Studies involving sample source:Culture media
| Study ID | Study Title | Species | Institute |
|---|---|---|---|
| ST002473 | Linking bacterial metabolites to disease-associated microbes to uncover mechanisms of host-microbial interactions in intestinal inflammation. Veillonella parvula media profiling of IBD drug metabolites | Veillonella parvula | Broad Institute of MIT and Harvard |
| ST003119 | Bleach protects algal crops from novel pathogen but increases stress tolerance traits and virulence factors within the associated bacterial microbiome | Algae | National Renewable Energy Lab |
| ST003332 | Increased Cholesterol Synthesis Drives Neurotoxicity in Patient Stem Cell-Derived Model of Multiple Sclerosis - media metabolomics | Human | University of Colorado Denver |
| ST003485 | Tryptophan metabolite profiling of cell supernatants (culture media) from TNBC cell lines with either overexpression or stable knockdown of TDO2. | Human | University of Colorado Anschutz Medical Campus |
| ST003486 | Tryptophan metabolite profiling of cell supernatants (culture media) from TNBC cell line BT549 grown in suspension with TDO inhibition. | Human | University of Colorado Anschutz Medical Campus |
| ST003488 | Tryptophan metabolite profiling of cell supernatants (culture media) from TNBC cell line BT549 grown in suspension with TDO2 knockdown and IDO1 compensation. | Human | University of Colorado Anschutz Medical Campus |
| ST003489 | Tryptophan pathway profiling of culture media from TNBC cell line MDA-MB-231 +/- inhibitors of the TDO/IDO pathway. | Human | University of Colorado Anschutz Medical Campus |
| ST003490 | Metabolomics of culture media from TNBC cell line MDA-MB-453 +/- TDO2/IDO1 dual inhibition | Human | University of Colorado Anschutz Medical Campus |
| ST003491 | Tryptophan/indole profiling of culture media from TNBC cell line SUM159PT with stable TDO2 overexpression. | Human | University of Colorado Anschutz Medical Campus |
| ST003570 | Hepatocytes transform fructose into polar metabolites that are selectively utilized by cancer cells | Human | Washington University in St. Louis |
| ST003570 | Hepatocytes transform fructose into polar metabolites that are selectively utilized by cancer cells | Mouse | Washington University in St. Louis |
| ST003571 | Hepatocytes transform fructose into lipids that can metabolized by cancer cells | Human | Washington University in St. Louis |
| ST003571 | Hepatocytes transform fructose into lipids that can metabolized by cancer cells | Mouse | Washington University in St. Louis |
| ST003830 | Overcoming resistance to immunotherapy by targeting CD38 in human tumor explants - Extracellular metabolomics of B7.H3 human CAR-T cells | Human | Massachusetts General Hospital |
| ST003885 | Respiration defects limit serine synthesis required for lung cancer growth and survival - Effect of Polg mutation in NSCLC tumor derived lines (TDCLs) | Mouse | Rutgers University |
| ST003887 | Respiration defects limit serine synthesis required for lung cancer growth and survival - Effect of Polg mutation in NSCLC conditioned medium | Mouse | Rutgers Cancer Institute |
| ST003925 | Assessing the impact of SLC7A11 silencing on oxidative stress in amoeboid disseminating cancer cells | Human | The Institute of Cancer Research London |
| ST004259 | Phytate enhances gut Parasutterella colonization to alleviate radiation injury via anti-inflammatory and antioxidant effects | Human | Chinese Academy of Medical Sciences |
| ST004351 | Interactions with bacteria shape diatom adaptation to carbon concentration changes | Phaeodactylum tricornutum, Loktanella vestfoldensis | Chinese Academy of Sciences |
| ST004395 | Extracellular polar Metabolomics on Lymphoblastoid cell lines (LCL) between individuals with Fragile X Syndrome (FXS) and from typically developing (TD) male controls. | Human | UMass Chan Medical School |
| ST004397 | [¹³C₅,¹⁵N₂]-glutamine stable isotope tracing in TD, FXS2 (partial FMRP), and FXS1 (no FMRP) from Lymphoblastoid cell lines (LCL) | Human | UMass Chan Medical School |
| ST004400 | Extracellular polar metabolomics on media neural progenitor cells (NPCs) generated using dual SMAD inhibition method from FXS and CRISPR edited isogenic rescue induced pluripotent stem cells (iPSCs) | Human | UMass Chan Medical School |
| ST004401 | Polar metabolomics on extracellular media of induced pluripotent stem cells (iPSC) derived forebrain excitatory neurons generated from a FXS and CRISPR edited isogenic control. | Human | UMass Chan Medical School |
| ST004402 | Polar metabolomics on intracellular media of induced pluripotent stem cells (iPSC) derived forebrain excitatory neurons generated from a FXS and CRISPR edited isogenic control. | Human | UMass Chan Medical School |
| ST004403 | Polar metabolomics on cell pellets and extracellular media of 4-week iPSC derived forebrain excitatory neurons generated from a FXS and CRISPR edited isogenic control. | Human | UMass Chan Medical School |
| ST004404 | L-Glutamine-13C5,15N2 stable isotope tracing on cell and media of 4-week iPSC derived forebrain excitatory neurons generated from a FXS and CRISPR edited isogenic control. | Human | UMass Chan Medical School |
