<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pannkuk EL</submitter><funding>NIAID NIH HHS</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>Division of Intramural Research, National Institute of Allergy and Infectious Diseases</funding><pagination>5145-5155</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9109602</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(11)</volume><pubmed_abstract>An important component of ionizing radiation (IR) exposure after a radiological incident may include low-dose rate (LDR) exposures either externally or internally, such as from &lt;sup>137&lt;/sup>Cs deposition. In this study, a novel irradiation system, VAriable Dose-rate External &lt;sup>137&lt;/sup>Cs irradiatoR (VADER), was used to expose male and female mice to a variable LDR irradiation over a 30 d time span to simulate fall-out-type exposures in addition to biofluid collection from a reference dose rate (0.8 Gy/min). Radiation markers were identified by untargeted metabolomics and random forests. Mice exposed to LDR exposures were successfully identified from control groups based on their urine and serum metabolite profiles. In addition to metabolites commonly perturbed after IR exposure, we id</pubmed_abstract><journal>Journal of proteome research</journal><pubmed_title>Biofluid Metabolomics of Mice Exposed to External Low-Dose Rate Radiation in a Novel Irradiation System, the Variable Dose-Rate External &lt;sup>137&lt;/sup>Cs Irradiator.</pubmed_title><pmcid>PMC9109602</pmcid><funding_grant_id>U19 AI067773</funding_grant_id><funding_grant_id>P30 CA051008</funding_grant_id><funding_grant_id>P30CA051008</funding_grant_id><pubmed_authors>Laiakis EC</pubmed_authors><pubmed_authors>Brenner DJ</pubmed_authors><pubmed_authors>Amundson SA</pubmed_authors><pubmed_authors>Morton SR</pubmed_authors><pubmed_authors>Garty GY</pubmed_authors><pubmed_authors>Fornace AJ</pubmed_authors><pubmed_authors>Pujol-Canadell M</pubmed_authors><pubmed_authors>Girgis M</pubmed_authors><pubmed_authors>Ghandhi SA</pubmed_authors><pubmed_authors>Pannkuk EL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Biofluid Metabolomics of Mice Exposed to External Low-Dose Rate Radiation in a Novel Irradiation System, the Variable Dose-Rate External &lt;sup>137&lt;/sup>Cs Irradiator.</name><description>An important component of ionizing radiation (IR) exposure after a radiological incident may include low-dose rate (LDR) exposures either externally or internally, such as from &lt;sup>137&lt;/sup>Cs deposition. In this study, a novel irradiation system, VAriable Dose-rate External &lt;sup>137&lt;/sup>Cs irradiatoR (VADER), was used to expose male and female mice to a variable LDR irradiation over a 30 d time span to simulate fall-out-type exposures in addition to biofluid collection from a reference dose rate (0.8 Gy/min). Radiation markers were identified by untargeted metabolomics and random forests. Mice exposed to LDR exposures were successfully identified from control groups based on their urine and serum metabolite profiles. In addition to metabolites commonly perturbed after IR exposure, we id</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2025-04-04T07:45:23.532Z</modification><creation>2025-04-04T07:45:23.532Z</creation></dates><accession>S-EPMC9109602</accession><cross_references><pubmed>34585931</pubmed><doi>10.1021/acs.jproteome.1c00638</doi></cross_references></HashMap>