Uncoupling of the base excision and nucleotide incision repair pathways reveals thier respective biological roles

Proceedings of the National Academy of Sciences of the United States of America

Volumn 103, Issue 8, 2006, Pages 2564-2569

  Ishchenko, Alexander A ^a   Deprez, Eric ^a   Wlaksimenko, Andrei ^a,b   Brochon, Jean Claude ^a   Tauc, Patrick ^a   Saparbaev, Murat K ^a  

^a CNRS   (France)

^b BioAlliance Pharma   (France)

Author keywords

anomeric 2 deoxyadenosine; 3 blocking groups; Apurinic apyrimidinic endonuclease; Oxidative DNA damage; Tert butyl hydroperoxide

Indexed keywords

BLEOMYCIN; CHELATING AGENT; DEOXYADENOSINE DERIVATIVE; DNA; DNA (APURINIC OR APYRIMIDINIC SITE) LYASE; DNA GLYCOSYLTRANSFERASE; EDETIC ACID; HYDROGEN PEROXIDE; METAL ION; OLIGONUCLEOTIDE; SMALL INTERFERING RNA; TERT BUTYL HYDROPEROXIDE; ZINC ION;

ANIMAL CELL; ARTICLE; CATALYSIS; CELL STRAIN 3T3; DNA DAMAGE; DNA REPAIR; ENZYME ACTIVITY; ENZYME SPECIFICITY; ENZYME SUBSTRATE; ESCHERICHIA COLI; EXCISION REPAIR; FLOW CYTOMETRY; HELA CELL; HUMAN; HUMAN CELL; MUTAGENESIS; NONHUMAN; PLASMID; PRIORITY JOURNAL;

ANIMALS; CELLS, CULTURED; CHELATING AGENTS; DEOXYADENOSINES; DEOXYRIBONUCLEASE IV (PHAGE T4-INDUCED); DNA; DNA DAMAGE; DNA REPAIR; DNA-(APURINIC OR APYRIMIDINIC SITE) LYASE; DRUG RESISTANCE, BACTERIAL; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; HUMANS; MICE; MUTATION; OXIDANTS; OXIDATION-REDUCTION; SUBSTRATE SPECIFICITY; ZINC;

ANIMALIA; ESCHERICHIA COLI;

EID: 33644546374     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0508582103     Document Type: Article

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