Nucleotide excision repair-dependent dna double-strand break formation and atm signaling activation in mammalian quiescent cells*

HIGHLIGHTS

• who: Mitsuo Wakasugi from the In a clonogenic survival assay, appropriate numbers of asynchronously growing or, arrested SuSa/T-n and AT OS/T-n cells were plated into, mm dishes in triplicate per each sample and incubated for , h to attach to the dishesAfter washing with PBS(⫺) twice, the cells were irradiated with various doses of UV and incubated for, weeks. The colonies formed were fixed with ethanol, stained with, % Giemsa solution, and counted under a stereomicroscope (Olympus, Tokyo, Japan have published the research: Nucleotide Excision Repair-dependent DNA Double-strand Break Formation and ATM Signaling . . .
  

   

  

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