Found: 5
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Inactivating TDP2 missense mutation in siblings with congenital abnormalities reminiscent of fanconi anemia.
- Published in:
- Human Genetics, 2023, v. 142, n. 9, p. 1417, doi. 10.1007/s00439-023-02589-3
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- Article
Pathogenic ARH3 mutations result in ADP-ribose chromatin scars during DNA strand break repair.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-17069-9
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- Publication type:
- Article
Novel PNKP mutations associated with reduced DNA single‐strand break repair and severe microcephaly, seizures, and developmental delay.
- Published in:
- Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 1, p. 1, doi. 10.1002/mgg3.2295
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- Article
Unrepaired base excision repair intermediates in template DNA strands trigger replication fork collapse and PARP inhibitor sensitivity.
- Published in:
- EMBO Journal, 2023, v. 42, n. 18, p. 1, doi. 10.15252/embj.2022113190
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- Article
Inhibition of vacuolar ATPase attenuates the TRAIL-induced activation of caspase-8 and modulates the trafficking of TRAIL receptosomes.
- Published in:
- FEBS Journal, 2013, v. 280, n. 14, p. 3436, doi. 10.1111/febs.12347
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- Article