Repair protein persistence at DNA lesions characterizes XPF defect with Cockayne syndrome features

The structure-specific ERCC1-XPF endonuclease plays a key role in DNA damage excision by nucleotide excision repair (NER) and interstrand crosslink repair. Mutations in this complex can either cause xeroderma pigmentosum (XP) or XP combined with Cockayne syndrome (XPCS-complex) or Fanconi anemia. Ho...

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Detalhes bibliográficos
Publicado no:Nucleic Acids Res
Main Authors: Sabatella, Mariangela, Theil, Arjan F, Ribeiro-Silva, Cristina, Slyskova, Jana, Thijssen, Karen, Voskamp, Chantal, Lans, Hannes, Vermeulen, Wim
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2018
Assuntos:
Genome Integrity, Repair and Replication
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6182131/
https://ncbi.nlm.nih.gov/pubmed/30165384
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gky774
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