-
1
-
-
69949151386
-
Factors underlying sensitivity of cancers to small-molecule kinase inhibitors
-
Janne PA, Gray N, Settleman J (2009) Factors underlying sensitivity of cancers to small-molecule kinase inhibitors. Nat Rev Drug Discov 8: 709-723.
-
(2009)
Nat Rev Drug Discov
, vol.8
, pp. 709-723
-
-
Janne, P.A.1
Gray, N.2
Settleman, J.3
-
2
-
-
57749188299
-
Targeting cancer with small molecule kinase inhibitors
-
Zhang J, Yang PL, Gray NS (2009) Targeting cancer with small molecule kinase inhibitors. Nat Rev Cancer 9: 28-39.
-
(2009)
Nat Rev Cancer
, vol.9
, pp. 28-39
-
-
Zhang, J.1
Yang, P.L.2
Gray, N.S.3
-
3
-
-
0029947186
-
Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr-Abl positive cells
-
Druker BJ, Tamura S, Buchdunger E, Ohno S, Segal GM, et al. (1996) Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr-Abl positive cells. Nat Med 2: 561-566.
-
(1996)
Nat Med
, vol.2
, pp. 561-566
-
-
Druker, B.J.1
Tamura, S.2
Buchdunger, E.3
Ohno, S.4
Segal, G.M.5
-
4
-
-
13844251975
-
Characterization of AMN107, a selective inhibitor of native and mutant Bcr-Abl
-
Weisberg E, Manley PW, Breitenstein W, Bruggen J, Cowan-Jacob SW, et al. (2005) Characterization of AMN107, a selective inhibitor of native and mutant Bcr-Abl. Cancer Cell 7: 129-141.
-
(2005)
Cancer Cell
, vol.7
, pp. 129-141
-
-
Weisberg, E.1
Manley, P.W.2
Breitenstein, W.3
Bruggen, J.4
Cowan-Jacob, S.W.5
-
5
-
-
3142676436
-
Overriding imatinib resistance with a novel ABL kinase inhibitor
-
Shah NP, Tran C, Lee FY, Chen P, Norris D, et al. (2004) Overriding imatinib resistance with a novel ABL kinase inhibitor. Science 305: 399-401.
-
(2004)
Science
, vol.305
, pp. 399-401
-
-
Shah, N.P.1
Tran, C.2
Lee, F.Y.3
Chen, P.4
Norris, D.5
-
6
-
-
29244482571
-
Targeting the kinase activity of the BCR-ABL fusion protein in patients with chronic myeloid leukemia
-
Giles FJ, Cortes JE, Kantarjian HM (2005) Targeting the kinase activity of the BCR-ABL fusion protein in patients with chronic myeloid leukemia. Curr Mol Med 5: 615-623.
-
(2005)
Curr Mol Med
, vol.5
, pp. 615-623
-
-
Giles, F.J.1
Cortes, J.E.2
Kantarjian, H.M.3
-
7
-
-
33748885930
-
Novel tyrosine kinase inhibitors in chronic myelogenous leukemia
-
Jabbour E, Cortes J, Kantarjian H (2006) Novel tyrosine kinase inhibitors in chronic myelogenous leukemia. Curr Opin Oncol 18: 578-583.
-
(2006)
Curr Opin Oncol
, vol.18
, pp. 578-583
-
-
Jabbour, E.1
Cortes, J.2
Kantarjian, H.3
-
8
-
-
14644425319
-
Mechanisms of BCR-ABL in the pathogenesis of chronic myelogenous leukaemia
-
Ren R (2005) Mechanisms of BCR-ABL in the pathogenesis of chronic myelogenous leukaemia. Nat Rev Cancer 5: 172-183.
-
(2005)
Nat Rev Cancer
, vol.5
, pp. 172-183
-
-
Ren, R.1
-
10
-
-
0035800507
-
Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification
-
Gorre ME, Mohammed M, Ellwood K, Hsu N, Paquette R, et al. (2001) Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification. Science 293: 876-880.
-
(2001)
Science
, vol.293
, pp. 876-880
-
-
Gorre, M.E.1
Mohammed, M.2
Ellwood, K.3
Hsu, N.4
Paquette, R.5
-
11
-
-
0001686739
-
Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukemia
-
Shah NP, Nicoll JM, Nagar B, Gorre ME, Paquette RL, et al. (2002) Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukemia. Cancer Cell 2: 117-125.
-
(2002)
Cancer Cell
, vol.2
, pp. 117-125
-
-
Shah, N.P.1
Nicoll, J.M.2
Nagar, B.3
Gorre, M.E.4
Paquette, R.L.5
-
12
-
-
33845444046
-
Five-year follow-up of patients receiving imatinib for chronic myeloid leukemia
-
Druker BJ, Guilhot F, O'Brien SG, Gathmann I, Kantarjian H, et al. (2006) Five-year follow-up of patients receiving imatinib for chronic myeloid leukemia. N Engl J Med 355: 2408-2417.
-
(2006)
N Engl J Med
, vol.355
, pp. 2408-2417
-
-
Druker, B.J.1
Guilhot, F.2
O'Brien, S.G.3
Gathmann, I.4
Kantarjian, H.5
-
13
-
-
0037459344
-
Mechanisms of autoinhibition and STI-571/imatinib resistance revealed by mutagenesis of BCR-ABL
-
Azam M, Latek RR, Daley GQ (2003) Mechanisms of autoinhibition and STI-571/imatinib resistance revealed by mutagenesis of BCR-ABL. Cell 112: 831-843.
-
(2003)
Cell
, vol.112
, pp. 831-843
-
-
Azam, M.1
Latek, R.R.2
Daley, G.Q.3
-
14
-
-
34548548332
-
Crystal structure of the T315I Abl mutant in complex with the aurora kinases inhibitor PHA-739358
-
Modugno M, Casale E, Soncini C, Rosettani P, Colombo R, et al. (2007) Crystal structure of the T315I Abl mutant in complex with the aurora kinases inhibitor PHA-739358. Cancer Res 67: 7987-7990.
-
(2007)
Cancer Res
, vol.67
, pp. 7987-7990
-
-
Modugno, M.1
Casale, E.2
Soncini, C.3
Rosettani, P.4
Colombo, R.5
-
15
-
-
34548169642
-
Crystal structure of the T315I mutant of AbI kinase
-
Zhou T, Parillon L, Li F, Wang Y, Keats J, et al. (2007) Crystal structure of the T315I mutant of AbI kinase. Chem Biol Drug Des 70: 171-181.
-
(2007)
Chem Biol Drug Des
, vol.70
, pp. 171-181
-
-
Zhou, T.1
Parillon, L.2
Li, F.3
Wang, Y.4
Keats, J.5
-
16
-
-
33845806858
-
In vitro and in vivo activity of SKI-606, a novel Src-Abl inhibitor, against imatinibresistant Bcr-Abl+ neoplastic cells
-
Puttini M, Coluccia AM, Boschelli F, Cleris L, Marchesi E, et al. (2006) In vitro and in vivo activity of SKI-606, a novel Src-Abl inhibitor, against imatinibresistant Bcr-Abl+ neoplastic cells. Cancer Res 66: 11314-11322.
-
(2006)
Cancer Res
, vol.66
, pp. 11314-11322
-
-
Puttini, M.1
Coluccia, A.M.2
Boschelli, F.3
Cleris, L.4
Marchesi, E.5
-
17
-
-
19944428353
-
Discovery of N-(2-chloro-6-methyl- phenyl)-2-(6-(4-(2-hydroxyethyl)- piperazin-1-yl)-2-methylpyrimidin-4- ylamino)thiazole-5-carboxamide (BMS-354825), a dual Src/Abl kinase inhibitor with potent antitumor activity in preclinical assays
-
Lombardo LJ, Lee FY, Chen P, Norris D, Barrish JC, et al. (2004) Discovery of N-(2-chloro-6-methyl- phenyl)-2-(6-(4-(2-hydroxyethyl)- piperazin-1-yl)-2-methylpyrimidin-4- ylamino)thiazole-5-carboxamide (BMS-354825), a dual Src/Abl kinase inhibitor with potent antitumor activity in preclinical assays. J Med Chem 47: 6658-6661.
-
(2004)
J Med Chem
, vol.47
, pp. 6658-6661
-
-
Lombardo, L.J.1
Lee, F.Y.2
Chen, P.3
Norris, D.4
Barrish, J.C.5
-
18
-
-
43749086323
-
SGX393 inhibits the CML mutant Bcr-AblT315I and preempts in vitro resistance when combined with nilotinib or dasatinib
-
O'Hare T, Eide CA, Tyner JW, Corbin AS, Wong MJ, et al. (2008) SGX393 inhibits the CML mutant Bcr-AblT315I and preempts in vitro resistance when combined with nilotinib or dasatinib. Proc Natl Acad Sci U S A 105: 5507-5512.
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, pp. 5507-5512
-
-
O'Hare, T.1
Eide, C.A.2
Tyner, J.W.3
Corbin, A.S.4
Wong, M.J.5
-
19
-
-
68549115413
-
9-(Arenethenyl)purines as dual Src/Abl kinase inhibitors targeting the inactive conformation: Design, synthesis, and biological evaluation
-
Huang WS, Zhu X, Wang Y, Azam M, Wen D, et al. (2009) 9-(Arenethenyl)purines as dual Src/Abl kinase inhibitors targeting the inactive conformation: design, synthesis, and biological evaluation. J Med Chem 52: 4743-4756.
-
(2009)
J Med Chem
, vol.52
, pp. 4743-4756
-
-
Huang, W.S.1
Zhu, X.2
Wang, Y.3
Azam, M.4
Wen, D.5
-
20
-
-
65549152514
-
Equally potent inhibition of c-Src and Abl by compounds that recognize inactive kinase conformations
-
Seeliger MA, Ranjitkar P, Kasap C, Shan Y, Shaw DE, et al. (2009) Equally potent inhibition of c-Src and Abl by compounds that recognize inactive kinase conformations. Cancer Res 69: 2384-2392.
-
(2009)
Cancer Res
, vol.69
, pp. 2384-2392
-
-
Seeliger, M.A.1
Ranjitkar, P.2
Kasap, C.3
Shan, Y.4
Shaw, D.E.5
-
21
-
-
77953636478
-
Discovery of a small-molecule type II inhibitor of wild-type and gatekeeper mutants of BCRABL, PDGFRalpha, Kit, and Src kinases: Novel type II inhibitor of gatekeeper mutants
-
Weisberg E, Choi HG, Ray A, Barrett R, Zhang J, et al. (2010) Discovery of a small-molecule type II inhibitor of wild-type and gatekeeper mutants of BCRABL, PDGFRalpha, Kit, and Src kinases: novel type II inhibitor of gatekeeper mutants. Blood 115: 4206-4216.
-
(2010)
Blood
, vol.115
, pp. 4206-4216
-
-
Weisberg, E.1
Choi, H.G.2
Ray, A.3
Barrett, R.4
Zhang, J.5
-
22
-
-
70350507997
-
AP24534, a pan-BCR-ABL inhibitor for chronic myeloid leukemia, potently inhibits the T315I mutant and overcomes mutation-based resistance
-
O'Hare T, Shakespeare WC, Zhu X, Eide CA, Rivera VM, et al. (2009) AP24534, a pan-BCR-ABL inhibitor for chronic myeloid leukemia, potently inhibits the T315I mutant and overcomes mutation-based resistance. Cancer Cell 16: 401-412.
-
(2009)
Cancer Cell
, vol.16
, pp. 401-412
-
-
O'Hare, T.1
Shakespeare, W.C.2
Zhu, X.3
Eide, C.A.4
Rivera, V.M.5
-
23
-
-
47249120855
-
Inhibitors of ABL and the ABL-T315I mutation
-
Noronha G, Cao J, Chow CP, Dneprovskaia E, Fine RM, et al. (2008) Inhibitors of ABL and the ABL-T315I mutation. Curr Top Med Chem 8: 905-921.
-
(2008)
Curr Top Med Chem
, vol.8
, pp. 905-921
-
-
Noronha, G.1
Cao, J.2
Chow, C.P.3
Dneprovskaia, E.4
Fine, R.M.5
-
24
-
-
33644889108
-
Allosteric inhibitors of Bcr-abl-dependent cell proliferation
-
Adrian FJ, Ding Q, Sim T, Velentza A, Sloan C, et al. (2006) Allosteric inhibitors of Bcr-abl-dependent cell proliferation. Nat Chem Biol 2: 95-102.
-
(2006)
Nat Chem Biol
, vol.2
, pp. 95-102
-
-
Adrian, F.J.1
Ding, Q.2
Sim, T.3
Velentza, A.4
Sloan, C.5
-
25
-
-
75749146563
-
Targeting Bcr-Abl by combining allosteric with ATP-binding-site inhibitors
-
Zhang J, Adrian FJ, Jahnke W, Cowan-Jacob SW, Li AG, et al. (2010) Targeting Bcr-Abl by combining allosteric with ATP-binding-site inhibitors. Nature 463: 501-506.
-
(2010)
Nature
, vol.463
, pp. 501-506
-
-
Zhang, J.1
Adrian, F.J.2
Jahnke, W.3
Cowan-Jacob, S.W.4
Li, A.G.5
-
26
-
-
53549104402
-
Activation of tyrosine kinases by mutation of the gatekeeper threonine
-
Azam M, Seeliger MA, Gray NS, Kuriyan J, Daley GQ (2008) Activation of tyrosine kinases by mutation of the gatekeeper threonine. Nat Struct Mol Biol 15: 1109-1118.
-
(2008)
Nat Struct Mol Biol
, vol.15
, pp. 1109-1118
-
-
Azam, M.1
Seeliger, M.A.2
Gray, N.S.3
Kuriyan, J.4
Daley, G.Q.5
-
27
-
-
60849134578
-
Conformational disturbance in Abl kinase upon mutation and deregulation
-
Iacob RE, Pene-Dumitrescu T, Zhang J, Gray NS, Smithgall TE, et al. (2009) Conformational disturbance in Abl kinase upon mutation and deregulation. Proc Natl Acad Sci U S A 106: 1386-1391.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 1386-1391
-
-
Iacob, R.E.1
Pene-Dumitrescu, T.2
Zhang, J.3
Gray, N.S.4
Smithgall, T.E.5
-
28
-
-
0023571161
-
Nucleotide sequence of testis-derived c-abl cDNAs: Implications for testis-specific transcription and abl oncogene activation
-
Oppi C, Shore SK, Reddy EP (1987) Nucleotide sequence of testis-derived c-abl cDNAs: implications for testis-specific transcription and abl oncogene activation. Proc Natl Acad Sci U S A 84: 8200-8204.
-
(1987)
Proc Natl Acad Sci U S A
, vol.84
, pp. 8200-8204
-
-
Oppi, C.1
Shore, S.K.2
Reddy, E.P.3
-
29
-
-
28844458822
-
High yield bacterial expression of active c-Abl and c-Src tyrosine kinases
-
Seeliger MA, Young M, Henderson MN, Pellicena P, King DS, et al. (2005) High yield bacterial expression of active c-Abl and c-Src tyrosine kinases. Protein Sci 14: 3135-3139.
-
(2005)
Protein Sci
, vol.14
, pp. 3135-3139
-
-
Seeliger, M.A.1
Young, M.2
Henderson, M.N.3
Pellicena, P.4
King, D.S.5
-
30
-
-
51549121010
-
High-speed and highresolution UPLC separation at zero degrees Celsius
-
Wales TE, Fadgen KE, Gerhardt GC, Engen JR (2008) High-speed and highresolution UPLC separation at zero degrees Celsius. Anal Chem 80: 6815-6820.
-
(2008)
Anal Chem
, vol.80
, pp. 6815-6820
-
-
Wales, T.E.1
Fadgen, K.E.2
Gerhardt, G.C.3
Engen, J.R.4
-
31
-
-
33644761306
-
Hydrogen exchange mass spectrometry for the analysis of protein dynamics
-
Wales TE, Engen JR (2006) Hydrogen exchange mass spectrometry for the analysis of protein dynamics. Mass Spectrom Rev 25: 158-170.
-
(2006)
Mass Spectrom Rev
, vol.25
, pp. 158-170
-
-
Wales, T.E.1
Engen, J.R.2
-
32
-
-
0020855355
-
Hydrogen exchange and structural dynamics of proteins and nucleic acids
-
Englander SW, Kallenbach NR (1983) Hydrogen exchange and structural dynamics of proteins and nucleic acids. Q Rev Biophys 16: 521-655.
-
(1983)
Q Rev Biophys
, vol.16
, pp. 521-655
-
-
Englander, S.W.1
Kallenbach, N.R.2
-
33
-
-
33751337111
-
Semi-automated data processing of hydrogen exchange mass spectra using HX-Express
-
Weis DD, Engen JR, Kass IJ (2006) Semi-automated data processing of hydrogen exchange mass spectra using HX-Express. J Am Soc Mass Spectrom 17: 1700-1703.
-
(2006)
J Am Soc Mass Spectrom
, vol.17
, pp. 1700-1703
-
-
Weis, D.D.1
Engen, J.R.2
Kass, I.J.3
-
34
-
-
33745777632
-
UPLC/MS(E); a new approach for generating molecular fragment information for biomarker structure elucidation
-
Plumb RS, Johnson KA, Rainville P, Smith BW, Wilson ID, et al. (2006) UPLC/MS(E); a new approach for generating molecular fragment information for biomarker structure elucidation. Rapid Commun Mass Spectrom 20: 1989-1994.
-
(2006)
Rapid Commun Mass Spectrom
, vol.20
, pp. 1989-1994
-
-
Plumb, R.S.1
Johnson, K.A.2
Rainville, P.3
Smith, B.W.4
Wilson, I.D.5
-
35
-
-
15744380263
-
Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibition
-
Ohren JF, Chen H, Pavlovsky A, Whitehead C, Zhang E, et al. (2004) Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibition. Nat Struct Mol Biol 11: 1192-1197.
-
(2004)
Nat Struct Mol Biol
, vol.11
, pp. 1192-1197
-
-
Ohren, J.F.1
Chen, H.2
Pavlovsky, A.3
Whitehead, C.4
Zhang, E.5
-
36
-
-
77954615408
-
MK-2206, an allosteric Akt inhibitor, enhances antitumor efficacy by standard chemotherapeutic agents or molecular targeted drugs in vitro and in vivo
-
Hirai H, Sootome H, Nakatsuru Y, Miyama K, Taguchi S, et al. (2010) MK-2206, an allosteric Akt inhibitor, enhances antitumor efficacy by standard chemotherapeutic agents or molecular targeted drugs in vitro and in vivo. Mol Cancer Ther 9: 1956-1967.
-
(2010)
Mol Cancer Ther
, vol.9
, pp. 1956-1967
-
-
Hirai, H.1
Sootome, H.2
Nakatsuru, Y.3
Miyama, K.4
Taguchi, S.5
-
37
-
-
0001640528
-
Di- and triphosphopyridine nucleotide isocitric dehydrogenases in yeast
-
Kornberg A, Pricer WE, Jr. (1951) Di- and triphosphopyridine nucleotide isocitric dehydrogenases in yeast. J Biol Chem 189: 123-136.
-
(1951)
J Biol Chem
, vol.189
, pp. 123-136
-
-
Kornberg, A.1
Pricer Jr., W.E.2
-
38
-
-
33745283618
-
The structure of Dasatinib (BMS-354825) bound to activated ABL kinase domain elucidates its inhibitory activity against imatinib-resistant ABL mutants
-
Tokarski JS, Newitt JA, Chang CY, Cheng JD, Wittekind M, et al. (2006) The structure of Dasatinib (BMS-354825) bound to activated ABL kinase domain elucidates its inhibitory activity against imatinib-resistant ABL mutants. Cancer Res 66: 5790-5797.
-
(2006)
Cancer Res
, vol.66
, pp. 5790-5797
-
-
Tokarski, J.S.1
Newitt, J.A.2
Chang, C.Y.3
Cheng, J.D.4
Wittekind, M.5
-
39
-
-
33750989362
-
2-aminothiazole as a novel kinase inhibitor template. Structure-activity relationship studies toward the discovery of N-(2-chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1- piperazinyl)]-2-methyl-4-pyrimidinyl]amino)]-1,3-thiazole-5-carboxamide (dasatinib, BMS-354825) as a potent pan-Src kinase inhibitor
-
Das J, Chen P, Norris D, Padmanabha R, Lin J, et al. (2006) 2-aminothiazole as a novel kinase inhibitor template. Structure-activity relationship studies toward the discovery of N-(2-chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1- piperazinyl)]-2-methyl-4-pyrimidinyl]amino)]-1,3-thiazole-5-carboxamide (dasatinib, BMS-354825) as a potent pan-Src kinase inhibitor. J Med Chem 49: 6819-6832.
-
(2006)
J Med Chem
, vol.49
, pp. 6819-6832
-
-
Das, J.1
Chen, P.2
Norris, D.3
Padmanabha, R.4
Lin, J.5
-
40
-
-
49649108911
-
Solution conformations and dynamics of ABL kinase-inhibitor complexes determined by NMR substantiate the different binding modes of imatinib/nilotinib and dasatinib
-
Vajpai N, Strauss A, Fendrich G, Cowan-Jacob SW, Manley PW, et al. (2008) Solution conformations and dynamics of ABL kinase-inhibitor complexes determined by NMR substantiate the different binding modes of imatinib/nilotinib and dasatinib. J Biol Chem 283: 18292-18302.
-
(2008)
J Biol Chem
, vol.283
, pp. 18292-18302
-
-
Vajpai, N.1
Strauss, A.2
Fendrich, G.3
Cowan-Jacob, S.W.4
Manley, P.W.5
-
41
-
-
33947384902
-
In silico profiling of tyrosine kinases binding specificity and drug resistance using Monte Carlo simulations with the ensembles of protein kinase crystal structures
-
Verkhivker GM (2007) In silico profiling of tyrosine kinases binding specificity and drug resistance using Monte Carlo simulations with the ensembles of protein kinase crystal structures. Biopolymers 85: 333-348.
-
(2007)
Biopolymers
, vol.85
, pp. 333-348
-
-
Verkhivker, G.M.1
-
42
-
-
0030199899
-
Mass spectrometric determination of isotopic exchange rates of amide hydrogens located on the surfaces of proteins
-
Dharmasiri K, Smith DL (1996) Mass spectrometric determination of isotopic exchange rates of amide hydrogens located on the surfaces of proteins. Anal Chem 68: 2340-2344.
-
(1996)
Anal Chem
, vol.68
, pp. 2340-2344
-
-
Dharmasiri, K.1
Smith, D.L.2
-
43
-
-
75749148378
-
Investigating solution-phase protein structure and dynamics by hydrogen exchange mass spectrometry
-
Morgan CR, Engen JR (2009) Investigating solution-phase protein structure and dynamics by hydrogen exchange mass spectrometry. Curr Protoc Protein Sci Chapter 17: Unit 17 16: 11-17.
-
(2009)
Curr Protoc Protein Sci Chapter 17: Unit
, vol.17
, Issue.16
, pp. 11-17
-
-
Morgan, C.R.1
Engen, J.R.2
-
44
-
-
70350365399
-
Nmyristoylated c-Abl tyrosine kinase localizes to the endoplasmic reticulum upon binding to an allosteric inhibitor
-
Choi Y, Seeliger MA, Panjarian SB, Kim H, Deng X, et al. (2009) Nmyristoylated c-Abl tyrosine kinase localizes to the endoplasmic reticulum upon binding to an allosteric inhibitor. J Biol Chem 284: 29005-29014.
-
(2009)
J Biol Chem
, vol.284
, pp. 29005-29014
-
-
Choi, Y.1
Seeliger, M.A.2
Panjarian, S.B.3
Kim, H.4
Deng, X.5
-
45
-
-
33644871166
-
Organization of the SH3-SH2 unit in active and inactive forms of the c-Abl tyrosine kinase
-
Nagar B, Hantschel O, Seeliger M, Davies JM, Weis WI, et al. (2006) Organization of the SH3-SH2 unit in active and inactive forms of the c-Abl tyrosine kinase. Mol Cell 21: 787-798.
-
(2006)
Mol Cell
, vol.21
, pp. 787-798
-
-
Nagar, B.1
Hantschel, O.2
Seeliger, M.3
Davies, J.M.4
Weis, W.I.5
-
46
-
-
31644438945
-
Structure of the kinase domain of an imatinib-resistant Abl mutant in complex with the Aurora kinase inhibitor VX-680
-
Young MA, Shah NP, Chao LH, Seeliger M, Milanov ZV, et al. (2006) Structure of the kinase domain of an imatinib-resistant Abl mutant in complex with the Aurora kinase inhibitor VX-680. Cancer Res 66: 1007-1014.
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(2006)
Cancer Res
, vol.66
, pp. 1007-1014
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Young, M.A.1
Shah, N.P.2
Chao, L.H.3
Seeliger, M.4
Milanov, Z.V.5
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