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Article

Repriming of DNA synthesis at stalled replication forks by human PrimPol

17 Nov 2013

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 24240614
DOI: 10.1038/nsmb.2719

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Repriming of DNA synthesis at stalled replication forks by human PrimPolPMID 24240614Read ↗

PRIMPOL ensures robust handoff between on-the-fly and post-replicative DNA lesion bypassSemantic proximity Read ↗

PrimPol is required for the maintenance of efficient nuclear and mitochondrial DNA replication in human cellsSemantic proximity Read ↗

PrimPol is required for the maintenance of efficient nuclear and mitochondrial DNA replication in human cellsSemantic proximity Read ↗

Human CST complex restricts excessive PrimPol repriming upon UV induced replication stress by suppressing p21Semantic proximity Read ↗

S phase R-loop formation is restricted by PrimPol-mediated reprimingSemantic proximity Read ↗

Tolerating DNA damage by repriming: Gap filling in the spotlightSemantic proximity Read ↗

Models for human telomere C-strand fill-in by CST–Polα-primaseSemantic proximity Read ↗

Pol η is required for DNA replication during nucleotide deprivation by hydroxyureaSemantic proximity Read ↗

Roles of POL3, POL2 and PMS1 genes in maintaining accurate DNA replication.Semantic proximity Read ↗

Translesion activity of PrimPol on DNA with cisplatin and DNA–protein cross-linksSemantic proximity Read ↗

Nucleases Acting at Stalled Forks: How to Reboot the Replication Program with a Few ShortcutsSemantic proximity Read ↗

Translesion DNA Synthesis and Reinitiation of DNA Synthesis in Chemotherapy ResistanceSemantic proximity Read ↗

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