Defective global genome repair in XPC mice is associated with skin cancer susceptibility but not with sensitivity to UVB induced erythema and edema

Journal of Investigative Dermatology

Volumn 110, Issue 4, 1998, Pages 405-409

  Berg, R J W ^a   Ruven, H J T ^a   Sands, A T ^a   De Gruijl, F R ^a   Mullenders, L H F ^a  

^a UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

Cockayne syndrome; Cyclobutane pyrimidine dimers; Pyrimidine 6 4 pyrimidone photoproducts; Transcription coupled repair.

Indexed keywords

CYCLOBUTANE DERIVATIVE; PYRIMIDINE DERIVATIVE;

ANIMAL CELL; ANIMAL MODEL; ARTICLE; CANCER RISK; COCKAYNE SYNDROME; DNA DAMAGE; EDEMA; EMBRYO; ERYTHEMA; FEMALE; GENETIC PREDISPOSITION; GENOME; MALE; MOUSE; NONHUMAN; PHOTOSENSITIVITY; PRIORITY JOURNAL; SKIN CANCER; SKIN CARCINOGENESIS; TRANSCRIPTION REGULATION; ULTRAVIOLET B RADIATION; ULTRAVIOLET IRRADIATION; XERODERMA PIGMENTOSUM;

EID: 0031920594     PISSN: 0022202X     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1523-1747.1998.00173.x     Document Type: Article

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