Opposite roles of ERK and p38 mitogen-activated protein kinases in cadmium-induced genotoxicity and mitotic arrest

Chemical Research in Toxicology

Volumn 14, Issue 9, 2001, Pages 1193-1202

  Chao, J I ^a,b   Yang, J ^a,b  

^a NATIONAL TSING HUA UNIVERSITY   (Taiwan)

^b Hsinchu Hospital   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

2 (2 AMINO 3 METHOXYPHENYL)CHROMONE; 4 (4 FLUOROPHENYL) 2 (4 HYDROXYPHENYL) 5 (4 PYRIDYL)IMIDAZOLE; CADMIUM; CYCLIN B1; GUANINE NUCLEOTIDE BINDING PROTEIN; MITOGEN ACTIVATED PROTEIN KINASE; MITOGEN ACTIVATED PROTEIN KINASE INHIBITOR; PEROXIDE; PROTEIN CDC2; SYNAPTOPHYSIN; UNCLASSIFIED DRUG;

APOPTOSIS; ARTICLE; CELL CYCLE PHASE; CELL SURVIVAL; CELL VIABILITY; CONCENTRATION RESPONSE; CONTROLLED STUDY; CYTOTOXICITY; ENZYME ACTIVATION; FLOW CYTOMETRY; GENETIC STABILITY; GENOTOXICITY; HUMAN; HUMAN CELL; MICRONUCLEUS; MITOSIS INHIBITION; MOLECULAR STABILITY; SIGNAL TRANSDUCTION; TUMOR CELL LINE;

ADENOCARCINOMA; APOPTOSIS; CADMIUM; DNA DAMAGE; FLOW CYTOMETRY; HUMANS; LUNG NEOPLASMS; MITOGEN-ACTIVATED PROTEIN KINASES; MITOSIS; P38 MITOGEN-ACTIVATED PROTEIN KINASES; TUMOR CELLS, CULTURED;

EID: 0034808509     PISSN: 0893228X     EISSN: None     Source Type: Journal    
DOI: 10.1021/tx010041o     Document Type: Article

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