List of Studies ( Metabolite:Ophthalmic acid)
Study_id | Analysis_id | Study_title | Source | Species | Disease | Institute | Units(range) |
---|---|---|---|---|---|---|---|
ST002971 | AN004880 | Untargeted metabolomics of bioluminescent cell at T24h | Bacterial cells | Bacteria | Vidyasirimedhi Institute of Science and Technology | abundance | |
ST001680 | AN002739 | Metabolome of NAFLD in high fat diet mouse model | Liver | Mouse | Fatty liver disease | Weill Cornell Medicine | Abundance |
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 | |
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 |
ST002759 | AN004479 | Metabolic responses of normal rat kidneys to a high salt intake (Kidney cortex) | Kidney cortex | Rat | Medical College of Wisconsin | Area | |
ST002759 | AN004480 | Metabolic responses of normal rat kidneys to a high salt intake (Kidney cortex) | Kidney cortex | Rat | Medical College of Wisconsin | Area | |
ST002760 | AN004483 | Metabolic responses of normal rat kidneys to a high salt intake (Kidney outer medulla) | Kidney outer medulla | Rat | Medical College of Wisconsin | Area | |
ST002760 | AN004484 | Metabolic responses of normal rat kidneys to a high salt intake (Kidney outer medulla) | Kidney outer medulla | Rat | Medical College of Wisconsin | Area | |
ST002761 | AN004487 | Metabolic responses of normal rat kidneys to a high salt intake (Urine) | Urine | Rat | Medical College of Wisconsin | Area | |
ST003066 | AN005022 | Heritability of RBC metabolites: baseline correlation of metabolites and markers of RBC health and stability | Erythrocytes | Human | University of Iowa | area under curve | |
ST001143 | AN001882 | Microbial depletion and ozone exposure - Lung tissue (part I) | Lung | Mouse | Asthma | Harvard School of Public Health | Area under curve |
ST001144 | AN001886 | Microbial depletion and ozone exposure - serum (part II) | Blood | Mouse | Asthma | Harvard School of Public Health | Area under curve |
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. |
ST003088 | AN005051 | Metabolome changes in embryonic CSF (Part 10) | Blood | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST003088 | AN005051 | Metabolome changes in embryonic CSF (Part 10) | CSF | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST003088 | AN005051 | Metabolome changes in embryonic CSF (Part 10) | Liver | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST001153 | AN001903 | Erythrocyte adenosine A2B receptor-mediated AMPK activation: Counteracting CKD by promoting oxygen delivery | Blood | Mouse | Kidney disease | University of Texas Health Science Center McGovern Medical School | AU |
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. |
ST002287 | AN003739 | Enhanced systemic commensal E. coli immunogenicity through minor alteration of the metabolic profile | Bacterial cells | E. coli | University of Calgary | AUC | |
ST002465 | AN004021 | Map of microbially induced metabolic changes across diverse body sites in mice - Mouse Data | Blood | Mouse | University of Calgary | AUC | |
ST002465 | AN004021 | Map of microbially induced metabolic changes across diverse body sites in mice - Mouse Data | Intestine | Mouse | University of Calgary | AUC | |
ST002465 | AN004021 | Map of microbially induced metabolic changes across diverse body sites in mice - Mouse Data | Liver | Mouse | University of Calgary | AUC | |
ST002465 | AN004021 | Map of microbially induced metabolic changes across diverse body sites in mice - Mouse Data | Peritoneal fluid | Mouse | University of Calgary | AUC | |
ST002465 | AN004021 | Map of microbially induced metabolic changes across diverse body sites in mice - Mouse Data | Spleen | Mouse | University of Calgary | AUC | |
ST002465 | AN004021 | Map of microbially induced metabolic changes across diverse body sites in mice - Mouse Data | Urine | Mouse | University of Calgary | 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 |
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 | |
ST000042 | AN000065 | BALF Control vs ALI by RPLC-MS | Lung | 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 |
ST000044 | AN000069 | 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 | |
ST000105 | AN000174 | 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 |
ST000106 | AN000176 | IWMS Study 1:Weight comparison of obese and lean patients | Blood | Human | Obesity | University of Michigan | Counts |
ST000841 | AN001350 | Metabolomics of muscle in insulin sensitive and resistant obese indivduals. | Muscle | Human | Obesity | University of Michigan | Counts |
ST000842 | AN001357 | Muscle and plasma before and after exercise | Blood | Human | Obesity | University of Michigan | Counts |
ST001688 | AN002756 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism (part-II) | Bacterial cells | Bacteria | Stanford University | Counts | |
ST001671 | AN002727 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism | Bacterial cells | Bacteria | Stanford University | counts (area) | |
ST001671 | AN002728 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism | Bacterial cells | Bacteria | Stanford University | counts (area) | |
ST001671 | AN002729 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism | Bacterial cells | Bacteria | Stanford University | counts (area) | |
ST001688 | AN002757 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism (part-II) | Bacterial cells | Bacteria | Stanford University | counts (area) | |
ST001688 | AN002758 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism (part-II) | Bacterial cells | Bacteria | Stanford University | counts (area) | |
ST000508 | AN000778 | Metabolic Profiling of Date Palm Fruits | Plant | Date palm | Weill Cornell Medicine in Qatar | Counts per second | |
ST000867 | AN001396 | Metabolic Profiling of Date Palm Fruits (part II) | Date palm fruit | Date palm | Weill Cornell Medicine in Qatar | Counts per second | |
ST001402 | AN002344 | Ontogeny related changes in the pediatric liver metabolome | Liver | Human | Moffitt Cancer Center | estimated abundances | |
ST002539 | AN004181 | 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) |
ST002555 | AN004207 | Ethnicity-Specific Differences in Ovarian Cancer Metabolic Signatures | Cultured cells | Human | Cancer | University of Oklahoma Health Sciences Center | Fold change over standard |
ST002016 | AN003284 | Metabolomics of COVID patients | Blood | Human | COVID-19 | University of Virginia | intensity |
ST001788 | AN002899 | β-Adrenergic regulation of metabolism in macrophages (part-IV) | Macrophages | Human | Monash University | Intensity | |
ST002459 | AN004011 | 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 | |
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 | AN004450 | Biomolecular condensates create phospholipid-enriched microenvironments (Part 4) | Liver | Mouse | Cornell University | Ion abundance | |
ST002751 | AN004464 | Biomolecular condensates create phospholipid-enriched microenvironments (Part 5) | Liver | Mouse | Cornell University | Ion abundance (peak area) | |
ST001775 | AN002882 | Plasma metabolomics of diverse mouse strains infected with Plasmodium chabaudi | Blood | Mouse | Malaria | Stanford University | ion counts |
ST002349 | AN004096 | Biomolecular condensates create phospholipid-enriched microenvironments (Part 1) | Liver | Mouse | Cornell University | Ion counts | |
ST002352 | AN004098 | Biomolecular condensates create phospholipid-enriched microenvironments (Part 2) | Liver | Mouse | Cornell University | Ion counts | |
ST002822 | AN004599 | Effect of ERR Agonist in Mouse Heart Post Pressure Overload | Heart | Mouse | Baylor College of Medicine | log transformed data | |
ST002212 | AN003616 | Human fecal metabolome profiles under 3 different dietary terms | Feces | Human | Keio University | µmol/g | |
ST002477 | AN004046 | Neutrophil metabolomics in COVID-19 | Neutrophils | Human | COVID-19 | UT Southwestern Medical Center | MS reading |
ST003349 | AN005485 | An integrated LC-MS analysis of the biometric characteristics of different time cohorts of race walkers - targeted | Blood | Human | The First Affiliated Hospital of Dalian Medical University | ng/mL | |
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 | |
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 |
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 |
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 |
ST002775 | AN004518 | Zebrafish Retina Regeneration Metabolomics - 3 Days Post Crush | Eye tissue | Zebrafish | Eye disease | University of Miami | Normalized Concentrations |
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 | |
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 |
ST001865 | AN003024 | Systemic metabolite changes due to Hypoxia | Blood | Mouse | Northwestern University | Peak | |
ST001866 | AN003027 | Systemic metabolite changes due to PHD inhibition | Blood | Mouse | Northwestern University | Peak | |
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 | |
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 | |
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 |
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 |
ST002242 | AN003660 | Hypoxia promotes osteogenesis via regulating the acetyl-CoA-mediated mito-nuclear communication. | Cultured cells | Mouse | CECAD Research Center | peak area | |
ST002361 | AN003855 | UCP2-dependent redox-sensing in POMC neurons regulates feeding | Cultured cells | Mouse | Columbia University | peak area | |
ST002361 | AN003856 | UCP2-dependent redox-sensing in POMC neurons regulates feeding | Cultured cells | Mouse | Columbia University | 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 |
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 | |
ST000040 | AN000060 | Heatshock response of C. elegans using IROA (I) | Worms | C. elegans | University of Florida | Peak area | |
ST000040 | AN000061 | Heatshock response of C. elegans using IROA (I) | Worms | C. elegans | University of Florida | 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 |
ST000260 | AN000413 | Analysis of DJ-1 Knockout Mouse Brains | Brain | Mouse | National Insitute on Aging | Peak area | |
ST000335 | AN000541 | Metabolomics of bovine uterine fluid at the onset of conceptus elongation | Uterus | Cow | University of Florida | Peak area | |
ST000689 | AN001063 | Influence of Noxa knockdown on cell metabolism | Cultured cells | Human | University of Michigan | Peak area | |
ST000689 | AN001064 | Influence of Noxa knockdown on cell metabolism | Cultured cells | Human | University of Michigan | Peak area | |
ST000692 | AN001069 | Metabolites produced by strains associated with inflammation | Bacterial cells | Treponema | Inflammation | University of Michigan | Peak area |
ST000692 | AN001070 | Metabolites produced by strains associated with inflammation | Bacterial cells | Treponema | Inflammation | University of Michigan | Peak area |
ST000693 | AN001071 | 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 | |
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 | AN001073 | Differences in bile acids composition between ASCL5 knockout and floxed mice. | Intestine | Mouse | 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 | AN001079 | Brain-Immune system-Gut Interaction in Chronic Mild Stress (CMS +/- Lacto) | Mouse | Stress | 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 | AN001081 | Cytokines correlation with metabolomic profiling of psoriatic and normal skin | Keratinocytes | Human | University of Michigan | Peak area | |
ST000697 | AN001082 | Cytokines correlation with metabolomic profiling of psoriatic and normal skin | Keratinocytes | Human | University of Michigan | Peak area | |
ST000724 | AN001134 | Red squirrels age related changes | Blood | Squirrel | University of Michigan | Peak area | |
ST000724 | AN001135 | Red squirrels age related changes | Blood | Squirrel | University of Michigan | Peak area | |
ST000741 | AN001155 | Metabolite-phenotype link in X-linked Adrenoleukodystrophy (fibroblast cell culture) | Cultured cells | Human | Adrenoleukodystrophy | 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 |
ST000745 | AN001167 | Metabolomics of mice inoculated with human microbiota | Blood | Mouse | University of Michigan | Peak area | |
ST000745 | AN001168 | Metabolomics of mice inoculated with human microbiota | Blood | Mouse | University of Michigan | Peak area | |
ST000746 | AN001170 | Metabolomics of mice inoculated with human stool | Blood | Mouse | University of Michigan | Peak area | |
ST000748 | AN001172 | 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 | |
ST000756 | AN001187 | Metabolomics of cilia and modulation of renal microcirculation | Blood | Rat | University of Michigan | Peak area | |
ST000758 | AN001191 | Effects of caloric restriction in HCR/LCR rats | Rat | University of Michigan | Peak area | ||
ST000775 | AN001223 | Michigan Biomarkers for Refractory Depression (Bluebird) metabolomics pilot study | Blood | Human | Depression | University of Michigan | Peak area |
ST001157 | AN001915 | The gut microbiota plays a central role to modulate the plasma metabolome in response to chronic Angiotensin II infusion (part-I) | Blood | Mouse | Johns Hopkins University School of Medicine | Peak area | |
ST001218 | AN002031 | Wild type versus TRACK Mice on regular chow and Vitamin A deprived diet | Kidney | Mouse | Cancer | weill cornell medicine | Peak area |
ST001335 | AN002224 | Air Pollution, Placenta Function, and Birth Outcomes in Los Angeles in the Placental Assessment in Response to ENvironmenTal pollution study (PARENTs) cohort | Blood | Human | Environmental exposure | Emory University | 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 | |
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 |
ST003031 | AN004968 | Early time-restricted eating improves markers of cardiometabolic health but has no impact on nutrient absorption in healthy adults | Blood | Human | California Polytechnic State University, San Luis Obispo | 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 | |
ST002754 | AN004468 | Metabolomics analysis of maternal obesity model | Blood | Mouse | Fatty liver disease | University of Bonn | Peak Area |
ST002776 | AN004520 | Zebrafish Optic Nerve Regeneration, Tectum Metabolomics - 3 Days Post Crush | Eye tissue | Zebrafish | Eye disease | University of Miami | 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 |
ST002984 | AN004903 | 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 | AN001083 | Metabolomics analysis of Sirt5 knockdown (KD) melanoma | Human | University of Michigan | Peak area normalized | ||
ST000698 | AN001084 | Metabolomics analysis of Sirt5 knockdown (KD) melanoma | Human | University of Michigan | Peak area normalized | ||
ST000722 | AN001129 | Metabolomics of Diapause in Aedes albopictus | Eggs | Mosquito | University of Michigan | Peak area normalized | |
ST000742 | AN001157 | Metabolite-phenotype link in X-linked Adrenoleukodystrophy (part II) | Brain | Human | Adrenoleukodystrophy | University of Michigan | Peak area normalized |
ST002066 | AN003365 | 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 |
ST002412 | AN003931 | Metabolic effects of the protein kinase R | Macrophages | Mouse | Hudson | peak height | |
ST002792 | AN004542 | Chemoproteomics validates selective targeting of Plasmodium M1 alanyl aminopeptidase as a cross-species strategy to treat malaria | Blood | Plasmodium falciparum | Malaria | Monash University | peak height |
ST003036 | AN004978 | Identifying and mathematically modeling the time-course of extracellular metabolic markers associated with resistance to ceftolozane/tazobactam in Pseudomonas aeruginosa - Part 2 | Bacterial cells | Pseudomonas aeruginosa | Bacterial infection | Monash Institute of Pharmaceutical Sciences | 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 |
ST003053 | AN005007 | Providing insight into the mechanism of action of Cationic Lipidated Oligomers (CLOs) using metabolomics | Bacterial cells | Staphylococcus aureus | Bacterial infection | Monash University | peak height |
ST003144 | AN005159 | On-target, dual aminopeptidase inhibition provides cross-species antimalarial activity | Blood | Plasmodium falciparum | Malaria | Monash University | peak height |
ST000352 | AN000572 | Metabolic profiling reveals biochemical pathways and potential biomarkers associated with the pathogenesis of Krabbe disease | Brain | Mouse | Krabbe disease | University at Buffalo | 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 |
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 | |
ST002832 | AN004626 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Bacteroides fragilis | Stanford University | Peak height | |
ST002832 | AN004626 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Bacteroides thetaiotaomicron | Stanford University | Peak height | |
ST002832 | AN004626 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Bacteroides uniformis | Stanford University | Peak height | |
ST002832 | AN004626 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Blautia producta | Stanford University | Peak height | |
ST002832 | AN004626 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Clostridium clostridioforme | Stanford University | Peak height | |
ST002832 | AN004626 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Clostridium hathewayi | Stanford University | Peak height | |
ST002832 | AN004626 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Clostridium hylemonae | Stanford University | Peak height | |
ST002832 | AN004626 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Clostridium scindens | Stanford University | Peak height | |
ST002832 | AN004626 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Clostridium symbiosum | Stanford University | Peak height | |
ST002832 | AN004626 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Enterococcus faecalis | Stanford University | Peak height | |
ST002832 | AN004626 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Enterococcus faecium | Stanford University | Peak height | |
ST002832 | AN004626 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Enterococcus hirae | Stanford University | Peak height | |
ST002832 | AN004626 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Escherichia fergusonii | Stanford University | Peak height | |
ST002832 | AN004626 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Flavonifractor plautii | Stanford University | Peak height | |
ST002832 | AN004626 | Resource competition predicts assembly of in vitro gut bacterial communities- HILIC | Bacterial cells | Parabacteroides distasonis | Stanford University | Peak height | |
ST003179 | AN005221 | Property and Activity Refinement of Dihydroquinazolinone-3-carboxamides as Orally Efficacious Antimalarials that Target PfATP4 | Plasmodium cells | Plasmodium falciparum | Malaria | Monash University | Peak height |
ST001048 | AN001716 | Pediatric Inner-City Environmental Exposures at School and Home and Asthma Study | Urine | Human | Asthma | Icahn School of Medicine at Mount Sinai | Peak intensity |
ST001201 | AN001998 | Peroxide antimalarial treatment timecourse on trophozoite-stage P. falciparum parasites | Cultured cells | Human | Malaria | Monash University | Peak intensity |
ST001201 | AN001998 | 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 |
ST001373 | AN002293 | Targeting Sirt2 reprograms T cell metabolism for effective immune response | Spleen | Mouse | Moffitt Cancer Center | Peak intensity | |
ST001547 | AN002576 | β-Adrenergic regulation of metabolism in macrophages | Macrophages | Human | Monash University | 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) | |
ST000452 | AN000708 | The alpha-1A adrenergic receptor agonist A61603 reduces cardiac polyunsaturated fatty acid-Serum raw data | Blood | 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 |
ST001745 | AN002838 | Metabolomic profiling of the rat hippocampus across developmental ages and after learning | Brain | Rat | New York University | pmoles/l | |
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 |
ST001835 | AN002977 | Use of Integrated Metabolomics, Transcriptomics, and Signal Protein Profile to Characterize the Effector Function and Associated Metabotype of Polarized Macrophage Phenotypes | Blood | Human | Idaho Veterans Research and Education Foundation | raw area count | |
ST001683 | AN002747 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism. | Blood | Mouse | Stanford University | Raw ion count (peak area) | |
ST001683 | AN002747 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism. | Feces | Mouse | Stanford University | Raw ion count (peak area) | |
ST001683 | AN002747 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism. | Intestine | Mouse | Stanford University | Raw ion count (peak area) | |
ST001683 | AN002747 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism. | Urine | Mouse | Stanford University | Raw ion count (peak area) | |
ST001683 | AN002748 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism. | Blood | Mouse | Stanford University | Raw ion count (peak area) | |
ST001683 | AN002748 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism. | Feces | Mouse | Stanford University | Raw ion count (peak area) | |
ST001683 | AN002748 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism. | Intestine | Mouse | Stanford University | Raw ion count (peak area) | |
ST001683 | AN002748 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism. | Urine | Mouse | Stanford University | Raw ion count (peak area) | |
ST001683 | AN002749 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism. | Blood | Mouse | Stanford University | Raw ion count (peak area) | |
ST001683 | AN002749 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism. | Feces | Mouse | Stanford University | Raw ion count (peak area) | |
ST001683 | AN002749 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism. | Intestine | Mouse | Stanford University | Raw ion count (peak area) | |
ST001683 | AN002749 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism. | Urine | Mouse | Stanford University | Raw ion count (peak area) | |
ST003132 | AN005139 | Untargeted Metabolomics on Mouse colonic mucosa | Colonic mucosa | Mouse | University College Cork | Raw Peak Area | |
ST003281 | AN005375 | Phosphate availability conditions caspofungin tolerance, capsule attachment and titan cell formation in Cryptococcus neoformans | Fungal cells | Cryptococcus neoformans | Meningoencephalitis | 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 | |
ST002837 | AN004637 | Bacterial tryptophan metabolites increased by prebiotic galactooligosaccharide reduce microglial reactivity and are associated with lower anxiety-like behavior (Blood) | Blood | Mouse | Anxiety | National Center for Advancing Translational Sciences | 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 | |
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 | |
ST002584 | AN004256 | Metabolomics analysis of ALDH1L1-expressing HuH7 cell lines. | Cultured cells | Human | Cancer | Tohoku Medical and Pharmaceutical University | Relative Area |
ST003298 | AN005402 | Annual changes on metabolomics profile in latex | Latex | Plant | Sumitomo Riko Co., Ltd. | Relative Area | |
ST002263 | AN003696 | Intermittent fasting induces rapid hepatocyte proliferation to maintain the hepatostat | Liver | Mouse | Stanford University | relative counts | |
ST002263 | AN003697 | Intermittent fasting induces rapid hepatocyte proliferation to maintain the hepatostat | Liver | Mouse | Stanford University | relative counts | |
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 |
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 | |
ST002513 | AN004139 | 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 | |
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 | |
ST002231 | AN003641 | 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 |
ST000815 | AN001291 | db/db WT ozone and air exposed mice | Lung | Mouse | Ozone Stress | Harvard School of Public Health | total ion counts |
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 |
ST002171 | AN003557 | Serum metabolome of specific-pathogen-free mice fed with five distinct rodent diets with varying fiber content and source. | Blood | Mouse | Luxembourg Institute of Health | uM | |
ST000093 | AN000148 | Metabolomics Analysis of Frontal Fibrosing Alopecia | Scalp | Human | Alopecia | Case Western Reserve University | Unspecified |
ST001253 | AN002081 | Phenotyping Mouse blood metabolites in day and night in type 2 diabetes | Blood | Mouse | Diabetes | Indiana University School of Medicine | VolNormImp Area counts |