Titanium dioxide particles phosphorylate histone H2AX independent of ROS production

Mutation Research - Genetic Toxicology and Environmental Mutagenesis

Volumn 742, Issue 1-2, 2012, Pages 84-91

  Toyooka, Tatsushi ^a   Amano, Takeharu ^a   Ibuki, Yuko ^a  

^a UNIVERSITY OF SHIZUOKA   (Japan)

Author keywords

H2AX; Nanoparticles; Nanotoxicity; ROS; TiO 2

Indexed keywords

DNA; HISTONE H2AX; HYDROGEN PEROXIDE; PHOSPHORYLATED HISTONE H2AX; REACTIVE OXYGEN METABOLITE; SERUM ALBUMIN; TITANIUM DIOXIDE; UNCLASSIFIED DRUG;

ARTICLE; CANCER CELL CULTURE; CELL CYCLE PHASE; CONTROLLED STUDY; DNA DAMAGE; FLOW CYTOMETRY; GENOTOXICITY; HUMAN; HUMAN CELL; LUNG ADENOCARCINOMA; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN PHOSPHORYLATION;

BIOLOGICAL MARKERS; CELL CYCLE; CELL LINE, TUMOR; DNA DAMAGE; HISTONES; HUMANS; NANOPARTICLES; PARTICLE SIZE; PHOSPHORYLATION; REACTIVE OXYGEN SPECIES; TITANIUM;

BOVINAE;

EID: 84856079653     PISSN: 13835718     EISSN: 18793592     Source Type: Journal    
DOI: 10.1016/j.mrgentox.2011.12.015     Document Type: Article

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