-
1
-
-
76149118435
-
Small-molecule pan-IAP antagonists: A patent review
-
Flygare JA, Fairbrother WJ. Small-molecule pan-IAP antagonists: a patent review. Expert Opin Ther Pat 2010;20:251-67.
-
(2010)
Expert Opin Ther Pat
, vol.20
, pp. 251-267
-
-
Flygare, J.A.1
Fairbrother, W.J.2
-
2
-
-
77954930632
-
IAPs: From caspase inhibitors to modulators of NF-kappaB, inflammation and cancer
-
Gyrd-Hansen M, Meier P. IAPs: from caspase inhibitors to modulators of NF-kappaB, inflammation and cancer. Nat Rev Cancer 2010;10: 561-74.
-
(2010)
Nat Rev Cancer
, vol.10
, pp. 561-574
-
-
Gyrd-Hansen, M.1
Meier, P.2
-
3
-
-
54249123632
-
IAP-targeted therapies for cancer
-
LaCasse EC, Mahoney DJ, Cheung HH, Plenchette S, Baird S, Korneluk RG. IAP-targeted therapies for cancer. Oncogene 2008;27:6252-75.
-
(2008)
Oncogene
, vol.27
, pp. 6252-6275
-
-
LaCasse, E.C.1
Mahoney, D.J.2
Cheung, H.H.3
Plenchette, S.4
Baird, S.5
Korneluk, R.G.6
-
4
-
-
0034616945
-
Smac, a mitochondrial protein that promotes cytochrome c-dependent caspase activation by eliminating IAP inhibition
-
Du C, Fang M, Li Y, Li L, Wang X. Smac, a mitochondrial protein that promotes cytochrome c-dependent caspase activation by eliminating IAP inhibition. Cell 2000;102:33-42.
-
(2000)
Cell
, vol.102
, pp. 33-42
-
-
Du, C.1
Fang, M.2
Li, Y.3
Li, L.4
Wang, X.5
-
5
-
-
0034616942
-
Identification of DIABLO, a mammalian protein that promotes apoptosis by binding to and antagonizing IAP proteins
-
Verhagen AM, Ekert PG, Pakusch M, Silke J, Connolly LM, Reid GE, et al. Identification of DIABLO, a mammalian protein that promotes apoptosis by binding to and antagonizing IAP proteins. Cell 2000;102:43-53.
-
(2000)
Cell
, vol.102
, pp. 43-53
-
-
Verhagen, A.M.1
Ekert, P.G.2
Pakusch, M.3
Silke, J.4
Connolly, L.M.5
Reid, G.E.6
-
6
-
-
4444243683
-
A small molecule smac mimic potentiates TRAIL- and TNFalpha-mediated cell death
-
DOI 10.1126/science.1098231
-
Li L, Thomas RM, Suzuki H, De Brabander JK, Wang X, Harran PG. A small molecule Smac mimic potentiates TRAIL- and TNFalpha-mediated cell death. Science 2004;305:1471-4. (Pubitemid 39167668)
-
(2004)
Science
, vol.305
, Issue.5689
, pp. 1471-1474
-
-
Li, L.1
Thomas, R.M.2
Suzuki, H.3
De Brabander, J.K.4
Wang, X.5
Harran, P.G.6
-
7
-
-
56449103218
-
SM-164: A novel, bivalent Smac mimetic that induces apoptosis and tumor regression by concurrent removal of the blockade of cIAP-1/2 and XIAP
-
Lu J, Bai L, Sun H, Nikolovska-Coleska Z, McEachern D, Qiu S, et al. SM-164: a novel, bivalent Smac mimetic that induces apoptosis and tumor regression by concurrent removal of the blockade of cIAP-1/2 and XIAP. Cancer Res 2008;68:9384-93.
-
(2008)
Cancer Res
, vol.68
, pp. 9384-9393
-
-
Lu, J.1
Bai, L.2
Sun, H.3
Nikolovska-Coleska, Z.4
McEachern, D.5
Qiu, S.6
-
8
-
-
35948994157
-
Autocrine TNFalpha Signaling Renders Human Cancer Cells Susceptible to Smac-Mimetic-Induced Apoptosis
-
DOI 10.1016/j.ccr.2007.08.029, PII S1535610807002619
-
Petersen SL, Wang L, Yalcin-Chin A, Li L, Peyton M, Minna J, et al. Autocrine TNFalpha signaling renders human cancer cells susceptible to Smac-mimetic-induced apoptosis. Cancer Cell 2007;12:445-56. (Pubitemid 350064365)
-
(2007)
Cancer Cell
, vol.12
, Issue.5
, pp. 445-456
-
-
Petersen, S.L.1
Wang, L.2
Yalcin-Chin, A.3
Li, L.4
Peyton, M.5
Minna, J.6
Harran, P.7
Wang, X.8
-
9
-
-
36148954336
-
IAP Antagonists Target cIAP1 to Induce TNFalpha-Dependent Apoptosis
-
DOI 10.1016/j.cell.2007.10.037, PII S0092867407013578
-
Vince JE, Wong WW,Khan N, Feltham R, Chau D, Ahmed AU, et al. IAP antagonists target cIAP1 to induce TNFalpha-dependent apoptosis. Cell 2007;131:682-93. (Pubitemid 350103599)
-
(2007)
Cell
, vol.131
, Issue.4
, pp. 682-693
-
-
Vince, J.E.1
Wong, W.W.-L.2
Khan, N.3
Feltham, R.4
Chau, D.5
Ahmed, A.U.6
Benetatos, C.A.7
Chunduru, S.K.8
Condon, S.M.9
McKinlay, M.10
Brink, R.11
Leverkus, M.12
Tergaonkar, V.13
Schneider, P.14
Callus, B.A.15
Koentgen, F.16
Vaux, D.L.17
Silke, J.18
-
10
-
-
36048999753
-
IAP Antagonists Induce Autoubiquitination of c-IAPs, NF-kappaB Activation, and TNFalpha-Dependent Apoptosis
-
DOI 10.1016/j.cell.2007.10.030, PII S0092867407013487
-
Varfolomeev E, Blankenship JW, Wayson SM, Fedorova AV, Kayagaki N, et al. IAP antagonists induce autoubiquitination of c-IAPs, NF-kappaB activation, and TNFalpha-dependent apoptosis. Cell 2007;131:669-81. (Pubitemid 350087204)
-
(2007)
Cell
, vol.131
, Issue.4
, pp. 669-681
-
-
Varfolomeev, E.1
Blankenship, J.W.2
Wayson, S.M.3
Fedorova, A.V.4
Kayagaki, N.5
Garg, P.6
Zobel, K.7
Dynek, J.N.8
Elliott, L.O.9
Wallweber, H.J.A.10
Flygare, J.A.11
Fairbrother, W.J.12
Deshayes, K.13
Dixit, V.M.14
Vucic, D.15
-
11
-
-
37549000486
-
A Smac mimetic rescue screen reveals roles for inhibitor of apoptosis proteins in tumor necrosis factor-alpha signaling
-
Gaither A, Porter D, Yao Y, Borawski J, Yang G, Donovan J, et al. A Smac mimetic rescue screen reveals roles for inhibitor of apoptosis proteins in tumor necrosis factor-alpha signaling. Cancer Res 2007;67:11493-8.
-
(2007)
Cancer Res
, vol.67
, pp. 11493-11498
-
-
Gaither, A.1
Porter, D.2
Yao, Y.3
Borawski, J.4
Yang, G.5
Donovan, J.6
-
12
-
-
70350228525
-
Down-regulation of c-FLIP Enhances death of cancer cells by smac mimetic compound
-
Cheung HH, Mahoney DJ, Lacasse EC, Korneluk RG. Down-regulation of c-FLIP Enhances death of cancer cells by smac mimetic compound. Cancer Res 2009;69:7729-38.
-
(2009)
Cancer Res
, vol.69
, pp. 7729-7738
-
-
Cheung, H.H.1
Mahoney, D.J.2
Lacasse, E.C.3
Korneluk, R.G.4
-
13
-
-
78650403056
-
Smac mimetic compounds potentiate interleukin-1{beta}-mediated cell death
-
Cheung HH, Beug ST, St Jean M, Brewster A, Kelly NL, Wang S, et al. Smac mimetic compounds potentiate interleukin-1{beta}-mediated cell death. J Biol Chem 2010;285:40612-23.
-
(2010)
J Biol Chem
, vol.285
, pp. 40612-40623
-
-
Cheung, H.H.1
Beug, S.T.2
St Jean, M.3
Brewster, A.4
Kelly, N.L.5
Wang, S.6
-
14
-
-
77955376177
-
Overcoming cancer cell resistance to Smac mimetic induced apoptosis by modulating cIAP-2 expression
-
Petersen SL, Peyton M, Minna JD, Wang X. Overcoming cancer cell resistance to Smac mimetic induced apoptosis by modulating cIAP-2 expression. Proc Natl Acad Sci U S A 2010;107:11936-41.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 11936-11941
-
-
Petersen, S.L.1
Peyton, M.2
Minna, J.D.3
Wang, X.4
-
15
-
-
37049019494
-
Design, synthesis, and characterization of a potent, nonpeptide, cell-permeable, bivalent smac mimetic that concurrently targets both the BIR2 and BIR3 domains in XIAP
-
DOI 10.1021/ja074725f
-
Sun H, Nikolovska-Coleska Z, Lu J, Meagher JL, Yang CY, Qiu S, et al. Design, synthesis, and characterization of a potent, nonpeptide, cell-permeable, bivalent Smac mimetic that concurrently targets both the BIR2 and BIR3 domains in XIAP. J Am Chem Soc 2007;129:15279-94. (Pubitemid 350247811)
-
(2007)
Journal of the American Chemical Society
, vol.129
, Issue.49
, pp. 15279-15294
-
-
Sun, H.1
Nikolovska-Coleska, Z.2
Lu, J.3
Meagher, J.L.4
Yang, C.-Y.5
Qiu, S.6
Tomita, Y.7
Ueda, Y.8
Jiang, S.9
Krajewski, K.10
Roller, P.P.11
Stuckey, J.A.12
Wang, S.13
-
16
-
-
79954504195
-
A potent and orally active antagonist (SM-406/AT-406) of multiple inhibitor of apoptosis proteins (IAPs) in clinical development for cancer treatment
-
Cai Q, Sun H, Peng Y, Lu J, Nikolovska-Coleska Z, McEachern D, et al. A potent and orally active antagonist (SM-406/AT-406) of multiple inhibitor of apoptosis proteins (IAPs) in clinical development for cancer treatment. J Med Chem 2011;54:2714-26.
-
(2011)
J Med Chem
, vol.54
, pp. 2714-2726
-
-
Cai, Q.1
Sun, H.2
Peng, Y.3
Lu, J.4
Nikolovska-Coleska, Z.5
McEachern, D.6
-
17
-
-
0021118703
-
Quantitative analysis of dose-effect relationships: The combined effects of multiple drugs or enzyme inhibitors
-
Chou TC, Talalay P. Quantitative analysis of dose-effect relationships: the combined effects of multiple drugs or enzyme inhibitors. Adv Enzyme Regul 1984;22:27-55.
-
(1984)
Adv Enzyme Regul
, vol.22
, pp. 27-55
-
-
Chou, T.C.1
Talalay, P.2
-
18
-
-
20844462896
-
LRIG1 restricts growth factor signaling by enhancing receptor ubiquitylation and degradation
-
Gur G, Rubin C, Katz M, Amit I, Citri A, Nilsson J, et al. LRIG1 restricts growth factor signaling by enhancing receptor ubiquitylation and degradation. EMBO J 2004;23:3270-81.
-
(2004)
EMBO J
, vol.23
, pp. 3270-3281
-
-
Gur, G.1
Rubin, C.2
Katz, M.3
Amit, I.4
Citri, A.5
Nilsson, J.6
-
19
-
-
38149041753
-
Lrig1 is an endogenous inhibitor of Ret receptor tyrosine kinase activation, downstream signaling, and biological responses to GDNF
-
Ledda F, Bieraugel O, Fard SS, Vilar M, Paratcha G. Lrig1 is an endogenous inhibitor of Ret receptor tyrosine kinase activation, downstream signaling, and biological responses to GDNF. J Neurosci 2008;28:39-49.
-
(2008)
J Neurosci
, vol.28
, pp. 39-49
-
-
Ledda, F.1
Bieraugel, O.2
Fard, S.S.3
Vilar, M.4
Paratcha, G.5
-
20
-
-
54249104578
-
Suppression of the negative regulator LRIG1 contributes to ErbB2 overexpression in breast cancer
-
Miller JK, Shattuck DL, Ingalla EQ, Yen L, Borowsky AD, Young LJ, et al. Suppression of the negative regulator LRIG1 contributes to ErbB2 overexpression in breast cancer. Cancer Res 2008;68:8286-94.
-
(2008)
Cancer Res
, vol.68
, pp. 8286-8294
-
-
Miller, J.K.1
Shattuck, D.L.2
Ingalla, E.Q.3
Yen, L.4
Borowsky, A.D.5
Young, L.J.6
-
21
-
-
33847181657
-
LRIG1 is a novel negative regulator of the Met receptor and opposes Met and Her2 synergy
-
Shattuck DL, Miller JK, Laederich M, Funes M, Petersen H, Carraway KL 3rd, et al. LRIG1 is a novel negative regulator of the Met receptor and opposes Met and Her2 synergy. Mol Cell Biol 2007;27:1934-46.
-
(2007)
Mol Cell Biol
, vol.27
, pp. 1934-1946
-
-
Shattuck, D.L.1
Miller, J.K.2
Laederich, M.3
Funes, M.4
Petersen, H.5
Carraway III, K.L.6
-
22
-
-
68949144565
-
Upregulation of LRIG1 suppresses malignant glioma cell growth by attenuating EGFR activity
-
Ye F, Gao Q, Xu T, Zeng L, Ou Y, Mao F, et al. Upregulation of LRIG1 suppresses malignant glioma cell growth by attenuating EGFR activity. J Neurooncol 2009;94:183-94.
-
(2009)
J Neurooncol
, vol.94
, pp. 183-194
-
-
Ye, F.1
Gao, Q.2
Xu, T.3
Zeng, L.4
Ou, Y.5
Mao, F.6
-
23
-
-
79958154460
-
Regulation of epidermal growth factor receptor signalling by inducible feedback inhibitors
-
Segatto O, Anastasi S, Alema S. Regulation of epidermal growth factor receptor signalling by inducible feedback inhibitors. J Cell Sci 2011;124:1785-93.
-
(2011)
J Cell Sci
, vol.124
, pp. 1785-1793
-
-
Segatto, O.1
Anastasi, S.2
Alema, S.3
-
24
-
-
8744267487
-
The leucine-rich repeat protein LRIG1 is a negative regulator of ErbB family receptor tyrosine kinases
-
DOI 10.1074/jbc.M409703200
-
Laederich MB, Funes-Duran M, Yen L, Ingalla E, Wu X, Carraway KL 3rd, et al. The leucine-rich repeat protein LRIG1 is a negative regulator of ErbB family receptor tyrosine kinases. J Biol Chem 2004;279:47050-6. (Pubitemid 39518360)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.45
, pp. 47050-47056
-
-
Laederich, M.B.1
Funes-Duran, M.2
Yen, L.3
Ingalla, E.4
Wu, X.5
Carraway III, K.L.6
Sweeney, C.7
-
25
-
-
52949087545
-
LRIG1 negatively regulates the oncogenic EGF receptor mutant EGFR-vIII
-
Stutz MA, Shattuck DL, Laederich MB, Carraway KL 3rd, Sweeney C. LRIG1 negatively regulates the oncogenic EGF receptor mutant EGFR-vIII. Oncogene 2008;27:5741-52.
-
(2008)
Oncogene
, vol.27
, pp. 5741-5752
-
-
Stutz, M.A.1
Shattuck, D.L.2
Laederich, M.B.3
Carraway III, K.L.4
Sweeney, C.5
-
26
-
-
33846281874
-
A soluble ectodomain of LRIG1 inhibits cancer cell growth by attenuating basal and ligand-dependent EGFR activity
-
DOI 10.1038/sj.onc.1209803, PII 1209803
-
Goldoni S, Iozzo RA, Kay P, Campbell S, McQuillan A, Agnew C, et al. A soluble ectodomain of LRIG1 inhibits cancer cell growth by attenuating basal and ligand-dependent EGFR activity. Oncogene 2007;26:368-81. (Pubitemid 46122827)
-
(2007)
Oncogene
, vol.26
, Issue.3
, pp. 368-381
-
-
Goldoni, S.1
Iozzo, R.A.2
Kay, P.3
Campbell, S.4
McQuillan, A.5
Agnew, C.6
Zhu, J.-X.7
Keene, D.R.8
Reed, C.C.9
Iozzo, R.V.10
-
27
-
-
19644367829
-
Negative regulation of receptor tyrosine kinases: Unexpected links to c-Cbl and receptor ubiquitylation
-
DOI 10.1038/sj.cr.7290268
-
Rubin C, Gur G, Yarden Y. Negative regulation of receptor tyrosine kinases: unexpected links to c-Cbl and receptor ubiquitylation. Cell Res 2005;15:66-71. (Pubitemid 41653969)
-
(2005)
Cell Research
, vol.15
, Issue.1
, pp. 66-71
-
-
Rubin, C.1
Gur, G.2
Yarden, Y.3
-
28
-
-
33747047561
-
Single-cell expression profiling of human epidermal stem and transit-amplifying cells: Lrig1 is a regular of stem cell quiescence
-
DOI 10.1073/pnas.0601886103
-
Jensen KB, Watt FM. Single-cell expression profiling of human epidermal stem and transit-amplifying cells: Lrig1 is a regulator of stem cell quiescence. Proc Natl Acad Sci U S A 2006;103:11958-63. (Pubitemid 44215793)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.32
, pp. 11958-11963
-
-
Jensen, K.B.1
Watt, F.M.2
-
29
-
-
65349166258
-
Lrig1 expression defines a distinct multipotent stem cell population in mammalian epidermis
-
Jensen KB, Collins CA, Nascimento E, Tan DW, Frye M, Itami S, et al. Lrig1 expression defines a distinct multipotent stem cell population in mammalian epidermis. Cell Stem Cell 2009;4:427-39.
-
(2009)
Cell Stem Cell
, vol.4
, pp. 427-439
-
-
Jensen, K.B.1
Collins, C.A.2
Nascimento, E.3
Tan, D.W.4
Frye, M.5
Itami, S.6
-
30
-
-
77952800807
-
Receptor tyrosine kinase coactivation networks in cancer
-
Xu AM, Huang PH. Receptor tyrosine kinase coactivation networks in cancer. Cancer Res 2010;70:3857-60.
-
(2010)
Cancer Res
, vol.70
, pp. 3857-3860
-
-
Xu, A.M.1
Huang, P.H.2
-
31
-
-
77956621143
-
Akt-RSK-S6 kinase signaling networks activated by oncogenic receptor tyrosine kinases
-
Moritz A, Li Y, Guo A, Villen J, Wang Y, MacNeill J, et al. Akt-RSK-S6 kinase signaling networks activated by oncogenic receptor tyrosine kinases. Sci Signal 2010;3:ra64.
-
(2010)
Sci Signal
, vol.3
-
-
Moritz, A.1
Li, Y.2
Guo, A.3
Villen, J.4
Wang, Y.5
MacNeill, J.6
-
32
-
-
77953896432
-
Cell signaling by receptor tyrosine kinases
-
Lemmon MA, Schlessinger J. Cell signaling by receptor tyrosine kinases. Cell 2010;141:1117-34.
-
(2010)
Cell
, vol.141
, pp. 1117-1134
-
-
Lemmon, M.A.1
Schlessinger, J.2
-
33
-
-
77956042544
-
SRC: A century of science brought to the clinic
-
Aleshin A, Finn RS. SRC: a century of science brought to the clinic. Neoplasia 2010;12:599-607.
-
(2010)
Neoplasia
, vol.12
, pp. 599-607
-
-
Aleshin, A.1
Finn, R.S.2
-
34
-
-
10744228765
-
A Selective Small Molecule Inhibitor of c-Met Kinase Inhibits c-Met-Dependent Phenotypes in Vitro and Exhibits Cytoreductive Antitumor Activity in Vivo
-
Christensen JG, Schreck R, Burrows J, Kuruganti P, Chan E, Le P, et al. A selective small molecule inhibitor of c-Met kinase inhibits c-Met-dependent phenotypes in vitro and exhibits cytoreductive antitumor activity in vivo. Cancer Res 2003;63:7345-55. (Pubitemid 37413476)
-
(2003)
Cancer Research
, vol.63
, Issue.21
, pp. 7345-7355
-
-
Christensen, J.G.1
Schreck, R.2
Burrows, J.3
Kuruganti, P.4
Chan, E.5
Le, P.6
Chen, J.7
Wang, X.8
Ruslim, L.9
Blake, R.10
Lipson, K.E.11
Ramphal, J.12
Do, S.13
Cui, J.J.14
Cherrington, J.M.15
Mendel, D.B.16
-
35
-
-
70350230210
-
Inhibition of tumor cell growth, invasion, and metastasis by EXEL-2880 (XL880, GSK1363089), a novel inhibitor of HGF and VEGF receptor tyrosine kinases
-
Qian F, Engst S, Yamaguchi K, Yu P, Won KA, Mock L, et al. Inhibition of tumor cell growth, invasion, and metastasis by EXEL-2880 (XL880, GSK1363089), a novel inhibitor of HGF and VEGF receptor tyrosine kinases. Cancer Res 2009;69:8009-16.
-
(2009)
Cancer Res
, vol.69
, pp. 8009-8016
-
-
Qian, F.1
Engst, S.2
Yamaguchi, K.3
Yu, P.4
Won, K.A.5
Mock, L.6
-
36
-
-
34249324494
-
An orally available small-molecule inhibitor of c-Met, PF-2341066, exhibits cytoreductive antitumor efficacy through antiproliferative and antiangiogenic mechanisms
-
Zou HY, Li Q, Lee JH, Arango ME, McDonnell SR, Yamazaki S, et al. An orally available small-molecule inhibitor of c-Met, PF-2341066, exhibits cytoreductive antitumor efficacy through antiproliferative and antiangiogenic mechanisms. Cancer Res 2007;67:4408-17.
-
(2007)
Cancer Res
, vol.67
, pp. 4408-4417
-
-
Zou, H.Y.1
Li, Q.2
Lee, J.H.3
Arango, M.E.4
McDonnell, S.R.5
Yamazaki, S.6
-
37
-
-
0037439689
-
SKI-606, a 4-anilino-3-quinolinecarbonitrile dual inhibitor of Src and Abl kinases, is a potent antiproliferative agent against chronic myelogenous leukemia cells in culture and causes regression of K562 xenografts in nude mice
-
Golas JM, Arndt K, Etienne C, Lucas J, Nardin D, Gibbons J, et al. SKI- 606, a 4-anilino-3-quinolinecarbonitrile dual inhibitor of Src and Abl kinases, is a potent antiproliferative agent against chronic myelogenous leukemia cells in culture and causes regression of K562 xenografts in nude mice. Cancer Res 2003;63:375-81. (Pubitemid 36152495)
-
(2003)
Cancer Research
, vol.63
, Issue.2
, pp. 375-381
-
-
Golas, J.M.1
Arndt, K.2
Etienne, C.3
Lucas, J.4
Nardin, D.5
Gibbons, J.6
Frost, P.7
Ye, F.8
Boschelli, D.H.9
Boschelli, F.10
-
38
-
-
33845806858
-
+ neoplastic cells
-
DOI 10.1158/0008-5472.CAN-06-1199
-
Puttini M, Coluccia AM, Boschelli F, Cleris L, Marchesi E, Donella- Deana A, et al. In vitro and in vivo activity of SKI-606, a novel Src-Abl inhibitor, against imatinib-resistant Bcr-Abl+ neoplastic cells. Cancer Res 2006;66:11314-22. (Pubitemid 46009962)
-
(2006)
Cancer Research
, vol.66
, Issue.23
, pp. 11314-11322
-
-
Puttini, M.1
Coluccia, A.M.L.2
Boschelli, F.3
Cleris, L.4
Marchesi, E.5
Donella-Deana, A.6
Ahmed, S.7
Redaelli, S.8
Piazza, R.9
Magistroni, V.10
Andreoni, F.11
Scapozza, L.12
Formelli, F.13
Gambacorti-Passerini, C.14
-
39
-
-
51349124367
-
Resistance of human glioblastoma multiforme cells to growth factor inhibitors is overcome by blockade of inhibitor of apoptosis proteins
-
Ziegler DS, Wright RD, Kesari S, Lemieux ME, Tran MA, Jain M, et al. Resistance of human glioblastoma multiforme cells to growth factor inhibitors is overcome by blockade of inhibitor of apoptosis proteins. J Clin Invest 2008;118:3109-22.
-
(2008)
J Clin Invest
, vol.118
, pp. 3109-3122
-
-
Ziegler, D.S.1
Wright, R.D.2
Kesari, S.3
Lemieux, M.E.4
Tran, M.A.5
Jain, M.6
-
40
-
-
34447308516
-
Potentiation of antileukemic therapies by Smac mimetic, LBW242: Effects on mutant FLT3-expressing cells
-
DOI 10.1158/1535-7163.MCT-06-0810
-
Weisberg E, Kung AL, Wright RD, Moreno D, Catley L, Ray A, et al. Potentiation of antileukemic therapies by Smac mimetic, LBW242: effects on mutant FLT3-expressing cells. Mol Cancer Ther 2007;6:1951-61. (Pubitemid 47052485)
-
(2007)
Molecular Cancer Therapeutics
, vol.6
, Issue.7
, pp. 1951-1961
-
-
Weisberg, E.1
Kung, A.L.2
Wright, R.D.3
Moreno, D.4
Catley, L.5
Ray, A.6
Zawel, L.7
Tran, M.8
Cools, J.9
Gilliland, G.10
Mitsiades, C.11
McMillin, D.W.12
Jiang, J.13
Hall-Meyers, E.14
Griffin, J.D.15
-
41
-
-
78650305755
-
Smac mimetics: Implications for enhancement of targeted therapies in leukemia
-
Weisberg E, Ray A, Barrett R, Nelson E, Christie AL, Porter D, et al. Smac mimetics: implications for enhancement of targeted therapies in leukemia. Leukemia 2010;24:2100-9.
-
(2010)
Leukemia
, vol.24
, pp. 2100-2109
-
-
Weisberg, E.1
Ray, A.2
Barrett, R.3
Nelson, E.4
Christie, A.L.5
Porter, D.6
-
42
-
-
74049121619
-
Targeting inhibitor of apoptosis proteins in combination with ErbB antagonists in breast cancer
-
Foster FM, Owens TW, Tanianis-Hughes J, Clarke RB, Brennan K, Bundred NJ, et al. Targeting inhibitor of apoptosis proteins in combination with ErbB antagonists in breast cancer. Breast Cancer Res 2009;11:R41.
-
(2009)
Breast Cancer Res
, vol.11
-
-
Foster, F.M.1
Owens, T.W.2
Tanianis-Hughes, J.3
Clarke, R.B.4
Brennan, K.5
Bundred, N.J.6
-
43
-
-
77952490280
-
TNF-alpha, IL-6, and IL-1 expression is inhibited by GAS6 in monocytes/macrophages
-
Alciato F, Sainaghi PP, Sola D, Castello L, Avanzi GC. TNF-alpha, IL-6, and IL-1 expression is inhibited by GAS6 in monocytes/macrophages. J Leukoc Biol 2010;87:869-75.
-
(2010)
J Leukoc Biol
, vol.87
, pp. 869-875
-
-
Alciato, F.1
Sainaghi, P.P.2
Sola, D.3
Castello, L.4
Avanzi, G.C.5
-
44
-
-
77649092142
-
Ron receptor tyrosine kinase negatively regulates TNFalpha production in alveolar macrophages by inhibiting NF-kappaB activity and Adam17 production
-
Nikolaidis NM, Gray JK, Gurusamy D, Fox W, Stuart WD, et al. Ron receptor tyrosine kinase negatively regulates TNFalpha production in alveolar macrophages by inhibiting NF-kappaB activity and Adam17 production. Shock 2010;33:197-204.
-
(2010)
Shock
, vol.33
, pp. 197-204
-
-
Nikolaidis, N.M.1
Gray, J.K.2
Gurusamy, D.3
Fox, W.4
Stuart, W.D.5
-
45
-
-
33746894720
-
Twist mediates suppression of inflammation by type I IFNs and Axl
-
DOI 10.1084/jem.20051725
-
Sharif MN, Sosic D, Rothlin CV, Kelly E, Lemke G, Olson EN, et al. Twist mediates suppression of inflammation by type I IFNs and Axl. J Exp Med 2006;203:1891-901. (Pubitemid 44188464)
-
(2006)
Journal of Experimental Medicine
, vol.203
, Issue.8
, pp. 1891-1901
-
-
Sharif, M.N.1
Sosic, D.2
Rothlin, C.V.3
Kelly, E.4
Lemke, G.5
Olson, E.N.6
Ivashkiv, L.B.7
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