Bis(1H-indol-2yl)methanones Are Effective Inhibitors of Mutated FLT3 Tyrosine Kinase, Overcome Resistance to PKC412A In Vitro and Show Synergy with Chemotherapy

Heidel, Florian and Mirea, Fian K. and Breitenbucher, Frank and Dove, Stefan and Huber, Christoph and Bohmer, Frank D. and Fischer, Thomas (2006) Bis(1H-indol-2yl)methanones Are Effective Inhibitors of Mutated FLT3 Tyrosine Kinase, Overcome Resistance to PKC412A In Vitro and Show Synergy with Chemotherapy. BLOOD, 108 (11): 1369. 399A. ISSN 0006-4971

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Item Type: Article
Subjects: 600 Technology > 610 Medical sciences Medicine
600 Technology > 615 Pharmacy
Divisions: Chemistry and Pharmacy > Institute of Pharmacy
Depositing User: Petra Gürster
Date Deposited: 04 Mar 2021 10:17
Last Modified: 04 Mar 2021 10:17
URI: https://pred.uni-regensburg.de/id/eprint/33759

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