<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ngo LP</submitter><funding>NIEHS NIH HHS</funding><pagination>89-99</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8477454</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>174</volume><pubmed_abstract>Although DNA repair is known to impact susceptibility to cancer and other diseases, relatively few population studies have been performed to evaluate DNA repair kinetics in people due to the difficulty of assessing DNA repair in a high-throughput manner. Here we use the CometChip, a high-throughput comet assay, to explore inter-individual variation in repair of oxidative damage to DNA, a known risk factor for aging, cancer and other diseases. DNA repair capacity after H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub>-induced DNA oxidation damage was quantified in peripheral blood mononuclear cells (PBMCs). For 10 individuals, blood was drawn at several times over the course of 4-6 weeks. In addition, blood was drawn once from each of 56 individuals. DNA damage levels were quantified prior to exposure to H&lt;sub>2&lt;</pubmed_abstract><journal>Free radical biology &amp; medicine</journal><pubmed_title>CometChip analysis of human primary lymphocytes enables quantification of inter-individual differences in the kinetics of repair of oxidative DNA damage.</pubmed_title><pmcid>PMC8477454</pmcid><funding_grant_id>U01 ES029520</funding_grant_id><funding_grant_id>P30 ES000002</funding_grant_id><funding_grant_id>DP1 ES022576</funding_grant_id><funding_grant_id>P30 ES002109</funding_grant_id><funding_grant_id>P42 ES027707</funding_grant_id><pubmed_authors>Samson LD</pubmed_authors><pubmed_authors>Nagel ZD</pubmed_authors><pubmed_authors>Ngo LP</pubmed_authors><pubmed_authors>Mazzucato P</pubmed_authors><pubmed_authors>Engelward BP</pubmed_authors><pubmed_authors>Kaushal S</pubmed_authors><pubmed_authors>Chaim IA</pubmed_authors><pubmed_authors>Ricciardi C</pubmed_authors></additional><is_claimable>false</is_claimable><name>CometChip analysis of human primary lymphocytes enables quantification of inter-individual differences in the kinetics of repair of oxidative DNA damage.</name><description>Although DNA repair is known to impact susceptibility to cancer and other diseases, relatively few population studies have been performed to evaluate DNA repair kinetics in people due to the difficulty of assessing DNA repair in a high-throughput manner. Here we use the CometChip, a high-throughput comet assay, to explore inter-individual variation in repair of oxidative damage to DNA, a known risk factor for aging, cancer and other diseases. DNA repair capacity after H&lt;sub>2&lt;/sub>O&lt;sub>2&lt;/sub>-induced DNA oxidation damage was quantified in peripheral blood mononuclear cells (PBMCs). For 10 individuals, blood was drawn at several times over the course of 4-6 weeks. In addition, blood was drawn once from each of 56 individuals. DNA damage levels were quantified prior to exposure to H&lt;sub>2&lt;</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2025-04-04T10:27:49.439Z</modification><creation>2025-04-04T10:27:49.439Z</creation></dates><accession>S-EPMC8477454</accession><cross_references><pubmed>34324980</pubmed><doi>10.1016/j.freeradbiomed.2021.07.033</doi></cross_references></HashMap>