Base excision repair facilitates a functional relationship between guanine oxidation and histone demethylation

Antioxidants and Redox Signaling

Volumn 18, Issue 18, 2013, Pages 2429-2443

  Li, Jianfeng ^a,b   Braganza, Andrea ^a,b   Sobol, Robert W ^a,b,c  

^a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF PITTSBURGH CANCER INSTITUTE   (United States)

^c UNIVERSITY OF PITTSBURGH GRADUATE SCHOOL OF PUBLIC HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GUANINE; HISTONE; HYDROGEN PEROXIDE; LYSINE SPECIFIC DEMETHYLASE 1; METHYLTRANSFERASE; SINGLE STRANDED DNA; UNCLASSIFIED DRUG;

ALKYLATION; CELL METABOLISM; CHEMOTHERAPY; DEAMINATION; DEMETHYLATION; DNA DAMAGE; DNA METHYLATION; ENVIRONMENTAL EXPOSURE; ENZYME ACTIVITY; EPIGENETICS; EXCISION REPAIR; GENE EXPRESSION REGULATION; HISTONE DEMETHYLATION; HISTONE MODIFICATION; HUMAN; OXIDATION; PRIORITY JOURNAL; REVIEW; SINGLE STRANDED DNA BREAK; TRANSCRIPTION REGULATION;

ANIMALS; DEOXYGUANOSINE; DNA; DNA REPAIR; EPIGENESIS, GENETIC; ESTROGENS; GUANINE; HISTONES; HUMANS; METHYLATION; OXIDATION-REDUCTION; PROTEIN PROCESSING, POST-TRANSLATIONAL; PROTO-ONCOGENE PROTEINS C-MYC;

MAMMALIA;

EID: 84878569702     PISSN: 15230864     EISSN: 15577716     Source Type: Journal    
DOI: 10.1089/ars.2012.5107     Document Type: Review

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