Assembly of nuclear matrix–bound protein complexes involved in non-homologous end joining is induced by inhibition of DNA topoisomerase II
Author:
Publisher
Wiley
Subject
Cell Biology,Clinical Biochemistry,Physiology
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1. Hypersensitivity of Nonhomologous DNA End-joining Mutants to VP-16 and ICRF-193
2. Genetic evidence for involvement of two distinct nonhomologous end-joining pathways in repair of topoisomerase II-mediated DNA damage
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1. The genetic sequences prone to copy number variation and single nucleotide polymorphism are linked to the repair of the poisoned DNA topoisomerase II;2020-09-03
2. A role for the p53 tumour suppressor in regulating the balance between homologous recombination and non-homologous end joining;Open Biology;2016-09
3. Reduced DNA double-strand break repair capacity and risk of squamous cell carcinoma of the head and neck—A case-control study;DNA Repair;2016-04
4. The effects of anti-DNA topoisomerase II drugs, etoposide and ellipticine, are modified in root meristem cells of Allium cepa by MG132, an inhibitor of 26S proteasomes;Plant Physiology and Biochemistry;2015-11
5. Heat-shock induced γH2AX foci are associated with the nuclear matrix only in S-phase cells;Doklady Biochemistry and Biophysics;2013-05
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