Anti-Werner's syndrome helicase WRN 抗体 (ab200)

ab200 を使用した論文を発表された方は、こちらまでお知らせください。データシートに掲載させていただきます。

ab200 は 20 報の論文で使用されています。

  • Gong Y  et al. PHF11 promotes DSB resection, ATR signaling, and HR. Genes Dev 31:46-58 (2017). WB ; Mouse . PubMed: 28115467
  • Palermo V  et al. CDK1 phosphorylates WRN at collapsed replication forks. Nat Commun 7:12880 (2016). PubMed: 27634057
  • Matino D  et al. IDO1 suppresses inhibitor development in hemophilia A treated with factor VIII. J Clin Invest 125:3766-81 (2015). PubMed: 26426076
  • 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). Human . PubMed: 26622343
  • Silva BA  et al. DNA damage to a single chromosome end delays anaphase onset. J Biol Chem 289:22771-84 (2014). ICC/IF . PubMed: 24982423
  • 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). WB ; Human . PubMed: 22576367
  • 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). WB, ICC/IF ; Human . PubMed: 21558802
  • 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). ICC/IF ; Human . PubMed: 19559722
  • 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). WB ; Human . PubMed: 18682526
  • Kusumoto R  et al. Werner protein cooperates with the XRCC4-DNA ligase IV complex in end-processing. Biochemistry 47:7548-56 (2008). PubMed: 18558713
  • 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). PubMed: 17173071
  • 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). PubMed: 17599064
  • 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). ELISA, IP ; Human . PubMed: 17118963
  • 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). PubMed: 16723399
  • 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). PubMed: 15995249
  • 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). PubMed: 16223718
  • 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). PubMed: 15498034
  • 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). PubMed: 12633936
  • Baynton K  et al. WRN interacts physically and functionally with the recombination mediator protein RAD52. J Biol Chem 278:36476-86 (2003). PubMed: 12750383
  • 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). PubMed: 11380620