-
1
-
-
51849111556
-
PI3K pathway alterations in cancer: Variations on a theme
-
18794884 10.1038/onc.2008.245 1:CAS:528:DC%2BD1cXhtFWiurzI
-
Yuan TL, Cantley LC (2008) PI3K pathway alterations in cancer: variations on a theme. Oncogene 27:5497-5510
-
(2008)
Oncogene
, vol.27
, pp. 5497-5510
-
-
Yuan, T.L.1
Cantley, L.C.2
-
2
-
-
11144358645
-
High frequency of mutations of the PIK3CA gene in human cancers
-
15016963 10.1126/science.1096502 1:CAS:528:DC%2BD2cXjsVGmsbk%3D
-
Samuels Y, Wang Z, Bardelli A, Silliman N, Ptak J, Szabo S, Yan H, Gazdar A, Powell SM, Riggins GJ, Willson JK, Markowitz S, Kinzler KW, Vogelstein B, Velculescu VE (2004) High frequency of mutations of the PIK3CA gene in human cancers. Science 304:554
-
(2004)
Science
, vol.304
, pp. 554
-
-
Samuels, Y.1
Wang, Z.2
Bardelli, A.3
Silliman, N.4
Ptak, J.5
Szabo, S.6
Yan, H.7
Gazdar, A.8
Powell, S.M.9
Riggins, G.J.10
Willson, J.K.11
Markowitz, S.12
Kinzler, K.W.13
Vogelstein, B.14
Velculescu, V.E.15
-
3
-
-
51849128358
-
Class i PI3K in oncogenic cellular transformation
-
18794883 10.1038/onc.2008.244 1:CAS:528:DC%2BD1cXhtFWiur%2FP
-
Zhao L, Vogt PK (2008) Class I PI3K in oncogenic cellular transformation. Oncogene 27:5486-5496
-
(2008)
Oncogene
, vol.27
, pp. 5486-5496
-
-
Zhao, L.1
Vogt, P.K.2
-
4
-
-
77949881462
-
The PI3K pathway as drug target in human cancer
-
20085938 10.1200/JCO.2009.25.3641 1:CAS:528:DC%2BC3cXktF2lt7w%3D
-
Courtney KD, Corcoran RB, Engelman JA (2010) The PI3K pathway as drug target in human cancer. J Clin Oncol 28:1075-1083
-
(2010)
J Clin Oncol
, vol.28
, pp. 1075-1083
-
-
Courtney, K.D.1
Corcoran, R.B.2
Engelman, J.A.3
-
5
-
-
0032506011
-
The lipid phosphatase activity of PTEN is critical for its tumor supressor function
-
9811831 10.1073/pnas.95.23.13513 1:CAS:528:DyaK1cXnsVGgsL4%3D
-
Myers MP, Pass I, Batty IH, Van der Kaay J, Stolarov JP, Hemmings BA, Wigler MH, Downes CP, Tonks NK (1998) The lipid phosphatase activity of PTEN is critical for its tumor supressor function. Proc Natl Acad Sci U S A 95:13513-13518
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 13513-13518
-
-
Myers, M.P.1
Pass, I.2
Batty, I.H.3
Van Der Kaay, J.4
Stolarov, J.P.5
Hemmings, B.A.6
Wigler, M.H.7
Downes, C.P.8
Tonks, N.K.9
-
6
-
-
67749122122
-
Targeting PI3K signalling in cancer: Opportunities, challenges and limitations
-
19629070 10.1038/nrc2664 1:CAS:528:DC%2BD1MXovFylsrg%3D
-
Engelman JA (2009) Targeting PI3K signalling in cancer: opportunities, challenges and limitations. Nat Rev Cancer 9:550-562
-
(2009)
Nat Rev Cancer
, vol.9
, pp. 550-562
-
-
Engelman, J.A.1
-
7
-
-
75849118878
-
Targeting the PI3K signaling pathway in cancer
-
20006486 10.1016/j.gde.2009.11.002 1:CAS:528:DC%2BC3cXhslWktrc%3D
-
Wong KK, Engelman JA, Cantley LC (2010) Targeting the PI3K signaling pathway in cancer. Curr Opin Genet Dev 20:87-90
-
(2010)
Curr Opin Genet Dev
, vol.20
, pp. 87-90
-
-
Wong, K.K.1
Engelman, J.A.2
Cantley, L.C.3
-
8
-
-
0032475861
-
Negative regulation of PKB/Akt-dependent cell survival by the tumor suppressor PTEN
-
9778245 10.1016/S0092-8674(00)81780-8 1:CAS:528:DyaK1cXmslWlsr0%3D
-
Stambolic V, Suzuki A, de la Pompa JL, Brothers GM, Mirtsos C, Sasaki T, Ruland J, Penninger JM, Siderovski DP, Mak TW (1998) Negative regulation of PKB/Akt-dependent cell survival by the tumor suppressor PTEN. Cell 95:29-39
-
(1998)
Cell
, vol.95
, pp. 29-39
-
-
Stambolic, V.1
Suzuki, A.2
De La Pompa, J.L.3
Brothers, G.M.4
Mirtsos, C.5
Sasaki, T.6
Ruland, J.7
Penninger, J.M.8
Siderovski, D.P.9
Mak, T.W.10
-
9
-
-
0030799706
-
Dual role of phosphatidylinositol-3,4,5-trisphosphate in the activation of protein kinase B
-
9228007 10.1126/science.277.5325.567 1:CAS:528:DyaK2sXkvVCgtbs%3D
-
Stokoe D, Stephens LR, Copeland T, Gaffney PR, Reese CB, Painter GF, Holmes AB, McCormick F, Hawkins PT (1997) Dual role of phosphatidylinositol-3,4, 5-trisphosphate in the activation of protein kinase B. Science 277:567-570
-
(1997)
Science
, vol.277
, pp. 567-570
-
-
Stokoe, D.1
Stephens, L.R.2
Copeland, T.3
Gaffney, P.R.4
Reese, C.B.5
Painter, G.F.6
Holmes, A.B.7
McCormick, F.8
Hawkins, P.T.9
-
10
-
-
0030904561
-
The PI 3-kinase/Akt signaling pathway delivers an anti-apoptotic signal
-
9087425 10.1101/gad.11.6.701 1:CAS:528:DyaK2sXisVCrsrc%3D
-
Kennedy SG, Wagner AJ, Conzen SD, Jordan J, Bellacosa A, Tsichlis PN, Hay N (1997) The PI 3-kinase/Akt signaling pathway delivers an anti-apoptotic signal. Genes Dev 11:701-713
-
(1997)
Genes Dev
, vol.11
, pp. 701-713
-
-
Kennedy, S.G.1
Wagner, A.J.2
Conzen, S.D.3
Jordan, J.4
Bellacosa, A.5
Tsichlis, P.N.6
Hay, N.7
-
11
-
-
0032578999
-
Protein kinase B kinases that mediate phosphatidylinositol 3,4,5-trisphosphate-dependent activation of protein kinase B
-
9445477 10.1126/science.279.5351.710 1:CAS:528:DyaK1cXovValug%3D%3D
-
Stephens L, Anderson K, Stokoe D, Erdjument-Bromage H, Painter GF, Holmes AB, Gaffney PR, Reese CB, McCormick F, Tempst P, Coadwell J, Hawkins PT (1998) Protein kinase B kinases that mediate phosphatidylinositol 3,4,5-trisphosphate- dependent activation of protein kinase B. Science 279:710-714
-
(1998)
Science
, vol.279
, pp. 710-714
-
-
Stephens, L.1
Anderson, K.2
Stokoe, D.3
Erdjument-Bromage, H.4
Painter, G.F.5
Holmes, A.B.6
Gaffney, P.R.7
Reese, C.B.8
McCormick, F.9
Tempst, P.10
Coadwell, J.11
Hawkins, P.T.12
-
12
-
-
44349119736
-
Angiogenesis selectively requires the p110alpha isoform of PI3K to control endothelial cell migration
-
18449193 10.1038/nature06892 1:CAS:528:DC%2BD1cXmsVKqtb4%3D
-
Graupera M, Guillermet-Guibert J, Foukas LC, Phng LK, Cain RJ, Salpekar A, Pearce W, Meek S, Millan J, Cutillas PR, Smith AJ, Ridley AJ, Ruhrberg C, Gerhardt H, Vanhaesebroeck B (2008) Angiogenesis selectively requires the p110alpha isoform of PI3K to control endothelial cell migration. Nature 453:662-666
-
(2008)
Nature
, vol.453
, pp. 662-666
-
-
Graupera, M.1
Guillermet-Guibert, J.2
Foukas, L.C.3
Phng, L.K.4
Cain, R.J.5
Salpekar, A.6
Pearce, W.7
Meek, S.8
Millan, J.9
Cutillas, P.R.10
Smith, A.J.11
Ridley, A.J.12
Ruhrberg, C.13
Gerhardt, H.14
Vanhaesebroeck, B.15
-
13
-
-
53049087363
-
Effects of the dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor NVP-BEZ235 on the tumor vasculature: Implications for clinical imaging
-
18701483 10.1158/0008-5472.CAN-08-1044 1:CAS:528:DC%2BD1cXpslKnu7w%3D
-
Schnell CR, Stauffer F, Allegrini PR, O'Reilly T, McSheehy PM, Dartois C, Stumm M, Cozens R, Littlewood-Evans A, Garcia-Echeverria C, Maira SM (2008) Effects of the dual phosphatidylinositol 3-kinase/mammalian target of rapamycin inhibitor NVP-BEZ235 on the tumor vasculature: implications for clinical imaging. Cancer Res 68:6598-6607
-
(2008)
Cancer Res
, vol.68
, pp. 6598-6607
-
-
Schnell, C.R.1
Stauffer, F.2
Allegrini, P.R.3
O'Reilly, T.4
McSheehy, P.M.5
Dartois, C.6
Stumm, M.7
Cozens, R.8
Littlewood-Evans, A.9
Garcia-Echeverria, C.10
Maira, S.M.11
-
14
-
-
77952243758
-
Development of phosphoinositide-3 kinase pathway inhibitors for advanced cancer
-
20425592 10.1007/s11912-010-0091-6 1:CAS:528:DC%2BC3cXht1Cjsb%2FN
-
Cleary JM, Shapiro GI (2010) Development of phosphoinositide-3 kinase pathway inhibitors for advanced cancer. Curr Oncol Rep 12:87-94
-
(2010)
Curr Oncol Rep
, vol.12
, pp. 87-94
-
-
Cleary, J.M.1
Shapiro, G.I.2
-
15
-
-
51849098272
-
Drug discovery approaches targeting the PI3K/Akt pathway in cancer
-
18794885 10.1038/onc.2008.246 1:CAS:528:DC%2BD1cXhtFWiur3J
-
Garcia-Echeverria C, Sellers WR (2008) Drug discovery approaches targeting the PI3K/Akt pathway in cancer. Oncogene 27:5511-5526
-
(2008)
Oncogene
, vol.27
, pp. 5511-5526
-
-
Garcia-Echeverria, C.1
Sellers, W.R.2
-
17
-
-
66149126085
-
Antitumor efficacy of the novel RAF inhibitor GDC-0879 is predicted by BRAFV600E mutational status and sustained extracellular signal-regulated kinase/mitogen-activated protein kinase pathway suppression
-
19276360 10.1158/0008-5472.CAN-08-3563 1:CAS:528:DC%2BD1MXjvVWisbk%3D
-
Hoeflich KP, Herter S, Tien J, Wong L, Berry L, Chan J, O'Brien C, Modrusan Z, Seshagiri S, Lackner M, Stern H, Choo E, Murray L, Friedman LS, Belvin M (2009) Antitumor efficacy of the novel RAF inhibitor GDC-0879 is predicted by BRAFV600E mutational status and sustained extracellular signal-regulated kinase/mitogen-activated protein kinase pathway suppression. Cancer Res 69:3042-3051
-
(2009)
Cancer Res
, vol.69
, pp. 3042-3051
-
-
Hoeflich, K.P.1
Herter, S.2
Tien, J.3
Wong, L.4
Berry, L.5
Chan, J.6
O'Brien, C.7
Modrusan, Z.8
Seshagiri, S.9
Lackner, M.10
Stern, H.11
Choo, E.12
Murray, L.13
Friedman, L.S.14
Belvin, M.15
-
18
-
-
34447530785
-
An HTS approach to screen for antagonists of the nuclear export machinery using high content cell-based assays
-
17638533 10.1089/adt.2007.058 1:CAS:528:DC%2BD2sXnvFajsrc%3D
-
Zanella F, Rosado A, Blanco F, Henderson BR, Carnero A, Link W (2007) An HTS approach to screen for antagonists of the nuclear export machinery using high content cell-based assays. Assay Drug Dev Technol 5:333-341
-
(2007)
Assay Drug Dev Technol
, vol.5
, pp. 333-341
-
-
Zanella, F.1
Rosado, A.2
Blanco, F.3
Henderson, B.R.4
Carnero, A.5
Link, W.6
-
19
-
-
54349088758
-
Chemical genetic analysis of FOXO nuclear-cytoplasmic shuttling by using image-based cell screening
-
18756565 10.1002/cbic.200800255 1:CAS:528:DC%2BD1cXht1CltrbI
-
Zanella F, Rosado A, Garcia B, Carnero A, Link W (2008) Chemical genetic analysis of FOXO nuclear-cytoplasmic shuttling by using image-based cell screening. Chembiochem 9:2229-2237
-
(2008)
Chembiochem
, vol.9
, pp. 2229-2237
-
-
Zanella, F.1
Rosado, A.2
Garcia, B.3
Carnero, A.4
Link, W.5
-
20
-
-
70350518100
-
Chemical interrogation of FOXO3a nuclear translocation identifies potent and selective inhibitors of phosphoinositide 3-kinases
-
19690175 10.1074/jbc.M109.038984 1:CAS:528:DC%2BD1MXht1SqsbvF
-
Link W, Oyarzabal J, Serelde BG, Albarran MI, Rabal O, Cebria A, Alfonso P, Fominaya J, Renner O, Peregrina S, Soilan D, Ceballos PA, Hernandez AI, Lorenzo M, Pevarello P, Granda TG, Kurz G, Carnero A, Bischoff JR (2009) Chemical interrogation of FOXO3a nuclear translocation identifies potent and selective inhibitors of phosphoinositide 3-kinases. J Biol Chem 284:28392-28400
-
(2009)
J Biol Chem
, vol.284
, pp. 28392-28400
-
-
Link, W.1
Oyarzabal, J.2
Serelde, B.G.3
Albarran, M.I.4
Rabal, O.5
Cebria, A.6
Alfonso, P.7
Fominaya, J.8
Renner, O.9
Peregrina, S.10
Soilan, D.11
Ceballos, P.A.12
Hernandez, A.I.13
Lorenzo, M.14
Pevarello, P.15
Granda, T.G.16
Kurz, G.17
Carnero, A.18
Bischoff, J.R.19
-
21
-
-
0032583125
-
Integration of endothelial cells in multicellular spheroids prevents apoptosis and induces differentiation
-
9832561 10.1083/jcb.143.5.1341 1:CAS:528:DyaK1cXnvVKkurc%3D
-
Korff T, Augustin HG (1998) Integration of endothelial cells in multicellular spheroids prevents apoptosis and induces differentiation. J Cell Biol 143:1341-1352
-
(1998)
J Cell Biol
, vol.143
, pp. 1341-1352
-
-
Korff, T.1
Augustin, H.G.2
-
22
-
-
2942726155
-
The ins and outs of FoxO shuttling: Mechanisms of FoxO translocation and transcriptional regulation
-
10.1042/BJ20040167
-
Van Der Heide LP, Hoekman MF, Smidt MP (2004) The ins and outs of FoxO shuttling: mechanisms of FoxO translocation and transcriptional regulation. Biochem J 380:297-309
-
(2004)
Biochem J
, vol.380
, pp. 297-309
-
-
Van Der Heide, L.P.1
Hoekman, M.F.2
Smidt, M.P.3
-
23
-
-
62349102223
-
Using multiplexed regulation of luciferase activity and GFP translocation to screen for FOXO modulators
-
19243599 10.1186/1471-2121-10-14
-
Zanella F, Rosado A, Garcia B, Carnero A, Link W (2009) Using multiplexed regulation of luciferase activity and GFP translocation to screen for FOXO modulators. BMC Cell Biol 10:14
-
(2009)
BMC Cell Biol
, vol.10
, pp. 14
-
-
Zanella, F.1
Rosado, A.2
Garcia, B.3
Carnero, A.4
Link, W.5
-
24
-
-
34250823572
-
Pharmacologic characterization of a potent inhibitor of class i phosphatidylinositide 3-kinases
-
17575152 10.1158/0008-5472.CAN-06-4615 1:CAS:528:DC%2BD2sXmsFCqtr0%3D
-
Raynaud FI, Eccles S, Clarke PA, Hayes A, Nutley B, Alix S, Henley A, Di-Stefano F, Ahmad Z, Guillard S, Bjerke LM, Kelland L, Valenti M, Patterson L, Gowan S, de Haven Brandon A, Hayakawa M, Kaizawa H, Koizumi T, Ohishi T, Patel S, Saghir N, Parker P, Waterfield M, Workman P (2007) Pharmacologic characterization of a potent inhibitor of class I phosphatidylinositide 3-kinases. Cancer Res 67:5840-5850
-
(2007)
Cancer Res
, vol.67
, pp. 5840-5850
-
-
Raynaud, F.I.1
Eccles, S.2
Clarke, P.A.3
Hayes, A.4
Nutley, B.5
Alix, S.6
Henley, A.7
Di-Stefano, F.8
Ahmad, Z.9
Guillard, S.10
Bjerke, L.M.11
Kelland, L.12
Valenti, M.13
Patterson, L.14
Gowan, S.15
De Haven Brandon, A.16
Hayakawa, M.17
Kaizawa, H.18
Koizumi, T.19
Ohishi, T.20
Patel, S.21
Saghir, N.22
Parker, P.23
Waterfield, M.24
Workman, P.25
more..
-
25
-
-
56549093146
-
The discovery of the benzhydroxamate MEK inhibitors CI-1040 and PD 0325901
-
18952427 10.1016/j.bmcl.2008.10.054 1:CAS:528:DC%2BD1cXhsVWjsL%2FI
-
Barrett SD, Bridges AJ, Dudley DT, Saltiel AR, Fergus JH, Flamme CM, Delaney AM, Kaufman M, LePage S, Leopold WR, Przybranowski SA, Sebolt-Leopold J, Van Becelaere K, Doherty AM, Kennedy RM, Marston D, Howard WA Jr, Smith Y, Warmus JS, Tecle H (2008) The discovery of the benzhydroxamate MEK inhibitors CI-1040 and PD 0325901. Bioorg Med Chem Lett 18:6501-6504
-
(2008)
Bioorg Med Chem Lett
, vol.18
, pp. 6501-6504
-
-
Barrett, S.D.1
Bridges, A.J.2
Dudley, D.T.3
Saltiel, A.R.4
Fergus, J.H.5
Flamme, C.M.6
Delaney, A.M.7
Kaufman, M.8
Lepage, S.9
Leopold, W.R.10
Przybranowski, S.A.11
Sebolt-Leopold, J.12
Van Becelaere, K.13
Doherty, A.M.14
Kennedy, R.M.15
Marston, D.16
Howard, Jr.W.A.17
Smith, Y.18
Warmus, J.S.19
Tecle, H.20
more..
-
26
-
-
0035476866
-
The characterization of novel, dual ErbB-2/EGFR, tyrosine kinase inhibitors: Potential therapy for cancer
-
11585755 1:CAS:528:DC%2BD3MXnsVeht70%3D
-
Rusnak DW, Affleck K, Cockerill SG, Stubberfield C, Harris R, Page M, Smith KJ, Guntrip SB, Carter MC, Shaw RJ, Jowett A, Stables J, Topley P, Wood ER, Brignola PS, Kadwell SH, Reep BR, Mullin RJ, Alligood KJ, Keith BR, Crosby RM, Murray DM, Knight WB, Gilmer TM, Lackey K (2001) The characterization of novel, dual ErbB-2/EGFR, tyrosine kinase inhibitors: potential therapy for cancer. Cancer Res 61:7196-7203
-
(2001)
Cancer Res
, vol.61
, pp. 7196-7203
-
-
Rusnak, D.W.1
Affleck, K.2
Cockerill, S.G.3
Stubberfield, C.4
Harris, R.5
Page, M.6
Smith, K.J.7
Guntrip, S.B.8
Carter, M.C.9
Shaw, R.J.10
Jowett, A.11
Stables, J.12
Topley, P.13
Wood, E.R.14
Brignola, P.S.15
Kadwell, S.H.16
Reep, B.R.17
Mullin, R.J.18
Alligood, K.J.19
Keith, B.R.20
Crosby, R.M.21
Murray, D.M.22
Knight, W.B.23
Gilmer, T.M.24
Lackey, K.25
more..
-
27
-
-
52449106253
-
The identification of 2-(1 H-indazol-4-yl)-6-(4-methanesulfonyl- piperazin-1-ylmethyl)-4-morpholin -4-yl-thieno[3,2-d]pyrimidine (GDC-0941) as a potent, selective, orally bioavailable inhibitor of class i PI3 kinase for the treatment of cancer
-
18754654 10.1021/jm800295d 1:CAS:528:DC%2BD1cXhtVCmsr7E
-
Folkes AJ, Ahmadi K, Alderton WK, Alix S, Baker SJ, Box G, Chuckowree IS, Clarke PA, Depledge P, Eccles SA, Friedman LS, Hayes A, Hancox TC, Kugendradas A, Lensun L, Moore P, Olivero AG, Pang J, Patel S, Pergl-Wilson GH, Raynaud FI, Robson A, Saghir N, Salphati L, Sohal S, Ultsch MH, Valenti M, Wallweber HJ, Wan NC, Wiesmann C, Workman P, Zhyvoloup A, Zvelebil MJ, Shuttleworth SJ (2008) The identification of 2-(1 H-indazol-4-yl)-6-(4-methanesulfonyl-piperazin-1- ylmethyl)-4-morpholin -4-yl-thieno[3,2-d]pyrimidine (GDC-0941) as a potent, selective, orally bioavailable inhibitor of class I PI3 kinase for the treatment of cancer. J Med Chem 51:5522-5532
-
(2008)
J Med Chem
, vol.51
, pp. 5522-5532
-
-
Folkes, A.J.1
Ahmadi, K.2
Alderton, W.K.3
Alix, S.4
Baker, S.J.5
Box, G.6
Chuckowree, I.S.7
Clarke, P.A.8
Depledge, P.9
Eccles, S.A.10
Friedman, L.S.11
Hayes, A.12
Hancox, T.C.13
Kugendradas, A.14
Lensun, L.15
Moore, P.16
Olivero, A.G.17
Pang, J.18
Patel, S.19
Pergl-Wilson, G.H.20
Raynaud, F.I.21
Robson, A.22
Saghir, N.23
Salphati, L.24
Sohal, S.25
Ultsch, M.H.26
Valenti, M.27
Wallweber, H.J.28
Wan, N.C.29
Wiesmann, C.30
Workman, P.31
Zhyvoloup, A.32
Zvelebil, M.J.33
Shuttleworth, S.J.34
more..
-
28
-
-
67651155960
-
Biological properties of potent inhibitors of class i phosphatidylinositide 3-kinases: From PI-103 through PI-540, PI-620 to the oral agent GDC-0941
-
19584227 10.1158/1535-7163.MCT-08-1200 1:CAS:528:DC%2BD1MXosVynuro%3D
-
Raynaud FI, Eccles SA, Patel S, Alix S, Box G, Chuckowree I, Folkes A, Gowan S, De Haven Brandon A, Di Stefano F, Hayes A, Henley AT, Lensun L, Pergl-Wilson G, Robson A, Saghir N, Zhyvoloup A, McDonald E, Sheldrake P, Shuttleworth S, Valenti M, Wan NC, Clarke PA, Workman P (2009) Biological properties of potent inhibitors of class I phosphatidylinositide 3-kinases: from PI-103 through PI-540, PI-620 to the oral agent GDC-0941. Mol Cancer Ther 8:1725-1738
-
(2009)
Mol Cancer Ther
, vol.8
, pp. 1725-1738
-
-
Raynaud, F.I.1
Eccles, S.A.2
Patel, S.3
Alix, S.4
Box, G.5
Chuckowree, I.6
Folkes, A.7
Gowan, S.8
De Haven Brandon, A.9
Di Stefano, F.10
Hayes, A.11
Henley, A.T.12
Lensun, L.13
Pergl-Wilson, G.14
Robson, A.15
Saghir, N.16
Zhyvoloup, A.17
McDonald, E.18
Sheldrake, P.19
Shuttleworth, S.20
Valenti, M.21
Wan, N.C.22
Clarke, P.A.23
Workman, P.24
more..
-
29
-
-
51849111524
-
NVP-BEZ235, a dual PI3K/mTOR inhibitor, prevents PI3K signaling and inhibits the growth of cancer cells with activating PI3K mutations
-
18829560 10.1158/0008-5472.CAN-08-1385 1:CAS:528:DC%2BD1cXhtF2msLrK
-
Serra V, Markman B, Scaltriti M, Eichhorn PJ, Valero V, Guzman M, Botero ML, Llonch E, Atzori F, Di Cosimo S, Maira M, Garcia-Echeverria C, Parra JL, Arribas J, Baselga J (2008) NVP-BEZ235, a dual PI3K/mTOR inhibitor, prevents PI3K signaling and inhibits the growth of cancer cells with activating PI3K mutations. Cancer Res 68:8022-8030
-
(2008)
Cancer Res
, vol.68
, pp. 8022-8030
-
-
Serra, V.1
Markman, B.2
Scaltriti, M.3
Eichhorn, P.J.4
Valero, V.5
Guzman, M.6
Botero, M.L.7
Llonch, E.8
Atzori, F.9
Di Cosimo, S.10
Maira, M.11
Garcia-Echeverria, C.12
Parra, J.L.13
Arribas, J.14
Baselga, J.15
-
30
-
-
77956280407
-
PIK3CA mutation uncouples tumor growth and cyclin D1 regulation from MEK/ERK and mutant KRAS signaling
-
20699365 10.1158/0008-5472.CAN-10-0409 1:CAS:528:DC%2BC3cXhtV2rsLbJ
-
Halilovic E, She QB, Ye Q, Pagliarini R, Sellers WR, Solit DB, Rosen N (2010) PIK3CA mutation uncouples tumor growth and cyclin D1 regulation from MEK/ERK and mutant KRAS signaling. Cancer Res 70:6804-6814
-
(2010)
Cancer Res
, vol.70
, pp. 6804-6814
-
-
Halilovic, E.1
She, Q.B.2
Ye, Q.3
Pagliarini, R.4
Sellers, W.R.5
Solit, D.B.6
Rosen, N.7
-
31
-
-
70449995469
-
Identifying genotype-dependent efficacy of single and combined PI3K- and MAPK-pathway inhibition in cancer
-
19805051 10.1073/pnas.0907325106 1:CAS:528:DC%2BD1MXhsVWrsbvJ
-
Sos ML, Fischer S, Ullrich R, Peifer M, Heuckmann JM, Koker M, Heynck S, Stuckrath I, Weiss J, Fischer F, Michel K, Goel A, Regales L, Politi KA, Perera S, Getlik M, Heukamp LC, Ansen S, Zander T, Beroukhim R, Kashkar H, Shokat KM, Sellers WR, Rauh D, Orr C, Hoeflich KP, Friedman L, Wong KK, Pao W, Thomas RK (2009) Identifying genotype-dependent efficacy of single and combined PI3K- and MAPK-pathway inhibition in cancer. Proc Natl Acad Sci U S A 106:18351-18356
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 18351-18356
-
-
Sos, M.L.1
Fischer, S.2
Ullrich, R.3
Peifer, M.4
Heuckmann, J.M.5
Koker, M.6
Heynck, S.7
Stuckrath, I.8
Weiss, J.9
Fischer, F.10
Michel, K.11
Goel, A.12
Regales, L.13
Politi, K.A.14
Perera, S.15
Getlik, M.16
Heukamp, L.C.17
Ansen, S.18
Zander, T.19
Beroukhim, R.20
Kashkar, H.21
Shokat, K.M.22
Sellers, W.R.23
Rauh, D.24
Orr, C.25
Hoeflich, K.P.26
Friedman, L.27
Wong, K.K.28
Pao, W.29
Thomas, R.K.30
more..
|