List of Studies ( Metabolite:Maleamate)
Study_id | Analysis_id | Study_title | Source | Species | Disease | Institute | Units(range) |
---|---|---|---|---|---|---|---|
ST000509 | AN000780 | Metabolic changes to maternal rat liver tissue during and post-pregnancy | Liver | Rat | University of Colorado, Denver | 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 |
ST002759 | AN004479 | 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 | |
ST003087 | AN005048 | Metabolome changes in embryonic CSF (Part 9) | CSF | Mouse | Autism | Boston Children's Hospital, Harvard Medical School | a.u. |
ST002289 | AN003741 | Map of microbially induced metabolic changes across diverse body sites in mice - Bacterial culture data | Bacterial cells | Bacteria | University of Calgary | AUC | |
ST000044 | AN000068 | Pilot experiment looking for the existence of certain molecules in pancreatic cancer cells | Pancreas | Human | Cancer | University of Michigan | Counts |
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) | |
ST001897 | AN003078 | A local source of insulin in the eye governed by phagocytosis and starvation | Eye tissue | Mouse | University of Virginia | intensity | |
ST002797 | AN004551 | Fetal metabolic adaptations to cardiovascular stress in twin-twin transfusion syndrome | Amniotic fluid | Human | Twin-twin transfusion syndrome | University of Texas Health Science Center at Houston | intensity |
ST001788 | AN002900 | β-Adrenergic regulation of metabolism in macrophages (part-IV) | Macrophages | Human | Monash University | Intensity | |
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 | ||
ST002775 | AN004517 | Zebrafish Retina Regeneration Metabolomics - 3 Days Post Crush | Eye tissue | Zebrafish | Eye disease | University of Miami | Normalized Concentrations |
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 | |
ST001747 | AN002843 | Lung metabolomics after ischemic acute kidney injury reveals increased oxidative stress, altered energy production, and ATP depletion | Lung | Mouse | Acute kidney injury | University of Colorado Anschutz Medical Campus | peak area |
ST000010 | AN000025 | Lung Cancer Cells 4 | Lung | Human | Cancer | University of Michigan | Peak area |
ST000164 | AN000257 | Metabolomic analysis of normal and diabetic mouse bone marrow under PBS or metformin treatment | Bone marrow | Mouse | Diabetes | New York 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 | |
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 | |
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 | |
ST000697 | AN001081 | Cytokines correlation with metabolomic profiling of psoriatic and normal skin | Keratinocytes | Human | 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 |
ST001218 | AN002031 | Wild type versus TRACK Mice on regular chow and Vitamin A deprived diet | Kidney | Mouse | Cancer | weill cornell medicine | Peak area |
ST001658 | AN002706 | Control of Topoisomerase II Activity and Chemotherapeutic Inhibition by TCA Cycle Metabolites | Yeast cells | Yeast | Cancer | Johns Hopkins University | 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 |
ST002776 | AN004519 | Zebrafish Optic Nerve Regeneration, Tectum Metabolomics - 3 Days Post Crush | Eye tissue | Zebrafish | Eye disease | University of Miami | Peak Area |
ST001937 | AN003150 | Comprehensive plasma metabolomics and lipidomics based management of benign and malignant solitary pulmonary nodules | Blood | Human | Cancer | China Pharmaceutical University | peak height |
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 |
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 |
ST000403 | AN000643 | Metabolomics-based elucidation of active metabolic pathways in erythrocytes and HSC-derived reticulocytes | Cells | Human | Monash Institute of Pharmaceutical Sciences, Monash University | Peak height | |
ST000539 | AN000819 | Metabolomics-based elucidation of active metabolic pathways in erythrocytes and HSC-derived reticulocytes (part II) | Cells | Human | Monash Institute of Pharmaceutical Sciences, Monash University | Peak height | |
ST000546 | AN000833 | 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 |
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 |
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 |
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 |
ST001547 | AN002576 | β-Adrenergic regulation of metabolism in macrophages | Macrophages | Human | Monash University | Peak intensity | |
ST001549 | AN002581 | β-Adrenergic regulation of metabolism in macrophages (part-III) | Macrophages | Human | Monash University | Peak intensity | |
ST000925 | AN001518 | MuRF1-Related Metabolomic Changes in Stretched and Unloaded HL-1 Cells | Cardiomyocyte cells | Mouse | University of North Carolina | Peak values (Log transformed) | |
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 |
ST002094 | AN003420 | 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 | 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) | |
ST001377 | AN002297 | Stirred suspension bioreactors maintain naïve pluripotency of human pluripotent stem cells (hPSCs) | Stem cells | Human | University of Calgary | relative signal intensity compared to media only | |
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 |
ST002551 | AN004200 | Metabolomics dataset of CNTF induced axon regeneration in mice post optic nerve crush | Eye tissue | Mouse | Eye disease | University of Miami | µg/ml |
ST002551 | AN004201 | Metabolomics dataset of CNTF induced axon regeneration in mice post optic nerve crush | Eye tissue | Mouse | Eye disease | University of Miami | µg/ml |
ST002111 | AN003454 | Metabolomics dataset of optogenetic axon regenerative mouse model post optic nerve crush | Eye tissue | Mouse | Eye disease | University of Miami | µg/mL |