-
1
-
-
0042626302
-
The serine/threonine kinase Pim-2 is a transcriptionally regulated apoptotic inhibitor
-
Fox CJ, Hammerman PS, Cinalli RM, et al. The serine/threonine kinase Pim-2 is a transcriptionally regulated apoptotic inhibitor. Genes Dev 2003;17:1841-1854
-
(2003)
Genes Dev
, vol.17
, pp. 1841-1854
-
-
Fox, C.J.1
Hammerman, P.S.2
Cinalli, R.M.3
-
2
-
-
0026019439
-
The pim-1 oncogene encodes two related protein-serine/threonine kinases by alternative initiation at AUG and CUG
-
Saris CJ, Domen J, Berns A. The pim-1 oncogene encodes two related protein-serine/threonine kinases by alternative initiation at AUG and CUG. EMBO J 1991;10: 655-664
-
(1991)
EMBO J
, vol.10
, pp. 655-664
-
-
Saris, C.J.1
Domen, J.2
Berns, A.3
-
3
-
-
0021233675
-
Murine leukemia virus-induced t-cell lymphomagenesis: Integration of proviruses in a distinct chromosomal region
-
Cuypers HT, Selten G, Quint W, et al. Murine leukemia virus-induced t-cell lymphomagenesis: integration of proviruses in a distinct chromosomal region. Cell 1984;37:141-150
-
(1984)
Cell
, vol.37
, pp. 141-150
-
-
Cuypers, H.T.1
Selten, G.2
Quint, W.3
-
4
-
-
0028988929
-
Proviral tagging in E-myc transgenic mice lacking the Pim-1 proto-oncogene leads to compensatory activation of Pim-2
-
Van Der Lugt NMT, Domen J, Verhoeven E, et al. Proviral tagging in E-myc transgenic mice lacking the Pim-1 proto-oncogene leads to compensatory activation of Pim-2. EMBO J 1995;14:2536-2544
-
(1995)
EMBO J
, vol.14
, pp. 2536-2544
-
-
Van Der Lugt, N.M.T.1
Domen, J.2
Verhoeven, E.3
-
5
-
-
33846701190
-
Proto-oncogene, Pim-3 with serine/ threonine kinase activity, is aberrantly expressed in human colon cancer cells and can prevent Bad-mediated apoptosis
-
Popivanova BK, Li Y-Y, Zheng H, et al. Proto-oncogene, Pim-3 with serine/ threonine kinase activity, is aberrantly expressed in human colon cancer cells and can prevent Bad-mediated apoptosis. Cancer Sci 2007;98:321-328
-
(2007)
Cancer Sci
, vol.98
, pp. 321-328
-
-
Popivanova, B.K.1
Li, Y.-Y.2
Zheng, H.3
-
6
-
-
2942700011
-
Mice deficient for all PIM kinases display reduced body size and impaired responses to hematopoietic growth factors
-
Mikkers H, Nawijn M, Allen J, et al. Mice deficient for all PIM kinases display reduced body size and impaired responses to hematopoietic growth factors. Mol Cell Biol 2004;24:6104-6115
-
(2004)
Mol Cell Biol
, vol.24
, pp. 6104-6115
-
-
Mikkers, H.1
Nawijn, M.2
Allen, J.3
-
7
-
-
0032497808
-
The human Pim-2 proto-oncogene and its testicular expression
-
Baytel D, Shalom S, Madgar I, et al. The human Pim-2 proto-oncogene and its testicular expression. Biochim Biophys Acta 1998;1442:274-285
-
(1998)
Biochim Biophys Acta
, vol.1442
, pp. 274-285
-
-
Baytel, D.1
Shalom, S.2
Madgar, I.3
-
9
-
-
3943048638
-
Pim-1 expression in prostatic intraepithelial neoplasia and human prostate cancer
-
Valdman A, Fang X, Pang ST, et al. Pim-1 expression in prostatic intraepithelial neoplasia and human prostate cancer. Prostate 2004;60:367-371
-
(2004)
Prostate
, vol.60
, pp. 367-371
-
-
Valdman, A.1
Fang, X.2
Pang, S.T.3
-
10
-
-
30044433786
-
The 44 kDa Pim-1 kinase directly interacts with tyrosine kinase Etk/BMX and protects human prostate cancer cells from apoptosis induced by chemotherapeutic drugs
-
Xie Y, Xu K, Dai B, et al. The 44 kDa Pim-1 kinase directly interacts with tyrosine kinase Etk/BMX and protects human prostate cancer cells from apoptosis induced by chemotherapeutic drugs. Oncogene 2006;25:70-78
-
(2006)
Oncogene
, vol.25
, pp. 70-78
-
-
Xie, Y.1
Xu, K.2
Dai, B.3
-
11
-
-
33746122005
-
Pim-3, a proto-oncogene with serine/ threonine kinase activity, is aberrantly expressed in human pancreatic cancer and phosphorylates Bad to block Bad-mediated apoptosis in human pancreatic cancer cell lines
-
Li Y-Y, Popivanova BK, Nagai Y, et al. Pim-3, a proto-oncogene with serine/ threonine kinase activity, is aberrantly expressed in human pancreatic cancer and phosphorylates Bad to block Bad-mediated apoptosis in human pancreatic cancer cell lines. Cancer Res 2006;66:6741-6747
-
(2006)
Cancer Res
, vol.66
, pp. 6741-6747
-
-
Li, Y.-Y.1
Popivanova, B.K.2
Nagai, Y.3
-
12
-
-
11144354804
-
Increased expression of the hPim-2 gene in human chronic lymphocytic leukemia and non-Hodgkin lymphoma
-
Cohen AM, Grinblat B, Bessler H, et al. Increased expression of the hPim-2 gene in human chronic lymphocytic leukemia and non-Hodgkin lymphoma. Leuk Lymphoma 2004;45:951-955
-
(2004)
Leuk Lymphoma
, vol.45
, pp. 951-955
-
-
Cohen, A.M.1
Grinblat, B.2
Bessler, H.3
-
13
-
-
0037105582
-
A molecular compendium of genes expressed in multiple myeloma
-
Claudio JO, Masih-Kahn E, Tang H, et al. A molecular compendium of genes expressed in multiple myeloma. Blood 2002;100:2175-2186
-
(2002)
Blood
, vol.100
, pp. 2175-2186
-
-
Claudio, J.O.1
Masih-Kahn, E.2
Tang, H.3
-
14
-
-
20044379405
-
Structural basis of constitutive activity and a unique nucleotide binding mode of human Pim-1 kinase
-
Qian KC, Wang L, Hickey ER, et al. Structural basis of constitutive activity and a unique nucleotide binding mode of human Pim-1 kinase. J Biol Chem 2005;280:6130-6137
-
(2005)
J Biol Chem
, vol.280
, pp. 6130-6137
-
-
Qian, K.C.1
Wang, L.2
Hickey, E.R.3
-
15
-
-
26444448463
-
The survival kinases Akt and Pim as potential pharmacological targets
-
Amaravadi R, Thompson CB. The survival kinases Akt and Pim as potential pharmacological targets. J Clin Invest 2005;115:2618-2624
-
(2005)
J Clin Invest
, vol.115
, pp. 2618-2624
-
-
Amaravadi, R.1
Thompson, C.B.2
-
17
-
-
0033451992
-
Synergistic roles for Pim-1 and c-Myc in STAT3-mediated cell cycle progression and antiapoptosis
-
Shirogane G, Fukada T, Muller JMM, et al. Synergistic roles for Pim-1 and c-Myc in STAT3-mediated cell cycle progression and antiapoptosis. Immunity 1999;11:709-719
-
(1999)
Immunity
, vol.11
, pp. 709-719
-
-
Shirogane, G.1
Fukada, T.2
Muller, J.M.M.3
-
18
-
-
0033560095
-
Interferon-alpha activates multiple STAT proteins and upregulates proliferation-associated IL-2Ralpha, c-myc, and pim-1 genes in human T cells
-
Matikainen S, Sareneva T, Ronni T, et al. Interferon-alpha activates multiple STAT proteins and upregulates proliferation-associated IL-2Ralpha, c-myc, and pim-1 genes in human T cells. Blood 1999;93:1980-1991
-
(1999)
Blood
, vol.93
, pp. 1980-1991
-
-
Matikainen, S.1
Sareneva, T.2
Ronni, T.3
-
20
-
-
0242580961
-
The PIM-2 kinase phosphorylates BAD on serine 112 and reverses BAD-induced cell death
-
Yan B, Zemskova M, Holder S, et al. The PIM-2 kinase phosphorylates BAD on serine 112 and reverses BAD-induced cell death. J Biol Chem 2003;278:45358-45367
-
(2003)
J Biol Chem
, vol.278
, pp. 45358-45367
-
-
Yan, B.1
Zemskova, M.2
Holder, S.3
-
21
-
-
3343007095
-
Pim-1 kinase promotes inactivation of the pro-apoptotic Bad protein by phosphorylating it on the Ser112 gatekeeper site
-
Aho TLT, Sandholm J, Peltola K, et al. Pim-1 kinase promotes inactivation of the pro-apoptotic Bad protein by phosphorylating it on the Ser112 gatekeeper site. FEBS Lett 2004;571:43-49
-
(2004)
FEBS Lett
, vol.571
, pp. 43-49
-
-
Aho, T.L.T.1
Sandholm, J.2
Peltola, K.3
-
22
-
-
32944458740
-
Pim kinases phosphorylate multiple sites on Bad and promote 14-3-3 binding and dissociation from Bcl-XL
-
Macdonald A, Campbell DG, Toth R, et al. Pim kinases phosphorylate multiple sites on Bad and promote 14-3-3 binding and dissociation from Bcl-XL. BMC Cell Biology 2006;7:1-14
-
(2006)
BMC Cell Biology
, vol.7
, pp. 1-14
-
-
MacDonald, A.1
Campbell, D.G.2
Toth, R.3
-
23
-
-
76149134020
-
Bad is a BH3-containing protein that forms an inactivating dimer with Bcl-xL
-
Kelekar A, Chang BS, Harlan JE, et al. Bad is a BH3-containing protein that forms an inactivating dimer with Bcl-xL. Mol Cell Biol 1997;17:740-746
-
(1997)
Mol Cell Biol
, vol.17
, pp. 740-746
-
-
Kelekar, A.1
Chang, B.S.2
Harlan, J.E.3
-
24
-
-
70349576526
-
Protein synthesis is resistant to rapamycin and constitutes a promising therapeutic target in acute myeloid leukemia
-
Tamburini J, Green AS, Bardet V, et al. Protein synthesis is resistant to rapamycin and constitutes a promising therapeutic target in acute myeloid leukemia. Blood 2009;114:1618-1627
-
(2009)
Blood
, vol.114
, pp. 1618-1627
-
-
Tamburini, J.1
Green, A.S.2
Bardet, V.3
-
25
-
-
0043127142
-
The pims and outs of survival signaling: Role for the Pim-2 protein kinase in the suppression of apoptosis by cytokines
-
White E. The pims and outs of survival signaling: role for the Pim-2 protein kinase in the suppression of apoptosis by cytokines. Genes & Dev 2003;17:1813-1816
-
(2003)
Genes & Dev
, vol.17
, pp. 1813-1816
-
-
White, E.1
-
26
-
-
33746637660
-
Current development of mTOR inhibitors as anticancer agents
-
Faivre S, Kroemer G, Raymond E. Current development of mTOR inhibitors as anticancer agents. Nat Rev Drug Discovery 2006;5:671-688
-
(2006)
Nat Rev Drug Discovery
, vol.5
, pp. 671-688
-
-
Faivre, S.1
Kroemer, G.2
Raymond, E.3
-
27
-
-
33645745475
-
Targeting PIM kinases impairs survival of hematopoietic cells transformed by kinase inhibitor-sensitive and kinase inhibitor-resistant forms of Fms-like tyrosine kinase 3 and BCR/ABL
-
Adam M, Pogacic V, Bendit M, et al. Targeting PIM kinases impairs survival of hematopoietic cells transformed by kinase inhibitor-sensitive and kinase inhibitor-resistant forms of Fms-like tyrosine kinase 3 and BCR/ABL. Cancer Res 2006;66:3828-3835
-
(2006)
Cancer Res
, vol.66
, pp. 3828-3835
-
-
Adam, M.1
Pogacic, V.2
Bendit, M.3
-
28
-
-
0034658541
-
Roles of STAT3 in mediating the cell growth, differentiation and survival signals relayed through the IL-6 family of cytokine receptors
-
Hirano T, Ishihara K, Hibi M. Roles of STAT3 in mediating the cell growth, differentiation and survival signals relayed through the IL-6 family of cytokine receptors. Oncogene 2000;19:2548-2556
-
(2000)
Oncogene
, vol.19
, pp. 2548-2556
-
-
Hirano, T.1
Ishihara, K.2
Hibi, M.3
-
29
-
-
9144225473
-
The ongogenic serine/threonine kinase Pim-1 phosphorylates and inhibits the activity of Cdc25C-associated Kinase 1 (C-TAK1)
-
Bachmann M, Hennemann H, Xing PX, et al. The ongogenic serine/threonine kinase Pim-1 phosphorylates and inhibits the activity of Cdc25C-associated Kinase 1 (C-TAK1). J Biol Chem 2004;279:48319-48328
-
(2004)
J Biol Chem
, vol.279
, pp. 48319-48328
-
-
Bachmann, M.1
Hennemann, H.2
Xing, P.X.3
-
32
-
-
13244278180
-
The Pim kinases control rapamycin-resistant T cell survival and activation
-
Fox J, Hammerman PS, Thompson CB. The Pim kinases control rapamycin-resistant T cell survival and activation. J Exp Med 2005;201:259-266
-
(2005)
J Exp Med
, vol.201
, pp. 259-266
-
-
Fox, J.1
Hammerman, P.S.2
Thompson, C.B.3
-
35
-
-
65149094214
-
Structure-based design of 3-aryl-6-amino-triazolo[4,3-b]pyridazine inhibitors of Pim-1 kinase
-
Grey R, Pierce AC, Bemis GW, et al. Structure-based design of 3-aryl-6-amino-triazolo[4,3-b]pyridazine inhibitors of Pim-1 kinase. Bioorg Med Chem Lett 2009;19:3019-3022
-
(2009)
Bioorg Med Chem Lett
, vol.19
, pp. 3019-3022
-
-
Grey, R.1
Pierce, A.C.2
Bemis, G.W.3
-
37
-
-
76149118368
-
-
SGI-1776 is an inhibitor of PIM kinases, a family of oncoproteins that promote tumor cell survival Available from[Last accessed 2 September 2009]
-
SGI-1776 is an inhibitor of PIM kinases, a family of oncoproteins that promote tumor cell survival. SuperGen Pipeline. Available from: http://www.supergen.com/ whatwedo/product.html?productId=2. [Last accessed 2 September 2009]
-
SuperGen Pipeline
-
-
-
38
-
-
19744365702
-
A small molecule-kinase interaction map for clinical kinase inhibitors
-
Fabian MA, Biffs WH, Treiber DK, et al. A small molecule-kinase interaction map for clinical kinase inhibitors. Nature Biotech 2005;23:329-336
-
(2005)
Nature Biotech
, vol.23
, pp. 329-336
-
-
Fabian, M.A.1
Biffs, W.H.2
Treiber, D.K.3
-
39
-
-
38049155899
-
A systematic interaction map of validated kinase inhibitors with Ser/Thr kinases
-
Fedorov O, Marsden B, Pogacic V, et al. A systematic interaction map of validated kinase inhibitors with Ser/Thr kinases. Proc Natl Acad Sci USA 2007;104:20523-20528
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 20523-20528
-
-
Fedorov, O.1
Marsden, B.2
Pogacic, V.3
-
40
-
-
28144464847
-
Structural basis of inhibitor specificity of the human protooncogene proviral insertion site in moloney murine leukemia virus (PIM-1) kinase
-
Bullock AN, Debreczeni JE, Fedorov OY, et al. Structural basis of inhibitor specificity of the human protooncogene proviral insertion site in moloney murine leukemia virus (PIM-1) kinase. J Med Chem 2005;48:7604-7614
-
(2005)
J Med Chem
, vol.48
, pp. 7604-7614
-
-
Bullock, A.N.1
Debreczeni, J.E.2
Fedorov, O.Y.3
-
41
-
-
34547132324
-
Structural analysis identifies imidazo [1,2-b]pyridazines as PIM kinase inhibitors with in vitro antileukemic activity
-
Pogacic V, Bullock AN, Fedorov O, et al. Structural analysis identifies imidazo [1,2-b]pyridazines as PIM kinase inhibitors with in vitro antileukemic activity. Cancer Res 2007;67:6916-6924
-
(2007)
Cancer Res
, vol.67
, pp. 6916-6924
-
-
Pogacic, V.1
Bullock, A.N.2
Fedorov, O.3
-
47
-
-
71049189242
-
Discovery of 3H-Benzo[4,5]thieno[3,2-d] pyrimidine-4-ones as potent, highly selective, and orally bioavailable inhibitors of the human protooncogene proviral insertion site in moloney murine leukemia virus (PIM) kinases
-
Tao Z-F, Hasvold L, Leverson JD, et al. Discovery of 3H-Benzo[4,5] thieno[3,2-d] pyrimidine-4-ones as potent, highly selective, and orally bioavailable inhibitors of the human protooncogene proviral insertion site in moloney murine leukemia virus (PIM) kinases. J Med Chem 2009;52:6621-6636
-
(2009)
J Med Chem
, vol.52
, pp. 6621-6636
-
-
Tao, Z.-F.1
Hasvold, L.2
Leverson, J.D.3
-
52
-
-
64549120239
-
Hit to lead account of the discovery of a new class of inhibitors of Pim kinases and crystallographic studies revealing an unusual kinase binding mode
-
Qian K, Wang L, Cywin CL, et al. Hit to lead account of the discovery of a new class of inhibitors of Pim kinases and crystallographic studies revealing an unusual kinase binding mode. J Med Chem 2009;52:1814-1827
-
(2009)
J Med Chem
, vol.52
, pp. 1814-1827
-
-
Qian, K.1
Wang, L.2
Cywin, C.L.3
-
54
-
-
59449108140
-
Synthesis and evaluation of novel inhibitors of Pim-1 and Pim-2 protein kinases
-
Xia Z, Knaak C, Ma J, et al. Synthesis and evaluation of novel inhibitors of Pim-1 and Pim-2 protein kinases. J Med Chem 2009;52:74-86
-
(2009)
J Med Chem
, vol.52
, pp. 74-86
-
-
Xia, Z.1
Knaak, C.2
Ma, J.3
-
55
-
-
7844224790
-
N-(2-Benzoylphenyl)-L-tyrosine PPARgamma agonists. 1. Discovery of a novel series of potent antihyperglycemic and antihyperlipidemic agents
-
Henke BR, Blanchard SG, Brackeen MF, et al. N-(2-Benzoylphenyl)-L- tyrosine PPARgamma agonists. 1. Discovery of a novel series of potent antihyperglycemic and antihyperlipidemic agents. J Med Chem 1998;41:5020-5036
-
(1998)
J Med Chem
, vol.41
, pp. 5020-5036
-
-
Henke, B.R.1
Blanchard, S.G.2
Brackeen, M.F.3
-
56
-
-
0030567857
-
Nonthiazolidinedione antihyperglycemic agents. 1: Alpha-heteroatom substituted beta-phenylpropanoic acids
-
Buckle DR, Cantello BCC, Cawthorne MA, et al. Nonthiazolidinedione antihyperglycemic agents. 1: alpha-heteroatom substituted beta-phenylpropanoic acids. Bioorg Med Chem Lett 1996;6:2121-2126
-
(1996)
Bioorg Med Chem Lett
, vol.6
, pp. 2121-2126
-
-
Buckle, D.R.1
Cantello, B.C.C.2
Cawthorne, M.A.3
-
60
-
-
0035413617
-
Chemical inhibitors of protein kinases
-
Bridges AJ. Chemical inhibitors of protein kinases. Chem Rev 2001;101:2541-2571
-
(2001)
Chem Rev
, vol.101
, pp. 2541-2571
-
-
Bridges, A.J.1
-
61
-
-
34547689097
-
Comparative molecular field analysis of flavonoid inhibitors of the PIM-1 kinase
-
Holder S, Lilly M, Brown ML. Comparative molecular field analysis of flavonoid inhibitors of the PIM-1 kinase. Biorg Med Chem 2007;15:6463-6473
-
(2007)
Biorg Med Chem
, vol.15
, pp. 6463-6473
-
-
Holder, S.1
Lilly, M.2
Brown, M.L.3
-
62
-
-
33846805635
-
Characterization of a potent and selective small-molecule inhibitor of the PIM1 kinase
-
Holder S, Zemskova M, Zhang C, et al. Characterization of a potent and selective small-molecule inhibitor of the PIM1 kinase. Mol Cancer Ther 2007;6:163-172
-
(2007)
Mol Cancer Ther
, vol.6
, pp. 163-172
-
-
Holder, S.1
Zemskova, M.2
Zhang, C.3
-
72
-
-
84954208573
-
Structural aspects of kinases and their inhibitors
-
Kubinyi H, Müller G, editors, Wiley-VCH Verlag GmbH & Co.
-
Buijsman, R. Structural aspects of kinases and their inhibitors. In: Kubinyi H, Müller G, editors, Chemogenomics in drug discovery. Wiley-VCH Verlag GmbH & Co.; 2004. p. 191-217
-
(2004)
Chemogenomics in Drug Discovery
, pp. 191-217
-
-
Buijsman, R.1
-
73
-
-
17144422830
-
Pim-1 ligand-bound structures reveal the mechanism of serine/threonine kinase inhibition by LY294002
-
Jacobs MD, Black J, Futer O, et al. Pim-1 ligand-bound structures reveal the mechanism of serine/threonine kinase inhibition by LY294002. J Biol Chem 2005;280:13728-13734
-
(2005)
J Biol Chem
, vol.280
, pp. 13728-13734
-
-
Jacobs, M.D.1
Black, J.2
Futer, O.3
-
74
-
-
76149117485
-
-
Available from[Last accessed 2 September 2009]
-
Available from: http://www.rcsb.org/ pdb/home/home.do. [Last accessed 2 September 2009]
-
-
-
-
75
-
-
41149093037
-
Docking study yields four novel inhibitors of the protooncogene Pim-1 kinase
-
Pierce AC, Jacobs M, Stuver-Moody C. Docking study yields four novel inhibitors of the protooncogene Pim-1 kinase. J Med Chem 2008;51:1972-1975
-
(2008)
J Med Chem
, vol.51
, pp. 1972-1975
-
-
Pierce, A.C.1
Jacobs, M.2
Stuver-Moody, C.3
-
76
-
-
0036893503
-
Kinase inhibitors and the case for CHO hydrogen bonds in protein-ligand binding
-
Pierce AC, Sandretto KL, Bemis, GW. Kinase inhibitors and the case for CHO hydrogen bonds in protein-ligand binding. Proteins Struct Funct Genet 2002;49:567-576
-
(2002)
Proteins Struct Funct Genet
, vol.49
, pp. 567-576
-
-
Pierce, A.C.1
Sandretto, K.L.2
Bemis, G.W.3
-
77
-
-
33847058740
-
Identification and structure-activity relationships of substituted pyridones as inhibitors of Pim-1 kinase
-
Cheney IW, Yan S, Appleby T, et al. Identification and structure-activity relationships of substituted pyridones as inhibitors of Pim-1 kinase. Biorg Med Chem Lett 2007;17:1679-1683
-
(2007)
Biorg Med Chem Lett
, vol.17
, pp. 1679-1683
-
-
Cheney, I.W.1
Yan, S.2
Appleby, T.3
-
78
-
-
48649100754
-
4-(1H-Indazol-5-yl)-6-phenylpyrimidin-2 (1H)-one analogs as potent CDC7 inhibitors
-
Shafer CM, Lindvall M, Bellamacina C, et al. 4-(1H-Indazol-5-yl)-6- phenylpyrimidin-2 (1H)-one analogs as potent CDC7 inhibitors. Bioorg Med Chem Lett 2008;18:4482-4485
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 4482-4485
-
-
Shafer, C.M.1
Lindvall, M.2
Bellamacina, C.3
-
81
-
-
33646489986
-
Expression, purification, crystallization and preliminary crystallographic analysis of human Pim-1 kinase
-
Qian KC, Studts J, Wang L, et al. Expression, purification, crystallization and preliminary crystallographic analysis of human Pim-1 kinase. Acta Crystallogr Sect F Struct Biol Cryst Commun 2005;61:96-99
-
(2005)
Acta Crystallogr Sect F Struct Biol Cryst Commun
, vol.61
, pp. 96-99
-
-
Qian, K.C.1
Studts, J.2
Wang, L.3
-
83
-
-
16244377514
-
Crystal structures of proto-oncogene kinase Pim1: A target of aberrant somatic hypermutations in diffuse large cell lymphoma
-
Kumar A, Mandiyan V, Suzuki Y, et al. Crystal structures of proto-oncogene kinase Pim1: a target of aberrant somatic hypermutations in diffuse large cell lymphoma. J Mol Biol 2005;348:183-193
-
(2005)
J Mol Biol
, vol.348
, pp. 183-193
-
-
Kumar, A.1
Mandiyan, V.2
Suzuki, Y.3
-
84
-
-
0037032835
-
The protein kinase complement of the human genome
-
Manning G, Whyte DB, Martinez R, et al. The protein kinase complement of the human genome. Science 2002;298:1912-1934
-
(2002)
Science
, vol.298
, pp. 1912-1934
-
-
Manning, G.1
Whyte, D.B.2
Martinez, R.3
-
85
-
-
0034383949
-
The regulation of protein function by multisite phosphorylation-a 25 year update
-
Cohen P. The regulation of protein function by multisite phosphorylation-a 25 year update. Trends Biochem Sci 2000;25:596-601
-
(2000)
Trends Biochem Sci
, vol.25
, pp. 596-601
-
-
Cohen, P.1
-
86
-
-
69949151386
-
Factors underlying sensitivity of cancers to small-molecule kinase inhibitors
-
Jänne PA, Gray N, Settleman J. Factors underlying sensitivity of cancers to small-molecule kinase inhibitors. Nat Rev Drug Discov 2009;8:709-723
-
(2009)
Nat Rev Drug Discov
, vol.8
, pp. 709-723
-
-
Jänne, P.A.1
Gray, N.2
Settleman, J.3
-
87
-
-
64349099558
-
Kinase domain mutations in cancer: Implications for small molecule drug design strategies
-
Bikker JA, Brooijmans N, Wissner A, et al. Kinase domain mutations in cancer: implications for small molecule drug design strategies. J Med Chem 2009;52:1493-1509
-
(2009)
J Med Chem
, vol.52
, pp. 1493-1509
-
-
Bikker, J.A.1
Brooijmans, N.2
Wissner, A.3
-
88
-
-
57749188299
-
Targeting cancer with small molecule kinase inhibitors
-
Zhang J, Yang PL, Gray NS. Targeting cancer with small molecule kinase inhibitors. Nat Rev Cancer 2009;9:28-39
-
(2009)
Nat Rev Cancer
, vol.9
, pp. 28-39
-
-
Zhang, J.1
Yang, P.L.2
Gray, N.S.3
-
89
-
-
66749134594
-
Targeting innate immunity protein kinase signalling in inflammation
-
Gaestel M, Kotlyarov A, Kracht M. Targeting innate immunity protein kinase signalling in inflammation. Nat Rev Drug Discovery 2009;8:480-499
-
(2009)
Nat Rev Drug Discovery
, vol.8
, pp. 480-499
-
-
Gaestel, M.1
Kotlyarov, A.2
Kracht, M.3
-
90
-
-
76149109066
-
Anti-inflammatory agents as cancer therapeutics
-
Khosrow K. Anti-inflammatory agents as cancer therapeutics. Adv Pharmacol 2009;57:31-89
-
(2009)
Adv Pharmacol
, vol.57
, pp. 31-89
-
-
Khosrow, K.1
-
93
-
-
63449124343
-
The selectivity of inhibitors of protein kinase CK2: An update
-
Pagano MA, Bain J, Kazimierczuk Z, et al. The selectivity of inhibitors of protein kinase CK2: an update. Biochem J 2008;415:353-365
-
(2008)
Biochem J
, vol.415
, pp. 353-365
-
-
Pagano, M.A.1
Bain, J.2
Kazimierczuk, Z.3
-
94
-
-
0034306450
-
Specificity and mechanism of action of some commonly used protein kinase inhibitors
-
Davies SP, Reddy H, Caivano M, et al. Specificity and mechanism of action of some commonly used protein kinase inhibitors. Biochem J 2000;351:95-105
-
(2000)
Biochem J
, vol.351
, pp. 95-105
-
-
Davies, S.P.1
Reddy, H.2
Caivano, M.3
-
95
-
-
0036568813
-
Joining the cell survival squad: An emerging role for protein kinase CK2
-
Ahmed K, Gerber DA, Cochet C. Joining the cell survival squad: an emerging role for protein kinase CK2. Trends Cell Biol 2002;12:226-230
-
(2002)
Trends Cell Biol
, vol.12
, pp. 226-230
-
-
Ahmed, K.1
Gerber, D.A.2
Cochet, C.3
-
96
-
-
0033018831
-
Protein kinase CK2 and its role in cellular proliferation, development and pathology
-
Guerra B, Issinger O-G. Protein kinase CK2 and its role in cellular proliferation, development and pathology. Electrophoresis 1999;20:391-408
-
(1999)
Electrophoresis
, vol.20
, pp. 391-408
-
-
Guerra, B.1
Issinger, O.-G.2
-
97
-
-
32044466838
-
Exploiting the PI3K/AKT pathway for cancer drug discovery
-
Hennessy BT, Smith DL, Ram PT, et al. Exploiting the PI3K/AKT pathway for cancer drug discovery. Nat Rev Drug Discov 2005;4:988-1004
-
(2005)
Nat Rev Drug Discov
, vol.4
, pp. 988-1004
-
-
Hennessy, B.T.1
Smith, D.L.2
Ram, P.T.3
-
98
-
-
24944563309
-
Protein kinase Ce is a predictive biomarker of aggressive breast cancer and a validated target for RNA interference anticancer therapy
-
Pan Q, Bao LW, Kleer CG, et al. Protein kinase Ce is a predictive biomarker of aggressive breast cancer and a validated target for RNA interference anticancer therapy. Cancer Res 2005;65:8366-8371
-
(2005)
Cancer Res
, vol.65
, pp. 8366-8371
-
-
Pan, Q.1
Bao, L.W.2
Kleer, C.G.3
|