| C56BL6 WT or TRIFKO BMDM stimulated with different TLRs (part-III) (ST001343) |
University of California, Los Angeles |
Mus musculus |
ESI |
576 |
| Timecourse of C56BL6 BMDM stimulated with different TLRs (part-I) (ST001342) |
University of California, Los Angeles |
Mus musculus |
ESI |
864 |
| C56BL6 BMDM stimulated with different TLRs W/O acetylated LDL (part-II) (ST001341) |
University of California, Los Angeles |
Mus musculus |
ESI |
929 |
| Effect of high-fat diet and bile acid treatment on serum and tissue lipidomes in mice (ST001336) |
QIMR Berghofer Medical Research Institute |
Mus musculus |
ESI |
411 |
| Deadly Duality of PEBP1: Shutting off Necroptosis, Turning on Ferroptosis (ST001334) |
University of Pittsburgh |
Mus musculus |
ESI |
30 |
| LCMS lipid and acyl-carnitine analysis (ST001332) |
University of Cambridge |
Caenorhabditis elegans |
ESI |
125 |
| SS-31 and NMN: Two Paths to Improve Metabolism and Function in Aged Hearts (ST001329) |
University of Washington |
Mus musculus |
ESI |
23 |
| Mitochondrial Lipid Profiles in Traumatic Optic Neuropathy (ST001327) |
University of Miami |
Mus musculus |
ESI |
33 |
| Obesity and Poor Diet as Susceptibility Factors for Secondhand Smoke in Childhood Asthma (ST001325) |
University of Michigan |
Homo sapiens |
ESI |
147 |
| Metabolomics Adaptation of Juvenile Pacific Abalone Haliotis discus hannai to Heat Stress (ST001324) |
Institute of Oceanology, Chinese Academy of Sciences |
Haliotis discus hannai |
ESI |
123 |
| Effect of high-fat diet on serum lipidome in mice (ST001323) |
QIMR Berghofer Medical Research Institute |
Mus musculus |
ESI |
270 |
| Maternal adiposity alters the human milk metabolome: a link between non-glucose monosaccharides and infant adiposity (ST001322) |
University of California, Davis |
Homo sapiens |
EI |
35 |
| Dynamics of Exposure, Phthalates, and Asthma in a Randomized Trial (DEPART) (ST001317) |
Icahn School of Medicine at Mount Sinai |
Homo sapiens |
ESI |
46 |
| Retargeting azithromycin-like compounds as antimalarials with dual modality (ST001315) |
Monash University |
Plasmodium falciparum |
ESI |
114 |
| Lipid expression in serum after early life exposure to an endocrine disruptor and a Western Diet at 240 days postnatal (part-IV) (ST001313) |
Baylor College of Medicine |
Rattus norvegicus |
ESI |
204 |
| Lipid expression in serum after early lifer exposure to an endocrine disruptor at 70 days postnatal (part-III) (ST001312) |
Baylor College of Medicine |
Rattus norvegicus |
ESI |
204 |
| Lipid expression in liver after early lifer exposure to an endocrine disruptor at 70 days postnatal (part-II) (ST001311) |
Baylor College of Medicine |
Rattus norvegicus |
ESI |
131 |
| Multi-omics analysis delineates the distinct functions of sub-cellular acetyl-CoA pools in Toxoplasma gondii (ST001304) |
Monash University |
Toxoplasma gondii |
ESI |
202 |
| Luminal metabolome profiles of human microbiota-associated (HMA) mice treated with anti-IL-22 antibody or control antibody (ST001301) |
University of Michigan |
Mus musculus |
ESI |
25 |
| Luminal metabolome profiles ofUC-HMA mice transplanted with a healthy human-derived fecal microbiota (FMT). (ST001300) |
University of Michigan |
Mus musculus |
ESI |
34 |
| Metabolomics of blood plasma and kidney tissue from control (db/m) and diabetic (db/db) mice. (ST001292) |
University of Michigan |
Mus musculus |
ESI |
868 |
| Regulated accumulation of desmosterol integrates macrophage lipid metabolism and inflammatory responses (ST001289) |
LIPID MAPS |
Mus musculus |
Other |
272 |
| Subcellular organelle lipidomics in TLR-4-activated macrophages (ST001288) |
LIPID MAPS |
Mus musculus |
ESI |
228 |
| Lipid composition of isolated lipid droplets from the functional bovine corpus luteum (ST001286) |
University of Nebraska Medical Center |
Bos taurus |
ESI |
363 |
| Nitric Oxide (NO) effect on mitochondrial metabolic rewiring in M1 Macrophages (ST001283) |
National Cancer Institute |
Mus musculus |
EI |
28 |
| Role of Hi1a in mitochondrial metabolic rewiring in M1 Macrophages (ST001282) |
National Cancer Institute |
Mus musculus |
EI |
50 |
| Development and Characterisation of a Novel Class of Aroyl Guanidine Containing Anti-Trypanosomal Compounds (ST001276) |
Monash University |
Trypanosoma brucei brucei |
ESI |
207 |
| Metabolomics-based profiling of the mode of action of Pathogen Box compounds in Trypanosoma brucei (part-II) (ST001275) |
Monash University |
Trypanosoma brucei brucei |
ESI |
339 |
| Metabolomics-based profiling of the mode of action of Pathogen Box compounds in Trypanosoma brucei (part-I) (ST001274) |
Monash University |
Trypanosoma brucei brucei |
ESI |
214 |
| Lipidomics Dataset of Sonication-Induced Traumatic Optic Neuropathy in Mice (ST001273) |
University of Miami |
Mus musculus |
ESI |
108 |
| Growth cone memebrane and growth cone particulate lipidomics (ST001272) |
University of Miami |
Mus musculus |
ESI |
940 |
| Exosomal lipids for classifying early and late stage non-small cell lung cancer (ST001269) |
University of Kentucky |
Homo sapiens |
ESI |
482 |
| Mass spectrometry-based lipidomics of oral squamous cell carcinoma tissue reveals aberrant cholesterol and glycerophospholipid metabolism (ST001267) |
University of Helsinki |
Homo sapiens |
ESI |
1370 |
| Comparative metabolomics of MCF-7 breast cancer cells using different extraction solvents assessed by mass spectroscopy (ST001265) |
Sharjah Institute for Medical Research |
Homo sapiens |
EI |
24 |
| Targeted Metabolomic Analysis in Patients with Wilson Disease Reveals Dysregulated Choline, Methionine and Aromatic Amino Acid Metabolism: Implications for Hepatic and Neurological Phenotypes (ST001259) |
University of California, Davis |
Homo sapiens |
ESI |
63 |
| Phenotyping Mouse blood metabolites in day and night in type 2 diabetes (ST001253) |
Indiana University School of Medicine |
Mus musculus |
ESI |
336 |
| Eicosanoid profiles of dermal fibroblasts (part-I) (ST001252) |
University of South Florida |
Mus musculus |
MALDI |
21 |
| The effects of a training program encompassing cold exposure, breathing exercises, and meditation on plasma metabomics during experimental human endotoxemia (ST001251) |
Radboud University Medical Centre |
Homo sapiens |
ESI |
90 |
| Luminal metabolome profiles of mice developed dextran sulfate sodium (DSS) colitis (ST001250) |
University of Michigan |
Mus musculus |
ESI |
30 |
| TFPa/HADHA is required for fatty acid beta-oxidation and cardiolipin re-modeling in human cardiomyocytes (part-I) (ST001246) |
University of California, Davis |
Homo sapiens |
ESI |
166 |
| Luteal lipids regulate progesterone production and may modulate immune cell function during the estrous cycle and pregnancy (ST001245) |
University of California, Davis |
Bos taurus |
ESI |
70 |
| Global Metabolic Analysis Trisomy 21 - Cohort 3, CSF (ST001242) |
University of Colorado Denver |
Homo sapiens |
ESI |
26 |
| Global Metabolic Analysis Trisomy 21 - Cohort 3, Plasma (ST001241) |
University of Colorado Denver |
Homo sapiens |
ESI |
50 |
| Global Metabolic Analysis Trisomy 21 - Cohort 2 (ST001240) |
University of Colorado Denver |
Homo sapiens |
ESI |
40 |
| Metabolic responses to PD1 immune-checkpoint blockade and association with therapeutic benefits - Part III (ST001237) |
Broad Institute of MIT and Harvard |
Homo sapiens |
ESI |
89 |
| Metabolic responses to PD1 immune-checkpoint blockade and association with therapeutic benefits - Part II (ST001236) |
Broad Institute of MIT and Harvard |
Homo sapiens |
ESI |
89 |
| Metabolic responses to PD1 immune-checkpoint blockade and association with therapeutic benefits - Part I (ST001235) |
Broad Institute of MIT and Harvard |
Homo sapiens |
ESI |
32 |
| The effect of weaning stress, sex and temperament on fecal microbiota and metabolites in Brahman calves. (ST001234) |
Texas A&M University |
Bos indicus |
EI |
29 |
| Aquamin and Prevention of Colon Cancer (part-V) (ST001229) |
University of Michigan |
Homo sapiens |
ESI |
20 |
| Vaginal swab lipidome profiles at 48 h reflect the fat composition of neonatal diet during first two days postnatal (ST001224) |
Purdue University |
Sus scrofa |
ESI |
32 |