Gong Y et al.PHF11 promotes DSB resection, ATR signaling, and HR.Genes Dev 31:46-58 (2017).
Palermo V et al.CDK1 phosphorylates WRN at collapsed replication forks.Nat Commun 7:12880 (2016).
Matino D et al.IDO1 suppresses inhibitor development in hemophilia A treated with factor VIII.J Clin Invest 125:3766-81 (2015).
Li P et al.Methylation of Werner syndrome protein is associated with the occurrence and development of invasive meningioma via the regulation of Myc and p53 expression.Exp Ther Med 10:498-502 (2015).
Silva BA et al.DNA damage to a single chromosome end delays anaphase onset.J Biol Chem 289:22771-84 (2014).
Barefield C & Karlseder J The BLM helicase contributes to telomere maintenance through processing of late-replicating intermediate structures.Nucleic Acids Res 40:7358-67 (2012).
Trego KS et al.The DNA repair endonuclease XPG interacts directly and functionally with the WRN helicase defective in Werner syndrome.Cell Cycle 10:1998-2007 (2011).
Rusin M et al.Resveratrol induces senescence-like growth inhibition of U-2 OS cells associated with the instability of telomeric DNA and upregulation of BRCA1.Mech Ageing Dev 130:528-37 (2009).
Selak N et al.The Bloom's syndrome helicase (BLM) interacts physically and functionally with p12, the smallest subunit of human DNA polymerase delta.Nucleic Acids Res 36:5166-79 (2008).
Kusumoto R et al.Werner protein cooperates with the XRCC4-DNA ligase IV complex in end-processing.Biochemistry 47:7548-56 (2008).
Jiao R et al.The Werner syndrome protein is required for recruitment of chromatin assembly factor 1 following DNA damage.Oncogene 26:3811-22 (2007).
Chan KL et al.BLM is required for faithful chromosome segregation and its localization defines a class of ultrafine anaphase bridges.EMBO J 26:3397-409 (2007).
Otterlei M et al.Werner syndrome protein participates in a complex with RAD51, RAD54, RAD54B and ATR in response to ICL-induced replication arrest.J Cell Sci 119:5137-46 (2006).
Agrelo R et al.Epigenetic inactivation of the premature aging Werner syndrome gene in human cancer.Proc Natl Acad Sci U S A 103:8822-7 (2006).
Friedemann J et al.Nuclear DNA helicase II (RNA helicase A) interacts with Werner syndrome helicase and stimulates its exonuclease activity.J Biol Chem : (2005).
Zhang N et al.The Pso4 mRNA splicing and DNA repair complex interacts with WRN for processing of DNA interstrand cross-links.J Biol Chem 280:40559-67 (2005).
Bordi L et al.Expression of Werner and Bloom syndrome genes is differentially regulated by in vitro HIV-1 infection of peripheral blood mononuclear cells.Clin Exp Immunol 138:251-8 (2004).
Rodríguez-López AM et al.Characterisation of the interaction between WRN, the helicase/exonuclease defective in progeroid Werner's syndrome, and an essential replication factor, PCNA.Mech Ageing Dev 124:167-74 (2003).
Baynton K et al.WRN interacts physically and functionally with the recombination mediator protein RAD52.J Biol Chem 278:36476-86 (2003).
Sakamoto S et al.Werner helicase relocates into nuclear foci in response to DNA damaging agents and co-localizes with RPA and Rad51.Genes Cells 6:421-30 (2001).