List of Studies ( Metabolite:dUMP)
Study_id | Analysis_id | Study_title | Source | Species | Disease | Institute | Units(range) |
---|---|---|---|---|---|---|---|
ST001680 | AN002738 | Metabolome of NAFLD in high fat diet mouse model | Liver | Mouse | Fatty liver disease | Weill Cornell Medicine | Abundance |
ST001447 | AN002418 | Metabolomics of lung injury after allogeneic hematopoietic cell transplantation - Colon ICMS | Intestine | Mouse | Graft versus host disease | University of Kentucky | abundance & normalized peak area |
ST001453 | AN002428 | Metabolomics of lung injury after allogeneic hematopoietic cell transplantation - Liver ICMS | Liver | Human | Graft versus host disease | University of Kentucky | abundance & normalized peak area |
ST001470 | AN002446 | Metabolomics of lung injury after allogeneic hematopoietic cell transplantation - Lung ICMS | Mouse | Graft versus host disease | University of Kentucky | abundance & normalized peak area | |
ST001472 | AN002448 | Metabolomics of lung injury after allogeneic hematopoietic cell transplantation - Small Intestines ICMS | SI | Mouse | Graft versus host disease | University of Kentucky | abundance & normalized peak area |
ST001712 | AN002787 | Metabolomics analysis of plasma from a mouse model of astrocytoma subjected to radiotherapy | Blood | Mouse | Cancer | National Cancer Institute | 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 |
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 |
ST002179 | AN003569 | 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 |
ST002123 | AN003476 | GCN2 regulates mitochondrial OXPHOS in HSPCs under proliferation conditions. | Bone marrow | Mouse | Sun Yat-sen University | AU | |
ST002250 | AN003676 | Ramadan diurnal intermittent fasting is associated with significant plasma metabolomics changes in overweight and obese subjects: A prospective cohort study | Blood | Human | Obesity | University of Sharjah | AU |
ST002910 | AN004779 | Identifying the impact of RelA overexpression in triple negative breast cancer cells using mass spectroscopy-based proteomics and metabolomics analysis | Cultured cells | Human | Cancer | Sharjah Institute for Medical Research | AU |
ST003026 | AN004961 | Untargeted Metabolomics Reveals Unique Biomolecular Signatures in Overweight and Obesity Using UHPLC-ESI-QTOF-MS Analysis | Blood | Human | Obesity | Sharjah Institute for Medical Research | AU |
ST003039 | AN004986 | A Non-Targeted Metabolomics Comparative Study on Plasma of Pfizer and Sinopharm COVID- 19 Vaccinated individuals, Assessed by (TIMS-QTOF) Mass Spectrometry. | Blood | Human | COVID-19 | Sharjah Institute for Medical Research | AU |
ST003201 | AN005251 | Molecular signatures of xenograft colon cancer models treated with topotecan: A Mass Spectrometry-Based Study | Blood | Mouse | Cancer | Sharjah Institute for Medical Research | AU |
ST002373 | AN003868 | Extracellular metabolome of activated CD8+ T cells | Cultured cells | Mouse | Johns Hopkins University | AUC | |
ST001850 | AN002997 | Unbiased LC-MS-based metabolomics analysis for both whole cell and mitochondria metabolites to gain an insight into the role of Tug1/PGC1 axis on metabolite profiles in podocytes | Epithelial cells | Mouse | University of Texas MD Anderson Cancer Center | AUC/ngDNA | |
ST001074 | AN001756 | Open source discovery of starting points for next generation chemoprotective antimalarial drugs (Biofocus 1) | Parasite | Human | Pennsylvania State University | Average Peak Area | |
ST002121 | AN003473 | Functional metabolic molecule were identified as novel therapeutic targets to facilitate gemcitabine treatment against pancreatic cancer (Tumor tissues metabolomics) | Tissue | Mouse | Cancer | Shanghai Center for Systems Biomedicine, Shanghai Jiaotong University | counts |
ST000041 | AN000063 | High PUFA diet in humans | Blood | 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 | AN000144 | Caloric Restriction vs drugs | Blood | Mouse | University of Michigan | Counts | |
ST000105 | AN000173 | SCOR Metabolomics | Blood | Human | University of Chicago | Counts | |
ST000106 | AN000176 | IWMS Study 1:Weight comparison of obese and lean patients | Blood | Human | Obesity | University of Michigan | Counts |
ST000946 | AN001552 | Untargeted Metabolomics of T1 Participants | Blood | Human | Environmental exposure | University of Michigan | Counts |
ST000946 | AN001553 | Untargeted Metabolomics of T1 Participants | Blood | Human | Environmental exposure | 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) | |
ST002869 | AN004703 | Identifying Biodegradation Pathways of Cetrimonium Bromide (CTAB) Using Metagenome, Metatranscriptome, and Metabolome Tri-omics Integration | Water | Bacteria | Environmental exposure | Arizona State University | counts per second |
ST001897 | AN003078 | A local source of insulin in the eye governed by phagocytosis and starvation | Eye tissue | Mouse | University of Virginia | intensity | |
ST002016 | AN003285 | Metabolomics of COVID patients | Blood | Human | COVID-19 | University of Virginia | intensity |
ST003343 | AN005478 | Proteomic and metabolomic profiling of methicillin resistant versus methicillin sensitive Staphylococcus aureus using a simultaneous extraction protocol | Bacterial cells | Staphylococcus aureus | Bacterial infection | Mohammed Bin Rashid University of Medicine and Health Science | intensity |
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 | |
ST000441 | AN000692 | Metabolomic Profiling of the Malaria Box Reveals Antimalarial Target Pathways | Plasmodium cells | Plasmodium falciparum | Malaria | Pennsylvania State University | log2 fold change vs untreated |
ST001474 | AN004409 | Metabolomics of lung injury after allogeneic hematopoietic cell transplantation - Spleen ICMS | Multiple tissues | Mouse | Graft versus host disease | University of Kentucky | natural abundance corrected and dry residue normalized peak area |
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 |
ST000367 | AN000601 | Distinctly perturbed metabolic networks underlie differential tumor tissue damages induced by immune modulator b-glucan in a two-case ex vivo non-small cell lung cancer study | Lung | Human | Cancer | University of Kentucky | normalized corrected peak area |
ST002009 | AN003275 | Metabolomics analysis of stress erythroid progenitors | Stem cells | Mouse | Inflammation | Pennsylvania State University | Normalized peak area |
ST002361 | AN003855 | UCP2-dependent redox-sensing in POMC neurons regulates feeding | Cultured cells | Mouse | Columbia University | peak area | |
ST002371 | AN003866 | High-resolution metabolomics analysis of NLRP3 inflammasome activated macrophages | Macrophages | Mouse | Inflammation | Wake Forest School of Medicine | peak area |
ST002536 | AN004172 | Effectors enabling adaptation to mitochondrial complex I loss in Hürthle cell carcinoma | Thyroid | Human | Cancer | Broad Institute of MIT and Harvard | peak area |
ST002658 | AN004330 | MoTrPAC: Endurance exercise training study in young adult rats, Rat Kidney Powder - Untargeted Reversed-Phase Positive | Kidney | Rat | University of Michigan | 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 |
ST000009 | AN000024 | Mixed meal tolerance | Human | University of Michigan | Peak area | ||
ST000010 | AN000026 | Lung Cancer Cells 4 | Lung | Human | Cancer | University of Michigan | Peak area |
ST000011 | AN000028 | African Metabolomics | Human | 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 | |
ST000292 | AN000466 | LC-MS Based Approaches to Investigate Metabolomic Differences in the Plasma of Young Women after Drinking Cranberry Juice or Apple Juice | Blood | Human | University of Florida | Peak area | |
ST000692 | AN001069 | 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 | 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 | |
ST000695 | AN001076 | Pilot metabolomics study of aromatase inhibitor associated arthralgias | Blood | Human | Arthralgia | 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 | |
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 | |
ST000725 | AN001136 | Metabolome, body composition, and muscle performance in children | Blood | Human | University of Michigan | Peak area | |
ST000725 | AN001137 | Metabolome, body composition, and muscle performance in children | Blood | 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 |
ST000749 | AN001174 | Rat amniotic fluid metabolomics | Amniotic fluid | Rat | University of Michigan | Peak area | |
ST000750 | AN001176 | Rat amniotic fluid metabolomics (part II) | Amniotic fluid | Rat | University of Michigan | Peak area | |
ST000751 | AN001178 | Mouse placentas-DEHP exposure (part II) | Placenta | Mouse | University of Michigan | Peak area | |
ST000751 | AN001179 | Mouse placentas-DEHP exposure (part II) | Placenta | Mouse | University of Michigan | Peak area | |
ST000756 | AN001186 | Metabolomics of cilia and modulation of renal microcirculation | Blood | Rat | University of Michigan | Peak area | |
ST000758 | AN001190 | Effects of caloric restriction in HCR/LCR rats | Rat | University of Michigan | Peak area | ||
ST000758 | AN001191 | Effects of caloric restriction in HCR/LCR rats | Rat | University of Michigan | Peak area | ||
ST000823 | AN001306 | Metabolic profiling of cyst fluid from patients with Intraductal Pancreatic Mucinous Neoplasm (part II) | Cyst fluid | Human | Cancer | University of Michigan | Peak area |
ST000823 | AN001307 | Metabolic profiling of cyst fluid from patients with Intraductal Pancreatic Mucinous Neoplasm (part II) | Cyst fluid | Human | Cancer | University of Michigan | Peak area |
ST001031 | AN001691 | Metabolome analysis on multi-connected biparental chromosome segment substitution line populations in rice | Plant | Rice | Huazhong Agricultural University | 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 |
ST001441 | AN002408 | Metabolomics of patient-derived fibroblasts | Fibroblast cells | Human | Mitochondrial disease | North Carolina State University | Peak area |
ST001611 | AN002646 | 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 | AN002646 | 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 |
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 | |
ST002505 | AN004127 | 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 |
ST000691 | AN001067 | Metabolomics of diabetic nephropathy | Blood | Human | Diabetes | University of Michigan | Peak area normalized |
ST000691 | AN001067 | Metabolomics of diabetic nephropathy | Blood | Human | Kidney disease | University of Michigan | Peak area normalized |
ST000705 | AN001096 | Slow Aging Mice Plasma Metabolomics | Blood | Mouse | University of Michigan | Peak area normalized | |
ST000721 | AN001128 | Metabolomic Profiles of Recovery from Traumatic Brain Injury | Blood | Human | Trauma | University of Michigan | Peak area normalized |
ST000722 | AN001130 | Metabolomics of Diapause in Aedes albopictus | Eggs | Mosquito | University of Michigan | Peak area normalized | |
ST000726 | AN001139 | Polycystic Ovarian Syndrome(PCOS) metabolomics | Blood | Human | Polycystic ovary syndrome | University of Michigan | Peak area normalized |
ST000744 | AN001163 | Metabolomics of intensive weight management clinic (IWMC) weight loss | Human | Diabetes | University of Michigan | Peak area normalized | |
ST000759 | AN001195 | Age and exercise effect on metabolomics in rats | Rat | University of Michigan | Peak area normalized | ||
ST000763 | AN001201 | Untargeted metabolomics and lipidomics of scleroderma PAH discovery cohort | Blood | Human | Scleroderma | University of Michigan | Peak area normalized |
ST000818 | AN001297 | Integrated nutrigenomic and metabolomic analysis of Africans with variable diet | Blood | Human | Heart disease | University of Michigan | Peak area normalized |
ST001325 | AN002206 | Obesity and Poor Diet as Susceptibility Factors for Secondhand Smoke in Childhood Asthma | Blood | Human | Asthma | University of Michigan | Peak area normalized |
ST001149 | AN001896 | Plasmodium Niemann-Pick Type C1-Related Protein is a Druggable Target Required for Parasite Membrane Homeostasis | Cultured cells | Plasmodium falciparum | Malaria | Pennsylvania State University | Peak Area Post-Blank Subtraction |
ST002926 | AN004799 | Multi-“omics” analysis reveals the orphan P. falciparum protein kinase PfPK8 regulates multi-gene family expression | Blood | Plasmodium falciparum | Malaria | Monash University | 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 |
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 | |
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 |
ST001754 | AN002857 | Metabolomic Analysis of Canine Diabetes (part-II) | Blood | Dog | Diabetes | University of Florida | Peak Height |
ST000356 | AN000583 | GC/MS and LC/MS metabolomics profiling for breast cancer serum data and control serum data | Blood | Human | Cancer | University of Hawaii Cancer Center | Peak intensity |
ST002541 | AN004187 | 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 | AN004189 | 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 | |
ST002281 | AN003725 | Metabolite patterns between isogenic normal hiPSCs and Trisomy hiPSC | iPSC cells | Human | Down syndrome | Guangdong provincial people's hospital | pmoles/l |
ST001008 | AN001650 | Multi-Platform Physiologic and Metabolic Phenotyping Reveals Microbial Toxicity (part II) | Intestine | Mouse | Pennsylvania State University | 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 | |
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 | |
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 | |
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) | |
ST000047 | AN000082 | Identification of altered metabolic pathways in Alzheimer's disease, mild cognitive impairment and cognitively normals using Metabolomics (CSF) | Cerebrospinal fluid | Human | Alzheimers disease | Mayo Clinic | Raw MS Intensities |
ST002584 | AN004255 | Metabolomics analysis of ALDH1L1-expressing HuH7 cell lines. | Cultured cells | Human | Cancer | Tohoku Medical and Pharmaceutical University | relative area |
ST002719 | AN004408 | Comparison of metabolic of A549 cells before and after Gossypol acetate (GAA) treatment | Lung | Human | Cancer | Hangzhou Institute of Medicine (HIM), University of Chinese Academy of Sciences (Zhejiang Cancer Hospital), Chinese Academy of Sciences | relative intensity |
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 |
ST002111 | AN003454 | Metabolomics dataset of optogenetic axon regenerative mouse model post optic nerve crush | Eye tissue | Mouse | Eye disease | University of Miami | µg/mL |