Mutator phenotype of mammalian cells due to deficiency of NEIL1 DNA glycosylase, an oxidized base-specific repair enzyme

DNA Repair

Volumn 7, Issue 8, 2008, Pages 1213-1220

  Maiti, Amit K ^a,b   Boldogh, Istvan ^a   Spratt, Heidi ^b   Mitra, Sankar ^a,b   Hazra, Tapas K ^a,b  

^a University of Texas Medical Branch School of Medicine   (United States)

^b UNIVERSITY OF TEXAS MEDICAL BRANCH   (United States)

Author keywords

BER; Hprt; Mutagenesis; NEIL1; Oxidative stress

Indexed keywords

DNA GLYCOSYLTRANSFERASE; HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE; NEIL1 PROTEIN; NEIL2 PROTEIN; SINGLE STRANDED DNA;

ANIMAL CELL; ARTICLE; CELL STRAIN V 79; CONTROLLED STUDY; DNA DAMAGE; DNA REPLICATION; ENZYME DEFICIENCY; GENE MUTATION; HUMAN; HUMAN CELL; NONHUMAN; OXIDATIVE STRESS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN GLYCOSYLATION;

ANIMALS; BASE SEQUENCE; CELL LINE; CRICETINAE; CRICETULUS; DNA DAMAGE; DNA GLYCOSYLASES; DNA PRIMERS; HUMANS; HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE; MUTATION; OLIGONUCLEOTIDES, ANTISENSE; OXIDATION-REDUCTION; PHENOTYPE;

CRICETULUS GRISEUS; MAMMALIA;

EID: 46649089126     PISSN: 15687864     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dnarep.2008.03.025     Document Type: Article

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