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Volumn 15, Issue 2, 1999, Pages 209-216
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The administration schedule of cyclin-dependent kinase inhibitor gene therapy and etoposide chemotherapy is a major determinant of cytotoxicity.
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Author keywords
[No Author keywords available]
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Indexed keywords
ANTINEOPLASTIC AGENT;
CDKN1A PROTEIN, HUMAN;
CYCLIN DEPENDENT KINASE;
CYCLIN DEPENDENT KINASE INHIBITOR 1A;
CYCLINE;
DNA TOPOISOMERASE (ATP HYDROLYSING);
ENZYME INHIBITOR;
ETOPOSIDE;
ARTICLE;
BONE TUMOR;
CELL CYCLE;
CELL SURVIVAL;
DNA DAMAGE;
DRUG ADMINISTRATION;
DRUG ANTAGONISM;
DRUG EFFECT;
GENE THERAPY;
GENETICS;
HUMAN;
METHODOLOGY;
OSTEOSARCOMA;
TUMOR SUPPRESSOR GENE;
ANTINEOPLASTIC AGENTS, PHYTOGENIC;
BONE NEOPLASMS;
CELL CYCLE;
CELL SURVIVAL;
CYCLIN-DEPENDENT KINASE INHIBITOR P21;
CYCLIN-DEPENDENT KINASES;
CYCLINS;
DNA DAMAGE;
DNA TOPOISOMERASES, TYPE II;
DRUG ADMINISTRATION SCHEDULE;
ENZYME INHIBITORS;
ETOPOSIDE;
GENE THERAPY;
GENES, P16;
HUMANS;
OSTEOSARCOMA;
MLCS;
MLOWN;
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EID: 0033175624
PISSN: 10196439
EISSN: None
Source Type: Journal
DOI: 10.3892/ijo.15.2.209 Document Type: Article |
Times cited : (15)
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References (0)
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