Polymerase η deficiency in the xeroderma pigmentosum variant uncovers an overlap between the S phase checkpoint and double-strand break repair

Ítems similars

• UV-induced replication arrest in the xeroderma pigmentosum variant leads to DNA double-strand breaks, γ-H2AX formation, and Mre11 relocalization
  per: Limoli, Charles L., et al.
  Publicat: (2002)
• Molecular analysis of mutations in DNA polymerase η in xeroderma pigmentosum-variant patients
  per: Broughton, Bernard C., et al.
  Publicat: (2002)
• Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes.
  per: Greenhaw, G A, et al.
  Publicat: (1992)
• Enzyme Defect in Xeroderma Pigmentosum
  per: Cleaver, J. E.
  Publicat: (1970)
• Domain structure, localization, and function of DNA polymerase η, defective in xeroderma pigmentosum variant cells
  per: Kannouche, Patricia, et al.
  Publicat: (2001)