These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
675 related articles for article (PubMed ID: 19039322)
1. Global target profile of the kinase inhibitor bosutinib in primary chronic myeloid leukemia cells. Remsing Rix LL; Rix U; Colinge J; Hantschel O; Bennett KL; Stranzl T; Müller A; Baumgartner C; Valent P; Augustin M; Till JH; Superti-Furga G Leukemia; 2009 Mar; 23(3):477-85. PubMed ID: 19039322 [TBL] [Abstract][Full Text] [Related]
2. SKI-606, a 4-anilino-3-quinolinecarbonitrile dual inhibitor of Src and Abl kinases, is a potent antiproliferative agent against chronic myelogenous leukemia cells in culture and causes regression of K562 xenografts in nude mice. Golas JM; Arndt K; Etienne C; Lucas J; Nardin D; Gibbons J; Frost P; Ye F; Boschelli DH; Boschelli F Cancer Res; 2003 Jan; 63(2):375-81. PubMed ID: 12543790 [TBL] [Abstract][Full Text] [Related]
3. Bosutinib: a dual SRC/ABL kinase inhibitor for the treatment of chronic myeloid leukemia. Keller G; Schafhausen P; Brummendorf TH Expert Rev Hematol; 2009 Oct; 2(5):489-97. PubMed ID: 21083014 [TBL] [Abstract][Full Text] [Related]
4. Selective pyrrolo-pyrimidine inhibitors reveal a necessary role for Src family kinases in Bcr-Abl signal transduction and oncogenesis. Wilson MB; Schreiner SJ; Choi HJ; Kamens J; Smithgall TE Oncogene; 2002 Nov; 21(53):8075-88. PubMed ID: 12444544 [TBL] [Abstract][Full Text] [Related]
5. Synergism between bosutinib (SKI-606) and the Chk1 inhibitor (PF-00477736) in highly imatinib-resistant BCR/ABL⁺ leukemia cells. Nguyen T; Hawkins E; Kolluri A; Kmieciak M; Park H; Lin H; Grant S Leuk Res; 2015 Jan; 39(1):65-71. PubMed ID: 25465126 [TBL] [Abstract][Full Text] [Related]
6. In vitro and in vivo activity of SKI-606, a novel Src-Abl inhibitor, against imatinib-resistant Bcr-Abl+ neoplastic cells. Puttini M; Coluccia AM; Boschelli F; Cleris L; Marchesi E; Donella-Deana A; Ahmed S; Redaelli S; Piazza R; Magistroni V; Andreoni F; Scapozza L; Formelli F; Gambacorti-Passerini C Cancer Res; 2006 Dec; 66(23):11314-22. PubMed ID: 17114238 [TBL] [Abstract][Full Text] [Related]
7. An update on dual Src/Abl inhibitors. Musumeci F; Schenone S; Brullo C; Botta M Future Med Chem; 2012 Apr; 4(6):799-822. PubMed ID: 22530642 [TBL] [Abstract][Full Text] [Related]
8. Persistent Cdk2 inactivation drives growth arrest of BCR-ABL-expressing cells in response to dual inhibitor of SRC and ABL kinases SKI606. Mancini M; Brusa G; Zuffa E; Corrado P; Martinelli G; Grafone T; Barbieri E; Santucci MA Leuk Res; 2007 Jul; 31(7):979-87. PubMed ID: 17129604 [TBL] [Abstract][Full Text] [Related]
9. Structural and spectroscopic analysis of the kinase inhibitor bosutinib and an isomer of bosutinib binding to the Abl tyrosine kinase domain. Levinson NM; Boxer SG PLoS One; 2012; 7(4):e29828. PubMed ID: 22493660 [TBL] [Abstract][Full Text] [Related]
10. Cotreatment with vorinostat (suberoylanilide hydroxamic acid) enhances activity of dasatinib (BMS-354825) against imatinib mesylate-sensitive or imatinib mesylate-resistant chronic myelogenous leukemia cells. Fiskus W; Pranpat M; Balasis M; Bali P; Estrella V; Kumaraswamy S; Rao R; Rocha K; Herger B; Lee F; Richon V; Bhalla K Clin Cancer Res; 2006 Oct; 12(19):5869-78. PubMed ID: 17020995 [TBL] [Abstract][Full Text] [Related]
20. Three novel patient-derived BCR/ABL mutants show different sensitivity to second and third generation tyrosine kinase inhibitors. Redaelli S; Mologni L; Rostagno R; Piazza R; Magistroni V; Ceccon M; Viltadi M; Flynn D; Gambacorti-Passerini C Am J Hematol; 2012 Nov; 87(11):E125-8. PubMed ID: 23044928 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]