List of Studies ( Metabolite:Methyl nicotinamide)
| Study_id | Analysis_id | Study_title | Source | Species | Disease | Institute | Analysis Type |
|---|---|---|---|---|---|---|---|
| ST004321 | AN007199 | Food intake-independent metabolic alterations in cachectic C26 mice compared to non-cachectic C26 mice | Blood | Mouse | Cancer | Harvard School of Public Health | LC-MS |
| ST004135 | AN006855 | The SLC1A1/EAAT3 Dicarboxylic Amino Acid Transporter is an Epigenetically Dysregulated Nutrient Carrier that Sustains Oncogenic Metabolic Programs | Cultured cells | Human | Cancer | Cleveland Clinic | LC-MS |
| ST004092 | AN006782 | SLC45A4 Knockout cells have lowered GABA production | Cultured cells | Human | Cancer | Rutgers University | LC-MS |
| ST003893 | AN006395 | Respiration defects limit serine synthesis required for lung cancer growth and survival - NSCLC rewires glycolytic metabolism to synthesize more serine from glucose (Tumors) | Tumor tissue | Mouse | Cancer | Rutgers University | LC-MS |
| ST003893 | AN006395 | Respiration defects limit serine synthesis required for lung cancer growth and survival - NSCLC rewires glycolytic metabolism to synthesize more serine from glucose (Tumors) | Tumor tissue | Mouse | Lung cancer | Rutgers University | LC-MS |
| ST003890 | AN006390 | Respiration defects limit serine synthesis required for lung cancer growth and survival - Effect of Polg mutation in NSCLC Tissues_Liver | Liver | Mouse | Cancer | Rutgers University | LC-MS |
| ST003890 | AN006390 | Respiration defects limit serine synthesis required for lung cancer growth and survival - Effect of Polg mutation in NSCLC Tissues_Liver | Liver | Mouse | Lung cancer | Rutgers University | LC-MS |
| ST003887 | AN006384 | Respiration defects limit serine synthesis required for lung cancer growth and survival - Effect of Polg mutation in NSCLC conditioned medium | Culture media | Mouse | Cancer | Rutgers Cancer Institute | LC-MS |
| ST003887 | AN006384 | Respiration defects limit serine synthesis required for lung cancer growth and survival - Effect of Polg mutation in NSCLC conditioned medium | Culture media | Mouse | Lung cancer | Rutgers Cancer Institute | LC-MS |
| ST003886 | AN006382 | Respiration defects limit serine synthesis required for lung cancer growth and survival - Effect of Polg mutation in NSCLC TDCLs | Cultured cells | Mouse | Cancer | Rutgers Cancer Institute | LC-MS |
| ST003886 | AN006382 | Respiration defects limit serine synthesis required for lung cancer growth and survival - Effect of Polg mutation in NSCLC TDCLs | Cultured cells | Mouse | Lung cancer | Rutgers Cancer Institute | LC-MS |
| ST003885 | AN006381 | Respiration defects limit serine synthesis required for lung cancer growth and survival - Effect of Polg mutation in NSCLC tumor derived lines (TDCLs) | Culture media | Mouse | Cancer | Rutgers University | LC-MS |
| ST003885 | AN006381 | Respiration defects limit serine synthesis required for lung cancer growth and survival - Effect of Polg mutation in NSCLC tumor derived lines (TDCLs) | Culture media | Mouse | Lung cancer | Rutgers University | LC-MS |
| ST003884 | AN006379 | Respiration defects limit serine synthesis required for lung cancer growth and survival - Effect of Polg mutation in NSCLC Em tumor derived cell lines (TDCLs) | Tumor cells | Mouse | Cancer | Rutgers Cancer Institute | LC-MS |
| ST003884 | AN006379 | Respiration defects limit serine synthesis required for lung cancer growth and survival - Effect of Polg mutation in NSCLC Em tumor derived cell lines (TDCLs) | Tumor cells | Mouse | Lung cancer | Rutgers Cancer Institute | LC-MS |
| ST003883 | AN006377 | Respiration defects limit serine synthesis required for lung cancer growth and survival - Effect of Polg mutation in NSCLC Tissues | Blood | Mouse | Cancer | Rutgers University | LC-MS |
| ST003883 | AN006377 | Respiration defects limit serine synthesis required for lung cancer growth and survival - Effect of Polg mutation in NSCLC Tissues | Blood | Mouse | Lung cancer | Rutgers University | LC-MS |
| ST003883 | AN006377 | Respiration defects limit serine synthesis required for lung cancer growth and survival - Effect of Polg mutation in NSCLC Tissues | Lung | Mouse | Cancer | Rutgers University | LC-MS |
| ST003883 | AN006377 | Respiration defects limit serine synthesis required for lung cancer growth and survival - Effect of Polg mutation in NSCLC Tissues | Lung | Mouse | Lung cancer | Rutgers University | LC-MS |
| ST003883 | AN006377 | Respiration defects limit serine synthesis required for lung cancer growth and survival - Effect of Polg mutation in NSCLC Tissues | Tumor tissue | Mouse | Cancer | Rutgers University | LC-MS |
| ST003883 | AN006377 | Respiration defects limit serine synthesis required for lung cancer growth and survival - Effect of Polg mutation in NSCLC Tissues | Tumor tissue | Mouse | Lung cancer | Rutgers University | LC-MS |
| ST003846 | AN006321 | Hepatic Coenzyme Q (CoQ) Deficiency Drives Reverse Electron Transport and Disrupts Hepatic Metabolic Homeostasis in Obesity | Liver | Mouse | Obesity | Harvard School of Public Health | LC-MS |
| ST003665 | AN006022 | The effects of cystine limitation stress adaptation (CLSA) on metabolomics changes in pancreatic cancer cells (PANC1) | Cultured cells | Human | Cancer | Pennsylvania State University | LC-MS |
| ST003638 | AN005975 | The effects of cystine limitation stress adaptation (CLSA) on metabolomics changes in pancreatic cancer cells (MiaPaCa-2) | Pancreas | Human | Cancer | Pennsylvania State University | LC-MS |
| 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 | LC-MS |
| ST003264 | AN005348 | SLC25A48 controls mitochondrial choline import and metabolism | Blood | Mouse | Harvard Medical School | LC-MS | |
| ST002936 | AN004815 | O-GlcNAcase activity maintains stress granules for proximity-enhanced ATP production to ensure recovery from stress (Part 2) | Cultured cells | Human | Zhejiang University | LC-MS | |
| ST002906 | AN004769 | Polar metabolite levels in K562 cells following short-term folate depletion | Cultured cells | Human | Anemia | Boston Children's Hospital, Harvard Medical School | LC-MS |
| ST002824 | AN004606 | Leukemia inhibitory factor suppresses hepatic de novo lipogenesis and induces cachexia | Blood | Mouse | Cancer | Rutgers University | LC-MS |
| 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 | Other |
| ST002431 | AN003957 | MS profiling of the Long Term Evolution Experiment | Bacterial cells | Escherichia coli | Rutgers University | LC-MS | |
| ST002374 | AN003869 | Metabolomics analysis of WT vs. GOT1 knockout CD8+ T cells | Cultured cells | Mouse | Johns Hopkins University | LC-MS | |
| ST002373 | AN003868 | Extracellular metabolome of activated CD8+ T cells | Cultured cells | Mouse | Johns Hopkins University | LC-MS | |
| ST002053 | AN003343 | Resistance to NaFAc of in vitro maturated Toxoplasma gondii bradyzoites in human myotubes. | Myotubes | Toxoplasma gondii | Parasitic infection | Robert Koch-Institute | LC-MS |
| ST001908 | AN003105 | Post Acute Myocardial Infarction Left Ventricular Remodeling Bio marker Analysis (PAMILA) | Blood | Human | Heart disease | National University of Singapore | LC-MS |
| ST001309 | AN002178 | Metabolite expression in liver after early life exposure to an endocrine disruptor at 240 days postnatal (part-I) | Liver | Rat | Environmental exposure | Baylor College of Medicine | LC-MS |
| ST000614 | AN000939 | Tobacco-specific carcinogens in Bladder Cancer | Bladder | Human | Cancer | Baylor College of Medicine | LC-MS |
