List of Studies ( Metabolite:O-Acetylserine)
Study_id | Analysis_id | Study_title | Source | Species | Disease | Institute | Units(range) |
---|---|---|---|---|---|---|---|
ST001041 | AN001706 | Development of a weaned pig model of enterotoxigenic E.coli-induced environmental enteropathy | Feces | Pig | Texas A&M University | - | |
ST002405 | AN003919 | Stool global metabolite levels in peanut allergy (Part 2) | Feces | Human | Peanut allergy | Icahn School of Medicine at Mount Sinai | Absolute Intensity |
ST001680 | AN002739 | Metabolome of NAFLD in high fat diet mouse model | Liver | Mouse | Fatty liver disease | Weill Cornell Medicine | Abundance |
ST001062 | AN001736 | Arabidopsis Nit1 knockout metabolomics | Plant | Arabidopsis thaliana | University of California, Davis | Arbitrary units | |
ST002831 | AN004624 | Folate depletion upregulates heme synthesis | Cultured cells | Human | Anemia | Boston Children's Hospital, Harvard Medical School | Arbitrary Units |
ST002179 | AN003568 | Impact of nitisinone on the cerebrospinal fluid metabolome of a murine model of alkaptonuria | Cerebrospinal fluid | Mouse | Genetic disease | University of Liverpool Institute of Life Course & Medical Sciences | area |
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 |
ST002760 | AN004486 | 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 | |
ST000450 | AN000705 | Metabolic features of chronic fatigue syndrome | Blood | Human | Myalgic encephalomyelitis/chronic fatigue syndrome | University of California, San Diego | Area under curve |
ST000617 | AN000947 | Validation of the application of targeted metabolomic appraoch in the diagnosis of CFS | Blood | Human | Myalgic encephalomyelitis/chronic fatigue syndrome | University of California, San Diego | Area under 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. |
ST003087 | AN005049 | Metabolome changes in embryonic CSF (Part 9) | CSF | 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. |
ST002123 | AN003476 | GCN2 regulates mitochondrial OXPHOS in HSPCs under proliferation conditions. | Bone marrow | Mouse | Sun Yat-sen University | AU | |
ST003175 | AN005211 | Inactivation of mitochondrial MUL1 E3 ubiquitin ligase inhibits lipogenesis and prevents diet-induced obesity in mice | Liver | Mouse | Obesity; Diabetes; Liver disease | University of Florida | 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. |
ST002373 | AN003868 | Extracellular metabolome of activated CD8+ T cells | Cultured cells | Mouse | Johns Hopkins 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 | |
ST003028 | AN004964 | Chronic stress dampens Lactobacillus johnsonii-mediated tumor suppression to enhance colorectal cancer progression | Colon | Mouse | Cancer | China Pharmaceutical University | count per second (cps) |
ST000044 | AN000069 | Pilot experiment looking for the existence of certain molecules in pancreatic cancer cells | Pancreas | Human | Cancer | University of Michigan | Counts |
ST000979 | AN001603 | Metabolomic profiles in healthy research cats receiving clindamycin with a synbiotic or a placebo: a randomized, controlled trial | Feces | Cat | Antibiotic resistance | University of California, Davis | Counts |
ST000981 | AN001607 | Metabolomic profiles in healthy research cats receiving clindamycin with a synbiotic or a placebo: a randomized, controlled trial (Part II) | Feces | Cat | Antibiotic resistance | University of California, Davis | Counts |
ST001688 | AN002756 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism (part-II) | Bacterial cells | Bacteria | Stanford University | Counts | |
ST003362 | AN005505 | 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 | AN005507 | 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 |
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) | |
ST001688 | AN002757 | A gut microbe-focused metabolomics pipeline enables mechanistic interrogation of microbiome metabolism (part-II) | Bacterial cells | Bacteria | Stanford University | counts (area) | |
ST002201 | AN003604 | Multi-omics profiling of 5 Arabidopsis accessions in response to combined water and nitrogen deficiencies. | Plant | Arabidopsis thaliana | Stress | INRAE | µg/mg FW and arbitrary/mg FW |
ST001980 | AN003230 | Metabolomic profiles in S. mutans, S. gordonii, and S. oralis cells treated with D-tagatose | Bacterial cells | Streptococcus | Osaka University | intensity | |
ST001788 | AN002900 | β-Adrenergic regulation of metabolism in macrophages (part-IV) | Macrophages | Human | Monash University | Intensity | |
ST002010 | AN003276 | Chemoresistant Ovarian Cancer Global Metabolomics | Cultured cells | Human | Cancer | The University of South Australia | Intensity |
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 | |
ST001188 | AN001980 | P. falciparum infected erythrocytes | Cultured cells | Plasmodium falciparum | Malaria | University of Melbourne | ion count |
ST002824 | AN004605 | Leukemia inhibitory factor suppresses hepatic de novo lipogenesis and induces cachexia | Blood | Mouse | Cancer | Rutgers University | Ion counts |
ST002956 | AN004855 | An application of automated LLE extraction in determine the age and HFD effects in adult mice in metabolomic, lipidomic, and proteomic | Blood | Mouse | Calico Life Sciences | Log2(Top Peak Area) | |
ST002419 | AN003940 | Metabolomic changes in growth of E. colik at four timespoints in MOPS rich and minimum medium | Bacterial cells | E. coli | Duke Kunshan University | mmol/L | |
ST002212 | AN003616 | Human fecal metabolome profiles under 3 different dietary terms | Feces | Human | Keio University | µmol/g | |
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 | ||
ST001324 | AN002203 | Metabolomics Adaptation of Juvenile Pacific Abalone Haliotis discus hannai to Heat Stress | Pacific Abalone | Institute of Oceanology, Chinese Academy of Sciences | mV*s | ||
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 | |
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 |
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 | |
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 |
ST003312 | AN005424 | Integrative analysis of serum and fecal metabolome and the microbiome that herald Crohn Disease flare - serum | Blood | Human | Inflammatory bowel disease; Crohn disease | Sheba hospital | normalized metabolite percentage per sample |
ST002132 | AN003487 | Optimization of Imputation Strategies for High-Resolution Gas Chromatography-Mass Spectrometry (HR GC-MS) Metabolomics Data | Blood | Baboon | Wake Forest School of Medicine | Normalized Peak abundances | |
ST002132 | AN003487 | Optimization of Imputation Strategies for High-Resolution Gas Chromatography-Mass Spectrometry (HR GC-MS) Metabolomics Data | Liver | Baboon | Wake Forest School of Medicine | Normalized Peak abundances | |
ST002009 | AN003275 | Metabolomics analysis of stress erythroid progenitors | Stem cells | Mouse | Inflammation | Pennsylvania State University | 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 |
ST002012 | AN003286 | Untargeted primary metabolite profiling in Arabidopsis thaliana | Leaves | Arabidopsis thaliana | Salk Institute for Biological Studies | normalized peak height | |
ST002012 | AN003286 | Untargeted primary metabolite profiling in Arabidopsis thaliana | Roots | Arabidopsis thaliana | Salk Institute for Biological Studies | normalized peak height | |
ST002026 | AN003296 | Metabolomics Analysis of Blood Plasma and Stool from Six Week Flaxseed Dietary Intervention in Postmenopausal Women (Stool/GC) | 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 |
ST001985 | AN003236 | Profiling Plasmodium falciparum parasites and human red blood cells after treatment with MMV693183 | Blood | Human | Malaria | Pennsylvania State University | Peak Abundance (normalized, blank subtracted, and corrected for baseline noise) |
ST001985 | AN003236 | Profiling Plasmodium falciparum parasites and human red blood cells after treatment with MMV693183 | Blood | Plasmodium falciparum | Malaria | Pennsylvania State University | Peak Abundance (normalized, blank subtracted, and corrected for baseline noise) |
ST001985 | AN003236 | Profiling Plasmodium falciparum parasites and human red blood cells after treatment with MMV693183 | Cultured cells | Human | Malaria | Pennsylvania State University | Peak Abundance (normalized, blank subtracted, and corrected for baseline noise) |
ST001985 | AN003236 | Profiling Plasmodium falciparum parasites and human red blood cells after treatment with MMV693183 | Cultured cells | Plasmodium falciparum | Malaria | Pennsylvania State University | Peak Abundance (normalized, blank subtracted, and corrected for baseline noise) |
ST002024 | AN003294 | Plasmodium falciparum stable-isotope carbon labeling to explore metabolic consequences of keto–acid dehydrogenase disruption | Cultured cells | Plasmodium falciparum | Malaria | Pennsylvania State University | Peak Abundance (normalized, blank subtracted, and corrected for baseline noise) |
ST001780 | AN002890 | Comparative analysis of metabolomic profiles in cerebrospinal fluid before and after endurance exercise | Cerebrospinal fluid | Human | UCSD School of Medicine | peak area | |
ST001789 | AN002901 | Acute metabolomic changes of plasma in response to endurance exercise | Blood | Human | University of California, San Diego | peak area | |
ST002007 | AN003270 | Isotope tracing analysis of stress erythroid progenitors | Cultured cells | Mouse | Inflammation | Pennsylvania State University | 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 |
ST002966 | AN004873 | Metabolomics reveal the pathway of benzylisoquinoline alkaloids in Corydalis yanhusuo bulbs | Plant | Plant | Chongqing Academy of Chinese Materia Medica, Chongqing, China | peak area | |
ST000117 | AN000198 | Metabolomics analysis of multiple metabolic functions in the YjgF/YER057c/UK114 (Rid) protein family GC-MS (Part 1) | Bacterial cells | E. coli | University of California, Davis | Peak area | |
ST000117 | AN000198 | Metabolomics analysis of multiple metabolic functions in the YjgF/YER057c/UK114 (Rid) protein family GC-MS (Part 1) | Bacterial cells | Salmonella | University of California, Davis | Peak area | |
ST000118 | AN000199 | Metabolomics analysis of multiple metabolic functions in the YjgF/YER057c/UK114 (Rid) protein family GCMS (part 2) | Bacterial cells | E. coli | University of California, Davis | Peak area | |
ST000118 | AN000199 | Metabolomics analysis of multiple metabolic functions in the YjgF/YER057c/UK114 (Rid) protein family GCMS (part 2) | Bacterial cells | Salmonella | University of California, Davis | Peak area | |
ST000235 | AN000353 | Sprague Dawley rats Nicotine alters brain oxidative metabolism | Brain | Rat | University of Florida | Peak area | |
ST000270 | AN000432 | Metabolomics in AML | Blood | Human | University of Florida | Peak area | |
ST000307 | AN000487 | Targeting CRBN to alter CD8 T cell metabolism | Cells | Mouse | University of Florida | Peak area | |
ST000701 | AN001089 | Differences in metabolism in mouse embryonic fibroblasts (control vs SCF-beta-TrCP knockout) | Cultured cells | Mouse | University of Michigan | Peak area | |
ST000746 | AN001169 | Metabolomics of mice inoculated with human stool | Blood | Mouse | University of Michigan | Peak area | |
ST000746 | AN001170 | Metabolomics of mice inoculated with human stool | Blood | Mouse | University of Michigan | Peak area | |
ST000814 | AN001288 | Hormones & Cognition/Aging/Placebo | Blood | Human | University of Michigan | Peak area | |
ST001071 | AN001753 | Guinea Grass Untargeted Metabolomic Profiling | Plant | Guinea Grass | University of Illinois at Urbana-Champaign (UIUC) | 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 |
ST001262 | AN002095 | The impact of tobacco smoke exposure and environmental exposures on the pulmonary microbiome of critically ill children | Urine | Human | Emory University | Peak area | |
ST001420 | AN002375 | Metabolomic analysis of patients with recurrent angina | Blood | Human | Angina | University of California, San Diego | Peak area |
ST001935 | AN003146 | Metabolomic profiling of spontaneous macaque model for diabetes mellitus | Blood | Macaque monkey | Diabetes | Xiamen University | Peak area |
ST001935 | AN003146 | Metabolomic profiling of spontaneous macaque model for diabetes mellitus | Liver | Macaque monkey | Diabetes | Xiamen University | Peak area |
ST002382 | AN003881 | Deep multi-omic profiling reveals extensive mitochondrial remodeling driven by glycemia in early diabetic kidney disease | Kidney | Rat | Diabetes | The University of Melbourne | Peak area |
ST002772 | AN004512 | Day-night fluctuations in Cerebrospinal fluid metabolomics | Cerebrospinal fluid | Rat | University of Copenhagen | Peak area | |
ST002846 | AN004664 | Apolipoprotein E suppresses hyperlipidemia-driven hematopoiesis & inflammation by controlling mitochondrial metabolism | Macrophages | Mouse | Hyperlipidemia | Northwestern University | 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 |
ST002499 | AN004106 | Metabolomics analysis of stress erythroid progenitors (Part 2) | Stem cells | Mouse | Inflammation | Pennsylvania State University | peak area normalized to IS and cell number |
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 |
ST002104 | AN003439 | Chemoresistant Cancer Cell Lines are Characterized by Migratory, Amino Acid Metabolism, Protein Catabolism and IFN1 Signalling Perturbations | Cultured cells | Human | Cancer | Future Industries Institute | peak height |
ST002412 | AN003932 | Metabolic effects of the protein kinase R | Macrophages | Mouse | Hudson | peak height | |
ST002698 | AN004373 | Systemic host inflammation induces stage-specific transcriptomic modification and slower maturation in malaria parasites | Infected Red Blood Cells | Plasmodium berghei | Malaria | Peter Doherty Institute for Infection and Immunity | peak height |
ST003024 | AN004959 | Identifying and mathematically modeling the time-course of extracellular metabolic markers associated with resistance to ceftolozane/tazobactam in Pseudomonas aeruginosa - Part 1 | Bacterial cells | Bacteria | Monash Institute of Pharmaceutical Sciences | peak height | |
ST000243 | AN000380 | Metabolomic-based investigation on the effects of antifungal agents in Candida albicans | Yeast cells | Candida albicans | University of Florida | Peak height | |
ST000568 | AN000875 | Metabolomic study on a schizophrenia and type 2 diabetes susceptibility gene | Blood | Human | Diabetes | Shanghai Jiao Tong University Affiliated Sixth People’s Hospital | Peak height |
ST000886 | AN001443 | Mechanism Behind Stay Green Trait in Bread Wheat (Triticum aestivum L.) | Plant | Wheat | University of Florida | Peak height | |
ST000919 | AN001506 | Investigating Eicosanoids Implications on the Blood Pressure Response to Thiazide Diuretics | Blood | Human | University of Florida | Peak height | |
ST000954 | AN001564 | Explore Metabolites and Pathways Associated Increased Airway Hyperresponsiveness in Asthma | Blood | Human | Asthma | University of Florida | Peak height |
ST001088 | AN001773 | Physiological and metabolic response of crab megalopae and juveniles to ocean acidification | Muscle | Crab | NOAA NWFSC | 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 |
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 | |
ST003160 | AN005185 | New class of heterospirocyclic compounds present strong and rapid activity against artemisinin- and multidrug-resistant P. falciparum parasites | Plasmodium cells | Plasmodium falciparum | Malaria | Monash University | Peak height |
ST003179 | AN005222 | Property and Activity Refinement of Dihydroquinazolinone-3-carboxamides as Orally Efficacious Antimalarials that Target PfATP4 | Plasmodium cells | Plasmodium falciparum | Malaria | Monash University | Peak height |
ST001754 | AN002857 | Metabolomic Analysis of Canine Diabetes (part-II) | Blood | Dog | Diabetes | University of Florida | Peak Height |
ST001495 | AN002478 | Effects of Synbiotic Administration on Fecal Microbiome and Metabolomic Profiles of Dogs receiving Antibiotics | Feces | Dog | University of California, Davis | Peak height normalized with creatinine | |
ST001633 | AN002669 | Aromatic amino acid metabolism by the anaerobic gut bacterium Clostridium sporogenes (part-II) | Urine | Mouse | Stanford University | Peak height normalized with creatinine | |
ST002556 | AN004211 | Blood metabolomics and impacted cellular mechanisms during transition into lactation in dairy cows that develop metritis | Blood | Cow | Infection | University of Florida | peak heights |
ST002556 | AN004211 | Blood metabolomics and impacted cellular mechanisms during transition into lactation in dairy cows that develop metritis | Blood | Cow | Inflammation | University of Florida | peak heights |
ST002994 | AN004918 | Integrating uterine metabolome and microbiome data to advance the understanding of metritis development in dairy cows | Uterine fluid | Cow | Bacterial infection | University of Florida | peak heights |
ST002493 | AN004085 | Composition of raw plant-based food items Pilot Study | Plant | Plants | Massachusetts Institute of Technology | peak intensity | |
ST000569 | AN000876 | Effect of minimal and complex media on the metabolite profiles | Bacterial cells | Yeast | Graduate school of Korea University | Peak intensity | |
ST001373 | AN002293 | Targeting Sirt2 reprograms T cell metabolism for effective immune response | Spleen | Mouse | Moffitt Cancer Center | Peak intensity | |
ST001382 | AN002303 | Distinct metabolic states of a cell guide alternate fates of mutational buffering through altered proteostasis | Bacterial cells | E. coli | CSIR National Chemical Laboratory | Peak intensity | |
ST001527 | AN002548 | Lung cancer metabolomics analysis | Tumor cells | Human | Cancer | University of Louisville | Peak intensity |
ST001547 | AN002577 | β-Adrenergic regulation of metabolism in macrophages | Macrophages | Human | Monash University | Peak intensity | |
ST001548 | AN002579 | β-Adrenergic regulation of metabolism in macrophages (part-II) | Macrophages | Human | Monash University | Peak intensity | |
ST001549 | AN002580 | β-Adrenergic regulation of metabolism in macrophages (part-III) | Macrophages | Human | Monash University | 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 | |
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 |
ST001299 | AN002163 | Metatranscriptomic Analysis of the Mouse Gut Microbiome Response to the Persistent Organic Pollutant 2,3,7,8-Tetrachlorodibenzofuran | Intestine | Mouse | The Pennsylvania State University (Penn State) | ppm | |
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 | |
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 |
ST002805 | AN004561 | IL-1β-mediated adaptive re-programming of endogenous human cardiac fibroblasts to cells with immune features during fibrotic remodeling | Cultured cells | Human | Pulmonary hypertension | Brown University | Q3 Peak Area (area under curve) |
ST002094 | AN003421 | Commensal intestinal microbiota regulates host luminal proteolytic activity and intestinal barrier integrity through β-glucuronidase activity (Part 1) | Feces | Human | Irritable bowel syndrome | Mayo Clinic | raw intensity |
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) | |
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 |
ST002206 | AN003609 | Lipolysis-derived Lipids Determine Autophagy Initiation during Fasting | Worms | C. elegans | Seoul National University | relative area | |
ST002107 | AN003447 | 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 |
ST003350 | AN005491 | Dissecting the Genetic Basis of UV-B Responsive Metabolites in Rice | Leaves | Rice | Industrial Crops Institute of Hubei Academy of Agricultural Sciences | Relative intensity | |
ST002729 | AN004423 | 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 |
ST001970 | AN003212 | Analytical methodology for a metabolome atlas of goat’s plasma, milk and feces using 1H-NMR and UHPLC-HRMS:MS/milk | Milk | Goat | INSERM | SI | |
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 |
ST002082 | AN003397 | Predicting dying: a study of the metabolic changes and the dying process in patients with lung cancer | Urine | Human | Cancer | University of Liverpool Institute of Life Course & Medical Sciences | Values are raw peak area |