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The hSSB1 orthologue Obfc2b is essential for skeletogenesis but dispensable for the DNA damage response in vivo
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Analysis of protein dynamics at active, stalled, and collapsed replication forks
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hSSB1 rapidly binds at the sites of DNA double-strand breaks and is required for the efficient recruitment of the MRN complex
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hSSB1 interacts directly with the MRN complex stimulating its recruitment to DNA double-strand breaks and its endo-nuclease activity
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PARP is activated at stalled forks to mediate Mre11-dependent replication restart and recombination
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hSSB1 and hSSB2 Form Similar Multiprotein Complexes That Participate in DNA Damage Response
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Human RPA phosphorylation by ATR stimulates DNA synthesis and prevents ssDNA accumulation during DNA-replication stress
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Single-stranded DNA-binding protein hSSB1 is critical for genomic stability
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