The Cerebro-oculo-facio-skeletal Syndrome Point Mutation F231L in the ERCC1 DNA Repair Protein Causes Dissociation of the ERCC1-XPF Complex

Những quyển sách tương tự

• Single-stranded DNA Binding by the Helix-Hairpin-Helix Domain of XPF Protein Contributes to the Substrate Specificity of the ERCC1-XPF Protein Complex
  Bằng: Das, Devashish, et al.
  Được phát hành: (2017)
• Function and Interactions of ERCC1-XPF in DNA Damage Response
  Bằng: Faridounnia, Maryam, et al.
  Được phát hành: (2018)
• First Reported Patient with Human ERCC1 Deficiency Has Cerebro-Oculo-Facio-Skeletal Syndrome with a Mild Defect in Nucleotide Excision Repair and Severe Developmental Failure
  Bằng: Jaspers, Nicolaas G. J., et al.
  Được phát hành: (2007)
• Mapping of interaction domains between human repair proteins ERCC1 and XPF.
  Bằng: de Laat, W L, et al.
  Được phát hành: (1998)
• Cerebro-Oculo-Facio-Skeletal Syndrome with a Nucleotide Excision–Repair Defect and a Mutated XPD Gene, with Prenatal Diagnosis in a Triplet Pregnancy
  Bằng: Graham, Jr., John M., et al.
  Được phát hành: (2001)