The founding members of xeroderma pigmentosum group G produce XPG protein with severely impaired endonuclease activity

Journal of Investigative Dermatology

Volumn 118, Issue 2, 2002, Pages 344-351

  Lalle, Philippe ^a   Nouspikel, Thierry ^a   Constantinou, Angelos ^a   Thorel, Fabrizio ^a   Clarkson, Stuart G ^a  

^a UNIVERSITY OF GENEVA MEDICAL SCHOOL   (Switzerland)

Author keywords

Cockayne syndrome; DNA repair; Nucleotide excision repair; Transcription coupled repair

Indexed keywords

AMINO ACID; ENDONUCLEASE; PROTEIN; UNCLASSIFIED DRUG; XERODERMA PIGMENTOSUM PROTEIN;

ALLELE; ALTERNATIVE RNA SPLICING; AMINO ACID COMPOSITION; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; ARTICLE; COCKAYNE SYNDROME; CONTROLLED STUDY; DISEASE ASSOCIATION; DISEASE SEVERITY; ENZYME ACTIVITY; GENE DELETION; GENE MUTATION; GENETIC STABILITY; HUMAN; HUMAN CELL; INTRON; OXIDATIVE STRESS; PHOTOSENSITIVITY DISORDER; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN STABILITY; SKIN FIBROBLAST; XERODERMA PIGMENTOSUM;

EID: 0036180585     PISSN: 0022202X     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.0022-202x.2001.01673.x     Document Type: Article

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