1
|
The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity.
|
Nature
|
2012
|
31.78
|
2
|
Requirement of Src kinases Lyn, Hck and Fgr for BCR-ABL1-induced B-lymphoblastic leukemia but not chronic myeloid leukemia.
|
Nat Genet
|
2004
|
3.96
|
3
|
Identification of NVP-TAE684, a potent, selective, and efficacious inhibitor of NPM-ALK.
|
Proc Natl Acad Sci U S A
|
2006
|
3.83
|
4
|
Targeting Bcr-Abl by combining allosteric with ATP-binding-site inhibitors.
|
Nature
|
2010
|
3.39
|
5
|
Synthesis, structure-activity relationships, and in vivo efficacy of the novel potent and selective anaplastic lymphoma kinase (ALK) inhibitor 5-chloro-N2-(2-isopropoxy-5-methyl-4-(piperidin-4-yl)phenyl)-N4-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diamine (LDK378) currently in phase 1 and phase 2 clinical trials.
|
J Med Chem
|
2013
|
3.27
|
6
|
Expansion of Bcr-Abl-positive leukemic stem cells is dependent on Hedgehog pathway activation.
|
Cancer Cell
|
2008
|
3.01
|
7
|
Interfering with resistance to smoothened antagonists by inhibition of the PI3K pathway in medulloblastoma.
|
Sci Transl Med
|
2010
|
2.86
|
8
|
Essential role of stromally induced hedgehog signaling in B-cell malignancies.
|
Nat Med
|
2007
|
2.62
|
9
|
An efficient rapid system for profiling the cellular activities of molecular libraries.
|
Proc Natl Acad Sci U S A
|
2006
|
2.51
|
10
|
A general strategy for creating "inactive-conformation" abl inhibitors.
|
Chem Biol
|
2006
|
2.27
|
11
|
Loss of the tumor suppressor Snf5 leads to aberrant activation of the Hedgehog-Gli pathway.
|
Nat Med
|
2010
|
1.77
|
12
|
B-Raf kinase inhibitors for cancer treatment.
|
Curr Opin Investig Drugs
|
2007
|
1.67
|
13
|
Allosteric inhibition of SHP2 phosphatase inhibits cancers driven by receptor tyrosine kinases.
|
Nature
|
2016
|
1.52
|
14
|
Protein kinase C inhibitor sotrastaurin selectively inhibits the growth of CD79 mutant diffuse large B-cell lymphomas.
|
Cancer Res
|
2011
|
1.30
|
15
|
Maintenance of adenomatous polyposis coli (APC)-mutant colorectal cancer is dependent on Wnt/beta-catenin signaling.
|
Proc Natl Acad Sci U S A
|
2011
|
1.29
|
16
|
Clinical stage EGFR inhibitors irreversibly alkylate Bmx kinase.
|
Bioorg Med Chem Lett
|
2008
|
1.17
|
17
|
Inhibitors of the Abl kinase directed at either the ATP- or myristate-binding site.
|
Biochim Biophys Acta
|
2010
|
1.16
|
18
|
The Polycomb group protein Bmi-1 is essential for the growth of multiple myeloma cells.
|
Cancer Res
|
2010
|
1.09
|
19
|
The ITK-SYK fusion oncogene induces a T-cell lymphoproliferative disease in mice mimicking human disease.
|
Cancer Res
|
2010
|
1.01
|
20
|
A type-II kinase inhibitor capable of inhibiting the T315I "gatekeeper" mutant of Bcr-Abl.
|
J Med Chem
|
2010
|
0.96
|
21
|
A conserved salt bridge in the G loop of multiple protein kinases is important for catalysis and for in vivo Lyn function.
|
Mol Cell
|
2009
|
0.96
|
22
|
The effects of Bcr-Abl on C/EBP transcription-factor regulation and neutrophilic differentiation are reversed by the Abl kinase inhibitor imatinib mesylate.
|
Blood
|
2002
|
0.93
|
23
|
Trisomy 12 and elevated GLI1 and PTCH1 transcript levels are biomarkers for Hedgehog-inhibitor responsiveness in CLL.
|
Blood
|
2011
|
0.92
|
24
|
NAMPT is the cellular target of STF-31-like small-molecule probes.
|
ACS Chem Biol
|
2014
|
0.90
|
25
|
Role of p21(WAF1/CIP1) as an attenuator of both proliferative and drug-induced apoptotic signals in BCR-ABL-transformed hematopoietic cells.
|
Ann Hematol
|
2007
|
0.88
|
26
|
Hedgehog pathway activation in chronic myeloid leukemia.
|
Cell Cycle
|
2010
|
0.88
|
27
|
Allosteric inhibition of BCR-ABL.
|
Cell Cycle
|
2010
|
0.85
|
28
|
Src family tyrosine kinases phosphorylate Flt3 on juxtamembrane tyrosines and interfere with receptor maturation in a kinase-dependent manner.
|
Ann Hematol
|
2007
|
0.79
|
29
|
Total synthesis of 6-deoxypladienolide D and Assessment of Splicing Inhibitory Activity in a Mutant SF3B1 cancer cell line.
|
Org Lett
|
2014
|
0.78
|
30
|
Measuring the tyrosine kinase activity: a review of biochemical and cellular assay technologies.
|
Expert Opin Drug Discov
|
2008
|
0.76
|