drug Resistant Acinetobacter baumannii | Bacterial cells | Acinetobacter baumannii | Bacterial infection | Monash University | peak height |
ST003521 | AN005783 | Metabolic Profiling Unveils Enhanced Antibacterial Synergy of Polymyxin B and Teixobactin against Multi-Drug Resistant Acinetobacter baumannii | Bacterial cells | Acinetobacter baumannii | Bacterial infection | Monash University | peak height |
ST000239 | AN000369 | Sexual antagonism in exuded non-volatile metabolites in C. purpureus | Plant | Moss | University of Florida | Peak height | |
ST000243 | AN000379 | Metabolomic-based investigation on the effects of antifungal agents in Candida albicans | Yeast cells | Candida albicans | University of Florida | Peak height | |
ST000403 | AN000642 | Metabolomics-based elucidation of active metabolic pathways in erythrocytes and HSC-derived reticulocytes | Cells | Human | Monash Institute of Pharmaceutical Sciences, Monash University | Peak height | |
ST000414 | AN000655 | Metabolomics-based screening of the Malaria Box reveals both novel and established mechanisms of action | Cells | Plasmodium falciparum | Malaria | Monash Institute of Pharmaceutical Sciences, Monash University | Peak height |
ST000539 | AN000818 | Metabolomics-based elucidation of active metabolic pathways in erythrocytes and HSC-derived reticulocytes (part II) | Cells | Human | Monash Institute of Pharmaceutical Sciences, Monash University | Peak height | |
ST000546 | AN000832 | Multi-omics based identification of specific biochemical changes associated with PfKelch13-mutant artemisinin resistant Plasmodium | Cells | Plasmodium falciparum | Malaria | Monash Institute of Pharmaceutical Sciences, Monash University | Peak height |
ST000564 | AN000866 | 2014 Biotron Experiment Metabolites (part II) | Maize kernel | Maize | University of Florida | Peak height | |
ST000955 | AN001566 | Effects of ODC inhibition on T cell metabolism | Cultured cells | Mouse | Cancer | University of Florida | Peak height |
ST001033 | AN001694 | Determination of mode of action of anti-malalrial drugs using untargeted metabolomics | Cultured cells | Plasmodium falciparum | Malaria | Monash University | Peak height |
ST001122 | AN001847 | Identification of urine metabolites in patients with interstitial cystitis using untargeted metabolomics (part II) | Urine | Human | Interstitial cystitis | University of California, Davis | Peak height |
ST001211 | AN002017 | Metabolomic Markers of Methotrexate Response, In Vitro | Cultured cells | Human | University Of Kansas | Peak height | |
ST001274 | AN002115 | Metabolomics-based profiling of the mode of action of Pathogen Box compounds in Trypanosoma brucei (part-I) | Cultured cells | Trypanosoma brucei | Sleeping sickness | Monash University | Peak height |
ST001276 | AN002117 | Development and Characterisation of a Novel Class of Aroyl Guanidine Containing Anti-Trypanosomal Compounds | Cultured cells | Trypanosoma brucei | Sleeping sickness | Monash University | Peak height |
ST001637 | AN002675 | A Metabolome Atlas of the Aging Mouse Brain | Brain | Mouse | University of California, Davis | Peak height | |
ST001888 | AN003057 | A Metabolome Atlas of the Aging Mouse Brain (Study part II) | Brain | Mouse | University of California, Davis | Peak height | |
ST001928 | AN003136 | Metabolomics profiles of premenopausal women are different based on O-desmethylangolensin metabotype | Urine | Human | George Mason University | Peak height | |
ST002832 | AN004625 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Bacteroides fragilis | Stanford University | Peak height | |
ST002832 | AN004625 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Bacteroides thetaiotaomicron | Stanford University | Peak height | |
ST002832 | AN004625 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Bacteroides uniformis | Stanford University | Peak height | |
ST002832 | AN004625 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Blautia producta | Stanford University | Peak height | |
ST002832 | AN004625 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Clostridium clostridioforme | Stanford University | Peak height | |
ST002832 | AN004625 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Clostridium hathewayi | Stanford University | Peak height | |
ST002832 | AN004625 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Clostridium hylemonae | Stanford University | Peak height | |
ST002832 | AN004625 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Clostridium scindens | Stanford University | Peak height | |
ST002832 | AN004625 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Clostridium symbiosum | Stanford University | Peak height | |
ST002832 | AN004625 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Enterococcus faecalis | Stanford University | Peak height | |
ST002832 | AN004625 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Enterococcus faecium | Stanford University | Peak height | |
ST002832 | AN004625 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Enterococcus hirae | Stanford University | Peak height | |
ST002832 | AN004625 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Escherichia fergusonii | Stanford University | Peak height | |
ST002832 | AN004625 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Flavonifractor plautii | Stanford University | Peak height | |
ST002832 | AN004625 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Parabacteroides distasonis | Stanford University | Peak height | |
ST003356 | AN005497 | Noninvasive multiomic measurement of cell type repertoires in human urine | Urine | Human | Urinary tract infection | CZ Biohub | Peak height |
ST001794 | AN002911 | Metabolomics Analysis of Time-Series Gastrointestinal Lumen Samples | Intestine | Human | University of California, Davis | Peak Height Intensity | |
ST001815 | AN002945 | Metabolic Markers of Methotrexate Response in Juvenile Idiopathic Arthritis | Blood | Human | Arthritis | University Of Kansas | Peak Height Intensity |
ST001154 | AN001944 | A comprehensive plasma metabolomics dataset for a cohort of mouse knockouts within the International Mouse Phenotyping Consortium | Blood | Mouse | University of California | Peak height normalized with creatinine | |
ST002815 | AN004582 | Investigation of metabolism in hypertrophic cardiomyopathy - HILIC | Heart | Mouse | Cardiomyopathy | University of California, San Francisco | peak heights |
ST002950 | AN004838 | Investigate the impact of feeding time on the hexosamine biosynthetic pathway (HBP) in the mouse liver and heart using targeted metabolomics: biogenic amines | Heart | Mouse | University of California, Davis | peak heights | |
ST002950 | AN004838 | Investigate the impact of feeding time on the hexosamine biosynthetic pathway (HBP) in the mouse liver and heart using targeted metabolomics: biogenic amines | Liver | Mouse | University of California, Davis | peak heights | |
ST002493 | AN004086 | Composition of raw plant-based food items Pilot Study | Plant | Plants | Massachusetts Institute of Technology | peak intensity | |
ST003112 | AN005111 | Glucose Hypometabolism Prompts RAN Translation and Exacerbates C9orf72-related ALS/FTD Phenotypes | Brain | Mouse | Neurodegenerative Disorder | Thomas Jefferson University | peak intensity |
ST003113 | AN005098 | Inhibition of Asparagine Synthetase Effectively Retards Polycystic Kidney Disease Progression, investigated with targeted tracing metabolomics analysis in MEF cells using 15N2-glutamine. | Cultured cells | Mouse | Kidney disease | San Raffaele University | peak intensity |
ST003113 | AN005099 | Inhibition of Asparagine Synthetase Effectively Retards Polycystic Kidney Disease Progression, investigated with targeted tracing metabolomics analysis in MEF cells using 15N2-glutamine. | Cultured cells | Mouse | Kidney disease | San Raffaele University | peak intensity |
ST003118 | AN005112 | Glucose Hypometabolism Prompts RAN Translation and Exacerbates C9orf72-related ALS/FTD Phenotypes - Study 2 | Brain | Mouse | Neurodegenerative Disorder | Thomas Jefferson University | peak intensity |
ST000614 | AN000941 | Tobacco-specific carcinogens in Bladder Cancer | Bladder | Human | Cancer | Baylor College of Medicine | Peak intensity |
ST001201 | AN001999 | Peroxide antimalarial treatment timecourse on trophozoite-stage P. falciparum parasites | Cultured cells | Human | Malaria | Monash University | Peak intensity |
ST001201 | AN001999 | Peroxide antimalarial treatment timecourse on trophozoite-stage P. falciparum parasites | Cultured cells | Plasmodium falciparum | Malaria | Monash University | Peak intensity |
ST001202 | AN002000 | Peroxide antimalarial treatment timecourse on ring-stage P. falciparum parasites | Cultured cells | Human | Malaria | Monash University | Peak intensity |
ST001202 | AN002000 | Peroxide antimalarial treatment timecourse on ring-stage P. falciparum parasites | Cultured cells | Plasmodium falciparum | Malaria | Monash University | Peak intensity |
ST001204 | AN002004 | Peroxide antimalarial extended treatment timecourse on trophozoite-stage P. falciparum parasites | Cultured cells | Human | Malaria | Monash University | Peak intensity |
ST001204 | AN002004 | Peroxide antimalarial extended treatment timecourse on trophozoite-stage P. falciparum parasites | Cultured cells | Plasmodium falciparum | Malaria | Monash University | Peak intensity |
ST001205 | AN002006 | Peroxide antimalarial treatment of K13-mutant and -wildtype P. falciparum parasites | Cultured cells | Human | Malaria | Monash University | Peak intensity |
ST001205 | AN002006 | Peroxide antimalarial treatment of K13-mutant and -wildtype P. falciparum parasites | Cultured cells | Plasmodium falciparum | Malaria | Monash University | Peak intensity |
ST001549 | AN002580 | β-Adrenergic regulation of metabolism in macrophages (part-III) | Macrophages | Human | Monash University | Peak intensity | |
ST001692 | AN002762 | Perfluoroalkyl substances and lipid composition in human milk | Breast milk | Human | Environmental exposure | Icahn School of Medicine at Mount Sinai | Peak intensity |
ST002270 | AN003710 | Xenopus tropicalis glycolysis and PPP inhibition | Tail | Western clawed frog | University of Washington | Peak intensity | |
ST002541 | AN004186 | Methionine restriction constrains lipoylation and activates mitochondria for nitrogenic synthesis of amino acids (Part 1) | Yeast cells | Yeast | Life Sciences Institute, ZheJiang University | Peak intensity | |
ST002542 | AN004188 | Methionine restriction constrains lipoylation and activates mitochondria for nitrogenic synthesis of amino acids (Part 2) | Yeast cells | Yeast | Life Sciences Institute, ZheJiang University | Peak intensity | |
ST002872 | AN004708 | Comparative multi-omics analyses of cardiac mitochondrial stress in three mouse models of frataxin deficiency | Heart | Mouse | Cardiomyopathy | Weill Cornell Medicine | Peak intensity |
ST002872 | AN004708 | Comparative multi-omics analyses of cardiac mitochondrial stress in three mouse models of frataxin deficiency | Heart | Mouse | Friedreichs Ataxia | Weill Cornell Medicine | Peak intensity |
ST002068 | AN003370 | Mutant CHCHD10 causes an extensive metabolic rewiring that precedes OXPHOS dysfunction in a murine model of mitochondrial cardiomyopathy | Heart | Mouse | Heart disease | Weill Cornell Medicine | Peak Intensity |
ST002068 | AN003371 | Mutant CHCHD10 causes an extensive metabolic rewiring that precedes OXPHOS dysfunction in a murine model of mitochondrial cardiomyopathy | Heart | Mouse | Heart disease | Weill Cornell Medicine | Peak Intensity |
ST003126 | AN005125 | Effect of high fat diet on heart metabolome of CHCHD10 mutant mice | Heart | Mouse | Cardiomyopathy | Weill Cornell Medicine | Peak Intensity |
ST003128 | AN005128 | Effect of high fat diet on serum lipidome and metabolome in CHCHD10 Mutant Mice | Blood | Mouse | Cardiomyopathy | Weill Cornell Medicine | Peak Intensity |
ST000451 | AN000707 | The alpha-1A adrenergic receptor agonist A61603 reduces cardiac polyunsaturated fatty acid-Heart raw data | Muscle | Mouse | University of North Carolina | Peak values (scaled) | |
ST003313 | AN005425 | Integrative analysis of serum and fecal metabolome and the microbiome that herald Crohn Disease flare - feces | Feces | Human | Inflammatory bowel disease; Crohn disease | Sheba hospital | percentage of metabolites per sample |
ST001135 | AN001860 | Different dose exposure of OPC-163493 on HepG2 cells (part-I) | Hep G2 cells | Human | Diabetes | Otsuka Pharmaceuticals | pmol/1000000 cells |
ST002743 | AN004447 | Metabolomics comparison of lung fibroblasts from Pteropus alecto and Homo sapiens | Cultured cells | Black flying fox fruit bat | Duke-NUS Medical School | pmol/10^6 cells | |
ST002743 | AN004447 | Metabolomics comparison of lung fibroblasts from Pteropus alecto and Homo sapiens | Cultured cells | Human | Duke-NUS Medical School | pmol/10^6 cells | |
ST001745 | AN002838 | Metabolomic profiling of the rat hippocampus across developmental ages and after learning | Brain | Rat | New York University | pmoles/l | |
ST002281 | AN003725 | Metabolite patterns between isogenic normal hiPSCs and Trisomy hiPSC | iPSC cells | Human | Down syndrome | Guangdong provincial people's hospital | pmoles/l |
ST002793 | AN004544 | Interspecies metabolite transfer fuels methionine metabolism of Fusobacterium nucleatum to stimulate volatile methyl mercaptan production | Bacterial cells | Fusobacterium nucleatum | Halitosis | Osaka University | pmol/ODml |
ST002793 | AN004544 | Interspecies metabolite transfer fuels methionine metabolism of Fusobacterium nucleatum to stimulate volatile methyl mercaptan production | Bacterial cells | Fusobacterium nucleatum | Periodontitis | Osaka University | pmol/ODml |
ST001759 | AN002866 | Application of the redox metabolite detection method for mouse liver | Liver | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001760 | AN002867 | Application of the redox metabolite detection method for mouse kidney | Kidney | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001761 | AN002868 | Application of the redox metabolite detection method for mouse biofluids | Cerebrospinal fluid | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001762 | AN002869 | Application of the redox metabolite detection method for mouse kidney (part II) | Kidney | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001763 | AN002870 | Application of the redox metabolite detection method for mouse liver (part II) | Liver | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001764 | AN002871 | Application of the redox metabolite detection method for profiling redox state following pharmacologic perturbation with methotrexate | Cultured cells | Human | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001765 | AN002872 | Optimization of redox metabolite detection in mammalian cells (part I) | Cultured cells | Human | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001766 | AN002873 | Application of the redox metabolite detection method for mammalian tissues (part I) | Kidney | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001766 | AN002873 | Application of the redox metabolite detection method for mammalian tissues (part I) | Liver | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001768 | AN002875 | Application of the redox metabolite detection method for mammalian tissues (part III) | Kidney | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001768 | AN002875 | Application of the redox metabolite detection method for mammalian tissues (part III) | Liver | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001769 | AN002876 | Application of the redox metabolite detection method for profiling redox state following pharmacologic perturbations of redox balance in cells (part I) | Cultured cells | Human | Boston Childrens Hospital | ppm | |
ST001770 | AN002877 | Application of the redox metabolite detection method for profiling redox state following pharmacologic perturbations of redox balance in cells (part II) | Cultured cells | Human | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001771 | AN002878 | Application of the redox metabolite detection method for profiling redox state following pharmacologic perturbations of redox balance in cells (part III) | Cultured cells | Human | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001772 | AN002879 | Optimization of redox metabolite detection in mammalian cells (part II) | Cultured cells | Human | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001773 | AN002880 | Application of the redox metabolite detection method for mouse biofluids (part II) | Blood | Mouse | Boston Children's Hospital, Harvard Medical School | ppm | |
ST001974 | AN003222 | Anti-oxidative metabolism measurement in mammalian cells and tissues by quantitative LC/MS method (I) | Cerebrospinal fluid | Mouse | Cancer | Boston Children's Hospital, Harvard Medical School | ppm |
ST001975 | AN003223 | Anti-oxidative metabolism measurement in mammalian cells and tissues by quantitative LC/MS method (II) | Cerebrospinal fluid | Mouse | Cancer | Boston Children's Hospital, Harvard Medical School | ppm |
ST001976 | AN003224 | Anti-oxidation metabolism measurement in mammalian cells and tissues by quantitative LC/MS method (III) | Cerebrospinal fluid | Mouse | Cancer | Boston Children's Hospital, Harvard Medical School | ppm |
ST001977 | AN003225 | Anti-oxidative metabolism measurement in mammalian cells and tissues by quantitative LC/MS method (IV) | Cerebrospinal fluid | Human | Cancer | Boston Children's Hospital, Harvard Medical School | ppm |
ST001978 | AN003226 | Anti-oxidation metabolism measurement in mammalian cells and tissues by quantitative LC/MS method (V) | Cerebrospinal fluid | Human | Cancer | Boston Children's Hospital, Harvard Medical School | ppm |
ST001979 | AN003228 | Anti-oxidation metabolism measurement in mammalian cells and tissues by quantitative LC/MS method (VI) | Cerebrospinal fluid | Mouse | Cancer | Boston Children's Hospital, Harvard Medical School | ppm |
ST003080 | AN005038 | Metabolome changes in embryonic CSF (Part 2) | CSF | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | ppm |
ST002159 | AN003535 | Chemotaxonomic patterns in intracellular metabolites of marine microbial plankton | Plankton | Marine plankton | University of Washington | presence (1), absence (0), or background level (NA) | |
ST001983 | AN003234 | Metabolomic Fingerprinting of Human High Grade Serous Ovarian Carcinoma Cell Lines | Ovarian cancer cells | Human | Cancer | University of Oklahoma Health Sciences Center | ratio |
ST003495 | AN005735 | Hepatocyte Period 1 dictates oxidative substrate selection independent of the core circadian clock | Liver | Mouse | Washington University in St. Louis | Raw Area | |
ST003132 | AN005139 | Untargeted Metabolomics on Mouse colonic mucosa | Colonic mucosa | Mouse | University College Cork | Raw Peak Area | |
ST003101 | AN005072 | Parallel pheromonal, metabolite, and lipid analyses reveal patterns associated with early life transitions and ovary activation in honey bee (Apis mellifera) queens | Bee heads | Honey bee | Life Sciences Institute, The University of British Columbia | Rel Abundance | |
ST001404 | AN002346 | Ontogeny related changes in the pediatric liver metabolome (part-III) | Liver | Human | Moffitt Cancer Center | Relative Abundance | |
ST001730 | AN002815 | Mitochondrial ATP fuels ABC transporter-mediated drug efflux in cancer chemoresistance | Cultured cells | Human | Cancer | University of Colorado Denver | Relative Abundance |
ST001731 | AN002817 | Mitochondrial ATP fuels ABC transporter-mediated drug efflux in cancer chemoresistance (part-II) | Cultured cells | Human | Cancer | University of Colorado Denver | Relative Abundance |
ST001732 | AN002819 | Mitochondrial ATP fuels ABC transporter-mediated drug efflux in cancer chemoresistance (part-III) | Cultured cells | Human | Cancer | University of Colorado Anschutz Medical Campus | Relative Abundance |
ST002206 | AN003609 | Lipolysis-derived Lipids Determine Autophagy Initiation during Fasting | Worms | C. elegans | Seoul National University | relative area | |
ST001439 | AN002403 | Metabolites in contents of small intestine in wild type and DAOG181R/G181R mice | Intestine | Mouse | KEIO University School of Medicine | relative_area | |
ST000384 | AN000619 | Metabolomic profiles in P. gingivalis cells treated with pABA | Bacterial cells | Porphyromonas | Osaka University Graduate School of Dentistry | Relative Area | |
ST001178 | AN001954 | Metabolomic analysis of C2C12 myoblasts induced by the transcriptional factor FOXO1 | Muscle | Mouse | Kyoto Prefectural University | Relative Area | |
ST001668 | AN002720 | D-Allulose effects on hepatic metabolomics profile in rodents | Liver | Rat | Matsutani Chemical Industry Co., Ltd. | Relative Area | |
ST001684 | AN002751 | An overexpression of lipoprotein lipase leads to an alteration in the skeletal muscle metabolome in transgenic rabbits | Muscle | Rabbit | Saga University | Relative Area | |
ST002584 | AN004256 | Metabolomics analysis of ALDH1L1-expressing HuH7 cell lines. | Cultured cells | Human | Cancer | Tohoku Medical and Pharmaceutical University | Relative Area |
ST002263 | AN003696 | Intermittent fasting induces rapid hepatocyte proliferation to maintain the hepatostat | Liver | Mouse | Stanford University | relative counts | |
ST002106 | AN003444 | Genetic and chemical validation of Plasmodium falciparum aminopeptidase PfA-M17 as a drug target in the hemoglobin digestion pathway (Part 1) | Blood | Plasmodium falciparum | Malaria | Monash University | relative intensity |
ST002107 | AN003446 | Genetic and chemical validation of Plasmodium falciparum aminopeptidase PfA-M17 as a drug target in the hemoglobin digestion pathway (Part 2) | Blood | Plasmodium falciparum | Malaria | Monash University | relative intensity |
ST002108 | AN003448 | Genetic and chemical validation of Plasmodium falciparum aminopeptidase PfA-M17 as a drug target in the hemoglobin digestion pathway (Part 3) | Blood | Plasmodium falciparum | Malaria | Monash University | relative intensity |
ST002309 | AN003771 | Targeting malaria parasites with novel derivatives of azithromycin | Blood | Plasmodium falciparum | Malaria | Monash University | relative intensity |
ST001167 | AN001929 | Comprehensive Profiling by Non-targeted Stable Isotope Tracing Capillary Electrophoresis-Mass Spectrometry | Cultured cells | Human | Cancer | Dalian Institute Of Chemical Physics, Chinese Academy Of Sciences | Relative intensity after normalization |
ST002510 | AN004133 | Strain supernatants: Strain diversity of Eggerthella lenta metabolites in defined media | Bacterial culture supernatant | Eggerthella lenta | University of California, San Francisco | relative ion counts | |
ST002512 | AN004136 | Gnotobiotic mice: Metabolites in intestinal contents of germ-free mice colonized with strains of gut bacterium Eggerthella lenta | Intestine | Mouse | University of California, San Francisco | relative ion counts | |
ST002513 | AN004138 | Gnotobiotic mice: Metabolites in serum of germ-free mice colonized with strains of gut bacterium Eggerthella lenta | Blood | Mouse | University of California, San Francisco | relative ion counts | |
ST002729 | AN004424 | Improved Endurance Capacity of Diabetic Mice during SGLT2 Inhibition: Potential Role of AICARP, an Endogenous AMPK Activator. | Muscle | Mouse | Diabetes | Medical Institute of Bioregulation, Kyushu University | relative peak area |
ST002434 | AN003965 | Metabolomics analysis of heart from CHCHD10S59L/+ KI mice | Heart | Mouse | ALS | INSERM | relative units |
ST001869 | AN003031 | WNK463 Inhibition on Right Ventricular metabolomics | Heart | Rat | Hypertension | University of Minnesota | relative value |
ST001870 | AN003032 | Effects of GP130 Antagonism on Right Ventricular Metabolism in Monocrotaline Rats | Heart | Rat | University of Minnesota | relative value | |
ST001175 | AN001950 | Multi-omics analysis demonstrates unique mode of action of a potent new antimalarial compound, JPC-3210, against Plasmodium falciparum | Plasmodium cells | Plasmodium falciparum | Malaria | Monash University | Signal Intensity |
ST001304 | AN002172 | Multi-omics analysis delineates the distinct functions of sub-cellular acetyl-CoA pools in Toxoplasma gondii | Fibroblast cells | Toxoplasma gondii | Parasitic infection | Monash University | Signal Intensity |
ST001315 | AN002189 | Retargeting azithromycin-like compounds as antimalarials with dual modality | Blood | Plasmodium falciparum | Malaria | Monash University | Signal Intensity |
ST001198 | AN001994 | Targeted LC-MS/MS Analysis of Soluble Metabolites in the MeOH:H2O Phase (part-IV) | Bacterial cells | Synechococcus | Colorado State University | spectral abundance per cell | |
ST002231 | AN003640 | Metabolomics Analysis of HOG-EV and HOG-R132H Cells with and without BAY 2402234 Treatment | Cultured cells | Human | Cancer | UT Southwestern Medical Center | TIC-Corrected Peak Area |
ST003161 | AN005186 | Diet-omics in the Study of Urban and Rural Crohn disease Evolution (SOURCE) cohort | Feces | Human | Inflammatory bowel disease | Sheba hospital | TSS normalized values |
ST002246 | AN003666 | Longitudinal fecal metabolomic profiles from mothers and their infants in the EDIA study | Feces | Human | Broad Institute of MIT and Harvard | Unitless Abundances | |
ST002212 | AN003616 | Human fecal metabolome profiles under 3 different dietary terms | Feces | Human | Keio University | µmol/g | |
ST003267 | AN005352 | FDX2-KO induces global down-regulation of iron-sulfur cluster-containing proteins and senescence-like growth arrest or death in ovarian cancer cells | Cultured cells | Human | Cancer | Tohoku University | μmol/g-protein |