A multistep damage recognition mechanism for global genomic nucleotide excision repair

Genes and Development

Volumn 15, Issue 5, 2001, Pages 507-521

  Sugasawa, K ^a   Okamoto, T ^a   Shimizu, Y ^a   Masutani, C ^a   Iwai, S ^a   Hanaoka, F ^a  

^a RIKEN   (Japan)

Author keywords

Damage recognition; Nucleotide excision repair; Xeroderma pigmentosum; XPC HR23B complex

Indexed keywords

ARTICLE; DNA DAMAGE; DNA REPLICATION; EXCISION REPAIR; HUMAN; HUMAN CELL; PRIORITY JOURNAL; PROTEIN DNA BINDING; XERODERMA PIGMENTOSUM;

BASE PAIR MISMATCH; DEOXYRIBONUCLEASE I; DNA DAMAGE; DNA FOOTPRINTING; DNA REPAIR; DNA-BINDING PROTEINS; GENOME, HUMAN; HUMANS; MODELS, BIOLOGICAL; NUCLEIC ACID CONFORMATION; PLASMIDS; PROTEIN BINDING; PYRIMIDINE DIMERS; TUMOR CELLS, CULTURED;

MAMMALIA;

EID: 0035282109     PISSN: 08909369     EISSN: None     Source Type: Journal    
DOI: 10.1101/gad.866301     Document Type: Article

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55. Order of assembly of human DNA repair excision nuclease
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59. The xeroderma pigmentosum group C protein complex XPC-HR23B plays an important role in the recruitment of transcription factor IIH to damaged DNA