Opposite-base dependent excision of 5-formyluracil from DNA by hSMUG1

International Journal of Radiation Biology

Volumn 85, Issue 5, 2009, Pages 413-420

  Knvælsrud, Ingeborg ^a   Slupphaug, Geir ^b   Leiros, Ingar ^c   Matsuda, Akira ^d   Ruoff, Peter ^a   Bjelland, Svein ^a  

^a UNIVERSITY OF STAVANGER   (Norway)

^b NORWEGIAN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Norway)

^c UNIVERSITY OF TROMSØ   (Norway)

^d HOKKAIDO UNIVERSITY   (Japan)

Author keywords

DNA damage; DNA repair; Mutation; Reactive oxygen species

Indexed keywords

5 FORMYLURACIL; DNA; PHOSPHORUS 32; SODIUM HYDROXIDE; THYMINE DERIVATIVE; UNCLASSIFIED DRUG; URACIL DNA GLYCOSIDASE; 5-FORMYLURACIL; DRUG DERIVATIVE; SMUG1 PROTEIN, HUMAN; URACIL;

ARTICLE; AUTORADIOGRAPHY; CONTROLLED STUDY; DNA CLEAVAGE; DNA DAMAGE; DNA SEQUENCE; ELECTROPHORESIS; EXCISION REPAIR; HUMAN; HUMAN CELL; IONIZING RADIATION; PRIORITY JOURNAL; ANIMAL; BASE PAIRING; CHEMICAL STRUCTURE; CHEMISTRY; DNA REPAIR; ENZYME ACTIVE SITE; GENETICS; KINETICS; METABOLISM; MOUSE; MUTATION; NUCLEOTIDE SEQUENCE; RAT;

MAMMALIA;

ANIMALS; BASE PAIRING; BASE SEQUENCE; CATALYTIC DOMAIN; DNA; DNA REPAIR; HUMANS; KINETICS; MICE; MODELS, MOLECULAR; MUTATION; RATS; URACIL; URACIL-DNA GLYCOSIDASE;

EID: 67649871036     PISSN: 09553002     EISSN: 13623095     Source Type: Journal    
DOI: 10.1080/09553000902818915     Document Type: Article

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