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Oncogene

Volumn 21, Issue 22, 2002, Pages 3571-3578

Global genome repair of 8-oxog in hamster cells requires a functional csb gene product

(5) Sunesen, Morten a,c Stevnsner, Tinna a Brosh, Robert M b Dianov, Grigory L b,d Bohr, Vilhelm A b

a AARHUS UNIVERSITY (Denmark)

b NATIONAL INSTITUTE ON AGING (United States)

c INSTITUT PASTEUR (France)

d MRC Radiation And Genome Stability Unit (United Kingdom)

Author keywords

Cockayne syndrome; DNA instability; Oxidative DNA damage; Repair

Indexed keywords

GENE PRODUCT; RNA POLYMERASE;

ANIMAL CELL; ARTICLE; BASE MISPAIRING; COCKAYNE SYNDROME; DNA DAMAGE; DNA REPAIR; GENOME ANALYSIS; HAMSTER; MOLECULAR CLONING; NERVE DEGENERATION; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; TRANSCRIPTION REGULATION;

ADENOSINE TRIPHOSPHATASES; AMINO ACID SEQUENCE; ANIMALS; CELL LINE; CELL SURVIVAL; CRICETINAE; DNA HELICASES; DNA REPAIR; DNA-FORMAMIDOPYRIMIDINE GLYCOSYLASE; GENOME; GUANOSINE; LIGHT; MOLECULAR SEQUENCE DATA; MUTATION; N-GLYCOSYL HYDROLASES; PHOTOSENSITIZING AGENTS; PROTEIN STRUCTURE, TERTIARY; PYRROLIDINES; QUINOLIZINES; SEQUENCE ALIGNMENT; TETRAHYDROFOLATE DEHYDROGENASE;

ANIMALIA; CRICETINAE;

EID: 0037118577 PISSN: 09509232 EISSN: None Source Type: Journal
DOI: 10.1038/sj.onc.1205443 Document Type: Article

Times cited : (43)

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