-
1
-
-
17144405643
-
Mitotic kinesins: prospects for antimitotic drug discovery
-
Bergnes, G., Brejc, K., and Belmont, L. (2005). Mitotic kinesins: prospects for antimitotic drug discovery. Curr Top Med Chem. 5 (2), 127-145.
-
(2005)
Curr Top Med Chem.
, vol.5
, Issue.2
, pp. 127-145
-
-
Bergnes, G.1
Brejc, K.2
Belmont, L.3
-
3
-
-
0032100685
-
A homologue of Drosophila aurora kinase is oncogenic and amplified in human colorectal cancers
-
Bischoff, J. R., Anderson, L., Zhu, Y., et al. (1998). A homologue of Drosophila aurora kinase is oncogenic and amplified in human colorectal cancers. EMBO J. 17 (11), 3052-3065.
-
(1998)
EMBO J.
, vol.17
, Issue.11
, pp. 3052-3065
-
-
Bischoff, J.R.1
Anderson, L.2
Zhu, Y.3
-
4
-
-
3042716081
-
A single amino acid exchange inverts susceptibility of related receptor tyrosine kinases for the ATP site inhibitor STI-571
-
Böhmer, F. D., Karagyozov, L., Uecker, A., et al. (2003). A single amino acid exchange inverts susceptibility of related receptor tyrosine kinases for the ATP site inhibitor STI-571. J Biol Chem. 278 (7), 5148-5155.
-
(2003)
J Biol Chem.
, vol.278
, Issue.7
, pp. 5148-5155
-
-
Böhmer, F.D.1
Karagyozov, L.2
Uecker, A.3
-
5
-
-
33847724638
-
Aurora-A regulation of nuclear factor-kappaB signaling by phosphorylation of IkappaBalpha
-
Briassouli, P., Chan, F., Savage, K., et al. (2007). Aurora-A regulation of nuclear factor-kappaB signaling by phosphorylation of IkappaBalpha. Cancer Res. 67 (4), 1689-1695.
-
(2007)
Cancer Res.
, vol.67
, Issue.4
, pp. 1689-1695
-
-
Briassouli, P.1
Chan, F.2
Savage, K.3
-
6
-
-
39049166077
-
Aurora kinase inhibitors: identification and preclinical validation of their biomarkers
-
Carpinelli, P., and Moll, J. (2008). Aurora kinase inhibitors: identification and preclinical validation of their biomarkers. Expert Opin Ther Targets. 12 (1), 69-80.
-
(2008)
Expert Opin Ther Targets.
, vol.12
, Issue.1
, pp. 69-80
-
-
Carpinelli, P.1
Moll, J.2
-
7
-
-
37549071104
-
PHA-739358, a potent inhibitor of Aurora kinases with a selective target inhibition profile relevant to cancer
-
Carpinelli, P., Ceruti, R., Giorgini, M. L., et al. (2007). PHA-739358, a potent inhibitor of Aurora kinases with a selective target inhibition profile relevant to cancer. Mol Cancer Ther. 6 (12 Pt 1), 3158-3168.
-
(2007)
Mol Cancer Ther.
, vol.6
, Issue.1-12 PT
, pp. 3158-3168
-
-
Carpinelli, P.1
Ceruti, R.2
Giorgini, M.L.3
-
8
-
-
34247615972
-
Structural basis for potent inhibition of the Aurora kinases and a T315I multi-drug resistant mutant form of Abl kinase by VX-680
-
Cheetham, G. M., Charlton, P. A., Golec, J. M., et al. (2007). Structural basis for potent inhibition of the Aurora kinases and a T315I multi-drug resistant mutant form of Abl kinase by VX-680. Cancer Lett. 251 (2), 323-329.
-
(2007)
Cancer Lett.
, vol.251
, Issue.2
, pp. 323-329
-
-
Cheetham, G.M.1
Charlton, P.A.2
Golec, J.M.3
-
9
-
-
59349101062
-
Phase I study of the pan aurora kinases (AKs) inhibitor PHA-739358 administered as a 24 h infusion without/ with G-CSF in a 14-day cycle in patients with advanced solid tumors
-
Cohen, R. B., Jones, S. F., von Mehren, M., et al. (2008). Phase I study of the pan aurora kinases (AKs) inhibitor PHA-739358 administered as a 24 h infusion without/ with G-CSF in a 14-day cycle in patients with advanced solid tumors. J Clin Oncol. 26(Suppl), Abst 2520.
-
(2008)
J Clin Oncol
, vol.14
, Issue.9
, pp. 969-985
-
-
Cohen, R.B.1
Jones, S.F.2
Von Mehren, M.3
-
10
-
-
34247612847
-
Targeting cell cycle kinases for cancer therapy
-
De Carcer, G., Perez de Castro, I., and Malumbres, M. (2007). Targeting cell cycle kinases for cancer therapy. Curr Med Chem. 14 (9), 969-985.
-
(2007)
Curr Med Chem.
, vol.14
, Issue.9
, pp. 969-985
-
-
De Carcer, G.1
Perez De Castro, I.2
Malumbres, M.3
-
11
-
-
65349152111
-
Phase I study of the Aurora kinases (AKs) inhibitor PHA-739358 administered as a 6 and 3-h IV infusion on days 1, 8, 15 every 4 wks in patients with advanced solid tumors
-
De Jonge, M., Steeghs, N., Verweij, J., et al. (2008). Phase I study of the Aurora kinases (AKs) inhibitor PHA-739358 administered as a 6 and 3-h IV infusion on days 1, 8, 15 every 4 wks in patients with advanced solid tumors. J Clin Oncol. 26 (Suppl), Abst 3507.
-
(2008)
J Clin Oncol.
, vol.26
, Issue.SUPPL
, pp. 3507
-
-
Jonge, D.M.1
Steeghs, N.2
Verweij, J.3
-
12
-
-
1542287231
-
Tension between two kinetochores suffices for their bi-orientation on the mitotic spindle
-
Dewar, H., Tanaka, K., Nasmyth, K., et al. (2004). Tension between two kinetochores suffices for their bi-orientation on the mitotic spindle. Nature. 428 (6978), 93-97.
-
(2004)
Nature.
, vol.428
, Issue.6978
, pp. 93-97
-
-
Dewar, H.1
Tanaka, K.2
Nasmyth, K.3
-
13
-
-
24944573674
-
Aurora-A/STK15 T+91A is a general low penetrance cancer susceptibility gene: a meta-analysis of multiple cancer types
-
Ewart-Toland, A., Dai, Q., Gao, Y. T., et al. (2005). Aurora-A/STK15 T+91A is a general low penetrance cancer susceptibility gene: a meta-analysis of multiple cancer types. Carcinogenesis. 26 (8), 1368-1373.
-
(2005)
Carcinogenesis.
, vol.26
, Issue.8
, pp. 1368-1373
-
-
Ewart-Toland, A.1
Dai, Q.2
Gao, Y.T.3
-
15
-
-
20944437351
-
Potent and selective Aurora inhibitors identified by the expansion of a novel scaffold for protein kinase inhibition
-
Fancelli, D., Berta, D., Bindi, S., et al. (2005a). Potent and selective Aurora inhibitors identified by the expansion of a novel scaffold for protein kinase inhibition. J Med Chem. 48 (8), 3080-3084.
-
(2005)
J Med Chem.
, vol.48
, Issue.8
, pp. 3080-3084
-
-
Fancelli, D.1
Berta, D.2
Bindi, S.3
-
17
-
-
33845367377
-
1,4,5,6-Tetrahydropyrrolo[3,4-c ]pyrazoles:identification of a potent Aurora kinase inhibitor with a favorable antitumor kinase inhibition profile
-
Fancelli, D., Moll, J., Varasi, M., et al. (2006). 1,4,5,6-Tetrahydropyrrolo[3,4-c ]pyrazoles:identification of a potent Aurora kinase inhibitor with a favorable antitumor kinase inhibition profile. J Med Chem. 49 (24), 7247-7251.
-
(2006)
J Med Chem.
, vol.49
, Issue.24
, pp. 7247-7251
-
-
Fancelli, D.1
Moll, J.2
Varasi, M.3
-
18
-
-
33846988313
-
Roles of Aurora kinases in mitosis and tumorigenesis
-
Fu, J., Bian, M., Jiang, Q., et al. (2007). Roles of Aurora kinases in mitosis and tumorigenesis . Mol Cancer Res. 5 (1), 1-10.
-
(2007)
Mol Cancer Res.
, vol.5
, Issue.1
, pp. 1-10
-
-
Fu, J.1
Bian, M.2
Jiang, Q.3
-
19
-
-
45749115811
-
Midzone activation of Aurora B in anaphase produces an intracellular phosphorylation gradient
-
Fuller, B. G., Lampson, M. A., Foley, E. A., et al. (2008). Midzone activation of Aurora B in anaphase produces an intracellular phosphorylation gradient. Nature. 453 (7198), 1132-1136.
-
(2008)
Nature.
, vol.453
, Issue.7198
, pp. 1132-1136
-
-
Fuller, B.G.1
Lampson, M.A.2
Foley, E.A.3
-
20
-
-
41549122837
-
Aurora kinases as anticancer drug targets
-
Gautschi, O., Heighway, J., Mack, P. C., et al. (2008). Aurora kinases as anticancer drug targets. Clin Cancer Res. 14 (6), 1639-1648.
-
(2008)
Clin Cancer Res.
, vol.14
, Issue.6
, pp. 1639-1648
-
-
Gautschi, O.1
Heighway, J.2
Mack, P.C.3
-
21
-
-
33846240316
-
MK-0457, a novel kinase inhibitor, is active in patients with chronic myeloid leukemia or acute lymphocytic leukemia with the T315I BCR-ABL mutation
-
Giles, F. J., Cortes, J., Jones, D., et al. (2007). MK-0457, a novel kinase inhibitor, is active in patients with chronic myeloid leukemia or acute lymphocytic leukemia with the T315I BCR-ABL mutation. Blood. 109 (2), 500-502.
-
(2007)
Blood.
, vol.109
, Issue.2
, pp. 500-502
-
-
Giles, F.J.1
Cortes, J.2
Jones, D.3
-
22
-
-
0028938482
-
Mutations in Aurora prevent centrosome separation leading to the formation of monopolar spindles
-
Glover, D. M., Leibowitz, M. H., McLean, D. A., et al. (1995). Mutations in Aurora prevent centrosome separation leading to the formation of monopolar spindles. Cell. 81 (1), 95-105.
-
(1995)
Cell.
, vol.81
, Issue.1
, pp. 95-105
-
-
Glover, D.M.1
Leibowitz, M.H.2
McLean, D.A.3
-
23
-
-
43249111278
-
Simultaneous targeting of Aurora kinases and Bcr-Abl kinase by the small molecule inhibitor PHA-739358 is effective against imatinib-resistant BCR-ABL mutations including T315I
-
Gontarewicz, A., Balabanov, S., Keller, G., et al. (2008). Simultaneous targeting of Aurora kinases and Bcr-Abl kinase by the small molecule inhibitor PHA-739358 is effective against imatinib-resistant BCR-ABL mutations including T315I. Blood. 111 (8), 4355-4364.
-
(2008)
Blood.
, vol.111
, Issue.8
, pp. 4355-4364
-
-
Gontarewicz, A.1
Balabanov, S.2
Keller, G.3
-
24
-
-
0035962664
-
Histone H3 phosphorylation and cell division
-
Hans, F., and Dimitrov, S. (2001). Histone H3 phosphorylation and cell division. Oncogene. 20 (24), 3021-3027.
-
(2001)
Oncogene.
, vol.20
, Issue.24
, pp. 3021-3027
-
-
Hans, F.1
Dimitrov, S.2
-
25
-
-
2342639645
-
VX-680, a potent and selective small-molecule inhibitor of the Aurora kinases, suppresses tumor growth in vivo
-
Harrington, E. A., Bebbington, D., Moore, J., et al. (2004). VX-680, a potent and selective small-molecule inhibitor of the Aurora kinases, suppresses tumor growth in vivo. Nat Med. 10 (3), 262-267.
-
(2004)
Nat Med.
, vol.10
, Issue.3
, pp. 262-267
-
-
Harrington, E.A.1
Bebbington, D.2
Moore, J.3
-
26
-
-
0141429171
-
Aurora-A and an interacting activator, the LIM protein Ajuba, are required for mitotic commitment in human cells
-
Hirota, T., Kunitoku, N., Sasayama, T., et al. (2003). Aurora-A and an interacting activator, the LIM protein Ajuba, are required for mitotic commitment in human cells. Cell. 114 (5), 585-598.
-
(2003)
Cell.
, vol.114
, Issue.5
, pp. 585-598
-
-
Hirota, T.1
Kunitoku, N.2
Sasayama, T.3
-
27
-
-
38349016567
-
Targeted therapy in chronic myeloid leukemia
-
Jabbour, E., Cortes, J. E., Ghanem, H., O ' Brien, S., and Kantarjian, H. M. (2008). Targeted therapy in chronic myeloid leukemia. Expert Rev Anticancer Ther. 8 (1), 99-110.
-
(2008)
Expert Rev Anticancer Ther.
, vol.8
, Issue.1
, pp. 99-110
-
-
Jabbour, E.1
Cortes, J.E.2
Ghanem, H.3
O'Brien, S.4
Kantarjian, H.M.5
-
28
-
-
0036045353
-
Fibroblast growth factors in cancer: therapeutic possibilities
-
Jeffers, M., LaRochelle, W. J., and Lichenstein, H. S. (2002). Fibroblast growth factors in cancer: therapeutic possibilities. Expert Opin Ther Targets. 6 (4), 469-482.
-
(2002)
Expert Opin Ther Targets.
, vol.6
, Issue.4
, pp. 469-482
-
-
Jeffers, M.1
LaRochelle, W.J.2
Lichenstein, H.S.3
-
29
-
-
0036083301
-
Mechanism of action of antitumor drugs that interact with microtubules and tubulin
-
Jordan, M. A. (2002). Mechanism of action of antitumor drugs that interact with microtubules and tubulin. Curr Med Chem Anticancer Agents. 2 (1), 1-17.
-
(2002)
Curr Med Chem Anticancer Agents.
, vol.2
, Issue.1
, pp. 1-17
-
-
Jordan, M.A.1
-
30
-
-
1942438028
-
Microtubules as a target for anticancer drugs
-
Jordan, M. A., and Wilson, L. (2004). Microtubules as a target for anticancer drugs. Nat Rev Cancer. 4 (4), 253-265.
-
(2004)
Nat Rev Cancer.
, vol.4
, Issue.4
, pp. 253-265
-
-
Jordan, M.A.1
Wilson, L.2
-
31
-
-
0038341158
-
The Aurora kinases: role in cell transformation and tumorigenesis
-
Katayama, H., Brinkley, W. R., and Sen, S. (2003). The Aurora kinases: role in cell transformation and tumorigenesis. Cancer Metastasis Rev. 22 (4), 451-464.
-
(2003)
Cancer Metastasis Rev.
, vol.22
, Issue.4
, pp. 451-464
-
-
Katayama, H.1
Brinkley, W.R.2
Sen, S.3
-
32
-
-
9144251019
-
Phosphorylation by Aurora kinase A induces Mdm2-mediated destabilization and inhibition of p53
-
Katayama, H., Sasai, K., Kawai, H., et al. (2004). Phosphorylation by Aurora kinase A induces Mdm2-mediated destabilization and inhibition of p53. Nat Genet. 36 (1), 55-62.
-
(2004)
Nat Genet.
, vol.36
, Issue.1
, pp. 55-62
-
-
Katayama, H.1
Sasai, K.2
Kawai, H.3
-
33
-
-
0141768273
-
Function and regulation of Aurora/Ipl1p kinase family in cell division
-
Ke, Y. W., Dou, Z., Zhang, J., and Yao, X. B. (2003). Function and regulation of Aurora/Ipl1p kinase family in cell division. Cell Res. 13 (2), 69-81.
-
(2003)
Cell Res.
, vol.13
, Issue.2
, pp. 69-81
-
-
Ke, Y.W.1
Dou, Z.2
Zhang, J.3
Yao, X.B.4
-
34
-
-
13844317894
-
EGFR mutation and resistance of non-small-cell lung cancer to gefitinib
-
Kobayashi, S., Boggon, T. J., Dayaram, T., et al. (2005). EGFR mutation and resistance of non-small-cell lung cancer to gefitinib. N Engl J Med. 352 (8), 786-792.
-
(2005)
N Engl J Med.
, vol.352
, Issue.8
, pp. 786-792
-
-
Kobayashi, S.1
Boggon, T.J.2
Dayaram, T.3
-
35
-
-
17744373695
-
The RET proto-oncogene: a molecular therapeutic target in thyroid cancer
-
Kodama, Y., Asai, N., Kawai, K., et al. (2005). The RET proto-oncogene: a molecular therapeutic target in thyroid cancer. Cancer Sci. 96 (3), 143-148.
-
(2005)
Cancer Sci.
, vol.96
, Issue.3
, pp. 143-148
-
-
Kodama, Y.1
Asai, N.2
Kawai, K.3
-
36
-
-
0037135979
-
Human TPX2 is required for targeting Aurora-A kinase to the spindle
-
Kufer, T. A., Sillje, H. H., Korner, R., et al. (2002). Human TPX2 is required for targeting Aurora-A kinase to the spindle. J Cell Biol. 158 (4), 617-623.
-
(2002)
J Cell Biol.
, vol.158
, Issue.4
, pp. 617-623
-
-
Kufer, T.A.1
Sillje, H.H.2
Korner, R.3
-
37
-
-
10644227569
-
Aurora-A abrogation of p53 DNA binding and transactivation activity by phosphorylation of serine 215
-
Liu, Q., Kaneko, S., Yang, L., et al. (2004). Aurora-A abrogation of p53 DNA binding and transactivation activity by phosphorylation of serine 215. J Biol Chem. 279 (50), 52175-52182.
-
(2004)
J Biol Chem.
, vol.279
, Issue.50
, pp. 52175-52182
-
-
Liu, Q.1
Kaneko, S.2
Yang, L.3
-
38
-
-
34247259822
-
Antitumor activity of MLN8054, an orally active small-molecule inhibitor of Aurora A kinase
-
Manfredi, M. G., Ecsedy, J. A., Meetze, K. A., et al. (2007). Antitumor activity of MLN8054, an orally active small-molecule inhibitor of Aurora A kinase. Proc Natl Acad Sci USA. 104 (10), 4106-4111.
-
(2007)
Proc Natl Acad Sci USA.
, vol.104
, Issue.10
, pp. 4106-4111
-
-
Manfredi, M.G.1
Ecsedy, J.A.2
Meetze, K.A.3
-
39
-
-
34548548332
-
Crystal structure of the T315I Abl mutant in complex with the Aurora kinases inhibitor PHA-739358
-
Modugno, M., Casale, E., Soncini, C., et al. (2007). Crystal structure of the T315I Abl mutant in complex with the Aurora kinases inhibitor PHA-739358. Cancer Res. 67 (17), 7987-7990.
-
(2007)
Cancer Res.
, vol.67
, Issue.17
, pp. 7987-7990
-
-
Modugno, M.1
Casale, E.2
Soncini, C.3
-
40
-
-
34347405054
-
Maximal chromosome compaction occurs by axial shortening in anaphase and depends on Aurora kinase
-
Mora-Bermúdez, F., Gerlich, D., and Ellenberg, J. (2007). Maximal chromosome compaction occurs by axial shortening in anaphase and depends on Aurora kinase. Nat Cell Biol. 9 (7), 822-831.
-
(2007)
Nat Cell Biol.
, vol.9
, Issue.7
, pp. 822-831
-
-
Mora-Bermúdez, F.1
Gerlich, D.2
Ellenberg, J.3
-
41
-
-
0037018843
-
The kinase activity of Aurora B is required for kinetochore-microtubule interactions during mitosis
-
Murata-Hori, M., and Wang, Y. L. (2002). The kinase activity of Aurora B is required for kinetochore-microtubule interactions during mitosis. Curr Biol. 12 (11), 894-899.
-
(2002)
Curr Biol.
, vol.12
, Issue.11
, pp. 894-899
-
-
Murata-Hori, M.1
Wang, Y.L.2
-
42
-
-
0038156100
-
Mutation, SNP, and isoform analysis of fibroblast growth factor receptor 3 (FGFR3) in 150 newly diagnosed multiple myeloma patients
-
Onwuazor, O. N., Wen, X. Y., Wang, D. Y., et al. (2003). Mutation, SNP, and isoform analysis of fibroblast growth factor receptor 3 (FGFR3) in 150 newly diagnosed multiple myeloma patients. Blood. 102 (2), 772-773.
-
(2003)
Blood.
, vol.102
, Issue.2
, pp. 772-773
-
-
Onwuazor, O.N.1
Wen, X.Y.2
Wang, D.Y.3
-
43
-
-
2942522534
-
3-Aminopyrazole inhibitors of CDK2/cyclin A as antitumor agents
-
Pevarello, P., Brasca, M. G., Amici, R., et al. (2004). 3-Aminopyrazole inhibitors of CDK2/cyclin A as antitumor agents. 1. Lead finding. J Med Chem. 47 (13), 3367-3380.
-
(2004)
1. Lead finding. J Med Chem.
, vol.47
, Issue.13
, pp. 3367-3380
-
-
Pevarello, P.1
Brasca, M.G.2
Amici, R.3
-
44
-
-
33645220356
-
HEF1-Aurora A interactions: points of dialog between the cell cycle and cell attachment signaling networks
-
Pugacheva, E. N., and Golemis, E. A. (2006). HEF1-Aurora A interactions: points of dialog between the cell cycle and cell attachment signaling networks. Cell Cycle. 5 (4), 384-391.
-
(2006)
Cell Cycle.
, vol.5
, Issue.4
, pp. 384-391
-
-
Pugacheva, E.N.1
Golemis, E.A.2
-
45
-
-
21644465065
-
Over-expression of Aurora-A targets cytoplasmic polyadenylation element binding protein and promotes mRNA polyadenylation of Cdk1 and cyclin B1
-
Sasayama, T., Marumoto, T., Kunitoku, N., et al. (2005). Over-expression of Aurora-A targets cytoplasmic polyadenylation element binding protein and promotes mRNA polyadenylation of Cdk1 and cyclin B1. Genes Cells. 10 (7), 627-638.
-
(2005)
Genes Cells.
, vol.10
, Issue.7
, pp. 627-638
-
-
Sasayama, T.1
Marumoto, T.2
Kunitoku, N.3
-
46
-
-
39049126024
-
Inhibitors of cyclin dependent kinases:useful targets for cancer treatment
-
Sharma, P. S., Sharma, R., and Tyagi, R. (2008). Inhibitors of cyclin dependent kinases:useful targets for cancer treatment. Curr Cancer Drug Targets. 8 (1), 53-75.
-
(2008)
Curr Cancer Drug Targets.
, vol.8
, Issue.1
, pp. 53-75
-
-
Sharma, P.S.1
Sharma, R.2
Tyagi, R.3
-
47
-
-
0842282616
-
Predictive pharmacokinetic-pharmacodynamic modeling of tumor growth kinetics in xenograft models after administration of anticancer agents
-
Simeoni, M., Magni, P., Cammia, C., et al. (2004). Predictive pharmacokinetic-pharmacodynamic modeling of tumor growth kinetics in xenograft models after administration of anticancer agents. Cancer Res. 64 (3), 1094-1101.
-
(2004)
Cancer Res.
, vol.64
, Issue.3
, pp. 1094-1101
-
-
Simeoni, M.1
Magni, P.2
Cammia, C.3
-
48
-
-
33746080016
-
PHA-680632, a novel Aurora kinase inhibitor with potent antitumoral activity
-
Soncini, C., Carpinelli, P., Gianellini, L., et al. (2006). PHA-680632, a novel Aurora kinase inhibitor with potent antitumoral activity. Clin Cancer Res. 12 (13), 4080-4089.
-
(2006)
Clin Cancer Res.
, vol.12
, Issue.13
, pp. 4080-4089
-
-
Soncini, C.1
Carpinelli, P.2
Gianellini, L.3
-
49
-
-
34548217817
-
Aurora-C-T191D is a hyperactive Aurora-C mutant
-
Spengler, D. (2007). Aurora-C-T191D is a hyperactive Aurora-C mutant. Cell Cycle. 6 (14), 1803-1804.
-
(2007)
Cell Cycle.
, vol.6
, Issue.14
, pp. 1803-1804
-
-
Spengler, D.1
-
50
-
-
33749824425
-
Functional analyses and molecular modeling of two c-Kit mutations responsible for imatinib secondary resistance in GIST patients
-
Tamborini, E., Pricl, S., Negri, T., et al. (2006). Functional analyses and molecular modeling of two c-Kit mutations responsible for imatinib secondary resistance in GIST patients. Oncogene. 25 (45), 6140-6146.
-
(2006)
Oncogene.
, vol.25
, Issue.45
, pp. 6140-6146
-
-
Tamborini, E.1
Pricl, S.2
Negri, T.3
-
51
-
-
34548407864
-
FGFR3 protein expression and its relationship to mutation status and prognostic variables in bladder cancer
-
Tomlinson, D. C., Baldo, O., Harnden, P., et al. (2007). FGFR3 protein expression and its relationship to mutation status and prognostic variables in bladder cancer. J Pathol. 213 (1), 91-98.
-
(2007)
J Pathol.
, vol.213
, Issue.1
, pp. 91-98
-
-
Tomlinson, D.C.1
Baldo, O.2
Harnden, P.3
-
56
-
-
5044236233
-
Sequence and structural analysis of kinase ATP pocket residues
-
Vulpetti, A., and Bosotti, R. (2004). Sequence and structural analysis of kinase ATP pocket residues. Farmaco. 59 (10), 759-765.
-
(2004)
Farmaco.
, vol.59
, Issue.10
, pp. 759-765
-
-
Vulpetti, A.1
Bosotti, R.2
-
57
-
-
34250739960
-
AZD1152, a selective inhibitor of Aurora B kinase, inhibits human tumor xenograft growth by inducing apoptosis
-
Wilkinson, R. W., Odedra, R., Heaton, S. P., et al. (2007). AZD1152, a selective inhibitor of Aurora B kinase, inhibits human tumor xenograft growth by inducing apoptosis . Clin Cancer Res. 13 (12), 3682-3688.
-
(2007)
Clin Cancer Res.
, vol.13
, Issue.12
, pp. 3682-3688
-
-
Wilkinson, R.W.1
Odedra, R.2
Heaton, S.P.3
-
58
-
-
20444426846
-
Mitotic requirement for Aurora A kinase is bypassed in the absence of Aurora B kinase
-
Yang, H., Burke, T., Dempsey, J., et al. (2005). Mitotic requirement for Aurora A kinase is bypassed in the absence of Aurora B kinase. FEBS Lett. 579 (16), 3385-3391.
-
(2005)
FEBS Lett.
, vol.579
, Issue.16
, pp. 3385-3391
-
-
Yang, H.1
Burke, T.2
Dempsey, J.3
-
59
-
-
0031714080
-
Tumour amplified kinase STK15/BTAK induces centrosome amplification, aneuploidy and transformation
-
Zhou, H., Kuang, J., Zhong, L., et al. (1998). Tumour amplified kinase STK15/BTAK induces centrosome amplification, aneuploidy and transformation. Nat Genet. 20 (2), 189-193
-
(1998)
Nat Genet.
, vol.20
, Issue.2
, pp. 189-193
-
-
Zhou, H.1
Kuang, J.2
Zhong, L.3
|