Published in EMBO Rep on July 01, 2000
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TRF2 promotes, remodels and protects telomeric Holliday junctions. EMBO J (2009) 1.42
Direct association of Bloom's syndrome gene product with the human mismatch repair protein MLH1. Nucleic Acids Res (2001) 1.41
Requirement of Rrm3 helicase for repair of spontaneous DNA lesions in cells lacking Srs2 or Sgs1 helicase. Mol Cell Biol (2004) 1.40
Control of translocations between highly diverged genes by Sgs1, the Saccharomyces cerevisiae homolog of the Bloom's syndrome protein. Mol Cell Biol (2006) 1.40
ATR and ATM differently regulate WRN to prevent DSBs at stalled replication forks and promote replication fork recovery. EMBO J (2010) 1.39
Different quaternary structures of human RECQ1 are associated with its dual enzymatic activity. PLoS Biol (2007) 1.36
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Replication fork regression in vitro by the Werner syndrome protein (WRN): holliday junction formation, the effect of leading arm structure and a potential role for WRN exonuclease activity. Nucleic Acids Res (2007) 1.13
The Werner and Bloom syndrome proteins help resolve replication blockage by converting (regressed) holliday junctions to functional replication forks. Biochemistry (2011) 1.11
Unique and important consequences of RECQ1 deficiency in mammalian cells. Cell Cycle (2008) 1.09
The Bloom's syndrome helicase stimulates the activity of human topoisomerase IIIalpha. Nucleic Acids Res (2002) 1.08
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The dynamics of homologous pairing during mating type interconversion in budding yeast. PLoS Genet (2006) 1.07
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Analysis of the Xenopus Werner syndrome protein in DNA double-strand break repair. J Cell Biol (2005) 0.98
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Molecular cooperation between the Werner syndrome protein and replication protein A in relation to replication fork blockage. J Biol Chem (2010) 0.97
Telomeric protein TRF2 protects Holliday junctions with telomeric arms from displacement by the Werner syndrome helicase. Nucleic Acids Res (2010) 0.97
Identification and characterization of a Drosophila ortholog of WRN exonuclease that is required to maintain genome integrity. Aging Cell (2008) 0.96
Resolving branched DNA intermediates with structure-specific nucleases during replication in eukaryotes. Chromosoma (2013) 0.95
Replication stress induces specific enrichment of RECQ1 at common fragile sites FRA3B and FRA16D. Mol Cancer (2013) 0.94
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Identification and characterization of SMARCAL1 protein complexes. PLoS One (2013) 0.93
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The genetic consequences of ablating helicase activity and the Top3 interaction domain of Sgs1. DNA Repair (Amst) (2008) 0.91
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RECQL5 plays co-operative and complementary roles with WRN syndrome helicase. Nucleic Acids Res (2012) 0.89
WRN participates in translesion synthesis pathway through interaction with NBS1. Mech Ageing Dev (2010) 0.89
RPA alleviates the inhibitory effect of vinylphosphonate internucleotide linkages on DNA unwinding by BLM and WRN helicases. Nucleic Acids Res (2004) 0.89
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