Mutation in the ATP-binding site of BCR-ABL in a patient with chronic myeloid leukaemia with increasing resistance to STI571
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2002.03708.x/fullpdf
Reference10 articles.
1. BCR-ABL gene mutations in relation to clinical resistance of Philadelphia-positive leukaemia to STI571;Von Bubnoff;Lancet,2002
2. The tyrosine kinase inhibitor CGP57148B selectively inhibits the growth of BCR-ABL-positive cells;Deininger;Blood,1997
3. Activity of a specific inhibitor of the BCR-ABL tyrosine kinase in the blast crisis of chronic myeloid leukemia and acute lymphoblastic leukemia with the Philadelphia chromosome;Druker;New England Journal of Medicine,2001a
4. Efficacy and safety of a specific inhibitor of the BCR-ABL tyrosine kinase in chronic myeloid leukemia;Druker;New England Journal of Medicine,2001b
5. Role of alpha1 acid glycoprotein in the in vivo resistance of human BCR-ABL (+) leukemic cells to the abl inhibitor STI571;Gambacorti-Passerini;Journal of the National Cancer Institute,2000
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