Distinct roles of XRCC4 and Ku80 in non-homologous end-joining of endonuclease- and ionizing radiation-induced DNA double-strand breaks

Lignende værker

• Defects in XRCC4 and KU80 differentially affect the joining of distal nonhomologous ends
  af: Guirouilh-Barbat, Josée, et al.
  Udgivet: (2007)
• Dynamic assembly of end-joining complexes requires interaction between Ku70/80 and XRCC4
  af: Mari, Pierre-Olivier, et al.
  Udgivet: (2006)
• The alternative end-joining pathway for repair of DNA double-strand breaks requires PARP1 but is not dependent upon microhomologies
  af: Mansour, Wael Y., et al.
  Udgivet: (2010)
• Hierarchy of nonhomologous end-joining, single-strand annealing and gene conversion at site-directed DNA double-strand breaks
  af: Mansour, Wael Y., et al.
  Udgivet: (2008)
• Human RECQ1 Interacts with Ku70/80 and Modulates DNA End-Joining of Double-Strand Breaks
  af: Parvathaneni, Swetha, et al.
  Udgivet: (2013)