Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
19 Pt 1
pubmed:dateCreated
2005-10-5
pubmed:abstractText
Chronic myeloid leukemia (CML) is effectively treated with imatinib. However, reactivation of Bcr-Abl via kinase domain mutations that reduce sensitivity to imatinib can cause relapse. As combination therapy is frequently used to prevent emergence of resistance, the combination of imatinib with an inhibitor of imatinib-resistant Bcr-Abl mutants (e.g., Src/Abl inhibitors AP23848 and BMS-354825) was investigated.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/AP23848, http://linkedlifedata.com/resource/pubmed/chemical/Adenosine Triphosphate, http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents, http://linkedlifedata.com/resource/pubmed/chemical/Phosphotyrosine, http://linkedlifedata.com/resource/pubmed/chemical/Piperazines, http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase Inhibitors, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-abl, http://linkedlifedata.com/resource/pubmed/chemical/Pyrimidines, http://linkedlifedata.com/resource/pubmed/chemical/Thiazoles, http://linkedlifedata.com/resource/pubmed/chemical/dasatinib, http://linkedlifedata.com/resource/pubmed/chemical/imatinib, http://linkedlifedata.com/resource/pubmed/chemical/src-Family Kinases
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1078-0432
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
11
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
6987-93
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:16203792-Adenosine Triphosphate, pubmed-meshheading:16203792-Animals, pubmed-meshheading:16203792-Antineoplastic Agents, pubmed-meshheading:16203792-Cell Proliferation, pubmed-meshheading:16203792-Dose-Response Relationship, Drug, pubmed-meshheading:16203792-Drug Resistance, Neoplasm, pubmed-meshheading:16203792-Genetic Vectors, pubmed-meshheading:16203792-Hematopoietic Stem Cells, pubmed-meshheading:16203792-Humans, pubmed-meshheading:16203792-Immunoblotting, pubmed-meshheading:16203792-Inhibitory Concentration 50, pubmed-meshheading:16203792-Leukemia, Myelogenous, Chronic, BCR-ABL Positive, pubmed-meshheading:16203792-Mice, pubmed-meshheading:16203792-Mutation, pubmed-meshheading:16203792-Phosphotyrosine, pubmed-meshheading:16203792-Piperazines, pubmed-meshheading:16203792-Point Mutation, pubmed-meshheading:16203792-Protein Kinase Inhibitors, pubmed-meshheading:16203792-Protein Structure, Tertiary, pubmed-meshheading:16203792-Proto-Oncogene Proteins c-abl, pubmed-meshheading:16203792-Pyrimidines, pubmed-meshheading:16203792-Stem Cells, pubmed-meshheading:16203792-Thiazoles, pubmed-meshheading:16203792-Time Factors, pubmed-meshheading:16203792-src-Family Kinases
pubmed:year
2005
pubmed:articleTitle
Combined Abl inhibitor therapy for minimizing drug resistance in chronic myeloid leukemia: Src/Abl inhibitors are compatible with imatinib.
pubmed:affiliation
Howard Hughes Medical Institute, Oregon Health and Science University, Portland 97239, USA. oharet@ohsu.edu
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural