The DNA damage signal for Mdm2 regulation, Trp53 induction, and sunburn cell formation in vivo originates from actively transcribed genes

Journal of Investigative Dermatology

Volumn 117, Issue 5, 2001, Pages 1234-1240

  Brash, Douglas E ^a   Wikonkal, Norbert M ^a,b,f   Remenyik, Eva ^a,b   Van der Horst, Gijsbertus T J ^c   Friedberg, Errol C ^d   Cheo, David L ^d,g   Van Steeg, Harry ^e   Westerman, Anja ^e   Van Kranen, Henk J ^e  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF DEBRECEN   (Hungary)

^c ERASMUS MEDICAL CENTER   (Netherlands)

^d UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^e NATIONAL INSTITUTE FOR PUBLIC HEALTH AND THE ENVIRONMENT   (Netherlands)

^f SEMMELWEIS UNIVERSITY   (Hungary)

^g Invitrogen Corporation   (United States)

Author keywords

Apoptosis; Cockayne syndrome; Mdm2 protein; MeSH; Protein p53; Ultraviolet rays; Xeroderma pigmentosum

Indexed keywords

ANIMAL CELL; APOPTOSIS; ARTICLE; CANCER INHIBITION; CELL MUTANT; CONTROLLED STUDY; DNA DAMAGE; DNA REPAIR; ERYTHEMA; EXCISION REPAIR; GENE CONTROL; GENE TARGETING; GENETIC STABILITY; GENETIC STRAIN; GENETIC TRANSCRIPTION; GENOME; HOMOZYGOSITY; IN VIVO STUDY; KERATINOCYTE; MOUSE; NONHUMAN; PRECANCER; PRIORITY JOURNAL; QUANTITATIVE GENETICS; SUNBURN; ULTRAVIOLET B RADIATION; WILD TYPE;

EID: 0035725421     PISSN: 0022202X     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.0022-202X.2001.01554.x     Document Type: Article

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