<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Brunner S</submitter><funding>Laserlab-Europe</funding><funding>European Regional Development Fund</funding><pagination>1609971</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8966514</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27</volume><pubmed_abstract>The quantitative detection of radiation caused DNA double-strand breaks (DSB) by immunostained γ-H2AX foci using direct stochastic optical reconstruction microscopy (dSTORM) provides a deeper insight into the DNA repair process at nanoscale in a time-dependent manner. Glioblastoma (U251) cells were irradiated with 250 keV X-ray at 0, 2, 5, 8 Gy dose levels. Cell cycle phase distribution and apoptosis of U251 cells upon irradiation was assayed by flow cytometry. We studied the density, topology and volume of the γ-H2AX foci with 3D confocal microscopy and the dSTORM superresolution method. A pronounced increase in γ-H2AX foci and cluster density was detected by 3D confocal microscopy after 2 Gy, at 30 min postirradiation, but both returned to the control level at 24 h. Meanwhile, at 24 h a </pubmed_abstract><journal>Pathology oncology research : POR</journal><pubmed_title>Analysis of Ionizing Radiation Induced DNA Damage by Superresolution dSTORM Microscopy.</pubmed_title><pmcid>PMC8966514</pmcid><funding_grant_id>871124</funding_grant_id><funding_grant_id>GINOP-2.3.6-15-2015-00001</funding_grant_id><pubmed_authors>Varga D</pubmed_authors><pubmed_authors>Bozo R</pubmed_authors><pubmed_authors>Szabo ER</pubmed_authors><pubmed_authors>Erdelyi M</pubmed_authors><pubmed_authors>Hideghety K</pubmed_authors><pubmed_authors>Molnar R</pubmed_authors><pubmed_authors>Brunner S</pubmed_authors><pubmed_authors>Puskas LG</pubmed_authors><pubmed_authors>Gemes N</pubmed_authors><pubmed_authors>Tokes T</pubmed_authors><pubmed_authors>Szebeni GJ</pubmed_authors><pubmed_authors>Polanek R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Analysis of Ionizing Radiation Induced DNA Damage by Superresolution dSTORM Microscopy.</name><description>The quantitative detection of radiation caused DNA double-strand breaks (DSB) by immunostained γ-H2AX foci using direct stochastic optical reconstruction microscopy (dSTORM) provides a deeper insight into the DNA repair process at nanoscale in a time-dependent manner. Glioblastoma (U251) cells were irradiated with 250 keV X-ray at 0, 2, 5, 8 Gy dose levels. Cell cycle phase distribution and apoptosis of U251 cells upon irradiation was assayed by flow cytometry. We studied the density, topology and volume of the γ-H2AX foci with 3D confocal microscopy and the dSTORM superresolution method. A pronounced increase in γ-H2AX foci and cluster density was detected by 3D confocal microscopy after 2 Gy, at 30 min postirradiation, but both returned to the control level at 24 h. Meanwhile, at 24 h a </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2025-08-23T03:04:54.182Z</modification><creation>2025-04-06T14:52:09.101Z</creation></dates><accession>S-EPMC8966514</accession><cross_references><pubmed>35370480</pubmed><doi>10.3389/pore.2021.1609971</doi></cross_references></HashMap>