Formation and longevity of idarubicin-induced DNA topoisomerase II cleavable complexes in K562 human leukaemia cells-Reference-Cited by-同舟云学术

Formation and longevity of idarubicin-induced DNA topoisomerase II cleavable complexes in K562 human leukaemia cells

Published:2002-05 Issue:10 Volume:63 Page:1807-1815
ISSN:0006-2952
Container-title:Biochemical Pharmacology
language:en
Short-container-title:Biochemical Pharmacology

Author:

Willmore Elaine,Errington Fiona,Tilby Michael J.,Austin Caroline A.

Publisher

Elsevier BV

Subject

Pharmacology,Biochemistry

Reference42 articles.

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3. The use of an oral chemotherapy (idarubicin and etoposide) in the treatment of acute myeloid leukaemia in the elderly: a report of toxicity and efficacy;Jackson;Leukaemia,1997

4. Idarubicin: a brief overview on pharmacology and clinical use;Borchmann;Int. J. Clin. Pharmacol. Ther.,1997

5. Comparative evaluation of the intracellular accumulation and DNA binding of idarubicin and daunorubicin in sensitive and multidrug-resistant human leukaemia K562 cells;Bogush;Anticancer Res.,1996

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