<p>U2OS cells expressing NBS1-GFP were irradiated with Ti ions (LET ∼270 keV/µm) under a low angle resulting in a streak-shaped foci pattern along the ion trajectory (red arrow). At time 0 s the fluorescence tag of the proteins in a small part of the streak are bleached with a short and intense laser pulse (cyan arrow). Fluorescence recovery in the bleached region represents the protein exchange at the DNA damage. Selected time frames are shown. Time labels correspond to the time after bleaching.</p
The formation of DNA lesions poses a constant threat to cellular stability. Repair of endogenously a...
Traditionally, the kinetics of DNA repair have been estimated using immunocytochemistry by labeling ...
We have established an experimental scheme to evaluate the repair efficiency of non-DSB type of clus...
<p>Cells were irradiated with Sm ions (LET 10290 keV/µm) at 0 s generating DNA damage along their tr...
To study the dynamics of protein recruitment to DNA lesions, ion beams can be used to generate extre...
The response of cells to ionizing radiation-induced DNA double-strand breaks (DSB) is determined by ...
<p>(<b>A</b>) FRAP data from the nucleoplasm of U2OS cells stably expressing GFP-lamin A. GFP-lamin ...
Cellular response to radiation damage is made by a complex network of pathways and feedback loops w...
Radiation-induced damage to the genomic DNA of cells may lead to errors in transcription and replica...
High-linear energy transfer (LET) ion irradiation of cell nuclei induces complex and severe DNA lesi...
<p>(<b>A</b>) A region of interest of ∼4 μm<sup>2</sup> was photo-bleached and the fluorescence reco...
<p>(A) Representative images illustrating fluorescence recovery of Chtop-GFP after photobleaching in...
<p>A–E: snapshots of a cell during data acquisition; A: the cell before photobleaching (panel labele...
Here we show how to measure the mobility of transcription factors using fluorescence recovery after ...
The most deleterious DNA lesions induced by ionizing radiation are clustered DNA double-strand break...
The formation of DNA lesions poses a constant threat to cellular stability. Repair of endogenously a...
Traditionally, the kinetics of DNA repair have been estimated using immunocytochemistry by labeling ...
We have established an experimental scheme to evaluate the repair efficiency of non-DSB type of clus...
<p>Cells were irradiated with Sm ions (LET 10290 keV/µm) at 0 s generating DNA damage along their tr...
To study the dynamics of protein recruitment to DNA lesions, ion beams can be used to generate extre...
The response of cells to ionizing radiation-induced DNA double-strand breaks (DSB) is determined by ...
<p>(<b>A</b>) FRAP data from the nucleoplasm of U2OS cells stably expressing GFP-lamin A. GFP-lamin ...
Cellular response to radiation damage is made by a complex network of pathways and feedback loops w...
Radiation-induced damage to the genomic DNA of cells may lead to errors in transcription and replica...
High-linear energy transfer (LET) ion irradiation of cell nuclei induces complex and severe DNA lesi...
<p>(<b>A</b>) A region of interest of ∼4 μm<sup>2</sup> was photo-bleached and the fluorescence reco...
<p>(A) Representative images illustrating fluorescence recovery of Chtop-GFP after photobleaching in...
<p>A–E: snapshots of a cell during data acquisition; A: the cell before photobleaching (panel labele...
Here we show how to measure the mobility of transcription factors using fluorescence recovery after ...
The most deleterious DNA lesions induced by ionizing radiation are clustered DNA double-strand break...
The formation of DNA lesions poses a constant threat to cellular stability. Repair of endogenously a...
Traditionally, the kinetics of DNA repair have been estimated using immunocytochemistry by labeling ...
We have established an experimental scheme to evaluate the repair efficiency of non-DSB type of clus...